Variant report

Variant	nsv1040650
Chromosome Location	chr11:108859584-109174553
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1005)
CpG islands
(count:489)
Chromatin interactive
region (count:23)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1005 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:108979879-108980350	HepG2	liver:	n/a	n/a
2	ATF1	chr11:109004252-109004258	K562	blood:	n/a	n/a
3	ATF2	chr11:108976753-108977364	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr11:108910987-108911437	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr11:108911022-108911451	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr11:109038474-109038475	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr11:109065685-109065713	K562	blood:	n/a	n/a
8	BACH1	chr11:108976878-108977607	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr11:108914217-108914418	GM12878	blood:	n/a	n/a
10	BATF	chr11:109003950-109004190	GM12878	blood:	n/a	n/a
11	BATF	chr11:109162375-109162631	GM12878	blood:	n/a	chr11:109162484-109162495
12	BATF	chr11:108914188-108914419	GM12878	blood:	n/a	n/a
13	BCL11A	chr11:108914180-108914452	GM12878	blood:	n/a	chr11:108914250-108914259
14	BHLHE40	chr11:108979897-108980294	HepG2	liver:	n/a	n/a
15	BHLHE40	chr11:109065685-109065712	K562	blood:	n/a	n/a
16	BHLHE40	chr11:108979895-108980135	HepG2	liver:	n/a	n/a
17	BRCA1	chr11:109065685-109065885	GM12878	blood:	n/a	n/a
18	CEBPB	chr11:109008949-109009318	A549	lung:	n/a	n/a
19	CEBPB	chr11:109008995-109009303	IMR90	lung:	n/a	n/a
20	CEBPB	chr11:108997876-108998093	HepG2	liver:	n/a	chr11:108997936-108997947
21	CEBPB	chr11:108906092-108906392	H1-hESC	embryonic stem cell:	n/a	chr11:108906201-108906212
22	CEBPB	chr11:108939439-108939612	HepG2	liver:	n/a	chr11:108939510-108939521
23	CEBPB	chr11:108933263-108933534	HepG2	liver:	n/a	n/a
24	CEBPB	chr11:108933204-108933537	IMR90	lung:	n/a	n/a
25	CEBPB	chr11:109064622-109064955	A549	lung:	n/a	chr11:109064793-109064804
26	CEBPB	chr11:108871358-108871592	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr11:108997869-108998011	A549	lung:	n/a	chr11:108997936-108997947
28	CEBPB	chr11:109015096-109015265	HepG2	liver:	n/a	n/a
29	CEBPB	chr11:109093162-109093293	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr11:108906187-108906219	HepG2	liver:	n/a	chr11:108906201-108906212
31	CEBPB	chr11:109064615-109064974	IMR90	lung:	n/a	chr11:109064793-109064804
32	CEBPB	chr11:108939447-108939579	K562	blood:	n/a	chr11:108939510-108939521
33	CEBPB	chr11:109138162-109138362	HepG2	liver:	n/a	chr11:109138213-109138224 chr11:109138236-109138247
34	CEBPB	chr11:109040272-109040308	HepG2	liver:	n/a	n/a
35	CEBPB	chr11:108961566-108961568	IMR90	lung:	n/a	n/a
36	CEBPB	chr11:109009013-109009200	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr11:109093060-109093402	HepG2	liver:	n/a	n/a
38	CEBPB	chr11:109064618-109064979	HepG2	liver:	n/a	chr11:109064793-109064804
39	CEBPB	chr11:108918761-108919039	IMR90	lung:	n/a	chr11:108918880-108918891 chr11:108918878-108918891 chr11:108918880-108918891
40	CEBPB	chr11:109009016-109009288	A549	lung:	n/a	n/a
41	CEBPB	chr11:109138052-109138427	Hela-S3	cervix:	n/a	chr11:109138213-109138224 chr11:109138236-109138247
42	CEBPB	chr11:109064707-109064907	H1-hESC	embryonic stem cell:	n/a	chr11:109064793-109064804
43	CEBPB	chr11:109138067-109138403	A549	lung:	n/a	chr11:109138213-109138224 chr11:109138236-109138247
44	CEBPB	chr11:109064712-109064965	K562	blood:	n/a	chr11:109064793-109064804
45	CHD2	chr11:109065593-109065784	K562	blood:	n/a	n/a
46	CHD2	chr11:108976790-108977395	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr11:109003242-109003633	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr11:108994901-108995043	HepG2	liver:	n/a	n/a
49	CREB1	chr11:108911088-108911360	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTBP2	chr11:108976914-108977735	H1-hESC	embryonic stem cell:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:108991744-108991794	GM12891	blood:	n/a
2	chr11:108991744-108991794	GM12891	blood:	n/a
3	chr11:108906099-108906149	HEK293	kidney:	embryo
4	chr11:109172798-109172848	MCF-7	breast:	n/a
5	chr11:108991744-108991794	GM06990	blood:	n/a
6	chr11:109002818-109002868	HRE	kidney:	n/a
7	chr11:108906099-108906149	HAEpiC	amniotic membrane:	n/a
8	chr11:108991744-108991794	T-47D	breast:	n/a
9	chr11:108991744-108991794	AG09309	skin:	n/a
10	chr11:109172798-109172848	IMR90	lung:	fetal
11	chr11:108918285-108918335	H1-hESC	embryonic stem cell:	embryo
12	chr11:108918285-108918335	HMEC	breast:	n/a
13	chr11:108991744-108991794	PFSK-1	brain:	n/a
14	chr11:108991744-108991794	H1-hESC	embryonic stem cell:	embryo
15	chr11:109002818-109002868	NT2-D1	testis:	n/a
16	chr11:109172798-109172848	RPTEC	kidney:	n/a
17	chr11:108994504-108994554	GM19239	blood:	n/a
18	chr11:108991744-108991794	HRCEpiC	kidney:	n/a
19	chr11:109002818-109002868	PrEC	prostate:	n/a
20	chr11:109172798-109172848	U87	brain:	n/a
21	chr11:109002818-109002868	HRPEpiC	eye:	n/a
22	chr11:108918285-108918335	U87	brain:	n/a
23	chr11:108994504-108994554	IMR90	lung:	fetal
24	chr11:109172798-109172848	Hepatocyte	liver:	n/a
25	chr11:108983607-108983657	MCF10A-Er-Src	breast:	n/a
26	chr11:108909215-108909265	Caco-2	colon:	n/a
27	chr11:108906099-108906149	NT2-D1	testis:	n/a
28	chr11:108983607-108983657	HMEC	breast:	n/a
29	chr11:108918285-108918335	GM12878	blood:	n/a
30	chr11:109172798-109172848	GM12878	blood:	n/a
31	chr11:108983607-108983657	AG09319	gingival:	n/a
32	chr11:108994504-108994554	A549	lung:	n/a
33	chr11:108991744-108991794	Caco-2	colon:	n/a
34	chr11:108906099-108906149	HNPCEpiC	eye:	n/a
35	chr11:108983607-108983657	HRPEpiC	eye:	n/a
36	chr11:108991744-108991794	MCF-7	breast:	n/a
37	chr11:108991744-108991794	A549	lung:	n/a
38	chr11:109172798-109172848	H1-hESC	embryonic stem cell:	embryo
39	chr11:108918285-108918335	NHDF-neo	bronchial:	n/a
40	chr11:109002818-109002868	SK-N-SH	brain:	n/a
41	chr11:108906099-108906149	Jurkat	blood:	n/a
42	chr11:108906099-108906149	HUVEC	blood vessel:	n/a
43	chr11:108991744-108991794	NHBE	bronchial:	n/a
44	chr11:108909215-108909265	IMR90	lung:	fetal
45	chr11:108994504-108994554	U87	brain:	n/a
46	chr11:108909215-108909265	RPTEC	kidney:	n/a
47	chr11:108983607-108983657	NT2-D1	testis:	n/a
48	chr11:109172798-109172848	HL-60	blood:	n/a
49	chr11:108906099-108906149	LNCaP	prostate:	n/a
50	chr11:109002818-109002868	HMEC	breast:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:108936870..108939701-chr11:108941192..108943026,2	K562	blood:
2	chr11:108905168..108907464-chr11:108909151..108912288,3	K562	blood:
3	chr11:109125816..109127319-chr11:109129668..109132140,2	K562	blood:
4	chr11:108989018..108990754-chr11:108993164..108995394,2	K562	blood:
5	chr11:108936870..108939701-chr11:108941192..108943026,2	K562	blood:
6	chr11:108905323..108906917-chr11:108910788..108913428,2	K562	blood:
7	chr11:109035278..109038191-chr11:109041487..109043368,2	K562	blood:
8	chr11:109118774..109120383-chr11:109121444..109124055,2	K562	blood:
9	chr11:108873859..108875938-chr11:108935111..108937056,2	K562	blood:
10	chr11:109118774..109120383-chr11:109121444..109124055,2	K562	blood:
11	chr11:108927357..108928938-chr11:108932482..108934210,2	K562	blood:
12	chr11:108905323..108906917-chr11:108910788..108913428,2	K562	blood:
13	chr11:109034615..109037015-chr11:109038018..109041527,3	K562	blood:
14	chr11:108899961..108902009-chr11:108909481..108912314,2	K562	blood:
15	chr11:108905168..108907464-chr11:108909151..108912288,3	K562	blood:
16	chr11:108989018..108990754-chr11:108993164..108995394,2	K562	blood:
17	chr11:108927357..108928938-chr11:108932482..108934210,2	K562	blood:
18	chr11:108899961..108902009-chr11:108909481..108912314,2	K562	blood:
19	chr11:108873859..108875938-chr11:108935111..108937056,2	K562	blood:
20	chr11:109125816..109127319-chr11:109129668..109132140,2	K562	blood:
21	chr11:109127805..109129868-chr11:109133707..109135749,2	K562	blood:
22	chr11:109034615..109037015-chr11:109038018..109041527,3	K562	blood:
23	chr11:109035278..109038191-chr11:109041487..109043368,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EXPH5-1	chr11:108873192-108873299	ENSG00000255528
2	lnc-EXPH5-1	chr11:108908470-108908694	ENSG00000255528

No data

Variant related genes	Relation type
ENSG00000255528	TF binding region
ENSG00000264997	TF binding region
RNU6-654P	TF binding region
RNA5SP349	TF binding region
ENSG00000255528	CpG island
ENSG00000264997	CpG island
RNU6-654P	CpG island
RNA5SP349	CpG island
ENSG00000264997	chromatin interactions

Extended variants
information (count: 9063 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:9063 , 50 per page) page: 1 2 3 4 5 6 7 ... 182

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10890917	chr11:108859584-108859585	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536891950	chr11:108859599-108859600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187017205	chr11:108859600-108859601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs369179755	chr11:108859631-108859632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142932188	chr11:108859646-108859647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536706175	chr11:108859657-108859658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs78859850	chr11:108859696-108859697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs79378072	chr11:108859697-108859698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs539039057	chr11:108859704-108859705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557818312	chr11:108859708-108859709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145189265	chr11:108859719-108859720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559916529	chr11:108859730-108859731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200300039	chr11:108859738-108859739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs533922149	chr11:108859848-108859849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556737634	chr11:108859867-108859868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554954830	chr11:108859876-108859877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373889156	chr11:108859967-108859968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs139018905	chr11:108860025-108860026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573839100	chr11:108860075-108860076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs116674257	chr11:108860081-108860082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562619715	chr11:108860089-108860090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12362999	chr11:108860105-108860106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577903662	chr11:108860143-108860144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141918475	chr11:108860155-108860156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs146305926	chr11:108860160-108860161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10789701	chr11:108860176-108860177	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs376666598	chr11:108860182-108860183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs113664475	chr11:108860195-108860196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs139589065	chr11:108860208-108860209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561864707	chr11:108860209-108860210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs529435544	chr11:108860223-108860224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs149595378	chr11:108860258-108860259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192363731	chr11:108860265-108860266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs144538717	chr11:108860285-108860286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551392204	chr11:108860293-108860294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566428107	chr11:108860337-108860338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs533778338	chr11:108860339-108860340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs61912831	chr11:108860346-108860347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182113921	chr11:108860373-108860374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567385040	chr11:108860379-108860380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537630037	chr11:108860380-108860381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556364073	chr11:108860418-108860419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566892100	chr11:108860419-108860420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs116857063	chr11:108860424-108860425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148465825	chr11:108860435-108860436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572869385	chr11:108860474-108860475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540254334	chr11:108860488-108860489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572375985	chr11:108860583-108860584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561823355	chr11:108860627-108860628	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529420186	chr11:108860634-108860635	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	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
Chronic lymphocytic leukemia	21546498	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
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
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
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
Prostate cancer	18632612	CNVD
Renal cell carcinoma	21668985	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:737 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:108857000-108861000	Weak transcription	Aorta	Aorta
2	chr11:108857000-108862800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:108858000-108860600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr11:108860600-108861200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
5	chr11:108861000-108861400	ZNF genes & repeats	Aorta	Aorta
6	chr11:108861400-108862600	Weak transcription	Aorta	Aorta
7	chr11:108862600-108862800	Enhancers	Aorta	Aorta
8	chr11:108862600-108863200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr11:108865000-108865200	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr11:108865000-108866600	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr11:108865200-108865600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr11:108865200-108866000	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr11:108865400-108866400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr11:108865600-108866000	Active TSS	Monocytes-CD14+_RO01746	blood
15	chr11:108866000-108866400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
16	chr11:108866400-108866600	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr11:108871600-108871800	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr11:108872200-108872600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr11:108872400-108872600	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr11:108881400-108881800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr11:108884000-108884200	Bivalent Enhancer	Esophagus	oesophagus
22	chr11:108885400-108887800	Enhancers	HUVEC	blood vessel
23	chr11:108885600-108886200	Enhancers	NH-A	brain
24	chr11:108885600-108886800	Enhancers	Muscle Satellite Cultured Cells	--
25	chr11:108885600-108887000	Enhancers	Osteobl	bone
26	chr11:108886200-108886600	Flanking Active TSS	NH-A	brain
27	chr11:108886200-108886800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr11:108886200-108887400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr11:108886200-108887600	Enhancers	NHEK	skin
30	chr11:108886200-108887800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr11:108886400-108886600	Enhancers	A549	lung
32	chr11:108886400-108886800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr11:108886600-108886800	Enhancers	NH-A	brain
34	chr11:108889800-108890800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr11:108892200-108892400	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr11:108892600-108893600	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr11:108892600-108894600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr11:108893400-108893600	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr11:108893600-108894000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
40	chr11:108893600-108894200	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr11:108893600-108894200	Enhancers	Osteobl	bone
42	chr11:108893800-108894200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr11:108894000-108894400	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr11:108894200-108903800	Weak transcription	Osteobl	bone
45	chr11:108897000-108898000	Enhancers	HSMM	muscle
46	chr11:108897200-108899000	Enhancers	Muscle Satellite Cultured Cells	--
47	chr11:108897600-108897800	Enhancers	A549	lung
48	chr11:108897800-108898800	Weak transcription	A549	lung
49	chr11:108898800-108899000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr11:108898800-108899200	Enhancers	A549	lung

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