Variant report

Variant	rs73477457
Chromosome Location	chr6:70410237-70410238
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs56666938	1.00[AFR][1000 genomes]
rs6455341	1.00[AMR][1000 genomes]
rs6917742	1.00[AMR][1000 genomes]
rs6919250	1.00[AMR][1000 genomes]
rs6934751	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73481729	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73481746	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73481760	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73481771	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73485505	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73485528	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73485534	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73485552	1.00[AFR][1000 genomes]
rs73486006	1.00[AMR][1000 genomes]
rs73486025	1.00[AMR][1000 genomes]
rs73486045	1.00[AMR][1000 genomes]
rs73486048	1.00[AMR][1000 genomes]
rs7762910	1.00[AMR][1000 genomes]
rs7763838	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886140	chr6:70354682-70728202	Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv830682	chr6:70397851-70592883	Weak transcription Strong transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:70378800-70416800	Weak transcription	Fetal Kidney	kidney
2	chr6:70378800-70430800	Weak transcription	Fetal Stomach	stomach
3	chr6:70378800-70430800	Weak transcription	Spleen	Spleen
4	chr6:70378800-70435200	Weak transcription	Psoas Muscle	Psoas
5	chr6:70379000-70428400	Weak transcription	Ovary	ovary
6	chr6:70379000-70435400	Weak transcription	Fetal Brain Male	brain
7	chr6:70379600-70431000	Weak transcription	Rectal Smooth Muscle	rectum
8	chr6:70380400-70430600	Weak transcription	Fetal Intestine Small	intestine
9	chr6:70380600-70455600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr6:70380800-70467800	Weak transcription	K562	blood
11	chr6:70382200-70435400	Weak transcription	Brain Angular Gyrus	brain
12	chr6:70382400-70430200	Weak transcription	Small Intestine	intestine
13	chr6:70383800-70431000	Weak transcription	Lung	lung
14	chr6:70384000-70415800	Weak transcription	Fetal Lung	lung
15	chr6:70384200-70428400	Weak transcription	Aorta	Aorta
16	chr6:70384200-70431000	Weak transcription	Fetal Muscle Leg	muscle
17	chr6:70384600-70417400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr6:70385000-70421600	Weak transcription	Fetal Intestine Large	intestine
19	chr6:70387600-70415600	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr6:70388000-70423400	Weak transcription	Left Ventricle	heart
21	chr6:70396200-70412200	Strong transcription	Primary B cells from peripheral blood	blood
22	chr6:70397200-70415600	Weak transcription	Primary T cells from cord blood	blood
23	chr6:70397800-70439000	Weak transcription	Fetal Heart	heart
24	chr6:70398000-70423000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr6:70400800-70430800	Weak transcription	Pancreas	Pancrea
26	chr6:70402000-70412000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr6:70402000-70430800	Weak transcription	Esophagus	oesophagus
28	chr6:70402200-70435200	Weak transcription	Brain Anterior Caudate	brain
29	chr6:70402800-70430800	Weak transcription	Fetal Muscle Trunk	muscle
30	chr6:70403000-70429800	Weak transcription	NHDF-Ad	bronchial
31	chr6:70403200-70415400	Weak transcription	HSMM	muscle
32	chr6:70403400-70432200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr6:70403800-70412600	Weak transcription	HSMMtube	muscle
34	chr6:70403800-70422800	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr6:70404200-70447400	Weak transcription	Hela-S3	cervix
36	chr6:70404400-70410800	Strong transcription	Monocytes-CD14+_RO01746	blood
37	chr6:70404400-70420000	Weak transcription	NHLF	lung
38	chr6:70404600-70410600	Strong transcription	Primary T helper cells fromperipheralblood	blood
39	chr6:70404600-70433800	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr6:70405000-70411800	Strong transcription	Primary T helper cells PMA-I stimulated	--
41	chr6:70405000-70432200	Weak transcription	Fetal Brain Female	brain
42	chr6:70405000-70468400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr6:70405400-70434600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr6:70405600-70427600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr6:70405600-70446400	Weak transcription	HepG2	liver
46	chr6:70406000-70411000	Strong transcription	Liver	Liver
47	chr6:70406000-70411400	Strong transcription	Adipose Nuclei	Adipose
48	chr6:70406000-70411800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr6:70406000-70430800	Weak transcription	Thymus	Thymus
50	chr6:70406000-70433600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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