| Tag | Content |
|---|
EnhancerAtlas ID | HS078-00093 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr1:2528130-2529430 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PLAG1 | MA0163.1 | chr1:2529066-2529080 | CCCCCTAGGGCCTC | - | 7.06 | | SP1 | MA0079.4 | chr1:2529019-2529034 | CTGACCCCGCCCCCT | + | 6.26 | | SP4 | MA0685.1 | chr1:2529019-2529036 | CTGACCCCGCCCCCTAC | + | 6.26 | | TCF3 | MA0522.2 | chr1:2528554-2528564 | AACACCTGCT | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGTGGGGCCA CCCGATCATC CCACGGGCCC CCACGTCAGC CTTCCCAGGC CTGGCGTGGG 60
GCCCTGGGCT TACGGGGTGA GCAGACCCAC CTATCCTCAG CCTCAGGGTG CCCCGGGGCT 120
AGCGGGGGCA CGGGATGATC TCAGCCTCAC CTCTGGGTGC TGCTGCGGCG GGGGGAAGGA 180
TGGGCATGGT ATTGTGATTG GGGAACTTCC GCAGACTGAG AGCTGGGCCT TTACCCTGAG 240
GAGTTGGGGG GGTTCCTCCC CGGCCCCTGT CCTGGTTGTC TGGCTGGACT CTGCTCTCCA 300
GGACTCCAGC CCCAGTCTCA AGGCACAGGG CTGGCGCTGA CCCCAGAGCA AGGCCTGGGA 360
CCACGTCCCT CTCAGCCACC AGCTCCCAGG GCCCTGGTCT CTCCATTGTT GAAGCAGCTG 420
TGAGAACACC TGCTCATCTG TCCCCAGGGA CACAGGAGCA CGAGACTCTG GGCCCCAGAC 480
TCAGGCAAAG CCCAGGGAGC ACTCTGCCCA GCGTCCTGCC ACACCTTCTG GGCTGCAGGA 540
CTTCCTGCCC TTTAGGAAAG GGAGGCAGCC CTTTCTTCCT CCCCAAAGCT CCTAGACTCA 600
GTGCCCCCCT GACGCTTGAC TCACAGATGT CTCTGACCTA CCCCCCCATG GCAACAGGAG 660
GCTTGACTTG CCCCCAGCTT GCCTCTGCCT CAGTCTCCCC ATTGCAGTGG GGACCTCTGT 720
CCCTCCCATT ACTCTAACAA AGGTCTTGAG AGTCCCGACT CCCCTCTGCC CTTAGCCCCT 780
ATACCCAATC CCTCAGCTGC TGCGGTCAAC ACCTCCCCTG CGTCTGTGTG TCTGCCAGCA 840
CCATGGCCAA GCCTGTCACC TCACCTGGGT GACCACATCG GCCTCCATGC TGACCCCGCC 900
CCCTACTCAA CTCACTCTCC CCAGAACAGC CAGAATCCCC CTAGGGCCTC CCTGCGGTTC 960
CTTGTCTCCA CCCTCACCCC AGCCCTGGAG CAGCCACAGT GACTACAGGA GCAGCATATC 1020
TGACCGCGTC TCTGCTCTTA GCACCCCTGC GGCTTTCAGA CAGGGAGTAC AATCCAAACC 1080
GGCTGCTGTG GCCCGTGGTC ACCTCGCCTC CCTCCCTGCC ATCTTCTCCT TCCTGTCCGC 1140
TGCTGACCAC GGGTCCGGCC CCTGCCTGCT CCTGCCTCTG GCCTCTGCAC TGGCACTGGC 1200
TGTTTCTGCT CCCGGGAAAT CACCCCGCCG CCTCTTCAGG CCTTTAAGGT CTCAAATGTC 1260
GCCTCCCCGG AGCAGTGCTC CCTGTCCTCG TCCCTCCCTG 1300
|
