Variant report

Variant	rs7248419
Chromosome Location	chr19:21358343-21358344
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10406253	0.87[EUR][1000 genomes]
rs10407190	0.87[EUR][1000 genomes]
rs11668640	0.87[EUR][1000 genomes]
rs12980860	0.87[EUR][1000 genomes]
rs2115498	0.93[EUR][1000 genomes]
rs2358807	0.88[EUR][1000 genomes]
rs2358808	0.89[ASN][1000 genomes]
rs29703	0.80[ASN][1000 genomes]
rs29705	0.80[ASN][1000 genomes]
rs29722	0.83[ASN][1000 genomes]
rs29725	0.85[ASN][1000 genomes]
rs29728	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs29729	0.87[ASN][1000 genomes]
rs388229	0.88[ASN][1000 genomes]
rs416001	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6511202	0.85[EUR][1000 genomes]
rs6511204	0.83[EUR][1000 genomes]
rs6511205	0.87[EUR][1000 genomes]
rs8101918	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3385528	chr19:21030777-21495566	Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers 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	32 gene(s)	inside rSNPs	diseases
2	nsv960811	chr19:21200306-21371757	Strong transcription Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	esv3399352	chr19:21232738-21423323	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	esv3518033	chr19:21278465-21747567	Strong transcription Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
5	esv3518034	chr19:21278465-21747567	ZNF genes & repeats Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
6	esv3414204	chr19:21301761-21839451	ZNF genes & repeats Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
7	nsv911414	chr19:21355473-21454672	Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr19:21325400-21361800	Weak transcription	Small Intestine	intestine
2	chr19:21325600-21365800	Weak transcription	Brain Angular Gyrus	brain
3	chr19:21326000-21361000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr19:21326800-21361800	Weak transcription	Stomach Mucosa	stomach
5	chr19:21331000-21371000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr19:21333000-21373000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr19:21333400-21364800	Weak transcription	HUVEC	blood vessel
8	chr19:21334600-21360800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr19:21335000-21365000	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr19:21335800-21362800	Weak transcription	Psoas Muscle	Psoas
11	chr19:21336000-21362000	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr19:21336200-21361800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr19:21336200-21361800	Weak transcription	Stomach Smooth Muscle	stomach
14	chr19:21336600-21360600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr19:21339400-21361000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr19:21339400-21361000	Weak transcription	NHDF-Ad	bronchial
17	chr19:21341800-21361600	Weak transcription	Colon Smooth Muscle	Colon
18	chr19:21342800-21362600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
19	chr19:21343400-21358600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr19:21343600-21359800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr19:21344200-21359000	Strong transcription	Primary B cells from cord blood	blood
22	chr19:21345400-21358600	Weak transcription	Colonic Mucosa	Colon
23	chr19:21345400-21359200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr19:21345400-21361400	Weak transcription	Spleen	Spleen
25	chr19:21345600-21363000	Weak transcription	HepG2	liver
26	chr19:21348400-21359200	Strong transcription	HUES48 Cell Line	embryonic stem cell
27	chr19:21348600-21359200	Strong transcription	HUES64 Cell Line	embryonic stem cell
28	chr19:21348600-21359800	Strong transcription	Primary T helper cells fromperipheralblood	blood
29	chr19:21348600-21366400	Weak transcription	Brain Substantia Nigra	brain
30	chr19:21349000-21359000	Strong transcription	HUES6 Cell Line	embryonic stem cell
31	chr19:21349400-21358800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr19:21349400-21359800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr19:21349600-21359800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr19:21349600-21370600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr19:21349800-21358400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr19:21349800-21360000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr19:21349800-21360200	Strong transcription	Duodenum Mucosa	Duodenum
38	chr19:21349800-21363200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr19:21350000-21358800	Strong transcription	Adipose Nuclei	Adipose
40	chr19:21350000-21360400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr19:21350000-21360800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr19:21350200-21362000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr19:21351400-21363800	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
44	chr19:21351800-21358600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
45	chr19:21351800-21358600	Strong transcription	Primary T helper naive cells from peripheral blood	blood
46	chr19:21351800-21358600	Strong transcription	Rectal Mucosa Donor 29	rectum
47	chr19:21352000-21361200	Strong transcription	Cortex derived primary cultured neurospheres	brain
48	chr19:21352200-21359800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr19:21352200-21363800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr19:21353000-21362800	Weak transcription	Hela-S3	cervix

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links