Variant report

Variant	rs1503194
Chromosome Location	chrX:105100928-105100929
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs209109	0.91[CEU][hapmap];1.00[TSI][hapmap]
rs382243	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[LWK][hapmap];0.86[MEX][hapmap];0.81[MKK][hapmap];1.00[TSI][hapmap];0.90[YRI][hapmap]
rs400049	1.00[CEU][hapmap]
rs445086	1.00[CEU][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap]
rs7063036	1.00[CEU][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:105083200-105101200	Weak transcription	Fetal Muscle Trunk	muscle
2	chrX:105094400-105101800	Weak transcription	Fetal Muscle Leg	muscle
3	chrX:105096200-105136600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chrX:105098200-105102800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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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

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