Tag | Content |
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EnhancerAtlas ID | HS095-32657 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chrX:152892870-152894340 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TEAD1 | MA0090.2 | chrX:152893368-152893378 | ATGGAATGTG | - | 6.02 | ZNF263 | MA0528.1 | chrX:152894286-152894307 | GGGGGAGGGGGCAAGGGAAGG | + | 6.53 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_35416 | chrX:152886816-152894923 | HepG2 |
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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 |
GH0XI153621 | chrX | 152887213 | 152894348 |
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Enhancer Sequence | GCCCATGATC CTGTCAGGAG ATCAATCTCC CTTCCAGCAT GTTTTCAGTT TTTTACTGTA 60 AAGAATTGCA AACACATGCC CAACCTAGAG AGGATGACAG GGCACACCGG CCCCGCCGGC 120 GGTCCTCACA CAGCCCTCTC TCCTCTCCAC TCCCCTTAAT GTGGCCCCGA GGCCTGGGGC 180 CTCCTGAGAG AGGCACCTCC ATCTGCCTTA AGCAGGGACA GGGCCTTCCA GGCAGCAAAC 240 CCGGGTTCAG AACCTGGACC CTTGTCTACA CCAGCCAGGG CTGGAGGTTG GCCCTCTCAG 300 CCTGGGGACT CATAGGGGTG CCCGAAACTC CAGGAATCAG CCCCCTGGGC CCCCACTGGG 360 CCAGGTCAAA GTCAGTGTGG GTGGGAGGTA TTTGCAAGAT CGCCATGCAG GAAGTAGGGT 420 CCCAGGGAGA GGACAGGCCC AGACAGCCAT CGCCGCAGGC ATCTGCCCAC ATGGAAAGCA 480 AGGCGGTAAG CAGAGGCGAT GGAATGTGTG TCAACACCGT GCAAAGGGCC AGTGTGGCCG 540 GGGCTGGGGC AGCGAGGGCG GCAGCCAGGG GCCTCAAGGG GCGGGCAAGA GGCCCGGGAG 600 GCTGGGACTG CCAGGAAGGA AGCCAGCTGC TCAGCCTGGG GCGCCCTCCC CGAGGCCTGC 660 CCGCTCCCTA CCAGCCAGAC TTCTAGCCAA GCTCCAGAGC TGGGAGCCCA GCTGCCCACC 720 TAGCATCTCA CAGGGATGGC CTTGCACACT ACACACCTCC ACCCAAGTGG AGCAATTCTG 780 TACATTCAAG TACAATTCAG TTGTACAATT CTGTACAATT CAAGTACATT CTCAAGTGTA 840 CTTGAGCAAT TTCTGATGCC GAGCTCCCCT GCCGCGCCAC ATCTATAGTG GCTCCAGGTG 900 CGGTTGCCTC TTCTCTCCAC ACCCCTCCCG GGAGCACACA CGCAGGCATG TAGGCTGCTC 960 CAAGGGGTTC TGGAAGGCTC TGGCCCTTTC TTCTTCAGCA ACCTCCTAAG GGGCTGGGTG 1020 AGGAGTGAGC GGCCAACACA CATACATGCA TACACACACA CGTACACTAG CCTCTGCATT 1080 TCATATACAT GTGAAAATCA TTTGCTCCCC AATGCAGGTA ACATGAGAGG CTGGGCCCTG 1140 CAGCTCTGAG GCTGTCTGCA CAAACAGATC CTGAGAGAGA ATAGCCTCAA GGGGTCTGTC 1200 AGCCTGTGGC CAAGTCAGAT GGTCACGTCC TGTTTGCCCT GGGTGACTGG TCCAGAGGTG 1260 GGCCTCCCCG TGAGGACTCG ACTGCTAGGG CCAGCAACCA GCACTGAATG CCCGTGGCCC 1320 AGGTATGGGG CAGAGTGCCT CCCTCCCTCC CCCAGCAGGC CTGCCTCACC AGGACCCTCT 1380 CACCCACACT CTGGAGGGTA CACAGGGCCA AGAGCCGGGG GAGGGGGCAA GGGAAGGGAT 1440 TAGCCCCAGG CAGCCAGCTA AAACGGGGTC 1470
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