Tag | Content |
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EnhancerAtlas ID | HS095-26081 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr6:41734490-41735640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESX1 | MA0644.1 | chr6:41735052-41735062 | ACCAATTAAC | + | 6.02 | Stat6 | MA0520.1 | chr6:41734765-41734780 | ATTTCTGAGGAAATG | - | 7.85 | ZNF263 | MA0528.1 | chr6:41735000-41735021 | GGAGCAGGGGGTGGAGGAGAC | + | 6.53 |
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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 |
GH06I041766 | chr6 | 41734169 | 41737506 |
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Enhancer Sequence | CCTGAAGGGC TCACACAGGC CCTCCCCACC CTTGCCTCCG CCCTCCCTAT ACCTTTCTGA 60 AAGCCCACGG GTGCCTCATT ACAAGACCCC CCACCTGTGA GTAGGACACC CCTTGAAGAT 120 ATTGGTCAGA GAGCGCCCCA GAGCTCAGGA AGCCTAAGCT CTGAGGGCCT CCCATGAGGC 180 TGATTTGCTC TCTGGAGAGG CAGGCAGGGG CGAGTGAAGT CAAGCCTCTT CTTGCACACC 240 TGCTCTGGCC TCTCCCGTCG ACACAACCAG GAGCCATTTC TGAGGAAATG AGAGTAGAGG 300 GGCAGAGTTG GTAGGTGGGC ATAGGGCAGG CCCCAGGGGA GAGCAGGTTC ACCCTATAGT 360 TAACTGGGAA AGGCCTTGGC TTGGATTTCA GGATTCCTGA GTGGGAGCAC TGGAATGTGA 420 TCCCCTGCTG GGACTCAATC CAGGGAGAAG CACCCAACAC AGTCTCCCTG CAGCCCACCT 480 GAGAGAATGA GGCTCCTTCA GGCCAGGCAG GGAGCAGGGG GTGGAGGAGA CACACGACAG 540 GCATCCAGCC CTAGCCCAAG CCACCAATTA ACTTCATGGC CTGAGGCAAG TTACGTCACC 600 TCTTGGCCTG TTTCCTCCTC TGTACAGTGA TGATAACATC CCGCCAGTGA GGCCTGATAA 660 ATATTCGACA AGGCCCTGTG GAAAGCTGAC TGTGTTTATA CCCTTGTAAA GTGCTATTAT 720 TACCCGGGGG GACCTTGGGA AGGGCCCCTC CTGGTCTGAC CTGAAATGTC ACTCCCAGAC 780 AGGATGCTGG ATCCTGTCCT TTCCTGAGGG CAGCCCAGGG GTGGGTAGGG CCTGTTTCTA 840 AAGAAGAGAA CCCAGCACTC GGCAAACATG CACTGATGCT GGTGATGATC TTTGGATGAT 900 GATGGTGATG GAAACTGATT CCATCTGTGC ACCACAGCCT GACGGCAGGG CGGGCTCAAA 960 CACAGGGGCG GCAGTTACCC TCCTGGGCAT CGCTCCCACC CACCCCTTCC CGCCAGGAAA 1020 GCTGTCCACT CACACCCTGT CCTTCCCTCG AGAGGAAAAT TCCTGTAGTA GACCTCATGG 1080 GCCAGAGGCA GTGACCAGGG GAGGGGACAG GAAAGGTTGG GGGCCACACT GAGCTGGAAG 1140 TCGACTCCTT 1150
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