Variant report

Variant	nsv949520
Chromosome Location	chr9:98204199-98238358
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:549)
CpG islands
(count:427)
Chromatin interactive
region (count:46)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:549 , 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	chr9:98215314-98215388	K562	blood:	n/a	n/a
2	ARID3A	chr9:98205859-98206018	K562	blood:	n/a	n/a
3	ARID3A	chr9:98214579-98214712	K562	blood:	n/a	n/a
4	ARID3A	chr9:98224854-98225426	K562	blood:	n/a	n/a
5	ATF1	chr9:98224654-98225251	K562	blood:	n/a	n/a
6	ATF2	chr9:98224457-98225273	GM12878	blood:	n/a	n/a
7	ATF2	chr9:98224649-98225239	GM12878	blood:	n/a	n/a
8	ATF3	chr9:98224774-98225257	K562	blood:	n/a	n/a
9	BACH1	chr9:98227166-98227236	K562	blood:	n/a	n/a
10	BACH1	chr9:98224894-98225069	K562	blood:	n/a	n/a
11	BATF	chr9:98224780-98225220	GM12878	blood:	n/a	n/a
12	BATF	chr9:98208520-98208810	GM12878	blood:	n/a	n/a
13	BATF	chr9:98208505-98208801	GM12878	blood:	n/a	n/a
14	BATF	chr9:98224831-98225171	GM12878	blood:	n/a	n/a
15	BCL11A	chr9:98224728-98225264	GM12878	blood:	n/a	chr9:98225195-98225204
16	BCL11A	chr9:98224740-98225225	GM12878	blood:	n/a	chr9:98225195-98225204
17	BCL3	chr9:98224804-98225467	K562	blood:	n/a	chr9:98225195-98225204
18	BCL3	chr9:98224832-98225231	GM12878	blood:	n/a	chr9:98225195-98225204
19	BCLAF1	chr9:98224534-98225309	GM12878	blood:	n/a	chr9:98225195-98225204
20	BCLAF1	chr9:98224502-98225248	GM12878	blood:	n/a	chr9:98225195-98225204
21	BHLHE40	chr9:98214485-98214824	K562	blood:	n/a	n/a
22	BHLHE40	chr9:98215350-98215409	K562	blood:	n/a	n/a
23	BHLHE40	chr9:98204524-98204570	K562	blood:	n/a	n/a
24	BHLHE40	chr9:98224564-98225398	K562	blood:	n/a	n/a
25	BHLHE40	chr9:98208583-98208944	GM12878	blood:	n/a	n/a
26	BHLHE40	chr9:98224478-98225574	GM12878	blood:	n/a	n/a
27	BHLHE40	chr9:98223976-98224105	K562	blood:	n/a	n/a
28	BHLHE40	chr9:98210286-98210522	GM12878	blood:	n/a	n/a
29	CBX3	chr9:98224396-98225508	K562	blood:	n/a	n/a
30	CBX3	chr9:98224692-98225259	K562	blood:	n/a	n/a
31	CCNT2	chr9:98224778-98225492	K562	blood:	n/a	chr9:98225171-98225191 chr9:98225271-98225280
32	CEBPB	chr9:98219991-98220380	IMR90	lung:	n/a	chr9:98220176-98220193 chr9:98220177-98220190
33	CEBPB	chr9:98214152-98214240	HepG2	liver:	n/a	n/a
34	CEBPB	chr9:98224783-98225209	K562	blood:	n/a	n/a
35	CEBPB	chr9:98204995-98205284	HepG2	liver:	n/a	chr9:98205147-98205158
36	CEBPB	chr9:98224660-98225226	GM12878	blood:	n/a	n/a
37	CEBPB	chr9:98221567-98221811	IMR90	lung:	n/a	n/a
38	CEBPB	chr9:98210387-98210708	H1-hESC	embryonic stem cell:	n/a	chr9:98210634-98210647
39	CEBPB	chr9:98216885-98217055	K562	blood:	n/a	n/a
40	CEBPB	chr9:98224804-98225223	GM12878	blood:	n/a	n/a
41	CEBPB	chr9:98224798-98225320	K562	blood:	n/a	n/a
42	CEBPB	chr9:98215326-98215541	K562	blood:	n/a	n/a
43	CEBPD	chr9:98224641-98225442	K562	blood:	n/a	n/a
44	CEBPD	chr9:98224818-98225434	K562	blood:	n/a	n/a
45	CHD1	chr9:98224386-98225214	GM12878	blood:	n/a	n/a
46	CHD1	chr9:98225475-98225550	GM12878	blood:	n/a	n/a
47	CHD2	chr9:98210337-98210627	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr9:98224930-98225160	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr9:98224440-98225583	GM12878	blood:	n/a	chr9:98225271-98225281
50	CHD2	chr9:98224863-98225284	K562	blood:	n/a	chr9:98225271-98225281

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:98213755-98213805	HL-60	blood:	n/a
2	chr9:98221975-98222025	Hepatocyte	liver:	n/a
3	chr9:98212061-98212111	PFSK-1	brain:	n/a
4	chr9:98213755-98213805	HEK293	kidney:	embryo
5	chr9:98206966-98207016	HEEpiC	esophagus:	n/a
6	chr9:98212061-98212111	NH-A	brain:	n/a
7	chr9:98212061-98212111	HRE	kidney:	n/a
8	chr9:98215821-98215871	Hela-S3	cervix:	n/a
9	chr9:98212061-98212111	PrEC	prostate:	n/a
10	chr9:98210236-98210286	T-47D	breast:	n/a
11	chr9:98212061-98212111	Jurkat	blood:	n/a
12	chr9:98206966-98207016	MCF-7	breast:	n/a
13	chr9:98215821-98215871	IMR90	lung:	fetal
14	chr9:98206966-98207016	HUVEC	blood vessel:	n/a
15	chr9:98210236-98210286	AG10803	skin:	n/a
16	chr9:98215821-98215871	HUVEC	blood vessel:	n/a
17	chr9:98206966-98207016	NH-A	brain:	n/a
18	chr9:98221975-98222025	AG09319	gingival:	n/a
19	chr9:98212061-98212111	NT2-D1	testis:	n/a
20	chr9:98213755-98213805	AG10803	skin:	n/a
21	chr9:98206966-98207016	HCT-116	colon:	n/a
22	chr9:98221975-98222025	BE2_C	brain:	n/a
23	chr9:98210236-98210286	SK-N-SH	brain:	n/a
24	chr9:98221619-98221669	Hela-S3	cervix:	n/a
25	chr9:98210236-98210286	U87	brain:	n/a
26	chr9:98210236-98210286	K562	blood:	n/a
27	chr9:98215821-98215871	HRCEpiC	kidney:	n/a
28	chr9:98212061-98212111	HCF	heart:	n/a
29	chr9:98210236-98210286	NT2-D1	testis:	n/a
30	chr9:98221619-98221669	HNPCEpiC	eye:	n/a
31	chr9:98221619-98221669	AG10803	skin:	n/a
32	chr9:98212061-98212111	HRCEpiC	kidney:	n/a
33	chr9:98215821-98215871	HCT-116	colon:	n/a
34	chr9:98215821-98215871	PANC-1	pancreas:	n/a
35	chr9:98221975-98222025	SK-N-SH_RA	brain:	n/a
36	chr9:98206966-98207016	Hepatocyte	liver:	n/a
37	chr9:98212061-98212111	AG09319	gingival:	n/a
38	chr9:98215821-98215871	AG04450	lung:	fetal
39	chr9:98215821-98215871	HCPEpiC	choroid plexus:	n/a
40	chr9:98206966-98207016	GM12892	blood:	n/a
41	chr9:98206966-98207016	IMR90	lung:	fetal
42	chr9:98221975-98222025	BJ	skin:	n/a
43	chr9:98210236-98210286	GM12878	blood:	n/a
44	chr9:98215821-98215871	BE2_C	brain:	n/a
45	chr9:98210236-98210286	HL-60	blood:	n/a
46	chr9:98215821-98215871	LNCaP	prostate:	n/a
47	chr9:98215821-98215871	SK-N-SH_RA	brain:	n/a
48	chr9:98210236-98210286	HCF	heart:	n/a
49	chr9:98215821-98215871	HIPEpiC	eye:	n/a
50	chr9:98213755-98213805	MCF10A-Er-Src	breast:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:98227014..98229023-chr9:98271434..98274318,2	MCF-7	breast:
2	chr9:98214310..98216415-chr9:98227721..98230889,3	MCF-7	breast:
3	chr9:98200946..98203462-chr9:98205677..98208531,4	K562	blood:
4	chr9:98227321..98228997-chr9:98229888..98232177,2	K562	blood:
5	chr9:98233664..98236470-chr9:98268989..98270628,2	K562	blood:
6	chr12:53297243..53298949-chr9:98222802..98225552,2	MCF-7	breast:
7	chr9:98223412..98227347-chr9:98253313..98257210,3	K562	blood:
8	chr9:98187807..98190501-chr9:98217714..98219257,2	MCF-7	breast:
9	chr9:98210481..98212145-chr9:98266993..98269582,2	K562	blood:
10	chr9:98207334..98210169-chr9:98211282..98214476,3	K562	blood:
11	chr9:98219926..98222684-chr9:98235733..98238442,2	K562	blood:
12	chr9:98211125..98213950-chr9:98219693..98221314,2	MCF-7	breast:
13	chr9:98218910..98222494-chr9:98224731..98227835,5	K562	blood:
14	chr9:98202595..98206584-chr9:98206995..98209232,3	MCF-7	breast:
15	chr9:98223555..98229775-chr9:98269693..98275962,10	K562	blood:
16	chr9:98202143..98207025-chr9:98207845..98211987,5	K562	blood:
17	chr9:98077820..98081322-chr9:98214829..98218712,4	K562	blood:
18	chr9:98210280..98213178-chr9:98213473..98216650,4	K562	blood:
19	chr9:98199109..98200665-chr9:98217953..98219861,2	K562	blood:
20	chr9:98214310..98216415-chr9:98227721..98230889,3	MCF-7	breast:
21	chr9:98222216..98224760-chr9:98225950..98227870,2	MCF-7	breast:
22	chr9:98222977..98229750-chr9:98267050..98274823,12	K562	blood:
23	chr9:98222888..98225027-chr9:98277335..98280257,3	K562	blood:
24	chr9:98202595..98206584-chr9:98206995..98209232,3	MCF-7	breast:
25	chr9:98228127..98229820-chr9:98239088..98240889,2	K562	blood:
26	chr9:98197509..98199344-chr9:98205458..98207531,2	MCF-7	breast:
27	chr9:98195732..98198631-chr9:98215123..98217873,2	K562	blood:
28	chr9:98190412..98192872-chr9:98202167..98205058,2	K562	blood:
29	chr9:98233432..98236653-chr9:98236835..98241063,4	MCF-7	breast:
30	chr9:98233432..98236653-chr9:98236835..98241063,4	MCF-7	breast:
31	chr9:98141744..98142409-chr9:98210461..98211518,3	MCF-7	breast:
32	chr9:98223864..98226761-chr9:98228381..98231062,3	K562	blood:
33	chr9:98187259..98193172-chr9:98208629..98217669,12	MCF-7	breast:
34	chr9:98223181..98225027-chr9:98277335..98280257,2	K562	blood:
35	chr9:98187665..98189990-chr9:98203397..98205232,2	MCF-7	breast:
36	chr9:98209521..98214013-chr9:98214744..98218073,4	K562	blood:
37	chr9:98210232..98214386-chr9:98264282..98269915,4	K562	blood:
38	chr9:98218003..98222058-chr9:98271885..98274474,3	K562	blood:
39	chr9:98218196..98221051-chr9:98231021..98232882,2	K562	blood:
40	chr9:98197131..98198876-chr9:98214885..98216623,2	K562	blood:
41	chr9:98223864..98226761-chr9:98228381..98231062,3	K562	blood:
42	chr9:98236732..98239700-chr9:98240483..98242788,2	MCF-7	breast:
43	chr9:98202143..98207025-chr9:98207845..98211987,5	K562	blood:
44	chr9:98201937..98203643-chr9:98208903..98210438,2	K562	blood:
45	chr9:98206913..98208735-chr9:98254383..98256847,2	MCF-7	breast:
46	chr9:98195671..98199206-chr9:98203414..98207469,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf3-6	chr9:98207060-98208373	NONHSAT133370

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PTCH1	hsa-miR-212-3p	chr9:98208705-98208699

Variant related genes	Relation type
PTCH1	TF binding region
PTCH1	CpG island
ENSG00000170421	chromatin interactions
ENSG00000271314	chromatin interactions
ENSG00000158169	chromatin interactions
ENSG00000237857	chromatin interactions
ENSG00000185920	chromatin interactions
ENSG00000271155	chromatin interactions

Extended variants
information (count: 1554 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1554 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs357563	chr9:98204199-98204200	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
2	rs573513254	chr9:98204205-98204206	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs541928172	chr9:98204222-98204223	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs563804268	chr9:98204224-98204225	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs148196786	chr9:98204230-98204231	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs372633452	chr9:98204239-98204240	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs552532577	chr9:98204268-98204269	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs564517159	chr9:98204280-98204281	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs528773394	chr9:98204319-98204320	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs547351894	chr9:98204356-98204357	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs568642261	chr9:98204363-98204364	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs536050245	chr9:98204371-98204372	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs550365242	chr9:98204383-98204384	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs56041614	chr9:98204385-98204386	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs539207476	chr9:98204443-98204444	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs186193478	chr9:98204469-98204470	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs544976516	chr9:98204482-98204483	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs572543101	chr9:98204492-98204493	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs16909856	chr9:98204493-98204494	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs555261692	chr9:98204497-98204498	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs573452075	chr9:98204536-98204537	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs189155569	chr9:98204551-98204552	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs562581643	chr9:98204555-98204556	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs531604782	chr9:98204572-98204573	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs575689055	chr9:98204593-98204594	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs114343848	chr9:98204594-98204595	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs112191650	chr9:98204603-98204604	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs561265780	chr9:98204608-98204609	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs374683959	chr9:98204615-98204616	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs367845477	chr9:98204660-98204661	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs547269154	chr9:98204669-98204670	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs562378129	chr9:98204699-98204700	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs529602236	chr9:98204712-98204713	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs376391716	chr9:98204713-98204714	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs551152921	chr9:98204715-98204716	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs141552230	chr9:98204757-98204758	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs528257300	chr9:98204791-98204792	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs16909859	chr9:98204792-98204793	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs182051894	chr9:98204802-98204803	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs116808917	chr9:98204818-98204819	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs533544350	chr9:98204819-98204820	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs576638942	chr9:98204834-98204835	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs186465730	chr9:98204837-98204838	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs190849352	chr9:98204861-98204862	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs373001451	chr9:98204946-98204947	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs150482595	chr9:98204955-98204956	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs114664581	chr9:98204971-98204972	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs577795375	chr9:98205012-98205013	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs35246192	chr9:98205112-98205113	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs546284712	chr9:98205148-98205149	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
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
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
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
overgrowth syndrome	16570072	CNVD
Effusion lymphoma	18079361	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Neurodevelopmental disorder	22521361	CNVD
Basal cell carcinoma	21518781	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1525 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:98189600-98210800	Weak transcription	Right Atrium	heart
2	chr9:98189800-98206600	Weak transcription	Pancreas	Pancrea
3	chr9:98194800-98206600	Weak transcription	Left Ventricle	heart
4	chr9:98196800-98206600	Weak transcription	Fetal Muscle Leg	muscle
5	chr9:98196800-98207000	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr9:98197000-98204600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr9:98197000-98206600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr9:98197000-98206600	Weak transcription	Duodenum Mucosa	Duodenum
9	chr9:98197000-98206600	Weak transcription	Fetal Muscle Trunk	muscle
10	chr9:98197000-98207200	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr9:98197200-98204200	Weak transcription	Fetal Stomach	stomach
12	chr9:98197200-98204400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr9:98197200-98204400	Weak transcription	Fetal Intestine Large	intestine
14	chr9:98197200-98204600	Weak transcription	Fetal Lung	lung
15	chr9:98197200-98205000	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr9:98197200-98206600	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr9:98197200-98206600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr9:98197200-98207000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr9:98197200-98207200	Weak transcription	Placenta	Placenta
20	chr9:98197200-98207600	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr9:98197200-98208800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr9:98197400-98205000	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr9:98197800-98204800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr9:98197800-98209400	Weak transcription	Fetal Heart	heart
25	chr9:98198000-98206600	Weak transcription	Brain Hippocampus Middle	brain
26	chr9:98198000-98207200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr9:98198000-98207200	Weak transcription	Brain Substantia Nigra	brain
28	chr9:98198000-98207400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr9:98200600-98207200	Weak transcription	HepG2	liver
30	chr9:98200800-98204600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr9:98200800-98211800	Weak transcription	Fetal Brain Male	brain
32	chr9:98201600-98207000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr9:98202000-98204400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr9:98202000-98224600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr9:98202200-98204400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr9:98202400-98206600	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr9:98202600-98204400	Weak transcription	Fetal Intestine Small	intestine
38	chr9:98202800-98207800	Weak transcription	Hela-S3	cervix
39	chr9:98203000-98204800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr9:98203000-98207200	Weak transcription	HSMM	muscle
41	chr9:98203200-98205200	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr9:98203200-98206600	Weak transcription	Brain Anterior Caudate	brain
43	chr9:98203200-98206600	Weak transcription	Lung	lung
44	chr9:98203200-98206800	Weak transcription	Gastric	stomach
45	chr9:98203200-98207000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr9:98203200-98207000	Weak transcription	Fetal Brain Female	brain
47	chr9:98203200-98207200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr9:98203200-98207200	Weak transcription	Fetal Kidney	kidney
49	chr9:98203200-98207200	Weak transcription	Rectal Mucosa Donor 29	rectum
50	chr9:98203200-98207600	Weak transcription	Duodenum Smooth Muscle	Duodenum

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