Tag | Content |
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EnhancerAtlas ID | HS116-10634 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr14:59658410-59659370 |
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) |
KLF4 | MA0039.3 | chr14:59658752-59658763 | AGAGGGTGTGG | - | 6.02 |
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| 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 |
GH14I059192 | chr14 | 59658719 | 59659190 |
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Enhancer Sequence | CTGAACCAGG CATTTCTAGA TTTCTCTCAG TTGCACTATC CTTGGCCCAG ATAATCTTCC 60 CAGGAGGTGT GTGACACGTG AATAGGGAGA GACACCAAGA GAAAGATACC CAGAAGCCTT 120 TGCCAGGCCA CCAGTGTCTC CCAGAAGAGC TGGGAGACAA TAGTCCTCTC ACCTGAGGCA 180 GAGCCGTTCC GTAAACAGGA TCAGTTGTTT CAGGCTGGTT GATGTGAAAG AAATGTGAAA 240 GAACATTTGC CCAATATTTG TAACATGTTA CCATCCAGTA GTCTGATTCT GTGGGTTTTC 300 AGGAGCATAA ATTAGTAAAT TAGTGAGGAG GTGTGATAAT GAAGAGGGTG TGGTGGGTCA 360 CATCCTTGGG TGGTGCTTAC AGGAGCTCCA TGAATAGGTG CTAAGGAATT TGAATCCTGG 420 CTTTCTTGTT TTGTGGACAT GTTCTGCTTG TTAAGGGGTG TGTGTGTGTG TGTGTGTGTG 480 TGTGTGTGTG TGTGTGTGTG TGGTTTTGAG CTACTTTGTT TAAAAGGCTG CTTTTAGTGT 540 TGGCACTATG GTCCTTAAAA CAAATAAGGT GTTTACAAGC AAAAGTTCTG ATTGAAAGTG 600 TTTCATTTTG TAAATATTTG GGAGATGGCA TAAAGAGAAA CTTGAGGTCT TGTGTGAAAA 660 CACTTTAAAG TTGCAGCTGT TGGACCAGAG GAAACATGCT TTTCCAACAA AGCTTGGTAT 720 CCTTGAGTGC CCTAGGTGTT TGGTTCAGGA AATAATCACA GAGCTTGTAA CTGCTGTGGG 780 GCCCTCCCTG GCTTCAAGCC GTGCTCTGGT ATTTCCAGTG TTAAGTCTAT CCTTATATTG 840 CCGGAAACAA AGCAAGGTGT CCAACTTGGG TTAGCAAACT TGTTTTCTCT CTAGAGGGGA 900 CACCAGTCAA AATAGAAGTT CTATATTCTG TTGTGATTTT TTCCTCTTTG GATGAGGAAT 960
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