Variant report

Variant	rs61838240
Chromosome Location	chr1:223512135-223512136
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	chr1:223510081..223513953-chr1:223514794..223517151,3	K562	blood:
2	chr1:223503941..223506228-chr1:223511294..223513326,2	MCF-7	breast:

Extended variants
information (count: 55 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10495206	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10495207	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10907376	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11261264	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12123148	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12140453	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12564615	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1400959	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1547788	0.82[EUR][1000 genomes]
rs17162008	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17163824	0.84[EUR][1000 genomes]
rs17163825	0.83[EUR][1000 genomes]
rs17163827	0.91[EUR][1000 genomes]
rs17163828	0.85[EUR][1000 genomes]
rs17163831	0.83[EUR][1000 genomes]
rs17480087	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17480344	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17518349	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17518363	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17539269	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17539583	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17577742	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17578168	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17578203	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1772280	0.83[EUR][1000 genomes]
rs34150324	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35318812	0.84[EUR][1000 genomes]
rs61838208	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61838209	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61838210	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61838229	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61838230	0.94[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61838231	0.94[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61838234	0.82[EUR][1000 genomes]
rs61838235	0.82[EUR][1000 genomes]
rs61838236	0.84[EUR][1000 genomes]
rs61838237	0.84[EUR][1000 genomes]
rs61838238	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61838239	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61838241	0.84[EUR][1000 genomes]
rs61838243	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61838246	0.83[EUR][1000 genomes]
rs61838249	0.84[EUR][1000 genomes]
rs61838250	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61838252	0.83[EUR][1000 genomes]
rs61839867	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61839878	0.81[AMR][1000 genomes]
rs7536652	0.82[EUR][1000 genomes]
rs7541162	0.81[EUR][1000 genomes]
rs870486	0.84[EUR][1000 genomes]
rs9442042	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9442046	0.81[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
rs61838240	SUSD4	cis	Heart Left Ventricle	GTEx

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:223497200-223512600	Weak transcription	Pancreas	Pancrea
2	chr1:223505600-223512600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr1:223505600-223514800	Weak transcription	Right Atrium	heart
4	chr1:223505600-223521400	Weak transcription	Primary T cells from cord blood	blood
5	chr1:223505800-223513000	Weak transcription	Fetal Lung	lung
6	chr1:223506600-223526000	Weak transcription	Esophagus	oesophagus
7	chr1:223510800-223512800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr1:223511200-223513200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr1:223511200-223513600	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr1:223511200-223517600	Weak transcription	Psoas Muscle	Psoas
11	chr1:223511800-223514200	Enhancers	Brain Angular Gyrus	brain
12	chr1:223511800-223515600	Enhancers	Left Ventricle	heart
13	chr1:223511800-223515800	Enhancers	Ovary	ovary
14	chr1:223511800-223527000	Enhancers	Fetal Heart	heart
15	chr1:223512000-223512400	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr1:223512000-223512600	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr1:223512000-223512600	Enhancers	Right Ventricle	heart
18	chr1:223512000-223513000	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr1:223512000-223513600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr1:223512000-223513800	Weak transcription	Fetal Thymus	thymus

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links