Variant report

Variant	rs7766706
Chromosome Location	chr6:165784920-165784921
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs1706115	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1706117	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1706118	0.92[ASN][1000 genomes]
rs1706121	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1706123	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1740807	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1740811	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1740812	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs479290	0.89[ASN][1000 genomes]
rs480219	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs480275	0.89[ASN][1000 genomes]
rs482128	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs483088	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs485667	0.87[ASN][1000 genomes]
rs486002	0.89[ASN][1000 genomes]
rs487489	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs489431	0.89[ASN][1000 genomes]
rs491253	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs495725	0.83[ASN][1000 genomes]
rs499235	0.89[ASN][1000 genomes]
rs500017	0.90[ASN][1000 genomes]
rs5003411	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs502012	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs507362	0.90[ASN][1000 genomes]
rs509909	0.89[ASN][1000 genomes]
rs512584	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs518034	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs521211	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs522241	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs525984	0.87[ASN][1000 genomes]
rs528450	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs529247	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs536502	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs536526	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs536555	0.89[ASN][1000 genomes]
rs537436	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs540913	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs547304	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs550108	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs554575	0.88[ASN][1000 genomes]
rs557104	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs557916	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs564788	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs572280	0.86[ASN][1000 genomes]
rs574295	0.87[ASN][1000 genomes]
rs575092	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs575669	0.89[ASN][1000 genomes]
rs579312	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs580810	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs688805	0.82[ASN][1000 genomes]
rs7744356	0.84[ASN][1000 genomes]
rs7744357	0.82[ASN][1000 genomes]
rs7753220	0.82[ASN][1000 genomes]
rs9459398	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432982	chr6:165528589-165835589	Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
2	nsv605245	chr6:165542686-165845903	Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
3	nsv1031648	chr6:165544569-165841029	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
4	nsv432983	chr6:165554403-165851585	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
5	esv3417270	chr6:165682773-166023032	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
6	nsv886928	chr6:165722345-166197889	Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:165744800-165801200	Weak transcription	Hela-S3	cervix
2	chr6:165745600-165802800	Weak transcription	Fetal Heart	heart
3	chr6:165747400-165802600	Weak transcription	HSMMtube	muscle
4	chr6:165747600-165853000	Weak transcription	A549	lung
5	chr6:165763800-165789600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr6:165763800-165797000	Weak transcription	Right Ventricle	heart
7	chr6:165763800-165797600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr6:165764400-165813400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr6:165769800-165789000	Weak transcription	Ovary	ovary
10	chr6:165769800-165791800	Weak transcription	Left Ventricle	heart
11	chr6:165771600-165788000	Weak transcription	HSMM	muscle
12	chr6:165772000-165835800	Weak transcription	Fetal Kidney	kidney
13	chr6:165776200-165798800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr6:165777000-165788400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr6:165777400-165791200	Weak transcription	Fetal Brain Female	brain
16	chr6:165777800-165789600	Weak transcription	Brain Germinal Matrix	brain
17	chr6:165779200-165788000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr6:165779800-165805000	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr6:165784800-165785400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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