Tag | Content |
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EnhancerAtlas ID | HS190-00961 |
Organism | Homo sapiens |
Tissue/cell | Treg_cell |
Coordinate | chr1:169648200-169649140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TCF7L2 | MA0523.1 | chr1:169649001-169649015 | AAACTTCAAAGGGA | + | 6.74 | ZNF263 | MA0528.1 | chr1:169648621-169648642 | GGAGGAGGGTCAGAGTGAGGA | + | 6.43 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_10569 | chr1:169647849-169652512 | CD19_Primary | SE_11089 | chr1:169642623-169653758 | CD20 | SE_18548 | chr1:169647785-169652059 | CD4p_CD25-_Il17-_PMAstim_Th | SE_39546 | chr1:169647775-169648776 | Jurkat | SE_58649 | chr1:169639952-169681619 | Ly1 | SE_58866 | chr1:169645496-169682054 | Ly3 | SE_62308 | chr1:169636484-169681753 | Tonsil | SE_66316 | chr1:169647775-169648776 | 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: 2 | ID | Chromosome | Start | End |
GH01I169678 | chr1 | 169647776 | 169648776 | GH01I169679 | chr1 | 169648865 | 169651709 |
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Enhancer Sequence | CATTTTAATT CAAGCTTTAA AACTGCTAAA TAAAATGTGC TCCAATTTCT ATATTGACAG 60 ACATACCTTC CTAATGAGCT GGGGTTCGAA TTTAGAAATC TTTGATGCTT CAGAGTCCAC 120 ACTGAAATGT GGAGGCACAT AGTGAGTTGG TCCCCAGCCT TCAGTCCACC CACCTTCTCT 180 TTACTAAATC ACCTTTCACA TACATGTATG AACACCCCAG CCTCCAAGTC CAAACCCTAA 240 ACAAAATGGG ACACCCTTGT GCATACACAG AGACACAGCC CATCCTCAGG AAAACCTGGA 300 AAAGTCCATA CAAGTTCTGG AAGCAAGCTT GGGACGGTTT CAGTAGTGTG GTCTATAAGG 360 GAGGCCTCAG AAGACAGGTT TTCTTAATTC TGTGAACTTC TCCCACAGTA GAAAGGGTGC 420 TGGAGGAGGG TCAGAGTGAG GACTTCTAAA GCATGGGTCC TGAGTAGGGG CCACTCTTGC 480 CCAAGTCTAA GAAGGGTACT AGAATAGCAC ACTACTACTA GATACTAGAA CCCAGATACA 540 AGCACAGGTC TTCTGAAATT AATAATAATA ATAACTATTA CCATTATTAT ACCAGTAGCT 600 GTCATTTATT TAGTGCTTAT TATTTGCCAG TCACTGTTCT AAATTCTTTA CATGTATTAT 660 ACAACTGCCA TATAACTGCC ATATGAGGGA TGTACCCTCA TTGTCACCAT TTTACCGATG 720 AGAAAACTGG CATAAAACGT TTAAGTAACT TGTCCAAGTT ACAGAGCTTA GTGAAGCCAC 780 AATGTTGCTC AATTTGCTCT CAAACTTCAA AGGGATGGGA AGGACACCTA AGTCATAGAG 840 TCTTTAAGAA TCAGAGCTAG AAGGAATCTT AGATGTTATC TAGTCAGCCT CCTCCCATTA 900 CAGTCCAAGA GAAGATGGCC CTGAGTTACT TGTAGCTATT 940
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