Variant report

Variant	rs67238056
Chromosome Location	chr1:59056827-59056828
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:59041326..59044486-chr1:59056548..59059729,7	MCF-7	breast:
2	chr1:59039068..59041052-chr1:59055428..59057682,2	MCF-7	breast:
3	chr1:59049910..59054215-chr1:59054903..59060265,8	MCF-7	breast:
4	chr1:59055381..59057219-chr1:59060297..59061966,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000184292	Chromatin interaction

Extended variants
information (count: 60 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10889104	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11207260	0.81[EUR][1000 genomes]
rs11207262	0.81[EUR][1000 genomes]
rs11207264	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11207265	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11207266	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11207267	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11207268	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11581594	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11582299	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11583248	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11584788	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11589214	0.81[EUR][1000 genomes]
rs11589236	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11590757	0.81[EUR][1000 genomes]
rs12067296	0.81[EUR][1000 genomes]
rs12067565	0.81[EUR][1000 genomes]
rs12068196	0.83[ASN][1000 genomes]
rs12068201	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12068391	0.81[EUR][1000 genomes]
rs12068457	0.81[EUR][1000 genomes]
rs12068597	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12069688	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12077340	0.81[EUR][1000 genomes]
rs12087583	0.80[ASN][1000 genomes]
rs12092564	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12097882	0.81[EUR][1000 genomes]
rs12406405	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12568356	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17117873	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17117877	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17372425	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17461345	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs232841	0.80[ASN][1000 genomes]
rs232842	0.80[ASN][1000 genomes]
rs232844	0.80[ASN][1000 genomes]
rs232847	0.80[ASN][1000 genomes]
rs34023272	0.81[EUR][1000 genomes]
rs34135541	0.81[EUR][1000 genomes]
rs3893156	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3893157	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs41313363	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs59607787	0.81[EUR][1000 genomes]
rs59924197	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs61779295	0.80[ASN][1000 genomes]
rs61779296	0.80[ASN][1000 genomes]
rs6663327	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6664314	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6666138	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6666304	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6690139	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6704300	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs67264345	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs67443104	0.81[EUR][1000 genomes]
rs67538366	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67673245	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs67805407	0.81[EUR][1000 genomes]
rs68192782	0.81[EUR][1000 genomes]
rs7547070	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003930	chr1:58930444-59157038	Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs67238056	TACSTD2	cis	Whole Blood	GTEx

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:59049400-59057800	Weak transcription	Gastric	stomach
2	chr1:59050600-59057400	Weak transcription	Right Atrium	heart
3	chr1:59051200-59063400	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr1:59051800-59057600	Weak transcription	A549	lung
5	chr1:59052000-59057200	Weak transcription	Hela-S3	cervix
6	chr1:59052200-59057000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr1:59052400-59058000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr1:59052600-59057800	Weak transcription	NH-A	brain
9	chr1:59052600-59057800	Weak transcription	NHLF	lung
10	chr1:59052800-59057200	Weak transcription	HSMMtube	muscle
11	chr1:59052800-59057400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr1:59052800-59057400	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr1:59052800-59057400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr1:59052800-59057400	Weak transcription	Esophagus	oesophagus
15	chr1:59052800-59057400	Weak transcription	Ovary	ovary
16	chr1:59052800-59057400	Weak transcription	HSMM	muscle
17	chr1:59052800-59057600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr1:59053000-59057200	Weak transcription	HUVEC	blood vessel
19	chr1:59053000-59057600	Weak transcription	Osteobl	bone
20	chr1:59054400-59059400	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr1:59054800-59057600	Weak transcription	Placenta	Placenta
22	chr1:59054800-59057800	Weak transcription	Spleen	Spleen
23	chr1:59055000-59060000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr1:59055200-59058200	Weak transcription	Fetal Lung	lung
25	chr1:59055400-59057000	Weak transcription	NHEK	skin
26	chr1:59056000-59057200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr1:59056000-59057200	Weak transcription	NHDF-Ad	bronchial
28	chr1:59056000-59059400	Enhancers	Pancreas	Pancrea
29	chr1:59056200-59057400	Weak transcription	Lung	lung
30	chr1:59056200-59057800	Weak transcription	Psoas Muscle	Psoas
31	chr1:59056400-59058000	Weak transcription	Fetal Stomach	stomach
32	chr1:59056400-59058200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr1:59056400-59059400	Enhancers	HMEC	breast
34	chr1:59056600-59057200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr1:59056800-59058800	Enhancers	Aorta	Aorta
36	chr1:59056800-59058800	Enhancers	Fetal Muscle Leg	muscle
37	chr1:59056800-59059400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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