Tag | Content |
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EnhancerAtlas ID | HS098-57221 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr9:38035370-38037950 |
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) |
ESRRB | MA0141.3 | chr9:38036035-38036046 | TCAAGGTCATA | + | 6.62 | Esrra | MA0592.2 | chr9:38036034-38036045 | CTCAAGGTCAT | + | 6.02 | Esrrg | MA0643.1 | chr9:38036035-38036045 | TCAAGGTCAT | + | 6.02 | PRDM1 | MA0508.2 | chr9:38035493-38035503 | TCACTTTCAC | + | 6.02 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_00446 | chr9:38035274-38037855 | Adipose_Nuclei | SE_01843 | chr9:38035849-38037381 | Aorta | SE_02310 | chr9:38035164-38037218 | Astrocytes | SE_04803 | chr9:38037075-38038316 | Brain_Cingulate_Gyrus | SE_05785 | chr9:38036275-38041022 | Brain_Hippocampus_Middle | SE_23246 | chr9:38034914-38035808 | Colon_Crypt_1 | SE_26555 | chr9:38035522-38037321 | Esophagus | SE_28791 | chr9:38029759-38035765 | Fetal_Intestine_Large | SE_33929 | chr9:38035258-38037356 | HCC1954 | SE_34811 | chr9:38034088-38040783 | HeLa | SE_36884 | chr9:38035316-38037082 | HMEC | SE_38030 | chr9:38034960-38040717 | HUVEC | SE_38998 | chr9:38035048-38039881 | IMR90 | SE_40993 | chr9:38037427-38040848 | Left_Ventricle | SE_42283 | chr9:38037522-38040704 | Lung | SE_44329 | chr9:38035017-38039025 | NHDF-Ad | SE_44779 | chr9:38035042-38040081 | NHLF | SE_45758 | chr9:38034875-38040105 | Osteoblasts | SE_47196 | chr9:38029911-38057164 | Panc1 | SE_48861 | chr9:38036997-38040800 | Right_Atrium | SE_51847 | chr9:38035299-38037355 | Skeletal_Muscle_Myoblast | SE_55662 | chr9:38034844-38039953 | u87 | SE_57367 | chr9:38035126-38035751 | VACO_503 | SE_57367 | chr9:38036342-38036769 | VACO_503 | SE_63571 | chr9:38035287-38037494 | HSMM | SE_64986 | chr9:38035005-38037312 | NHEK | SE_65279 | chr9:38035619-38036887 | Pancreatic_islets | SE_65279 | chr9:38037547-38039359 | Pancreatic_islets | SE_67542 | chr9:38034844-38039953 | u87 |
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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 |
GH09I038035 | chr9 | 38035151 | 38041531 |
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Enhancer Sequence | TTTGCCACTA GAAACTCTAT AGTCCTCCTG AGATTTTTAT GGTACCCTGA AGCATAGGAC 60 TGGGGATAGG GGAGCCAGTG TTGAAGGGGT TGCTCCAACC TTATAAAACT GCATCCCTCC 120 CTCTCACTTT CACAGGCTGC TCAGTGAGAG AGGTTCTCCA CCTCTTTCCC CAGTGGCATG 180 TGAAAGGTTG GGTGCCATGG GAGAAGCACA GAATCACATC CTGAAGTTCA GCAATGCCCA 240 CGGTGGGGTA GGTCTTGGGG ACAGAAGGAC AAAGCTCAGT CAGTGTCTAC CTTCCATGAG 300 TGGATAATCT AGGGAGAGGT CAGCAACCCT CTCCTGTAAA TTACCATATA GAAAATATTT 360 TAGGTTCCTG AGGGTCATAC AGTACTCCTG GTTTAGTCCA GTGATTCTCA ACATAGCTGC 420 ACATCAGAAA AACTCCTGGG GAGCTTTTAC AATGCACCAT GCCTAAGTTT GGCCCCCAGA 480 AATTCTGATT TAAGTGGCCC AAGGTGGGGC CTGGGATTAG TATTTCTAAA AGCTCCCCTA 540 GGAGCTTGGA TACAATCCAT CCAAGACTGA GAATCACTCT CTGGTCTCCA GCAGAAACAG 600 GCGCGTGCAA AACCTCAGCA TTATCCCCAG TGATTTCCCA AACCCAGCGA GGGGAAGTGA 660 CTCGCTCAAG GTCATACAGT GAGTCAAGAG GCAAAGAATC TGAGCCCAAG ATCTTCTCCC 720 TGCAGCACCC AGGCACAGAC AGGCCCAAAC TCCTGTTCCA GAGCTTGGGA TACCAGGCCT 780 TCTTGCTCAA GCCCTGCTGC CCCATAAGGT GAAGACCCCA GAGAAACACC AGCCACATTC 840 GCCCCGACCC ACTCTAACGC ATGGGGCACT GCCCTCTCTC CAGACCAAAC CTCAACGAGG 900 TAGAACTAAC AGGGGAATGA ATTTCTAAAA CAGCCACATT TTAACCAAAA TTGCTAACAG 960 TTTATTAGCA TCTGGGAGGA ACAAAAGTTA GGGCTGTAAA AACTGTATTT CTTCAGTCCT 1020 AACAAGCGCA GCCACAGCAA ACTCTTTACC AATGACACCA CTAAAGACTT GCCAAAACGT 1080 GCCGCCTGCC TAGAGCTCTG CCCACGCAGG ACTTGGGCAC AAGGAACCCC CAGAGCCCTT 1140 GGGAATGTTG CAAGAGCTTG GCTGAGGCTG GGTGGCCACT GGCGGCGATG ATCTCAACGT 1200 CTACAGAGCA AATGAGCTCC GAAAGACAGG GCAGACCCAG GCATCCCCCG CCTAGCAGGA 1260 GCTCTGCTAG TGGAGATAAC TGGAGAGTCT CTGAGCCCCA GACTCTCTGG GGTTCTCTCC 1320 ATTGAGCCAC AGGACAGTGA GGGACTTGAG AGAGCAAGGA TGGGAGAAGC TGAATAATAA 1380 TACAAGAAAT ACTGAGAGCA GCTACCAGGG ACTATGCTCA GTTCTTTTAA TACAACATCC 1440 CTATGGATTT GATTCTCATA TTGTCCCCAT TTTACAGATG AAAAAAACCA AGGCATGGGG 1500 TGGCTGGATA ACATGTCCAA GGTCACCAAA GCAGTTAAGT TGCAGAGCCC TGACTCAAAC 1560 TCGGGTGCTG TCTCTTAATC TTATGCTCAA CAGACTTAGA AGTGACTCTA CTATGAAACT 1620 CCTCCCTGCA GAGACAGCAA AATAGACCCA GAGAGAGCAA GGGACTGGTG CAGGACCCCG 1680 CAGCACGGGA GCTGGGGTAA AAGCAGTTCT GTGTACTGCC CTGTAGACAG CCTGGCTTTG 1740 GGCCCTACTA GGCTGACACA ACTCCCTCTT TTCCCGGAGA AGAATCCTGC GATCTCCTTA 1800 TGACACAACA GTGGGCTCAA ACAAGAGAAC TGGAGAAAGA GATGGCACAC AGGGCTCTTG 1860 TCTGTAGTCT GTGTAAAGTA CCAATTGCTG GAGTACTCCG TGTCATTTGG AAACTTCCTA 1920 TCTTACCTCC ATATAGGCCC ATGGTCAACA GGGCTGTGAG CTTGTTTCCG ACACCTGCCC 1980 CCACCACTGC CCGCTCCAGT CACACGCAGA GTCACCAGCC CCCAACTTCC CCAGGGGGTC 2040 TTCACTCATA CTGTGCCCTT CTCTCTTCTC TGATCACTGC ATGTTCAAAT TCTATCTAAC 2100 CTCCAATGCT CGGCACATGA GAACATGAGC TCTAGAGTGA AATGTGGGTT GAAATCCACA 2160 CTGTGTCACC TTGAGAAGTT TGCTCAACCT CTCTGGGCCT CAGTTTCTTC ACTATAAAGT 2220 GGGGATAGTA ACAGAACCCA CCTCAGTGCT TGGCAACAGG AGGGGCTCAA CTGTGTGTCA 2280 TTATCATCGA TTCAGCCCCC ATGTACCATT CTGAGAACCC CACCTCCGCT AGAAGTGAGC 2340 CTCTCTCCTC TGAGCCCTGA AGTTCTGTCT GCTCCTCCAT TCAGCCTCCC TGGGCTGACC 2400 TTGGGGCAGA TCCTGTGCTG GGCTCTGGAA CATAGAGCAG AAGGAGTGGT CCTTCCTGCA 2460 GGAGACACAG GCTCATTGGG GGATAGCCAC AGGCTCACAA ATAGGCATGA CACAAGGTGG 2520 CTGGGCTAGA AGAGGAGCTA AAAAGTGACA TTTCACATTC TGTCACACTC TAACAAGATT 2580
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