| Tag | Content |
|---|
EnhancerAtlas ID | HS059-27130 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr2:191583130-191584590 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr2:191584206-191584218 | ACTATAAATAGA | + | 6.22 | | MEF2B | MA0660.1 | chr2:191584206-191584218 | ACTATAAATAGA | + | 6.37 | | Stat6 | MA0520.1 | chr2:191583762-191583777 | ATTTCCCAGGAAAGG | - | 6.15 |
|
| | 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 |
| GH02I190717 | chr2 | 191582084 | 191584601 |
|
Enhancer Sequence | TCCTGCCTTT ACTTCAAGTC GTCCTGCCTT TCCAGATGGA ACCAATGTAC TTCTTACATA 60
TGTTGATTGA TGTCTCATGT CTCCCTAAAA TGTATAAAAC CAAGCTGTGC CCCGACCACA 120
TTGGGCACAT GTCTTCAGGA CTTCCTGAGG CTGTGTCATG GGTGCATCCT CAACCTTGGC 180
AAAATAAACT TTCTAAATTA ACCGAGCCCT GTCTCAGACC TTCAGCGTTC ACAGACTATA 240
CCGAATCGGG CTGTTAATCT TTGAAAGTGA CTGGAACCCT AGAGATCTAA CCAAGATATT 300
GTCAGGGAAC TCAGCAGAGA GATCGTGAAC ATGGCAGAAC TGAAGGCAAG TGACTGTAGA 360
AAAATAAATT ATTTCACGCC TGTACTTCCT ACGAACAAGG ATTGTTTAGT AAACTAGATG 420
TGGTAGCCAC GATTTTCATG ATCAACAGAG TGGCAACAGG CAAGACTGAA TGATGGGGCT 480
TTGGGGAATT GCACTGGCGA TGAATCACCC TGAGATTATG CAGGTGGGGT TTCCCCTGAA 540
GGGACTGGAA CTGCTCACTG CCAGCTGTCC TCAGAAGAGG TCAGTCATGG GGCGGGAAAT 600
CAGAATGCTG GGACTAGAGT CAGTCTGACT GGATTTCCCA GGAAAGGTGA CTGTTGAGTC 660
CCCAGGGCAC TTCCTCCTGG AGGGGGAAGG ACCTGTGCCT GGCACTGACT TATTCTCTGT 720
TTTCTGTTTC CTTTCCATTG TCCCTGAACC TTTATTGTGA TCTGATCAGT GTCTCAAATA 780
TTTTGACTTC TGATGTCCTG AGAGGAATTA AGGGGAAAGG TCCACAACCA ACCCCTGAGG 840
CAAAGCAGAG GAGGGTTATG ACTTCTGTCC TCAGGCCACA GCAGTGGTGG CAGCCACAGG 900
CACCAGCTGA GAACAGCTTT GCCCCAGAGG GACCAGTTTC TGAATACACA TGACAGAGCA 960
CCTTGAGAGA GTCTCAAGAT TCTTTAGCAG AACAGGGGAC ACTGGGAGTA GGGGCAGAGG 1020
GCACTCATTT TTGTCAATAA AACTAGTGTG AGTCAAACTA CGATGGCTTC AGTTACACTA 1080
TAAATAGAAT TATCAAACAA GGGGACAAGC TCCTTGTCCC TACAAGTGCT TAAAAAATAA 1140
ATATTTTTCT TTTAAGGAGT TTTCTAATGG TGTTCCTATG ACATTAATTT ATTAAACATT 1200
TAACATACTT TGCACTTACT GTATATCAAG CATTGTGCTA GGTTCCTTAC ATACAATTTC 1260
TATTAATAAC CTGGTTTTGT AGTTGAGGAA ACAGAAGCTT ACAAAGTGAA ATAAGTTGCC 1320
TTAGGTCTTG CAAATAATCA GTAGTAGAGA CCCCCAAAGG TGAGCACACT AGAATACACC 1380
AGCCTAGTCG GGGAGGATGA CCATCATGGA AAACCACTCA CTGATGGAGA TGTGCACAAA 1440
TTGTTTTGGG CGCATATGAC 1460
|
