Tag | Content |
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EnhancerAtlas ID | HS048-00452 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr1:18454530-18455220 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Hnf4a | MA0114.3 | chr1:18454963-18454979 | TCTGGACTCTGACCCC | - | 6.58 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 18454800 | 18455095 | chr1 | 18455105 | 18455200 |
| Enhancer Sequence | GAGATTAGTG ATACTCTTGG ATATTATTAT TATTGTTGTT AGCTAATACT AATGGATAAC 60 TTACTACTCG TTTATCCAAT ATTTATTGGT CTCCTACTGT GTGCCTGGGA GGTGGTTCTG 120 AACAGGAGGC AAGAGCTTTG GCTGCATGGG CTGACATTCT GGTGGATGAG ACAAGAATAA 180 ACATATGGAT AAATAACCTA CTTCTGGCTG TGAACCTCTG TGAGGGGAGT AAAGCAGGGC 240 TGTGGGATTG TGAGGGACTC AGGAGCAGAG CAGCTTCTCT AGATTGGGTG GTCAAGGAAG 300 GCTTCTGGGA GGAGGTGCCT TATGAGATGA GTAGGGAAGA AAATAGCAGG AAAAGTCTGG 360 CTCAGCCCTG GTGTTGGCGT CTCCTGGCCA GGGCGTATGT TTGTAGCTGA TTCCTTCCCT 420 GGATGGGGCC TTCTCTGGAC TCTGACCCCA TTGCTGGGAA TCTGTCACTG GTAATTCCCT 480 CCCACCAGTG ATGCAAGCTC AGCTGGCCCA TGACAGTGTC CCCTTTGGCC CTGGGGAGAC 540 CCGAGGAAAG AGCATTCCAG GCCCCAGGGA AGCAATTCTA GACCTGTTCT TATTTAATTC 600 TTGCAGAACT CCACGTGGTG GGCCCTACTG TATTCTCCAT TTGCAGATGA GGAGACTGAG 660 ACTCAGAGAT GAAACTCCCC TAGTGGGTTT 690
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