Tag | Content |
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EnhancerAtlas ID | HS180-50131 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr9:126982770-126984260 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr9:126983886-126983901 | ACTGGCCTTGAATTT | - | 6.42 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_09686 | chr9:126975691-126986742 | CD14 | SE_59974 | chr9:126945864-126986288 | Ly4 |
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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 |
GH09I124220 | chr9 | 126982280 | 126986678 |
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Enhancer Sequence | AACAGAAGAG AAAACTGAGG CATGGAGAGA TCAAGTCACG CAACTAGTAA ATGGCAGAGC 60 TGATCTGAAC CAAACTGTTG GGCTCCTAAG TCCCACCCTT AACCATTACA CTATGCCCCC 120 TTCCCATTTC ACCATCAACA GCTCTCTCCC CAGTCAGCCT CACTCAAGCT CAACGCCGCT 180 CTCCTTCTCA GAATTTTACC CAGGGCCTCC AACTCAGATC AATAACCAGC ATCTGCTCCC 240 AAGGGTAACA CCTGACACCT GACTTCTCAC CTTTTTCCCA GGCCTGGGGC CCTGGAGTCA 300 CCAGGGTTTG AGTCCTGACT TTGCCCATTT TCCAGCCGTG GAGCTTGTAG AAGGCACTTC 360 TCTTCCTAAA GCTTCCGTTT CCTCCACTGC AGCATGGGGA GGGAGGCTTG TCCTAAATTT 420 GTTGGCCTGT GGTGGAGACA ATTTGAAGCC ACACTCACGG AGCAGGTCAC ACTGGAAGCG 480 TATGTGTGTT CAGTGTGTTC CCTGGAAGCG TATGTGTGTT CAGTCCATGA AACTCTGATC 540 AACAGTTAAT CATATCCCCA GAGTCCTGGG GACACTGCCA AGTATTTCTT TGCTTTTCCC 600 AACACGTTCT CAGCCCCTGC AGTGTGCATC GTGGGCAAGT GTGCTGGGCA GTCCTGTGTG 660 CTTGCCCCTC TCCTGCAAAC TGCTTTTCCC AGTTTCCTTT GCCAACTGGC TTCCTGTTAG 720 GTTGGGCCAA GGGGAAGCAC TGGCAGGAGA TTGGAGCATG GGAGGAGGGG ACAATCTGGG 780 TATTTCTCCC TCCCTCTGCT TAGGGAGGGA GTGGGAGTGG CCTTTCCCCA GCACAGGCTG 840 CTCTCTTCTG TGTCTTTGGC TGCTCTAGAA CCACCCGGTC ATCTGCAGTT CCAAGTCTCC 900 AGGTGGCTCT GATGATTCAA GTTACTCCTG GGCAGTATCA CTGCCTCTTC CTTTTGTCTC 960 TCCACCCCTA AGTGGTAGCA CCTTTTGCCA TTGTGGAACA AGCACTTGCC TCACCATTTG 1020 CTGTTTGGCT TTTCAGCTCT TCCCTCTTCC AGGTAACCAA TTCCCTATAT TAAATTTCCT 1080 CTGTTGGAAA TACCTAGAGT GGTTTCTGTT TTTCTGACTG GCCTTGAATT TTACAGCGGG 1140 CATCTTTGGC CCAAGAATTG TCTCTCTCTT CTCCACTTAC AGAGTTTTTA TCCTAGAGGG 1200 GCAGCATCAG ACCCCTGAGG GCATGTCACA GGCGGGACTA ATGGAAGAGG CTCTAGCTCC 1260 TTCTAGCTCT TTGCAGTAAA CTTACTACAA GACAGCAAAG CTTTCTCATG CTACCACTGA 1320 CTGTCTCTTG TGACATAGGT GGAGTAGCAT TGCGCTACTC TGCTGTCTCT CTACTTCACC 1380 TTCCTGAAGA CTTATTGCAC AAAGGGTGGG TGGAGCTGTC GAGAACCAGG GGAGAGAAGA 1440 AAGTAGTGAA GGGGGCAAAG AAGCCCTTCC TGGCACACTA GCAAAGTGCC 1490
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