Variant report

Variant	rs187748717
Chromosome Location	chr2:33954747-33954748
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	NRF1	chr2:33954694-33954832	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:33954735-33954785	Caco-2	colon:	n/a
2	chr2:33954735-33954785	HUVEC	blood vessel:	n/a
3	chr2:33954735-33954785	HCM	heart:	n/a
4	chr2:33954735-33954785	BJ	skin:	n/a
5	chr2:33954735-33954785	HEEpiC	esophagus:	n/a
6	chr2:33954735-33954785	GM19239	blood:	n/a
7	chr2:33954735-33954785	HAEpiC	amniotic membrane:	n/a
8	chr2:33954735-33954785	PrEC	prostate:	n/a
9	chr2:33954735-33954785	GM12891	blood:	n/a
10	chr2:33954735-33954785	MCF-7	breast:	n/a
11	chr2:33954735-33954785	SK-N-SH_RA	brain:	n/a
12	chr2:33954735-33954785	T-47D	breast:	n/a
13	chr2:33954735-33954785	AG04449	skin:	fetal
14	chr2:33954735-33954785	RPTEC	kidney:	n/a
15	chr2:33954735-33954785	Hela-S3	cervix:	n/a
16	chr2:33954735-33954785	AG09309	skin:	n/a
17	chr2:33954735-33954785	NH-A	brain:	n/a
18	chr2:33954735-33954785	CMK	blood:	n/a
19	chr2:33954735-33954785	Jurkat	blood:	n/a
20	chr2:33954735-33954785	HNPCEpiC	eye:	n/a
21	chr2:33954735-33954785	K562	blood:	n/a
22	chr2:33954735-33954785	LNCaP	prostate:	n/a
23	chr2:33954735-33954785	Hepatocyte	liver:	n/a
24	chr2:33954735-33954785	HCF	heart:	n/a
25	chr2:33954735-33954785	ECC-1	luminal epithelium:	n/a
26	chr2:33954735-33954785	HIPEpiC	eye:	n/a
27	chr2:33954735-33954785	ProgFib	skin:	n/a
28	chr2:33954735-33954785	U87	brain:	n/a
29	chr2:33954735-33954785	HCT-116	colon:	n/a
30	chr2:33954735-33954785	SK-N-MC	brain:	n/a
31	chr2:33954735-33954785	HEK293	kidney:	embryo
32	chr2:33954735-33954785	PANC-1	pancreas:	n/a
33	chr2:33954735-33954785	HPAEpiC	pulmonary alveolar:	n/a
34	chr2:33954735-33954785	HRCEpiC	kidney:	n/a
35	chr2:33954735-33954785	H1-hESC	embryonic stem cell:	embryo
36	chr2:33954735-33954785	HRPEpiC	eye:	n/a
37	chr2:33954735-33954785	HepG2	liver:	n/a
38	chr2:33954735-33954785	NHDF-neo	bronchial:	n/a
39	chr2:33954735-33954785	SKMC	muscle:	n/a
40	chr2:33954735-33954785	A549	lung:	n/a
41	chr2:33954735-33954785	SAEC	small airway:	n/a
42	chr2:33954735-33954785	GM06990	blood:	n/a
43	chr2:33954735-33954785	AG09319	gingival:	n/a
44	chr2:33954735-33954785	AoSMC	blood vessel:	n/a
45	chr2:33954735-33954785	AG10803	skin:	n/a
46	chr2:33954735-33954785	NHBE	bronchial:	n/a
47	chr2:33954735-33954785	BE2_C	brain:	n/a
48	chr2:33954735-33954785	MCF10A-Er-Src	breast:	n/a
49	chr2:33954735-33954785	HCPEpiC	choroid plexus:	n/a
50	chr2:33954735-33954785	IMR90	lung:	fetal

No data

Variant related genes	Relation type
MYADML	TF binding region
MYADML	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	esv3350238	chr2:33849408-33979026	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv873793	chr2:33936701-33988173	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
3	nsv873794	chr2:33936701-34103546	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv873795	chr2:33939941-34064746	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv214925	chr2:33951155-33959435	Enhancers ZNF genes & repeats Weak transcription	TF binding region CpG island	1 gene(s)	inside rSNPs	n/a
6	nsv873796	chr2:33953186-33981501	Enhancers ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

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

No data

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