Tag | Content |
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EnhancerAtlas ID | HS108-08051 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr11:72194500-72195210 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFG | MA0659.1 | chr11:72194637-72194658 | AGCTTGCTGAGTCAGTATTTT | + | 6 | MAFK | MA0496.2 | chr11:72194638-72194657 | GCTTGCTGAGTCAGTATTT | + | 6.27 | MAFK | MA0496.2 | chr11:72194638-72194657 | GCTTGCTGAGTCAGTATTT | - | 6 |
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| 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 |
GH11I072483 | chr11 | 72194197 | 72195590 |
|
Enhancer Sequence | CACCTGCCTT AGCCTCCCAA AGTGGTGGGA TTACAGGAGT GAGCCATCAC GCCCGGCCAC 60 GAAGTGATAT TTTTAACCCC ATATTATATG AGAGGAAGTA GATCTCAGAA CATGAGTGTT 120 ATAGTCCAGG TTTGCACAGC TTGCTGAGTC AGTATTTTAA CTCAGGGCTA TGTGTCTGAT 180 TCCAGCACCT CCCTCTGCAC CCGTATTAGA ACACATTGAG AAGGCTCCCC AAGCCATGCC 240 TCCTGTTGGC CTATCTCTCG CTGATCTGCT CCACAGTGGA ACCCTCACAT GCATCTACAT 300 GTTTCAGACA AGGCTCTGGG CACCCAAAGA TTAACAAGAC AGACCCAGAG CTTGCTTTCA 360 TAGAGCCCAC AGTTAGGGGG TGCTCAGGGA AGACAGCTGT TCAAACAACT CATTCCAGAA 420 GTTGTTATGT ACAATTGTGC TGACTGCTAG AAAGGAAAAG CACGGGACAG GAAGTTGTGA 480 AATAGTTTCA GGGAAGCCAT ACTTGTGTAG GAAGTCAGGT CGAACTTCAT GGGAAAGGGG 540 AATTTAGGCT GAGAGTTCAA AATTGAATAG CAGTTGATTG AGCAGTGAGT CATGGAGGAA 600 CTGTCTATAC TAGAAATGAA AAGGCTTTGA GGCTGGGAAA GAACTTGGCC CTAATGGTCA 660 GAAGGGTGAA GGGCAGTGAG CAAGGGATAA ATAATAAAAA TCATAATTCA 710
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