| Tag | Content |
|---|
EnhancerAtlas ID | HS147-00955 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:31288650-31290300 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX1 | MA0509.2 | chr1:31289183-31289199 | CGTCGCCATGGTAACC | + | 7.02 | | RFX1 | MA0509.2 | chr1:31289183-31289199 | CGTCGCCATGGTAACC | - | 7.02 | | RFX2 | MA0600.2 | chr1:31289183-31289199 | CGTCGCCATGGTAACC | + | 7.07 | | RFX2 | MA0600.2 | chr1:31289183-31289199 | CGTCGCCATGGTAACC | - | 7.25 | | RFX5 | MA0510.2 | chr1:31289183-31289199 | CGTCGCCATGGTAACC | - | 6.99 | | RFX5 | MA0510.2 | chr1:31289183-31289199 | CGTCGCCATGGTAACC | + | 7.03 |
|
| | 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 |
| GH01I030815 | chr1 | 31288762 | 31291050 |
|
Enhancer Sequence | CGTGGCTACA AAGTGTCAAG TCAGGGTCAC CTCCCAGGCC AGTCCGAAAG CAAGCCTCAG 60
GGCCTGGAGA TCCTCTGAAA CAGGGCGTAC CTGGGGCATG GTGTGCACAT GGTGGAGTGA 120
ACAGATCAGA ACTCAGAGAA TAGCTGGGCC AGGGAGAAAC AGAGTGAAGA GAATGCAGCA 180
CCAGGACCAA AACAGACCAG GACACCGAAA CAGAATGGGC AGGACATTGA GCAGCAGCCA 240
TGTAAAGACT TGCTCTCAAT TTGCCTAAAT ATGAGAGAAT TGTGGGTCTC TGTGTCCTGG 300
ATTGATGCGG GATCCTGAAG CCACTCAATG GCCTCTGCAT GCCAGAATCC CATCCTGCTG 360
CCCTTCAGGA CTCTCCCTGC CCCTGCCAAG GTGGAGGGGT GGGTGCTCAG ACAGCAGAGT 420
GACCACCCGG GCACCTCCTC GGGATGCTGC GGCCAGGGGA CGCAATGCAT CAGCAGGTGG 480
GCTGGGGTCC AGGCCCATCC TGGAAAAGGC CGGCTGCAAG TTTCCATGGA GCCCGTCGCC 540
ATGGTAACCA AGCCTCCGCG GCAGGACTCC AGCAGAGCCA GGAAAGACAA GCTCCTTTCT 600
TGTCCATATC CCAGGAGCCT GCAGGAGGGG GGCGGAGGGA AGTGGGGACA ATCAGGCTTT 660
CTGAACCAGG ATGGGGGTGG GGGCAGAGAG AAGCGGAGGC TGTCTTCCTG CTCAATGGGT 720
CAGCTATAAA CTGCCAGAAC GTGGCACCCT ATTTCACGCC TCTGTGATTT GCTCGTGCTC 780
TTCTCTCCCC TGGAATGCCC TCCCCCACCC TTGTCTCCCT GGAGCGCTCC CAGCTGTCAT 840
CTGTGCCTCA CTGACCCTTC TGGGCAGAGT CAGTCCTTCC CTCCTCTGGT CACCTTTCAC 900
ATATCCCCAG GGTGTCTGGC TCACCCACAG GCTTGGGGCG TGTGGTGGTG GTAAGAGCAC 960
AAGCTCTGGA ATCAGGGAGA TCTGAGTCAC ATCCCAGCTC TGCCATGAAC ATGTCAGTGA 1020
CTCTAAGTAA GCCACTTATC CTCTCTAAGC CTCTACTTCC TGCTCAATGG GTCAGGACTC 1080
ACTGAGCTCA ATGCTCAATG GGTCATTCCT CATCTGCCAT CTTCCAGCTG TGTGATCTTG 1140
AGTAAGTTTC CAAACCTCTC TGAGGCTCAG TTTCTTCTTC TGAAAAGTGA GGTGATGTCC 1200
GTGAGGTGCT TGATGCACAC CTTGCATGTA ATAAATGTCA CTGATTGTTC TCATGTGTAG 1260
TGAGCGCTTC CTCTCTGCCC CCTGGGGAGT GGACTTCCAG TCCCTGCCAG GCCTGGTTTA 1320
TCCCCGAGCT TACACTCAGG CTCCCAACCC CTATACTAAG CCCTCCCCTC TGCCAGGAGT 1380
CCTGGCCTGG CATTGTCCAT GCCTTTCAGA GTAGGGTCTT TGAGAGGCAC GAACTTTCCC 1440
TGCCCAGAGC AGGGACTGGC ACACCACACA GAGCTGACAT TTCCAGTCTG ACATCTGAGA 1500
GCAAGCATTG TGAAGGAGAA TAGATTCCAC GAGAGCTTCC TGACAGCAGG GTCAGCCTTT 1560
GGGCTGCGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTA TGGCTGTCAG CAAACGCTCT 1620
AACATGCACA CACAAACACA TATGTGTACT 1650
|
