Tag | Content |
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EnhancerAtlas ID | HS193-20461 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr20:19737890-19740110 |
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) |
Myod1 | MA0499.1 | chr20:19739280-19739293 | AGGGACAGCTGGA | - | 6.16 | NRF1 | MA0506.1 | chr20:19738661-19738672 | CGCGCAGGCGC | - | 6.14 | ZNF263 | MA0528.1 | chr20:19738850-19738871 | CCTTCCTCCTCTTCCTCCTCC | - | 10.77 | ZNF263 | MA0528.1 | chr20:19738853-19738874 | TCCTCCTCTTCCTCCTCCTCC | - | 11.13 | ZNF263 | MA0528.1 | chr20:19738837-19738858 | CCTCCTTTCTCCCCCTTCCTC | - | 6.05 | ZNF263 | MA0528.1 | chr20:19738789-19738810 | AGCCCTTCCCTCCCCTCCTCC | - | 6.24 | ZNF263 | MA0528.1 | chr20:19738807-19738828 | TCCTCTTTCCTCTCCTCTCCC | - | 6.2 | ZNF263 | MA0528.1 | chr20:19738838-19738859 | CTCCTTTCTCCCCCTTCCTCC | - | 6.63 | ZNF263 | MA0528.1 | chr20:19738814-19738835 | TCCTCTCCTCTCCCCTCCCCT | - | 6.69 | ZNF263 | MA0528.1 | chr20:19738828-19738849 | CTCCCCTCCCCTCCTTTCTCC | - | 6.71 | ZNF263 | MA0528.1 | chr20:19738795-19738816 | TCCCTCCCCTCCTCCTCTTTC | - | 6.81 | ZNF263 | MA0528.1 | chr20:19738804-19738825 | TCCTCCTCTTTCCTCTCCTCT | - | 7.12 | ZNF263 | MA0528.1 | chr20:19738819-19738840 | TCCTCTCCCCTCCCCTCCCCT | - | 7.1 | ZNF263 | MA0528.1 | chr20:19738844-19738865 | TCTCCCCCTTCCTCCTCTTCC | - | 7.27 | ZNF263 | MA0528.1 | chr20:19738824-19738845 | TCCCCTCCCCTCCCCTCCTTT | - | 7.2 | ZNF263 | MA0528.1 | chr20:19738831-19738852 | CCCTCCCCTCCTTTCTCCCCC | - | 7.53 | ZNF263 | MA0528.1 | chr20:19738841-19738862 | CTTTCTCCCCCTTCCTCCTCT | - | 7.67 | ZNF263 | MA0528.1 | chr20:19738862-19738883 | TCCTCCTCCTCCTCTTGCTCC | - | 8.28 | ZNF263 | MA0528.1 | chr20:19738792-19738813 | CCTTCCCTCCCCTCCTCCTCT | - | 8.56 | ZNF263 | MA0528.1 | chr20:19738847-19738868 | CCCCCTTCCTCCTCTTCCTCC | - | 8.64 | ZNF263 | MA0528.1 | chr20:19738856-19738877 | TCCTCTTCCTCCTCCTCCTCT | - | 9.38 | ZNF263 | MA0528.1 | chr20:19738865-19738886 | TCCTCCTCCTCTTGCTCCTCC | - | 9.44 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_25320 | chr20:19737341-19740094 | Colon_Crypt_3 | SE_27220 | chr20:19737317-19742104 | Esophagus | SE_33568 | chr20:19737077-19740559 | H2171 | SE_37230 | chr20:19737239-19743420 | HSMMtube | SE_40908 | chr20:19737269-19742041 | Left_Ventricle | SE_42706 | chr20:19737283-19741946 | Lung |
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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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Enhancer Sequence | CTGTCCAAAA CAACCGTCTC TCTGACACCT TCGAGGTGTC CCTTTGTCTC TTTGAGGTTC 60 CCTCCGTGAC ACTGGCTACT TTGTAACTCT AACACTGTCA GCAATTAATT CCCAAAGGTG 120 AGGTCCCCGT GGGAAGTGGG AAAACCCAGC GAATCACCAG GGACCCGCCT GATTCCGAAA 180 AGGCTGGATG CTGGCTGGGA ACCGGCCCCG CAGCTCCGGC GTCCCCGCCT GCCTGCGCGG 240 CCTTCAGCTG GGGTTACGGA GGGCTCCCAG CGCCGATCCA AACCGCGTTC CAGGCGGGGT 300 GGGCGGGCCC CTGGCCAGCG AGGCCGAAGC AAAACAACCC GCCCAGGCGT CCAGAGCGTA 360 TCCAACCCTG GAGAACCTGC CCCGGAACCA AGAGCCGCAG CCAGCTCAGG CCTCTCGAGT 420 GGGGCCTTTC CAGCCCCTGC AACAGATCCC GGGATCTGTA GTTGGGCGGA GGGGCTCGTT 480 ATGGGAAAGG GGTGCGTGCG CGTTTGTGCT AAAACAAGAA AGGCAAGAAT CTCCGAGAAC 540 AAAACTCTGG TCCTCGCCTG GCCGGGGACC GCAGAAGACA GGGGCGGCAG CGCCAAGGCG 600 GGTCAGGGGC CGGTCCAGCC AAGTTTGCTC CGGCTTAGAT AAACTTTCTG ATGGCAGTTT 660 TTCCTGGTTG CAGCCTGGGT TCCTTGTAAC AGGGTAAGCG TAGCGGGTGG TTGTCAAGAG 720 GGGCGGAGGC TGGCGGTTAC AGGGAATGGA GGGATGGGCC GGACCTGGGG TCGCGCAGGC 780 GCCTTGGTCG CTGCCTCCGA TCCGATCACC CCCGCCCCAT CTCCTCTGCG AGCTCAGGAA 840 GGTGGCTGGG GGAGGGGGAT GGCTCCCTAC TGCCGAGGGA CGGCCCGAGG CAAACACAAA 900 GCCCTTCCCT CCCCTCCTCC TCTTTCCTCT CCTCTCCCCT CCCCTCCCCT CCTTTCTCCC 960 CCTTCCTCCT CTTCCTCCTC CTCCTCTTGC TCCTCCCGGG CGGGGAAACC CAGCCCCGCG 1020 CTCGTCTTTG GGGCCACCGG TCGCCCCCGC CTCCGGGACC TGCGGGGAGG GCCCGCGAGA 1080 GGTAAGGGGC GGTGGCAGCG GAGACCCCAC CCCCTGTGCC CGCACCTAGA GAGCCCGGAG 1140 AGGCTCCGGG CACGGGCGGG GCTCTCTGGG GTTCCAGACG TGGGTGCTGC TGTGCGCACT 1200 CTCTCCCTAC TCCGGAGGGG ACTTGAGGAA GACAGCCAGA GCGCGTCCTC GGGGATCGTG 1260 GGGAACGGAA GGGGGAAGGG GGATCAGGGA GTGGGGACAA GGGGCAGAGT GACATTCCGG 1320 AGCGCGAGGT GGCCGCTGGT CCCGGCAGGG TCACCGGGTG TCCTCAGCTG ACCTGTGCGG 1380 GGCTGGGGTG AGGGACAGCT GGAGGGTGCA GGCACTATGG CTCGAGGTGC GGAGGTGCGG 1440 GTGTGCGTGC GTGTGCACCG GACGGAGTTT GGTAGGGACC TTTGAGGAGT TCTACCTGCA 1500 GGGCTGCCTG TGGGGTGTCA AGTGCTCCCT GCGCCTGAGC GCGCGGGTCA GACCCGGTGT 1560 CGCACAGCTT TGATCCCCAG CGCGGACCCC ACTGGTGAGT CCAGCCAGTG TGCAGGGCAG 1620 ATGCTCCGAC CGGAGATTTC CTCCCCCGGG TGGAAAAGCA GGAGGGTTGT TGTGTCCGGG 1680 CAGGGGGCAC TTGGGCTGTC GCGGTGATTG ATGGCTGCGC AGCGGGCGGA GGAGGAGCCC 1740 CGGATTCCTG CCGGGAAGGG ACGGGGCCAC TTTCCCACTT TGAGGCCTCC CCGCCCCCTT 1800 CTGGGCTTGG CCTCCACCCT TGGCCTGGGC TCCCACCAGC TCGGCGTCCA CCCACCGGCG 1860 GTGGCGCGCC CCTCGACCGC GCGGGGACAG CAGGATTTGC AGAAGTTCAG CTTGAAAGCC 1920 TATGATATGT TGCCAAGAAA TACAGGGCAA GATCGGTCCC CTGGGCCCTG AGAGGCGCCT 1980 GTCTTCTCAG AGCTCTTAAA TCCCTGGGGC TTTCCTAATT CCGCAGTGTA GCGGCACTTC 2040 CTTGCGCGGT TTTGGGCACA TTGGGGTTTC TTAGGAACAC GCTGTCATCG GTAAGGAAAC 2100 ATCAGAGTAC TCTTCGACCA AAAGGACTGT AAATACTGAA GCAAAAAGAA ACACTTGCTG 2160 GGAGTGCAAA GGGCTTACTG GGAAAAAAGA AACACACAGG GCAGCACTCC ATCATTAAGA 2220
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