Variant report

Variant	rs62087367
Chromosome Location	chr18:9509837-9509838
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10468796	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10468797	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10853380	0.94[ASN][1000 genomes]
rs11663979	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11664312	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12386073	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12386075	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12386078	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12454651	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12454987	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12457895	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1561997	0.95[ASN][1000 genomes]
rs16955157	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2028660	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2061692	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2241943	0.95[ASN][1000 genomes]
rs28510500	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4798819	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58103465	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58651706	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs59277394	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62086154	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62087375	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7234529	0.88[ASN][1000 genomes]
rs7235585	0.88[ASN][1000 genomes]
rs7238922	0.93[ASN][1000 genomes]
rs73395727	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[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	nsv916373	chr18:9026803-9592201	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
2	nsv1056407	chr18:9144345-9553764	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	nsv1062025	chr18:9287249-9552470	Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
4	nsv543643	chr18:9287249-9552470	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	nsv833585	chr18:9401630-9597291	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
6	nsv428005	chr18:9401658-9542396	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:9477000-9514000	Weak transcription	NH-A	brain
2	chr18:9477200-9513800	Weak transcription	HSMM	muscle
3	chr18:9478000-9522400	Weak transcription	Hela-S3	cervix
4	chr18:9479000-9514000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr18:9479000-9533200	Weak transcription	Aorta	Aorta
6	chr18:9479000-9533600	Weak transcription	Gastric	stomach
7	chr18:9480200-9513800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr18:9483000-9513800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr18:9492600-9514000	Weak transcription	Rectal Smooth Muscle	rectum
10	chr18:9495000-9518000	Weak transcription	Liver	Liver
11	chr18:9495000-9518000	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr18:9495200-9530400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr18:9495200-9533600	Weak transcription	Right Ventricle	heart
14	chr18:9495400-9512800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr18:9495400-9514000	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr18:9495400-9524000	Weak transcription	Spleen	Spleen
17	chr18:9495400-9534000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr18:9495800-9514000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr18:9495800-9517000	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr18:9496000-9513800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr18:9496800-9534000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr18:9497400-9532600	Weak transcription	Colonic Mucosa	Colon
23	chr18:9497600-9517200	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr18:9497800-9513800	Weak transcription	NHEK	skin
25	chr18:9498400-9523200	Weak transcription	Esophagus	oesophagus
26	chr18:9499400-9525000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr18:9500800-9535000	Weak transcription	Fetal Heart	heart
28	chr18:9502000-9514000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr18:9502200-9514000	Weak transcription	Dnd41	blood
30	chr18:9502200-9519800	Weak transcription	Brain Angular Gyrus	brain
31	chr18:9503000-9513600	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr18:9503000-9517200	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr18:9503600-9513800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr18:9503800-9513000	Weak transcription	Fetal Muscle Leg	muscle
35	chr18:9503800-9513600	Weak transcription	Primary T cells from cord blood	blood
36	chr18:9503800-9514000	Weak transcription	Fetal Brain Female	brain
37	chr18:9503800-9517400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr18:9504000-9512800	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr18:9504000-9513600	Weak transcription	Primary B cells from cord blood	blood
40	chr18:9504000-9515200	Weak transcription	Brain Hippocampus Middle	brain
41	chr18:9505000-9513800	Weak transcription	HepG2	liver
42	chr18:9505200-9513000	Weak transcription	Fetal Intestine Large	intestine
43	chr18:9505200-9524600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr18:9505400-9513600	Weak transcription	Primary hematopoietic stem cells	blood
45	chr18:9505600-9513600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr18:9505800-9513800	Weak transcription	Stomach Mucosa	stomach
47	chr18:9506200-9517200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr18:9506400-9522400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr18:9506600-9513600	Weak transcription	Adipose Nuclei	Adipose
50	chr18:9506600-9513800	Weak transcription	HUES64 Cell Line	embryonic stem cell

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