Variant report

Variant	rs1771318
Chromosome Location	chr1:225696144-225696145
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10799310	0.83[EUR][1000 genomes]
rs12071529	0.86[EUR][1000 genomes]
rs1222434	0.90[AFR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1222439	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1336480	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1360958	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1764345	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1764347	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1890999	0.88[EUR][1000 genomes]
rs1891000	0.82[AMR][1000 genomes]
rs2035916	0.87[EUR][1000 genomes]
rs4233220	0.83[EUR][1000 genomes]
rs4554690	0.82[EUR][1000 genomes]
rs475794	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs481746	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs499385	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs516323	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs525062	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs526221	0.80[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs544404	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs544430	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs566085	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs59363938	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6692054	0.83[EUR][1000 genomes]
rs72750896	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7545317	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs954534	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9651009	0.82[EUR][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	nsv832714	chr1:225592333-225805396	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	esv2756886	chr1:225665694-225703485	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
3	esv2759003	chr1:225665694-225703485	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv4720	chr1:225673218-225718009	Genic enhancers Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:225663200-225696400	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr1:225666000-225696800	Weak transcription	Esophagus	oesophagus
3	chr1:225669800-225696800	Weak transcription	Pancreas	Pancrea
4	chr1:225672200-225696800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr1:225672200-225696800	Weak transcription	Brain Germinal Matrix	brain
6	chr1:225674400-225696800	Weak transcription	Aorta	Aorta
7	chr1:225676200-225696400	Weak transcription	Gastric	stomach
8	chr1:225677200-225696400	Weak transcription	Brain Angular Gyrus	brain
9	chr1:225677200-225696400	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr1:225677200-225696400	Weak transcription	Brain Substantia Nigra	brain
11	chr1:225677200-225696400	Weak transcription	Colon Smooth Muscle	Colon
12	chr1:225677200-225696600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:225677200-225696600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr1:225677200-225696600	Weak transcription	Psoas Muscle	Psoas
15	chr1:225677200-225703600	Weak transcription	Fetal Brain Female	brain
16	chr1:225680200-225696200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:225680800-225696200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr1:225681200-225696200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr1:225681800-225699800	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr1:225683000-225696800	Weak transcription	Lung	lung
21	chr1:225683400-225696600	Weak transcription	Right Ventricle	heart
22	chr1:225684200-225696800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr1:225686800-225696200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr1:225686800-225696400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr1:225686800-225696400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr1:225686800-225696400	Weak transcription	Stomach Smooth Muscle	stomach
27	chr1:225686800-225699800	Weak transcription	Adipose Nuclei	Adipose
28	chr1:225687000-225696600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr1:225687000-225705000	Weak transcription	Spleen	Spleen
30	chr1:225687400-225704400	Weak transcription	Fetal Stomach	stomach
31	chr1:225688000-225696600	Weak transcription	Brain Cingulate Gyrus	brain
32	chr1:225688600-225704600	Weak transcription	Placenta	Placenta
33	chr1:225688800-225696400	Weak transcription	Brain Hippocampus Middle	brain
34	chr1:225688800-225696400	Weak transcription	Fetal Intestine Large	intestine
35	chr1:225688800-225696400	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr1:225688800-225696600	Weak transcription	Fetal Intestine Small	intestine
37	chr1:225688800-225711400	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr1:225689200-225696600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr1:225689200-225696600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
40	chr1:225689200-225696600	Weak transcription	Fetal Muscle Trunk	muscle
41	chr1:225689200-225696600	Weak transcription	Ovary	ovary
42	chr1:225689200-225696600	Weak transcription	HSMMtube	muscle
43	chr1:225689200-225721000	Weak transcription	Duodenum Mucosa	Duodenum
44	chr1:225689800-225696400	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr1:225691000-225696600	Weak transcription	Right Atrium	heart
46	chr1:225691000-225706200	Weak transcription	Primary B cells from cord blood	blood
47	chr1:225691200-225705000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr1:225692400-225696200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
49	chr1:225692600-225704800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr1:225693200-225702800	Weak transcription	Pancreatic Islets	Pancreatic Islet

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