Tag | Content |
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EnhancerAtlas ID | HS116-16879 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr19:11252200-11255100 |
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) |
KLF16 | MA0741.1 | chr19:11253321-11253332 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr19:11253322-11253332 | GGGGCGGGGC | - | 6.02 | RREB1 | MA0073.1 | chr19:11253305-11253325 | GGGGCGGGGGTGGGATGGGG | - | 6.36 | SP4 | MA0685.1 | chr19:11253318-11253335 | GATGGGGGCGGGGCCGG | - | 6.11 | TFAP2A | MA0003.3 | chr19:11254073-11254084 | TGCCTGAGGCT | - | 6.32 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_00404 | chr19:11252239-11255117 | Adipose_Nuclei | SE_01196 | chr19:11252554-11254634 | Adrenal_Gland | SE_01676 | chr19:11252175-11254872 | Aorta | SE_26153 | chr19:11252419-11254868 | Duodenum_Smooth_Muscle | SE_26820 | chr19:11252176-11254854 | Esophagus | SE_30142 | chr19:11252410-11254998 | Fetal_Muscle | SE_32185 | chr19:11252162-11254848 | Gastric | SE_34530 | chr19:11252077-11255141 | HCT-116 | SE_35072 | chr19:11251558-11255461 | HeLa | SE_37121 | chr19:11252319-11256706 | HSMMtube | SE_38721 | chr19:11252321-11255143 | HUVEC | SE_39292 | chr19:11252171-11256472 | IMR90 | SE_40759 | chr19:11252142-11254992 | Left_Ventricle | SE_42281 | chr19:11252143-11255130 | Lung | SE_44509 | chr19:11252576-11254785 | NHDF-Ad | SE_44970 | chr19:11252454-11255142 | NHLF | SE_46645 | chr19:11252599-11253277 | Ovary | SE_46645 | chr19:11253365-11254513 | Ovary | SE_47998 | chr19:11252823-11253312 | Pancreas | SE_47998 | chr19:11253358-11254455 | Pancreas | SE_48638 | chr19:11252197-11254999 | Right_Atrium | SE_49703 | chr19:11252414-11253276 | Right_Ventricle | SE_49703 | chr19:11253364-11254711 | Right_Ventricle | SE_53189 | chr19:11252493-11254613 | Small_Intestine | SE_54664 | chr19:11252303-11254861 | Stomach_Smooth_Muscle |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr19 | 11253262 | 11253482 | chr19 | 11253991 | 11254271 | chr19 | 11252544 | 11254576 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I011140 | chr19 | 11251653 | 11257081 |
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Enhancer Sequence | CTGACCTCGT GATCTGCTTG CCTCAGCCTG CCAAAGTGCT GGGATTACAG GGGTGAGCCA 60 CTGTGCCCGG CTGCGATCTG TTTCTTTTAA CCGTAAACTG GGAAGAACTT TGACCACCTC 120 TTAGTCCAGA ACTATCAGGG AAGGGGCACT GAATGCCAGG CTGGAGGAGG GTTGCATGAA 180 AGGCTTGACC CCAGCTACTC AGGAGGCTGA GGCAGAAGGA CTGTTTGACC TGATGAATTC 240 GAGGCTGCAG TGAGGCTGTG ATCGCGCCAC TGCACTCCAG CCTAGGCAAT AGAGTGAGAC 300 CCTGTCTCTA AAAAAAAAAA AAAAAAAATG GCTCAGCCAT CCCAAGCTGC TCCCAGCTGC 360 CTGCCCCTCT AGGTGGCCCC CACTACTGGC CTGAGGATGC ACTTTATCCC CGCCAGGGCC 420 TGAGGAGTCC TGGGGAAAGG TACCCAAGTC TAGTCCTCAG GAGAAGCCGC CCAGGGAGCA 480 CTAGGGCCCG AGGAAGGGTT CAACCTCGAG ACTCCATAGC CCCTGGGCTC CCGTCCCCAG 540 AAACACCAGT TACGAGCAGG GGGCTGGCCA TGGTGTGAAT TCATGACCTG CACACCTCTT 600 GCCGTAATGA CTAAGTGGCT AGAGCTTCAG GCTGCCCCAC TGCTGCCCTC TGGAGCTCGA 660 GCAGGTGCAG GTGTGGGTGC CCACCCTGGC TTGGCCTCTT CTCACCTGGG TGGCTTCGGA 720 CACAGGGTGG ACTCCTCAAA GGGGCTGCTT CCCATCTGAG AAGCCAGCAT AATCCTCCAG 780 GGGCTACTGA TATACACACG CTGCCCCTGG TCCTGAGTTA GATCACCCTG CCCCTAGGGA 840 GGGCTTGGGG GCTTCACTGC TGAAGTTCAG ACTCCAGGGT GGTCCTTGTC CTGTGTGCCT 900 CAGTTTCCCC ATCTGTAAAA TGGATGGTCC TGGGGCTGAG CCTCAGTGCT GCAGGGACTA 960 GTGTGGAACC CTGTGTCCTG GTGCCTGAAA CCTTACTCCC ACCTCAGCAG GGCTGGGCTG 1020 AGCCATCAGC AAGCCTCTGG CCGGCCTCCA TCATTCAGGA AAGAGCCGGT GGCTGAAGGC 1080 ACAGCTCTCA GAGGGAGAAC AAACGGGGGC GGGGGTGGGA TGGGGGCGGG GCCGGAGGCC 1140 ACCGGCCTCA GGCTGTCCTG GGCATCCAGC CAGTGCTGGG CAGTGAGTCA GGGGCCAGGC 1200 ATGTGGAGTG GGGCCTCTCC CAGCCCCGGA GATCAGGCAC CTCCCGGAAC CCGCCTGCTG 1260 GGCCCCCACC AGGCCGCGTT CCTCTCCCAC TCGCTCTCCC CATAGAGGGG ACCCTGGACC 1320 TGCCTGGGGG GGACGAGGAT GGGGATGTGG CTGGTGGGCA CAGGGCCTCT CTGAGCCCCG 1380 GCACAGGCCG CCTGATGGGA CCGTCTCTTC CTTGGGGAAA CTGAGGCCCA GGTTGCTGGG 1440 GTGGAGGGGA TGTGGAGTGA CAGGGCAGGG CAATGGCTCC TCGGCCCCCT CCGGGAACAA 1500 AGCCAGGTCA TTCCTGTGGG GAGGGAGCGC CAACCCCAGG GTTGGGGGGG GCACGGGCCC 1560 TGGGTCAGGG GTACAGATAA GCCTGGGCTC CCAGAACCCT TGTCACAGCG GCACCCCTGC 1620 CCCATGCCTG CTTTCTCTCC AGGGCACTCA GAGCTGCAGT TTGCAGGACG AGAGGGAGAC 1680 GTGCCCAATC CCCCCATCCC AGGACGCTCA GCCGTGCGTG GGCTGGGCCC ACTCCACTCC 1740 CGGCGCCCAC AGTTGCCCCA GTGAACCGGC CAGTGGAGGC ATCCTGTCCC GTGTGCGGGA 1800 AAGGAATGAC CGCCAAGGTG ACAGCAGCGC TTAGCCAACC CTGGCGCTGA CACCTGACTT 1860 GCAAACTGCT CCCTGCCTGA GGCTTCAAGG CAGGCGAGAG GCTTTGTGTG TGTGACTTCC 1920 TCCCCGAAGG GACACTGGCA ACAGCTGGAG ACATTTCCTG TTGTTAAGGC TGAGGGGGAG 1980 CTGCTGGCAT TTGGTGGGTG GAGGCCAGGG ATGACGTTAA CTGTTCTACT ACGCCCAGGA 2040 CAGCCCCCAA CACACACAAC AGCCTGGCCC AATGTCACGA GAGCTGAGGT GGAACAGCCC 2100 TGTTCTGCTT CAGGTCTTCA GGTCTTTGGG GGTCAAGGAT GCAAATAGAG GACTCTGCTC 2160 CCAATTCAGC TCACATAAAA GAACCGGCCG GGCGCTGTCG CTCATGCCTA TAATCCCAGC 2220 GCTTTGGGAG GCCGAAGTGG GAGGATCGCT TGAGCCCAGG AGTTTGAGAC CAGCCTGGGT 2280 AACATAGCAA GATCCCATTT CTACGAAAGT ACAAAAATTA CCTGGGCACG GTGGCATGCA 2340 CCTGTAGTCC CAGCGGCTTG GGAGGCTGAG GTGGGAAGTT TGCTTGAGCC CAGGAGGTTG 2400 AGGCTGCAGT GAGCCGAGAT CATGCCAGTG CACTCCAGCC TCGGCGACAG AGTTAGACTC 2460 TATCTCAAAA AAGAAAAAAG AGAGAAAACC CACCAACTTG GAAAATTAAA ACAGCCCCAA 2520 GGGCATCTAG GAACAGTTAA CTGCACATCT AAACCCAGGC CCGCCGTTCT TAGAAGCTCT 2580 GCAAGCTGCA TGGACTGACT CCTGACATTT CAGGGCTAGA CTCAAAAATC CCTTTAAAAA 2640 AATTTTGTTT CTGAGACGGA GTTTCACTCT TGTCCAAGCT GGAGTGGAAT GGCACGATCT 2700 CGGCTCACTG CAACCTCCAC CTCCTGGGTT CAAGTAAGTC TCCTGCCACA GCCTCCAGAG 2760 TAGCTGGGAT TACAGGTGCC CGCCACCATG CCTGGCTAAC TTGTATTTTT AGTAGAGATG 2820 GGGTTTCACC ATGTTGGCCA GACTGGTCTT GAACTCCTGA TGTCAGGTGA CCCACCTGCC 2880 TTGGCCTCCC AATGTTGCTG 2900
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