Tag | Content |
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EnhancerAtlas ID | HS051-20070 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr3:129344920-129347380 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr3:129346391-129346409 | GGAGGGAGGGAGGGAGGG | + | 6.03 | EWSR1-FLI1 | MA0149.1 | chr3:129346395-129346413 | GGAGGGAGGGAGGGAGGG | + | 6.03 | KLF5 | MA0599.1 | chr3:129345584-129345594 | GGGGCGGGGC | - | 6.02 | PLAG1 | MA0163.1 | chr3:129346117-129346131 | CCCCCTTGGGCCCT | - | 6.39 | ZNF263 | MA0528.1 | chr3:129346379-129346400 | TGGGGAGGCGAAGGAGGGAGG | + | 6.17 | ZNF263 | MA0528.1 | chr3:129346392-129346413 | GAGGGAGGGAGGGAGGGAGGG | + | 7.97 | ZNF263 | MA0528.1 | chr3:129346388-129346409 | GAAGGAGGGAGGGAGGGAGGG | + | 8.94 |
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| Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
SE_00112 | chr3:129340805-129347842 | Adipose_Nuclei | SE_00978 | chr3:129344947-129347229 | Adrenal_Gland | SE_01893 | chr3:129345011-129347468 | Aorta | SE_04322 | chr3:129343992-129347508 | Brain_Anterior_Caudate | SE_05345 | chr3:129343446-129347451 | Brain_Cingulate_Gyrus | SE_05951 | chr3:129340827-129347709 | Brain_Hippocampus_Middle | SE_07365 | chr3:129343956-129347550 | Brain_Hippocampus_Middle_150 | SE_09767 | chr3:129342751-129347601 | CD14 | SE_26494 | chr3:129343406-129347432 | Duodenum_Smooth_Muscle | SE_27065 | chr3:129344848-129347446 | Esophagus | SE_29874 | chr3:129343657-129347429 | Fetal_Muscle | SE_31569 | chr3:129341039-129347353 | Gastric | SE_37506 | chr3:129343906-129347484 | HSMMtube | SE_37994 | chr3:129339897-129347523 | HUVEC | SE_40701 | chr3:129340197-129347529 | Left_Ventricle | SE_42115 | chr3:129332899-129347478 | Lung | SE_46476 | chr3:129343823-129347545 | Osteoblasts | SE_47266 | chr3:129343410-129347403 | Panc1 | SE_48609 | chr3:129340064-129347458 | Right_Atrium | SE_50249 | chr3:129340253-129347425 | Sigmoid_Colon | SE_51354 | chr3:129340749-129347601 | Skeletal_Muscle | SE_52687 | chr3:129344833-129347492 | Small_Intestine | SE_53375 | chr3:129340176-129347496 | Spleen | SE_62855 | chr3:129293187-129347490 | Tonsil | SE_65523 | chr3:129341199-129347466 | Pancreatic_islets | SE_68869 | chr3:129343741-129347394 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr3 | 129346400 | 129346825 | chr3 | 129346331 | 129346490 | chr3 | 129345321 | 129345603 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I129621 | chr3 | 129340226 | 129347832 |
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Enhancer Sequence | GCAGTGAGCC GAGATTGCGC CACTGCACTC CTGGGACAGA CAGAGTGAGA CTGTCTCAAA 60 AAAAAAAAAA AAAAAAAAAG TCAAATGTAG ACACGTGCAT CCTGGCAATC CCACGTCTAG 120 ATATTGGAAT AAAATTAAAA CACAGGTCCA TAAAAACCTG TACAGATGCT TGTCACAGCT 180 CCATTGATAA TTTCTGCAAT CTGGAAACAA GCCAAGTGTC CCTGGGCTGG TGAAGAGGTA 240 AACACATGGA GGCCTCCATA CAATGGAACG AAAAGGAACA GCCTCTTGAT ACTCCGACAC 300 AAGGATGCAT CTCCAAGCCA GGCTGGAAAG GCTCCACGCT GCAGGATCCC ATGTACATGC 360 TGTTTGGAAA AGGCCAGGCC ACAGGACGGG ACACAGATGG GTAGTTGCCA GGGCTAGGGC 420 TGGGGCTGGG GGGAGGGACT GACTGGGAAG GGCCACCAGG GAATTTTCTG GTTGCTGGGA 480 ATGTTCCATG TCTTGTTCAG AGCATTTACA GGGTATAAAC GTGCAAAGTT TACCAGACTT 540 CACATTTGAG ATCTGAGGCC ACTTCTCCTG ATGTAAATTA TAACTCAATG AATAAAAGTT 600 TTTAAAAACA ACCCAGTTCC ATACTCGCCA GCCTGTGCCA GGTTCTTAGC CTGGGGACAG 660 AGCTGGGGCG GGGCGGGTCC CTGCTTTCTG ACCGGCAGGG GTGGGAGGGG CCCAGGCTGG 720 GGTGCTGCGA AGGCAACCCA GGGAGGGCGC CCGAGCCCCG CCCAGGCCAG GCCCCAGGCT 780 CTCCCGTGCT CCCGCCCCGC AGAGAGAGGC CGGAAGCGGC CCCGGAGGGC CCATTGTCCG 840 CGCTTCCGTT CCGGCTCCGC CTCGTCCTCC CGCGGCCAGA GGTGCGACCT CTGAGCCCCT 900 GGCCAGCTCC CAGCCGGCCT AGGGGGGCGG GGGCACGGGG CGGAGGTCCC GCAGCCCGTG 960 CTCGTCCCGC CTCGCTTGGA GGGAGCAAGG GCTCCGAGCC CTGGGCCCAG GTCCTGTGCC 1020 TCCGCTTCCC CGGCTGCGGG TACACCCCCA GCTTCCCGAG CCCCCCGGGC CCTCGCTGCT 1080 CCACCCAGAA GTTGCGGTGA CTGCGGCCCC AGCACCCCGT TCCCTGGCCG GGCATCACTT 1140 GCGCAGCATG CTGCCCCCAG AGGACAGGGC TACAGTTAGT CGCCCACACC TCATTCACCC 1200 CCTTGGGCCC TTGAGCGTCT TAGAAGCCGC AGATGCCAAG GAGGGGACGC TGCCTCGCGG 1260 ATGGTCACTT GGGAGCAAAG CTGGGGACTA AAGGAACCAG GGACAGAGAT TCCTGCTCTC 1320 GCCAAATTGG CCGCTCTGGG CCAGGCACTG AGGACACACC GCGAAGCCGG ATAGCCAGGT 1380 CCTGTCCTCA GGGCCCTGTC CGGAAGAGGA CTGGGCAGCC TCGAGTCCGC GGCAATGAAT 1440 GAATGTTCAA TTGCACAGAT GGGGAGGCGA AGGAGGGAGG GAGGGAGGGA GGGCAGTCGC 1500 TTGGGCGGTC ATTGGAGGCT CTGGGAGGCT ATGCGCCGGC AAGAAGCAGC GGGGTGGAGG 1560 CAGCCCTGCG GGAGTCGGCG AGGGCCGCGT GGATGTGCTC GGTGGTTTTG AGGCCAGTGG 1620 CTGGAGGGGC GTGAGAGTGG GAGACCAGAC TTGAGGGGAG TGGCTGGAGT TGAGACTCAA 1680 ATCCAAGAAG GAAACGGTGG GGCTTGGACC ACTTGCCTAC TGAGAAAAAT GGAAGTCGGG 1740 AAGGCTTTAG ATCTAGTCGC GCTTGGTCAC TTCCGTCTCC GGGCCTCAGC TTCCCAGGTT 1800 GTAGAAAGCA TCAGGGTTGG AGGCTCTGAA ATTCTGGCTC CTCTCAAGCC AAGATTAGTA 1860 TGACTTCATT TTGGTTGTGC AAGAAATGGG CCTGCAGCGG TTCGCAGAGG CAGAGGGACC 1920 TAAGCTTGAA GGGCAATCAA ACCGGCGTAG GCAGGAACGT CGGGAGCCCA GACCCCAGGC 1980 AGGGAGTTTA AGGTCTTGGA CACAGAGGGT GCGCTCCTCG AAGCAGCCAC AAAGCGGTGA 2040 CAGAGACCAG GCTTACGTTT TGTTTTGAAA TAATTTCAAA GTAACAGAAA AGCCGTGAGA 2100 ATAGTTCCGA GAACTGCCTC CCTTATTAAT GCAGATTCAC CAAGCTTTAA CATTCTGCTC 2160 CCCAGCCCTT GCATATTCAA GCCCCCATTG CAAGCATCGG AGAGTAAGTT GCAGGCGCGA 2220 TGGCCCTTGA ACCCTAAGTC CTCCAATGTG TATTGCCCAA GAACAAGGAC ATTCTATTGC 2280 ACAACCCCAG TGGTTTTCAA GATCGAGTGA TTTAACCATA ATACAATAAT TTAATCTGCA 2340 CAACCTTACT CAAATATCAC CAAATGTCGC AACGAGGTCT TTTATAGCAC ATCCCCTTCC 2400 CATCCCCATC CAGGAGCCAC GCCAGGATCA CATTTGTAAA TTTAATTATT ATTATTTAAG 2460
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