Tag | Content |
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EnhancerAtlas ID | HS098-14697 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:120064430-120065920 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RFX2 | MA0600.2 | chr12:120065658-120065674 | CATTGCTATGGCAACA | - | 6.18 | RFX2 | MA0600.2 | chr12:120065658-120065674 | CATTGCTATGGCAACA | + | 6.19 | RFX5 | MA0510.2 | chr12:120065658-120065674 | CATTGCTATGGCAACA | - | 6.44 | RFX5 | MA0510.2 | chr12:120065658-120065674 | CATTGCTATGGCAACA | + | 6.52 |
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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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Enhancer Sequence | GTAAAATGTC CTTGCTAGGG TATTTTATCA GAAGGCACAT GATGTCATTT GGTCAAGATT 60 CTCTTATTAT TAAAGGGAGA AGAACAGTAT CTGGCCTTCA TTTCAGCAGC AAGCAGTCTC 120 TGAATACCTC TTCTTTGCCT GGCAGTGTAC TATGTCCTGC AGACCTCAAA GATGCCCTCA 180 AAAACTTCAC ATTCTGTGGG GAAACAGAAA TATTCATGCA CTCATTCAGT CAATAACATA 240 TTTCTTGAGC TCCAACAATG TGCCAGACAC CACTCTAAGT ACTAGAAACA AGGATGATAT 300 TTAAATATTT AACAAGTTTG GCATGAGCAC AGAATCAGAG AAGATGCTCT GCTGAGCCCA 360 ATAACCCTTA AGTTGCTGGA TCATGGGGAA ACCGGGGAAA AGGCAGAGGA GCAAGTGGGA 420 TGGCTGGGAT ATTGGGGAAG GCGGACAAGC TTCAGAGTAG CTGCTATTTA TCAGTGAGTA 480 CAGAGTATTT CAACATTTTA ACAGCTGGGA ATGACAGCCG TGGCTTGGGC ATGGAGATGA 540 AAAATTCAGC CAAGGTCCCT GACCTCATGG ATTGACCTTC TAGTGCAGGA GTGGGCGAAC 600 TTCTTTGGTA AATGACCAAA TAGTAAATAT TTTTGGCCTT GCAGGCCCTA CATTCTCTGG 660 ACAGAGAGGC AAAGTCCCAA CTACTCAACT CTGTCTTTGT AGCACAAAAG TAGTGTGTCA 720 GTCCATTTTG CACTGCTATA AAGAAATACC TAACACTGAA TGATTTATAA AGAAAGGAGG 780 TTTGTTTGGT GCATGGTTCT GCAGGCTAAA CAAACATGGC GCCAGTATCT TCTTCCGGTG 840 AGGACTCAGG AAGCCTTTAC TCATTGTGGA AAGCAAGGGG AAAACAATTG TGTCATGTGG 900 CAAGACAGAG AGAGAGAGCA AGAGAACGAT GCCAGGCTCT TTTAAACAAC CAGCTCACAC 960 ATGAACTAAC AGAGTGAGAA CTCATTACTG CAGGGAGGGC ACCAAGCCAT TAATGAGGGT 1020 CTGCCCCCTG ACCACAACAT CTCCCACCAG GCCCCACCTC CAACATTGGG GATCACGTTT 1080 ACACATGAGA TTTGGAGGGA ACAAACATCC AAACTGAGGT AGGAGGCGGG ACTTGACTCC 1140 AGACCAGATT GAAGACCGGC TGAAACAGGG AAAAGGCACT CAAAGCTCCT CTCCATAAGA 1200 CATGCTCACC AGTGCCATGA CAGTTTACCA TTGCTATGGC AACACCCAGA AGCTACCACC 1260 CCTTTCCAGG GCAATGACTC GGAAGTTGTC ACCCCTTTTC AGGGCCACGA CCCAGAAGTT 1320 ACTACCCCTT ATCTAAAAAT TTCTTAACAA CCTGCCCCTT AATTTACATA TAGTTAAAAG 1380 TGAGTATAAA TCTGACTGCA GCACTGCCCT GAGCTGCTGC TCTCAACACG CTACCTATGG 1440 GGTAGCCTTG CTCTGCAGGA GCAGTCATGG AGCTGTAACT CAACCAGGGC 1490
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