Tag | Content |
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EnhancerAtlas ID | HS149-01052 |
Organism | Homo sapiens |
Tissue/cell | NKC |
Coordinate | chr7:2076990-2079300 |
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: 2 | ID | Chromosome | Start | End |
GH07I002037 | chr7 | 2076900 | 2078235 | GH07I002039 | chr7 | 2079127 | 2079493 |
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Enhancer Sequence | CCAGGCACGC CTTGCTCTCC TGGACTACAC AGATACTGTG CTTCTTACAA ATGGAAGGCT 60 TGTGGCCGTC CTGCCTTCGG CGAGGCACCA TGTTCCCAAC AGCATGTGCT CCCTACACGG 120 CTCTGTCACA TCTGGTAATC CTCATGGCGT TTCAGACATT GTATCACTAT TATATCTGTT 180 GTGGTCTGTA ATGGGTGGTC TCTGATCTTA CTACTGTCAT TGATTCTGGG GCGCCACGTC 240 CTGACTGTAC TTCCGACATT GCATCACTGT TATGTCTGTT GTGGTCTGTG ATCGGCGGTC 300 TCCGATCTTA CTGCTGTCAT TGATTCTGGG ACGCCACACA CTATGCTCCT CAGACGGCAA 360 AAGCTTCACC GACCAACGCT GCTTGTGTCT GGCTGCTTCA CTGACCAGCC ATCTCCCTCC 420 CTCCCTCTCC TTGGGCCTCT CTATTCCCTG GGCGACACAA CAGTATTAAA ATCAGGCCAA 480 TTAATAACCC TACAACAGCC TCTAAGCATT CAAGAGAAAG GAAGAGTCGC ATGTCTCTCC 540 TTTAAACCAA AAGCTAGAAA GGATTAAGCT TAGTGAGGAA GGCGTGCCAA AAGCAAAGAT 600 AAGCCGAAAG CCAGGCCTCT CGTGCCAAAC AGCTCGCCAA GTTGTGAATG CAAAGGGAAA 660 GTTCTTGGAG GAAATTAAAA GTGCTGCTCC ACTGAACACA CCAACGATAA GAAAGTGAAA 720 CTGTCTTATT GCTGATACGG AGAAGTCTGA GTGGTCTGGA TAGATCAAAC CAGCCCCAAC 780 ATTCCCTTAA GTCAGAGCAA GTTCCACGAG GCTGAGAGAG GTGGGAAAGC TGCAGAATTC 840 AAGTCTGAAG CTAGCAGAGG TGGGTTCATG AGGTTTACAT TAAGAGGCAG TCCCCATCAC 900 ATAAAAGTAC AAGGTGAAGC CGCAAGTGCT GACGGAGAAG CTGCAGCAAG TTCTCCAGAA 960 GATCCAGCTA AGAGCACCAA TGAAGGTGGC CACACTAAAC ACCAGATTTG CAGTGCACAT 1020 AAAACAGCCT TCTGCTGGAA GATGCCGTCT AGGGCTTTTA CAGTTACAGA GGAGAAGTCG 1080 ATCCCTGCCT TCAAAGTTTC AGAGGACAAG CTGATGCTGT TAGGAGATAA TGAAGCTGAT 1140 GACTTTTTTT TTTTTTTTTT TTTTTTTTTT TGAGACACAG TCTCACTCAT TCTGTCACCC 1200 AGGCTGGAGC ACGGTGGCAC AATCTTGGCT CACTGCAACC TCCGCCTTCT GGGTTCAAGC 1260 AATTCTCCTG CCTCAGCCTC CCAAGTAGCC GGGATTACAA GTGTGTGCCA CCACGCCTCA 1320 CTAATTTTTT GTATTTTTAG TAGAGACAGG GTTTCACCAT GCTGGCCAGG ATGGTCTCGA 1380 ACTCCTGCTG ACCTCAAGTG ATCCGCCCAC CTCGACCTCT CAAAGTGCTG GGATTCCATG 1440 CATCAGCTAC TGTGCCTGAT CTAAGCTTTT TATTTTGATC CAATTACAGA TTCACTTGGA 1500 GCTATAAAAA ATAATACAGA GATCACAAGT AGCATTCATC CAGTTCCTCC CAATAGCAAC 1560 ATCTGGCACA ACTACAGCAC AGTATCACAA CCCGTATGCC GACAATGATA CAGTCAAGAT 1620 ACAGCACATT TCATCACCAC AAAAACCCCT CGGGTTGTCC GTTCACAGCC ACGATTCCTC 1680 CTGTGCGTCT CCGTAACTCA CGGCAGCCAT CCACAGGCTG TCTATCACTT CAGCCTTTTA 1740 ATAACGTCAT GCAAATGGGA TCATGCAGCA CACGACCTTC AGGGACTGGG CTCTTCGCTC 1800 CGCTAAACTC CCTGGAGATC TATTCAAGTA TGTTTATCCA CAGTGAATTC CTTCTTAGTC 1860 CTGAGTATTA CTCTGTGTGA CGGAGGCACT ACCGTTGTTT AACCATCACC ACCGAAGGAC 1920 ATCAGAATTC TTTCCAGTTT TTGGCCATTA TGCAAAAGCT GCTAGGAAGA GTCCTCTGTC 1980 GGGTTTTGTC CGAACCTCGG TTTTATTTCA CTGGAATCGA CACCCAGGAA TGCGACTGCT 2040 GGTCATATGG GAGCTGCAGT GCAGTTTTTA AGAAACCCTC GAGCTGGTTC CAGGGTGGCT 2100 GCACCCTGTC ACTCTCCCAT CAGCAAGGCA CCAGAGATGG AGTTTCTCTA CACACTGACT 2160 GGCATCTGAT GGTGTCCGTT TCTGAACTTT GACAGGTGTG CAGTGACACC TCACTGTGGT 2220 TTTAACTTGC ATTTCCCTCA TGACTAATGA TGTTGAACAT CTTTCCACGG GCTTAACTGT 2280 CATCTGTATA TGTTATTTGG TAAAAAGGTC 2310
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