Variant report

Variant	rs73041534
Chromosome Location	chr3:23431250-23431251
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NKIRAS1-5	chr3:23431152-23431400	NONHSAT088668

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

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10510538	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1054048	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12638508	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17405137	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55737333	0.86[EUR][1000 genomes]
rs57338964	0.89[EUR][1000 genomes]
rs57859482	0.86[AMR][1000 genomes]
rs58157906	0.90[AMR][1000 genomes]
rs59180179	0.89[EUR][1000 genomes]
rs59461083	0.89[EUR][1000 genomes]
rs61264520	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73041537	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73041557	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73041601	0.89[EUR][1000 genomes]
rs73043622	0.89[EUR][1000 genomes]
rs73043635	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73043648	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73043654	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73043677	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73043684	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73043689	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73043697	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73045614	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs73045642	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7632099	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002823	chr3:23277838-23623083	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1007373	chr3:23367952-23710331	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv876624	chr3:23385877-23483536	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv876625	chr3:23390301-23509597	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1012236	chr3:23408427-23469063	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1010032	chr3:23408985-23469063	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:23409200-23431800	Weak transcription	Aorta	Aorta
2	chr3:23420000-23433600	Weak transcription	Primary T cells from cord blood	blood
3	chr3:23425800-23432200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr3:23427000-23445000	Weak transcription	Right Ventricle	heart
5	chr3:23427600-23432000	Enhancers	Primary B cells from cord blood	blood
6	chr3:23428000-23431600	Weak transcription	Psoas Muscle	Psoas
7	chr3:23428000-23431800	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr3:23428400-23431400	Active TSS	Duodenum Mucosa	Duodenum
9	chr3:23428400-23431400	Active TSS	Rectal Mucosa Donor 29	rectum
10	chr3:23428600-23435400	Weak transcription	Brain Substantia Nigra	brain
11	chr3:23429800-23432200	Weak transcription	Liver	Liver
12	chr3:23429800-23445400	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr3:23430000-23432200	Enhancers	Primary B cells from peripheral blood	blood
14	chr3:23430400-23431400	Enhancers	H9 Cell Line	embryonic stem cell
15	chr3:23430600-23431400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr3:23430600-23431400	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr3:23430600-23431400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr3:23430600-23431400	Flanking Active TSS	GM12878-XiMat	blood
19	chr3:23430600-23431600	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr3:23430600-23431600	Weak transcription	Stomach Smooth Muscle	stomach
21	chr3:23430600-23431800	Enhancers	Fetal Thymus	thymus
22	chr3:23430800-23431600	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr3:23430800-23431600	Enhancers	H1 Cell Line	embryonic stem cell
24	chr3:23430800-23431800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr3:23430800-23433400	Weak transcription	Fetal Heart	heart
26	chr3:23431000-23431400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr3:23431000-23431800	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr3:23431000-23431800	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr3:23431000-23436200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr3:23431200-23431800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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