| Tag | Content |
|---|
EnhancerAtlas ID | HS053-07569 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr11:72194440-72195350 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
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 | | Nr2f6(var.2) | MA0728.1 | chr11:72194479-72194494 | CGATCTTTTGACCTC | - | 6.19 |
|
| | 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 | AGTAGAGATG GGGTTTCGCC ATGTGAGCCA GGATGGTCTC GATCTTTTGA CCTCGTGATC 60
CACCTGCCTT AGCCTCCCAA AGTGGTGGGA TTACAGGAGT GAGCCATCAC GCCCGGCCAC 120
GAAGTGATAT TTTTAACCCC ATATTATATG AGAGGAAGTA GATCTCAGAA CATGAGTGTT 180
ATAGTCCAGG TTTGCACAGC TTGCTGAGTC AGTATTTTAA CTCAGGGCTA TGTGTCTGAT 240
TCCAGCACCT CCCTCTGCAC CCGTATTAGA ACACATTGAG AAGGCTCCCC AAGCCATGCC 300
TCCTGTTGGC CTATCTCTCG CTGATCTGCT CCACAGTGGA ACCCTCACAT GCATCTACAT 360
GTTTCAGACA AGGCTCTGGG CACCCAAAGA TTAACAAGAC AGACCCAGAG CTTGCTTTCA 420
TAGAGCCCAC AGTTAGGGGG TGCTCAGGGA AGACAGCTGT TCAAACAACT CATTCCAGAA 480
GTTGTTATGT ACAATTGTGC TGACTGCTAG AAAGGAAAAG CACGGGACAG GAAGTTGTGA 540
AATAGTTTCA GGGAAGCCAT ACTTGTGTAG GAAGTCAGGT CGAACTTCAT GGGAAAGGGG 600
AATTTAGGCT GAGAGTTCAA AATTGAATAG CAGTTGATTG AGCAGTGAGT CATGGAGGAA 660
CTGTCTATAC TAGAAATGAA AAGGCTTTGA GGCTGGGAAA GAACTTGGCC CTAATGGTCA 720
GAAGGGTGAA GGGCAGTGAG CAAGGGATAA ATAATAAAAA TCATAATTCA TAGAGGTAAG 780
TGCAACTAAT GTTTCCACGT GTCTTATTCT AACCAATTCT GGTTAAGAAT ATGGGTTCTG 840
GAGCCAGACA GGCTGGGTTT GAATCCTAGC TCCACCATAT TGGTTGTATG GCACTGGGCA 900
AGTTCCACCT 910
|
