Tag | Content |
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EnhancerAtlas ID | HS060-19547 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr2:75038790-75040020 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF2 | MA0051.1 | chr2:75038912-75038930 | GGAAAGAGAAAGCAGAGC | + | 6.21 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAGGCAGGTT AGAAAGAGAT GATGAAGGTG TGGATGGTGG AGAAGAAGGG AGCGAGATGG 60 ATTTGAAGGG TTTAGGAGGG AGAAGCAACA GGGAGGAGAG GGGAAGAGCC CAATCCCAGC 120 CAGGAAAGAG AAAGCAGAGC CCTTGATGGT GGTTGTGGGG TGAGGTTCTT GGCTGCCATC 180 AGGGAGGAGA ACTTGAAAAC ATCTGGTCCA GTTGTGTGGC CTCTGCTACG GATGGACAGT 240 ACTGCCTGTC CCCTAAACTT TGTTCAGTGC TGAGACTTTT TGGAGGAACT TTTGGAAGAA 300 GATTTGAATT TTGAGTCTTA CAAAAAGTAC AATACTGTGC ATGTGTCCAT GCAGTCTGAG 360 AATCAGAAGT AAAACAACTC TTCTATCTGG GCTGTCAGAA AAGTTTTGTT TGAAAGTTCC 420 AACACAGTGC CTTTTCTTTT TTAATTTTTA TTTTAAGTTC AGGGGTACAT GTGCAGGATG 480 TGCAGGCTTT TTACATAGGT AAATGTGTGT TAAGGGAGTT TGTTGTACAG ATTATGTCAT 540 CGGCCAGGTA TTGAGCCTAG TATCCATTAG CTATTTTTCC TGATCCTCTC CTTTCTCCCA 600 CCCTCTGCCC TCCAGTAGGC CCCAGTGTGC GTTGTTCCCC CCTGTGTGTC CATGTGTCTA 660 TGTGACACAG TTCTTGGTAT TGCTAACAAA AATAAGCTTG AGTCCTGGGC TAAAATGACC 720 TATACAGATC CCTGACTGTC GAGAATTGTG AAGGATTTGA GATTTTGCTG TACTTGCAAG 780 CTAACAAGCC TGACTCACAG ATGCCAACAG AAGACAGAAG ACTCCTGGGT CAGAGGCAAA 840 GAACAGGTTA GTACTTAAGT AATAGCAGCA GCCTAGTATC CCTATTTTTG CATTGGTTCC 900 TCAAACCTCA ATTTCCACAG GGTGACAAAA GACCCAGGTA ATTCTTGCAC TTGTTGTGGG 960 TTACATTATA AGAGAGGAAT TCCAGGCTTA GTGAACTCAA ATCTTTTGTG ATGGGCCAGG 1020 TGCGGTGGCT CACATCTGGA ATCCCAGCAC TTTGGGAGGC TGAGGTGGGA GAATTGCTTG 1080 AGCCCAGAAG TTGGAGGCAG CCTGGGCAAC ATGATGAAAC CCCATCTCTA CAAAAAATAC 1140 AAAAATAGTC AGGGGTGGTA GCATGCACCT ATGGTCCCAG CTACCTGGGT GGCTAAGGTA 1200 GGAGGACGGC TTGAGCCGGG GAGGTCGAGG 1230
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