| Tag | Content |
|---|
EnhancerAtlas ID | HS060-29650 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr6:33646620-33647650 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HEY2 | MA0649.1 | chr6:33647633-33647643 | GACACGTGCC | + | 6.02 | | Npas2 | MA0626.1 | chr6:33647633-33647643 | GACACGTGCC | - | 6.02 | | SCRT1 | MA0743.1 | chr6:33647062-33647077 | AGACACCTGTTGAGT | - | 6.17 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGGCGGGGCT GAGGGGTGCT CAGGCATCTT GGGGTGGGGG ACCGGAGCAG AGGCTTGGCG 60
GGAAGGCCAC AGAGTTAGAG AAGTCAGACG GTGGGTCACA AAAGGAACAC TCAGCTGCTG 120
ACCATGGAGG GGACGCAGAG GGAGAAGTGA GGCTGCAGAT GTGGTAGAAC TCAGCCTGTG 180
GGCCTGATAG AACTCAAGCA GGGTCCCAGT AGCATCAGGC ACCTAGCAGA ACTCAGACAA 240
CAGGCCAGAA AGAAATCAAG CATGCATTCC TTGTCACTTG TCGTCGTTTA TTTAAAATCA 300
GGAAGCACCT GCTACGTGCC ACGGACTGTA CATGCATGGG GGACATCAGC TGAGTGTCAG 360
CTCCTGGGGG GCACGGGCAG GGACCCCATC CTTTGTGTGC ATCGCCAGGG CCCCAGTGTG 420
TGGCGCATAG TAGGTTCTCA ACAGACACCT GTTGAGTGAA GGCACGAAGG ATACAGGGCT 480
GAGTCTAAAT CTGGAACAGA CGTGGTCCCT GCCCCTGAGC ATCTGACAGT GTAGGCGGCA 540
GGGGGAGAAA GAAGCAAACA CTGAAGGGAG ATTAGGACAT CATAAACAAG ACATGATGTG 600
CTGGAACTGC TGTACAGTGT TAGTTTTATT AATTTCTATT ATTATATTAC TGCGAATAAT 660
GCAGTCGCTG GCACGAGAGG TGTGTGCTCA GTGAGGAGGG TTTAAGTAAC TGCTGCGGGA 720
GCACAGGGGA GGGAGGGGGT GAGCAAGGCG GGATTAGCGA GGCTTCCTGG AGGAAGCTGC 780
CTCTGAGATG ACCCCTATGG GACTTCTTTC CAGTGGGGAG AAGCGGGGAC TTTCTGGGTC 840
ATGGGGTCAA TATCTCTGCT GGCAGAGGGC CTGAGACATC AGCTGGGGAA CCCCCAAATC 900
CCAGCCAGGG GAGGGTTTTC CTGATTTCAG GTAAGGGCTG TGGTCAGAGT CCCAGTTTCT 960
CCCTGGTAAG CAACGGAGAG GAGAGCCCAG GGCTTGCTGG ACCGAGAGAG TGTGACACGT 1020
GCCCCCTCCC 1030
|
