Tag | Content |
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EnhancerAtlas ID | HS180-50227 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr9:130338000-130338980 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Stat4 | MA0518.1 | chr9:130338619-130338633 | CTTCCAGGAAGGGG | + | 6.29 |
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| Number of super-enhancer constituents: 13 | ID | Coordinate | Tissue/cell |
SE_09759 | chr9:130337879-130339132 | CD14 | SE_23282 | chr9:130338049-130339039 | Colon_Crypt_1 | SE_26528 | chr9:130337898-130339044 | Esophagus | SE_31422 | chr9:130337892-130339080 | Gastric | SE_33582 | chr9:130337963-130339059 | H2171 | SE_34621 | chr9:130315344-130339309 | HeLa | SE_41594 | chr9:130338007-130338931 | LNCaP | SE_47474 | chr9:130338046-130338372 | Pancreas | SE_50184 | chr9:130337947-130339149 | Sigmoid_Colon | SE_52507 | chr9:130337997-130339028 | Small_Intestine | SE_55718 | chr9:130334592-130338872 | u87 | SE_63440 | chr9:130298563-130342452 | NCI-H69 | SE_67516 | chr9:130334592-130338872 | u87 |
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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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Enhancer Sequence | GTTTCACCAT ATTGATCAGG CTGGTCTCAA ACTCCTGAGC TCAGGTGATC CGCCCGCCTT 60 GGCTCCCACA GTGCTGGGAT TACAGGCGTG AGCCACCGTG CCTGGCTGTG TGAAACATGG 120 ATTTTTTTCC CGCATCTTGC CCCACCAAGC AGCATTCAGC CTTCAACCTC AGCTAATTAC 180 CCTTCATCAG AGAGGACATT TCTGCACCCT GCCCCCCTAC TAGGTCAGGC CTGCCATTAT 240 TATCACCCCC TCCCCAGTGT CCTAAACTCC TCCTTCATGG CAAGCATCAC ATTCAACATG 300 ATTTTGTGTG TGTGCAATTA TCTGTTTAAA TAAATCTTTC TCTCTGAGGA CCAGGACTGT 360 CCTCCTTCGA CATGACATCA CTAGCGTCAG TCGCAATGGG AGCTTGAGGG AGCACGTATG 420 ATGTGCAGAA CACTATCCTG GGCACTGGAG GGGAACGTGA CAGTGAGGGA CCCACCTGGT 480 CCTTGGGACC TCACAGGTTT GTTCATAGAC CTATACTGAA ACACTCATGC CTGCAGTGGC 540 CATGACACAT CATGGGGTAC AAAGTCCCTT CTATAGTGCA TGTGGGCCTC TGCTACTGTG 600 CAGAGCTTCT GCTTGTAAAC TTCCAGGAAG GGGGTGCCTT ACCGCCTTCC CAGGCACAAA 660 TTCCGTGGTT GGATCCAACA GCACTGAAGT CAGGCAGGGG GCCGCTGAAG TGCCAGCAGA 720 CAGGCAGGGA GTGAGAAATA ACTTCAGGAT GATAAAGATA ATGGAAGCGC CCGTTCATTG 780 CAGGCTCCTG TGCTCAGTTC AGTGCTTTAT AGCTTCTGCC TCATTGAATG GTCACAACTT 840 TTGGGGAACA CCCACTTTAC AGGAGAGAAA ACTGAGGCTT CATGAGGTAT AAGTAAGAGA 900 TGAGGATGAG ATCAGGCACA GTGGCTCACG CCTGTAATCC CAACACTTTG GGAGGCTGAG 960 GCAGGAGGAT CGCTTGAGCC 980
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