Variant report

Variant	rs73038947
Chromosome Location	chr1:175193057-175193058
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:175165193..175167023-chr1:175191805..175194752,2	K562	blood:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs12066900	1.00[EUR][1000 genomes]
rs12074601	1.00[EUR][1000 genomes]
rs2157566	1.00[EUR][1000 genomes]
rs2861278	1.00[EUR][1000 genomes]
rs4650736	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4650737	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4650738	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4651393	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs4651397	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4651401	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs4651403	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4651442	1.00[EUR][1000 genomes]
rs60264525	1.00[EUR][1000 genomes]
rs60781969	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs61553406	1.00[EUR][1000 genomes]
rs6685421	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73032419	1.00[EUR][1000 genomes]
rs73032430	1.00[EUR][1000 genomes]
rs73032442	1.00[EUR][1000 genomes]
rs73032445	1.00[EUR][1000 genomes]
rs73034615	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73036233	1.00[EUR][1000 genomes]
rs73036254	1.00[EUR][1000 genomes]
rs73038926	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73038929	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73038933	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73038939	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73046091	1.00[EUR][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	nsv949473	chr1:175151666-175391741	Enhancers ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:175188200-175195000	Enhancers	Placenta	Placenta
2	chr1:175188800-175194200	Weak transcription	GM12878-XiMat	blood
3	chr1:175189800-175193200	Weak transcription	Primary B cells from cord blood	blood
4	chr1:175190600-175196000	Weak transcription	Right Atrium	heart
5	chr1:175190800-175196400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr1:175190800-175201200	Weak transcription	Psoas Muscle	Psoas
7	chr1:175191400-175194400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr1:175191600-175195400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr1:175191600-175199200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr1:175191800-175193400	Weak transcription	Fetal Stomach	stomach
11	chr1:175191800-175195600	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr1:175191800-175196600	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr1:175192000-175196000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr1:175192200-175193800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr1:175192600-175200200	Enhancers	Primary B cells from peripheral blood	blood
16	chr1:175192800-175195600	Weak transcription	Spleen	Spleen

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