| Tag | Content |
|---|
EnhancerAtlas ID | HS147-39109 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr7:106410560-106411580 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr7:106410735-106410747 | TCTAAAAATAGT | + | 6.02 | | RUNX1 | MA0002.2 | chr7:106411179-106411190 | AAACCACAGAA | - | 6.32 | | SOX10 | MA0442.2 | chr7:106411287-106411298 | AAAACAAAGAA | + | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I106765 | chr7 | 106406261 | 106411934 |
|
Enhancer Sequence | AATAGAAAAA GAGATAGTAA GAGAAATCTT CACTTACTCT GAATGACTTC AAAACTTCTG 60
TTAATACAAA TTCTATCCCA AAGTATCAAA AGAGTTTGCA GATGAGATCA GAGAACTGCT 120
CCTGAGAATC AAGGAGAATG GAAAAGGTGA CTAATGGCTG GAAAATGTTT CTACTTCTAA 180
AAATAGTGAA AGAATGAGAT CTGTATGTAA ACTGATGAGC CTCATGCAGA CGCCAAACAA 240
AATTCTAAAA TGGATGATTT GTAGGCAAGA TACAGTAAAC AAATACTAAC CAGTGTGAAT 300
TCACTAAGAA CAAGTCATGC CAACCAGTCT CACTTCTTTT CTTAGATTTG GTTGCCTGTG 360
TGTCAGGAGG AAGGCATGCA CATGGTATGC CTTGGTTTTA GCATAGCATT TGCCAAATAT 420
CGTGATGCAC ACCTTTTGTT GTTAAGATGG AGGAATGAGG GCCCAGGTAA CAGCAAGATG 480
ACTGGTGGTT TGCTGCATAG TTAGGCATTC AATGTCACCC AAAGAATATT GGCCAAAGAC 540
TTGACTTCCA CCTTAAAAGG CAAACTCCAA GAATTTATGA TTTGCTCATT TCTGTTCAAT 600
ATTTTTGTCA AAAACATGAA AACCACAGAA TGCATGTTTA TGAATATTTC AATTTAAAAA 660
TTAGGGAGAC AGAGCTAATA CACGAGGAGA CAATTCAAAA CTATTTCTTC ATATAGAAAT 720
CAGGCCCAAA ACAAAGAAAA TACAAATTAT TTGGGATAAA CATAAGGCCA AAAAAAAAGA 780
GAGAGACAGA GAGACTAATA ATACCAATAG CTTACATTTA TTGAACAGTT ACTATGCATT 840
ATATAGTCAC ATGCCATATA TACATATGTT TTGAGACTGG ATCTTGCTCT GTTGCCCAGG 900
CTGGAGTGCA ATGGCACAAT CTTAGCTCAC TGCAACCTCC CCGTCCCAGG CTCAAGCAGT 960
CCTCCCACCT CAGCCTCCCG ATAGCTAAGA CTACAGGCAC GTCACCATGT TTGGCTAATT 1020
|
