Tag | Content |
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EnhancerAtlas ID | HS180-01660 | Organism | Homo sapiens | Tissue/cell | Small_intestine | Coordinate | chr1:51415770-51416750 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:51416433-51416451 | TCTTCCTTCCTTCCTTCC | - | 10.05 | EWSR1-FLI1 | MA0149.1 | chr1:51416429-51416447 | TTTCTCTTCCTTCCTTCC | - | 6.22 | EWSR1-FLI1 | MA0149.1 | chr1:51416437-51416455 | CCTTCCTTCCTTCCTGAA | - | 6.47 | FOSL1 | MA0477.1 | chr1:51416630-51416641 | AGTGACTCATG | + | 6.14 | NKX2-5 | MA0063.2 | chr1:51416679-51416689 | ACCACTTGAG | + | 6.02 | Zfx | MA0146.2 | chr1:51416662-51416676 | GAGGCCGAGGCGGG | - | 6.01 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAAAGTGCTG GGAATACAGG TGGGAGCCAC CACACCTGTC CCAGATCACC ATTTTATAGA 60 CTGAATAAAT GAAGCCTACA AAAGGCAAAT GACTTTCTCA AAGAACCACA GCTAAGAAAA 120 CCTAAAACAA AACAAAAAGA CAACAGCTAC AGCCAGTCTA CCTAAGTACA ATGTTCTAAC 180 AACTGCCCCT TATGGAGGTG TAACCACATA TTGCCACCTA GCAGGCATTC AAACACTCCA 240 GCCCTCTGAA TTTACTAAAA CCTAGAAAAG TACTGATTTC ATGGGGGGAG CGGAGAAATA 300 ACTTTACCTT AAATGCCCAG ACAGTAAATA TTTTAGGCTT GTAAGGCCAT TAAAATCTCT 360 GTCTCAACTA CTCATCTCTG TCACTCTAGC AAGAAAACCA CCACAGATAA AGGTAAATGA 420 ACGGGTATGG CTGTGTTGCA ATAAATCCTT ATTTATAAAA ACAGGCAGCT GGCCTGCAAG 480 ATATAGTTTG CTGACCCCTG ATCTACAAGG TCCATAAAAC CAGTCAGGCA AACAACAGGC 540 ATCAACTCTA TCATACTCAG CTAATCTAGA GACACTATGT GCATTCCAAG GCTTCTGAAC 600 ACCTGTGAAC ACAGAAGCAT GGCACTAAAT GGTAAACAAG GAATAGACAA AGTGCCACCT 660 TTCTCTTCCT TCCTTCCTTC CTGAAGATCT ACTACATGAC AGCCAAGCAC TGCTAATTTA 720 TTTTATACGT AAGTTTCCTC ATTTGTAGAA ATTTCTAAAG AGCAGTTTTT GTTTTCTTCA 780 AGAACTCCAA GCTGACAAAT TAGCTGGAAA ATGAACACTC TTATATGTAC CTGGATAAAA 840 TATTTGTTTC AGCCAGGCAA AGTGACTCAT GCCTGAAATC CCAGCACTTT GGGAGGCCGA 900 GGCGGGCAGA CCACTTGAGG TCAGGAGTTC GAGACCAGAC TGGCCAACAT GGTGAAACCC 960 CATCTCCACT AAAAATATTT 980
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