Tag | Content |
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EnhancerAtlas ID | HS116-00491 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr1:19716630-19718980 |
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) |
CTCF | MA0139.1 | chr1:19717998-19718017 | CGTCCAGCAGAGGGCTCTG | + | 6 | NEUROD2 | MA0668.1 | chr1:19717661-19717671 | GCCATATGGT | + | 6.02 | TEAD1 | MA0090.2 | chr1:19717870-19717880 | CACATTCCAT | + | 6.02 | TFAP4 | MA0691.1 | chr1:19717593-19717603 | AACAGCTGAT | + | 6.02 |
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| Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
SE_01631 | chr1:19716172-19718011 | Aorta | SE_01631 | chr1:19718069-19719052 | Aorta | SE_04046 | chr1:19716514-19718685 | Brain_Anterior_Caudate | SE_05077 | chr1:19716739-19718770 | Brain_Cingulate_Gyrus | SE_05833 | chr1:19716201-19720492 | Brain_Hippocampus_Middle | SE_18410 | chr1:19716176-19720317 | CD4p_CD25-_Il17-_PMAstim_Th | SE_25786 | chr1:19716549-19718828 | Duodenum_Smooth_Muscle | SE_26537 | chr1:19716179-19720568 | Esophagus | SE_28013 | chr1:19716841-19718501 | Fetal_Intestine | SE_28668 | chr1:19716604-19718754 | Fetal_Intestine_Large | SE_31164 | chr1:19716409-19719128 | Fetal_Thymus | SE_31447 | chr1:19716397-19718506 | Gastric | SE_42185 | chr1:19716243-19719159 | Lung | SE_45720 | chr1:19716651-19718686 | Osteoblasts | SE_46635 | chr1:19716568-19717616 | Ovary | SE_46635 | chr1:19718098-19718452 | Ovary | SE_48688 | chr1:19716506-19718426 | Right_Atrium | SE_50058 | chr1:19716289-19720556 | Sigmoid_Colon | SE_51211 | chr1:19716277-19718925 | Skeletal_Muscle | SE_52345 | chr1:19716229-19719127 | Small_Intestine | SE_54550 | chr1:19716169-19718904 | Stomach_Smooth_Muscle | SE_65446 | chr1:19716642-19717397 | Pancreatic_islets | SE_65446 | chr1:19717662-19720701 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 19717195 | 19718433 | chr1 | 19716796 | 19717030 | chr1 | 19717212 | 19718898 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I019389 | chr1 | 19716333 | 19720569 |
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Enhancer Sequence | AACCAGTCCC TACACTCATC TGAACCCCGG CCCCCGCCCC CTACTCATGT CGAGTGCTTA 60 GAGCAGTGGA AGAAATCACA TTAAGTGTCA CAGACCATGG GTTTGTACAG TGATTTAAAT 120 GAAACGACAG GTCCAAACAA AGCCGAGAGT TCACTTTGGG GTGCATGTGG CACTGGCTCT 180 GTCGCCTCCA AAGCCAGGGA GGGCCTCTGA GGAGGAGGAG CGGTGCTGAC ACGCGGCAGC 240 CGGATGGTTT CTGTCTAAAC CACCCATCTG AACTGCCTAA CGGCCTTGGA GGGAAGGTTC 300 AGATAACACC AAAGGTGTCA GACCAATCCA GGCTGTTGGG GGGATTTAAA CATAATTCCC 360 AGTGACTTGG AATAATAAAC ACTACACTGG TCAGGACAGT GCCTGCCGTC TTTCTGGTGG 420 GAGTTCAGGG CTCCACCAGT TCCTCTGCTG CCACAGGAGT GTGCCCACCC CAGGGAGCAG 480 GAGCCACAAG TCCTTCACCA CCGATACTTT TGCCGGGCTC GGTGGTACCC AGGAGGCCAC 540 TGGAAAGACG GGTGGGGAGT GGGTAAAGTG AACTAGGGCA GGGAAAAGAA AAAACCCCAG 600 AAGGTAGAAG GTAAGGGAGA GACTAGGATG CCATTGGCAA CGGCCTCAGG TGACACCTGA 660 ATAATAATCC GTGGAAGGAC CAGGTGATCG TAATAGCCCT GCCCTGCGTG GCAGGCACTA 720 TGCTAGCAGC TCTCCCTGCC CTTCCCTATG ATCCTGACAA TGGCTCTTCA CACAGACACG 780 CACTCCAGTC CTTGTTTTAA AGAAGGGGAA ACAGGGCCTT AGAGAAATAA CTTGACCGGA 840 GCCACGCAGC TACGGGCCAA TGTCTGAGGA AGGACATGCA GTTATATACA GCACAGCTAG 900 GTTCAAAAAG AAACTGCTTT TCCCAAACTG AACACTTTTT TTTTTTCTTA AATCATCCAA 960 CCCAACAGCT GATCACACGA AGAGATACAA ATCAGAAGTT TCCGGCCACA AGTGAGGTTC 1020 GTGTTTGTGC CGCCATATGG TTCTACTTTG CCTCTTCCTC TTCTCCATTA GTTATTAATG 1080 TTGAAAAAAA TTGTTCAACC AGAAAAAGAA ACTTGAGATG AACCCTTAAA AAAAGCACAA 1140 AAGCCAGAGC AGCTCAGACC CACGGAGTCT AACCCACGGC GCCCTTGTCT TTAAGAAGTG 1200 CACCCTTGTA CCTCGGTTTT TTAAAAAATG GCCAAATGAA CACATTCCAT CTTTTGATCT 1260 GCCTGTTGGC CGAGAGCCCA CCACCAGCAA GATAGGAATC AAAAACAGAT TCTGCGTACT 1320 TGGGTGCACT CAGAGGAAAC TGCCACGCCA GAATGCTGCA GCTGCCGACG TCCAGCAGAG 1380 GGCTCTGTGA CAATTTGTTC CTTTTATTTT TCCAGAAGGC CCAAAACTTT CTTAAAAAGA 1440 TAAAAGAGCA TTTCAAGTGG CACATACACT CGTGTCAGAA ACAAAATATA CAGTGTGGCA 1500 TTCTGTAAAA ACACCAACCT CGAAACCGAA CAGGTTCAAA TCCTCGGTCA GTCACTTGCT 1560 GGCTGAGTGT AACCTTCCTA AGTCTCTGGA ACTGGGGGTT ACAACATCCA TGTCAAGGAG 1620 AAATTCACAC TGTTCCATAA ACCCCGAATG CCCGCTCCAG GCCCGTGTCA GGTGCAAGGG 1680 CTCAGCACGG GAAGAGATGG ACATGGGCGG CCCTGCTCTG ACAGCAAAGT CCAGCCACAG 1740 AGGCATCTCC AAGAGGCAAG GGTAGGCCAG GCATGGTGGC TCACGCCTGT AACCAGCACT 1800 TTGGGAGGCT GAGGAGGGTG GATCACTTGA GTTCAGGAGT TCAAGACCAG CCTGGCCAAT 1860 GTGGCAAAAC CCCATCTCTA CTAAAAATAT ACAAAAATTA GCCAGGTGTG GTGGTGCATG 1920 CCTATAATCC CAGCTACTCA GGAGGCCGAA GCAGGAGAAT CACTTGAATC TGGGAGATAG 1980 AGGTTGCCGT GAGCCAAGAC TGTGTCACTG CACTGTAGCC TGTGCGACAC AGAGAGACTC 2040 TGTCTCAAGG TAAAAAAAAA AAAAAAAAAA GAGGCAGGAA GCGAACCTGC AGGAGACGAC 2100 AGAAGGGGGT TGCTGTGGGG GCAAGTCAGC AGTCTAGGAG GTGGCACAGA GATGACATGT 2160 GAATAATGAC CAAGGAGCCG GCCCTCCAAG ACTGCAGGGA AAAATAACAG GGGCATCCCA 2220 AGAAGAGGGA AGAGCTGGCA TGAGGCTCTG CTGCAGAGGC CACTGAGGCA AGTGCAAGAA 2280 CAGAGAGGAG CAAAGCGCGG CTGGAGTGAG ACCCAGTGAG GCAGCACGCA GCACCTCCTG 2340 GGTCACTCCA 2350
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