Tag | Content |
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EnhancerAtlas ID | HS002-05645 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr2:191582900-191584210 |
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) |
Stat6 | MA0520.1 | chr2:191583762-191583777 | ATTTCCCAGGAAAGG | - | 6.15 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 191583077 | 191583133 | chr2 | 191583583 | 191583867 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I190717 | chr2 | 191582084 | 191584601 |
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Enhancer Sequence | TTGCGAAAGG AAAATATCTT GGGCTTCCAA AATCACTAAG GAAAACTCAA GCTGGAAACT 60 GCTTAGGGCA AACGTGTCTC GCATTCTATT CGCAGTCTCC CCTCTGCTCA CTGAGATAGA 120 TTCATATCTG ACTTGCCTCC TTTGGAAAGG CTAATCAGAA ATCCAGAAGA ATGTAACCGT 180 TTGTGTATCA GCTATCTGTG ACCTGGAAGC TCCCTCCCCG CTTCGAGTCT TCCTGCCTTT 240 ACTTCAAGTC GTCCTGCCTT TCCAGATGGA ACCAATGTAC TTCTTACATA TGTTGATTGA 300 TGTCTCATGT CTCCCTAAAA TGTATAAAAC CAAGCTGTGC CCCGACCACA TTGGGCACAT 360 GTCTTCAGGA CTTCCTGAGG CTGTGTCATG GGTGCATCCT CAACCTTGGC AAAATAAACT 420 TTCTAAATTA ACCGAGCCCT GTCTCAGACC TTCAGCGTTC ACAGACTATA CCGAATCGGG 480 CTGTTAATCT TTGAAAGTGA CTGGAACCCT AGAGATCTAA CCAAGATATT GTCAGGGAAC 540 TCAGCAGAGA GATCGTGAAC ATGGCAGAAC TGAAGGCAAG TGACTGTAGA AAAATAAATT 600 ATTTCACGCC TGTACTTCCT ACGAACAAGG ATTGTTTAGT AAACTAGATG TGGTAGCCAC 660 GATTTTCATG ATCAACAGAG TGGCAACAGG CAAGACTGAA TGATGGGGCT TTGGGGAATT 720 GCACTGGCGA TGAATCACCC TGAGATTATG CAGGTGGGGT TTCCCCTGAA GGGACTGGAA 780 CTGCTCACTG CCAGCTGTCC TCAGAAGAGG TCAGTCATGG GGCGGGAAAT CAGAATGCTG 840 GGACTAGAGT CAGTCTGACT GGATTTCCCA GGAAAGGTGA CTGTTGAGTC CCCAGGGCAC 900 TTCCTCCTGG AGGGGGAAGG ACCTGTGCCT GGCACTGACT TATTCTCTGT TTTCTGTTTC 960 CTTTCCATTG TCCCTGAACC TTTATTGTGA TCTGATCAGT GTCTCAAATA TTTTGACTTC 1020 TGATGTCCTG AGAGGAATTA AGGGGAAAGG TCCACAACCA ACCCCTGAGG CAAAGCAGAG 1080 GAGGGTTATG ACTTCTGTCC TCAGGCCACA GCAGTGGTGG CAGCCACAGG CACCAGCTGA 1140 GAACAGCTTT GCCCCAGAGG GACCAGTTTC TGAATACACA TGACAGAGCA CCTTGAGAGA 1200 GTCTCAAGAT TCTTTAGCAG AACAGGGGAC ACTGGGAGTA GGGGCAGAGG GCACTCATTT 1260 TTGTCAATAA AACTAGTGTG AGTCAAACTA CGATGGCTTC AGTTACACTA 1310
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