Variant report

Variant	rs6853079
Chromosome Location	chr4:99443611-99443612
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	chr4:99441293..99445376-chr4:99447706..99451023,3	K562	blood:
2	chr4:99413602..99415848-chr4:99442433..99444375,2	K562	blood:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10004753	0.95[YRI][hapmap];0.82[AFR][1000 genomes]
rs10489125	0.82[JPT][hapmap]
rs10516433	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10516434	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11945713	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13116201	0.95[YRI][hapmap];0.80[AFR][1000 genomes]
rs1554849	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs17498778	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17499015	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17564872	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.95[YRI][hapmap];0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17564998	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4699642	0.94[YRI][hapmap]
rs4699645	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4699654	0.82[JPT][hapmap]
rs56221164	1.00[ASN][1000 genomes]
rs59150136	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60026821	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs60947018	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6532740	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[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]
rs6532746	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs6817773	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6830136	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6840239	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6840610	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6846101	0.90[ASN][1000 genomes]
rs7666585	0.82[JPT][hapmap]
rs7667273	0.82[JPT][hapmap]
rs7667608	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7676155	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7688849	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7689116	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7689289	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[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]
rs9761395	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[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	nsv529623	chr4:98501338-99460166	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	esv2754250	chr4:99094922-99527122	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1004181	chr4:99208152-99529576	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:99434400-99443800	Weak transcription	Aorta	Aorta
2	chr4:99436600-99446400	Weak transcription	Left Ventricle	heart
3	chr4:99438800-99452000	Enhancers	Fetal Heart	heart
4	chr4:99439600-99445800	Enhancers	Ovary	ovary
5	chr4:99439800-99443800	Weak transcription	Fetal Brain Female	brain
6	chr4:99440400-99443800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr4:99440400-99458400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr4:99440800-99443800	Weak transcription	Primary B cells from cord blood	blood
9	chr4:99441200-99446400	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr4:99441600-99443800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr4:99441800-99446400	Weak transcription	Spleen	Spleen
12	chr4:99442200-99446000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr4:99442200-99446000	Enhancers	NHEK	skin
14	chr4:99442200-99450600	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr4:99442400-99444600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr4:99442400-99444800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr4:99442400-99445800	Enhancers	Brain Cingulate Gyrus	brain
18	chr4:99442400-99446600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr4:99442400-99446800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr4:99442600-99443800	Enhancers	Dnd41	blood
21	chr4:99442600-99444000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
22	chr4:99442600-99444000	Enhancers	Osteobl	bone
23	chr4:99442600-99444400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr4:99442600-99444800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
25	chr4:99442600-99445200	Enhancers	HMEC	breast
26	chr4:99442600-99445400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr4:99442600-99445400	Enhancers	HSMM	muscle
28	chr4:99442600-99445600	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr4:99442600-99445600	Enhancers	Brain Substantia Nigra	brain
30	chr4:99442600-99445600	Enhancers	NHLF	lung
31	chr4:99442600-99445800	Enhancers	Rectal Smooth Muscle	rectum
32	chr4:99442600-99446000	Enhancers	Brain Angular Gyrus	brain
33	chr4:99442600-99446000	Enhancers	Brain Germinal Matrix	brain
34	chr4:99442600-99446000	Enhancers	Fetal Lung	lung
35	chr4:99442600-99446000	Enhancers	Fetal Stomach	stomach
36	chr4:99442600-99446600	Enhancers	Brain Hippocampus Middle	brain
37	chr4:99442600-99446800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr4:99442600-99447400	Enhancers	Brain Anterior Caudate	brain
39	chr4:99442800-99444000	Enhancers	Primary T helper naive cells from peripheral blood	blood
40	chr4:99442800-99444200	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr4:99442800-99444400	Enhancers	HSMMtube	muscle
42	chr4:99442800-99445800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr4:99442800-99445800	Enhancers	A549	lung
44	chr4:99443000-99446800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr4:99443200-99443800	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr4:99443200-99444000	Enhancers	Primary T cells from cord blood	blood
47	chr4:99443200-99444000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
48	chr4:99443200-99444200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr4:99443200-99444400	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr4:99443200-99444600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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