Variant report

Variant	rs11758187
Chromosome Location	chr6:149215090-149215091
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10499259	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11756841	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11757486	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11758175	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11758230	0.99[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11759833	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1340498	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1340499	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1351698	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1351699	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1545840	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1545841	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1545842	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17079511	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1817508	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34443186	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35526080	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35748463	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35946167	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56904209	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62426104	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62426110	0.99[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][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	nsv1032690	chr6:149206106-149398712	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv464074	chr6:149211090-149242095	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv604844	chr6:149211090-149242095	Enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149193200-149218800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr6:149199400-149215600	Weak transcription	Spleen	Spleen
3	chr6:149207800-149219400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr6:149207800-149221400	Weak transcription	Primary hematopoietic stem cells	blood
5	chr6:149207800-149237400	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr6:149208000-149217200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr6:149208000-149229800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr6:149209000-149247600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr6:149209800-149230800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr6:149210000-149218000	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr6:149210000-149220800	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr6:149210200-149230200	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr6:149210200-149240200	Weak transcription	Primary B cells from cord blood	blood
14	chr6:149210400-149226200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr6:149210400-149235000	Weak transcription	Primary B cells from peripheral blood	blood
16	chr6:149210800-149226000	Weak transcription	Esophagus	oesophagus
17	chr6:149211000-149216600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr6:149211000-149221000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr6:149211000-149221400	Weak transcription	Lung	lung
20	chr6:149211600-149226400	Weak transcription	Left Ventricle	heart
21	chr6:149211600-149255400	Weak transcription	Stomach Smooth Muscle	stomach
22	chr6:149212200-149230200	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr6:149212600-149219800	Weak transcription	Ovary	ovary
24	chr6:149212600-149222200	Weak transcription	Aorta	Aorta
25	chr6:149212600-149225000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr6:149212800-149216800	Weak transcription	Stomach Mucosa	stomach
27	chr6:149213200-149233400	Weak transcription	Fetal Heart	heart
28	chr6:149213400-149222400	Weak transcription	Gastric	stomach
29	chr6:149214400-149215400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr6:149214800-149215200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr6:149214800-149215200	Strong transcription	Fetal Stomach	stomach
32	chr6:149215000-149215200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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