| Tag | Content |
|---|
EnhancerAtlas ID | HS076-51686 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr7:100015280-100016730 |
Target genes | | Number: 40 | 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 | CAGTGAGCCA AGATCATGCC ACTGCACTCT AGCCTGGGCA ACAGAGTGAG ACTCCATCTA 60
AAAAAAAAAA AAATTATATG TACTGTATTT TATATCATTT GTTGCTCAAA CGCCTAGGAA 120
TAGAAGTATA CCTAAGAATG GCTGAAATGT CAGACTGTTC TCTTCAGCCT CATGAACTTA 180
TGGAAAAGCC TTCATAGAGG TTTTTGGTTT TTTGGTTTTT GGTTTTTGTT TTTTGGTTTT 240
TTTTTGAGAC AGAGTCTTGC TCTGTCGCCC AGGCTGGAGT GAGGTGGCGA AATCTCGGCT 300
CACTGCAACT TCCGCCTCCC AGGTTCAAGC GATTCTCGTG CCTCAGCCTC CTGAGTAGCT 360
GGGACTAGAG GTGCACGCCA CCACGCCTGG CTAATTTTTA TATTTTTAGT AGAGACGGGG 420
TTTCACCATG TTGGGCAGGC TGGTCTTGAA CTCCTGACCT CAAGTGATCC ACCCGCCTTG 480
GCCTCCCAAA GTGCTGGGAT TACAGGCATG AGCCACTGCA CCTGGCCTCC CTCACTGCGT 540
TCTTTATTCC AAAAACTAAA TCTCTAACCA CATGCAAAAT CGGTATTAGA AACTGAAATT 600
TGCAAGGGTA TGTACCCTAA GTTTTTCAAA TCTAGGGAAA ACAATTTTAT CTTATTTGAA 660
GTTGTTTGTA AATACATGGA AACGAATTTT AACTGCATTT TAAAAATTTA GGGCCAGGCA 720
CTGTAGCTCA CGTCTACAAT CCCAACACTT TGGGAGGCTG AAATGGGAGA ATCGTTTGCA 780
GCCATGAGTT CAAGACCAGC CTGGGCAACA TAGCAAGACC TCATCTCTAC AAAAAGTAAA 840
AATTAAAACA ACAGGCTGGG TGCAGTGGCT TACACATGTA ATCCCAGCAC TGAGAGGCTG 900
AGGTGGGCAG ATCACTTGAG GTCAAGAGTT CGAGACCAGC CTGGCCAGCC TGGTGAAACC 960
TTGCCTCTAC TAAAAATACA AAAATTAGCC AGGCGTGGTG GTGGGCGCCT GTAATCCCAG 1020
CTACTCAGGA GGCTGAGGCA GGGGAATCAC TTGAACCTGG GAGGCAGATG CTGAAGTGAG 1080
CTGAGATCAT ATCACTGCCC TCCAGCCTGG GTGACAGAAC AAGATTCCAT CTCAAAAAAA 1140
AAAAAATAAT AAATAAGTAA ATAAATAACA ACAAAAATCC CATAATGGCT TGAAAATTTA 1200
GTTAAGACTA TATATAAATT CTGAAGTCAA TGTAATCCAC TTTTTCTAAA AATATGTACC 1260
CTTTATCTAA GGTGGTTTAG CTATAGTCCT GTTGACAGAT GATGAAGTAT TTTTAAAATA 1320
TGTTGAAGTC TCATCTAATA TTACCTTATT TAGAAGATGG GAGAGAAAGA GAGAAGCTGT 1380
CAGACTTAAC TCTCCCTCTC AGGTAACAGT CACTGCTTAA CTGAAACCCT TTTTCTCTTA 1440
CTACATGCCA 1450
|
