Variant report

Variant	rs664245
Chromosome Location	chr6:101334709-101334710
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:101333797..101336056-chr6:101337811..101340573,2	MCF-7	breast:
2	chr6:101333586..101335134-chr6:101338753..101340690,2	K562	blood:
3	chr6:101328677..101332841-chr6:101334376..101338552,5	K562	blood:
4	chr6:101325336..101331866-chr6:101332086..101337094,13	K562	blood:

Variant related genes	Relation type
ENSG00000112249	Chromatin interaction
ENSG00000260000	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1069049	0.93[JPT][hapmap]
rs12174782	0.93[CHB][hapmap];0.93[JPT][hapmap]
rs12530388	0.93[CHB][hapmap]
rs4840159	0.80[CHB][hapmap]
rs592436	0.92[CHB][hapmap];0.93[JPT][hapmap];0.83[AMR][1000 genomes]
rs618919	0.83[AMR][1000 genomes]
rs657915	0.93[JPT][hapmap]
rs6919745	0.93[CHB][hapmap];0.93[JPT][hapmap]
rs6934256	1.00[CHB][hapmap];0.93[JPT][hapmap]
rs705599	0.92[CHB][hapmap];0.93[JPT][hapmap]
rs705605	0.93[CHB][hapmap];0.93[JPT][hapmap];0.81[AMR][1000 genomes]
rs705606	0.80[AMR][1000 genomes]
rs705607	0.92[CHB][hapmap];0.93[JPT][hapmap];0.81[AMR][1000 genomes]
rs705608	0.93[CHB][hapmap];0.93[JPT][hapmap];0.81[AMR][1000 genomes]
rs705610	0.83[AMR][1000 genomes]
rs7739574	0.93[JPT][hapmap]
rs7750098	0.93[JPT][hapmap]
rs7771570	0.80[CHB][hapmap]
rs846775	0.81[AMR][1000 genomes]
rs846794	0.93[CHB][hapmap];0.93[JPT][hapmap]
rs846797	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes]
rs846798	0.92[CHB][hapmap];0.93[JPT][hapmap];0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949535	chr6:100740293-101469052	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer 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	16 gene(s)	inside rSNPs	diseases
2	nsv1020692	chr6:101136992-101426071	ZNF genes & repeats Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv886457	chr6:101158950-101487473	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv1020400	chr6:101172705-101981665	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv538390	chr6:101172705-101981665	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv1019213	chr6:101225650-101623140	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
7	nsv538391	chr6:101225650-101623140	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
8	esv2763587	chr6:101277874-101510491	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 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	chr6:101329800-101335000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr6:101329800-101340600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:101330200-101340000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr6:101330400-101339000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr6:101330600-101335000	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr6:101330800-101339000	Weak transcription	K562	blood
7	chr6:101331600-101339000	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr6:101331600-101340000	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr6:101331600-101340000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr6:101332800-101335400	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr6:101333400-101335400	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr6:101333600-101339600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr6:101333800-101335000	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr6:101334200-101339000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr6:101334200-101339400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr6:101334400-101334800	Weak transcription	HUES64 Cell Line	embryonic stem cell

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