Tag | Content |
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EnhancerAtlas ID | HS104-47381 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr5:68214930-68217280 |
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) |
IRF1 | MA0050.2 | chr5:68215115-68215136 | AAAAAAAAAAAGAAAGAAAAG | - | 6.41 | Nr2f6(var.2) | MA0728.1 | chr5:68215883-68215898 | TGACCTCTTGACTTG | - | 6.35 | REST | MA0138.2 | chr5:68216826-68216847 | CTTAGCACCCGGGCCAGCAGC | + | 6.16 | YY1 | MA0095.2 | chr5:68215853-68215865 | GCAGCCATCTTG | - | 6.74 |
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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 |
GH05I068920 | chr5 | 68216568 | 68221116 |
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Enhancer Sequence | CCGTCTCTAC TAAAAATACA AAAAATTAGC CTGGCATGGT GGCGAGCGCC TGTAGTCCCA 60 CCTACTTGGG AGGCTGAGGC AAGAGAATGG CGTGAACCCA GAAGGTGGAG CTTGCAGTGA 120 GCCGAGATTG CACCACTCAC TGCACTCCAG CCTGGGCGAC AGAGCAAGAC TCCATCTCAA 180 AAAAAAAAAA AAAAAAGAAA GAAAAGAAAA GAAACAAGAT GGAATCAGTA AGGTCAGATT 240 TCTCTGTTAT AATTTTTGCA AGGCAGTTTC AATGACAAGA GTACTTTATG AAGAACTGGA 300 CACACTACAG GCTCTTAAAA AATAAACATA ATAAGCCATA TATAATTTGA TGTTTAAAAT 360 ATAAAGAAAA ATGCTTTCTT ATTGCACCTG AGTGTCATGG AGCCAATTCA TACACAAGTT 420 AGAGACTTCT GACCTAGAGC CTCTTTCTGA ACTAAGAAAT CATAGAAAAC CATGAATTGA 480 TTCTCCCTTC TTTGTGGGCC TTGGTCTTAC ACGTATCTTT CAGCAGTCCA CTTCAGTTCT 540 CTTACTCTTG TCCTGACACG GATATAAGCT ACTGACAGAA ATCATCAGTG ATGGGATCAC 600 ACAGAGGGTA GAGTGAGAAG ATATGACTGT GGTGCCCATT CTTTACAGCA ATTTCTCAGC 660 CCAGGCTAAA ACTGTGAAAA GAAGAGGAAG AGAGGGTCCT CGGGAAAAGT ATGTTAGCAG 720 TGGCGAGTAT CCGAGTCACC AGCAGCATAT CCATACAGGT CTACAGCAAC CTCAGTTCTT 780 GCCTCCTCAG AAGAAAGAAT TTGACTGAGA GGCATAAGGC AGAAAAAGAG ACTGAGGCAA 840 GTTTTAGAAC AGAAGTGAAA GTTTATTAAA AAGCTTTAGA ACACGAACGA AAAGAAAGTA 900 AAGTACACTT GGAAGAGGGC CAAGCAGCCA TCTTGCAGGA CAAGTGCAAG GTTTGACCTC 960 TTGACTTGGG GTTTTATATG TTGCCATTCT TCCAGGGTCT TACATCCCTC CTCTCTTGAT 1020 TATTCCCTTG GGGTGAGCTG CCCACACAGC ACAGTAGCCT ACTAGCATTT GGGAGGTAAG 1080 CAAGCGCAGT GTGTTTACTG GAGTTGTATG CATGCCTACC TGAGGTGTTC TTCCCTTTAT 1140 GGCCTCTGAA GGTCATAATA TACCAGTTAA ACTCCACCAT TTTGCCTCTT AATGCGCATG 1200 CTTGGGCCCA TTTGCCCAAC TCCTGAGATC TTATTGGTAA GCTGCTGATC ACCAGTTTCA 1260 GATGGTTGAC AAGCAGTTTC TCAATTGCTG AAAATACTGA CAATGGACAG ATTAATAGGA 1320 GAAAAGGCAG ACTAATTTAT TGAATGTACA TAAACCCAGC ATGATTCCCC AACAACCCAA 1380 TGGGGCACAG ATGTTTATAT ACCCTTCTTC ACAGGGGATG GGGAAGTTGG GGAATGTATG 1440 CAATTCTTTA AAGGGGTAGT AAATGATTAT TAGGGAGAAT GAATGGACCA GGGAGCCAAA 1500 AATTATTGGG AAACTGCCTT TCCCTGGCAC TGGCTGTGAC CAATTATTAT TTTAGAGACA 1560 GCTTAACAAC TGCCTGACCA TCACCTGATG GTTTCCTGCT GAGAGGTGAC AGTGTGCTGG 1620 CAGCCCTCGC TCGCTCTCGG CACCTCCTCG GCCTTGGCGC CCACTCTGGC CACACTTGAG 1680 GAGCCCTTCA GCCCACCACT GCACTATGGG AGCCCCTTTC TGGGCTGGTT GAGACCACAG 1740 CCAGCTTCCT CTGCTTGCAG GGAGGTGCGG AGGAGAGGCG CGGAAGGGAA CCGGGGCTGC 1800 GCGCAGCAGA CCAGCTCGAG TTCGGGGTGG GCATGGGCTC GGCGGGCCCC GCACTCAGAG 1860 CAGCCGGCCG GCACCCGCGG CCAGGGCAGT GAGGGGCTTA GCACCCGGGC CAGCAGCTGC 1920 GGAGGGTGCA CCAGGTCCCC CAGCAGAGCC GGCCCGCTGG CACTGCGCTC AAATTCTCGC 1980 AGGGTCTCAG CTGCCTCCCT GTGGGGCAGG GCTCAGGAAC TGCAGCCTGC CATGCCCAAG 2040 CCTCCCCCTA GCCGTGGGCT CCTGCGCGGC CTGAACCTCC CCGAGGAGCA CAGCTCCCTA 2100 CTCCACGGCA CCTGGTCCCA TCAGCCGCTC AAGGCCTGAG GAGTGCGGGT GCGCAGCGCA 2160 GGACTGGCGG GCAGCTCTGC CTGCAGCCCC CGGTGTGGGA TCCACTGGGC TCCTGAGTCT 2220 AGTGGGGACT TGGAGAACCT TTATGTCTAG CTGAGGGATT GTAAATACAC CAATCAGCAC 2280 TCTGTGTCTA GCTCAAGGTT TGTAAACATA CCAATCAGCA CCCTGTGTCT AACTCAAGGT 2340 TTGTAAATGC 2350
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