Variant report

Variant	esv3395928
Chromosome Location	chr11:58806208-58850452
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	chr11:58831671-58832143	GM12878	blood:	n/a	n/a
3	ATF2	chr11:58831402-58832419	GM12878	blood:	n/a	n/a
4	BACH1	chr11:58825972-58826213	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr11:58826199-58826498	GM12878	blood:	n/a	n/a
6	BATF	chr11:58818940-58819193	GM12878	blood:	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	chr11:58831416-58832275	GM12878	blood:	n/a	chr11:58831926-58831934
10	BCL11A	chr11:58818899-58819262	GM12878	blood:	n/a	chr11:58819091-58819100
11	BCL11A	chr11:58818878-58819275	GM12878	blood:	n/a	chr11:58819091-58819100
12	BCL11A	chr11:58831483-58831904	GM12878	blood:	n/a	n/a
13	BCL11A	chr11:58831528-58832157	GM12878	blood:	n/a	n/a
14	BCL3	chr11:58831794-58832281	GM12878	blood:	n/a	n/a
15	BHLHE40	chr11:58825938-58826278	GM12878	blood:	n/a	n/a
16	BHLHE40	chr11:58820953-58821000	K562	blood:	n/a	n/a
17	BHLHE40	chr11:58826040-58826162	K562	blood:	n/a	n/a
18	BRCA1	chr11:58825950-58826184	GM12878	blood:	n/a	n/a
19	CEBPB	chr11:58827942-58827984	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr11:58825987-58826187	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr11:58835714-58835923	HepG2	liver:	n/a	chr11:58835780-58835791
22	CEBPB	chr11:58835627-58835890	IMR90	lung:	n/a	chr11:58835780-58835791
23	CEBPB	chr11:58841369-58841519	IMR90	lung:	n/a	n/a
24	CEBPB	chr11:58835676-58835875	K562	blood:	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	chr11:58825822-58826232	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr11:58826018-58826077	K562	blood:	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	chr11:58820639-58820705	GM10248	blood:	n/a	n/a
33	CTCF	chr11:58820881-58821070	MCF-7	breast:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
34	CTCF	chr11:58820940-58821090	AoAF	blood vessel:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
35	CTCF	chr11:58820775-58821162	IMR90	lung:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
36	CTCF	chr11:58825852-58826271	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr11:58820880-58821030	HCPEpiC	choroid plexus:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
38	CTCF	chr11:58843660-58843810	GM12869	blood:	n/a	n/a
39	CTCF	chr11:58826000-58826150	AG04449	skin:	n/a	n/a
40	CTCF	chr11:58825962-58826217	MCF-7	breast:	n/a	n/a
41	CTCF	chr11:58820040-58820123	GM10248	blood:	n/a	n/a
42	CTCF	chr11:58820580-58820730	GM12878	blood:	n/a	n/a
43	CTCF	chr11:58820900-58821050	GM12864	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
44	CTCF	chr11:58820790-58821140	A549	lung:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
45	CTCF	chr11:58820860-58821010	GM12865	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
46	CTCF	chr11:58820889-58821070	GM13976	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
47	CTCF	chr11:58825911-58826191	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr11:58820858-58821084	HepG2	liver:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
49	CTCF	chr11:58826000-58826150	BJ	skin:	n/a	n/a
50	CTCF	chr11:58820860-58821010	HCT-116	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	chr11:58826073-58826123	HEK293	kidney:	embryo
2	chr11:58830424-58830474	HEEpiC	esophagus:	n/a
3	chr11:58830857-58830907	T-47D	breast:	n/a
4	chr11:58826073-58826123	HEK293	kidney:	embryo
5	chr11:58830424-58830474	HEEpiC	esophagus:	n/a
6	chr11:58830857-58830907	T-47D	breast:	n/a
7	chr11:58830355-58830405	AoSMC	blood vessel:	n/a
8	chr11:58828174-58828224	PFSK-1	brain:	n/a
9	chr11:58826475-58826525	PrEC	prostate:	n/a
10	chr11:58830355-58830405	U87	brain:	n/a
11	chr11:58806952-58807002	HMEC	breast:	n/a
12	chr11:58830191-58830241	GM19239	blood:	n/a
13	chr11:58806952-58807002	MCF-7	breast:	n/a
14	chr11:58826414-58826464	Caco-2	colon:	n/a
15	chr11:58825714-58825764	RPTEC	kidney:	n/a
16	chr11:58828174-58828224	Hepatocyte	liver:	n/a
17	chr11:58826073-58826123	HRCEpiC	kidney:	n/a
18	chr11:58826110-58826160	H1-hESC	embryonic stem cell:	embryo
19	chr11:58825714-58825764	NH-A	brain:	n/a
20	chr11:58826475-58826525	SAEC	small airway:	n/a
21	chr11:58826073-58826123	HCM	heart:	n/a
22	chr11:58830355-58830405	LNCaP	prostate:	n/a
23	chr11:58830610-58830660	CMK	blood:	n/a
24	chr11:58828174-58828224	GM06990	blood:	n/a
25	chr11:58810187-58810237	CMK	blood:	n/a
26	chr11:58825714-58825764	SAEC	small airway:	n/a
27	chr11:58830610-58830660	GM06990	blood:	n/a
28	chr11:58825870-58825920	HRE	kidney:	n/a
29	chr11:58830355-58830405	AG09309	skin:	n/a
30	chr11:58826110-58826160	HCPEpiC	choroid plexus:	n/a
31	chr11:58806952-58807002	Jurkat	blood:	n/a
32	chr11:58810187-58810237	AG09319	gingival:	n/a
33	chr11:58826110-58826160	PrEC	prostate:	n/a
34	chr11:58828174-58828224	AG09309	skin:	n/a
35	chr11:58826073-58826123	NHDF-neo	bronchial:	n/a
36	chr11:58833356-58833406	HRCEpiC	kidney:	n/a
37	chr11:58826073-58826123	AG04449	skin:	fetal
38	chr11:58810187-58810237	AG09309	skin:	n/a
39	chr11:58830424-58830474	SKMC	muscle:	n/a
40	chr11:58830857-58830907	ProgFib	skin:	n/a
41	chr11:58830857-58830907	MCF10A-Er-Src	breast:	n/a
42	chr11:58810187-58810237	ProgFib	skin:	n/a
43	chr11:58826073-58826123	HIPEpiC	eye:	n/a
44	chr11:58830424-58830474	HL-60	blood:	n/a
45	chr11:58830424-58830474	HRE	kidney:	n/a
46	chr11:58830355-58830405	ovcar-3	ovarian:	n/a
47	chr11:58833356-58833406	HUVEC	blood vessel:	n/a
48	chr11:58828174-58828224	PANC-1	pancreas:	n/a
49	chr11:58830355-58830405	HCM	heart:	n/a
50	chr11:58826110-58826160	RPTEC	kidney:	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	chr11:58818733-58818781	ENSG00000255240.1
2	lnc-GLYATL2-2	chr11:58825845-58825923	ENSG00000255240.1
3	lnc-GLYATL2-2	chr11:58822768-58822919	ENSG00000255240.1
4	lnc-GLYATL2-2	chr11:58818733-58818781	NR_033853
5	lnc-GLYATL2-2	chr11:58825845-58825925	NR_033853
6	lnc-GLYATL2-2	chr11:58825845-58826132	ENSG00000255240.1
7	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
8	lnc-GLYATL2-2	chr11:58820930-58821099	NR_033853
9	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
10	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1

Variant related genes	Relation type
ENSG00000255240	TF binding region
GLYATL1P3	TF binding region
GLYATL1P4	TF binding region
ENSG00000255240	CpG island
GLYATL1P3	CpG island
GLYATL1P4	CpG island
ENSG00000189057	chromatin interactions

Extended variants
information (count: 1574 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1574 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs151078867	chr11:58806243-58806244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs189104527	chr11:58806247-58806248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs200713628	chr11:58806248-58806249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528632584	chr11:58806252-58806253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs11229763	chr11:58806327-58806328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs546904656	chr11:58806331-58806332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs562202030	chr11:58806332-58806333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs199499437	chr11:58806348-58806349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs529289685	chr11:58806385-58806386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs10792215	chr11:58806390-58806391	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs529910655	chr11:58806395-58806396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs60763754	chr11:58806396-58806397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs569224205	chr11:58806400-58806401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556258849	chr11:58806402-58806403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551880472	chr11:58806456-58806457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183629134	chr11:58806466-58806467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs371560768	chr11:58806506-58806507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs12362597	chr11:58806527-58806528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs555640179	chr11:58806556-58806557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs4373955	chr11:58806666-58806667	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs535465616	chr11:58806667-58806668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188385566	chr11:58806708-58806709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555920706	chr11:58806739-58806740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs144941103	chr11:58806756-58806757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs544724816	chr11:58806791-58806792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs559780648	chr11:58806800-58806801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs370613072	chr11:58806802-58806803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs140938214	chr11:58806831-58806832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540423005	chr11:58806848-58806849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs562301469	chr11:58806875-58806876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs1961876	chr11:58806884-58806885	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs551237431	chr11:58806892-58806893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs562895875	chr11:58806897-58806898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs533332392	chr11:58806906-58806907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551917109	chr11:58806914-58806915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs78967894	chr11:58806931-58806932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs144589381	chr11:58806943-58806944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs114369932	chr11:58806952-58806953	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs181158053	chr11:58806953-58806954	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs535679889	chr11:58806965-58806966	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs185067950	chr11:58806988-58806989	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs10896904	chr11:58807029-58807030	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs556394737	chr11:58807045-58807046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs189929532	chr11:58807047-58807048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs182048305	chr11:58807111-58807112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs553452258	chr11:58807118-58807119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs571854821	chr11:58807137-58807138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs542695216	chr11:58807139-58807140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141816985	chr11:58807169-58807170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs367681729	chr11:58807195-58807196	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:343 , 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	chr11:58804600-58807400	Weak transcription	Primary B cells from peripheral blood	blood
3	chr11:58805000-58825200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr11:58805200-58825400	Weak transcription	Primary hematopoietic stem cells	blood
5	chr11:58806200-58807400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr11:58806200-58807800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr11:58807400-58808000	Strong transcription	Primary B cells from peripheral blood	blood
8	chr11:58808000-58808200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr11:58808000-58808600	Enhancers	Stomach Mucosa	stomach
10	chr11:58808000-58810800	Weak transcription	Primary B cells from peripheral blood	blood
11	chr11:58810600-58811400	Strong transcription	Primary B cells from cord blood	blood
12	chr11:58810800-58811800	Strong transcription	Primary B cells from peripheral blood	blood
13	chr11:58811400-58818200	Weak transcription	Primary B cells from cord blood	blood
14	chr11:58811800-58816200	Weak transcription	Primary B cells from peripheral blood	blood
15	chr11:58813600-58825200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr11:58815400-58824400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr11:58816200-58818200	Strong transcription	Primary B cells from peripheral blood	blood
18	chr11:58816600-58816800	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr11:58816800-58817000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr11:58817000-58817200	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr11:58817000-58817200	Enhancers	Fetal Intestine Large	intestine
22	chr11:58817000-58818200	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr11:58817200-58821800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr11:58817200-58825200	Weak transcription	Liver	Liver
25	chr11:58817200-58825400	Weak transcription	Fetal Intestine Large	intestine
26	chr11:58817400-58819400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr11:58817400-58822000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr11:58818200-58818600	Genic enhancers	Primary B cells from peripheral blood	blood
29	chr11:58818200-58819400	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr11:58818200-58820200	Enhancers	Primary B cells from cord blood	blood
31	chr11:58818600-58825200	Enhancers	Primary B cells from peripheral blood	blood
32	chr11:58818800-58819400	Enhancers	GM12878-XiMat	blood
33	chr11:58819200-58819400	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr11:58819400-58820600	Weak transcription	GM12878-XiMat	blood
35	chr11:58819400-58821200	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr11:58819400-58822000	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr11:58819400-58822600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr11:58820200-58820800	Weak transcription	Primary B cells from cord blood	blood
39	chr11:58820600-58821200	Enhancers	GM12878-XiMat	blood
40	chr11:58820800-58822200	Enhancers	Primary B cells from cord blood	blood
41	chr11:58821200-58821400	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr11:58821200-58821600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr11:58821200-58825400	Weak transcription	GM12878-XiMat	blood
44	chr11:58821400-58822200	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr11:58821600-58822400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr11:58821800-58822600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr11:58821800-58822800	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr11:58822000-58822600	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr11:58822000-58822800	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr11:58822200-58823200	Enhancers	HUES48 Cell Line	embryonic stem cell

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