Variant report

Variant	rs26484
Chromosome Location	chr5:96016569-96016570
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:96016371..96018531-chr5:96023831..96025876,2	K562	blood:
2	chr5:96001057..96002966-chr5:96015196..96017728,2	K562	blood:
3	chr5:96001506..96003727-chr5:96014793..96017258,2	MCF-7	breast:

Extended variants
information (count: 34 )
Associated
traits (count: 15 )

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10045215	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10067766	0.85[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs10075736	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1421911	0.85[CHB][hapmap];0.95[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.92[ASN][1000 genomes]
rs151835	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs151904	1.00[JPT][hapmap]
rs152005	1.00[ASW][hapmap];0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs152014	0.93[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs152017	0.89[CHB][hapmap];0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs152020	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2351245	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs26482	0.95[CHB][hapmap];0.95[CHD][hapmap];0.80[GIH][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs26483	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs26485	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs26503	1.00[JPT][hapmap]
rs26504	1.00[JPT][hapmap]
rs28040	0.92[ASN][1000 genomes]
rs28093	0.83[CHB][hapmap];0.85[CHD][hapmap];0.86[JPT][hapmap]
rs28104	0.83[CHB][hapmap];0.86[JPT][hapmap]
rs31248	0.81[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs31249	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs31250	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4267886	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4590196	0.85[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs6556937	0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs6860934	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs6897588	0.85[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7704167	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7705824	0.90[CHD][hapmap];0.80[GIH][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs7733671	0.95[CHB][hapmap];0.95[CHD][hapmap];0.80[GIH][hapmap];1.00[JPT][hapmap];0.92[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	nsv1024964	chr5:95742124-96065492	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
2	nsv537811	chr5:95742124-96065492	Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
3	nsv1015173	chr5:95987366-96153392	Genic enhancers Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
4	nsv432755	chr5:95987984-96657483	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases

mRNA abundance (count:15)

SNP	Gene	Cis/trans	Tissue	Source
rs26484	CAST	cis	parietal	SCAN
rs26484	CTC-506B8.1	cis	Whole Blood	GTEx
rs26484	CAST	cis	Adipose Subcutaneous	GTEx
rs26484	CAST	cis	Nerve Tibial	GTEx
rs26484	CAST	cis	lymphoblastoid	seeQTL
rs26484	CAST	cis	multi-tissue	Pritchard
rs26484	CTC-506B8.1	cis	Adipose Subcutaneous	GTEx
rs26484	CTC-506B8.1	cis	Artery Tibial	GTEx
rs26484	CAST	cis	Esophagus Muscularis	GTEx
rs26484	CAST	Cis_1M	lymphoblastoid	RTeQTL
rs26484	CAST	cis	Whole Blood	GTEx
rs26484	CTC-506B8.1	cis	Esophagus Muscularis	GTEx
rs26484	CAST	cis	lung	GTEx
rs26484	CAST	cis	cerebellum	SCAN
rs26484	CAST	cis	Artery Tibial	GTEx

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:95999400-96018200	Weak transcription	Fetal Muscle Trunk	muscle
2	chr5:95999400-96038000	Weak transcription	Fetal Stomach	stomach
3	chr5:95999600-96016600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr5:95999600-96016600	Weak transcription	HSMMtube	muscle
5	chr5:95999600-96026000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr5:95999600-96028200	Weak transcription	Aorta	Aorta
7	chr5:95999600-96037800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr5:95999600-96038000	Weak transcription	Fetal Lung	lung
9	chr5:95999800-96022800	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr5:95999800-96024600	Weak transcription	Fetal Heart	heart
11	chr5:96000400-96018400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr5:96000800-96037600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr5:96001600-96037000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr5:96002400-96018400	Weak transcription	Psoas Muscle	Psoas
15	chr5:96002400-96027800	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr5:96002400-96037600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr5:96002400-96038200	Weak transcription	Esophagus	oesophagus
18	chr5:96003000-96022800	Weak transcription	Stomach Smooth Muscle	stomach
19	chr5:96004800-96028200	Weak transcription	Lung	lung
20	chr5:96004800-96036600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr5:96005000-96038000	Weak transcription	Ovary	ovary
22	chr5:96005000-96038200	Weak transcription	Gastric	stomach
23	chr5:96005600-96021400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr5:96005600-96027800	Weak transcription	Left Ventricle	heart
25	chr5:96007400-96016600	Weak transcription	Right Atrium	heart
26	chr5:96007400-96018200	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr5:96007400-96018400	Weak transcription	Colonic Mucosa	Colon
28	chr5:96007400-96022200	Weak transcription	Right Ventricle	heart
29	chr5:96007400-96025400	Weak transcription	Pancreas	Pancrea
30	chr5:96007600-96027800	Weak transcription	Fetal Intestine Large	intestine
31	chr5:96008000-96018000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr5:96009200-96037600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr5:96011000-96017000	Strong transcription	Primary T cells fromperipheralblood	blood
34	chr5:96012000-96026400	Weak transcription	NHLF	lung
35	chr5:96012200-96021400	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr5:96012200-96022800	Weak transcription	HUVEC	blood vessel
37	chr5:96012400-96023400	Weak transcription	Primary T cells from cord blood	blood
38	chr5:96013000-96016800	Strong transcription	Duodenum Mucosa	Duodenum
39	chr5:96013000-96037800	Weak transcription	Primary hematopoietic stem cells	blood
40	chr5:96013400-96021800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr5:96013400-96022400	Weak transcription	Primary T helper cells PMA-I stimulated	--
42	chr5:96013600-96031400	Weak transcription	Stomach Mucosa	stomach
43	chr5:96013800-96018400	Weak transcription	NHDF-Ad	bronchial
44	chr5:96013800-96021200	Weak transcription	Placenta	Placenta
45	chr5:96013800-96022400	Weak transcription	Small Intestine	intestine
46	chr5:96013800-96037600	Weak transcription	Rectal Smooth Muscle	rectum
47	chr5:96014000-96023200	Weak transcription	Liver	Liver
48	chr5:96014000-96030800	Weak transcription	HSMM	muscle
49	chr5:96014800-96016800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr5:96014800-96027400	Weak transcription	Fetal Intestine Small	intestine

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