Tag | Content |
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EnhancerAtlas ID | HS187-22272 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr7:2076620-2079420 |
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) |
IRF1 | MA0050.2 | chr7:2077695-2077716 | GATAAGAAAGTGAAACTGTCT | - | 6.45 |
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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: 3 | ID | Chromosome | Start | End |
GH07I002038 | chr7 | 2076661 | 2076750 | GH07I002037 | chr7 | 2076900 | 2078235 | GH07I002039 | chr7 | 2079127 | 2079493 |
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Enhancer Sequence | AGCACGAGCT TCCGCGTGCC CACCCACGCG CAGAAGACCT CCACCTGCCG CATGCTCCTC 60 CCACAGCTCC CCCCACAGCA TGAGCTTCCA CGCGCCCACG AAGGTGTCCA GCCATGCAGC 120 AAACGTGGAT CAGGCCCAGG TACACATCAG ATCTCACCGG TTCCAGTGCC TTCTGCCACG 180 TGGAAATTTC GGCTCCTTCT TTGTCTTCTT AATAGACTCT TCTTTTTTTT TTTTTTTTTT 240 AGAACGGGTT TAGATTTAGA AGAATGGAGA AGATGGTAGA GACTTTTCAC ATATTCCACA 300 CCCAGGTGCC CCACTGTTAA CATCTTACAC GAGCACAGTG TGCTGGCCAC AATAAGGAGC 360 CAGCATGGAC CCAGGCACGC CTTGCTCTCC TGGACTACAC AGATACTGTG CTTCTTACAA 420 ATGGAAGGCT TGTGGCCGTC CTGCCTTCGG CGAGGCACCA TGTTCCCAAC AGCATGTGCT 480 CCCTACACGG CTCTGTCACA TCTGGTAATC CTCATGGCGT TTCAGACATT GTATCACTAT 540 TATATCTGTT GTGGTCTGTA ATGGGTGGTC TCTGATCTTA CTACTGTCAT TGATTCTGGG 600 GCGCCACGTC CTGACTGTAC TTCCGACATT GCATCACTGT TATGTCTGTT GTGGTCTGTG 660 ATCGGCGGTC TCCGATCTTA CTGCTGTCAT TGATTCTGGG ACGCCACACA CTATGCTCCT 720 CAGACGGCAA AAGCTTCACC GACCAACGCT GCTTGTGTCT GGCTGCTTCA CTGACCAGCC 780 ATCTCCCTCC CTCCCTCTCC TTGGGCCTCT CTATTCCCTG GGCGACACAA CAGTATTAAA 840 ATCAGGCCAA TTAATAACCC TACAACAGCC TCTAAGCATT CAAGAGAAAG GAAGAGTCGC 900 ATGTCTCTCC TTTAAACCAA AAGCTAGAAA GGATTAAGCT TAGTGAGGAA GGCGTGCCAA 960 AAGCAAAGAT AAGCCGAAAG CCAGGCCTCT CGTGCCAAAC AGCTCGCCAA GTTGTGAATG 1020 CAAAGGGAAA GTTCTTGGAG GAAATTAAAA GTGCTGCTCC ACTGAACACA CCAACGATAA 1080 GAAAGTGAAA CTGTCTTATT GCTGATACGG AGAAGTCTGA GTGGTCTGGA TAGATCAAAC 1140 CAGCCCCAAC ATTCCCTTAA GTCAGAGCAA GTTCCACGAG GCTGAGAGAG GTGGGAAAGC 1200 TGCAGAATTC AAGTCTGAAG CTAGCAGAGG TGGGTTCATG AGGTTTACAT TAAGAGGCAG 1260 TCCCCATCAC ATAAAAGTAC AAGGTGAAGC CGCAAGTGCT GACGGAGAAG CTGCAGCAAG 1320 TTCTCCAGAA GATCCAGCTA AGAGCACCAA TGAAGGTGGC CACACTAAAC ACCAGATTTG 1380 CAGTGCACAT AAAACAGCCT TCTGCTGGAA GATGCCGTCT AGGGCTTTTA CAGTTACAGA 1440 GGAGAAGTCG ATCCCTGCCT TCAAAGTTTC AGAGGACAAG CTGATGCTGT TAGGAGATAA 1500 TGAAGCTGAT GACTTTTTTT TTTTTTTTTT TTTTTTTTTT TGAGACACAG TCTCACTCAT 1560 TCTGTCACCC AGGCTGGAGC ACGGTGGCAC AATCTTGGCT CACTGCAACC TCCGCCTTCT 1620 GGGTTCAAGC AATTCTCCTG CCTCAGCCTC CCAAGTAGCC GGGATTACAA GTGTGTGCCA 1680 CCACGCCTCA CTAATTTTTT GTATTTTTAG TAGAGACAGG GTTTCACCAT GCTGGCCAGG 1740 ATGGTCTCGA ACTCCTGCTG ACCTCAAGTG ATCCGCCCAC CTCGACCTCT CAAAGTGCTG 1800 GGATTCCATG CATCAGCTAC TGTGCCTGAT CTAAGCTTTT TATTTTGATC CAATTACAGA 1860 TTCACTTGGA GCTATAAAAA ATAATACAGA GATCACAAGT AGCATTCATC CAGTTCCTCC 1920 CAATAGCAAC ATCTGGCACA ACTACAGCAC AGTATCACAA CCCGTATGCC GACAATGATA 1980 CAGTCAAGAT ACAGCACATT TCATCACCAC AAAAACCCCT CGGGTTGTCC GTTCACAGCC 2040 ACGATTCCTC CTGTGCGTCT CCGTAACTCA CGGCAGCCAT CCACAGGCTG TCTATCACTT 2100 CAGCCTTTTA ATAACGTCAT GCAAATGGGA TCATGCAGCA CACGACCTTC AGGGACTGGG 2160 CTCTTCGCTC CGCTAAACTC CCTGGAGATC TATTCAAGTA TGTTTATCCA CAGTGAATTC 2220 CTTCTTAGTC CTGAGTATTA CTCTGTGTGA CGGAGGCACT ACCGTTGTTT AACCATCACC 2280 ACCGAAGGAC ATCAGAATTC TTTCCAGTTT TTGGCCATTA TGCAAAAGCT GCTAGGAAGA 2340 GTCCTCTGTC GGGTTTTGTC CGAACCTCGG TTTTATTTCA CTGGAATCGA CACCCAGGAA 2400 TGCGACTGCT GGTCATATGG GAGCTGCAGT GCAGTTTTTA AGAAACCCTC GAGCTGGTTC 2460 CAGGGTGGCT GCACCCTGTC ACTCTCCCAT CAGCAAGGCA CCAGAGATGG AGTTTCTCTA 2520 CACACTGACT GGCATCTGAT GGTGTCCGTT TCTGAACTTT GACAGGTGTG CAGTGACACC 2580 TCACTGTGGT TTTAACTTGC ATTTCCCTCA TGACTAATGA TGTTGAACAT CTTTCCACGG 2640 GCTTAACTGT CATCTGTATA TGTTATTTGG TAAAAAGGTC TGTCTATATC TTTTGCTTGT 2700 TTGCTAATTA GGTGTGTCTG TTTTGTTTTT CTATTACTGA GTTTTGAGAG TTTTCTCATC 2760 TATTACAGAT AACAAATCGT CTTTGTCAGA TATGAAGCTT 2800
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