| Tag | Content |
|---|
EnhancerAtlas ID | HS175-05490 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr12:6997200-6998380 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr12:6997249-6997261 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr12:6997253-6997265 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr12:6997257-6997269 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr12:6997955-6997967 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr12:6998250-6998262 | GTTTGTTTGTTT | + | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr12:6998165-6998180 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 6998304 | 6998380 | | chr12 | 6997600 | 6997800 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I006885 | chr12 | 6994734 | 6997295 |
|
Enhancer Sequence | AACACATTCC ACATGCATTG ACTGTCAGGC TTCGTTGCTT CCATTACCTG TTTGTTTGTT 60
TGTTTGTTTA TTTATTTATT TATTGAGACA GGGTCTTGCT GTATCACCCA GGCTGGAGTG 120
CAGTAGCATG AGCATGGCTC ACTGCAGCCT CAACTTTCCC AGGCACAGGT GATCCTCCTG 180
CCTGCACCTC CTGAGTAGCT GGGACTACAG GTGCACACCA CCACGTTCAG CTAATTTTCT 240
GCAGAGATGA GGTCTTGCCA TGTTGCCCAG GCTGGTCTTG AACTCTTGGA CTCAAGAGAT 300
CTGCAGCCTC CCAAAGTGCT GGGATTACAG GCGTGAGACA CCACACCTGG CCTCCCATTG 360
CCTGTTTAAA TAGAAATGAT GCAACTAGCA ATATGGAAGG ACTTCCAGAT CTTTACCACA 420
TTAAGATTAG GGTCAGCATC CATGGCTCTG GGAGTCAAGG GAGAATCTCA GCCTAATGTA 480
TGTGGCTTTG AAACAGCAAA TAATGCTTAG ATCAGCAGAG TGAAGGATGG AGTCATGTTG 540
GGACAGGAAA CCTTCATTCA GCGCCTTTAT GAGCACATTC ATAAAGTGTG TGGTACATCA 600
GTGTGGTATT GTTGTGTCCT GCAGCACAAA GCCAGATTTT TTCTCTTTGA GGTCCTGCTT 660
GACTTCTAGA ATGAAGATAT TTGAAACTGA ATCAGGGAAA GTACTACAGT CACCCAGGAC 720
TTTGCATTTG ATTGCTAGAG CACAGGCAGG TTTTTGTTTG TTTGTTTTTT TTGACAGTCT 780
CGCTCTGCAG CCGCGGCTGG AGTAAAGTGG CTCAATCTCT GCTCACTGCA AACTCTCCCT 840
CCCAGGTTCA AGCAATTCTG TCTCAGCCTC CCGAGTAGCT GGGATTACAG GGGTGTGCCA 900
CCATGCCTGG CTAATTTTTG TATTTTTAAT AGAGATGGGG TTTCACTGTG TTGGCCAGGC 960
TGTCTTGAAC TCCTGACCTC AAGTGCTCTG CCCATCTCAG CCTCCCAAAG GCTGGGATTA 1020
CAGGTGTGAG CCACCGTACC GCCGTTTTTT GTTTGTTTGT TTTGTTTTTT TTTTTAAAGG 1080
GCACCAGGAT TTGTAGAATG ACAGCCCTGT AGAACTACAC TGCCCCTGCA CTTGGGGGCA 1140
AGGGCAAAGG GTGGAGGGGA ATAGCATTCA GAAGATCATG 1180
|
