Tag | Content |
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EnhancerAtlas ID | HS188-05187 |
Organism | Homo sapiens |
Tissue/cell | Th2 |
Coordinate | chr17:4383250-4386430 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr17:4383970-4383988 | GGAAGGGTGGAAGGAGGG | + | 7.04 | NR2C2 | MA0504.1 | chr17:4384890-4384905 | AGAGGGCAGAGGGCA | + | 6.62 | Nr2f6(var.2) | MA0728.1 | chr17:4385401-4385416 | CGATCTCTTGACCTC | - | 6 | PLAG1 | MA0163.1 | chr17:4385424-4385438 | CCCCCCTTGGCCTC | - | 6.06 | ZEB1 | MA0103.3 | chr17:4384160-4384171 | CCCACCTGCCC | + | 6.14 | ZNF263 | MA0528.1 | chr17:4384335-4384356 | GGGTGAGGAGGGTGAGGGAGG | + | 6.58 | ZNF263 | MA0528.1 | chr17:4384329-4384350 | GGAGCAGGGTGAGGAGGGTGA | + | 6.72 | ZNF263 | MA0528.1 | chr17:4383967-4383988 | GGGGGAAGGGTGGAAGGAGGG | + | 6.77 | ZNF263 | MA0528.1 | chr17:4384338-4384359 | TGAGGAGGGTGAGGGAGGGGA | + | 7.18 |
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| Number of super-enhancer constituents: 19 | ID | Coordinate | Tissue/cell |
SE_23583 | chr17:4382378-4385214 | Colon_Crypt_1 | SE_23583 | chr17:4385402-4387697 | Colon_Crypt_1 | SE_24329 | chr17:4382476-4385188 | Colon_Crypt_2 | SE_24329 | chr17:4385419-4387592 | Colon_Crypt_2 | SE_26970 | chr17:4382504-4384084 | Esophagus | SE_26970 | chr17:4384372-4385197 | Esophagus | SE_28097 | chr17:4378603-4387608 | Fetal_Intestine | SE_29102 | chr17:4378472-4387704 | Fetal_Intestine_Large | SE_31567 | chr17:4382469-4385277 | Gastric | SE_31567 | chr17:4385380-4387675 | Gastric | SE_42277 | chr17:4383361-4385251 | Lung | SE_42277 | chr17:4385387-4387616 | Lung | SE_53037 | chr17:4381447-4385287 | Small_Intestine | SE_53037 | chr17:4385363-4387724 | Small_Intestine | SE_53662 | chr17:4384026-4385141 | Spleen | SE_57545 | chr17:4382493-4385202 | VACO_503 | SE_57545 | chr17:4385406-4386959 | VACO_503 | SE_57914 | chr17:4384151-4385051 | VACO_9m | SE_65581 | chr17:4383216-4387811 | Pancreatic_islets |
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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 |
GH17I004475 | chr17 | 4378469 | 4387600 |
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Enhancer Sequence | CATTTTCTAT CCCCCAAAGA AATCATGGTG CCCTAGAATC TGGGTTTGAA AGGGTTATGG 60 GCATGTATAG TCGTTGAATC TGTCAACAAA CCCTGCTTGA ATACTACTGT GGATGGGGTG 120 CTCACTCCCT GCCAAGATGT CTGCCCCTCC CCGGCAGATC CCCTGACCCC TCCCCACGGC 180 CCAGGCCCAG CGAGTGTGGA GAGGCCTGCC CTGTCTTTGG CTCCTGGGTG AGTGGATCAG 240 CTGCAGGACT GGCAGGTCTT CCCTGCCCCT CCCTCCAGAC AGGAGACTTG GGCTCCAGCC 300 CAGAGTCAGC CGCAGACCTG CTACATGGCC CTGGGCCTCA GTTTCCTTGT CTATAAAAGG 360 GGTAATCACC ACCTGCCCGG TAGGGTGAGC AAGGCGGCCT CCAGGAATGC TCAGGAAAGG 420 GGAAGGCATT GGCAAATGTT TTATTCATGG GATTGTCCAC TTTTAGGCTC AGGGAGATTA 480 ACATCCCCCC AGCATAGCTG GTTCTCTCTG AGGTGGTCCA AACAGAGCTG CACCTGCCCC 540 CACAGCTTCC CTGGCCTGCC CCCCACGGCG CAGCTCCCTC TTCCACATGA CAGCCCCACA 600 GATATGTGAA GGCTGCACCC GTGTCCCCCA GCGTCTGCAT TTGTAAGAAT GATTAACCTG 660 GCAGAGCCAG GCTCTTTGTG GGGTTAAAGA GGAGAGTGTG TGCTGGAGAG GGCGGGTGGG 720 GGAAGGGTGG AAGGAGGGTT AGGGGCTGGC CAGCTGCACA GTTTTACCCA TTTGGGGAGC 780 TGCCCAGGGA GCCGGCTGGA CAGGAACCAG CCCACCTCAG GGCTCCCTGT GGCCCTTCCT 840 TGGCTTGGAG GCCTCCAGCC ACAATGCTTT GCACCACCAT CCCAGAGCCT CCCGCCCCCT 900 TCCCTGCCTT CCCACCTGCC CGGAGCCCCG TGGCCAAAGA TGCCTTTTGG CCTTCGGGGA 960 TCAGAGCTGA GCAATCCTTG TAGCCCCTAT AGTTCGGTTC CTCCATGTTG CTGCTTCCTC 1020 CCTGTAAAGG CAGGTGGTGG GGGAGCCGTT CTGTGCAGTG GAGGGGCAGA TGCCAGCTTG 1080 GAGCAGGGTG AGGAGGGTGA GGGAGGGGAA GCAGGACACC GAGGGTAGAC AATTCCCTTG 1140 AGGAGCTGAG CTGACAGGAG CAAAGGGCAT GGTAGCTGGA GTTGGCAGAA GATCCCAGGA 1200 AGCTGGCATT GCTTTTCAAG AGGGGAGGAC AGAACAGCCT CCAGGGAGCA GAGAGGGGCA 1260 AGCAGGAGGA GAGAGGGGGC CATGTTTGAG GGTGAGCTGG GGGTGGAATC CAGCACTGGG 1320 GGAGGAAGTG GCCTCCCAGC AGAGCAGGGG CAGGAAGTGT GTGGGGACAG GGTCTGTGGC 1380 AGGAAGTAGA GGAAGGTCCC CTTTGCCGGC CGGCACTGGC TCCTGAGACA GGAGATCGGC 1440 TTCTCTTTCA GCAGGGGCCC AGGGAGGGAG GAGGCCTTAG GGTGTGTGTG AACAGGGTCC 1500 ACAGAACAAG GGAGCAGGAA GCTAAGGGCA GGGCACGTTC ACGTGAACAG CTTTGGGCGG 1560 CCAAGAAAGC CACGAGGAGC TGATAGGAAA ATGGGTGGAA ACTGCAGGTG TCTGGGTGGT 1620 TGGAGCCTGT GGGTTAGGTC AGAGGGCAGA GGGCAGCAGA GCCCAGGCTC GAGGACTCTG 1680 CAGCAGCCCA TCTGCTCCCA CTCCCAGCCT GGCTCCTCAC TAGCTGTGTG ACCCTGGCCA 1740 AGTGACTGAA CCTCTCTGGG TCTTGGTTTG CTCACCTGTC CAGTAGGTAG AGCGGTGGCA 1800 ACCACCATTG ACACCCCAGG CTATAAGGAT AGAATGAACT CACACCTGCG TCCTGCAGAT 1860 TCCTGAGTGG GCGTGTGGGC CCCACTGACT TCCAGATCAT CCCTTCCTTG GGACACTGCT 1920 CTCTCTCTCT CTTTTTTTTT TTTTTTACTT TTGAGACGGA GTCTCGCACT GTCGCCAGGC 1980 TGGAGTGCAG TGGTGCGATC TCAGCTCACT GCGACCTCTG CCTCCTGGGT TCAAGCGATT 2040 CTCCTGCCTC AGCCTCCTGA ATAGCTGGGA CTACAGGCAT GCGCCACCAC GCCCAGCTAA 2100 TTTTTGTATT TTTAGTAGAG ACGGGGTTCA CCATGTTGGC CAGGATGGTC TCGATCTCTT 2160 GACCTCATGA TCCGCCCCCC TTGGCCTCCC AGAATGCTGG GATTATAGGT GTGAGCCACT 2220 GCGCCTGTCC AGGACACTGT TCTCTTTGAT GCCATCTCCA CAATGGGGAG AATCCAGGTT 2280 ATCTCTGGAG AAGGGACCTC AGGGGCTCTC CGGTCCGGTG GCTTGGAGAC GTCATTGTGC 2340 ATGAGAGTCA GATTTGAGGG AGCTTGTGAC AAACCCAGAT TCCAGGCCCT GTGTCCTCTG 2400 AGTCTGATTC AGTGGGTCCG TGCTGGGGTC CAGGGACCTG CATTTCTGAT GAACTTCCCA 2460 AGTGATCCTG CCGTAGCATT CCGTAGAGCA CGCTTTGAGA ACACTGGTCT CACGCCGCAA 2520 GCTCCCCAGT CCATAAATGC TTTGCCAAAT TCTAGCCATC CCCTTGTTGA CATACGCCTC 2580 CAATGGGGAG CTCGTTCTGC ATACCTCGGG CAGCCCCTGC CTCTCGGGGG GTTTCTGTTG 2640 ATGAAAATGA TTTGGTTCAG TCACAGCCAA GACCCACCTC TGCCAGCCTC CCCTTGGCCC 2700 CGCTGGGCCA TAGAGGGGCC CTGCTCCCTG GAGACTGAGA TCGTGTCCCC TGAACCCGCA 2760 TCTCCCCAGG CAGAGCTCCC TGCCTCCCGA AACCTAGTCA TGAGGTCTTC AGCTCCCTCC 2820 CAGCCCTGCT GTCTGTCCCC GCCCCACTCA GGATGGCCCA GAGCCAGCTC ACCCCAATCC 2880 CCCTCCAGGC AGGGGACAGT GTAAGCAAAG GTGTGGAGGG AGGATCCCAG GGGCACGATC 2940 TCTGGATCCC AACCAGTTGG GGGGCTAGAG CAGAAGGGGA GCTCATTCCC TCTTTCTCAG 3000 CCCTGTCCTC TGGGGTCCTG GAATCCAGCC ACAGGCTCAT CTCCCACCCC TCAGCAGACG 3060 TCCCCACAGT TCCCCGGAGA GTTGTCACCT CTGCGTTCTC CCCCTGCCCC AGGTCTCCAT 3120 GCTTCCCTGC TCAGCCTCTG CCCCCCAGGT AGCTGTCTGC TCACTGGCCT GTCTCACCCT 3180
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