Variant report

Variant	rs566325660
Chromosome Location	chr6:29343835-29343836
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RAD21	chr6:29343758-29344127	MCF-7	breast:	n/a	chr6:29343951-29343970
2	SMC3	chr6:29343730-29344143	GM12878	blood:	n/a	n/a
3	CTCF	chr6:29343822-29344082	K562	blood:	n/a	chr6:29343952-29343973 chr6:29343950-29343968
4	RAD21	chr6:29343713-29344272	HCT-116	colon:	n/a	chr6:29343951-29343970
5	RAD21	chr6:29343760-29344097	SK-N-SH_RA	brain:	n/a	chr6:29343951-29343970
6	CTCF	chr6:29343707-29344164	MCF-7	breast:	n/a	chr6:29343952-29343973 chr6:29343950-29343968
7	CTCF	chr6:29343740-29343890	NHEK	skin:	n/a	n/a
8	RAD21	chr6:29343699-29344172	HepG2	liver:	n/a	chr6:29343951-29343970
9	CTCF	chr6:29343664-29344257	SK-N-SH	brain:	n/a	chr6:29343952-29343973 chr6:29343950-29343968
10	CTCF	chr6:29343816-29344034	SK-N-SH_RA	brain:	n/a	chr6:29343952-29343973 chr6:29343950-29343968
11	RAD21	chr6:29343808-29344144	GM12878	blood:	n/a	chr6:29343951-29343970
12	CTCF	chr6:29343724-29344261	HCT-116	colon:	n/a	chr6:29343952-29343973 chr6:29343950-29343968
13	ZNF143	chr6:29343809-29344104	GM12878	blood:	n/a	n/a
14	CTCF	chr6:29343820-29343970	HMEC	breast:	n/a	chr6:29343950-29343968
15	CTCF	chr6:29343800-29343950	BE2_C	brain:	n/a	n/a
16	RAD21	chr6:29343790-29344176	H1-hESC	embryonic stem cell:	n/a	chr6:29343951-29343970
17	RAD21	chr6:29343644-29344183	HCT-116	colon:	n/a	chr6:29343951-29343970
18	RAD21	chr6:29343761-29344080	A549	lung:	n/a	chr6:29343951-29343970
19	RAD21	chr6:29343835-29344236	HepG2	liver:	n/a	chr6:29343951-29343970
20	CTCF	chr6:29343720-29343870	GM12873	blood:	n/a	n/a
21	RAD21	chr6:29343729-29344216	H1-hESC	embryonic stem cell:	n/a	chr6:29343951-29343970
22	RAD21	chr6:29343799-29344087	GM12878	blood:	n/a	chr6:29343951-29343970
23	RAD21	chr6:29343749-29344193	MCF-7	breast:	n/a	chr6:29343951-29343970
24	CTCF	chr6:29343790-29344139	GM12878	blood:	n/a	chr6:29343952-29343973 chr6:29343950-29343968
25	CTCF	chr6:29343820-29343970	A549	lung:	n/a	chr6:29343950-29343968
26	CTCF	chr6:29343800-29343950	HBMEC	blood vessel:	n/a	n/a
27	RAD21	chr6:29343756-29344097	H1-hESC	embryonic stem cell:	n/a	chr6:29343951-29343970

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:29343538..29344515-chr6:29556985..29557870,6	MCF-7	breast:
2	chr6:29343821..29344378-chr6:29664074..29664947,2	MCF-7	breast:

Variant related genes	Relation type
OR12D3	TF binding region

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv601215	chr6:28946920-29348297	ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
2	nsv1018937	chr6:28956136-29366175	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
3	nsv1020683	chr6:29225146-29353408	Bivalent Enhancer Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv830624	chr6:29274525-29445565	Enhancers Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	nsv966676	chr6:29326915-29365789	Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv883527	chr6:29342825-29354799	Enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv519453	chr6:29343355-29351873	Enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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