| ID: 130061740 | ATAC-STARR-seq lymphoblastoid active region 12814 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76737032..76737081) | | |
| ID: 130061739 | ATAC-STARR-seq lymphoblastoid silent region 9024 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76710987..76711196) | | |
| ID: 129664149 | ReSE screen-validated silencer GRCh37_chr17:74736456-74736653 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76740374..76740571) | | |
| ID: 127888048 | OCT4-NANOG hESC enhancer GRCh37_chr17:74800558-74801081 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76804476..76804999) | | |
| ID: 127888047 | H3K4me1 hESC enhancer GRCh37_chr17:74752181-74752680 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76756099..76756598) | | |
| ID: 127888046 | H3K4me1 hESC enhancer GRCh37_chr17:74751679-74752180 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76755597..76756098) | | |
| ID: 127888045 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:74732487-74733112 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76736405..76737030) | | |
| ID: 127888044 | H3K4me1 hESC enhancer GRCh37_chr17:74725107-74725737 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76729025..76729655) | | |
| ID: 127888043 | H3K4me1 hESC enhancer GRCh37_chr17:74723821-74724449 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76727739..76728367) | | |
| ID: 127888042 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:74722561-74723190 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76726479..76727219) | | |
| ID: 106480551 | RNA, U6 small nuclear 97, pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76752912..76753013) | | |
| ID: 106480313 | RNY4 pseudogene 36 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76703632..76703727, complement) | | |
| ID: 101928514 | long intergenic non-protein coding RNA 2080 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76799044..76807102) | | |
| ID: 693221 | microRNA 636 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76736450..76736548, complement) | MIRN636, hsa-mir-636 | |
| ID: 439921 | matrix remodeling associated 7 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76672551..76710965, complement) | | |
| ID: 124512 | methyltransferase 23, arginine [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76726041..76733881) | C17orf95, MRT44 | 615262 |
| ID: 79157 | major facilitator superfamily domain containing 11 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76736634..76803805) | ET | 620346 |
| ID: 23210 | jumonji domain containing 6, arginine demethylase and lysine hydroxylase [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76712836..76726606, complement) | PSR, PTDSR, PTDSR1 | 604914 |
| ID: 6427 | serine and arginine rich splicing factor 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76734115..76737411, complement) | PR264, SC-35, SC35, SFRS2, SFRS2A, SRp30b | 600813 |