Variant report

Variant	rs11666138
Chromosome Location	chr19:37851667-37851668
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11667853	1.00[EUR][1000 genomes]
rs11667866	1.00[EUR][1000 genomes]
rs11668217	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11668546	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11671057	1.00[EUR][1000 genomes]
rs11672064	1.00[EUR][1000 genomes]
rs11672330	1.00[AMR][1000 genomes]
rs2216690	1.00[EUR][1000 genomes]
rs4483965	1.00[AMR][1000 genomes]
rs61741499	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs8106641	1.00[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	nsv918028	chr19:37020645-38014526	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	esv2757695	chr19:37794850-38051606	Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	esv2758759	chr19:37794850-38051606	ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
4	nsv1057688	chr19:37828019-37988253	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv9718	chr19:37839070-37852872	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:37826200-37853200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr19:37826600-37856200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr19:37826600-37861600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr19:37826800-37852600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr19:37826800-37853400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr19:37827000-37853400	Weak transcription	Stomach Mucosa	stomach
7	chr19:37828000-37855800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr19:37830000-37853600	Strong transcription	HUES64 Cell Line	embryonic stem cell
9	chr19:37830800-37853200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr19:37832600-37852200	Weak transcription	Fetal Thymus	thymus
11	chr19:37832800-37852400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr19:37836800-37852000	Weak transcription	Aorta	Aorta
13	chr19:37837800-37852200	Weak transcription	Right Ventricle	heart
14	chr19:37839000-37852800	Weak transcription	Brain Substantia Nigra	brain
15	chr19:37839600-37853200	Weak transcription	Hela-S3	cervix
16	chr19:37839800-37853600	Weak transcription	Fetal Heart	heart
17	chr19:37840200-37852000	Weak transcription	Esophagus	oesophagus
18	chr19:37840200-37852000	Weak transcription	NHEK	skin
19	chr19:37840200-37852200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr19:37840400-37853200	Weak transcription	NH-A	brain
21	chr19:37840600-37852400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr19:37840800-37852400	Weak transcription	Brain Angular Gyrus	brain
23	chr19:37840800-37853200	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr19:37841000-37852000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr19:37841200-37855200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr19:37842600-37855400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
27	chr19:37842800-37856600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr19:37843800-37855800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr19:37843800-37857600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
30	chr19:37844000-37857000	ZNF genes & repeats	Liver	Liver
31	chr19:37844200-37852000	Weak transcription	Pancreas	Pancrea
32	chr19:37845400-37855800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
33	chr19:37845600-37853200	Strong transcription	HUES6 Cell Line	embryonic stem cell
34	chr19:37845600-37853600	Strong transcription	Fetal Muscle Trunk	muscle
35	chr19:37845600-37855800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr19:37845800-37853000	Weak transcription	NHLF	lung
37	chr19:37846200-37853200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr19:37846200-37856400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr19:37846400-37852000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr19:37846400-37854600	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
41	chr19:37846600-37853600	Strong transcription	Skeletal Muscle Female	skeletal muscle
42	chr19:37847000-37852800	Strong transcription	Muscle Satellite Cultured Cells	--
43	chr19:37847000-37854200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr19:37847200-37852400	Weak transcription	Colon Smooth Muscle	Colon
45	chr19:37847400-37852400	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr19:37847600-37852800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr19:37847600-37852800	ZNF genes & repeats	Fetal Intestine Large	intestine
48	chr19:37847800-37852800	Weak transcription	Fetal Brain Male	brain
49	chr19:37847800-37853000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr19:37847800-37854800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood

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