Tag | Content |
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EnhancerAtlas ID | HS052-28144 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr4:4482410-4484040 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr4:4482474-4482493 | TATCCACTAGATGGCAACA | + | 6.28 | ZNF263 | MA0528.1 | chr4:4483746-4483767 | CTCCCTGCTCCTGCCTCCTCC | - | 6.19 |
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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 |
GH04I004480 | chr4 | 4482329 | 4483127 |
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Enhancer Sequence | TTCAAGAATC AGTAATAGGG TACAATAAAC TCCAAACATA CTAAGGCAGC CACATACTTC 60 CCATTATCCA CTAGATGGCA ACACAAGTAT TAGAGCAGCA GTAATAACAG GACCTCTCAA 120 AAACAGCAGT TTTTTCCCAA GGACTTTAAA AATTTCTCTG ATTCTTTTGA TCTGGAATCA 180 AAGGATTAAT AAAGGTTCAC CATTCTGTGC AGGAGGAAGC TGAAATGAGA TTGTTTTTAA 240 GCATACATAT GCACTACAGA TGAGTTGAGT CCAGGAATAT TCTGAAACAC TGCACTCTAG 300 GCAGATTCCA CACAAAGGGA GCTCTGGGAG CATGGCTGCC AGCTGCCATC CCAGGCGGCA 360 GGCCCAGCTT TGTTTTTATG TGTCACCCAC AGAACAGCCT TGCTAGCTGT TCCTTCGTGG 420 GTGTTTTGTG AATTACCCAA AGCACGATAT ACTGTACAAC AAAAACCCTG GTACAAAATG 480 ATGGGATTCT TCTCAAAGAG CGACCGCATT CTGACTGTGG GGAGAGTTCA AAGCAGTCGG 540 CAAGTGTCCT TTGCTGATCA CAGCAGTGGT TTGACTTGCA AACCCCCTCA CCCTTCCCAG 600 GATGATAGAA ATTCTGTTCT GCTGGCACTC ACAACACTTC CAACAAAGAC CTGATTGATT 660 ATGGAACACT AAGTACTGAT TTGCATAATT TGCCTCTGCA AGAAACAAGC ATTGTTCAAG 720 ATTAAAGAGA CTCCAGTAGG TCCCTCTGGC ATATTGTAAA AAGGTCCCTG TAACACAAAA 780 TCATTATTTT TTTTTCATTC AATCAGTGGA CACAGCTTGC TGTTCAGTTA GTATGCAGCC 840 AAAGGCACAG CCAGAAAAAC CACTGCTGTA TGTTTGCCAA CTACTGACAA GTTAAAGTGA 900 TTTTTCACAA GGATCATGTA CCCAAGTTTA ATTTGGAGCC CACTGACTAA ATTCCGAGTC 960 TAACTCCTTT CACTCTTAAT TGAAAAATGC ATCAATAGCA ATTACTAAGT CAGAGCTAAA 1020 AGTTCAGAAC TAACACACCT CTGGAGCATG TTGACCTGCT GATGTCACAG TGGGGACTGT 1080 CTGAGTCCTA TCCCTGTGCA AAAGAAGCTC CCCAGTGACC AATCACCCAC AAAAGAGGCT 1140 AGCACAGCCA CAGACATTCC ACTGTGCTCA GGACCACAGC AGCGAGTTTG TTGAGGGAAT 1200 ACATAAAGGA ACTGTTCCTT TCTCGCTTTC TTCTTTTCTT TCAGCAGTTG TTGAGTAAGC 1260 AACTCCTGTC ACTTTCCCCC AATTCCTACT GAGGGGGACA CTCTTCACCA GGCCTCACCA 1320 AACTCGGATG GCTCTCCTCC CTGCTCCTGC CTCCTCCTTC CTTGTCCCCT CCTGAAGCAC 1380 TAGCCTCCCT CGGGTTCCAG AACACCACTG TCTCTAGGTT CTTTTCTAAA ACCTATAACT 1440 CCTTTTCTTC ACCTTCATTC ATTCCCTCTC TGCCTTTGTT AATCTCTGAA ACTTCTTGTA 1500 AGTTCAGCCC TTGGCTCTTT CTTTACATGT TCTTGCTAAG CTCACTCATT CCAATCCATA 1560 GCTTTATTTA CTGTCTACAT GAATTGTCCA CCCAGCCGCT GCCTCCCTCC TGTGTTCAAG 1620 CTGAGTGTAT 1630
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