Variant report

Variant	rs877506
Chromosome Location	chr14:69028349-69028350
allele	C/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:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:68938535..68940820-chr14:69027924..69029987,2	MCF-7	breast:
2	chr14:68995172..68997333-chr14:69028182..69030145,2	MCF-7	breast:
3	chr14:68998490..69000612-chr14:69028274..69029938,2	MCF-7	breast:
4	chr14:69023246..69027101-chr14:69028219..69030991,3	MCF-7	breast:
5	chr14:69027264..69032673-chr14:69034374..69038789,10	MCF-7	breast:
6	chr14:69019342..69021876-chr14:69025131..69028551,3	MCF-7	breast:
7	chr14:69027252..69028985-chr14:69183923..69186800,2	MCF-7	breast:
8	chr14:69027748..69038857-chr14:69257974..69264472,24	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000182185	Chromatin interaction
ENSG00000185650	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs1023530	0.95[CEU][hapmap]
rs11158750	1.00[CEU][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs12586230	0.81[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12588940	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12590644	0.95[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12882030	1.00[CEU][hapmap];0.82[YRI][hapmap];0.81[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs17105837	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2842333	0.91[CEU][hapmap];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869154	chr14:68366754-69041768	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv832822	chr14:68874640-69060272	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	esv1795754	chr14:69017623-69079110	Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv1832715	chr14:69017623-69079110	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69017400-69030400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:69018200-69029600	Weak transcription	Fetal Intestine Small	intestine
3	chr14:69019400-69028400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr14:69019800-69029800	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr14:69020400-69028400	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr14:69020400-69030000	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr14:69021000-69036200	Weak transcription	Brain Germinal Matrix	brain
8	chr14:69021200-69028400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr14:69021200-69028400	Weak transcription	Fetal Kidney	kidney
10	chr14:69021200-69028600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr14:69021400-69030000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr14:69022000-69028600	Weak transcription	Thymus	Thymus
13	chr14:69022200-69031400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr14:69022400-69028400	Weak transcription	Right Ventricle	heart
15	chr14:69022400-69028600	Weak transcription	Stomach Mucosa	stomach
16	chr14:69022400-69029800	Weak transcription	NH-A	brain
17	chr14:69022600-69028400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr14:69022600-69029400	Weak transcription	HMEC	breast
19	chr14:69022600-69032600	Weak transcription	NHDF-Ad	bronchial
20	chr14:69022800-69029200	Weak transcription	NHEK	skin
21	chr14:69023200-69028400	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr14:69023200-69029200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr14:69023200-69029400	Weak transcription	Aorta	Aorta
24	chr14:69024200-69029600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr14:69025200-69028800	Weak transcription	Primary B cells from peripheral blood	blood
26	chr14:69025200-69029000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr14:69025200-69031200	Weak transcription	HUVEC	blood vessel
28	chr14:69025400-69028400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr14:69025400-69029000	Weak transcription	Spleen	Spleen
30	chr14:69025400-69029800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr14:69026400-69033600	Enhancers	Ovary	ovary
32	chr14:69027200-69033400	Enhancers	Liver	Liver
33	chr14:69027400-69029800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr14:69027400-69029800	Enhancers	HepG2	liver
35	chr14:69027400-69030000	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr14:69027600-69028800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr14:69027600-69030200	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr14:69027600-69030400	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr14:69027600-69032000	Enhancers	Colon Smooth Muscle	Colon
40	chr14:69027600-69032600	Enhancers	Fetal Stomach	stomach
41	chr14:69027600-69032800	Enhancers	Fetal Muscle Trunk	muscle
42	chr14:69027600-69033000	Enhancers	Primary T cells from cord blood	blood
43	chr14:69027600-69033400	Enhancers	Placenta	Placenta
44	chr14:69027600-69033600	Enhancers	Fetal Muscle Leg	muscle
45	chr14:69027800-69033400	Enhancers	Lung	lung
46	chr14:69027800-69033400	Enhancers	Pancreas	Pancrea
47	chr14:69027800-69033600	Enhancers	Fetal Thymus	thymus
48	chr14:69028000-69028600	Enhancers	A549	lung
49	chr14:69028000-69028600	Enhancers	HSMM	muscle
50	chr14:69028000-69029600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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