Variant report

Variant	nsv934176
Chromosome Location	chr9:6517535-6644738
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1752)
CpG islands
(count:244)
Chromatin interactive
region (count:31)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1752 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:6530270-6530987	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:6585150-6585539	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:6552110-6552393	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:6585226-6585461	K562	blood:	n/a	n/a
5	ARID3A	chr9:6542871-6542968	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:6568252-6568419	K562	blood:	n/a	n/a
7	ARID3A	chr9:6641775-6641951	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:6590416-6591246	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:6592072-6592556	HepG2	liver:	n/a	n/a
10	ATF1	chr9:6594559-6594926	K562	blood:	n/a	n/a
11	ATF2	chr9:6620437-6621001	GM12878	blood:	n/a	n/a
12	ATF2	chr9:6566455-6566850	GM12878	blood:	n/a	n/a
13	ATF2	chr9:6630782-6631440	GM12878	blood:	n/a	n/a
14	ATF2	chr9:6597976-6598892	GM12878	blood:	n/a	n/a
15	ATF2	chr9:6598244-6598868	GM12878	blood:	n/a	n/a
16	ATF2	chr9:6632332-6633189	GM12878	blood:	n/a	n/a
17	ATF2	chr9:6575185-6575710	GM12878	blood:	n/a	n/a
18	ATF2	chr9:6605130-6605645	GM12878	blood:	n/a	n/a
19	BATF	chr9:6598389-6598834	GM12878	blood:	n/a	chr9:6598659-6598670
20	BATF	chr9:6632442-6633016	GM12878	blood:	n/a	n/a
21	BATF	chr9:6630698-6631421	GM12878	blood:	n/a	chr9:6630833-6630842
22	BATF	chr9:6598357-6598887	GM12878	blood:	n/a	chr9:6598659-6598670
23	BATF	chr9:6592868-6593086	GM12878	blood:	n/a	n/a
24	BATF	chr9:6566437-6566727	GM12878	blood:	n/a	n/a
25	BATF	chr9:6620458-6620655	GM12878	blood:	n/a	n/a
26	BCL11A	chr9:6632471-6632972	GM12878	blood:	n/a	n/a
27	BCL11A	chr9:6605220-6605551	GM12878	blood:	n/a	n/a
28	BCL11A	chr9:6594611-6594793	GM12878	blood:	n/a	n/a
29	BCL11A	chr9:6598377-6598720	GM12878	blood:	n/a	n/a
30	BCL11A	chr9:6598313-6598874	GM12878	blood:	n/a	n/a
31	BCL11A	chr9:6575318-6575518	GM12878	blood:	n/a	n/a
32	BCL11A	chr9:6605232-6605584	GM12878	blood:	n/a	n/a
33	BCL11A	chr9:6632584-6632927	GM12878	blood:	n/a	n/a
34	BCL3	chr9:6558003-6558364	GM12878	blood:	n/a	n/a
35	BCL3	chr9:6566337-6566811	GM12878	blood:	n/a	n/a
36	BCL3	chr9:6598339-6598796	GM12878	blood:	n/a	n/a
37	BCL3	chr9:6575300-6575684	GM12878	blood:	n/a	n/a
38	BCL3	chr9:6632539-6633018	GM12878	blood:	n/a	n/a
39	BCLAF1	chr9:6575167-6575735	GM12878	blood:	n/a	n/a
40	BCLAF1	chr9:6632444-6633343	GM12878	blood:	n/a	n/a
41	BCLAF1	chr9:6605192-6605673	GM12878	blood:	n/a	n/a
42	BCLAF1	chr9:6598022-6598904	GM12878	blood:	n/a	n/a
43	BCLAF1	chr9:6632431-6632955	GM12878	blood:	n/a	n/a
44	BCLAF1	chr9:6598356-6598906	GM12878	blood:	n/a	n/a
45	BCLAF1	chr9:6630775-6631290	GM12878	blood:	n/a	n/a
46	BHLHE40	chr9:6549190-6549255	K562	blood:	n/a	n/a
47	BHLHE40	chr9:6598319-6598809	GM12878	blood:	n/a	n/a
48	BHLHE40	chr9:6640333-6640626	HepG2	liver:	n/a	n/a
49	BHLHE40	chr9:6630905-6631327	GM12878	blood:	n/a	n/a
50	BHLHE40	chr9:6590771-6591126	HepG2	liver:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6532828-6532878	HCM	heart:	n/a
2	chr9:6644603-6644653	HNPCEpiC	eye:	n/a
3	chr9:6552115-6552165	A549	lung:	n/a
4	chr9:6644603-6644653	IMR90	lung:	fetal
5	chr9:6644369-6644419	HIPEpiC	eye:	n/a
6	chr9:6532828-6532878	HUVEC	blood vessel:	n/a
7	chr9:6552115-6552165	BE2_C	brain:	n/a
8	chr9:6644603-6644653	SAEC	small airway:	n/a
9	chr9:6532828-6532878	SK-N-SH_RA	brain:	n/a
10	chr9:6644369-6644419	AoSMC	blood vessel:	n/a
11	chr9:6532828-6532878	HCF	heart:	n/a
12	chr9:6644369-6644419	PrEC	prostate:	n/a
13	chr9:6552115-6552165	NB4	blood:	n/a
14	chr9:6644603-6644653	SK-N-SH_RA	brain:	n/a
15	chr9:6644369-6644419	GM19239	blood:	n/a
16	chr9:6552115-6552165	GM12892	blood:	n/a
17	chr9:6532828-6532878	GM12892	blood:	n/a
18	chr9:6532828-6532878	HNPCEpiC	eye:	n/a
19	chr9:6644369-6644419	ovcar-3	ovarian:	n/a
20	chr9:6532828-6532878	GM19239	blood:	n/a
21	chr9:6552115-6552165	GM06990	blood:	n/a
22	chr9:6532828-6532878	SK-N-SH	brain:	n/a
23	chr9:6532828-6532878	AG10803	skin:	n/a
24	chr9:6532828-6532878	GM12891	blood:	n/a
25	chr9:6644369-6644419	HEEpiC	esophagus:	n/a
26	chr9:6644603-6644653	HEEpiC	esophagus:	n/a
27	chr9:6644603-6644653	AG09309	skin:	n/a
28	chr9:6644369-6644419	Hepatocyte	liver:	n/a
29	chr9:6552115-6552165	HCM	heart:	n/a
30	chr9:6644603-6644653	SK-N-MC	brain:	n/a
31	chr9:6644603-6644653	HAEpiC	amniotic membrane:	n/a
32	chr9:6552115-6552165	K562	blood:	n/a
33	chr9:6644369-6644419	GM12892	blood:	n/a
34	chr9:6644369-6644419	SK-N-SH_RA	brain:	n/a
35	chr9:6644369-6644419	NT2-D1	testis:	n/a
36	chr9:6552115-6552165	HRPEpiC	eye:	n/a
37	chr9:6644603-6644653	BE2_C	brain:	n/a
38	chr9:6644603-6644653	Hepatocyte	liver:	n/a
39	chr9:6552115-6552165	HIPEpiC	eye:	n/a
40	chr9:6532828-6532878	HIPEpiC	eye:	n/a
41	chr9:6644369-6644419	NHBE	bronchial:	n/a
42	chr9:6644369-6644419	ECC-1	luminal epithelium:	n/a
43	chr9:6644369-6644419	HCF	heart:	n/a
44	chr9:6644369-6644419	Caco-2	colon:	n/a
45	chr9:6552115-6552165	ovcar-3	ovarian:	n/a
46	chr9:6552115-6552165	RPTEC	kidney:	n/a
47	chr9:6532828-6532878	AG04450	lung:	fetal
48	chr9:6644369-6644419	Hela-S3	cervix:	n/a
49	chr9:6532828-6532878	NHBE	bronchial:	n/a
50	chr9:6552115-6552165	ECC-1	luminal epithelium:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:6605288..6608151-chr9:6611363..6613701,3	K562	blood:
2	chr9:6627812..6629680-chr9:6632614..6635740,3	MCF-7	breast:
3	chr9:6639393..6643031-chr9:6644244..6646064,4	MCF-7	breast:
4	chr9:6605288..6608151-chr9:6611363..6613701,3	K562	blood:
5	chr9:6410972..6413613-chr9:6564070..6565701,2	MCF-7	breast:
6	chr9:6640659..6642824-chr9:6643049..6645706,2	MCF-7	breast:
7	chr9:6411889..6413422-chr9:6565833..6568598,2	K562	blood:
8	chr9:6516849..6518888-chr9:6521453..6523458,2	K562	blood:
9	chr9:6550978..6552657-chr9:6561789..6563568,2	K562	blood:
10	chr9:6533272..6535800-chr9:6681069..6683891,2	K562	blood:
11	chr9:6354058..6354828-chr9:6567905..6568745,4	MCF-7	breast:
12	chr9:6523722..6524445-chr9:6667595..6668159,2	K562	blood:
13	chr9:6623651..6625727-chr9:6679924..6681530,2	MCF-7	breast:
14	chr9:6550978..6552657-chr9:6561789..6563568,2	K562	blood:
15	chr9:6585232..6587306-chr9:6664888..6666750,2	MCF-7	breast:
16	chr9:6570923..6573857-chr9:6574160..6576030,2	K562	blood:
17	chr9:6615911..6617907-chr9:6681150..6682978,2	MCF-7	breast:
18	chr9:6588736..6590830-chr9:6680231..6682699,2	MCF-7	breast:
19	chr9:6562859..6565330-chr9:6565433..6569047,3	K562	blood:
20	chr9:6624229..6626158-chr9:6679853..6681433,2	MCF-7	breast:
21	chr9:6570923..6573857-chr9:6574160..6576030,2	K562	blood:
22	chr9:6354258..6354771-chr9:6567896..6568668,2	MCF-7	breast:
23	chr9:6584834..6585802-chr9:6667386..6668426,5	MCF-7	breast:
24	chr9:6579960..6582259-chr9:6679731..6681701,2	MCF-7	breast:
25	chr9:6627812..6629680-chr9:6632614..6635740,3	MCF-7	breast:
26	chr9:6593764..6596429-chr9:6597405..6599828,2	MCF-7	breast:
27	chr9:6639721..6642651-chr9:6680043..6682884,2	MCF-7	breast:
28	chr9:6516849..6518888-chr9:6521453..6523458,2	K562	blood:
29	chr9:6593764..6596429-chr9:6597405..6599828,2	MCF-7	breast:
30	chr9:6590828..6592705-chr9:6679350..6681430,2	MCF-7	breast:
31	chr9:6641084..6643158-chr9:6652442..6654682,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UHRF2-5	chr9:6568844-6569360	NONHSAT130143
2	lnc-UHRF2-4	chr9:6542094-6542350	NONHSAT130139
3	lnc-UHRF2-3	chr9:6529539-6529917	NONHSAT130138

No data

Variant related genes	Relation type
ENSG00000236924	TF binding region
ENSG00000237158	TF binding region
RN7SL25P	TF binding region
ENSG00000206147	TF binding region
ENSG00000252110	TF binding region
GLDC	TF binding region
ENSG00000236924	CpG island
ENSG00000237158	CpG island
RN7SL25P	CpG island
ENSG00000206147	CpG island
ENSG00000252110	CpG island
GLDC	CpG island
ENSG00000237158	chromatin interactions
ENSG00000252110	chromatin interactions
ENSG00000178445	chromatin interactions
ENSG00000236924	chromatin interactions
ENSG00000147854	chromatin interactions

Extended variants
information (count: 7047 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:7047 , 50 per page) page: 1 2 3 4 5 6 7 ... 141

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12350603	chr9:6517539-6517540	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547185778	chr9:6517582-6517583	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs372470193	chr9:6517648-6517649	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs532977446	chr9:6517681-6517682	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs528103731	chr9:6517727-6517728	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187748467	chr9:6517730-6517731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569880360	chr9:6517768-6517769	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537035245	chr9:6517783-6517784	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555112950	chr9:6517856-6517857	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs12553538	chr9:6517865-6517866	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs538008405	chr9:6517882-6517883	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs534661131	chr9:6517892-6517893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553115884	chr9:6517932-6517933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369332161	chr9:6517961-6517962	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs578190278	chr9:6517962-6517963	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191368177	chr9:6518003-6518004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183074746	chr9:6518005-6518006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557609081	chr9:6518023-6518024	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575879655	chr9:6518051-6518052	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542997950	chr9:6518053-6518054	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs377140120	chr9:6518063-6518064	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs561171584	chr9:6518072-6518073	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572904046	chr9:6518077-6518078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs375618415	chr9:6518083-6518084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs540287944	chr9:6518127-6518128	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565061316	chr9:6518131-6518132	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs35182724	chr9:6518206-6518207	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs551321166	chr9:6518209-6518210	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187796355	chr9:6518216-6518217	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530761852	chr9:6518261-6518262	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542333657	chr9:6518262-6518263	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560957123	chr9:6518309-6518310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs10975620	chr9:6518319-6518320	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs537782487	chr9:6518341-6518342	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567232803	chr9:6518347-6518348	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534619020	chr9:6518374-6518375	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs10975621	chr9:6518422-6518423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546688965	chr9:6518429-6518430	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192062677	chr9:6518438-6518439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528051865	chr9:6518441-6518442	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546494763	chr9:6518455-6518456	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557336050	chr9:6518501-6518502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12346169	chr9:6518514-6518515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201462425	chr9:6518618-6518619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs376327100	chr9:6518629-6518630	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs142904030	chr9:6518642-6518643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs62566156	chr9:6518659-6518660	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536497361	chr9:6518665-6518666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568156059	chr9:6518688-6518689	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200839813	chr9:6518705-6518706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
Prostate cancer	18632612	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
early-passage human iPS cells	21368824	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	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

Chromatin state (count:1835 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6463600-6518400	Weak transcription	Fetal Brain Male	brain
2	chr9:6498800-6554400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr9:6499000-6528400	Weak transcription	Pancreas	Pancrea
4	chr9:6506200-6518600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr9:6506400-6521800	Weak transcription	Colon Smooth Muscle	Colon
6	chr9:6506400-6530600	Weak transcription	Gastric	stomach
7	chr9:6506800-6519200	Weak transcription	Fetal Kidney	kidney
8	chr9:6507000-6523800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr9:6507000-6524800	Weak transcription	Brain Hippocampus Middle	brain
10	chr9:6507000-6534400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr9:6507200-6522400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr9:6507800-6521800	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr9:6508000-6520200	Weak transcription	Fetal Intestine Small	intestine
14	chr9:6508200-6519400	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr9:6508200-6521800	Weak transcription	Fetal Stomach	stomach
16	chr9:6508400-6519600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr9:6508400-6521000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr9:6508400-6521800	Weak transcription	Primary B cells from cord blood	blood
19	chr9:6508400-6523600	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr9:6508400-6525000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr9:6508400-6526400	Weak transcription	Rectal Smooth Muscle	rectum
22	chr9:6508400-6526600	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr9:6508400-6528200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr9:6508400-6530600	Weak transcription	Left Ventricle	heart
25	chr9:6508600-6524200	Weak transcription	Stomach Smooth Muscle	stomach
26	chr9:6508600-6537800	Weak transcription	HMEC	breast
27	chr9:6508600-6538200	Weak transcription	NHEK	skin
28	chr9:6508800-6518600	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr9:6508800-6519000	Weak transcription	Dnd41	blood
30	chr9:6508800-6520200	Weak transcription	Fetal Muscle Leg	muscle
31	chr9:6508800-6521400	Weak transcription	Primary hematopoietic stem cells	blood
32	chr9:6508800-6521800	Weak transcription	GM12878-XiMat	blood
33	chr9:6508800-6523800	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr9:6508800-6526600	Weak transcription	HSMM	muscle
35	chr9:6509000-6519200	Weak transcription	Fetal Intestine Large	intestine
36	chr9:6509000-6520200	Weak transcription	Liver	Liver
37	chr9:6509000-6521600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr9:6509000-6521800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr9:6509000-6521800	Weak transcription	Adipose Nuclei	Adipose
40	chr9:6509400-6521800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr9:6509800-6525000	Weak transcription	Osteobl	bone
42	chr9:6509800-6530200	Weak transcription	A549	lung
43	chr9:6510000-6521800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr9:6510000-6521800	Weak transcription	Fetal Brain Female	brain
45	chr9:6510400-6558800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr9:6510600-6522200	Weak transcription	NHDF-Ad	bronchial
47	chr9:6510600-6525000	Weak transcription	NH-A	brain
48	chr9:6510600-6543000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr9:6510800-6521200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr9:6511000-6518600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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