| Tag | Content |
|---|
EnhancerAtlas ID | HS048-05826 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr11:1354250-1355450 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr11:1354660-1354675 | GGGGTACAAAGGTCA | + | 6.07 | | Pou2f3 | MA0627.1 | chr11:1354564-1354580 | TTGTATGCAAATCATA | + | 7.38 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGGGATGGTG CCAAACCATG AGAAACCACT CCCACGATCT AATCACCTCC CACCAGGCCC 60
CACCTCCAGC ATTGGGGATT ACAATTTGAC ATGAGATTTG GGTGGGGACA CAGATCCAAA 120
CTATATCACC TATGAAAACA GAAGGCAGGT CAGTGGGCTG CAGAGAGAGA GTGGAGGGAG 180
AGGGCGGGAG GAAGGTAAGC GGCACTGGAG GCTTGGGGGG GTCTGTTTAT TATCTCGATT 240
GTGGTGATGC TTTTGGTGTC ATTTGCAAAA GGCAAAACAT ATCAACTGAT AACACTTTAG 300
ATAAATGCGG CTTGTTGTAT GCAAATCATA CTTCAGCTAG CTGCTGAAAG AGAGATGTAT 360
ACCTACAAAA CACCACACAC ACAGGAAGAT GCCTGCGTAG TTAAGGGACT GGGGTACAAA 420
GGTCAGCATT GAACCAGGGG CTGAGTTCTG CAGTAGGAGT GGGGCCCCAC AGCAGGAAGC 480
AAGCTGAATA TACACAGAGA CTGTTAGGAC CATGCAATGG CACGGGTGGC CACAGCCACC 540
AAGAGAGCCA GACCGGGGCC AGCAGTGCAG CAGGAGCTGC ACCAAGGAGC TGCCCTGTCG 600
AGGAGAAGTC TAGAAACTAC AGCCAAGGAC TGGCCCTGAA TATCTCATTC CGGAAGCAAT 660
TCCAAGGGAA GCCCAGCCTT GGCTGCTCAG CAAAGGTGAC TCAGAGCAGC GGTCCATCCT 720
GCCATGCACA GACTAGCAGC CCTCTCTGGG CAGAGGGACT TCAGGATGCA CCAAATTCAT 780
GCACTTGGTT CAAGCAGTTT CAGAAATTTG CAGTCTGCTT GCTCTCTCTC CCAGATGAGC 840
TTTAGGCAAA GATGTTCTTT TGAGGCACCA GATATGTCCT CTCCTTGCTC ATGGTCAAGG 900
TGGCTGAGAG CTGCTGCCGG GTACTGAAGC CCTTGACCAC ATGGGCACTG CTCATGGGAC 960
GTCCTCGAAG CTGTCCCTGA AGGACGTCCC TGGAGAGCCG CCAGGGAGCC TGTCCACCTC 1020
CTACCTGGCT CGGCCAGCCC CAATTTCAGC GCACAGGGTT CCTCCACCTC TCAGTTCTCA 1080
TGAATGATGC TGCAATGAAC ATGCAACATG GGTGTGCAAA TATCTCCTCA AGACCCTGCC 1140
TTCAACTCGA TGTCATTCCT TTTTATGGCC GGATAATATT CCGTTGGATG GATGCAGCCC 1200
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