Variant report

Variant	rs61095714
Chromosome Location	chr18:39545872-39545873
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr18:39543831..39546776-chr18:39549951..39551574,2	K562	blood:
2	chr18:39541005..39543575-chr18:39545049..39547363,2	K562	blood:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs11873469	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs11873602	0.90[AFR][1000 genomes]
rs11874766	0.88[AFR][1000 genomes]
rs11874775	0.86[AFR][1000 genomes]
rs11874814	0.93[AFR][1000 genomes]
rs11874830	0.97[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs11876547	0.97[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs11876578	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs11877901	0.94[AFR][1000 genomes]
rs1540057	0.89[AFR][1000 genomes]
rs16975441	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs16975447	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs16975466	0.99[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs16975521	0.97[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs56411890	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs56751463	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs56979511	0.91[AFR][1000 genomes]
rs57208863	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs58298297	0.97[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs58881642	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs6507453	0.89[AFR][1000 genomes]
rs6507454	0.93[AFR][1000 genomes]
rs6650669	0.89[AFR][1000 genomes]
rs7229485	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs7237185	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs7237815	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs7240066	0.93[AFR][1000 genomes]
rs7241399	0.89[AFR][1000 genomes]
rs7245131	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs7343027	0.87[AFR][1000 genomes]
rs73451096	0.87[AMR][1000 genomes]
rs73454573	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs73454580	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs73454581	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs73454593	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs73454596	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs73454602	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs73950814	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs8084037	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs8088187	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs8089142	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs8095945	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1066869	chr18:38742896-39680723	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv543685	chr18:38742896-39680723	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv949609	chr18:39126941-40070286	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
4	nsv431979	chr18:39255558-39696452	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
5	nsv1066029	chr18:39322920-39623625	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv543686	chr18:39322920-39623625	Strong transcription Weak transcription Active TSS Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv909566	chr18:39327962-39688452	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
8	esv34153	chr18:39398768-39872265	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
9	nsv909567	chr18:39470190-39652939	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
10	nsv909568	chr18:39491873-39768746	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:39536000-39547000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr18:39536000-39547000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr18:39536000-39547000	Weak transcription	Left Ventricle	heart
4	chr18:39536000-39547200	Weak transcription	Esophagus	oesophagus
5	chr18:39536000-39621800	Weak transcription	Stomach Mucosa	stomach
6	chr18:39536200-39547000	Weak transcription	Right Ventricle	heart
7	chr18:39536200-39547000	Weak transcription	Thymus	Thymus
8	chr18:39536200-39548000	Weak transcription	Colonic Mucosa	Colon
9	chr18:39536200-39552400	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr18:39536200-39564800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr18:39536200-39568600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr18:39536400-39552400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr18:39536400-39578200	Weak transcription	A549	lung
14	chr18:39536800-39546800	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr18:39536800-39547000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr18:39536800-39547000	Weak transcription	Aorta	Aorta
17	chr18:39536800-39547000	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr18:39536800-39547000	Weak transcription	Spleen	Spleen
19	chr18:39536800-39580000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr18:39536800-39633600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr18:39537000-39547600	Weak transcription	Fetal Brain Male	brain
22	chr18:39537400-39546600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr18:39537400-39547000	Strong transcription	HSMM	muscle
24	chr18:39537400-39547200	Weak transcription	Colon Smooth Muscle	Colon
25	chr18:39537400-39552400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr18:39537400-39553000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr18:39537400-39555800	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr18:39537600-39547000	Weak transcription	Rectal Smooth Muscle	rectum
29	chr18:39537600-39552200	Strong transcription	Primary monocytes fromperipheralblood	blood
30	chr18:39537600-39552800	Strong transcription	HUES64 Cell Line	embryonic stem cell
31	chr18:39537600-39553200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr18:39537800-39547000	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr18:39538600-39546800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr18:39538600-39547000	Weak transcription	Brain Germinal Matrix	brain
35	chr18:39538600-39548400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr18:39539000-39547000	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr18:39539200-39546800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr18:39539200-39547000	Weak transcription	NHEK	skin
39	chr18:39539400-39548200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
40	chr18:39539600-39548200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr18:39540200-39548200	Strong transcription	K562	blood
42	chr18:39541000-39546800	Weak transcription	Fetal Stomach	stomach
43	chr18:39541000-39547000	Weak transcription	Fetal Intestine Small	intestine
44	chr18:39541000-39547000	Weak transcription	Pancreas	Pancrea
45	chr18:39541400-39547000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr18:39541600-39549600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr18:39542400-39546200	Strong transcription	Duodenum Smooth Muscle	Duodenum
48	chr18:39542400-39547000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
49	chr18:39542400-39548200	Strong transcription	Duodenum Mucosa	Duodenum
50	chr18:39542400-39548200	Strong transcription	Rectal Mucosa Donor 29	rectum

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