Tag | Content |
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EnhancerAtlas ID | HS145-02991 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr10:35262070-35263250 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2C | MA0524.2 | chr10:35262272-35262284 | TGCCCTAGGGCA | + | 6.92 | TFAP2C | MA0524.2 | chr10:35262272-35262284 | TGCCCTAGGGCA | - | 6.92 |
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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 |
GH10I034973 | chr10 | 35262513 | 35263505 |
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Enhancer Sequence | GTATCAGAGA GCACTGTCGA GCATGATTGT GTAGAAGTGT TAGACTCAGT TTACTCTAGC 60 AGACCTGACC TCCGGGACCA GCCTTGGGCA TCAGTAGACT GGGAACTACA CGTGGACGGG 120 AGCAGCTTCA TCAACCCACA AGGAGAGAGA GGTGCAGGGT GTGCGGTGGT AACCCTGGAC 180 ACTGTTGTTG AAGCCAGATC ATTGCCCTAG GGCACTTCAG CCCAGAAAGC TGAACTCATT 240 GCTTTAATTC GGGCCTTAGA ACTCAGTGAA GGTAAGACTG TAAACGTTTA CACTGATTCT 300 CCGTATGCCT TTTTAACCCT TCAAGTGCAT GGAACATGAT ATAAAGAAAA GGGCCTATTG 360 AACTCTGGGG GAAAAGACAT AAAATATCAA CAAGAAATCT TGCAATTATT AGAAGCAGTA 420 TGGAAACCCC ACAAGGTGTC AGTTATGCAT TGCAGAGGAC ACCAGCGAGC TTCCACCTTG 480 GTGGGTTTGG GGAATTCCCT CGCTGACCCA GAGGCTCGAA AAGCAGCAAC TGCCCCCTTC 540 CGGGCATCAG TCACAGCCCC TCTGCTCCCT CAAGCACCTG ATCTTGCACC TACTTATTCT 600 AAAGAAAAGG ACTTTCTCCA GGAAGATGGA GGACAAGTGA TGCAGGAAGG ATGGATTTGG 660 TTACCAGATG GGAGAGTAGC TGTGCCACAG CTGTTAGGAG CTGCAGTTGT ACTGGCTGTG 720 CATAAAACCA CCCATCTAGG CCAGGAGTCA CTTGAAAAGT TGTTAGGCTG GTATTTCTAC 780 ATCTCACATT TGTCAGCCCC TGCCAAAATA GTGACGCAGC AGTGTGTTAC CTGCTGACAG 840 CATAATGCGA GGCAAGGTCC AGCCATTCCA CCCGGCATAC AGGCTTATGG AGCAGCCCCC 900 TTTGAAGATC TCCAGGTAGA TTCCACAGAG ATGCCAAAGT GTGGAGGTAA CAAGTATTTA 960 CTAGTTCTCA TGTGTGCCTA CTCTGGGTGG GTGGAGGCTT ATCCAACATG AACTGAGAAA 1020 GCTCGTGAAG TAACCCGTGT GCTTCTTCGA GATCTTATTC CTAGATTTGG ACTGCCCTTA 1080 CGGATCGGCT CAGATAACGG GCCGGCATTT GTGGCTGACT TGATACAGAA GACAGCAAAG 1140 GTATTGGGGA TCACATGGAA ACTGCATGCC GCCTACCAGC 1180
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