Variant report

Variant	rs73535828
Chromosome Location	chr8:9449905-9449906
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:9436374..9438118-chr8:9448298..9450020,2	K562	blood:

Extended variants
information (count: 95 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:92)

rs_ID	r²[population]
rs10086535	0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10090277	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10090998	0.82[EUR][1000 genomes]
rs10090999	0.82[EUR][1000 genomes]
rs10093972	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10105767	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10105968	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11249940	0.88[EUR][1000 genomes]
rs11249944	0.82[EUR][1000 genomes]
rs11984920	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11988208	0.84[EUR][1000 genomes]
rs11991831	0.82[EUR][1000 genomes]
rs11995167	0.84[EUR][1000 genomes]
rs12234900	0.84[EUR][1000 genomes]
rs12234999	0.84[EUR][1000 genomes]
rs12235001	0.84[EUR][1000 genomes]
rs28499425	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28562614	0.82[EUR][1000 genomes]
rs28675389	0.84[EUR][1000 genomes]
rs33944167	0.86[EUR][1000 genomes]
rs34614689	0.84[EUR][1000 genomes]
rs35052906	0.88[EUR][1000 genomes]
rs35721526	0.96[EUR][1000 genomes]
rs36036709	0.92[EUR][1000 genomes]
rs4319098	0.90[EUR][1000 genomes]
rs4348499	0.88[EUR][1000 genomes]
rs4380943	0.90[EUR][1000 genomes]
rs4383973	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4474027	0.96[EUR][1000 genomes]
rs4612344	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4629869	0.96[EUR][1000 genomes]
rs5002814	0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs5002815	0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs5018578	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55924085	0.82[EUR][1000 genomes]
rs57000316	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs57024674	0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs57331392	0.94[EUR][1000 genomes]
rs57482128	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs57580633	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs57987233	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs58458097	0.94[EUR][1000 genomes]
rs58596872	0.88[EUR][1000 genomes]
rs58981097	0.84[EUR][1000 genomes]
rs59201801	0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs59268701	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs59519630	0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs59940446	0.98[EUR][1000 genomes]
rs60051555	0.94[EUR][1000 genomes]
rs60078276	0.92[EUR][1000 genomes]
rs60222666	0.88[EUR][1000 genomes]
rs60857446	0.82[EUR][1000 genomes]
rs60942347	0.86[EUR][1000 genomes]
rs61594550	0.94[EUR][1000 genomes]
rs61682841	0.96[EUR][1000 genomes]
rs6422356	0.84[EUR][1000 genomes]
rs6601358	0.86[EUR][1000 genomes]
rs6984737	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6987746	0.80[EUR][1000 genomes]
rs6990116	0.86[EUR][1000 genomes]
rs7000182	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7001395	0.86[EUR][1000 genomes]
rs7002917	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7009596	0.84[EUR][1000 genomes]
rs7009863	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7014218	0.86[EUR][1000 genomes]
rs7016632	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7018268	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7018348	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73523222	0.92[EUR][1000 genomes]
rs73523224	0.96[EUR][1000 genomes]
rs73523249	0.94[EUR][1000 genomes]
rs73537955	0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73537959	0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73537971	0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73539904	0.96[EUR][1000 genomes]
rs73539907	0.96[EUR][1000 genomes]
rs7815297	0.86[EUR][1000 genomes]
rs7815378	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7815506	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7815644	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7818016	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7821007	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7825464	0.86[ASN][1000 genomes]
rs7827395	0.84[EUR][1000 genomes]
rs7829677	0.86[ASN][1000 genomes]
rs7837344	0.92[EUR][1000 genomes]
rs7837923	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7840161	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7846023	0.88[EUR][1000 genomes]
rs9644705	0.86[EUR][1000 genomes]
rs9644706	0.82[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	nsv530864	chr8:9097498-9914548	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv497927	chr8:9097611-9544519	Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv981863	chr8:9446521-9455100	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:9414400-9459600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:9417200-9450000	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr8:9427400-9450000	Weak transcription	Thymus	Thymus
4	chr8:9428200-9466200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr8:9428400-9450000	Weak transcription	Psoas Muscle	Psoas
6	chr8:9429000-9450000	Weak transcription	Fetal Kidney	kidney
7	chr8:9431000-9450000	Weak transcription	Colon Smooth Muscle	Colon
8	chr8:9433600-9461000	Weak transcription	Fetal Stomach	stomach
9	chr8:9434800-9459000	Weak transcription	Primary B cells from cord blood	blood
10	chr8:9435400-9465600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr8:9435400-9468400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr8:9435600-9450000	Weak transcription	Small Intestine	intestine
13	chr8:9435600-9457600	Weak transcription	Fetal Muscle Leg	muscle
14	chr8:9435600-9472400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr8:9435800-9459400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr8:9435800-9465400	Weak transcription	Lung	lung
17	chr8:9435800-9465600	Weak transcription	Pancreas	Pancrea
18	chr8:9435800-9472600	Weak transcription	HSMMtube	muscle
19	chr8:9437400-9468000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr8:9438000-9450000	Weak transcription	K562	blood
21	chr8:9439200-9450000	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr8:9439200-9450000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr8:9439400-9472400	Weak transcription	HSMM	muscle
24	chr8:9439600-9450000	Weak transcription	Adipose Nuclei	Adipose
25	chr8:9439600-9450600	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr8:9439600-9465600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr8:9440400-9454800	Weak transcription	GM12878-XiMat	blood
28	chr8:9440600-9465600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr8:9440800-9450000	Weak transcription	Primary B cells from peripheral blood	blood
30	chr8:9441200-9460600	Weak transcription	Fetal Intestine Large	intestine
31	chr8:9442600-9450000	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr8:9442600-9465400	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr8:9445400-9450000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr8:9445400-9459800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr8:9446400-9451000	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr8:9446800-9450800	Enhancers	Brain Hippocampus Middle	brain
37	chr8:9447000-9451000	Enhancers	Brain Anterior Caudate	brain
38	chr8:9447000-9451000	Enhancers	Brain Substantia Nigra	brain
39	chr8:9447600-9465400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr8:9447800-9450000	Weak transcription	Left Ventricle	heart
41	chr8:9447800-9450600	Weak transcription	Gastric	stomach
42	chr8:9447800-9457600	Weak transcription	Right Atrium	heart
43	chr8:9448000-9450800	Enhancers	Dnd41	blood
44	chr8:9448000-9459600	Weak transcription	Fetal Intestine Small	intestine
45	chr8:9448200-9450200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr8:9448200-9450400	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr8:9448400-9450000	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr8:9448400-9450200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr8:9448400-9450800	Enhancers	Primary T helper cells PMA-I stimulated	--
50	chr8:9448400-9451000	Enhancers	Primary T helper cells fromperipheralblood	blood

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