Variant report

Variant	rs6683206
Chromosome Location	chr1:154418088-154418089
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:154377603..154379181-chr1:154416383..154418263,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000160712	Chromatin interaction
ENSG00000228013	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs10908838	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11265612	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12118770	0.80[EUR][1000 genomes]
rs12129500	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4553185	0.83[EUR][1000 genomes]
rs4845371	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4845619	0.83[EUR][1000 genomes]
rs4845625	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs59632925	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6427658	0.82[EUR][1000 genomes]
rs6667434	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6686750	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6689306	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6689393	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6694258	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6694817	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7526131	0.80[EUR][1000 genomes]
rs7536152	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7549250	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7549338	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7553796	0.83[AMR][1000 genomes];0.86[EUR][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	nsv999364	chr1:153622634-154419436	Strong transcription Genic enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	286 gene(s)	inside rSNPs	diseases
2	nsv535175	chr1:153622634-154419436	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	286 gene(s)	inside rSNPs	diseases
3	nsv948413	chr1:153974621-154797272	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
4	nsv1000402	chr1:153991106-154527053	Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	106 gene(s)	inside rSNPs	diseases
5	nsv521887	chr1:154236570-154684106	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6683206	TDRD10	cis	lung	GTEx

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:154403200-154426000	Weak transcription	Brain Angular Gyrus	brain
2	chr1:154406000-154423200	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr1:154406200-154425600	Weak transcription	Primary B cells from cord blood	blood
4	chr1:154407600-154418600	Weak transcription	Ovary	ovary
5	chr1:154408600-154420600	Weak transcription	Brain Hippocampus Middle	brain
6	chr1:154408600-154425800	Weak transcription	Brain Substantia Nigra	brain
7	chr1:154408800-154420600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr1:154408800-154420600	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr1:154408800-154421000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr1:154408800-154425600	Weak transcription	Brain Cingulate Gyrus	brain
11	chr1:154409200-154420600	Weak transcription	Gastric	stomach
12	chr1:154409200-154425800	Weak transcription	Right Atrium	heart
13	chr1:154409400-154424600	Weak transcription	Stomach Mucosa	stomach
14	chr1:154410800-154418600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
15	chr1:154410800-154418800	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr1:154412600-154425800	Weak transcription	Psoas Muscle	Psoas
17	chr1:154412800-154425800	Weak transcription	HepG2	liver
18	chr1:154413000-154419600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr1:154413200-154422600	Weak transcription	Primary B cells from peripheral blood	blood
20	chr1:154413600-154418800	Genic enhancers	Colon Smooth Muscle	Colon
21	chr1:154413600-154419600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr1:154413800-154418800	Genic enhancers	Primary T helper cells fromperipheralblood	blood
23	chr1:154414400-154424400	Strong transcription	Primary monocytes fromperipheralblood	blood
24	chr1:154414400-154424400	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr1:154414600-154424400	Strong transcription	Primary neutrophils fromperipheralblood	blood
26	chr1:154414600-154426000	Weak transcription	Thymus	Thymus
27	chr1:154414800-154418200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr1:154414800-154418400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr1:154414800-154419000	Genic enhancers	Primary T cells fromperipheralblood	blood
30	chr1:154414800-154436000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr1:154415000-154418400	Weak transcription	Placenta	Placenta
32	chr1:154415000-154418600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr1:154415000-154418600	Weak transcription	HSMM	muscle
34	chr1:154415000-154418800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr1:154415000-154418800	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr1:154415000-154420600	Weak transcription	Pancreas	Pancrea
37	chr1:154415200-154418600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr1:154415200-154418600	Strong transcription	Duodenum Smooth Muscle	Duodenum
39	chr1:154415200-154419200	Genic enhancers	Primary T helper cells PMA-I stimulated	--
40	chr1:154415200-154419200	Strong transcription	Lung	lung
41	chr1:154415200-154420800	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr1:154415200-154424000	Weak transcription	Fetal Stomach	stomach
43	chr1:154415600-154419200	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr1:154415600-154419200	Genic enhancers	Stomach Smooth Muscle	stomach
45	chr1:154415800-154419400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr1:154415800-154425800	Weak transcription	Esophagus	oesophagus
47	chr1:154416000-154418400	Weak transcription	Fetal Lung	lung
48	chr1:154416200-154418400	Strong transcription	Rectal Smooth Muscle	rectum
49	chr1:154416200-154435800	Strong transcription	Liver	Liver
50	chr1:154416400-154420600	Weak transcription	Rectal Mucosa Donor 31	rectum

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