Tag | Content |
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EnhancerAtlas ID | HS129-08292 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr12:14989040-14990410 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr12:14990217-14990230 | GAAGCTTCTAGAA | - | 6.28 | STAT1 | MA0137.3 | chr12:14990124-14990135 | TTTCTGGGAAA | + | 6.02 | STAT3 | MA0144.2 | chr12:14990124-14990135 | TTTCTGGGAAA | + | 6.32 |
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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 |
GH12I014834 | chr12 | 14986938 | 14991193 |
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Enhancer Sequence | TGAAGTGTGG CAGCAAAACT AGCATGAATT TCTTTTTCCT TCTTCACAAT TCCACAGGTA 60 GAAGATTCAT TTTTACAGTA GATCTTAGCA ACCTCAGCAT ACAATTTTTT CTTTCTTTCT 120 ATTAAGTTGA GAACTTTAAA CTTTTCATTC AAAGGAGGCG CTTTCTCTTG GGCATATCTG 180 AATCTCCAAG ATCACTATTC TTTCACTTTG GGGCCATTAT GAAATAAAAT GAGGGTCACT 240 TGAAAACAAA CACTGCAGTA CCGAGACAGC AGATCTGATA ACCGAGAGGG CTACTAAGTG 300 ACTCACAGTG TAGACTGTGG ATGATTCACA TCCCAAGAGG GAAGGCACAA GATTTCATCA 360 CACCACTCAG AATGGCATAC CATTTAAAAC TTAGGAATTC TTTATCTCTG GAATTGTCCA 420 TTTAATATAT TCTGCGGGTA ACTGAAACCA GAGAAAGCAA AACCATAGGT AAGGGGGCAT 480 TACTGCAATT TTTTGCCCTC AACTAAATGA CTGTGATGCT AACTAGCCAA TGGCAGATGA 540 GGCTTAGGTA GGTCAGGTAG AACCAGAGGA TGGACCAGCC TTCTCTGCAA CCCTTAGTCA 600 GAGTCTGGGA TCAAAGGAAG AAAGGCATCC CTGCAATGTG AGCTTATTCC TCTCCTTCTT 660 TTACCTTCCC AGATAGTTTC GTAGCTGTGG AGGGTGAGAA AATGCTCCAA TTCCAGCTCT 720 TGGCTGATTA TATGATGCCT CTGACCTATC TCTTCCCTCT TCACTTCAAT TTATAAAGAA 780 AATATTAAGT TGAGAACTTT AAACTTTTCA TTCAAAGGAG GCACTTTCTC TTGGGCATAT 840 CTGAATCACC AAGATCACTA TTCTTGCACT TTGGGGCCAT TATGAAATAA AATGAGGGTC 900 ACTTGAAAAC AAACACTGCA ATACCGAGAC AGCAGATCTG ATCACTGAGA GGGCTACTAA 960 GTGACTCACA GTGTAGACTG TGGATCCCCC AAACAACGGG ATGATTCACA TCATGACCAG 1020 TGGTATTTTT ATTCTGCCGT TTACAAGCTT TTCTGCATGG CCACACAAGC TTCTAATTGA 1080 TAAATTTCTG GGAAAAATTT AGTTACGGTA ACTCACATTG CAAGTGACCA TGTTGATCAT 1140 TTACATTGTG ACAACAGCTT ACTTTTGACT AGGGGTTGAA GCTTCTAGAA TATCTTCCCT 1200 TCTTCAAATA TTGGAACTGT TTTTAATTAA TTGTGTTAGA TGGTCATGTA GTCTAAGGCT 1260 CAGATTGCTT AGAGGTATAT TCACCATCAT TCATTCACTC ATTCAACAAA ATAGGCTGGG 1320 CACTTCTATG TGCCAGAGGA CTGAAGTTAG TAATAGCTAA CACTAATTTA 1370
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