Tag | Content |
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EnhancerAtlas ID | HS048-30164 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr5:135429550-135431350 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr5:135430431-135430446 | TGGACTTTGAACTTG | - | 6.89 | Hnf4a | MA0114.3 | chr5:135430429-135430445 | GCTGGACTTTGAACTT | - | 6.88 |
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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: 1 | ID | Chromosome | Start | End |
GH05I136093 | chr5 | 135429548 | 135431175 |
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Enhancer Sequence | ATTCCATTTT AATCAGTAAT TGTTCATTTC CTGTTCCTTG GTTAATTAAA CAAAATTGCA 60 GTTTTTACAT CATAACTTCC TTAAAATATT CCATTTTAGA GACCTCTTGT TGTTCTTCCA 120 TTAGAACTGC CTCCATAGGT GTAATCAGTG CCTGTTGGGG ACATGGCTTC CCTCCTTAAA 180 ATAGCCTGTG AACTTTTTTT CTCCAAAACA TTGAGAGTTT CCTCTCCTGT TAAATTATCT 240 CCTGCTATTT AGTATCGTTG AGGAAAAGTC TAATACAGGC CTGATTTTTG TTCTTTTTTG 300 GGGATCCAGT TTTTTTCTCC AGTGCCTAGT AAGCACTCAG AAAGCAGTGC CTACGATTGG 360 GTGGCTCATG GGGCAGCTTC TCTCTTTATT AGAAAAAGAG ATATCTTACA AGTGGTTGCC 420 TCCACTGAGA TCAGTTGGAA ACTCCCCATT ATCTCATTTA TGTCCCCATT TTCTCCCTGC 480 AGCCCAAACA ATCAGCCTTT GGACTTTATC TAGGCTGTCA CAGATGGAGA GTCCCCCTGA 540 TGTCCGGAAT CATTGCCCAA CAGTCTGGTG TCTAATGTTC TAATGAAATG TCATATTTCA 600 TCATTTGTTT GCATGGATAT GTCTGTGAGA AAATGGTTTT GGGGGAGGAG AAATGATTCA 660 GTATAATAGT TAAACTGCTT AATTGCAAAC AATATAAACT CTGTTATTTT ATTTGATAGT 720 TATTGGGAAG CTCCAAGAAG GGCTGGACAA ATTAGAGAAG CAGGCTTAGA AAATGGGTAG 780 GAACTAATGG AGGTGGGATG GTAGGGAACT CCACTATGAA AACAGTCTGA TTATGACATG 840 TTGCCTGTTC TGCTGTTCCC AGACACTCAC CGTGCTGCTG CTGGACTTTG AACTTGGCTA 900 CTGCCACCAT AAATAGTCAC TGACTGTACC TGAATCTTTG TGCCACTGCC TGGCCTCATA 960 TGCAGCAGGC AGAGTATAAT TATTCCCCAT TTGGGCTTTC TCAGTGGCAA GGGGGCTCAG 1020 TCTCTCTCAA AGACATGCAG AATAAAGAAG TCTCCCCCAA AGAAGGGGGT TTTATATTCT 1080 GGGCAGCTAA AAATTGGCAT GTGTTATCTA GGCAAACGTC AGTAGACTTC TGATTTCTAT 1140 CACTAAGTAG CAGCCTTCGA TTCTGCTGGA GATTGTGATA CATCCCAAAA GATGACGAGG 1200 CAGAGGTTGT CGCTGCCCTG CTCATCCTCT CTGCACTCAC CCCTACCAGC AGAGGTGATT 1260 CTTTCCAACA CCTGCAGCTC TCTGCCAGCT GCAGAAGCAC ACTTGACCTC TCCCCGGGAC 1320 AAGCAGGAAG AGCCAGATAC CTGATGCCCC TTGATTCAGT TCTCATCCAA CAATTCGATA 1380 TGGCCATGAT GAATGAATAC CATAGCTTCC GTGTCCCACA GCTGGGGTAA CTCTGGGGTG 1440 TGTACTACAT TGTTTCCCAG CAAGATTAGT CCCAGCTGTC CACAGTGAGA AGTGGCATGA 1500 TAAGACACCC TTTCTTACCT GTCTCACTTC TGCACACCCC TACTTGTAGG CCTGCAGATC 1560 TCCTGCCAAC TAAGCTACTG GCACTTGAAT ACTTGCCTTA GGGTCTGCTC TTAGATTTGC 1620 TCAAACTAAC ACAGTTGGTG AAGCCCTGTT GAGTAGTCAA GAGTACTTGG AATAAAAGGA 1680 CAAGGCAGAA GAGTTCCTGA TCTTATTCTC ACTTCCCACT TAAAGTTTTT GAAGAAGTGG 1740 ATTATCCTGA AATTCTACCC TGCGTAAGCC CTTTGACCCA GTCTTTTCCC TCGTAGTTGT 1800
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