Variant report

Variant	rs73692227
Chromosome Location	chr8:89331430-89331431
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10504846	0.98[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs10955556	0.81[ASN][1000 genomes]
rs11986810	0.86[ASN][1000 genomes]
rs12114224	0.98[ASN][1000 genomes]
rs16880720	0.98[ASN][1000 genomes]
rs16880925	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16880935	0.98[ASN][1000 genomes]
rs17667732	0.98[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs17667749	0.98[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs17667787	0.98[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs17667853	0.98[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs17667883	0.98[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs17729077	0.90[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs17729255	0.90[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs17729512	0.98[ASN][1000 genomes]
rs17729596	0.98[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs1915018	0.82[ASN][1000 genomes]
rs1915019	0.82[ASN][1000 genomes]
rs28904573	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28904574	0.90[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs28986476	0.97[ASN][1000 genomes]
rs28986490	0.98[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs28986498	0.98[ASN][1000 genomes]
rs36013966	0.83[ASN][1000 genomes]
rs3844198	0.86[ASN][1000 genomes]
rs5016164	0.90[EUR][1000 genomes]
rs55888684	0.98[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs56053776	0.98[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs56165694	0.93[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs56322839	0.98[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs57279787	0.98[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs57749754	0.98[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs58695872	0.98[ASN][1000 genomes]
rs58755914	0.98[ASN][1000 genomes]
rs59122715	0.88[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs59544142	0.95[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs61160643	0.88[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs7000030	0.98[ASN][1000 genomes]
rs7003179	0.98[ASN][1000 genomes]
rs7013819	0.86[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs73692211	0.86[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs73692213	0.90[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs73692214	0.98[ASN][1000 genomes]
rs73692215	0.98[ASN][1000 genomes]
rs73692216	0.98[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs73692217	0.98[ASN][1000 genomes]
rs73692218	0.87[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs73692219	0.97[ASN][1000 genomes]
rs73692222	0.98[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs73692223	0.98[ASN][1000 genomes]
rs73692224	0.98[ASN][1000 genomes]
rs73692225	0.98[ASN][1000 genomes]
rs73692226	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7816934	0.90[ASN][1000 genomes]
rs7817311	0.98[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs7818066	0.90[EUR][1000 genomes]
rs7833834	0.80[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs7837860	0.85[ASN][1000 genomes]
rs7843531	0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029898	chr8:88837956-89606641	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv1030028	chr8:89060085-89733470	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1019111	chr8:89186908-89475460	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv831386	chr8:89209788-89403546	Enhancers Genic enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:89320600-89331800	Weak transcription	Left Ventricle	heart
2	chr8:89320800-89337600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr8:89321800-89333400	Weak transcription	Fetal Brain Male	brain
4	chr8:89324400-89336200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr8:89326600-89338200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr8:89327000-89332200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr8:89327200-89331800	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr8:89327200-89336200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr8:89327400-89331800	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr8:89327400-89332000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr8:89327400-89332800	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr8:89327400-89332800	Weak transcription	Rectal Smooth Muscle	rectum
13	chr8:89327400-89336000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr8:89327400-89336000	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr8:89327600-89332600	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr8:89330600-89332600	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr8:89330600-89333200	Enhancers	Fetal Heart	heart
18	chr8:89331000-89331600	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr8:89331000-89332400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr8:89331000-89333400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr8:89331200-89331800	Enhancers	NHDF-Ad	bronchial
22	chr8:89331200-89332000	Active TSS	Aorta	Aorta
23	chr8:89331200-89332000	Enhancers	Colon Smooth Muscle	Colon
24	chr8:89331200-89332600	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr8:89331200-89332600	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr8:89331200-89332800	Weak transcription	Brain Angular Gyrus	brain
27	chr8:89331200-89333200	Enhancers	NH-A	brain
28	chr8:89331200-89333200	Enhancers	Osteobl	bone
29	chr8:89331400-89332600	Weak transcription	Fetal Brain Female	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links