| Tag | Content |
|---|
EnhancerAtlas ID | HS147-25127 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr2:242471550-242473380 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr2:242471796-242471811 | TGGCCTTTGGACCCG | - | 6.48 | | IRF1 | MA0050.2 | chr2:242473117-242473138 | TTTTTCTTTCTTTTTTTTTTT | + | 6.59 | | ZNF263 | MA0528.1 | chr2:242472072-242472093 | TGGGGAGGGGCTGGAGGAGGG | + | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCATGCCCGG CCCTGTATGT TAATTTTTAA ATGAAAGCTT TTAAATTAAT AATTCCTAAA 60
TGTCATCCCA TATGGAGTCA GTGTCCAGAT TTCCTATCTG TACATAGGAT TTCCCAAGAG 120
CAACTGCATA CCATTGGTTC ACACTTCCAT CCCTCCACAC CTGTTTCCTT GTCTCTTAAC 180
TCTCTTTTTG CCCCTGCAAC GGAGCAGCGG AGGATATCGA GCCTCCAGTC TGTGGAGGCC 240
ACAAACTGGC CTTTGGACCC GGTGCCACCT CCCTGTTCCT CAGCGCCCTT CTCCTGCGCT 300
TGGCAGTAGG TGGCAAGGCT CGTGGGCTTC TTGGCTTCTG TGGGAAGCCC ACCTCCTCTC 360
CCGCAAGCCC AGGTGGTCTT TATCAGACTG CACACTCCCT CAAGTTGGGG TACAGTGGTG 420
TGATGGTGGC ACATCTTCCT GGAAAGTCCC ATACCCCAGG GTGTCTAAGG ACACCCCACC 480
AGGCCCCCAG CCCCGTCTCC TGCAGAAGCT GCAGCTTGGC CTTGGGGAGG GGCTGGAGGA 540
GGGCAAAGCC CCCAGGATGG GTGAGCACCA CCCTCCAACC AGGGGCCACG GAAACGGAGG 600
GAAGAGGAGA TGTGGAGACA ACAAGCAGGG CTGCCTCGCC CGGGGGAGCT GAGGGCCCAG 660
AGCCAGCTGA CCCACCACGC CAAAGCAAGT TCAGCCTCAG TCCCACCGGA GTGCCACGAC 720
TGGGCAAGCC ACCCCTCCAG TACAAACCCC CAAGTCAGAG GGGCACGGCC GCAGGGTGGC 780
AGCAGCTCTG TCACTGCCCT GGGCTGCACA TTTGGCTGTA GGCCTCACGG ATGAGGACCT 840
TGCCCTTTTG CAGACCTCCA GGTGTGACTC CAGCCAGGGC CCCGTGACGG AGCCTCCAAT 900
GGGTCCCACC GGTCCGTCCG CTCAGCAGCT GCTTCTGGAA GGCCATCATC AGCTCCGCCG 960
GTCCGTCCGT TCGGCAGCTG CTTCTGGAAG GCCACCATCA GCTCCCCAGC CCCTTCACTC 1020
ACTGTCCCTT GAGGGGTTCC AGGAGGCCAT GGCTGAGAGG TGCTGCAGCC AGGAGTGCAG 1080
ACCCCATCGC AGGGAGGACA GATCACTCCC CCACGACACA AGGAAGGCCA CCCCGAGGTG 1140
TGGGGGCAGG CCTGGGGGTC TCACTTCTGG GACTACGACC ATGCTCTTCC TCCAGGTCGC 1200
CCACCTTCCT CCTTAGCACA GGGCCCCAGG TCACAGAATG ACTCAGGCCT GGGAGCTGGG 1260
TGAGGGCGAG GACTTCCCCA GGGCTGCTCC AGACCTGGGT TTTCTCAGCC CACTGCCCTC 1320
ACCAATTGTT AACCTTAGTG GCTGCCCTTT GTGTGGTCCA GCGGATCCCA CAACCACCGG 1380
AAGGCACCAG GGATCTCTGC AGGCCCCCCC CCAGCCCCTG CCACCTCTCC CTCTTGCTGC 1440
CAGTCAGGGA GTAGCTACTC AATGCACCTG CTTCATCAAG GTATCCATGC CAGCTGCAGG 1500
GTGCCCCTGT GCACCTTCTG TCCTTAAGAG CTGGCCCAGG GTGGCATCCC CCCACCAGAG 1560
TAAGTCTTTT TTCTTTCTTT TTTTTTTTTT TTAGACGGAG TCTTGCACTG TCGCCCAGGC 1620
TGGAGTCAGC TGGAGTCAGC TGGTGTGGTC TCAGCTCACT GCAAGCTCCG ACTCCTGGGT 1680
TCAAGCGATT CTCCTGCCTC AGCCTGCCAA GCAGCTGGGA CTACAGGCAC CCGCCACCAC 1740
ACCCGGCTAA TTTTTTGTAT TTTCAGTACA GACGGGGTTT CCCCGTGTTA GCCAGGATGG 1800
TCTCGATCTC CTGACCTCGT GATCCGCCCG 1830
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