| Tag | Content |
|---|
EnhancerAtlas ID | HS108-41618 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr9:131417660-131418810 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr9:131418777-131418788 | CCTTCCCGCCC | - | 6.62 | | IRF1 | MA0050.2 | chr9:131417795-131417816 | AAAAAAAAAGAGAAAGAAACC | - | 6.56 | | ZEB1 | MA0103.3 | chr9:131418387-131418398 | GCGCAGGTGGG | - | 6.62 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCGCCTGTAG TCCCAGCTAC TAGGGAGGCT GAGGCAGGAG AATGGCATAA ACCCGGGAGG 60
CGGAGCTTGC AGTGAGCAGA GATCGCGCCA TTGCACTCCA GCCCGGGCGA CAGAGCGAGA 120
CTCCGTCTCC AAAAAAAAAA AAAAGAGAAA GAAACCAAGT AGCGCCGAAA CCAAGTAGCT 180
GGCACTACTA CACTCCAGCC TGGGCGACAG AGTGAGACTC TGTCTCAAAA AAAAGAAAAA 240
AAAGAAGGCC GGGCGCGGTG GCTCACGCCT GTAATCCCAG CACTTTGGAA GGCCGAGGAG 300
GGCGGATCAC GAGGACAGGA GATGGAAACC ATTCTGGCTA ACACTGTGAA ACCCCGTCTC 360
TACTAAAAAA TACAAAAAAA TTAGCCAGGC GTGCTGGCGG CCGCCTGTAG TCCCAGCTAC 420
TGGGGAGGCT GGGGCAGGAG AATGGCGTGA ACCTGGGAGG CGGAGTTTGC AGTGAGCCGA 480
GTTCGCGCCA CTGCACTCCA GCCTGGGCGA CAGAGCGAGA CTGTCTCAAA AAAAAAAAAA 540
AAAAGCCTGA ACGCGGTGGC TCACACCTGT AATCCCAGCA CTTTGGGAGG CCGAGGAAGG 600
AGGACAGCTT AAGCCCAGGA GTTGGAGACC AGCCAGGGCA ACACATGGAG ACCCCATCTC 660
TACAAGATAA TAAATAAATA AACAGCCAGC GTGGTGGCCC GCGCCTGAGG TCCCAGATAC 720
TCTGGATGCG CAGGTGGGAG GATCGCTCAG CACCGGGGGC TGAGGCTGCA GTGAGCCGAG 780
ATCGCACCAC TGCACTCCAG CCTGGGCGAC AGAGCGAGAC CCTGTTCAAA AAAAAAAACA 840
CAAAACAAAA CCAAAAAAAG TTGTTTGAAA TGCTTAAAAA CTACAGTTCA CACAAAATCC 900
TTCAAAACGT GGGATCCTTG GAGGTGTTTT GTTTTTCCAC TTTTTGTTGT TAAAAAATGG 960
GCCGAAAGTA TCCTCTGGGT CAGTTTCTGT GGAATAAACT GTAAAGGCAA ACGGTGGGAC 1020
GCCCGAACCC GCCCGGCAGC CACGGTGGGA CGCCCGAACC CGCCCGGCAG CCACGGTGGG 1080
ACGCCCGAAC CCGCCCGGCA GCCGCGCTGC GACCCCGCCT TCCCGCCCGC GTCGCTCCGC 1140
GCGGGGCCCG 1150
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