| Tag | Content |
|---|
EnhancerAtlas ID | HS059-43477 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr7:100015310-100016730 |
Target genes | | Number: 36 | Name | Ensembl ID |
|
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 | AGCCTGGGCA ACAGAGTGAG ACTCCATCTA AAAAAAAAAA AAATTATATG TACTGTATTT 60
TATATCATTT GTTGCTCAAA CGCCTAGGAA TAGAAGTATA CCTAAGAATG GCTGAAATGT 120
CAGACTGTTC TCTTCAGCCT CATGAACTTA TGGAAAAGCC TTCATAGAGG TTTTTGGTTT 180
TTTGGTTTTT GGTTTTTGTT TTTTGGTTTT TTTTTGAGAC AGAGTCTTGC TCTGTCGCCC 240
AGGCTGGAGT GAGGTGGCGA AATCTCGGCT CACTGCAACT TCCGCCTCCC AGGTTCAAGC 300
GATTCTCGTG CCTCAGCCTC CTGAGTAGCT GGGACTAGAG GTGCACGCCA CCACGCCTGG 360
CTAATTTTTA TATTTTTAGT AGAGACGGGG TTTCACCATG TTGGGCAGGC TGGTCTTGAA 420
CTCCTGACCT CAAGTGATCC ACCCGCCTTG GCCTCCCAAA GTGCTGGGAT TACAGGCATG 480
AGCCACTGCA CCTGGCCTCC CTCACTGCGT TCTTTATTCC AAAAACTAAA TCTCTAACCA 540
CATGCAAAAT CGGTATTAGA AACTGAAATT TGCAAGGGTA TGTACCCTAA GTTTTTCAAA 600
TCTAGGGAAA ACAATTTTAT CTTATTTGAA GTTGTTTGTA AATACATGGA AACGAATTTT 660
AACTGCATTT TAAAAATTTA GGGCCAGGCA CTGTAGCTCA CGTCTACAAT CCCAACACTT 720
TGGGAGGCTG AAATGGGAGA ATCGTTTGCA GCCATGAGTT CAAGACCAGC CTGGGCAACA 780
TAGCAAGACC TCATCTCTAC AAAAAGTAAA AATTAAAACA ACAGGCTGGG TGCAGTGGCT 840
TACACATGTA ATCCCAGCAC TGAGAGGCTG AGGTGGGCAG ATCACTTGAG GTCAAGAGTT 900
CGAGACCAGC CTGGCCAGCC TGGTGAAACC TTGCCTCTAC TAAAAATACA AAAATTAGCC 960
AGGCGTGGTG GTGGGCGCCT GTAATCCCAG CTACTCAGGA GGCTGAGGCA GGGGAATCAC 1020
TTGAACCTGG GAGGCAGATG CTGAAGTGAG CTGAGATCAT ATCACTGCCC TCCAGCCTGG 1080
GTGACAGAAC AAGATTCCAT CTCAAAAAAA AAAAAATAAT AAATAAGTAA ATAAATAACA 1140
ACAAAAATCC CATAATGGCT TGAAAATTTA GTTAAGACTA TATATAAATT CTGAAGTCAA 1200
TGTAATCCAC TTTTTCTAAA AATATGTACC CTTTATCTAA GGTGGTTTAG CTATAGTCCT 1260
GTTGACAGAT GATGAAGTAT TTTTAAAATA TGTTGAAGTC TCATCTAATA TTACCTTATT 1320
TAGAAGATGG GAGAGAAAGA GAGAAGCTGT CAGACTTAAC TCTCCCTCTC AGGTAACAGT 1380
CACTGCTTAA CTGAAACCCT TTTTCTCTTA CTACATGCCA 1420
|
