Tag | Content |
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EnhancerAtlas ID | HS116-17786 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr2:24657140-24659500 |
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) |
MIXL1 | MA0662.1 | chr2:24658558-24658568 | TCTAATTAAC | + | 6.02 | Myog | MA0500.1 | chr2:24659041-24659052 | GACAGCTGCAG | + | 6.62 | Tcf12 | MA0521.1 | chr2:24659041-24659052 | GACAGCTGCAG | + | 6.14 |
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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 |
GH02I024433 | chr2 | 24656789 | 24659939 |
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Enhancer Sequence | GGATTACAGG CATGAGCCAC TATGCCCAGC CCGTATTTGT TTTTTTTTCT CCAAGCCATT 60 GCCTGCAGAC AGCAGCCATG CTCGCTGTCT CTGTTTTTCC CCTATCCTTG CTCAACCTAG 120 GCTGAGCCCT CCCAGGGCCC TCTGTGTATG TTTGTTAGTG AGGAAGTGTC TGTTAGAAGA 180 AAGGGTCTGA AAGGTTCAAT TAGAGACTCA AGATCTGTGG GGTTCCCAGC TGTCCCTGGA 240 GCAAGGTACC CTTGACAGCC AGTCTATGGT CTATGAGAGC GTGAAGTTGA TTCCTTTTCC 300 TCCAGCTTCC TTTGGGTCTT TCCCCAACCT GGCCTTGGGC AAGGCTGACT CTGGGTTGCT 360 TTTCTGTTGC TGTTACTCCC TGGAATTGGA CCCATAGTTT GAGCCTCCTC TGGAAAAGGG 420 ATCACAAGTC TCTCCTTACA CTGCTGGCTC CAGGTCACCT CCTGTAGGCC AGGCCTGGGG 480 GGTGGAGTTG GCCAGAGCAC TAAACTATCT GGGGTATGCT CTGGGCCTCT TGGCTGAGAA 540 GGCCAAAACA CTCACCATCA GCTCTGCTAT TTTCTCTCTC CCCAGGACCT GGGGAGAAAG 600 GAGGAAGAGC CACTTCTCTT ATCACTGTCT TTGGCTGGTC TCATCCATTC CTCTTCCATC 660 CTTCATGCCT CCTCCTCTCT CTGTGTCATG GTCCCCATTT TTTTCTCCCT GATCACTGTC 720 CCTCTGACAG TGTTTCTGAC TTCCAGAGTT CATTTTGAGG CCTCTCTTCC TCATCTTCTC 780 TCCTTTCCCA CCTAGACCGA GCTCTTGTCA GCCCACCTTT CTGTTTCTGG CTGTTTCCAC 840 TGTTGTTCCC TGTCCGCAGA GCAAACGGGG CAGGGAGGCG ATGCCACCCT TGTGGGCCCG 900 GCAGGGAGCT GGGTGATTTT TAAGCGTTTT TCTCATTTTA AGGGCTAGGT GATAGAATGG 960 TTGCCTGAGG CCCCACCTCA GAAGCTGGCC TAGGGTCCCG ACAGGAGTTG TCTCACACTC 1020 CGTCCCACGG AACTGGGGGT GAGGTGGTGG CAGTGCTGGC ATCAGACCAT AACATAAAGG 1080 GAGTAGCTGA AGCCCTCCGA AGTAGGCCAC GCCTGCGCCA TTGCACAGTT CGGAGCTCTC 1140 CCATCAGCCC TTCCGAGTGC ACTGCCTCAA GTCGCACATC CAAAGTGAAA TGTGGGTGTT 1200 TTAATCACTG AAGAGAATCC TTAATGCTGC TCCTTCAGCA CATAGCTGTC TCTCCTGTGC 1260 CAGGAACCGC AGGGAGCCTA TTGCTTTCCA TCCTGAACTG GATCCAGAAG CGTTAGGTGA 1320 GGCTCAATAC AATTTTCAGT TGTTATCATG GGAGGCCCTT AGAGACGCTT CTCAGTTCTA 1380 GCAATTAGCC ACACAGGGGT CAACCAAGTG TTCTCAGCTC TAATTAACAG CTGTGTTGAA 1440 TCTGGGACAC ATAGAATTCC TTTGGGGACG CACTCTTCAA ACAGAAACAA AGCCAGAATA 1500 GCAAGCTCTT TCCTCCTTAT CAGAGGCTAT GAAGTATGAA AATGACTGCT GAGGGGATTC 1560 TTAATGAAAA TACCGGGAAG CTGAGTGGCC TCCGGGCTGC ATGTATGAAT TTAAAGGCAA 1620 AAAGACAATC TCAGCTTGAC TATGAAGTTA TCTGCTGGGG CTCAGGAGGC TCTGGGGAGC 1680 GCTGGGGGAA TTAGGTGCCT CTTAGCTCCA CTCCCAGAGC CCGGTACACC CAGCAGGCTA 1740 CATGATAATC ATCACCACAC AAATCAAAGG CTTGATCTCT GGCTTCAAAA GGAAAAGGAA 1800 CAGGAACAGG ATACTCTCTG TTGGGACTCC TGCTCTGAGC GGGAACTATG CTGATGCCTG 1860 TTCAAGTTGT TCCCTGGGTA TTTTGGCTTC TTGCCCTGCC TGACAGCTGC AGGAGTTCTG 1920 TAAGAAATCT GAGGGAGAAT TTCCTTTGCA ACCATGACTG AGAACCCAGG ATCAAGAGCT 1980 TTGCAGACAG AAAAGACATT ACCCTTCGAA TATCCCAAGC CATCTATTAG GGTCAGCAAG 2040 CAGCCGGCAA AAAGCGGGGC AGCTGGTGGT CCAGCCCTGG GTGGAGAAAG TGGATTCCAT 2100 CGGGAAACAG CCAGTTGAAG TTTTCTTTAC TAACTGAGAG CAAATGCACC GAGGCATTTA 2160 AAAATAAGCA TATGTTCATA CTGGAATATT TCAAATGAAC AGAAACAACA CCTAAGGCCC 2220 AGATCGATAA ATATTAACTT TGTGACACAT TTACTTCACA ACTTTTTCTA AACAATTTGG 2280 TATACATTAA AACCTACCCC TTCTTCCCCT GGCTCCACTC CCCACTCCCA TCCTGAAGTT 2340 AGTAGGTATT TTTCTATGTA 2360
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