| Tag | Content |
|---|
EnhancerAtlas ID | HS098-14362 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:106214040-106215050 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr12:106214778-106214793 | TGCTATTTTTGTAAA | - | 6.13 | | NR3C1 | MA0113.3 | chr12:106214402-106214419 | AAGGACATTGTGTTCTG | - | 6.06 | | NR3C1 | MA0113.3 | chr12:106214402-106214419 | AAGGACATTGTGTTCTG | + | 6.08 | | NR3C2 | MA0727.1 | chr12:106214402-106214419 | AAGGACATTGTGTTCTG | - | 6.3 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I105820 | chr12 | 106213956 | 106215826 |
|
Enhancer Sequence | CCCAGGATGG CAGTGTTTAT GTGACTTGAG TTCTTGGCTA AAGCTGTGTT AGCAAGTGTA 60
CATCCTGTGT ACAGAGAGGA AGGTGTGTGT GGACTTTAAA CCATTCCCCA GGTATGGTTC 120
CATGGCTTTT CCAGCCTAGC TCATTCTTAT TTCTTTCTCC CTCTTGTCCT CACTCTTGGC 180
AGTTTCTTCT CTGGTGGCCT GCTAAGAGTT ACAAGTTCAT TAGCAGCATC AACTCAAAGA 240
GAGATCAAAT CTGTGGAGAC CCTTGCTCTT TGAGCACCTT GCCTGCAGCC CTTAAGCTGA 300
CATGCACTGC AGATGGCCCG AGCTGGGTGG AGGGCATACT GTACAGAAGG AGGATACAAG 360
CCAAGGACAT TGTGTTCTGT CTCTAATCAA ACCCCATTAA GTGGCAAATT CCTCTATTCA 420
AAAGTTTTCA TAGGATGGTA CTTTCAAAAG AACTCCAGCT GGTTAAACTT AGGGCCTGAA 480
ATAAATCCAG TCTAATAATT CGATCTGGCT CTGGGCCTGC CACATCCTTT CGATGGAAGA 540
ACTCAATGCA TTTTCATTCA TTAGGGGCCT CCTCTCAATG TTGACTCAGA GGTAGGCCAC 600
AAAATTCTTT GCTTGTGTTG GCCTTGAGAG GACTGGGTCA CTTAATGAAA CAAGTAGCTT 660
CCAGTGTGTC CCTGGCTGTT AACGCAACCT CCTCATGCTT GCTGGTGCAT TTTCAGAGCT 720
TGATTGTGCA AGAAATATTG CTATTTTTGT AAATGGTTTG GCCTCTGCAG TCATTAACCT 780
GGCATTTCTC CCCCGTGGAG GGGAAACATC ATGTGTCCAT TGATTCCTTC TTTTGTTTGT 840
AAGCTGTTTG CAAAAGAAAG CCCTCAAAAA AAGTCCTTTC TCCCTGCATC TTGTCATTAG 900
TACCAACATG GAATTTCTTC TAGTTACTTT TATCAACTTA CTAAGTAATA TTTTTCAGAA 960
TATTTAGCAG TATTTTCCTG GTTCTTTCAA GTCTCTTGGC TGCTGGAGTA 1010
|
