Variant report

Variant	nsv1025800
Chromosome Location	chr9:8712487-9030627
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	chr9:8961022-8961768	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:8868744-8869021	HepG2	liver:	n/a	n/a
3	ATF2	chr9:8858467-8859172	H1-hESC	embryonic stem cell:	n/a	chr9:8858876-8858890 chr9:8858878-8858889
4	ATF2	chr9:8858576-8859063	H1-hESC	embryonic stem cell:	n/a	chr9:8858876-8858890 chr9:8858878-8858889
5	ATF2	chr9:8734663-8735065	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr9:8734880-8735045	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr9:8868710-8869028	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr9:8895967-8895969	A549	lung:	n/a	n/a
9	BHLHE40	chr9:8961130-8961628	HepG2	liver:	n/a	n/a
10	BRCA1	chr9:8961431-8961631	HepG2	liver:	n/a	n/a
11	BRCA1	chr9:8855216-8855273	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr9:8961184-8961759	HepG2	liver:	n/a	n/a
13	CEBPB	chr9:8889203-8889415	K562	blood:	n/a	chr9:8889298-8889307 chr9:8889298-8889307 chr9:8889298-8889307 chr9:8889296-8889307
14	CEBPB	chr9:9010741-9010996	A549	lung:	n/a	chr9:9010892-9010905 chr9:9010894-9010903 chr9:9010892-9010903
15	CEBPB	chr9:8926157-8926470	IMR90	lung:	n/a	chr9:8926304-8926313 chr9:8926302-8926313 chr9:8926304-8926315
16	CEBPB	chr9:8765139-8765438	HepG2	liver:	n/a	chr9:8765314-8765325
17	CEBPB	chr9:8889118-8889488	A549	lung:	n/a	chr9:8889298-8889307 chr9:8889298-8889307 chr9:8889298-8889307 chr9:8889296-8889307
18	CEBPB	chr9:8992944-8993144	HepG2	liver:	n/a	n/a
19	CEBPB	chr9:8765147-8765485	IMR90	lung:	n/a	chr9:8765314-8765325
20	CEBPB	chr9:8910663-8910909	HepG2	liver:	n/a	n/a
21	CEBPB	chr9:8961081-8961810	HepG2	liver:	n/a	n/a
22	CEBPB	chr9:8791919-8792041	A549	lung:	n/a	n/a
23	CEBPB	chr9:9006505-9006741	HepG2	liver:	n/a	n/a
24	CEBPB	chr9:8899375-8899382	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr9:8987639-8987844	H1-hESC	embryonic stem cell:	n/a	chr9:8987749-8987758 chr9:8987747-8987758 chr9:8987747-8987760
26	CEBPB	chr9:8782263-8782583	HepG2	liver:	n/a	chr9:8782419-8782430
27	CEBPB	chr9:8996279-8996542	HepG2	liver:	n/a	n/a
28	CEBPB	chr9:8810067-8810317	HepG2	liver:	n/a	chr9:8810172-8810183 chr9:8810174-8810185 chr9:8810174-8810185
29	CEBPB	chr9:8775818-8775879	K562	blood:	n/a	chr9:8775851-8775862
30	CEBPB	chr9:8990176-8990287	H1-hESC	embryonic stem cell:	n/a	chr9:8990232-8990245 chr9:8990232-8990243
31	CEBPB	chr9:8862470-8862814	HepG2	liver:	n/a	chr9:8862647-8862660 chr9:8862648-8862659 chr9:8862649-8862658 chr9:8862647-8862658 chr9:8862647-8862660
32	CEBPB	chr9:8862492-8862809	A549	lung:	n/a	chr9:8862647-8862660 chr9:8862648-8862659 chr9:8862649-8862658 chr9:8862647-8862658 chr9:8862647-8862660
33	CEBPB	chr9:8765187-8765410	K562	blood:	n/a	chr9:8765314-8765325
34	CEBPB	chr9:8863911-8864232	H1-hESC	embryonic stem cell:	n/a	chr9:8864067-8864078 chr9:8864066-8864079
35	CEBPB	chr9:8782348-8782559	K562	blood:	n/a	chr9:8782419-8782430
36	CEBPB	chr9:8765144-8765459	A549	lung:	n/a	chr9:8765314-8765325
37	CEBPB	chr9:8961188-8961617	HepG2	liver:	n/a	n/a
38	CEBPB	chr9:8862489-8862789	H1-hESC	embryonic stem cell:	n/a	chr9:8862647-8862660 chr9:8862648-8862659 chr9:8862649-8862658 chr9:8862647-8862658 chr9:8862647-8862660
39	CEBPB	chr9:8782267-8782532	H1-hESC	embryonic stem cell:	n/a	chr9:8782419-8782430
40	CEBPB	chr9:8961294-8961477	HepG2	liver:	n/a	n/a
41	CEBPB	chr9:8990081-8990286	A549	lung:	n/a	chr9:8990232-8990245 chr9:8990232-8990243
42	CEBPB	chr9:8833571-8833682	H1-hESC	embryonic stem cell:	n/a	chr9:8833624-8833637 chr9:8833625-8833636 chr9:8833624-8833637 chr9:8833624-8833637
43	CEBPB	chr9:8889126-8889470	H1-hESC	embryonic stem cell:	n/a	chr9:8889298-8889307 chr9:8889298-8889307 chr9:8889298-8889307 chr9:8889296-8889307
44	CEBPB	chr9:9010715-9011060	HepG2	liver:	n/a	chr9:9010892-9010905 chr9:9010894-9010903 chr9:9010892-9010903
45	CEBPB	chr9:8946121-8946175	A549	lung:	n/a	n/a
46	CEBPB	chr9:8782287-8782568	A549	lung:	n/a	chr9:8782419-8782430
47	CEBPB	chr9:8765224-8765372	H1-hESC	embryonic stem cell:	n/a	chr9:8765314-8765325
48	CEBPB	chr9:8945985-8946238	HepG2	liver:	n/a	chr9:8946106-8946117
49	CEBPB	chr9:8822586-8822914	HepG2	liver:	n/a	chr9:8822735-8822746
50	CEBPB	chr9:8926156-8926446	HepG2	liver:	n/a	chr9:8926304-8926313 chr9:8926302-8926313 chr9:8926304-8926315

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:8857502-8857552	Caco-2	colon:	n/a
2	chr9:8713437-8713487	PrEC	prostate:	n/a
3	chr9:8857502-8857552	AG09319	gingival:	n/a
4	chr9:8858259-8858309	SAEC	small airway:	n/a
5	chr9:8852055-8852105	U87	brain:	n/a
6	chr9:8856695-8856745	HRPEpiC	eye:	n/a
7	chr9:8852055-8852105	NB4	blood:	n/a
8	chr9:8835149-8835199	HAEpiC	amniotic membrane:	n/a
9	chr9:8713664-8713714	SK-N-MC	brain:	n/a
10	chr9:8858259-8858309	CMK	blood:	n/a
11	chr9:8858259-8858309	NHBE	bronchial:	n/a
12	chr9:8857491-8857541	AG10803	skin:	n/a
13	chr9:8858259-8858309	Jurkat	blood:	n/a
14	chr9:8713664-8713714	PrEC	prostate:	n/a
15	chr9:8713437-8713487	ovcar-3	ovarian:	n/a
16	chr9:8713437-8713487	ProgFib	skin:	n/a
17	chr9:8856695-8856745	NT2-D1	testis:	n/a
18	chr9:8835149-8835199	ECC-1	luminal epithelium:	n/a
19	chr9:8713788-8713838	HUVEC	blood vessel:	n/a
20	chr9:8857502-8857552	AG09309	skin:	n/a
21	chr9:8713788-8713838	NHDF-neo	bronchial:	n/a
22	chr9:8857486-8857536	PFSK-1	brain:	n/a
23	chr9:8857491-8857541	SK-N-SH	brain:	n/a
24	chr9:8857502-8857552	ProgFib	skin:	n/a
25	chr9:8858259-8858309	LNCaP	prostate:	n/a
26	chr9:8713664-8713714	AG04450	lung:	fetal
27	chr9:8713437-8713487	NHBE	bronchial:	n/a
28	chr9:8857486-8857536	HRPEpiC	eye:	n/a
29	chr9:8835149-8835199	PrEC	prostate:	n/a
30	chr9:8858644-8858694	Hela-S3	cervix:	n/a
31	chr9:8857491-8857541	NHBE	bronchial:	n/a
32	chr9:8857486-8857536	HL-60	blood:	n/a
33	chr9:8857486-8857536	HepG2	liver:	n/a
34	chr9:8858259-8858309	A549	lung:	n/a
35	chr9:8858574-8858624	MCF-7	breast:	n/a
36	chr9:8858644-8858694	AG09309	skin:	n/a
37	chr9:8857502-8857552	GM12878	blood:	n/a
38	chr9:8857486-8857536	GM06990	blood:	n/a
39	chr9:8857502-8857552	PFSK-1	brain:	n/a
40	chr9:8858574-8858624	GM06990	blood:	n/a
41	chr9:8858259-8858309	U87	brain:	n/a
42	chr9:8713664-8713714	AoSMC	blood vessel:	n/a
43	chr9:8713437-8713487	SAEC	small airway:	n/a
44	chr9:8852055-8852105	NH-A	brain:	n/a
45	chr9:8852055-8852105	GM06990	blood:	n/a
46	chr9:8856695-8856745	Caco-2	colon:	n/a
47	chr9:8858259-8858309	AoSMC	blood vessel:	n/a
48	chr9:8713664-8713714	GM06990	blood:	n/a
49	chr9:8857486-8857536	MCF10A-Er-Src	breast:	n/a
50	chr9:8858644-8858694	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:7569797..7570734-chr9:8895690..8896630,4	MCF-7	breast:
2	chr9:8868603..8871582-chr9:8873717..8875264,2	K562	blood:
3	chr3:136824772..136825295-chr9:8731189..8731885,2	MCF-7	breast:
4	chr9:7569880..7570683-chr9:8895710..8896327,2	MCF-7	breast:
5	chr9:8868603..8871582-chr9:8873717..8875264,2	K562	blood:
6	chr9:8485590..8486306-chr9:8895648..8896453,2	MCF-7	breast:
7	chr9:7844225..7844973-chr9:8895548..8896327,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KDM4C-8	chr9:8858130-8858323	ENSG00000225706
2	lnc-KDM4C-9	chr9:8936079-8936179	ENSG00000234021
3	lnc-KDM4C-17	chr9:8848134-8848323	ucscGeneNc_uc003zku_1
4	lnc-KDM4C-9	chr9:8962800-8963077	ENSG00000234021
5	lnc-KDM4C-9	chr9:8958722-8958848	ENSG00000234021
6	lnc-KDM4C-9	chr9:8962124-8962189	ENSG00000234021
7	lnc-KDM4C-8	chr9:8859956-8861724	ENSG00000225706
8	lnc-KDM4C-17	chr9:8849956-8851724	ucscGeneNc_uc003zku_1
9	lnc-KDM4C-8	chr9:8858134-8858323	ENSG00000225706
10	lnc-KDM4C-8	chr9:8860782-8862255	ENSG00000225706

Variant related genes	Relation type
ENSG00000251699	TF binding region
RNU7-185P	TF binding region
ENSG00000212695	TF binding region
PTPRD	TF binding region
ENSG00000234021	TF binding region
ENSG00000225706	TF binding region
ENSG00000251699	CpG island
RNU7-185P	CpG island
ENSG00000212695	CpG island
PTPRD	CpG island
ENSG00000234021	CpG island
ENSG00000225706	CpG island
ENSG00000153707	chromatin interactions
PLEC	miRNA target sites
CCDC76	miRNA target sites
WHSC1L1	miRNA target sites
HNRNPK	miRNA target sites

Extended variants
information (count: 12723 )
Associated
traits (count: 128 )

Variant overlapped rSNPs/rCNVs (count:12723 , 50 per page) page: 1 2 3 4 5 6 7 ... 255

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79642990	chr9:8712498-8712499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs117846167	chr9:8712510-8712511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs538123720	chr9:8712549-8712550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556420477	chr9:8712577-8712578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs10815925	chr9:8712601-8712602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs368644212	chr9:8712603-8712604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs75141215	chr9:8712671-8712672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs553925451	chr9:8712687-8712688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572457181	chr9:8712709-8712710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545990628	chr9:8712733-8712734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557899538	chr9:8712734-8712735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191391019	chr9:8712735-8712736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs10977257	chr9:8712737-8712738	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs111231345	chr9:8712763-8712764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs374791498	chr9:8712782-8712783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181132158	chr9:8712805-8712806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529243500	chr9:8712836-8712837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370247866	chr9:8712858-8712859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs541022610	chr9:8712868-8712869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs62528774	chr9:8712869-8712870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186100567	chr9:8712911-8712912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141246542	chr9:8712931-8712932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs13294608	chr9:8712945-8712946	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs189737128	chr9:8712964-8712965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375581202	chr9:8712989-8712990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs138050607	chr9:8712994-8712995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs550004381	chr9:8713021-8713022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs35154124	chr9:8713054-8713055	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs149507020	chr9:8713075-8713076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs75224924	chr9:8713086-8713087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539893821	chr9:8713150-8713151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557947765	chr9:8713168-8713169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576643901	chr9:8713205-8713206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs577725272	chr9:8713207-8713208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369621231	chr9:8713214-8713215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143108781	chr9:8713247-8713248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545590422	chr9:8713271-8713272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555644984	chr9:8713307-8713308	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs573932554	chr9:8713317-8713318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7857358	chr9:8713332-8713333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577546055	chr9:8713339-8713340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112272736	chr9:8713343-8713344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183455343	chr9:8713353-8713354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs117429409	chr9:8713357-8713358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548061200	chr9:8713374-8713375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187842397	chr9:8713385-8713386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561955771	chr9:8713394-8713395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529509456	chr9:8713419-8713420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs10977258	chr9:8713420-8713421	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs190756251	chr9:8713459-8713460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:128)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	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
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	21811587	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	20668451	CNVD
Schizophrenia	20838587	CNVD
Glioblastoma	18772890	CNVD
Glioblastoma multiforme	21390271	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Renal cell carcinoma	21215367	CNVD
small cell lung cancer	21764851	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Mental retardation	17847001	CNVD
Cutaneous squamous cell carcinomas	17420988	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD

Chromatin state (count:2888 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8699600-8717800	Weak transcription	Primary hematopoietic stem cells	blood
2	chr9:8700800-8718000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr9:8704400-8731800	Weak transcription	Fetal Lung	lung
4	chr9:8706800-8714400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr9:8706800-8718000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr9:8710600-8733600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr9:8711800-8713400	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr9:8712000-8715800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr9:8712000-8716600	Weak transcription	Brain Angular Gyrus	brain
10	chr9:8712000-8718200	Weak transcription	Brain Cingulate Gyrus	brain
11	chr9:8712200-8717800	Weak transcription	Brain Hippocampus Middle	brain
12	chr9:8712400-8714400	Weak transcription	Brain Substantia Nigra	brain
13	chr9:8714400-8714600	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr9:8714400-8714800	Enhancers	Brain Substantia Nigra	brain
15	chr9:8714600-8715000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr9:8714800-8717400	Weak transcription	Brain Substantia Nigra	brain
17	chr9:8715000-8718600	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr9:8715200-8715400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr9:8715400-8723000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr9:8715600-8719000	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr9:8715600-8720200	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr9:8715800-8716000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr9:8715800-8716200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr9:8715800-8716200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr9:8715800-8716200	Enhancers	Fetal Brain Female	brain
26	chr9:8715800-8716400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr9:8715800-8716600	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr9:8715800-8716600	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr9:8716000-8716200	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr9:8716000-8716400	Enhancers	H1 Cell Line	embryonic stem cell
31	chr9:8716000-8717000	Enhancers	H9 Cell Line	embryonic stem cell
32	chr9:8716000-8718000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr9:8716200-8717200	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr9:8716200-8717400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr9:8716200-8717800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr9:8716200-8720200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr9:8716200-8732600	Weak transcription	Fetal Brain Female	brain
38	chr9:8716400-8717400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr9:8716400-8718000	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr9:8716400-8719400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr9:8716600-8717000	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr9:8716600-8717200	Enhancers	Brain Angular Gyrus	brain
43	chr9:8716600-8717600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr9:8717000-8717800	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr9:8717000-8718200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr9:8717000-8721000	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr9:8717200-8717600	Weak transcription	Brain Angular Gyrus	brain
48	chr9:8717200-8718600	Enhancers	Muscle Satellite Cultured Cells	--
49	chr9:8717200-8719200	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr9:8717200-8721000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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