Variant report

Variant	rs10939130
Chromosome Location	chr4:26676687-26676688
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:26667642..26669884-chr4:26673933..26676753,2	K562	blood:
2	chr4:26674755..26676897-chr4:26682042..26683729,2	K562	blood:

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10014273	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs10031954	0.95[ASN][1000 genomes]
rs10470786	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10805265	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs11737510	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13117759	0.95[ASN][1000 genomes]
rs13353547	0.95[ASN][1000 genomes]
rs1641558	0.90[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1641560	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1641561	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs166353	1.00[YRI][hapmap];0.90[AMR][1000 genomes]
rs1686374	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1686383	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16878551	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs1994551	0.89[JPT][hapmap]
rs2309414	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs260941	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs260942	1.00[CHB][hapmap];0.82[JPT][hapmap];0.91[ASN][1000 genomes]
rs260944	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs260947	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs260951	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs260954	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs260955	1.00[CHB][hapmap];0.90[JPT][hapmap];0.83[ASN][1000 genomes]
rs4235020	0.95[ASN][1000 genomes]
rs4416469	1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[EUR][1000 genomes]
rs6831895	0.95[ASN][1000 genomes]
rs6833757	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7656543	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7670323	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7672066	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7681685	0.89[AMR][1000 genomes]
rs7690923	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9997756	0.95[ASN][1000 genomes]
rs9997999	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][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	nsv522423	chr4:26625185-26706342	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv878768	chr4:26625185-26766687	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv524115	chr4:26631178-26706342	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:26629200-26680800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr4:26640000-26691400	Weak transcription	Colon Smooth Muscle	Colon
3	chr4:26642400-26697400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr4:26642800-26680000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:26642800-26680800	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr4:26656800-26679200	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr4:26657600-26676800	Weak transcription	Pancreas	Pancrea
8	chr4:26657600-26678400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr4:26657600-26679200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr4:26657600-26680600	Weak transcription	Brain Hippocampus Middle	brain
11	chr4:26657800-26678600	Weak transcription	Fetal Lung	lung
12	chr4:26658400-26679800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr4:26658400-26679800	Weak transcription	Fetal Intestine Small	intestine
14	chr4:26659000-26677600	Weak transcription	Dnd41	blood
15	chr4:26659600-26687600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr4:26660000-26680800	Weak transcription	Esophagus	oesophagus
17	chr4:26660200-26679800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr4:26660200-26680200	Weak transcription	Fetal Brain Male	brain
19	chr4:26660600-26689000	Weak transcription	HMEC	breast
20	chr4:26660800-26679200	Weak transcription	NHEK	skin
21	chr4:26660800-26691400	Weak transcription	Psoas Muscle	Psoas
22	chr4:26661000-26680400	Weak transcription	Liver	Liver
23	chr4:26662800-26680000	Weak transcription	Fetal Brain Female	brain
24	chr4:26663200-26678000	Weak transcription	Fetal Stomach	stomach
25	chr4:26663200-26680600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr4:26663200-26680600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr4:26663400-26680200	Weak transcription	Brain Cingulate Gyrus	brain
28	chr4:26663400-26680800	Weak transcription	Lung	lung
29	chr4:26663600-26678000	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr4:26663600-26678200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr4:26663600-26679800	Weak transcription	Primary T cells from cord blood	blood
32	chr4:26663600-26680000	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr4:26663600-26680400	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr4:26663600-26680400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr4:26663600-26680600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr4:26663600-26680800	Weak transcription	Fetal Muscle Trunk	muscle
37	chr4:26663600-26684000	Weak transcription	Fetal Kidney	kidney
38	chr4:26663600-26691800	Weak transcription	Right Ventricle	heart
39	chr4:26663800-26677800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr4:26663800-26677800	Weak transcription	Adipose Nuclei	Adipose
41	chr4:26663800-26678800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr4:26663800-26680200	Weak transcription	Fetal Intestine Large	intestine
43	chr4:26663800-26691200	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr4:26663800-26691400	Weak transcription	Stomach Smooth Muscle	stomach
45	chr4:26663800-26694000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr4:26664000-26678000	Weak transcription	HSMMtube	muscle
47	chr4:26664000-26678600	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr4:26664000-26679800	Weak transcription	Primary B cells from cord blood	blood
49	chr4:26664000-26679800	Weak transcription	Primary T helper cells fromperipheralblood	blood
50	chr4:26664800-26680600	Weak transcription	Ovary	ovary

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