| Tag | Content |
|---|
EnhancerAtlas ID | HS147-25740 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr20:34023330-34025070 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| INSM1 | MA0155.1 | chr20:34024107-34024119 | CGCCCCCTGGCA | - | 6.74 | | SP2 | MA0516.2 | chr20:34024273-34024290 | GAGGGGGAGGGACTTGC | - | 6.18 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr20 | 34024717 | 34024788 | | chr20 | 34023940 | 34024013 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH20I035435 | chr20 | 34023199 | 34023580 |
|
Enhancer Sequence | CTCAAATTCT CAGCTGCTTC CACCATCCCT TAAAGGAGAC CTTGGTGCTC TTGTTATGCA 60
GATGAGGCAC AGAGATGGGG AGTGACTTGA CTAAGGTCAC ACAGCAAGTT AATGACAAAG 120
CTGGTCCACA CTGACCTACA GCCCAATTTT CCTGGCTTTC CAGTGCAAGG ATTTTGTTGC 180
CTATGTGTCT TACTCTCCTG AGCATGTGTG TGTGTTACAG TTGTATGCAT GTGTGTGATT 240
GGGTTCATAT GTGAATATGA AAGAGTGTAT ACGTTAATGA CGCATTATAT GTATAAATGA 300
TTGGGCTTGT GTGACTATTT GAAGAGCACA TATATGTCTG TATATGCATG ATTGATCTTG 360
TGTGTGTATG TAAGAAGGTG TGTGTGCACA TGCATATGTG TGTGATTCGG CATGTGTGTA 420
CGTGTGTGAT TCAGCACGTG TGTGTGTGAG TCAGCATGCA TGTACATGTG TGATTCAGCA 480
TGTGTGTATA AACATAAGGC TATGTATGTG TATGTGAGAA GCTCAGTAGT ATCTCCGAAT 540
CAGCATGCCC TCCTTCCTAA ATTGCAATTT GCCATTGGGG AGCTTTCATA TATTGCTCTA 600
GAAGGTGACT AATTAGGCCT TTAAACTCCC CGTCTCCCCC TCTCCAAGCT CCCTTAGTGC 660
TGGGGGGCAC ACGGACTTAT TTTATGAGCC CCCAAGGGGT CACAGCTTTC CCTGGCTGGG 720
CAGGCAGCCA GACCACCTCC CCCACCTCAG CCAGACCTGC TGCCTCTGTG CCTCCCCCGC 780
CCCCTGGCAG CCCCCTCCAG GCCAGCTCTA ATGAGGAGCC TCTCCCACCC TCTGACCCCT 840
CCCCCACCCT GCCAGCCTAG GACCAGAGCA AATGAGCTGC AGGCAACTTG AGCGACCAAC 900
AGCCCACCTC CCTCTTCACA CTAGGAAGAA ACTGAGGCCC TGAGAGGGGG AGGGACTTGC 960
TTAGATCACA CAGCAAGTGG AGAGGAAAAG CTGCAACAGT AACATTAGGT GGGCCGAGAG 1020
AGACAGAGGG GAGCAGGTAG TCTCTGGAGT TAATGAGGAG AATGAGGCAT GTTCAGGACA 1080
GCATCTAAAG TTTTCATGTT GGAAGGGCTC TCAGAAACCA CCCTGTCCAA CCCCATATAG 1140
GTGTACAGAT GGGAAAACGG AGACCCCAAG TGAGAAGGAG CTTTCCCAAG GTCATACTGC 1200
GAGTTAGGCC CTGGGTCTGC TCCCTCCCCA TGTATCTGAA CATCATTCCA TGACTCCAAG 1260
ATGCCCCATT TACTGTGTGC ACCTCTCTTG CCTCCTCTAT CCCCTTGCCT GAGGGCAAAG 1320
TTGCAGAAGC ATGGGGACCT CAAGATTCAT TTCTTTCTCT GCCGTCTGAG ACCGCCTACA 1380
AACCTGTGGA GCTTGGAAAG TTCGGCCAGC CCAGCAGGTA CAGATGCACA ACTGAGCAAT 1440
CAAGTCTCGG AATCTGGTCT CCAACTCTGC CACGAACTGG CAGGTCTTGT CTCTTCTCTA 1500
GGCTTTAGTG CCCACTCTGC ACCTTGCAGG CGTTGGACCT GGTGCTTCCT AGGTGCCCTC 1560
CAGCCCTGAT GTGTGGGCAG CCTAGGATCT GCTATGTGTG AGATATGTGT CAGTGTCCCC 1620
AGACACCCAC CCCGGGCCAG ATGCACACAG TGTCTCCCAC CAGGGCAGTG CCAGGGCTTT 1680
GAAAGCCCCT CCATTCATGC AGATGCCCCT CCCTCTGAGC CGTGCCCCTG CCACCCCGCC 1740
|
