ID: 127405813 | H3K4me1 hESC enhancer GRCh37_chr6:31513919-31514418 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31546142..31546641) | | |
ID: 127405812 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:31461392-31462273 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31493615..31494496) | | |
ID: 127405811 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:31456015-31456724 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31488238..31488947) | | |
ID: 127405810 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:31455304-31456014 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31487527..31488237) | | |
ID: 127405809 | H3K4me1 hESC enhancer GRCh37_chr6:31442899-31443399 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31475122..31475622) | | |
ID: 126859649 | MED14-independent group 3 enhancer GRCh37_chr6:31509210-31510409 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31541433..31542660) | | |
ID: 106478957 | DDX39B antisense RNA 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31542304..31543138) | | |
ID: 102725068 | MICB divergent transcript [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31479918..31494794, complement) | TCONS_00012692 | |
ID: 100532737 | ATP6V1G2-DDX39B readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31530219..31546848, complement) | | |
ID: 100287329 | uncharacterized LOC100287329 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31559571..31572703, complement) | | |
ID: 100129921 | ribosomal protein L15 pseudogene 4 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31528072..31528721) | Em:AC006046.2, RPL15_4_680 | |
ID: 692233 | small nucleolar RNA, C/D box 117 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31536374..31536449, complement) | U83 | |
ID: 692199 | small nucleolar RNA, C/D box 84 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31541101..31541178, complement) | U84 | |
ID: 401250 | mitochondrial coiled-coil domain 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31528962..31530232) | | 609624 |
ID: 352961 | HLA complex group 26 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31471229..31472408) | 3.8-1, NCRNA00191, bCX205D4.4, bPG181B23.4 | |
ID: 7919 | DExD-box helicase 39B [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31530226..31542003, complement) | BAT1, D6S81E, UAP56 | 142560 |
ID: 5491 | peptidylprolyl isomerase A pseudogene 9 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31518977..31520330, complement) | PPIP9 | |
ID: 4795 | NFKB inhibitor like 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31546851..31558829) | IKBL, NFKBIL | 601022 |
ID: 4277 | MHC class I polypeptide-related sequence B [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31494918..31511124) | PERB11.2 | 602436 |
ID: 534 | ATPase H+ transporting V1 subunit G2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31544444..31546742, complement) | ATP6G, ATP6G2, NG38, VMA10 | 606853 |