Tag | Content |
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EnhancerAtlas ID | HS191-25088 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr22:50339960-50341900 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PLAG1 | MA0163.1 | chr22:50340609-50340623 | GAGGCCCAAAGGGG | + | 6.37 | PLAG1 | MA0163.1 | chr22:50341608-50341622 | GGGGGCCACGGGGG | + | 7.1 |
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| Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
SE_03028 | chr22:50341487-50344026 | Bladder | SE_10530 | chr22:50338855-50340155 | CD19_Primary | SE_11301 | chr22:50337371-50340370 | CD20 | SE_17545 | chr22:50337358-50341301 | CD4p_CD25-_CD45RAp_Naive | SE_17909 | chr22:50337253-50340777 | CD4p_CD25-_CD45ROp_Memory | SE_23129 | chr22:50340142-50347336 | Colon_Crypt_1 | SE_23738 | chr22:50340192-50347293 | Colon_Crypt_2 | SE_24687 | chr22:50340156-50348528 | Colon_Crypt_3 | SE_26808 | chr22:50341423-50346477 | Esophagus | SE_28169 | chr22:50340100-50347261 | Fetal_Intestine | SE_29459 | chr22:50340194-50347426 | Fetal_Intestine_Large | SE_31381 | chr22:50340030-50364844 | Gastric | SE_34375 | chr22:50340613-50344021 | HCT-116 | SE_35007 | chr22:50337640-50340278 | HeLa | SE_35007 | chr22:50341530-50344029 | HeLa | SE_35554 | chr22:50341650-50344088 | HepG2 | SE_41617 | chr22:50340249-50340536 | LNCaP | SE_42159 | chr22:50339996-50364887 | Lung | SE_47471 | chr22:50340157-50349301 | Pancreas | SE_50117 | chr22:50339205-50347666 | Sigmoid_Colon | SE_52469 | chr22:50340730-50346981 | Small_Intestine | SE_56937 | chr22:50340142-50346911 | VACO_400 | SE_58096 | chr22:50340895-50342014 | VACO_9m | SE_61206 | chr22:50315437-50364432 | HBL1 | SE_61985 | chr22:50315627-50364432 | Toledo | SE_62450 | chr22:50318672-50364388 | Tonsil | SE_65335 | chr22:50340176-50344048 | Pancreatic_islets | SE_68380 | chr22:50327316-50364640 | TC32 | SE_68381 | chr22:50327316-50364640 | TC32 | SE_68382 | chr22:50327316-50364640 | TC32 | SE_69071 | chr22:50340249-50341775 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 50340250 | 50341213 | chr22 | 50340274 | 50341177 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I049942 | chr22 | 50336159 | 50349619 |
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Enhancer Sequence | CCCAGCTACT CAGGAGGCTG AGGCAGGAGA ATCACTTGAA CCCGGGAGGT GGAGGTTGCA 60 GTGAGCTGAG ATCACACCAC TGCACTCCAG CCTGGGCAAA AGAGTGAGAC TCCATCACAA 120 AAAAAAAAAG ACTTTGGATA AATATGTGTT GTCCAACAAC TTTGGATAAC AGAAAACACC 180 ACAACAAGTT GAGAAATGGA TTACAGAAAA AAGAACGAGC TTCGTACGTT AGCACCTATA 240 ATATCATTTC ATCCTGCATT TTGAACAATG AACCCTGAAT TCTCATGTGC GCTGGGCTCT 300 GCAAATCATG TGGCTGCTCC CCATAGTCAG GAAGGAGAGT GGGACTCAGG GGAGGAGGCA 360 GGATGAGCTG AGACCCAGGC TGCCTGTCCC TACCACTGAC CAGGACAGCG TTCCAGCCTC 420 CCCGTCTGCT CAGAATCTGC CCTGACCTGC TCCACACCCC CGCAGGCCCG CAGGGGAGGG 480 CAGAACTAGA AGGGACCAGC GCATAGGGAC CTGGGGGTGC TGGCACTGAG GTCTCTGGGC 540 CTGGGATGCT GACCTTCCCG GAGCCCTGAG CTGGGCCAGG ACGAGGTCTT CCCATCAGAC 600 TTGCCGCTGG CTAGGTGACC GGCCTGTCTC ACAGATGAAA ATATATTCTG AGGCCCAAAG 660 GGGGCCCAGA CCCTGACTTT GTGGCCCAGA GCCAGGTTCT CCCCATAACC AGCAGGCTTC 720 TTTACCCACA GGCCACTGTC CACCCAAGCC CCGCAGGCAG GAACCCTTGG TATTGGGTGG 780 CCCTGAGCTT GGGATTTGCC GCTGGCTGTG TGGCCCTTCG GAGCCAGTCC GGCACACCCG 840 CAGGCACACA CACATGCGCA CTCGCATACA GCCACAGATT ACACAGGCAC CAGCTTCCCG 900 GGAATCCATT TGTCATGCAA ATGCCCCTCC TGGGGCCCCT TGCCTCCCCA GAGCTGTGTC 960 TGTCCAGGGT GGGGCCCAGG TCCGTGGAGT CCTGCAGTTT CCTGGCCACA GCTATTGGCA 1020 ACTGAGGGAT GTCTCTCCAA AGAGGACCCA GATCCACGTC CAGGCTTGCC TGGGACCCGA 1080 TCCCTGCCCA GTGCGGGGGC TGCAGCCTCA AGGCCCAGTC TGGCCACCGC CAAGTCCACT 1140 GGGAGCCAAG TGTGGGTTCA TTCCCTCGTG GCTTCTGGTG CACCAGTGGG GTGGGGGGCC 1200 AGGCCTCTTT CCCTCCTTGG CTGCCTCAAA GCAAGAGGGA GGGACTCTCA GCCCTGTGCC 1260 CACCGACAGG CCCAGTCTCC ATTCCTCCTA AAGCCCCTCT ATGGCCCCCC AGCCCTTGGA 1320 GCTGAGCTTG TGAGAGCCGT CCCCTACAGG GTGGGCTCGG GAGGCAGAGC TGTGAGCCTG 1380 CTCCCCGCCC ACCCAGAGCC CAGCTGGGGC AGACCCAGGC ATCCAGGCCG GCAGGGTGAG 1440 CCTGTGCCCA GGTTGGGCAG CCCCCTATGC TGGGGGTGGC CAGGCTCTGG GCCTAAGTGC 1500 TGCCGGGAGA CAGGGTGGCT GGGCTCTGGG ATGCTGGCTG AGGGACACAG GCTCCCTCCT 1560 GTCCTCCGGG GCCAGTGGAC CCTGGGGCAG CCCCCATGCC TGCTGTCCTG TCCCCACACA 1620 GCCTGTGAAG CAGGCTCCAG GCACACATGG GGGCCACGGG GGCAGGTGGT CCAGACGGCT 1680 CTCAAGGCAA AGCTGGGAAC ACTGTCCCAT CCCTCTGGAA CCCGCCCTGG TGAGGGGTGC 1740 AGGGGCCCTC AGTGGCCACC TTATAGGACC GGGCACCGGG CACTTCATGA GGCTGTCTGC 1800 TCGGCCACAG CAGCCCTGCT GATGGAAGCC AGCCCTGGGC CCACTGCAGC TGAGCCACCC 1860 AGGGGCCTGG CCACCCAGAG CTTCCCTGAT AGGCTGCGCT GTGCCCGGAG CCCCCCAGTG 1920 ACTGTCTCCT GCCCAGCCAG 1940
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