| Tag | Content |
|---|
EnhancerAtlas ID | HS116-35451 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr9:131200720-131202000 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr9:131201074-131201093 | TGGCCACCAGAGGGCGCAA | + | 8.69 | | ESRRB | MA0141.3 | chr9:131201589-131201600 | TATGACCTTGA | - | 6.62 | | Esrra | MA0592.2 | chr9:131201590-131201601 | ATGACCTTGAG | - | 6.02 | | Esrrg | MA0643.1 | chr9:131201590-131201600 | ATGACCTTGA | - | 6.02 | | SOX10 | MA0442.2 | chr9:131201840-131201851 | AAAACAAAGAA | + | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 131200888 | 131201996 | | chr9 | 131201200 | 131201577 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I128438 | chr9 | 131200796 | 131201602 |
|
Enhancer Sequence | GAGGAGTCAG GCCGATCCAG CATCACCTCT GTGCTGGGTG ATCTTGGGTG GGTGCCATCC 60
CTTCCCTGGG CCTTAGTCTA CTCTTCGGTC ATTGTGGCTG GTTGGGTATA GAGTGGCCTA 120
GCCTGAGCCC GGCTCACAGT GAGTGCTCAC CTGTTGGGGC TGATGTGGTC ATCCCCGAAG 180
TCATTACCAG CCTCACCTTG CTGGTCAGGG TGGGCCCAGC CAGTCCAAGG GCTGCTGATG 240
TCCCCCGGCC CTTTGGATCA TCTCTTGTGC AGCTGAAACC CTGGCTTAGG GGAAGAGGAA 300
CCGCCTGGGA GGGGCTGGGG GAGATCCTGG GTTCCCCTCT GGCACTAACC AATGTGGCCA 360
CCAGAGGGCG CAAGGTGGCA GAGCCTGGAC TTGGCCAGGA TGCTCTCTGC TGGGTTGGGG 420
CCAACACCAG GAAGGAAGCA TGGGCCATAG GGAAGCTCCC ATTGGTGCTG GGGCAACCCG 480
CAGCAGCTCT GCGTCTTCTG CTCTTCTGAT GGGAACTGCA GGCCTCTCCC CTGGCCCCAG 540
AGAGTCGGGC TTCTGGGCCC AGCCGCTGTC TGTCATGCCT GCACTCAGGC AGCTGGAGGG 600
GTGGGAGGGG AGATGGCTCC TGGCCTTGGC CATGGCTGCT TTGGCTTCCA CCGTTCCTGC 660
TCCTCTTCCA TGTGGCCCCC TGACTTGGTT GTGTGAGCAC TCCAGTCCTG GCAGAGCCTG 720
ACAGGCACTC CCTGAGGTTG GGGTATCCCT TGGCTCTGTC CTGGGGTTGA GGTCCAGGAC 780
CTGGCACGGC TGTGAGAAGG ACCTTGGGCT GGAGCTGTGG ACTCGGTGCT TTATTCGTTC 840
TAAGATGAAA GTCATTCATT CTGGATGGCT ATGACCTTGA GCGACTCACT TCTCTCCAGG 900
CTCCAGGTGT CCCCTTCATT CATTTGTTAA CCTTTATTAA GCACCTCCCA TGGGCCGCAG 960
TCAGGCCCTG GGGATTCAGC AGTGAATGAA ACTGACAAAA CCCCTGACCT CATTAAACTG 1020
ACATTCTTTT TTTTCTTTTT TTTTTGTGGC GGAGTCTCAC TCTATCACCT TCTGTCACCA 1080
CACCCGGCCA AAACTGACAT CCTAATGAGG GATGCAGACA AAAACAAAGA AAGATCAGAG 1140
GGTGTGAATT GCTATAGAGA AAAATGAGAA GCGGAGAGAT ACAAAGTAAG ATCTGAGAAG 1200
TTAACACCTG AACAAAGACG CAGGAGTGGG CCAGGCATAG TTGCTCATGC CTGTAATCCT 1260
AGCACTTTGG AAGGCCTAAG 1280
|
