Tag | Content |
---|
EnhancerAtlas ID | HS018-05234 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr12:51895390-51896650 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr12:51896020-51896032 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr12:51896024-51896036 | GTTTGTTTGTTT | + | 6.32 | MEF2A | MA0052.3 | chr12:51895485-51895497 | TCTATTTTTAGT | - | 6.27 | MEF2B | MA0660.1 | chr12:51895485-51895497 | TCTATTTTTAGT | - | 6.32 | MEF2C | MA0497.1 | chr12:51895484-51895499 | TTCTATTTTTAGTTC | - | 7.13 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CAATAAATAT ATGAGTGCAG ATGTCTTTTT GACAGAACAA TTTATTTTCC TTTGGGTATA 60 TACCAAGTAA TGGGATTGTT GGGTCTAATG CTAGTTCTAT TTTTAGTTCT TTGAGAAATC 120 TCCAAACTGC TTTCCACAGG GGCTGAACTA ATTTGCATTC CCACCAACAG TGTAGAAGTG 180 TTCACTTTTC TCCACAACCA TGCCAAAGTC TGTTATTTTT TGACTTTTTA ATAATAGTCG 240 TTCTGACTGA TGTGAAATGG AGTCTCTTTG TGGTTCTGAT TTGCATCTCT GATGATGCAT 300 GATGTTGACC AGTTTTTAAT ATGTTTGTTG ACTGCTTGTA TGTCTTCTTT TAAGAAGTGT 360 CTGTTCATAT CCTTTGCCCT TTCGCTTCTA TGCACCAATA ACACCCAGGC TGAGAGTCAA 420 ACCAAGAACA CAATCCTGAC TACAGTAGCC ATAAAGAAAA TGAAATACCT GGGAATACAC 480 CTAATCAAAA ACATGAAAGC ACTCTCTAGA GGGAGAACTA CAAAACATTG CTGAAAGAAA 540 TCAGAGATGA TTCTCTGAAA AAGAAGTCAG ATTAGAAATG ATTCTCTGAA AAAGAAATCA 600 TCTCTGATTT CTTTCAGCAG TGTGTTTTTT GTTTGTTTGT TTGTTTTGAG ACAGAGTCTT 660 GCTCTGTCGC CAAGGCTGGA GGGCAATGGC ATGATTTCAG CTCACTACAA CCTCCTGCTC 720 CTGGGTTCGA GCGATTCTCC TACCTCAGCC TCCCGAGTAG CTGGGATTAC AGGTACCTGC 780 CATCACGCCT GGGCTAATTT TTGTATTTTT AGTAGAGACA AGGTTTTGCC ATGTTGACCA 840 GTCTGGTCTC GAACTCCTGA CCTCAAGTGA TCTGCCTGCC TTGGCCTCCC AAAGTGCTGG 900 GATTAAGGCA TGAGCCACTG TGCCTGACCT CTTTTTTTTT TTGAGATGGA GTCTCGCTCT 960 GTCGCCCAGG CTGGAGTGCA GTGGTGTTAA AAACTGGTCA ACATCATGCA TCATCAGACA 1020 TGCAAATCAG AACCACAAAG AGACTCCATT TCACATCAGT CAGAATTACT ATTATTAAAA 1080 AATCAAAAAG TAACAGACGT TGGCATGGTT GTGGAGTGCA GTGGTGTGAT CTCGGCCGAC 1140 TGCAACCTCT GCCTCCCAGG TTCAAGCGAT TCTCCTGCCT CAGCCTTCCT AGTAGCTGGA 1200 ACTACAGGCA TGCACCACCA CGCCCGACTA ATTTTTTTTT TTTTTTTTTT GAGATGGAGT 1260
|