Variant report

Variant	rs72734170
Chromosome Location	chr1:195710874-195710875
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	chr1:195707846..195709349-chr1:195709392..195711387,2	K562	blood:
2	chr1:195710497..195713809-chr1:195716668..195718919,3	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10801449	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10921892	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10921902	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11587693	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11587700	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11802328	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12074167	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12083340	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12083881	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1576764	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17626633	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17626902	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17672688	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17673134	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2895785	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2942913	0.87[ASN][1000 genomes]
rs2989981	0.87[ASN][1000 genomes]
rs4304556	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4335360	0.83[ASN][1000 genomes]
rs4514223	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55707019	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55894754	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56012771	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56024053	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs56067913	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72734142	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72734144	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72734150	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72734151	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72734153	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72734155	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72734156	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72734157	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72734159	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72734164	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72734165	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72734166	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72734169	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72736158	0.83[ASN][1000 genomes]
rs7415128	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv872894	chr1:195053221-195745968	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1009307	chr1:195368381-195726703	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv872932	chr1:195447286-195736070	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv872937	chr1:195493538-195849028	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv1007203	chr1:195672857-195902360	Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:195702800-195712200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr1:195708000-195712400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:195708800-195711200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr1:195709800-195711600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr1:195710600-195713600	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr1:195710800-195711000	Enhancers	Placenta Amnion	Placenta Amnion
7	chr1:195710800-195711200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr1:195710800-195711200	Enhancers	H1 Cell Line	embryonic stem cell
9	chr1:195710800-195711200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr1:195710800-195711200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:195710800-195711200	Enhancers	H9 Cell Line	embryonic stem cell
12	chr1:195710800-195711400	Active TSS	Primary T cells from cord blood	blood
13	chr1:195710800-195711600	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr1:195710800-195711600	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr1:195710800-195711600	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr1:195710800-195711600	Enhancers	iPS-20b Cell Line	embryonic stem cell

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