Variant report

Variant	esv3448189
Chromosome Location	chr18:30350054-30353852
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:144)
CpG islands
(count:1160)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:144 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr18:30349484-30350573	HepG2	liver:	n/a	n/a
2	BRCA1	chr18:30351008-30351125	HepG2	liver:	n/a	n/a
3	CEBPD	chr18:30351440-30351711	HepG2	liver:	n/a	n/a
4	CEBPD	chr18:30350155-30350704	HepG2	liver:	n/a	n/a
5	CHD1	chr18:30352051-30352232	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD1	chr18:30351193-30351527	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr18:30352230-30352327	HepG2	liver:	n/a	n/a
8	CHD2	chr18:30351305-30351662	HepG2	liver:	n/a	n/a
9	CHD2	chr18:30349596-30351039	HepG2	liver:	n/a	n/a
10	CHD2	chr18:30351912-30351993	HepG2	liver:	n/a	n/a
11	CTBP2	chr18:30350782-30352343	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTBP2	chr18:30349564-30350580	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr18:30350074-30350149	MCF-7	breast:	n/a	n/a
14	CTCF	chr18:30351500-30351650	HEK293	kidney:	n/a	n/a
15	CTCF	chr18:30350040-30350190	SK-N-SH_RA	brain:	n/a	n/a
16	ELF1	chr18:30350342-30350598	HepG2	liver:	n/a	n/a
17	ELF1	chr18:30351404-30351723	HepG2	liver:	n/a	n/a
18	EP300	chr18:30352531-30353547	ECC-1	luminal epithelium:	n/a	chr18:30352890-30352904
19	EP300	chr18:30352701-30353370	ECC-1	luminal epithelium:	n/a	chr18:30352890-30352904
20	FOXP2	chr18:30349540-30350301	PFSK-1	brain:	n/a	n/a
21	HDAC2	chr18:30350272-30350999	HepG2	liver:	n/a	n/a
22	HEY1	chr18:30352876-30353062	HepG2	liver:	n/a	n/a
23	HEY1	chr18:30351777-30352364	HepG2	liver:	n/a	n/a
24	HEY1	chr18:30350643-30351715	HepG2	liver:	n/a	n/a
25	HEY1	chr18:30349545-30351734	HepG2	liver:	n/a	n/a
26	HEY1	chr18:30349551-30350642	HepG2	liver:	n/a	n/a
27	HNF4A	chr18:30350630-30350922	HepG2	liver:	n/a	n/a
28	HNF4A	chr18:30350602-30350964	HepG2	liver:	n/a	n/a
29	HNF4A	chr18:30349321-30351064	HepG2	liver:	n/a	chr18:30349419-30349431
30	HNF4G	chr18:30350640-30350894	HepG2	liver:	n/a	n/a
31	HNF4G	chr18:30350272-30350627	HepG2	liver:	n/a	n/a
32	KAP1	chr18:30352692-30352991	U2OS	brain:	n/a	n/a
33	KAP1	chr18:30352645-30353085	HEK293	kidney:	n/a	n/a
34	MAX	chr18:30350366-30350869	HepG2	liver:	n/a	n/a
35	MAX	chr18:30349544-30350691	H1-hESC	embryonic stem cell:	n/a	n/a
36	MAX	chr18:30349515-30350254	ECC-1	luminal epithelium:	n/a	n/a
37	MAX	chr18:30349450-30350212	H1-hESC	embryonic stem cell:	n/a	n/a
38	MAX	chr18:30351043-30351812	ECC-1	luminal epithelium:	n/a	chr18:30351760-30351770
39	MAX	chr18:30349526-30350245	ECC-1	luminal epithelium:	n/a	n/a
40	MAX	chr18:30349575-30350084	MCF-7	breast:	n/a	n/a
41	MAZ	chr18:30353290-30353631	HepG2	liver:	n/a	n/a
42	MAZ	chr18:30349161-30350570	HepG2	liver:	n/a	n/a
43	MAZ	chr18:30351534-30351707	HepG2	liver:	n/a	n/a
44	MXI1	chr18:30349162-30351185	HepG2	liver:	n/a	n/a
45	MYBL2	chr18:30350150-30350605	HepG2	liver:	n/a	n/a
46	MYBL2	chr18:30350173-30350730	HepG2	liver:	n/a	n/a
47	MYBL2	chr18:30351080-30351761	HepG2	liver:	n/a	n/a
48	MYC	chr18:30350367-30350613	MCF-7	breast:	n/a	n/a
49	MYC	chr18:30349912-30350062	MCF-7	breast:	n/a	n/a
50	MYC	chr18:30349764-30350214	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:30351342-30351392	BJ	skin:	n/a
2	chr18:30351342-30351392	BJ	skin:	n/a
3	chr18:30350441-30350491	AG09319	gingival:	n/a
4	chr18:30353125-30353175	GM12891	blood:	n/a
5	chr18:30351214-30351264	HIPEpiC	eye:	n/a
6	chr18:30353000-30353050	PrEC	prostate:	n/a
7	chr18:30352297-30352347	GM06990	blood:	n/a
8	chr18:30350441-30350491	ProgFib	skin:	n/a
9	chr18:30352505-30352555	AG04449	skin:	fetal
10	chr18:30352975-30353025	AG09309	skin:	n/a
11	chr18:30353125-30353175	LNCaP	prostate:	n/a
12	chr18:30353283-30353333	HAEpiC	amniotic membrane:	n/a
13	chr18:30351472-30351522	K562	blood:	n/a
14	chr18:30353073-30353123	BE2_C	brain:	n/a
15	chr18:30351983-30352033	AG04450	lung:	fetal
16	chr18:30350935-30350985	CMK	blood:	n/a
17	chr18:30352782-30352832	K562	blood:	n/a
18	chr18:30350977-30351027	BJ	skin:	n/a
19	chr18:30350221-30350271	NHDF-neo	bronchial:	n/a
20	chr18:30350935-30350985	AoSMC	blood vessel:	n/a
21	chr18:30352505-30352555	MCF10A-Er-Src	breast:	n/a
22	chr18:30353125-30353175	HRE	kidney:	n/a
23	chr18:30353125-30353175	Hepatocyte	liver:	n/a
24	chr18:30350935-30350985	HCM	heart:	n/a
25	chr18:30353283-30353333	Jurkat	blood:	n/a
26	chr18:30350935-30350985	SK-N-SH	brain:	n/a
27	chr18:30350441-30350491	ovcar-3	ovarian:	n/a
28	chr18:30353283-30353333	RPTEC	kidney:	n/a
29	chr18:30353125-30353175	Hela-S3	cervix:	n/a
30	chr18:30353240-30353290	Hepatocyte	liver:	n/a
31	chr18:30353699-30353749	Jurkat	blood:	n/a
32	chr18:30352297-30352347	IMR90	lung:	fetal
33	chr18:30351214-30351264	AoSMC	blood vessel:	n/a
34	chr18:30352505-30352555	H1-hESC	embryonic stem cell:	embryo
35	chr18:30353073-30353123	Jurkat	blood:	n/a
36	chr18:30351983-30352033	HCT-116	colon:	n/a
37	chr18:30352782-30352832	Caco-2	colon:	n/a
38	chr18:30350221-30350271	HRE	kidney:	n/a
39	chr18:30353073-30353123	HCPEpiC	choroid plexus:	n/a
40	chr18:30352297-30352347	PFSK-1	brain:	n/a
41	chr18:30353073-30353123	Hela-S3	cervix:	n/a
42	chr18:30352975-30353025	T-47D	breast:	n/a
43	chr18:30353000-30353050	MCF-7	breast:	n/a
44	chr18:30353000-30353050	Jurkat	blood:	n/a
45	chr18:30353699-30353749	NHDF-neo	bronchial:	n/a
46	chr18:30352782-30352832	A549	lung:	n/a
47	chr18:30353699-30353749	HCPEpiC	choroid plexus:	n/a
48	chr18:30351342-30351392	HRE	kidney:	n/a
49	chr18:30352297-30352347	SK-N-SH_RA	brain:	n/a
50	chr18:30352505-30352555	NHBE	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr18:30295209..30296136-chr18:30349960..30350509,2	MCF-7	breast:
2	chr18:30348555..30351173-chr18:30358732..30360847,2	MCF-7	breast:

No data

Variant related genes	Relation type
KLHL14	TF binding region
KLHL14	CpG island
ENSG00000243355	chromatin interactions

Extended variants
information (count: 112 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:112 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145953799	chr18:30350078-30350079	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs574080093	chr18:30350148-30350149	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs530606540	chr18:30350149-30350150	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs139808282	chr18:30350156-30350157	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs61737324	chr18:30350165-30350166	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs144497896	chr18:30350169-30350170	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs529572390	chr18:30350207-30350208	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs548025298	chr18:30350237-30350238	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs374457457	chr18:30350240-30350241	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs201954195	chr18:30350255-30350256	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs200898606	chr18:30350256-30350257	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs371127442	chr18:30350259-30350260	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs569840558	chr18:30350261-30350262	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs200246592	chr18:30350339-30350340	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs12960414	chr18:30350364-30350365	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs148422296	chr18:30350372-30350373	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs187378728	chr18:30350404-30350405	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs143489425	chr18:30350405-30350406	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs201853926	chr18:30350448-30350449	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs142625977	chr18:30350462-30350463	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs376235337	chr18:30350466-30350467	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs150980438	chr18:30350510-30350511	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs199730436	chr18:30350530-30350531	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs553349281	chr18:30350540-30350541	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs201743738	chr18:30350560-30350561	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs148041357	chr18:30350651-30350652	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs563446207	chr18:30350664-30350665	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs369221461	chr18:30350683-30350684	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs530538870	chr18:30350752-30350753	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs572051795	chr18:30350772-30350773	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs112071499	chr18:30350784-30350785	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs111576896	chr18:30350905-30350906	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs560726054	chr18:30350968-30350969	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs114037252	chr18:30350978-30350979	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs141733409	chr18:30350987-30350988	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs192114706	chr18:30351030-30351031	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs564126666	chr18:30351068-30351069	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs559652748	chr18:30351104-30351105	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs185350575	chr18:30351126-30351127	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs551578006	chr18:30351155-30351156	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs189756857	chr18:30351207-30351208	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs77270535	chr18:30351224-30351225	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs549409338	chr18:30351298-30351299	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs7229745	chr18:30351310-30351311	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs535054045	chr18:30351312-30351313	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs192772902	chr18:30351316-30351317	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs374908947	chr18:30351323-30351324	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs113012489	chr18:30351336-30351337	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs578015293	chr18:30351337-30351338	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs538901681	chr18:30351359-30351360	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Esophageal squamous carcinoma	18350619	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Glioblastoma multiforme	21922591	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21297112	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	17002787	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	16912164	CNVD
Renal cell carcinoma	19150565	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19150955	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	21811587	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:448 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:30348800-30350200	Bivalent/Poised TSS	HepG2	liver
2	chr18:30348800-30351000	Bivalent/Poised TSS	Primary Natural Killer cells fromperipheralblood	blood
3	chr18:30348800-30353600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
4	chr18:30349000-30350200	Bivalent/Poised TSS	Fetal Kidney	kidney
5	chr18:30349200-30350600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr18:30349200-30351200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
7	chr18:30349200-30351600	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr18:30349200-30352600	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr18:30349200-30353600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
10	chr18:30349400-30350800	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr18:30349400-30351600	Bivalent/Poised TSS	Fetal Brain Female	brain
12	chr18:30349400-30352400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
13	chr18:30349400-30352600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
14	chr18:30349400-30352600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
15	chr18:30349400-30352600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
16	chr18:30349600-30350200	Flanking Active TSS	Ovary	ovary
17	chr18:30349600-30350200	Enhancers	Right Atrium	heart
18	chr18:30349600-30350400	Enhancers	Lung	lung
19	chr18:30349600-30350600	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
20	chr18:30349600-30350600	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
21	chr18:30349600-30350600	Flanking Bivalent TSS/Enh	Esophagus	oesophagus
22	chr18:30349600-30350600	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
23	chr18:30349600-30350600	Flanking Active TSS	Gastric	stomach
24	chr18:30349600-30350800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
25	chr18:30349600-30351000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr18:30349600-30351400	Flanking Active TSS	Right Ventricle	heart
27	chr18:30349600-30352000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
28	chr18:30349600-30352200	Bivalent/Poised TSS	Small Intestine	intestine
29	chr18:30349600-30352400	Active TSS	Pancreatic Islets	Pancreatic Islet
30	chr18:30349600-30352400	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
31	chr18:30349600-30352600	Bivalent/Poised TSS	Psoas Muscle	Psoas
32	chr18:30349800-30350200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
33	chr18:30349800-30350200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr18:30349800-30350200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
35	chr18:30349800-30350200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr18:30349800-30350200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
37	chr18:30349800-30350200	Flanking Bivalent TSS/Enh	Brain Angular Gyrus	brain
38	chr18:30349800-30350200	Flanking Bivalent TSS/Enh	Brain Anterior Caudate	brain
39	chr18:30349800-30350200	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
40	chr18:30349800-30350200	Flanking Bivalent TSS/Enh	NH-A	brain
41	chr18:30349800-30350400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
42	chr18:30349800-30350400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr18:30349800-30350400	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr18:30349800-30350400	Bivalent Enhancer	Fetal Intestine Small	intestine
45	chr18:30349800-30350600	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr18:30349800-30350600	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr18:30349800-30350600	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
48	chr18:30349800-30350600	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
49	chr18:30349800-30350600	Flanking Bivalent TSS/Enh	Brain Inferior Temporal Lobe	brain
50	chr18:30349800-30350600	Flanking Bivalent TSS/Enh	Brain Substantia Nigra	brain

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