Tag | Content |
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EnhancerAtlas ID | HS116-09802 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr13:50960460-50961790 |
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) |
SCRT1 | MA0743.1 | chr13:50961507-50961522 | ATGCAACAGGTAGCC | + | 6.08 | SCRT2 | MA0744.1 | chr13:50961507-50961520 | ATGCAACAGGTAG | + | 6.18 | Tcf12 | MA0521.1 | chr13:50960705-50960716 | CAGCAGCTGTT | - | 6.32 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_51476 | chr13:50958392-50963020 | Skeletal_Muscle | SE_61089 | chr13:50927585-50962248 | HBL1 |
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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 |
GH13I050385 | chr13 | 50959974 | 50961900 |
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Enhancer Sequence | TATTGTGAAA AGATACATTT CTTTTCCTCC TGTGGATCTT CCCCTCAGAA TTCCAGTTCT 60 AATTCTACTC CTTGTGTGAA CCCCTGAACA TGCACCCATG CCCATTCATT TTTCTGGGCC 120 CCTCACAGCA GCTCTAGCAC CTCCACCTAA AAGGATTGAA AGGGAAGATG AGACCCCATT 180 GCAGAATATT TGAAGTGGTT ACTCATCAGC CCTGTATATA CATATTAAAA TTCTCTGAGT 240 TGTTACAGCA GCTGTTGCAA CTGAAAATAA TTCAGCAAAC AGGATCATTT TCTGTGTAGT 300 TTATGGGCTC GGGAACAGTC CAGAAGCTTT GGAATTTGAG TTACTGTCAG CCCGCTGCTC 360 AGCCAATCTC CACATGTCAC AGGCTGGTAA TTTGATCTAC AGCTCCCTTG AAGTGAGTTT 420 GTACTGAACA CAGAAAGCTC TTTTTTCCCC CTTTTTGCCA AACGCTAAAT AGCCTTTTAT 480 GTGTGTCTTT TTTCCCCTTA CACAATCACG ATTTGATTCA ACAAAAATAT TACACACCTT 540 CTTCCTGAGG ATTTTGTGTC CTTTTCTTGG ACTCGCAGCT ACACATTTTG GGCAGCAAGT 600 TCCCTTGTTC CCTCGGCAGC TGCCTGCGCG CAGTCCTCCG GAGAGCCTAG GCCTGGGAGA 660 GACCGCCTTG GATTTAGCTG GGCCTAAGAA AACACAGGCA CAGCAGTGAG AAAAATATTA 720 TCTTCCAATT CCCCTTCCTT TCAAGACTCA GGAAATCTGC TTCTTTTCAG TGCTCTTATC 780 ACTGCTGTGA AGTTTTGATT TTTCCAATCT CCAGTGGTGG TTTAAAAGGA GCTTAGAGCA 840 GAAGCTGAAA GGGCCTCCTG TATTTAGAGA GCAGAAGCCC CACCTGCTGT CTCTGGGGCA 900 CCTCCCAGTG GCCAGGGCCA GGGGGTGTGT CTGATGATGG AGACAGTTGG AGCCACTTCA 960 GCACTGGCGC CGAGTTTATT TCATCTGCTG ATATTTAGAT TGTGGTGGGG AGGGCAGAAT 1020 GCCTGATGAT GCCGTCAGTT CACCACCATG CAACAGGTAG CCTGCTTTCC AGCTACTTTG 1080 CATGATATCC AGACTTTCTG GCATCAAGGC TTGGTGGCTC ACAGGGCTTG AGGCAACACT 1140 ACTCTGTAGC TTCCATTTTT TTTAGTGATT CCCTCACCGG TGGTGGATCT ACCTAAGATC 1200 ACAGTGGCCA CGGTGGTATG CTATTTTGGG TTACTGAAAA CTGAAACCTG TTTTTCGCTG 1260 AAGACAGTTT GCCTAACAGT TTAATAACCT TTATACTTAG AATATCAGGA GTCCTGTCTG 1320 TCTGATCAGC 1330
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