| Tag | Content |
|---|
EnhancerAtlas ID | HS108-41056 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr9:100921530-100923270 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PLAG1 | MA0163.1 | chr9:100922125-100922139 | CCCCCTTGGGCCCC | - | 8.42 | | ZNF143 | MA0088.2 | chr9:100923130-100923146 | CAGTGGATCATGGGAG | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATGTTGCCCA GGCTGGTCTC AACCTCCTGA TCTCAAGCAA TTCTCCTGTA GCTGCCTCTC 60
AAAGGTTGGG ATTAAAGGCG TGAGCCACTG CCCCTGGCCT CACATCACCC TCTGATGCTG 120
CCCATTCATT GCTGCCCTAC AGGATCAAGG CCAAATCCTT TGGCTTGGCA TTCAAGGCCT 180
CTGGCTGGGT CTCATTCCAT ATTCCAAGAT TCTTTTCTTC TAGCTCATCT AAACGGCACC 240
TTCCAGCTTC CCCAGCACCT GCTCTTGCAT CTCCAGCCCT CTGGCTCTTT GCCCGTCCCT 300
CTCCTTCTGC TTGGCTTGCC ATTCCCATGC CCCCACCTCC TGTTCCCATC TCCACAAATC 360
CAAATCCGCC CCTTCCCTAG CTCCCAAGCC ACTTCCTCCA GAGAGTCCTC CTTGATATCC 420
CAAGTAGCAG AGATCTCGCT CTCCTCTGTT CCCTGACAGC CACCTCTCCC CTTGCCTTTA 480
GCCCTTGACA CTGTCTACCC TGATTTGGGG TTCAGGGTCA GTTCTCATTT TCTCTGCTGG 540
CTTGGAGCTT CCTCAGAGAA GGCTCTGCTC CAGGAGTGTC CAGCACAGTG TCTATCCCCC 600
TTGGGCCCCC ACCTTCCCCA CTTAGGGGAA GGCAGGTTTG GCTGGGCCTA CGCTGGTCAA 660
GATAAAGAAG ATGCTCACCC AGCCCACACG GCTGACCCAT GAGGCTCTTC TCTGTGCTCA 720
ATTCCTCAGA ACGAGATTAC ACTGTGTGAC CTCAGGCAAG TCATAGCGAT AAGGGCCTGA 780
CCCCTGAGGC AAGCCCTTTA GACAGCACCA GGTAGCACGT CAGTCTTGCA GGGGCTTGTG 840
TATCCCATAA AGCTCAGAAA TTCCAACTCT CCTTTCGGGA GCTTTGCCCT AAACCCTGGC 900
TGCATTTGCC AGAGCTACAG GAAGCTGCAC AGAATGTAGG GATGGACTGA CTAATTAATG 960
CCCATGTGAT TCCAGAAAGG ATTTAAGAAG ACTCACAAAA ATAGAACACA AGATAGAAGG 1020
AAATGAAAAA GCTACAAGAG AAAAAATAGG GACACAAGGA AAATGCAGGT AAAAAGAGAT 1080
CACCTGAAAC GCAGGAGGAG TTAAGCTAGG TGTGCGGCCA GGTCCACCAC ACAGAGGAGG 1140
TAGACCTCAG ATTTGGCTCT GAGCTTCCTA GTGGCCAATT CAACAAGGAA AAGAGAATCA 1200
GAAAGGGATT TATTTGGTGT CTATAAGATA AAAGCCACAA GTTGCTAAGG AGCAGCACAT 1260
CTTTTCTCTA TAGTGAGTTT TGAGAGAAAT GGGTACTGGG GGTCCCCTTG GAAAGAAACA 1320
ACAAGGACAA ATGACCTCCC TAGGGTCTTG GCAACTTGGT GGCAGTGGAG GAGCCACCTT 1380
GGGCCTGGGC TCGGGTGGGA AAGCAAGGAG CAAATCAGCA GGCTCCGCTC CAGGCCCCCC 1440
CACTCCTCCC TCACCTTGAG CAACTGCTGG GGGTGGCGGG AGTGCACCTG TCTGTGGCAG 1500
CTGGTGATGC TCACCAGACG TCCCATTGCT CCCCTCATGT CCAGGCCCCT TCCAGTCAGG 1560
CAGCCATAGC ACACATCACT GCCTCCTATG ACCCGTTAGC CAGTGGATCA TGGGAGGCAG 1620
TGATGTGTGT CACTTCCAGG CCAAAGCACA TGAGACCTGC CTGTGACCCT CTAGGACTCT 1680
CGTCCTTGGC CAAAGGGATG AGAAGGGTGC ATGTTTCAGA TGGTGCATCT ATAAGGTAGT 1740
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