Tag | Content |
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EnhancerAtlas ID | HS050-59445 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr6:109750120-109751040 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Crem | MA0609.1 | chr6:109750522-109750532 | TTACGTCATA | - | 6.02 | FOXP2 | MA0593.1 | chr6:109750291-109750302 | AAGTAAACAAA | + | 6.62 | OLIG2 | MA0678.1 | chr6:109750272-109750282 | ACCATATGGT | + | 6.02 | OLIG2 | MA0678.1 | chr6:109750272-109750282 | ACCATATGGT | - | 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: 1 | ID | Chromosome | Start | End |
GH06I109428 | chr6 | 109749967 | 109750980 |
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Enhancer Sequence | GACACCATTA AACTTCCCTG CGCATCAAGA TATTATCTTT ATGAGATAGT CCAGAATAGA 60 TAGTTCTGAA AATGCCAATA AGAGTTCAAA TGAATGCAAC ACAAGGTAAT GTCCCAGTCA 120 TCTAGCAGCC AAACAGGCAA GCATATTTAT CTACCATATG GTTCTAACCG GAAGTAAACA 180 AATCCCTGGG TTTTATTCAG GAAGAAAAGT CCACCCTCTG TGCAAAAAAA ATCTATTGTC 240 TCTGGAACGC TTCATGACTA TCCTCTATCC TCACTGCCAC GAATTATTTC GGGCTTTCAT 300 TATGTCCAGC CCATGCTGCT ATCCAATCCC CTGCTCCCAA GCTCTCCCCT ACTCCAGCCT 360 GCTTCTGCAC AGACCTAAAC ATTTTTCCAG AAAAACAGAG GATTACGTCA TACTCTTTTA 420 TGGAAAGCTC TGTTGGTTCA GTTTCCTTCT GGATAAAATC CAACTCCTTC GTTCAGATGG 480 ACAATAAATC ATAACCCAGC CTCAATCTTT CTTTAGGATC TATTGGATTT TTTTTTTCCT 540 AATTAAAATC TGAGTACCCT TCCTATCTGG GGAACTCCTC ACAGGGTCCC ACCACCTTCA 600 CTAGAACCTA AAGGGGCCAG ATTCTCCCTC TCCCCATGCT GAGAGCACCA GGTTTTGGGA 660 ATATGACCTA GCCTTGCCAG CTAGGTGCTC CTGCCTGGGC TTAGGTCTCC AGGGAGTGAT 720 GAAAAGACAC TGAAGCATTG AACAGTTAAT CTCATTGAAG GTGGAGGTGT GAACAAGGGC 780 CAGCAGTGCC ATGGCAGTTC CCTGGCAGCA CATCCCTGCA GTGTGACTCT GGCCATGTCT 840 TCCTGCTGCC AGGCCTCATT GGTTCCCGCC TGTTTTCCAA AGCTGTTGTC CAGCTTTCCT 900 GTCAATTGTG AGATAACAGC 920
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