Tag | Content |
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EnhancerAtlas ID | HS092-09612 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr11:68316590-68317890 |
Target genes | Number: 14 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr11:68317470-68317480 | GCCCCGCCCC | + | 6.02 | Stat6 | MA0520.1 | chr11:68316750-68316765 | ATTTCTTTGGAAATG | - | 6.54 | ZNF263 | MA0528.1 | chr11:68316656-68316677 | TCCCCCTCCCTTTCTTCCCTT | - | 6.24 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 68316715 | 68316777 | chr11 | 68317308 | 68317583 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I068549 | chr11 | 68317141 | 68318630 |
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Enhancer Sequence | TCAGGTGATC CGCCCGCCTG GGCCTCCCAA AGTGCTGGGA TTACAGGCGT GAGCCACTGC 60 TCCCGGTCCC CCTCCCTTTC TTCCCTTTCT CAGAAGCTTT GCAGAACCAT GCTTCAGTCT 120 ATCCGTCTTT AATACTAACC TGCAACCTTA GAACTTACTC ATTTCTTTGG AAATGAGTTT 180 TGTTGAGAAT GCTAATTGTT ATTTAAGACC TCAAGGACTA GGAGGGCCTA TGAGGAGGAA 240 GGTCTTTCAG GTGGTGCCCA GGGCAGGGCA TGTTCCAGTG AGGTAGGGAG GTGTGCCAGG 300 TGTGCATTTA TGTGATGGTG TCAGGGCTGG ATTTGTTGGT GACCCAGGCA CTGTGATCAC 360 TGTGAGTAAA CAGCTGGGTG TATCTAGTGG GTGTCCTGGG ACTTGTCTGT TGGCAGGGAC 420 CTTAAATTGG GACACCTGTT TCCTTTTGGG TGTGTCTTTG TAGATGTATC TTTTCCCAAA 480 AGAGGTTGAG GATTCTGGGG AAGACTGAGG ACAGGGAGGG GGTTATCACC TTTATATTGG 540 AATTATCATA GGGAGAGATT TATTCAGGAT GGTTTACTGG AACCAGTTTA TTCCTTTGGT 600 TGCTTCTGGG TTCAAGTTTA GGACCTGTCT GGTTTCCAAA GGAATCAGTG TGTTTCTGGA 660 GAGAGAGAGC GATAGGAGGT TGATAAAGGT GTAGGTTGGG GAAAGGTTAG TTAGAAACCC 720 CTAAATGTCT TTTGATTTTG TGGATCCACA GTCGGAGATG ACTACAGAAG TGGGCTTGGA 780 ATGTAGGTGC CTGTGAATAG CTGTGGAGAC AGCAGGAGTC TGGGATTGAT TAGTTCGCCG 840 CCTGGAAAGT TTCCTGGTTT CTCCTGTAGT GGTCAGGAAT GCCCCGCCCC TCACATAGAT 900 GTTTACTCTC CTCTGTTTCG GGACATTATT ACTCAAAGAA TGGTCCTAGA CATCACTTGT 960 GAGCTTGTTA GAGATCTGTA ATCTCAGGTC TCTTCCTTGG CCTACTGAAT CAGAATATAC 1020 ATTTGAACAA GATTCTCGGA GAATTTGTGT GCACATTTTA AAACAGATAT TAAAATATGA 1080 AGTTGGGCCT CTACCTCTGT GGTGCCTACC TAATAGCTTC ACATTTTCCT TTGTTTGGTG 1140 TTTTCGTTGA GCAGCCAGAG AGTGTCAGGG TTTCTTCTCT GTTCCTTAAG CAAATTGTGT 1200 TTGATTTCTG CCCCCGCTGC CCGCCCTAGT CTCCTTTAGC TTTCCGGGCT TTTTATGAGC 1260 AGAGGAGGGG TGGTGTCCTT TCTAGGTAGT GAGCTGCCTT 1300
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