Variant report

Variant	rs11850847
Chromosome Location	chr14:65933798-65933799
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	chr14:65879676..65881204-chr14:65933662..65936142,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000033170	Chromatin interaction

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs10138765	0.83[EUR][1000 genomes]
rs11844747	1.00[CEU][hapmap];0.85[CHB][hapmap];0.82[JPT][hapmap];0.89[EUR][1000 genomes]
rs11845794	1.00[CEU][hapmap];0.80[CHB][hapmap]
rs11849252	1.00[CEU][hapmap]
rs11849862	1.00[CEU][hapmap];0.85[CHB][hapmap];0.81[JPT][hapmap];0.83[EUR][1000 genomes]
rs11850160	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs11850163	1.00[CEU][hapmap]
rs11851013	1.00[CEU][hapmap];0.83[JPT][hapmap];0.87[EUR][1000 genomes]
rs11851772	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12431420	1.00[CEU][hapmap];0.85[CHB][hapmap];0.82[JPT][hapmap];0.91[EUR][1000 genomes]
rs12433827	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12434585	1.00[CEU][hapmap];0.83[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12434854	0.81[CHB][hapmap];0.82[JPT][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12435908	1.00[CEU][hapmap]
rs12437427	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17246007	0.87[EUR][1000 genomes]
rs17246035	1.00[CEU][hapmap];0.85[CHB][hapmap];0.82[JPT][hapmap];0.89[EUR][1000 genomes]
rs17246042	0.89[EUR][1000 genomes]
rs17246259	0.81[EUR][1000 genomes]
rs17826580	1.00[CEU][hapmap];0.83[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17826724	1.00[CEU][hapmap]
rs17826736	1.00[CEU][hapmap]
rs17826790	0.83[EUR][1000 genomes]
rs17826796	0.83[EUR][1000 genomes]
rs1953417	1.00[CEU][hapmap];0.85[CHB][hapmap];0.82[JPT][hapmap];0.89[EUR][1000 genomes]
rs1998035	1.00[CEU][hapmap];0.85[CHB][hapmap];0.82[JPT][hapmap]
rs2073294	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs2152375	1.00[CEU][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2184602	1.00[CEU][hapmap];0.83[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2268957	1.00[CEU][hapmap];0.85[CHB][hapmap];0.82[JPT][hapmap]
rs2268958	1.00[CEU][hapmap];0.82[CHB][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap]
rs28668545	0.81[EUR][1000 genomes]
rs56156482	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs57201867	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs57451368	0.85[EUR][1000 genomes]
rs58032513	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs58115860	0.89[EUR][1000 genomes]
rs59117465	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs59204447	0.85[EUR][1000 genomes]
rs59561356	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs59676254	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs59685862	0.89[EUR][1000 genomes]
rs59822422	0.89[EUR][1000 genomes]
rs59921977	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs60396689	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs60554055	0.85[EUR][1000 genomes]
rs60852857	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60927973	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs60942639	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs61315421	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61533229	0.87[EUR][1000 genomes]
rs7140261	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7145574	1.00[CEU][hapmap];0.82[CHB][hapmap];0.83[JPT][hapmap];0.89[EUR][1000 genomes]
rs7150362	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs7150564	0.89[EUR][1000 genomes]
rs7153679	1.00[CEU][hapmap];0.81[CHB][hapmap];0.87[JPT][hapmap];0.85[EUR][1000 genomes]
rs73268512	0.81[EUR][1000 genomes]
rs73268521	0.85[EUR][1000 genomes]
rs73268524	0.83[EUR][1000 genomes]
rs73282213	0.81[EUR][1000 genomes]
rs73282250	0.81[EUR][1000 genomes]
rs73282260	0.83[EUR][1000 genomes]
rs73284121	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73284133	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73284143	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs73286118	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73286169	0.89[EUR][1000 genomes]
rs73286173	0.81[EUR][1000 genomes]
rs8005309	1.00[CEU][hapmap];0.82[CHB][hapmap];0.83[JPT][hapmap];0.89[EUR][1000 genomes]
rs8018909	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs884247	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9635251	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[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	nsv1036403	chr14:65724229-66208114	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv1043943	chr14:65782466-66698411	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
3	nsv542120	chr14:65782466-66698411	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
4	nsv1039168	chr14:65811750-66308343	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
5	esv3366524	chr14:65924360-66423862	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
6	nsv976347	chr14:65929311-65939441	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65898400-65935600	Weak transcription	Gastric	stomach
2	chr14:65905800-65936600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr14:65911200-65942400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr14:65913800-65942400	Weak transcription	Left Ventricle	heart
5	chr14:65917200-65936600	Weak transcription	Pancreas	Pancrea
6	chr14:65918600-65935600	Weak transcription	Fetal Stomach	stomach
7	chr14:65920400-65937800	Weak transcription	Ovary	ovary
8	chr14:65920800-65942400	Weak transcription	Stomach Mucosa	stomach
9	chr14:65922200-65936400	Weak transcription	Placenta	Placenta
10	chr14:65923200-65934800	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr14:65923200-65936000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr14:65923200-65938200	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr14:65923400-65935800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr14:65923400-65937000	Weak transcription	Brain Germinal Matrix	brain
15	chr14:65923400-65938000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr14:65923400-65945000	Weak transcription	NHDF-Ad	bronchial
17	chr14:65924000-65937600	Weak transcription	Fetal Brain Female	brain
18	chr14:65924200-65936600	Weak transcription	Lung	lung
19	chr14:65924400-65935400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr14:65924600-65935400	Weak transcription	Fetal Intestine Small	intestine
21	chr14:65925200-65936000	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr14:65925800-65943200	Weak transcription	Thymus	Thymus
23	chr14:65926000-65938200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr14:65927600-65934800	Weak transcription	Fetal Lung	lung
25	chr14:65927600-65935400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr14:65927600-65936600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr14:65927600-65936600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr14:65928000-65936200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr14:65928200-65936400	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr14:65928200-65936400	Weak transcription	Fetal Intestine Large	intestine
31	chr14:65928600-65935400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr14:65928600-65935600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr14:65928600-65936600	Weak transcription	Adipose Nuclei	Adipose
34	chr14:65928600-65936800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr14:65928600-65936800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
36	chr14:65928600-65937400	Weak transcription	Small Intestine	intestine
37	chr14:65928600-65949400	Weak transcription	Psoas Muscle	Psoas
38	chr14:65928800-65937000	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr14:65928800-65938800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr14:65929000-65936200	Weak transcription	Brain Hippocampus Middle	brain
41	chr14:65929000-65936600	Weak transcription	Primary T helper cells fromperipheralblood	blood
42	chr14:65929200-65934600	Weak transcription	Brain Substantia Nigra	brain
43	chr14:65929200-65934800	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr14:65929200-65935200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr14:65929200-65936400	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr14:65929200-65936400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr14:65929200-65936800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr14:65929200-65937200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr14:65929200-65937200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
50	chr14:65929200-65939800	Weak transcription	Primary hematopoietic stem cells	blood

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