Tag | Content |
---|
EnhancerAtlas ID | HS145-12296 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr2:28600040-28601860 |
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 |
|
| 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 |
|
| 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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH02I028376 | chr2 | 28599357 | 28606748 |
|
Enhancer Sequence | TGGCCCCACG TGCGAGGTGA GGGCAGAGTG GGCGAGGTCC CTTGGGGTGG GAGGCCTGGC 60 CCTCCTGACG GTGAGGGCAG GGTGCGGCCA GCAGTAGTTG GGAGGTGCGG GAGGCTCCTG 120 CTCGCTGGCT GGGCAGGGTG GGGCAGGGCG GGGCAGGCAC TGGGAACAGG GTGACCTGGA 180 CACCGCGACC TGCGATCATT GAACGAGGCA CGCAGCGGTG GTGGTGGAGA TAGGGAGACC 240 CTCTGTGCCG GGGGGACCCT CACCAAGGTG GGCACCCTCT GAGCCTCCCG CCCCGCTAGC 300 TTCCCCTTGG CCACCTCTAG GCAGCTTCCA GCAAGGATGT TCCTTCTCCC TCCCAACAGG 360 CCCTCACCTG GAGCCTGCTC GGACCTGCCC TCTCCACAAA GCATGGTAGC AACTCCCTGG 420 GGCAGAAAGT GTCTCTTCTG AAAGCAAGAC AAGAGTTTAA TGAAGCCCTA AACGCGCACA 480 GTTGAGCCTG AAATTAGGGT GGTGAAGGGA GGGGAAGAAG GCAGTTGAGG ACATGGGGGC 540 TTCAGCCCAG CCCTGCCCCA GCTGAGCAAA GCAACCTGCA AGCAAACATT TGCAGAGCCC 600 GAGGGCTTGG TTACAAAACA TTTCTGACCT AGAAAGGGGA GAATGCCACG TTCCCTTCCC 660 CCCAGACTCA GGTTTGGGGA GTGGTGTTGG GGTTTGGGGT TAATTTGGAA AGGGGGAACC 720 AACAGGTAAA GAGAGGCCAC CTCTGAAGGT GGATGCCTGG GTCTCTGAGG GTGTGGGGGG 780 AAGCATGGGT CTGCCCGGAC TGAAGCTGGG CAGGTGGGAA CCCTCCCCAC CCTGAGAGGG 840 AGGGAAGGAG GGAGGACACT GAGGGCTGCT GGGCTCTAGG TAAGCCAGTC AGACTGCACA 900 CACAGGTGTG CCAGGGCTGG GACTCCTGCC CAGGACACCC AGCACCGCTC TACCAGGTGG 960 GCAAAGCTCA TTCTGCTCCC CAAAGAGGAA GGGAGTGGCC AGCCCTGAAG GGAGTGGCCA 1020 GCCCTGATTG ACACAACCAG CTGGGCTCCT GGCTTTAGGG ACAAAGCAAC TGAGACTTGC 1080 TTTTACCAAT GGTTGCAGGC ATCTGGACAA CTGGCAGTGT TGAAGGGAGC ACTGGCCTCA 1140 GCCCCTCTCT ATCCTGTCCC CAGGTCTCCC CAAAATGCTG CTGAGACATT CAAACCGCAG 1200 CCTCCTCCTT TACCTGGTAA TTGATCCTCT TTTGCCCTGC AACTTGGGTT TGGTCTTAAT 1260 TTGCCAGGCA CTAAAGGCAA GAAGAGACGG GCAGGAGGGC GTGTTATCGC TTGTCTCCGG 1320 GCACAGAGGC TGTTGCAACA GAGCTCCTGA GTGCGTGTAA GAGTGCACGC GTGTAGCAGA 1380 GGAAGGGAAC AGGCTGCACA TGGGGTGGAG GATGGGTGCC AGCTTTCCTC CCTTGTGTGT 1440 GCCTATGGCA GGGGGAGGGT CACTGGGCTG ATTTCTGTCC CTGAGGCAGG AGACCCCAGG 1500 ACACAAAACA GACCCAGCAA GGCCTCTGTA GCTGCAGCCG GTGCCTGAGC TGCTCAGCCT 1560 CCCTGTGCTG ACTGACACTG ACTGAAGCTG GTCTCATAGC CCAACTCGTA GCTTCTCAGC 1620 CAGTCTTGAC TGGCACCTGC CTGGCAGCCC ATTGACCACT TAGTGGAGAT GGTATGACAC 1680 CCTGGGGGCT AGAAGCTGGT TGTAGGTTCT TTGACTTTAA GGGACTATCT TCTAAAGAGG 1740 CCAAAGTAGG CACCTTTGCT GGTGGCTCTG GCAGAGCTGC GGAAGCAGCA GCTCAAGTTC 1800 TGCCTTGAAG CTGAGTCCAT 1820
|