Variant report

Variant	rs35328461
Chromosome Location	chr19:18572616-18572617
allele	A/C/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	chr19:18571434..18574065-chr19:18793013..18794622,2	K562	blood:
2	chr19:18558274..18559892-chr19:18572198..18574398,2	MCF-7	breast:
3	chr19:18561406..18562774-chr19:18571386..18573287,9	MCF-7	breast:
4	chr19:18571221..18574796-chr19:18667687..18669982,3	MCF-7	breast:
5	chr19:18552236..18554463-chr19:18572240..18574871,2	K562	blood:
6	chr19:18570477..18573833-chr19:18762488..18765349,3	K562	blood:
7	chr19:18555475..18558086-chr19:18572096..18574064,2	K562	blood:
8	chr19:18534057..18535915-chr19:18572174..18573934,2	MCF-7	breast:
9	chr19:18571067..18573112-chr19:18583342..18585104,3	K562	blood:
10	chr19:18530437..18532393-chr19:18572390..18574377,2	MCF-7	breast:
11	chr19:18571458..18573058-chr19:18682527..18684220,2	MCF-7	breast:
12	chr19:18561436..18562624-chr19:18572175..18573129,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000130511	Chromatin interaction
ENSG00000105662	Chromatin interaction
ENSG00000221983	Chromatin interaction
ENSG00000105656	Chromatin interaction
ENSG00000105700	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10403002	1.00[AMR][1000 genomes]
rs11574806	0.87[EUR][1000 genomes]
rs16982418	1.00[EUR][1000 genomes]
rs16982427	1.00[EUR][1000 genomes]
rs16982429	1.00[EUR][1000 genomes]
rs16982485	1.00[EUR][1000 genomes]
rs2314669	0.87[EUR][1000 genomes]
rs34078075	1.00[EUR][1000 genomes]
rs34868531	1.00[EUR][1000 genomes]
rs58410315	1.00[EUR][1000 genomes]
rs58604797	1.00[EUR][1000 genomes]
rs58723610	1.00[EUR][1000 genomes]
rs58842178	1.00[EUR][1000 genomes]
rs59511380	1.00[EUR][1000 genomes]
rs59549953	1.00[EUR][1000 genomes]
rs60687616	1.00[EUR][1000 genomes]
rs61743938	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61743954	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7247603	0.87[EUR][1000 genomes]
rs73523072	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73523074	0.87[EUR][1000 genomes]
rs8101976	1.00[EUR][1000 genomes]
rs8102397	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532614	chr19:18033043-18573963	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	204 gene(s)	inside rSNPs	diseases
2	esv3323899	chr19:18343484-18620429	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers 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	162 gene(s)	inside rSNPs	diseases
3	nsv911274	chr19:18440942-18691942	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
4	nsv1057795	chr19:18453362-18883844	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
5	nsv543925	chr19:18453362-18883844	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
6	nsv428018	chr19:18454891-18663981	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
7	nsv911275	chr19:18484922-18586759	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
8	nsv1060687	chr19:18522527-18643218	Genic enhancers Strong transcription Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
9	nsv532615	chr19:18534867-18796031	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18553400-18579000	Weak transcription	Fetal Kidney	kidney
2	chr19:18553800-18578000	Strong transcription	Primary neutrophils fromperipheralblood	blood
3	chr19:18554000-18577600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr19:18556800-18574800	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr19:18562200-18580200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr19:18562200-18580600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr19:18562800-18580800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr19:18566000-18574400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr19:18566200-18574000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr19:18566200-18574000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr19:18566400-18572800	Strong transcription	Primary T cells from cord blood	blood
12	chr19:18566400-18572800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr19:18566400-18575600	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr19:18566400-18575800	Strong transcription	Primary T cells fromperipheralblood	blood
15	chr19:18566600-18572800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr19:18566600-18575600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr19:18566800-18572800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr19:18566800-18573800	Strong transcription	Primary B cells from cord blood	blood
19	chr19:18566800-18574000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr19:18566800-18575000	Strong transcription	HepG2	liver
21	chr19:18566800-18577200	Strong transcription	Primary B cells from peripheral blood	blood
22	chr19:18566800-18577600	Strong transcription	Primary monocytes fromperipheralblood	blood
23	chr19:18567000-18573800	Genic enhancers	Placenta	Placenta
24	chr19:18567000-18573800	Strong transcription	Dnd41	blood
25	chr19:18567000-18575800	Strong transcription	Thymus	Thymus
26	chr19:18567000-18577400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr19:18567200-18573200	Genic enhancers	Right Ventricle	heart
28	chr19:18567200-18573800	Genic enhancers	Fetal Muscle Trunk	muscle
29	chr19:18567400-18572800	Enhancers	Psoas Muscle	Psoas
30	chr19:18567400-18572800	Genic enhancers	NHDF-Ad	bronchial
31	chr19:18567400-18573000	Genic enhancers	Fetal Muscle Leg	muscle
32	chr19:18567600-18572800	Genic enhancers	Muscle Satellite Cultured Cells	--
33	chr19:18567800-18578200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr19:18568200-18583800	Weak transcription	Fetal Brain Male	brain
35	chr19:18568600-18573200	Strong transcription	K562	blood
36	chr19:18569000-18573000	Strong transcription	Fetal Brain Female	brain
37	chr19:18569200-18572800	Strong transcription	HUES6 Cell Line	embryonic stem cell
38	chr19:18569400-18572800	Strong transcription	Cortex derived primary cultured neurospheres	brain
39	chr19:18569600-18575000	Weak transcription	Primary hematopoietic stem cells	blood
40	chr19:18569800-18572800	Enhancers	Right Atrium	heart
41	chr19:18569800-18573000	Strong transcription	H9 Cell Line	embryonic stem cell
42	chr19:18569800-18573000	Genic enhancers	Lung	lung
43	chr19:18570000-18572800	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr19:18570000-18572800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr19:18570000-18572800	Genic enhancers	Duodenum Mucosa	Duodenum
46	chr19:18570200-18572800	Enhancers	Fetal Heart	heart
47	chr19:18570600-18572800	Strong transcription	H1 Cell Line	embryonic stem cell
48	chr19:18570600-18573000	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr19:18570800-18572800	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr19:18570800-18572800	Genic enhancers	Colonic Mucosa	Colon

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