Tag | Content |
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EnhancerAtlas ID | HS105-51059 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr20:62641670-62642630 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr20:62642441-62642452 | AATGAGTCAGA | - | 6.32 | GFI1 | MA0038.2 | chr20:62642108-62642120 | TGCAGTGATTTT | - | 6.11 | Myod1 | MA0499.1 | chr20:62642580-62642593 | TGCAGCTGTCCCC | + | 7.12 | Myog | MA0500.1 | chr20:62642579-62642590 | CTGCAGCTGTC | - | 6.62 | Tcf12 | MA0521.1 | chr20:62642579-62642590 | CTGCAGCTGTC | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH20I064009 | chr20 | 62641065 | 62643254 |
|
Enhancer Sequence | GGTGAGTCTG GCGGGCTCAG GGCCACCAGA GCCCAAAGTG GCCAAGGCCT GAGCCCAGGT 60 TCAGTGTCTG GAAGTGATGA TACAAGTGGA GCATTGAGCT CACTCAGGCT GCAATTTCTG 120 GGAGCAGAAG GCCCTGTGGA ACCCCAGGAT GCCGTTCTGT ACATAGCCGC TAGGCAGGGT 180 GGTCAGTGGC CTCAGCTAGC TGTGCTCTTA ATGGACGTGC AGGGAGAATC TTAGCTCATA 240 CCTGACCACT GCAGAAAATT CTCTGTTGGG CAGTTGCTCA GGGGCCATTT CCTCTCAGCA 300 GCCCAGAGTT TGTCATGGGA GCCGAAGGTG GCAGCGTGAT AGAAAACATT GCTTTCTGTC 360 AGCTCCGCAT GACTGCTCTT TGCCTCTAAG CTAAGTGGGA TTTCTTTGGT TTTAAGCATT 420 CCAGTTCACA GCATTCTGTG CAGTGATTTT TAGTCTTGGT TTTATGATAC CTAGTATGTC 480 TTTAATTATC CTAAGGGGTA TTGTGAAATT CTCCAAACAA CATTAATCTT ATTTTATTTA 540 CATAAAAATG AATAAAGCCC GTACACATCT TAGGGATGGA ATGCTGCAGA ACCAAGGGTC 600 TGGGAACTTC AGGAGGCTGA ACACCCTTCT GTGTGTTTAG CCTGTGAGGG CAGTAGCCTC 660 ATCCTGCTCG TCTGTGCCAG CCCCTGGTAT CAGGTCTGGC GTGCTGTGTG CCTGGAGGCT 720 GTGTTTGTGA ACATTCAACT GAGAATCTTT TGATGCTCAC GAGAGTCACT AAATGAGTCA 780 GAAGCATAAA GGAACAGTTG GTCAGGTGAG AAGTGCTGCT GTGGACACTT CTCAGGCCAT 840 GTTCAGATGG TTCTCGAGAG CTAAGAAAGA ACGTGGTGGC CAACGCTGGA GGGTGGGTCG 900 CTGTCTGGCC TGCAGCTGTC CCCCCAGCAC AGTGTCCTCT CCTTTTTCTC GTGTCCTCTC 960
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