Tag | Content |
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EnhancerAtlas ID | HS060-19741 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr2:97628070-97629480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr2:97628170-97628191 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 | REL | MA0101.1 | chr2:97628343-97628353 | GGGGATTTCC | + | 6.02 |
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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 |
GH02I096962 | chr2 | 97628301 | 97629334 | GH02I096963 | chr2 | 97629400 | 97630716 |
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Enhancer Sequence | CAGGAGAATT GCTTGAACCT GGGAGGTAGA GGTTGCAGTG AACCAAGACT GTGCCATTGC 60 ACTCCAGCCC TGGCAACAGT GCAAGACTTC GTCTCAAGAA AAAAAAAAAA AGAAAGAAAG 120 AAAGAAAGAA AAAAAAGCCT ATAAGAACTA GGCTAATCTA CAAAGGGGTC CTGTCCCTGT 180 CCCTAAAACC ATCTTTTAAA GGGACTTCTG TGATGCTGGC TGTAATGTAT GTGCATTATT 240 AAGAGTCCTG AGGCGACTCT TATACATCTA ATTGGGGATT TCCTGTGCAG CCTAGAGCTG 300 AGAATAAAGG ATGATGTTGT GGTTTAAATA TCTGCCTCTG CCCCAGGCTC AGCACACACG 360 CAAGGTCTTT TAACTTTAAG AAATGGAGAA TTGAGGATGT CACCCATTCA AGATGCAAGC 420 CGATTGTTAG AGCATGCACA GATGCTTGCT CGGGACTGTC AGGGGTCCTT TCTGTGACGG 480 GCAGTTGTGG CAATTAGATG ACGCCTTGTC TGGCAGGCAG TGGTCAGCCC CCACCCTAAG 540 CATCCCTTCC TGACCTGCAC CCCCTTCCCT GGCCCTATTC AGGGATGAAG AGGCTGCTGG 600 CTTTGTACAC TGGTGAATGA CTTTTGTAAA GCAGAAAGCT GAACAGTCCC ATCCAGATGA 660 TCCCACATCA AAACCACCAC CTCAAAGTGG CTGCTGTCAA AGAGGCTTTC TCAAAGCACC 720 ACTAGAAAAC GTCATGCGCC CAGCAAATTA CCAGTGTTTT CAAAGCCAGG ACTACCTTCT 780 GCGTTAAGCT GGTTGCACAG ATAACTTCCT TTCTGTGAGG AGTTTCAAAA CATCCAAGCC 840 ATGACTTCCG GAATGCTGGA GGTACTCAGT AGAAAGATAC AGAGCTGGAA GAATTACTCT 900 TGCTGCAGAG ATTTTTAAAA AGGTTTTAAA AGGTTTGATT CCATGGCTAT GTAGCTAGTG 960 AGTGGAGAAC CTGGAAACCA AATCCATGCA CCTCAGCTCA GAGAGAAAGT TGCTTTCATC 1020 AAATATAATG CTGCCAAAGT GCTCTTGCCG AGGAAGGCCT TTGGCCCTAA ACACGCTAAT 1080 TAAATTCAGT CTACATGCCC CACCATGCCC ATCCACATGC TTCCTGCAAC ATCAGACAGG 1140 AAGCAGCACC TGCCTCGTGG GAGTCCATGT GGGACGTCAT GGCCGGCTGC CTTTCCCTGG 1200 AACTCTGGGC AGTGTGTGAG GAGCTCTCTT TGTCCACCTG GGACGGCTGC TCAAATCCCA 1260 ACACATTCCT AAACTTTCAC CATAAAAACT GGCACCAGTC AGGAGGCAGG GGTCCTTCTA 1320 ATTTGGGCCA GGCAAAGTAC AGCCTGCAGG CCGAGTCCTG TGTGGGGCCT GTTTCTGCAA 1380 CAAGGGCTCA CTGCAGCACA GCCATGCGCC 1410
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