Variant report

Variant	nsv1031214
Chromosome Location	chr5:17382604-17427825
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:516)
CpG islands
(count:306)
Chromatin interactive
region (count:18)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:516 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:17398657-17398856	K562	blood:	n/a	n/a
2	ARID3A	chr5:17400080-17400209	K562	blood:	n/a	n/a
3	ATF1	chr5:17400131-17400411	K562	blood:	n/a	n/a
4	ATF1	chr5:17415654-17415786	K562	blood:	n/a	n/a
5	ATF1	chr5:17413435-17413764	K562	blood:	n/a	n/a
6	ATF1	chr5:17400709-17401396	K562	blood:	n/a	n/a
7	ATF1	chr5:17398236-17399036	K562	blood:	n/a	n/a
8	ATF2	chr5:17401891-17402229	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr5:17425371-17425899	GM12878	blood:	n/a	n/a
10	ATF2	chr5:17425402-17425976	GM12878	blood:	n/a	n/a
11	ATF2	chr5:17426396-17426854	GM12878	blood:	n/a	n/a
12	BACH1	chr5:17413521-17413685	K562	blood:	n/a	chr5:17413586-17413600
13	BACH1	chr5:17400938-17402146	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr5:17415528-17415532	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr5:17425526-17425766	GM12878	blood:	n/a	n/a
16	BATF	chr5:17413423-17413703	GM12878	blood:	n/a	chr5:17413589-17413600
17	BCL3	chr5:17401782-17402305	A549	lung:	n/a	chr5:17402272-17402281
18	BCL3	chr5:17398488-17398790	GM12878	blood:	n/a	n/a
19	BHLHE40	chr5:17402043-17402129	A549	lung:	n/a	n/a
20	BHLHE40	chr5:17425193-17426019	GM12878	blood:	n/a	n/a
21	BHLHE40	chr5:17398695-17398915	K562	blood:	n/a	n/a
22	BHLHE40	chr5:17413480-17413606	GM12878	blood:	n/a	n/a
23	BHLHE40	chr5:17400134-17400222	K562	blood:	n/a	n/a
24	BHLHE40	chr5:17413400-17413989	K562	blood:	n/a	n/a
25	BRCA1	chr5:17406577-17407006	Hela-S3	cervix:	n/a	n/a
26	CCNT2	chr5:17413432-17413642	K562	blood:	n/a	n/a
27	CCNT2	chr5:17400128-17400357	K562	blood:	n/a	n/a
28	CCNT2	chr5:17400915-17401502	K562	blood:	n/a	n/a
29	CEBPB	chr5:17394857-17395075	IMR90	lung:	n/a	chr5:17395016-17395027
30	CEBPB	chr5:17401143-17401427	A549	lung:	n/a	chr5:17401288-17401299
31	CEBPB	chr5:17382473-17382661	A549	lung:	n/a	n/a
32	CEBPB	chr5:17401160-17401435	K562	blood:	n/a	chr5:17401288-17401299
33	CEBPB	chr5:17401207-17401412	IMR90	lung:	n/a	chr5:17401288-17401299
34	CEBPB	chr5:17394964-17395100	K562	blood:	n/a	chr5:17395016-17395027
35	CEBPB	chr5:17418161-17418572	MCF-7	breast:	n/a	n/a
36	CEBPB	chr5:17401122-17401406	HepG2	liver:	n/a	chr5:17401288-17401299
37	CEBPB	chr5:17406732-17406967	IMR90	lung:	n/a	n/a
38	CEBPB	chr5:17411605-17411851	A549	lung:	n/a	chr5:17411694-17411707 chr5:17411696-17411707 chr5:17411696-17411707 chr5:17411694-17411707
39	CEBPB	chr5:17401122-17401458	K562	blood:	n/a	chr5:17401288-17401299
40	CEBPB	chr5:17405238-17405440	Hela-S3	cervix:	n/a	chr5:17405385-17405396 chr5:17405383-17405396
41	CEBPB	chr5:17406636-17407035	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr5:17398657-17398694	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr5:17394910-17395080	A549	lung:	n/a	chr5:17395016-17395027
44	CEBPB	chr5:17401115-17402025	H1-hESC	embryonic stem cell:	n/a	chr5:17401288-17401299
45	CEBPB	chr5:17406735-17407070	A549	lung:	n/a	n/a
46	CEBPB	chr5:17411531-17411914	IMR90	lung:	n/a	chr5:17411694-17411707 chr5:17411696-17411707 chr5:17411696-17411707 chr5:17411694-17411707
47	CEBPB	chr5:17394873-17395134	HepG2	liver:	n/a	chr5:17395016-17395027
48	CEBPB	chr5:17418170-17418517	MCF-7	breast:	n/a	n/a
49	CEBPB	chr5:17413506-17413705	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr5:17402299-17402631	H1-hESC	embryonic stem cell:	n/a	chr5:17402304-17402316 chr5:17402458-17402471

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:17414184-17414234	HNPCEpiC	eye:	n/a
2	chr5:17414184-17414234	HNPCEpiC	eye:	n/a
3	chr5:17427098-17427148	HAEpiC	amniotic membrane:	n/a
4	chr5:17401890-17401940	SAEC	small airway:	n/a
5	chr5:17400323-17400373	BE2_C	brain:	n/a
6	chr5:17414184-17414234	ProgFib	skin:	n/a
7	chr5:17414184-17414234	GM19239	blood:	n/a
8	chr5:17400323-17400373	HRPEpiC	eye:	n/a
9	chr5:17427098-17427148	HMEC	breast:	n/a
10	chr5:17395952-17396002	A549	lung:	n/a
11	chr5:17427098-17427148	LNCaP	prostate:	n/a
12	chr5:17427098-17427148	HCM	heart:	n/a
13	chr5:17400323-17400373	BJ	skin:	n/a
14	chr5:17395952-17396002	SKMC	muscle:	n/a
15	chr5:17401890-17401940	HUVEC	blood vessel:	n/a
16	chr5:17414184-17414234	HCPEpiC	choroid plexus:	n/a
17	chr5:17401890-17401940	HepG2	liver:	n/a
18	chr5:17400323-17400373	RPTEC	kidney:	n/a
19	chr5:17400323-17400373	SK-N-SH	brain:	n/a
20	chr5:17395952-17396002	HCM	heart:	n/a
21	chr5:17395952-17396002	HCT-116	colon:	n/a
22	chr5:17395952-17396002	HRCEpiC	kidney:	n/a
23	chr5:17400323-17400373	SK-N-MC	brain:	n/a
24	chr5:17414184-17414234	AG04449	skin:	fetal
25	chr5:17414184-17414234	NT2-D1	testis:	n/a
26	chr5:17400323-17400373	IMR90	lung:	fetal
27	chr5:17414184-17414234	LNCaP	prostate:	n/a
28	chr5:17400323-17400373	HRE	kidney:	n/a
29	chr5:17414184-17414234	AG09319	gingival:	n/a
30	chr5:17401890-17401940	HRPEpiC	eye:	n/a
31	chr5:17414184-17414234	SK-N-SH_RA	brain:	n/a
32	chr5:17395952-17396002	HepG2	liver:	n/a
33	chr5:17400323-17400373	HUVEC	blood vessel:	n/a
34	chr5:17414184-17414234	HIPEpiC	eye:	n/a
35	chr5:17395952-17396002	ProgFib	skin:	n/a
36	chr5:17414184-17414234	SK-N-SH	brain:	n/a
37	chr5:17427098-17427148	HNPCEpiC	eye:	n/a
38	chr5:17427098-17427148	AG04449	skin:	fetal
39	chr5:17400323-17400373	HRCEpiC	kidney:	n/a
40	chr5:17414184-17414234	RPTEC	kidney:	n/a
41	chr5:17427098-17427148	HEEpiC	esophagus:	n/a
42	chr5:17427098-17427148	AG10803	skin:	n/a
43	chr5:17395952-17396002	HRE	kidney:	n/a
44	chr5:17414184-17414234	AG10803	skin:	n/a
45	chr5:17427098-17427148	MCF10A-Er-Src	breast:	n/a
46	chr5:17427098-17427148	HCPEpiC	choroid plexus:	n/a
47	chr5:17400323-17400373	ProgFib	skin:	n/a
48	chr5:17400323-17400373	NHDF-neo	bronchial:	n/a
49	chr5:17414184-17414234	Hela-S3	cervix:	n/a
50	chr5:17395952-17396002	SK-N-MC	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:17399274..17401360-chr5:17404322..17406946,2	MCF-7	breast:
2	chr5:17216804..17218598-chr5:17393185..17395511,2	MCF-7	breast:
3	chr5:17365516..17367373-chr5:17399549..17401386,2	K562	blood:
4	chr5:17216329..17216875-chr5:17413138..17413983,2	MCF-7	breast:
5	chr5:17215642..17218111-chr5:17382482..17385091,2	MCF-7	breast:
6	chr5:17422805..17424378-chr5:17424436..17427431,2	MCF-7	breast:
7	chr5:17393977..17396441-chr5:17404895..17406641,2	MCF-7	breast:
8	chr5:17413771..17415306-chr5:17416901..17419149,2	MCF-7	breast:
9	chr5:17393977..17396441-chr5:17404895..17406641,2	MCF-7	breast:
10	chr5:17379053..17381282-chr5:17384689..17387126,2	MCF-7	breast:
11	chr5:17413771..17415306-chr5:17416901..17419149,2	MCF-7	breast:
12	chr5:17422805..17424378-chr5:17424436..17427431,2	MCF-7	breast:
13	chr5:17401084..17403430-chr5:17409103..17412028,2	K562	blood:
14	chr5:17215792..17218205-chr5:17402099..17403683,2	MCF-7	breast:
15	chr5:17401084..17403430-chr5:17409103..17412028,2	K562	blood:
16	chr5:17391442..17394133-chr5:17400985..17402513,2	MCF-7	breast:
17	chr5:17391442..17394133-chr5:17400985..17402513,2	MCF-7	breast:
18	chr5:17399274..17401360-chr5:17404322..17406946,2	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BASP1-3	chr5:17404535-17404838	XLOC_004308
2	lnc-MYO10-3	chr5:17384952-17385549	XLOC_004746
3	lnc-BASP1-3	chr5:17404535-17404701	XLOC_004308
4	lnc-MYO10-3	chr5:17387311-17387419	XLOC_004746
5	lnc-BASP1-3	chr5:17404005-17404178	XLOC_004308
6	lnc-MYO10-3	chr5:17387311-17387419	ENSG00000250822
7	lnc-BASP1-3	chr5:17404217-17404429	XLOC_004308
8	lnc-BASP1-3	chr5:17404039-17404474	NONHSAT100631
9	lnc-BASP1-3	chr5:17404040-17404197	XLOC_004308
10	lnc-BASP1-3	chr5:17412001-17412207	XLOC_004308
11	lnc-BASP1-3	chr5:17412000-17412207	NONHSAT100631
12	lnc-MYO10-3	chr5:17384952-17385549	ENSG00000250822
13	lnc-BASP1-3	chr5:17404213-17404838	XLOC_004308
14	lnc-BASP1-3	chr5:17404534-17404840	NONHSAT100631
15	lnc-BASP1-3	chr5:17404535-17404838	XLOC_004308
16	lnc-BASP1-3	chr5:17404098-17404197	NONHSAT100634
17	lnc-BASP1-3	chr5:17404667-17404840	XLOC_004308
18	lnc-BASP1-3	chr5:17404128-17404197	XLOC_004308
19	lnc-BASP1-3	chr5:17404255-17404460	XLOC_004308

No data

Variant related genes	Relation type
ENSG00000248455	TF binding region
ENSG00000250822	TF binding region
ENSG00000248455	CpG island
ENSG00000250822	CpG island
ENSG00000215196	chromatin interactions
ENSG00000176788	chromatin interactions
GTF2H1	miRNA target sites
RAD51	miRNA target sites
MMP2	miRNA target sites
RNF41	miRNA target sites
MMP24	miRNA target sites
GXYLT1	miRNA target sites

Extended variants
information (count: 1606 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1606 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560796320	chr5:17382648-17382649	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs184199888	chr5:17382674-17382675	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs539973963	chr5:17382681-17382682	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs559906953	chr5:17382686-17382687	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs7728024	chr5:17382703-17382704	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs188805083	chr5:17382732-17382733	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs569148109	chr5:17382750-17382751	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs568012192	chr5:17382781-17382782	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs569275011	chr5:17382860-17382861	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs113737593	chr5:17382888-17382889	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs370795220	chr5:17382894-17382895	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs140218124	chr5:17382905-17382906	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs1500510	chr5:17382906-17382907	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs112674585	chr5:17382915-17382916	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs150310955	chr5:17382945-17382946	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs182261433	chr5:17382949-17382950	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs540049022	chr5:17382992-17382993	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs556547429	chr5:17383007-17383008	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs137914336	chr5:17383009-17383010	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs1500509	chr5:17383037-17383038	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs537227412	chr5:17383040-17383041	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs554534197	chr5:17383089-17383090	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs372837764	chr5:17383100-17383101	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs558663414	chr5:17383175-17383176	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs186613302	chr5:17383176-17383177	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs559820649	chr5:17383180-17383181	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs532139927	chr5:17383198-17383199	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs558514103	chr5:17383207-17383208	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs191812200	chr5:17383237-17383238	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs184750133	chr5:17383241-17383242	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs200873885	chr5:17383244-17383245	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs201896886	chr5:17383245-17383246	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs111681045	chr5:17383254-17383255	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs188823098	chr5:17383262-17383263	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs548226097	chr5:17383324-17383325	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs11133897	chr5:17383334-17383335	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs75211478	chr5:17383389-17383390	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs201012253	chr5:17383391-17383392	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs62350501	chr5:17383392-17383393	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs527686900	chr5:17383393-17383394	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs369707442	chr5:17383437-17383438	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs148973435	chr5:17383482-17383483	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs547868769	chr5:17383508-17383509	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs371674651	chr5:17383512-17383513	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs145765536	chr5:17383535-17383536	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs139379121	chr5:17383561-17383562	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs192923715	chr5:17383577-17383578	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs201256468	chr5:17383609-17383610	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs5866252	chr5:17383655-17383656	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs397883595	chr5:17383667-17383668	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	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
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21364760	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Myoepithelioma	18604193	CNVD
Lung cancer	16740712	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Melanoma	22183965	CNVD
Renal cell carcinoma	18194544	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:537 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:17375800-17387000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:17379200-17383000	Enhancers	A549	lung
3	chr5:17379400-17382800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr5:17380400-17384200	Weak transcription	Colon Smooth Muscle	Colon
5	chr5:17380800-17383200	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr5:17381000-17383000	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr5:17381000-17384200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr5:17381200-17384200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr5:17381800-17382800	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr5:17382200-17383800	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr5:17382400-17384200	Weak transcription	Primary B cells from peripheral blood	blood
12	chr5:17382800-17384000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr5:17383000-17383800	Weak transcription	A549	lung
14	chr5:17383800-17384000	Enhancers	A549	lung
15	chr5:17383800-17384200	Enhancers	Fetal Brain Male	brain
16	chr5:17383800-17385400	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr5:17384000-17384200	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr5:17384000-17384600	Weak transcription	A549	lung
19	chr5:17384000-17384800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr5:17384000-17385400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr5:17384200-17384600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr5:17384200-17384600	Enhancers	Primary B cells from peripheral blood	blood
23	chr5:17384200-17385200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr5:17384200-17385400	Enhancers	Colon Smooth Muscle	Colon
25	chr5:17384200-17386800	Weak transcription	Fetal Brain Male	brain
26	chr5:17384600-17384800	Enhancers	A549	lung
27	chr5:17384800-17387400	Weak transcription	A549	lung
28	chr5:17385400-17387200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr5:17386800-17387400	Enhancers	Fetal Brain Male	brain
30	chr5:17387000-17387600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr5:17387400-17387600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr5:17387400-17387600	Enhancers	A549	lung
33	chr5:17393800-17394600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr5:17394000-17395600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr5:17394200-17394400	Enhancers	A549	lung
36	chr5:17394400-17394600	Enhancers	Placenta	Placenta
37	chr5:17394400-17394800	ZNF genes & repeats	A549	lung
38	chr5:17394600-17394800	Enhancers	Ovary	ovary
39	chr5:17394600-17396000	Weak transcription	Placenta	Placenta
40	chr5:17394800-17395200	Weak transcription	A549	lung
41	chr5:17394800-17396000	Weak transcription	Ovary	ovary
42	chr5:17395200-17395400	Enhancers	Fetal Kidney	kidney
43	chr5:17395200-17395400	Enhancers	A549	lung
44	chr5:17395200-17395400	Enhancers	NHLF	lung
45	chr5:17395200-17395400	Enhancers	Osteobl	bone
46	chr5:17395200-17396000	Enhancers	Fetal Stomach	stomach
47	chr5:17395400-17396400	Weak transcription	Fetal Kidney	kidney
48	chr5:17395400-17396400	Weak transcription	Osteobl	bone
49	chr5:17395400-17397800	Weak transcription	A549	lung
50	chr5:17395400-17397800	Weak transcription	NHLF	lung

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