| Tag | Content |
|---|
EnhancerAtlas ID | HS065-04671 |
Organism | Homo sapiens |
Tissue/cell | GM18508 |
Coordinate | chr7:100015200-100016570 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr7:100015726-100015741 | TGAACTCCTGACCTC | - | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr7:100016197-100016212 | GAGGTCAAGAGTTCG | + | 6.24 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CACGGTGGCA TGCACCTGTA GTCCCAGCTT CTCGGGAGGC TGAGGCAGGA GAATTTCTTG 60
AACCTGGGAG GCGGAAGTTG CAGTGAGCCA AGATCATGCC ACTGCACTCT AGCCTGGGCA 120
ACAGAGTGAG ACTCCATCTA AAAAAAAAAA AAATTATATG TACTGTATTT TATATCATTT 180
GTTGCTCAAA CGCCTAGGAA TAGAAGTATA CCTAAGAATG GCTGAAATGT CAGACTGTTC 240
TCTTCAGCCT CATGAACTTA TGGAAAAGCC TTCATAGAGG TTTTTGGTTT TTTGGTTTTT 300
GGTTTTTGTT TTTTGGTTTT TTTTTGAGAC AGAGTCTTGC TCTGTCGCCC AGGCTGGAGT 360
GAGGTGGCGA AATCTCGGCT CACTGCAACT TCCGCCTCCC AGGTTCAAGC GATTCTCGTG 420
CCTCAGCCTC CTGAGTAGCT GGGACTAGAG GTGCACGCCA CCACGCCTGG CTAATTTTTA 480
TATTTTTAGT AGAGACGGGG TTTCACCATG TTGGGCAGGC TGGTCTTGAA CTCCTGACCT 540
CAAGTGATCC ACCCGCCTTG GCCTCCCAAA GTGCTGGGAT TACAGGCATG AGCCACTGCA 600
CCTGGCCTCC CTCACTGCGT TCTTTATTCC AAAAACTAAA TCTCTAACCA CATGCAAAAT 660
CGGTATTAGA AACTGAAATT TGCAAGGGTA TGTACCCTAA GTTTTTCAAA TCTAGGGAAA 720
ACAATTTTAT CTTATTTGAA GTTGTTTGTA AATACATGGA AACGAATTTT AACTGCATTT 780
TAAAAATTTA GGGCCAGGCA CTGTAGCTCA CGTCTACAAT CCCAACACTT TGGGAGGCTG 840
AAATGGGAGA ATCGTTTGCA GCCATGAGTT CAAGACCAGC CTGGGCAACA TAGCAAGACC 900
TCATCTCTAC AAAAAGTAAA AATTAAAACA ACAGGCTGGG TGCAGTGGCT TACACATGTA 960
ATCCCAGCAC TGAGAGGCTG AGGTGGGCAG ATCACTTGAG GTCAAGAGTT CGAGACCAGC 1020
CTGGCCAGCC TGGTGAAACC TTGCCTCTAC TAAAAATACA AAAATTAGCC AGGCGTGGTG 1080
GTGGGCGCCT GTAATCCCAG CTACTCAGGA GGCTGAGGCA GGGGAATCAC TTGAACCTGG 1140
GAGGCAGATG CTGAAGTGAG CTGAGATCAT ATCACTGCCC TCCAGCCTGG GTGACAGAAC 1200
AAGATTCCAT CTCAAAAAAA AAAAAATAAT AAATAAGTAA ATAAATAACA ACAAAAATCC 1260
CATAATGGCT TGAAAATTTA GTTAAGACTA TATATAAATT CTGAAGTCAA TGTAATCCAC 1320
TTTTTCTAAA AATATGTACC CTTTATCTAA GGTGGTTTAG CTATAGTCCT 1370
|
