Tag | Content |
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EnhancerAtlas ID | HS118-09681 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr2:28600120-28602320 |
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 | chr2:28600540-28600561 | GGTGAAGGGAGGGGAAGAAGG | + | 6.5 | 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: 3 | Chromosome | Start | End |
chr2 | 28600400 | 28601600 | 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 | GGTGCGGCCA GCAGTAGTTG GGAGGTGCGG GAGGCTCCTG CTCGCTGGCT GGGCAGGGTG 60 GGGCAGGGCG GGGCAGGCAC TGGGAACAGG GTGACCTGGA CACCGCGACC TGCGATCATT 120 GAACGAGGCA CGCAGCGGTG GTGGTGGAGA TAGGGAGACC CTCTGTGCCG GGGGGACCCT 180 CACCAAGGTG GGCACCCTCT GAGCCTCCCG CCCCGCTAGC TTCCCCTTGG CCACCTCTAG 240 GCAGCTTCCA GCAAGGATGT TCCTTCTCCC TCCCAACAGG CCCTCACCTG GAGCCTGCTC 300 GGACCTGCCC TCTCCACAAA GCATGGTAGC AACTCCCTGG GGCAGAAAGT GTCTCTTCTG 360 AAAGCAAGAC AAGAGTTTAA TGAAGCCCTA AACGCGCACA GTTGAGCCTG AAATTAGGGT 420 GGTGAAGGGA GGGGAAGAAG GCAGTTGAGG ACATGGGGGC TTCAGCCCAG CCCTGCCCCA 480 GCTGAGCAAA GCAACCTGCA AGCAAACATT TGCAGAGCCC GAGGGCTTGG TTACAAAACA 540 TTTCTGACCT AGAAAGGGGA GAATGCCACG TTCCCTTCCC CCCAGACTCA GGTTTGGGGA 600 GTGGTGTTGG GGTTTGGGGT TAATTTGGAA AGGGGGAACC AACAGGTAAA GAGAGGCCAC 660 CTCTGAAGGT GGATGCCTGG GTCTCTGAGG GTGTGGGGGG AAGCATGGGT CTGCCCGGAC 720 TGAAGCTGGG CAGGTGGGAA CCCTCCCCAC CCTGAGAGGG AGGGAAGGAG GGAGGACACT 780 GAGGGCTGCT GGGCTCTAGG TAAGCCAGTC AGACTGCACA CACAGGTGTG CCAGGGCTGG 840 GACTCCTGCC CAGGACACCC AGCACCGCTC TACCAGGTGG GCAAAGCTCA TTCTGCTCCC 900 CAAAGAGGAA GGGAGTGGCC AGCCCTGAAG GGAGTGGCCA GCCCTGATTG ACACAACCAG 960 CTGGGCTCCT GGCTTTAGGG ACAAAGCAAC TGAGACTTGC TTTTACCAAT GGTTGCAGGC 1020 ATCTGGACAA CTGGCAGTGT TGAAGGGAGC ACTGGCCTCA GCCCCTCTCT ATCCTGTCCC 1080 CAGGTCTCCC CAAAATGCTG CTGAGACATT CAAACCGCAG CCTCCTCCTT TACCTGGTAA 1140 TTGATCCTCT TTTGCCCTGC AACTTGGGTT TGGTCTTAAT TTGCCAGGCA CTAAAGGCAA 1200 GAAGAGACGG GCAGGAGGGC GTGTTATCGC TTGTCTCCGG GCACAGAGGC TGTTGCAACA 1260 GAGCTCCTGA GTGCGTGTAA GAGTGCACGC GTGTAGCAGA GGAAGGGAAC AGGCTGCACA 1320 TGGGGTGGAG GATGGGTGCC AGCTTTCCTC CCTTGTGTGT GCCTATGGCA GGGGGAGGGT 1380 CACTGGGCTG ATTTCTGTCC CTGAGGCAGG AGACCCCAGG ACACAAAACA GACCCAGCAA 1440 GGCCTCTGTA GCTGCAGCCG GTGCCTGAGC TGCTCAGCCT CCCTGTGCTG ACTGACACTG 1500 ACTGAAGCTG GTCTCATAGC CCAACTCGTA GCTTCTCAGC CAGTCTTGAC TGGCACCTGC 1560 CTGGCAGCCC ATTGACCACT TAGTGGAGAT GGTATGACAC CCTGGGGGCT AGAAGCTGGT 1620 TGTAGGTTCT TTGACTTTAA GGGACTATCT TCTAAAGAGG CCAAAGTAGG CACCTTTGCT 1680 GGTGGCTCTG GCAGAGCTGC GGAAGCAGCA GCTCAAGTTC TGCCTTGAAG CTGAGTCCAT 1740 TTGCTTTCCC CCTTCCCGGG ACAGACGCGG AATCCTACCA CAGTTATCCC ATCACCGAAT 1800 CAAAGGTATC ATGGGGGGTG ACGACCAGTG GGCAGGGGGT CAGAAGAGGC CCTGGGATCA 1860 CTCAGTGCAG ACTCCTTCGC CGCCTTCCTC CTCAGCACCC CTACCTCTCT TGGTTTCCTG 1920 TGGCTGCTAT AACAGAGGAC CACAAACTTG GTGGTTTAAA ATAACAGACT CTTCCTCTTT 1980 CACAGTTCTG GAGGCCAGAA GTCGGAAATC AAGGTGTCGG CAGGGCCTCG CTCCCTCTGG 2040 AGGCCCTAGG GAGATCCATT CCTCATCACT TCCAGCTTCT GGAGCTGTCA GCATTCTTTA 2100 GCTTGTCCCT GCATCTGTCT CTGCTCTGTC TTTGTGAGGC CTTCTCTGTG TGCGTCATCT 2160 CCCTCTACCC CACTCTTATA AGGATACTTC CTGTTGAATT 2200
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