Variant report

Variant	nsv456147
Chromosome Location	chr14:22073473-22305071
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1835)
CpG islands
(count:1648)
Chromatin interactive
region (count:24)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1835 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:22100505-22100805	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:22179625-22179926	K562	blood:	n/a	n/a
3	ARID3A	chr14:22236446-22236646	K562	blood:	n/a	n/a
4	ARID3A	chr14:22179625-22179949	HepG2	liver:	n/a	n/a
5	ATF1	chr14:22109400-22109600	K562	blood:	n/a	n/a
6	BACH1	chr14:22143914-22143985	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr14:22239915-22240160	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr14:22091049-22091050	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr14:22080493-22080730	GM12878	blood:	n/a	n/a
10	BATF	chr14:22080421-22080820	GM12878	blood:	n/a	n/a
11	BHLHE40	chr14:22236428-22236693	K562	blood:	n/a	n/a
12	BHLHE40	chr14:22236359-22236692	GM12878	blood:	n/a	n/a
13	BHLHE40	chr14:22080385-22080812	GM12878	blood:	n/a	chr14:22080447-22080460 chr14:22080443-22080464
14	BRCA1	chr14:22191831-22191884	HepG2	liver:	n/a	n/a
15	CEBPB	chr14:22179643-22180005	K562	blood:	n/a	chr14:22179946-22179959
16	CEBPB	chr14:22126294-22126423	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr14:22124752-22125048	K562	blood:	n/a	chr14:22124889-22124900
18	CEBPB	chr14:22107189-22107485	HepG2	liver:	n/a	chr14:22107316-22107327
19	CEBPB	chr14:22100593-22100707	K562	blood:	n/a	chr14:22100629-22100640
20	CEBPB	chr14:22187935-22188129	HepG2	liver:	n/a	n/a
21	CEBPB	chr14:22124746-22125041	HepG2	liver:	n/a	chr14:22124889-22124900
22	CEBPB	chr14:22126286-22126507	HepG2	liver:	n/a	n/a
23	CEBPB	chr14:22115279-22115699	MCF-7	breast:	n/a	chr14:22115409-22115422 chr14:22115409-22115420 chr14:22115409-22115422 chr14:22115409-22115422 chr14:22115411-22115422
24	CEBPB	chr14:22115304-22115582	A549	lung:	n/a	chr14:22115409-22115422 chr14:22115409-22115420 chr14:22115409-22115422 chr14:22115409-22115422 chr14:22115411-22115422
25	CEBPB	chr14:22100525-22100771	HepG2	liver:	n/a	chr14:22100629-22100640
26	CEBPB	chr14:22126297-22126473	A549	lung:	n/a	n/a
27	CEBPB	chr14:22249926-22250066	HepG2	liver:	n/a	n/a
28	CEBPB	chr14:22115274-22115574	HepG2	liver:	n/a	chr14:22115409-22115422 chr14:22115409-22115420 chr14:22115409-22115422 chr14:22115409-22115422 chr14:22115411-22115422
29	CEBPB	chr14:22171581-22171967	MCF-7	breast:	n/a	chr14:22171736-22171749
30	CEBPB	chr14:22131108-22131332	IMR90	lung:	n/a	n/a
31	CEBPB	chr14:22220403-22220709	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr14:22179638-22180002	HepG2	liver:	n/a	chr14:22179946-22179959
33	CEBPB	chr14:22179639-22179945	A549	lung:	n/a	n/a
34	CEBPB	chr14:22179577-22179993	MCF-7	breast:	n/a	chr14:22179946-22179959
35	CEBPB	chr14:22100462-22100825	HepG2	liver:	n/a	chr14:22100629-22100640
36	CEBPB	chr14:22278968-22279088	HepG2	liver:	n/a	chr14:22279034-22279045
37	CEBPB	chr14:22249065-22249134	HepG2	liver:	n/a	n/a
38	CEBPB	chr14:22270575-22270843	HepG2	liver:	n/a	chr14:22270690-22270701
39	CEBPB	chr14:22147887-22147981	H1-hESC	embryonic stem cell:	n/a	chr14:22147955-22147966
40	CEBPB	chr14:22100514-22100851	HepG2	liver:	n/a	chr14:22100629-22100640
41	CEBPB	chr14:22115287-22115570	K562	blood:	n/a	chr14:22115409-22115422 chr14:22115409-22115420 chr14:22115409-22115422 chr14:22115409-22115422 chr14:22115411-22115422
42	CEBPB	chr14:22115230-22115604	MCF-7	breast:	n/a	chr14:22115409-22115422 chr14:22115409-22115420 chr14:22115409-22115422 chr14:22115409-22115422 chr14:22115411-22115422
43	CEBPB	chr14:22179640-22179981	IMR90	lung:	n/a	chr14:22179946-22179959
44	CEBPB	chr14:22080468-22080701	HepG2	liver:	n/a	chr14:22080639-22080650
45	CEBPB	chr14:22162653-22162767	HepG2	liver:	n/a	chr14:22162686-22162697
46	CEBPB	chr14:22179641-22179994	H1-hESC	embryonic stem cell:	n/a	chr14:22179946-22179959
47	CEBPB	chr14:22162533-22162719	H1-hESC	embryonic stem cell:	n/a	chr14:22162686-22162697
48	CEBPB	chr14:22220415-22220731	HepG2	liver:	n/a	n/a
49	CEBPB	chr14:22179110-22179134	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr14:22131065-22131322	HepG2	liver:	n/a	n/a

(count:1648 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:22131976-22132026	Hepatocyte	liver:	n/a
2	chr14:22131976-22132026	Hepatocyte	liver:	n/a
3	chr14:22089641-22089691	HIPEpiC	eye:	n/a
4	chr14:22217085-22217135	HCF	heart:	n/a
5	chr14:22292347-22292397	SKMC	muscle:	n/a
6	chr14:22191827-22191877	AG04450	lung:	fetal
7	chr14:22191761-22191811	BJ	skin:	n/a
8	chr14:22191382-22191432	HNPCEpiC	eye:	n/a
9	chr14:22218494-22218544	HEEpiC	esophagus:	n/a
10	chr14:22111727-22111777	Hela-S3	cervix:	n/a
11	chr14:22265369-22265419	Jurkat	blood:	n/a
12	chr14:22217085-22217135	Hela-S3	cervix:	n/a
13	chr14:22236598-22236648	NB4	blood:	n/a
14	chr14:22103082-22103132	SKMC	muscle:	n/a
15	chr14:22089641-22089691	HUVEC	blood vessel:	n/a
16	chr14:22103310-22103360	HNPCEpiC	eye:	n/a
17	chr14:22090709-22090759	BJ	skin:	n/a
18	chr14:22103310-22103360	HMEC	breast:	n/a
19	chr14:22292347-22292397	AG09309	skin:	n/a
20	chr14:22103504-22103554	Hepatocyte	liver:	n/a
21	chr14:22279816-22279866	AG09309	skin:	n/a
22	chr14:22131976-22132026	HRPEpiC	eye:	n/a
23	chr14:22132021-22132071	HCT-116	colon:	n/a
24	chr14:22217085-22217135	GM19239	blood:	n/a
25	chr14:22132021-22132071	GM12878	blood:	n/a
26	chr14:22279816-22279866	SK-N-SH	brain:	n/a
27	chr14:22191382-22191432	AoSMC	blood vessel:	n/a
28	chr14:22090709-22090759	SAEC	small airway:	n/a
29	chr14:22103310-22103360	Hela-S3	cervix:	n/a
30	chr14:22236519-22236569	SKMC	muscle:	n/a
31	chr14:22132021-22132071	Jurkat	blood:	n/a
32	chr14:22241537-22241587	Caco-2	colon:	n/a
33	chr14:22111727-22111777	U87	brain:	n/a
34	chr14:22236519-22236569	PrEC	prostate:	n/a
35	chr14:22241537-22241587	HCM	heart:	n/a
36	chr14:22292347-22292397	T-47D	breast:	n/a
37	chr14:22236519-22236569	HL-60	blood:	n/a
38	chr14:22216296-22216346	K562	blood:	n/a
39	chr14:22191856-22191906	PANC-1	pancreas:	n/a
40	chr14:22103031-22103081	SK-N-SH_RA	brain:	n/a
41	chr14:22216296-22216346	HCPEpiC	choroid plexus:	n/a
42	chr14:22241537-22241587	HCF	heart:	n/a
43	chr14:22131976-22132026	U87	brain:	n/a
44	chr14:22292347-22292397	HUVEC	blood vessel:	n/a
45	chr14:22236519-22236569	AG09319	gingival:	n/a
46	chr14:22110278-22110328	U87	brain:	n/a
47	chr14:22131976-22132026	A549	lung:	n/a
48	chr14:22236519-22236569	CMK	blood:	n/a
49	chr14:22236018-22236068	GM12891	blood:	n/a
50	chr14:22216296-22216346	SKMC	muscle:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:22295303..22297076-chr14:22298582..22300710,2	K562	blood:
2	chr14:22217192..22217714-chr14:22336654..22337322,2	MCF-7	breast:
3	chr14:22191619..22192367-chr14:22202463..22203027,2	MCF-7	breast:
4	chr13:69008871..69009371-chr14:22109098..22109604,2	MCF-7	breast:
5	chr14:22025433..22026344-chr14:22109433..22110015,2	MCF-7	breast:
6	chr14:22295303..22297076-chr14:22298582..22300710,2	K562	blood:
7	chr14:22236090..22236721-chr14:22293035..22293909,3	MCF-7	breast:
8	chr14:22256716..22259521-chr14:22263376..22264997,2	MCF-7	breast:
9	chr14:22074721..22076475-chr14:22089369..22091494,2	MCF-7	breast:
10	chr14:22031087..22032606-chr14:22098992..22101506,2	MCF-7	breast:
11	chr14:22202912..22203435-chr14:22216852..22217387,2	MCF-7	breast:
12	chr14:22081094..22083875-chr14:22197364..22199332,2	MCF-7	breast:
13	chr14:22202912..22203435-chr14:22216852..22217387,2	MCF-7	breast:
14	chr14:22109038..22109779-chr14:22179252..22179808,3	MCF-7	breast:
15	chr14:22081094..22083875-chr14:22197364..22199332,2	MCF-7	breast:
16	chr14:22140885..22141748-chr5:66767836..66768488,2	MCF-7	breast:
17	chr14:22109038..22109779-chr14:22179252..22179808,3	MCF-7	breast:
18	chr14:22264815..22265316-chr14:22293406..22294027,2	MCF-7	breast:
19	chr14:22179693..22180223-chr14:22202227..22202999,2	MCF-7	breast:
20	chr14:22179693..22180223-chr14:22202227..22202999,2	MCF-7	breast:
21	chr14:22256716..22259521-chr14:22263376..22264997,2	MCF-7	breast:
22	chr14:22073139..22075335-chr14:22078669..22080896,2	K562	blood:
23	chr14:22238003..22239945-chr14:22252615..22254697,2	MCF-7	breast:
24	chr14:22238003..22239945-chr14:22252615..22254697,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4E2-2	chr14:22297692-22297743	NONHSAT035707
2	lnc-OR4E2-2	chr14:22297937-22298223	NONHSAT035707
3	lnc-OR10G2-3	chr14:22080078-22080535	NONHSAT035699
4	lnc-OR10G2-1	chr14:22184112-22184486	ENSG00000248358
5	lnc-OR10G2-2	chr14:22117944-22118553	NONHSAT035700
6	lnc-AE000662.92.1-10	chr14:22237068-22237313	NONHSAT035705
7	lnc-OR10G2-1	chr14:22183018-22183212	ENSG00000248358

No data

Variant related genes	Relation type
ENSG00000256385	TF binding region
RPL4P1	TF binding region
OR4E2	TF binding region
TRAV6	TF binding region
TRAV1-1	TF binding region
TRAV8-1	TF binding region
OR10G1P	TF binding region
ENSG00000222776	TF binding region
TRAV3	TF binding region
ARL6IP1P1	TF binding region
TRAV2	TF binding region
TRAV4	TF binding region
TRAV7	TF binding region
TRAV10	TF binding region
TRAV11	TF binding region
TRAV5	TF binding region
ENSG00000248358	TF binding region
ENSG00000256350	TF binding region
TRAV9-1	TF binding region
TRAV12-1	TF binding region
OR10G2	TF binding region
OR4E1	TF binding region
TRAV1-2	TF binding region
ENSG00000256385	CpG island
RPL4P1	CpG island
OR4E2	CpG island
TRAV6	CpG island
TRAV1-1	CpG island
TRAV8-1	CpG island
OR10G1P	CpG island
ENSG00000222776	CpG island
TRAV3	CpG island
ARL6IP1P1	CpG island
TRAV2	CpG island
TRAV4	CpG island
TRAV7	CpG island
TRAV10	CpG island
TRAV11	CpG island
TRAV5	CpG island
ENSG00000248358	CpG island
ENSG00000256350	CpG island
TRAV9-1	CpG island
TRAV12-1	CpG island
OR10G2	CpG island
OR4E1	CpG island
TRAV1-2	CpG island
ENSG00000255569	chromatin interactions
ENSG00000211788	chromatin interactions
ENSG00000256737	chromatin interactions
ENSG00000256385	chromatin interactions
ENSG00000211784	chromatin interactions
ENSG00000211777	chromatin interactions

Extended variants
information (count: 4862 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:4862 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12435291	chr14:22073473-22073474	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs35879562	chr14:22073485-22073486	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs531763425	chr14:22073503-22073504	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs528266286	chr14:22073513-22073514	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs192369658	chr14:22073542-22073543	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs137980576	chr14:22073552-22073553	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs370547039	chr14:22073558-22073559	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs530966330	chr14:22073566-22073567	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs78568220	chr14:22073581-22073582	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs183209276	chr14:22073601-22073602	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs567499564	chr14:22073615-22073616	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs149414094	chr14:22073617-22073618	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs201852526	chr14:22073650-22073651	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs74242618	chr14:22073651-22073652	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs200154727	chr14:22073652-22073653	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs192010512	chr14:22073685-22073686	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs71419157	chr14:22073688-22073689	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs532977990	chr14:22073692-22073693	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs552487090	chr14:22073739-22073740	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs368552341	chr14:22073751-22073752	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs372616664	chr14:22073794-22073795	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs35628489	chr14:22073823-22073824	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs368347542	chr14:22073890-22073891	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs566448501	chr14:22073901-22073902	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs139773086	chr14:22073919-22073920	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs184462849	chr14:22073934-22073935	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs117305217	chr14:22073938-22073939	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs139583760	chr14:22073948-22073949	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs115818010	chr14:22073967-22073968	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs190096150	chr14:22073978-22073979	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs545212448	chr14:22074036-22074037	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs565223289	chr14:22074047-22074048	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs192903812	chr14:22074059-22074060	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs72686040	chr14:22074093-22074094	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs561352840	chr14:22074105-22074106	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs189292125	chr14:22074106-22074107	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs61971835	chr14:22074140-22074141	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs576726536	chr14:22074156-22074157	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs146063521	chr14:22074189-22074190	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs180927013	chr14:22074283-22074284	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs61482390	chr14:22074331-22074332	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs369280745	chr14:22074356-22074357	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs548571476	chr14:22074372-22074373	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs199754645	chr14:22074385-22074386	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs111484656	chr14:22074386-22074387	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs56107795	chr14:22074398-22074399	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs7153247	chr14:22074463-22074464	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs74034941	chr14:22074492-22074493	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs553142747	chr14:22074511-22074512	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs545068714	chr14:22074533-22074534	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Autism	22495311	CNVD
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD
Mortal	21835882	CNVD
Breast cancer	21858162	CNVD
Autism	22102821	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Schizophrenia	23813976	CNVD
Barrett''s syndrome	19417022	CNVD

Chromatin state (count:385 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:22072800-22074800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr14:22080000-22080800	Enhancers	GM12878-XiMat	blood
3	chr14:22080400-22081000	Enhancers	Pancreas	Pancrea
4	chr14:22080800-22081000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr14:22080800-22081200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr14:22081000-22085600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr14:22081200-22081600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr14:22081600-22081800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr14:22081600-22082800	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr14:22081800-22085600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr14:22082200-22082600	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr14:22082400-22082800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr14:22082800-22085600	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr14:22082800-22085600	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr14:22085400-22086000	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr14:22085400-22086000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr14:22085600-22085800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr14:22085600-22086000	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr14:22085600-22086000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr14:22085600-22086000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr14:22085600-22086200	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr14:22085600-22086200	Enhancers	H1 Cell Line	embryonic stem cell
23	chr14:22085600-22086200	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr14:22085600-22086600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr14:22085800-22086000	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr14:22085800-22086200	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr14:22086000-22086600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr14:22105800-22106800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr14:22106000-22106800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr14:22107200-22107600	Enhancers	HepG2	liver
31	chr14:22110200-22112000	Active TSS	Primary T cells fromperipheralblood	blood
32	chr14:22110800-22111800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
33	chr14:22111000-22111200	Enhancers	Primary T cells from cord blood	blood
34	chr14:22111000-22111800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
35	chr14:22111000-22112000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr14:22111000-22112000	Enhancers	H1 Cell Line	embryonic stem cell
37	chr14:22111000-22112000	Enhancers	H9 Cell Line	embryonic stem cell
38	chr14:22111000-22112200	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr14:22111000-22112200	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr14:22111000-22112200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr14:22111000-22112200	Active TSS	Fetal Thymus	thymus
42	chr14:22111200-22112000	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr14:22111200-22112000	Active TSS	Primary T cells from cord blood	blood
44	chr14:22111200-22112400	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr14:22111400-22111800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr14:22111400-22111800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr14:22111400-22112600	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr14:22111600-22111800	Bivalent Enhancer	Hela-S3	cervix
49	chr14:22111600-22112000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr14:22111600-22112200	Enhancers	HUES64 Cell Line	embryonic stem cell

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