Variant report

Variant	rs1633923
Chromosome Location	chr19:35705625-35705626
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:35705153..35708046-chr19:35947064..35948602,2	MCF-7	breast:
2	chr19:35703283..35706238-chr19:35738621..35741297,3	MCF-7	breast:
3	chr19:35705011..35706655-chr19:35719234..35721990,2	K562	blood:
4	chr19:35699017..35701710-chr19:35704867..35706681,2	K562	blood:
5	chr19:35703379..35705750-chr19:35757891..35759671,2	K562	blood:
6	chr19:35634307..35636181-chr19:35704870..35707266,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000105699	Chromatin interaction
ENSG00000177558	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11084807	0.87[EUR][1000 genomes]
rs12461622	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12978960	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1614514	0.85[CEU][hapmap];0.82[EUR][1000 genomes]
rs1688009	0.95[ASN][1000 genomes]
rs1688014	1.00[CEU][hapmap];0.89[JPT][hapmap]
rs2018697	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4805115	0.94[EUR][1000 genomes]
rs4806113	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs517986	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs565918	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6510471	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs6510472	0.89[JPT][hapmap]
rs7250545	1.00[CEU][hapmap];0.89[JPT][hapmap];0.82[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432045	chr19:35556260-36520760	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
2	nsv1060100	chr19:35658505-36170042	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv543993	chr19:35658505-36170042	Enhancers Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
4	nsv1067541	chr19:35698638-35712439	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv1066553	chr19:35698638-35749563	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
6	esv2763203	chr19:35700047-35738400	Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:35693400-35707000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
2	chr19:35694200-35708200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr19:35698000-35708200	Enhancers	Primary B cells from peripheral blood	blood
4	chr19:35698000-35708200	Enhancers	Primary T helper cells fromperipheralblood	blood
5	chr19:35698200-35708000	Enhancers	Primary B cells from cord blood	blood
6	chr19:35699200-35708000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr19:35700600-35707200	Enhancers	Primary hematopoietic stem cells	blood
8	chr19:35701200-35709400	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr19:35702200-35706000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr19:35703200-35707000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
11	chr19:35703400-35705800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr19:35703600-35706000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
13	chr19:35704200-35706200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
14	chr19:35704400-35706000	Enhancers	Fetal Heart	heart
15	chr19:35704400-35706200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr19:35704600-35705800	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr19:35704600-35705800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr19:35704600-35705800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr19:35704600-35705800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr19:35704600-35705800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr19:35704600-35705800	Enhancers	Fetal Intestine Small	intestine
22	chr19:35704600-35705800	Enhancers	HMEC	breast
23	chr19:35704600-35706000	Enhancers	Fetal Intestine Large	intestine
24	chr19:35704600-35706000	Enhancers	Fetal Muscle Leg	muscle
25	chr19:35704600-35706000	Enhancers	Right Atrium	heart
26	chr19:35704600-35706200	Enhancers	K562	blood
27	chr19:35704600-35706800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr19:35704600-35706800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr19:35704600-35708000	Enhancers	NHDF-Ad	bronchial
30	chr19:35704800-35705800	Enhancers	HepG2	liver
31	chr19:35704800-35706000	Enhancers	Right Ventricle	heart
32	chr19:35705000-35705800	Enhancers	Adipose Nuclei	Adipose
33	chr19:35705000-35705800	Enhancers	Colon Smooth Muscle	Colon
34	chr19:35705000-35705800	Enhancers	NHEK	skin
35	chr19:35705000-35706600	Enhancers	Primary T cells from cord blood	blood
36	chr19:35705000-35708000	Enhancers	Primary T cells fromperipheralblood	blood
37	chr19:35705000-35708000	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr19:35705000-35709400	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr19:35705200-35705800	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr19:35705200-35705800	Enhancers	GM12878-XiMat	blood
41	chr19:35705200-35706000	Enhancers	Stomach Smooth Muscle	stomach
42	chr19:35705200-35706000	Enhancers	Spleen	Spleen
43	chr19:35705200-35707800	Weak transcription	Gastric	stomach
44	chr19:35705200-35708600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr19:35705200-35709600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr19:35705200-35711200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr19:35705400-35706000	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr19:35705400-35706000	Enhancers	Hela-S3	cervix
49	chr19:35705400-35707600	Weak transcription	Lung	lung
50	chr19:35705400-35709000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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