| Tag | Content |
|---|
EnhancerAtlas ID | HS187-06150 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr12:102217640-102218620 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN | MA0488.1 | chr12:102218136-102218149 | ATGACATCATTTG | - | 6.18 | | JUND(var.2) | MA0492.1 | chr12:102218135-102218150 | GATGACATCATTTGA | - | 6.16 | | MEF2C | MA0497.1 | chr12:102217640-102217655 | ATATTAAAAATAGAA | + | 6.14 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I101821 | chr12 | 102215595 | 102220178 |
|
Enhancer Sequence | ATATTAAAAA TAGAAACAAT CTACTTTACA ACTTCTAGAG CAAGGTAAAG GGCTAACAGC 60
TATCACAGAC ACAATGTCAC CAGTAAAGCC AGGGAGAGGA AATGGGTTTT GACTGAAGCC 120
AGTGTCTTCA AGACATCTGT TGTTCCGGCC CTTCTTTGGG TAACAGCCTT GTGATTATCT 180
TCTGAAGCTC TCCTCTCAGT TCACGTGGTT CAGTTGAGAC TGACAGCCCC ACCCACTCCC 240
CTATTTCTGG AGACGATCCC AGTGGTTAAC AAGGGTATAA CAAGGGCACT CATTCCTCTG 300
GCTAGGCAGG CAGCCCTGGG TCTAGTTGGC ACTAATGAGA AAGAAAAGCT ATCTTTCTGC 360
TGCAGTTACT GAACTGGTAG AACAGAAGGT GGGGTTGCCA GCAGCAATCC TTGTTCTCAT 420
ATGAGGAGAG CTTGCTGAGA AGTAAACTAA AGAGGGGAAG GCAGAGGTGA GAAACAGGGA 480
CAAAAAGAGA TTCCTGATGA CATCATTTGA GCACCTCGAT CCACTCCTGC CAGAAATTTC 540
ACCATATATA TATATATATA TATATATATA TTTTCTTTTT TTTTTTTTTT TTTTTGGTTA 600
ACCTTTTTGT TTTGTTTTGT TTGAGACAGA GCCTCACTCT GTCGCCCAAG CTGGAGTGCA 660
GTGGCACAAT CTTGGCTCAC TGCAACATCT GCCTCCAGGG TTCAAGCGAT TCTCCTGCCT 720
CAGCCTACCA AGTAGCTGGG ACTACAGGCA TGCACCACCA CGCCCAGTTA ATTTTTGTAT 780
TTTTTGTAGA GACAGGGTTT CACCATGTTG GCCAGGCTGC TTTCGAACTC GCCTTGGCCT 840
CCCAAAGTGC TGGGATTACA CACATGAGCC ACCACACCTG GCCTCATCCT ATATTTTTCA 900
ATTATCCCAG TTAACAAACT GGTTAATAAT AAACTAGTTA ATAAGCTAGG TCTGAGTTGG 960
GAGTCTGTCA CTTGCAACCT 980
|
