Tag | Content |
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EnhancerAtlas ID | HS048-16258 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr17:48205760-48206620 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr17:48205993-48206011 | GGGAGAAAGGGAGGCAGG | + | 6.35 | HNF4G | MA0484.1 | chr17:48205974-48205989 | TGACCTTTGACCCTT | - | 6.69 | NR2C2 | MA0504.1 | chr17:48205974-48205989 | TGACCTTTGACCCTT | - | 7.7 | Nr2f6 | MA0677.1 | chr17:48205974-48205988 | TGACCTTTGACCCT | - | 7.82 | Rxra | MA0512.2 | chr17:48205974-48205988 | TGACCTTTGACCCT | - | 7.95 | ZNF263 | MA0528.1 | chr17:48206039-48206060 | GAAGGAGAAAGGAAGAAAGGG | + | 6.19 | ZNF263 | MA0528.1 | chr17:48206246-48206267 | GAGGGTGGGAGAGAAGGGAGA | + | 6.21 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCCTCTCCTT CCAAAACTGA GCCTAGAAAA ATTAGACACC AAACCCGCCC CCACTCTCAC 60 TCCCACACAC ACCCCGCACA CTCTCTCACA CACACACACA CACACACACA CACACACCCC 120 CATTCAGCCA GGTAACTGCA CAAGGGTGGG ATTGAACCGG TTCCTCTGGA TACCCTTCCC 180 CCCAAGGCTT CCAATCCTGG AGAAGGAGCA CCAATGACCT TTGACCCTTC TCTGGGAGAA 240 AGGGAGGCAG GTGAGCTCAC AGCCTCTTGG GACCCAGGAG AAGGAGAAAG GAAGAAAGGG 300 CGCACAATTC CTGGGGAGGG AGCGGGAGCG GGAGCGGAAG GAAGTGAGGA GTAGGAAGAA 360 GCAGAGACAG ACACACAAAC TGGCGGAGAG TCCACAGGGC TGCTGAGAAG AAAGAGATCA 420 CACCGAGAGT GGGGCCACGG GAACTGGCAC TGGGAACAAG GGCTTCCGCC GCTCTAAGTG 480 ACGCCCGAGG GTGGGAGAGA AGGGAGAAGC CCTTCGGGCA GGCGATAGGA AAGGGCCCCT 540 GAAGAGGAGA AAGCGACAGA GAGAAGTGCA ACTGGGAGAG GCCGGGAAGA GGTGGATGGG 600 AAAGGAGACT AGCGGTCGGG GAGGCAGTTG TGGAGCCAGA GAGGTGGTCC CCCCTTCCCA 660 TATCGCCGGC CGTCCACTGG CCCCAGGCTT GGGGTAGTCC TCAGGAGTCG GGCACCCCCT 720 CAAAGCACTG TTGGAGATGG GGTGAGGTTG GGGACAGGGC ACCTACTCCA CTCTCAGAGC 780 CCTTCTCCCC AGTCAGAGCC CGGTGGCTAG TTTCTCTCCA AACCATCAGC ACAACTCCCC 840 GCCGGGCAAG AAAGAGTTAA 860
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