Tag | Content |
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EnhancerAtlas ID | HS116-03138 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr1:226558690-226560120 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr1:226558841-226558851 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr1:226558841-226558851 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr1:226558841-226558851 | ATTTTCCATT | + | 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 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I226370 | chr1 | 226557758 | 226559380 |
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Enhancer Sequence | ACACACTCCT GAACTTATGG ACTTACATTC AAATCAATGC TGTCCCTTTC AGATCAGTCA 60 CCTCCAACAA ATATTGCTAC TGCTCATATC TTGGGAACTG CCTGCCATCA AGAGAAGCTG 120 CAGTGGAAGA AGCATGAGAT CTGCAGCCTT CATTTTCCAT TTGTTAAGTG GGGCCACCTT 180 CCTTAAAAGG CACTCACTCC CTTTTGCGAG CAGCCCTGCC TATTTGGCTC AGCCCCTGCG 240 TGGAGACACC TGTGTACCAA TGGGCCCCAC ACTCTGTATC CTGAGACATC GTCTCTGGGG 300 CTTTGCCAAT AGACCCTTCT GAGCTCCCTG GGGGCCGTGA CTGCGCCTTT CCATTTCTGC 360 ATGTCCAGCA CTTCCTGCAG TGCTTGGAAC AAAGAACTGA ACAAGAATCT TAGAAATGGA 420 ACTGCTATGG TGATAAAATT AAATAAAAGG ATGTGAAAAG TGCTCACAGC TCATCAGACA 480 CCTACCAGGA GCCAACAGCT TCTAATAACA TCCACAAGCC CTGGCATGGG CTTCCCTGTA 540 CCCTCAACAC TGCAAACTCC ATCCTAAGGG AAGATCTGAT TTCTGGCAAG AATTAAGTAG 600 CCGGAGCCAC ATCTGGGGAA GAAGGTGGAT AATCTATTTC AAGCCAAGAA CAAGGTACAA 660 TAAAAGAACA GAGTGACTTT GGTATGGACC CTCAATCAGC TCTGAAAGCA ATTCTCAAGA 720 AGGAATCCCA AAAGAAGTTC TGACGGCAGA GCATGGCCAG AGTGAGGGCA GAGCTCTGAA 780 GGGCGCGACA TTTTCCACGC TGTATAATTC TGGTGTTTAT GTAAAAAAAA GAAAATACCT 840 AGTTTCCCTA ATTGTACACC CCTCAAAACA TACGCACAGA CTAAAAATAA GAGGTGGGCT 900 CCATCCACAC AGGCCGCCCT CACTACTGGA AAAGAAACTC AGGCACAGCG CTGGACAGCG 960 GGCTGGGAGC AGTGGCTCCA CAGCTGCCCA GTTGAGAGAG AAACAGAAAA GTGGGAGAAA 1020 CACCTTGGCA CTGGGGACCC ACGAGCCCCA GCTGCAGCCA GGAGGAGGCT TCTAGGGCTG 1080 CAGCCTGGAA CCCTGCCCCC TGCCATGTGT CGTGACTGCC CGGAACCCAT TCCCTTCTGG 1140 ACTCAGGATG TGCCCTCCTC ACAGGGAGAG TCAGGTTCCC CTGGTGCTGG GGATGAAGCC 1200 CCGAGGGCCA CTGTGTCTAC TTCTCCACAT GGTTACCCCA ATCCCACGTG GACCCCGCTG 1260 AGGTCAGGAG TGGGCACCCC GCTTTCCACA CACTTCCAGC TAGCTGCCTT TTAGCTTGTT 1320 TCAGCAAGCA GCGCCCCTGT CCCTTTTCTT CCTGCTAAAC TAGTTACCTG TCCAGTGAAA 1380 AACATTAAAA TGTCATTTCA GGCTGGGGGC CATGGCTCAT GCCTGTAATC 1430
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