Variant report

Variant	rs11782590
Chromosome Location	chr8:95970158-95970159
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:95961511..95965084-chr8:95968441..95972141,5	K562	blood:
2	chr8:95960008..95964622-chr8:95970124..95974538,6	MCF-7	breast:

Variant related genes	Relation type
ENSG00000253878	Chromatin interaction
ENSG00000164938	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10098025	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10504939	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11774085	0.81[AFR][1000 genomes]
rs11776186	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11778553	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11779282	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11779698	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11780130	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11781397	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11781757	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11782818	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11783262	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11783878	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11783985	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11784140	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11784212	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11787303	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13250762	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17665714	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17665737	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2904889	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3802191	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3802192	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs57890591	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs58282276	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs58314911	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs60003497	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61591488	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs896848	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]

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	nsv1017301	chr8:95273503-96248352	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	nsv539680	chr8:95273503-96248352	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS 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 miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv532338	chr8:95296118-95971825	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
4	nsv508520	chr8:95939373-96140068	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	nsv818645	chr8:95967838-95974373	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11782590	INTS8	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:95962200-95977800	Weak transcription	Hela-S3	cervix
2	chr8:95962400-95971400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr8:95962600-95970600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr8:95962800-95972400	Weak transcription	Aorta	Aorta
5	chr8:95962800-95974200	Weak transcription	Gastric	stomach
6	chr8:95962800-95975800	Weak transcription	Right Ventricle	heart
7	chr8:95962800-95977000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr8:95962800-95979800	Weak transcription	Fetal Muscle Trunk	muscle
9	chr8:95962800-95980200	Weak transcription	Ovary	ovary
10	chr8:95962800-95980600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr8:95963000-95971200	Weak transcription	Fetal Intestine Small	intestine
12	chr8:95963000-95971400	Weak transcription	Primary B cells from cord blood	blood
13	chr8:95963000-95975800	Weak transcription	Fetal Stomach	stomach
14	chr8:95963000-95980400	Weak transcription	HSMM	muscle
15	chr8:95963400-95970200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr8:95963400-95974200	Weak transcription	Psoas Muscle	Psoas
17	chr8:95963600-95971400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr8:95963600-95972400	Weak transcription	NHLF	lung
19	chr8:95963600-95973800	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr8:95963600-95974000	Weak transcription	Esophagus	oesophagus
21	chr8:95963600-95977800	Weak transcription	HUVEC	blood vessel
22	chr8:95963600-95979600	Weak transcription	A549	lung
23	chr8:95963800-95970800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr8:95963800-95973800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr8:95963800-95979400	Weak transcription	Colon Smooth Muscle	Colon
26	chr8:95964000-95970200	Weak transcription	Fetal Muscle Leg	muscle
27	chr8:95964000-95971000	Weak transcription	Primary B cells from peripheral blood	blood
28	chr8:95964200-95970200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr8:95964200-95970400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr8:95964200-95971400	Weak transcription	Fetal Intestine Large	intestine
31	chr8:95964400-95971000	Weak transcription	HMEC	breast
32	chr8:95964400-95972000	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr8:95964400-95973600	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr8:95964400-95973800	Weak transcription	Osteobl	bone
35	chr8:95964400-95976000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr8:95964400-95980000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr8:95964400-96002200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr8:95964600-95970200	Weak transcription	Stomach Smooth Muscle	stomach
39	chr8:95964600-95970200	Weak transcription	Thymus	Thymus
40	chr8:95964600-95970400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr8:95964600-95970800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr8:95964600-95971000	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr8:95964600-95971200	Weak transcription	HepG2	liver
44	chr8:95964600-95972000	Weak transcription	Fetal Lung	lung
45	chr8:95964600-95972000	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr8:95964600-95973600	Weak transcription	Lung	lung
47	chr8:95964600-95979400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr8:95964600-95980200	Weak transcription	Brain Substantia Nigra	brain
49	chr8:95964600-95980600	Weak transcription	Fetal Brain Female	brain
50	chr8:95964600-95992800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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