Variant report

Variant	rs1128863
Chromosome Location	chrX:154356862-154356863
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs12387365	1.00[CEU][hapmap]
rs1448032	1.00[GIH][hapmap]
rs17052027	1.00[CEU][hapmap];0.87[TSI][hapmap]
rs3599	1.00[CEU][hapmap];0.87[TSI][hapmap]
rs5940367	1.00[CEU][hapmap];0.87[TSI][hapmap]
rs5940453	1.00[CEU][hapmap];0.87[TSI][hapmap]
rs5945137	0.90[ASW][hapmap];1.00[GIH][hapmap];0.84[LWK][hapmap]
rs5987093	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.81[YRI][hapmap]
rs7881389	1.00[GIH][hapmap]

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:154307800-154357400	Weak transcription	Brain Hippocampus Middle	brain

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links