Variant report

Variant	nsv909694
Chromosome Location	chr18:61766039-61986584
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:666)
CpG islands
(count:305)
Chromatin interactive
region (count:9)
LncRNA
region (count:37)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:666 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr18:61940883-61941395	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr18:61869447-61869901	GM12878	blood:	n/a	n/a
3	ATF2	chr18:61767625-61767949	GM12878	blood:	n/a	n/a
4	BACH1	chr18:61801624-61802143	H1-hESC	embryonic stem cell:	n/a	chr18:61801798-61801812
5	BACH1	chr18:61833159-61833548	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr18:61767609-61767957	GM12878	blood:	n/a	chr18:61767813-61767823 chr18:61767812-61767823
7	BATF	chr18:61767565-61768085	GM12878	blood:	n/a	chr18:61767578-61767586 chr18:61767813-61767823 chr18:61767812-61767823
8	BCL11A	chr18:61767395-61767989	GM12878	blood:	n/a	chr18:61767815-61767824 chr18:61767816-61767825
9	BCL11A	chr18:61940948-61941245	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr18:61801638-61801844	H1-hESC	embryonic stem cell:	n/a	chr18:61801800-61801809 chr18:61801801-61801810
11	BCL11A	chr18:61767583-61767877	GM12878	blood:	n/a	chr18:61767815-61767824 chr18:61767816-61767825
12	BCL11A	chr18:61940890-61941305	H1-hESC	embryonic stem cell:	n/a	n/a
13	BHLHE40	chr18:61870675-61870753	GM12878	blood:	n/a	n/a
14	BHLHE40	chr18:61842749-61842935	GM12878	blood:	n/a	n/a
15	BHLHE40	chr18:61767666-61768345	GM12878	blood:	n/a	n/a
16	BHLHE40	chr18:61794405-61795010	GM12878	blood:	n/a	n/a
17	BHLHE40	chr18:61972110-61972116	GM12878	blood:	n/a	n/a
18	BRCA1	chr18:61869031-61869036	GM12878	blood:	n/a	n/a
19	BRCA1	chr18:61801379-61801960	Hela-S3	cervix:	n/a	n/a
20	CCNT2	chr18:61858063-61858380	K562	blood:	n/a	n/a
21	CEBPB	chr18:61783166-61783540	HepG2	liver:	n/a	chr18:61783346-61783357
22	CEBPB	chr18:61877208-61877497	HepG2	liver:	n/a	chr18:61877336-61877349 chr18:61877335-61877352
23	CEBPB	chr18:61921633-61921944	HepG2	liver:	n/a	n/a
24	CEBPB	chr18:61767590-61767840	IMR90	lung:	n/a	chr18:61767715-61767728 chr18:61767716-61767727 chr18:61767715-61767726
25	CEBPB	chr18:61810885-61811013	HepG2	liver:	n/a	n/a
26	CEBPB	chr18:61875847-61876144	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr18:61877303-61877444	A549	lung:	n/a	chr18:61877336-61877349 chr18:61877335-61877352
28	CEBPB	chr18:61875851-61876154	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr18:61792636-61792951	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr18:61783218-61783438	K562	blood:	n/a	chr18:61783346-61783357
31	CEBPB	chr18:61792622-61792960	IMR90	lung:	n/a	n/a
32	CEBPB	chr18:61953948-61954069	HepG2	liver:	n/a	n/a
33	CEBPB	chr18:61870273-61870546	A549	lung:	n/a	chr18:61870374-61870383 chr18:61870374-61870383 chr18:61870374-61870383 chr18:61870374-61870383
34	CEBPB	chr18:61776195-61776411	HepG2	liver:	n/a	chr18:61776247-61776258
35	CEBPB	chr18:61967966-61967990	A549	lung:	n/a	n/a
36	CEBPB	chr18:61870224-61870527	IMR90	lung:	n/a	chr18:61870374-61870383 chr18:61870374-61870383 chr18:61870374-61870383 chr18:61870374-61870383
37	CEBPB	chr18:61870202-61870548	H1-hESC	embryonic stem cell:	n/a	chr18:61870374-61870383 chr18:61870374-61870383 chr18:61870374-61870383 chr18:61870374-61870383
38	CEBPB	chr18:61870207-61870536	HepG2	liver:	n/a	chr18:61870374-61870383 chr18:61870374-61870383 chr18:61870374-61870383 chr18:61870374-61870383
39	CEBPB	chr18:61967008-61967184	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr18:61783166-61783528	IMR90	lung:	n/a	chr18:61783346-61783357
41	CEBPB	chr18:61778281-61778554	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr18:61924821-61925085	IMR90	lung:	n/a	chr18:61924939-61924950
43	CEBPB	chr18:61921707-61921830	IMR90	lung:	n/a	n/a
44	CEBPB	chr18:61921652-61921957	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr18:61870297-61870487	ECC-1	luminal epithelium:	n/a	chr18:61870374-61870383 chr18:61870374-61870383 chr18:61870374-61870383 chr18:61870374-61870383
46	CEBPB	chr18:61875882-61876124	IMR90	lung:	n/a	n/a
47	CEBPB	chr18:61861939-61862191	HepG2	liver:	n/a	n/a
48	CEBPB	chr18:61783183-61783534	Hela-S3	cervix:	n/a	chr18:61783346-61783357
49	CEBPB	chr18:61801554-61801992	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr18:61940797-61941332	H1-hESC	embryonic stem cell:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:61817088-61817138	HepG2	liver:	n/a
2	chr18:61816543-61816593	SAEC	small airway:	n/a
3	chr18:61817320-61817370	SAEC	small airway:	n/a
4	chr18:61816636-61816686	HIPEpiC	eye:	n/a
5	chr18:61816543-61816593	PFSK-1	brain:	n/a
6	chr18:61816543-61816593	PrEC	prostate:	n/a
7	chr18:61817320-61817370	NHDF-neo	bronchial:	n/a
8	chr18:61816636-61816686	T-47D	breast:	n/a
9	chr18:61816543-61816593	HMEC	breast:	n/a
10	chr18:61817243-61817293	ProgFib	skin:	n/a
11	chr18:61816543-61816593	ProgFib	skin:	n/a
12	chr18:61817243-61817293	NB4	blood:	n/a
13	chr18:61817088-61817138	AG10803	skin:	n/a
14	chr18:61816636-61816686	HCF	heart:	n/a
15	chr18:61816636-61816686	Hela-S3	cervix:	n/a
16	chr18:61817088-61817138	HEK293	kidney:	embryo
17	chr18:61817243-61817293	NT2-D1	testis:	n/a
18	chr18:61817088-61817138	HRPEpiC	eye:	n/a
19	chr18:61817320-61817370	PANC-1	pancreas:	n/a
20	chr18:61816543-61816593	H1-hESC	embryonic stem cell:	embryo
21	chr18:61817320-61817370	ProgFib	skin:	n/a
22	chr18:61816543-61816593	HUVEC	blood vessel:	n/a
23	chr18:61817088-61817138	PANC-1	pancreas:	n/a
24	chr18:61817243-61817293	AG09309	skin:	n/a
25	chr18:61816543-61816593	HAEpiC	amniotic membrane:	n/a
26	chr18:61817088-61817138	GM19239	blood:	n/a
27	chr18:61816636-61816686	AG10803	skin:	n/a
28	chr18:61817088-61817138	A549	lung:	n/a
29	chr18:61817243-61817293	HPAEpiC	pulmonary alveolar:	n/a
30	chr18:61817243-61817293	HEK293	kidney:	embryo
31	chr18:61816636-61816686	BE2_C	brain:	n/a
32	chr18:61817320-61817370	MCF-7	breast:	n/a
33	chr18:61817320-61817370	ovcar-3	ovarian:	n/a
34	chr18:61817243-61817293	SK-N-SH	brain:	n/a
35	chr18:61816636-61816686	GM06990	blood:	n/a
36	chr18:61817088-61817138	HUVEC	blood vessel:	n/a
37	chr18:61817243-61817293	HRCEpiC	kidney:	n/a
38	chr18:61817088-61817138	HMEC	breast:	n/a
39	chr18:61817243-61817293	Caco-2	colon:	n/a
40	chr18:61817243-61817293	IMR90	lung:	fetal
41	chr18:61816636-61816686	NHBE	bronchial:	n/a
42	chr18:61817243-61817293	AoSMC	blood vessel:	n/a
43	chr18:61817243-61817293	HepG2	liver:	n/a
44	chr18:61817243-61817293	LNCaP	prostate:	n/a
45	chr18:61817243-61817293	HL-60	blood:	n/a
46	chr18:61816543-61816593	HIPEpiC	eye:	n/a
47	chr18:61816543-61816593	MCF10A-Er-Src	breast:	n/a
48	chr18:61817320-61817370	AG04450	lung:	fetal
49	chr18:61816543-61816593	ovcar-3	ovarian:	n/a
50	chr18:61816636-61816686	GM19239	blood:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:61854165..61855797-chr18:61857298..61859309,2	MCF-7	breast:
2	chr12:23330560..23331349-chr18:61953012..61953772,2	MCF-7	breast:
3	chr18:61901489..61903388-chr18:61925678..61927439,2	K562	blood:
4	chr18:61854165..61855797-chr18:61857298..61859309,2	MCF-7	breast:
5	chr18:61788364..61791257-chr18:61797699..61800240,2	K562	blood:
6	chr18:61818770..61820270-chr4:129731857..129734037,3	K562	blood:
7	chr18:61818770..61820270-chr4:129732434..129734037,2	K562	blood:
8	chr18:61786877..61787630-chr18:61997133..61998068,4	MCF-7	breast:
9	chr18:61788364..61791257-chr18:61797699..61800240,2	K562	blood:

(count:37 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SERPINB3-1	chr18:61816009-61816260	NR_027245
2	lnc-SERPINB3-2	chr18:61925453-61925754	ENSG00000266952.1
3	lnc-SERPINB8-2	chr18:61826097-61826222	ENSG00000236392.2
4	lnc-SERPINB3-2	chr18:61880318-61882281	NR_033983
5	lnc-SERPINB8-5	chr18:61916536-61916628	NR_033881
6	lnc-SERPINB3-1	chr18:61806691-61806803	NONHSAT059686
7	lnc-SERPINB3-2	chr18:61927150-61927290	ENSG00000266952.1
8	lnc-SERPINB3-2	chr18:61925453-61925754	NR_033983
9	lnc-SERPINB8-2	chr18:61826092-61826222	ENSG00000236392
10	lnc-SERPINB8-5	chr18:61961162-61961350	NR_033881
11	lnc-SERPINB3-2	chr18:61927150-61927290	NR_033983
12	lnc-SERPINB8-2	chr18:61823449-61823500	ENSG00000236392.2
13	lnc-SERPINB8-5	chr18:61771325-61771469	ENSG00000267134.1
14	lnc-SERPINB8-5	chr18:61955030-61955127	ENSG00000267134.1
15	lnc-SERPINB3-2	chr18:61880320-61882281	XLOC_012865
16	lnc-SERPINB3-1	chr18:61778898-61779044	NONHSAT059684
17	lnc-SERPINB8-5	chr18:61916536-61916628	ENSG00000267134.1
18	lnc-SERPINB8-5	chr18:61771325-61771469	NR_033881
19	lnc-SERPINB8-5	chr18:61794619-61794673	ENSG00000267134.1
20	lnc-SERPINB3-1	chr18:61778089-61778341	NONHSAT059684
21	lnc-SERPINB3-1	chr18:61816009-61816108	ENSG00000179676
22	lnc-SERPINB8-2	chr18:61814443-61814604	ENSG00000236392
23	lnc-SERPINB3-2	chr18:61925453-61925754	XLOC_012865
24	lnc-SERPINB8-5	chr18:61961162-61961350	ENSG00000267134.1
25	lnc-SERPINB8-2	chr18:61826330-61826533	ENSG00000236392.2
26	lnc-SERPINB3-1	chr18:61816009-61816289	NONHSAT059684
27	lnc-SERPINB3-1	chr18:61816009-61816264	ENSG00000179676
28	lnc-SERPINB8-2	chr18:61823458-61823500	ENSG00000236392
29	lnc-SERPINB3-2	chr18:61927150-61927290	XLOC_012865
30	lnc-SERPINB8-2	chr18:61823449-61823500	ENSG00000236392
31	lnc-SERPINB3-1	chr18:61806687-61806803	ENSG00000179676
32	lnc-SERPINB8-2	chr18:61826330-61826533	ENSG00000236392
33	lnc-SERPINB3-1	chr18:61816009-61816289	NONHSAT059686
34	lnc-SERPINB3-2	chr18:61880317-61882281	ENSG00000266952.1
35	lnc-SERPINB8-5	chr18:61794619-61794673	NR_033881
36	lnc-SERPINB8-2	chr18:61826097-61826528	ENSG00000236392
37	lnc-SERPINB8-5	chr18:61955030-61955127	NR_033881

No data

Variant related genes	Relation type
ENSG00000267134	TF binding region
ENSG00000236392	TF binding region
ENSG00000266952	TF binding region
LINC00305	TF binding region
ENSG00000267134	CpG island
ENSG00000236392	CpG island
ENSG00000266952	CpG island
LINC00305	CpG island
ENSG00000077684	chromatin interactions
ENSG00000266952	chromatin interactions

Extended variants
information (count: 6090 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:6090 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2613658	chr18:61766039-61766040	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs111564066	chr18:61766042-61766043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs116967920	chr18:61766057-61766058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556131424	chr18:61766062-61766063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs4517884	chr18:61766067-61766068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs77494309	chr18:61766087-61766088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537987481	chr18:61766102-61766103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs552734110	chr18:61766167-61766168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186470629	chr18:61766225-61766226	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs188891061	chr18:61766230-61766231	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs181670093	chr18:61766253-61766254	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs577515901	chr18:61766296-61766297	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs185572668	chr18:61766301-61766302	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs113593345	chr18:61766305-61766306	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs531909995	chr18:61766327-61766328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs541966527	chr18:61766328-61766329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs372375189	chr18:61766335-61766336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75605107	chr18:61766417-61766418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs527289805	chr18:61766425-61766426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs375837414	chr18:61766453-61766454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2676670	chr18:61766454-61766455	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs148195727	chr18:61766499-61766500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533114976	chr18:61766508-61766509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112240334	chr18:61766560-61766561	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs550031905	chr18:61766600-61766601	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs369102410	chr18:61766606-61766607	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs533846151	chr18:61766630-61766631	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs535606011	chr18:61766653-61766654	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs554652352	chr18:61766663-61766664	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs568169294	chr18:61766682-61766683	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs191370700	chr18:61766683-61766684	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs534027274	chr18:61766713-61766714	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs141551288	chr18:61766721-61766722	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs575003505	chr18:61766742-61766743	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs183127248	chr18:61766750-61766751	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs565451203	chr18:61766815-61766816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534144054	chr18:61766876-61766877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs150904135	chr18:61766885-61766886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs4941243	chr18:61766946-61766947	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs76530920	chr18:61766949-61766950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs2850714	chr18:61766976-61766977	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs369444266	chr18:61767085-61767086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs2850688	chr18:61767127-61767128	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs140235884	chr18:61767133-61767134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs143980785	chr18:61767188-61767189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs532919619	chr18:61767192-61767193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs186078818	chr18:61767210-61767211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190948661	chr18:61767264-61767265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs610433	chr18:61767315-61767316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs529056852	chr18:61767316-61767317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
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
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
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
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
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
Invasive pancreatic ductal carcinoma	16982739	CNVD
Colorectal cancer	21297112	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	19150955	CNVD
Acute myeloid leukemia	21251322	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Medulloblastoma	16783165	CNVD
Burkitt''s lymphoma	18698080	CNVD
Colorectal cancer	16774939	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Glioblastoma	21080181	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Colorectal cancer	16912164	CNVD
Intracranial aneurysm	16715129	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Gastric cancer	22539939	CNVD
Ovarian cancer	20844748	CNVD
Squamous cell cancer	20885788	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cancer	20164919	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	21811587	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:744 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:61763000-61774200	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr18:61766600-61768000	Enhancers	Fetal Kidney	kidney
3	chr18:61766800-61768400	Enhancers	GM12878-XiMat	blood
4	chr18:61767800-61769000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr18:61770400-61770800	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr18:61776000-61778000	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr18:61776800-61778000	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr18:61777600-61778800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr18:61777800-61779000	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr18:61778000-61778400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr18:61778000-61778400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
12	chr18:61778000-61778400	Enhancers	Placenta	Placenta
13	chr18:61778000-61778800	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr18:61778000-61778800	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr18:61778000-61778800	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr18:61778000-61779000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr18:61778000-61779000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr18:61778000-61779000	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr18:61778400-61778800	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr18:61778400-61778800	Weak transcription	Placenta	Placenta
21	chr18:61778400-61779400	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr18:61778800-61779000	Enhancers	Placenta	Placenta
23	chr18:61778800-61780000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr18:61778800-61783200	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr18:61778800-61783200	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr18:61778800-61783800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr18:61779000-61782200	Weak transcription	Placenta	Placenta
28	chr18:61779000-61783200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr18:61779400-61779600	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr18:61780000-61780200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr18:61780800-61781000	Enhancers	H9 Cell Line	embryonic stem cell
32	chr18:61780800-61783200	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr18:61782200-61782800	Enhancers	Placenta	Placenta
34	chr18:61783200-61783600	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr18:61783200-61785200	Enhancers	H1 Cell Line	embryonic stem cell
36	chr18:61783200-61785200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr18:61783200-61785600	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr18:61783200-61785600	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr18:61783200-61785600	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr18:61783200-61785600	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr18:61783400-61784000	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr18:61783600-61784600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
43	chr18:61783800-61785000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr18:61783800-61785200	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr18:61784000-61784200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
46	chr18:61784000-61784400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr18:61784000-61784600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr18:61784000-61784800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr18:61784000-61784800	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr18:61784000-61785200	Enhancers	H9 Cell Line	embryonic stem cell

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