Tag | Content |
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EnhancerAtlas ID | HS051-15454 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr2:68952620-68955460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr2:68954051-68954072 | TTTTCCTTTCTGTTTTTTTTC | + | 6.23 | ZNF263 | MA0528.1 | chr2:68954968-68954989 | GATGGAGAAGGAGAGGGAGAG | + | 6.32 | ZNF263 | MA0528.1 | chr2:68952895-68952916 | TTATCTTCCCCTTCCTCCTTT | - | 6.58 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_09157 | chr2:68953069-68955306 | CD14 | SE_10171 | chr2:68953600-68954979 | CD19_Primary | SE_11846 | chr2:68953525-68955379 | CD3 | SE_13123 | chr2:68954045-68955431 | CD34_Primary_RO01480 | SE_13358 | chr2:68952452-68955565 | CD34_Primary_RO01536 | SE_14164 | chr2:68952650-68953527 | CD34_Primary_RO01549 | SE_14164 | chr2:68953580-68955128 | CD34_Primary_RO01549 | SE_14434 | chr2:68953539-68955487 | CD4_Memory_Primary_7pool | SE_15442 | chr2:68953589-68955201 | CD4_Memory_Primary_8pool | SE_16342 | chr2:68952552-68955240 | CD4_Naive_Primary_8pool | SE_17374 | chr2:68953427-68955400 | CD4p_CD25-_CD45RAp_Naive | SE_17790 | chr2:68952762-68955597 | CD4p_CD25-_CD45ROp_Memory | SE_18271 | chr2:68953025-68955670 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19336 | chr2:68953357-68955448 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20020 | chr2:68953833-68955187 | CD56 | SE_22313 | chr2:68952804-68955599 | CD8_primiary | SE_25454 | chr2:68952602-68955573 | DND41 | SE_31134 | chr2:68953335-68955594 | Fetal_Thymus | SE_39426 | chr2:68952643-68955604 | Jurkat | SE_53380 | chr2:68953588-68955181 | Spleen | SE_55534 | chr2:68954271-68955017 | Thymus | SE_58353 | chr2:68936255-69037867 | Ly1 | SE_58815 | chr2:68915194-69067159 | Ly3 | SE_60486 | chr2:68936463-69018341 | DHL6 | SE_60993 | chr2:68936154-69024001 | HBL1 | SE_62221 | chr2:68936470-69037652 | Tonsil | SE_66438 | chr2:68952643-68955604 | Jurkat |
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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 |
GH02I068726 | chr2 | 68953318 | 68955619 |
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Enhancer Sequence | CAATTTTTTT CTTTTCTTTT CTTTTAGAGA TGGGGCCTCA ACTGTGTTGA CCAAGCTGTT 60 TAGAATTCCT GGGCTCAAGT CATCCTCCTC AGCCTCCCAA AGTGCTGGGA TTACAGGCAT 120 GAGCCACCAT GCCCAGCCTG ATTATTTAAA AGTATACATC AAATCAAGGC ACTCCTCTGC 180 TGTAAACCTC ACTCTAAGCA AAAGCCAAAG TTCCAGCAAA GTCCTATGAA GCCCCATACA 240 ATTCGTCCCC TATTACCTTG TTGACCCATC TCTTGTTATC TTCCCCTTCC TCCTTTTGCT 300 GTGAACACAA GACCTCCTTG GGGTCTCTTG AAGTGCTAGG CCTCCTCTCA CCTCTGGCAG 360 AGCTCTTGCA CTCACACCTC CATCTGCTGG AAGGTTCTCC CACATAGGTT TACCTGGCTC 420 ATTCTCAACC TGGCTTAGGT CTTTACTCAA ATGTCACCTA TTCTGTGAAA TGTCACCTTC 480 GCTGTCCAAC TATTTAAAAA TGCAATCTCC CTCCCCTCTC CCCTCAATCT GACATTTCTT 540 TCACCCCTTC CCGTAGCACT TTTTCTTTTT CTCCACAGCC CTTACCACCA TCTAACACGT 600 TACATTTATT TCACTTATTT ATTTTCTTGT CTCTTTCCTC ATTAGAACAA GCTCCACAAA 660 AGCAGGCGTT TTCATCTGTC TTCTTGTTGG CTGTGTTCTC AGCACCTAGA GCACTGCCTG 720 ATCCCTAATA GGTGAACGGT TCCTTTATAT TTGTTGAATG AATGAGTGGC AGGAGGCAGA 780 GTGGGTCTAT TATGTGGAAA TATATGAGAT TGTTCTTGCC AGTCAAAAGC TGTCAAATAT 840 TGGCAGCTTC ACGTGGTTCA AATTAATGTA ACGTAATACA GAACAATGGC CAAAAGGAGG 900 TGTTACGTGA GGGACATTTG CTCCTGATTT GCTCAGTGTG CTCCTTCCTG TTGGAAAACA 960 TGAGATTCTT TTATAATCCC CTGGGAACGA ATTTCCCATA TAAATAGACA TTTCCCTTCC 1020 TGAGCCCATC ATTCACAGAG CAGCCTTCTT CCAGGTAGAG CACCAGCAGT AATAATGCCC 1080 GTCTTGGCCT TCAGGCCTCC AGATATAAAT TTTTTGGCTA TGGGACAATT TTTTTTGGCT 1140 ATGGGACACT TAGAAAAAAT AAAGATCAAT AGACTATCAA ACTGTAGCCA GACATCAGAT 1200 CCAATGCCAG GGACCTTGGC AAAGGTGACA TCAGTAACGA GAGGAGGTGC CTCCAACTGA 1260 CTGCTCAGGG CTGGGAGGAA CAAGCCTCTG TGGTCTGAGC CCAGGAGCCT GCACCCCATC 1320 CACTGGGCTC ACACAGAGTG TTCAGAGCCC AGAAATCTCT TCCTCTGCCA GGTCTGCCTC 1380 TGCTGAGCTT GCAAAAAGGC ATAGTCCTAT TGCACAAATC TTTTTTTTTT CTTTTCCTTT 1440 CTGTTTTTTT TCCATATACC CAAGGGAATG GGAATAAAAC CTTAATTTTG TGCCTTGTAA 1500 ATACAGCTTT TAAAAAGATA TAGACTATTA AAATCCAAAT AAAAAAGATC TTTACGTTTG 1560 GTGTCTCCAA ATGCTATATT CCAGGACGTA CATGCTGAGG CATCTGTCAG TCAAGACCAC 1620 AAGATACAGC CATCCGGCCT ATGCACTTAG TATTTGCTAA AAGCGTGGTT ACTGGTTGAG 1680 TGCGTCTGCA ACACGGGGGC CCACGTTCAA ATGCCTGCAC GAGCCAGGTG GGAAATACAA 1740 GCGAGTGAAA CTGGCTGACT CACGGCCACA AAGAAATGTG TTTCCTCCCA ATCTGCTTGA 1800 CTTCAGGCCA TCTTTTTTTC CCCTCACTTT TGGTTAAGAT GTGGGTACAA AAAGTATTAT 1860 GCTTTTCTTC TTAAATCTAT TAGAAGGAAA ATATCAATAC AAGTGTGACC ACAATAGCAC 1920 CTGGCACAGT CTCCCAGGAA TGTAAAGGTT TGTGCCAATT TAGGGCACTT GATCTGCCTC 1980 AGAGGGTCTG CCTCTGCGGA GCTTCCATCT GCTGATTAAC AGGGCATCAC CCTACTTCAC 2040 AAAGGCCTGT GTTCAGAGAA ACCTCCCCCG GCTTTGTGCC ATGGCCAGGG ACCTCCTGAC 2100 AAAGGTAGAC CCTCACCTTC TGACTCTCCT GGAGTCTGTT CTTCACTCTG ACCCAAACTA 2160 TGTCAAGTTC AGAAAACTGA TTTCTGCCTC TCCCTCCATC CATTTATCTG ATGCTCATCC 2220 GTGAGGCAGC TGGAATAGGA TTGCTCCATT CCCCTGCCCA GGCATTGTTT TAAATCCCTG 2280 CAGAAAACAA CAGCTACAAC CATCATGGTA ATGAGGGATG ACGGTGACAA CCACAACCTG 2340 GAGAGCTCGA TGGAGAAGGA GAGGGAGAGA TCTGGTGACA AGTGACTCTC TTCAGCAGAT 2400 CTAATCACTC CTAGAAAGAT GTGACTGCCT TTTCATGCAC AGCATCACTT AAAAGTTCTA 2460 GAGAACTAGG CAAGGGGTAG GGGAAATGCA GCTGAAGTAC ATAGAAAAAA GTCTGCTGGA 2520 AATTTGAAAT GATACTGAGT ACAATGTACA TCAGAAAGAT TAAATGGAAA TAAGGCAAAA 2580 GTAGGAAAGT TTCAGTCAAA GTTGAAGGCT TGAGTTTTAG CTGGATGTGG TCTTGAGGAA 2640 ATGCAGGTTC AGTGGGACTA CATCATCGGA TGTTTCACGA AGCAGGAATT CTGCTTTGGA 2700 AAACCAAACC AGCCAATAAG CAAATGAAAA GATGCTTAAC ATCATTAGTC ATCAGGGAAA 2760 TGCAAATCAA AACCCCAATG AGATAATAAC ATTTCATCCT AACCATCCAC TAGAATGGCT 2820 AAAATAAAAA AAGACTGATG 2840
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