Variant report

Variant	nsv825933
Chromosome Location	chr11:58815698-58854802
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	chr11:58831786-58832150	GM12878	blood:	n/a	chr11:58831926-58831934
6	BATF	chr11:58831416-58832275	GM12878	blood:	n/a	chr11:58831926-58831934
7	BATF	chr11:58831471-58831776	GM12878	blood:	n/a	n/a
8	BATF	chr11:58826199-58826498	GM12878	blood:	n/a	n/a
9	BATF	chr11:58818940-58819193	GM12878	blood:	n/a	n/a
10	BCL11A	chr11:58831483-58831904	GM12878	blood:	n/a	n/a
11	BCL11A	chr11:58818878-58819275	GM12878	blood:	n/a	chr11:58819091-58819100
12	BCL11A	chr11:58831528-58832157	GM12878	blood:	n/a	n/a
13	BCL11A	chr11:58818899-58819262	GM12878	blood:	n/a	chr11:58819091-58819100
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	chr11:58835714-58835923	HepG2	liver:	n/a	chr11:58835780-58835791
21	CEBPB	chr11:58827942-58827984	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr11:58825987-58826187	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr11:58835627-58835890	IMR90	lung:	n/a	chr11:58835780-58835791
24	CEBPB	chr11:58852160-58852235	HepG2	liver:	n/a	n/a
25	CEBPB	chr11:58850700-58850889	HepG2	liver:	n/a	n/a
26	CEBPB	chr11:58841369-58841519	IMR90	lung:	n/a	n/a
27	CHD1	chr11:58821218-58821270	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD1	chr11:58825963-58826312	GM12878	blood:	n/a	n/a
29	CHD2	chr11:58825822-58826232	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr11:58826018-58826077	K562	blood:	n/a	n/a
31	CHD2	chr11:58825891-58826300	GM12878	blood:	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	chr11:58825952-58826356	GM19239	blood:	n/a	n/a
35	CTCF	chr11:58826020-58826170	HL-60	blood:	n/a	n/a
36	CTCF	chr11:58820840-58820990	AG09319	gingival:	n/a	chr11:58820969-58820985 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
37	CTCF	chr11:58826020-58826170	HEK293	kidney:	n/a	n/a
38	CTCF	chr11:58826020-58826170	GM12864	blood:	n/a	n/a
39	CTCF	chr11:58820860-58821010	GM12869	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
40	CTCF	chr11:58820791-58821130	Spleen_OC	spleen:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
41	CTCF	chr11:58825917-58826236	Lung_OC	lung:	n/a	n/a
42	CTCF	chr11:58820940-58821090	HCFaa	heart:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
43	CTCF	chr11:58826020-58826170	HFF-Myc	foreskin:	n/a	n/a
44	CTCF	chr11:58820860-58821010	GM12867	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
45	CTCF	chr11:58820880-58821030	GM12873	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
46	CTCF	chr11:58826040-58826190	AG09309	skin:	n/a	n/a
47	CTCF	chr11:58820856-58821105	GM12892	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
48	CTCF	chr11:58825891-58826269	GM19238	blood:	n/a	n/a
49	CTCF	chr11:58820860-58821010	HFF-Myc	foreskin:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
50	CTCF	chr11:58820940-58821090	GM12866	blood:	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	chr11:58826414-58826464	HCT-116	colon:	n/a
2	chr11:58826414-58826464	HCT-116	colon:	n/a
3	chr11:58830355-58830405	HCPEpiC	choroid plexus:	n/a
4	chr11:58830191-58830241	SK-N-SH	brain:	n/a
5	chr11:58830857-58830907	CMK	blood:	n/a
6	chr11:58828174-58828224	HCM	heart:	n/a
7	chr11:58830355-58830405	BE2_C	brain:	n/a
8	chr11:58830424-58830474	GM19239	blood:	n/a
9	chr11:58825870-58825920	HCT-116	colon:	n/a
10	chr11:58830857-58830907	Jurkat	blood:	n/a
11	chr11:58826475-58826525	PFSK-1	brain:	n/a
12	chr11:58830857-58830907	GM12891	blood:	n/a
13	chr11:58826475-58826525	AG10803	skin:	n/a
14	chr11:58830355-58830405	NHBE	bronchial:	n/a
15	chr11:58830857-58830907	HAEpiC	amniotic membrane:	n/a
16	chr11:58830191-58830241	U87	brain:	n/a
17	chr11:58830191-58830241	MCF10A-Er-Src	breast:	n/a
18	chr11:58826110-58826160	NH-A	brain:	n/a
19	chr11:58825714-58825764	SAEC	small airway:	n/a
20	chr11:58826073-58826123	NHDF-neo	bronchial:	n/a
21	chr11:58828174-58828224	SAEC	small airway:	n/a
22	chr11:58830610-58830660	NT2-D1	testis:	n/a
23	chr11:58830424-58830474	PrEC	prostate:	n/a
24	chr11:58826475-58826525	Hela-S3	cervix:	n/a
25	chr11:58830191-58830241	HCM	heart:	n/a
26	chr11:58828174-58828224	HNPCEpiC	eye:	n/a
27	chr11:58825714-58825764	HMEC	breast:	n/a
28	chr11:58833356-58833406	HMEC	breast:	n/a
29	chr11:58825870-58825920	RPTEC	kidney:	n/a
30	chr11:58825870-58825920	U87	brain:	n/a
31	chr11:58825714-58825764	HUVEC	blood vessel:	n/a
32	chr11:58830424-58830474	AG04450	lung:	fetal
33	chr11:58826073-58826123	HCM	heart:	n/a
34	chr11:58830424-58830474	HUVEC	blood vessel:	n/a
35	chr11:58830610-58830660	HUVEC	blood vessel:	n/a
36	chr11:58826110-58826160	HMEC	breast:	n/a
37	chr11:58826073-58826123	HCT-116	colon:	n/a
38	chr11:58833356-58833406	SAEC	small airway:	n/a
39	chr11:58825714-58825764	AG10803	skin:	n/a
40	chr11:58830191-58830241	HCPEpiC	choroid plexus:	n/a
41	chr11:58830424-58830474	RPTEC	kidney:	n/a
42	chr11:58830610-58830660	Jurkat	blood:	n/a
43	chr11:58826073-58826123	MCF-7	breast:	n/a
44	chr11:58826073-58826123	SK-N-SH	brain:	n/a
45	chr11:58833356-58833406	HepG2	liver:	n/a
46	chr11:58825714-58825764	RPTEC	kidney:	n/a
47	chr11:58826110-58826160	MCF10A-Er-Src	breast:	n/a
48	chr11:58825870-58825920	ProgFib	skin:	n/a
49	chr11:58828174-58828224	GM12891	blood:	n/a
50	chr11:58830424-58830474	AG09319	gingival:	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	chr11:58822768-58822919	ENSG00000255240.1
2	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
3	lnc-GLYATL2-2	chr11:58825845-58825923	ENSG00000255240.1
4	lnc-GLYATL2-2	chr11:58825845-58825925	NR_033853
5	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1
6	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1
7	lnc-GLYATL2-2	chr11:58820930-58821099	NR_033853
8	lnc-GLYATL2-2	chr11:58818733-58818781	NR_033853
9	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
10	lnc-GLYATL2-2	chr11:58825845-58826132	ENSG00000255240.1

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: 1358 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:1358 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192032351	chr11:58815733-58815734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs75349508	chr11:58815765-58815766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548476270	chr11:58815856-58815857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs114560548	chr11:58815928-58815929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144218204	chr11:58815966-58815967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148303473	chr11:58815974-58815975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184540592	chr11:58816011-58816012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190216007	chr11:58816020-58816021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs141554458	chr11:58816035-58816036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs568269558	chr11:58816092-58816093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs535596322	chr11:58816098-58816099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370597502	chr11:58816106-58816107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs193243384	chr11:58816188-58816189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185736725	chr11:58816230-58816231	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs146394712	chr11:58816237-58816238	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540502083	chr11:58816241-58816242	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139784328	chr11:58816325-58816326	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370128697	chr11:58816391-58816392	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560156975	chr11:58816421-58816422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554998517	chr11:58816422-58816423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573398845	chr11:58816427-58816428	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs10792216	chr11:58816457-58816458	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs146134560	chr11:58816473-58816474	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531140025	chr11:58816477-58816478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546450914	chr11:58816520-58816521	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545975082	chr11:58816530-58816531	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139082459	chr11:58816537-58816538	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189369037	chr11:58816538-58816539	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531018066	chr11:58816554-58816555	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs546779754	chr11:58816612-58816613	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568614142	chr11:58816643-58816644	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529393630	chr11:58816644-58816645	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs551042052	chr11:58816705-58816706	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs149911096	chr11:58816706-58816707	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530360916	chr11:58816709-58816710	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs144871005	chr11:58816724-58816725	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs533831830	chr11:58816792-58816793	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554934285	chr11:58816867-58816868	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs573439433	chr11:58816892-58816893	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181012121	chr11:58816973-58816974	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557156517	chr11:58817005-58817006	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575762842	chr11:58817008-58817009	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538856394	chr11:58817024-58817025	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185358229	chr11:58817067-58817068	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188559216	chr11:58817077-58817078	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181401153	chr11:58817138-58817139	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185833140	chr11:58817165-58817166	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529435819	chr11:58817166-58817167	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568656983	chr11:58817198-58817199	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551064650	chr11:58817222-58817223	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

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

Chromatin state (count:337 , 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	chr11:58811400-58818200	Weak transcription	Primary B cells from cord blood	blood
4	chr11:58811800-58816200	Weak transcription	Primary B cells from peripheral blood	blood
5	chr11:58813600-58825200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr11:58815400-58824400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr11:58816200-58818200	Strong transcription	Primary B cells from peripheral blood	blood
8	chr11:58816600-58816800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr11:58816800-58817000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr11:58817000-58817200	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr11:58817000-58817200	Enhancers	Fetal Intestine Large	intestine
12	chr11:58817000-58818200	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr11:58817200-58821800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr11:58817200-58825200	Weak transcription	Liver	Liver
15	chr11:58817200-58825400	Weak transcription	Fetal Intestine Large	intestine
16	chr11:58817400-58819400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr11:58817400-58822000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr11:58818200-58818600	Genic enhancers	Primary B cells from peripheral blood	blood
19	chr11:58818200-58819400	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr11:58818200-58820200	Enhancers	Primary B cells from cord blood	blood
21	chr11:58818600-58825200	Enhancers	Primary B cells from peripheral blood	blood
22	chr11:58818800-58819400	Enhancers	GM12878-XiMat	blood
23	chr11:58819200-58819400	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr11:58819400-58820600	Weak transcription	GM12878-XiMat	blood
25	chr11:58819400-58821200	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr11:58819400-58822000	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr11:58819400-58822600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr11:58820200-58820800	Weak transcription	Primary B cells from cord blood	blood
29	chr11:58820600-58821200	Enhancers	GM12878-XiMat	blood
30	chr11:58820800-58822200	Enhancers	Primary B cells from cord blood	blood
31	chr11:58821200-58821400	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr11:58821200-58821600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr11:58821200-58825400	Weak transcription	GM12878-XiMat	blood
34	chr11:58821400-58822200	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr11:58821600-58822400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr11:58821800-58822600	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr11:58821800-58822800	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr11:58822000-58822600	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr11:58822000-58822800	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr11:58822200-58823200	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr11:58822200-58824400	Weak transcription	Primary B cells from cord blood	blood
42	chr11:58822400-58823200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr11:58822600-58823200	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr11:58822600-58825200	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr11:58822800-58825200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr11:58822800-58825200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr11:58823200-58825200	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr11:58823200-58825200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr11:58823200-58825600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr11:58824400-58824600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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