| Tag | Content |
|---|
EnhancerAtlas ID | HS024-00458 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr1:31288000-31290280 |
Target genes | |
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 | CCCATTCCCA CCTCAAGGCC TTTGTCCCTG CCTGGGTCTC TCTTCCCTCT CGTAGCTGGC 60
TCTTCCCATT ATGCGGCTCT CTCATCCTTG TGTGTCATTT GCTCAGAGAG ATTGTCCCTG 120
AGCACTCATC CTCTTTAAGA ACATCGTCCC CACCCATCAC CCTCTATCTC AACACTCTAC 180
TTACAATGCG TTGTATTATT ATTTGCTCTT TTTACCCATC TCCCCCAGTA GGTGCTCTGT 240
AAGGGCAGAA ACCAGGTCCT CACACCATCG GTGCATGATA AAAATTAACT GACCAAATAA 300
CACGGTGGTA CCCTCTTCAA GGCAACTTCG GAGTCAGACA TGCCTACGTT CTCCTTCCTG 360
CTCTGCCACA TGTGTGACCC TGGACAGGGT CCTCCATCCT CTTGGCCTCA GTGTCTTTGC 420
CAGCAAACTG GGAATAAGAA TCCTGTGTCA TGGGGTTGTC ATAAGGGGGA AATGAGATGA 480
CGTAAGTGCA GTTCTTAGCA TAATAAATGC ATTCAAAGCA AATAAAAAGT GCTCAGTAAA 540
TGCAGATATT ATTAAGCATA TTTGTTGGAT GAACAAGCAA TCCCATAAAG CACGTGTTTA 600
GAGACGTGGA ACCCAAGACT CCGGAAGAGG GAGCGACTTG TTCCAGGTTG CGTGGCTACA 660
AAGTGTCAAG TCAGGGTCAC CTCCCAGGCC AGTCCGAAAG CAAGCCTCAG GGCCTGGAGA 720
TCCTCTGAAA CAGGGCGTAC CTGGGGCATG GTGTGCACAT GGTGGAGTGA ACAGATCAGA 780
ACTCAGAGAA TAGCTGGGCC AGGGAGAAAC AGAGTGAAGA GAATGCAGCA CCAGGACCAA 840
AACAGACCAG GACACCGAAA CAGAATGGGC AGGACATTGA GCAGCAGCCA TGTAAAGACT 900
TGCTCTCAAT TTGCCTAAAT ATGAGAGAAT TGTGGGTCTC TGTGTCCTGG ATTGATGCGG 960
GATCCTGAAG CCACTCAATG GCCTCTGCAT GCCAGAATCC CATCCTGCTG CCCTTCAGGA 1020
CTCTCCCTGC CCCTGCCAAG GTGGAGGGGT GGGTGCTCAG ACAGCAGAGT GACCACCCGG 1080
GCACCTCCTC GGGATGCTGC GGCCAGGGGA CGCAATGCAT CAGCAGGTGG GCTGGGGTCC 1140
AGGCCCATCC TGGAAAAGGC CGGCTGCAAG TTTCCATGGA GCCCGTCGCC ATGGTAACCA 1200
AGCCTCCGCG GCAGGACTCC AGCAGAGCCA GGAAAGACAA GCTCCTTTCT TGTCCATATC 1260
CCAGGAGCCT GCAGGAGGGG GGCGGAGGGA AGTGGGGACA ATCAGGCTTT CTGAACCAGG 1320
ATGGGGGTGG GGGCAGAGAG AAGCGGAGGC TGTCTTCCTG CTCAATGGGT CAGCTATAAA 1380
CTGCCAGAAC GTGGCACCCT ATTTCACGCC TCTGTGATTT GCTCGTGCTC TTCTCTCCCC 1440
TGGAATGCCC TCCCCCACCC TTGTCTCCCT GGAGCGCTCC CAGCTGTCAT CTGTGCCTCA 1500
CTGACCCTTC TGGGCAGAGT CAGTCCTTCC CTCCTCTGGT CACCTTTCAC ATATCCCCAG 1560
GGTGTCTGGC TCACCCACAG GCTTGGGGCG TGTGGTGGTG GTAAGAGCAC AAGCTCTGGA 1620
ATCAGGGAGA TCTGAGTCAC ATCCCAGCTC TGCCATGAAC ATGTCAGTGA CTCTAAGTAA 1680
GCCACTTATC CTCTCTAAGC CTCTACTTCC TGCTCAATGG GTCAGGACTC ACTGAGCTCA 1740
ATGCTCAATG GGTCATTCCT CATCTGCCAT CTTCCAGCTG TGTGATCTTG AGTAAGTTTC 1800
CAAACCTCTC TGAGGCTCAG TTTCTTCTTC TGAAAAGTGA GGTGATGTCC GTGAGGTGCT 1860
TGATGCACAC CTTGCATGTA ATAAATGTCA CTGATTGTTC TCATGTGTAG TGAGCGCTTC 1920
CTCTCTGCCC CCTGGGGAGT GGACTTCCAG TCCCTGCCAG GCCTGGTTTA TCCCCGAGCT 1980
TACACTCAGG CTCCCAACCC CTATACTAAG CCCTCCCCTC TGCCAGGAGT CCTGGCCTGG 2040
CATTGTCCAT GCCTTTCAGA GTAGGGTCTT TGAGAGGCAC GAACTTTCCC TGCCCAGAGC 2100
AGGGACTGGC ACACCACACA GAGCTGACAT TTCCAGTCTG ACATCTGAGA GCAAGCATTG 2160
TGAAGGAGAA TAGATTCCAC GAGAGCTTCC TGACAGCAGG GTCAGCCTTT GGGCTGCGTG 2220
TGTGTGTGTG TGTGTGTGTG TGTGTGTGTA TGGCTGTCAG CAAACGCTCT AACATGCACA 2280
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