Variant report

Variant	nsv566032
Chromosome Location	chr14:104657760-104769149
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1014)
CpG islands
(count:4282)
Chromatin interactive
region (count:51)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1014 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr14:104766727-104766924	K562	blood:	n/a	n/a
2	BACH1	chr14:104692678-104692680	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr14:104717532-104718237	GM12878	blood:	n/a	n/a
4	BCL3	chr14:104733500-104733914	GM12878	blood:	n/a	n/a
5	BCL3	chr14:104713332-104713671	GM12878	blood:	n/a	n/a
6	BCL3	chr14:104755490-104755662	GM12878	blood:	n/a	n/a
7	BCL3	chr14:104733530-104733887	GM12878	blood:	n/a	n/a
8	BCL3	chr14:104733084-104733421	GM12878	blood:	n/a	n/a
9	BCL3	chr14:104754712-104755473	GM12878	blood:	n/a	n/a
10	BCL3	chr14:104754737-104756137	GM12878	blood:	n/a	chr14:104756045-104756058
11	BCL3	chr14:104733046-104733417	GM12878	blood:	n/a	n/a
12	BCL3	chr14:104755664-104755989	GM12878	blood:	n/a	n/a
13	BHLHE40	chr14:104667654-104667658	K562	blood:	n/a	n/a
14	BHLHE40	chr14:104689367-104689702	K562	blood:	n/a	chr14:104689550-104689559 chr14:104689549-104689558 chr14:104689549-104689558
15	BHLHE40	chr14:104733203-104733312	K562	blood:	n/a	n/a
16	BRCA1	chr14:104762913-104763304	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr14:104741821-104742162	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr14:104760931-104761615	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr14:104755929-104756620	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr14:104712001-104712378	HCT-116	colon:	n/a	n/a
21	CBX3	chr14:104711995-104712385	HCT-116	colon:	n/a	n/a
22	CEBPB	chr14:104748127-104748195	HepG2	liver:	n/a	n/a
23	CEBPB	chr14:104721710-104721853	A549	lung:	n/a	chr14:104721796-104721807
24	CEBPB	chr14:104721705-104721905	K562	blood:	n/a	chr14:104721796-104721807
25	CEBPB	chr14:104755978-104756796	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr14:104698470-104698783	K562	blood:	n/a	chr14:104698625-104698636
27	CEBPB	chr14:104738331-104738554	HepG2	liver:	n/a	chr14:104738399-104738410
28	CEBPB	chr14:104762929-104763352	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr14:104713013-104713344	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr14:104698451-104698818	HepG2	liver:	n/a	chr14:104698625-104698636
31	CEBPB	chr14:104741273-104742573	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr14:104738332-104738532	IMR90	lung:	n/a	chr14:104738399-104738410
33	CEBPB	chr14:104698447-104698823	IMR90	lung:	n/a	chr14:104698625-104698636
34	CEBPB	chr14:104745687-104746247	Hela-S3	cervix:	n/a	chr14:104745796-104745807
35	CEBPB	chr14:104759885-104761832	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr14:104738254-104738516	A549	lung:	n/a	chr14:104738399-104738410
37	CEBPB	chr14:104698445-104698820	A549	lung:	n/a	chr14:104698625-104698636
38	CEBPB	chr14:104721659-104721859	HepG2	liver:	n/a	chr14:104721796-104721807
39	CEBPB	chr14:104766604-104766963	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr14:104760514-104760678	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr14:104759827-104760202	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr14:104742073-104742481	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr14:104734458-104734543	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr14:104756031-104756587	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr14:104760913-104761660	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr14:104706780-104707033	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr14:104762980-104763598	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr14:104693333-104693497	H1-hESC	embryonic stem cell:	n/a	chr14:104693423-104693441 chr14:104693425-104693433 chr14:104693426-104693434
49	CTCF	chr14:104690791-104691140	GM12878	blood:	n/a	chr14:104690948-104690957 chr14:104690942-104690960 chr14:104690945-104690955 chr14:104690944-104690957 chr14:104690937-104690958 chr14:104690943-104690959 chr14:104690944-104690957
50	CTCF	chr14:104713156-104713180	Hela-S3	cervix:	n/a	n/a

(count:4282 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:104746687-104746737	MCF10A-Er-Src	breast:	n/a
2	chr14:104665702-104665752	Hepatocyte	liver:	n/a
3	chr14:104668772-104668822	AG04450	lung:	fetal
4	chr14:104733813-104733863	AoSMC	blood vessel:	n/a
5	chr14:104696387-104696437	AG04450	lung:	fetal
6	chr14:104735644-104735694	SK-N-MC	brain:	n/a
7	chr14:104690882-104690932	HAEpiC	amniotic membrane:	n/a
8	chr14:104668827-104668877	GM12878	blood:	n/a
9	chr14:104666047-104666097	Hepatocyte	liver:	n/a
10	chr14:104680011-104680061	ProgFib	skin:	n/a
11	chr14:104741448-104741498	K562	blood:	n/a
12	chr14:104674859-104674909	PFSK-1	brain:	n/a
13	chr14:104746687-104746737	MCF10A-Er-Src	breast:	n/a
14	chr14:104665702-104665752	Hepatocyte	liver:	n/a
15	chr14:104668772-104668822	AG04450	lung:	fetal
16	chr14:104733813-104733863	AoSMC	blood vessel:	n/a
17	chr14:104696387-104696437	AG04450	lung:	fetal
18	chr14:104735644-104735694	SK-N-MC	brain:	n/a
19	chr14:104690882-104690932	HAEpiC	amniotic membrane:	n/a
20	chr14:104668827-104668877	GM12878	blood:	n/a
21	chr14:104666047-104666097	Hepatocyte	liver:	n/a
22	chr14:104680011-104680061	ProgFib	skin:	n/a
23	chr14:104741448-104741498	K562	blood:	n/a
24	chr14:104674859-104674909	PFSK-1	brain:	n/a
25	chr14:104666047-104666097	U87	brain:	n/a
26	chr14:104768316-104768366	HPAEpiC	pulmonary alveolar:	n/a
27	chr14:104743900-104743950	HCPEpiC	choroid plexus:	n/a
28	chr14:104736574-104736624	GM06990	blood:	n/a
29	chr14:104685248-104685298	MCF-7	breast:	n/a
30	chr14:104679960-104680010	HL-60	blood:	n/a
31	chr14:104687369-104687419	GM19239	blood:	n/a
32	chr14:104735644-104735694	BJ	skin:	n/a
33	chr14:104690151-104690201	HIPEpiC	eye:	n/a
34	chr14:104744006-104744056	HRE	kidney:	n/a
35	chr14:104665702-104665752	NHBE	bronchial:	n/a
36	chr14:104668921-104668971	AG09319	gingival:	n/a
37	chr14:104744168-104744218	HRCEpiC	kidney:	n/a
38	chr14:104687369-104687419	AG04449	skin:	fetal
39	chr14:104734272-104734322	HMEC	breast:	n/a
40	chr14:104744006-104744056	GM12878	blood:	n/a
41	chr14:104662709-104662759	HL-60	blood:	n/a
42	chr14:104758477-104758527	HNPCEpiC	eye:	n/a
43	chr14:104734272-104734322	NHDF-neo	bronchial:	n/a
44	chr14:104682988-104683038	LNCaP	prostate:	n/a
45	chr14:104736574-104736624	HAEpiC	amniotic membrane:	n/a
46	chr14:104696387-104696437	AoSMC	blood vessel:	n/a
47	chr14:104705293-104705343	BE2_C	brain:	n/a
48	chr14:104663241-104663291	HEEpiC	esophagus:	n/a
49	chr14:104696220-104696270	CMK	blood:	n/a
50	chr14:104669834-104669884	K562	blood:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:104756389..104758056-chr14:104758774..104761093,2	MCF-7	breast:
2	chr14:104623348..104624079-chr14:104760154..104761091,2	MCF-7	breast:
3	chr14:104747853..104750552-chr14:104755271..104758240,2	MCF-7	breast:
4	chr14:104649230..104653061-chr14:104657794..104660199,5	MCF-7	breast:
5	chr14:104603438..104604496-chr14:104718718..104719807,9	MCF-7	breast:
6	chr14:104746362..104748538-chr14:104754609..104757132,3	MCF-7	breast:
7	chr14:104746362..104748538-chr14:104754609..104757132,3	MCF-7	breast:
8	chr14:104646912..104648600-chr14:104679599..104681696,2	MCF-7	breast:
9	chr14:104651259..104651765-chr14:104760560..104761404,2	MCF-7	breast:
10	chr14:104750633..104755093-chr14:104756730..104760416,4	MCF-7	breast:
11	chr14:104617545..104619541-chr14:104760413..104762032,2	MCF-7	breast:
12	chr14:104736178..104738016-chr14:104740822..104743657,2	MCF-7	breast:
13	chr14:104655728..104658058-chr14:104665902..104667845,2	MCF-7	breast:
14	chr14:104688070..104688871-chr4:134164467..134165082,2	MCF-7	breast:
15	chr14:104722882..104724563-chr14:104724745..104727407,2	MCF-7	breast:
16	chr14:104750633..104755093-chr14:104756730..104760416,4	MCF-7	breast:
17	chr14:104651310..104653934-chr14:104676245..104678161,2	MCF-7	breast:
18	chr14:104649534..104651729-chr14:104660798..104662472,2	MCF-7	breast:
19	chr14:104570906..104573518-chr14:104661055..104663991,2	MCF-7	breast:
20	chr14:104655728..104658058-chr14:104665902..104667845,2	MCF-7	breast:
21	chr14:104747853..104750552-chr14:104755271..104758240,2	MCF-7	breast:
22	chr14:104762292..104764129-chr14:104770564..104772247,2	MCF-7	breast:
23	chr14:104768093..104769693-chr14:104774112..104776117,2	MCF-7	breast:
24	chr14:104723993..104726216-chr14:104758223..104760086,2	K562	blood:
25	chr14:104756422..104758689-chr14:104761247..104763793,2	MCF-7	breast:
26	chr14:104603795..104604545-chr14:104760161..104761480,5	MCF-7	breast:
27	chr14:104600334..104603089-chr14:104739484..104741726,2	MCF-7	breast:
28	chr14:104736178..104738016-chr14:104740822..104743657,2	MCF-7	breast:
29	chr14:104694080..104694805-chr14:105030047..105031033,2	MCF-7	breast:
30	chr14:104641001..104643795-chr14:104659198..104661496,2	MCF-7	breast:
31	chr14:104723993..104726216-chr14:104758223..104760086,2	K562	blood:
32	chr14:104728779..104730960-chr14:104733381..104735361,2	K562	blood:
33	chr14:104747907..104749438-chr14:104962689..104965288,2	K562	blood:
34	chr14:104694371..104697146-chr14:104809063..104811864,2	MCF-7	breast:
35	chr14:104665772..104667960-chr14:104672753..104674404,2	MCF-7	breast:
36	chr14:104709839..104712329-chr14:104712351..104715124,2	MCF-7	breast:
37	chr14:104698677..104700498-chr14:104705265..104708074,2	MCF-7	breast:
38	chr14:104689890..104692418-chr14:104695085..104697901,2	K562	blood:
39	chr14:104756389..104758056-chr14:104758774..104761093,2	MCF-7	breast:
40	chr14:104698677..104700498-chr14:104705265..104708074,2	MCF-7	breast:
41	chr14:104575830..104578279-chr14:104758176..104760324,2	MCF-7	breast:
42	chr14:104728779..104730960-chr14:104733381..104735361,2	K562	blood:
43	chr14:104637815..104640571-chr14:104677890..104680782,2	MCF-7	breast:
44	chr14:104603676..104604415-chr14:104760235..104760804,2	MCF-7	breast:
45	chr14:104665772..104667960-chr14:104672753..104674404,2	MCF-7	breast:
46	chr14:104722882..104724563-chr14:104724745..104727407,2	MCF-7	breast:
47	chr14:104760654..104761549-chr14:104836417..104836978,2	MCF-7	breast:
48	chr14:104654038..104657382-chr14:104659420..104664106,7	MCF-7	breast:
49	chr14:104603553..104604461-chr14:104718749..104719349,2	MCF-7	breast:
50	chr14:104756422..104758689-chr14:104761247..104763793,2	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C14orf144-1	chr14:104756355-104756432	NONHSAT040253
2	lnc-C14orf144-1	chr14:104689931-104690153	ENSG00000258913
3	lnc-RP11-614O9.3.1-3	chr14:104753936-104755057	NONHSAT040254
4	lnc-C14orf144-1	chr14:104689744-104690153	XLOC_010948
5	lnc-C14orf144-1	chr14:104689951-104690153	ENSG00000258913
6	lnc-C14orf144-1	chr14:104753823-104753890	NONHSAT040253
7	lnc-C14orf144-1	chr14:104747468-104747661	NONHSAT040253
8	lnc-KIF26A-1	chr14:104674355-104676114	XLOC_010947
9	lnc-KIF26A-1	chr14:104672529-104672929	XLOC_010947
10	lnc-RP11-614O9.3.1-3	chr14:104755476-104756432	NONHSAT040254
11	lnc-C14orf144-1	chr14:104741681-104741966	ENSG00000258913
12	lnc-C14orf144-1	chr14:104689921-104690153	ENSG00000258913
13	lnc-C14orf144-1	chr14:104754171-104754406	ENSG00000258913
14	lnc-C14orf144-1	chr14:104709434-104710084	ENSG00000258913
15	lnc-RP11-614O9.3.1-3	chr14:104755902-104756432	NONHSAT040255
16	lnc-C14orf144-1	chr14:104753823-104753890	ENSG00000258913
17	lnc-KIF26A-1	chr14:104672215-104672264	XLOC_010947
18	lnc-C14orf144-1	chr14:104709434-104709704	XLOC_010948

No data

Variant related genes	Relation type
ENSG00000258913	TF binding region
C14orf144	TF binding region
ENSG00000258913	CpG island
C14orf144	CpG island
ENSG00000258748	chromatin interactions
ENSG00000228032	chromatin interactions
ENSG00000166183	chromatin interactions
ENSG00000258913	chromatin interactions
ENSG00000207568	chromatin interactions
PDE3B	miRNA target sites
BRWD1	miRNA target sites

Extended variants
information (count: 5489 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:5489 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs947006	chr14:104657760-104657761	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs57482160	chr14:104657762-104657763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559589150	chr14:104657801-104657802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528125690	chr14:104657822-104657823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186751984	chr14:104657823-104657824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs149364852	chr14:104657830-104657831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112631353	chr14:104657831-104657832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530584846	chr14:104657861-104657862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550403760	chr14:104657878-104657879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570102553	chr14:104657879-104657880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567497247	chr14:104657887-104657888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536042972	chr14:104657896-104657897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536047654	chr14:104657904-104657905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191150404	chr14:104657905-104657906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566342930	chr14:104657914-104657915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546522897	chr14:104657920-104657921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534721689	chr14:104657927-104657928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs60651195	chr14:104657928-104657929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577725431	chr14:104658025-104658026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs543464847	chr14:104658030-104658031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs147463079	chr14:104658062-104658063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs573795309	chr14:104658098-104658099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs12892055	chr14:104658127-104658128	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs574288907	chr14:104658233-104658234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs573146747	chr14:104658271-104658272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139835551	chr14:104658272-104658273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564825313	chr14:104658291-104658292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530622302	chr14:104658295-104658296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550448932	chr14:104658304-104658305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561026766	chr14:104658309-104658310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145342080	chr14:104658338-104658339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549527990	chr14:104658342-104658343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs77643529	chr14:104658345-104658346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534947617	chr14:104658354-104658355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs147649361	chr14:104658376-104658377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577917594	chr14:104658438-104658439	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs148690334	chr14:104658439-104658440	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs116546889	chr14:104658522-104658523	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs557208855	chr14:104658523-104658524	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs537555798	chr14:104658524-104658525	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs151185688	chr14:104658544-104658545	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs553098139	chr14:104658549-104658550	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs76227554	chr14:104658558-104658559	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs28621042	chr14:104658568-104658569	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs183804742	chr14:104658587-104658588	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs117419921	chr14:104658604-104658605	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs543228838	chr14:104658612-104658613	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs544175284	chr14:104658647-104658648	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs115760998	chr14:104658656-104658657	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs114237733	chr14:104658660-104658661	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:112)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	17426248	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ependymoma	19289631	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1117 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104643800-104662200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr14:104652600-104660400	Weak transcription	Spleen	Spleen
3	chr14:104655000-104661400	Weak transcription	Fetal Brain Male	brain
4	chr14:104656200-104658400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr14:104656200-104662200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr14:104656200-104669200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr14:104657200-104665400	Weak transcription	Fetal Brain Female	brain
8	chr14:104657400-104657800	Enhancers	Liver	Liver
9	chr14:104658000-104658200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr14:104658400-104659000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr14:104658800-104659200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
12	chr14:104659000-104660400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr14:104660400-104660600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr14:104660400-104660600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr14:104660400-104661000	Enhancers	Spleen	Spleen
16	chr14:104660600-104661200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr14:104660600-104661800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr14:104661000-104663000	Weak transcription	Spleen	Spleen
19	chr14:104661200-104663400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr14:104661400-104661600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr14:104661400-104661600	Enhancers	Fetal Brain Male	brain
22	chr14:104661400-104663600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
23	chr14:104661600-104661800	Enhancers	Brain Germinal Matrix	brain
24	chr14:104661600-104662000	Weak transcription	Fetal Brain Male	brain
25	chr14:104661800-104663200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr14:104661800-104663400	Flanking Active TSS	Brain Germinal Matrix	brain
27	chr14:104662000-104662600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr14:104662000-104663400	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr14:104662000-104663400	Enhancers	Esophagus	oesophagus
30	chr14:104662000-104663800	Enhancers	Fetal Brain Male	brain
31	chr14:104662000-104664000	Enhancers	Fetal Lung	lung
32	chr14:104662200-104662400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr14:104662200-104662400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
34	chr14:104662200-104662600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr14:104662200-104662600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr14:104662200-104662600	Bivalent Enhancer	Stomach Mucosa	stomach
37	chr14:104662200-104662800	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr14:104662200-104663400	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr14:104662200-104663400	Bivalent Enhancer	Fetal Muscle Leg	muscle
40	chr14:104662200-104663600	Bivalent Enhancer	Fetal Stomach	stomach
41	chr14:104662400-104662600	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr14:104662400-104662800	Enhancers	Fetal Kidney	kidney
43	chr14:104662400-104663000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr14:104662400-104663200	Enhancers	Gastric	stomach
45	chr14:104662400-104663400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr14:104662400-104663600	Enhancers	Primary B cells from peripheral blood	blood
47	chr14:104662600-104663400	Bivalent Enhancer	Brain Hippocampus Middle	brain
48	chr14:104662800-104663000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr14:104662800-104663200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr14:104662800-104663400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast

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