Variant report

Variant	rs3845779
Chromosome Location	chr2:37189123-37189124
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:37183461..37185242-chr2:37187560..37189178,2	MCF-7	breast:
2	chr2:37186145..37190956-chr2:37191183..37194668,5	K562	blood:

Variant related genes	Relation type
ENSG00000115808	Chromatin interaction

Extended variants
information (count: 78 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs1008838	0.86[CHB][hapmap]
rs10166161	0.93[ASN][1000 genomes]
rs10182741	1.00[CHB][hapmap];0.89[ASN][1000 genomes]
rs10185737	0.91[ASN][1000 genomes]
rs10189328	1.00[CHB][hapmap]
rs10189918	0.89[ASN][1000 genomes]
rs10201963	1.00[CHB][hapmap];0.82[ASN][1000 genomes]
rs10202311	0.93[ASN][1000 genomes]
rs10209808	0.89[ASN][1000 genomes]
rs10490659	1.00[CHB][hapmap];0.93[CHD][hapmap]
rs10495868	1.00[CHB][hapmap]
rs10865120	0.86[CHB][hapmap]
rs11124552	1.00[CHB][hapmap];0.93[CHD][hapmap];0.81[ASN][1000 genomes]
rs11674211	1.00[CHB][hapmap];0.89[ASN][1000 genomes]
rs11675109	1.00[CHB][hapmap]
rs11676225	1.00[CHB][hapmap];0.93[CHD][hapmap]
rs11678303	1.00[CHB][hapmap]
rs11682966	1.00[CHB][hapmap];0.93[CHD][hapmap]
rs11685600	0.93[ASN][1000 genomes]
rs11686605	0.84[ASN][1000 genomes]
rs11691236	0.88[ASN][1000 genomes]
rs11887829	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11904023	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12328274	0.82[ASN][1000 genomes]
rs12479195	1.00[CHB][hapmap]
rs12616770	0.88[ASN][1000 genomes]
rs12624290	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs13385627	0.81[ASN][1000 genomes]
rs13385823	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13401327	1.00[CHB][hapmap]
rs13413438	1.00[CHB][hapmap];0.89[ASN][1000 genomes]
rs13424317	0.86[ASN][1000 genomes]
rs17020005	1.00[CHB][hapmap]
rs17020069	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs17020072	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs17020074	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs17020084	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs1861433	1.00[CHB][hapmap]
rs1861436	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs2216106	0.82[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap]
rs2540919	0.86[CHB][hapmap]
rs2541000	0.86[CHB][hapmap]
rs2691104	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs2691109	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs2691110	1.00[CHB][hapmap]
rs2691114	1.00[CHB][hapmap]
rs2691115	1.00[CHB][hapmap]
rs2691116	1.00[CHB][hapmap]
rs2691118	1.00[CHB][hapmap]
rs2717494	1.00[CHB][hapmap]
rs2717501	1.00[CHB][hapmap]
rs2717505	1.00[CHB][hapmap];0.82[CHD][hapmap]
rs2717509	1.00[CHB][hapmap]
rs2717510	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs2717511	1.00[CHB][hapmap]
rs2717512	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs2717518	1.00[CHB][hapmap]
rs2717522	0.82[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap]
rs28718824	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs35622893	0.81[ASN][1000 genomes]
rs3770775	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.96[GIH][hapmap];0.95[TSI][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs41486347	1.00[CHB][hapmap];0.93[CHD][hapmap]
rs4635515	1.00[CHB][hapmap]
rs4670651	0.86[CHB][hapmap]
rs59854977	0.89[ASN][1000 genomes]
rs6544048	0.81[CEU][hapmap]
rs723673	1.00[CHB][hapmap]
rs73924949	0.91[ASN][1000 genomes]
rs73924952	0.89[ASN][1000 genomes]
rs7562109	0.85[CHB][hapmap];0.86[CHD][hapmap]
rs7579735	0.81[ASN][1000 genomes]
rs7581702	1.00[CHB][hapmap]
rs998321	0.82[ASW][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1004483	chr2:36875235-37356812	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv535644	chr2:36875235-37356812	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv428395	chr2:36990348-37300352	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv456363	chr2:37109281-37235324	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
5	nsv581470	chr2:37109281-37235324	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs3845779	EIF2AK2	cis	parietal	SCAN

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37132400-37192400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr2:37134600-37192400	Weak transcription	Fetal Stomach	stomach
3	chr2:37143400-37191000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr2:37143800-37191800	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr2:37150200-37191800	Weak transcription	Fetal Thymus	thymus
6	chr2:37152400-37191800	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr2:37154600-37191800	Weak transcription	Fetal Intestine Large	intestine
8	chr2:37158200-37192000	Weak transcription	Ovary	ovary
9	chr2:37158600-37191800	Weak transcription	Fetal Lung	lung
10	chr2:37159000-37191800	Weak transcription	Primary hematopoietic stem cells	blood
11	chr2:37165000-37190800	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr2:37165600-37191800	Weak transcription	Fetal Intestine Small	intestine
13	chr2:37166600-37191600	Weak transcription	Dnd41	blood
14	chr2:37168600-37191800	Weak transcription	Thymus	Thymus
15	chr2:37176200-37191800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr2:37178600-37191200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr2:37178600-37191800	Weak transcription	Rectal Smooth Muscle	rectum
18	chr2:37178800-37191600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr2:37178800-37191600	Weak transcription	Duodenum Mucosa	Duodenum
20	chr2:37179000-37190200	Weak transcription	Placenta	Placenta
21	chr2:37179000-37190400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr2:37179000-37190800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr2:37179000-37191600	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr2:37179200-37190800	Weak transcription	Gastric	stomach
25	chr2:37179200-37191200	Weak transcription	HSMMtube	muscle
26	chr2:37179200-37191600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr2:37179200-37191600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr2:37179200-37191600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr2:37179200-37191800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr2:37179200-37191800	Weak transcription	Fetal Muscle Leg	muscle
31	chr2:37179200-37191800	Weak transcription	Right Atrium	heart
32	chr2:37179200-37192000	Weak transcription	HSMM	muscle
33	chr2:37179200-37192800	Weak transcription	Lung	lung
34	chr2:37179400-37191400	Weak transcription	Primary T cells from cord blood	blood
35	chr2:37179400-37191800	Weak transcription	Osteobl	bone
36	chr2:37179600-37191800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr2:37179800-37190000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr2:37180000-37190200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr2:37180000-37191600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr2:37180000-37191600	Weak transcription	HUVEC	blood vessel
41	chr2:37180000-37192000	Weak transcription	Fetal Kidney	kidney
42	chr2:37180200-37190000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr2:37180200-37191800	Weak transcription	Brain Anterior Caudate	brain
44	chr2:37180400-37190200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr2:37180400-37190200	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr2:37180400-37191000	Weak transcription	Primary B cells from peripheral blood	blood
47	chr2:37180400-37191800	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr2:37180400-37191800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr2:37180400-37191800	Weak transcription	Primary B cells from cord blood	blood
50	chr2:37180600-37191800	Weak transcription	A549	lung

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