Tag | Content |
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EnhancerAtlas ID | HS048-20429 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr2:60667490-60668960 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr2:60668928-60668943 | AAGATCAAGGCCAGT | + | 6.03 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_09302 | chr2:60665482-60669657 | CD14 | SE_10188 | chr2:60665450-60669087 | CD19_Primary | SE_11372 | chr2:60663587-60688215 | CD20 | SE_59393 | chr2:60656758-60679029 | Ly3 |
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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 |
GH02I060438 | chr2 | 60665688 | 60668063 |
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Enhancer Sequence | TTGCACTGAG ACATAATCTC TGGTGTGTTC ATTCTCTTAC ATTTAGATTA ATTATAAAAC 60 ATTGTCACCA GAATATTAAA GTAATGTTTA ATACACAGAA GGGAATAAGG TACTCTGGAA 120 AATGCATAAT TTCCCTATGA TGATTTTGCC AGTTGCATGC AATATGATCT TTTGATTGCC 180 AGCTATAGAA ATATTGTGAC TAAGCTTTCA CTAGCTTTTT ATTTTTGCAA CCATCCTGTC 240 ATAGCACTTT GAAAACTGTA AGCTTGGCCC ATCAAAAAAA AAAAAAAAAA ACAACCAAGA 300 GTGCCCATGC TAAAGATTTC TGTCAGCTTG GTTCCAAAGA AGGGAGATGA TAGGAGAGGG 360 TGAGCCTTGT ACGGGCAGCA CCTTCCACTT CAGCAAGCCT AACACAGCTG GGTGGTGGAG 420 AAAGGATGGA CTCTTACCCT CTGTACAGGC CCAACACACA TGCACACCCA TACACACACA 480 CACACACACA CACACGTCCT TTGAACATGG GAAGGTGTCA ACATTCCTAA ATGGAAATCT 540 CAAGTCCTCT CACTTGCTTC AGATTTTCCA AGCTCTACTG CAGCCATACA CCCCGGAGGA 600 ATCATCTGAA TCAACACCGA GTCACAGCTA GCAGAACTCT CCTTGCTGGC AGTGGCTGAA 660 ATGGGACCAA CATTCCTCAG GGGGCTGCTC CTGGGGATTG GTTACCTCCC TCTAGATACT 720 GGGCTCCATC CTTGGCTGTG TTGGTTAAAA ACCAAGTGTC GTTACCAGCG GAGGGCTCCT 780 GTCCTTCGAG GTCTCTCTCC AGGTCTCCAC AGGTGAAACT TTTCCACGAT GATAATCATT 840 TAAAAAATAA TCACAGTAAT AGCAGAAGGA GCACTCCAAC CCATCCGTCT TCCCAGCACA 900 CTCACTGGGC AAGTTGGTAA CCCCATGCTT CTGTCACACC ACCAAGAATG CTGGTAGAAT 960 TCTCAGTGTG TTTTAAAACT AAAATTAATT TTTAAATGTG TTTTCTGTTT ATCCATGCCC 1020 CCTAATGGCA ATGCACCCAG CACCTATTAT CTTGTTTCTA TTCTCTTCAA GGCCTCCTAC 1080 GTCTCTCTGA CCTCTACCCT CTGCTCTTCG AAAATATACT GGATGTGAAA AGCCCTCTCA 1140 ACCCCAAAAG GCTCAAAGTC TTGTAGCTTA ATTACCTTTC CATTTGCAAC ACGGAGGCCC 1200 CTTGGGTCAG AATTCAATGT GATTTCCAGT AGGAGAGGGG ATAGGTTTAC TTGGCTCCAG 1260 CCCACCCCAC ATCTGTTCTA TAGACACAAG GACCCCCTAG GCCAGGAGAG GATATATGCT 1320 AACCTTTGCT GGCCTGGCTT TCTAGCCTTT ACCTTTAACT CCAGGAGAAG AGTGGGAGCC 1380 CAGAGTGAAT ACAGCTTCTG AGGATAAGAC TACAGAAACT AGAGGATAAT GACTATCAAA 1440 GATCAAGGCC AGTAATGTCA TTGAGATCGT 1470
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