Tag | Content |
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EnhancerAtlas ID | HS050-15692 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr12:48430680-48432160 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF2 | MA0051.1 | chr12:48432045-48432063 | TATTTGGTTTCACTTTGG | - | 6.4 | ZNF263 | MA0528.1 | chr12:48431450-48431471 | GGAGGTGGAGGAGAGGGAGGG | + | 7.95 |
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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: 1 | ID | Chromosome | Start | End |
GH12I048036 | chr12 | 48430576 | 48432183 |
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Enhancer Sequence | GCCTGTCCAA GTGAGTGAGG GGATGTGAGA TGGTCTCAAG CTCTGGCGAA AGGCCTCCTC 60 ACCTTATTGG CTGGGGTGTA GGATGGTACA TGGAACTGAG GGGCGTGGGA GGTGGAGGAT 120 GGTCCTCTGG TGAGAAGGGG AATGGCTGAC GAGAGATAGG CATCTCCACA CTACCAGGGC 180 CAGAGCTGTG GGGCTTGGAG ACTCCATTCA AGAGTCCTGT AGTTCCCTTT CCTAGCCAGA 240 CCCAAAGGAC CTTCTCTGGT GCTGAGATCT TCAGAGAAAT GCTCAGAGCT CCTCAGGAGA 300 CCTTGCTGCT AGGGTTTGGT CACTATTCTC TGTTGCAATT TGCCTTGAGA GAGCCCAAGT 360 GGGTGCCTCC CCTCTGACTT AGATCTAGAA AGCCAGGGTT TTGAAGCCCA AAGAGGCTAG 420 CCTCTCTTTC CATGAGAGTT GAGCCCATTT TCTGAGCAGA CACAGGAGAG CTGTTGGCTC 480 AGGGCAGGCA AGGAAAGGCT TCGTGAGCCA AGGGAAAACA ATTAGGAGTA ATTACCATCA 540 AGAGAGGCCT CCAGTGAGGG GTGAGGGTGG GAAAGGCTGT CTGTTGAAGA GGAAGATGAA 600 AGTGGCAGAC TGATTTTGGG GATGAAATAG GAGAGAGGGC AGGAGGAGGG GTTGAGCCAG 660 AATGTGTGCT GTCTTCCTTC TCCAGTAACA GGGCGGCACC CCTCCCCCTC AGTCTGTAGC 720 TGAACTAACT TCCGCCTCTA CAGGGCAGAG GGGCTCAGTG TATGGGGGTG GGAGGTGGAG 780 GAGAGGGAGG GCACAAGGCT CTGCATTCCT GACATTCTCA AACCAGTAGG AATGGCCGAG 840 GAAACTCCAT GCTGAAGAGA CAGAGCGGGA GACACAGACC GAGGCAAAAA GATAAAATGG 900 AGCACTAGAA ATGTTTCCAA ATTCCTACAA GTATAGGTCC CCAGGTCATC CCCAGAGAGG 960 GCCACCGCCT GGCACACTGG ATTCCTGAGG CCGTCGGTGG GGACAGGCTG AATCCACTTG 1020 ATGTCTCCCT ACCTCACCAC CTTCAATCCC TAGCCTTCCC CTTTCTGGAT TCAGACTAGA 1080 GACCTTGAGG GAAAAGAGGT TTGCTAATGT GCACAGCCAA GAGCAGAGGA TGAAAGGAGG 1140 AGCCAAAAAG AAAAAGGACA GACAGGAAAG GGTTGTCATG GGAGAGGTGA GGAGAATTCC 1200 TTGTTATCCC TGTCTGGAGA AGCCAAGAGA AAGTGAACCA ATGACAGAGG GACCTCCTCA 1260 TTCCCCTTGA CTTCCAAACT ATGATGAAAA GACAAATAAG GACCTCAATG TTGCTCACGA 1320 GAGAAAAGCA GAAGATGACT TTGAGAACTT TGTCAAAGGT TCTCTTATTT GGTTTCACTT 1380 TGGTCGAGTC CCCTTGGAGT CTAGGTCAGG CGTTTTTCCT GTTGAGATGA AGTCGTGTGG 1440 CCACGTGGAA GCAGCAGATT CTAGCACTTT TAGGGGTCTT 1480
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