Variant report

Variant	rs11667844
Chromosome Location	chr19:19775740-19775741
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:19625322..19628012-chr19:19773852..19776193,2	K562	blood:
2	chr19:19748686..19750462-chr19:19773488..19775987,2	K562	blood:
3	chr19:19647870..19650487-chr19:19773815..19776020,2	MCF-7	breast:
4	chr19:19748686..19750462-chr19:19772850..19775987,3	K562	blood:
5	chr19:19636166..19641062-chr19:19772143..19775843,4	MCF-7	breast:
6	chr19:19751259..19757786-chr19:19771999..19776232,8	K562	blood:
7	chr19:19496290..19497914-chr19:19774313..19776411,2	MCF-7	breast:
8	chr19:19649331..19652417-chr19:19771491..19776120,6	K562	blood:
9	chr19:19651192..19652936-chr19:19774066..19776214,2	MCF-7	breast:
10	chr19:19751259..19758144-chr19:19770384..19776332,14	K562	blood:
11	chr19:19772164..19776257-chr19:19777737..19781997,10	MCF-7	breast:
12	chr19:19752144..19756505-chr19:19773208..19775858,7	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000258674	Chromatin interaction
ENSG00000160161	Chromatin interaction
ENSG00000250067	Chromatin interaction
ENSG00000167491	Chromatin interaction
ENSG00000178093	Chromatin interaction
ENSG00000089639	Chromatin interaction
ENSG00000186010	Chromatin interaction
ENSG00000181896	Chromatin interaction

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10405234	0.86[EUR][1000 genomes]
rs10423311	0.86[EUR][1000 genomes]
rs11667828	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11670710	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12983292	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2288867	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs28635562	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4808976	0.86[EUR][1000 genomes]
rs7249670	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs8107058	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	esv1828240	chr19:19591146-19900900	Weak transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	nsv1063273	chr19:19591146-20061367	ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription 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	67 gene(s)	inside rSNPs	diseases
3	nsv911309	chr19:19727042-19784891	Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
4	nsv911310	chr19:19753882-19784891	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases
5	esv3330851	chr19:19755507-19852881	Strong transcription Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:19774000-19776000	Active TSS	Placenta	Placenta
2	chr19:19774200-19779000	Weak transcription	Fetal Heart	heart
3	chr19:19774800-19779000	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr19:19775000-19778400	Weak transcription	Spleen	Spleen
5	chr19:19775200-19775800	Enhancers	Primary T killer memory cells from peripheral blood	blood
6	chr19:19775200-19776200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr19:19775200-19776200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr19:19775200-19776200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr19:19775200-19776800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr19:19775200-19776800	Weak transcription	HepG2	liver
11	chr19:19775200-19777600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr19:19775200-19777600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr19:19775200-19778200	Weak transcription	Liver	Liver
14	chr19:19775200-19778400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr19:19775200-19778400	Weak transcription	Duodenum Mucosa	Duodenum
16	chr19:19775200-19778800	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr19:19775200-19778800	Weak transcription	HUVEC	blood vessel
18	chr19:19775200-19779000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr19:19775200-19779000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr19:19775200-19779000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr19:19775200-19779000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr19:19775200-19779000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr19:19775200-19779000	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr19:19775200-19779000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr19:19775200-19779000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr19:19775200-19779000	Weak transcription	Brain Angular Gyrus	brain
27	chr19:19775200-19779000	Weak transcription	Brain Anterior Caudate	brain
28	chr19:19775200-19779000	Weak transcription	Brain Cingulate Gyrus	brain
29	chr19:19775200-19779000	Weak transcription	Brain Germinal Matrix	brain
30	chr19:19775200-19779000	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr19:19775200-19779000	Weak transcription	Brain Substantia Nigra	brain
32	chr19:19775200-19779000	Weak transcription	Colonic Mucosa	Colon
33	chr19:19775200-19779000	Weak transcription	Colon Smooth Muscle	Colon
34	chr19:19775200-19779000	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr19:19775200-19779000	Weak transcription	Fetal Brain Male	brain
36	chr19:19775200-19779000	Weak transcription	Fetal Brain Female	brain
37	chr19:19775200-19779000	Weak transcription	Fetal Stomach	stomach
38	chr19:19775200-19779000	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr19:19775200-19779000	Weak transcription	Psoas Muscle	Psoas
40	chr19:19775200-19779000	Weak transcription	Right Ventricle	heart
41	chr19:19775200-19779000	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr19:19775200-19779000	Weak transcription	HSMMtube	muscle
43	chr19:19775200-19779000	Weak transcription	NH-A	brain
44	chr19:19775200-19779000	Weak transcription	NHLF	lung
45	chr19:19775200-19779200	Weak transcription	Stomach Mucosa	stomach
46	chr19:19775200-19779200	Weak transcription	A549	lung
47	chr19:19775200-19779200	Weak transcription	NHDF-Ad	bronchial
48	chr19:19775400-19775800	ZNF genes & repeats	Fetal Intestine Large	intestine
49	chr19:19775400-19776000	Enhancers	Primary B cells from peripheral blood	blood
50	chr19:19775400-19777400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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