Variant report

Variant	esv1794580
Chromosome Location	chr11:94224060-94227993
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:538)
CpG islands
(count:1038)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:538 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:94226621-94227809	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:94226817-94227053	K562	blood:	n/a	n/a
3	ARID3A	chr11:94226313-94226540	K562	blood:	n/a	n/a
4	ATF1	chr11:94226839-94227255	K562	blood:	n/a	n/a
5	ATF2	chr11:94227299-94227715	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr11:94226566-94227214	GM12878	blood:	n/a	n/a
7	ATF2	chr11:94226652-94227512	GM12878	blood:	n/a	n/a
8	ATF2	chr11:94226438-94227189	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr11:94226375-94227236	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr11:94226529-94227423	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr11:94226647-94227663	K562	blood:	n/a	n/a
12	BHLHE40	chr11:94226945-94227545	GM12878	blood:	n/a	n/a
13	BRCA1	chr11:94226675-94227414	GM12878	blood:	n/a	chr11:94227016-94227025
14	BRCA1	chr11:94226371-94227630	H1-hESC	embryonic stem cell:	n/a	chr11:94227016-94227025
15	BRCA1	chr11:94226782-94227267	HepG2	liver:	n/a	chr11:94227016-94227025
16	BRCA1	chr11:94226214-94228062	Hela-S3	cervix:	n/a	chr11:94227016-94227025
17	CBX3	chr11:94226404-94227578	K562	blood:	n/a	n/a
18	CCNT2	chr11:94227031-94227510	K562	blood:	n/a	chr11:94227089-94227098
19	CEBPB	chr11:94227274-94227398	K562	blood:	n/a	n/a
20	CEBPB	chr11:94226446-94227029	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr11:94226437-94227421	Hela-S3	cervix:	n/a	chr11:94227066-94227074
22	CHD1	chr11:94227248-94227585	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD1	chr11:94226299-94226643	GM12878	blood:	n/a	n/a
24	CHD1	chr11:94226844-94227595	GM12878	blood:	n/a	chr11:94227016-94227025
25	CHD1	chr11:94226278-94227020	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr11:94226306-94227671	GM12878	blood:	n/a	chr11:94227016-94227025
27	CHD2	chr11:94226396-94227568	HepG2	liver:	n/a	chr11:94227016-94227025
28	CHD2	chr11:94226349-94227541	K562	blood:	n/a	chr11:94227016-94227025
29	CHD2	chr11:94226388-94227648	Hela-S3	cervix:	n/a	chr11:94227016-94227025
30	CHD2	chr11:94226427-94227776	H1-hESC	embryonic stem cell:	n/a	chr11:94227016-94227025
31	CREB1	chr11:94226488-94227658	HepG2	liver:	n/a	n/a
32	CREB1	chr11:94226821-94227301	ECC-1	luminal epithelium:	n/a	n/a
33	CREB1	chr11:94226893-94227217	A549	lung:	n/a	n/a
34	CREB1	chr11:94226788-94227293	A549	lung:	n/a	n/a
35	CREB1	chr11:94226423-94227560	GM12878	blood:	n/a	n/a
36	CTBP2	chr11:94226538-94227547	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr11:94227240-94227390	AG04449	skin:	n/a	chr11:94227306-94227314
38	CTCF	chr11:94227340-94227490	GM12871	blood:	n/a	chr11:94227410-94227423
39	CTCF	chr11:94227300-94227450	NHEK	skin:	n/a	chr11:94227410-94227423 chr11:94227306-94227314
40	CTCF	chr11:94227520-94227670	NHLF	lung:	n/a	n/a
41	CTCF	chr11:94226360-94226510	GM12872	blood:	n/a	n/a
42	CTCF	chr11:94226680-94226830	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr11:94227273-94227353	GM12891	blood:	n/a	chr11:94227306-94227314
44	CTCF	chr11:94227280-94227430	HCPEpiC	choroid plexus:	n/a	chr11:94227410-94227423 chr11:94227306-94227314
45	CTCF	chr11:94227300-94227450	SK-N-SH_RA	brain:	n/a	chr11:94227410-94227423 chr11:94227306-94227314
46	CTCF	chr11:94227380-94227530	GM06990	blood:	n/a	chr11:94227410-94227423
47	CTCF	chr11:94226580-94226730	HMEC	breast:	n/a	n/a
48	CTCF	chr11:94227340-94227490	HMEC	breast:	n/a	chr11:94227410-94227423
49	CTCF	chr11:94227240-94227390	GM12872	blood:	n/a	chr11:94227306-94227314
50	CTCF	chr11:94227280-94227430	HUVEC	blood vessel:	n/a	chr11:94227410-94227423 chr11:94227306-94227314

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:94227320-94227370	HEK293	kidney:	embryo
2	chr11:94227320-94227370	HEK293	kidney:	embryo
3	chr11:94227380-94227430	PrEC	prostate:	n/a
4	chr11:94226767-94226817	SK-N-SH	brain:	n/a
5	chr11:94226537-94226587	NH-A	brain:	n/a
6	chr11:94226925-94226975	ovcar-3	ovarian:	n/a
7	chr11:94227125-94227175	MCF-7	breast:	n/a
8	chr11:94227180-94227230	HL-60	blood:	n/a
9	chr11:94227006-94227056	HNPCEpiC	eye:	n/a
10	chr11:94227380-94227430	MCF-7	breast:	n/a
11	chr11:94226925-94226975	HMEC	breast:	n/a
12	chr11:94227038-94227088	ECC-1	luminal epithelium:	n/a
13	chr11:94227320-94227370	HRPEpiC	eye:	n/a
14	chr11:94227180-94227230	Hela-S3	cervix:	n/a
15	chr11:94227125-94227175	AG09319	gingival:	n/a
16	chr11:94224044-94224094	HCT-116	colon:	n/a
17	chr11:94224044-94224094	AG04450	lung:	fetal
18	chr11:94226537-94226587	Caco-2	colon:	n/a
19	chr11:94227109-94227159	BJ	skin:	n/a
20	chr11:94227106-94227156	T-47D	breast:	n/a
21	chr11:94227180-94227230	AG09319	gingival:	n/a
22	chr11:94226925-94226975	HEEpiC	esophagus:	n/a
23	chr11:94227583-94227633	HRPEpiC	eye:	n/a
24	chr11:94226925-94226975	PANC-1	pancreas:	n/a
25	chr11:94226767-94226817	RPTEC	kidney:	n/a
26	chr11:94227038-94227088	HUVEC	blood vessel:	n/a
27	chr11:94227109-94227159	SKMC	muscle:	n/a
28	chr11:94227583-94227633	NT2-D1	testis:	n/a
29	chr11:94227081-94227131	NT2-D1	testis:	n/a
30	chr11:94227109-94227159	HCT-116	colon:	n/a
31	chr11:94227380-94227430	HNPCEpiC	eye:	n/a
32	chr11:94227380-94227430	NH-A	brain:	n/a
33	chr11:94227583-94227633	H1-hESC	embryonic stem cell:	embryo
34	chr11:94226991-94227041	SK-N-SH	brain:	n/a
35	chr11:94227183-94227233	AG09309	skin:	n/a
36	chr11:94227583-94227633	K562	blood:	n/a
37	chr11:94227180-94227230	AG04450	lung:	fetal
38	chr11:94226991-94227041	HCPEpiC	choroid plexus:	n/a
39	chr11:94227081-94227131	U87	brain:	n/a
40	chr11:94227125-94227175	HAEpiC	amniotic membrane:	n/a
41	chr11:94227081-94227131	GM12878	blood:	n/a
42	chr11:94227125-94227175	HEK293	kidney:	embryo
43	chr11:94224044-94224094	AoSMC	blood vessel:	n/a
44	chr11:94227183-94227233	HRPEpiC	eye:	n/a
45	chr11:94227411-94227461	A549	lung:	n/a
46	chr11:94226925-94226975	Caco-2	colon:	n/a
47	chr11:94226925-94226975	PrEC	prostate:	n/a
48	chr11:94226767-94226817	MCF-7	breast:	n/a
49	chr11:94226537-94226587	CMK	blood:	n/a
50	chr11:94226991-94227041	ovcar-3	ovarian:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:93860234..93863458-chr11:94225545..94228425,3	K562	blood:
2	chr11:94226544..94227246-chr17:33904994..33905713,2	Hela-S3	cervix:
3	chr11:94225979..94229384-chr11:94230397..94235421,9	K562	blood:
4	chr11:94226287..94227152-chr12:49524847..49525416,2	Hela-S3	cervix:
5	chr11:94226700..94227357-chr19:7293430..7294141,2	Hela-S3	cervix:
6	chr11:94223520..94226395-chr11:94275795..94278274,2	K562	blood:
7	chr11:94219714..94224180-chr11:94224527..94226991,4	MCF-7	breast:
8	chr11:94180184..94182302-chr11:94227182..94229296,2	K562	blood:
9	chr11:94219618..94222085-chr11:94222930..94224543,2	K562	blood:
10	chr11:94225466..94228271-chr11:94275709..94278301,3	K562	blood:
11	chr11:94222232..94224873-chr11:94225304..94228914,3	K562	blood:
12	chr11:94200661..94202892-chr11:94224214..94225865,2	K562	blood:
13	chr11:94217826..94221118-chr11:94222264..94225071,4	K562	blood:
14	chr11:94213347..94215361-chr11:94222222..94224695,2	K562	blood:
15	chr11:94226137..94228706-chr11:94300541..94302920,2	K562	blood:
16	chr11:93914625..93916953-chr11:94227203..94228744,2	MCF-7	breast:
17	chr11:93473689..93475609-chr11:94224502..94227416,2	K562	blood:
18	chr11:94226771..94229140-chr11:94275887..94279295,4	K562	blood:

No data

Variant related genes	Relation type
ANKRD49	TF binding region
MRE11A	TF binding region
ANKRD49	CpG island
MRE11A	CpG island
ENSG00000196371	chromatin interactions
ENSG00000110218	chromatin interactions
ENSG00000168876	chromatin interactions
ENSG00000134627	chromatin interactions
ENSG00000123416	chromatin interactions
ENSG00000171105	chromatin interactions
ENSG00000182919	chromatin interactions
ENSG00000006125	chromatin interactions
ENSG00000108733	chromatin interactions
ENSG00000258017	chromatin interactions
ENSG00000166012	chromatin interactions
ENSG00000020922	chromatin interactions

Extended variants
information (count: 157 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:157 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1061945	chr11:94224060-94224061	Weak transcription Strong transcription	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs111633777	chr11:94224065-94224066	Weak transcription Strong transcription	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs190031653	chr11:94224071-94224072	Weak transcription Strong transcription	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs372068015	chr11:94224075-94224076	Weak transcription Strong transcription	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs145218439	chr11:94224079-94224080	Weak transcription Strong transcription	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs149101834	chr11:94224115-94224116	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs200118981	chr11:94224141-94224142	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs556654467	chr11:94224142-94224143	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs575339131	chr11:94224145-94224146	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs373719420	chr11:94224160-94224161	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs201715733	chr11:94224167-94224168	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs560756378	chr11:94224207-94224208	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs104895020	chr11:94224231-94224232	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs540157985	chr11:94224234-94224235	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs3758784	chr11:94224245-94224246	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs556240226	chr11:94224267-94224268	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs1009455	chr11:94224274-94224275	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs142904422	chr11:94224287-94224288	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs151068346	chr11:94224320-94224321	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs562651178	chr11:94224365-94224366	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs531642273	chr11:94224392-94224393	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs142381479	chr11:94224488-94224489	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs372486717	chr11:94224499-94224500	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs571265128	chr11:94224523-94224524	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs539040577	chr11:94224546-94224547	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs61893736	chr11:94224579-94224580	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs567075155	chr11:94224697-94224698	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs554144569	chr11:94224734-94224735	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs534469296	chr11:94224786-94224787	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs571852284	chr11:94224791-94224792	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs552922084	chr11:94224807-94224808	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs570745325	chr11:94224829-94224830	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs185450305	chr11:94224848-94224849	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs13447590	chr11:94224881-94224882	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs574833982	chr11:94224885-94224886	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs535555169	chr11:94224900-94224901	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs554313034	chr11:94224919-94224920	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs12708333	chr11:94224929-94224930	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs548001885	chr11:94224956-94224957	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs13447589	chr11:94224991-94224992	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs12290689	chr11:94224995-94224996	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs13447588	chr11:94225027-94225028	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs5793685	chr11:94225062-94225063	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs398097724	chr11:94225063-94225064	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs13447587	chr11:94225079-94225080	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs562354875	chr11:94225082-94225083	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs397509351	chr11:94225127-94225128	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs35693442	chr11:94225155-94225156	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs529770290	chr11:94225164-94225165	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs548329795	chr11:94225166-94225167	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	21062444	CNVD
Cancer	21499728	CNVD
Breast cancer	19181860	CNVD
Breast cancer	17603634	CNVD
Mantle cell lymphoma	19029149	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:533 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:94157400-94226200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:94157600-94226400	Weak transcription	Esophagus	oesophagus
3	chr11:94162800-94225800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr11:94167400-94226400	Weak transcription	Small Intestine	intestine
5	chr11:94179000-94226000	Weak transcription	Colonic Mucosa	Colon
6	chr11:94180600-94225800	Weak transcription	Brain Substantia Nigra	brain
7	chr11:94181000-94226400	Weak transcription	Pancreas	Pancrea
8	chr11:94183600-94225800	Weak transcription	NHLF	lung
9	chr11:94184400-94225800	Weak transcription	NHDF-Ad	bronchial
10	chr11:94194600-94225000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr11:94194600-94225000	Weak transcription	Fetal Brain Male	brain
12	chr11:94197400-94224600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr11:94197600-94225600	Weak transcription	Fetal Heart	heart
14	chr11:94198400-94224400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr11:94203000-94225800	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr11:94206600-94225800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr11:94206600-94226000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr11:94206800-94226000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr11:94208000-94224600	Strong transcription	HUES64 Cell Line	embryonic stem cell
20	chr11:94208000-94225600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr11:94210200-94226200	Weak transcription	Aorta	Aorta
22	chr11:94211200-94226200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr11:94213400-94224600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
24	chr11:94214200-94225200	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr11:94214200-94226000	Weak transcription	HSMMtube	muscle
26	chr11:94216000-94225800	Weak transcription	Osteobl	bone
27	chr11:94216800-94226400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr11:94217000-94225800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr11:94217000-94226400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr11:94217000-94226400	Weak transcription	Gastric	stomach
31	chr11:94217000-94226600	Weak transcription	Spleen	Spleen
32	chr11:94218000-94225800	Weak transcription	Colon Smooth Muscle	Colon
33	chr11:94218200-94225000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr11:94218200-94225200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr11:94218200-94225400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr11:94219000-94225400	Weak transcription	Fetal Intestine Small	intestine
37	chr11:94220000-94225000	Weak transcription	HUVEC	blood vessel
38	chr11:94220800-94225400	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr11:94221400-94224600	Strong transcription	Hela-S3	cervix
40	chr11:94221400-94225800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr11:94221600-94225200	Weak transcription	Psoas Muscle	Psoas
42	chr11:94222000-94225800	Weak transcription	Brain Anterior Caudate	brain
43	chr11:94222000-94225800	Weak transcription	Fetal Kidney	kidney
44	chr11:94222600-94225400	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr11:94222600-94225800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr11:94222600-94226200	Weak transcription	Right Ventricle	heart
47	chr11:94223000-94225800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr11:94223200-94226000	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr11:94223400-94225800	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr11:94223400-94225800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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