Tag | Content |
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EnhancerAtlas ID | HS184-27191 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr7:661100-663380 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr7:663015-663028 | TTCCAGAACCTTC | + | 6.3 | SREBF1 | MA0595.1 | chr7:661282-661292 | GTGGGGTGAT | - | 6.02 | TFAP2A | MA0003.3 | chr7:662031-662042 | TGCCTGAGGCT | - | 6.32 | Znf423 | MA0116.1 | chr7:661822-661837 | GCCACCTAAGGGGGA | + | 6.33 |
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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 |
GH07I000621 | chr7 | 661052 | 662082 |
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Enhancer Sequence | ACCTTGTACT CCCAAAGCAA GAATTCAGCT CACCCCCACT TTGGAAGGAG CATGACCATC 60 TCCAATCTGC CACAATTCCC AAGGACTCCA CGTTTTCCAC TTAATTCCTG AACCCCCAGG 120 ATCCCGAGTT TGCAACCCTT CCCTAAGGGG CTCACTATTG AGCAGTGGTG ACAGATGCTT 180 GTGTGGGGTG ATGTCACAGC AGGTGGGGTC ATCCCCATGA CAGATGCTTC CTGGCCATCA 240 CCTCATCATG TGTGGTACAA GTCCCAACCT TGCCTGGAGG GACCCAGGGG ACTGAGTTTC 300 TGAAGAGTTA AGCCATCTGT AAAATGGGCA CAGTAACACT CTCAGCCTCT AAAGCAGCAG 360 GGAGGACTCA GTGATCATGA GGCTTGTGAA GCACTCAGCA GAATAAGGGG CTCCCACGGT 420 CAGCAGCTGC TGCCATAGTG TCTGCTGGTT CCAAACCCCA TGCAGCCGCT CCCCCAGTGC 480 TGCTAGAAGG GTCACACATG TCCCAGAATC CCCCAGGAGT GATGCAAATG GAGCGGCCCA 540 TGCCCCGATC TCAGCCAGTC TCTTCACCAC TCTGGCTTTT TTATTCCTTT TTGTTGGCTT 600 ACATTGCTAA TATATTGTGG AACTGCAGCC AGAGGTGGCC TGACAGGTAA ACACCTCCCC 660 GCCCTCACCC ATGCAAAGAA ACCTGCTGAA GCAAACAGGT TCAGCCAGTT CTCAGAGCCG 720 AGGCCACCTA AGGGGGACAA CAGAAAGGAT GGGCACCCAC AGCCCCTCAA AGCTGCACCT 780 CAGACCCGAG CACCAGGTGC CTGCCAAGGC TGGGCATGCA TTCAGAAGAG CAGCGAGGTG 840 AGGGGTGGCA GCAAGGACCC CCGCGCCACA CAGGGCCTCC CGCTCACTCC TCCCGCTCCA 900 ACAATCTGCA TTTCTGTATG TTAGAAATGT CTGCCTGAGG CTAAAAGAAA TAAAGAATTT 960 TTGTGACTTT TAAACAAAAG CATCATGACA TTGACCTGGG AGAACATGAA TGTGCTAGGA 1020 TCGTATCCAG TAATAAAGAA GGCAAACTGA GTTATTAGCA CTTCCAACAT GTCTGATCTT 1080 TAGTTTTTTT CAACTCTCTA TTTTGAAAAT CTTTGAACCT TCCTAGGGAT GGAAGGGGGA 1140 TGTCAGAGTC AGGACACGGG TTGTTATTCC CCCTCCCATG ATGTCAAAGA GCAGAACACA 1200 CAGAGGCACA TATGCACCAA CAGTAGGTCT GCAGAGAATG TGCATATGTG TATTGACAAG 1260 GAGCAGACGG GAATGATGAG TGAAGAAAAC AGAACATTTA CCAAAAAGGA CCCCGCTGAA 1320 GGCAGAACAC TTGTTCCAGC GCATACTAAT ATGTTTTTCT GACTTCTTAT GTTTTTCAAC 1380 ATGACGCTAT CCAGGGGGAA AGAGTGGCCT GCTCAGTCTG TCCTCCTTTA GAAGTGGTTC 1440 TGAAAGACCT AGACATGCTG CCCTCGCTGG GGAAGAACCT CTCTCCATTG CGGATTTAAA 1500 CCTTAGGTCA ATGTTATTTA AGGAAAGGAA GTGGCCTAAA CCCTTGGGCA GACCCTGGGT 1560 GCTGGCATCA CGGTCCTATC TCTTCTGTCC CAGCCCAAGA CCCAGGGTTC CCATCTGCTG 1620 GGATCCCAGC GCCCCAGACA CAGCATCCTG GCTTGTGTTT AGCCTCTTCC ACTGTTTAGG 1680 TGAAGGCTTG TTCCGTGACT CTGTTGACTA CAAGTTTCCA AAAAATTCTC TCTAAATAGC 1740 AATAACTCAG TCCTGGCATC ATGGAAAGCA GAGCTCCTGC TCCCGGCTGG GGTGCCAACA 1800 GCACGGTGTT CTCAAATCCC CTGGGACCCT CGGCCACACT CTTGACTGTG GGTCTGGTTC 1860 CTAACCACAA ACATGTGGTA ACAACAATTC TCTCTCTGGC CAAACTTTAG TCAGGTTCCA 1920 GAACCTTCTT CTAGGCCCAT CTGTACTTCC TTGTAAAATA ATCCTGCCAA ATCAGTTCAG 1980 CCAGAACCGA TCACCCACCA TAATCAATAT GTGATCATCT TTGATATCTG ATCATCCTCA 2040 GTGTCTGATC AGGCTCCTCA CACCCACCAC CCCATGGGGG ATGTCTGGTC ACCCTGGCCT 2100 CTCTTCAGCA ACAATCCTGT TAGGTCAGTG AAGCCAGAAC CCCCCAGCCC CTGGTGTTTC 2160 CTCTCGGTCA TTTTCCATCC ACTGCCACTT AGGTGGAAAT TCTCACGTTC TCATCTCATA 2220 TTCGGAGGCA AGCCCAAGCT CCTTCCTCCA CCGCAAGACC CCATTGCAGT GATCCCTGTA 2280
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