Tag | Content |
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EnhancerAtlas ID | HS043-03673 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr1:206754490-206755620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:206754991-206755009 | GGAAGGAAGGAAGGAAAG | + | 10.53 | EWSR1-FLI1 | MA0149.1 | chr1:206754999-206755017 | GGAAGGAAAGAAAGAAAG | + | 6.95 | EWSR1-FLI1 | MA0149.1 | chr1:206755177-206755195 | TGAAGGGAGGAAGGTAGG | + | 7.01 | EWSR1-FLI1 | MA0149.1 | chr1:206754987-206755005 | AAAAGGAAGGAAGGAAGG | + | 7.95 | EWSR1-FLI1 | MA0149.1 | chr1:206754995-206755013 | GGAAGGAAGGAAAGAAAG | + | 8.46 | ZNF263 | MA0528.1 | chr1:206754996-206755017 | GAAGGAAGGAAAGAAAGAAAG | + | 6.02 | ZNF263 | MA0528.1 | chr1:206754992-206755013 | GAAGGAAGGAAGGAAAGAAAG | + | 6.03 | ZNF263 | MA0528.1 | chr1:206754964-206754985 | GGGGGAGAGAGAGAGAGAGAA | + | 6.38 |
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| Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
SE_09327 | chr1:206745188-206758382 | CD14 | SE_10603 | chr1:206747310-206756416 | CD19_Primary | SE_11004 | chr1:206727079-206757887 | CD20 | SE_11917 | chr1:206750311-206757762 | CD3 | SE_14503 | chr1:206746009-206758997 | CD4_Memory_Primary_7pool | SE_16490 | chr1:206750757-206757114 | CD4_Naive_Primary_8pool | SE_16959 | chr1:206748089-206757504 | CD4p_CD225int_CD127p_Tmem | SE_17411 | chr1:206724289-206760065 | CD4p_CD25-_CD45RAp_Naive | SE_17843 | chr1:206723887-206758306 | CD4p_CD25-_CD45ROp_Memory | SE_18269 | chr1:206723684-206769868 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19128 | chr1:206746389-206766399 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20034 | chr1:206746357-206757932 | CD56 | SE_20823 | chr1:206746904-206757454 | CD8_Memory_7pool | SE_22080 | chr1:206746077-206757652 | CD8_Naive_8pool | SE_22390 | chr1:206744356-206757869 | CD8_primiary | SE_31229 | chr1:206751813-206754781 | Fetal_Thymus | SE_31229 | chr1:206755155-206757244 | Fetal_Thymus | SE_50667 | chr1:206747343-206754765 | Sigmoid_Colon | SE_53261 | chr1:206746644-206756568 | Small_Intestine | SE_53552 | chr1:206746429-206757806 | Spleen | SE_59167 | chr1:206727342-206757447 | Ly3 | SE_62534 | chr1:206724532-206763666 | Tonsil | SE_65624 | chr1:206752745-206755870 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I206573 | chr1 | 206746529 | 206757654 |
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Enhancer Sequence | TTATCTGTGA AATAAGAATG ACATACATAG TATGTAAGAG AAGGTATGTG AAAGTACCCA 60 GCACAGGCTG TTATTAATAG GTCAGGACCC CTTGGGGAGA GTACAGCGGG AGCAGACAGG 120 CCAGGGAACG ATGCCACGAT GGAAAGAGGA TGTCAGAAGC TGGGTGCGGT GGCTCACACC 180 TGTAATGCCA GCACTTTGGG AGGCCAAGGC GGATGGATCA TTTGAGGTCA GGAGTTCGAC 240 ATCAGCCTGG CCAATATGGT GAAATCCCGT CTCTACTAAA AAATACAAAA ATTAGCTGGG 300 TGTGGTGGTG CGCACCTGTA ATCCCAGCTA CTTGGGAGGC TGAGGCAGGA GAATTGCTTG 360 AACCTGGGAG GCAGAGATTG CAGTCAGCCA AGATCGTGCC ACCGCATTCC AGCCTGGGTG 420 ACAGAGGGAG ACGAAAGAAA AGAAAGAAAG AAAGAGAGAG AGACAGAGAG AGAGGGGGGA 480 GAGAGAGAGA GAGAAAGAAA AGGAAGGAAG GAAGGAAAGA AAGAAAGGAG GATGTCAGCT 540 GTGCTGAGGG GTTGGAGGTG GGAGGCTGGA GCCACGCCAG CTCCTCTTGG CAGCCAGAGC 600 CTGACATTGC ATCGGTTCTG TGGGATTGGA AAGTGGAAGG AAGTGATGGC AGGTTGTTCA 660 GGGTGGCGTG TCTCCCACAT GGCTTGCTGA AGGGAGGAAG GTAGGGCAAA GCTCTGTCAC 720 GGAGGGGGGG CCCTGTTGTG TTCCGCGGGG TGGTGGTGTG ACGTCGCGGC AGCTGTGAAA 780 TTCCCCAGCC AAACCCAGAC ACCCACAGGA CAGTGTCAGA TGGTGTCAGA GTCATCCCTC 840 ACTGGGCCTC AGTTTCCTCA TTTACCAAAG GAGAATCCTG ATCCACCCCA AGTCTGCTAC 900 ACTTGAACGT CAGGCAAATT CTGGGTGGGT TCTGACCAAC CAGTTCCCAC ACTCCCAGCC 960 ACTCAGGGAC AGTGTGAAGA TAAAACCGGG AGGTGGGTAA CAGTGAACTT GAGAGAGAGC 1020 CAGAGAACTG ACTGAGGGAC AGTGGCTTCG ACCCCAGAAT TCACCCCTGT ATTGTCTCTA 1080 CAAGGTGAGG GCCATTGACC TCAATCTCCT CAATTTCATT GTTCACTTAT 1130
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