ID: 130067637 | ATAC-STARR-seq lymphoblastoid active region 19191 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43812400..43812669) | | |
ID: 129664874 | ReSE screen-validated silencer GRCh37_chr22:44207707-44207948 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43811827..43812068) | | |
ID: 127896580 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:44320245-44320987 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43924365..43925107) | | |
ID: 127896579 | H3K27ac hESC enhancer GRCh37_chr22:44319500-44320244 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43923620..43924364) | | |
ID: 127896578 | H3K4me1 hESC enhancer GRCh37_chr22:44317583-44318083 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43921703..43922203) | | |
ID: 127896577 | H3K4me1 hESC enhancer GRCh37_chr22:44301043-44301543 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43905163..43905663) | | |
ID: 127896576 | H3K4me1 hESC enhancer GRCh37_chr22:44279103-44279833 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43883223..43883953) | | |
ID: 127896575 | H3K4me1 hESC enhancer GRCh37_chr22:44256209-44256708 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43860329..43860828) | | |
ID: 127896574 | H3K4me1 hESC enhancer GRCh37_chr22:44247635-44248134 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43851755..43852254) | | |
ID: 127896573 | H3K4me1 hESC enhancer GRCh37_chr22:44240991-44241816 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43845111..43845936) | | |
ID: 127896572 | H3K4me1 hESC enhancer GRCh37_chr22:44223866-44224628 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43827986..43828748) | | |
ID: 127896571 | H3K4me1 hESC enhancer GRCh37_chr22:44215896-44216537 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43820016..43820657) | | |
ID: 127896570 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:44208791-44209592 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43812911..43813712) | | |
ID: 126863162 | MED14-independent group 3 enhancer GRCh37_chr22:44293320-44294519 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43897440..43898639) | | |
ID: 121627950 | Sharpr-MPRA regulatory region 5125 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43945810..43946203) | | |
ID: 114004363 | Sharpr-MPRA regulatory region 15126 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43867849..43868143) | | |
ID: 105373058 | EFCAB6 divergent transcript [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43812422..43817902) | | |
ID: 150379 | patatin like phospholipase domain containing 5 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43879678..43892013, complement) | GS2L, dJ388M5, dJ388M5.4 | 611589 |
ID: 80339 | patatin like phospholipase domain containing 3 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43923805..43947582) | ADPN, C22orf20, iPLA(2)epsilon | 609567 |
ID: 64800 | EF-hand calcium binding domain 6 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43528778..43812305, complement) | DJBP, HSCBCIP1, dJ185D5.1 | 619664 |