Tag | Content |
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EnhancerAtlas ID | HS047-16823 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr19:11252140-11255030 |
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 | TTTTTGTATT TTTAGTAGAG ACGGGAGTTT CACCATCTTG GCCAGGCTGG TCTCGAACTC 60 CTGACCTCGT GATCTGCTTG CCTCAGCCTG CCAAAGTGCT GGGATTACAG GGGTGAGCCA 120 CTGTGCCCGG CTGCGATCTG TTTCTTTTAA CCGTAAACTG GGAAGAACTT TGACCACCTC 180 TTAGTCCAGA ACTATCAGGG AAGGGGCACT GAATGCCAGG CTGGAGGAGG GTTGCATGAA 240 AGGCTTGACC CCAGCTACTC AGGAGGCTGA GGCAGAAGGA CTGTTTGACC TGATGAATTC 300 GAGGCTGCAG TGAGGCTGTG ATCGCGCCAC TGCACTCCAG CCTAGGCAAT AGAGTGAGAC 360 CCTGTCTCTA AAAAAAAAAA AAAAAAAATG GCTCAGCCAT CCCAAGCTGC TCCCAGCTGC 420 CTGCCCCTCT AGGTGGCCCC CACTACTGGC CTGAGGATGC ACTTTATCCC CGCCAGGGCC 480 TGAGGAGTCC TGGGGAAAGG TACCCAAGTC TAGTCCTCAG GAGAAGCCGC CCAGGGAGCA 540 CTAGGGCCCG AGGAAGGGTT CAACCTCGAG ACTCCATAGC CCCTGGGCTC CCGTCCCCAG 600 AAACACCAGT TACGAGCAGG GGGCTGGCCA TGGTGTGAAT TCATGACCTG CACACCTCTT 660 GCCGTAATGA CTAAGTGGCT AGAGCTTCAG GCTGCCCCAC TGCTGCCCTC TGGAGCTCGA 720 GCAGGTGCAG GTGTGGGTGC CCACCCTGGC TTGGCCTCTT CTCACCTGGG TGGCTTCGGA 780 CACAGGGTGG ACTCCTCAAA GGGGCTGCTT CCCATCTGAG AAGCCAGCAT AATCCTCCAG 840 GGGCTACTGA TATACACACG CTGCCCCTGG TCCTGAGTTA GATCACCCTG CCCCTAGGGA 900 GGGCTTGGGG GCTTCACTGC TGAAGTTCAG ACTCCAGGGT GGTCCTTGTC CTGTGTGCCT 960 CAGTTTCCCC ATCTGTAAAA TGGATGGTCC TGGGGCTGAG CCTCAGTGCT GCAGGGACTA 1020 GTGTGGAACC CTGTGTCCTG GTGCCTGAAA CCTTACTCCC ACCTCAGCAG GGCTGGGCTG 1080 AGCCATCAGC AAGCCTCTGG CCGGCCTCCA TCATTCAGGA AAGAGCCGGT GGCTGAAGGC 1140 ACAGCTCTCA GAGGGAGAAC AAACGGGGGC GGGGGTGGGA TGGGGGCGGG GCCGGAGGCC 1200 ACCGGCCTCA GGCTGTCCTG GGCATCCAGC CAGTGCTGGG CAGTGAGTCA GGGGCCAGGC 1260 ATGTGGAGTG GGGCCTCTCC CAGCCCCGGA GATCAGGCAC CTCCCGGAAC CCGCCTGCTG 1320 GGCCCCCACC AGGCCGCGTT CCTCTCCCAC TCGCTCTCCC CATAGAGGGG ACCCTGGACC 1380 TGCCTGGGGG GGACGAGGAT GGGGATGTGG CTGGTGGGCA CAGGGCCTCT CTGAGCCCCG 1440 GCACAGGCCG CCTGATGGGA CCGTCTCTTC CTTGGGGAAA CTGAGGCCCA GGTTGCTGGG 1500 GTGGAGGGGA TGTGGAGTGA CAGGGCAGGG CAATGGCTCC TCGGCCCCCT CCGGGAACAA 1560 AGCCAGGTCA TTCCTGTGGG GAGGGAGCGC CAACCCCAGG GTTGGGGGGG GCACGGGCCC 1620 TGGGTCAGGG GTACAGATAA GCCTGGGCTC CCAGAACCCT TGTCACAGCG GCACCCCTGC 1680 CCCATGCCTG CTTTCTCTCC AGGGCACTCA GAGCTGCAGT TTGCAGGACG AGAGGGAGAC 1740 GTGCCCAATC CCCCCATCCC AGGACGCTCA GCCGTGCGTG GGCTGGGCCC ACTCCACTCC 1800 CGGCGCCCAC AGTTGCCCCA GTGAACCGGC CAGTGGAGGC ATCCTGTCCC GTGTGCGGGA 1860 AAGGAATGAC CGCCAAGGTG ACAGCAGCGC TTAGCCAACC CTGGCGCTGA CACCTGACTT 1920 GCAAACTGCT CCCTGCCTGA GGCTTCAAGG CAGGCGAGAG GCTTTGTGTG TGTGACTTCC 1980 TCCCCGAAGG GACACTGGCA ACAGCTGGAG ACATTTCCTG TTGTTAAGGC TGAGGGGGAG 2040 CTGCTGGCAT TTGGTGGGTG GAGGCCAGGG ATGACGTTAA CTGTTCTACT ACGCCCAGGA 2100 CAGCCCCCAA CACACACAAC AGCCTGGCCC AATGTCACGA GAGCTGAGGT GGAACAGCCC 2160 TGTTCTGCTT CAGGTCTTCA GGTCTTTGGG GGTCAAGGAT GCAAATAGAG GACTCTGCTC 2220 CCAATTCAGC TCACATAAAA GAACCGGCCG GGCGCTGTCG CTCATGCCTA TAATCCCAGC 2280 GCTTTGGGAG GCCGAAGTGG GAGGATCGCT TGAGCCCAGG AGTTTGAGAC CAGCCTGGGT 2340 AACATAGCAA GATCCCATTT CTACGAAAGT ACAAAAATTA CCTGGGCACG GTGGCATGCA 2400 CCTGTAGTCC CAGCGGCTTG GGAGGCTGAG GTGGGAAGTT TGCTTGAGCC CAGGAGGTTG 2460 AGGCTGCAGT GAGCCGAGAT CATGCCAGTG CACTCCAGCC TCGGCGACAG AGTTAGACTC 2520 TATCTCAAAA AAGAAAAAAG AGAGAAAACC CACCAACTTG GAAAATTAAA ACAGCCCCAA 2580 GGGCATCTAG GAACAGTTAA CTGCACATCT AAACCCAGGC CCGCCGTTCT TAGAAGCTCT 2640 GCAAGCTGCA TGGACTGACT CCTGACATTT CAGGGCTAGA CTCAAAAATC CCTTTAAAAA 2700 AATTTTGTTT CTGAGACGGA GTTTCACTCT TGTCCAAGCT GGAGTGGAAT GGCACGATCT 2760 CGGCTCACTG CAACCTCCAC CTCCTGGGTT CAAGTAAGTC TCCTGCCACA GCCTCCAGAG 2820 TAGCTGGGAT TACAGGTGCC CGCCACCATG CCTGGCTAAC TTGTATTTTT AGTAGAGATG 2880 GGGTTTCACC 2890
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