Tag | Content |
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EnhancerAtlas ID | HS098-29361 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:28600750-28601800 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr2:28600874-28600892 | AGAGGGAGGGAAGGAGGG | + | 6.03 | EWSR1-FLI1 | MA0149.1 | chr2:28600878-28600896 | GGAGGGAAGGAGGGAGGA | + | 6.05 | ZEB1 | MA0103.3 | chr2:28600847-28600858 | GGGCAGGTGGG | - | 6.14 | ZNF263 | MA0528.1 | chr2:28600875-28600896 | GAGGGAGGGAAGGAGGGAGGA | + | 7.39 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_02920 | chr2:28599561-28601101 | Bladder | SE_02920 | chr2:28601345-28602276 | Bladder | SE_09457 | chr2:28600588-28602584 | CD14 | SE_18763 | chr2:28601601-28602332 | CD4p_CD25-_Il17-_PMAstim_Th | SE_20015 | chr2:28600839-28603526 | CD56 | SE_22508 | chr2:28601257-28603053 | CD8_primiary | SE_23078 | chr2:28598089-28602675 | Colon_Crypt_1 | SE_23736 | chr2:28598363-28602327 | Colon_Crypt_2 | SE_24706 | chr2:28597998-28602775 | Colon_Crypt_3 | SE_25842 | chr2:28599329-28605934 | Duodenum_Smooth_Muscle | SE_26550 | chr2:28598695-28603580 | Esophagus | SE_27724 | chr2:28599333-28602272 | Fetal_Intestine | SE_28654 | chr2:28599422-28602161 | Fetal_Intestine_Large | SE_29693 | chr2:28600789-28602243 | Fetal_Muscle | SE_31386 | chr2:28598655-28606836 | Gastric | SE_33745 | chr2:28599607-28603153 | H2171 | SE_34659 | chr2:28599324-28602394 | HeLa | SE_36417 | chr2:28599847-28602208 | HMEC | SE_48134 | chr2:28600160-28602310 | Psoas_Muscle | SE_50076 | chr2:28598606-28603073 | Sigmoid_Colon | SE_51112 | chr2:28600641-28602370 | Skeletal_Muscle | SE_52349 | chr2:28598286-28606435 | Small_Intestine | SE_53354 | chr2:28601073-28602344 | Spleen | SE_55359 | chr2:28601399-28601909 | Thymus | SE_62927 | chr2:28581266-28660518 | Tonsil | SE_64959 | chr2:28600200-28602183 | NHEK | SE_65553 | chr2:28601380-28602038 | 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 |
GH02I028376 | chr2 | 28599357 | 28606748 |
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Enhancer Sequence | AGGGGGAACC AACAGGTAAA GAGAGGCCAC CTCTGAAGGT GGATGCCTGG GTCTCTGAGG 60 GTGTGGGGGG AAGCATGGGT CTGCCCGGAC TGAAGCTGGG CAGGTGGGAA CCCTCCCCAC 120 CCTGAGAGGG AGGGAAGGAG GGAGGACACT GAGGGCTGCT GGGCTCTAGG TAAGCCAGTC 180 AGACTGCACA CACAGGTGTG CCAGGGCTGG GACTCCTGCC CAGGACACCC AGCACCGCTC 240 TACCAGGTGG GCAAAGCTCA TTCTGCTCCC CAAAGAGGAA GGGAGTGGCC AGCCCTGAAG 300 GGAGTGGCCA GCCCTGATTG ACACAACCAG CTGGGCTCCT GGCTTTAGGG ACAAAGCAAC 360 TGAGACTTGC TTTTACCAAT GGTTGCAGGC ATCTGGACAA CTGGCAGTGT TGAAGGGAGC 420 ACTGGCCTCA GCCCCTCTCT ATCCTGTCCC CAGGTCTCCC CAAAATGCTG CTGAGACATT 480 CAAACCGCAG CCTCCTCCTT TACCTGGTAA TTGATCCTCT TTTGCCCTGC AACTTGGGTT 540 TGGTCTTAAT TTGCCAGGCA CTAAAGGCAA GAAGAGACGG GCAGGAGGGC GTGTTATCGC 600 TTGTCTCCGG GCACAGAGGC TGTTGCAACA GAGCTCCTGA GTGCGTGTAA GAGTGCACGC 660 GTGTAGCAGA GGAAGGGAAC AGGCTGCACA TGGGGTGGAG GATGGGTGCC AGCTTTCCTC 720 CCTTGTGTGT GCCTATGGCA GGGGGAGGGT CACTGGGCTG ATTTCTGTCC CTGAGGCAGG 780 AGACCCCAGG ACACAAAACA GACCCAGCAA GGCCTCTGTA GCTGCAGCCG GTGCCTGAGC 840 TGCTCAGCCT CCCTGTGCTG ACTGACACTG ACTGAAGCTG GTCTCATAGC CCAACTCGTA 900 GCTTCTCAGC CAGTCTTGAC TGGCACCTGC CTGGCAGCCC ATTGACCACT TAGTGGAGAT 960 GGTATGACAC CCTGGGGGCT AGAAGCTGGT TGTAGGTTCT TTGACTTTAA GGGACTATCT 1020 TCTAAAGAGG CCAAAGTAGG CACCTTTGCT 1050
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