Tag | Content |
---|
EnhancerAtlas ID | HS187-13364 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:68952680-68955400 |
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 |
|
| 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 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH02I068726 | chr2 | 68953318 | 68955619 |
|
Enhancer Sequence | TAGAATTCCT GGGCTCAAGT CATCCTCCTC AGCCTCCCAA AGTGCTGGGA TTACAGGCAT 60 GAGCCACCAT GCCCAGCCTG ATTATTTAAA AGTATACATC AAATCAAGGC ACTCCTCTGC 120 TGTAAACCTC ACTCTAAGCA AAAGCCAAAG TTCCAGCAAA GTCCTATGAA GCCCCATACA 180 ATTCGTCCCC TATTACCTTG TTGACCCATC TCTTGTTATC TTCCCCTTCC TCCTTTTGCT 240 GTGAACACAA GACCTCCTTG GGGTCTCTTG AAGTGCTAGG CCTCCTCTCA CCTCTGGCAG 300 AGCTCTTGCA CTCACACCTC CATCTGCTGG AAGGTTCTCC CACATAGGTT TACCTGGCTC 360 ATTCTCAACC TGGCTTAGGT CTTTACTCAA ATGTCACCTA TTCTGTGAAA TGTCACCTTC 420 GCTGTCCAAC TATTTAAAAA TGCAATCTCC CTCCCCTCTC CCCTCAATCT GACATTTCTT 480 TCACCCCTTC CCGTAGCACT TTTTCTTTTT CTCCACAGCC CTTACCACCA TCTAACACGT 540 TACATTTATT TCACTTATTT ATTTTCTTGT CTCTTTCCTC ATTAGAACAA GCTCCACAAA 600 AGCAGGCGTT TTCATCTGTC TTCTTGTTGG CTGTGTTCTC AGCACCTAGA GCACTGCCTG 660 ATCCCTAATA GGTGAACGGT TCCTTTATAT TTGTTGAATG AATGAGTGGC AGGAGGCAGA 720 GTGGGTCTAT TATGTGGAAA TATATGAGAT TGTTCTTGCC AGTCAAAAGC TGTCAAATAT 780 TGGCAGCTTC ACGTGGTTCA AATTAATGTA ACGTAATACA GAACAATGGC CAAAAGGAGG 840 TGTTACGTGA GGGACATTTG CTCCTGATTT GCTCAGTGTG CTCCTTCCTG TTGGAAAACA 900 TGAGATTCTT TTATAATCCC CTGGGAACGA ATTTCCCATA TAAATAGACA TTTCCCTTCC 960 TGAGCCCATC ATTCACAGAG CAGCCTTCTT CCAGGTAGAG CACCAGCAGT AATAATGCCC 1020 GTCTTGGCCT TCAGGCCTCC AGATATAAAT TTTTTGGCTA TGGGACAATT TTTTTTGGCT 1080 ATGGGACACT TAGAAAAAAT AAAGATCAAT AGACTATCAA ACTGTAGCCA GACATCAGAT 1140 CCAATGCCAG GGACCTTGGC AAAGGTGACA TCAGTAACGA GAGGAGGTGC CTCCAACTGA 1200 CTGCTCAGGG CTGGGAGGAA CAAGCCTCTG TGGTCTGAGC CCAGGAGCCT GCACCCCATC 1260 CACTGGGCTC ACACAGAGTG TTCAGAGCCC AGAAATCTCT TCCTCTGCCA GGTCTGCCTC 1320 TGCTGAGCTT GCAAAAAGGC ATAGTCCTAT TGCACAAATC TTTTTTTTTT CTTTTCCTTT 1380 CTGTTTTTTT TCCATATACC CAAGGGAATG GGAATAAAAC CTTAATTTTG TGCCTTGTAA 1440 ATACAGCTTT TAAAAAGATA TAGACTATTA AAATCCAAAT AAAAAAGATC TTTACGTTTG 1500 GTGTCTCCAA ATGCTATATT CCAGGACGTA CATGCTGAGG CATCTGTCAG TCAAGACCAC 1560 AAGATACAGC CATCCGGCCT ATGCACTTAG TATTTGCTAA AAGCGTGGTT ACTGGTTGAG 1620 TGCGTCTGCA ACACGGGGGC CCACGTTCAA ATGCCTGCAC GAGCCAGGTG GGAAATACAA 1680 GCGAGTGAAA CTGGCTGACT CACGGCCACA AAGAAATGTG TTTCCTCCCA ATCTGCTTGA 1740 CTTCAGGCCA TCTTTTTTTC CCCTCACTTT TGGTTAAGAT GTGGGTACAA AAAGTATTAT 1800 GCTTTTCTTC TTAAATCTAT TAGAAGGAAA ATATCAATAC AAGTGTGACC ACAATAGCAC 1860 CTGGCACAGT CTCCCAGGAA TGTAAAGGTT TGTGCCAATT TAGGGCACTT GATCTGCCTC 1920 AGAGGGTCTG CCTCTGCGGA GCTTCCATCT GCTGATTAAC AGGGCATCAC CCTACTTCAC 1980 AAAGGCCTGT GTTCAGAGAA ACCTCCCCCG GCTTTGTGCC ATGGCCAGGG ACCTCCTGAC 2040 AAAGGTAGAC CCTCACCTTC TGACTCTCCT GGAGTCTGTT CTTCACTCTG ACCCAAACTA 2100 TGTCAAGTTC AGAAAACTGA TTTCTGCCTC TCCCTCCATC CATTTATCTG ATGCTCATCC 2160 GTGAGGCAGC TGGAATAGGA TTGCTCCATT CCCCTGCCCA GGCATTGTTT TAAATCCCTG 2220 CAGAAAACAA CAGCTACAAC CATCATGGTA ATGAGGGATG ACGGTGACAA CCACAACCTG 2280 GAGAGCTCGA TGGAGAAGGA GAGGGAGAGA TCTGGTGACA AGTGACTCTC TTCAGCAGAT 2340 CTAATCACTC CTAGAAAGAT GTGACTGCCT TTTCATGCAC AGCATCACTT AAAAGTTCTA 2400 GAGAACTAGG CAAGGGGTAG GGGAAATGCA GCTGAAGTAC ATAGAAAAAA GTCTGCTGGA 2460 AATTTGAAAT GATACTGAGT ACAATGTACA TCAGAAAGAT TAAATGGAAA TAAGGCAAAA 2520 GTAGGAAAGT TTCAGTCAAA GTTGAAGGCT TGAGTTTTAG CTGGATGTGG TCTTGAGGAA 2580 ATGCAGGTTC AGTGGGACTA CATCATCGGA TGTTTCACGA AGCAGGAATT CTGCTTTGGA 2640 AAACCAAACC AGCCAATAAG CAAATGAAAA GATGCTTAAC ATCATTAGTC ATCAGGGAAA 2700 TGCAAATCAA AACCCCAATG 2720
|