Variant report

Variant	rs10210215
Chromosome Location	chr2:182654171-182654172
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:182653773..182656641-chr2:182670969..182672673,2	K562	blood:
2	chr2:182647541..182657734-chr2:182753295..182760748,23	MCF-7	breast:
3	chr2:182652862..182655320-chr2:182765271..182767272,2	MCF-7	breast:
4	chr2:182653817..182655921-chr2:182755914..182757576,2	K562	blood:
5	chr2:182653727..182657745-chr2:182674412..182677081,4	MCF-7	breast:
6	chr2:182645215..182647741-chr2:182652412..182654174,2	K562	blood:
7	chr2:182646086..182659083-chr2:182754079..182762654,36	MCF-7	breast:
8	chr2:182649909..182651915-chr2:182653150..182656385,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000138434	Chromatin interaction
ENSG00000260742	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10165936	1.00[CEU][hapmap]
rs10166812	1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10173114	1.00[CEU][hapmap]
rs10176061	1.00[CEU][hapmap]
rs10176613	1.00[CEU][hapmap];0.93[CHB][hapmap];0.86[JPT][hapmap];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10176757	1.00[CEU][hapmap]
rs10179363	1.00[CEU][hapmap];0.81[AFR][1000 genomes]
rs10179547	1.00[CEU][hapmap]
rs10199645	1.00[CEU][hapmap]
rs10200243	1.00[CEU][hapmap]
rs10201303	1.00[CEU][hapmap]
rs10221891	1.00[CEU][hapmap]
rs13404156	1.00[CEU][hapmap]
rs13425734	1.00[CEU][hapmap]
rs1528024	1.00[CEU][hapmap]
rs1528025	1.00[CEU][hapmap]
rs1528027	1.00[CEU][hapmap]
rs16867498	1.00[CEU][hapmap]
rs16867509	1.00[CEU][hapmap]
rs1881158	1.00[CEU][hapmap]
rs1881159	1.00[CEU][hapmap];0.85[YRI][hapmap];0.84[AFR][1000 genomes]
rs2059702	1.00[CEU][hapmap]
rs2288330	1.00[CEU][hapmap]
rs2303554	1.00[CEU][hapmap]
rs2368224	1.00[CEU][hapmap];0.92[CHB][hapmap];0.85[JPT][hapmap];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3731693	1.00[CEU][hapmap]
rs3815877	1.00[CEU][hapmap]
rs3815878	1.00[CEU][hapmap]
rs6433943	1.00[CEU][hapmap]
rs6707164	1.00[CEU][hapmap]
rs6720109	1.00[CEU][hapmap]
rs6720702	1.00[CEU][hapmap]
rs6735322	1.00[CEU][hapmap]
rs6736766	1.00[CEU][hapmap]
rs6748354	1.00[CEU][hapmap]
rs6751685	1.00[CEU][hapmap]
rs6754192	1.00[CEU][hapmap]
rs6755017	1.00[CEU][hapmap]
rs7557969	1.00[CEU][hapmap];0.89[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]
rs7562680	1.00[CEU][hapmap]
rs7580410	1.00[CEU][hapmap]
rs7603721	1.00[CEU][hapmap]
rs7608942	1.00[CEU][hapmap]
rs9807949	1.00[CEU][hapmap];0.93[CHB][hapmap];0.86[JPT][hapmap];0.95[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9808112	1.00[CEU][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9808113	0.84[AFR][1000 genomes]

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	nsv1005870	chr2:181968637-182921439	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv536063	chr2:181968637-182921439	Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv1001558	chr2:182590009-182732738	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10210215	LOC647288///LOC730587	trans	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:182642200-182657200	Enhancers	Hela-S3	cervix
2	chr2:182646600-182654800	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr2:182648000-182657200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr2:182648600-182657200	Enhancers	HMEC	breast
5	chr2:182648800-182654600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr2:182648800-182657000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr2:182649200-182656200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr2:182649600-182654800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr2:182649600-182657200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr2:182650000-182655400	Enhancers	NHEK	skin
11	chr2:182650200-182657000	Enhancers	Fetal Intestine Large	intestine
12	chr2:182650800-182654800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr2:182651000-182655600	Weak transcription	HSMMtube	muscle
14	chr2:182651000-182655800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr2:182651200-182656800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr2:182651200-182657000	Enhancers	Primary hematopoietic stem cells	blood
17	chr2:182651200-182657200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr2:182651400-182654800	Weak transcription	HSMM	muscle
19	chr2:182652000-182654600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr2:182652000-182654800	Weak transcription	Pancreas	Pancrea
21	chr2:182652000-182655400	Weak transcription	Placenta	Placenta
22	chr2:182652200-182657400	Enhancers	HUVEC	blood vessel
23	chr2:182652400-182655600	Weak transcription	Fetal Kidney	kidney
24	chr2:182652400-182657200	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr2:182652800-182654200	Weak transcription	Stomach Mucosa	stomach
26	chr2:182652800-182654800	Weak transcription	Thymus	Thymus
27	chr2:182652800-182654800	Weak transcription	K562	blood
28	chr2:182653000-182654800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr2:182653000-182654800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr2:182653200-182654400	Weak transcription	Dnd41	blood
31	chr2:182653200-182654600	Weak transcription	Fetal Thymus	thymus
32	chr2:182653200-182654800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr2:182653400-182654800	Enhancers	Rectal Mucosa Donor 29	rectum
34	chr2:182653400-182656000	Enhancers	Osteobl	bone
35	chr2:182653400-182657400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr2:182653600-182654400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr2:182653600-182655600	Enhancers	Muscle Satellite Cultured Cells	--
38	chr2:182653600-182656400	Enhancers	Liver	Liver
39	chr2:182653600-182657200	Enhancers	NH-A	brain
40	chr2:182653600-182657200	Enhancers	NHDF-Ad	bronchial
41	chr2:182653600-182657200	Enhancers	NHLF	lung
42	chr2:182653600-182657400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr2:182653800-182654800	Weak transcription	Fetal Intestine Small	intestine
44	chr2:182653800-182654800	Enhancers	A549	lung
45	chr2:182653800-182656800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr2:182654000-182654400	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr2:182654000-182654400	Weak transcription	HepG2	liver
48	chr2:182654000-182654800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr2:182654000-182654800	Weak transcription	Duodenum Mucosa	Duodenum

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