Variant report

Variant	nsv533545
Chromosome Location	chr9:43386522-43686949
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:743)
CpG islands
(count:183)
Chromatin interactive
region (count:0)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:743 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

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	BACH1	chr9:43456004-43456520	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr9:43418592-43418991	GM12878	blood:	n/a	chr9:43418699-43418707
5	BATF	chr9:43391498-43391789	GM12878	blood:	n/a	n/a
6	BATF	chr9:43393256-43393475	GM12878	blood:	n/a	n/a
7	BATF	chr9:43445858-43446598	GM12878	blood:	n/a	n/a
8	BATF	chr9:43653838-43653993	GM12878	blood:	n/a	n/a
9	BATF	chr9:43529040-43529422	GM12878	blood:	n/a	n/a
10	BATF	chr9:43391601-43391805	GM12878	blood:	n/a	n/a
11	BATF	chr9:43392171-43392418	GM12878	blood:	n/a	n/a
12	BATF	chr9:43393230-43393466	GM12878	blood:	n/a	n/a
13	BATF	chr9:43397934-43398253	GM12878	blood:	n/a	n/a
14	BATF	chr9:43418541-43419033	GM12878	blood:	n/a	chr9:43418699-43418707
15	BATF	chr9:43397875-43398296	GM12878	blood:	n/a	n/a
16	BATF	chr9:43446919-43447105	GM12878	blood:	n/a	n/a
17	BATF	chr9:43488473-43488768	GM12878	blood:	n/a	chr9:43488642-43488653
18	BATF	chr9:43445830-43446625	GM12878	blood:	n/a	n/a
19	BCL11A	chr9:43392237-43392400	GM12878	blood:	n/a	n/a
20	BCL11A	chr9:43445830-43446611	GM12878	blood:	n/a	n/a
21	BCL11A	chr9:43432708-43432921	GM12878	blood:	n/a	n/a
22	BCL11A	chr9:43393221-43393463	GM12878	blood:	n/a	n/a
23	BCL11A	chr9:43397937-43398236	GM12878	blood:	n/a	n/a
24	BCL11A	chr9:43418681-43418913	GM12878	blood:	n/a	n/a
25	BCL11A	chr9:43445889-43446516	GM12878	blood:	n/a	n/a
26	BCL11A	chr9:43446717-43446938	GM12878	blood:	n/a	n/a
27	BCL11A	chr9:43415815-43416061	GM12878	blood:	n/a	n/a
28	BHLHE40	chr9:43505744-43505995	A549	lung:	n/a	n/a
29	CEBPB	chr9:43475810-43476027	IMR90	lung:	n/a	chr9:43475938-43475951 chr9:43475938-43475951
30	CEBPB	chr9:43686226-43687047	A549	lung:	n/a	chr9:43686435-43686447
31	CEBPB	chr9:43475824-43476024	A549	lung:	n/a	chr9:43475938-43475951 chr9:43475938-43475951
32	CTCF	chr9:43653760-43653910	GM12865	blood:	n/a	n/a
33	CTCF	chr9:43686500-43686650	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr9:43594301-43594313	NHEK	skin:	n/a	n/a
35	CTCF	chr9:43653760-43653910	GM12874	blood:	n/a	n/a
36	CTCF	chr9:43653825-43653977	Kidney_OC	kidney:	n/a	chr9:43653906-43653927 chr9:43653907-43653920 chr9:43653904-43653922 chr9:43653905-43653921 chr9:43653909-43653919
37	CTCF	chr9:43392340-43392490	GM12864	blood:	n/a	n/a
38	CTCF	chr9:43684713-43685132	K562	blood:	n/a	chr9:43684809-43684822 chr9:43684811-43684819
39	CTCF	chr9:43497957-43498272	A549	lung:	n/a	chr9:43498167-43498185
40	CTCF	chr9:43498080-43498230	A549	lung:	n/a	chr9:43498167-43498185
41	CTCF	chr9:43686499-43687160	A549	lung:	n/a	chr9:43686883-43686904 chr9:43686882-43686898
42	CTCF	chr9:43392306-43392390	GM12878	blood:	n/a	n/a
43	CTCF	chr9:43653832-43653982	K562	blood:	n/a	chr9:43653906-43653927 chr9:43653907-43653920 chr9:43653904-43653922 chr9:43653905-43653921 chr9:43653909-43653919
44	CTCF	chr9:43392155-43392488	K562	blood:	n/a	n/a
45	CTCF	chr9:43392360-43392510	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr9:43498040-43498190	HCFaa	heart:	n/a	chr9:43498167-43498185
47	CTCF	chr9:43658422-43658478	GM13976	blood:	n/a	n/a
48	CTCF	chr9:43392380-43392530	GM12873	blood:	n/a	n/a
49	CTCF	chr9:43392320-43392470	GM06990	blood:	n/a	n/a
50	CTCF	chr9:43498095-43498221	Hela-S3	cervix:	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	GM19239	blood:	n/a
2	chr9:43525320-43525370	SK-N-MC	brain:	n/a
3	chr9:43525320-43525370	U87	brain:	n/a
4	chr9:43525320-43525370	HEEpiC	esophagus:	n/a
5	chr9:43525948-43525998	HL-60	blood:	n/a
6	chr9:43631161-43631211	ProgFib	skin:	n/a
7	chr9:43631161-43631211	IMR90	lung:	fetal
8	chr9:43631161-43631211	HCF	heart:	n/a
9	chr9:43525948-43525998	HCT-116	colon:	n/a
10	chr9:43525948-43525998	GM06990	blood:	n/a
11	chr9:43631161-43631211	SK-N-SH	brain:	n/a
12	chr9:43525320-43525370	K562	blood:	n/a
13	chr9:43525948-43525998	HRE	kidney:	n/a
14	chr9:43525948-43525998	GM12878	blood:	n/a
15	chr9:43525320-43525370	Caco-2	colon:	n/a
16	chr9:43631161-43631211	RPTEC	kidney:	n/a
17	chr9:43525320-43525370	HCPEpiC	choroid plexus:	n/a
18	chr9:43525948-43525998	HMEC	breast:	n/a
19	chr9:43631161-43631211	AG10803	skin:	n/a
20	chr9:43525948-43525998	A549	lung:	n/a
21	chr9:43525948-43525998	PFSK-1	brain:	n/a
22	chr9:43631161-43631211	MCF-7	breast:	n/a
23	chr9:43525948-43525998	Jurkat	blood:	n/a
24	chr9:43525320-43525370	IMR90	lung:	fetal
25	chr9:43525320-43525370	CMK	blood:	n/a
26	chr9:43525320-43525370	SKMC	muscle:	n/a
27	chr9:43525948-43525998	HCM	heart:	n/a
28	chr9:43631161-43631211	HCPEpiC	choroid plexus:	n/a
29	chr9:43631161-43631211	ovcar-3	ovarian:	n/a
30	chr9:43525320-43525370	HRE	kidney:	n/a
31	chr9:43525948-43525998	U87	brain:	n/a
32	chr9:43525320-43525370	H1-hESC	embryonic stem cell:	embryo
33	chr9:43631161-43631211	ECC-1	luminal epithelium:	n/a
34	chr9:43525320-43525370	HAEpiC	amniotic membrane:	n/a
35	chr9:43525320-43525370	HEK293	kidney:	embryo
36	chr9:43631161-43631211	NH-A	brain:	n/a
37	chr9:43631161-43631211	PANC-1	pancreas:	n/a
38	chr9:43525948-43525998	HepG2	liver:	n/a
39	chr9:43525320-43525370	HNPCEpiC	eye:	n/a
40	chr9:43525320-43525370	ovcar-3	ovarian:	n/a
41	chr9:43525320-43525370	MCF10A-Er-Src	breast:	n/a
42	chr9:43525320-43525370	SK-N-SH	brain:	n/a
43	chr9:43525320-43525370	HL-60	blood:	n/a
44	chr9:43631161-43631211	LNCaP	prostate:	n/a
45	chr9:43525320-43525370	Hela-S3	cervix:	n/a
46	chr9:43525320-43525370	AG09309	skin:	n/a
47	chr9:43631161-43631211	AG04449	skin:	fetal
48	chr9:43525320-43525370	HepG2	liver:	n/a
49	chr9:43525320-43525370	HIPEpiC	eye:	n/a
50	chr9:43525948-43525998	HCF	heart:	n/a

No data

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNTNAP3B-6	chr9:43399987-43401315	NONHSAT131358
2	lnc-ANKRD20A3-13	chr9:43627769-43628378	NONHSAT131362
3	lnc-ANKRD20A3-13	chr9:43628634-43628694	NONHSAT131362
4	lnc-CNTNAP3B-2	chr9:43617727-43618056	NONHSAT131361
5	lnc-ANKRD20A3-13	chr9:43629020-43629117	NONHSAT131362
6	lnc-CNTNAP3B-5	chr9:43403148-43403646	NONHSAT131359

No data

Variant related genes	Relation type
ENSG00000239986	TF binding region
ENSG00000223512	TF binding region
ENSG00000269474	TF binding region
ATP5A1P5	TF binding region
SPATA31A6	TF binding region
CNTNAP3B	TF binding region
ENSG00000239986	CpG island
ENSG00000223512	CpG island
ENSG00000269474	CpG island
ATP5A1P5	CpG island
SPATA31A6	CpG island
CNTNAP3B	CpG island

Extended variants
information (count: 2563 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2563 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149231140	chr9:43396426-43396427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs587609276	chr9:43396453-43396454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs587682828	chr9:43396500-43396501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs587764438	chr9:43396512-43396513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187673239	chr9:43396523-43396524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs587717386	chr9:43396529-43396530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs587727299	chr9:43396547-43396548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs191968618	chr9:43396572-43396573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs587680295	chr9:43396602-43396603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs587756731	chr9:43396603-43396604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs587656849	chr9:43396625-43396626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs143023934	chr9:43396635-43396636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs587770334	chr9:43396637-43396638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs4961788	chr9:43396655-43396656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs3007473	chr9:43396678-43396679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185734020	chr9:43396697-43396698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs587722703	chr9:43396701-43396702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs587601059	chr9:43396704-43396705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs587645517	chr9:43396717-43396718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs587710612	chr9:43396753-43396754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs375080471	chr9:43396755-43396756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs587684617	chr9:43396759-43396760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs587762435	chr9:43396765-43396766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs587614963	chr9:43396768-43396769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs587692696	chr9:43396771-43396772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs587724038	chr9:43396793-43396794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs587625723	chr9:43396840-43396841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs75769817	chr9:43396852-43396853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs4961872	chr9:43396853-43396854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs587737108	chr9:43396867-43396868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs587636450	chr9:43396875-43396876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs587690014	chr9:43396879-43396880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs372369939	chr9:43396902-43396903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs4246160	chr9:43396938-43396939	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs4246161	chr9:43396940-43396941	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs587750497	chr9:43396947-43396948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs11261848	chr9:43396957-43396958	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs200653208	chr9:43396959-43396960	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs199977370	chr9:43396964-43396965	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs587652282	chr9:43396972-43396973	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs188651557	chr9:43396987-43396988	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs5002504	chr9:43396993-43396994	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs141709357	chr9:43396995-43396996	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs4961873	chr9:43397019-43397020	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs587737738	chr9:43397044-43397045	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs587596595	chr9:43397055-43397056	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs12336916	chr9:43397089-43397090	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs587690657	chr9:43397116-43397117	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs587704406	chr9:43397132-43397133	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs587600147	chr9:43397136-43397137	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Lung cancer	17086460	CNVD
Rhabdomyosarcoma	16790082	CNVD

Chromatin state (count:272 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:43396400-43399000	Enhancers	Primary B cells from peripheral blood	blood
2	chr9:43399000-43400000	Weak transcription	Primary B cells from peripheral blood	blood
3	chr9:43400000-43400200	Enhancers	Primary B cells from peripheral blood	blood
4	chr9:43400600-43401000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr9:43400800-43401000	Enhancers	Osteobl	bone
6	chr9:43401000-43401600	Weak transcription	Osteobl	bone
7	chr9:43401600-43402400	Enhancers	Osteobl	bone
8	chr9:43433600-43433800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
9	chr9:43441400-43441800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr9:43445600-43446600	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr9:43445600-43446600	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr9:43445800-43446200	Enhancers	Osteobl	bone
13	chr9:43445800-43446600	Enhancers	A549	lung
14	chr9:43446000-43446600	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr9:43450400-43450800	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr9:43450800-43454000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr9:43451600-43452000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr9:43451600-43452600	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr9:43451600-43453400	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr9:43452400-43452600	Enhancers	H1 Cell Line	embryonic stem cell
21	chr9:43452600-43453000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr9:43452600-43453200	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr9:43452600-43454000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr9:43452600-43455400	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr9:43452800-43453000	Enhancers	H9 Cell Line	embryonic stem cell
26	chr9:43453200-43453400	Weak transcription	Primary neutrophils fromperipheralblood	blood
27	chr9:43453400-43453800	Active TSS	Monocytes-CD14+_RO01746	blood
28	chr9:43453400-43454200	Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr9:43453400-43454400	Active TSS	Primary neutrophils fromperipheralblood	blood
30	chr9:43453600-43454000	Active TSS	H9 Cell Line	embryonic stem cell
31	chr9:43453600-43454000	Active TSS	Fetal Brain Female	brain
32	chr9:43453600-43454200	Active TSS	HUES48 Cell Line	embryonic stem cell
33	chr9:43454000-43454400	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr9:43454000-43456800	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr9:43454200-43454400	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr9:43454200-43454400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr9:43454400-43454600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
38	chr9:43454400-43454600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
39	chr9:43454400-43455400	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr9:43454400-43455400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr9:43454400-43455400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr9:43454600-43456800	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr9:43455400-43455600	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr9:43455400-43455800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
45	chr9:43455400-43455800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr9:43455400-43455800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr9:43455400-43456000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr9:43455400-43456000	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr9:43455400-43456200	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr9:43455400-43457000	Enhancers	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links