Variant report

Variant	rs73257211
Chromosome Location	chr6:166969049-166969050
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11963778	0.89[AMR][1000 genomes]
rs11964118	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11969154	1.00[AMR][1000 genomes]
rs11969174	1.00[AMR][1000 genomes]
rs11969176	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11970618	0.89[AMR][1000 genomes]
rs16899123	0.89[AMR][1000 genomes]
rs16899126	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16899129	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16899150	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16899151	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16899157	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57647994	1.00[AMR][1000 genomes]
rs59061765	0.89[AMR][1000 genomes]
rs60005152	1.00[AMR][1000 genomes]
rs61045375	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73255201	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73257221	1.00[AMR][1000 genomes]
rs73257223	1.00[AMR][1000 genomes]
rs73257240	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73257242	0.89[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3490076	chr6:166727901-167306743	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
2	esv3490077	chr6:166727901-167306743	Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
3	nsv886941	chr6:166907173-166996991	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA	5 gene(s)	inside rSNPs	diseases
4	nsv5592	chr6:166958317-167002951	Weak transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166947400-166969400	Weak transcription	Aorta	Aorta
2	chr6:166955200-166970600	Weak transcription	Pancreas	Pancrea
3	chr6:166955200-166970600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr6:166960000-166972800	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr6:166961200-166970400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr6:166964800-166972000	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr6:166965000-166969200	Enhancers	Fetal Brain Male	brain
8	chr6:166965600-166971000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr6:166965800-166972400	Enhancers	Fetal Muscle Leg	muscle
10	chr6:166966000-166969800	Enhancers	Fetal Stomach	stomach
11	chr6:166966000-166973600	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr6:166966000-166974200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr6:166966200-166969600	Enhancers	HSMM	muscle
14	chr6:166966200-166970000	Enhancers	Brain Hippocampus Middle	brain
15	chr6:166966200-166971200	Enhancers	Left Ventricle	heart
16	chr6:166966200-166978000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr6:166966400-166970400	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr6:166966400-166970800	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr6:166966600-166969800	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr6:166966600-166970000	Enhancers	Brain Anterior Caudate	brain
21	chr6:166966600-166970200	Enhancers	Right Ventricle	heart
22	chr6:166966600-166970800	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr6:166966800-166970400	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr6:166967000-166969600	Weak transcription	Stomach Smooth Muscle	stomach
25	chr6:166967000-166971200	Enhancers	Brain Angular Gyrus	brain
26	chr6:166967200-166970000	Enhancers	Skeletal Muscle Female	skeletal muscle
27	chr6:166967400-166969200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr6:166967400-166969400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr6:166967400-166969800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr6:166967600-166969400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr6:166967600-166969400	Enhancers	Fetal Heart	heart
32	chr6:166967600-166970400	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr6:166967600-166970600	Enhancers	HUVEC	blood vessel
34	chr6:166967600-166971000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr6:166967600-166971000	Enhancers	Adipose Nuclei	Adipose
36	chr6:166967600-166971000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
37	chr6:166967600-166971800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr6:166967800-166969600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr6:166967800-166969600	Weak transcription	NHEK	skin
40	chr6:166967800-166969800	Enhancers	Brain Cingulate Gyrus	brain
41	chr6:166967800-166970000	Weak transcription	Duodenum Mucosa	Duodenum
42	chr6:166968000-166969200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr6:166968000-166969600	Enhancers	Muscle Satellite Cultured Cells	--
44	chr6:166968000-166969800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr6:166968000-166969800	Weak transcription	Rectal Smooth Muscle	rectum
46	chr6:166968000-166970000	Enhancers	NHDF-Ad	bronchial
47	chr6:166968000-166972000	Enhancers	Spleen	Spleen
48	chr6:166968000-166972800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr6:166968200-166969200	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr6:166968200-166969600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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