Tag | Content |
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EnhancerAtlas ID | HS080-02593 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr1:179890530-179891900 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:179891129-179891150 | TCTTTCTTTCTTTTTTCTTTT | + | 6.11 | ZNF263 | MA0528.1 | chr1:179891669-179891690 | CTTTCCCCACCCCCATCCCCC | - | 6.21 |
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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: 2 | ID | Chromosome | Start | End |
GH01I179921 | chr1 | 179890421 | 179890570 | GH01I179922 | chr1 | 179890681 | 179890950 |
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Enhancer Sequence | TTTCTTTTGG CAGTGTAAAC AAGCAGTTAC ATTAAATACG TAAAGATAAT GCATTATTCT 60 GCTATTTTGT CCTTATCAAG ATCATGTAGT AAAATTTTGT GGTATAAGAG GATAGTGTTT 120 TTCCCTAAGG AAGAGGATTT TATTGGCATT AACCACCAAA GATGGGGTTC CTGAGCCTGG 180 AAAACCAAGC TGAGAAGGCT GCCATTGACT GGAAAAGGAG GAAATTCCTC CCTTGAATGC 240 CCTCTTTCTG GCCTGGATTC TGAGAATTCC TTGTGTGTTT AAGGACCCTT GTGGGTGGTA 300 GAGAAACTAG TTCCTGTCAC CTGAGCATAA ACAGAAGAAC CCCTTTGTAC TCTACACCCC 360 AGACATAATG AACTACTTGC AATTTCCTAA ACACATCATT CACTTGTCTT TTGCACATTC 420 TTAGACTCTT GGAATACTTC ATTTCCTGCC CTCTCGCTTT CTCCAATCTC ATGTTCTGCT 480 AATTTTTATT TGTCCTTAAA GTCTTCGTTT TCTTAGGGCA GCACTTCAGT GAAATCTTTC 540 ATAATTCCCT TCCCCCAGAT ACTATTTTAG GTGCCTCCTG TTTTTTTTCT TTCTTTCTTT 600 CTTTCTTTCT TTTTTCTTTT TCTTTTTTTG GTAGCTTAAA CAATAAGACC TTTATTGTTA 660 CAAAACCCAG CAGCGTGAGG AGTTCCTGGG TTGGGTGAAT TAGAGGCTGG AAAAATTCAT 720 CGCAAGCATT ACAAGATAAC CAATGATACC CCTGATGAAA GAAAACCTCT GCAAACTGCT 780 AGCTGAAGCC AGCTCCTGTC CTTTTATCCA AAACTGGGTA GTGTCCAGCC AAACCATTTT 840 GGGGGTTGAA TGAGTCACTT CAAAGGGCTC AAATGACTGG TGAATCTTCC AGATAAAAGG 900 AGAGAACACA GACTTTCCTG CGCATTTTAA AGTGACTGAG GTGCTCCACA CTCTGATTTA 960 TCCTTTATTA CCCTGTGGCA GCATTAGCAT ACCCCTGCTA CCACATGCAT CTTGCAAGCA 1020 GTGATGTGTC ATCAATATAT GCACCGTGGC AATCACAGAA TGCTCAAATA TTTATTGAAT 1080 AAAAAGAGCA AGCCATACCT AATTATAGCT AGGTAAGTTG CATCTTAGTG TTTTATTTGC 1140 TTTCCCCACC CCCATCCCCC ATTACGCCTA AGCCCTATCT AAAAGTTGTA TATAACTCAT 1200 CTGGGTTTAG CAATGCTATG AATAAGGAAA AACAAAGAGG ACCAATCTAC GCCGTGGAAG 1260 GGAAATGCAC TTCTCTGATA GAGACAGTGA TCATTACAGG TCCTCAAGGG AAAGGTGGAA 1320 TATCAAGGGA AAAGACTGGG AAGCTGTGAG GTCTTTCCAC AGTGATATTT 1370
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