Variant report

Variant	rs10930874
Chromosome Location	chr2:180305196-180305197
allele	C/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]
rs10179194	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10497539	0.89[ASN][1000 genomes]
rs12467818	0.97[ASN][1000 genomes]
rs16866729	0.88[ASN][1000 genomes]
rs72964238	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180293800-180307800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:180294200-180306600	Weak transcription	Liver	Liver
3	chr2:180294200-180307400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr2:180294600-180305600	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr2:180299800-180308400	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr2:180300000-180305800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr2:180300200-180305800	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr2:180300400-180305600	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr2:180300400-180306000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr2:180303800-180307800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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