Tag | Content |
---|
EnhancerAtlas ID | HS018-02143 | Organism | Homo sapiens | Tissue/cell | CD19+ | Coordinate | chr1:226960150-226961560 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr1:226960771-226960783 | GTTTGTTTGTTT | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 226960219 | 226960370 | chr1 | 226960200 | 226961461 |
| | Number: 1 | ID | Chromosome | Start | End |
GH01I226772 | chr1 | 226960302 | 226960501 |
| Enhancer Sequence | ATATTTATTG ACTAAGTTAA TGAAAGTAAG CCATGATTTA AAGAAGCTAC CCACTGAACC 60 CCATGATAGA ATTCAAGGGC TGTCTACCAT AGTTGAAAAG ACTTCTCTCT GTCAAAGGGA 120 ACTATTGTCT TGTGACTACT TCCCTGAAGG TAGCATGTCT GACCACATAA CAAGGGTGGG 180 ATGACCTCCA CCAAAGAGGC TGGGCCAATG CTAATGATGC AGGCCGGAGG CAGAGGGCAC 240 CAGCCACCAG GCACTCCTTG CCACCCCCAT AGCAGGGACA TCATAAAATG TCTGGGTTTC 300 CCCGGAGGCC AGCAAACAAA GGAACAACTG CCTTTTGGAG TAAGTAATCC TGATACTGCA 360 TGTAGTCCAA GGCACACAGA AGGAATCCCT CTGGCAGATA AACCGTAGAG TTGCACAGCA 420 AGAGGGACCT TACAAATGAT CTAAGACTGT GCTTTTGTTT TCAGGATGAG GAAACAGAAG 480 CCTGTAAAGG TGAAAGGAAT TGTCCAAGGT CCCGTGGTTA GTACAGAAAC TAGAAACTGG 540 AAGTAGAACC CAGATCGCTT TCTGAGTCCC CTGAGACTTT GCATATGCTG AATGATTATA 600 AATGATTATA AATAAGTCTT TGTTTGTTTG TTTTTTGAGA CGGAGTCTCC TGCAGCAGCA 660 CTCTGTAACC TATCTCGGCT CACTGCAACC TCCACCTCCC AGGCTCAAGC GATTCTCCTG 720 CCTCAGCTTC CCGAGTAGCT GGGATTACAG GCATGTGCCA CCATGCCCAG CTAATTTTTG 780 TATTTTTAGT AGAGACAGGG TTTCACCATG TTGGCCAGGC TACCCTCGAA CTCCTGGCCT 840 CAAGTGATCT GCCACCTTCA GCCTCCCACA GTGCTGGGAT TACAGCCATG AGCCACTGCA 900 CCCGGCCATA AATAAATCTT AAATCTGATT GAAGGACCCA ACTTCAATAC TTGGAGGTGA 960 TGTCATTAAC CTTAGCAGGT GGGCTCCACA TTTTATCTTT AGCTTCCTAT AAATATGCTC 1020 TAGAGAAGCT TTGGTTTGGG GGTAATCAGA GGTGGAAGCC TCAGGACAGA CCCAGCTTCT 1080 GTTGCCTGGA ACCCTCCATG CTCAGGATGG GCCCTGGTGC CCGGGACCTG GATGCAGACC 1140 CATTGCAGAG GTCTGCTGCA TTTCCTCCAG AGTAGGACAG CAAAATGAGT TGATTTCATG 1200 TTCTGTTCAT CAAAACAAGT GGCCTTCTGA GCCCATCAGC TTCTCAAGGA TTCTCTCCCT 1260 GTAGTGGTTG TCACGGCCAC TGTGCATTTT CTGAATCTCA CCACTTCCAG CCACCAGTCT 1320 GCTAGGGTGG CCTTTTCCAA CCCTATGACA ATGTTTAGCA CTATTATTGG AGAATTTCTA 1380 ACTGACTTGA TGCTGTTGCC ATCTGTTTTT 1410
|
| |
|
|
|