Variant report

Variant	rs9386028
Chromosome Location	chr6:143539833-143539834
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:143533693..143535662-chr6:143539028..143541980,2	K562	blood:

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10484581	1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs10484582	1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs10484583	1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs12055523	1.00[ASW][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap];1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs12055848	0.85[AMR][1000 genomes]
rs12176429	1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs1424924	1.00[AFR][1000 genomes]
rs1593289	1.00[AFR][1000 genomes]
rs17072283	1.00[JPT][hapmap]
rs17072288	1.00[JPT][hapmap]
rs17072338	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs17072347	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs17072349	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs17072381	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs17072390	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs17072404	1.00[AFR][1000 genomes]
rs17072408	1.00[AFR][1000 genomes]
rs17072410	1.00[AFR][1000 genomes]
rs17072450	1.00[AFR][1000 genomes]
rs17072501	1.00[AFR][1000 genomes]
rs17072541	1.00[AFR][1000 genomes]
rs17072544	1.00[AFR][1000 genomes]
rs17629061	1.00[JPT][hapmap]
rs2328475	1.00[AFR][1000 genomes]
rs4458714	1.00[ASW][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes]
rs4482993	1.00[AFR][1000 genomes]
rs4895603	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes]
rs4895604	1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs4895608	1.00[AFR][1000 genomes]
rs4895610	1.00[AFR][1000 genomes]
rs4896625	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4896630	0.85[AMR][1000 genomes]
rs4896631	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs4896654	1.00[AFR][1000 genomes]
rs6932032	1.00[JPT][hapmap]
rs7452873	1.00[AFR][1000 genomes]
rs7765576	1.00[JPT][hapmap]
rs7769247	1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap];0.92[AMR][1000 genomes]
rs9321895	1.00[JPT][hapmap];0.85[AMR][1000 genomes]
rs9321896	1.00[AFR][1000 genomes]
rs9373380	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9373382	1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs9373383	1.00[AFR][1000 genomes]
rs9376728	1.00[JPT][hapmap]
rs9376732	1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs9376733	1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs9376734	1.00[JPT][hapmap];1.00[AFR][1000 genomes]
rs9376735	1.00[JPT][hapmap];1.00[AFR][1000 genomes]
rs9376736	0.83[GIH][hapmap]
rs9386029	1.00[JPT][hapmap];0.85[AMR][1000 genomes]
rs9390062	1.00[JPT][hapmap]
rs9390071	1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs9399431	1.00[AFR][1000 genomes]
rs9403453	1.00[JPT][hapmap]
rs9403454	1.00[JPT][hapmap]
rs9403465	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9403467	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9403469	1.00[ASW][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs9403470	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs9403471	1.00[JPT][hapmap];1.00[AFR][1000 genomes]
rs9403472	1.00[JPT][hapmap];1.00[AFR][1000 genomes]
rs9403473	1.00[AFR][1000 genomes]
rs9403474	1.00[JPT][hapmap];1.00[AFR][1000 genomes]
rs9403476	1.00[JPT][hapmap];1.00[AFR][1000 genomes]

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	esv275228	chr6:143539833-143549921	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:143514200-143545400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr6:143514400-143545200	Weak transcription	HMEC	breast
3	chr6:143516000-143545600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr6:143525600-143544200	Weak transcription	HepG2	liver
5	chr6:143525800-143545800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr6:143527400-143552000	Weak transcription	Brain Angular Gyrus	brain
7	chr6:143527400-143578800	Weak transcription	Brain Hippocampus Middle	brain
8	chr6:143533800-143542000	Weak transcription	Colon Smooth Muscle	Colon
9	chr6:143535000-143540400	Weak transcription	Fetal Intestine Large	intestine
10	chr6:143535000-143540600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:143535000-143541000	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr6:143535000-143541000	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr6:143535000-143541000	Weak transcription	Fetal Intestine Small	intestine
14	chr6:143535000-143541600	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr6:143535000-143541600	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr6:143535000-143544200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr6:143535000-143544200	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr6:143535000-143545200	Weak transcription	Pancreas	Pancrea
19	chr6:143535000-143549600	Weak transcription	Lung	lung
20	chr6:143535000-143551000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr6:143535000-143568000	Weak transcription	Aorta	Aorta
22	chr6:143536000-143543000	Weak transcription	Ovary	ovary
23	chr6:143536000-143543000	Weak transcription	Right Atrium	heart
24	chr6:143536200-143546000	Weak transcription	Right Ventricle	heart
25	chr6:143536600-143542800	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr6:143537000-143543000	Weak transcription	Fetal Muscle Leg	muscle
27	chr6:143537600-143542000	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr6:143537600-143542800	Weak transcription	Fetal Lung	lung
29	chr6:143537800-143542000	Weak transcription	Rectal Smooth Muscle	rectum
30	chr6:143537800-143542400	Weak transcription	Stomach Smooth Muscle	stomach
31	chr6:143537800-143547200	Strong transcription	K562	blood
32	chr6:143538000-143540400	Weak transcription	Left Ventricle	heart
33	chr6:143538000-143542400	Weak transcription	Fetal Stomach	stomach
34	chr6:143538000-143542400	Weak transcription	Psoas Muscle	Psoas
35	chr6:143538000-143542600	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr6:143539000-143543200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr6:143539400-143542000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr6:143539600-143540200	Strong transcription	Liver	Liver
39	chr6:143539800-143542800	Enhancers	Fetal Heart	heart

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