ID: 56979 | PR/SET domain 9 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (23507155..23528093) | KMT8B, MEISETZ, MSBP3, PFM6, ZNF899 | 609760 |
ID: 8878 | sequestosome 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (179806393..179838078) | A170, DMRV, EBIAP, FTDALS3, NADGP, OSIL, PDB3, ZIP3, p60, p62, p62B | 601530 |
ID: 4904 | Y-box binding protein 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (42682418..42703805) | BP-8, CBF-A, CSDA2, CSDB, DBPB, EFI-A, MDR-NF1, NSEP-1, NSEP1, YB-1, YB1 | 154030 |
ID: 107980440 | ABL breakpoint recombination region [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (130710129..130854140) | | |
ID: 107963955 | BCR-ABL major-breakpoint cluster region [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (23289649..23292626) | | |
ID: 10155 | tripartite motif containing 28 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (58544064..58550715) | KAP1, PPP1R157, RNF96, TF1B, TIF1B, TIF1beta | 601742 |
ID: 107548103 | MS32 minisatellite repeat instability region [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (236096118..236097991) | | |
ID: 110594336 | MS1 minisatellite repeat instability region [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (31428806..31434663) | | |
ID: 107963951 | BCR-ABL minor-breakpoint cluster region [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (23217698..23253190) | | |
ID: 10516 | fibulin 5 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (91869411..91947694, complement) | ADCL2, ARCL1A, ARMD3, CMT1H, DANCE, EVEC, FIBL-5, HNARMD, UP50 | 604580 |
ID: 106780800 | CYP21A2 recombination region [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32037872..32041144) | | |
ID: 908 | chaperonin containing TCP1 subunit 6A [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (56051765..56063989) | CCT-zeta, CCT-zeta-1, CCT6, Cctz, HTR3, MoDP-2, TCP-1-zeta, TCP20, TCPZ, TTCP20 | 104613 |
ID: 51142 | coiled-coil-helix-coiled-coil-helix domain containing 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (56101573..56106476, complement) | C7orf17, MIX17B, MNRR1, NS2TP, PARK22 | 616244 |
ID: 109623491 | MS31A repeat instability region [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (1271210..1273139) | | |
ID: 110599567 | D7S22 minisatellite repeat instability region [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (158150063..158151575) | | |
ID: 107652445 | meiotic recombination hotspot SHOX [Homo sapiens (human)] | Chromosome X, NC_000023.11 (633053..636275); Chromosome Y, NC_000024.10 (633053..636275) | | |
ID: 90780 | pygopus family PHD finger 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (154957026..154961782, complement) | 1190004M21Rik | 606903 |
ID: 105943586 | distal CMT1A-REP [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (14170534..14194724) | | |
ID: 108004539 | CYP21A1P recombination region [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32005826..32008652) | | |
ID: 108004538 | AZFa HERV15yq2 recombination region [Homo sapiens (human)] | Chromosome Y, NC_000024.10 (13111541..13122314) | | |