Variant report

Variant	esv3459073
Chromosome Location	chr2:209233591-209247266
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	chr2:209238240-209238613	K562	blood:	n/a	n/a
2	ARID3A	chr2:209233745-209234164	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:209235877-209236505	K562	blood:	n/a	n/a
4	ARID3A	chr2:209238174-209238580	HepG2	liver:	n/a	n/a
5	ATF1	chr2:209235807-209236248	K562	blood:	n/a	n/a
6	BHLHE40	chr2:209235865-209236444	K562	blood:	n/a	n/a
7	CCNT2	chr2:209243607-209243784	K562	blood:	n/a	n/a
8	CCNT2	chr2:209235684-209236200	K562	blood:	n/a	n/a
9	CEBPB	chr2:209235790-209236138	K562	blood:	n/a	n/a
10	CEBPB	chr2:209238250-209238569	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr2:209233734-209234186	Hela-S3	cervix:	n/a	chr2:209233922-209233933
12	CEBPB	chr2:209233870-209234062	HepG2	liver:	n/a	chr2:209233922-209233933
13	CEBPB	chr2:209234443-209234834	IMR90	lung:	n/a	n/a
14	CEBPB	chr2:209233738-209234200	HepG2	liver:	n/a	chr2:209233922-209233933
15	CEBPB	chr2:209233827-209234132	A549	lung:	n/a	chr2:209233922-209233933
16	CEBPB	chr2:209233720-209234122	A549	lung:	n/a	chr2:209233922-209233933
17	CEBPB	chr2:209233813-209234182	IMR90	lung:	n/a	chr2:209233922-209233933
18	CEBPB	chr2:209233818-209234101	HepG2	liver:	n/a	chr2:209233922-209233933
19	CEBPB	chr2:209233800-209234152	MCF-7	breast:	n/a	chr2:209233922-209233933
20	CEBPB	chr2:209233797-209234153	A549	lung:	n/a	chr2:209233922-209233933
21	CEBPB	chr2:209235768-209236174	K562	blood:	n/a	n/a
22	CEBPB	chr2:209233774-209234153	MCF-7	breast:	n/a	chr2:209233922-209233933
23	CEBPD	chr2:209235812-209236227	K562	blood:	n/a	n/a
24	CEBPD	chr2:209235741-209236189	K562	blood:	n/a	n/a
25	CREB1	chr2:209235820-209236371	K562	blood:	n/a	n/a
26	CTCF	chr2:209238300-209238450	GM12869	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
27	CTCF	chr2:209238208-209238541	SK-N-SH_RA	brain:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
28	CTCF	chr2:209238320-209238470	HA-sp	spinal cord:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
29	CTCF	chr2:209238166-209238545	T-47D	breast:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
30	CTCF	chr2:209238280-209238430	HCM	heart:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
31	CTCF	chr2:209238256-209238504	HepG2	liver:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
32	CTCF	chr2:209238300-209238450	HCFaa	heart:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
33	CTCF	chr2:209238340-209238490	NHEK	skin:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
34	CTCF	chr2:209238251-209238505	LNCaP	prostate:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
35	CTCF	chr2:209238340-209238490	K562	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
36	CTCF	chr2:209238273-209238481	GM19240	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
37	CTCF	chr2:209238320-209238470	HAc	cerebellar:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
38	CTCF	chr2:209238300-209238450	HVMF	connective:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
39	CTCF	chr2:209238240-209238390	A549	lung:	n/a	n/a
40	CTCF	chr2:209238262-209238626	HCT-116	colon:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
41	CTCF	chr2:209238320-209238470	HPF	lung:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
42	CTCF	chr2:209238256-209238500	Pancreas_OC	pancreas:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
43	CTCF	chr2:209238235-209238586	K562	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
44	CTCF	chr2:209240551-209240587	ProgFib	skin:	n/a	n/a
45	CTCF	chr2:209238300-209238450	HUVEC	blood vessel:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
46	CTCF	chr2:209237710-209237736	MCF-7	breast:	n/a	n/a
47	CTCF	chr2:209238242-209238498	ProgFib	skin:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
48	CTCF	chr2:209238082-209238602	HCT-116	colon:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
49	CTCF	chr2:209238280-209238430	HCPEpiC	choroid plexus:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
50	CTCF	chr2:209238259-209238506	Kidney_OC	kidney:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:209240193-209240243	SAEC	small airway:	n/a
2	chr2:209240193-209240243	HEEpiC	esophagus:	n/a
3	chr2:209240193-209240243	PFSK-1	brain:	n/a
4	chr2:209242596-209242646	MCF-7	breast:	n/a
5	chr2:209240193-209240243	GM06990	blood:	n/a
6	chr2:209240193-209240243	Jurkat	blood:	n/a
7	chr2:209240193-209240243	HAEpiC	amniotic membrane:	n/a
8	chr2:209240193-209240243	HMEC	breast:	n/a
9	chr2:209242596-209242646	BJ	skin:	n/a
10	chr2:209240193-209240243	HNPCEpiC	eye:	n/a
11	chr2:209242596-209242646	NT2-D1	testis:	n/a
12	chr2:209240193-209240243	Hela-S3	cervix:	n/a
13	chr2:209242596-209242646	A549	lung:	n/a
14	chr2:209242596-209242646	ovcar-3	ovarian:	n/a
15	chr2:209240193-209240243	NHBE	bronchial:	n/a
16	chr2:209242596-209242646	GM12891	blood:	n/a
17	chr2:209240193-209240243	PrEC	prostate:	n/a
18	chr2:209240193-209240243	RPTEC	kidney:	n/a
19	chr2:209242596-209242646	SK-N-SH_RA	brain:	n/a
20	chr2:209242596-209242646	IMR90	lung:	fetal
21	chr2:209242596-209242646	U87	brain:	n/a
22	chr2:209240193-209240243	BJ	skin:	n/a
23	chr2:209242596-209242646	AG10803	skin:	n/a
24	chr2:209242596-209242646	NHBE	bronchial:	n/a
25	chr2:209242596-209242646	HMEC	breast:	n/a
26	chr2:209242596-209242646	HCM	heart:	n/a
27	chr2:209240193-209240243	GM12891	blood:	n/a
28	chr2:209240193-209240243	A549	lung:	n/a
29	chr2:209242596-209242646	HCPEpiC	choroid plexus:	n/a
30	chr2:209240193-209240243	NB4	blood:	n/a
31	chr2:209240193-209240243	AoSMC	blood vessel:	n/a
32	chr2:209242596-209242646	HL-60	blood:	n/a
33	chr2:209240193-209240243	CMK	blood:	n/a
34	chr2:209242596-209242646	AG04449	skin:	fetal
35	chr2:209240193-209240243	BE2_C	brain:	n/a
36	chr2:209242596-209242646	PFSK-1	brain:	n/a
37	chr2:209242596-209242646	HAEpiC	amniotic membrane:	n/a
38	chr2:209240193-209240243	HEK293	kidney:	embryo
39	chr2:209242596-209242646	AG09309	skin:	n/a
40	chr2:209242596-209242646	PrEC	prostate:	n/a
41	chr2:209240193-209240243	HCPEpiC	choroid plexus:	n/a
42	chr2:209242596-209242646	HCT-116	colon:	n/a
43	chr2:209240193-209240243	AG09309	skin:	n/a
44	chr2:209242596-209242646	AG09319	gingival:	n/a
45	chr2:209242596-209242646	GM06990	blood:	n/a
46	chr2:209240193-209240243	HIPEpiC	eye:	n/a
47	chr2:209242596-209242646	HUVEC	blood vessel:	n/a
48	chr2:209242596-209242646	Hepatocyte	liver:	n/a
49	chr2:209240193-209240243	HRE	kidney:	n/a
50	chr2:209240193-209240243	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:209244985..209246550-chr2:209250823..209252697,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000265454	TF binding region
ENSG00000265454	CpG island

Extended variants
information (count: 476 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:476 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116725194	chr2:209233630-209233631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs555630190	chr2:209233639-209233640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571178518	chr2:209233658-209233659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183648896	chr2:209233672-209233673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs143063982	chr2:209233685-209233686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs576440023	chr2:209233686-209233687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535566596	chr2:209233706-209233707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs555874210	chr2:209233718-209233719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs575867910	chr2:209233728-209233729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs572328092	chr2:209233759-209233760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs151199718	chr2:209233877-209233878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs13390265	chr2:209233915-209233916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140255856	chr2:209233934-209233935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs150377282	chr2:209233968-209233969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs372341092	chr2:209233975-209233976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs59863990	chr2:209233992-209233993	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs138201838	chr2:209234024-209234025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs531582310	chr2:209234060-209234061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs34110985	chr2:209234092-209234093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs373090197	chr2:209234093-209234094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs199954817	chr2:209234095-209234096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190201476	chr2:209234152-209234153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs143045831	chr2:209234178-209234179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs182600581	chr2:209234184-209234185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186729580	chr2:209234185-209234186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs551448386	chr2:209234325-209234326	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs550488892	chr2:209234335-209234336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs7590641	chr2:209234337-209234338	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs536074686	chr2:209234341-209234342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555564019	chr2:209234352-209234353	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs572517970	chr2:209234387-209234388	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs13003574	chr2:209234420-209234421	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs190382792	chr2:209234527-209234528	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs571401583	chr2:209234548-209234549	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs138419944	chr2:209234576-209234577	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs557939800	chr2:209234583-209234584	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs181206095	chr2:209234605-209234606	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs7604977	chr2:209234616-209234617	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs35549934	chr2:209234641-209234642	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs185584864	chr2:209234692-209234693	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs28386802	chr2:209234694-209234695	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs190300495	chr2:209234738-209234739	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs562389356	chr2:209234892-209234893	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs540984157	chr2:209234895-209234896	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs564060012	chr2:209234897-209234898	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs533002145	chr2:209234906-209234907	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs182113273	chr2:209234927-209234928	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs529298816	chr2:209234928-209234929	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs372965514	chr2:209234934-209234935	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs529431700	chr2:209234943-209234944	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	CNVD
Renal cell carcinoma	18765545	CNVD
Ovarian cancer	19193619	CNVD
Non-small cell lung cancer	18676828	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Urothelial cell carcinoma	18451213	CNVD
Acute lymphoblastic leukemia	22237106	CNVD

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209220200-209235200	Weak transcription	K562	blood
2	chr2:209224800-209234200	Weak transcription	Placenta	Placenta
3	chr2:209226000-209234200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr2:209228800-209234000	Weak transcription	Osteobl	bone
5	chr2:209229200-209234600	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr2:209233000-209234400	Enhancers	Liver	Liver
7	chr2:209233000-209240200	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr2:209233200-209234800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr2:209233400-209236600	Enhancers	HepG2	liver
10	chr2:209233800-209236600	Enhancers	NHDF-Ad	bronchial
11	chr2:209234000-209234400	Enhancers	Adipose Nuclei	Adipose
12	chr2:209234000-209236000	Weak transcription	Pancreas	Pancrea
13	chr2:209234000-209236200	Enhancers	Osteobl	bone
14	chr2:209234000-209236600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr2:209234200-209234800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr2:209234200-209235000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr2:209234200-209235000	Enhancers	Placenta	Placenta
18	chr2:209234200-209236200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr2:209234400-209234800	Flanking Active TSS	Liver	Liver
20	chr2:209234600-209234800	Enhancers	Muscle Satellite Cultured Cells	--
21	chr2:209234600-209234800	Enhancers	NH-A	brain
22	chr2:209234800-209235200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr2:209234800-209235400	Active TSS	Liver	Liver
24	chr2:209234800-209235800	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr2:209235000-209235800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr2:209235200-209236400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr2:209235200-209236600	Enhancers	K562	blood
28	chr2:209235400-209236200	Flanking Active TSS	Liver	Liver
29	chr2:209235800-209236000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr2:209235800-209236000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr2:209235800-209236000	Enhancers	Muscle Satellite Cultured Cells	--
32	chr2:209235800-209236000	Enhancers	HSMM	muscle
33	chr2:209236000-209240200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr2:209238600-209238800	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr2:209238800-209240000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr2:209239000-209241600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr2:209239800-209241600	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr2:209240000-209240400	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr2:209240000-209241000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
40	chr2:209240000-209241200	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr2:209240000-209241400	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr2:209240000-209241400	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr2:209240000-209241600	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr2:209240200-209240800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr2:209240200-209241000	Enhancers	H1 Cell Line	embryonic stem cell
46	chr2:209240200-209241000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr2:209240200-209241000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr2:209240200-209241000	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr2:209240400-209240800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr2:209240400-209241200	Enhancers	HUES6 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links