Tag | Content |
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EnhancerAtlas ID | HS108-00141 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr1:3826910-3828390 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZEB1 | MA0103.3 | chr1:3827019-3827030 | CCCACCTGCGC | + | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH01I003910 | chr1 | 3826913 | 3828381 |
| Enhancer Sequence | CCGAGAGTCT CCCAAGGACA ATGGAGAAGC AGGATGCGCG GGCTCAGAAG CAATGCGGCC 60 CCCCAGCACT GCATGCCCAG CCACCCCAAC TTCTAGGCAG CTGCAGGCTC CCACCTGCGC 120 AGAGAATAGG CTGTTCACCT GCAACGGCGG CTGGCGCCGG GGGAGGTGGG CGTTCTGGGA 180 GAGGAGGAGC CCCTGGCTGC ATGGCTGTGC CGTGGGTGGT GCCGTGGACC TGCTGGTGGC 240 CGAGTCCCTC TGAGGGCTGC ATGTTTTGAG GGGACCCTGG CTTTGGCCTG GCATGGACCC 300 TCTTGCGCAG ATCATCTCGT GATTCTCCTG GCAACCCTGT GAGACGGACG GGTTCTTTCA 360 TTGCCCACTG TTGGCACCTG GGGAGATGGA GGAGCACAGA GGGGACACAC CTTGCTCAGG 420 ATCACACAGC AAGGAGGTGC CAAGGTCGAG TTGGACCTGG ACTCCCCACT TTCACGGCCA 480 TGTGGGTCTC TGCAGGGCAC CCTTCCTGGA GGAGGACCGG TGCAGACCCC TGTTGAGTAG 540 GGGACAGCCG CCTGGAGAAC CACCCTTGGC CGCCTTAGGT AGGTGCCAGC GCAGGTGTCT 600 GCAGTCCTGA CGCCAGGGGG CAGGATGAGA CAGGGGAACG AAGTCGGTGC GGCAGGCGTG 660 GCGGCCTCGC CGGTCTTTTC CTGGGACGCT CTCAGGATGG CTCTCGGAGG GTGCCCGGGC 720 GGCAGGCAGG GCTCAGAATG CGGCTCCGTT GCTCACTAAC GGCCTTCAGA GTCTTCTGAG 780 CAGTCCAGGA TGGGGGCAGC AGCTGCCTCT GTAGAGAATG TGAATCTTTG GCTTCTCAGG 840 TATCCAACAC CTTGGCAAGC ACCAGGGAGT GAAATCACTG AATTAAGAAT GTGTTTGTGA 900 GAAGTGGCAG CTGCTTCCCG CTGGGGCTCA GGGAGGGAGT TGCGGGCTGG GCCGGGGGCT 960 GCTGAGCTCC GTGTCCACTG CTGTCTGGTC TGGAAACAGC GTGAATCCCG GTGACCGCCG 1020 CTCCCTCCCA GGCTGTCCCG GCAGGTTCTG AGCTGGTGAG AGGGATTTCA GGGTGGTGGG 1080 TGCTGTGCTG AGGCTTTGCT CCCCTGCTGG GTTGAGTGTC TGCAGCCGCC CCCACATCCC 1140 CCGCTTTGCT AGTCTTTTCC TTCACGCAGC CTTTGCTGCC CAGGGGGACC CACCCCAGCT 1200 GTTCTCGGGA GCCCAGCCCC TCTGCAGAGT TCTTTAGGCT GCTCCTACCC AGAGGGACCT 1260 TCCCAGCAGG TGGGCCTAGC TTCAGATCTC CAAGTCTGTG GTGGCCCCCA CCCACTGAGA 1320 CCCAGGAGGC CCAGCGGGAC TTGGGGTTCA GGCCAAGGTT TGTCTGGCTC CCTCCTTCCT 1380 CCTTCCAGGC ACGTTGTCTA GAAATCACCT CATCTCTTAC AGGTCACCAG TTAATTGTGT 1440 TGGAGGAAGC TCTGGGATGT ACGGGTCTGA ATGGCCCACA 1480
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