Tag | Content |
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EnhancerAtlas ID | HS104-40188 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr3:39788720-39791340 |
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) |
Foxd3 | MA0041.1 | chr3:39789997-39790009 | GTTTGTTTGTTT | + | 6.32 | ZNF263 | MA0528.1 | chr3:39789060-39789081 | GGAGAAGGCTGAGAAGGAGGA | + | 6.51 |
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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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Enhancer Sequence | GCCTAACCAT TGAGTTATAT TTCTTCCAAC AAGTGACATT TAGGAATATT GAGAGTTATT 60 TTTTGTGTTC ATTCTTGGGA TAAAGAATAC CATATATTAG GCTAGTAATA TAAATGTTTG 120 GGTTGCCTAT TCTAGATACC CTTCATGGAG CCATTGGGTT CATTCCAATG CGATGTGAGT 180 ATTGGCTGCT AATGGCTCCC AGATGTTCCT GTCCACTGAG AAGAATTTCT TTTGGCCAAG 240 GCAACTTCAC TCTGGAAATG GCTGAAAGTT ACGTCTTCTC CTCAGAAGTA GCTCATGGCC 300 AATGACTAAT ATACGATCTA AGTACTGAGT TGTTAAAAGA GGAGAAGGCT GAGAAGGAGG 360 ATACAGAAAA TAGCAAAATG GCTGTTTCTT CCCCAGGGGC CATCCTTTAT AGCTTAGCCA 420 AATGGCCCAC CTTTGATCAT TCTTCTCCCC AAAGGAATGA AGTGTAACAT TTACATCAAT 480 GTCCACCTCC ACAATGGGTA GAAGGCAAGG CAATGGGCTG AGCAGGAGAC ATAGAATCTA 540 AAAGCTGAAA AACCCTGGAA AGGGTAAGAA AAGTAATTTC TTGGGGGGAG GGGGGACAAC 600 TGGCAGCAAG AATTATGGAG ACTGCATTGG AGCACACAAT GCTCCTTGGG AAGTCCAAGG 660 TTAGAGATTC AATACTTAAA AATGCATCTG GAACCATTGC AGAAGCAGAA CTAAAATTAG 720 CTGCAATTGA TAATAAGAAT TCTTACATAA AAATAACAAT AGTAAAAATT AACAATAGCT 780 ACTGTTGATT GAGCACCTGC CAAATGTGAG GTTCAGTGCC AGATTATTTA CATTTATTCA 840 TCATTATCCC TGCAACAAAT ATGGAAGGCT GGACTGAGCC AATGCCCATC TCTTTTCACA 900 AGGCCAGCTT GCCTCCTATT CCATGACAAA CACCTGCAGG AAAGAATAGA GTGGAATGGG 960 CAGAACAAAA GAGAAATGGA ACCTAGAGTA TCATTTCCTC CTCCTTAGTG CACATGCCTG 1020 GCATGTGCAG CCAATAATTA GTCACTCAAT AAATATTTGA AAAGGAAATG AACAACTAGA 1080 AGTTTAGATA ACAAACTTTA ATGGTTAATT TTGGATGGTG GGGCCGGGAG CTACATTTTC 1140 CTTGGTGTTT TCCCCAAGCT TTCTGCATTA AATTTATACT TATGTAAATT GTAAAACTCT 1200 GAGCATATAT AACTATATGC CAACATTGAA ATATTTTGAA AATTATGATC ACTTTAATTC 1260 CTAAATGAAG AGGTTTTGTT TGTTTGTTTC TTGTATACAT AAGGCTTTCC TGTATATCAC 1320 TTAGGCCTTA ACTTTTTTGT ACACACAGAT TCTGGGTTGC AGAAATGCCT CCTAAAACAT 1380 CTACTTTTGG CACCAACTAC AGCAGGGTGC CATTGTGAAA ACCACTCTGA ATCCCAAATT 1440 GAGGGCTGCT GCAGCCTTTT CCAGGGGAAG AGGACTGCTG TTTAGGGCAC CTCGTCTCCT 1500 GATCTCCTGA TCTTTTGAAA AGGGGCTTCT ATTTTTGTTT ATGGACATGC AGATGTCTTT 1560 AAAAGAGAAA GAGTCCTAAA CATCTCTTTT AAATCACTGA CCCATGTTTC TTAATAGCCA 1620 GCAATGAACA AGGGAATTCC CAGCAAATGT GATGGTAGTC ACATCCAAAA ATTAGAAAGC 1680 TAAGGCATCT ACTTAGATTA AAATATGCCT GGGTGTCGGC CCTGTTTTCT GTGGTAGTAA 1740 TATATTTTCT GTCCTCATGA CTCAGCCTGT AATAGCCAGT AATGAAGTAA ATAATTCCCA 1800 GCAAATGTGA CAGCAGTCAG ATTGAAAAAT TAGTAAGCTA AGACATCTAC TTTGTTTATA 1860 ATATACCTGA GTGTCATGGC TCAGTTTCCT GGAATCACCC CCAGAAATTC TACCCTTACG 1920 TTGGATAAAT GAAAATGCTC TGGAATGTCA CTTTTTGTTC CCCAGCAAAC CACTCTCTGA 1980 CAAGCAATTG GTCCTCTGCC AGGTGACCTT GACCCAAAAG CTGAACCATG CTTCCACTGT 2040 TCATAGATGA AGAAACTGAG GCTCAGAGAA CTTCTGCCAG GGAGCACAGC TCGTTGAGAG 2100 CAAGTCTGAA ATAAGTGACC AGGTTTCCTG ATTGTCTTCT CCTATTTCTG TGGTAGCCAT 2160 GGAAGAGGAG TTGGTCCTGG CTCTTCTGGA AACTTCTGAG TCCAGAAGTC ACTCTACACT 2220 CTTCTCTCAT TGGACCCTCT TCATCCACAC ACCAACACCT TCCTCCTTGA AGCATTCAAC 2280 CTGTGGCCCA CCTTTCCTGG TAGCTGCCCT CCCTCCCCAG TCCTCAGCTG ATGTCTCTCC 2340 TGCCTGCTCA TAGGAGTTGG AGGTACTCCC TCCTGTACCT CCTTTGGTAC CCCACAGAGC 2400 TCCAGGGCCA GCCCAGCCCT TTGGAGACCA CTTTTCTCTG ATCCTCCATC CTGCAGGTAG 2460 TGTCTTTGTT TGAGCCTCCT CCTCTCAGGG TGAATGCTTT TTTCAGCTGT AGTTTAATGA 2520 ATCTCAAACC AGGCTCTGGA TGAGTTGCTT CAGTCAGGAG CTTAGAAACA ACACATCTCC 2580 TAACACTTGC TGCTTGCCAT GTTCTCAGCC ATTCCCTTTT 2620
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