Tag | Content |
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EnhancerAtlas ID | HS101-18691 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr17:41543060-41544640 |
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) |
ZNF263 | MA0528.1 | chr17:41543233-41543254 | TTCTCCTTCTCCTTCTTCTTC | - | 6.47 | ZNF263 | MA0528.1 | chr17:41543230-41543251 | TTCTTCTCCTTCTCCTTCTTC | - | 6.67 | ZNF263 | MA0528.1 | chr17:41543224-41543245 | TTCTTCTTCTTCTCCTTCTCC | - | 6.7 | ZNF263 | MA0528.1 | chr17:41543227-41543248 | TTCTTCTTCTCCTTCTCCTTC | - | 7.12 |
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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: 2 | ID | Chromosome | Start | End |
GH17I043465 | chr17 | 41543160 | 41544056 | GH17I043466 | chr17 | 41544338 | 41544724 |
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Enhancer Sequence | TTTCAAAATG TTGCCTGCTT GCAATTTTCC CAGAATTTCT GAAGACAGAC ACATTTTTTC 60 TAGCCCTGTA ATCTTCTCAG ATTTGAGCTG GAAATCAGAA TAAGGACTGA GTACTGCCCC 120 TTTCACTCAC CAAACAGATT ACTTCCCTGC AATCAGTAAA CAACTTCTTC TTCTTCTCCT 180 TCTCCTTCTT CTTCTTTTTT TGATGGAGTC TTGCTGCAAT GCCCCGGCTG GAGTGCAGTG 240 GCACCATCTC GGCTCACTGC AATCTCTGCT TCCCGGGTTC AAGTGATTCT CTTGCCTCAG 300 CCTCCTGAGT AGCTGGGACT GCAAGCATGT GCCACCATGC CCAGCTAATT TTTGTATTTT 360 TAGTGGAGAC AGAGGTTTCA CCATATTGGC CACTCCAACT CCTGAGCTCA AGTGATCCGC 420 CCACCTCGGC CTCCTAAAGT GCAGGGATTA CAGGTGTGAG GCACCATGCC CAGCCCAATA 480 AACATCTTTT GCCTGCAGAG CTTGCCACGT GTTCCAGGTT TTTCTGAGTT AGTAGGAGTC 540 AGGCATCTCC TGAGTGACTT GGCCAGACAA GTGGATGTTA ATGAGTGACT GATGAGAAAA 600 CATGGGAACA ATTGCCCCTG CTGGATGTCC CAGTGTGCAG GAGAAGCTGT GCTGATATCT 660 GTGCTCAGGA CTCTTTGGAA TGCCATTATG ATTTTATGCA CCAAGGTGTA TTATTGTATT 720 GTAAGGGTTT CGGTTACCCT TAAGGGCTTG CAATTAATTT TCATTTGTCC TAGTCTTTTA 780 CAAGAGGGTT ACAAATGGCT CCTTTCCTAG TGTTCTACAA AAGTCTTTCC TTTTAAAATA 840 GTGCCCTATG ACACAGACAC GTGGTCCTAG AGCTTGTGTA ATTTTTTTTT TTTTTTTTTA 900 GACGGAGTCT CGCTCTGTGC AGTGGCCAGA TCTCGGCTCA CTGCAAGCTC CGCCTCCCGG 960 GTTCATGCCA TTCTCCTGCC TCAGCCTCCC CAGTAACTGG GACTACAGGT GCCTGCCACC 1020 ATACCTGGCT AATTTTTTGT ATTTTTAGTA GAGATGGGGT TTCACCGTGT TAGCCAGGAT 1080 GGTCTTGATC TCCTGACCTC GTGATCCGCC CGCCTCAGCC TCCCAAAGTG CTGGGATTAC 1140 AGGTGTGAGC CACCGCGCCC GGCCGAGCCT GTGTAATTTT AGGCTGGAGT CCTGCTAGCA 1200 CTGGAAAGCT TTGCCCTCAT TATAAATGGT CAACTTGGCC TTCTGATTTC TAAGTTCATC 1260 TCCTGATGAT TTTGGCAAGT ATCAATAAAT TATCTGGAGA CTGCTTACCA ACGTAGGGGG 1320 ACTGACATGA TTTAAAATCC AGTGTCTTCA CTTGAGGTTT GAGTGATCAA CCAAAGTTTA 1380 GCTGTCCTAA GAAGCCCTGC TTCAAAATCC TTTCCTGGCC GGGCGTGGTG GCTCAAGCCT 1440 GTAATGCCAG CACTTGAGGG GACCAAGGCT GGAGGATTGC TTAAGCTCGG AAGTTTGAGA 1500 CTGGCCTGGG CAACATAGTG AGGCTCTGTC TCTACAAAAG ATACAAAAAA TCCTTTCCAG 1560 CATGTTCTCA TCTTTCCTGG 1580
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