Tag | Content |
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EnhancerAtlas ID | HS104-41882 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr3:127993140-127994700 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr3:127994241-127994256 | AGGGCTGTGTGACCT | - | 6.51 | FOXF2 | MA0030.1 | chr3:127993748-127993762 | CTTGTTTACCTTCA | - | 6.27 | KLF13 | MA0657.1 | chr3:127993649-127993667 | AAGACACGCCCCTCTGTA | + | 6.84 |
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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 |
GH03I128273 | chr3 | 127992831 | 127995113 |
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Enhancer Sequence | TGCCTTCCTC CGAGTCGCAG CAAAGAGGAG GAGGAAAGGG GCAAGCTGCT CTAGAGCACG 60 CACGCATGTG GGCGCAGTCA CCACAGGAAG CCTCAGCCCC TGCACCCTCT ACATGGAGCC 120 CTGGCAGTCA GGCAGCACTC AGTGGTTGCT GGGGGAGCAG ATGTGGAGGT GCCAAATGTG 180 GCGCGGGTAG GGAGTGTGGC TGGCCTCTGG ACATCCCCTG TAGAAGCCAC ATGTTGAGGG 240 AGCCTAGGTC GGTGTGGGCC CTGGCCCAGG GTGGCCTTGG GACACTCCCA GGGCAGCTGT 300 AGCACCCTAC AAGTTGTCGT ATGAAAACCA CTCTAACTTA TACGTGCTTT TGGGTGGAAT 360 TAAATGAGTT TTATTGTTTC TAGGACAAGA TAGGGATTTG ATTAGAAACA ACATTTATGG 420 AATGCCAGGG CTGGTTCCCA TCCACTGTGC CCTGCAGGAA CACAGAGTCT TGGGTCCCAG 480 GCATAAACGG CCAGCTGTGT GACTGGGGCA AGACACGCCC CTCTGTATGG CCAGGCCACC 540 TTCTTAAATA AGTAAGAACA GCCTTCAGGT GGGAATGGTT CTTCCCAAGG GCCATTTGCT 600 TTCACAATCT TGTTTACCTT CAGTGGTCAG TTAAGTTTCA AGGGGAAACT GTGACTCAGG 660 CCAGTGGAAT TGTCAGATGC AGAAGCAAGG GGTGAGATGG ATGCGGGCTT GCTGGGCTTA 720 CCGAAACTTG TATGCCTGTA GGCCTCTGGG GGTGCAGTCA TTTCCTCCCT CTAGCTGTGG 780 GCTGCGGTGC CTTTGGAATA GGATGCGCAT GTCATCGAGG GGTCTAGCAG TGACCTGAGG 840 ACTGGCAGGA CCTCGATACT GGGGCCCAAA GCGGTTTCCT CTCCTGGGAA ATGGGTGCCC 900 AGCCAGTGTC AGAGCCCCAG CTGGGAGTGG CCTTGGTGCA GAAAATGCTG TGTAAATGGC 960 AATTGACAGT GCCAGGTTGT GCCCAATGCA AGCATGGGTG CTGCCTGGTC CACAAAGGAG 1020 TATCTGATCT TTGACTGTCT GAAGACCACT GCCTTTCTAG GTTGGAAGCA AGCTCTGATT 1080 CAGATGAAAG TGTGGCCATG CAGGGCTGTG TGACCTCAGC TTGCACACCC ATGAAGCCAG 1140 CCCTGCCCAC AACCTTTCCA GATACTGTTG ATGCGTGTCA TGTCGGGGAC TGGAGTCCCT 1200 GACAGGTATC AGAGCCCAAG CTGGCCCTGG GGGAGCCCTC AGTGGGGCTG GGGTGGTCAG 1260 GCAGGCAGCT GTTTCTTCAT ATGGGGAAGG CACTGAGTGA ACATGGCTTC CAGAGTGTGG 1320 TGGGGGCACT GGAAGGGCTC CAACCCTGCT TCCCAGGCAA GGCGACTGAA GCTGAGTCTC 1380 AGAGAAGGCA GAGGGCTTTG CCCAGGCATT CTGAGCAGAA GGAACAGTAT GTGCTAAAGC 1440 CCAGAGGCGA GAGAGTGTCT GGCATGACTG AGGTAAACAT GGAGCTCCTT GCAGAGAGTC 1500 TGAGAAGTGG GGTGGTTCGT AGGTGGTTGT GGTCATCTCT GAAAGGGCAG TAGGGAGGAT 1560
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