Variant report

Variant	rs17763641
Chromosome Location	chr6:71498546-71498547
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10447360	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1084382	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1084385	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1084386	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1333966	1.00[LWK][hapmap]
rs1413353	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs2347624	1.00[CHB][hapmap]
rs2460694	1.00[ASN][1000 genomes]
rs2504742	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs2504746	1.00[ASN][1000 genomes]
rs4235862	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6455381	1.00[ASN][1000 genomes]
rs7740106	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7750570	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs782003	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs9294880	1.00[ASN][1000 genomes]
rs9346399	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs9446297	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932111	chr6:70736835-71633094	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer 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 target site	31 gene(s)	inside rSNPs	diseases
2	nsv1027049	chr6:70961610-71561488	Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv524328	chr6:70961833-71558805	Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv917312	chr6:70961903-71601688	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:71444800-71523600	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr6:71447800-71500600	Weak transcription	Brain Cingulate Gyrus	brain
3	chr6:71466400-71508800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr6:71468800-71532200	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr6:71473000-71515600	Weak transcription	Left Ventricle	heart
6	chr6:71473800-71520200	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr6:71474600-71568800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr6:71474800-71515000	Weak transcription	Duodenum Mucosa	Duodenum
9	chr6:71475000-71515200	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr6:71481800-71515000	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr6:71482200-71515600	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr6:71483000-71515200	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr6:71487600-71515600	Weak transcription	Thymus	Thymus
14	chr6:71489000-71506000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr6:71489000-71517400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr6:71489000-71521800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr6:71489200-71517800	Weak transcription	Fetal Thymus	thymus
18	chr6:71489400-71515000	Weak transcription	Liver	Liver
19	chr6:71489600-71515600	Weak transcription	Primary T cells from cord blood	blood
20	chr6:71490400-71515600	Weak transcription	Pancreas	Pancrea
21	chr6:71491800-71526200	Weak transcription	HSMM	muscle
22	chr6:71492000-71504000	Weak transcription	Primary B cells from cord blood	blood
23	chr6:71492000-71522200	Weak transcription	Brain Angular Gyrus	brain
24	chr6:71492400-71508800	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr6:71492400-71563600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr6:71492800-71515600	Weak transcription	Aorta	Aorta
27	chr6:71493000-71515600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr6:71493000-71526000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr6:71493200-71502000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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