Tag | Content |
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EnhancerAtlas ID | HS052-26367 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr3:63863050-63864720 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr3:63863733-63863751 | TGAAAGAAAGAAGGAAGG | + | 6.56 | EWSR1-FLI1 | MA0149.1 | chr3:63863737-63863755 | AGAAAGAAGGAAGGATGG | + | 6.73 | EWSR1-FLI1 | MA0149.1 | chr3:63863741-63863759 | AGAAGGAAGGATGGCAGG | + | 6.75 | EWSR1-FLI1 | MA0149.1 | chr3:63863745-63863763 | GGAAGGATGGCAGGCAGG | + | 7.46 | TCF7L2 | MA0523.1 | chr3:63864572-63864586 | GCTCTTTGATCTTT | - | 6.04 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 63863794 | 63864299 | chr3 | 63864575 | 63864655 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I063878 | chr3 | 63863677 | 63863876 |
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Enhancer Sequence | TCCAATAAAA TATACTTTGA AATGCATGCT TAGAAGTAAG GGTAGAAGAG TGGTAGAAAT 60 GGGTACATAG TGTGAACCAA ATTTTGTTAA TCCTACTGCT TGTCAGACTG CCCGCCAGGT 120 GTTGCCTTCA GGCTGATGAG AGCTGCCTGG CCCTTTGGCC AGCTTTGGCT GATTTGCAGC 180 AGAGCATCTT TTCTTAGACA ACTGTCTATA TCTGTCTGTG TCTTTATCTT AGCAACTGTT 240 TCTTGTCAGC TCCAAATGCC TGCTGGTTGC AGAGAGAGAC ATTTGGGGTC CTTGTTGGAG 300 TGGCTTATTG ATATGAGCCA TAAGTTCTTA TCAACCCCGT GGAAAAATTC TTTAAATCAG 360 CTCTTATTCA AAAGAATGCC CGAATATTCA CAAATATAGT ATCCTTCAGA TTACTTGCAC 420 CAAGTAACAG CAAGGTATTT AGAGACTCCC AGGTGATTTC AATTAACATC TAACCTCAAA 480 TCCGGTCTCC TTGGTAAGAG AAAAATCCAG AGAAGGAGCT CAAAGCAGAT TATGGTATAA 540 GCATATGCCA GTCCTCTCCT GTGGAAAAAG AAAAGTGCTA ATCTGGTCAG AACTGTTAAA 600 GAGACAGGCA AGGCTGAGCA CAGCAGAATT CTCTCATCCT GTTCATCTTT TGCATTAGTG 660 CAGAAAAAAG ATTTATCTCA GGATGAAAGA AAGAAGGAAG GATGGCAGGC AGGTGGCTAG 720 TAATAGGAGA TGGTTGGTTC TCTTCCTCTC TGCCTGGGCT AGTGGTAAGC AGGTCCTCAG 780 GTCTGAAAAA CTAGTAAAAG TGAAGTGACA CACAGGGCAG CTTCCCCAGG CAGTGATACA 840 ACTTGTTGGT ATTCAGTGTG AAAATACAAA GCTGACTTTG ATTCCTTGCC ATCAGCCAGA 900 GGAAACCCTG GAGAAGTAGG AGGCAGTGGC ATCTCTTTGT AAACATTTTA TTCTTGACAA 960 GTAACAGACT CCTACCTAGA GAATTGTAAG CGTTGGCCCC TCCATTCTGC CAGCTGTCTT 1020 TCAAGAGCAC TCTCAGTATT CTCCTGCACT GACCAGTTTA AAAGGTGTCG TTTCTGCTCC 1080 CATGCAGTGC TTGGTGTGAA GGAATTAATT TGCAAGATGA ATAACCATTG TGATAACTGC 1140 TCACATGCAA AGGAGAGAGA TTGCTGATTT TACAGGTGTG TGGTTTGCTT TCTTAGATCT 1200 GGCAGGAAAC AGAGTCCAAC TCAGATGGTT TAAGAGACTT TAAATGAAAG AATTATTTTC 1260 AGAAGGACGG GCAGAGTTCA GGATGACATG GGTTTCTGTC ACCTAGAAAC TAATAGGAAT 1320 GGCAAGCTGT TATCACTGCT AGATCTGAGG GAGCAAAGAG AAGAAATAGT GTTACTGGAG 1380 TCTAGTGAGA GCTGGTGCCA TAGTGGATGG GCTGTTAAGA CAGGAGCTAT AGTACTAGAG 1440 GCATTCAGCC ACTGCCAGAA AAGGGAGCCC AGAGCAGGGA GGGAACAAGG AGGGAATATT 1500 CTCCTCTCTG ACTTTTTTCT TTGCTCTTTG ATCTTTTTCC AGTGCCTTCT ATTGGCCAGA 1560 CTCACCTGGA AGCTGGCCAG CAGGTGAATC TATGATGCTG CCCATAGAGG TCAGCCTCTT 1620 GGGACTCAGC AGGGCCCAGT ATGGTGGAAA GTTGGTCTGG GGGTGGAAAG 1670
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