| Tag | Content |
|---|
EnhancerAtlas ID | HS098-57682 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr9:90872760-90873980 |
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 | chr9:90873036-90873057 | TTAATGCTGATTCTGCATTTC | + | 6.56 | | MAFG | MA0659.1 | chr9:90873036-90873057 | TTAATGCTGATTCTGCATTTC | - | 6.68 | | MAFK | MA0496.2 | chr9:90873037-90873056 | TAATGCTGATTCTGCATTT | + | 6.44 | | MAFK | MA0496.2 | chr9:90873037-90873056 | TAATGCTGATTCTGCATTT | - | 6.63 |
|
| | 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 |
| GH09I088257 | chr9 | 90871951 | 90874154 |
|
Enhancer Sequence | GTGTCTGGAT AACACAATGA AAGCATGCTT GCCTGCTGGA TTGTACAGAC CAAGCCCCTC 60
AGCATGCACA AATGGTTATC TTCAGTCACT TATACTTCCT AAGTTACCAG AATAACCTTG 120
CACTCTCTCT CCCTTTGGCA ACACAAACCT CATAGATTGG AAAATAGTCT TTTCTGCTGT 180
CTTAATGCTT GCTTGCTTTC TATTCAAAAA CTACTGCATG ACTATACAGC ATTTGAAACT 240
CACTGTCTGA TTGGAATTTG GGAAACATTG GCTTTCTTAA TGCTGATTCT GCATTTCCTG 300
CTGAAATTGA GCTCTCAGCT TTGAGCAGTC CCACTGAAAC CAGGGGCAGC CAGCCGGATT 360
CTCTGCAAGT CAGGAAATGA GAGCCAGACT CCCTTGCTTG TCTCTATGGA CACTGGAGTC 420
GGTTTCCCTT CCTGGGCAGA TGAAAGGGTG AGGTCATTGC ACATGATTGA GTGGTGGAGA 480
AACTCAGCCT TCTAGAAACT AAGACCAAGC AATCATCTCA CAAGAAAACA TTTTGGAAGC 540
TAGGTTTTCA TCAACAACAT TAAATAAATC ACTGGTTTTT AAAGACCGGT AAACCCCAAT 600
GGCAGTCTGT CTGGATTTGT TCTAAAACTT AAAGCATGAG TTTTGCTTGT AAATGAGAGT 660
TCCCTGAAAT GCCAGCAAAA AAAAAAAAAA AAAAAAGCAA ACCCAATCCT TTGGGTAATA 720
GGAACCACAA CAAGGAAAAA TAGGAACCGC AACAAGGAAA AACATTTTTT TAAATAAATA 780
AAACATTTCA TGTTTATCCT CAGCAATTTC GTGTTTAAAA GAAACAAACT CTACAACTGC 840
TCAGCATTCT TCACAAGGAA GGTGTGCCTT CAGCCTCCCG GAAAAGTCTC TCGGCTGGTA 900
TGACCTGGCC TGTTGCCGGG AAAAAGTGAG ATTTGGCAGA CACGGGCGTC GGGACAGCCT 960
GCATGGTTAC TGGACTGCAA GGTCTGGCCC CGTCAAAGCA GACAGCTCTA TTATCCCCAC 1020
AGCCTGCAGA ACTGGGGTCA GGCGTGTCCT GATGCTGGAT CTCTGCCCTC CTTCTCCCGG 1080
TTCTCACCCT GTAGGTGTCG GATTTGACCA TTTGCACAAC AACCCTCACG TTGTCATTCC 1140
CAGATCCTCA TTGGTGCATT GTTCTTTTTG TTTATAGTAA ACTTTATTTT TTTAGAGCAG 1200
TTTCAGGTTC ACAGCAAAAA 1220
|
