Variant report

Variant	rs73264341
Chromosome Location	chr14:31060768-31060769
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:31060440..31063351-chr14:31089762..31092777,3	MCF-7	breast:
2	chr14:31055576..31058014-chr14:31058559..31061042,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000092108	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs12100621	1.00[AMR][1000 genomes]
rs57216699	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57549139	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57618174	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57677010	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58653311	0.83[AFR][1000 genomes]
rs60350877	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60353606	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60362029	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60727186	0.83[AFR][1000 genomes]
rs73251132	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73251134	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73251145	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73251146	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73251151	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73251156	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73251167	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73251168	1.00[AMR][1000 genomes]
rs73251169	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73251177	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73251179	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73251181	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73251184	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73251188	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73251199	0.83[AFR][1000 genomes]
rs73253017	0.83[AFR][1000 genomes]
rs73254546	0.83[AFR][1000 genomes]
rs73254548	0.83[AFR][1000 genomes]
rs73254552	0.83[AFR][1000 genomes]
rs73254553	0.83[AFR][1000 genomes]
rs73254554	0.83[AFR][1000 genomes]
rs73254555	0.83[AFR][1000 genomes]
rs73254556	0.83[AFR][1000 genomes]
rs73254560	0.83[AFR][1000 genomes]
rs73254565	0.83[AFR][1000 genomes]
rs73254568	0.83[AFR][1000 genomes]
rs73254580	0.83[AFR][1000 genomes]
rs73254583	0.83[AFR][1000 genomes]
rs73254586	0.83[AFR][1000 genomes]
rs73254588	0.83[AFR][1000 genomes]
rs73254589	0.83[AFR][1000 genomes]
rs73255979	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73255992	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73258111	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73258118	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73258119	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73264309	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73264311	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73264321	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73264329	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73264330	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73264333	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73264346	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73264352	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73264358	1.00[AMR][1000 genomes]
rs73264362	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv564169	chr14:30819087-31541494	Strong transcription Genic enhancers ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv1036419	chr14:30969616-31224226	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv901581	chr14:30978745-31585289	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31029000-31071800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:31029200-31071800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr14:31032000-31067400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr14:31032400-31067200	Weak transcription	Fetal Stomach	stomach
5	chr14:31033800-31070000	Weak transcription	Lung	lung
6	chr14:31040200-31069800	Weak transcription	Rectal Smooth Muscle	rectum
7	chr14:31043000-31079600	Weak transcription	Gastric	stomach
8	chr14:31043000-31090600	Weak transcription	Small Intestine	intestine
9	chr14:31045000-31070000	Weak transcription	Aorta	Aorta
10	chr14:31045800-31067400	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr14:31046800-31069800	Weak transcription	Fetal Kidney	kidney
12	chr14:31047000-31069800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr14:31047000-31079600	Weak transcription	Pancreas	Pancrea
14	chr14:31047200-31063600	Weak transcription	Fetal Intestine Small	intestine
15	chr14:31048600-31060800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr14:31049600-31079600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr14:31050200-31079800	Weak transcription	Brain Angular Gyrus	brain
18	chr14:31050800-31067800	Weak transcription	Ovary	ovary
19	chr14:31051800-31064600	Strong transcription	HSMM	muscle
20	chr14:31051800-31079600	Weak transcription	Fetal Brain Male	brain
21	chr14:31052000-31077400	Weak transcription	Psoas Muscle	Psoas
22	chr14:31053600-31079800	Weak transcription	Brain Substantia Nigra	brain
23	chr14:31053800-31067600	Weak transcription	Brain Anterior Caudate	brain
24	chr14:31053800-31070200	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr14:31053800-31090600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr14:31054200-31090400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
27	chr14:31054400-31066800	Weak transcription	Brain Germinal Matrix	brain
28	chr14:31054600-31062800	Strong transcription	Monocytes-CD14+_RO01746	blood
29	chr14:31054600-31063400	Strong transcription	A549	lung
30	chr14:31054600-31066800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr14:31054600-31068000	Weak transcription	HSMMtube	muscle
32	chr14:31054800-31063800	Strong transcription	HUES64 Cell Line	embryonic stem cell
33	chr14:31054800-31066800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr14:31054800-31066800	Weak transcription	Fetal Intestine Large	intestine
35	chr14:31054800-31072000	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr14:31054800-31087200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr14:31055000-31086800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr14:31055200-31062800	Strong transcription	Primary T helper cells PMA-I stimulated	--
39	chr14:31055200-31062800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr14:31055200-31063000	Strong transcription	HUES6 Cell Line	embryonic stem cell
41	chr14:31055200-31063000	Strong transcription	Primary hematopoietic stem cells	blood
42	chr14:31055200-31065000	Strong transcription	Osteobl	bone
43	chr14:31055400-31063000	Strong transcription	Primary monocytes fromperipheralblood	blood
44	chr14:31055400-31063800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr14:31055400-31067400	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr14:31055400-31069800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr14:31055400-31070000	Weak transcription	Colonic Mucosa	Colon
48	chr14:31055600-31088000	Strong transcription	HUES48 Cell Line	embryonic stem cell
49	chr14:31056000-31063400	Strong transcription	Dnd41	blood
50	chr14:31056200-31063600	Strong transcription	iPS-20b Cell Line	embryonic stem cell

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