Variant report

Variant	rs61838235
Chromosome Location	chr1:223509717-223509718
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:223504054..223506980-chr1:223508583..223510799,2	K562	blood:
2	chr1:223508432..223510410-chr1:223512972..223514710,2	K562	blood:
3	chr1:223497129..223500114-chr1:223509294..223511393,2	K562	blood:

Extended variants
information (count: 65 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10495206	0.81[EUR][1000 genomes]
rs10495207	0.83[EUR][1000 genomes]
rs1518040	0.81[AFR][1000 genomes]
rs1547788	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1619227	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1713220	0.90[AMR][1000 genomes]
rs17162008	0.83[EUR][1000 genomes]
rs17163789	0.82[AFR][1000 genomes]
rs17163816	0.83[AFR][1000 genomes]
rs17163818	0.87[AFR][1000 genomes]
rs17163824	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17163825	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17163828	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17163831	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17480087	0.81[EUR][1000 genomes]
rs17480344	0.81[EUR][1000 genomes]
rs17539269	0.81[EUR][1000 genomes]
rs17539583	0.82[EUR][1000 genomes]
rs17578168	0.82[EUR][1000 genomes]
rs17578203	0.82[EUR][1000 genomes]
rs1829308	0.85[AFR][1000 genomes]
rs1829309	0.85[AFR][1000 genomes]
rs1850562	0.80[AFR][1000 genomes]
rs1935037	0.81[AFR][1000 genomes]
rs2096082	0.80[AFR][1000 genomes]
rs2176504	0.80[AFR][1000 genomes]
rs2176505	0.80[AFR][1000 genomes]
rs2176506	0.82[AFR][1000 genomes]
rs2459849	0.90[AMR][1000 genomes]
rs2487521	0.90[AMR][1000 genomes]
rs2678377	0.90[AMR][1000 genomes]
rs34468460	0.81[AFR][1000 genomes]
rs34572097	0.87[AFR][1000 genomes]
rs35318812	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4661238	0.80[AFR][1000 genomes]
rs4661239	0.80[AFR][1000 genomes]
rs61838210	0.81[EUR][1000 genomes]
rs61838229	0.81[EUR][1000 genomes]
rs61838230	0.82[EUR][1000 genomes]
rs61838231	0.82[EUR][1000 genomes]
rs61838234	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61838236	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61838237	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61838238	0.82[EUR][1000 genomes]
rs61838239	0.82[EUR][1000 genomes]
rs61838240	0.82[EUR][1000 genomes]
rs61838241	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61838243	0.82[EUR][1000 genomes]
rs61838246	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61838249	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61838250	0.84[EUR][1000 genomes]
rs6604709	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs66531524	0.83[AFR][1000 genomes]
rs66768536	0.80[AFR][1000 genomes]
rs66867621	0.82[AFR][1000 genomes]
rs67707169	0.81[AFR][1000 genomes]
rs7536652	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7541162	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7555607	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs825127	0.88[AFR][1000 genomes]
rs870486	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9442046	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012537	chr1:222755091-223512243	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	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
3	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:1)

SNP	Gene	Cis/trans	Tissue	Source
rs61838235	SUSD4	cis	Heart Left Ventricle	GTEx

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:223497200-223512600	Weak transcription	Pancreas	Pancrea
2	chr1:223497400-223510400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr1:223505600-223511800	Weak transcription	Ovary	ovary
4	chr1:223505600-223512600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr1:223505600-223514800	Weak transcription	Right Atrium	heart
6	chr1:223505600-223521400	Weak transcription	Primary T cells from cord blood	blood
7	chr1:223505800-223513000	Weak transcription	Fetal Lung	lung
8	chr1:223506600-223526000	Weak transcription	Esophagus	oesophagus
9	chr1:223506800-223509800	Weak transcription	Fetal Heart	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links