Tag | Content |
---|
EnhancerAtlas ID | HS187-06538 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr13:21049450-21051060 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr13:21050176-21050194 | GGCAGGAAGGAAGGAAAC | + | 7.53 | NFKB1 | MA0105.4 | chr13:21049845-21049858 | AGGGGAATCACCT | - | 6.22 | NFKB1 | MA0105.4 | chr13:21049845-21049858 | AGGGGAATCACCT | + | 6.5 |
|
| 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 |
GH13I020474 | chr13 | 21048535 | 21051757 |
|
Enhancer Sequence | TGATTCCACC TTTGGGCTCT GGGGTGAGAT CTTTATCCTG TCATTTCTAA ACAGATAATC 60 CATTCAGTCA TCAACAAATG TTTATTAAGT TCCTGCCTCA TGCCAGGCAC TGTTTTAGGT 120 ACTGGAAAAA CAGCAGTAGA TAAAGCAATC AAAAATATTC CTGAGGTGTG CAGGCAAAAA 180 TGATTGGGGG TGGAGAGTGG GTATGGCATG GAATAAATAC TAGCACCCAC TTTACGGGGG 240 TGTCGTGAGG ACTGAAGTGG GTCATTTTGT GTTAAGAGTG TGGCACAGGA CCTGGTCCAT 300 GGTAAGGGAT GGATGCACAG TAGTTCCCAT TAGCTGCGGG TCATAGGCCA AGACTAAAGA 360 AGAGCCATAT CAGCCTCAGG AGGCCTTGGG AACAGAGGGG AATCACCTGA TGCTGTGCAA 420 CTGGCTCTGG CCAGGCTCAG AGAAACCAGG GACCCTTTCA GCGGAAGATT CCCACCCACC 480 ACCTACCAAC TAGGATGGCA AGATAGCAAG TGCCTTCAAA CGCGAGCAAA GCAAGAAGCA 540 AAAGGCCGCA GGACGAGTCC CGGTGACATA TCCACAAATC ACAGGCAGAG AGCCTGTTAA 600 AGGAAGGCTG TGTAAGTGTA CTCAGTCAGT GGAAAGTGGA CTTGCTCCAG GAAGGCCACA 660 GCCTCATCCT GGCCTGTGTC ACCTGCCCCA CGCACACGGC AGTTCCGGGG CAGGTCCTGC 720 GCACGCGGCA GGAAGGAAGG AAACCACAGT AGGTCTCTCA GAGGAAACCA CAGTAGCAGC 780 CTCCTCTGCC AAAACAACAG AAATAGCTAC TCCAGTGTCC CAGGTGTCTT CCCACACACA 840 AATGTGCAAT GCGATACTTG CTGAACGCCA GGGCCTCTGA AAGGCAGGAA GGTAATTAGC 900 TGGGAGTGGT GGCATGTGCC TATAATCCCA GCTACCAGGA GGCTGAGGCA AGAGAATCAC 960 TGGAACCCGG GAGGCAGAGG CTGCAGTGAG CCAAGATCGC GCCACTGCAC TACAGCCTGG 1020 GTGACAGAGC AAAACTCCAT CTCAAAAAAA AAAAAAAAAA GGAAAAACGA AAGGCAGGAA 1080 GGTCTCTGCT GGGCAGCAGG GACTGATACA GGTCAACCAG ACCCATAAGA GGTGAAAGGC 1140 CGCCCCTTGA AAGAAACCTT TTGATTTCCC CCAGTGGTTC AAACAGACTT ACTGGGCAAC 1200 AAGTCTTTGA ATATTGACTT TCAAATGAAA ATAAACACAG CAAGGCAGCT CTGCGTCAGC 1260 AGATATGCTC CCAGCGTGCT GATACCGCTA GGTGAGCAGC AGGGAGCCCA AGCCGGAAGA 1320 AAAACATGCA GCAGGGCCAG CACCGAGTTC TGCAGGTGTC CCTTACTTTT CATTAACATG 1380 AAGCTCCCAG ATTCCCGCTT ATGCCTCATA CCTCTTAAAA ACGCAGGCTC AGCAGGGCGA 1440 GGTAGCTTAT GCCTGCAATT CCAGCACTTT GGGAGGCCAA GCTGGAGGAT TGTTTAGGCC 1500 CAGGAGTTCA AGACCAGCTT GGACAACACA GTGAGACCTC GACTCTACTA AAAAATTACC 1560 TGGGTGTAGG CCGGGTGCGG TGGCTCACGC CTGTAATCCC AGCACTTTGG 1610
|