Tag | Content |
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EnhancerAtlas ID | HS110-02630 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr2:28599510-28602070 |
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: 2 | Chromosome | Start | End |
chr2 | 28600400 | 28601600 | chr2 | 28600937 | 28601380 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I028376 | chr2 | 28599357 | 28606748 |
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Enhancer Sequence | AGGGAACACA GCACTTACAG AATGAAATGG GGGCGGTGCA CGTAGCATTT TCTTTTGGGG 60 ACAATGCTAA AAGCTCTATT ACAGTTTTCC TCACAGCCTG CCCAGCCTTG ATAGAAGTAA 120 TATCTCATGT CTGTGTAGCC TTTTACCTAA GTGAGCAACA GGCTTTCTCT CCTACGTTAT 180 GTCTTTCCAT TCCCCTGGAC ACCTCAGGGA ACAGGTATAG TACCCTCAAT TTACGGACGG 240 GGAGACTGAG GCTCAGAAAG ATGCAGTAAT CTGCTGGAGG ACACACAGGT AGTAAGGGGC 300 AAACCCAGGC CTCGAAGCCA GCAGGCCCTT TGAGACATGC TTCTCTAGAA AGTTTCACCC 360 CATGGAGTCC TTCCTGGGAC CAGTACAAGG CAGGTCCGTC CTAGTGGTTG GGAGTGTGGT 420 CACCACGTGC CTGCGTTGAG GGTCTGGATC ACAGAGCCCA CTTTCTGGAT CCTTTTCCTC 480 CTCTCGAGGG CCCCAGGAGG GTGGGCAAGG TCTCTTGGAA TGGGGGGGCC TGGCCCCACG 540 TGCGAGGTGA GGGCAGAGTG GGCGAGGTCC CTTGGGGTGG GAGGCCTGGC CCTCCTGACG 600 GTGAGGGCAG GGTGCGGCCA GCAGTAGTTG GGAGGTGCGG GAGGCTCCTG CTCGCTGGCT 660 GGGCAGGGTG GGGCAGGGCG GGGCAGGCAC TGGGAACAGG GTGACCTGGA CACCGCGACC 720 TGCGATCATT GAACGAGGCA CGCAGCGGTG GTGGTGGAGA TAGGGAGACC CTCTGTGCCG 780 GGGGGACCCT CACCAAGGTG GGCACCCTCT GAGCCTCCCG CCCCGCTAGC TTCCCCTTGG 840 CCACCTCTAG GCAGCTTCCA GCAAGGATGT TCCTTCTCCC TCCCAACAGG CCCTCACCTG 900 GAGCCTGCTC GGACCTGCCC TCTCCACAAA GCATGGTAGC AACTCCCTGG GGCAGAAAGT 960 GTCTCTTCTG AAAGCAAGAC AAGAGTTTAA TGAAGCCCTA AACGCGCACA GTTGAGCCTG 1020 AAATTAGGGT GGTGAAGGGA GGGGAAGAAG GCAGTTGAGG ACATGGGGGC TTCAGCCCAG 1080 CCCTGCCCCA GCTGAGCAAA GCAACCTGCA AGCAAACATT TGCAGAGCCC GAGGGCTTGG 1140 TTACAAAACA TTTCTGACCT AGAAAGGGGA GAATGCCACG TTCCCTTCCC CCCAGACTCA 1200 GGTTTGGGGA GTGGTGTTGG GGTTTGGGGT TAATTTGGAA AGGGGGAACC AACAGGTAAA 1260 GAGAGGCCAC CTCTGAAGGT GGATGCCTGG GTCTCTGAGG GTGTGGGGGG AAGCATGGGT 1320 CTGCCCGGAC TGAAGCTGGG CAGGTGGGAA CCCTCCCCAC CCTGAGAGGG AGGGAAGGAG 1380 GGAGGACACT GAGGGCTGCT GGGCTCTAGG TAAGCCAGTC AGACTGCACA CACAGGTGTG 1440 CCAGGGCTGG GACTCCTGCC CAGGACACCC AGCACCGCTC TACCAGGTGG GCAAAGCTCA 1500 TTCTGCTCCC CAAAGAGGAA GGGAGTGGCC AGCCCTGAAG GGAGTGGCCA GCCCTGATTG 1560 ACACAACCAG CTGGGCTCCT GGCTTTAGGG ACAAAGCAAC TGAGACTTGC TTTTACCAAT 1620 GGTTGCAGGC ATCTGGACAA CTGGCAGTGT TGAAGGGAGC ACTGGCCTCA GCCCCTCTCT 1680 ATCCTGTCCC CAGGTCTCCC CAAAATGCTG CTGAGACATT CAAACCGCAG CCTCCTCCTT 1740 TACCTGGTAA TTGATCCTCT TTTGCCCTGC AACTTGGGTT TGGTCTTAAT TTGCCAGGCA 1800 CTAAAGGCAA GAAGAGACGG GCAGGAGGGC GTGTTATCGC TTGTCTCCGG GCACAGAGGC 1860 TGTTGCAACA GAGCTCCTGA GTGCGTGTAA GAGTGCACGC GTGTAGCAGA GGAAGGGAAC 1920 AGGCTGCACA TGGGGTGGAG GATGGGTGCC AGCTTTCCTC CCTTGTGTGT GCCTATGGCA 1980 GGGGGAGGGT CACTGGGCTG ATTTCTGTCC CTGAGGCAGG AGACCCCAGG ACACAAAACA 2040 GACCCAGCAA GGCCTCTGTA GCTGCAGCCG GTGCCTGAGC TGCTCAGCCT CCCTGTGCTG 2100 ACTGACACTG ACTGAAGCTG GTCTCATAGC CCAACTCGTA GCTTCTCAGC CAGTCTTGAC 2160 TGGCACCTGC CTGGCAGCCC ATTGACCACT TAGTGGAGAT GGTATGACAC CCTGGGGGCT 2220 AGAAGCTGGT TGTAGGTTCT TTGACTTTAA GGGACTATCT TCTAAAGAGG CCAAAGTAGG 2280 CACCTTTGCT GGTGGCTCTG GCAGAGCTGC GGAAGCAGCA GCTCAAGTTC TGCCTTGAAG 2340 CTGAGTCCAT TTGCTTTCCC CCTTCCCGGG ACAGACGCGG AATCCTACCA CAGTTATCCC 2400 ATCACCGAAT CAAAGGTATC ATGGGGGGTG ACGACCAGTG GGCAGGGGGT CAGAAGAGGC 2460 CCTGGGATCA CTCAGTGCAG ACTCCTTCGC CGCCTTCCTC CTCAGCACCC CTACCTCTCT 2520 TGGTTTCCTG TGGCTGCTAT AACAGAGGAC CACAAACTTG 2560
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