Variant report

Variant	nsv1018416
Chromosome Location	chr9:14846753-14921247
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:14868526-14869963	HepG2	liver:	n/a	chr9:14869168-14869184 chr9:14869167-14869183
2	ARID3A	chr9:14882074-14882476	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:14888518-14888791	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:14893420-14893599	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:14899812-14900038	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:14908366-14908878	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:14913278-14913856	HepG2	liver:	n/a	n/a
8	ATF3	chr9:14846813-14847157	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr9:14899853-14900153	K562	blood:	n/a	chr9:14899992-14900003
10	CEBPB	chr9:14884179-14884475	HepG2	liver:	n/a	n/a
11	CEBPB	chr9:14905488-14905648	HepG2	liver:	n/a	chr9:14905524-14905535
12	CEBPB	chr9:14899873-14900096	HepG2	liver:	n/a	chr9:14899992-14900003
13	CEBPB	chr9:14868569-14869669	HepG2	liver:	n/a	n/a
14	CEBPB	chr9:14899731-14900204	HepG2	liver:	n/a	chr9:14899992-14900003
15	CEBPB	chr9:14877121-14877303	HepG2	liver:	n/a	n/a
16	CEBPB	chr9:14899811-14900187	HepG2	liver:	n/a	chr9:14899992-14900003
17	CEBPB	chr9:14899804-14900187	HepG2	liver:	n/a	chr9:14899992-14900003
18	CEBPD	chr9:14899872-14900130	HepG2	liver:	n/a	n/a
19	CEBPD	chr9:14868715-14869298	HepG2	liver:	n/a	n/a
20	CEBPD	chr9:14899837-14900073	HepG2	liver:	n/a	n/a
21	CEBPD	chr9:14869355-14869588	HepG2	liver:	n/a	n/a
22	CHD1	chr9:14910224-14910402	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr9:14910010-14910438	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr9:14846857-14847057	HepG2	liver:	n/a	n/a
25	CHD2	chr9:14868700-14869330	HepG2	liver:	n/a	n/a
26	CHD2	chr9:14846832-14847123	H1-hESC	embryonic stem cell:	n/a	n/a
27	CREB1	chr9:14846723-14847119	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr9:14846754-14847104	K562	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
29	CTCF	chr9:14846803-14847117	GM19238	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
30	CTCF	chr9:14904778-14904843	ProgFib	skin:	n/a	n/a
31	CTCF	chr9:14846779-14847104	NHEK	skin:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
32	CTCF	chr9:14846835-14847102	K562	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
33	CTCF	chr9:14888953-14889222	MCF-7	breast:	n/a	n/a
34	CTCF	chr9:14882635-14882707	Lung_OC	lung:	n/a	n/a
35	CTCF	chr9:14846900-14847050	AG04449	skin:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
36	CTCF	chr9:14846900-14847050	AoAF	blood vessel:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
37	CTCF	chr9:14846860-14847010	GM12869	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
38	CTCF	chr9:14846800-14846950	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr9:14846780-14846930	HFF-Myc	foreskin:	n/a	n/a
40	CTCF	chr9:14888940-14889090	HCM	heart:	n/a	n/a
41	CTCF	chr9:14846860-14847010	GM12870	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
42	CTCF	chr9:14863460-14863610	AG10803	skin:	n/a	chr9:14863553-14863574 chr9:14863556-14863564 chr9:14863551-14863569
43	CTCF	chr9:14846900-14847050	AG09319	gingival:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
44	CTCF	chr9:14846860-14847010	RPTEC	kidney:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
45	CTCF	chr9:14846745-14847152	H1-hESC	embryonic stem cell:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
46	CTCF	chr9:14846840-14846990	HRPEpiC	eye:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846949-14846965 chr9:14846943-14846964
47	CTCF	chr9:14846799-14847116	GM12878	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
48	CTCF	chr9:14846880-14847030	HPF	lung:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
49	CTCF	chr9:14847245-14847309	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr9:14846860-14847010	GM12801	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:14910315-14910365	H1-hESC	embryonic stem cell:	embryo
2	chr9:14910315-14910365	H1-hESC	embryonic stem cell:	embryo
3	chr9:14883945-14883995	NH-A	brain:	n/a
4	chr9:14910315-14910365	GM12892	blood:	n/a
5	chr9:14910689-14910739	HAEpiC	amniotic membrane:	n/a
6	chr9:14910689-14910739	SK-N-SH_RA	brain:	n/a
7	chr9:14908132-14908182	BE2_C	brain:	n/a
8	chr9:14910315-14910365	HL-60	blood:	n/a
9	chr9:14883945-14883995	GM12878	blood:	n/a
10	chr9:14908132-14908182	NH-A	brain:	n/a
11	chr9:14883945-14883995	HPAEpiC	pulmonary alveolar:	n/a
12	chr9:14883945-14883995	GM19239	blood:	n/a
13	chr9:14883945-14883995	MCF10A-Er-Src	breast:	n/a
14	chr9:14910315-14910365	AG10803	skin:	n/a
15	chr9:14910689-14910739	HRPEpiC	eye:	n/a
16	chr9:14910315-14910365	RPTEC	kidney:	n/a
17	chr9:14908132-14908182	RPTEC	kidney:	n/a
18	chr9:14910689-14910739	HRE	kidney:	n/a
19	chr9:14908132-14908182	ECC-1	luminal epithelium:	n/a
20	chr9:14908132-14908182	GM19239	blood:	n/a
21	chr9:14910315-14910365	PFSK-1	brain:	n/a
22	chr9:14883945-14883995	GM12891	blood:	n/a
23	chr9:14910315-14910365	HCPEpiC	choroid plexus:	n/a
24	chr9:14883945-14883995	Jurkat	blood:	n/a
25	chr9:14910315-14910365	HAEpiC	amniotic membrane:	n/a
26	chr9:14910315-14910365	HRCEpiC	kidney:	n/a
27	chr9:14908132-14908182	NB4	blood:	n/a
28	chr9:14910315-14910365	IMR90	lung:	fetal
29	chr9:14910689-14910739	PFSK-1	brain:	n/a
30	chr9:14910689-14910739	U87	brain:	n/a
31	chr9:14908132-14908182	SKMC	muscle:	n/a
32	chr9:14883945-14883995	BE2_C	brain:	n/a
33	chr9:14910689-14910739	MCF-7	breast:	n/a
34	chr9:14908132-14908182	AG04450	lung:	fetal
35	chr9:14910689-14910739	PrEC	prostate:	n/a
36	chr9:14910315-14910365	NT2-D1	testis:	n/a
37	chr9:14910315-14910365	SK-N-SH	brain:	n/a
38	chr9:14908132-14908182	HUVEC	blood vessel:	n/a
39	chr9:14910689-14910739	AG04449	skin:	fetal
40	chr9:14910689-14910739	HCT-116	colon:	n/a
41	chr9:14908132-14908182	ovcar-3	ovarian:	n/a
42	chr9:14883945-14883995	Caco-2	colon:	n/a
43	chr9:14910689-14910739	HEK293	kidney:	embryo
44	chr9:14910315-14910365	U87	brain:	n/a
45	chr9:14910315-14910365	AG04449	skin:	fetal
46	chr9:14910689-14910739	CMK	blood:	n/a
47	chr9:14910689-14910739	HNPCEpiC	eye:	n/a
48	chr9:14883945-14883995	PrEC	prostate:	n/a
49	chr9:14908132-14908182	SAEC	small airway:	n/a
50	chr9:14910315-14910365	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:14897379..14899021-chr9:14903144..14904953,2	MCF-7	breast:
2	chr9:14914097..14915785-chr9:14923708..14925930,2	K562	blood:
3	chr9:14691985..14694492-chr9:14845348..14847282,2	MCF-7	breast:
4	chr9:14843588..14845441-chr9:14847451..14849631,2	K562	blood:
5	chr20:52274228..52274993-chr9:14900093..14900641,2	MCF-7	breast:
6	chr9:14846510..14847037-chr9:15142689..15143560,2	MCF-7	breast:
7	chr9:14850312..14853276-chr9:14856165..14857741,2	MCF-7	breast:
8	chr9:14897379..14899021-chr9:14903144..14904953,2	MCF-7	breast:
9	chr9:14842932..14845441-chr9:14846633..14848951,2	K562	blood:

Variant related genes	Relation type
RNU6-1260P	TF binding region
FREM1	TF binding region
RNU6-1260P	CpG island
FREM1	CpG island
ENSG00000251960	chromatin interactions
ENSG00000199814	chromatin interactions
ENSG00000175893	chromatin interactions

Extended variants
information (count: 3682 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:3682 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191207178	chr9:14846753-14846754	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs140305360	chr9:14846773-14846774	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs372702488	chr9:14846780-14846781	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs373770485	chr9:14846781-14846782	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs112530713	chr9:14846837-14846838	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs545232332	chr9:14846849-14846850	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs183462091	chr9:14846860-14846861	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs532477401	chr9:14846866-14846867	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs547806357	chr9:14846894-14846895	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs566105538	chr9:14846924-14846925	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs530199869	chr9:14846938-14846939	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs575651580	chr9:14846939-14846940	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs138033323	chr9:14846964-14846965	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs187954716	chr9:14846965-14846966	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs10810270	chr9:14846993-14846994	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs149547024	chr9:14846994-14846995	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs369150832	chr9:14847039-14847040	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs535375660	chr9:14847042-14847043	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs553331454	chr9:14847114-14847115	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs571743607	chr9:14847158-14847159	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs113961764	chr9:14847167-14847168	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs10810271	chr9:14847175-14847176	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs192778341	chr9:14847195-14847196	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs183694733	chr9:14847278-14847279	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs114255481	chr9:14847295-14847296	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs13293940	chr9:14847297-14847298	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs13295210	chr9:14847298-14847299	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs532280601	chr9:14847304-14847305	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs541369181	chr9:14847421-14847422	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs36230117	chr9:14847425-14847426	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs12376219	chr9:14847428-14847429	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs57269628	chr9:14847431-14847432	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs200137062	chr9:14847432-14847433	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs60709864	chr9:14847433-14847434	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs28468394	chr9:14847436-14847437	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs62536619	chr9:14847467-14847468	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs559747011	chr9:14847507-14847508	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs192399950	chr9:14847552-14847553	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs142681376	chr9:14847626-14847627	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs76595440	chr9:14847630-14847631	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs531076803	chr9:14847634-14847635	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs571212176	chr9:14847637-14847638	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs571052745	chr9:14847665-14847666	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs532333942	chr9:14847716-14847717	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs534971765	chr9:14847724-14847725	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs147382072	chr9:14847731-14847732	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs184564034	chr9:14847745-14847746	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs79308147	chr9:14847761-14847762	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs76306390	chr9:14847780-14847781	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs568889633	chr9:14847789-14847790	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:882 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14779800-14853200	Weak transcription	Placenta	Placenta
2	chr9:14801800-14857200	Strong transcription	HepG2	liver
3	chr9:14807400-14868600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr9:14809200-14847600	Weak transcription	Fetal Intestine Small	intestine
5	chr9:14810400-14849600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr9:14823400-14848400	Weak transcription	Duodenum Mucosa	Duodenum
7	chr9:14824000-14852800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr9:14826000-14849600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr9:14833400-14860600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr9:14837400-14846800	Strong transcription	Fetal Lung	lung
11	chr9:14838600-14854000	Strong transcription	Fetal Kidney	kidney
12	chr9:14840600-14851400	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr9:14842000-14847400	Strong transcription	Fetal Muscle Trunk	muscle
14	chr9:14842200-14852400	Weak transcription	Brain Hippocampus Middle	brain
15	chr9:14842800-14848400	Weak transcription	Aorta	Aorta
16	chr9:14843200-14848000	Weak transcription	Adipose Nuclei	Adipose
17	chr9:14843400-14850600	Weak transcription	Fetal Stomach	stomach
18	chr9:14843400-14851000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr9:14843400-14868800	Weak transcription	Pancreas	Pancrea
20	chr9:14843600-14846800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr9:14844400-14853000	Strong transcription	Fetal Muscle Leg	muscle
22	chr9:14845000-14849800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr9:14846000-14848000	Weak transcription	Colon Smooth Muscle	Colon
24	chr9:14846200-14850200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr9:14846200-14850800	Weak transcription	Fetal Intestine Large	intestine
26	chr9:14846800-14849200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr9:14846800-14850600	Genic enhancers	Fetal Lung	lung
28	chr9:14847400-14848200	Weak transcription	Fetal Muscle Trunk	muscle
29	chr9:14847600-14848400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr9:14847600-14848400	Weak transcription	Fetal Brain Male	brain
31	chr9:14848000-14851600	Strong transcription	Colon Smooth Muscle	Colon
32	chr9:14848000-14853000	Strong transcription	Adipose Nuclei	Adipose
33	chr9:14848200-14852400	Strong transcription	Fetal Muscle Trunk	muscle
34	chr9:14848400-14848800	ZNF genes & repeats	Fetal Brain Male	brain
35	chr9:14848400-14849400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr9:14848400-14851800	Strong transcription	Aorta	Aorta
37	chr9:14848400-14852600	Strong transcription	Duodenum Mucosa	Duodenum
38	chr9:14848800-14849600	Weak transcription	Fetal Brain Male	brain
39	chr9:14849200-14850800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr9:14849400-14850400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr9:14849600-14849800	Enhancers	Fetal Brain Male	brain
42	chr9:14849600-14850200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr9:14849600-14850400	Enhancers	Primary hematopoietic stem cells	blood
44	chr9:14849600-14869000	Weak transcription	Small Intestine	intestine
45	chr9:14849800-14850200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr9:14849800-14850200	Active TSS	Fetal Brain Male	brain
47	chr9:14850200-14853200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr9:14850200-14857000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr9:14850200-14859000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr9:14850200-14869000	Weak transcription	Fetal Brain Male	brain

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