Variant report

Variant	rs371882359
Chromosome Location	chr14:22103726-22103727
allele	A/C
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	chr14:22103726-22103776	SK-N-SH	brain:	n/a
2	chr14:22103726-22103776	SK-N-MC	brain:	n/a
3	chr14:22103726-22103776	BE2_C	brain:	n/a
4	chr14:22103726-22103776	SKMC	muscle:	n/a
5	chr14:22103726-22103776	HepG2	liver:	n/a
6	chr14:22103726-22103776	HCT-116	colon:	n/a
7	chr14:22103726-22103776	HUVEC	blood vessel:	n/a
8	chr14:22103726-22103776	Hela-S3	cervix:	n/a
9	chr14:22103726-22103776	T-47D	breast:	n/a
10	chr14:22103726-22103776	AG09309	skin:	n/a
11	chr14:22103726-22103776	HPAEpiC	pulmonary alveolar:	n/a
12	chr14:22103726-22103776	HCPEpiC	choroid plexus:	n/a
13	chr14:22103726-22103776	NH-A	brain:	n/a
14	chr14:22103726-22103776	AG04449	skin:	fetal
15	chr14:22103726-22103776	HCM	heart:	n/a
16	chr14:22103726-22103776	SK-N-SH_RA	brain:	n/a
17	chr14:22103726-22103776	SAEC	small airway:	n/a
18	chr14:22103726-22103776	ProgFib	skin:	n/a
19	chr14:22103726-22103776	PFSK-1	brain:	n/a
20	chr14:22103726-22103776	H1-hESC	embryonic stem cell:	embryo
21	chr14:22103726-22103776	U87	brain:	n/a
22	chr14:22103726-22103776	MCF10A-Er-Src	breast:	n/a
23	chr14:22103726-22103776	BJ	skin:	n/a
24	chr14:22103726-22103776	HL-60	blood:	n/a
25	chr14:22103726-22103776	ovcar-3	ovarian:	n/a
26	chr14:22103726-22103776	RPTEC	kidney:	n/a
27	chr14:22103726-22103776	IMR90	lung:	fetal
28	chr14:22103726-22103776	AoSMC	blood vessel:	n/a
29	chr14:22103726-22103776	A549	lung:	n/a
30	chr14:22103726-22103776	Hepatocyte	liver:	n/a
31	chr14:22103726-22103776	PANC-1	pancreas:	n/a
32	chr14:22103726-22103776	NHBE	bronchial:	n/a
33	chr14:22103726-22103776	MCF-7	breast:	n/a
34	chr14:22103726-22103776	CMK	blood:	n/a
35	chr14:22103726-22103776	Jurkat	blood:	n/a
36	chr14:22103726-22103776	GM19239	blood:	n/a
37	chr14:22103726-22103776	HRE	kidney:	n/a
38	chr14:22103726-22103776	HNPCEpiC	eye:	n/a
39	chr14:22103726-22103776	HEK293	kidney:	embryo
40	chr14:22103726-22103776	GM12892	blood:	n/a
41	chr14:22103726-22103776	HMEC	breast:	n/a
42	chr14:22103726-22103776	NHDF-neo	bronchial:	n/a
43	chr14:22103726-22103776	ECC-1	luminal epithelium:	n/a
44	chr14:22103726-22103776	Caco-2	colon:	n/a
45	chr14:22103726-22103776	HRCEpiC	kidney:	n/a
46	chr14:22103726-22103776	K562	blood:	n/a
47	chr14:22103726-22103776	GM12891	blood:	n/a
48	chr14:22103726-22103776	PrEC	prostate:	n/a
49	chr14:22103726-22103776	AG10803	skin:	n/a
50	chr14:22103726-22103776	HEEpiC	esophagus:	n/a

No data

Variant related genes	Relation type
OR10G2	CpG island

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530769	chr14:21407536-22139126	Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
2	esv2422459	chr14:21931624-22169502	Genic enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
3	nsv1042309	chr14:22042511-22866936	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
4	nsv456147	chr14:22073473-22305071	Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
5	nsv563851	chr14:22073473-22305071	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
6	nsv901479	chr14:22102800-22146832	Enhancers Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 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
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