Variant report

Variant	esv3427756
Chromosome Location	chr2:233661496-233680721
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	CBX3	chr2:233667119-233667348	K562	blood:	n/a	n/a
2	CEBPB	chr2:233679886-233679925	H1-hESC	embryonic stem cell:	n/a	chr2:233679893-233679904
3	CEBPB	chr2:233679748-233680075	HepG2	liver:	n/a	chr2:233679893-233679904
4	CEBPB	chr2:233672635-233672964	HepG2	liver:	n/a	chr2:233672797-233672808
5	CEBPB	chr2:233679737-233680066	IMR90	lung:	n/a	chr2:233679893-233679904
6	CEBPB	chr2:233672709-233672949	A549	lung:	n/a	chr2:233672797-233672808
7	CTCF	chr2:233674100-233674250	HRE	kidney:	n/a	n/a
8	CTCF	chr2:233674190-233674315	Medullo	brain:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
9	CTCF	chr2:233674209-233674227	Gliobla	brain:	n/a	n/a
10	CTCF	chr2:233674118-233674319	HepG2	liver:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
11	CTCF	chr2:233674237-233674277	Pancreas_OC	pancreas:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
12	CTCF	chr2:233674140-233674290	NB4	blood:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
13	CTCF	chr2:233674170-233674323	Hela-S3	cervix:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
14	CTCF	chr2:233674240-233674390	RPTEC	kidney:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
15	CTCF	chr2:233674229-233674236	Pancreas_OC	pancreas:	n/a	n/a
16	CTCF	chr2:233678380-233678390	Kidney_OC	kidney:	n/a	n/a
17	CTCF	chr2:233674120-233674270	AG09319	gingival:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
18	CTCF	chr2:233674120-233674270	GM12870	blood:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
19	CTCF	chr2:233674164-233674339	HUVEC	blood vessel:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
20	CTCF	chr2:233674180-233674330	GM12874	blood:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
21	CTCF	chr2:233674216-233674304	GM10266	blood:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
22	CTCF	chr2:233674160-233674310	GM12873	blood:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
23	CTCF	chr2:233674179-233674285	GM12878	blood:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
24	CTCF	chr2:233674240-233674390	GM12865	blood:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
25	CTCF	chr2:233674040-233674190	RPTEC	kidney:	n/a	n/a
26	CTCF	chr2:233674207-233674228	MCF-7	breast:	n/a	n/a
27	CTCF	chr2:233674191-233674310	Spleen_OC	spleen:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
28	CTCF	chr2:233674160-233674310	HRPEpiC	eye:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
29	CTCF	chr2:233674100-233674250	HEK293	kidney:	n/a	n/a
30	CTCF	chr2:233675368-233675418	Pancreas_OC	pancreas:	n/a	n/a
31	CTCF	chr2:233674233-233674248	Gliobla	brain:	n/a	n/a
32	CTCF	chr2:233674252-233674295	LNCaP	prostate:	n/a	n/a
33	CTCF	chr2:233674200-233674350	HPAF	blood vessel:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
34	CTCF	chr2:233674179-233674281	MCF-7	breast:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
35	CTCF	chr2:233674200-233674350	SAEC	small airway:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
36	CTCF	chr2:233674160-233674310	GM12871	blood:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
37	CTCF	chr2:233674134-233674334	K562	blood:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
38	CTCF	chr2:233674160-233674310	HRE	kidney:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
39	CTCF	chr2:233674180-233674330	HCPEpiC	choroid plexus:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
40	CTCF	chr2:233674077-233674419	GM12878	blood:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
41	CTCF	chr2:233674260-233674410	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr2:233674088-233674345	A549	lung:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
43	CTCF	chr2:233674160-233674310	A549	lung:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
44	CTCF	chr2:233674219-233674293	GM13977	blood:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
45	CTCF	chr2:233662320-233662470	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr2:233674180-233674330	HVMF	connective:	n/a	chr2:233674244-233674265 chr2:233674247-233674255 chr2:233674243-233674259 chr2:233674242-233674260
47	CTCF	chr2:233675362-233675367	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr2:233674080-233674230	HMEC	breast:	n/a	n/a
49	CUX1	chr2:233671189-233671264	K562	blood:	n/a	n/a
50	CUX1	chr2:233667177-233667304	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:233680285-233680335	GM12878	blood:	n/a
2	chr2:233680285-233680335	IMR90	lung:	fetal
3	chr2:233680285-233680335	T-47D	breast:	n/a
4	chr2:233680285-233680335	GM12891	blood:	n/a
5	chr2:233680285-233680335	MCF10A-Er-Src	breast:	n/a
6	chr2:233680285-233680335	NHBE	bronchial:	n/a
7	chr2:233680285-233680335	AG09319	gingival:	n/a
8	chr2:233680285-233680335	HEEpiC	esophagus:	n/a
9	chr2:233680285-233680335	SAEC	small airway:	n/a
10	chr2:233680285-233680335	HUVEC	blood vessel:	n/a
11	chr2:233680285-233680335	SKMC	muscle:	n/a
12	chr2:233680285-233680335	HAEpiC	amniotic membrane:	n/a
13	chr2:233680285-233680335	HIPEpiC	eye:	n/a
14	chr2:233680285-233680335	AG04450	lung:	fetal
15	chr2:233680285-233680335	HRPEpiC	eye:	n/a
16	chr2:233680285-233680335	ovcar-3	ovarian:	n/a
17	chr2:233680285-233680335	SK-N-SH_RA	brain:	n/a
18	chr2:233680285-233680335	ProgFib	skin:	n/a
19	chr2:233680285-233680335	HepG2	liver:	n/a
20	chr2:233680285-233680335	Hepatocyte	liver:	n/a
21	chr2:233680285-233680335	AG10803	skin:	n/a
22	chr2:233680285-233680335	Jurkat	blood:	n/a
23	chr2:233680285-233680335	NT2-D1	testis:	n/a
24	chr2:233680285-233680335	HL-60	blood:	n/a
25	chr2:233680285-233680335	U87	brain:	n/a
26	chr2:233680285-233680335	NH-A	brain:	n/a
27	chr2:233680285-233680335	ECC-1	luminal epithelium:	n/a
28	chr2:233680285-233680335	BJ	skin:	n/a
29	chr2:233680285-233680335	HRE	kidney:	n/a
30	chr2:233680285-233680335	PANC-1	pancreas:	n/a
31	chr2:233680285-233680335	PFSK-1	brain:	n/a
32	chr2:233680285-233680335	PrEC	prostate:	n/a
33	chr2:233680285-233680335	Caco-2	colon:	n/a
34	chr2:233680285-233680335	HPAEpiC	pulmonary alveolar:	n/a
35	chr2:233680285-233680335	SK-N-SH	brain:	n/a
36	chr2:233680285-233680335	BE2_C	brain:	n/a
37	chr2:233680285-233680335	HNPCEpiC	eye:	n/a
38	chr2:233680285-233680335	HCPEpiC	choroid plexus:	n/a
39	chr2:233680285-233680335	A549	lung:	n/a
40	chr2:233680285-233680335	GM19239	blood:	n/a
41	chr2:233680285-233680335	K562	blood:	n/a
42	chr2:233680285-233680335	HMEC	breast:	n/a
43	chr2:233680285-233680335	CMK	blood:	n/a
44	chr2:233680285-233680335	NHDF-neo	bronchial:	n/a
45	chr2:233680285-233680335	HRCEpiC	kidney:	n/a
46	chr2:233680285-233680335	AoSMC	blood vessel:	n/a
47	chr2:233680285-233680335	HCT-116	colon:	n/a
48	chr2:233680285-233680335	MCF-7	breast:	n/a
49	chr2:233680285-233680335	GM06990	blood:	n/a
50	chr2:233680285-233680335	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:233670766..233673483-chr2:233675178..233677384,2	MCF-7	breast:
2	chr2:233625989..233627596-chr2:233662051..233663810,2	MCF-7	breast:
3	chr2:233422671..233424995-chr2:233680170..233682627,2	K562	blood:
4	chr2:233679964..233682809-chr2:233685559..233687469,2	MCF-7	breast:

Variant related genes	Relation type
GIGYF2	TF binding region
GIGYF2	CpG island
ENSG00000204120	chromatin interactions

Extended variants
information (count: 719 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:719 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs283467	chr2:233661526-233661527	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs567963578	chr2:233661550-233661551	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs540662511	chr2:233661569-233661570	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs560283036	chr2:233661654-233661655	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs532682505	chr2:233661689-233661690	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs74827722	chr2:233661727-233661728	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182403188	chr2:233661765-233661766	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs11394783	chr2:233661790-233661791	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs397723991	chr2:233661800-233661801	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs397822987	chr2:233661801-233661802	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs79644779	chr2:233661802-233661803	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs571978507	chr2:233661826-233661827	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567272490	chr2:233661839-233661840	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540646600	chr2:233661868-233661869	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564204920	chr2:233661899-233661900	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs115832348	chr2:233661904-233661905	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548193450	chr2:233661908-233661909	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148054315	chr2:233661924-233661925	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186938970	chr2:233661928-233661929	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs143704106	chr2:233661957-233661958	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10933410	chr2:233661994-233661995	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs111876596	chr2:233662021-233662022	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs115248899	chr2:233662066-233662067	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs569200441	chr2:233662104-233662105	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs533838643	chr2:233662120-233662121	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547395785	chr2:233662187-233662188	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs148403782	chr2:233662199-233662200	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs201948659	chr2:233662200-233662201	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs372540940	chr2:233662201-233662202	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs67221198	chr2:233662236-233662237	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs376904994	chr2:233662246-233662247	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs375329603	chr2:233662261-233662262	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs571450943	chr2:233662307-233662308	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs367853310	chr2:233662333-233662334	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs557142241	chr2:233662371-233662372	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs115880474	chr2:233662375-233662376	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs191789733	chr2:233662376-233662377	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs570095497	chr2:233662410-233662411	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs13425525	chr2:233662427-233662428	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs138785735	chr2:233662441-233662442	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs541069662	chr2:233662442-233662443	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs142806893	chr2:233662488-233662489	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs577816683	chr2:233662490-233662491	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs150851141	chr2:233662510-233662511	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs563491802	chr2:233662536-233662537	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529059624	chr2:233662537-233662538	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs542437777	chr2:233662552-233662553	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs559638861	chr2:233662574-233662575	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs34388285	chr2:233662578-233662579	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs149979910	chr2:233662640-233662641	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	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
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
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	22429812	CNVD
Bladder cancer	21909424	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
prenatal diagnosis	22389664	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mental retardation	20152051	CNVD
Cancer	21183584	CNVD
Albright''s disease	22277900	CNVD
Brachydactyly-Mental Retardation Syndrome	22470819	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Colorectal cancer	19359472	CNVD
Autism	18414403	CNVD
Pancreatic cancer	17952125	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:741 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:233641400-233662400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:233642000-233667200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr2:233648600-233664000	Strong transcription	Fetal Muscle Trunk	muscle
4	chr2:233648800-233666800	Strong transcription	HSMM	muscle
5	chr2:233648800-233668000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr2:233649000-233680600	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr2:233649200-233663000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr2:233649200-233665800	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr2:233649400-233663000	Strong transcription	Primary B cells from peripheral blood	blood
10	chr2:233649400-233663400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr2:233649400-233665400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr2:233649400-233666000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr2:233649400-233667600	Strong transcription	Fetal Thymus	thymus
14	chr2:233649600-233663200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr2:233649600-233666800	Strong transcription	HepG2	liver
16	chr2:233649800-233666400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr2:233649800-233667000	Strong transcription	Primary T helper cells PMA-I stimulated	--
18	chr2:233650000-233662200	Strong transcription	Fetal Brain Female	brain
19	chr2:233650000-233662800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr2:233650000-233663400	Strong transcription	HUES48 Cell Line	embryonic stem cell
21	chr2:233650800-233664200	Strong transcription	Primary T cells fromperipheralblood	blood
22	chr2:233651000-233662400	Strong transcription	Left Ventricle	heart
23	chr2:233651200-233662200	Strong transcription	Cortex derived primary cultured neurospheres	brain
24	chr2:233651200-233662200	Strong transcription	Osteobl	bone
25	chr2:233651200-233663400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr2:233651200-233664600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr2:233651200-233668000	Strong transcription	Primary T helper cells fromperipheralblood	blood
28	chr2:233651400-233662800	Strong transcription	HUES6 Cell Line	embryonic stem cell
29	chr2:233651400-233665600	Strong transcription	Primary hematopoietic stem cells	blood
30	chr2:233651400-233668000	Strong transcription	Liver	Liver
31	chr2:233651600-233663400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
32	chr2:233651800-233661800	Strong transcription	Duodenum Smooth Muscle	Duodenum
33	chr2:233651800-233662200	Strong transcription	Muscle Satellite Cultured Cells	--
34	chr2:233651800-233662400	Strong transcription	H1 Cell Line	embryonic stem cell
35	chr2:233651800-233662600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr2:233651800-233663200	Strong transcription	Primary neutrophils fromperipheralblood	blood
37	chr2:233651800-233663200	Strong transcription	Fetal Muscle Leg	muscle
38	chr2:233651800-233663200	Strong transcription	Placenta	Placenta
39	chr2:233651800-233663400	Strong transcription	GM12878-XiMat	blood
40	chr2:233651800-233664000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
41	chr2:233651800-233664200	Strong transcription	HUES64 Cell Line	embryonic stem cell
42	chr2:233651800-233665600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr2:233651800-233666000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr2:233651800-233668000	Strong transcription	Dnd41	blood
45	chr2:233652000-233662400	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
46	chr2:233652000-233664600	Strong transcription	Adipose Nuclei	Adipose
47	chr2:233652200-233666400	Strong transcription	Primary T cells from cord blood	blood
48	chr2:233652400-233661800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr2:233652400-233666600	Strong transcription	Primary B cells from cord blood	blood
50	chr2:233653400-233661600	Strong transcription	Rectal Mucosa Donor 31	rectum

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