Tag | Content |
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EnhancerAtlas ID | HS139-28230 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr2:28600600-28602310 |
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: 28 | 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 | chr2:28600287-28600833 | Thymus | 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: 2 | Chromosome | Start | End |
chr2 | 28600937 | 28601380 | chr2 | 28601800 | 28602147 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I028376 | chr2 | 28599357 | 28606748 |
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Enhancer Sequence | GCTGAGCAAA GCAACCTGCA AGCAAACATT TGCAGAGCCC GAGGGCTTGG TTACAAAACA 60 TTTCTGACCT AGAAAGGGGA GAATGCCACG TTCCCTTCCC CCCAGACTCA GGTTTGGGGA 120 GTGGTGTTGG GGTTTGGGGT TAATTTGGAA AGGGGGAACC AACAGGTAAA GAGAGGCCAC 180 CTCTGAAGGT GGATGCCTGG GTCTCTGAGG GTGTGGGGGG AAGCATGGGT CTGCCCGGAC 240 TGAAGCTGGG CAGGTGGGAA CCCTCCCCAC CCTGAGAGGG AGGGAAGGAG GGAGGACACT 300 GAGGGCTGCT GGGCTCTAGG TAAGCCAGTC AGACTGCACA CACAGGTGTG CCAGGGCTGG 360 GACTCCTGCC CAGGACACCC AGCACCGCTC TACCAGGTGG GCAAAGCTCA TTCTGCTCCC 420 CAAAGAGGAA GGGAGTGGCC AGCCCTGAAG GGAGTGGCCA GCCCTGATTG ACACAACCAG 480 CTGGGCTCCT GGCTTTAGGG ACAAAGCAAC TGAGACTTGC TTTTACCAAT GGTTGCAGGC 540 ATCTGGACAA CTGGCAGTGT TGAAGGGAGC ACTGGCCTCA GCCCCTCTCT ATCCTGTCCC 600 CAGGTCTCCC CAAAATGCTG CTGAGACATT CAAACCGCAG CCTCCTCCTT TACCTGGTAA 660 TTGATCCTCT TTTGCCCTGC AACTTGGGTT TGGTCTTAAT TTGCCAGGCA CTAAAGGCAA 720 GAAGAGACGG GCAGGAGGGC GTGTTATCGC TTGTCTCCGG GCACAGAGGC TGTTGCAACA 780 GAGCTCCTGA GTGCGTGTAA GAGTGCACGC GTGTAGCAGA GGAAGGGAAC AGGCTGCACA 840 TGGGGTGGAG GATGGGTGCC AGCTTTCCTC CCTTGTGTGT GCCTATGGCA GGGGGAGGGT 900 CACTGGGCTG ATTTCTGTCC CTGAGGCAGG AGACCCCAGG ACACAAAACA GACCCAGCAA 960 GGCCTCTGTA GCTGCAGCCG GTGCCTGAGC TGCTCAGCCT CCCTGTGCTG ACTGACACTG 1020 ACTGAAGCTG GTCTCATAGC CCAACTCGTA GCTTCTCAGC CAGTCTTGAC TGGCACCTGC 1080 CTGGCAGCCC ATTGACCACT TAGTGGAGAT GGTATGACAC CCTGGGGGCT AGAAGCTGGT 1140 TGTAGGTTCT TTGACTTTAA GGGACTATCT TCTAAAGAGG CCAAAGTAGG CACCTTTGCT 1200 GGTGGCTCTG GCAGAGCTGC GGAAGCAGCA GCTCAAGTTC TGCCTTGAAG CTGAGTCCAT 1260 TTGCTTTCCC CCTTCCCGGG ACAGACGCGG AATCCTACCA CAGTTATCCC ATCACCGAAT 1320 CAAAGGTATC ATGGGGGGTG ACGACCAGTG GGCAGGGGGT CAGAAGAGGC CCTGGGATCA 1380 CTCAGTGCAG ACTCCTTCGC CGCCTTCCTC CTCAGCACCC CTACCTCTCT TGGTTTCCTG 1440 TGGCTGCTAT AACAGAGGAC CACAAACTTG GTGGTTTAAA ATAACAGACT CTTCCTCTTT 1500 CACAGTTCTG GAGGCCAGAA GTCGGAAATC AAGGTGTCGG CAGGGCCTCG CTCCCTCTGG 1560 AGGCCCTAGG GAGATCCATT CCTCATCACT TCCAGCTTCT GGAGCTGTCA GCATTCTTTA 1620 GCTTGTCCCT GCATCTGTCT CTGCTCTGTC TTTGTGAGGC CTTCTCTGTG TGCGTCATCT 1680 CCCTCTACCC CACTCTTATA AGGATACTTC 1710
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