Variant report

Variant	rs10425846
Chromosome Location	chr19:35703320-35703321
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:35703283..35706238-chr19:35738621..35741297,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000105699	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10403023	0.96[ASN][1000 genomes]
rs12982723	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1633924	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1688010	0.98[ASN][1000 genomes]
rs1688011	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1688012	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17541474	0.85[EUR][1000 genomes]
rs17613706	0.89[EUR][1000 genomes]
rs28579145	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34461963	0.86[EUR][1000 genomes]
rs34979825	0.84[EUR][1000 genomes]
rs36101648	0.81[EUR][1000 genomes]
rs487554	0.98[ASN][1000 genomes]
rs495570	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs498342	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs521055	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs534481	0.98[ASN][1000 genomes]
rs538182	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs540818	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs565818	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62111445	0.88[EUR][1000 genomes]
rs7247282	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8182468	0.96[ASN][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:59 , 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	chr19:35694000-35704400	Enhancers	Primary T cells fromperipheralblood	blood
3	chr19:35694200-35708200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr19:35696600-35704600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr19:35696800-35704600	Weak transcription	Colonic Mucosa	Colon
6	chr19:35697400-35704600	Weak transcription	Small Intestine	intestine
7	chr19:35698000-35708200	Enhancers	Primary B cells from peripheral blood	blood
8	chr19:35698000-35708200	Enhancers	Primary T helper cells fromperipheralblood	blood
9	chr19:35698200-35708000	Enhancers	Primary B cells from cord blood	blood
10	chr19:35699200-35708000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr19:35700400-35704200	Enhancers	Primary T cells from cord blood	blood
12	chr19:35700600-35707200	Enhancers	Primary hematopoietic stem cells	blood
13	chr19:35701200-35709400	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr19:35701400-35705600	Enhancers	Fetal Thymus	thymus
15	chr19:35701800-35703400	Enhancers	Esophagus	oesophagus
16	chr19:35701800-35703400	Enhancers	Thymus	Thymus
17	chr19:35701800-35703400	Enhancers	HepG2	liver
18	chr19:35701800-35703800	Enhancers	Placenta	Placenta
19	chr19:35702000-35704600	Weak transcription	Left Ventricle	heart
20	chr19:35702000-35704600	Weak transcription	K562	blood
21	chr19:35702000-35705000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr19:35702200-35706000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr19:35702400-35703400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
24	chr19:35702400-35703400	Enhancers	Right Atrium	heart
25	chr19:35702400-35703600	Enhancers	Fetal Muscle Leg	muscle
26	chr19:35702400-35703800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
27	chr19:35702400-35704600	Enhancers	GM12878-XiMat	blood
28	chr19:35702600-35703400	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr19:35702600-35703400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
30	chr19:35702600-35703400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
31	chr19:35702600-35703400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr19:35702600-35703400	Enhancers	Lung	lung
33	chr19:35702600-35703600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
34	chr19:35702600-35703600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
35	chr19:35702600-35703600	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr19:35702600-35703600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr19:35702600-35703800	Enhancers	HUVEC	blood vessel
38	chr19:35702600-35704600	Enhancers	Duodenum Mucosa	Duodenum
39	chr19:35702600-35704600	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr19:35702800-35703400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr19:35702800-35703400	Enhancers	Spleen	Spleen
42	chr19:35702800-35704600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr19:35702800-35705600	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr19:35703000-35703400	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr19:35703000-35703400	Enhancers	Brain Hippocampus Middle	brain
46	chr19:35703000-35703400	Enhancers	Duodenum Smooth Muscle	Duodenum
47	chr19:35703000-35703400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
48	chr19:35703000-35703600	Enhancers	Rectal Smooth Muscle	rectum
49	chr19:35703000-35704200	Weak transcription	Stomach Mucosa	stomach
50	chr19:35703000-35704600	Weak transcription	Fetal Muscle Trunk	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links