ID: 132090120 | Neanderthal introgressed variant-containing enhancer experimental_29464 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53896213..53896382) | | |
ID: 132090119 | Neanderthal introgressed variant-containing enhancer experimental_29460 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53896016..53896185) | | |
ID: 132090118 | Neanderthal introgressed variant-containing enhancer experimental_29403 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53867819..53867988) | | |
ID: 130008001 | ATAC-STARR-seq lymphoblastoid active region 6430 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53975277..53975426) | | |
ID: 129663153 | ReSE screen-validated silencer GRCh37_chr12:54355207-54355431 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53961423..53961647) | | |
ID: 127882492 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:54368136-54368730 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53974352..53974946) | | |
ID: 127824279 | H3K4me1 hESC enhancer GRCh37_chr12:54360165-54361069 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53966381..53967285) | | |
ID: 127824278 | H3K4me1 hESC enhancer GRCh37_chr12:54345326-54345913 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53951542..53952129) | | |
ID: 127824277 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:54321787-54322624 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53928003..53928840) | | |
ID: 126861532 | MED14-independent group 3 enhancer GRCh37_chr12:54261991-54263190 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53868207..53869406) | | |
ID: 126861531 | BRD4-independent group 4 enhancer GRCh37_chr12:54242057-54243256 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53848273..53849472) | | |
ID: 108228199 | HOXC11-HOXC10 intergenic CAGE-defined high expression enhancer [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53978916..53979430) | | |
ID: 107105350 | NUP98-HOXC11 recombination region [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53973793..53975180) | | |
ID: 106479224 | RN7SK pseudogene 289 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53816185..53816479) | | |
ID: 105378250 | uncharacterized LOC105378250 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53739594..53898384) | | |
ID: 105369775 | uncharacterized LOC105369775 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53953385..53956427, complement) | | |
ID: 100874366 | HOXC13 antisense RNA [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53935328..53939643, complement) | HOXC-AS5 | |
ID: 100874365 | HOXC cluster antisense RNA 3 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53983951..53985519, complement) | | |
ID: 100124700 | HOX transcript antisense RNA [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53962312..53974954, complement) | HOXAS, HOXC-AS4, HOXC11-AS1, NCRNA00072 | 611400 |
ID: 3229 | homeobox C13 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53938831..53946544) | ECTD9, HOX3, HOX3G | 142976 |