Tag | Content |
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EnhancerAtlas ID | HS110-04005 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr6:1182690-1184080 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr6:1183356-1183367 | TCAAGGTCATT | + | 6.32 | Esrra | MA0592.2 | chr6:1183355-1183366 | TTCAAGGTCAT | + | 6.62 | Esrrg | MA0643.1 | chr6:1183356-1183366 | TCAAGGTCAT | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I001183 | chr6 | 1183581 | 1183730 |
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Enhancer Sequence | CAACAAAGGG TTATTGTTGC CAAGTTCCTG CCAAATGTTA TTTTCCTAAG TTAGTGTGTT 60 GGTGGTGGTG GCGGTGTTTT TTCTGGCCAA AGCCTGAACA AAGAATTCCA GATGGCAACA 120 TGGAGTGGGA AAGCCTCATC ACCGTAGACC AAAATTCTCC CAAAGTCCAA AGAAGATTGG 180 GAAATCCTTT TAAAATATTT CCTTTGGATG GAGGAAGGGA GTGGGTACCA CAGGAAATGT 240 AAAGTAGGAA ATAACGGCGA TTTAACTTAA CTTTAGGGTA AATTCTTTGA GGATATTAAT 300 TCATTTCTTA AAACTTAGAA TGTGCTTCCC CCACCCCCAA GGAGGAACAC CAATGCAAGG 360 CCTGGGCAAA GCACAAGGTT CTCACTAAGC GCTAGTTGAA CTGAGCAAAA CTGACCCCCA 420 GAGCACAGAG TAAGTATGAC AGAAATGACA TCGACAATGA CCAGCTCATT AAGCTCTTCT 480 GCAGGTTTCA GTCTCTGCAC TGAGCACTTC ACGCGTATCA TCAGATCCTG CAACAACCCC 540 ATGACAACCT TATTTCTTCC TTGATTCTTA GCTATAGAAA TTCAGTCTCA GAGAGGTTAG 600 AGACTTTCCT TCATCACAGA GCCAGTCAGT CACAGAGCTG GGATCAACCC CAGATCTGTC 660 TCACTTTCAA GGTCATTTTC TACCACCGCA CTGAGAAACC TGAGTAAAGT CCCAAAACTC 720 CACCTTCACA TCAATAGGTC ACTAAAACAA TCAATGTGTA AGATTAAGCT TGGCCAACAG 780 AGGAATTCTG ACCAATGTGA AACTACCGGT CGAGAAACTC AGGAAGATAC CTACTGTGTT 840 GGGAAATCAC AGGACATTCT GTGTAACAAA GTTCAGTGTT ACGGGGTAAA AACTAAAACA 900 CCCAACAAGC CAGTGAGGGT CACTTGTATA ACTGAGGCTC CACGTTTCCA CTGGAGGAGC 960 CGAGTGTGCA GGGGTGTGGT GCAGCGCCTC ACACAGCCTT ACGCAGGAAT GTAGTTGGCA 1020 CACCCTTCTT TCTCCCTAGC CAGCAGAAAA AAATGCAGAT ACGCAGATTG AAAGTATAAA 1080 TGTAAAAATT GCTTAATTCA TTGTTAAATA TTCTTATAGC TATCAGATGT AATGACAAAG 1140 ACAGACAATG CCAGAAGTCA TGTTTTCACA ACTCTTTAGA AAAGAAAATA AGACAGTAAA 1200 GATCTGGAAA GCACGTAATT ACAGGCTGCA AGTGCAATTT TGTTGCATGA GAGTGACCTG 1260 CCTCCACCCC CAGTCTCCAC CATCCTTTGG ACTTATCCTT TATAAGCTGA AGACTGCTAT 1320 ATCACTCCCA AAGTCTCTAC TGAGCTGCTA AACCATACAT CCAATTAGCT TTCAGATGGC 1380 TCCAGTTACA 1390
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