Variant report

Variant	nsv915873
Chromosome Location	chr11:58766189-58846911
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:776)
CpG islands
(count:916)
Chromatin interactive
region (count:3)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:776 , 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	ARID3A	chr11:58792609-58792905	HepG2	liver:	n/a	n/a
2	ATF1	chr11:58779639-58779652	K562	blood:	n/a	n/a
3	ATF2	chr11:58831402-58832419	GM12878	blood:	n/a	n/a
4	ATF2	chr11:58831671-58832143	GM12878	blood:	n/a	n/a
5	ATF2	chr11:58825833-58826405	GM12878	blood:	n/a	n/a
6	BACH1	chr11:58825972-58826213	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr11:58831471-58831776	GM12878	blood:	n/a	n/a
8	BATF	chr11:58831786-58832150	GM12878	blood:	n/a	chr11:58831926-58831934
9	BATF	chr11:58826199-58826498	GM12878	blood:	n/a	n/a
10	BATF	chr11:58818940-58819193	GM12878	blood:	n/a	n/a
11	BATF	chr11:58831416-58832275	GM12878	blood:	n/a	chr11:58831926-58831934
12	BCL11A	chr11:58818878-58819275	GM12878	blood:	n/a	chr11:58819091-58819100
13	BCL11A	chr11:58818899-58819262	GM12878	blood:	n/a	chr11:58819091-58819100
14	BCL11A	chr11:58831528-58832157	GM12878	blood:	n/a	n/a
15	BCL11A	chr11:58831483-58831904	GM12878	blood:	n/a	n/a
16	BCL3	chr11:58831794-58832281	GM12878	blood:	n/a	n/a
17	BHLHE40	chr11:58826040-58826162	K562	blood:	n/a	n/a
18	BHLHE40	chr11:58820953-58821000	K562	blood:	n/a	n/a
19	BHLHE40	chr11:58825938-58826278	GM12878	blood:	n/a	n/a
20	BHLHE40	chr11:58792570-58792935	HepG2	liver:	n/a	chr11:58792752-58792765 chr11:58792748-58792769
21	BRCA1	chr11:58825950-58826184	GM12878	blood:	n/a	n/a
22	CEBPB	chr11:58780472-58780728	HepG2	liver:	n/a	chr11:58780597-58780608
23	CEBPB	chr11:58767588-58767695	A549	lung:	n/a	n/a
24	CEBPB	chr11:58825987-58826187	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr11:58827942-58827984	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr11:58767634-58767824	Hela-S3	cervix:	n/a	chr11:58767688-58767699 chr11:58767686-58767697
27	CEBPB	chr11:58767565-58767768	HepG2	liver:	n/a	chr11:58767688-58767699 chr11:58767686-58767697
28	CEBPB	chr11:58767586-58767847	H1-hESC	embryonic stem cell:	n/a	chr11:58767688-58767699 chr11:58767686-58767697
29	CEBPB	chr11:58779256-58779450	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr11:58835676-58835875	K562	blood:	n/a	chr11:58835780-58835791
31	CEBPB	chr11:58841369-58841519	IMR90	lung:	n/a	n/a
32	CEBPB	chr11:58774084-58774291	HepG2	liver:	n/a	chr11:58774243-58774254
33	CEBPB	chr11:58767676-58767679	K562	blood:	n/a	n/a
34	CEBPB	chr11:58835627-58835890	IMR90	lung:	n/a	chr11:58835780-58835791
35	CEBPB	chr11:58835714-58835923	HepG2	liver:	n/a	chr11:58835780-58835791
36	CHD1	chr11:58825963-58826312	GM12878	blood:	n/a	n/a
37	CHD1	chr11:58821218-58821270	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr11:58825822-58826232	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr11:58826018-58826077	K562	blood:	n/a	n/a
40	CHD2	chr11:58825891-58826300	GM12878	blood:	n/a	n/a
41	CREB1	chr11:58845805-58846333	GM12878	blood:	n/a	n/a
42	CREB1	chr11:58845766-58846361	GM12878	blood:	n/a	n/a
43	CTCF	chr11:58820840-58820990	GM12874	blood:	n/a	chr11:58820969-58820985 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
44	CTCF	chr11:58843660-58843810	GM12869	blood:	n/a	n/a
45	CTCF	chr11:58825953-58826185	GM20000	blood:	n/a	n/a
46	CTCF	chr11:58820650-58820688	GM12878	blood:	n/a	n/a
47	CTCF	chr11:58826000-58826150	HCFaa	heart:	n/a	n/a
48	CTCF	chr11:58820940-58821090	HCFaa	heart:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
49	CTCF	chr11:58825883-58826276	K562	blood:	n/a	n/a
50	CTCF	chr11:58820860-58821010	MCF-7	breast:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58825714-58825764	Hepatocyte	liver:	n/a
2	chr11:58825714-58825764	Hepatocyte	liver:	n/a
3	chr11:58830191-58830241	GM12878	blood:	n/a
4	chr11:58825714-58825764	SK-N-MC	brain:	n/a
5	chr11:58830424-58830474	AG09309	skin:	n/a
6	chr11:58826414-58826464	MCF10A-Er-Src	breast:	n/a
7	chr11:58830355-58830405	BE2_C	brain:	n/a
8	chr11:58806952-58807002	K562	blood:	n/a
9	chr11:58828174-58828224	AG09319	gingival:	n/a
10	chr11:58830191-58830241	HCM	heart:	n/a
11	chr11:58826475-58826525	NHBE	bronchial:	n/a
12	chr11:58830191-58830241	SK-N-SH	brain:	n/a
13	chr11:58830610-58830660	NHBE	bronchial:	n/a
14	chr11:58825714-58825764	PANC-1	pancreas:	n/a
15	chr11:58830355-58830405	BJ	skin:	n/a
16	chr11:58830191-58830241	K562	blood:	n/a
17	chr11:58830424-58830474	ECC-1	luminal epithelium:	n/a
18	chr11:58806952-58807002	AG10803	skin:	n/a
19	chr11:58830424-58830474	HRE	kidney:	n/a
20	chr11:58830610-58830660	LNCaP	prostate:	n/a
21	chr11:58826073-58826123	PANC-1	pancreas:	n/a
22	chr11:58810187-58810237	Hepatocyte	liver:	n/a
23	chr11:58830857-58830907	ovcar-3	ovarian:	n/a
24	chr11:58830355-58830405	HL-60	blood:	n/a
25	chr11:58833356-58833406	LNCaP	prostate:	n/a
26	chr11:58826414-58826464	AG04449	skin:	fetal
27	chr11:58825870-58825920	GM06990	blood:	n/a
28	chr11:58826110-58826160	HMEC	breast:	n/a
29	chr11:58825714-58825764	HCM	heart:	n/a
30	chr11:58825870-58825920	SK-N-SH_RA	brain:	n/a
31	chr11:58826475-58826525	SK-N-SH	brain:	n/a
32	chr11:58826073-58826123	NH-A	brain:	n/a
33	chr11:58826073-58826123	T-47D	breast:	n/a
34	chr11:58826414-58826464	AG10803	skin:	n/a
35	chr11:58825714-58825764	IMR90	lung:	fetal
36	chr11:58825714-58825764	NT2-D1	testis:	n/a
37	chr11:58830857-58830907	GM06990	blood:	n/a
38	chr11:58830355-58830405	HMEC	breast:	n/a
39	chr11:58833356-58833406	HRE	kidney:	n/a
40	chr11:58810187-58810237	SK-N-SH_RA	brain:	n/a
41	chr11:58828174-58828224	NT2-D1	testis:	n/a
42	chr11:58830857-58830907	NHBE	bronchial:	n/a
43	chr11:58826110-58826160	AoSMC	blood vessel:	n/a
44	chr11:58830355-58830405	NHDF-neo	bronchial:	n/a
45	chr11:58830424-58830474	HL-60	blood:	n/a
46	chr11:58830355-58830405	NHBE	bronchial:	n/a
47	chr11:58825870-58825920	HCPEpiC	choroid plexus:	n/a
48	chr11:58825870-58825920	NH-A	brain:	n/a
49	chr11:58833356-58833406	HCM	heart:	n/a
50	chr11:58830191-58830241	Hela-S3	cervix:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:58830364..58831268-chr11:58873992..58874927,2	HCT-116	colon:
2	chr11:58762969..58764487-chr11:58768997..58771127,2	K562	blood:
3	chr11:58399679..58402149-chr11:58838160..58840024,2	K562	blood:

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

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

No data

Variant related genes	Relation type
ENSG00000255240	TF binding region
GLYATL1P4	TF binding region
ENSG00000254786	TF binding region
ENSG00000255240	CpG island
GLYATL1P4	CpG island
ENSG00000254786	CpG island
ENSG00000189057	chromatin interactions

Extended variants
information (count: 3048 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:3048 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557738556	chr11:58766249-58766250	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs386753960	chr11:58766264-58766265	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs7946908	chr11:58766266-58766267	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs558923251	chr11:58766284-58766285	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs10896889	chr11:58766296-58766297	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs541920622	chr11:58766313-58766314	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs141257192	chr11:58766314-58766315	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs112316581	chr11:58766322-58766323	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570377915	chr11:58766451-58766452	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs113942490	chr11:58766485-58766486	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs369565884	chr11:58766524-58766525	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs537412804	chr11:58766525-58766526	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs372333462	chr11:58766600-58766601	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs559017270	chr11:58766623-58766624	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs10896890	chr11:58766639-58766640	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs377476850	chr11:58766655-58766656	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs191128172	chr11:58766735-58766736	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs577202576	chr11:58766736-58766737	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs574500234	chr11:58766740-58766741	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs117342245	chr11:58766752-58766753	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs563215074	chr11:58766781-58766782	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs367846058	chr11:58766882-58766883	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545378212	chr11:58766895-58766896	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563778786	chr11:58766899-58766900	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528189773	chr11:58766943-58766944	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546334122	chr11:58766944-58766945	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs117624725	chr11:58766959-58766960	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10896891	chr11:58767017-58767018	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs548821375	chr11:58767023-58767024	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs76756281	chr11:58767070-58767071	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541038610	chr11:58767125-58767126	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376178090	chr11:58767126-58767127	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs143927602	chr11:58767127-58767128	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564481932	chr11:58767203-58767204	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs533491707	chr11:58767210-58767211	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs533495979	chr11:58767229-58767230	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs558980150	chr11:58767248-58767249	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs147237575	chr11:58767347-58767348	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535020462	chr11:58767364-58767365	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs180691300	chr11:58767407-58767408	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550427380	chr11:58767416-58767417	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541638843	chr11:58767420-58767421	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556772393	chr11:58767467-58767468	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs11229723	chr11:58767505-58767506	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs544693957	chr11:58767508-58767509	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529461617	chr11:58767523-58767524	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs199601537	chr11:58767556-58767557	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs185350145	chr11:58767576-58767577	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs377135616	chr11:58767600-58767601	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs548318175	chr11:58767611-58767612	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58757400-58766600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr11:58758600-58766400	Weak transcription	Primary B cells from cord blood	blood
3	chr11:58760400-58767000	Weak transcription	GM12878-XiMat	blood
4	chr11:58761000-58769200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr11:58762400-58766400	Weak transcription	Primary B cells from peripheral blood	blood
6	chr11:58764800-58775200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr11:58765600-58766400	Enhancers	Liver	Liver
8	chr11:58765600-58767800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr11:58765800-58766200	Strong transcription	Primary hematopoietic stem cells	blood
10	chr11:58766200-58769000	Weak transcription	Primary hematopoietic stem cells	blood
11	chr11:58766400-58766600	Enhancers	Stomach Mucosa	stomach
12	chr11:58766400-58766800	Flanking Active TSS	Liver	Liver
13	chr11:58766400-58767600	Enhancers	Primary B cells from cord blood	blood
14	chr11:58766400-58767600	Enhancers	Primary B cells from peripheral blood	blood
15	chr11:58766600-58767200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
16	chr11:58766600-58767400	Enhancers	Sigmoid Colon	Sigmoid Colon
17	chr11:58766600-58768000	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr11:58766600-58768000	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr11:58766800-58767200	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr11:58766800-58767800	Enhancers	Liver	Liver
21	chr11:58767000-58767400	Enhancers	GM12878-XiMat	blood
22	chr11:58767200-58767400	Enhancers	Stomach Mucosa	stomach
23	chr11:58767200-58774000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr11:58767600-58770000	Weak transcription	Primary B cells from cord blood	blood
25	chr11:58767600-58776400	Weak transcription	Primary B cells from peripheral blood	blood
26	chr11:58767800-58769200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr11:58767800-58771200	Weak transcription	Liver	Liver
28	chr11:58769000-58770600	Enhancers	Primary hematopoietic stem cells	blood
29	chr11:58769200-58770400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr11:58769200-58770400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr11:58770000-58771600	Strong transcription	Primary B cells from cord blood	blood
32	chr11:58770400-58773600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr11:58770400-58774400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr11:58770600-58775200	Weak transcription	Primary hematopoietic stem cells	blood
35	chr11:58771200-58772200	Enhancers	Liver	Liver
36	chr11:58771600-58776600	Weak transcription	Primary B cells from cord blood	blood
37	chr11:58772200-58772600	Weak transcription	Liver	Liver
38	chr11:58772600-58773600	Enhancers	Liver	Liver
39	chr11:58773600-58776000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr11:58773600-58776000	Weak transcription	Liver	Liver
41	chr11:58774000-58774200	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr11:58774200-58774600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr11:58774400-58775200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr11:58774600-58774800	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr11:58774800-58775800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr11:58775200-58778600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr11:58775200-58780000	Enhancers	Primary hematopoietic stem cells	blood
48	chr11:58775200-58781000	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr11:58775800-58776000	Active TSS	Primary hematopoietic stem cells short term culture	blood
50	chr11:58776000-58777200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood

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