ID: 127269112 | H3K4me1 hESC enhancer GRCh37_chr1:47697093-47698066 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (47231421..47232394) | | |
ID: 127269111 | NANOG-H3K4me1 hESC enhancer GRCh37_chr1:47696119-47697092 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (47230447..47231420) | | |
ID: 127269110 | H3K4me1 hESC enhancer GRCh37_chr1:47694965-47695926 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (47229293..47230254) | | |
ID: 127269109 | H3K4me1 hESC enhancer GRCh37_chr1:47694003-47694964 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (47228331..47229292) | | |
ID: 127269108 | NANOG-H3K4me1 hESC enhancer GRCh37_chr1:47673792-47674378 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (47208120..47208706) | | |
ID: 127269107 | H3K4me1 hESC enhancer GRCh37_chr1:47657113-47658062 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (47191441..47192390) | | |
ID: 127269106 | H3K4me1 hESC enhancer GRCh37_chr1:47644793-47645294 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (47179121..47179622) | | |
ID: 122056864 | Sharpr-MPRA regulatory region 12212 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (47190317..47190611) | | |
ID: 122056863 | Sharpr-MPRA regulatory region 13342 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (47173877..47174171) | | |
ID: 111429629 | GATA motif-containing MPRA enhancer 229 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (47181248..47181392) | | |
ID: 105378701 | CYP4A22 antisense RNA 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (47095540..47179623, complement) | ncRNA-a3 | |
ID: 100874253 | long intergenic non-protein coding RNA 853 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (47179250..47180339) | PDZK1IP1-AS1, ncRNA-a4 | |
ID: 100873219 | MT-ND1 pseudogene 34 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (47164492..47165872, complement) | | |
ID: 284541 | cytochrome P450 family 4 subfamily A member 22 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (47137441..47149727) | | 615341 |
ID: 10158 | PDZK1 interacting protein 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (47183582..47190036, complement) | DD96, MAP17, SPAP | 607178 |
ID: 6886 | TAL bHLH transcription factor 1, erythroid differentiation factor [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (47216290..47232335, complement) | SCL, TCL5, bHLHa17, tal-1 | 187040 |