Variant report

Variant	nsv1047504
Chromosome Location	chr11:58805608-58847365
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	chr11:58831416-58832275	GM12878	blood:	n/a	chr11:58831926-58831934
6	BATF	chr11:58831471-58831776	GM12878	blood:	n/a	n/a
7	BATF	chr11:58818940-58819193	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	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	chr11:58820953-58821000	K562	blood:	n/a	n/a
17	BHLHE40	chr11:58825938-58826278	GM12878	blood:	n/a	n/a
18	BRCA1	chr11:58825950-58826184	GM12878	blood:	n/a	n/a
19	CEBPB	chr11:58835676-58835875	K562	blood:	n/a	chr11:58835780-58835791
20	CEBPB	chr11:58835627-58835890	IMR90	lung:	n/a	chr11:58835780-58835791
21	CEBPB	chr11:58841369-58841519	IMR90	lung:	n/a	n/a
22	CEBPB	chr11:58827942-58827984	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr11:58825987-58826187	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr11:58835714-58835923	HepG2	liver:	n/a	chr11:58835780-58835791
25	CHD1	chr11:58821218-58821270	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD1	chr11:58825963-58826312	GM12878	blood:	n/a	n/a
27	CHD2	chr11:58826018-58826077	K562	blood:	n/a	n/a
28	CHD2	chr11:58825822-58826232	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr11:58825891-58826300	GM12878	blood:	n/a	n/a
30	CREB1	chr11:58845766-58846361	GM12878	blood:	n/a	n/a
31	CREB1	chr11:58845805-58846333	GM12878	blood:	n/a	n/a
32	CTCF	chr11:58825980-58826130	GM12866	blood:	n/a	n/a
33	CTCF	chr11:58826000-58826150	AG09319	gingival:	n/a	n/a
34	CTCF	chr11:58820880-58821030	WERI-Rb-1	eye:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
35	CTCF	chr11:58820754-58821158	H1-hESC	embryonic stem cell:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
36	CTCF	chr11:58820775-58821162	IMR90	lung:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
37	CTCF	chr11:58820858-58821084	HepG2	liver:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
38	CTCF	chr11:58820854-58821102	GM19239	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
39	CTCF	chr11:58826020-58826170	GM12870	blood:	n/a	n/a
40	CTCF	chr11:58825962-58826305	MCF-7	breast:	n/a	n/a
41	CTCF	chr11:58820940-58821090	AoAF	blood vessel:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
42	CTCF	chr11:58820920-58821070	WI-38	lung:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
43	CTCF	chr11:58820840-58820990	HL-60	blood:	n/a	chr11:58820969-58820985 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
44	CTCF	chr11:58820860-58821010	GM12864	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
45	CTCF	chr11:58820642-58820718	GM10266	blood:	n/a	n/a
46	CTCF	chr11:58820880-58821150	A549	lung:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
47	CTCF	chr11:58820845-58821120	GM19238	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
48	CTCF	chr11:58820771-58821119	K562	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
49	CTCF	chr11:58826000-58826150	AG04450	lung:	n/a	n/a
50	CTCF	chr11:58820900-58821050	Caco-2	colon:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58825870-58825920	RPTEC	kidney:	n/a
2	chr11:58826073-58826123	SK-N-SH_RA	brain:	n/a
3	chr11:58825870-58825920	RPTEC	kidney:	n/a
4	chr11:58826073-58826123	SK-N-SH_RA	brain:	n/a
5	chr11:58830610-58830660	AG04449	skin:	fetal
6	chr11:58825714-58825764	IMR90	lung:	fetal
7	chr11:58830610-58830660	T-47D	breast:	n/a
8	chr11:58830191-58830241	AG10803	skin:	n/a
9	chr11:58825714-58825764	MCF10A-Er-Src	breast:	n/a
10	chr11:58825714-58825764	GM12891	blood:	n/a
11	chr11:58826110-58826160	T-47D	breast:	n/a
12	chr11:58806952-58807002	LNCaP	prostate:	n/a
13	chr11:58830424-58830474	ProgFib	skin:	n/a
14	chr11:58826475-58826525	HIPEpiC	eye:	n/a
15	chr11:58830191-58830241	Hela-S3	cervix:	n/a
16	chr11:58826110-58826160	HRPEpiC	eye:	n/a
17	chr11:58826110-58826160	HPAEpiC	pulmonary alveolar:	n/a
18	chr11:58826475-58826525	SK-N-MC	brain:	n/a
19	chr11:58810187-58810237	GM12892	blood:	n/a
20	chr11:58806952-58807002	AG04450	lung:	fetal
21	chr11:58830610-58830660	HNPCEpiC	eye:	n/a
22	chr11:58830857-58830907	Jurkat	blood:	n/a
23	chr11:58806952-58807002	PANC-1	pancreas:	n/a
24	chr11:58826110-58826160	Jurkat	blood:	n/a
25	chr11:58806952-58807002	HepG2	liver:	n/a
26	chr11:58810187-58810237	HUVEC	blood vessel:	n/a
27	chr11:58833356-58833406	CMK	blood:	n/a
28	chr11:58830355-58830405	U87	brain:	n/a
29	chr11:58830191-58830241	CMK	blood:	n/a
30	chr11:58826414-58826464	SK-N-SH	brain:	n/a
31	chr11:58830857-58830907	T-47D	breast:	n/a
32	chr11:58833356-58833406	SK-N-SH_RA	brain:	n/a
33	chr11:58826414-58826464	ovcar-3	ovarian:	n/a
34	chr11:58833356-58833406	AG04449	skin:	fetal
35	chr11:58830610-58830660	GM12878	blood:	n/a
36	chr11:58830424-58830474	Hela-S3	cervix:	n/a
37	chr11:58830355-58830405	SAEC	small airway:	n/a
38	chr11:58828174-58828224	SAEC	small airway:	n/a
39	chr11:58830424-58830474	T-47D	breast:	n/a
40	chr11:58826073-58826123	SAEC	small airway:	n/a
41	chr11:58833356-58833406	HRCEpiC	kidney:	n/a
42	chr11:58826475-58826525	AG09309	skin:	n/a
43	chr11:58826414-58826464	LNCaP	prostate:	n/a
44	chr11:58825870-58825920	NH-A	brain:	n/a
45	chr11:58825714-58825764	HNPCEpiC	eye:	n/a
46	chr11:58830355-58830405	HRE	kidney:	n/a
47	chr11:58810187-58810237	HIPEpiC	eye:	n/a
48	chr11:58830610-58830660	NH-A	brain:	n/a
49	chr11:58810187-58810237	AG04449	skin:	fetal
50	chr11:58830610-58830660	HMEC	breast:	n/a

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

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

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

Extended variants
information (count: 1479 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1479 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2849734	chr11:58805608-58805609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs569741929	chr11:58805680-58805681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535971654	chr11:58805711-58805712	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557145529	chr11:58805712-58805713	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141826339	chr11:58805717-58805718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs545978724	chr11:58805719-58805720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558084577	chr11:58805745-58805746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2849735	chr11:58805786-58805787	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs2720333	chr11:58805814-58805815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs189713716	chr11:58805818-58805819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs12290612	chr11:58805820-58805821	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs544312457	chr11:58805825-58805826	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562404564	chr11:58805828-58805829	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531138729	chr11:58805829-58805830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182373925	chr11:58805840-58805841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187000473	chr11:58805843-58805844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs113376864	chr11:58805844-58805845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528793204	chr11:58805868-58805869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546866217	chr11:58805872-58805873	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568462067	chr11:58805905-58805906	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534607435	chr11:58805909-58805910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs2954130	chr11:58805914-58805915	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2954131	chr11:58805920-58805921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2954132	chr11:58805937-58805938	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535445351	chr11:58805965-58805966	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs145677545	chr11:58805986-58805987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569204556	chr11:58805999-58806000	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539935177	chr11:58806023-58806024	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182821381	chr11:58806079-58806080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558021107	chr11:58806082-58806083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573055824	chr11:58806096-58806097	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188373958	chr11:58806111-58806112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs118004976	chr11:58806116-58806117	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs193180390	chr11:58806122-58806123	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs114053110	chr11:58806143-58806144	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562501582	chr11:58806155-58806156	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185490858	chr11:58806182-58806183	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577358670	chr11:58806199-58806200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs151078867	chr11:58806243-58806244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs189104527	chr11:58806247-58806248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs200713628	chr11:58806248-58806249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs528632584	chr11:58806252-58806253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs11229763	chr11:58806327-58806328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546904656	chr11:58806331-58806332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs562202030	chr11:58806332-58806333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs199499437	chr11:58806348-58806349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529289685	chr11:58806385-58806386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs10792215	chr11:58806390-58806391	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs529910655	chr11:58806395-58806396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs60763754	chr11:58806396-58806397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

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	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58782800-58810600	Weak transcription	Primary B cells from cord blood	blood
2	chr11:58804600-58806200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr11:58804600-58807400	Weak transcription	Primary B cells from peripheral blood	blood
4	chr11:58805000-58806200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr11:58805000-58825200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr11:58805200-58825400	Weak transcription	Primary hematopoietic stem cells	blood
7	chr11:58806200-58807400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr11:58806200-58807800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr11:58807400-58808000	Strong transcription	Primary B cells from peripheral blood	blood
10	chr11:58808000-58808200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr11:58808000-58808600	Enhancers	Stomach Mucosa	stomach
12	chr11:58808000-58810800	Weak transcription	Primary B cells from peripheral blood	blood
13	chr11:58810600-58811400	Strong transcription	Primary B cells from cord blood	blood
14	chr11:58810800-58811800	Strong transcription	Primary B cells from peripheral blood	blood
15	chr11:58811400-58818200	Weak transcription	Primary B cells from cord blood	blood
16	chr11:58811800-58816200	Weak transcription	Primary B cells from peripheral blood	blood
17	chr11:58813600-58825200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr11:58815400-58824400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr11:58816200-58818200	Strong transcription	Primary B cells from peripheral blood	blood
20	chr11:58816600-58816800	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr11:58816800-58817000	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr11:58817000-58817200	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr11:58817000-58817200	Enhancers	Fetal Intestine Large	intestine
24	chr11:58817000-58818200	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr11:58817200-58821800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr11:58817200-58825200	Weak transcription	Liver	Liver
27	chr11:58817200-58825400	Weak transcription	Fetal Intestine Large	intestine
28	chr11:58817400-58819400	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr11:58817400-58822000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr11:58818200-58818600	Genic enhancers	Primary B cells from peripheral blood	blood
31	chr11:58818200-58819400	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr11:58818200-58820200	Enhancers	Primary B cells from cord blood	blood
33	chr11:58818600-58825200	Enhancers	Primary B cells from peripheral blood	blood
34	chr11:58818800-58819400	Enhancers	GM12878-XiMat	blood
35	chr11:58819200-58819400	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr11:58819400-58820600	Weak transcription	GM12878-XiMat	blood
37	chr11:58819400-58821200	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr11:58819400-58822000	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr11:58819400-58822600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr11:58820200-58820800	Weak transcription	Primary B cells from cord blood	blood
41	chr11:58820600-58821200	Enhancers	GM12878-XiMat	blood
42	chr11:58820800-58822200	Enhancers	Primary B cells from cord blood	blood
43	chr11:58821200-58821400	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr11:58821200-58821600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr11:58821200-58825400	Weak transcription	GM12878-XiMat	blood
46	chr11:58821400-58822200	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr11:58821600-58822400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr11:58821800-58822600	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr11:58821800-58822800	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr11:58822000-58822600	Enhancers	HUES6 Cell Line	embryonic stem cell

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