Tag | Content |
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EnhancerAtlas ID | HS104-60449 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr9:38087670-38088900 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr9:38088136-38088155 | TGGCCACAAGGGGGCGAGA | + | 6.68 | FOSL2 | MA0478.1 | chr9:38088451-38088462 | GGATGACTCAG | + | 6.32 | JUNB | MA0490.1 | chr9:38088451-38088462 | GGATGACTCAG | + | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 38087887 | 38088363 | chr9 | 38088375 | 38088802 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I038088 | chr9 | 38088061 | 38088210 |
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Enhancer Sequence | TCTTCTTCCT TTCCTTCTGT TTTCAAAAGA CTTCCTGTCT CCCAAAGACC AATTTGATTA 60 TTTTCTCGCT GGGACCTCCA CAGCTACATT ACCCCATTTC TTAATTCTTG AAGTTCTTGG 120 CACAGTCTAA TTTGAACCAC AAATTATTAA ATTTTTGATG AGTGCTTCAG CTGCCCTTTA 180 TTGGCTGTAA CTTCCCGCCA TGGACTGCAT CCTCATCCAC AGATTGATCG CCTTTGACTG 240 GTGCTCAAGA ATCCTTGGGA GTTGATGGAC TGATGAATCA AACGGGGAGT CTGAGGCTGC 300 CATGGACAAT TAAATGGGAG AGCAGGAGTG GAGAAGAGTT AGTGCTGCCC AAGTAACGGT 360 CATCCAGGAA TAAGGAAGCC TTTTGAGAAA TAATAATCAA GCTGGCTCAA ATGCACTTGG 420 CACACATGGG GTGGACCCTG AGTCCCAGGT GGTGCACCTC TCCGAGTGGC CACAAGGGGG 480 CGAGAGAGGG CATGGTCCAG GTGCCAAAAT ATTGCTGTGG CTGTGGGGTC AGCCAGCTGG 540 CTGGTCCGCT AGTTGAGCCC TGGCTGGAAG GGGAATCTTG GCCTAGGTGA TTTGCACAGG 600 ATAAAGTGGG CCTCCAACCA GAAGGCCTAG GAAGCAGCGT GCCTGGACCA AGGTTAGGAA 660 AGCCCAAGGA TGAACAGACG GATGGCAAAC ATTGATAAAC ATCTAAGAAT AGGAGCTAGA 720 ATCTCCAAAA TTAAACCAGC AAGTGAATGT CCAGTGACCC ACATATTCTG CTAAGGATGG 780 GGGATGACTC AGTGTCCTGG AGAAGGAAGC AGGAAGCCCA GGCATAGTAC AGTGGCAAGG 840 ACTGAGTCTG GGAGGCAGGG GTCTGGAGTC TGATCTCTAA CCTTGTAGTT CCTCAATCCT 900 GTGTCTATGG CCCCTGATGA AAGCTCGTAC TGTGTGTCCT TAGGTGATGA CCTCTCCCTC 960 TCTGAGCCTC AGGTGTCTCA TCTTACCAAA TAAGTTTGAT GTCTGGAGAC TGAGAGACCA 1020 GCCCCACCCT TGCACTGGGC ACCATGATGA CCAGGGTTCC TTTCAGTTTC AATGGTCTCT 1080 GAGTGACATG AACAAAACAG TTAGTTGGCT GCAAAGACCA TGTCTTTCTC ACTTCTGCCT 1140 GTGTACACCT GCTTTCTTTA CAACTTTTGA GGAGGCCCTG GTCCTTTGGG ACCAGGATTG 1200 TTCAGACCTT TGTAGAAGCT GAGCAGTATA 1230
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