Tag | Content |
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EnhancerAtlas ID | HS108-38754 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr8:11645050-11646230 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr8:11645388-11645399 | CATGAGTCACC | - | 6.62 | JUND | MA0491.1 | chr8:11645388-11645399 | CATGAGTCACC | - | 6.02 |
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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 |
GH08I011787 | chr8 | 11645422 | 11645475 | GH08I011790 | chr8 | 11645681 | 11645830 |
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Enhancer Sequence | TTGTGAGAGT GAAGCTGAAA ACACTGGCTG ATATTTCTGG CTTTCCTTTA TTCTTCTCTT 60 TTTTTTTTTT TTTTTTTTGA GACAGGGTCT CACTCTGTTG CCCAGGCTGG AGTACAGTGG 120 TGTGACCATG GCTCACTGCA GCCTTGACCT CCCGGGCTCA GGTGATCCTT CCACCTCAGC 180 CGCCCTAGTA GCTGGGACTA CAGGTGTGCA CCACTATGCC TGGCTAATTT TTGTATTTTT 240 GTATAGAGGG AGACTCACCA TGTTGTCCCA GGTGGTCTCG AACTGCAGGC CTGAAGTGAT 300 CCACTTGCTT TGGCCTCCCA AAATGCTGGG ATAACAGGCA TGAGTCACCA TGCCCGGCCT 360 CCTCTGTCTT AAATGACTGA CAATTGTCAA CAGTGCAGAG AGCCACTTGA TGGCAGACCA 420 AGTCTCTTGT ACTGAAGGCT CCTCCCGCAC GGGGTGCTCT CCCTGTGTCG AGGGCTGTGT 480 CTCCCCCACC CAGTTCTCAC CACTTCGCTT ACTTCTTGCA CATGATCTAC AAAACAACAC 540 ATGAAGACAG GTCCTCAACC TTGTTGTCCT TAAGTTATAG ATGAGAAAAC GGAAGAGTCT 600 AGAGAGGCTG AGGACCTCGC CTAAGCTCAC ACAGTTAACA AGGGCCAGAG CCACACCGGA 660 GTCAGCTCTG GCTGCCGAAA TGTGCCCTAG GGGAGGTGAC TCAAACAGCA GACTTATTTC 720 TTATAGTTCT GGAGCCTGGG AAGTCCAAGA TCAAGGGCTG GCTGACTCAG TTCCTCTGCT 780 AGATCACACT GGGCATTAGG GCTTTATATG TGAATTTTAA GGGAACACAA TTCAGTCTGT 840 TACAGGCTAC AAAGGAATTT GGGAGAAAAT CCTCAACTTC TCAAAGGTCG TCTCCTCCCA 900 CTCTTGAAAA AACATACAAT AGCTTATAAA AACCTCACTT TCCCTTCATG AAGGCCTGGA 960 TTTAAGAAAA AATGAATAAA ACCTCAATTC CAGAATAGAC GATGGGAAAA TATTGAATAA 1020 TGGATTTATT TGTATTTAGA AGGGTAGAAG AGCATACTCA TGCACTTGTG TGTATATATG 1080 CACATATATA AAATATGTAA CATCAAAGAA TGTGGGCCAG GCGTGGTGGC TTATGCCTGT 1140 AATCCCAGCA CTTTGGGAGG CAAGGCAGGT GGATAACCTG 1180
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