Variant report

Variant	nsv1027371
Chromosome Location	chr9:43505840-44273229
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2915)
CpG islands
(count:854)
Chromatin interactive
region (count:1)
LncRNA
region (count:27)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2915 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:44108136-44108696	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:44118677-44118886	HepG2	liver:	n/a	n/a
3	ATF1	chr9:43939526-43939892	K562	blood:	n/a	n/a
4	ATF3	chr9:43939586-43939712	K562	blood:	n/a	n/a
5	BACH1	chr9:44227257-44227630	K562	blood:	n/a	n/a
6	BACH1	chr9:43686226-43686817	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr9:44227184-44227631	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr9:44072537-44072807	GM12878	blood:	n/a	chr9:44072668-44072679
9	BATF	chr9:44124043-44124400	GM12878	blood:	n/a	n/a
10	BATF	chr9:44110695-44110955	GM12878	blood:	n/a	n/a
11	BATF	chr9:44070573-44070887	GM12878	blood:	n/a	n/a
12	BATF	chr9:44145517-44145676	GM12878	blood:	n/a	n/a
13	BATF	chr9:44088928-44089261	GM12878	blood:	n/a	chr9:44088983-44088991
14	BATF	chr9:44124132-44124352	GM12878	blood:	n/a	n/a
15	BATF	chr9:44086306-44086516	GM12878	blood:	n/a	n/a
16	BATF	chr9:44108339-44108646	GM12878	blood:	n/a	chr9:44108541-44108552
17	BATF	chr9:44243686-44243967	GM12878	blood:	n/a	n/a
18	BATF	chr9:44065378-44065708	GM12878	blood:	n/a	n/a
19	BATF	chr9:43714519-43714714	GM12878	blood:	n/a	n/a
20	BATF	chr9:43844088-43844411	GM12878	blood:	n/a	n/a
21	BATF	chr9:44072527-44072766	GM12878	blood:	n/a	chr9:44072668-44072679
22	BATF	chr9:44105673-44105873	GM12878	blood:	n/a	n/a
23	BATF	chr9:44125333-44125599	GM12878	blood:	n/a	n/a
24	BATF	chr9:44108035-44108219	GM12878	blood:	n/a	n/a
25	BATF	chr9:44070553-44070898	GM12878	blood:	n/a	n/a
26	BATF	chr9:44076866-44077089	GM12878	blood:	n/a	n/a
27	BATF	chr9:44108319-44108733	GM12878	blood:	n/a	chr9:44108541-44108552
28	BATF	chr9:44030085-44030326	GM12878	blood:	n/a	n/a
29	BATF	chr9:44112676-44113049	GM12878	blood:	n/a	n/a
30	BATF	chr9:44176537-44176725	GM12878	blood:	n/a	n/a
31	BATF	chr9:43925013-43925176	GM12878	blood:	n/a	n/a
32	BATF	chr9:44108799-44108996	GM12878	blood:	n/a	n/a
33	BATF	chr9:44065395-44065684	GM12878	blood:	n/a	n/a
34	BATF	chr9:44245375-44245745	GM12878	blood:	n/a	n/a
35	BATF	chr9:43529040-43529422	GM12878	blood:	n/a	n/a
36	BATF	chr9:44030553-44030791	GM12878	blood:	n/a	n/a
37	BATF	chr9:44245139-44246113	GM12878	blood:	n/a	n/a
38	BATF	chr9:44082194-44082452	GM12878	blood:	n/a	n/a
39	BATF	chr9:44030517-44030875	GM12878	blood:	n/a	n/a
40	BATF	chr9:44107144-44107983	GM12878	blood:	n/a	n/a
41	BATF	chr9:44012526-44012769	GM12878	blood:	n/a	n/a
42	BATF	chr9:44125369-44125590	GM12878	blood:	n/a	n/a
43	BATF	chr9:44088871-44089267	GM12878	blood:	n/a	chr9:44088983-44088991
44	BATF	chr9:43653838-43653993	GM12878	blood:	n/a	n/a
45	BATF	chr9:43875906-43876190	GM12878	blood:	n/a	n/a
46	BATF	chr9:44100518-44100936	GM12878	blood:	n/a	chr9:44100637-44100647
47	BATF	chr9:44095589-44095794	GM12878	blood:	n/a	n/a
48	BATF	chr9:44086267-44086535	GM12878	blood:	n/a	n/a
49	BATF	chr9:44030053-44030338	GM12878	blood:	n/a	n/a
50	BATF	chr9:44063096-44063309	GM12878	blood:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:44227339-44227389	AG09319	gingival:	n/a
2	chr9:44118236-44118286	HCF	heart:	n/a
3	chr9:43525320-43525370	NHBE	bronchial:	n/a
4	chr9:44227339-44227389	HUVEC	blood vessel:	n/a
5	chr9:43860027-43860077	HAEpiC	amniotic membrane:	n/a
6	chr9:44119823-44119873	U87	brain:	n/a
7	chr9:43525948-43525998	U87	brain:	n/a
8	chr9:43525948-43525998	MCF10A-Er-Src	breast:	n/a
9	chr9:44118014-44118064	HUVEC	blood vessel:	n/a
10	chr9:43915234-43915284	H1-hESC	embryonic stem cell:	embryo
11	chr9:43631161-43631211	HCPEpiC	choroid plexus:	n/a
12	chr9:43631161-43631211	SAEC	small airway:	n/a
13	chr9:44118236-44118286	HUVEC	blood vessel:	n/a
14	chr9:43525948-43525998	GM19239	blood:	n/a
15	chr9:43860965-43861015	MCF10A-Er-Src	breast:	n/a
16	chr9:44227210-44227260	PrEC	prostate:	n/a
17	chr9:43631161-43631211	Caco-2	colon:	n/a
18	chr9:43525320-43525370	GM06990	blood:	n/a
19	chr9:44118915-44118965	NHBE	bronchial:	n/a
20	chr9:44120147-44120197	CMK	blood:	n/a
21	chr9:44118236-44118286	HCPEpiC	choroid plexus:	n/a
22	chr9:43860027-43860077	AG09309	skin:	n/a
23	chr9:44119823-44119873	HAEpiC	amniotic membrane:	n/a
24	chr9:44119413-44119463	Jurkat	blood:	n/a
25	chr9:43860965-43861015	HRCEpiC	kidney:	n/a
26	chr9:44120147-44120197	LNCaP	prostate:	n/a
27	chr9:44227210-44227260	Hela-S3	cervix:	n/a
28	chr9:44119413-44119463	GM12878	blood:	n/a
29	chr9:43525320-43525370	HCM	heart:	n/a
30	chr9:44118236-44118286	GM19239	blood:	n/a
31	chr9:44227210-44227260	NB4	blood:	n/a
32	chr9:43915234-43915284	ProgFib	skin:	n/a
33	chr9:44119823-44119873	NH-A	brain:	n/a
34	chr9:44119823-44119873	HRCEpiC	kidney:	n/a
35	chr9:43631161-43631211	HPAEpiC	pulmonary alveolar:	n/a
36	chr9:44227339-44227389	HIPEpiC	eye:	n/a
37	chr9:44118915-44118965	HRE	kidney:	n/a
38	chr9:44118236-44118286	K562	blood:	n/a
39	chr9:43525948-43525998	GM12891	blood:	n/a
40	chr9:43860027-43860077	GM06990	blood:	n/a
41	chr9:43860027-43860077	Caco-2	colon:	n/a
42	chr9:44227339-44227389	HCT-116	colon:	n/a
43	chr9:43631161-43631211	PFSK-1	brain:	n/a
44	chr9:44227210-44227260	SKMC	muscle:	n/a
45	chr9:43525948-43525998	HRPEpiC	eye:	n/a
46	chr9:43860027-43860077	NHDF-neo	bronchial:	n/a
47	chr9:44227210-44227260	CMK	blood:	n/a
48	chr9:44118014-44118064	AG04449	skin:	fetal
49	chr9:43915234-43915284	GM19239	blood:	n/a
50	chr9:44120147-44120197	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:107699957..107700478-chr9:44227430..44227950,2	MCF-7	breast:

(count:27 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM75A6-1	chr9:44144869-44145101	XLOC_007696
2	lnc-FAM75A6-3	chr9:44260422-44263319	ENSG00000233424.2
3	lnc-ANKRD20A3-13	chr9:43629020-43629117	NONHSAT131362
4	lnc-FAM75A6-3	chr9:44260052-44260139	ENSG00000233424.2
5	lnc-FAM75A6-7	chr9:44046989-44047817	NONHSAT131371
6	lnc-FAM75A6-3	chr9:44256580-44256817	ENSG00000233424.2
7	lnc-CNTNAP3B-2	chr9:43617727-43618056	NONHSAT131361
8	lnc-CNTNAP3B-3	chr9:44011053-44011839	NONHSAT131369
9	lnc-FAM75A6-6	chr9:43830636-43831108	NONHSAT131365
10	lnc-FAM75A6-5	chr9:43802781-43803039	NONHSAT131363
11	lnc-FAM75A6-6	chr9:43833702-43835037	NONHSAT131365
12	lnc-FAM75A6-2	chr9:44182692-44183417	XLOC_007697
13	lnc-ANKRD20A3-13	chr9:43628634-43628694	NONHSAT131362
14	lnc-FAM75A6-3	chr9:44256189-44256817	ENSG00000233424
15	lnc-FAM75A6-2	chr9:44181550-44181732	XLOC_007697
16	lnc-RP11-160N1.10.1-8	chr9:43822729-43822779	NONHSAT131364
17	lnc-ANKRD20A3-13	chr9:43627769-43628378	NONHSAT131362
18	lnc-RP11-160N1.10.1-8	chr9:43875989-43876034	NONHSAT131364
19	lnc-FAM75A6-1	chr9:44136621-44137011	XLOC_007696
20	lnc-RP11-160N1.10.1-8	chr9:43844144-43844200	NONHSAT131364
21	lnc-FAM75A6-8	chr9:44075932-44076173	NONHSAT131372
22	lnc-RP11-160N1.10.1-8	chr9:43828157-43828221	NONHSAT131364
23	lnc-RP11-160N1.10.1-8	chr9:43853497-43853563	NONHSAT131364
24	lnc-RP11-160N1.10.1-8	chr9:43861003-43861206	NONHSAT131364
25	lnc-RP11-160N1.10.1-8	chr9:43822613-43822699	NONHSAT131364
26	lnc-FAM75A6-3	chr9:44260052-44260139	ENSG00000233424
27	lnc-FAM75A6-3	chr9:44260422-44263319	ENSG00000233424

No data

Variant related genes	Relation type
ENSG00000204818	TF binding region
ENSG00000237207	TF binding region
ENSG00000229079	TF binding region
MEP1AP4	TF binding region
ENSG00000239986	TF binding region
CYP4F60P	TF binding region
ENSG00000170165	TF binding region
ENSG00000233424	TF binding region
ENSG00000270909	TF binding region
SNX18P5	TF binding region
SPATA31A6	TF binding region
ANKRD20A7P	TF binding region
RNU6-599P	TF binding region
CNN2P4	TF binding region
RN7SL343P	TF binding region
CNTNAP3B	TF binding region
ENSG00000204818	CpG island
ENSG00000237207	CpG island
ENSG00000229079	CpG island
MEP1AP4	CpG island
ENSG00000239986	CpG island
CYP4F60P	CpG island
ENSG00000170165	CpG island
ENSG00000233424	CpG island
ENSG00000270909	CpG island
SNX18P5	CpG island
SPATA31A6	CpG island
ANKRD20A7P	CpG island
RNU6-599P	CpG island
CNN2P4	CpG island
RN7SL343P	CpG island
CNTNAP3B	CpG island
ZBTB39	miRNA target sites

Extended variants
information (count: 8705 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:8705 , 50 per page) page: 1 2 3 4 5 6 7 ... 175

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562213416	chr9:43505860-43505861	Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532778293	chr9:43505861-43505862	Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs201029569	chr9:43505868-43505869	Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs530586204	chr9:43505931-43505932	Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551122579	chr9:43505941-43505942	Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560069980	chr9:43505948-43505949	Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs79489161	chr9:43505972-43505973	Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs149226679	chr9:43505978-43505979	Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549249836	chr9:43506074-43506075	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs567478166	chr9:43506076-43506077	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537992541	chr9:43506142-43506143	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545906192	chr9:43506144-43506145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571804394	chr9:43506147-43506148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181949828	chr9:43506150-43506151	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553925720	chr9:43506159-43506160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs572397507	chr9:43506166-43506167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs564005224	chr9:43506174-43506175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368357261	chr9:43506195-43506196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536555993	chr9:43506201-43506202	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183788524	chr9:43506203-43506204	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143020621	chr9:43506204-43506205	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs377303187	chr9:43506236-43506237	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148185048	chr9:43506266-43506267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565119859	chr9:43506291-43506292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546178759	chr9:43506339-43506340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs368241236	chr9:43506374-43506375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577344730	chr9:43506421-43506422	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374560196	chr9:43506425-43506426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112993889	chr9:43506468-43506469	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566077948	chr9:43506506-43506507	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545082326	chr9:43506518-43506519	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530329211	chr9:43506564-43506565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559931911	chr9:43506577-43506578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201392414	chr9:43506619-43506620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs527242887	chr9:43506660-43506661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548431617	chr9:43506695-43506696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561132228	chr9:43506707-43506708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs62555073	chr9:43506721-43506722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531622712	chr9:43506857-43506858	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs550030462	chr9:43506880-43506881	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs146945234	chr9:43506893-43506894	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs538798831	chr9:43506917-43506918	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs368841313	chr9:43506935-43506936	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs547831735	chr9:43506972-43506973	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs565946168	chr9:43506973-43506974	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs536624876	chr9:43506979-43506980	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs111966207	chr9:43506986-43506987	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs554856305	chr9:43506995-43506996	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs200749735	chr9:43507019-43507020	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs372724947	chr9:43507097-43507098	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Schizophrenia	20967226	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:597 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:43505400-43506000	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr9:43505400-43506400	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr9:43505400-43507000	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr9:43505600-43506000	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr9:43505600-43506000	Genic enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr9:43505600-43506200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr9:43505600-43507000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr9:43505800-43506000	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr9:43505800-43506200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr9:43506000-43506200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr9:43506000-43506800	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr9:43506000-43506800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr9:43506200-43506800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr9:43506400-43506800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr9:43506800-43507000	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr9:43506800-43507200	Active TSS	iPS-18 Cell Line	embryonic stem cell
17	chr9:43506800-43507400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr9:43506800-43507400	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr9:43507000-43507400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
20	chr9:43507000-43507400	Active TSS	iPS-20b Cell Line	embryonic stem cell
21	chr9:43507000-43508400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr9:43507200-43507400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
23	chr9:43507400-43507600	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr9:43507400-43508200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr9:43507400-43508200	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr9:43507600-43508000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr9:43507600-43508000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr9:43508000-43508800	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr9:43508200-43508600	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr9:43508200-43508800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr9:43508400-43508600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr9:43508600-43508800	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr9:43508800-43509800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr9:43509800-43510000	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr9:43581000-43583400	Active TSS	A549	lung
36	chr9:43581200-43581600	Enhancers	HUVEC	blood vessel
37	chr9:43581200-43582200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr9:43581600-43582800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr9:43582200-43582600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr9:43582400-43582800	Enhancers	Fetal Brain Male	brain
41	chr9:43582600-43583000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr9:43588400-43589000	Enhancers	HUVEC	blood vessel
43	chr9:43589000-43590200	Weak transcription	HUVEC	blood vessel
44	chr9:43590200-43590800	Enhancers	HUVEC	blood vessel
45	chr9:43590800-43593800	Weak transcription	HUVEC	blood vessel
46	chr9:43593800-43595000	Enhancers	HUVEC	blood vessel
47	chr9:43594200-43594600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr9:43594200-43595000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr9:43609400-43609800	Enhancers	HUVEC	blood vessel
50	chr9:43684200-43685200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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