ID: 130060849 | ATAC-STARR-seq lymphoblastoid active region 12172 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41812209..41812318) | | |
ID: 130060848 | ATAC-STARR-seq lymphoblastoid silent region 8500 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41811579..41812068) | | |
ID: 130060847 | ATAC-STARR-seq lymphoblastoid silent region 8499 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41786380..41786679) | | |
ID: 129664044 | ReSE screen-validated silencer GRCh37_chr17:39942255-39942467 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41786003..41786215) | | |
ID: 127886862 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:39956613-39957119 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41800361..41800867) | | |
ID: 127886861 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:39956106-39956612 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41799854..41800360) | | |
ID: 127886860 | H3K4me1 hESC enhancer GRCh37_chr17:39947785-39948448 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41791533..41792196) | | |
ID: 127886859 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:39932003-39932506 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41775751..41776254) | | |
ID: 127886858 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:39927964-39928467 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41771712..41772215) | | |
ID: 127886857 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:39927459-39927963 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41771207..41771711) | | |
ID: 127886856 | H3K4me1 hESC enhancer GRCh37_chr17:39889784-39890326 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41733532..41734074) | | |
ID: 127886855 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:39881045-39881584 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41724793..41725332) | | |
ID: 127886854 | OCT4-NANOG hESC enhancer GRCh37_chr17:39864421-39864948 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41708169..41708696) | | |
ID: 127886853 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:39861304-39862096 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41705052..41705844) | | |
ID: 127886852 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:39845747-39846655 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41689480..41690403) | | |
ID: 127886851 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:39844838-39845746 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41688586..41689494) | | |
ID: 125177475 | Sharpr-MPRA regulatory region 1334 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41717457..41717751) | | |
ID: 116276464 | CRISPRi-validated cis-regulatory element chr17.2540 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41792676..41793529) | | |
ID: 106480768 | RNA, 5S ribosomal pseudogene 442 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41718154..41718243) | RN5S442 | |
ID: 106479370 | RNA, 7SL, cytoplasmic 399, pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41730127..41730405, complement) | | |