Variant report

Variant	rs17163825
Chromosome Location	chr1:223523854-223523855
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:223523045..223525039-chr1:223526417..223529119,2	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10495207	0.85[EUR][1000 genomes]
rs11261264	0.81[EUR][1000 genomes]
rs12123148	0.80[EUR][1000 genomes]
rs12140453	0.81[EUR][1000 genomes]
rs1400961	0.81[JPT][hapmap]
rs1547788	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1619227	0.91[CEU][hapmap];0.80[CHB][hapmap];0.81[JPT][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1713220	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17162008	0.85[EUR][1000 genomes]
rs17163824	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17163827	0.82[EUR][1000 genomes]
rs17163828	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17163831	0.90[CEU][hapmap];0.80[CHB][hapmap];0.81[JPT][hapmap];0.95[MEX][hapmap];0.94[TSI][hapmap];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs17539583	0.83[EUR][1000 genomes]
rs17578168	0.83[EUR][1000 genomes]
rs17578203	0.87[TSI][hapmap];0.87[EUR][1000 genomes]
rs1772280	0.80[EUR][1000 genomes]
rs2459849	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2487521	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2678377	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34150324	0.81[EUR][1000 genomes]
rs35318812	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3820596	0.81[JPT][hapmap]
rs61838234	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61838235	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61838236	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61838237	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61838238	0.83[EUR][1000 genomes]
rs61838239	0.83[EUR][1000 genomes]
rs61838240	0.83[EUR][1000 genomes]
rs61838241	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61838243	0.83[EUR][1000 genomes]
rs61838246	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61838249	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61838250	0.85[EUR][1000 genomes]
rs61839867	0.81[EUR][1000 genomes]
rs6604709	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7536652	0.82[CEU][hapmap];0.85[CHB][hapmap];0.90[JPT][hapmap];0.95[MEX][hapmap];0.86[TSI][hapmap];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7541162	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7555607	0.91[CEU][hapmap];0.80[CHB][hapmap];0.81[JPT][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs870486	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs885279	0.81[JPT][hapmap]
rs9442046	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1000039	chr1:223429733-223527845	Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv1010798	chr1:223498145-223538989	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs17163825	SUSD4	cis	parietal	SCAN
rs17163825	SUSD4	cis	Heart Left Ventricle	GTEx
rs17163825	SUSD4	cis	cerebellum	SCAN

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:223506600-223526000	Weak transcription	Esophagus	oesophagus
2	chr1:223511800-223527000	Enhancers	Fetal Heart	heart
3	chr1:223514000-223526200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:223514400-223535800	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr1:223517600-223527400	Enhancers	Ovary	ovary
6	chr1:223522200-223525200	Weak transcription	Primary T cells from cord blood	blood
7	chr1:223523000-223524200	Enhancers	Stomach Mucosa	stomach
8	chr1:223523200-223524600	Enhancers	Fetal Muscle Leg	muscle
9	chr1:223523400-223524800	Enhancers	Gastric	stomach
10	chr1:223523400-223525400	Weak transcription	Brain Anterior Caudate	brain
11	chr1:223523600-223524000	Enhancers	Left Ventricle	heart
12	chr1:223523800-223524000	Enhancers	Fetal Lung	lung
13	chr1:223523800-223524200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland

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