Variant report

Variant	nsv880933
Chromosome Location	chr5:8467174-8688962
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:722)
CpG islands
(count:183)
Chromatin interactive
region (count:16)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:722 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:8546002-8546027	K562	blood:	n/a	n/a
2	ATF1	chr5:8578036-8578244	K562	blood:	n/a	n/a
3	BACH1	chr5:8667114-8667151	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr5:8622560-8622739	HepG2	liver:	n/a	n/a
5	BHLHE40	chr5:8474568-8474666	K562	blood:	n/a	n/a
6	CBX3	chr5:8470621-8470920	K562	blood:	n/a	n/a
7	CBX3	chr5:8470624-8470962	K562	blood:	n/a	n/a
8	CEBPB	chr5:8561200-8561508	HepG2	liver:	n/a	chr5:8561297-8561308
9	CEBPB	chr5:8609171-8609387	A549	lung:	n/a	chr5:8609323-8609334 chr5:8609323-8609336
10	CEBPB	chr5:8486303-8486352	HepG2	liver:	n/a	n/a
11	CEBPB	chr5:8676931-8677276	Hela-S3	cervix:	n/a	chr5:8677094-8677105
12	CEBPB	chr5:8676922-8677270	K562	blood:	n/a	chr5:8677094-8677105
13	CEBPB	chr5:8676917-8677291	HepG2	liver:	n/a	chr5:8677094-8677105
14	CEBPB	chr5:8661655-8661933	K562	blood:	n/a	chr5:8661784-8661795 chr5:8661784-8661797 chr5:8661784-8661797 chr5:8661784-8661797 chr5:8661758-8661771
15	CEBPB	chr5:8591862-8592128	H1-hESC	embryonic stem cell:	n/a	chr5:8591930-8591943 chr5:8591977-8591988
16	CEBPB	chr5:8587724-8588014	HepG2	liver:	n/a	n/a
17	CEBPB	chr5:8665158-8665231	K562	blood:	n/a	n/a
18	CEBPB	chr5:8576249-8576499	IMR90	lung:	n/a	chr5:8576391-8576402
19	CEBPB	chr5:8576166-8576478	H1-hESC	embryonic stem cell:	n/a	chr5:8576391-8576402
20	CEBPB	chr5:8591877-8592159	A549	lung:	n/a	chr5:8591930-8591943 chr5:8591977-8591988
21	CEBPB	chr5:8587655-8588007	IMR90	lung:	n/a	n/a
22	CEBPB	chr5:8676930-8677250	H1-hESC	embryonic stem cell:	n/a	chr5:8677094-8677105
23	CEBPB	chr5:8676915-8677281	A549	lung:	n/a	chr5:8677094-8677105
24	CEBPB	chr5:8576335-8576460	K562	blood:	n/a	chr5:8576391-8576402
25	CEBPB	chr5:8591878-8592107	HepG2	liver:	n/a	chr5:8591930-8591943 chr5:8591977-8591988
26	CEBPB	chr5:8576214-8576520	HepG2	liver:	n/a	chr5:8576391-8576402
27	CEBPB	chr5:8661685-8661922	A549	lung:	n/a	chr5:8661784-8661795 chr5:8661784-8661797 chr5:8661784-8661797 chr5:8661784-8661797 chr5:8661758-8661771
28	CEBPB	chr5:8541033-8541332	A549	lung:	n/a	chr5:8541208-8541219
29	CEBPB	chr5:8541037-8541334	HepG2	liver:	n/a	chr5:8541208-8541219
30	CEBPB	chr5:8587820-8587839	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr5:8609172-8609456	HepG2	liver:	n/a	chr5:8609323-8609334 chr5:8609323-8609336
32	CEBPB	chr5:8576225-8576508	Hela-S3	cervix:	n/a	chr5:8576391-8576402
33	CEBPB	chr5:8676872-8677292	IMR90	lung:	n/a	chr5:8677094-8677105
34	CREB1	chr5:8578003-8578275	GM12878	blood:	n/a	n/a
35	CREB1	chr5:8577953-8578368	GM12878	blood:	n/a	n/a
36	CREB1	chr5:8578018-8578250	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr5:8585380-8585530	MCF-7	breast:	n/a	n/a
38	CTCF	chr5:8650570-8650684	GM12892	blood:	n/a	n/a
39	CTCF	chr5:8585460-8585610	HL-60	blood:	n/a	n/a
40	CTCF	chr5:8474020-8474170	AG04450	lung:	n/a	n/a
41	CTCF	chr5:8474200-8474350	GM12866	blood:	n/a	n/a
42	CTCF	chr5:8650460-8650610	AG04449	skin:	n/a	n/a
43	CTCF	chr5:8585480-8585630	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr5:8585480-8585630	HEK293	kidney:	n/a	n/a
45	CTCF	chr5:8685900-8686050	SK-N-SH_RA	brain:	n/a	chr5:8686004-8686025 chr5:8686009-8686027
46	CTCF	chr5:8585480-8585630	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr5:8474020-8474170	HCT-116	colon:	n/a	n/a
48	CTCF	chr5:8585460-8585610	GM12864	blood:	n/a	n/a
49	CTCF	chr5:8522866-8523036	MCF-7	breast:	n/a	n/a
50	CTCF	chr5:8474075-8474159	HUVEC	blood vessel:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:8621010-8621060	AG09319	gingival:	n/a
2	chr5:8621010-8621060	NH-A	brain:	n/a
3	chr5:8621010-8621060	ProgFib	skin:	n/a
4	chr5:8621010-8621060	AG04449	skin:	fetal
5	chr5:8621221-8621271	CMK	blood:	n/a
6	chr5:8621221-8621271	HCM	heart:	n/a
7	chr5:8621221-8621271	IMR90	lung:	fetal
8	chr5:8621010-8621060	Hela-S3	cervix:	n/a
9	chr5:8621221-8621271	GM12892	blood:	n/a
10	chr5:8621221-8621271	PFSK-1	brain:	n/a
11	chr5:8621127-8621177	PrEC	prostate:	n/a
12	chr5:8621127-8621177	IMR90	lung:	fetal
13	chr5:8621127-8621177	SAEC	small airway:	n/a
14	chr5:8621127-8621177	GM06990	blood:	n/a
15	chr5:8621010-8621060	HIPEpiC	eye:	n/a
16	chr5:8621010-8621060	HCPEpiC	choroid plexus:	n/a
17	chr5:8621221-8621271	MCF10A-Er-Src	breast:	n/a
18	chr5:8621221-8621271	HUVEC	blood vessel:	n/a
19	chr5:8621010-8621060	NB4	blood:	n/a
20	chr5:8621010-8621060	BJ	skin:	n/a
21	chr5:8621127-8621177	AG09309	skin:	n/a
22	chr5:8621221-8621271	GM12878	blood:	n/a
23	chr5:8621221-8621271	HEEpiC	esophagus:	n/a
24	chr5:8621127-8621177	RPTEC	kidney:	n/a
25	chr5:8621010-8621060	HRCEpiC	kidney:	n/a
26	chr5:8621221-8621271	U87	brain:	n/a
27	chr5:8621221-8621271	A549	lung:	n/a
28	chr5:8621221-8621271	RPTEC	kidney:	n/a
29	chr5:8621127-8621177	HCT-116	colon:	n/a
30	chr5:8621221-8621271	HRCEpiC	kidney:	n/a
31	chr5:8621127-8621177	MCF-7	breast:	n/a
32	chr5:8621010-8621060	Jurkat	blood:	n/a
33	chr5:8621010-8621060	IMR90	lung:	fetal
34	chr5:8621127-8621177	ovcar-3	ovarian:	n/a
35	chr5:8621127-8621177	SK-N-SH	brain:	n/a
36	chr5:8621127-8621177	HRPEpiC	eye:	n/a
37	chr5:8621221-8621271	HIPEpiC	eye:	n/a
38	chr5:8621221-8621271	NHDF-neo	bronchial:	n/a
39	chr5:8621221-8621271	Hepatocyte	liver:	n/a
40	chr5:8621221-8621271	HEK293	kidney:	embryo
41	chr5:8621221-8621271	BJ	skin:	n/a
42	chr5:8621010-8621060	HRE	kidney:	n/a
43	chr5:8621010-8621060	PANC-1	pancreas:	n/a
44	chr5:8621127-8621177	PANC-1	pancreas:	n/a
45	chr5:8621127-8621177	NT2-D1	testis:	n/a
46	chr5:8621127-8621177	SK-N-MC	brain:	n/a
47	chr5:8621010-8621060	GM12878	blood:	n/a
48	chr5:8621010-8621060	HEEpiC	esophagus:	n/a
49	chr5:8621221-8621271	PrEC	prostate:	n/a
50	chr5:8621127-8621177	HUVEC	blood vessel:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:8593087..8595132-chr5:8597589..8599233,2	K562	blood:
2	chr5:8641727..8643790-chr5:8675458..8678330,2	K562	blood:
3	chr5:8593087..8595132-chr5:8597589..8599233,2	K562	blood:
4	chr5:8507041..8510012-chr5:8511674..8514146,2	K562	blood:
5	chr20:55143138..55143881-chr5:8652253..8652753,2	MCF-7	breast:
6	chr5:8507041..8510012-chr5:8511674..8514146,2	K562	blood:
7	chr5:8472940..8473440-chr7:72649624..72650127,2	Hela-S3	cervix:
8	chr5:8486955..8488830-chr5:8517823..8520241,2	MCF-7	breast:
9	chr5:8641727..8643790-chr5:8675458..8678330,2	K562	blood:
10	chr17:59817376..59818116-chr5:8562940..8563758,2	MCF-7	breast:
11	chr5:8455618..8458508-chr5:8467454..8469231,2	MCF-7	breast:
12	chr5:8461759..8464771-chr5:8466218..8469670,3	K562	blood:
13	chr5:8486955..8488830-chr5:8517823..8520241,2	MCF-7	breast:
14	chr5:8462445..8464940-chr5:8473267..8475894,2	K562	blood:
15	chr15:65588273..65588991-chr5:8674806..8675306,2	Hela-S3	cervix:
16	chr5:8456935..8459076-chr5:8488179..8490717,2	K562	blood:

(count:25 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTRR-15	chr5:8613189-8613331	l_2871_chr5:8578246-8630138_testes
2	lnc-MTRR-4	chr5:8533758-8534042	XLOC_004285
3	lnc-MTRR-15	chr5:8586758-8587042	l_2871_chr5:8578246-8630138_testes
4	lnc-SEMA5A-8	chr5:8633154-8633448	NONHSAT100304
5	lnc-MTRR-13	chr5:8614462-8614808	NONHSAT100301
6	lnc-MTRR-4	chr5:8528623-8528791	XLOC_004285
7	lnc-SEMA5A-7	chr5:8659876-8660171	NONHSAT100305
8	lnc-MTRR-4	chr5:8525247-8525456	XLOC_004285
9	lnc-MTRR-12	chr5:8510804-8510879	ucscGeneNc_uc003jei_2
10	lnc-MTRR-4	chr5:8525270-8525456	NONHSAT100297
11	lnc-MTRR-15	chr5:8629950-8630138	l_2871_chr5:8578246-8630138_testes
12	lnc-MTRR-15	chr5:8616097-8616381	l_2871_chr5:8578246-8630138_testes
13	lnc-MTRR-4	chr5:8528589-8528785	NONHSAT100296
14	lnc-MTRR-4	chr5:8560189-8560379	XLOC_004285
15	lnc-FASTKD3-1	chr5:8510562-8510671	ucscGeneNc_uc003jeh_1
16	lnc-MTRR-4	chr5:8533758-8533950	NONHSAT100297
17	lnc-MTRR-15	chr5:8578247-8578474	l_2871_chr5:8578246-8630138_testes
18	lnc-FASTKD3-1	chr5:8505336-8505393	ucscGeneNc_uc003jeh_1
19	lnc-MTRR-15	chr5:8581585-8581790	l_2871_chr5:8578246-8630138_testes
20	lnc-SEMA5A-6	chr5:8669130-8669362	NONHSAT100306
21	lnc-MTRR-4	chr5:8525291-8525456	XLOC_004285
22	lnc-MTRR-12	chr5:8513046-8516208	ucscGeneNc_uc003jei_2
23	lnc-MTRR-4	chr5:8525270-8525456	NONHSAT100296
24	lnc-MTRR-4	chr5:8528623-8528790	XLOC_004285
25	lnc-SEMA5A-5	chr5:8685693-8685928	NONHSAT100307

No data

Variant related genes	Relation type
ENSG00000248765	TF binding region
MTND6P2	TF binding region
ENSG00000249782	TF binding region
ENSG00000248765	CpG island
MTND6P2	CpG island
ENSG00000249782	CpG island
ENSG00000199568	chromatin interactions
ENSG00000247516	chromatin interactions
ENSG00000250037	chromatin interactions
ENSG00000249159	chromatin interactions
ENSG00000245729	chromatin interactions

Extended variants
information (count: 4656 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:4656 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13170576	chr5:8467174-8467175	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs567045555	chr5:8467183-8467184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562190083	chr5:8467188-8467189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs369787926	chr5:8467225-8467226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147441061	chr5:8467276-8467277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559446760	chr5:8467357-8467358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs114684861	chr5:8467364-8467365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529744765	chr5:8467388-8467389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138200148	chr5:8467408-8467409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs116680656	chr5:8467419-8467420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs11374328	chr5:8467430-8467431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs397754646	chr5:8467438-8467439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566116636	chr5:8467443-8467444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547561894	chr5:8467461-8467462	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs192360998	chr5:8467463-8467464	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs143630377	chr5:8467486-8467487	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs528906817	chr5:8467531-8467532	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs568812704	chr5:8467594-8467595	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs534233321	chr5:8467613-8467614	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs557635311	chr5:8467662-8467663	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs79057857	chr5:8467693-8467694	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs10512964	chr5:8467721-8467722	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs147181841	chr5:8467761-8467762	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs553442746	chr5:8467773-8467774	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs368537010	chr5:8467814-8467815	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs573271402	chr5:8467844-8467845	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs341893	chr5:8467900-8467901	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs555837612	chr5:8467901-8467902	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs575612751	chr5:8467912-8467913	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs544811168	chr5:8467926-8467927	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs75350441	chr5:8467963-8467964	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs533481803	chr5:8467973-8467974	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs532565572	chr5:8467978-8467979	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs184739165	chr5:8468030-8468031	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs547469780	chr5:8468062-8468063	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs140832514	chr5:8468106-8468107	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs142316461	chr5:8468108-8468109	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs921186	chr5:8468123-8468124	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs341892	chr5:8468144-8468145	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs568950067	chr5:8468145-8468146	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs187203624	chr5:8468173-8468174	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs192891228	chr5:8468197-8468198	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs341891	chr5:8468206-8468207	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs534128298	chr5:8468224-8468225	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs554111348	chr5:8468246-8468247	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs185444541	chr5:8468271-8468272	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs189499905	chr5:8468277-8468278	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs72733880	chr5:8468285-8468286	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs367632404	chr5:8468290-8468291	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs377354205	chr5:8468302-8468303	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
abnormal development	18461090	CNVD
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
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
T-cell prolymphocytic leukemia	17713554	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	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
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Melanoma	22183965	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Ovarian cancer	19193619	CNVD
Hepatocellular carcinoma	16785998	CNVD
Cancer	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intellectual disability	22102821	CNVD
Myelofibrosis	22110671	CNVD
Cri-du chat syndrome	16773131	CNVD
Cryptorchidism	21048976	CNVD
Glioblastoma multiforme	22286061	CNVD
Cervical cancer	16585170	CNVD
Mental retardation	16773131	CNVD
Non-small cell lung cancer	21829676	CNVD
Cri-du chat syndrome	22470819	CNVD
sporadic birth defects	19047251	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:236 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:8458400-8468400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:8458600-8468400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr5:8458600-8468400	Weak transcription	Esophagus	oesophagus
4	chr5:8458600-8468400	Weak transcription	Pancreas	Pancrea
5	chr5:8459800-8470200	Weak transcription	Aorta	Aorta
6	chr5:8463000-8468000	Weak transcription	Left Ventricle	heart
7	chr5:8463400-8469600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr5:8468400-8468600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr5:8468400-8468600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr5:8468400-8468600	ZNF genes & repeats	Esophagus	oesophagus
11	chr5:8468400-8468600	Enhancers	Pancreas	Pancrea
12	chr5:8468600-8470400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr5:8469600-8474000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
14	chr5:8469800-8474000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr5:8470000-8470400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr5:8470200-8471200	ZNF genes & repeats	Aorta	Aorta
17	chr5:8470400-8470800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
18	chr5:8470400-8471200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr5:8471200-8473200	Weak transcription	Aorta	Aorta
20	chr5:8473200-8473400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr5:8473200-8473400	ZNF genes & repeats	Aorta	Aorta
22	chr5:8473200-8475200	Enhancers	Fetal Intestine Large	intestine
23	chr5:8473200-8475200	Enhancers	Fetal Intestine Small	intestine
24	chr5:8473400-8473600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr5:8473400-8474000	Enhancers	H1 Cell Line	embryonic stem cell
26	chr5:8473800-8474200	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr5:8473800-8474800	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr5:8474000-8474400	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr5:8474000-8474800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr5:8474400-8474800	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr5:8474400-8475000	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr5:8474800-8475200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr5:8475200-8475800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr5:8475600-8476200	Enhancers	Brain Germinal Matrix	brain
35	chr5:8475600-8476600	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr5:8475800-8476200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr5:8475800-8476200	Active TSS	Brain Anterior Caudate	brain
38	chr5:8476000-8476400	Enhancers	Fetal Brain Male	brain
39	chr5:8481000-8481600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr5:8489400-8490800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr5:8491000-8492000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr5:8491200-8491800	Enhancers	NHDF-Ad	bronchial
43	chr5:8491200-8493200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr5:8493000-8494000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr5:8493400-8494200	Enhancers	Primary hematopoietic stem cells	blood
46	chr5:8496200-8496400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr5:8499800-8502000	Enhancers	NHDF-Ad	bronchial
48	chr5:8500400-8501400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr5:8500400-8501600	Enhancers	Osteobl	bone
50	chr5:8501000-8501600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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