Variant report

Variant	nsv891983
Chromosome Location	chr9:510546-634160
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1191)
CpG islands
(count:61)
Chromatin interactive
region (count:41)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1191 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:613790-614724	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:592251-592433	HepG2	liver:	n/a	n/a
3	ATF3	chr9:557723-558324	A549	lung:	n/a	n/a
4	BACH1	chr9:557912-558114	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr9:561382-561724	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr9:561269-561869	A549	lung:	n/a	n/a
7	BCL3	chr9:561341-561682	GM12878	blood:	n/a	n/a
8	BCL3	chr9:557812-558394	A549	lung:	n/a	n/a
9	BHLHE40	chr9:629150-629515	GM12878	blood:	n/a	n/a
10	BHLHE40	chr9:546835-547287	K562	blood:	n/a	n/a
11	BHLHE40	chr9:614452-614687	HepG2	liver:	n/a	n/a
12	BHLHE40	chr9:567560-567673	GM12878	blood:	n/a	n/a
13	BRCA1	chr9:613818-614198	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr9:589772-590180	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr9:618492-618642	H1-hESC	embryonic stem cell:	n/a	chr9:618588-618601 chr9:618588-618601 chr9:618588-618599 chr9:618590-618601
16	CEBPB	chr9:599945-600321	H1-hESC	embryonic stem cell:	n/a	chr9:600087-600098 chr9:600123-600134
17	CEBPB	chr9:599936-600484	Hela-S3	cervix:	n/a	chr9:600087-600098 chr9:600123-600134
18	CEBPB	chr9:599942-600395	HepG2	liver:	n/a	chr9:600087-600098 chr9:600123-600134
19	CEBPB	chr9:573616-573837	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr9:618520-618739	HepG2	liver:	n/a	chr9:618588-618601 chr9:618588-618601 chr9:618588-618599 chr9:618590-618601
21	CEBPB	chr9:599836-600408	MCF-7	breast:	n/a	chr9:600087-600098 chr9:600123-600134
22	CEBPB	chr9:530695-530959	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr9:599844-600456	A549	lung:	n/a	chr9:600087-600098 chr9:600123-600134
24	CEBPB	chr9:561474-561777	MCF-7	breast:	n/a	n/a
25	CEBPB	chr9:599921-600405	A549	lung:	n/a	chr9:600087-600098 chr9:600123-600134
26	CEBPB	chr9:563605-564145	A549	lung:	n/a	n/a
27	CEBPB	chr9:599936-600319	K562	blood:	n/a	chr9:600087-600098 chr9:600123-600134
28	CEBPB	chr9:561219-561918	A549	lung:	n/a	n/a
29	CEBPB	chr9:614904-615126	HepG2	liver:	n/a	chr9:614996-615007
30	CEBPB	chr9:599948-600356	MCF-7	breast:	n/a	chr9:600087-600098 chr9:600123-600134
31	CEBPB	chr9:530652-530956	A549	lung:	n/a	n/a
32	CEBPB	chr9:602928-603376	MCF-7	breast:	n/a	n/a
33	CEBPB	chr9:614887-615070	H1-hESC	embryonic stem cell:	n/a	chr9:614996-615007
34	CEBPB	chr9:561371-561765	A549	lung:	n/a	n/a
35	CEBPB	chr9:599971-600359	ECC-1	luminal epithelium:	n/a	chr9:600087-600098 chr9:600123-600134
36	CEBPB	chr9:589903-590000	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr9:599907-600250	ECC-1	luminal epithelium:	n/a	chr9:600087-600098 chr9:600123-600134
38	CEBPB	chr9:530490-531138	HCT-116	colon:	n/a	chr9:530982-530993 chr9:530982-530995 chr9:530982-530995 chr9:530982-530993
39	CEBPB	chr9:618469-618742	A549	lung:	n/a	chr9:618588-618601 chr9:618588-618601 chr9:618588-618599 chr9:618590-618601
40	CEBPB	chr9:599943-600381	IMR90	lung:	n/a	chr9:600087-600098 chr9:600123-600134
41	CEBPB	chr9:561463-561714	A549	lung:	n/a	n/a
42	CEBPB	chr9:602628-603112	MCF-7	breast:	n/a	n/a
43	CEBPB	chr9:573656-573820	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr9:604811-604854	A549	lung:	n/a	n/a
45	CEBPB	chr9:599889-600308	A549	lung:	n/a	chr9:600087-600098 chr9:600123-600134
46	CEBPB	chr9:618414-618785	IMR90	lung:	n/a	chr9:618588-618601 chr9:618588-618601 chr9:618588-618599 chr9:618590-618601
47	CEBPB	chr9:530749-531005	A549	lung:	n/a	chr9:530982-530993 chr9:530982-530995 chr9:530982-530995 chr9:530982-530993
48	CHD1	chr9:557966-558051	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr9:629243-629367	GM12878	blood:	n/a	n/a
50	CHD2	chr9:591485-591533	Hela-S3	cervix:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:574312-574362	HMEC	breast:	n/a
2	chr9:574312-574362	A549	lung:	n/a
3	chr9:574312-574362	PFSK-1	brain:	n/a
4	chr9:574312-574362	NHBE	bronchial:	n/a
5	chr9:574312-574362	NH-A	brain:	n/a
6	chr9:574312-574362	MCF-7	breast:	n/a
7	chr9:574312-574362	ECC-1	luminal epithelium:	n/a
8	chr9:574312-574362	BJ	skin:	n/a
9	chr9:574312-574362	HUVEC	blood vessel:	n/a
10	chr9:574312-574362	HEEpiC	esophagus:	n/a
11	chr9:574312-574362	HRCEpiC	kidney:	n/a
12	chr9:574312-574362	ovcar-3	ovarian:	n/a
13	chr9:574312-574362	K562	blood:	n/a
14	chr9:574312-574362	GM06990	blood:	n/a
15	chr9:574312-574362	HepG2	liver:	n/a
16	chr9:574312-574362	GM12891	blood:	n/a
17	chr9:574312-574362	IMR90	lung:	fetal
18	chr9:574312-574362	T-47D	breast:	n/a
19	chr9:574312-574362	NB4	blood:	n/a
20	chr9:574312-574362	SK-N-SH	brain:	n/a
21	chr9:574312-574362	HRE	kidney:	n/a
22	chr9:574312-574362	GM12878	blood:	n/a
23	chr9:574312-574362	HCM	heart:	n/a
24	chr9:574312-574362	NT2-D1	testis:	n/a
25	chr9:574312-574362	BE2_C	brain:	n/a
26	chr9:574312-574362	HAEpiC	amniotic membrane:	n/a
27	chr9:574312-574362	HEK293	kidney:	embryo
28	chr9:574312-574362	NHDF-neo	bronchial:	n/a
29	chr9:574312-574362	HCPEpiC	choroid plexus:	n/a
30	chr9:574312-574362	AG04450	lung:	fetal
31	chr9:574312-574362	PrEC	prostate:	n/a
32	chr9:574312-574362	HPAEpiC	pulmonary alveolar:	n/a
33	chr9:574312-574362	SAEC	small airway:	n/a
34	chr9:574312-574362	ProgFib	skin:	n/a
35	chr9:574312-574362	LNCaP	prostate:	n/a
36	chr9:574312-574362	GM19239	blood:	n/a
37	chr9:574312-574362	AG10803	skin:	n/a
38	chr9:574312-574362	MCF10A-Er-Src	breast:	n/a
39	chr9:574312-574362	RPTEC	kidney:	n/a
40	chr9:574312-574362	AG09309	skin:	n/a
41	chr9:574312-574362	AG09319	gingival:	n/a
42	chr9:574312-574362	HCF	heart:	n/a
43	chr9:574312-574362	CMK	blood:	n/a
44	chr9:574312-574362	SK-N-MC	brain:	n/a
45	chr9:574312-574362	HNPCEpiC	eye:	n/a
46	chr9:574312-574362	AoSMC	blood vessel:	n/a
47	chr9:574312-574362	Caco-2	colon:	n/a
48	chr9:574312-574362	HRPEpiC	eye:	n/a
49	chr9:574312-574362	Hepatocyte	liver:	n/a
50	chr9:574312-574362	Jurkat	blood:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:14226157..14227663-chr9:613613..615133,2	K562	blood:
2	chr9:613518..614436-chr9:806263..806822,2	MCF-7	breast:
3	chr9:581769..582694-chr9:763829..764743,4	MCF-7	breast:
4	chr9:581168..581745-chr9:613579..614471,2	MCF-7	breast:
5	chr9:581649..582215-chr9:998516..999103,2	MCF-7	breast:
6	chr9:581860..582832-chr9:613640..614518,3	MCF-7	breast:
7	chr10:14227179..14227880-chr9:613613..614133,4	MCF-7	breast:
8	chr9:613644..614435-chr9:753933..755128,3	MCF-7	breast:
9	chr9:581821..582545-chr9:807512..808214,2	MCF-7	breast:
10	chr9:487771..490019-chr9:514331..516293,2	MCF-7	breast:
11	chr9:582031..585321-chr9:586707..590039,3	K562	blood:
12	chr9:535330..537087-chr9:549296..551126,2	K562	blood:
13	chr9:469974..471479-chr9:511045..512830,2	K562	blood:
14	chr9:613348..614490-chr9:763793..765061,13	MCF-7	breast:
15	chr9:581168..581745-chr9:613579..614471,2	MCF-7	breast:
16	chr9:613541..614622-chr9:757205..758240,10	MCF-7	breast:
17	chr9:469326..471004-chr9:547085..549851,2	MCF-7	breast:
18	chr9:581860..582832-chr9:613640..614518,3	MCF-7	breast:
19	chr9:530586..533539-chr9:534026..536380,2	MCF-7	breast:
20	chr9:518740..521510-chr9:531283..533605,2	MCF-7	breast:
21	chr9:523311..524277-chr9:542856..543632,2	MCF-7	breast:
22	chr9:613814..614512-chr9:1017801..1018342,2	MCF-7	breast:
23	chr9:581438..583645-chr9:586871..590074,4	MCF-7	breast:
24	chr9:385789..386423-chr9:612104..612846,2	K562	blood:
25	chr9:613650..614569-chr9:806256..807252,7	MCF-7	breast:
26	chr9:581871..582698-chr9:763741..764739,5	MCF-7	breast:
27	chr9:512039..514160-chr9:515791..519174,3	K562	blood:
28	chr9:512039..514160-chr9:515791..519174,3	K562	blood:
29	chr9:613714..614307-chr9:893592..894180,2	MCF-7	breast:
30	chr9:582031..585321-chr9:586707..590039,3	K562	blood:
31	chr9:613586..614504-chr9:756894..758172,6	MCF-7	breast:
32	chr9:613569..614095-chr9:1100690..1101615,2	MCF-7	breast:
33	chr9:530586..533539-chr9:534026..536380,2	MCF-7	breast:
34	chr9:613026..614583-chr9:763698..764753,25	MCF-7	breast:
35	chr9:555602..557901-chr9:561314..563396,2	K562	blood:
36	chr9:518740..521510-chr9:531283..533605,2	MCF-7	breast:
37	chr9:535330..537087-chr9:549296..551126,2	K562	blood:
38	chr9:523311..524277-chr9:542856..543632,2	MCF-7	breast:
39	chr9:581438..583645-chr9:586871..590074,4	MCF-7	breast:
40	chr9:385596..386468-chr9:546637..547164,2	MCF-7	breast:
41	chr9:555602..557901-chr9:561314..563396,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DOCK8-2	chr9:547317-547341	ENSG00000226403.1
2	lnc-DOCK8-2	chr9:547038-547341	NONHSAT129931
3	lnc-DOCK8-2	chr9:549190-549531	ENSG00000226403.1
4	lnc-DOCK8-2	chr9:549107-549531	ENSG00000226403.1
5	lnc-DOCK8-2	chr9:547318-547341	ENSG00000226403.1
6	lnc-DOCK8-2	chr9:549107-549525	NONHSAT129931

No data

Variant related genes	Relation type
ENSG00000226403	TF binding region
RNU6-1327P	TF binding region
RN7SL412P	TF binding region
ENSG00000226403	CpG island
RNU6-1327P	CpG island
RN7SL412P	CpG island
ENSG00000107104	chromatin interactions
ENSG00000228115	chromatin interactions
ENSG00000227155	chromatin interactions

Extended variants
information (count: 7280 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:7280 , 50 per page) page: 1 2 3 4 5 6 7 ... 146

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7850663	chr9:510546-510547	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565710130	chr9:510584-510585	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188026927	chr9:510601-510602	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548346522	chr9:510625-510626	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113198121	chr9:510638-510639	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568172039	chr9:510644-510645	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536800208	chr9:510649-510650	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs373758787	chr9:510650-510651	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554729764	chr9:510651-510652	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570620757	chr9:510652-510653	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539755235	chr9:510656-510657	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552926800	chr9:510691-510692	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs7850873	chr9:510700-510701	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs541910162	chr9:510756-510757	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573237850	chr9:510776-510777	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192485776	chr9:510820-510821	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs7854730	chr9:510829-510830	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs556937585	chr9:510861-510862	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs7874553	chr9:510862-510863	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs183194639	chr9:510880-510881	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs533419883	chr9:510899-510900	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533438692	chr9:510947-510948	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540975857	chr9:510997-510998	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs7857770	chr9:511024-511025	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs528052922	chr9:511029-511030	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs548211661	chr9:511041-511042	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs116697047	chr9:511043-511044	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs530646743	chr9:511063-511064	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs114139138	chr9:511065-511066	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs187368777	chr9:511081-511082	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs142938006	chr9:511082-511083	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs7848411	chr9:511094-511095	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs58677638	chr9:511098-511099	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs75695144	chr9:511217-511218	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs552888312	chr9:511243-511244	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs566437180	chr9:511258-511259	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs535410340	chr9:511262-511263	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs555360336	chr9:511266-511267	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs145529649	chr9:511268-511269	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs544723673	chr9:511315-511316	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs12342353	chr9:511342-511343	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs568131957	chr9:511380-511381	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs192934374	chr9:511396-511397	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs115334403	chr9:511459-511460	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs560721513	chr9:511491-511492	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs533886111	chr9:511510-511511	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs12000995	chr9:511527-511528	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs184611985	chr9:511537-511538	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs561757168	chr9:511573-511574	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs148426659	chr9:511575-511576	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164920	CNVD
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-small cell lung cancer	16651412	CNVD

Chromatin state (count:2545 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:505800-512000	Weak transcription	Esophagus	oesophagus
2	chr9:506000-511200	Weak transcription	Adipose Nuclei	Adipose
3	chr9:506000-512000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr9:506000-520000	Weak transcription	Aorta	Aorta
5	chr9:506000-520200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr9:506200-517800	Weak transcription	Colonic Mucosa	Colon
7	chr9:506400-511000	Weak transcription	Brain Substantia Nigra	brain
8	chr9:506400-514400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr9:506400-519600	Weak transcription	Colon Smooth Muscle	Colon
10	chr9:506600-512000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr9:506600-512200	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr9:506600-514400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr9:506600-514600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr9:506600-517600	Weak transcription	Fetal Intestine Large	intestine
15	chr9:506600-517600	Weak transcription	Fetal Intestine Small	intestine
16	chr9:506800-511000	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr9:506800-511400	Weak transcription	Fetal Heart	heart
18	chr9:506800-511800	Weak transcription	Brain Hippocampus Middle	brain
19	chr9:506800-512000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr9:506800-512400	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr9:506800-517600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr9:506800-517600	Weak transcription	NHEK	skin
23	chr9:507000-510800	Weak transcription	A549	lung
24	chr9:507000-511000	Weak transcription	Duodenum Mucosa	Duodenum
25	chr9:507000-512000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr9:507000-512000	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr9:507000-512200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr9:507000-516600	Weak transcription	Left Ventricle	heart
29	chr9:507000-532600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr9:507400-511800	Weak transcription	Pancreas	Pancrea
31	chr9:508400-522400	Weak transcription	Fetal Muscle Leg	muscle
32	chr9:510400-511000	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr9:510800-511600	Strong transcription	A549	lung
34	chr9:511000-511400	Enhancers	Duodenum Mucosa	Duodenum
35	chr9:511000-512200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr9:511000-513200	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr9:511000-513400	Enhancers	Brain Substantia Nigra	brain
38	chr9:511200-511400	Enhancers	Small Intestine	intestine
39	chr9:511200-511600	Enhancers	Adipose Nuclei	Adipose
40	chr9:511400-512000	Enhancers	Fetal Heart	heart
41	chr9:511400-512000	Weak transcription	Small Intestine	intestine
42	chr9:511400-516000	Weak transcription	Duodenum Mucosa	Duodenum
43	chr9:511600-511800	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr9:511600-518200	Weak transcription	A549	lung
45	chr9:511800-512200	Enhancers	Pancreas	Pancrea
46	chr9:511800-513600	Enhancers	Brain Hippocampus Middle	brain
47	chr9:511800-513600	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr9:512000-512200	Genic enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr9:512000-512200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr9:512000-512200	Enhancers	Primary T helper naive cells from peripheral blood	blood

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