Tag | Content |
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EnhancerAtlas ID | HS116-10321 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr14:23514770-23516260 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr14:23515139-23515157 | GGAAGGTATGAGGGAAGG | + | 6.56 | JUN(var.2) | MA0489.1 | chr14:23514825-23514839 | ATGAGTCATTTCCC | - | 6.92 | Nr2f6(var.2) | MA0728.1 | chr14:23515923-23515938 | TGAACTCCTGACCTC | - | 6.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 23514978 | 23515378 | chr14 | 23515962 | 23516028 |
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| Number: 2 | ID | Chromosome | Start | End |
GH14I023047 | chr14 | 23514810 | 23515409 | GH14I023046 | chr14 | 23516010 | 23516609 |
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Enhancer Sequence | TAGACAAAGG CCAACATCCC ATTCCAATGC ACCCCTCACT GTCTAAGAGT AGCCCATGAG 60 TCATTTCCCC CATTTCTCTA CTAATTCCTG AAGGCTTGAT ACAGATATCA CGGTGAGACC 120 AAAGGGGCGG AGATCTTCCC CTTCCTGCCC CGAACCAGAA GACCTTGTCC TTCTGATGCC 180 CTGCTTGGGG TGGTGCCTAC CTCCTCACAG TCTCTGGAGA GTTCGGGGGG ATAGCCCGCT 240 CTTGCACAAG CCCTTGGACT GTCAGAGGTC CAGGCTTCCA GCCTTCAGCA GAGTAAATGA 300 CCTGAATTCC AGCACTAGAG GGAGGGGCCT TGTTCTCCTA CCTCCTGCTT GTCCTTATCA 360 AGCAGGTGGG GAAGGTATGA GGGAAGGTAT GTTCACATTG AAGCAGCTTT CCCCAGCTGC 420 CAGTACCCCA TACGAAGGGG GAGTCACAAG GACCTATCCT ACCTCGCCTA CCTGTGTGTG 480 CCTCTGGAGC CCTGGAGTTG AGAGGCCTGA GCTCTCATGC TGGTTCCTGG GTGGACCCCT 540 TCTCTGGACT TTGGGAGATA ATTGCAGTTC TGGCTCAGCT CCCACCTAGT TGACTGCTTC 600 TGTCCGTCAA CAGCCTGCCT CCCTGGTCCT CTCCCTCCTC CTTTGTGTTC TGCAAAGACT 660 AAGACCATGG CCTAGGGGAG AGTTAAAGGT GGGAGCAGCG GGCCCAGATT CAATGTGACT 720 GTCTCACTCT GGTCCGCCCT TTCCCCACTT GGCACTACGA GCCCCAGGAA AGGCTGGTTT 780 GTCCCCGCTG CTGCCTGCCA CCCCCATTAT TTTCCTAGTC CAGAATCCCC CTTCCTCTCT 840 TAGTCTTTTA TCCCTCCGGC CCTCTTCTCA GCAGCTCTCA CACTTCACCC TCTACTTCTC 900 CTGCCCATCT TGCCCTCTGA CCAATCCCTA TATCTTTTTT TTTTTTTTTT TTGAGACAGA 960 GTCTCGCTCT GTCACCCAGG CTGGAGCGCA GTGGCGCGAT CTTGGCTCAC TGCAACCTCC 1020 GCCTCCCAGA TTCAAGTGAT TCTCCTGCCT CAGCCTCCTG AGTAGCTGGG ACTACAGACA 1080 TGCGCCACCA TGCCCTGCTA ATTTTTTGTA TTTTTAGTAG AGATGGGGTT TCTACCATTG 1140 GCCAGGCTGG TCTTGAACTC CTGACCTCAA GTGATCCACC CGCCTCAGCC TCCCAAACTG 1200 CTGGATTTAC AGACAAGAGC CACCGCGCCT GGCTGAATCC TTATATCTTA ATTTTCTTGG 1260 ACCGCTTGAG ACCAACAGAG GACCCAGAAA GTTGGTGGTG AGAGTGGGGC AGAGTCATCA 1320 TCTCCTTACT CCCTCATGGA ATTAACCCAA GTCTTCCCCT ATCTAGAAGG AGGTGAAGTG 1380 TATTTTCCCC CAAGGAGAAA GGAGAATGAA CTGGGAGGCA ATAGGCTAGG CCTCGCCTCC 1440 CGTCCTTTGG GACGATGAAG CTTTGTATAG AAACCTGAGT GCAAAAACAG 1490
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