| Tag | Content |
|---|
EnhancerAtlas ID | HS062-00659 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr1:67965080-67966930 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:67966302-67966321 | GAGCGCCCTCTACAGGCCA | - | 7 | | Foxq1 | MA0040.1 | chr1:67966072-67966083 | TATAAACAATA | - | 6.32 | | HES2 | MA0616.2 | chr1:67965724-67965734 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr1:67965724-67965734 | GGCACGTGCC | - | 6.02 | | IRF1 | MA0050.2 | chr1:67965574-67965595 | TCTTTCTTTCTTTTTTTCTTT | + | 6.34 |
|
| | 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 |
| GH01I067500 | chr1 | 67966080 | 67966683 |
|
Enhancer Sequence | ATTTTTGTAT TTTTAGTAGA GACAGGGTTT CACCATGTTG GCCAGGCTGG TCTTGAACTC 60
CTGATCTCCA GTGATCCGCC TGCCTCAGCC TCCCAAAGTG CTGGGATTAC AGGGGTAAGC 120
CACCATCCCT GGCTGAAAGG TTTTTTGTTG TTGCTGAGAG AGTCTCACTC TGACTCCCAG 180
GCTGAAGTGC AGTGGTATGA TCATGGCTCA CTGCAGCCTC AATTTCCCAG GCTTAAGGGA 240
TCCTCCTGCC AAGGTCTACC AAAGTGCTGG GATTAGAGGT GTGAGGCATC ACGCCTAGCC 300
TAGATAGACG TTCTCGTACA CAGCAGTTCT TCAAGTATGT CCCGGAGTGG TGTCCTTGAG 360
ATACTTTCAG GGAATTCTCA AGATTTAACT ATTTTTTACT CTTACTCTCT CAGAGTACAT 420
AGTGGAGTTT TTCAGAGGTT ACCTGACTTG TGAAATTGAT AGGGACTCAC TGCAAAAGGA 480
AAATTCAGGT CTTTTCTTTC TTTCTTTTTT TCTTTTTTTT GAGATGGAGT CTCACTCTGT 540
CGCCCAGGCT GGAGTGCTGT GGTGCCATCT CGGCTCACTG CAAGCTCCGC CTCCCGGGTT 600
CAAGCGATTC TCCTGCCTCA GCCTTCTGAG TAGCTGGGAT TACAGGCACG TGCCGCCACG 660
CCAATTTTTG TATTTTTAGT AAAGACGGGG TTTCACCATA TTGGTCAGGC TGATCTCGAA 720
CTCCTGACCT CGTGATCCAC CTGCCTTGGC CTCCGAAAGT GCTCGGATTA CAGGCGTGAG 780
CCACCGCCCC TGGCTTAGGT CTTTTCTATT AAGACACACA TTAAAGGGAT TTGTAAAAAA 840
TGCATTTTTG GGGGGTTTTG GAAATTTTTT TTTTTGCAAA AATACTATTT ATGCTAATAT 900
TTAATTATTT ATTGTTGCTA TTTTTAAATG GGTATATGTT TTAAACATTT CTCATTATTA 960
ATTTCTAATA TGGTAAATAT CTATATAACC CATATAAACA ATAGCTCTTT GGGATCCTCA 1020
ATAATAAGAG TATAAAAGAG TCACGAGACC AAAAAGTGTG ATACCTACTG TTGGACATAA 1080
GTGCATTCAC CTGCTGGATG GCGTAAGGGC TGAAGGCTTT TCCCCATGCC CCGCGAAAAG 1140
CAATCAGCCA GCCATCCTCA CTCGCCCTGG AGGCCACGTA GCCGTGGCGC GTCCCAGGCT 1200
CGAGCTCCCT GGCCTGTGCT CAGAGCGCCC TCTACAGGCC AAGAGTGGAT CCCACACCAT 1260
TCTTGCTTGA ATCTACTGCT CTGGCTGAAC TTTTAGCCCA GGGGGAGTTT GAAGTTCGCG 1320
GCTGCCTGGC GCCTTGGAAC AGGCGATAGG CAGCATCTAC AAGCTTCATT TTCACAGGTG 1380
GGGGCTGCGG AATGGGGAAG CATCGTGCTG CAGTGACGAA ACCACTAAAC TGACCTGAAT 1440
CTTGGTCCTG GCTCAGTCCA CAACTAGGGT GGGGTCCCCT GACCTCCCTG GGTTTCAATT 1500
ACTCAGGAGG AAACAACCCA CAATGAACTA GCCACAAAGA TCCTTCTGGC TCTAGCAGCC 1560
TATGATTCTA GGTGCTAATT GTCCCCACGT CTTACCTAGA GAAGGGGCTT AGTTCCCTGG 1620
CTACTGCCTT TCAGAGCTAT CTTTGCTTTC GAGGTTTGGC TCAATAAGAA TCTGACTTCA 1680
GGATGGGTCT TTGCAGTTAT GGAGCTCATG GATTTTGTTC TTTAGCAAGT GCATTTTAAA 1740
ACACCTTCTC AACACTTCAT CGATTTATAA AGCAAATCAT AAGAAGCTGG CATTGGCTCA 1800
AGCTCTGGGC CAATATATGC ATTTTCTTAT TTGAGCCACA CCACAACCCT 1850
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