Variant report

Variant	rs2934730
Chromosome Location	chrX:55114262-55114263
allele	C/T
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	chrX:55114262-55114312	NH-A	brain:	n/a
2	chrX:55114262-55114312	GM12878	blood:	n/a
3	chrX:55114262-55114312	BE2_C	brain:	n/a
4	chrX:55114262-55114312	PFSK-1	brain:	n/a
5	chrX:55114262-55114312	K562	blood:	n/a
6	chrX:55114262-55114312	MCF-7	breast:	n/a
7	chrX:55114262-55114312	HUVEC	blood vessel:	n/a
8	chrX:55114262-55114312	HL-60	blood:	n/a
9	chrX:55114262-55114312	LNCaP	prostate:	n/a
10	chrX:55114262-55114312	BJ	skin:	n/a
11	chrX:55114262-55114312	ECC-1	luminal epithelium:	n/a
12	chrX:55114262-55114312	Hela-S3	cervix:	n/a
13	chrX:55114262-55114312	HRE	kidney:	n/a
14	chrX:55114262-55114312	T-47D	breast:	n/a
15	chrX:55114262-55114312	HRPEpiC	eye:	n/a
16	chrX:55114262-55114312	HAEpiC	amniotic membrane:	n/a
17	chrX:55114262-55114312	HCF	heart:	n/a
18	chrX:55114262-55114312	NT2-D1	testis:	n/a
19	chrX:55114262-55114312	HCPEpiC	choroid plexus:	n/a
20	chrX:55114262-55114312	GM12891	blood:	n/a
21	chrX:55114262-55114312	AG04450	lung:	fetal
22	chrX:55114262-55114312	HepG2	liver:	n/a
23	chrX:55114262-55114312	RPTEC	kidney:	n/a
24	chrX:55114262-55114312	HRCEpiC	kidney:	n/a
25	chrX:55114262-55114312	SAEC	small airway:	n/a
26	chrX:55114262-55114312	PrEC	prostate:	n/a
27	chrX:55114262-55114312	AG10803	skin:	n/a
28	chrX:55114262-55114312	H1-hESC	embryonic stem cell:	embryo
29	chrX:55114262-55114312	NHDF-neo	bronchial:	n/a
30	chrX:55114262-55114312	ProgFib	skin:	n/a
31	chrX:55114262-55114312	GM06990	blood:	n/a
32	chrX:55114262-55114312	AG04449	skin:	fetal
33	chrX:55114262-55114312	SKMC	muscle:	n/a
34	chrX:55114262-55114312	HCT-116	colon:	n/a
35	chrX:55114262-55114312	Caco-2	colon:	n/a
36	chrX:55114262-55114312	Jurkat	blood:	n/a
37	chrX:55114262-55114312	U87	brain:	n/a
38	chrX:55114262-55114312	Hepatocyte	liver:	n/a
39	chrX:55114262-55114312	GM19239	blood:	n/a
40	chrX:55114262-55114312	SK-N-SH_RA	brain:	n/a
41	chrX:55114262-55114312	HPAEpiC	pulmonary alveolar:	n/a
42	chrX:55114262-55114312	ovcar-3	ovarian:	n/a
43	chrX:55114262-55114312	HMEC	breast:	n/a
44	chrX:55114262-55114312	AG09319	gingival:	n/a
45	chrX:55114262-55114312	PANC-1	pancreas:	n/a
46	chrX:55114262-55114312	HNPCEpiC	eye:	n/a
47	chrX:55114262-55114312	AoSMC	blood vessel:	n/a
48	chrX:55114262-55114312	GM12892	blood:	n/a
49	chrX:55114262-55114312	NHBE	bronchial:	n/a
50	chrX:55114262-55114312	HEK293	kidney:	embryo

No data

Variant related genes	Relation type
PAGE2	CpG island

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv19730	chrX:55086753-55121905	Enhancers Bivalent Enhancer	TF binding region CpG island	3 gene(s)	inside rSNPs	n/a
2	esv3345340	chrX:55105625-55119598	Bivalent Enhancer	TF binding region CpG island	1 gene(s)	inside rSNPs	n/a
3	esv3430852	chrX:55105694-55114440	Inactive region	TF binding region CpG island	1 gene(s)	inside rSNPs	n/a

No data

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

No data

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