Tag | Content |
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EnhancerAtlas ID | HS182-01812 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:206754810-206756600 |
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 | NFIC | MA0161.2 | chr1:206755867-206755878 | TACTTGGCACA | + | 6.32 | 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_27304 | chr1:206755912-206765002 | Esophagus | SE_31229 | chr1:206755155-206757244 | Fetal_Thymus | 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 | SE_65624 | chr1:206756181-206757996 | 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 |
chr1 | 206754982 | 206755508 | chr1 | 206754868 | 206756159 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I206573 | chr1 | 206746529 | 206757654 |
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Enhancer Sequence | ATCCCAGCTA CTTGGGAGGC TGAGGCAGGA GAATTGCTTG AACCTGGGAG GCAGAGATTG 60 CAGTCAGCCA AGATCGTGCC ACCGCATTCC AGCCTGGGTG ACAGAGGGAG ACGAAAGAAA 120 AGAAAGAAAG AAAGAGAGAG AGACAGAGAG AGAGGGGGGA GAGAGAGAGA GAGAAAGAAA 180 AGGAAGGAAG GAAGGAAAGA AAGAAAGGAG GATGTCAGCT GTGCTGAGGG GTTGGAGGTG 240 GGAGGCTGGA GCCACGCCAG CTCCTCTTGG CAGCCAGAGC CTGACATTGC ATCGGTTCTG 300 TGGGATTGGA AAGTGGAAGG AAGTGATGGC AGGTTGTTCA GGGTGGCGTG TCTCCCACAT 360 GGCTTGCTGA AGGGAGGAAG GTAGGGCAAA GCTCTGTCAC GGAGGGGGGG CCCTGTTGTG 420 TTCCGCGGGG TGGTGGTGTG ACGTCGCGGC AGCTGTGAAA TTCCCCAGCC AAACCCAGAC 480 ACCCACAGGA CAGTGTCAGA TGGTGTCAGA GTCATCCCTC ACTGGGCCTC AGTTTCCTCA 540 TTTACCAAAG GAGAATCCTG ATCCACCCCA AGTCTGCTAC ACTTGAACGT CAGGCAAATT 600 CTGGGTGGGT TCTGACCAAC CAGTTCCCAC ACTCCCAGCC ACTCAGGGAC AGTGTGAAGA 660 TAAAACCGGG AGGTGGGTAA CAGTGAACTT GAGAGAGAGC CAGAGAACTG ACTGAGGGAC 720 AGTGGCTTCG ACCCCAGAAT TCACCCCTGT ATTGTCTCTA CAAGGTGAGG GCCATTGACC 780 TCAATCTCCT CAATTTCATT GTTCACTTAT CCTTCCCAGG GGGTGGGAGG AGGAGGGCAT 840 CTGGGAACAT ATGAGAAGAA TGAACACATG GTCTCACAGG AGGAACACAA TGGGACAGAC 900 CTGGAATTTC TGTTTCATTC TGTACATACT GACTGTAGGG TGTGAGGCAG GTTGCTAAAC 960 TTCTCTTAGT CTCAATAGTC TCACCTGTAA GATGGGGTAA TAAACTATCT TACAGACTTC 1020 TGGTTTGTGA GAATCATATG AGATAATGTA TGCCAAATAC TTGGCACAGA AGAAGTGCTA 1080 AGTAAATTCT AGGTGTCCCT GTGCCCAGTA GCGGTTTATC TCCTCTTTTA TGGTAGAGGG 1140 GGCTACAGCC CTTCATCCCT GCCAGTTCAC TCGTTCATTT GACAAATAGA TATTTACTTC 1200 TTGCTATGTG AAAAGCACTG TGGCAAGTGA TGTGGGGCCT GGACTGGTCT CTATGTGTCC 1260 TTGGTCCTTG GGATCTAAGA GAATTCTTGT CTTCCCGATC AGTAGTATAT ACTGGCACCA 1320 TGGGTAGACG CCTGTCCCTC CAGCTGTGTT GTTACTTCCT TGAGGAGACA GACCATGGCT 1380 TGTATTTCTT TGCATCTCCC ATAGCATCAA AGAAGCATCT TTTCCATAGC AGCTTTCCAT 1440 AAGCAAATGC GGCTCTGCTC ATTCACCAGA TTCATAGTCA GTGCCTGAGT GCCAGACGCT 1500 TTCACACTAA TCTCAAGACA AGCCTGTGCA GTAGGTATTG TTCCCATTTC ACAGATGAGG 1560 AGACTGAGGC TTAGAGAAAT CTGAGTTACT TCTCCAGGAG GGCTGGCTAG ACACTGGCAC 1620 AGCTGCAATT TGACCTCTCA TTGTCTCACT CCGAGTCCGT GCAGTTAGTT CCACTCTGCA 1680 GGGCTGGATG CTCACTTCTT GGTTAGAGAG GCTTTGGGGA GGGCGTGGTT GTTCCCTTTC 1740 TCACCCTGAG AACTACTACA CATCCACCTC CACTTCTGTG TCTCTTCCAG 1790
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