Variant report

Variant	nsv525747
Chromosome Location	chr2:209087335-209116753
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:311)
CpG islands
(count:183)
Chromatin interactive
region (count:32)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:311 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:209087199-209087560	K562	blood:	n/a	n/a
2	ARID3A	chr2:209111812-209112156	HepG2	liver:	n/a	n/a
3	ATF1	chr2:209087055-209087498	K562	blood:	n/a	n/a
4	ATF3	chr2:209087130-209087430	K562	blood:	n/a	n/a
5	BACH1	chr2:209115059-209115138	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr2:209099914-209100373	A549	lung:	n/a	n/a
7	BHLHE40	chr2:209087239-209087419	K562	blood:	n/a	n/a
8	CCNT2	chr2:209112875-209112995	K562	blood:	n/a	n/a
9	CEBPB	chr2:209110532-209110860	A549	lung:	n/a	chr2:209110668-209110679
10	CEBPB	chr2:209115102-209115453	HepG2	liver:	n/a	chr2:209115280-209115291
11	CEBPB	chr2:209110601-209110842	K562	blood:	n/a	chr2:209110668-209110679
12	CEBPB	chr2:209115102-209115457	A549	lung:	n/a	chr2:209115280-209115291
13	CEBPB	chr2:209115208-209115417	K562	blood:	n/a	chr2:209115280-209115291
14	CEBPB	chr2:209105438-209105722	HepG2	liver:	n/a	n/a
15	CEBPB	chr2:209086994-209087575	HCT-116	colon:	n/a	chr2:209087453-209087470
16	CEBPB	chr2:209090419-209090517	HepG2	liver:	n/a	chr2:209090459-209090470
17	CEBPB	chr2:209115093-209115513	MCF-7	breast:	n/a	chr2:209115280-209115291
18	CEBPB	chr2:209110506-209110821	Hela-S3	cervix:	n/a	chr2:209110668-209110679
19	CEBPB	chr2:209115158-209115365	HepG2	liver:	n/a	chr2:209115280-209115291
20	CEBPB	chr2:209115073-209115443	IMR90	lung:	n/a	chr2:209115280-209115291
21	CEBPB	chr2:209086952-209087445	K562	blood:	n/a	n/a
22	CEBPB	chr2:209111879-209112234	HepG2	liver:	n/a	chr2:209112058-209112069
23	CEBPB	chr2:209113891-209115695	Hela-S3	cervix:	n/a	chr2:209115280-209115291
24	CEBPB	chr2:209115060-209115548	MCF-7	breast:	n/a	chr2:209115280-209115291
25	CEBPB	chr2:209110530-209110863	HepG2	liver:	n/a	chr2:209110668-209110679
26	CEBPB	chr2:209105464-209105801	MCF-7	breast:	n/a	n/a
27	CEBPD	chr2:209115159-209115340	HepG2	liver:	n/a	n/a
28	CHD2	chr2:209099915-209100298	HepG2	liver:	n/a	n/a
29	CHD2	chr2:209104715-209104895	HepG2	liver:	n/a	n/a
30	CTCF	chr2:209106360-209106510	HFF-Myc	foreskin:	n/a	n/a
31	CTCF	chr2:209091692-209091779	GM13976	blood:	n/a	n/a
32	CTCF	chr2:209108332-209108352	Medullo	brain:	n/a	n/a
33	CTCF	chr2:209098063-209098127	GM13977	blood:	n/a	n/a
34	CTCF	chr2:209108260-209108410	A549	lung:	n/a	n/a
35	E2F4	chr2:209110646-209110846	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr2:209115090-209115311	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr2:209106978-209107171	MCF10A-Er-Src	breast:	n/a	n/a
38	ELK4	chr2:209114571-209114848	Hela-S3	cervix:	n/a	n/a
39	EP300	chr2:209115087-209115456	Hela-S3	cervix:	n/a	n/a
40	EP300	chr2:209114086-209114690	Hela-S3	cervix:	n/a	chr2:209114105-209114115 chr2:209114330-209114340 chr2:209114589-209114598
41	EP300	chr2:209093297-209093403	K562	blood:	n/a	chr2:209093358-209093372
42	EP300	chr2:209111668-209112248	HepG2	liver:	n/a	n/a
43	EP300	chr2:209087244-209087550	K562	blood:	n/a	n/a
44	EP300	chr2:209093368-209093469	GM12878	blood:	n/a	n/a
45	EP300	chr2:209089428-209089994	ECC-1	luminal epithelium:	n/a	n/a
46	EP300	chr2:209089159-209090178	ECC-1	luminal epithelium:	n/a	chr2:209089208-209089222
47	FOS	chr2:209115044-209115418	MCF10A-Er-Src	breast:	n/a	chr2:209115220-209115232
48	FOS	chr2:209089619-209089831	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr2:209087141-209087503	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr2:209089588-209089861	MCF10A-Er-Src	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:209092738-209092788	AG09309	skin:	n/a
2	chr2:209092738-209092788	ovcar-3	ovarian:	n/a
3	chr2:209116254-209116304	GM12891	blood:	n/a
4	chr2:209092738-209092788	K562	blood:	n/a
5	chr2:209092738-209092788	HL-60	blood:	n/a
6	chr2:209092738-209092788	AoSMC	blood vessel:	n/a
7	chr2:209116254-209116304	AG04450	lung:	fetal
8	chr2:209101221-209101271	HL-60	blood:	n/a
9	chr2:209116254-209116304	HEEpiC	esophagus:	n/a
10	chr2:209101221-209101271	HCM	heart:	n/a
11	chr2:209092738-209092788	HRPEpiC	eye:	n/a
12	chr2:209092738-209092788	HPAEpiC	pulmonary alveolar:	n/a
13	chr2:209116254-209116304	HIPEpiC	eye:	n/a
14	chr2:209092738-209092788	AG04450	lung:	fetal
15	chr2:209101221-209101271	HEEpiC	esophagus:	n/a
16	chr2:209116254-209116304	HMEC	breast:	n/a
17	chr2:209092738-209092788	SKMC	muscle:	n/a
18	chr2:209101221-209101271	Jurkat	blood:	n/a
19	chr2:209101221-209101271	ECC-1	luminal epithelium:	n/a
20	chr2:209116254-209116304	ProgFib	skin:	n/a
21	chr2:209101221-209101271	H1-hESC	embryonic stem cell:	embryo
22	chr2:209116254-209116304	GM12892	blood:	n/a
23	chr2:209092738-209092788	GM12891	blood:	n/a
24	chr2:209101221-209101271	HRE	kidney:	n/a
25	chr2:209116254-209116304	AoSMC	blood vessel:	n/a
26	chr2:209101221-209101271	PFSK-1	brain:	n/a
27	chr2:209092738-209092788	NT2-D1	testis:	n/a
28	chr2:209092738-209092788	HEEpiC	esophagus:	n/a
29	chr2:209116254-209116304	H1-hESC	embryonic stem cell:	embryo
30	chr2:209092738-209092788	NB4	blood:	n/a
31	chr2:209092738-209092788	HNPCEpiC	eye:	n/a
32	chr2:209116254-209116304	ECC-1	luminal epithelium:	n/a
33	chr2:209116254-209116304	SAEC	small airway:	n/a
34	chr2:209116254-209116304	HCF	heart:	n/a
35	chr2:209092738-209092788	HIPEpiC	eye:	n/a
36	chr2:209116254-209116304	HRE	kidney:	n/a
37	chr2:209101221-209101271	GM12878	blood:	n/a
38	chr2:209116254-209116304	U87	brain:	n/a
39	chr2:209116254-209116304	HRCEpiC	kidney:	n/a
40	chr2:209092738-209092788	HRE	kidney:	n/a
41	chr2:209101221-209101271	Caco-2	colon:	n/a
42	chr2:209092738-209092788	HAEpiC	amniotic membrane:	n/a
43	chr2:209116254-209116304	SK-N-SH_RA	brain:	n/a
44	chr2:209116254-209116304	SK-N-MC	brain:	n/a
45	chr2:209101221-209101271	MCF-7	breast:	n/a
46	chr2:209092738-209092788	NH-A	brain:	n/a
47	chr2:209101221-209101271	RPTEC	kidney:	n/a
48	chr2:209116254-209116304	HRPEpiC	eye:	n/a
49	chr2:209101221-209101271	SAEC	small airway:	n/a
50	chr2:209116254-209116304	HepG2	liver:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:209087250..209089681-chr2:209091533..209093570,2	MCF-7	breast:
2	chr2:209106089..209108636-chr2:209109749..209112220,2	MCF-7	breast:
3	chr2:209110703..209113505-chr2:209114518..209117084,3	K562	blood:
4	chr2:209105321..209107338-chr2:209107926..209110455,2	K562	blood:
5	chr2:209107973..209109717-chr2:209111459..209113433,2	K562	blood:
6	chr2:209101770..209103884-chr2:209108105..209109769,2	K562	blood:
7	chr2:209107973..209109717-chr2:209111459..209113433,2	K562	blood:
8	chr2:208488594..208490562-chr2:209093498..209095135,2	MCF-7	breast:
9	chr2:209106594..209109969-chr2:209113559..209115828,3	K562	blood:
10	chr2:209106594..209109969-chr2:209113559..209115828,3	K562	blood:
11	chr2:209104332..209106656-chr2:209130862..209133286,2	MCF-7	breast:
12	chr2:209105823..209107971-chr2:209113114..209114666,2	MCF-7	breast:
13	chr2:209116323..209123332-chr2:209127326..209134005,17	K562	blood:
14	chr2:209111236..209113082-chr2:209117522..209119533,2	MCF-7	breast:
15	chr2:209113508..209115266-chr2:209130064..209132288,2	MCF-7	breast:
16	chr2:209111341..209112901-chr2:209132498..209134029,2	K562	blood:
17	chr2:209094975..209096969-chr2:209118680..209120575,2	MCF-7	breast:
18	chr2:209106089..209108636-chr2:209109749..209112220,2	MCF-7	breast:
19	chr2:209101770..209103884-chr2:209108105..209109769,2	K562	blood:
20	chr2:209116323..209122695-chr2:209127326..209132568,14	K562	blood:
21	chr2:209109891..209111741-chr2:209118147..209121095,2	MCF-7	breast:
22	chr2:209095167..209097788-chr2:209102081..209104092,2	K562	blood:
23	chr2:209095167..209097788-chr2:209102081..209104092,2	K562	blood:
24	chr2:209110703..209113505-chr2:209114518..209117084,3	K562	blood:
25	chr2:209105321..209107338-chr2:209107926..209110455,2	K562	blood:
26	chr2:209105823..209107971-chr2:209113114..209114666,2	MCF-7	breast:
27	chr2:209095163..209099233-chr2:209117961..209120869,4	K562	blood:
28	chr2:209104117..209105753-chr2:209117843..209120211,2	MCF-7	breast:
29	chr2:209093824..209096542-chr2:209097199..209100673,3	K562	blood:
30	chr2:209058318..209061036-chr2:209107934..209110316,2	MCF-7	breast:
31	chr2:209109477..209111031-chr2:209118764..209120968,2	MCF-7	breast:
32	chr2:209115314..209118296-chr2:209118564..209121392,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IDH1-1	chr2:209086886-209087349	NONHSAT076633

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	IDH1	hsa-miR-30a-5p	chr2:209101662-209101656
2	IDH1	hsa-miR-30a-5p	chr2:209101688-209101709
3	IDH1	hsa-miR-30a-5p	chr2:209101657-209101678
4	IDH1	hsa-miR-30a-5p	chr2:209101749-209101743
5	IDH1	hsa-miR-30a-5p	chr2:209101744-209101765

Variant related genes	Relation type
IDH1	TF binding region
ENSG00000263524	TF binding region
IDH1-AS1	TF binding region
TPT1P2	TF binding region
IDH1	CpG island
ENSG00000263524	CpG island
IDH1-AS1	CpG island
TPT1P2	CpG island
ENSG00000263524	chromatin interactions
ENSG00000115020	chromatin interactions
ENSG00000144401	chromatin interactions
ENSG00000138413	chromatin interactions
ENSG00000231908	chromatin interactions
ENSG00000228111	chromatin interactions
DIAPH1	miRNA target sites

Extended variants
information (count: 1197 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1197 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4675743	chr2:209087335-209087336	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs372691907	chr2:209087349-209087350	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs376238929	chr2:209087356-209087357	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs562179122	chr2:209087368-209087369	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs199624939	chr2:209087373-209087374	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs527770043	chr2:209087374-209087375	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs546843979	chr2:209087375-209087376	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs117559802	chr2:209087389-209087390	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs113662193	chr2:209087410-209087411	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs113204871	chr2:209087424-209087425	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs552452831	chr2:209087451-209087452	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs111839989	chr2:209087494-209087495	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs140297467	chr2:209087506-209087507	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs112641239	chr2:209087538-209087539	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs181082726	chr2:209087565-209087566	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs185498891	chr2:209087574-209087575	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs188005435	chr2:209087607-209087608	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs112983521	chr2:209087608-209087609	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs113848923	chr2:209087615-209087616	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs533622974	chr2:209087631-209087632	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs113057019	chr2:209087654-209087655	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs553992100	chr2:209087657-209087658	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs376911825	chr2:209087704-209087705	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs113232220	chr2:209087735-209087736	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs113933197	chr2:209087754-209087755	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs577360382	chr2:209087772-209087773	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs150348866	chr2:209087816-209087817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs34199380	chr2:209087833-209087834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs376123279	chr2:209087851-209087852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs180922348	chr2:209087855-209087856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs138229929	chr2:209087916-209087917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs542276890	chr2:209087923-209087924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs111398755	chr2:209087944-209087945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs185179384	chr2:209087978-209087979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs527831939	chr2:209087984-209087985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541526615	chr2:209088002-209088003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs564529236	chr2:209088017-209088018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs111243007	chr2:209088050-209088051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs10171966	chr2:209088145-209088146	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs568142309	chr2:209088150-209088151	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs115548300	chr2:209088167-209088168	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs562819896	chr2:209088171-209088172	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs551297088	chr2:209088200-209088201	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs111673336	chr2:209088201-209088202	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs62193611	chr2:209088220-209088221	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs370943894	chr2:209088223-209088224	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs111491988	chr2:209088227-209088228	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs373669241	chr2:209088270-209088271	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs111598710	chr2:209088271-209088272	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs567717360	chr2:209088291-209088292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Breast cancer	17603634	CNVD
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
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
Glioblastoma	21080181	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
Papillary thyroid carcinoma	22161024	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	CNVD
Acute lymphoblastic leukemia	22237106	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
Pancreatic cancer	17952125	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Urothelial cell carcinoma	18451213	CNVD

Chromatin state (count:712 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209086600-209087600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr2:209086800-209087400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr2:209086800-209087600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr2:209086800-209087600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr2:209086800-209087600	Enhancers	K562	blood
6	chr2:209086800-209087600	Enhancers	NHEK	skin
7	chr2:209086800-209088200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr2:209086800-209088200	Enhancers	HMEC	breast
9	chr2:209087000-209087400	Enhancers	HSMM	muscle
10	chr2:209087000-209087600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr2:209087000-209087600	Enhancers	Osteobl	bone
12	chr2:209087000-209087800	Enhancers	Muscle Satellite Cultured Cells	--
13	chr2:209087200-209087600	Enhancers	NH-A	brain
14	chr2:209087400-209089600	Weak transcription	HSMM	muscle
15	chr2:209087400-209100000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr2:209087600-209089200	Weak transcription	Osteobl	bone
17	chr2:209087600-209089600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr2:209087600-209089600	Weak transcription	NHEK	skin
19	chr2:209087600-209103400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr2:209087800-209089200	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr2:209088200-209089200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr2:209088200-209089200	Weak transcription	HMEC	breast
23	chr2:209089200-209090000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr2:209089200-209090000	Enhancers	Muscle Satellite Cultured Cells	--
25	chr2:209089200-209090000	Enhancers	Osteobl	bone
26	chr2:209089200-209090200	Enhancers	HMEC	breast
27	chr2:209089600-209089800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr2:209089600-209090000	Enhancers	HSMM	muscle
29	chr2:209089600-209090000	Enhancers	NHEK	skin
30	chr2:209090000-209099800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr2:209090000-209103000	Weak transcription	Osteobl	bone
32	chr2:209090000-209104400	Weak transcription	NHEK	skin
33	chr2:209090200-209100600	Weak transcription	HMEC	breast
34	chr2:209091000-209102800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr2:209091400-209094000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr2:209092400-209093000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr2:209092400-209094000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr2:209092600-209093000	Enhancers	Spleen	Spleen
39	chr2:209093000-209118400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr2:209094800-209095400	Enhancers	Liver	Liver
41	chr2:209095000-209095200	Enhancers	HepG2	liver
42	chr2:209095200-209095400	Enhancers	Duodenum Mucosa	Duodenum
43	chr2:209095200-209101600	Weak transcription	HepG2	liver
44	chr2:209095400-209099000	Weak transcription	Liver	Liver
45	chr2:209095400-209101800	Weak transcription	Duodenum Mucosa	Duodenum
46	chr2:209096200-209104400	Weak transcription	HSMM	muscle
47	chr2:209096800-209097200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
48	chr2:209097000-209100000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr2:209097200-209099800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr2:209097200-209099800	Weak transcription	Sigmoid Colon	Sigmoid Colon

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