Variant report

Variant	nsv614551
Chromosome Location	chr9:71612891-71671116
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1776)
CpG islands
(count:1040)
Chromatin interactive
region (count:64)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1776 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:71635426-71635919	K562	blood:	n/a	n/a
2	ARID3A	chr9:71631852-71631872	K562	blood:	n/a	n/a
3	ARID3A	chr9:71634748-71635103	K562	blood:	n/a	n/a
4	ARID3A	chr9:71642563-71642873	K562	blood:	n/a	n/a
5	ARID3A	chr9:71614594-71614886	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:71650444-71651128	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:71650526-71650743	K562	blood:	n/a	n/a
8	ARID3A	chr9:71651502-71651839	K562	blood:	n/a	n/a
9	ATF1	chr9:71634756-71635094	K562	blood:	n/a	n/a
10	ATF1	chr9:71642591-71642873	K562	blood:	n/a	n/a
11	ATF1	chr9:71635543-71635967	K562	blood:	n/a	n/a
12	ATF1	chr9:71613777-71614153	K562	blood:	n/a	n/a
13	ATF2	chr9:71650422-71650822	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr9:71650325-71650801	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr9:71650292-71651027	A549	lung:	n/a	n/a
16	BACH1	chr9:71650535-71650996	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr9:71634639-71634975	K562	blood:	n/a	n/a
18	BCL3	chr9:71650984-71651685	A549	lung:	n/a	n/a
19	BCL3	chr9:71650464-71650985	GM12878	blood:	n/a	n/a
20	BCLAF1	chr9:71650456-71650942	GM12878	blood:	n/a	n/a
21	BCLAF1	chr9:71650320-71651006	GM12878	blood:	n/a	n/a
22	BHLHE40	chr9:71651417-71652026	K562	blood:	n/a	n/a
23	BHLHE40	chr9:71650466-71651197	K562	blood:	n/a	n/a
24	BHLHE40	chr9:71634550-71635063	K562	blood:	n/a	n/a
25	BHLHE40	chr9:71669163-71669440	GM12878	blood:	n/a	n/a
26	BHLHE40	chr9:71613664-71614154	K562	blood:	n/a	n/a
27	BHLHE40	chr9:71631696-71631742	K562	blood:	n/a	n/a
28	BHLHE40	chr9:71614468-71614941	GM12878	blood:	n/a	n/a
29	BHLHE40	chr9:71650493-71651530	GM12878	blood:	n/a	n/a
30	BHLHE40	chr9:71650290-71651580	HepG2	liver:	n/a	n/a
31	BHLHE40	chr9:71651819-71652051	HepG2	liver:	n/a	n/a
32	BHLHE40	chr9:71633440-71634093	K562	blood:	n/a	n/a
33	BHLHE40	chr9:71614430-71614874	K562	blood:	n/a	n/a
34	BRCA1	chr9:71650553-71650960	HepG2	liver:	n/a	n/a
35	BRCA1	chr9:71650525-71650755	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr9:71651018-71651389	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr9:71650370-71651092	H1-hESC	embryonic stem cell:	n/a	n/a
38	CBX3	chr9:71650416-71650740	K562	blood:	n/a	n/a
39	CBX3	chr9:71650395-71650842	K562	blood:	n/a	n/a
40	CBX3	chr9:71650265-71651368	HCT-116	colon:	n/a	n/a
41	CBX3	chr9:71634637-71635116	K562	blood:	n/a	n/a
42	CBX3	chr9:71634767-71635088	K562	blood:	n/a	n/a
43	CBX3	chr9:71614487-71615016	K562	blood:	n/a	n/a
44	CBX3	chr9:71644422-71644945	K562	blood:	n/a	n/a
45	CBX3	chr9:71644508-71644794	K562	blood:	n/a	n/a
46	CCNT2	chr9:71650338-71651360	K562	blood:	n/a	n/a
47	CCNT2	chr9:71623403-71623461	K562	blood:	n/a	n/a
48	CCNT2	chr9:71634748-71635750	K562	blood:	n/a	n/a
49	CEBPB	chr9:71622329-71622529	HepG2	liver:	n/a	chr9:71622451-71622462
50	CEBPB	chr9:71642667-71642952	HepG2	liver:	n/a	n/a

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:71627667-71627717	AG09309	skin:	n/a
2	chr9:71628906-71628956	GM12878	blood:	n/a
3	chr9:71651331-71651381	NT2-D1	testis:	n/a
4	chr9:71627667-71627717	AG09309	skin:	n/a
5	chr9:71628906-71628956	GM12878	blood:	n/a
6	chr9:71651331-71651381	NT2-D1	testis:	n/a
7	chr9:71651331-71651381	HCM	heart:	n/a
8	chr9:71669714-71669764	ECC-1	luminal epithelium:	n/a
9	chr9:71661107-71661157	AG09319	gingival:	n/a
10	chr9:71627667-71627717	ProgFib	skin:	n/a
11	chr9:71661107-71661157	HL-60	blood:	n/a
12	chr9:71651175-71651225	HAEpiC	amniotic membrane:	n/a
13	chr9:71650719-71650769	CMK	blood:	n/a
14	chr9:71669714-71669764	HAEpiC	amniotic membrane:	n/a
15	chr9:71650331-71650381	GM12891	blood:	n/a
16	chr9:71649195-71649245	GM12878	blood:	n/a
17	chr9:71650331-71650381	GM06990	blood:	n/a
18	chr9:71650237-71650287	IMR90	lung:	fetal
19	chr9:71650237-71650287	SK-N-MC	brain:	n/a
20	chr9:71650719-71650769	HRPEpiC	eye:	n/a
21	chr9:71661107-71661157	SK-N-SH	brain:	n/a
22	chr9:71649195-71649245	HUVEC	blood vessel:	n/a
23	chr9:71661107-71661157	SK-N-MC	brain:	n/a
24	chr9:71631514-71631564	A549	lung:	n/a
25	chr9:71649195-71649245	BE2_C	brain:	n/a
26	chr9:71650237-71650287	HL-60	blood:	n/a
27	chr9:71629130-71629180	HEEpiC	esophagus:	n/a
28	chr9:71623401-71623451	GM19239	blood:	n/a
29	chr9:71652532-71652582	ProgFib	skin:	n/a
30	chr9:71654823-71654873	HRCEpiC	kidney:	n/a
31	chr9:71623401-71623451	ProgFib	skin:	n/a
32	chr9:71652532-71652582	Jurkat	blood:	n/a
33	chr9:71627667-71627717	T-47D	breast:	n/a
34	chr9:71631514-71631564	AG09309	skin:	n/a
35	chr9:71651331-71651381	SK-N-SH_RA	brain:	n/a
36	chr9:71650331-71650381	MCF10A-Er-Src	breast:	n/a
37	chr9:71651175-71651225	HCPEpiC	choroid plexus:	n/a
38	chr9:71661107-71661157	BJ	skin:	n/a
39	chr9:71629130-71629180	CMK	blood:	n/a
40	chr9:71629130-71629180	HRE	kidney:	n/a
41	chr9:71627667-71627717	AG04449	skin:	fetal
42	chr9:71647192-71647242	SK-N-SH	brain:	n/a
43	chr9:71627667-71627717	GM19239	blood:	n/a
44	chr9:71649195-71649245	SK-N-MC	brain:	n/a
45	chr9:71650719-71650769	SAEC	small airway:	n/a
46	chr9:71623401-71623451	HRPEpiC	eye:	n/a
47	chr9:71669714-71669764	GM12878	blood:	n/a
48	chr9:71669714-71669764	BJ	skin:	n/a
49	chr9:71628906-71628956	PFSK-1	brain:	n/a
50	chr9:71651175-71651225	AG09309	skin:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:71634014..71636230-chr9:71638337..71641027,2	K562	blood:
2	chr9:71658862..71661009-chr9:71818957..71821038,2	K562	blood:
3	chr9:71634711..71636591-chr9:71649540..71651584,2	MCF-7	breast:
4	chr9:71199108..71199619-chr9:71642191..71643182,2	K562	blood:
5	chr9:71648859..71652807-chr9:71663115..71665569,4	MCF-7	breast:
6	chr9:71614377..71616166-chr9:71649558..71651998,2	MCF-7	breast:
7	chr9:71634014..71636921-chr9:71638059..71641027,2	K562	blood:
8	chr9:71319203..71320145-chr9:71614622..71615180,2	MCF-7	breast:
9	chr9:71649378..71651041-chr9:71654267..71655823,2	MCF-7	breast:
10	chr9:71634014..71636230-chr9:71638337..71641027,2	K562	blood:
11	chr9:71621939..71625091-chr9:71631557..71634181,3	K562	blood:
12	chr9:71199440..71199949-chr9:71642261..71643160,3	MCF-7	breast:
13	chr9:71612570..71616113-chr9:71618356..71621633,3	K562	blood:
14	chr9:71647332..71649670-chr9:71650617..71653266,2	K562	blood:
15	chr9:71640222..71642541-chr9:71649127..71652222,3	MCF-7	breast:
16	chr9:71649461..71652506-chr9:71658685..71662535,4	MCF-7	breast:
17	chr9:71649472..71654369-chr9:71735388..71737779,6	MCF-7	breast:
18	chr9:71644052..71646200-chr9:71649443..71653055,3	MCF-7	breast:
19	chr9:71621939..71625091-chr9:71631557..71634181,3	K562	blood:
20	chr9:71199122..71199719-chr9:71614348..71615097,4	MCF-7	breast:
21	chr9:71649461..71652506-chr9:71658685..71662535,4	MCF-7	breast:
22	chr9:71393142..71395397-chr9:71613352..71615098,2	K562	blood:
23	chr9:71642300..71643929-chr9:71644528..71647295,2	MCF-7	breast:
24	chr9:71622551..71625318-chr9:71628981..71631159,4	K562	blood:
25	chr9:71659255..71662171-chr9:71666375..71668806,2	K562	blood:
26	chr9:71197374..71198367-chr9:71614324..71614982,2	MCF-7	breast:
27	chr9:71587881..71589909-chr9:71610346..71613287,2	K562	blood:
28	chr9:71668853..71671288-chr9:71790657..71793201,2	MCF-7	breast:
29	chr9:71655862..71658846-chr9:71661896..71664645,2	MCF-7	breast:
30	chr9:71634014..71636921-chr9:71638059..71641027,2	K562	blood:
31	chr9:71459669..71460505-chr9:71614463..71615113,2	MCF-7	breast:
32	chr9:71668771..71670774-chr9:71790512..71793503,2	MCF-7	breast:
33	chr9:71627843..71630592-chr9:71632071..71633725,3	K562	blood:
34	chr9:71646520..71648758-chr9:71649618..71651156,2	MCF-7	breast:
35	chr9:71651891..71654666-chr9:71794283..71796361,2	MCF-7	breast:
36	chr9:71198223..71198730-chr9:71614318..71615145,2	MCF-7	breast:
37	chr9:71650420..71652084-chr9:71654261..71655791,2	MCF-7	breast:
38	chr9:71612099..71614210-chr9:71616099..71618792,2	MCF-7	breast:
39	chr9:71642108..71644566-chr9:71646491..71648725,2	K562	blood:
40	chr9:71651712..71654573-chr9:71656499..71659593,3	K562	blood:
41	chr9:71628740..71631389-chr9:71634679..71636239,2	K562	blood:
42	chr9:71668686..71669450-chr9:71838137..71838734,2	MCF-7	breast:
43	chr9:71653020..71654541-chr9:71659472..71661333,2	K562	blood:
44	chr9:71655862..71658846-chr9:71661896..71664645,2	MCF-7	breast:
45	chr9:71642108..71644566-chr9:71646491..71648725,2	K562	blood:
46	chr9:71642182..71645609-chr9:71649881..71653003,5	K562	blood:
47	chr9:71619036..71621267-chr9:71649234..71651665,2	K562	blood:
48	chr9:71612570..71616113-chr9:71618356..71621633,3	K562	blood:
49	chr9:71655778..71657735-chr9:71659824..71661960,2	K562	blood:
50	chr9:71182851..71183578-chr9:71614201..71614782,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKACG-4	chr9:71624143-71625000	ucscGeneNc_uc004ahk_2
2	lnc-PRKACG-4	chr9:71625289-71625403	ucscGeneNc_uc004ahk_2

No data

Variant related genes	Relation type
PRKACG	TF binding region
FXN	TF binding region
PRKACG	CpG island
FXN	CpG island
ENSG00000165060	chromatin interactions
ENSG00000187866	chromatin interactions
ENSG00000119139	chromatin interactions
ENSG00000165059	chromatin interactions

Extended variants
information (count: 2189 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2189 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs883751	chr9:71612891-71612892	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs533303174	chr9:71612907-71612908	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186749035	chr9:71612955-71612956	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs35888296	chr9:71612957-71612958	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs386734752	chr9:71612975-71612976	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542788542	chr9:71612988-71612989	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566194337	chr9:71613001-71613002	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529182351	chr9:71613008-71613009	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548686952	chr9:71613015-71613016	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs189678590	chr9:71613022-71613023	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs10120881	chr9:71613087-71613088	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs141990996	chr9:71613119-71613120	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571577153	chr9:71613133-71613134	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538805017	chr9:71613176-71613177	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574866720	chr9:71613214-71613215	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs148174017	chr9:71613222-71613223	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373835807	chr9:71613223-71613224	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182214411	chr9:71613336-71613337	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562839688	chr9:71613338-71613339	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs555464324	chr9:71613339-71613340	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs574023441	chr9:71613366-71613367	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs544283387	chr9:71613460-71613461	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs563155408	chr9:71613470-71613471	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs531738161	chr9:71613524-71613525	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs551809400	chr9:71613627-71613628	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs77433860	chr9:71613628-71613629	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs560351061	chr9:71613659-71613660	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs141998654	chr9:71613700-71613701	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs186148598	chr9:71613761-71613762	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs112506658	chr9:71613765-71613766	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs560823514	chr9:71613770-71613771	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs531299045	chr9:71613779-71613780	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs150670469	chr9:71613780-71613781	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs527930613	chr9:71613782-71613783	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs140890251	chr9:71613844-71613845	Enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs547562072	chr9:71613847-71613848	Enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs62569223	chr9:71613947-71613948	Enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs142753327	chr9:71613982-71613983	Enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs534029974	chr9:71613983-71613984	Enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs536512766	chr9:71614006-71614007	Enhancers Strong transcription Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs147367553	chr9:71614009-71614010	Enhancers Strong transcription Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs574059848	chr9:71614077-71614078	Enhancers Strong transcription Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs538204488	chr9:71614118-71614119	Enhancers Strong transcription Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs556160409	chr9:71614142-71614143	Enhancers Strong transcription Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs114374945	chr9:71614194-71614195	Enhancers Strong transcription Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs190960130	chr9:71614245-71614246	Enhancers Strong transcription Bivalent Enhancer Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs560311928	chr9:71614248-71614249	Enhancers Strong transcription Bivalent Enhancer Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs572259671	chr9:71614249-71614250	Enhancers Strong transcription Bivalent Enhancer Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs17407816	chr9:71614256-71614257	Enhancers Strong transcription Bivalent Enhancer Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs184189162	chr9:71614259-71614260	Enhancers Strong transcription Bivalent Enhancer Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17899364	CNVD
Mantle cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Epilepsy	22083797	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1669 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71594800-71628400	Weak transcription	Spleen	Spleen
2	chr9:71595200-71628000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:71595200-71631600	Weak transcription	Gastric	stomach
4	chr9:71595800-71626200	Weak transcription	Colonic Mucosa	Colon
5	chr9:71597200-71613000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr9:71597200-71626000	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr9:71598400-71613200	Weak transcription	Right Ventricle	heart
8	chr9:71598800-71623200	Weak transcription	Pancreas	Pancrea
9	chr9:71598800-71644600	Weak transcription	Right Atrium	heart
10	chr9:71599000-71613000	Weak transcription	Left Ventricle	heart
11	chr9:71603800-71614600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr9:71604200-71617800	Strong transcription	Fetal Intestine Large	intestine
13	chr9:71606800-71623000	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr9:71606800-71626800	Weak transcription	HepG2	liver
15	chr9:71607400-71630600	Weak transcription	Aorta	Aorta
16	chr9:71607600-71614200	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr9:71607600-71628000	Weak transcription	Lung	lung
18	chr9:71608400-71613600	Weak transcription	Duodenum Mucosa	Duodenum
19	chr9:71609200-71613000	Weak transcription	Fetal Intestine Small	intestine
20	chr9:71610000-71614600	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr9:71610400-71614600	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr9:71611000-71614600	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr9:71611600-71613400	Weak transcription	Primary B cells from cord blood	blood
24	chr9:71611600-71613800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
25	chr9:71611600-71614000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr9:71611600-71614600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr9:71611600-71616400	Weak transcription	Primary B cells from peripheral blood	blood
28	chr9:71611800-71613000	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr9:71611800-71613200	Weak transcription	GM12878-XiMat	blood
30	chr9:71611800-71613400	Weak transcription	Primary T cells from cord blood	blood
31	chr9:71611800-71613800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr9:71611800-71614600	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr9:71611800-71614600	Enhancers	Fetal Stomach	stomach
34	chr9:71611800-71615800	Enhancers	Fetal Heart	heart
35	chr9:71612000-71613000	Enhancers	Fetal Kidney	kidney
36	chr9:71612000-71613200	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr9:71612000-71613200	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr9:71612000-71613200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr9:71612000-71613800	Weak transcription	Primary T cells fromperipheralblood	blood
40	chr9:71612000-71614600	Enhancers	Primary hematopoietic stem cells	blood
41	chr9:71612000-71614600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr9:71612200-71613000	Weak transcription	Brain Cingulate Gyrus	brain
43	chr9:71612200-71613200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr9:71612200-71613200	Weak transcription	Adipose Nuclei	Adipose
45	chr9:71612200-71613200	Weak transcription	Monocytes-CD14+_RO01746	blood
46	chr9:71612200-71614000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr9:71612200-71614000	Enhancers	Fetal Brain Female	brain
48	chr9:71612200-71614600	Enhancers	Fetal Lung	lung
49	chr9:71612200-71614800	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr9:71612400-71614000	Weak transcription	Brain Substantia Nigra	brain

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