Variant report

Variant	rs9323448
Chromosome Location	chr14:64691456-64691457
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:64690892..64693639-chr14:64700268..64702860,3	MCF-7	breast:
2	chr14:64685399..64687983-chr14:64689618..64691623,2	K562	blood:

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10136955	0.86[YRI][hapmap]
rs10140457	0.80[AMR][1000 genomes]
rs10151446	1.00[CEU][hapmap]
rs11844444	0.84[EUR][1000 genomes]
rs11848293	0.84[EUR][1000 genomes]
rs17101676	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs17101718	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs17179096	0.92[EUR][1000 genomes]
rs17179194	0.92[EUR][1000 genomes]
rs45453691	0.92[EUR][1000 genomes]
rs73279598	0.84[EUR][1000 genomes]
rs8022631	0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv902019	chr14:64395569-64882380	Enhancers Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv456326	chr14:64420413-64754361	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv564905	chr14:64420413-64754361	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv902021	chr14:64647646-64715794	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
5	nsv1050378	chr14:64686543-64703012	Strong transcription Weak transcription Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:64664000-64699600	Weak transcription	Small Intestine	intestine
2	chr14:64664200-64698600	Weak transcription	HMEC	breast
3	chr14:64665400-64700200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr14:64666800-64699400	Strong transcription	Primary T helper cells fromperipheralblood	blood
5	chr14:64672800-64696600	Strong transcription	Primary T cells fromperipheralblood	blood
6	chr14:64674600-64696000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr14:64674600-64696200	Strong transcription	HUES64 Cell Line	embryonic stem cell
8	chr14:64674600-64696400	Strong transcription	HUES48 Cell Line	embryonic stem cell
9	chr14:64674600-64699800	Strong transcription	Liver	Liver
10	chr14:64674800-64692400	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr14:64674800-64692600	Strong transcription	Duodenum Smooth Muscle	Duodenum
12	chr14:64674800-64692800	Strong transcription	Primary T cells from cord blood	blood
13	chr14:64674800-64695800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr14:64674800-64696000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
15	chr14:64674800-64696000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
16	chr14:64674800-64696000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr14:64674800-64696200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr14:64674800-64696200	Strong transcription	Primary neutrophils fromperipheralblood	blood
19	chr14:64674800-64696200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr14:64674800-64696400	Strong transcription	Rectal Mucosa Donor 31	rectum
21	chr14:64674800-64696400	Strong transcription	Dnd41	blood
22	chr14:64674800-64696800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr14:64674800-64697600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr14:64674800-64698400	Strong transcription	HUES6 Cell Line	embryonic stem cell
25	chr14:64674800-64699000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr14:64674800-64700000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr14:64674800-64700600	Strong transcription	Fetal Intestine Large	intestine
28	chr14:64675000-64696400	Strong transcription	Primary T helper cells PMA-I stimulated	--
29	chr14:64675000-64696400	Strong transcription	Brain Germinal Matrix	brain
30	chr14:64675200-64696400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr14:64675400-64695200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr14:64675400-64696200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr14:64675600-64691800	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr14:64676600-64696200	Strong transcription	Rectal Mucosa Donor 29	rectum
35	chr14:64676800-64698800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr14:64677000-64698600	Weak transcription	NHLF	lung
37	chr14:64677000-64698800	Strong transcription	Duodenum Mucosa	Duodenum
38	chr14:64677000-64699400	Strong transcription	Sigmoid Colon	Sigmoid Colon
39	chr14:64677200-64691800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr14:64677200-64698600	Weak transcription	NHDF-Ad	bronchial
41	chr14:64677400-64697800	Strong transcription	Fetal Stomach	stomach
42	chr14:64677600-64698200	Strong transcription	Colonic Mucosa	Colon
43	chr14:64679800-64698200	Weak transcription	HUVEC	blood vessel
44	chr14:64679800-64698800	Weak transcription	NH-A	brain
45	chr14:64680600-64694800	Strong transcription	Fetal Intestine Small	intestine
46	chr14:64681200-64692600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr14:64681400-64692400	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr14:64681600-64698800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr14:64684400-64696800	Strong transcription	Adipose Nuclei	Adipose
50	chr14:64684400-64699600	Strong transcription	Placenta	Placenta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links