Tag | Content |
---|
EnhancerAtlas ID | HS108-23702 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr2:172486700-172488350 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr2:172488177-172488189 | CTCTGTTTACTT | - | 6.37 | FOXP2 | MA0593.1 | chr2:172488178-172488189 | TCTGTTTACTT | - | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TATTGAGGAG TATCAGAATA TGCCAACCTA AAATATGCCT ATTTGGCATT TGGCTTATTT 60 TGCGCTAAAG CCCGCTGAGA ACCAGAAGAC CAGGAAATTA CATTTAGAAA GTCAATTTAC 120 ATATAGAAAT GGTGCTTCCC TCTGTACCAG GAGGAAGAGG ATCCTTAACA ACTCCTATCA 180 ATGGAGAAGG TACTTCCATC TGCATAACAA ACCAATGACC CTTGTTTACC ATACTTTTCC 240 TGGTCACCTA CCCCTAACTT TCCTCCCCCA TGCAGAAGCC TAAAACTCTT CTTTCCTTGT 300 TTAAGCCTAA GATGATAGAA AGCCAACTTC TAACCACCTA ATGGAGTCAA TCAATTCTGA 360 ATATGCCCAT ATGTAAGCAC CAGGCATATG CTAATAAACA TCTGTTTATT TTTTTTTCTT 420 GTTAATCTGT CTTTAGCCAG CCTAATTTAT ATGGCACCAG CTGGAGAACT TAAGATGAGT 480 GAAAGAGGAG TTTTTTTCCT CCTCTACAGT ATCTATTTCT GCATTGGAAA TGGACCCACA 540 TATACACTTA AACACAGTCT TCTAAACCAC CCGGCATTCA AAGGTGACAT TGTCACCTAC 600 CAACCCCCAC ATCCAGTAAA CTCATTGCTT TAGATTGAAT TTCAGATCAT TTCATTGTGA 660 AAGAAAAATA AAAAGTAGGA ACTCCCAATT CATTATGCCA AAAGAGAAAA GTTAAGCTTG 720 AAAACTGAGT CACAAAAAAA CTGCCTTGCC TTTTGCTCCT AAACTGAAAG GTACAGATAA 780 AAGACCACAT GCCTCCACAG GGGACCTCCC ACCCTGACCC TGAAAATGAA AATTAACAGC 840 TTATCTCTAT GGGTGCAGGA CAAGAGTGAA GCAGGTGATA CAGAAGAAAA AACAAATTTT 900 CTTCCTTTCC TTTGGTATGA GCAGCTTCTC CCTTGAATCC CTCCCGCCTC GTGTGATTGT 960 ACCCTGCTCT GCAAGTTTTT ATGAGTTTAT AGGTTCCTGT TTTCTGTAAC TAGTGTCTGT 1020 AAGTCTGTTT TTCATCTGAG TAGCACCATG GAGGTCATGA GACATGCTTG AGCAATCTTA 1080 GATTGCAGCC ATCTGGGCGC CATAGTGGAG GACATGAGAT AAGATTGTGC AGGCATCTTG 1140 AGCAAGCCTA GATAACAGCC ACCTGGCCCA CATAGCAAGA GTCACATGAA AGCCTGAGTT 1200 ATGAGCCTGT CTCTGTTTGA TAAACTGCCT TTGTTCTGCT TCCGTAAACC CACTTTTGCG 1260 CCACTGCATT TCGAGCCACA GATGCATGTA TAAAAGTCAA GCCCTGTCTT TGTTTGGGTC 1320 TCAGCCTTCT GGATGCAAAT CCGCTGAGCT GGTGCACCTA AATAAAATCC TCCTGTCCCA 1380 CCTATTGGTC TCTCCAGTTC CTTCATTCCC GCAACAAGAG GAGATTAGAA ATCATCTCCC 1440 CTACTTTAGA CAAAGGCATA TTTGACTGCT TCATCTACTC TGTTTACTTT TTTTTTTGAG 1500 ACAAAGTGTC GCTCTGTTGC CAAAGCCAGA GTGCAGTGGC ACAATCTCAG CTCAATCTCA 1560 GCTCACTGCA ACCTCCACCT CCCGGGTTCA AGTGATGCTC CTGCCTCAGT CTCCTGAGTA 1620 GCTGGAATTA CAGGTACATG CCACCACACC 1650
|
| |
|
|
|