Tag | Content |
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EnhancerAtlas ID | HS050-48797 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr3:133778500-133779990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RELA | MA0107.1 | chr3:133778575-133778585 | GGAAATTCCC | - | 6.02 | RREB1 | MA0073.1 | chr3:133778909-133778929 | CCCCACAACACCCACAAACA | + | 8.21 |
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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 |
GH03I134060 | chr3 | 133779061 | 133779210 |
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Enhancer Sequence | GATATCATTC TGAATTCCAA CTGGATCAGG CCACAAAAGT AGGAGGTATG GAGAGCTATT 60 TTGTGGTGAC AACCAGGAAA TTCCCTAAAC GTCTTTTAAA AATACATTCC TGCTTGGTTA 120 TTTGCCCTCA TTTTAATGTG GAGGCAACAA TGAGAAGGAA AAGTCCCTGG CAATGGGCTC 180 CAGGGAACTT CGACTTCATG GTGGAAGCTG CAAATGCAGG CAGGTCCCAG CAGATGTGGC 240 TCCCTTCTCC CAGGTGCTTC CAGGCAGGCT GCTGAGAACC ATCTGCCCTG GGGGTCTTCC 300 AGGGACTCCT CAGACATGTG GGCTCCGGGC CAGCTCCTTT GTTGCCTCCC TACCCTGGAG 360 CTGCCTCCAC TGATAGAGGA CAGAAGATGG ATGTCTCTGG TCGCTCCAGC CCCACAACAC 420 CCACAAACAC AGGCTGCTAA TCCAGTCTTG GAACTGTCAG GAAAAGCCCA TTTTCATTTG 480 ATCCTTTGCA CAAATAGATT AGAGGCCACC GACCTTGACG TCTGAGCATT GTTCAGCTTG 540 TGTTAGAAAA CATCCATATT TAGGGCGGTT GGGAGAGGCA CGGAGGAGGG AGCAAAGGTC 600 CAAAACACTC ACTGAGAAGA CTTGACCAGG ACTGAACATT CACACCCAAG CTAAAGTCTG 660 AACTCTGAGC GCCATCCTAT GTCAAAAAGG ATTCCCTGTG GACCTGAAAC ACCCAAAACC 720 AGCAGCTACT GGGGAATGAA TGCTTTTCCA GGATCATCAG CTCCTTTTGG GCTCATCCCT 780 TCCATGCTGA CTGAGCTTGG GTGGCTGACC TTTTGTTTTC TTATATGTGG GAGGCAATTG 840 AGAGCAAGGC TGTGAGGCTG GAATTCAACC CCTCTCCCCA TGGCCCCAGG GTGTGTCCAT 900 GTGGGGCTGC CAGATACACA GGAAAGGAGA GAAGAGCTGG GAAATGTTGA CTCTGGATTT 960 TAGGCAGCCT GGGTCCTCCC TTTTTCCTAA ATCAGGACCC AGTCAAGTAA GGAGATTGCC 1020 TCTGACCATG TGCTGCAGCT TGACAGTAAC ATGACAATAG ACCAAAACCC ACAGTTACTC 1080 GAGGCAAACC TAGATTTTTA AGGGGAGTGT ATGTGGGTGG CCTTATTTTA CTGAGAAAAA 1140 CCTTGTTTTG TTTATATTTT TCCCCTTACT TTGCAGAAGA AATAAGATCC CTTCTACCAA 1200 GGTTGTCCGT GATTTCTACT TCATTACTTG ACTTGGAAAC TCTCCCAAGA GGGTTGATAT 1260 TCACAGTGTT GACATGTCGG TCTTGTTCTC CTGACCTTTA GCCTATATTG TTGACCAAAG 1320 CTGTTTAAAG GGCTCCCTGT GTGAAAGGAA GCTGGGGTCG GGTGATTCTC GGGAAGGCAA 1380 GAGAACAACA CCCCATCTCA TGACTAAATC AAAACTCAGC TCAGGACAGG AGGATCTAGG 1440 GCTGAGTGGC TGCAGCAGAG AGATGATCCC TAAGTGGAGA AGCGAGTCTG 1490
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