Variant report

Variant	rs62119675
Chromosome Location	chr19:39829648-39829649
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:39826340..39829691-chr19:39831267..39834495,5	K562	blood:
2	chr19:39826587..39828135-chr19:39829547..39831242,2	K562	blood:
3	chr19:39828912..39834348-chr19:39896525..39904623,14	K562	blood:
4	chr19:39822373..39824358-chr19:39828655..39830757,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000090924	Chromatin interaction
ENSG00000128016	Chromatin interaction
ENSG00000266559	Chromatin interaction
ENSG00000179134	Chromatin interaction
ENSG00000269246	Chromatin interaction
ENSG00000130755	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs40469	0.82[EUR][1000 genomes]
rs45591338	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs45613331	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs61736260	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62119672	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62119676	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62119678	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62119679	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62119680	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62119682	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62119685	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62119686	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62119687	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62119688	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62119689	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62119690	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62119692	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62119693	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62119695	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62119697	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62119698	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62119699	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62119700	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62119702	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62119721	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62119722	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62119723	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62122887	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62122888	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62122889	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62122891	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62122892	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432048	chr19:39572060-39850060	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv833830	chr19:39709538-39837846	Enhancers Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
3	nsv911679	chr19:39735106-39924129	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	198 gene(s)	inside rSNPs	diseases
4	nsv1058514	chr19:39744112-39902580	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	187 gene(s)	inside rSNPs	diseases
5	nsv911680	chr19:39792460-39924129	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	194 gene(s)	inside rSNPs	diseases
6	nsv911681	chr19:39797716-39856246	Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
7	esv10629	chr19:39811570-39886212	Flanking Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
8	nsv870133	chr19:39822160-39938468	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	233 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39818600-39831600	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr19:39823800-39831200	Weak transcription	A549	lung
3	chr19:39826400-39831400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr19:39826400-39831400	Weak transcription	Brain Angular Gyrus	brain
5	chr19:39826400-39831400	Weak transcription	Brain Anterior Caudate	brain
6	chr19:39826400-39831400	Weak transcription	Brain Cingulate Gyrus	brain
7	chr19:39826400-39831400	Weak transcription	Colon Smooth Muscle	Colon
8	chr19:39826600-39830400	Weak transcription	Fetal Intestine Small	intestine
9	chr19:39826600-39830600	Weak transcription	Liver	Liver
10	chr19:39826600-39830600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr19:39826600-39830600	Weak transcription	Fetal Intestine Large	intestine
12	chr19:39826600-39830800	Weak transcription	Lung	lung
13	chr19:39826600-39831400	Weak transcription	Small Intestine	intestine
14	chr19:39826600-39831600	Weak transcription	Esophagus	oesophagus
15	chr19:39826800-39831000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr19:39826800-39831200	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr19:39826800-39831400	Weak transcription	Brain Hippocampus Middle	brain
18	chr19:39826800-39831400	Weak transcription	Fetal Muscle Trunk	muscle
19	chr19:39826800-39831400	Weak transcription	Left Ventricle	heart
20	chr19:39826800-39831400	Weak transcription	Right Ventricle	heart
21	chr19:39826800-39831600	Weak transcription	Right Atrium	heart
22	chr19:39827000-39830400	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr19:39827000-39831200	Weak transcription	Placenta	Placenta
24	chr19:39827000-39831200	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr19:39827000-39831200	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr19:39827000-39831400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr19:39827000-39831400	Enhancers	Fetal Thymus	thymus
28	chr19:39827000-39831400	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr19:39827000-39831400	Weak transcription	NHLF	lung
30	chr19:39827200-39830400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr19:39827400-39831200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr19:39827400-39831400	Weak transcription	HUVEC	blood vessel
33	chr19:39827600-39831200	Weak transcription	Duodenum Mucosa	Duodenum
34	chr19:39828200-39830400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr19:39828400-39830000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr19:39828400-39830600	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr19:39828400-39831200	Weak transcription	HSMM	muscle
38	chr19:39828400-39831400	Weak transcription	Spleen	Spleen
39	chr19:39828600-39829800	Weak transcription	Thymus	Thymus
40	chr19:39828600-39830400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr19:39828600-39830400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr19:39828600-39830600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr19:39828600-39830800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr19:39828600-39831200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
45	chr19:39828600-39831200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr19:39828600-39831200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr19:39828600-39831600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr19:39828800-39830600	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr19:39828800-39830600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr19:39829200-39830200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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