Variant report

Variant	rs1864449
Chromosome Location	chr6:161122763-161122764
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:161122748-161122798	HRE	kidney:	n/a
2	chr6:161122748-161122798	HAEpiC	amniotic membrane:	n/a
3	chr6:161122748-161122798	SKMC	muscle:	n/a
4	chr6:161122748-161122798	HCF	heart:	n/a
5	chr6:161122748-161122798	GM19239	blood:	n/a
6	chr6:161122748-161122798	HCPEpiC	choroid plexus:	n/a
7	chr6:161122748-161122798	HIPEpiC	eye:	n/a
8	chr6:161122748-161122798	U87	brain:	n/a
9	chr6:161122748-161122798	GM12878	blood:	n/a
10	chr6:161122748-161122798	SK-N-SH	brain:	n/a
11	chr6:161122748-161122798	HRCEpiC	kidney:	n/a
12	chr6:161122748-161122798	H1-hESC	embryonic stem cell:	embryo
13	chr6:161122748-161122798	RPTEC	kidney:	n/a
14	chr6:161122748-161122798	HEEpiC	esophagus:	n/a
15	chr6:161122748-161122798	Jurkat	blood:	n/a
16	chr6:161122748-161122798	MCF-7	breast:	n/a
17	chr6:161122748-161122798	GM12892	blood:	n/a
18	chr6:161122748-161122798	NHBE	bronchial:	n/a
19	chr6:161122748-161122798	Caco-2	colon:	n/a
20	chr6:161122748-161122798	HL-60	blood:	n/a
21	chr6:161122748-161122798	T-47D	breast:	n/a
22	chr6:161122748-161122798	Hela-S3	cervix:	n/a
23	chr6:161122748-161122798	ovcar-3	ovarian:	n/a
24	chr6:161122748-161122798	HEK293	kidney:	embryo
25	chr6:161122748-161122798	HRPEpiC	eye:	n/a
26	chr6:161122748-161122798	SAEC	small airway:	n/a
27	chr6:161122748-161122798	LNCaP	prostate:	n/a
28	chr6:161122748-161122798	PFSK-1	brain:	n/a
29	chr6:161122748-161122798	MCF10A-Er-Src	breast:	n/a
30	chr6:161122748-161122798	HepG2	liver:	n/a
31	chr6:161122748-161122798	NH-A	brain:	n/a
32	chr6:161122748-161122798	K562	blood:	n/a
33	chr6:161122748-161122798	HNPCEpiC	eye:	n/a
34	chr6:161122748-161122798	HPAEpiC	pulmonary alveolar:	n/a
35	chr6:161122748-161122798	AG09309	skin:	n/a
36	chr6:161122748-161122798	HCM	heart:	n/a
37	chr6:161122748-161122798	Hepatocyte	liver:	n/a
38	chr6:161122748-161122798	CMK	blood:	n/a
39	chr6:161122748-161122798	SK-N-MC	brain:	n/a
40	chr6:161122748-161122798	PrEC	prostate:	n/a
41	chr6:161122748-161122798	NB4	blood:	n/a
42	chr6:161122748-161122798	IMR90	lung:	fetal
43	chr6:161122748-161122798	ProgFib	skin:	n/a
44	chr6:161122748-161122798	HUVEC	blood vessel:	n/a
45	chr6:161122748-161122798	GM06990	blood:	n/a
46	chr6:161122748-161122798	ECC-1	luminal epithelium:	n/a
47	chr6:161122748-161122798	AG04449	skin:	fetal
48	chr6:161122748-161122798	NHDF-neo	bronchial:	n/a
49	chr6:161122748-161122798	HCT-116	colon:	n/a
50	chr6:161122748-161122798	AG04450	lung:	fetal

No data

Variant related genes	Relation type
PLG	CpG island

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs1009124	0.96[ASN][1000 genomes]
rs10945684	0.96[ASN][1000 genomes]
rs1864450	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1950562	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1965091	1.00[ASN][1000 genomes]
rs2144723	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2163235	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2314851	0.87[ASN][1000 genomes]
rs4063598	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4252045	1.00[ASN][1000 genomes]
rs4252049	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4252065	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7452732	1.00[ASN][1000 genomes]
rs7772437	0.99[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	esv2758089	chr6:160372244-161234665	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	esv2759484	chr6:160372244-161234665	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	nsv605005	chr6:161069941-161152449	Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv981222	chr6:161121517-161135479	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:161120200-161122800	Weak transcription	Fetal Intestine Large	intestine
2	chr6:161121000-161122800	Enhancers	Liver	Liver
3	chr6:161122600-161124000	Enhancers	HepG2	liver

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