Variant report

Variant	rs9881603
Chromosome Location	chr3:159338124-159338125
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	chr3:159328334..159331919-chr3:159337516..159340133,3	K562	blood:

Extended variants
information (count: 89 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:88)

rs_ID	r²[population]
rs1004091	0.80[YRI][hapmap]
rs10154893	0.90[CHB][hapmap];0.92[JPT][hapmap];0.89[ASN][1000 genomes]
rs1030882	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11921824	0.83[JPT][hapmap]
rs11921827	0.83[JPT][hapmap]
rs12106839	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12107648	0.90[CHB][hapmap];0.95[CHD][hapmap];0.92[JPT][hapmap];0.93[ASN][1000 genomes]
rs13434009	0.92[JPT][hapmap]
rs1343824	0.93[ASN][1000 genomes]
rs1347671	0.90[CHB][hapmap];0.92[JPT][hapmap];0.87[ASN][1000 genomes]
rs1356925	0.90[CHB][hapmap];0.86[CHD][hapmap];0.82[ASN][1000 genomes]
rs1356926	0.90[CHB][hapmap]
rs1356927	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1437519	1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];0.90[MKK][hapmap];0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1437520	0.90[CHB][hapmap];0.95[CHD][hapmap];0.92[JPT][hapmap];0.87[ASN][1000 genomes]
rs16830453	0.80[CHB][hapmap]
rs16830454	0.80[CHB][hapmap]
rs16830480	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs16830484	0.90[CHB][hapmap]
rs16830510	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs16830519	1.00[CHB][hapmap];0.92[JPT][hapmap];0.89[ASN][1000 genomes]
rs16830523	0.90[CHB][hapmap];0.92[JPT][hapmap];0.89[ASN][1000 genomes]
rs16830534	0.91[ASN][1000 genomes]
rs16830546	0.92[JPT][hapmap];0.80[YRI][hapmap];0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16830575	0.83[JPT][hapmap]
rs16830579	0.83[JPT][hapmap]
rs16830581	0.83[JPT][hapmap]
rs1816621	0.80[CHB][hapmap];0.92[JPT][hapmap];0.87[ASN][1000 genomes]
rs1816622	0.83[JPT][hapmap]
rs1978830	0.83[JPT][hapmap]
rs1978831	0.90[CHB][hapmap]
rs2118321	0.90[CHB][hapmap]
rs28718721	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs28743043	0.89[ASN][1000 genomes]
rs2886621	0.83[JPT][hapmap]
rs3930053	0.90[CHB][hapmap];0.86[CHD][hapmap]
rs4494974	0.87[ASN][1000 genomes]
rs59556163	0.90[ASN][1000 genomes]
rs60665389	0.85[ASN][1000 genomes]
rs61018732	0.93[ASN][1000 genomes]
rs61036525	0.82[ASN][1000 genomes]
rs61373569	0.93[ASN][1000 genomes]
rs6769217	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs6772245	0.83[JPT][hapmap]
rs6796636	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs73012253	0.91[ASN][1000 genomes]
rs750688	0.83[JPT][hapmap]
rs7619259	0.90[CHB][hapmap];0.86[CHD][hapmap]
rs7625882	0.90[CHB][hapmap]
rs7629269	0.90[CHB][hapmap];0.86[CHD][hapmap]
rs7636120	0.90[CHB][hapmap]
rs7637524	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7650974	0.90[CHB][hapmap]
rs7653224	0.90[CHB][hapmap];0.86[CHD][hapmap]
rs9290045	0.90[CHB][hapmap];0.86[CHD][hapmap];0.81[ASN][1000 genomes]
rs9809076	0.83[JPT][hapmap]
rs9809681	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9814630	0.90[MKK][hapmap]
rs9817830	0.90[CHB][hapmap];0.82[ASN][1000 genomes]
rs9819000	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs9819080	0.90[CHB][hapmap];0.92[JPT][hapmap];0.91[ASN][1000 genomes]
rs9823562	0.82[ASN][1000 genomes]
rs9824363	0.90[CHB][hapmap];0.90[CHD][hapmap];0.92[JPT][hapmap];0.93[ASN][1000 genomes]
rs9826417	0.92[JPT][hapmap];0.83[ASN][1000 genomes]
rs9829229	0.90[CHB][hapmap];0.82[CHD][hapmap]
rs9829310	0.83[JPT][hapmap]
rs9832443	0.82[ASN][1000 genomes]
rs9833713	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9833762	0.90[CHB][hapmap]
rs9840484	0.90[CHB][hapmap]
rs9842465	0.81[CHD][hapmap];0.92[JPT][hapmap];0.83[ASN][1000 genomes]
rs9848763	0.90[CHB][hapmap];0.92[JPT][hapmap];0.87[ASN][1000 genomes]
rs9848897	0.90[CHB][hapmap];0.92[JPT][hapmap];0.87[ASN][1000 genomes]
rs9849705	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9851700	0.83[JPT][hapmap]
rs9852770	0.82[ASN][1000 genomes]
rs9857283	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9860690	1.00[CHB][hapmap];0.84[JPT][hapmap];0.82[ASN][1000 genomes]
rs9864641	0.82[ASN][1000 genomes]
rs9866095	0.90[CHB][hapmap];0.86[CHD][hapmap];0.82[ASN][1000 genomes]
rs9867212	0.82[JPT][hapmap]
rs9870872	0.91[ASN][1000 genomes]
rs9877425	0.82[JPT][hapmap]
rs9879792	0.83[JPT][hapmap]
rs9881499	0.90[CHB][hapmap];0.82[ASN][1000 genomes]
rs9882328	1.00[CHB][hapmap];0.92[JPT][hapmap];0.87[ASN][1000 genomes]
rs9882993	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs9883498	0.81[CHD][hapmap];0.91[JPT][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998949	chr3:158774806-159394550	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:159336400-159338200	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr3:159336400-159338600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr3:159336400-159340200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr3:159336400-159340200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr3:159336600-159338400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr3:159336600-159339200	Enhancers	HSMM	muscle
7	chr3:159336600-159340200	Enhancers	NHLF	lung
8	chr3:159336600-159340400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr3:159337000-159338200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr3:159337000-159338400	Enhancers	Osteobl	bone
11	chr3:159337000-159338600	Enhancers	Brain Hippocampus Middle	brain
12	chr3:159337000-159338800	Enhancers	Hela-S3	cervix
13	chr3:159337000-159339200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr3:159337000-159339400	Enhancers	HUVEC	blood vessel
15	chr3:159337000-159339400	Enhancers	NH-A	brain
16	chr3:159337000-159340200	Enhancers	NHDF-Ad	bronchial
17	chr3:159337200-159338600	Enhancers	HSMMtube	muscle
18	chr3:159337200-159339000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr3:159337200-159339200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr3:159337200-159339600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr3:159337200-159340000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr3:159337400-159339600	Weak transcription	Left Ventricle	heart
23	chr3:159337400-159339800	Weak transcription	Fetal Stomach	stomach
24	chr3:159337400-159339800	Weak transcription	Right Ventricle	heart
25	chr3:159337600-159338400	Enhancers	A549	lung
26	chr3:159337600-159339800	Weak transcription	Colon Smooth Muscle	Colon
27	chr3:159337600-159342800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr3:159337600-159344200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr3:159337800-159338600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
30	chr3:159337800-159338800	Weak transcription	Fetal Kidney	kidney
31	chr3:159338000-159338600	Enhancers	Brain Anterior Caudate	brain
32	chr3:159338000-159339200	Weak transcription	Liver	Liver
33	chr3:159338000-159339600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr3:159338000-159339600	Enhancers	HMEC	breast
35	chr3:159338000-159340000	Weak transcription	Aorta	Aorta

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