Tag | Content |
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EnhancerAtlas ID | HS050-17360 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr12:117295830-117296750 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REST | MA0138.2 | chr12:117296039-117296060 | CCTAGGACCATGGACAGCAGC | + | 7.44 | ZNF263 | MA0528.1 | chr12:117296576-117296597 | GGTGGAGGAGAGGGAGGGATG | + | 6.54 |
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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 |
GH12I116858 | chr12 | 117295961 | 117296110 |
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Enhancer Sequence | CCTGGGTGAC AGAGTGAGAC TCTGTCTCAA AATAAAATAG AAGAAGAAGA AGAAGTGGAA 60 AAGAAGTCCC CAGTATCCAA ATGAAGGCGG CTAAAAAAAA AAAAAAAAAA CGAACAAAAA 120 AACAGGAACT GGGCTCTAAG AGATGCGCAG GGCCAAAAAA AACCCAAAAA AAAACAAAAC 180 AGGAACTGGG GTCTAGGACA TGCGCACGGC CTAGGACCAT GGACAGCAGC CATTGGGGCC 240 AATGGGCTCC CCAGAGAAAC TTCCTACTCA AGCTACACCA ATAACAAAGA GAATAGGAAA 300 CGGACCCCCA AATTTGAAGA GATTGTATTT GTTTGTGGGA GATCAGGTGG GGGTGAGAAG 360 CTTCCAGAAA GGACTGGATC TCATTCGGAG TGTTGAAGTC CCGGGGGCTC CAGTCCCAGC 420 GGTTCCTGGC TCCCCACTCT CTGAGAGCAA GCAGCACCAT CAGAAATGAA GAGGCAAAAG 480 TCTCTTCATC TCATTATGCA GCAAGCTACC TAAACGATGA TCTCAGAGGC CTCCCTCTGC 540 TTGTACGGTC ACACACACAC ACACACACAC ACACACACAC ACACACACAC ACACACACTG 600 CTGTCTGCTG AAACCCGATA TGAGGTCTTT TTTAAAATTT ATTTCAAAGC CTCCCTCCCT 660 TTCTCTCTCT CTCTCTTCAC AGACGCTCTG CAGTGAAGCT AATCAAAATC AATGACTCCT 720 TGGCAGCCAG AGAAAAGTGG GGGAGCGGTG GAGGAGAGGG AGGGATGTTG CCAGCACTTT 780 GCACACTGTG GAAATATTTT TTAAAAAACA AGAACCACCC CACTATCTCA TGCAATCCAA 840 GTAATACAAC AGGAGAGATG GTGGAGACAA TATATACATA TATATCATGC TTCAATTTCC 900 TAATACAAAT GTCCATCAAG 920
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