Tag | Content |
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EnhancerAtlas ID | HS146-00407 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr1:37951020-37953260 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr1:37951953-37951973 | CCCTCCCCCACCCCCCCACA | + | 6.17 | TEAD1 | MA0090.2 | chr1:37951769-37951779 | ATGGAATGTG | - | 6.02 | ZEB1 | MA0103.3 | chr1:37951945-37951956 | CCCACCTGCCC | + | 6.14 | ZNF263 | MA0528.1 | chr1:37951491-37951512 | CTCCCCATCACCTCCTGCTCC | - | 6.3 |
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| Number of super-enhancer constituents: 37 | ID | Coordinate | Tissue/cell |
SE_00995 | chr1:37938982-37953203 | Adrenal_Gland | SE_01903 | chr1:37948265-37953245 | Aorta | SE_11493 | chr1:37938939-37953541 | CD20 | SE_17494 | chr1:37950569-37951665 | CD4p_CD25-_CD45RAp_Naive | SE_17494 | chr1:37952091-37953578 | CD4p_CD25-_CD45RAp_Naive | SE_17864 | chr1:37950020-37953616 | CD4p_CD25-_CD45ROp_Memory | SE_18659 | chr1:37951001-37951807 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19263 | chr1:37951954-37953461 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_22516 | chr1:37952028-37953269 | CD8_primiary | SE_23342 | chr1:37950876-37953399 | Colon_Crypt_1 | SE_23956 | chr1:37950885-37951843 | Colon_Crypt_2 | SE_23956 | chr1:37951956-37953284 | Colon_Crypt_2 | SE_26141 | chr1:37950907-37953499 | Duodenum_Smooth_Muscle | SE_26814 | chr1:37948794-37953411 | Esophagus | SE_27863 | chr1:37952290-37953288 | Fetal_Intestine | SE_28852 | chr1:37952149-37953486 | Fetal_Intestine_Large | SE_31547 | chr1:37938860-37953351 | Gastric | SE_34808 | chr1:37949489-37953812 | HeLa | SE_36403 | chr1:37952043-37953189 | HMEC | SE_37759 | chr1:37949654-37953790 | HSMMtube | SE_41638 | chr1:37947973-37951816 | LNCaP | SE_41638 | chr1:37951911-37953293 | LNCaP | SE_42562 | chr1:37938719-37953498 | Lung | SE_45338 | chr1:37950944-37951914 | NHLF | SE_45338 | chr1:37951966-37953371 | NHLF | SE_46585 | chr1:37950638-37953471 | Osteoblasts | SE_47620 | chr1:37950334-37951789 | Pancreas | SE_48484 | chr1:37948733-37953659 | Psoas_Muscle | SE_49357 | chr1:37949273-37953284 | Right_Atrium | SE_50165 | chr1:37948804-37953471 | Sigmoid_Colon | SE_52446 | chr1:37948920-37953379 | Small_Intestine | SE_54020 | chr1:37948718-37953674 | Spleen | SE_56449 | chr1:37950785-37953592 | u87 | SE_62625 | chr1:37936685-37953308 | Tonsil | SE_64577 | chr1:37951962-37953469 | NHEK | SE_65323 | chr1:37939205-37953672 | Pancreatic_islets | SE_67957 | chr1:37950785-37953592 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 37951442 | 37951953 | chr1 | 37952009 | 37953206 |
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Enhancer Sequence | AGCCTTGAGG CTGCCTGGAA AAAATAGGGA ATGTTCTCAC CCCTCTTCCC ATCCCAGCTG 60 CCAGCTGGCC ACAGCCTTGG GAGTTCATAC TTGCTTACTT GCTTCTTGAC CAGAGCTGAA 120 CTCTAAGCCA TTTGCTGCTT CTGCTGTGTG TGGGGAGGGA TGGGCAGTGG GCAGCAGGTC 180 CTGACTGGCT GTGCCGTGTC TGGAGGCCAA GTCTGGCCCT GCTGGTTCAC TGATAAGCCC 240 CGGCAAGGGT GGCAGAGCTC ATGTGGCAGG TGCCTGAGGG GCTGGGATCT AGGGAGGACT 300 GGTCAGTTCC ATGCCCCGCT GGCCTGAGCT TGCATCCTGT GCTTTCCAGG CAGGCTTAGA 360 TGCCCCTTCA GGCCTCTTTC TCAGTCTGCC AGGCAGAGTG ACTCCGAGGC TACCAGGCCC 420 AGTGCCCCAG CTGTGTTTCT TTCCCACGAA TTGGGCTTTA ACTCCAAAGT TCTCCCCATC 480 ACCTCCTGCT CCACTGCCCA TTCAAGCAGC TTAGGTAGGT GGTATTTGCT CACAGGGCCT 540 CAGTCTCCCC ACCTGTAAAA GGGACACAAT GGTCCTTGCC TCTTTCTAGA TTTGAGAGAA 600 TAACTCAGTT CCTGTGAAAG GAGGAGAGGG AGGGGTCCTG GATTCAAGCC CCCATCACTA 660 GCGATGCAGC CCTGGGCAAC CCACTTCCCT CTCAGAGCCT CAGCTTCCTG CCTCTTCAGA 720 GGCAGCTTCC CTCTGAGAGG GGGACAGGGA TGGAATGTGA CTCCTGCATG CTGGAAAAGA 780 TCAAATTCTG GGGAGCTGCC CCAGTTGCTC TTTCCTCCTC TTGTTTTCCT GGTTCCAGGA 840 GCCAGAAGCT GATGAGGAAA CCAGTAAGTA TGCAAATTCT GGCACTATTG GGAAATGATC 900 CTGGGGAGCT CACAGAGGAC AGCCTCCCAC CTGCCCTCCC CCACCCCCCC ACAGGCCCCC 960 CAACCTTGCC CTTGGGCTCT CACCAGCAGG GGCCGAACCC TGAGTTTTAT TGCGAGTTCT 1020 GTCTCGCACA CATGGGTTAA CCCCTCTTGG AGTGAAGCCA GGGTGACTAT GGCCAATCTG 1080 TCCTCAGAAA ACCTCCAGCC TCCCTAGCAG AGAGCAAACG AGCCCACAAT GGGATGAAAG 1140 ATCCCTGCTC TGGATGTCTC AGCCCAGTCC CCATCCCACT TCTCTAGAGT GGGGGAAACT 1200 CAGGAGTCCC CAAAGACCTG GGACCTAAGC TAGGAGCAGA ACTTTAGAGG TCCGGGGGAG 1260 CAGCTCTCCA ATCCCCCCAT CCCCGCCAGT GCTGCTCACA CCCCCCTCGT TGTAGTCTCC 1320 TGCAGGGGGG GACAGGTGGT GTCTGGGAAG GGGCCAGTAC TCCTCACCGC AGCTGCCACT 1380 TCCCTCATCT TCCCCCAGCA AAGCTCTCAG CCCTCCCTTC CCCATGCCTC CTGGAAAAGC 1440 CAGCATTTGT CTTCTGTACA CAGAAGGGAA AGACCCTAGC CCTGAGGGAG GTGCTGGGCA 1500 GGCCTCTACC AAGACAAGAG TGAGTGAGCA GCAGAGAAAG TGGGACTTGG GGGGCACATA 1560 TCTCTAGGAG CTGCAGGGAA GGAAGTGGTG CAATCAGCCT CAGCCCTGGG CCCAGCTGGT 1620 CCCTAGAGGA CGCTTCCCCA AAAGAAGGCA GCCCAAGGAC CCTAGCACTT TTGTCCCAGG 1680 GCTTCTCAAA CTTCTGGCTT TTTTTTTTTC TTGGACCATA GCAGAGTGGG TGGAGTAGAG 1740 GGTGGCAAGG GCCTGTTCTG GGGACCTCCC AGTTCATGGG AAGGGTGTGG GAGATTTGCC 1800 TGAAAGAGGC AGGAAGTAGG GCCCTACAAC TAAGGAAACC CAAGCCATCC CAGGCCATGG 1860 CATGTAAATC CTTCCAGCTA GTTCCTGAAG GGGAAGAGGC CCTAGGCTGT CATCCTGAGG 1920 TGTGGCCTTG TTAAGCTCCT CTCAAGGCAG CTGCTCGTGA TCTTCAACTG CTCATCCATT 1980 TAAGAGATGT CAGCAAAACG AGGTGGGAGG AAAGGATCAG GCGCCCCACC CCACACTAAG 2040 TTGGGCACAT TGCTGGGAGG TCAAGTCACT GGGAATGGTG CAAAGGCTCT AATTCTGGCT 2100 GCTCGTGGGC TGCTTGTGGG GCCGTGCCTG CCACCTGCCG GTGCTTCCTG GTACTGCTAC 2160 CCATGGAGCA GGGGCCTGCC CACCAGCTCT GGCCTGGAAA TGAAGGGCCT AGACACAAAG 2220 ATCTTCCAGC AGGATCTGAA 2240
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