Variant report

Variant	rs2691565
Chromosome Location	chr7:17951236-17951237
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:17882358..17885096-chr7:17950396..17953115,2	K562	blood:

Extended variants
information (count: 54 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10216315	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10227224	0.84[ASN][1000 genomes]
rs10227582	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10265373	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11983260	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1568815	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1568817	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1568818	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2691558	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2691560	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2691561	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2691562	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2691563	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2691564	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2691566	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2691567	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2691568	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2691569	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2691570	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2691571	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2691572	0.80[AMR][1000 genomes]
rs2691577	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2691578	0.83[ASN][1000 genomes]
rs2691579	0.81[ASN][1000 genomes]
rs2691580	0.82[ASN][1000 genomes]
rs2714854	0.80[AMR][1000 genomes]
rs2714855	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2714856	0.80[AMR][1000 genomes]
rs2714857	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2714859	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2714860	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2714861	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2714863	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2714864	0.88[ASN][1000 genomes]
rs2714865	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2714866	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2714867	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2714868	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2714869	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2714870	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2714878	0.90[EUR][1000 genomes]
rs4719525	0.83[ASN][1000 genomes]
rs4721671	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021524	chr7:17251148-17963307	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv533938	chr7:17254118-18040301	Weak transcription Enhancers Flanking Active TSS Strong transcription 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 lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv1024398	chr7:17630148-18545073	Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
4	nsv538764	chr7:17630148-18545073	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
5	nsv830913	chr7:17848480-18034218	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv1026629	chr7:17862477-18362404	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
7	nsv1025023	chr7:17865796-18357630	Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
8	nsv1030201	chr7:17898410-18491985	Enhancers Strong transcription Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
9	nsv887808	chr7:17920613-18150005	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
10	nsv1018517	chr7:17926468-18127372	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
11	nsv606357	chr7:17938491-18375245	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2691565	SNX13	cis	Adipose Subcutaneous	GTEx

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:17900400-17956600	Weak transcription	A549	lung
2	chr7:17903600-17953000	Weak transcription	Thymus	Thymus
3	chr7:17907200-17954800	Weak transcription	Spleen	Spleen
4	chr7:17911400-17977400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr7:17913000-17955800	Weak transcription	K562	blood
6	chr7:17927200-17955000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr7:17929200-17951400	Weak transcription	Fetal Intestine Large	intestine
8	chr7:17929200-17952200	Weak transcription	Fetal Muscle Leg	muscle
9	chr7:17929800-17951600	Weak transcription	Fetal Thymus	thymus
10	chr7:17929800-17954000	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr7:17930000-17952400	Weak transcription	Primary B cells from peripheral blood	blood
12	chr7:17930200-17951800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr7:17930200-17954200	Weak transcription	Placenta	Placenta
14	chr7:17938200-17951800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr7:17938800-17952800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr7:17941000-17951600	Weak transcription	Right Ventricle	heart
17	chr7:17941000-17952400	Weak transcription	Ovary	ovary
18	chr7:17941200-17952400	Weak transcription	Gastric	stomach
19	chr7:17941400-17958400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr7:17942800-17951800	Weak transcription	Left Ventricle	heart
21	chr7:17942800-17954800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr7:17942800-17954800	Weak transcription	Pancreas	Pancrea
23	chr7:17943200-17952400	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr7:17943400-17951400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr7:17943800-17952400	Weak transcription	Duodenum Mucosa	Duodenum
26	chr7:17943800-17956000	Weak transcription	Primary T cells from cord blood	blood
27	chr7:17944000-17953800	Weak transcription	Liver	Liver
28	chr7:17944000-17955400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr7:17944600-17952000	Weak transcription	Fetal Heart	heart
30	chr7:17944800-17955200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr7:17947000-17955200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr7:17947200-17954800	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr7:17947200-17955400	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr7:17947400-17951800	Weak transcription	Psoas Muscle	Psoas
35	chr7:17947400-17954800	Weak transcription	Small Intestine	intestine
36	chr7:17947400-17956600	Weak transcription	Fetal Lung	lung
37	chr7:17947400-17957400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
38	chr7:17947600-17953600	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr7:17948200-17961000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr7:17948400-17960800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr7:17948600-17962800	Weak transcription	Rectal Smooth Muscle	rectum
42	chr7:17949600-17954800	Weak transcription	Fetal Intestine Small	intestine
43	chr7:17950200-17951600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
44	chr7:17950200-17951800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr7:17950400-17955000	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr7:17950600-17955800	Weak transcription	Primary hematopoietic stem cells	blood
47	chr7:17950800-17951800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr7:17950800-17956800	Weak transcription	Primary B cells from cord blood	blood
49	chr7:17951200-17951600	Weak transcription	HUES64 Cell Line	embryonic stem cell

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