Variant report

Variant	rs1879149
Chromosome Location	chr8:120931825-120931826
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 87 )
Associated
traits (count: 13 )

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs10092845	0.83[EUR][1000 genomes]
rs10099088	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10102995	0.95[CEU][hapmap];1.00[JPT][hapmap]
rs10955942	0.85[EUR][1000 genomes]
rs11984773	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs11984866	0.86[CEU][hapmap];1.00[CHB][hapmap];0.85[EUR][1000 genomes]
rs11998247	0.87[CEU][hapmap];1.00[JPT][hapmap]
rs12541326	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12541733	1.00[CHB][hapmap]
rs12543242	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12545586	0.86[EUR][1000 genomes]
rs12548248	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12677306	1.00[CEU][hapmap];0.82[YRI][hapmap];0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12679478	0.95[CEU][hapmap];0.81[YRI][hapmap];0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13263147	0.86[EUR][1000 genomes]
rs13265513	1.00[CEU][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13265734	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13277786	0.90[EUR][1000 genomes]
rs13278508	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13280041	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs16893299	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2002377	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2017310	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2056305	1.00[CEU][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2139430	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2139431	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2176750	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2326432	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28461628	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28546392	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28600928	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35362581	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4073559	0.92[CEU][hapmap];0.85[EUR][1000 genomes]
rs4455866	0.82[ASN][1000 genomes]
rs4871010	0.91[CEU][hapmap];0.86[EUR][1000 genomes]
rs4871011	0.91[CEU][hapmap];0.86[EUR][1000 genomes]
rs4871786	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4871793	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4871795	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56177421	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62528673	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62528677	0.85[EUR][1000 genomes]
rs62528692	0.83[EUR][1000 genomes]
rs6469860	0.85[EUR][1000 genomes]
rs6469866	1.00[CEU][hapmap];0.81[YRI][hapmap];0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6469869	0.83[EUR][1000 genomes]
rs6469873	0.80[EUR][1000 genomes]
rs6469875	1.00[CEU][hapmap];0.96[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6469876	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6995862	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs6996081	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs6999911	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7000068	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7000488	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7004324	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7005888	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7007672	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7018038	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7388491	0.91[CEU][hapmap];0.87[EUR][1000 genomes]
rs7461170	0.90[CEU][hapmap];1.00[CHB][hapmap];0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7462839	0.85[AFR][1000 genomes]
rs7813263	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs7813430	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7823280	0.92[CEU][hapmap]
rs7838578	0.86[EUR][1000 genomes]
rs7845043	0.87[EUR][1000 genomes]
rs869340	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs869341	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9297607	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9649948	0.91[CEU][hapmap];0.85[EUR][1000 genomes]
rs9649949	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9987135	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9987139	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9987140	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9987142	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9987165	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9987297	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949368	chr8:120568034-121019872	Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv1021071	chr8:120589963-120968317	Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv891418	chr8:120600965-121301474	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
4	nsv465789	chr8:120636850-120994394	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
5	nsv612111	chr8:120636850-120994394	Flanking Active TSS Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
6	nsv427826	chr8:120642181-120953395	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
7	nsv1027974	chr8:120885478-121079658	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv539739	chr8:120885478-121079658	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv972194	chr8:120898451-120965081	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	nsv1018953	chr8:120910380-120954832	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:13)

SNP	Gene	Cis/trans	Tissue	Source
rs1879149	DSCC1	cis	Artery Tibial	GTEx
rs1879149	DEPDC6	cis	uninvolved skin	skin_eQTL
rs1879149	DSCC1	cis	Esophagus Muscularis	GTEx
rs1879149	DSCC1	cis	Nerve Tibial	GTEx
rs1879149	DEPTOR	cis	Esophagus Muscularis	GTEx
rs1879149	DSCC1	cis	Skin Sun Exposed Lower leg	GTEx
rs1879149	DSCC1	cis	Muscle Skeletal	GTEx
rs1879149	DSCC1	cis	lung	GTEx
rs1879149	DSCC1	cis	Thyroid	GTEx
rs1879149	DSCC1	cis	Artery Aorta	GTEx
rs1879149	DSCC1	cis	Adipose Subcutaneous	GTEx
rs1879149	DEPDC6	cis	lesional skin	skin_eQTL
rs1879149	DSCC1	cis	Cerebellum	GTEx

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:120920800-120932800	Weak transcription	Fetal Muscle Trunk	muscle
2	chr8:120923000-120935400	Enhancers	Stomach Mucosa	stomach
3	chr8:120923600-120932800	Weak transcription	Lung	lung
4	chr8:120925000-120932400	Weak transcription	Right Ventricle	heart
5	chr8:120925000-120932600	Weak transcription	Esophagus	oesophagus
6	chr8:120925200-120932600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr8:120926200-120932600	Weak transcription	Gastric	stomach
8	chr8:120926200-120944400	Weak transcription	Primary T cells from cord blood	blood
9	chr8:120927000-120933000	Enhancers	HepG2	liver
10	chr8:120927000-120934000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr8:120927200-120933200	Enhancers	Fetal Intestine Large	intestine
12	chr8:120927400-120933400	Enhancers	Fetal Intestine Small	intestine
13	chr8:120927600-120933000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr8:120927600-120933000	Enhancers	Duodenum Mucosa	Duodenum
15	chr8:120927600-120933200	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr8:120928400-120933600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr8:120928600-120933000	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr8:120928600-120933200	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr8:120928600-120933400	Enhancers	Fetal Muscle Leg	muscle
20	chr8:120928800-120933200	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr8:120929400-120932000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr8:120929800-120932800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr8:120930000-120932600	Weak transcription	Left Ventricle	heart
24	chr8:120930200-120932400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr8:120930200-120933000	Enhancers	Colonic Mucosa	Colon
26	chr8:120930400-120932200	Enhancers	Brain Hippocampus Middle	brain
27	chr8:120930400-120932400	Enhancers	Brain Angular Gyrus	brain
28	chr8:120930400-120933200	Enhancers	Primary hematopoietic stem cells	blood
29	chr8:120930600-120932400	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr8:120930600-120932400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr8:120931000-120933000	Enhancers	Colon Smooth Muscle	Colon
32	chr8:120931000-120933200	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr8:120931000-120933200	Enhancers	Liver	Liver
34	chr8:120931000-120933200	Enhancers	Fetal Brain Male	brain
35	chr8:120931000-120933200	Enhancers	Rectal Smooth Muscle	rectum
36	chr8:120931200-120932400	Enhancers	Brain Anterior Caudate	brain
37	chr8:120931200-120932400	Enhancers	Brain Cingulate Gyrus	brain
38	chr8:120931200-120932600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr8:120931200-120932600	Weak transcription	Pancreas	Pancrea
40	chr8:120931200-120932600	Weak transcription	Psoas Muscle	Psoas
41	chr8:120931200-120932800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr8:120931200-120933000	Enhancers	Duodenum Smooth Muscle	Duodenum
43	chr8:120931200-120933200	Enhancers	Adipose Nuclei	Adipose
44	chr8:120931400-120932600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr8:120931400-120933000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr8:120931400-120933200	Enhancers	Fetal Stomach	stomach
47	chr8:120931600-120932000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
48	chr8:120931600-120932400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr8:120931600-120932400	Enhancers	Ovary	ovary
50	chr8:120931600-120932800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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