Variant report

Variant	rs16963326
Chromosome Location	chr18:29984209-29984210
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr18:29982431..29984298-chr18:29998082..29999982,2	MCF-7	breast:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10048362	0.91[ASN][1000 genomes]
rs1037753	0.82[JPT][hapmap];0.82[ASN][1000 genomes]
rs10502587	0.86[JPT][hapmap]
rs10502596	1.00[CHB][hapmap];0.93[JPT][hapmap];0.91[ASN][1000 genomes]
rs11504782	0.81[ASN][1000 genomes]
rs11665147	0.86[CHB][hapmap];0.87[JPT][hapmap];0.82[ASN][1000 genomes]
rs11665150	0.86[CHB][hapmap];0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs11665190	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs11873325	1.00[CHB][hapmap];0.87[JPT][hapmap];0.91[ASN][1000 genomes]
rs13381088	1.00[CHB][hapmap];0.93[JPT][hapmap];0.91[ASN][1000 genomes]
rs13381344	0.86[CHB][hapmap];0.87[JPT][hapmap];0.83[ASN][1000 genomes]
rs16963270	0.80[ASN][1000 genomes]
rs16963287	0.81[CHB][hapmap]
rs16963289	0.86[CHB][hapmap];0.87[JPT][hapmap];0.82[ASN][1000 genomes]
rs16963334	1.00[CHB][hapmap];0.93[JPT][hapmap];0.92[ASN][1000 genomes]
rs1964517	0.80[ASN][1000 genomes]
rs2034968	0.86[CHB][hapmap];0.87[JPT][hapmap];0.80[ASN][1000 genomes]
rs2421462	0.81[CHB][hapmap]
rs28500590	0.92[ASN][1000 genomes]
rs3786308	1.00[CHB][hapmap];0.93[JPT][hapmap];0.91[ASN][1000 genomes]
rs3786310	1.00[CHB][hapmap];0.93[JPT][hapmap];0.91[ASN][1000 genomes]
rs3826611	1.00[CHB][hapmap];0.93[JPT][hapmap];0.91[ASN][1000 genomes]
rs41527551	0.86[CHB][hapmap];0.87[JPT][hapmap];0.80[ASN][1000 genomes]
rs56808255	0.84[ASN][1000 genomes]
rs59211646	0.92[ASN][1000 genomes]
rs7226639	0.93[JPT][hapmap];0.81[ASN][1000 genomes]
rs73958414	0.91[ASN][1000 genomes]
rs73958415	0.92[ASN][1000 genomes]
rs8097263	0.86[CHB][hapmap];0.87[JPT][hapmap];0.82[ASN][1000 genomes]
rs968099	0.87[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3347612	chr18:29975003-29990362	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29963600-29999200	Weak transcription	Fetal Kidney	kidney
2	chr18:29964800-29985400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr18:29966800-29985400	Weak transcription	Right Ventricle	heart
4	chr18:29967000-29986600	Weak transcription	Brain Angular Gyrus	brain
5	chr18:29981800-29986800	Weak transcription	Adipose Nuclei	Adipose
6	chr18:29982000-30005400	Weak transcription	Stomach Mucosa	stomach
7	chr18:29982600-29987000	Weak transcription	Brain Cingulate Gyrus	brain
8	chr18:29982600-29987200	Weak transcription	Fetal Heart	heart
9	chr18:29982800-29985600	Weak transcription	Colon Smooth Muscle	Colon
10	chr18:29982800-29985800	Weak transcription	Brain Substantia Nigra	brain
11	chr18:29982800-29987000	Weak transcription	Brain Hippocampus Middle	brain
12	chr18:29982800-29987000	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr18:29983000-29987200	Weak transcription	Ovary	ovary
14	chr18:29983800-29985200	Weak transcription	Pancreas	Pancrea
15	chr18:29983800-29987000	Weak transcription	Gastric	stomach
16	chr18:29983800-29987600	Weak transcription	Brain Anterior Caudate	brain
17	chr18:29984200-29985400	Weak transcription	HUES48 Cell Line	embryonic stem cell

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