Variant report

Variant	nsv916819
Chromosome Location	chr9:43468811-43836398
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:774)
CpG islands
(count:183)
Chromatin interactive
region (count:0)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:774 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:43498011-43498345	K562	blood:	n/a	n/a
2	BACH1	chr9:43686226-43686817	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr9:43653838-43653993	GM12878	blood:	n/a	n/a
4	BATF	chr9:43714519-43714714	GM12878	blood:	n/a	n/a
5	BATF	chr9:43488473-43488768	GM12878	blood:	n/a	chr9:43488642-43488653
6	BATF	chr9:43529040-43529422	GM12878	blood:	n/a	n/a
7	BHLHE40	chr9:43505744-43505995	A549	lung:	n/a	n/a
8	CEBPB	chr9:43772398-43772773	A549	lung:	n/a	n/a
9	CEBPB	chr9:43475810-43476027	IMR90	lung:	n/a	chr9:43475938-43475951 chr9:43475938-43475951
10	CEBPB	chr9:43475824-43476024	A549	lung:	n/a	chr9:43475938-43475951 chr9:43475938-43475951
11	CEBPB	chr9:43686226-43687047	A549	lung:	n/a	chr9:43686435-43686447
12	CTCF	chr9:43654220-43654370	A549	lung:	n/a	n/a
13	CTCF	chr9:43686740-43686890	HPAF	blood vessel:	n/a	n/a
14	CTCF	chr9:43750449-43750509	GM13976	blood:	n/a	n/a
15	CTCF	chr9:43653780-43653930	GM12869	blood:	n/a	chr9:43653906-43653927 chr9:43653907-43653920 chr9:43653904-43653922 chr9:43653905-43653921 chr9:43653909-43653919
16	CTCF	chr9:43516684-43516772	Kidney_OC	kidney:	n/a	n/a
17	CTCF	chr9:43686821-43686879	LNCaP	prostate:	n/a	n/a
18	CTCF	chr9:43533546-43533712	A549	lung:	n/a	n/a
19	CTCF	chr9:43693051-43693313	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr9:43686460-43686610	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr9:43756361-43756465	LNCaP	prostate:	n/a	n/a
22	CTCF	chr9:43498060-43498210	AG09309	skin:	n/a	chr9:43498167-43498185
23	CTCF	chr9:43684749-43684898	GM13976	blood:	n/a	chr9:43684809-43684822 chr9:43684811-43684819
24	CTCF	chr9:43789934-43790054	A549	lung:	n/a	n/a
25	CTCF	chr9:43820041-43820152	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr9:43653760-43653910	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr9:43749105-43749155	GM13977	blood:	n/a	n/a
28	CTCF	chr9:43743866-43743941	A549	lung:	n/a	n/a
29	CTCF	chr9:43498080-43498230	A549	lung:	n/a	chr9:43498167-43498185
30	CTCF	chr9:43497957-43498272	A549	lung:	n/a	chr9:43498167-43498185
31	CTCF	chr9:43808449-43808533	LNCaP	prostate:	n/a	n/a
32	CTCF	chr9:43835241-43835322	A549	lung:	n/a	n/a
33	CTCF	chr9:43692982-43693182	K562	blood:	n/a	n/a
34	CTCF	chr9:43769650-43769705	GM10248	blood:	n/a	n/a
35	CTCF	chr9:43736524-43736638	Spleen_OC	spleen:	n/a	n/a
36	CTCF	chr9:43638990-43639086	LNCaP	prostate:	n/a	n/a
37	CTCF	chr9:43777435-43777550	MCF-7	breast:	n/a	n/a
38	CTCF	chr9:43693120-43693270	HCM	heart:	n/a	n/a
39	CTCF	chr9:43653809-43653995	A549	lung:	n/a	chr9:43653906-43653927 chr9:43653907-43653920 chr9:43653904-43653922 chr9:43653905-43653921 chr9:43653909-43653919
40	CTCF	chr9:43498131-43498226	GM12892	blood:	n/a	chr9:43498167-43498185
41	CTCF	chr9:43686460-43686610	RPTEC	kidney:	n/a	n/a
42	CTCF	chr9:43716589-43716662	LNCaP	prostate:	n/a	n/a
43	CTCF	chr9:43653740-43653890	HMF	breast:	n/a	n/a
44	CTCF	chr9:43684920-43685070	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr9:43693036-43693250	LNCaP	prostate:	n/a	n/a
46	CTCF	chr9:43793772-43793799	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr9:43653760-43653910	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr9:43653825-43653977	Kidney_OC	kidney:	n/a	chr9:43653906-43653927 chr9:43653907-43653920 chr9:43653904-43653922 chr9:43653905-43653921 chr9:43653909-43653919
49	CTCF	chr9:43733843-43733904	Medullo	brain:	n/a	n/a
50	CTCF	chr9:43498060-43498210	HRPEpiC	eye:	n/a	chr9:43498167-43498185

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:43631161-43631211	NB4	blood:	n/a
2	chr9:43525320-43525370	HMEC	breast:	n/a
3	chr9:43525948-43525998	GM06990	blood:	n/a
4	chr9:43525320-43525370	SAEC	small airway:	n/a
5	chr9:43525320-43525370	HEK293	kidney:	embryo
6	chr9:43525320-43525370	LNCaP	prostate:	n/a
7	chr9:43525948-43525998	H1-hESC	embryonic stem cell:	embryo
8	chr9:43525948-43525998	SAEC	small airway:	n/a
9	chr9:43631161-43631211	HRCEpiC	kidney:	n/a
10	chr9:43525948-43525998	NB4	blood:	n/a
11	chr9:43631161-43631211	RPTEC	kidney:	n/a
12	chr9:43525948-43525998	PANC-1	pancreas:	n/a
13	chr9:43631161-43631211	NT2-D1	testis:	n/a
14	chr9:43525948-43525998	HNPCEpiC	eye:	n/a
15	chr9:43525320-43525370	PFSK-1	brain:	n/a
16	chr9:43525948-43525998	RPTEC	kidney:	n/a
17	chr9:43525320-43525370	HEEpiC	esophagus:	n/a
18	chr9:43631161-43631211	GM19239	blood:	n/a
19	chr9:43525948-43525998	GM12878	blood:	n/a
20	chr9:43525320-43525370	HAEpiC	amniotic membrane:	n/a
21	chr9:43525320-43525370	U87	brain:	n/a
22	chr9:43631161-43631211	SK-N-MC	brain:	n/a
23	chr9:43525320-43525370	SK-N-SH	brain:	n/a
24	chr9:43525320-43525370	GM06990	blood:	n/a
25	chr9:43525320-43525370	SKMC	muscle:	n/a
26	chr9:43631161-43631211	AG09319	gingival:	n/a
27	chr9:43631161-43631211	LNCaP	prostate:	n/a
28	chr9:43525948-43525998	GM12892	blood:	n/a
29	chr9:43525320-43525370	Jurkat	blood:	n/a
30	chr9:43631161-43631211	HCM	heart:	n/a
31	chr9:43631161-43631211	HCT-116	colon:	n/a
32	chr9:43631161-43631211	HIPEpiC	eye:	n/a
33	chr9:43525320-43525370	GM12891	blood:	n/a
34	chr9:43525948-43525998	GM19239	blood:	n/a
35	chr9:43525320-43525370	HIPEpiC	eye:	n/a
36	chr9:43525948-43525998	HRPEpiC	eye:	n/a
37	chr9:43525320-43525370	SK-N-SH_RA	brain:	n/a
38	chr9:43525320-43525370	A549	lung:	n/a
39	chr9:43525948-43525998	HRE	kidney:	n/a
40	chr9:43525948-43525998	K562	blood:	n/a
41	chr9:43631161-43631211	HAEpiC	amniotic membrane:	n/a
42	chr9:43631161-43631211	T-47D	breast:	n/a
43	chr9:43525320-43525370	T-47D	breast:	n/a
44	chr9:43631161-43631211	NH-A	brain:	n/a
45	chr9:43525948-43525998	ovcar-3	ovarian:	n/a
46	chr9:43525948-43525998	NH-A	brain:	n/a
47	chr9:43525948-43525998	HCF	heart:	n/a
48	chr9:43525948-43525998	MCF-7	breast:	n/a
49	chr9:43631161-43631211	HCPEpiC	choroid plexus:	n/a
50	chr9:43525320-43525370	HepG2	liver:	n/a

No data

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD20A3-13	chr9:43628634-43628694	NONHSAT131362
2	lnc-FAM75A6-5	chr9:43802781-43803039	NONHSAT131363
3	lnc-RP11-160N1.10.1-8	chr9:43822613-43822699	NONHSAT131364
4	lnc-ANKRD20A3-13	chr9:43629020-43629117	NONHSAT131362
5	lnc-FAM75A6-6	chr9:43833702-43835037	NONHSAT131365
6	lnc-RP11-160N1.10.1-8	chr9:43828157-43828221	NONHSAT131364
7	lnc-ANKRD20A3-13	chr9:43627769-43628378	NONHSAT131362
8	lnc-RP11-160N1.10.1-8	chr9:43822729-43822779	NONHSAT131364
9	lnc-FAM75A6-6	chr9:43830636-43831108	NONHSAT131365
10	lnc-CNTNAP3B-2	chr9:43617727-43618056	NONHSAT131361

No data

Variant related genes	Relation type
ENSG00000239986	TF binding region
ENSG00000270909	TF binding region
SPATA31A6	TF binding region
RN7SL343P	TF binding region
CNTNAP3B	TF binding region
ENSG00000239986	CpG island
ENSG00000270909	CpG island
SPATA31A6	CpG island
RN7SL343P	CpG island
CNTNAP3B	CpG island

Extended variants
information (count: 2480 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:2480 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191587687	chr9:43474478-43474479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs587735616	chr9:43474569-43474570	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs587629687	chr9:43474575-43474576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs2491531	chr9:43474629-43474630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs182989184	chr9:43474649-43474650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187528606	chr9:43474718-43474719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs192000238	chr9:43474756-43474757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs587600726	chr9:43474757-43474758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs184982984	chr9:43474769-43474770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575806368	chr9:43489007-43489008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546035482	chr9:43489009-43489010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs112254373	chr9:43489041-43489042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs532073642	chr9:43489139-43489140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs541105030	chr9:43489142-43489143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552054581	chr9:43489817-43489818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs200478614	chr9:43489819-43489820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs547658874	chr9:43489831-43489832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs201320460	chr9:43489844-43489845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs188633778	chr9:43489846-43489847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534837545	chr9:43489859-43489860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs79915011	chr9:43489860-43489861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs570121403	chr9:43489867-43489868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs568156962	chr9:43489871-43489872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535418506	chr9:43489887-43489888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs557236311	chr9:43489925-43489926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562144153	chr9:43489961-43489962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs138167139	chr9:43489962-43489963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs370537938	chr9:43489970-43489971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540037679	chr9:43489985-43489986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558102073	chr9:43490004-43490005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs149144948	chr9:43490005-43490006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541171924	chr9:43490011-43490012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200241865	chr9:43490189-43490190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs538997311	chr9:43490196-43490197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs201534118	chr9:43490231-43490232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs559478867	chr9:43490389-43490390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574493131	chr9:43490487-43490488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541796977	chr9:43490515-43490516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs571039452	chr9:43490547-43490548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs191540961	chr9:43490610-43490611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530749912	chr9:43490618-43490619	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201002402	chr9:43490641-43490642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2808903	chr9:43490648-43490649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552427912	chr9:43490659-43490660	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564175569	chr9:43490701-43490702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528280083	chr9:43490716-43490717	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2808902	chr9:43490717-43490718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2808901	chr9:43490755-43490756	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546698859	chr9:43490766-43490767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549653763	chr9:43490775-43490776	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
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
Oral squamous cell carcinoma	17134496	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	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
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	20409316	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Lung adenocarcinoma	17086460	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Lung cancer	17086460	CNVD
Rhabdomyosarcoma	16790082	CNVD

Chromatin state (count:222 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:43474400-43474800	Enhancers	A549	lung
2	chr9:43489000-43489200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr9:43489800-43490800	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr9:43489800-43491000	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr9:43490600-43491000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr9:43490600-43491000	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr9:43490600-43491000	Enhancers	NH-A	brain
8	chr9:43490600-43491200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr9:43490600-43491200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr9:43490600-43491200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr9:43490600-43491200	Enhancers	HUVEC	blood vessel
12	chr9:43490600-43491400	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr9:43490600-43492000	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr9:43490800-43491200	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr9:43490800-43491200	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr9:43491000-43493000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr9:43491200-43505400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr9:43491200-43505800	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr9:43491400-43491800	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr9:43491800-43492000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr9:43491800-43492000	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr9:43492000-43493000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr9:43492000-43493400	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr9:43492000-43493600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr9:43493000-43493800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr9:43493000-43493800	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr9:43493400-43493800	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr9:43493600-43493800	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr9:43505400-43505600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr9:43505400-43506000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr9:43505400-43506400	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr9:43505400-43507000	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr9:43505600-43506000	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr9:43505600-43506000	Genic enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr9:43505600-43506200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr9:43505600-43507000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr9:43505800-43506000	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr9:43505800-43506200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr9:43506000-43506200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr9:43506000-43506800	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr9:43506000-43506800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr9:43506200-43506800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr9:43506400-43506800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr9:43506800-43507000	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr9:43506800-43507200	Active TSS	iPS-18 Cell Line	embryonic stem cell
46	chr9:43506800-43507400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr9:43506800-43507400	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr9:43507000-43507400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
49	chr9:43507000-43507400	Active TSS	iPS-20b Cell Line	embryonic stem cell
50	chr9:43507000-43508400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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