| Tag | Content |
|---|
EnhancerAtlas ID | HS116-34446 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr9:34450580-34451920 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr9:34451284-34451302 | GTTCCCCTCCTTCCTTCC | - | 6.2 | | EWSR1-FLI1 | MA0149.1 | chr9:34451296-34451314 | CCTTCCTTCCTTTCTCCT | - | 6.84 | | EWSR1-FLI1 | MA0149.1 | chr9:34451292-34451310 | CCTTCCTTCCTTCCTTTC | - | 9.6 | | EWSR1-FLI1 | MA0149.1 | chr9:34451288-34451306 | CCCTCCTTCCTTCCTTCC | - | 9.72 | | Klf1 | MA0493.1 | chr9:34450852-34450863 | TGGGTGTGGCC | - | 6.62 | | RARA(var.2) | MA0730.1 | chr9:34451757-34451774 | TGACCTCTGAGTGATCT | - | 6.21 | | ZNF263 | MA0528.1 | chr9:34451292-34451313 | CCTTCCTTCCTTCCTTTCTCC | - | 6.1 | | ZNF263 | MA0528.1 | chr9:34451288-34451309 | CCCTCCTTCCTTCCTTCCTTT | - | 6.42 |
|
| | 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 |
| GH09I034450 | chr9 | 34450954 | 34451819 |
|
Enhancer Sequence | TAATTTTTGT ATTTTTAGTA GGGACGGGAT TTCAACATCT TGGCCAGGCT GTTCTTGAAC 60
TCCCGACCTG GTTATCCACC GCCTCGGCCT CCCAAAGTGC TGGGATTGCA GGCGTGAGCC 120
ACTGCGCCCG GCCAATTCAA TAAACCTTAA AATGCTCCTT CAGGTATTGT TCTCGATAGA 180
TGGGATGTAC TCTGCTTATA ACAGCCAAGA ATCTGATGGC TAAATCAGGC AAAACCAGGC 240
AAGGAGCCAC AGTCACTGGT CTTGTTTCTG CCTGGGTGTG GCCTCTTGTC ATATGTTTAG 300
ACTTAGGGCT GGAACGGTCA TTCAGAAAAC ACCATTCATA GCTGTATGTC CCCTCTTGCA 360
TGCACACTCA CATACCTCAC CGCCATCACA GAAACTTAAA ATTGACCTTC AATAACCAAA 420
CCATCCGATC CTCAATTTGC TATCTCTGAA TAACAATAAT AACAACAAAT ACAAGTACAG 480
ATTTGCTTGA ACTCTCTCCT GAGAATGTAA AGCCTAGGAG GAAACTCCTG CGGGCATGTG 540
TCTACCCTCT CTCCCAGGCC AGATGCTACA GGCCTCTTTC CTAGATGACT TCCCTACTCC 600
AGAGTCCCTC CCTGCAGCCA GAAGTTGATT TGGCTGTCCC ACAGTGAGGC CTGTGGATCA 660
TGTGCCAATT TCTAAACTCC AGAGCAGACT CAAATCCAGA GCTGGTTCCC CTCCTTCCTT 720
CCTTCCTTTC TCCTGCCCAG AAAGCCAGAT TCCCATCAGA GCCTATTTAA GAAACAATGA 780
CTTGGGACCC TGCTGAGCCA CACCTCTAGC TTCCTTCAAC CAGCACCTCT GGTTATCTGC 840
CTCAGCCCAA TTCTCCCCTT TCCACACGCT CTGGAGCTCC CTGAACCAGT TCTCCCAGGT 900
CTCTAGGAAG GCACGAAGCA GCTAAGCCCA AGAAGCTAAA TTTCCCATGT TCCCTTTCCA 960
GACACGAGGC TCCACCTGCC TTTTTAAGGA GGTGAGAGGG TCCCTGAGAC TAATCAGGTT 1020
TGAGTGAAGA AGCCTGTTTT CCATTTCTGC TCACTCTGGG CTATATAGGC AGTCAAGGGC 1080
AGCAGGCAGC TGGGGCTGGG AATGACTCAG CCTGAACCCC AGCTACCACA GAAGCACCTA 1140
CCCACAGAGG CCACACTGGG ACCTCTGAGA AGCCAAGTGA CCTCTGAGTG ATCTCACCCC 1200
AGAATTCTGC TCCTTTGGTA CACCTTGCCT GGAAGAAACG GTTGGGCTCT GCTTCCACCC 1260
AACTGCAGCT TTTCAGGCTG GTCTCAGAAA AGGAAAGTAC GTGTCCTTTT CCATTTTGAC 1320
ATCTTGCAGT GATGTAGTAA 1340
|
