Variant report

Variant	rs660385
Chromosome Location	chr21:46178687-46178688
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr21:46175791..46179741-chr21:46180006..46182976,4	K562	blood:
2	chr21:46177180..46179450-chr21:46200338..46203449,3	MCF-7	breast:
3	chr21:46178137..46180037-chr21:46220379..46223375,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000184787	Chromatin interaction
ENSG00000236519	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1060564	0.96[CHD][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs11569	0.96[CHD][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs13049333	0.86[JPT][hapmap]
rs180317	0.83[ASN][1000 genomes]
rs183518	0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs184633	0.81[ASN][1000 genomes]
rs235267	0.81[ASN][1000 genomes]
rs235269	0.80[ASN][1000 genomes]
rs235271	0.88[CHD][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs235272	0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs235275	0.84[CHD][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs235337	0.86[JPT][hapmap]
rs235352	0.86[JPT][hapmap];0.85[ASN][1000 genomes]
rs235353	0.85[ASN][1000 genomes]
rs235358	0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs235360	0.85[CHD][hapmap];0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs235361	0.84[ASN][1000 genomes]
rs235369	0.82[ASN][1000 genomes]
rs2838695	0.86[JPT][hapmap]
rs434608	0.98[ASN][1000 genomes]
rs657730	0.87[CHB][hapmap];0.93[JPT][hapmap];0.93[ASN][1000 genomes]
rs658637	0.87[CEU][hapmap];0.95[ASN][1000 genomes]
rs658657	0.87[CHB][hapmap];0.93[JPT][hapmap];0.92[ASN][1000 genomes]
rs690626	0.86[JPT][hapmap]
rs7280306	0.98[ASN][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	nsv916258	chr21:45995986-46624705	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	102 gene(s)	inside rSNPs	diseases
2	nsv913956	chr21:46096964-46279505	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
3	nsv1062245	chr21:46096964-46332587	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
4	nsv544478	chr21:46096964-46332587	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs660385	UBE2G2	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:46168000-46185800	Weak transcription	Right Atrium	heart
2	chr21:46171400-46183400	Weak transcription	Gastric	stomach
3	chr21:46173000-46180200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr21:46173000-46180800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr21:46176800-46178800	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr21:46178400-46180000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr21:46178600-46178800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr21:46178600-46179000	Enhancers	Fetal Lung	lung

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