| Tag | Content |
|---|
EnhancerAtlas ID | HS105-68745 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr6:36601140-36602550 |
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 | chr6:36602227-36602239 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr6:36602231-36602243 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr6:36602235-36602247 | GTTTGTTTGTTT | + | 6.32 | | PLAG1 | MA0163.1 | chr6:36601164-36601178 | CCCCCCTTGGCCTC | - | 6.06 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 36601713 | 36602187 | | chr6 | 36601686 | 36602297 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I036633 | chr6 | 36601360 | 36602547 |
|
Enhancer Sequence | GAACGTCTGA CCTCAGGCGA TCCACCCCCC TTGGCCTCCC AAAGTGCTAG GATTACAGGC 60
GCAGGCCACC GCGCCCGGCC AAATTTCAAT CTTGACTACA CAGTGGAATC ACCTGGGGAG 120
CTTTAGTGAC ATAATGACCA GTGCTGTCCA GGACGAGAAT CTCTGGGGTG AGGCCCAGGC 180
AGCAGTATTT TTAGAAGCTC TCCAGATGAA TGTAATGAGC ATGTCACTCC ATTGACATGC 240
ACTCAGGACA ATAACCACTG AAGGCTCCCT GTTTGACCAG AATGTTCTAG AGGAGCAGAA 300
TGGGACAGCC TGATTCATTT GGCTATTCCT CAGTCCTGGT GGGAATGAGA GAAGACTTGG 360
AGTCCAGAAA GGAGAGACTC TGAGGCCCTT CTTCTTCTTC TTCTTCTTTT TTTTTTTTTT 420
TGAGACAGAG TCTCGCTCTG TTTCCCAGGC TGGAGTGCAA TGGTGTGATC ATGGCTCACT 480
ACAGCCTTGA CCTCCTGGGG CTCAAGTGAT CCTCCTGTCT CAGCCTCCTG AGTAGCTGGG 540
ACTAAAGGCA CATGCCACTA CGCCTGGCTA GTTTTTTTAT TTTGTAGATA TGGGGGATCT 600
TGCTTTATTT CCCAGTTTGG TCTTGAACTC CTGGGCTCGA GTGGTCCTCC CGCTTCAGCC 660
TCCTAAAGTG ATAGGGTTAC AGGCATGAGC CACTGCACTT GGCCTTAGCC CCTACTTCTT 720
GAGAGGCCTC CGTGAGGGAC CAGGAAGCCT GCAGCCGTGA TGAGGCCCAG AGACCGTGGC 780
CGTTTGTTTT GGCATTTGCC CAGCAGGCAG TTCTGTGTGG AGCTGTGGCT CTTTTGTTTG 840
TGTGGTTTAA CTGTTGGCCC AGTTTTTCCA GTGCTGATTA GATATCCCTG TGAGCAGCAC 900
ATCCATTTCT AGTCCACAGG ATTCCTGAAA AAGGGGCCGA AACCGTTGTT TCTCTTAGCC 960
ATGAGGCAAG TCAGAGGTAC AGGGGGCCTG GCTCCTGCCT CTGTAACACT CCGAACCTCG 1020
AGTTTGAGGA TTCAGTGAGT CTATCAGTCA GGGTCCAGTC AGGATACACA AACCACACCA 1080
GTGTTTTGTT TGTTTGTTTG TTTGTTTGCT TGTTTTTGAG ACAAGATCTT GCTCTGTTGC 1140
CCAGGCTGGA GTGCAGTGGC ACAATCTGGG CTCACTGCAG CCTCAACTTC CTGGGCTCAA 1200
GCCATCCTCC CACCTCTGCC TCCCAAGTAG CTGGGACCAC AGGCATGCGC CTGCGAACAT 1260
GATTACATGC CGGGCACCGT AAGAGGCTAA TTTTTGTTTT TCTTGTAGAG ACGGCGTTTC 1320
ACCATGTTGC CCAGGCTGGT CTCAAACTCC TGGGCTCAAG GGATCGGCCT GCCTTGGCCT 1380
CCCAAAGTGC TGGGATTATA GGCGTAAGCC 1410
|
