Tag | Content |
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EnhancerAtlas ID | HS116-29570 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr6:43763880-43765200 |
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) |
ZNF263 | MA0528.1 | chr6:43763902-43763923 | TGCTCCCCTTCCTCCTCCCCA | - | 6.32 | ZNF263 | MA0528.1 | chr6:43763908-43763929 | CCTTCCTCCTCCCCAGCCTTC | - | 6.42 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_00396 | chr6:43764064-43765602 | Adipose_Nuclei | SE_40829 | chr6:43763899-43769361 | Left_Ventricle | SE_51234 | chr6:43764754-43768479 | Skeletal_Muscle | SE_57095 | chr6:43764707-43766691 | VACO_400 | SE_65246 | chr6:43762755-43768367 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I043798 | chr6 | 43764761 | 43764910 |
|
Enhancer Sequence | TGCGAGTTCT CAGTTGCTTT GCTGCTCCCC TTCCTCCTCC CCAGCCTTCT CACTGCTTTG 60 CTGCTGAGGT ATCCAGTGTA GACATTGTGT GTGGGCCCTC GTTCTGGATT TGTCCTCACT 120 TTCTGCCTGC AGCAGAGATC TGAAACAAAT TAGGAGCTCT CTGAGGGCAC AGGCAGTGTC 180 TCCCCCATCA GACTGGGAGC CTCCTTTGGA TTGAGTCCAT GTGACCTTGT AGCCAGGCCA 240 CTCCCCTTTC TCCTTTTCAT CGTGCTCTGG AGGACCTGGC GCTGACCCTC AAGGCTGACC 300 TTTTCCACAG GCTTAGCATA GCCTTCACTG CTGCTACCTG CAGAAGCTCT GAGAGAGCCT 360 CAGTAAACAT CCGTCTCCTC CTCCCTGATG ACCTGCCGGT GGGAATTCTC TTCCCCAGTC 420 CTCATTCTGC AGGCAGCTAT CTCCGAGTCC CTCAGGCTCT GGAAACTTCC AGTGGAAACA 480 ATTCTCTGGG AGCCAAGACC CCAGAGCTCT GGCTGGGGCT CTGTCACCAA CCAGCCCTGT 540 GACCTCAGGC AGCTCTTGGT TGTTCTCTGG GCCTCAGTGT CCCTACCTGT ACAATGGCAC 600 TATATCTAGC TTGCTGACCT TGGGGTAGGG TTTCCAAAAT GCACATTGTG ATCTATGTGG 660 GTCATGAAGT CGATTTAACA GCATGCAACC AGCATGATTC TTTTTCTTAA ATAGGAAGAG 720 AATAGGGCAG AAAATATTTA GTCTTGCATA GAGTAAGGGT AAGTATTGTT TCTTGAAACT 780 TGTGTGGAGT GTGTGTGTGT GTGTGTGTGT ACATGCGTTC TGGGTCATGA GGTAGGATAT 840 ATTTTTCAGG GGGGTTGTGG TAAAACAAAA AAGTAAGGAA GTCAGTACTG GAAGCTGTGA 900 CAGAAGGGTG ACGGTGGCAA CTGGAGACCC GGACGTGGTC TCTGCTACTT CTCCACGTCA 960 CGGAGATGAC AGGCCCACTT ACAACCTCCT GTCTGGGGTT CTTCCTTGCT CTCTTGAGTA 1020 GTCTTCCTGC CCTGCCTCTG CTGAGCTCAT GCCCCTCTCT ACCCAGAGCC CAGGGCCCTC 1080 CCAGCTGAGA GCTCTCAGGA GCTAGTCTGG TTCCCTGGGC CACTCCAATA AGAGAAGAAG 1140 ATTCTGGGAT CCACAGCCTG GTGGTGTCCA GTCTGCCCAG CTGCCTCCGG CCTGGTTCTG 1200 CCTCACGGTA ATAATACTGG ATTGGGAAAC TGAAGCTTGG GCCAAGTGGA GGAACATGGC 1260 TCCCTCCTAG CTTTCCCAAT GCCCCGTACC CTGGGAGGGA TACTCCTTAA CCCCTTCCTG 1320
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