Variant report

Variant	nsv897596
Chromosome Location	chr11:58818757-58855019
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:690)
CpG islands
(count:797)
Chromatin interactive
region (count:2)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:690 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:58825833-58826405	GM12878	blood:	n/a	n/a
2	ATF2	chr11:58831402-58832419	GM12878	blood:	n/a	n/a
3	ATF2	chr11:58831671-58832143	GM12878	blood:	n/a	n/a
4	BACH1	chr11:58825972-58826213	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr11:58831786-58832150	GM12878	blood:	n/a	chr11:58831926-58831934
6	BATF	chr11:58826199-58826498	GM12878	blood:	n/a	n/a
7	BATF	chr11:58818940-58819193	GM12878	blood:	n/a	n/a
8	BATF	chr11:58831471-58831776	GM12878	blood:	n/a	n/a
9	BATF	chr11:58831416-58832275	GM12878	blood:	n/a	chr11:58831926-58831934
10	BCL11A	chr11:58831483-58831904	GM12878	blood:	n/a	n/a
11	BCL11A	chr11:58818899-58819262	GM12878	blood:	n/a	chr11:58819091-58819100
12	BCL11A	chr11:58818878-58819275	GM12878	blood:	n/a	chr11:58819091-58819100
13	BCL11A	chr11:58831528-58832157	GM12878	blood:	n/a	n/a
14	BCL3	chr11:58831794-58832281	GM12878	blood:	n/a	n/a
15	BHLHE40	chr11:58826040-58826162	K562	blood:	n/a	n/a
16	BHLHE40	chr11:58825938-58826278	GM12878	blood:	n/a	n/a
17	BHLHE40	chr11:58820953-58821000	K562	blood:	n/a	n/a
18	BRCA1	chr11:58825950-58826184	GM12878	blood:	n/a	n/a
19	CEBPB	chr11:58825987-58826187	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr11:58850700-58850889	HepG2	liver:	n/a	n/a
21	CEBPB	chr11:58841369-58841519	IMR90	lung:	n/a	n/a
22	CEBPB	chr11:58852160-58852235	HepG2	liver:	n/a	n/a
23	CEBPB	chr11:58835676-58835875	K562	blood:	n/a	chr11:58835780-58835791
24	CEBPB	chr11:58835627-58835890	IMR90	lung:	n/a	chr11:58835780-58835791
25	CEBPB	chr11:58827942-58827984	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr11:58835714-58835923	HepG2	liver:	n/a	chr11:58835780-58835791
27	CHD1	chr11:58825963-58826312	GM12878	blood:	n/a	n/a
28	CHD1	chr11:58821218-58821270	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr11:58825891-58826300	GM12878	blood:	n/a	n/a
30	CHD2	chr11:58826018-58826077	K562	blood:	n/a	n/a
31	CHD2	chr11:58825822-58826232	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr11:58845766-58846361	GM12878	blood:	n/a	n/a
33	CREB1	chr11:58845805-58846333	GM12878	blood:	n/a	n/a
34	CTCF	chr11:58826000-58826150	HRE	kidney:	n/a	n/a
35	CTCF	chr11:58825980-58826130	HRE	kidney:	n/a	n/a
36	CTCF	chr11:58820860-58821010	GM12868	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
37	CTCF	chr11:58826000-58826150	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr11:58825852-58826271	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr11:58820621-58820756	Medullo	brain:	n/a	n/a
40	CTCF	chr11:58825881-58826206	A549	lung:	n/a	n/a
41	CTCF	chr11:58820858-58821103	GM19240	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
42	CTCF	chr11:58826000-58826150	K562	blood:	n/a	n/a
43	CTCF	chr11:58820740-58820890	HVMF	connective:	n/a	n/a
44	CTCF	chr11:58820883-58821075	MCF-7	breast:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
45	CTCF	chr11:58825934-58826195	K562	blood:	n/a	n/a
46	CTCF	chr11:58820500-58820650	GM12873	blood:	n/a	n/a
47	CTCF	chr11:58825956-58826204	LNCaP	prostate:	n/a	n/a
48	CTCF	chr11:58820340-58820490	GM12865	blood:	n/a	n/a
49	CTCF	chr11:58820850-58821102	Fibrobl	skin:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
50	CTCF	chr11:58820860-58821010	GM12866	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986

(count:797 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58833356-58833406	HIPEpiC	eye:	n/a
2	chr11:58830857-58830907	K562	blood:	n/a
3	chr11:58825714-58825764	IMR90	lung:	fetal
4	chr11:58825870-58825920	T-47D	breast:	n/a
5	chr11:58833356-58833406	HIPEpiC	eye:	n/a
6	chr11:58830857-58830907	K562	blood:	n/a
7	chr11:58825714-58825764	IMR90	lung:	fetal
8	chr11:58825870-58825920	T-47D	breast:	n/a
9	chr11:58830355-58830405	PrEC	prostate:	n/a
10	chr11:58833356-58833406	HCPEpiC	choroid plexus:	n/a
11	chr11:58830610-58830660	Caco-2	colon:	n/a
12	chr11:58830610-58830660	GM12891	blood:	n/a
13	chr11:58830857-58830907	U87	brain:	n/a
14	chr11:58830610-58830660	HNPCEpiC	eye:	n/a
15	chr11:58830191-58830241	HMEC	breast:	n/a
16	chr11:58825714-58825764	NT2-D1	testis:	n/a
17	chr11:58833356-58833406	T-47D	breast:	n/a
18	chr11:58833356-58833406	IMR90	lung:	fetal
19	chr11:58830191-58830241	HCM	heart:	n/a
20	chr11:58830424-58830474	HNPCEpiC	eye:	n/a
21	chr11:58825870-58825920	U87	brain:	n/a
22	chr11:58830355-58830405	BJ	skin:	n/a
23	chr11:58830857-58830907	HPAEpiC	pulmonary alveolar:	n/a
24	chr11:58826110-58826160	IMR90	lung:	fetal
25	chr11:58826073-58826123	SKMC	muscle:	n/a
26	chr11:58830355-58830405	U87	brain:	n/a
27	chr11:58826414-58826464	ECC-1	luminal epithelium:	n/a
28	chr11:58826110-58826160	MCF-7	breast:	n/a
29	chr11:58833356-58833406	NHDF-neo	bronchial:	n/a
30	chr11:58826414-58826464	CMK	blood:	n/a
31	chr11:58830857-58830907	AoSMC	blood vessel:	n/a
32	chr11:58826110-58826160	AoSMC	blood vessel:	n/a
33	chr11:58826110-58826160	ProgFib	skin:	n/a
34	chr11:58826110-58826160	NT2-D1	testis:	n/a
35	chr11:58825714-58825764	AG10803	skin:	n/a
36	chr11:58826073-58826123	HRCEpiC	kidney:	n/a
37	chr11:58826073-58826123	NHDF-neo	bronchial:	n/a
38	chr11:58830424-58830474	HCT-116	colon:	n/a
39	chr11:58830610-58830660	AG04449	skin:	fetal
40	chr11:58826414-58826464	U87	brain:	n/a
41	chr11:58830857-58830907	NHDF-neo	bronchial:	n/a
42	chr11:58825870-58825920	NHDF-neo	bronchial:	n/a
43	chr11:58825714-58825764	Jurkat	blood:	n/a
44	chr11:58828174-58828224	PFSK-1	brain:	n/a
45	chr11:58825870-58825920	IMR90	lung:	fetal
46	chr11:58825870-58825920	HRPEpiC	eye:	n/a
47	chr11:58830424-58830474	GM19239	blood:	n/a
48	chr11:58833356-58833406	HPAEpiC	pulmonary alveolar:	n/a
49	chr11:58828174-58828224	NT2-D1	testis:	n/a
50	chr11:58830424-58830474	HUVEC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:58399679..58402149-chr11:58838160..58840024,2	K562	blood:
2	chr11:58830364..58831268-chr11:58873992..58874927,2	HCT-116	colon:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLYATL2-2	chr11:58820930-58821099	NR_033853
2	lnc-GLYATL2-2	chr11:58822768-58822919	ENSG00000255240.1
3	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
4	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
5	lnc-GLYATL2-2	chr11:58825845-58825923	ENSG00000255240.1
6	lnc-GLYATL2-2	chr11:58818733-58818781	NR_033853
7	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1
8	lnc-GLYATL2-2	chr11:58825845-58825925	NR_033853
9	lnc-GLYATL2-2	chr11:58825845-58826132	ENSG00000255240.1
10	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1

No data

Variant related genes	Relation type
ENSG00000255240	TF binding region
GLYATL1P3	TF binding region
ENSG00000255240	CpG island
GLYATL1P3	CpG island
ENSG00000189057	chromatin interactions

Extended variants
information (count: 1271 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:1271 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4939253	chr11:58818757-58818758	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	mRNA abundance
2	rs545495464	chr11:58818763-58818764	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs553931439	chr11:58818764-58818765	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs112974544	chr11:58818780-58818781	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs485984	chr11:58818793-58818794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs192956378	chr11:58818800-58818801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542452842	chr11:58818838-58818839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs3824945	chr11:58818869-58818870	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs531526581	chr11:58818877-58818878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs543323276	chr11:58818900-58818901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs564911034	chr11:58818904-58818905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185625081	chr11:58818913-58818914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs544702090	chr11:58818924-58818925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs369373331	chr11:58818932-58818933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565822068	chr11:58818967-58818968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs188836058	chr11:58818975-58818976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs191100964	chr11:58818995-58818996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs571818743	chr11:58819025-58819026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs12226012	chr11:58819035-58819036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs10896906	chr11:58819040-58819041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs11229773	chr11:58819049-58819050	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs556541168	chr11:58819121-58819122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571621844	chr11:58819126-58819127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs183649054	chr11:58819151-58819152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs554125082	chr11:58819201-58819202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572238236	chr11:58819203-58819204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs542688624	chr11:58819252-58819253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs554362125	chr11:58819296-58819297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs188318686	chr11:58819302-58819303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs4499024	chr11:58819328-58819329	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs564986403	chr11:58819343-58819344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs71454361	chr11:58819367-58819368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532433654	chr11:58819375-58819376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs398045216	chr11:58819380-58819381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs371634165	chr11:58819381-58819382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs540705746	chr11:58819403-58819404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs181196833	chr11:58819406-58819407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs11827644	chr11:58819407-58819408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184100993	chr11:58819410-58819411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs11827646	chr11:58819423-58819424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs112408528	chr11:58819432-58819433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530109140	chr11:58819465-58819466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs565942793	chr11:58819526-58819527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs548276167	chr11:58819569-58819570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs114609803	chr11:58819570-58819571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs190189913	chr11:58819572-58819573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs181795830	chr11:58819586-58819587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs567521828	chr11:58819616-58819617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs146114071	chr11:58819647-58819648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs571885098	chr11:58819665-58819666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Cancer	20164919	CNVD

Chromatin state (count:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58805000-58825200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr11:58805200-58825400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr11:58813600-58825200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr11:58815400-58824400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr11:58817200-58821800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr11:58817200-58825200	Weak transcription	Liver	Liver
7	chr11:58817200-58825400	Weak transcription	Fetal Intestine Large	intestine
8	chr11:58817400-58819400	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr11:58817400-58822000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr11:58818200-58819400	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr11:58818200-58820200	Enhancers	Primary B cells from cord blood	blood
12	chr11:58818600-58825200	Enhancers	Primary B cells from peripheral blood	blood
13	chr11:58818800-58819400	Enhancers	GM12878-XiMat	blood
14	chr11:58819200-58819400	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr11:58819400-58820600	Weak transcription	GM12878-XiMat	blood
16	chr11:58819400-58821200	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr11:58819400-58822000	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr11:58819400-58822600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr11:58820200-58820800	Weak transcription	Primary B cells from cord blood	blood
20	chr11:58820600-58821200	Enhancers	GM12878-XiMat	blood
21	chr11:58820800-58822200	Enhancers	Primary B cells from cord blood	blood
22	chr11:58821200-58821400	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr11:58821200-58821600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr11:58821200-58825400	Weak transcription	GM12878-XiMat	blood
25	chr11:58821400-58822200	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr11:58821600-58822400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr11:58821800-58822600	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr11:58821800-58822800	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr11:58822000-58822600	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr11:58822000-58822800	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr11:58822200-58823200	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr11:58822200-58824400	Weak transcription	Primary B cells from cord blood	blood
33	chr11:58822400-58823200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr11:58822600-58823200	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr11:58822600-58825200	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr11:58822800-58825200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr11:58822800-58825200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr11:58823200-58825200	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr11:58823200-58825200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr11:58823200-58825600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr11:58824400-58824600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr11:58824400-58825200	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr11:58824400-58825200	Enhancers	Primary B cells from cord blood	blood
44	chr11:58824800-58825600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr11:58825200-58825400	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr11:58825200-58825400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
47	chr11:58825200-58825400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr11:58825200-58825400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr11:58825200-58825400	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr11:58825200-58825400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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