Tag | Content |
---|
EnhancerAtlas ID | HS108-07696 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr11:63919870-63922160 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr11:63920708-63920727 | GGGCTCCCCCTGCTGGCCC | - | 6.48 | EWSR1-FLI1 | MA0149.1 | chr11:63921564-63921582 | CCTTGCTGCTTTCCTCCC | - | 6.15 | Myod1 | MA0499.1 | chr11:63921418-63921431 | TGCAGCTGCCCCC | + | 6.08 | Nr5a2 | MA0505.1 | chr11:63921501-63921516 | AAGGTCAAGGTCACC | + | 7.16 | ZNF263 | MA0528.1 | chr11:63919877-63919898 | GAAGGAGGATCAGGGTGGGGG | + | 6.35 | ZNF263 | MA0528.1 | chr11:63919967-63919988 | TCTTCCTGTCCCTCCTTCTCT | - | 6.47 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 63919971 | 63920011 | chr11 | 63920247 | 63921734 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH11I064152 | chr11 | 63920194 | 63921854 |
|
Enhancer Sequence | GAGGCAGGAA GGAGGATCAG GGTGGGGGCA GAGGAACGGG CCTGGGGCTT GCACCCCCAC 60 ATCTCCTTTC TTGCCTCATC CAAGAATGCA AACCAGCTCT TCCTGTCCCT CCTTCTCTGG 120 GCACACAGGG CAGGCATGCT GGGGAAACCT CAGAGGCCCC TAGAATATCT TGTCCTGCTC 180 TCTTTGTTCA GGGAGGGAAA CTGAGGTCTG GGGAGGCTGA GGGACTGGCT CAGGCATCGC 240 AGACCTGGGT TGTGATGAAT TCAGCTCTGC CACTTTCCAG CAGCGTCCAC ATCTCTCTGG 300 GTCCCCCGTT TCTCCCTGAT TAGAACGGGG GTGAAGACGT CCCCTGCAGA ACAGCTCCGA 360 GCTTCCTCCC ACACACTAAG GCCAAGCCGG TTGGCAGCAC TCAGCCAGCG ACATTATCCA 420 TCAGTCCCAC CGCCAGTCAG TTCTGCCCTC ACTGTCACTG CATGCAGGCA GCGGGACAGC 480 TGTCCTCCTC CAGGAGCTGC AGGACCAAGT GGACCTGGCA CCTGTCCCCA ACATCCCCCC 540 CGGCAGCGGC TGAGGGCTCC CAGCATGACC AATGGGGTTG GAATCGTTCT CGTTTTACAG 600 ATGAGGAAAC CGGGGCTCAG GGAGGTTGGG AGGCCACCCT CACACAGCAG GGACTTGAGT 660 GAGGAGCCAG GCACCCCCCA CCCGCTCACA GACTCGGGGT CCACCCTGGC CGGCTCCCCT 720 TGCCTGAGCA CTGTCCCATG GGCTCCGCCT TCCCTTGGGG GTGGCACCAG GCACAGAAAC 780 CTGGAACCCG TCTCAGAAGG GCCCGCCCCG ACCGCGCCAG GCCAGGCTAG CAGCTCACGG 840 GCTCCCCCTG CTGGCCCGAG GCCGCCTGCA CACCCAGGCG CTCAGCCCAG CCTGGCACCC 900 TGGACCACAG GCTCCCGGGA TGGGGCAGCC CCCACGGCAA ACAGCAAAGG CTACAATTGA 960 GAAACTCAAA AAGCATCAAA AAATATGTAG AGGCGGGAGA GCAATTAGAG GAGGTGGTGA 1020 GAAAGGAAGG ACTGCAGCCT GGAAGCTTCT ATGCACATGG CAGTGAGGGG GACAGGTAGG 1080 TCCCTCCACA AATGTTCAGG GAGGTTGGGA GGCCACCCTC ACACAGCAGG GTGTTTTCCC 1140 GGCCAGAGTC ACTTCATCAT CCAGGCCTCC ATCTCCTCAT CTAACCACTG CTGGCAGGGG 1200 TGATAACAAC CCAAGGATGC TGAGAGCATT AGATGACAGA ACTCATGCAA GGGGCCCAGT 1260 CCAGAGTCCC TGCTGGATGC AAAGGTGGGG TCATCACAAA AGGCTAGGCC CACCCCTGGT 1320 CAGCCCCCAC TGCTGCTCAA GCCAGAGCCA CCTTTCCTGG CAGCCACTTC TGCCCCCTCT 1380 TCCATAAACA TGTTTGGGCA CGAGTAGGTC CTGCATTCAG TACCAGCGCT GCCACCTGCC 1440 AAGCCCACCT CCCAGAGGAC TCACTGCTGC AGGTCCCCCT CCACCAGGCT GTCCTGCCTG 1500 CCCTCAAATA ATCCCGTCCC CTCCCTCAAC GCCCGCATTC CACGCCCCTG CAGCTGCCCC 1560 CTCCTCTGCT GTCTCCACTT CTTCCCTCCC ATGCTCCCTT CAGTCCACCC AGTCTGGTCC 1620 CTCCTTCCAA CAAGGTCAAG GTCACCACAC CCCATGCAGC GGCCCCTCCT GCCTTCCCTG 1680 TGGACAGGAA GTGTCCTTGC TGCTTTCCTC CCTAGGTCTT CTAATCAGTT GCACAGATTC 1740 AAAACGCTCT TTAAGCAAGC AACCTCCGGG GCTGTCCCTC CACTCTCTTC TGAGCCTCTG 1800 ACCCCCACAG TGCCTGCCTG CTCTCATTCC CCAAAGCCCA GGCATGCAAA ACAGAACGTT 1860 TGACTCTTTC CCCCAAAACG TCATTTTTTT GTTGCTCCAT TCTTCCCTCT TTTTTACTCG 1920 AGACCCTGCA CCAGGGGTCC CTCCCTTTCC ATCCTCTTTT GGATTGATCC CCGTGACACC 1980 CTAGAAACCA AGCCTTCCTC TCACCCTCCA GGACTGAGCC TTCCTCATGG CTCCCTAGAT 2040 CCCACAGACG CTCCCAACTC CCAGCTGATC TCCGTGTGCA TCTCATCCCC ATCTGTTCCT 2100 TGACCGGCAG CCATGGATCC TGGGAACATA AATCAGGTGC CATCCCTCCT CTGTTCAAAA 2160 CTGCATTCAA ACGCCGGTCC TCTGGCCTCT CTCCCACCTC ACTCCCAATG CTGCCTCCCC 2220 CACTACACCA GTTCCCCAAA CAGCCAGGCT GCTTCCTGCC CCAGGCCCTT TGTACCTGCT 2280 GTGCTCTGCA 2290
|