Variant report

Variant	rs571077648
Chromosome Location	chr14:22218530-22218531
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	chr14:22218494-22218544	PrEC	prostate:	n/a
2	chr14:22218494-22218544	GM06990	blood:	n/a
3	chr14:22218494-22218544	PANC-1	pancreas:	n/a
4	chr14:22218494-22218544	HCT-116	colon:	n/a
5	chr14:22218494-22218544	HNPCEpiC	eye:	n/a
6	chr14:22218494-22218544	HCPEpiC	choroid plexus:	n/a
7	chr14:22218494-22218544	CMK	blood:	n/a
8	chr14:22218494-22218544	HRPEpiC	eye:	n/a
9	chr14:22218494-22218544	NHDF-neo	bronchial:	n/a
10	chr14:22218494-22218544	HRCEpiC	kidney:	n/a
11	chr14:22218494-22218544	HRE	kidney:	n/a
12	chr14:22218494-22218544	SK-N-SH	brain:	n/a
13	chr14:22218494-22218544	HIPEpiC	eye:	n/a
14	chr14:22218494-22218544	GM12892	blood:	n/a
15	chr14:22218494-22218544	K562	blood:	n/a
16	chr14:22218494-22218544	AG10803	skin:	n/a
17	chr14:22218494-22218544	NB4	blood:	n/a
18	chr14:22218494-22218544	BE2_C	brain:	n/a
19	chr14:22218494-22218544	AoSMC	blood vessel:	n/a
20	chr14:22218494-22218544	AG04449	skin:	fetal
21	chr14:22218494-22218544	HPAEpiC	pulmonary alveolar:	n/a
22	chr14:22218494-22218544	PFSK-1	brain:	n/a
23	chr14:22218494-22218544	U87	brain:	n/a
24	chr14:22218494-22218544	LNCaP	prostate:	n/a
25	chr14:22218494-22218544	NT2-D1	testis:	n/a
26	chr14:22218494-22218544	Hela-S3	cervix:	n/a
27	chr14:22218494-22218544	HAEpiC	amniotic membrane:	n/a
28	chr14:22218494-22218544	ECC-1	luminal epithelium:	n/a
29	chr14:22218494-22218544	AG09319	gingival:	n/a
30	chr14:22218494-22218544	SK-N-SH_RA	brain:	n/a
31	chr14:22218494-22218544	A549	lung:	n/a
32	chr14:22218494-22218544	HMEC	breast:	n/a
33	chr14:22218494-22218544	NH-A	brain:	n/a
34	chr14:22218494-22218544	NHBE	bronchial:	n/a
35	chr14:22218494-22218544	SAEC	small airway:	n/a
36	chr14:22218494-22218544	GM19239	blood:	n/a
37	chr14:22218494-22218544	T-47D	breast:	n/a
38	chr14:22218494-22218544	AG09309	skin:	n/a
39	chr14:22218494-22218544	ovcar-3	ovarian:	n/a
40	chr14:22218494-22218544	HCF	heart:	n/a
41	chr14:22218494-22218544	Jurkat	blood:	n/a
42	chr14:22218494-22218544	HL-60	blood:	n/a
43	chr14:22218494-22218544	AG04450	lung:	fetal
44	chr14:22218494-22218544	BJ	skin:	n/a
45	chr14:22218494-22218544	Caco-2	colon:	n/a
46	chr14:22218494-22218544	HCM	heart:	n/a
47	chr14:22218494-22218544	IMR90	lung:	fetal
48	chr14:22218494-22218544	H1-hESC	embryonic stem cell:	embryo
49	chr14:22218494-22218544	HepG2	liver:	n/a
50	chr14:22218494-22218544	GM12878	blood:	n/a

No data

Variant related genes	Relation type
RPL4P1	CpG island

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	nsv563852	chr14:22205447-22344160	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv976319	chr14:22218268-22220474	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:22217600-22218600	Enhancers	Fetal Thymus	thymus

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