Variant report

Variant	nsv1050346
Chromosome Location	chr11:104548749-104664665
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	ATF2	chr11:104576262-104577023	GM12878	blood:	n/a	n/a
2	BATF	chr11:104576557-104576905	GM12878	blood:	n/a	n/a
3	CEBPB	chr11:104630751-104630812	HepG2	liver:	n/a	chr11:104630758-104630769
4	CEBPB	chr11:104563447-104563746	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr11:104571351-104571838	IMR90	lung:	n/a	n/a
6	CEBPB	chr11:104550013-104550355	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr11:104592226-104592334	HepG2	liver:	n/a	n/a
8	CEBPB	chr11:104643625-104644063	IMR90	lung:	n/a	chr11:104643824-104643841
9	CEBPB	chr11:104601427-104601666	HepG2	liver:	n/a	chr11:104601561-104601570 chr11:104601559-104601572 chr11:104601560-104601571 chr11:104601597-104601608
10	CEBPB	chr11:104601432-104601743	IMR90	lung:	n/a	chr11:104601561-104601570 chr11:104601559-104601572 chr11:104601560-104601571 chr11:104601597-104601608
11	CEBPB	chr11:104662767-104663009	A549	lung:	n/a	chr11:104662933-104662944 chr11:104662933-104662946 chr11:104662935-104662946
12	CEBPB	chr11:104662811-104663019	HepG2	liver:	n/a	chr11:104662933-104662944 chr11:104662933-104662946 chr11:104662935-104662946
13	CEBPB	chr11:104584302-104584553	HepG2	liver:	n/a	chr11:104584443-104584454
14	CEBPB	chr11:104565834-104566127	IMR90	lung:	n/a	n/a
15	CEBPB	chr11:104565388-104566175	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr11:104571488-104571708	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr11:104596353-104596854	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr11:104663649-104663908	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr11:104643621-104644015	Hela-S3	cervix:	n/a	chr11:104643824-104643841
20	CEBPB	chr11:104565857-104566073	HepG2	liver:	n/a	n/a
21	CHD2	chr11:104643776-104643985	Hela-S3	cervix:	n/a	n/a
22	CREB1	chr11:104576585-104576883	GM12878	blood:	n/a	n/a
23	CTCF	chr11:104567727-104567800	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr11:104629695-104629723	GM12878	blood:	n/a	n/a
25	CTCF	chr11:104584370-104584376	GM10248	blood:	n/a	n/a
26	CTCF	chr11:104565020-104565170	BE2_C	brain:	n/a	chr11:104565124-104565133
27	CTCF	chr11:104629600-104629750	HEK293	kidney:	n/a	n/a
28	CTCF	chr11:104570380-104570530	HMF	breast:	n/a	n/a
29	CTCF	chr11:104628020-104628170	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr11:104629380-104629530	GM12870	blood:	n/a	n/a
31	CTCF	chr11:104578740-104578890	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr11:104609048-104609077	GM12878	blood:	n/a	n/a
33	CTCF	chr11:104609053-104609072	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr11:104629654-104629759	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr11:104627960-104628110	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr11:104628020-104628170	HRPEpiC	eye:	n/a	n/a
37	CTCF	chr11:104615626-104615665	GM13976	blood:	n/a	n/a
38	E2F4	chr11:104601818-104602188	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr11:104643656-104644076	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr11:104574005-104574092	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr11:104632032-104632232	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr11:104554232-104554322	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr11:104550570-104550727	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr11:104558741-104558988	MCF10A-Er-Src	breast:	n/a	n/a
45	EBF1	chr11:104576522-104576697	GM12878	blood:	n/a	n/a
46	EBF1	chr11:104602905-104603097	GM12878	blood:	n/a	chr11:104603020-104603033
47	EGR1	chr11:104643713-104644075	HCT-116	colon:	n/a	chr11:104643966-104643976 chr11:104643964-104643978 chr11:104643964-104643979 chr11:104643965-104643978 chr11:104643965-104643978 chr11:104643965-104643978 chr11:104643966-104643977
48	EGR1	chr11:104643755-104644273	HCT-116	colon:	n/a	chr11:104643966-104643976 chr11:104643964-104643978 chr11:104643964-104643979 chr11:104643965-104643978 chr11:104643965-104643978 chr11:104643965-104643978 chr11:104643966-104643977
49	EGR1	chr11:104576630-104576838	GM12878	blood:	n/a	n/a
50	EP300	chr11:104643257-104644408	SK-N-SH	brain:	n/a	chr11:104644127-104644134 chr11:104643619-104643628

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104576302-104576352	GM06990	blood:	n/a
2	chr11:104576302-104576352	GM06990	blood:	n/a
3	chr11:104621250-104621300	ProgFib	skin:	n/a
4	chr11:104643591-104643641	AG09309	skin:	n/a
5	chr11:104643591-104643641	CMK	blood:	n/a
6	chr11:104621250-104621300	HPAEpiC	pulmonary alveolar:	n/a
7	chr11:104576302-104576352	GM19239	blood:	n/a
8	chr11:104654124-104654174	BE2_C	brain:	n/a
9	chr11:104621250-104621300	H1-hESC	embryonic stem cell:	embryo
10	chr11:104654124-104654174	MCF-7	breast:	n/a
11	chr11:104643591-104643641	HNPCEpiC	eye:	n/a
12	chr11:104643591-104643641	BJ	skin:	n/a
13	chr11:104621250-104621300	PFSK-1	brain:	n/a
14	chr11:104643591-104643641	HRCEpiC	kidney:	n/a
15	chr11:104621250-104621300	AG09309	skin:	n/a
16	chr11:104654124-104654174	ovcar-3	ovarian:	n/a
17	chr11:104654124-104654174	AG09309	skin:	n/a
18	chr11:104654124-104654174	Jurkat	blood:	n/a
19	chr11:104643591-104643641	HEEpiC	esophagus:	n/a
20	chr11:104621250-104621300	AG09319	gingival:	n/a
21	chr11:104643591-104643641	HAEpiC	amniotic membrane:	n/a
22	chr11:104576302-104576352	IMR90	lung:	fetal
23	chr11:104621250-104621300	HUVEC	blood vessel:	n/a
24	chr11:104654124-104654174	HEEpiC	esophagus:	n/a
25	chr11:104654124-104654174	Hepatocyte	liver:	n/a
26	chr11:104643591-104643641	BE2_C	brain:	n/a
27	chr11:104576302-104576352	HCT-116	colon:	n/a
28	chr11:104576302-104576352	AG04449	skin:	fetal
29	chr11:104654124-104654174	HepG2	liver:	n/a
30	chr11:104643591-104643641	MCF10A-Er-Src	breast:	n/a
31	chr11:104654124-104654174	GM12891	blood:	n/a
32	chr11:104643591-104643641	RPTEC	kidney:	n/a
33	chr11:104643591-104643641	IMR90	lung:	fetal
34	chr11:104654124-104654174	NT2-D1	testis:	n/a
35	chr11:104576302-104576352	Hepatocyte	liver:	n/a
36	chr11:104643591-104643641	NH-A	brain:	n/a
37	chr11:104643591-104643641	GM12891	blood:	n/a
38	chr11:104576302-104576352	GM12892	blood:	n/a
39	chr11:104643591-104643641	HIPEpiC	eye:	n/a
40	chr11:104621250-104621300	K562	blood:	n/a
41	chr11:104654124-104654174	AG10803	skin:	n/a
42	chr11:104576302-104576352	PFSK-1	brain:	n/a
43	chr11:104654124-104654174	GM12878	blood:	n/a
44	chr11:104576302-104576352	T-47D	breast:	n/a
45	chr11:104643591-104643641	PFSK-1	brain:	n/a
46	chr11:104643591-104643641	LNCaP	prostate:	n/a
47	chr11:104643591-104643641	PrEC	prostate:	n/a
48	chr11:104621250-104621300	HCT-116	colon:	n/a
49	chr11:104621250-104621300	GM12878	blood:	n/a
50	chr11:104654124-104654174	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:104598989..104600834-chr11:104611335..104614012,2	K562	blood:
2	chr11:104625274..104625879-chr20:60553051..60553551,2	Hela-S3	cervix:
3	chr11:104625193..104625713-chr4:116457976..116458496,2	MCF-7	breast:
4	chr11:104524242..104527061-chr11:104559725..104562588,2	K562	blood:
5	chr11:104598989..104600834-chr11:104611335..104614012,2	K562	blood:

Variant related genes	Relation type
ENSG00000270449	TF binding region
ENSG00000270449	CpG island

Extended variants
information (count: 3764 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:3764 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527786004	chr11:104548780-104548781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559128361	chr11:104548783-104548784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569212841	chr11:104548813-104548814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537898065	chr11:104548879-104548880	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554840685	chr11:104548881-104548882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187169002	chr11:104548907-104548908	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs115401463	chr11:104548912-104548913	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548764764	chr11:104548936-104548937	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568821014	chr11:104548968-104548969	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191504631	chr11:104548976-104548977	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576646435	chr11:104548996-104548997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs112639592	chr11:104549003-104549004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562474195	chr11:104549017-104549018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181554648	chr11:104549034-104549035	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541419560	chr11:104549035-104549036	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs73625251	chr11:104549115-104549116	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs530387584	chr11:104549206-104549207	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs539034870	chr11:104549207-104549208	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs560652453	chr11:104549210-104549211	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs557345737	chr11:104549227-104549228	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs374175843	chr11:104549269-104549270	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs532781123	chr11:104549349-104549350	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs552636139	chr11:104549350-104549351	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs569293995	chr11:104549413-104549414	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs10895717	chr11:104549459-104549460	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs377633821	chr11:104549469-104549470	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs57498890	chr11:104549497-104549498	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs186224309	chr11:104549506-104549507	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs373449586	chr11:104549540-104549541	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs533805364	chr11:104549631-104549632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553687748	chr11:104549639-104549640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs17362426	chr11:104549684-104549685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs11825520	chr11:104549700-104549701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs1942509	chr11:104549702-104549703	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs189850579	chr11:104549716-104549717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs576005383	chr11:104549720-104549721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs541927445	chr11:104549766-104549767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571648855	chr11:104549787-104549788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs10502039	chr11:104549852-104549853	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs558034789	chr11:104549900-104549901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs73625259	chr11:104549918-104549919	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs565611752	chr11:104549950-104549951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs201082795	chr11:104549970-104549971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs201469483	chr11:104549972-104549973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs11378176	chr11:104549982-104549983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs202191895	chr11:104549983-104549984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs560812722	chr11:104549987-104549988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs532741635	chr11:104549992-104549993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs142004827	chr11:104550018-104550019	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563101893	chr11:104550026-104550027	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Melanoma	17363583	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Obesity	19966786	CNVD
Tetralogy of Fallot	22912587	CNVD
Prostate cancer	18632612	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:615 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104546000-104548800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr11:104546600-104549200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr11:104548800-104549200	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr11:104549000-104550600	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr11:104549000-104551400	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr11:104549200-104549600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
7	chr11:104549200-104549800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr11:104549200-104550000	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr11:104549200-104550600	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr11:104549200-104551200	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr11:104549200-104551200	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr11:104549400-104549800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr11:104549400-104549800	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr11:104549600-104551600	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr11:104550000-104550400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr11:104550400-104551000	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr11:104550600-104555600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr11:104550600-104557800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr11:104551000-104555400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr11:104551200-104555600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr11:104551200-104555800	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr11:104551400-104555400	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr11:104551600-104555600	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr11:104555400-104556200	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr11:104555400-104556200	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr11:104555600-104556000	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr11:104555600-104556200	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr11:104555600-104556200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr11:104555800-104556200	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr11:104556000-104557600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr11:104556200-104557200	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr11:104556200-104557200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr11:104556200-104557400	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr11:104556200-104557600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr11:104556200-104557800	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr11:104556400-104557800	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr11:104557200-104559600	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr11:104557200-104560000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr11:104557400-104558400	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr11:104557600-104559600	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr11:104557600-104559600	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr11:104557800-104558000	Enhancers	H1 Cell Line	embryonic stem cell
43	chr11:104557800-104559800	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr11:104557800-104559800	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr11:104558000-104558400	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr11:104558200-104559000	Enhancers	Primary hematopoietic stem cells	blood
47	chr11:104558200-104559800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr11:104558400-104558800	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr11:104558400-104559800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr11:104558600-104559000	Enhancers	Dnd41	blood

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