Variant report

Variant	nsv1047758
Chromosome Location	chr11:58790982-58847365
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	ARID3A	chr11:58792609-58792905	HepG2	liver:	n/a	n/a
2	ATF2	chr11:58825833-58826405	GM12878	blood:	n/a	n/a
3	ATF2	chr11:58831671-58832143	GM12878	blood:	n/a	n/a
4	ATF2	chr11:58831402-58832419	GM12878	blood:	n/a	n/a
5	BACH1	chr11:58825972-58826213	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr11:58831471-58831776	GM12878	blood:	n/a	n/a
7	BATF	chr11:58818940-58819193	GM12878	blood:	n/a	n/a
8	BATF	chr11:58831416-58832275	GM12878	blood:	n/a	chr11:58831926-58831934
9	BATF	chr11:58826199-58826498	GM12878	blood:	n/a	n/a
10	BATF	chr11:58831786-58832150	GM12878	blood:	n/a	chr11:58831926-58831934
11	BCL11A	chr11:58831483-58831904	GM12878	blood:	n/a	n/a
12	BCL11A	chr11:58818899-58819262	GM12878	blood:	n/a	chr11:58819091-58819100
13	BCL11A	chr11:58831528-58832157	GM12878	blood:	n/a	n/a
14	BCL11A	chr11:58818878-58819275	GM12878	blood:	n/a	chr11:58819091-58819100
15	BCL3	chr11:58831794-58832281	GM12878	blood:	n/a	n/a
16	BHLHE40	chr11:58826040-58826162	K562	blood:	n/a	n/a
17	BHLHE40	chr11:58825938-58826278	GM12878	blood:	n/a	n/a
18	BHLHE40	chr11:58792570-58792935	HepG2	liver:	n/a	chr11:58792752-58792765 chr11:58792748-58792769
19	BHLHE40	chr11:58820953-58821000	K562	blood:	n/a	n/a
20	BRCA1	chr11:58825950-58826184	GM12878	blood:	n/a	n/a
21	CEBPB	chr11:58835714-58835923	HepG2	liver:	n/a	chr11:58835780-58835791
22	CEBPB	chr11:58841369-58841519	IMR90	lung:	n/a	n/a
23	CEBPB	chr11:58835676-58835875	K562	blood:	n/a	chr11:58835780-58835791
24	CEBPB	chr11:58835627-58835890	IMR90	lung:	n/a	chr11:58835780-58835791
25	CEBPB	chr11:58825987-58826187	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr11:58827942-58827984	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr11:58825963-58826312	GM12878	blood:	n/a	n/a
28	CHD1	chr11:58821218-58821270	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr11:58825891-58826300	GM12878	blood:	n/a	n/a
30	CHD2	chr11:58825822-58826232	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr11:58826018-58826077	K562	blood:	n/a	n/a
32	CREB1	chr11:58845805-58846333	GM12878	blood:	n/a	n/a
33	CREB1	chr11:58845766-58846361	GM12878	blood:	n/a	n/a
34	CTCF	chr11:58826020-58826170	GM12868	blood:	n/a	n/a
35	CTCF	chr11:58825913-58826274	GM19240	blood:	n/a	n/a
36	CTCF	chr11:58820880-58821030	HPF	lung:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
37	CTCF	chr11:58826020-58826170	GM12801	blood:	n/a	n/a
38	CTCF	chr11:58820730-58821125	K562	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
39	CTCF	chr11:58825980-58826130	NHEK	skin:	n/a	n/a
40	CTCF	chr11:58825962-58826217	MCF-7	breast:	n/a	n/a
41	CTCF	chr11:58820940-58821090	HFF	foreskin:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
42	CTCF	chr11:58820880-58821030	GM12874	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
43	CTCF	chr11:58826000-58826150	HCM	heart:	n/a	n/a
44	CTCF	chr11:58825980-58826130	HCT-116	colon:	n/a	n/a
45	CTCF	chr11:58820740-58820890	HVMF	connective:	n/a	n/a
46	CTCF	chr11:58820845-58821120	GM19238	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
47	CTCF	chr11:58820920-58821070	Hela-S3	cervix:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
48	CTCF	chr11:58826040-58826190	AG09309	skin:	n/a	n/a
49	CTCF	chr11:58820856-58821105	GM12892	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
50	CTCF	chr11:58820840-58820990	AG09319	gingival:	n/a	chr11:58820969-58820985 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58828174-58828224	Jurkat	blood:	n/a
2	chr11:58830355-58830405	AG04450	lung:	fetal
3	chr11:58826110-58826160	BE2_C	brain:	n/a
4	chr11:58828174-58828224	Jurkat	blood:	n/a
5	chr11:58830355-58830405	AG04450	lung:	fetal
6	chr11:58826110-58826160	BE2_C	brain:	n/a
7	chr11:58830610-58830660	HRPEpiC	eye:	n/a
8	chr11:58830355-58830405	PrEC	prostate:	n/a
9	chr11:58826475-58826525	GM12878	blood:	n/a
10	chr11:58825870-58825920	HUVEC	blood vessel:	n/a
11	chr11:58830610-58830660	PFSK-1	brain:	n/a
12	chr11:58806952-58807002	HUVEC	blood vessel:	n/a
13	chr11:58826475-58826525	HMEC	breast:	n/a
14	chr11:58830857-58830907	PFSK-1	brain:	n/a
15	chr11:58830355-58830405	H1-hESC	embryonic stem cell:	embryo
16	chr11:58830857-58830907	U87	brain:	n/a
17	chr11:58826073-58826123	HAEpiC	amniotic membrane:	n/a
18	chr11:58826414-58826464	HPAEpiC	pulmonary alveolar:	n/a
19	chr11:58826110-58826160	NHBE	bronchial:	n/a
20	chr11:58826414-58826464	SK-N-SH	brain:	n/a
21	chr11:58825870-58825920	RPTEC	kidney:	n/a
22	chr11:58826414-58826464	HCT-116	colon:	n/a
23	chr11:58826110-58826160	HRE	kidney:	n/a
24	chr11:58806952-58807002	NH-A	brain:	n/a
25	chr11:58830610-58830660	ProgFib	skin:	n/a
26	chr11:58810187-58810237	Hela-S3	cervix:	n/a
27	chr11:58806952-58807002	HCF	heart:	n/a
28	chr11:58830191-58830241	SKMC	muscle:	n/a
29	chr11:58830355-58830405	HEEpiC	esophagus:	n/a
30	chr11:58825714-58825764	AoSMC	blood vessel:	n/a
31	chr11:58830857-58830907	ovcar-3	ovarian:	n/a
32	chr11:58826475-58826525	RPTEC	kidney:	n/a
33	chr11:58830191-58830241	HNPCEpiC	eye:	n/a
34	chr11:58806952-58807002	AG04449	skin:	fetal
35	chr11:58826110-58826160	PANC-1	pancreas:	n/a
36	chr11:58830424-58830474	HCPEpiC	choroid plexus:	n/a
37	chr11:58833356-58833406	K562	blood:	n/a
38	chr11:58825870-58825920	HRCEpiC	kidney:	n/a
39	chr11:58830424-58830474	MCF-7	breast:	n/a
40	chr11:58830610-58830660	CMK	blood:	n/a
41	chr11:58826475-58826525	HUVEC	blood vessel:	n/a
42	chr11:58826414-58826464	PFSK-1	brain:	n/a
43	chr11:58825870-58825920	AoSMC	blood vessel:	n/a
44	chr11:58830355-58830405	HAEpiC	amniotic membrane:	n/a
45	chr11:58826073-58826123	NT2-D1	testis:	n/a
46	chr11:58826073-58826123	LNCaP	prostate:	n/a
47	chr11:58806952-58807002	MCF10A-Er-Src	breast:	n/a
48	chr11:58830191-58830241	HCM	heart:	n/a
49	chr11:58830610-58830660	IMR90	lung:	fetal
50	chr11:58825714-58825764	AG09309	skin:	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	chr11:58820930-58821099	ENSG00000255240.1
2	lnc-GLYATL2-2	chr11:58825845-58826132	ENSG00000255240.1
3	lnc-GLYATL2-2	chr11:58820930-58821099	NR_033853
4	lnc-GLYATL2-2	chr11:58825845-58825923	ENSG00000255240.1
5	lnc-GLYATL2-2	chr11:58818733-58818781	NR_033853
6	lnc-GLYATL2-2	chr11:58822768-58822919	ENSG00000255240.1
7	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
8	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1
9	lnc-GLYATL2-2	chr11:58825845-58825925	NR_033853
10	lnc-GLYATL2-2	chr11:58818733-58818781	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: 2090 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:2090 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527897300	chr11:58790998-58790999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs370208792	chr11:58791023-58791024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs35613819	chr11:58791028-58791029	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs11229739	chr11:58791029-58791030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs398016191	chr11:58791035-58791036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs11229740	chr11:58791196-58791197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs149613268	chr11:58791217-58791218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571767474	chr11:58791230-58791231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192014476	chr11:58791243-58791244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553988779	chr11:58791338-58791339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs565839261	chr11:58791344-58791345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536085726	chr11:58791407-58791408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554832695	chr11:58791426-58791427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs115277970	chr11:58791435-58791436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543009306	chr11:58791471-58791472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558081068	chr11:58791474-58791475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs74643013	chr11:58791478-58791479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541088654	chr11:58791507-58791508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185365987	chr11:58791508-58791509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs555463205	chr11:58791519-58791520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10792214	chr11:58791521-58791522	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs538283033	chr11:58791523-58791524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541425591	chr11:58791611-58791612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190230036	chr11:58791625-58791626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs532091207	chr11:58791650-58791651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs7104357	chr11:58791673-58791674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs550500527	chr11:58791682-58791683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571629222	chr11:58791716-58791717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372347092	chr11:58791768-58791769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532420698	chr11:58791769-58791770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12803631	chr11:58791785-58791786	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs139544844	chr11:58791786-58791787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs578229994	chr11:58791812-58791813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs369632956	chr11:58791831-58791832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs143557733	chr11:58791844-58791845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs554390361	chr11:58791846-58791847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs569516794	chr11:58791911-58791912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs536905153	chr11:58791913-58791914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558444297	chr11:58791919-58791920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs9630207	chr11:58791939-58791940	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs534350286	chr11:58791946-58791947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs73485218	chr11:58791950-58791951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs75263190	chr11:58792016-58792017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs543205358	chr11:58792103-58792104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs147133455	chr11:58792133-58792134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs193245135	chr11:58792154-58792155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs185742993	chr11:58792160-58792161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs189369184	chr11:58792178-58792179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs565603852	chr11:58792188-58792189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs574297211	chr11:58792207-58792208	Enhancers Weak transcription	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:385 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58782800-58810600	Weak transcription	Primary B cells from cord blood	blood
2	chr11:58791800-58793600	Enhancers	Fetal Intestine Large	intestine
3	chr11:58792200-58792400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:58792200-58792600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr11:58792200-58792600	Enhancers	Fetal Intestine Small	intestine
6	chr11:58792200-58792600	Enhancers	Rectal Mucosa Donor 29	rectum
7	chr11:58792200-58792600	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr11:58792200-58792800	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr11:58792200-58792800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr11:58792200-58793000	Enhancers	Duodenum Mucosa	Duodenum
11	chr11:58792400-58793000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr11:58792400-58793000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr11:58792400-58793000	Enhancers	HepG2	liver
14	chr11:58792400-58793600	Enhancers	Liver	Liver
15	chr11:58792600-58793400	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr11:58792600-58796600	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr11:58793000-58796400	Weak transcription	Duodenum Mucosa	Duodenum
18	chr11:58793400-58794200	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr11:58793600-58795800	Weak transcription	Fetal Intestine Large	intestine
20	chr11:58794200-58796400	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr11:58795600-58796000	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr11:58795800-58797800	Enhancers	Fetal Intestine Large	intestine
23	chr11:58796000-58796200	Enhancers	Sigmoid Colon	Sigmoid Colon
24	chr11:58796000-58797400	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr11:58796000-58798600	Enhancers	Fetal Intestine Small	intestine
26	chr11:58796400-58797200	Enhancers	Duodenum Mucosa	Duodenum
27	chr11:58796400-58797200	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr11:58796400-58797400	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr11:58796600-58796800	Enhancers	Rectal Mucosa Donor 29	rectum
30	chr11:58796600-58797400	Enhancers	Stomach Mucosa	stomach
31	chr11:58796600-58797600	Enhancers	Colonic Mucosa	Colon
32	chr11:58797200-58797600	Flanking Active TSS	Duodenum Mucosa	Duodenum
33	chr11:58797200-58797800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
34	chr11:58797400-58797800	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr11:58797400-58797800	Enhancers	Sigmoid Colon	Sigmoid Colon
36	chr11:58797600-58797800	Flanking Active TSS	Colonic Mucosa	Colon
37	chr11:58797600-58797800	Enhancers	Duodenum Mucosa	Duodenum
38	chr11:58801400-58803200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr11:58803200-58804600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr11:58804400-58804600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr11:58804400-58804600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr11:58804600-58805000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr11:58804600-58806200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr11:58804600-58807400	Weak transcription	Primary B cells from peripheral blood	blood
45	chr11:58804800-58805000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr11:58804800-58805200	Enhancers	Primary hematopoietic stem cells	blood
47	chr11:58804800-58805200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr11:58805000-58805200	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr11:58805000-58806200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr11:58805000-58825200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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