Tag | Content |
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EnhancerAtlas ID | HS127-16277 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr2:28600480-28602990 |
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 | 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 | AAAGCAAGAC AAGAGTTTAA TGAAGCCCTA AACGCGCACA GTTGAGCCTG AAATTAGGGT 60 GGTGAAGGGA GGGGAAGAAG GCAGTTGAGG ACATGGGGGC TTCAGCCCAG CCCTGCCCCA 120 GCTGAGCAAA GCAACCTGCA AGCAAACATT TGCAGAGCCC GAGGGCTTGG TTACAAAACA 180 TTTCTGACCT AGAAAGGGGA GAATGCCACG TTCCCTTCCC CCCAGACTCA GGTTTGGGGA 240 GTGGTGTTGG GGTTTGGGGT TAATTTGGAA AGGGGGAACC AACAGGTAAA GAGAGGCCAC 300 CTCTGAAGGT GGATGCCTGG GTCTCTGAGG GTGTGGGGGG AAGCATGGGT CTGCCCGGAC 360 TGAAGCTGGG CAGGTGGGAA CCCTCCCCAC CCTGAGAGGG AGGGAAGGAG GGAGGACACT 420 GAGGGCTGCT GGGCTCTAGG TAAGCCAGTC AGACTGCACA CACAGGTGTG CCAGGGCTGG 480 GACTCCTGCC CAGGACACCC AGCACCGCTC TACCAGGTGG GCAAAGCTCA TTCTGCTCCC 540 CAAAGAGGAA GGGAGTGGCC AGCCCTGAAG GGAGTGGCCA GCCCTGATTG ACACAACCAG 600 CTGGGCTCCT GGCTTTAGGG ACAAAGCAAC TGAGACTTGC TTTTACCAAT GGTTGCAGGC 660 ATCTGGACAA CTGGCAGTGT TGAAGGGAGC ACTGGCCTCA GCCCCTCTCT ATCCTGTCCC 720 CAGGTCTCCC CAAAATGCTG CTGAGACATT CAAACCGCAG CCTCCTCCTT TACCTGGTAA 780 TTGATCCTCT TTTGCCCTGC AACTTGGGTT TGGTCTTAAT TTGCCAGGCA CTAAAGGCAA 840 GAAGAGACGG GCAGGAGGGC GTGTTATCGC TTGTCTCCGG GCACAGAGGC TGTTGCAACA 900 GAGCTCCTGA GTGCGTGTAA GAGTGCACGC GTGTAGCAGA GGAAGGGAAC AGGCTGCACA 960 TGGGGTGGAG GATGGGTGCC AGCTTTCCTC CCTTGTGTGT GCCTATGGCA GGGGGAGGGT 1020 CACTGGGCTG ATTTCTGTCC CTGAGGCAGG AGACCCCAGG ACACAAAACA GACCCAGCAA 1080 GGCCTCTGTA GCTGCAGCCG GTGCCTGAGC TGCTCAGCCT CCCTGTGCTG ACTGACACTG 1140 ACTGAAGCTG GTCTCATAGC CCAACTCGTA GCTTCTCAGC CAGTCTTGAC TGGCACCTGC 1200 CTGGCAGCCC ATTGACCACT TAGTGGAGAT GGTATGACAC CCTGGGGGCT AGAAGCTGGT 1260 TGTAGGTTCT TTGACTTTAA GGGACTATCT TCTAAAGAGG CCAAAGTAGG CACCTTTGCT 1320 GGTGGCTCTG GCAGAGCTGC GGAAGCAGCA GCTCAAGTTC TGCCTTGAAG CTGAGTCCAT 1380 TTGCTTTCCC CCTTCCCGGG ACAGACGCGG AATCCTACCA CAGTTATCCC ATCACCGAAT 1440 CAAAGGTATC ATGGGGGGTG ACGACCAGTG GGCAGGGGGT CAGAAGAGGC CCTGGGATCA 1500 CTCAGTGCAG ACTCCTTCGC CGCCTTCCTC CTCAGCACCC CTACCTCTCT TGGTTTCCTG 1560 TGGCTGCTAT AACAGAGGAC CACAAACTTG GTGGTTTAAA ATAACAGACT CTTCCTCTTT 1620 CACAGTTCTG GAGGCCAGAA GTCGGAAATC AAGGTGTCGG CAGGGCCTCG CTCCCTCTGG 1680 AGGCCCTAGG GAGATCCATT CCTCATCACT TCCAGCTTCT GGAGCTGTCA GCATTCTTTA 1740 GCTTGTCCCT GCATCTGTCT CTGCTCTGTC TTTGTGAGGC CTTCTCTGTG TGCGTCATCT 1800 CCCTCTACCC CACTCTTATA AGGATACTTC CTGTTGAATT GTGGGTCTGC CCAGATAATC 1860 CAAGAATCCA AGATGATCTC CTCCTCTCAA GATTCTTAAC CTCCTTACAT CTGCAAAGAC 1920 CCTTTTTCCA AATAAGCTCA CATTCACACG TTCCCGGGAT CTGGACACAG ACCTATCTTT 1980 TTGGGAGACC ACCATTCAAC CTGCTATACC ATTCAGTGGT TGGTAGGTTG TGGCTTAGAC 2040 CCCTCTAGTG ATGGGCGGCT CACTACTGCA TGAGTTGGCT CCATCTATGT CCAAACAGGT 2100 CTAATTATTT TAAAGTTCTT ACTTGGGTGG AGCTGAAATT TTGCTCAACA GGAACTTTTA 2160 CCCACTGGCC TTAGTTCTGG TCTTCAGAGT ACATACATCT AAATAAATAA ACCCTCCAAT 2220 CCCACCACCT CTGCCCCTGA TTACAAGGCA AAAACAAAAT GAGAAAAAGG ATGAATGGGC 2280 TTAGTTTTGA TACCAGGGAA AATGCAGAGA CTCCGGTCTC CCTGGTGGCC CTGTCCCTAG 2340 GACTTTGTGC CTGTTTCCTC GCCGTAACAC CAGAGAGTGG CCGAATCACC GTTTCATGGG 2400 ATGCTTTTGA GAAATGCATC CTGGAGAGTC CCAATTTGCA CTGGTACATT AAAGGCTCTG 2460 AGAAGTCCTA AGTAAAGAAA TCCACTTAAC CCCAATATTT TCCAAACTTA 2510
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