Tag | Content |
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EnhancerAtlas ID | HS116-35203 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr9:116903730-116904940 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr9:116904399-116904415 | TCTTATGTAAACAGAG | + | 6.23 | FOXP1 | MA0481.2 | chr9:116904403-116904415 | ATGTAAACAGAG | + | 6.32 | FOXP2 | MA0593.1 | chr9:116904403-116904414 | ATGTAAACAGA | + | 6.02 | ZNF263 | MA0528.1 | chr9:116903874-116903895 | TTCTCCTCTCCTGACTCCTCC | - | 6.64 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH09I114140 | chr9 | 116902964 | 116904012 | GH09I114141 | chr9 | 116904141 | 116904410 |
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Enhancer Sequence | GACTAGTGGC TACTATATTG AACAATGCAA GTCCTTAATA TAAGGATGAG AAAAACACCT 60 GCCCCCTCGT CCTGGGATGA GAAGGACCCC TAATGTGTGC ATAGAGCTTG GCAGATGAGA 120 GATGCTCACT GCTTCTTCAC TTCCTTCTCC TCTCCTGACT CCTCCAAATG AGATGAGTGT 180 CTTTGAGTGG AAGAATTTCC CTTTAGAGAC ATTCAACTCC CCTGTGGACA CTGGCTGGAG 240 AAGTGGATGA GTGGTAGGGG GAGAGACCCT GGGAGCTTCT GTGATGGACA GGCTCGGAGA 300 GCAGAGGACA AGGCCAGCTC AGAGAAGGAC AAAAATGACT GCATCTGCCA AATCCCACCT 360 CTATTTTTGG TGTTTACAGG CACTAGTGCT GGAAAGGGGC CCATCTTCGA AATTCCTTTT 420 CTTTGCATAG AGTGGTTAAG ATCATGGGCT CTAGAATCAG ATGGTTCTAG GTTAGTGTTT 480 CAGTTCCATT AGTTACCAGC TGTGAGACCT TGGGCAGGTT GCCAGCTTCT CTGCTACTCA 540 TCTGTAAAAG AAGCAGAATA ATGTCTACAT CTGAGGATTT TGTGAGTAAT CAATGAGCTA 600 ATATGTGCAA AGCTCTTTAC AGGAGACCCG GCAGATATCA AGTGCTTAAA AAACAGATGC 660 CACGGCCAAT CTTATGTAAA CAGAGCCTCT TAACGTCCAC GCCCATGCAG ACCAGAGTCC 720 AGTGAGATGT CTGCAAAGCC CATGATTCCA CATCTCCAGA CAATCTCTTT TTTGGTGGTC 780 TTCAGAGTGA GGCAGTGACC ACACACAGAA ACAAGTCCTG GTATCCTCAG ACGGCAGCTG 840 ACCCATCAAA TTTGACACTT GGAAGCCATC CTGAAGTTTC TAGTGCTTGG ATCTCCTTTC 900 CATTGCCCTT GCCAAATGGA AATCTCCTAG GACTCATCCA GAGGCAGGAG CTCTGAGGCC 960 TGGGGGCTCA GGGATGGCTG CCTCTCTGCG ACTTCTCACC CCTGGTCCTG GTGGAGTCTC 1020 CACTTTCCAG ACTCATTTTC CCTTCATTGT TTCCCCAGGC TGGAGGCGTC TGCAGATCAG 1080 CCCTGGTCAA AATGCCCAGC ACAGGAGCTG GCTTCCATAG GTCAGGGGCA GAGTAATCTT 1140 TGCTGAACTG GAAGAGCTAA AACTCAAAAA CTAACACCTG TCCCTGGTTA ATAGCCAAGG 1200 ATGACTTTCA 1210
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