Variant report

Variant	nsv1050218
Chromosome Location	chr14:34851521-34969433
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2000)
CpG islands
(count:854)
Chromatin interactive
region (count:128)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2000 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:34938206-34938421	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:34966093-34966592	K562	blood:	n/a	n/a
3	ARID3A	chr14:34966063-34967571	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:34967988-34968420	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:34905586-34905976	HepG2	liver:	n/a	chr14:34905782-34905798
6	ARID3A	chr14:34919326-34920261	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:34929903-34932054	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:34934231-34934837	K562	blood:	n/a	n/a
9	ARID3A	chr14:34906447-34906805	HepG2	liver:	n/a	n/a
10	ATF1	chr14:34965963-34966707	K562	blood:	n/a	n/a
11	ATF1	chr14:34934357-34934890	K562	blood:	n/a	n/a
12	ATF3	chr14:34966016-34966535	HepG2	liver:	n/a	n/a
13	ATF3	chr14:34966038-34966443	K562	blood:	n/a	n/a
14	ATF3	chr14:34894748-34894948	K562	blood:	n/a	n/a
15	ATF3	chr14:34934313-34934807	K562	blood:	n/a	n/a
16	BACH1	chr14:34931844-34931959	K562	blood:	n/a	n/a
17	BACH1	chr14:34858099-34858362	H1-hESC	embryonic stem cell:	n/a	chr14:34858182-34858196
18	BACH1	chr14:34934068-34935041	K562	blood:	n/a	n/a
19	BACH1	chr14:34934415-34934834	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr14:34966388-34966391	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr14:34930764-34932380	H1-hESC	embryonic stem cell:	n/a	n/a
22	BCL3	chr14:34965672-34966667	A549	lung:	n/a	chr14:34966277-34966286 chr14:34966278-34966287
23	BCL3	chr14:34965668-34967101	A549	lung:	n/a	chr14:34966277-34966286 chr14:34966278-34966287
24	BCLAF1	chr14:34930480-34931128	GM12878	blood:	n/a	n/a
25	BCLAF1	chr14:34931197-34931534	GM12878	blood:	n/a	chr14:34931198-34931211
26	BHLHE40	chr14:34934120-34934252	K562	blood:	n/a	n/a
27	BHLHE40	chr14:34934480-34934801	K562	blood:	n/a	n/a
28	BHLHE40	chr14:34931257-34931717	GM12878	blood:	n/a	n/a
29	BHLHE40	chr14:34966762-34967159	HepG2	liver:	n/a	n/a
30	BHLHE40	chr14:34894697-34895041	HepG2	liver:	n/a	n/a
31	BHLHE40	chr14:34931902-34932178	K562	blood:	n/a	n/a
32	BHLHE40	chr14:34968137-34968262	GM12878	blood:	n/a	n/a
33	BHLHE40	chr14:34930806-34932350	HepG2	liver:	n/a	n/a
34	BHLHE40	chr14:34960561-34960835	HepG2	liver:	n/a	n/a
35	BHLHE40	chr14:34894689-34894952	K562	blood:	n/a	n/a
36	BHLHE40	chr14:34965905-34966483	K562	blood:	n/a	n/a
37	BHLHE40	chr14:34966072-34966515	HepG2	liver:	n/a	n/a
38	BHLHE40	chr14:34931266-34931663	K562	blood:	n/a	n/a
39	BRCA1	chr14:34930066-34931920	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr14:34931610-34931870	H1-hESC	embryonic stem cell:	n/a	n/a
41	BRCA1	chr14:34965923-34966768	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr14:34903559-34903575	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr14:34931545-34931879	GM12878	blood:	n/a	n/a
44	BRCA1	chr14:34930926-34931871	HepG2	liver:	n/a	n/a
45	BRCA1	chr14:34906304-34906376	HepG2	liver:	n/a	n/a
46	CBX3	chr14:34889782-34890149	K562	blood:	n/a	n/a
47	CBX3	chr14:34880110-34880314	K562	blood:	n/a	n/a
48	CBX3	chr14:34880080-34880297	K562	blood:	n/a	n/a
49	CBX3	chr14:34889789-34890064	K562	blood:	n/a	n/a
50	CCNT2	chr14:34965901-34966514	K562	blood:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:34966313-34966363	H1-hESC	embryonic stem cell:	embryo
2	chr14:34931026-34931076	K562	blood:	n/a
3	chr14:34931458-34931508	NHDF-neo	bronchial:	n/a
4	chr14:34931803-34931853	NT2-D1	testis:	n/a
5	chr14:34931798-34931848	SK-N-SH_RA	brain:	n/a
6	chr14:34945225-34945275	GM12892	blood:	n/a
7	chr14:34966313-34966363	SK-N-SH	brain:	n/a
8	chr14:34931798-34931848	HNPCEpiC	eye:	n/a
9	chr14:34945475-34945525	GM06990	blood:	n/a
10	chr14:34902862-34902912	AG09319	gingival:	n/a
11	chr14:34931798-34931848	IMR90	lung:	fetal
12	chr14:34966313-34966363	NHDF-neo	bronchial:	n/a
13	chr14:34931458-34931508	AG09309	skin:	n/a
14	chr14:34931577-34931627	BJ	skin:	n/a
15	chr14:34945475-34945525	HMEC	breast:	n/a
16	chr14:34902862-34902912	HCT-116	colon:	n/a
17	chr14:34945475-34945525	GM12892	blood:	n/a
18	chr14:34931967-34932017	HMEC	breast:	n/a
19	chr14:34931391-34931441	BE2_C	brain:	n/a
20	chr14:34945225-34945275	PFSK-1	brain:	n/a
21	chr14:34931577-34931627	MCF-7	breast:	n/a
22	chr14:34945475-34945525	LNCaP	prostate:	n/a
23	chr14:34945475-34945525	Caco-2	colon:	n/a
24	chr14:34931822-34931872	HPAEpiC	pulmonary alveolar:	n/a
25	chr14:34931822-34931872	HIPEpiC	eye:	n/a
26	chr14:34931577-34931627	HCT-116	colon:	n/a
27	chr14:34931822-34931872	Caco-2	colon:	n/a
28	chr14:34906118-34906168	AG09319	gingival:	n/a
29	chr14:34945225-34945275	NT2-D1	testis:	n/a
30	chr14:34931577-34931627	NB4	blood:	n/a
31	chr14:34944819-34944869	SAEC	small airway:	n/a
32	chr14:34931803-34931853	HCM	heart:	n/a
33	chr14:34906118-34906168	PANC-1	pancreas:	n/a
34	chr14:34931798-34931848	BJ	skin:	n/a
35	chr14:34931967-34932017	AG10803	skin:	n/a
36	chr14:34931798-34931848	SKMC	muscle:	n/a
37	chr14:34931458-34931508	H1-hESC	embryonic stem cell:	embryo
38	chr14:34931577-34931627	A549	lung:	n/a
39	chr14:34945475-34945525	HUVEC	blood vessel:	n/a
40	chr14:34931577-34931627	GM12892	blood:	n/a
41	chr14:34945225-34945275	K562	blood:	n/a
42	chr14:34966313-34966363	HL-60	blood:	n/a
43	chr14:34944819-34944869	HNPCEpiC	eye:	n/a
44	chr14:34931577-34931627	GM19239	blood:	n/a
45	chr14:34966313-34966363	AG10803	skin:	n/a
46	chr14:34944819-34944869	Caco-2	colon:	n/a
47	chr14:34931967-34932017	LNCaP	prostate:	n/a
48	chr14:34906118-34906168	A549	lung:	n/a
49	chr14:34902862-34902912	HCF	heart:	n/a
50	chr14:34902862-34902912	HAEpiC	amniotic membrane:	n/a

(count:128 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:34938365..34940325-chr14:34941418..34943852,2	MCF-7	breast:
2	chr14:34875481..34877355-chr14:34884980..34887544,2	MCF-7	breast:
3	chr14:34898373..34900542-chr14:34902393..34904434,2	K562	blood:
4	chr14:34851488..34853508-chr14:35021790..35024186,2	MCF-7	breast:
5	chr14:34856634..34858180-chr14:35022480..35024837,2	K562	blood:
6	chr14:34843970..34846668-chr14:34868396..34870716,2	MCF-7	breast:
7	chr14:34800581..34801486-chr14:34967721..34968650,2	K562	blood:
8	chr14:34938365..34940325-chr14:34941418..34943852,2	MCF-7	breast:
9	chr14:34892965..34896052-chr14:34897017..34900393,3	K562	blood:
10	chr14:34959614..34962811-chr14:34966236..34969041,3	K562	blood:
11	chr14:34883972..34886715-chr14:34889275..34892253,2	K562	blood:
12	chr14:34893969..34896982-chr14:35022317..35025730,3	MCF-7	breast:
13	chr14:34853536..34855341-chr14:34855493..34858071,3	K562	blood:
14	chr14:34835401..34839083-chr14:34893653..34895439,3	MCF-7	breast:
15	chr14:34928753..34932995-chr14:34963537..34968945,14	MCF-7	breast:
16	chr14:34930470..34932730-chr14:35007965..35010227,2	K562	blood:
17	chr14:34923565..34925509-chr14:34925743..34927516,2	MCF-7	breast:
18	chr14:34933163..34934738-chr14:35003028..35005166,2	K562	blood:
19	chr14:34914730..34916776-chr14:34920765..34923718,2	MCF-7	breast:
20	chr14:34929195..34931958-chr14:34961926..34964418,2	MCF-7	breast:
21	chr14:34853536..34855341-chr14:34855493..34858071,3	K562	blood:
22	chr14:34892965..34896052-chr14:34897017..34900393,3	K562	blood:
23	chr14:34929806..34931757-chr14:34938226..34940059,2	K562	blood:
24	chr14:34904297..34907073-chr14:34966756..34968463,2	MCF-7	breast:
25	chr14:34965733..34968231-chr14:35022336..35025245,2	MCF-7	breast:
26	chr14:34841266..34842852-chr14:34928524..34930795,2	MCF-7	breast:
27	chr14:34952643..34954942-chr14:34966507..34969083,2	MCF-7	breast:
28	chr14:34909006..34911649-chr14:34913275..34915517,2	MCF-7	breast:
29	chr14:34932436..34934680-chr14:34965867..34967830,2	K562	blood:
30	chr14:34905214..34907538-chr14:34909131..34910921,2	K562	blood:
31	chr14:34930543..34933153-chr14:35015586..35017251,2	MCF-7	breast:
32	chr14:34933203..34935041-chr14:34939513..34941719,2	K562	blood:
33	chr14:34931264..34933781-chr14:35036806..35039605,2	K562	blood:
34	chr14:34916053..34917977-chr14:34929322..34931910,2	K562	blood:
35	chr14:34922503..34924704-chr14:35007891..35010342,2	MCF-7	breast:
36	chr14:34799548..34803609-chr14:34964477..34969425,6	MCF-7	breast:
37	chr14:34830829..34832701-chr14:34965153..34968151,2	MCF-7	breast:
38	chr14:34935994..34938322-chr14:34940821..34943431,3	K562	blood:
39	chr14:34927994..34930347-chr14:34965334..34966847,2	K562	blood:
40	chr14:34903790..34905906-chr14:35022727..35024666,2	MCF-7	breast:
41	chr14:34931011..34932642-chr14:34957315..34960104,2	K562	blood:
42	chr14:34931214..34931822-chr17:28443513..28444222,2	Hela-S3	cervix:
43	chr14:34957508..34960404-chr14:34964346..34966873,2	K562	blood:
44	chr14:34800596..34801300-chr14:34965892..34967188,3	MCF-7	breast:
45	chr14:34696743..34697572-chr14:34967866..34968659,3	MCF-7	breast:
46	chr14:34800908..34801526-chr14:34966566..34967258,2	MCF-7	breast:
47	chr14:34934706..34936748-chr14:34939832..34941960,2	MCF-7	breast:
48	chr14:34935994..34938322-chr14:34940821..34943431,3	K562	blood:
49	chr14:34963976..34965714-chr14:35019570..35022197,2	MCF-7	breast:
50	chr14:34894353..34897341-chr14:34909649..34911382,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPTSSA-2	chr14:34885893-34886808	NONHSAT036328
2	lnc-SPTSSA-1	chr14:34931922-34931980	NONHSAT036319

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C14orf147	hsa-miR-221-3p	chr14:34903356-34903378
2	C14orf147	hsa-miR-221-3p	chr14:34903362-34903355

Variant related genes	Relation type
ENSG00000223593	TF binding region
SPTSSA	TF binding region
EGLN3	TF binding region
ENSG00000237450	TF binding region
ENSG00000223593	CpG island
SPTSSA	CpG island
EGLN3	CpG island
ENSG00000237450	CpG island
ENSG00000158158	chromatin interactions
ENSG00000223593	chromatin interactions
ENSG00000129521	chromatin interactions
ENSG00000143368	chromatin interactions
ENSG00000129518	chromatin interactions
ENSG00000126653	chromatin interactions
ENSG00000206588	chromatin interactions
ENSG00000206596	chromatin interactions
ENSG00000165389	chromatin interactions
ENSG00000240463	chromatin interactions
ENSG00000199071	chromatin interactions
ENSG00000006652	chromatin interactions

Extended variants
information (count: 4096 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:4096 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2383593	chr14:34851521-34851522	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs575693158	chr14:34851533-34851534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559913009	chr14:34851596-34851597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs2104743	chr14:34851604-34851605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529191415	chr14:34851613-34851614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182625440	chr14:34851622-34851623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539240909	chr14:34851682-34851683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374931999	chr14:34851684-34851685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs117558266	chr14:34851700-34851701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs34869958	chr14:34851702-34851703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551597962	chr14:34851713-34851714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs77677485	chr14:34851727-34851728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs187753659	chr14:34851772-34851773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs191980427	chr14:34851803-34851804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574248304	chr14:34851830-34851831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183254465	chr14:34851883-34851884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556869445	chr14:34851886-34851887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs187868551	chr14:34851893-34851894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs544230352	chr14:34851902-34851903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs145044633	chr14:34851921-34851922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs115393531	chr14:34851925-34851926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs539930618	chr14:34851928-34851929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs138890558	chr14:34851970-34851971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs944128	chr14:34852018-34852019	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs78288692	chr14:34852095-34852096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs115287612	chr14:34852097-34852098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192346074	chr14:34852125-34852126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs34970438	chr14:34852146-34852147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs562913326	chr14:34852149-34852150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs370117550	chr14:34852171-34852172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs116025007	chr14:34852193-34852194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs78490062	chr14:34852195-34852196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs527799081	chr14:34852206-34852207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs17102490	chr14:34852217-34852218	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs371916100	chr14:34852282-34852283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs184450366	chr14:34852349-34852350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs2183312	chr14:34852356-34852357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs376493257	chr14:34852364-34852365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs567882055	chr14:34852438-34852439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536810870	chr14:34852551-34852552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556465735	chr14:34852628-34852629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs150835120	chr14:34852631-34852632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs538961261	chr14:34852678-34852679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs557776187	chr14:34852765-34852766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577177405	chr14:34852776-34852777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs539942299	chr14:34852786-34852787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs114701028	chr14:34852857-34852858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs573514938	chr14:34852865-34852866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs542446720	chr14:34852959-34852960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs112443279	chr14:34852962-34852963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Autism	22495311	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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Glioma	24330732	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:1762 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:34849000-34857800	Weak transcription	Esophagus	oesophagus
2	chr14:34849400-34853400	Enhancers	Hela-S3	cervix
3	chr14:34853400-34856000	Weak transcription	Hela-S3	cervix
4	chr14:34856000-34856200	Weak transcription	A549	lung
5	chr14:34856000-34857800	Enhancers	Hela-S3	cervix
6	chr14:34856200-34858400	Enhancers	A549	lung
7	chr14:34856800-34857600	Enhancers	NHEK	skin
8	chr14:34857000-34858600	Enhancers	HMEC	breast
9	chr14:34857600-34858400	Flanking Active TSS	NHEK	skin
10	chr14:34857800-34858000	Enhancers	Esophagus	oesophagus
11	chr14:34857800-34858000	Enhancers	Osteobl	bone
12	chr14:34857800-34858400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr14:34857800-34858400	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr14:34857800-34858400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr14:34857800-34858400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr14:34857800-34858600	Flanking Active TSS	Hela-S3	cervix
17	chr14:34858000-34858400	Enhancers	H1 Cell Line	embryonic stem cell
18	chr14:34858000-34858400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr14:34858400-34858600	Enhancers	NHEK	skin
20	chr14:34858400-34859400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr14:34858600-34859200	Enhancers	Hela-S3	cervix
22	chr14:34859600-34859800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr14:34869200-34870000	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr14:34869600-34870400	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr14:34870000-34870200	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr14:34870200-34870600	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
27	chr14:34870400-34872600	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr14:34870600-34872400	Weak transcription	Primary monocytes fromperipheralblood	blood
29	chr14:34872400-34874000	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr14:34872600-34872800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr14:34872600-34872800	Bivalent Enhancer	HepG2	liver
32	chr14:34872600-34873600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr14:34872600-34873800	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr14:34872600-34874000	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr14:34872800-34873200	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr14:34872800-34874200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr14:34873200-34873600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr14:34873200-34874000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr14:34873200-34875400	Enhancers	Primary hematopoietic stem cells	blood
40	chr14:34873600-34874000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr14:34874000-34874200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr14:34889400-34890600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
43	chr14:34889600-34890800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr14:34890600-34890800	Weak transcription	Monocytes-CD14+_RO01746	blood
45	chr14:34890800-34891200	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr14:34890800-34905800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr14:34891200-34902400	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr14:34892600-34892800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr14:34892600-34895800	Enhancers	Placenta	Placenta
50	chr14:34892800-34905400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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