Variant report

Variant	rs9487193
Chromosome Location	chr6:110030579-110030580
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1303981	0.82[AMR][1000 genomes]
rs13437149	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17070874	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2076929	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2295835	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2295836	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3823235	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6568587	0.91[AMR][1000 genomes]
rs6900091	1.00[AMR][1000 genomes]
rs6917383	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6917713	0.82[AMR][1000 genomes]
rs6925005	0.91[AMR][1000 genomes]
rs73535341	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7356790	1.00[AMR][1000 genomes]
rs7740192	1.00[AMR][1000 genomes]
rs7742066	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7743159	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7749605	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7753555	0.86[AMR][1000 genomes]
rs7765916	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7767805	0.90[AMR][1000 genomes]
rs7768577	0.82[AMR][1000 genomes]
rs7775092	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs927127	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs9372225	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9372226	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9374117	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9374121	0.85[ASN][1000 genomes]
rs9386817	0.82[AMR][1000 genomes]
rs9386833	1.00[AMR][1000 genomes]
rs9386835	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9386842	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9398214	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9398215	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9480990	0.90[AMR][1000 genomes]
rs9487186	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9487203	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949475	chr6:109907936-110160501	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv933105	chr6:109933270-110064342	ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
3	nsv817322	chr6:109933272-110070574	Strong transcription Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv830769	chr6:109944334-110078120	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv604485	chr6:109959269-110054486	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:110013000-110057000	Weak transcription	Left Ventricle	heart
2	chr6:110013000-110114400	Weak transcription	Right Ventricle	heart
3	chr6:110013200-110034000	Weak transcription	Fetal Stomach	stomach
4	chr6:110013200-110057000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr6:110013200-110057000	Weak transcription	Aorta	Aorta
6	chr6:110013400-110038600	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr6:110013600-110056000	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr6:110013600-110056800	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr6:110014000-110034400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr6:110014800-110034200	Weak transcription	Fetal Intestine Small	intestine
11	chr6:110018800-110034200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr6:110024200-110038800	Weak transcription	Thymus	Thymus
13	chr6:110024200-110056400	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr6:110025000-110034400	Weak transcription	Lung	lung
15	chr6:110025000-110057000	Weak transcription	Fetal Thymus	thymus
16	chr6:110027000-110038200	Weak transcription	Stomach Smooth Muscle	stomach
17	chr6:110027000-110040400	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr6:110027000-110052400	Weak transcription	Liver	Liver
19	chr6:110027000-110056400	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr6:110027600-110038600	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr6:110027800-110034200	Weak transcription	Spleen	Spleen
22	chr6:110027800-110038200	Weak transcription	Placenta	Placenta
23	chr6:110028000-110034200	Weak transcription	Brain Hippocampus Middle	brain
24	chr6:110028000-110036800	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr6:110028000-110038000	Weak transcription	Colon Smooth Muscle	Colon
26	chr6:110028000-110044000	Weak transcription	Brain Angular Gyrus	brain
27	chr6:110028000-110071200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr6:110028200-110032800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr6:110028200-110034400	Weak transcription	Brain Cingulate Gyrus	brain
30	chr6:110028200-110034600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr6:110028200-110034600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr6:110028200-110036200	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr6:110028200-110036200	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr6:110028200-110036800	Weak transcription	Adipose Nuclei	Adipose
35	chr6:110028200-110037600	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr6:110028200-110057200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr6:110028200-110080800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr6:110028400-110031000	Weak transcription	Primary B cells from cord blood	blood
39	chr6:110028400-110034200	Weak transcription	Primary T cells from cord blood	blood
40	chr6:110028400-110034200	Weak transcription	Brain Substantia Nigra	brain
41	chr6:110028400-110035000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr6:110029000-110036600	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr6:110030000-110035400	Weak transcription	Primary B cells from peripheral blood	blood

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