Tag | Content |
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EnhancerAtlas ID | HS108-41876 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr9:139233170-139234160 |
Target genes | Number: 19 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXC1 | MA0032.2 | chr9:139233422-139233433 | TATGTAAATAT | + | 6.62 | HSF1 | MA0486.2 | chr9:139233643-139233656 | GAATGTTCTGGAA | - | 6.62 |
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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: 1 | ID | Chromosome | Start | End |
GH09I136339 | chr9 | 139233761 | 139233910 |
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Enhancer Sequence | CGTGGGCGCG GACGCGGCGG GCAGACCCGG CCCGGCCCAC AGGCTGAATT ACCGCGGCCC 60 AGGCGAGGTG GCCTGGGTCC CATCCCCTGC TCTGCCACTG ACCATGCTGT GACCCAGGAG 120 TGGCAACGCC ACTGTGGGGA CTGAGCCAGA CAGTGTGGAC ATTGGGCCGG CCACTGACCC 180 CTGGCACAAG CGGGTGGGGT CCCCCTCCCA TCCCTCAATT CGCCACCCTG TTGCCCCCAC 240 CACCCATGTA TGTATGTAAA TATCACTCTC TGGAGAGAGA CAGGCTGGCA AACCACAGGC 300 CCCTAAGTAC TGTCTTGTGT GCAGGTCTGG GGTGGGTGGT GGCCGGAACA AGGGGCTCAG 360 AGCCACAGGC CTGTGGCCTT TCACAGGCAG CAGAGAGGAG AGGTCTTTTG AAAGGCTGCC 420 CTGCCTGGAG GCTTAAAAGT GGCCCAAGGT TTTCCTTTGT GGCGTGGTGA GGAGAATGTT 480 CTGGAATAGA CAGAGGTGCC GGTTGCACAG CATGAATGTA CAAAATGCCA GTGGATCGTC 540 CACGTGAAAA TGATCAAATT CCTGTTAGAC GCATTTCCCT CCAATATAAA AACAACCCCC 600 TCACCCAGTG ACTTGGAGGG TGCCCGTAAG GGTGGAGGGA GTGCAAGGGA GGAGGCTTGC 660 CGGCCGCCAG GGGGCGAGCG AGGCCAAGGG CCCAGAAACT GCCCGCAAAG GCAGAGCCGG 720 CCACAGGCCA GGTTGCTTGG ACTCTGCGCT AATCCTTTTA ATGGGAAGGA AAAAGGCAGA 780 GCTGATTGGG GCTTATGCTT GAAGGTGGCA GAATTTGTGG GAGGTCCAGC TGGGGGCATT 840 ATCCTGTCAT CCGGCCAATG CCCCTTGGGC CTGGGGGCCC CTGATGACCC TCGAAGCCAG 900 GGTCATGCTG GGGCCGTGAC CACCAGGGGA GGGGCTGGGG CTGGGGGCTG GCCTGGAGAG 960 GGCGGGTATG AATCTGGTCT CCCTCTCTGG 990
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