| Tag | Content |
|---|
EnhancerAtlas ID | HS118-19746 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr9:131814370-131815780 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF9 | MA0653.1 | chr9:131815666-131815681 | AGTTTCGCTTTTGTT | - | 6.52 | | Nkx2-5(var.2) | MA0503.1 | chr9:131815134-131815145 | CTTGAGTGCCT | - | 6.14 | | Zfx | MA0146.2 | chr9:131814645-131814659 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | 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 |
| GH09I129051 | chr9 | 131814117 | 131815639 |
|
Enhancer Sequence | CTGGGATTAT AGGCGTGAGC CACCGCGCCC AGCCTGTAAT TTATTTATTT TTAAGGTGTG 60
GCCTCACTCT GTTTTCCAGG CTGGAGTGCA GTGGCGTGAT CTTGGCTCAC TGCAGCCTCC 120
ACCTCCTGGG TTCAAGCGAT TCTGTCTCAG CCTCCTGAGA AGCCAGAGTC AGAGGTGCCT 180
GCCAGCACGC CCGGCTAATT TTTGTATTTT TAGTAGAGAT GGGGTTTTAC CATGTTGGCC 240
AGGGTGGTCT CGAACTCCTA ACTTCAAGTG ATCCACCCGC CTCGGCCTCC CAAAGTGCTG 300
GGATTACAGG CTTGAGCCAC CACACCCAGC CTACAGTGAA TATTTATTAT TGCAATATCA 360
GGAAAGGAAA ATGAAGTTAA AAGGCTAAAA TTTAAATTTT TGTGGCCAGG CACGGTGCCT 420
CACACCTGTA ATCCCAGCAC TTTGGGAGGC CGAGGCAGGA GGACCAGTTG AGCCCAGGAA 480
TTTGAGGGGA TGGGGCCACT TTTGGCAGCG GAGGTAGAAG GAGGAGGGAG GATTTCTCTG 540
CCTATTCCTC CCTCACCCTT GCCTTCATTC CTCTACCCGT GTGTCCCATT GGCCGAGAGC 600
CAGCTGGCAG GGGGACCTGG GAAACAGGTT GCAGAACAAG GGGAGGGCTG TGTCTGGCAC 660
AGCTGGTAAC AAGTTGAAGG TGTCCATGCT CTCTGTCCCT GCTGGGGCGT GAGCTCAGGA 720
TGTGAAGGTC AGGGAAATAC CTGAGGTTTG AAGTGACTCA AACCCTTGAG TGCCTGCAGT 780
TGCAGCTGCG TCAGGTCCTG TCTGCGAGTC GGCAGGGAAC GGGCACCTGT AGGAGTGTGT 840
TGGTGAGGGG GACTCAAGGG AGGTAGCTTT ATTTCCCAAA TTGTATTTCT TGCTAAAAAC 900
TATATCTGAA AATGATAGAA TTTGCATTGT TTTCCTTGTT GTGAAAGCAA TTACATATTC 960
CTTATCAAAT AATGAAAAGT ACAGAAATAG GAAAGAGAAG GGGGTGTAAA ATAGTCTGAT 1020
CCCAGACTCT GATCAGACAG CCCATGGTTG TGTGGTGTGG CACCCTCGGC CTCCTGGAGC 1080
ACTGGCGCTC TGTGGGGGCG CCAGCACCAG CTGTTCAGGC CTGGTCCATA GTAGGTGCTC 1140
AGTTAATGAT CTGTGGCATA TCTACATGCC AGGACGCCTA CAACCTTACA ATCCTACAAG 1200
GGGTGCCTGC AGCCCTTCAT CCAGGCATCA CCACTTTCTA TTCCTTCAGG CATTTTTTTC 1260
TGTCTATTGC TATAATTTTT TTTTTTTTTG AGACGGAGTT TCGCTTTTGT TGCCCAGGCT 1320
GGAGTGCAGT GGCGCAATCT TGGCTCACTG CAACTTCTGT CTCCCAGGTT CAAGCGATTC 1380
TCCTGCCTCA GCCTCCCGAG TAGTTTGGAT 1410
|
