Variant report

Variant	esv3381644
Chromosome Location	chr11:58822364-58866298
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:761)
CpG islands
(count:795)
Chromatin interactive
region (count:4)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:761 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:58864804-58864948	K562	blood:	n/a	n/a
2	ATF2	chr11:58825833-58826405	GM12878	blood:	n/a	n/a
3	ATF2	chr11:58831402-58832419	GM12878	blood:	n/a	n/a
4	ATF2	chr11:58864502-58864964	GM12878	blood:	n/a	n/a
5	ATF2	chr11:58831671-58832143	GM12878	blood:	n/a	n/a
6	BACH1	chr11:58825972-58826213	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr11:58862752-58863071	GM12878	blood:	n/a	n/a
8	BATF	chr11:58826199-58826498	GM12878	blood:	n/a	n/a
9	BATF	chr11:58831786-58832150	GM12878	blood:	n/a	chr11:58831926-58831934
10	BATF	chr11:58831416-58832275	GM12878	blood:	n/a	chr11:58831926-58831934
11	BATF	chr11:58831471-58831776	GM12878	blood:	n/a	n/a
12	BCL11A	chr11:58862711-58863079	GM12878	blood:	n/a	chr11:58862903-58862912
13	BCL11A	chr11:58831483-58831904	GM12878	blood:	n/a	n/a
14	BCL11A	chr11:58862690-58863069	GM12878	blood:	n/a	chr11:58862903-58862912
15	BCL11A	chr11:58831528-58832157	GM12878	blood:	n/a	n/a
16	BCL3	chr11:58831794-58832281	GM12878	blood:	n/a	n/a
17	BHLHE40	chr11:58865311-58865484	GM12878	blood:	n/a	n/a
18	BHLHE40	chr11:58825938-58826278	GM12878	blood:	n/a	n/a
19	BHLHE40	chr11:58826040-58826162	K562	blood:	n/a	n/a
20	BHLHE40	chr11:58862780-58863126	GM12878	blood:	n/a	n/a
21	BRCA1	chr11:58825950-58826184	GM12878	blood:	n/a	n/a
22	CEBPB	chr11:58852160-58852235	HepG2	liver:	n/a	n/a
23	CEBPB	chr11:58835627-58835890	IMR90	lung:	n/a	chr11:58835780-58835791
24	CEBPB	chr11:58861212-58861364	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr11:58835676-58835875	K562	blood:	n/a	chr11:58835780-58835791
26	CEBPB	chr11:58850700-58850889	HepG2	liver:	n/a	n/a
27	CEBPB	chr11:58825987-58826187	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr11:58835714-58835923	HepG2	liver:	n/a	chr11:58835780-58835791
29	CEBPB	chr11:58827942-58827984	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr11:58841369-58841519	IMR90	lung:	n/a	n/a
31	CHD1	chr11:58825963-58826312	GM12878	blood:	n/a	n/a
32	CHD2	chr11:58826018-58826077	K562	blood:	n/a	n/a
33	CHD2	chr11:58825891-58826300	GM12878	blood:	n/a	n/a
34	CHD2	chr11:58825822-58826232	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr11:58845766-58846361	GM12878	blood:	n/a	n/a
36	CREB1	chr11:58845805-58846333	GM12878	blood:	n/a	n/a
37	CTCF	chr11:58826020-58826170	GM12875	blood:	n/a	n/a
38	CTCF	chr11:58864700-58864850	Caco-2	colon:	n/a	chr11:58864789-58864805 chr11:58864791-58864804 chr11:58864788-58864806 chr11:58864790-58864811 chr11:58864791-58864799
39	CTCF	chr11:58825946-58826298	GM12891	blood:	n/a	n/a
40	CTCF	chr11:58864680-58864830	GM12871	blood:	n/a	chr11:58864789-58864805 chr11:58864791-58864804 chr11:58864788-58864806 chr11:58864790-58864811 chr11:58864791-58864799
41	CTCF	chr11:58825950-58826229	GM13977	blood:	n/a	n/a
42	CTCF	chr11:58825927-58826234	HepG2	liver:	n/a	n/a
43	CTCF	chr11:58826680-58826830	HEK293	kidney:	n/a	n/a
44	CTCF	chr11:58825948-58826257	ECC-1	luminal epithelium:	n/a	n/a
45	CTCF	chr11:58825924-58826243	NHEK	skin:	n/a	n/a
46	CTCF	chr11:58826020-58826170	NB4	blood:	n/a	n/a
47	CTCF	chr11:58864700-58864850	AG09319	gingival:	n/a	chr11:58864789-58864805 chr11:58864791-58864804 chr11:58864788-58864806 chr11:58864790-58864811 chr11:58864791-58864799
48	CTCF	chr11:58826020-58826170	GM12866	blood:	n/a	n/a
49	CTCF	chr11:58864660-58864810	GM12801	blood:	n/a	chr11:58864789-58864805 chr11:58864791-58864804 chr11:58864788-58864806 chr11:58864791-58864799
50	CTCF	chr11:58864529-58864998	A549	lung:	n/a	chr11:58864789-58864805 chr11:58864791-58864804 chr11:58864788-58864806 chr11:58864790-58864811 chr11:58864791-58864799

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58825870-58825920	NH-A	brain:	n/a
2	chr11:58826475-58826525	NT2-D1	testis:	n/a
3	chr11:58825870-58825920	NH-A	brain:	n/a
4	chr11:58826475-58826525	NT2-D1	testis:	n/a
5	chr11:58826073-58826123	HEK293	kidney:	embryo
6	chr11:58830610-58830660	NB4	blood:	n/a
7	chr11:58833356-58833406	ovcar-3	ovarian:	n/a
8	chr11:58828174-58828224	HRE	kidney:	n/a
9	chr11:58825870-58825920	HCM	heart:	n/a
10	chr11:58830857-58830907	PrEC	prostate:	n/a
11	chr11:58826475-58826525	PFSK-1	brain:	n/a
12	chr11:58830424-58830474	HUVEC	blood vessel:	n/a
13	chr11:58825714-58825764	HRE	kidney:	n/a
14	chr11:58830610-58830660	GM06990	blood:	n/a
15	chr11:58825870-58825920	GM19239	blood:	n/a
16	chr11:58830191-58830241	HAEpiC	amniotic membrane:	n/a
17	chr11:58825870-58825920	HMEC	breast:	n/a
18	chr11:58833356-58833406	U87	brain:	n/a
19	chr11:58830355-58830405	K562	blood:	n/a
20	chr11:58826475-58826525	HCM	heart:	n/a
21	chr11:58830355-58830405	A549	lung:	n/a
22	chr11:58826475-58826525	SK-N-MC	brain:	n/a
23	chr11:58826073-58826123	Caco-2	colon:	n/a
24	chr11:58830857-58830907	HCF	heart:	n/a
25	chr11:58830355-58830405	HUVEC	blood vessel:	n/a
26	chr11:58826073-58826123	SK-N-MC	brain:	n/a
27	chr11:58830857-58830907	Hela-S3	cervix:	n/a
28	chr11:58826073-58826123	AG10803	skin:	n/a
29	chr11:58825714-58825764	HCF	heart:	n/a
30	chr11:58833356-58833406	MCF10A-Er-Src	breast:	n/a
31	chr11:58826414-58826464	BJ	skin:	n/a
32	chr11:58826073-58826123	HMEC	breast:	n/a
33	chr11:58826475-58826525	HepG2	liver:	n/a
34	chr11:58830191-58830241	Hepatocyte	liver:	n/a
35	chr11:58828174-58828224	U87	brain:	n/a
36	chr11:58825714-58825764	SK-N-SH_RA	brain:	n/a
37	chr11:58833356-58833406	H1-hESC	embryonic stem cell:	embryo
38	chr11:58833356-58833406	BE2_C	brain:	n/a
39	chr11:58825870-58825920	T-47D	breast:	n/a
40	chr11:58833356-58833406	AG09319	gingival:	n/a
41	chr11:58826414-58826464	SKMC	muscle:	n/a
42	chr11:58828174-58828224	GM12878	blood:	n/a
43	chr11:58830191-58830241	SK-N-SH	brain:	n/a
44	chr11:58830610-58830660	HEEpiC	esophagus:	n/a
45	chr11:58828174-58828224	AG04450	lung:	fetal
46	chr11:58830424-58830474	HPAEpiC	pulmonary alveolar:	n/a
47	chr11:58830424-58830474	GM06990	blood:	n/a
48	chr11:58828174-58828224	AG10803	skin:	n/a
49	chr11:58830610-58830660	Jurkat	blood:	n/a
50	chr11:58830355-58830405	AG09309	skin:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:58864668..58865554-chr11:58903471..58904061,2	MCF-7	breast:
2	chr11:58399679..58402149-chr11:58838160..58840024,2	K562	blood:
3	chr11:58863409..58866220-chr11:58910202..58912249,2	K562	blood:
4	chr11:58830364..58831268-chr11:58873992..58874927,2	HCT-116	colon:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLYATL2-2	chr11:58822768-58822919	ENSG00000255240.1
2	lnc-GLYATL2-2	chr11:58825845-58825925	NR_033853
3	lnc-GLYATL2-2	chr11:58825845-58826132	ENSG00000255240.1
4	lnc-GLYATL2-2	chr11:58825845-58825923	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
ENSG00000166801	chromatin interactions
ENSG00000245571	chromatin interactions

Extended variants
information (count: 1609 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:1609 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562854396	chr11:58822379-58822380	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs576321066	chr11:58822394-58822395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542457804	chr11:58822400-58822401	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs550786244	chr11:58822427-58822428	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184757780	chr11:58822429-58822430	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533273401	chr11:58822440-58822441	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs531046377	chr11:58822462-58822463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562120629	chr11:58822487-58822488	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs368981888	chr11:58822513-58822514	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533590488	chr11:58822515-58822516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs189679445	chr11:58822596-58822597	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567059576	chr11:58822627-58822628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373530063	chr11:58822657-58822658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181604619	chr11:58822674-58822675	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185196747	chr11:58822684-58822685	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575711174	chr11:58822700-58822701	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs144802941	chr11:58822720-58822721	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs527416917	chr11:58822725-58822726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148632274	chr11:58822732-58822733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs6591504	chr11:58822800-58822801	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs540669713	chr11:58822841-58822842	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs189224082	chr11:58822850-58822851	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs540242	chr11:58822853-58822854	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs544350971	chr11:58822854-58822855	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs12270247	chr11:58822865-58822866	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs181910012	chr11:58822887-58822888	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs532938506	chr11:58822905-58822906	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs74718700	chr11:58822907-58822908	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs147343196	chr11:58822913-58822914	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs139465106	chr11:58822919-58822920	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs548598542	chr11:58822944-58822945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs118064264	chr11:58822951-58822952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531448988	chr11:58822954-58822955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs549567834	chr11:58822986-58822987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs186524274	chr11:58823010-58823011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539690520	chr11:58823024-58823025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs558372405	chr11:58823050-58823051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs188220092	chr11:58823057-58823058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs111587799	chr11:58823073-58823074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs112824228	chr11:58823074-58823075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs374483794	chr11:58823086-58823087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534473170	chr11:58823087-58823088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs555820086	chr11:58823128-58823129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538931616	chr11:58823210-58823211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs573911979	chr11:58823231-58823232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs550345	chr11:58823255-58823256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs556429407	chr11:58823261-58823262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs370811876	chr11:58823266-58823267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs578043035	chr11:58823315-58823316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs544839464	chr11:58823359-58823360	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:389 , 50 per page) page: 1 2 3 4 5 6 7 8

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	chr11:58817200-58825200	Weak transcription	Liver	Liver
6	chr11:58817200-58825400	Weak transcription	Fetal Intestine Large	intestine
7	chr11:58818600-58825200	Enhancers	Primary B cells from peripheral blood	blood
8	chr11:58819400-58822600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr11:58821200-58825400	Weak transcription	GM12878-XiMat	blood
10	chr11:58821600-58822400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr11:58821800-58822600	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr11:58821800-58822800	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr11:58822000-58822600	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr11:58822000-58822800	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr11:58822200-58823200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr11:58822200-58824400	Weak transcription	Primary B cells from cord blood	blood
17	chr11:58822400-58823200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr11:58822600-58823200	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr11:58822600-58825200	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr11:58822800-58825200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr11:58822800-58825200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr11:58823200-58825200	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr11:58823200-58825200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr11:58823200-58825600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr11:58824400-58824600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr11:58824400-58825200	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr11:58824400-58825200	Enhancers	Primary B cells from cord blood	blood
28	chr11:58824800-58825600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:58825200-58825400	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr11:58825200-58825400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
31	chr11:58825200-58825400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr11:58825200-58825400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr11:58825200-58825400	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr11:58825200-58825400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr11:58825200-58825400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr11:58825200-58825400	Enhancers	Liver	Liver
37	chr11:58825200-58825400	Enhancers	Fetal Thymus	thymus
38	chr11:58825200-58825400	Enhancers	Rectal Mucosa Donor 29	rectum
39	chr11:58825200-58825600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr11:58825200-58825600	Enhancers	Brain Cingulate Gyrus	brain
41	chr11:58825200-58825800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr11:58825200-58826000	Active TSS	ES-I3 Cell Line	embryonic stem cell
43	chr11:58825200-58826000	Active TSS	HUES48 Cell Line	embryonic stem cell
44	chr11:58825200-58826000	Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr11:58825200-58826200	Active TSS	Fetal Brain Female	brain
46	chr11:58825200-58826400	Flanking Active TSS	Primary B cells from cord blood	blood
47	chr11:58825200-58826400	Flanking Active TSS	Primary B cells from peripheral blood	blood
48	chr11:58825400-58825600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr11:58825400-58825600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr11:58825400-58825600	Enhancers	Primary monocytes fromperipheralblood	blood

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