Variant report

Variant	rs73277466
Chromosome Location	chr14:39764490-39764491
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:39763084..39765244-chr14:39767699..39769276,2	MCF-7	breast:

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs17109188	1.00[AMR][1000 genomes]
rs17109213	1.00[AMR][1000 genomes]
rs17109227	1.00[AMR][1000 genomes]
rs17109249	1.00[AMR][1000 genomes]
rs17109258	1.00[AMR][1000 genomes]
rs17109293	1.00[AMR][1000 genomes]
rs17109318	1.00[AMR][1000 genomes]
rs34909359	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56859252	1.00[AMR][1000 genomes]
rs57012657	1.00[AMR][1000 genomes]
rs57430547	1.00[AMR][1000 genomes]
rs57569191	1.00[AMR][1000 genomes]
rs58371839	1.00[AMR][1000 genomes]
rs58889517	1.00[AMR][1000 genomes]
rs59371684	1.00[AMR][1000 genomes]
rs59546917	1.00[AMR][1000 genomes]
rs59597680	1.00[AMR][1000 genomes]
rs59953702	1.00[AMR][1000 genomes]
rs60367463	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60601774	1.00[AMR][1000 genomes]
rs60921042	1.00[AMR][1000 genomes]
rs61176483	1.00[AMR][1000 genomes]
rs61549948	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61668966	1.00[AMR][1000 genomes]
rs7148519	1.00[AMR][1000 genomes]
rs73275040	1.00[AMR][1000 genomes]
rs73275059	1.00[AMR][1000 genomes]
rs73275062	1.00[AMR][1000 genomes]
rs73275075	1.00[AMR][1000 genomes]
rs73275076	1.00[AMR][1000 genomes]
rs73277428	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73277432	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73277440	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73277451	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73277467	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73277471	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73277473	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73277474	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73277475	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73277478	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73277496	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73277499	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73277501	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73279309	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73279392	1.00[AMR][1000 genomes]
rs73283432	1.00[AMR][1000 genomes]
rs73283442	1.00[AMR][1000 genomes]
rs73283453	1.00[AMR][1000 genomes]
rs73285541	1.00[AMR][1000 genomes]
rs73285564	1.00[AMR][1000 genomes]
rs73285569	1.00[AMR][1000 genomes]
rs73285591	1.00[AMR][1000 genomes]
rs73285598	1.00[AMR][1000 genomes]
rs73285599	1.00[AMR][1000 genomes]
rs73287518	1.00[AMR][1000 genomes]
rs73287521	1.00[AMR][1000 genomes]
rs73287541	1.00[AMR][1000 genomes]
rs73287554	1.00[AMR][1000 genomes]
rs73287555	1.00[AMR][1000 genomes]
rs73287560	1.00[AMR][1000 genomes]
rs73287572	1.00[AMR][1000 genomes]
rs73287574	1.00[AMR][1000 genomes]
rs73287602	1.00[AMR][1000 genomes]
rs73291562	1.00[AMR][1000 genomes]
rs73291565	1.00[AMR][1000 genomes]
rs73291581	1.00[AMR][1000 genomes]
rs73291596	1.00[AMR][1000 genomes]
rs73291598	1.00[AMR][1000 genomes]
rs73291685	1.00[AMR][1000 genomes]
rs73293309	1.00[AMR][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	nsv1053133	chr14:39657535-39770729	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1037183	chr14:39736939-39949233	Weak transcription Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv542048	chr14:39736939-39949233	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	nsv977461	chr14:39762414-39770640	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:39738200-39766200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr14:39738200-39813800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr14:39738800-39764800	Weak transcription	NHDF-Ad	bronchial
4	chr14:39739800-39766400	Weak transcription	Aorta	Aorta
5	chr14:39744600-39769800	Weak transcription	Pancreas	Pancrea
6	chr14:39746200-39776600	Weak transcription	K562	blood
7	chr14:39746400-39771200	Weak transcription	Fetal Heart	heart
8	chr14:39749400-39766400	Weak transcription	Right Ventricle	heart
9	chr14:39749400-39785400	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr14:39749600-39765200	Weak transcription	HUVEC	blood vessel
11	chr14:39749600-39771200	Weak transcription	Fetal Kidney	kidney
12	chr14:39752600-39769000	Weak transcription	Colon Smooth Muscle	Colon
13	chr14:39752600-39808200	Weak transcription	Stomach Mucosa	stomach
14	chr14:39755400-39775800	Strong transcription	Primary neutrophils fromperipheralblood	blood
15	chr14:39755400-39783400	Strong transcription	Liver	Liver
16	chr14:39755600-39767600	Strong transcription	Primary T cells fromperipheralblood	blood
17	chr14:39755600-39780400	Strong transcription	HepG2	liver
18	chr14:39755600-39797200	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr14:39756000-39764600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr14:39756000-39788600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr14:39756200-39776000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr14:39756200-39828400	Weak transcription	Brain Germinal Matrix	brain
23	chr14:39756400-39773200	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr14:39756400-39774000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr14:39756600-39819600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr14:39756800-39771200	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr14:39756800-39797800	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr14:39757000-39783400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr14:39757200-39773800	Strong transcription	Primary T helper cells fromperipheralblood	blood
30	chr14:39757400-39771200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr14:39757400-39796000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr14:39757400-39843800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr14:39758400-39767600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr14:39758600-39767400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr14:39758800-39766000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr14:39759400-39770200	Weak transcription	Colonic Mucosa	Colon
37	chr14:39759400-39801800	Weak transcription	NHLF	lung
38	chr14:39760000-39775800	Strong transcription	Primary T helper cells PMA-I stimulated	--
39	chr14:39760600-39765600	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
40	chr14:39760600-39767400	Strong transcription	Adipose Nuclei	Adipose
41	chr14:39760600-39767400	Strong transcription	Skeletal Muscle Female	skeletal muscle
42	chr14:39760800-39771200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr14:39761000-39775200	Strong transcription	Primary B cells from peripheral blood	blood
44	chr14:39761600-39773400	Strong transcription	Fetal Intestine Large	intestine
45	chr14:39761800-39771800	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr14:39762000-39765600	Strong transcription	HUES64 Cell Line	embryonic stem cell
47	chr14:39762200-39767000	Strong transcription	Osteobl	bone
48	chr14:39762200-39774200	Strong transcription	Duodenum Mucosa	Duodenum
49	chr14:39762400-39764800	Strong transcription	HUES48 Cell Line	embryonic stem cell
50	chr14:39762400-39765400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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