Variant report

Variant	esv2764156
Chromosome Location	chr9:19076894-19097008
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	chr9:19087872-19087966	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:19085298-19085650	HepG2	liver:	n/a	n/a
3	CTCF	chr9:19085460-19085610	A549	lung:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
4	CTCF	chr9:19085382-19085613	Hela-S3	cervix:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
5	CTCF	chr9:19085420-19085570	AoAF	blood vessel:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
6	CTCF	chr9:19085450-19085591	ProgFib	skin:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
7	CTCF	chr9:19085405-19085595	Gliobla	brain:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
8	CTCF	chr9:19085456-19085573	SK-N-SH_RA	brain:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
9	CTCF	chr9:19085420-19085570	GM12874	blood:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
10	CTCF	chr9:19085365-19085615	H1-hESC	embryonic stem cell:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
11	CTCF	chr9:19085367-19085608	SK-N-SH_RA	brain:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
12	CTCF	chr9:19085420-19085570	Caco-2	colon:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
13	CTCF	chr9:19085560-19085710	HCM	heart:	n/a	n/a
14	CTCF	chr9:19085440-19085590	WERI-Rb-1	eye:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
15	CTCF	chr9:19085360-19085510	AG09319	gingival:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
16	CTCF	chr9:19085480-19085630	NB4	blood:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
17	CTCF	chr9:19084260-19084410	HRE	kidney:	n/a	n/a
18	CTCF	chr9:19085318-19085711	GM12878	blood:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
19	CTCF	chr9:19085580-19085730	HFF	foreskin:	n/a	n/a
20	CTCF	chr9:19085375-19085652	H1-hESC	embryonic stem cell:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
21	CTCF	chr9:19085290-19085669	HepG2	liver:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
22	CTCF	chr9:19085400-19085611	HepG2	liver:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
23	CTCF	chr9:19085360-19085630	GM12878	blood:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
24	CTCF	chr9:19085380-19085530	HCFaa	heart:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
25	CTCF	chr9:19085400-19085550	AG10803	skin:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
26	CTCF	chr9:19085387-19085607	K562	blood:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
27	CTCF	chr9:19085429-19085585	MCF-7	breast:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
28	CTCF	chr9:19085360-19085510	HCM	heart:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
29	CTCF	chr9:19085460-19085610	AG09309	skin:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
30	CTCF	chr9:19085440-19085590	GM12872	blood:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
31	CTCF	chr9:19085447-19085547	Kidney_OC	kidney:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
32	CTCF	chr9:19085460-19085610	Hela-S3	cervix:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
33	CTCF	chr9:19085360-19085510	HFF	foreskin:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
34	CTCF	chr9:19085440-19085590	HUVEC	blood vessel:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
35	CTCF	chr9:19085420-19085570	SAEC	small airway:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
36	CTCF	chr9:19085435-19085608	Lung_OC	lung:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
37	CTCF	chr9:19085400-19085550	GM12874	blood:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
38	CTCF	chr9:19077040-19077190	GM12868	blood:	n/a	n/a
39	CTCF	chr9:19085460-19085610	HCT-116	colon:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
40	CTCF	chr9:19085440-19085590	HRE	kidney:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
41	CTCF	chr9:19085065-19085112	GM10266	blood:	n/a	n/a
42	CTCF	chr9:19085560-19085710	HVMF	connective:	n/a	n/a
43	CTCF	chr9:19085390-19085601	LNCaP	prostate:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
44	CTCF	chr9:19085357-19085573	A549	lung:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
45	CTCF	chr9:19085380-19085530	NHEK	skin:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
46	CTCF	chr9:19085445-19085603	NHEK	skin:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
47	CTCF	chr9:19085400-19085550	RPTEC	kidney:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
48	CTCF	chr9:19085395-19085606	GM12878	blood:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
49	CTCF	chr9:19085400-19085550	BJ	skin:	n/a	chr9:19085491-19085509 chr9:19085492-19085508
50	CTCF	chr9:19085520-19085670	NHDF-neo	bronchial:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:19084351-19084401	ProgFib	skin:	n/a
2	chr9:19084351-19084401	SAEC	small airway:	n/a
3	chr9:19084351-19084401	HRE	kidney:	n/a
4	chr9:19084351-19084401	HCT-116	colon:	n/a
5	chr9:19084351-19084401	HCPEpiC	choroid plexus:	n/a
6	chr9:19084351-19084401	PFSK-1	brain:	n/a
7	chr9:19084351-19084401	AG10803	skin:	n/a
8	chr9:19084351-19084401	AG09319	gingival:	n/a
9	chr9:19084351-19084401	ovcar-3	ovarian:	n/a
10	chr9:19084351-19084401	ECC-1	luminal epithelium:	n/a
11	chr9:19084351-19084401	T-47D	breast:	n/a
12	chr9:19084351-19084401	LNCaP	prostate:	n/a
13	chr9:19084351-19084401	NHDF-neo	bronchial:	n/a
14	chr9:19084351-19084401	NHBE	bronchial:	n/a
15	chr9:19084351-19084401	MCF-7	breast:	n/a
16	chr9:19084351-19084401	GM12878	blood:	n/a
17	chr9:19084351-19084401	AG09309	skin:	n/a
18	chr9:19084351-19084401	BJ	skin:	n/a
19	chr9:19084351-19084401	IMR90	lung:	fetal
20	chr9:19084351-19084401	K562	blood:	n/a
21	chr9:19084351-19084401	HPAEpiC	pulmonary alveolar:	n/a
22	chr9:19084351-19084401	GM06990	blood:	n/a
23	chr9:19084351-19084401	HNPCEpiC	eye:	n/a
24	chr9:19084351-19084401	HIPEpiC	eye:	n/a
25	chr9:19084351-19084401	U87	brain:	n/a
26	chr9:19084351-19084401	RPTEC	kidney:	n/a
27	chr9:19084351-19084401	HEEpiC	esophagus:	n/a
28	chr9:19084351-19084401	PrEC	prostate:	n/a
29	chr9:19084351-19084401	HMEC	breast:	n/a
30	chr9:19084351-19084401	GM12891	blood:	n/a
31	chr9:19084351-19084401	NT2-D1	testis:	n/a
32	chr9:19084351-19084401	SK-N-SH_RA	brain:	n/a
33	chr9:19084351-19084401	SK-N-SH	brain:	n/a
34	chr9:19084351-19084401	PANC-1	pancreas:	n/a
35	chr9:19084351-19084401	Jurkat	blood:	n/a
36	chr9:19084351-19084401	Hela-S3	cervix:	n/a
37	chr9:19084351-19084401	HCM	heart:	n/a
38	chr9:19084351-19084401	GM12892	blood:	n/a
39	chr9:19084351-19084401	HUVEC	blood vessel:	n/a
40	chr9:19084351-19084401	GM19239	blood:	n/a
41	chr9:19084351-19084401	Hepatocyte	liver:	n/a
42	chr9:19084351-19084401	HCF	heart:	n/a
43	chr9:19084351-19084401	AG04449	skin:	fetal
44	chr9:19084351-19084401	HL-60	blood:	n/a
45	chr9:19084351-19084401	SK-N-MC	brain:	n/a
46	chr9:19084351-19084401	H1-hESC	embryonic stem cell:	embryo
47	chr9:19084351-19084401	HAEpiC	amniotic membrane:	n/a
48	chr9:19084351-19084401	BE2_C	brain:	n/a
49	chr9:19084351-19084401	HepG2	liver:	n/a
50	chr9:19084351-19084401	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:19077380..19080397-chr9:19085594..19088171,3	K562	blood:
2	chr9:19084171..19086878-chr9:19096097..19098538,2	K562	blood:
3	chr9:19077380..19080397-chr9:19085594..19088171,3	K562	blood:
4	chr9:19090764..19093304-chr9:19100948..19103618,2	K562	blood:
5	chr9:19078940..19081412-chr9:19100972..19102814,2	K562	blood:
6	chr9:19084625..19086954-chr9:19229732..19232560,2	MCF-7	breast:
7	chr9:19085095..19085947-chr9:19174105..19174820,3	MCF-7	breast:
8	chr9:19089920..19092976-chr9:19101265..19103634,3	K562	blood:
9	chr9:19095602..19097894-chr9:19377705..19380132,2	MCF-7	breast:
10	chr9:19086054..19088942-chr9:19092129..19094506,2	K562	blood:
11	chr9:19084171..19086878-chr9:19096097..19098538,2	K562	blood:
12	chr9:19095545..19097905-chr9:19098403..19100459,2	K562	blood:

Variant related genes	Relation type
HAUS6	TF binding region
ENSG00000201118	TF binding region
HAUS6	CpG island
ENSG00000201118	CpG island
ENSG00000147874	chromatin interactions
ENSG00000137145	chromatin interactions

Extended variants
information (count: 1148 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1148 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545731587	chr9:19076920-19076921	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs191461735	chr9:19076949-19076950	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531653438	chr9:19076979-19076980	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564365251	chr9:19076990-19076991	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs182791995	chr9:19077028-19077029	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs7042340	chr9:19077031-19077032	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs72696470	chr9:19077093-19077094	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs529026656	chr9:19077106-19077107	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs186483945	chr9:19077112-19077113	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs111262719	chr9:19077117-19077118	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs75460995	chr9:19077118-19077119	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs558991783	chr9:19077120-19077121	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs112253696	chr9:19077126-19077127	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370783530	chr9:19077131-19077132	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs534720289	chr9:19077132-19077133	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs553363848	chr9:19077144-19077145	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs574468203	chr9:19077147-19077148	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149067210	chr9:19077198-19077199	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs557025579	chr9:19077205-19077206	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575105145	chr9:19077233-19077234	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143079123	chr9:19077272-19077273	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545936905	chr9:19077287-19077288	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564239108	chr9:19077290-19077291	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573127639	chr9:19077331-19077332	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs58750930	chr9:19077349-19077350	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540135299	chr9:19077389-19077390	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561771418	chr9:19077390-19077391	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190630183	chr9:19077394-19077395	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182807163	chr9:19077402-19077403	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375556992	chr9:19077404-19077405	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs562523762	chr9:19077414-19077415	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113018275	chr9:19077416-19077417	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs10963939	chr9:19077421-19077422	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs570939569	chr9:19077426-19077427	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535353686	chr9:19077458-19077459	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs187840771	chr9:19077470-19077471	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546973738	chr9:19077488-19077489	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs13291632	chr9:19077490-19077491	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs570350871	chr9:19077503-19077504	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140051888	chr9:19077514-19077515	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146905270	chr9:19077610-19077611	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539533939	chr9:19077619-19077620	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs117844419	chr9:19077634-19077635	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539604260	chr9:19077809-19077810	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572950437	chr9:19077822-19077823	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs557772640	chr9:19077824-19077825	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573066926	chr9:19077840-19077841	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540563133	chr9:19077870-19077871	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561924861	chr9:19077891-19077892	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573684752	chr9:19077917-19077918	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	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
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
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	22183965	CNVD
Myelofibrosis	22110671	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Pancreatic cancer	21811587	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:686 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:19051600-19101400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:19051800-19089000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr9:19052400-19077000	Weak transcription	Pancreas	Pancrea
4	chr9:19052800-19092400	Weak transcription	Fetal Brain Male	brain
5	chr9:19054400-19097800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
6	chr9:19054800-19098200	Strong transcription	HUES48 Cell Line	embryonic stem cell
7	chr9:19054800-19100800	Strong transcription	HUES64 Cell Line	embryonic stem cell
8	chr9:19055600-19082600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr9:19055600-19091200	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr9:19055800-19079800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr9:19055800-19085200	Strong transcription	Liver	Liver
12	chr9:19055800-19096800	Strong transcription	HUES6 Cell Line	embryonic stem cell
13	chr9:19055800-19098200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
14	chr9:19056000-19086000	Strong transcription	Primary T cells fromperipheralblood	blood
15	chr9:19056000-19091200	Strong transcription	Primary monocytes fromperipheralblood	blood
16	chr9:19056000-19096400	Strong transcription	Primary T helper cells fromperipheralblood	blood
17	chr9:19056000-19101200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr9:19056600-19094800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr9:19056600-19095200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr9:19056600-19095400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
21	chr9:19056600-19096000	Strong transcription	Primary T helper cells PMA-I stimulated	--
22	chr9:19056800-19083000	Strong transcription	Primary B cells from peripheral blood	blood
23	chr9:19056800-19096600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr9:19057200-19078200	Strong transcription	Primary B cells from cord blood	blood
25	chr9:19057600-19077000	Weak transcription	Esophagus	oesophagus
26	chr9:19062000-19102200	Weak transcription	Stomach Mucosa	stomach
27	chr9:19062800-19079000	Weak transcription	NHLF	lung
28	chr9:19063000-19077000	Weak transcription	Brain Angular Gyrus	brain
29	chr9:19063200-19077000	Weak transcription	Brain Cingulate Gyrus	brain
30	chr9:19066200-19077400	Strong transcription	Dnd41	blood
31	chr9:19066400-19083400	Strong transcription	Placenta	Placenta
32	chr9:19066400-19085600	Strong transcription	H1 Cell Line	embryonic stem cell
33	chr9:19066400-19096600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr9:19066800-19100400	Weak transcription	Fetal Heart	heart
35	chr9:19066800-19100800	Weak transcription	Small Intestine	intestine
36	chr9:19067000-19078400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr9:19067000-19084800	Weak transcription	Colonic Mucosa	Colon
38	chr9:19067400-19086600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr9:19068000-19077600	Strong transcription	A549	lung
40	chr9:19068800-19079800	Strong transcription	Fetal Muscle Leg	muscle
41	chr9:19068800-19085400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr9:19068800-19096800	Strong transcription	Fetal Thymus	thymus
43	chr9:19069800-19080800	Strong transcription	Fetal Lung	lung
44	chr9:19070000-19089400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr9:19070400-19090600	Weak transcription	Rectal Smooth Muscle	rectum
46	chr9:19071000-19077000	Weak transcription	Colon Smooth Muscle	Colon
47	chr9:19071200-19077200	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr9:19071200-19101200	Weak transcription	Psoas Muscle	Psoas
49	chr9:19071400-19086800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
50	chr9:19071800-19078200	Strong transcription	Brain Germinal Matrix	brain

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