Variant report

Variant	rs3731746
Chromosome Location	chr2:179430997-179430998
allele	A/C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs1007025	0.83[CEU][hapmap];0.84[GIH][hapmap]
rs12614435	0.91[CEU][hapmap];0.96[TSI][hapmap];0.89[EUR][1000 genomes]
rs12618265	0.83[CEU][hapmap];0.81[GIH][hapmap]
rs12998857	0.91[CEU][hapmap];0.90[TSI][hapmap]
rs1429094	0.84[EUR][1000 genomes]
rs1560221	0.81[JPT][hapmap]
rs16866373	0.83[CEU][hapmap]
rs16866397	0.83[CEU][hapmap];0.87[GIH][hapmap]
rs16866400	0.90[GIH][hapmap];0.81[JPT][hapmap]
rs16866406	0.83[CEU][hapmap];0.81[GIH][hapmap]
rs16866418	1.00[CHB][hapmap];0.91[CHD][hapmap];0.90[GIH][hapmap];0.80[TSI][hapmap];0.89[EUR][1000 genomes]
rs16866420	0.81[JPT][hapmap]
rs2042996	0.85[JPT][hapmap]
rs2129110	0.85[TSI][hapmap]
rs2163009	0.81[JPT][hapmap]
rs2288325	0.83[CEU][hapmap]
rs2288327	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2288569	0.81[GIH][hapmap]
rs2288571	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2303828	0.84[TSI][hapmap]
rs2303838	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];0.81[TSI][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2366751	0.81[JPT][hapmap]
rs2857265	0.83[CEU][hapmap];0.87[GIH][hapmap]
rs35112591	0.83[EUR][1000 genomes]
rs35504893	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3731748	0.83[CEU][hapmap];0.84[GIH][hapmap]
rs3731749	0.83[CEU][hapmap];0.87[GIH][hapmap]
rs3731750	0.85[JPT][hapmap]
rs3813250	0.81[JPT][hapmap]
rs3829746	0.81[JPT][hapmap]
rs3829747	0.83[CEU][hapmap];0.87[GIH][hapmap]
rs3829748	0.83[CEU][hapmap];0.87[GIH][hapmap]
rs4894029	0.81[JPT][hapmap]
rs6755456	0.91[CEU][hapmap]
rs744426	0.83[CEU][hapmap];0.87[GIH][hapmap]
rs7597154	0.83[CEU][hapmap]
rs890578	0.87[ASW][hapmap];0.91[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs957875	0.85[JPT][hapmap]
rs9808377	0.81[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834468	chr2:179351116-179533625	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	esv2757841	chr2:179409072-179608242	Active TSS ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	esv2759103	chr2:179409072-179608242	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:179388800-179441800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr2:179388800-179448800	Weak transcription	Small Intestine	intestine
3	chr2:179388800-179495800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr2:179393800-179439800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:179396000-179445400	Strong transcription	Right Ventricle	heart
6	chr2:179396600-179432400	Weak transcription	Fetal Kidney	kidney
7	chr2:179408000-179503000	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr2:179408200-179436200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr2:179409200-179439200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr2:179411000-179440000	Weak transcription	Brain Hippocampus Middle	brain
11	chr2:179411000-179466000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr2:179411200-179440200	Weak transcription	Colonic Mucosa	Colon
13	chr2:179412000-179441000	Weak transcription	Brain Cingulate Gyrus	brain
14	chr2:179413200-179435000	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr2:179413400-179437400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr2:179413600-179438200	Weak transcription	Duodenum Mucosa	Duodenum
17	chr2:179413600-179438800	Weak transcription	Brain Anterior Caudate	brain
18	chr2:179413600-179440000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr2:179413800-179436800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr2:179414000-179439000	Weak transcription	Brain Angular Gyrus	brain
21	chr2:179414000-179443400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr2:179414200-179431200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr2:179414200-179434800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr2:179414200-179435200	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr2:179414200-179439200	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr2:179414800-179471800	Weak transcription	Brain Substantia Nigra	brain
27	chr2:179417600-179434800	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr2:179417800-179441800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr2:179418200-179443200	Weak transcription	NHLF	lung
30	chr2:179418400-179439000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr2:179418400-179450200	Strong transcription	HSMMtube	muscle
32	chr2:179418600-179434200	Weak transcription	Osteobl	bone
33	chr2:179419600-179435400	Weak transcription	Primary T cells fromperipheralblood	blood
34	chr2:179422600-179434600	Weak transcription	HSMM	muscle
35	chr2:179424000-179442200	Genic enhancers	Skeletal Muscle Female	skeletal muscle
36	chr2:179424200-179442400	Strong transcription	Ovary	ovary
37	chr2:179424600-179443000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
38	chr2:179424800-179443000	ZNF genes & repeats	Primary T cells from cord blood	blood
39	chr2:179424800-179445200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr2:179425800-179440400	ZNF genes & repeats	Fetal Muscle Leg	muscle
41	chr2:179425800-179446800	Strong transcription	Primary neutrophils fromperipheralblood	blood
42	chr2:179426200-179442200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
43	chr2:179426400-179437200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr2:179427200-179433400	Strong transcription	Fetal Muscle Trunk	muscle
45	chr2:179427600-179431000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr2:179427600-179433200	ZNF genes & repeats	Primary B cells from peripheral blood	blood
47	chr2:179427600-179433200	Strong transcription	Psoas Muscle	Psoas
48	chr2:179427800-179433400	Strong transcription	Fetal Intestine Large	intestine
49	chr2:179427800-179443800	Strong transcription	Duodenum Smooth Muscle	Duodenum
50	chr2:179428000-179442200	Strong transcription	Liver	Liver

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