| ID: 132090532 | Neanderthal introgressed variant-containing enhancer experimental_50731 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10014104..10014273) | | |
| ID: 130063463 | ATAC-STARR-seq lymphoblastoid silent region 10050 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (9914666..9914755) | | |
| ID: 130063462 | ATAC-STARR-seq lymphoblastoid silent region 10049 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (9914546..9914645) | | |
| ID: 129664350 | ReSE screen-validated silencer GRCh37_chr19:10109314-10109542 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (9998638..9998866) | | |
| ID: 127890403 | H3K4me1 hESC enhancer GRCh37_chr19:10112675-10113174 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10001999..10002498) | | |
| ID: 127890402 | H3K4me1 hESC enhancer GRCh37_chr19:10112173-10112674 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10001497..10001998) | | |
| ID: 127890401 | H3K27ac hESC enhancer GRCh37_chr19:10063429-10064021 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (9952753..9953345) | | |
| ID: 127890400 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr19:10062835-10063428 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (9952159..9952752) | | |
| ID: 127890399 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:10047708-10048210 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (9937032..9937534) | | |
| ID: 127890398 | H3K4me1 hESC enhancer GRCh37_chr19:10046447-10047041 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (9935771..9936365) | | |
| ID: 126862852 | BRD4-independent group 4 enhancer GRCh37_chr19:10128438-10129637 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10017762..10018961) | | |
| ID: 125371474 | Sharpr-MPRA regulatory region 3549 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10000213..10000507) | | |
| ID: 124904636 | uncharacterized LOC124904636 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (9893490..9900522) | | |
| ID: 93145 | olfactomedin 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (9853718..9936515, complement) | NOE2, NOELIN2, NOELIN2_V1, OlfC | 617492 |
| ID: 50700 | retinol dehydrogenase 8 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10013483..10022279) | PRRDH, SDR28C2 | 608575 |
| ID: 50509 | collagen type V alpha 3 chain [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (9959561..10010504, complement) | | 120216 |