| Tag | Content |
|---|
EnhancerAtlas ID | HS069-00368 |
Organism | Homo sapiens |
Tissue/cell | GM18951 |
Coordinate | chr1:67965610-67967150 |
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 |
|
| | 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 | CTCACTCTGT CGCCCAGGCT GGAGTGCTGT GGTGCCATCT CGGCTCACTG CAAGCTCCGC 60
CTCCCGGGTT CAAGCGATTC TCCTGCCTCA GCCTTCTGAG TAGCTGGGAT TACAGGCACG 120
TGCCGCCACG CCAATTTTTG TATTTTTAGT AAAGACGGGG TTTCACCATA TTGGTCAGGC 180
TGATCTCGAA CTCCTGACCT CGTGATCCAC CTGCCTTGGC CTCCGAAAGT GCTCGGATTA 240
CAGGCGTGAG CCACCGCCCC TGGCTTAGGT CTTTTCTATT AAGACACACA TTAAAGGGAT 300
TTGTAAAAAA TGCATTTTTG GGGGGTTTTG GAAATTTTTT TTTTTGCAAA AATACTATTT 360
ATGCTAATAT TTAATTATTT ATTGTTGCTA TTTTTAAATG GGTATATGTT TTAAACATTT 420
CTCATTATTA ATTTCTAATA TGGTAAATAT CTATATAACC CATATAAACA ATAGCTCTTT 480
GGGATCCTCA ATAATAAGAG TATAAAAGAG TCACGAGACC AAAAAGTGTG ATACCTACTG 540
TTGGACATAA GTGCATTCAC CTGCTGGATG GCGTAAGGGC TGAAGGCTTT TCCCCATGCC 600
CCGCGAAAAG CAATCAGCCA GCCATCCTCA CTCGCCCTGG AGGCCACGTA GCCGTGGCGC 660
GTCCCAGGCT CGAGCTCCCT GGCCTGTGCT CAGAGCGCCC TCTACAGGCC AAGAGTGGAT 720
CCCACACCAT TCTTGCTTGA ATCTACTGCT CTGGCTGAAC TTTTAGCCCA GGGGGAGTTT 780
GAAGTTCGCG GCTGCCTGGC GCCTTGGAAC AGGCGATAGG CAGCATCTAC AAGCTTCATT 840
TTCACAGGTG GGGGCTGCGG AATGGGGAAG CATCGTGCTG CAGTGACGAA ACCACTAAAC 900
TGACCTGAAT CTTGGTCCTG GCTCAGTCCA CAACTAGGGT GGGGTCCCCT GACCTCCCTG 960
GGTTTCAATT ACTCAGGAGG AAACAACCCA CAATGAACTA GCCACAAAGA TCCTTCTGGC 1020
TCTAGCAGCC TATGATTCTA GGTGCTAATT GTCCCCACGT CTTACCTAGA GAAGGGGCTT 1080
AGTTCCCTGG CTACTGCCTT TCAGAGCTAT CTTTGCTTTC GAGGTTTGGC TCAATAAGAA 1140
TCTGACTTCA GGATGGGTCT TTGCAGTTAT GGAGCTCATG GATTTTGTTC TTTAGCAAGT 1200
GCATTTTAAA ACACCTTCTC AACACTTCAT CGATTTATAA AGCAAATCAT AAGAAGCTGG 1260
CATTGGCTCA AGCTCTGGGC CAATATATGC ATTTTCTTAT TTGAGCCACA CCACAACCCT 1320
ATTACCATTA TTCCCACTTT ACAGAGAGAA AAACAGAGGT CCAAGGAACT TAAGTAACTT 1380
GCCAAGATCC CAGAGCAACT GTATAGCAGA ACGGGAATTC AAAACCAAGC AGTCTGGTTC 1440
CACACCCACA ACACTATACC TAGCCCGGAT AATAAGAGTT TGCATTTTTT AAGGTTTGCT 1500
GTGTCCCTGG AGATTTACAT ACATTATCTC ATTCAATACA 1540
|
