Variant report

Variant	esv2764163
Chromosome Location	chr9:6637145-6673830
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:965)
CpG islands
(count:367)
Chromatin interactive
region (count:23)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:965 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:6667619-6667991	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:6673778-6673994	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:6645695-6646211	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:6664541-6665413	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:6641775-6641951	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:6667709-6667966	K562	blood:	n/a	n/a
7	ATF2	chr9:6673244-6673922	GM12878	blood:	n/a	n/a
8	ATF2	chr9:6654995-6655416	GM12878	blood:	n/a	n/a
9	ATF2	chr9:6654912-6655463	GM12878	blood:	n/a	n/a
10	ATF3	chr9:6664488-6664934	A549	lung:	n/a	n/a
11	ATF3	chr9:6664294-6664873	A549	lung:	n/a	n/a
12	BACH1	chr9:6645623-6645968	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr9:6667638-6667964	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr9:6644871-6645230	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr9:6656332-6656632	GM12878	blood:	n/a	n/a
16	BATF	chr9:6655058-6655371	GM12878	blood:	n/a	n/a
17	BCL11A	chr9:6655034-6655412	GM12878	blood:	n/a	n/a
18	BCL11A	chr9:6673323-6673715	GM12878	blood:	n/a	n/a
19	BCL11A	chr9:6673395-6673768	GM12878	blood:	n/a	n/a
20	BCL3	chr9:6664426-6665297	A549	lung:	n/a	chr9:6665033-6665042
21	BCL3	chr9:6664480-6665034	A549	lung:	n/a	n/a
22	BCLAF1	chr9:6667616-6668061	GM12878	blood:	n/a	n/a
23	BCLAF1	chr9:6646220-6646693	GM12878	blood:	n/a	n/a
24	BCLAF1	chr9:6645684-6646735	GM12878	blood:	n/a	chr9:6645822-6645831
25	BCLAF1	chr9:6654844-6655458	GM12878	blood:	n/a	n/a
26	BHLHE40	chr9:6654915-6655315	GM12878	blood:	n/a	n/a
27	BHLHE40	chr9:6673357-6673800	GM12878	blood:	n/a	n/a
28	BHLHE40	chr9:6646511-6647018	HepG2	liver:	n/a	n/a
29	BHLHE40	chr9:6645530-6646189	HepG2	liver:	n/a	n/a
30	BHLHE40	chr9:6645539-6646985	GM12878	blood:	n/a	n/a
31	BHLHE40	chr9:6646851-6646934	A549	lung:	n/a	n/a
32	BHLHE40	chr9:6640333-6640626	HepG2	liver:	n/a	n/a
33	BHLHE40	chr9:6664329-6665171	HepG2	liver:	n/a	n/a
34	BRCA1	chr9:6664464-6664732	HepG2	liver:	n/a	n/a
35	BRCA1	chr9:6664596-6664874	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr9:6662560-6662584	K562	blood:	n/a	n/a
37	CEBPB	chr9:6640356-6640570	HepG2	liver:	n/a	chr9:6640489-6640498
38	CEBPB	chr9:6641951-6642280	MCF-7	breast:	n/a	chr9:6642159-6642168 chr9:6642158-6642169 chr9:6642157-6642170 chr9:6642159-6642168 chr9:6642157-6642170 chr9:6642157-6642168 chr9:6642157-6642170 chr9:6642159-6642168 chr9:6642159-6642168
39	CEBPB	chr9:6640280-6640653	HepG2	liver:	n/a	chr9:6640489-6640498
40	CEBPB	chr9:6664587-6665287	HepG2	liver:	n/a	n/a
41	CEBPB	chr9:6642013-6642249	H1-hESC	embryonic stem cell:	n/a	chr9:6642159-6642168 chr9:6642158-6642169 chr9:6642157-6642170 chr9:6642159-6642168 chr9:6642157-6642170 chr9:6642157-6642168 chr9:6642157-6642170 chr9:6642159-6642168 chr9:6642159-6642168
42	CEBPB	chr9:6637458-6637625	Hela-S3	cervix:	n/a	chr9:6637505-6637516
43	CEBPB	chr9:6645730-6645913	HepG2	liver:	n/a	n/a
44	CEBPB	chr9:6641935-6642272	A549	lung:	n/a	chr9:6642159-6642168 chr9:6642158-6642169 chr9:6642157-6642170 chr9:6642159-6642168 chr9:6642157-6642170 chr9:6642157-6642168 chr9:6642157-6642170 chr9:6642159-6642168 chr9:6642159-6642168
45	CEBPB	chr9:6645827-6646639	GM12878	blood:	n/a	chr9:6646476-6646487
46	CEBPB	chr9:6641784-6642343	Hela-S3	cervix:	n/a	chr9:6642159-6642168 chr9:6642158-6642169 chr9:6642157-6642170 chr9:6642159-6642168 chr9:6642157-6642170 chr9:6642157-6642168 chr9:6642157-6642170 chr9:6642159-6642168 chr9:6642159-6642168
47	CEBPB	chr9:6640430-6640578	A549	lung:	n/a	chr9:6640489-6640498
48	CEBPB	chr9:6658749-6659061	IMR90	lung:	n/a	chr9:6658871-6658882
49	CEBPB	chr9:6654850-6655851	GM12878	blood:	n/a	n/a
50	CEBPB	chr9:6648282-6648509	Hela-S3	cervix:	n/a	chr9:6648394-6648405

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6644603-6644653	MCF-7	breast:	n/a
2	chr9:6644603-6644653	MCF-7	breast:	n/a
3	chr9:6645686-6645736	GM12878	blood:	n/a
4	chr9:6645736-6645786	CMK	blood:	n/a
5	chr9:6646386-6646436	HL-60	blood:	n/a
6	chr9:6645468-6645518	HL-60	blood:	n/a
7	chr9:6646386-6646436	ProgFib	skin:	n/a
8	chr9:6644603-6644653	NB4	blood:	n/a
9	chr9:6645686-6645736	CMK	blood:	n/a
10	chr9:6644603-6644653	AG10803	skin:	n/a
11	chr9:6644369-6644419	GM06990	blood:	n/a
12	chr9:6645686-6645736	NT2-D1	testis:	n/a
13	chr9:6644603-6644653	GM12891	blood:	n/a
14	chr9:6644603-6644653	GM12878	blood:	n/a
15	chr9:6646386-6646436	AG10803	skin:	n/a
16	chr9:6645736-6645786	ovcar-3	ovarian:	n/a
17	chr9:6646386-6646436	AG04449	skin:	fetal
18	chr9:6645736-6645786	HNPCEpiC	eye:	n/a
19	chr9:6646386-6646436	LNCaP	prostate:	n/a
20	chr9:6645468-6645518	HCT-116	colon:	n/a
21	chr9:6645736-6645786	HRPEpiC	eye:	n/a
22	chr9:6644369-6644419	ovcar-3	ovarian:	n/a
23	chr9:6645686-6645736	K562	blood:	n/a
24	chr9:6645468-6645518	NH-A	brain:	n/a
25	chr9:6645736-6645786	MCF-7	breast:	n/a
26	chr9:6644369-6644419	GM12892	blood:	n/a
27	chr9:6644369-6644419	SK-N-SH	brain:	n/a
28	chr9:6645686-6645736	A549	lung:	n/a
29	chr9:6644369-6644419	A549	lung:	n/a
30	chr9:6645736-6645786	U87	brain:	n/a
31	chr9:6645686-6645736	PANC-1	pancreas:	n/a
32	chr9:6645736-6645786	SK-N-SH_RA	brain:	n/a
33	chr9:6645736-6645786	A549	lung:	n/a
34	chr9:6644603-6644653	SKMC	muscle:	n/a
35	chr9:6645686-6645736	BJ	skin:	n/a
36	chr9:6644369-6644419	HUVEC	blood vessel:	n/a
37	chr9:6645468-6645518	ECC-1	luminal epithelium:	n/a
38	chr9:6645686-6645736	HEEpiC	esophagus:	n/a
39	chr9:6644603-6644653	T-47D	breast:	n/a
40	chr9:6644369-6644419	SK-N-SH_RA	brain:	n/a
41	chr9:6645686-6645736	ProgFib	skin:	n/a
42	chr9:6645736-6645786	HRCEpiC	kidney:	n/a
43	chr9:6645686-6645736	HNPCEpiC	eye:	n/a
44	chr9:6644603-6644653	HIPEpiC	eye:	n/a
45	chr9:6644369-6644419	HIPEpiC	eye:	n/a
46	chr9:6645686-6645736	NHDF-neo	bronchial:	n/a
47	chr9:6644603-6644653	K562	blood:	n/a
48	chr9:6645686-6645736	HCM	heart:	n/a
49	chr9:6646386-6646436	ECC-1	luminal epithelium:	n/a
50	chr9:6645468-6645518	AoSMC	blood vessel:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:6662765..6664429-chr9:6666367..6668579,2	MCF-7	breast:
2	chr9:6663029..6667664-chr9:6679639..6683357,9	MCF-7	breast:
3	chr9:6644301..6646741-chr9:6667847..6669482,2	MCF-7	breast:
4	chr9:6667615..6669315-chr9:6679006..6681464,2	K562	blood:
5	chr9:6643546..6649129-chr9:6652921..6657149,5	MCF-7	breast:
6	chr9:6656639..6659482-chr9:6662780..6664665,3	MCF-7	breast:
7	chr9:6654607..6656764-chr9:6663214..6664911,2	K562	blood:
8	chr9:6639393..6643031-chr9:6644244..6646064,4	MCF-7	breast:
9	chr9:6654607..6656764-chr9:6663214..6664911,2	K562	blood:
10	chr9:6656639..6659482-chr9:6662780..6664665,3	MCF-7	breast:
11	chr9:6641084..6643158-chr9:6652442..6654682,2	MCF-7	breast:
12	chr9:6652273..6654630-chr9:6673766..6675385,2	MCF-7	breast:
13	chr9:6641084..6643158-chr9:6652442..6654682,2	MCF-7	breast:
14	chr9:6640659..6642824-chr9:6643049..6645706,2	MCF-7	breast:
15	chr9:6354241..6354767-chr9:6667295..6668097,2	K562	blood:
16	chr9:6663663..6666675-chr9:6715678..6718421,3	MCF-7	breast:
17	chr9:6523722..6524445-chr9:6667595..6668159,2	K562	blood:
18	chr9:6672368..6674682-chr9:6676645..6678823,3	MCF-7	breast:
19	chr9:6639721..6642651-chr9:6680043..6682884,2	MCF-7	breast:
20	chr9:6665749..6668244-chr9:6673822..6675444,2	MCF-7	breast:
21	chr9:6662765..6664429-chr9:6666367..6668579,2	MCF-7	breast:
22	chr9:6584834..6585802-chr9:6667386..6668426,5	MCF-7	breast:
23	chr9:6585232..6587306-chr9:6664888..6666750,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KDM4C-5	chr9:6645882-6646085	NONHSAT130145
2	lnc-KDM4C-14	chr9:6661651-6661936	NONHSAT130147
3	lnc-KDM4C-14	chr9:6660407-6661044	NONHSAT130146
4	lnc-KDM4C-13	chr9:6663657-6663792	NONHSAT130148
5	lnc-KDM4C-5	chr9:6669544-6669728	NONHSAT130145
6	lnc-KDM4C-5	chr9:6669544-6669728	ENSG00000236924.1
7	lnc-KDM4C-14	chr9:6661783-6661845	NONHSAT130146
8	lnc-KDM4C-5	chr9:6645956-6646085	ENSG00000236924.1
9	lnc-KDM4C-5	chr9:6670425-6670635	ENSG00000236924.1
10	lnc-KDM4C-14	chr9:6661291-6661345	NONHSAT130146
11	lnc-KDM4C-13	chr9:6662424-6662810	NONHSAT130148
12	lnc-KDM4C-13	chr9:6663156-6663366	NONHSAT130148
13	lnc-KDM4C-5	chr9:6670425-6670690	NONHSAT130145

No data

Variant related genes	Relation type
ENSG00000236924	TF binding region
ENSG00000232946	TF binding region
RNF2P1	TF binding region
ENSG00000206147	TF binding region
ENSG00000229057	TF binding region
RN7SL123P	TF binding region
GLDC	TF binding region
ENSG00000236924	CpG island
ENSG00000232946	CpG island
RNF2P1	CpG island
ENSG00000206147	CpG island
ENSG00000229057	CpG island
RN7SL123P	CpG island
GLDC	CpG island
ENSG00000236924	chromatin interactions
ENSG00000232946	chromatin interactions
ENSG00000178445	chromatin interactions
ENSG00000225489	chromatin interactions

Extended variants
information (count: 2194 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:2194 , 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	rs555373181	chr9:6637179-6637180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs573276658	chr9:6637200-6637201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs148870359	chr9:6637202-6637203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs113770256	chr9:6637207-6637208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs112738370	chr9:6637255-6637256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs113915069	chr9:6637267-6637268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs79576744	chr9:6637308-6637309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs10115774	chr9:6637310-6637311	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs554683699	chr9:6637315-6637316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs561362931	chr9:6637359-6637360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191487874	chr9:6637382-6637383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547156903	chr9:6637393-6637394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs565330546	chr9:6637397-6637398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs71328199	chr9:6637405-6637406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs78813097	chr9:6637417-6637418	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs2918177	chr9:6637422-6637423	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs182115909	chr9:6637446-6637447	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs112801997	chr9:6637482-6637483	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs538936385	chr9:6637488-6637489	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs549002483	chr9:6637489-6637490	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs141083030	chr9:6637511-6637512	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs534281977	chr9:6637514-6637515	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs117150375	chr9:6637535-6637536	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs117502344	chr9:6637554-6637555	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs544810912	chr9:6637561-6637562	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs564688845	chr9:6637562-6637563	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs113895100	chr9:6637592-6637593	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs575015715	chr9:6637593-6637594	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs557566582	chr9:6637620-6637621	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs544259531	chr9:6637626-6637627	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs575727438	chr9:6637629-6637630	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs543355257	chr9:6637655-6637656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs554955779	chr9:6637669-6637670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs573277340	chr9:6637713-6637714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs186153166	chr9:6637752-6637753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs144885121	chr9:6637805-6637806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565393945	chr9:6637810-6637811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532686967	chr9:6637826-6637827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544355058	chr9:6637854-6637855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541539758	chr9:6637866-6637867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs78410955	chr9:6637876-6637877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190132961	chr9:6637912-6637913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs11788879	chr9:6637935-6637936	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs549266352	chr9:6637989-6637990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567179069	chr9:6637992-6637993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs370988761	chr9:6638015-6638016	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182679033	chr9:6638057-6638058	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs59012021	chr9:6638059-6638060	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs570896547	chr9:6638061-6638062	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538754925	chr9:6638081-6638082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	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
Disorders of sex development	21048976	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
Oral squamous cell carcinoma	17134496	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
Melanoma	18172304	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
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Dyslexia	22102821	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ependymoma	20639864	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:727 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6629200-6640200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr9:6631400-6641200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr9:6633200-6640400	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr9:6633400-6639800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr9:6633600-6639800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr9:6633600-6640000	Weak transcription	Fetal Kidney	kidney
7	chr9:6633600-6641000	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr9:6633600-6641000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr9:6633600-6641200	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr9:6633600-6641200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr9:6633600-6642600	Weak transcription	NHEK	skin
12	chr9:6633600-6643200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr9:6633800-6644200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr9:6634200-6637800	Enhancers	Placenta	Placenta
15	chr9:6634400-6639000	Weak transcription	HepG2	liver
16	chr9:6635200-6640000	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr9:6635800-6638400	Weak transcription	Liver	Liver
18	chr9:6635800-6639800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr9:6635800-6640200	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr9:6635800-6641200	Weak transcription	Fetal Intestine Large	intestine
21	chr9:6636600-6639800	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr9:6636800-6639200	Weak transcription	GM12878-XiMat	blood
23	chr9:6637000-6638000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr9:6637800-6640400	Weak transcription	Placenta	Placenta
25	chr9:6638000-6640200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr9:6638400-6641000	Enhancers	Liver	Liver
27	chr9:6639000-6640600	Enhancers	HepG2	liver
28	chr9:6639200-6639800	Enhancers	GM12878-XiMat	blood
29	chr9:6639200-6641000	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr9:6639800-6640400	Enhancers	Psoas Muscle	Psoas
31	chr9:6639800-6640600	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr9:6639800-6640600	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr9:6639800-6640600	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr9:6639800-6640800	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr9:6639800-6640800	Flanking Active TSS	GM12878-XiMat	blood
36	chr9:6639800-6642200	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr9:6640000-6640200	Enhancers	Fetal Kidney	kidney
38	chr9:6640000-6640600	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr9:6640000-6644200	Weak transcription	Fetal Brain Male	brain
40	chr9:6640200-6640800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr9:6640200-6641000	Weak transcription	Fetal Kidney	kidney
42	chr9:6640200-6641200	Enhancers	Esophagus	oesophagus
43	chr9:6640200-6641600	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr9:6640200-6642200	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr9:6640200-6642200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr9:6640400-6640600	Enhancers	H1 Cell Line	embryonic stem cell
47	chr9:6640400-6640600	Enhancers	Placenta	Placenta
48	chr9:6640400-6641200	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr9:6640400-6641600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr9:6640400-6644200	Weak transcription	Psoas Muscle	Psoas

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