Variant report

Variant	rs67921622
Chromosome Location	chr6:45942037-45942038
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10456555	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10456556	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10456557	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10807331	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10948268	0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10948269	0.87[ASN][1000 genomes]
rs10948271	0.83[ASN][1000 genomes]
rs12197310	0.87[ASN][1000 genomes]
rs12197333	0.85[ASN][1000 genomes]
rs12206357	0.85[ASN][1000 genomes]
rs1338467	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1338469	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1338472	0.87[ASN][1000 genomes]
rs1338473	0.87[ASN][1000 genomes]
rs1338474	0.87[ASN][1000 genomes]
rs1416168	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1416169	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1535109	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1555216	0.84[ASN][1000 genomes]
rs1555218	0.85[ASN][1000 genomes]
rs2021683	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2021684	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2021687	0.87[ASN][1000 genomes]
rs2039716	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2144162	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2144163	0.87[ASN][1000 genomes]
rs34495744	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35293483	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3777605	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3777606	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3777611	0.87[ASN][1000 genomes]
rs3777613	0.87[ASN][1000 genomes]
rs3777616	0.87[ASN][1000 genomes]
rs3777619	0.87[ASN][1000 genomes]
rs3777620	0.87[ASN][1000 genomes]
rs3777621	0.84[ASN][1000 genomes]
rs3777623	0.84[ASN][1000 genomes]
rs3777625	0.84[ASN][1000 genomes]
rs3777629	0.84[ASN][1000 genomes]
rs56968247	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs57300420	0.87[ASN][1000 genomes]
rs59981678	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6458484	0.85[ASN][1000 genomes]
rs6930840	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7764538	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7771614	0.84[ASN][1000 genomes]
rs7771749	0.84[ASN][1000 genomes]
rs9689318	0.84[ASN][1000 genomes]
rs9689699	0.85[ASN][1000 genomes]
rs9689703	0.85[ASN][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	nsv532024	chr6:45475088-45982640	Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv428482	chr6:45926644-46050182	Genic enhancers Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv885867	chr6:45936223-45982976	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:45938600-45942800	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr6:45938600-45943400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr6:45938600-45949800	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr6:45938600-45953200	Weak transcription	Lung	lung
5	chr6:45938800-45942800	Weak transcription	Fetal Intestine Small	intestine
6	chr6:45940200-45942200	Enhancers	Left Ventricle	heart
7	chr6:45941000-45942400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:45941000-45946800	Weak transcription	Right Atrium	heart
9	chr6:45941200-45946000	Weak transcription	Fetal Heart	heart
10	chr6:45941400-45942800	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr6:45941600-45945600	Weak transcription	Psoas Muscle	Psoas
12	chr6:45941600-45947000	Weak transcription	Right Ventricle	heart
13	chr6:45942000-45943400	Enhancers	Placenta	Placenta
14	chr6:45942000-45945400	Weak transcription	Skeletal Muscle Female	skeletal muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links