Variant report

Variant	nsv1050444
Chromosome Location	chr11:58404467-58434568
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	chr11:58421558-58421758	HepG2	liver:	n/a	n/a
2	ATF2	chr11:58414456-58415252	GM12878	blood:	n/a	n/a
3	ATF2	chr11:58414540-58415283	GM12878	blood:	n/a	n/a
4	BATF	chr11:58414703-58415208	GM12878	blood:	n/a	n/a
5	BATF	chr11:58414606-58415288	GM12878	blood:	n/a	n/a
6	BCL11A	chr11:58414626-58415247	GM12878	blood:	n/a	n/a
7	BCL11A	chr11:58414652-58415247	GM12878	blood:	n/a	n/a
8	BCL3	chr11:58433838-58434397	GM12878	blood:	n/a	n/a
9	BCL3	chr11:58414614-58415068	GM12878	blood:	n/a	n/a
10	BCL3	chr11:58433922-58434413	GM12878	blood:	n/a	n/a
11	BCLAF1	chr11:58414580-58415233	GM12878	blood:	n/a	n/a
12	BCLAF1	chr11:58414459-58415210	GM12878	blood:	n/a	n/a
13	BHLHE40	chr11:58408021-58408298	GM12878	blood:	n/a	n/a
14	BHLHE40	chr11:58421493-58421802	GM12878	blood:	n/a	n/a
15	BHLHE40	chr11:58414608-58415140	GM12878	blood:	n/a	n/a
16	BHLHE40	chr11:58421585-58421811	K562	blood:	n/a	n/a
17	CBX3	chr11:58426934-58427338	HCT-116	colon:	n/a	n/a
18	CBX3	chr11:58413372-58413619	K562	blood:	n/a	n/a
19	CBX3	chr11:58413363-58413588	K562	blood:	n/a	n/a
20	CEBPB	chr11:58422651-58422756	HepG2	liver:	n/a	n/a
21	CEBPB	chr11:58423829-58424184	A549	lung:	n/a	chr11:58423993-58424004 chr11:58423852-58423865
22	CEBPB	chr11:58418081-58418315	IMR90	lung:	n/a	n/a
23	CEBPB	chr11:58423843-58424164	K562	blood:	n/a	chr11:58423993-58424004 chr11:58423852-58423865
24	CEBPB	chr11:58423871-58424120	ECC-1	luminal epithelium:	n/a	chr11:58423993-58424004
25	CEBPB	chr11:58423831-58424205	Hela-S3	cervix:	n/a	chr11:58423993-58424004 chr11:58423852-58423865
26	CEBPB	chr11:58423825-58424188	HepG2	liver:	n/a	chr11:58423993-58424004 chr11:58423852-58423865
27	CEBPB	chr11:58423831-58424168	IMR90	lung:	n/a	chr11:58423993-58424004 chr11:58423852-58423865
28	CEBPB	chr11:58423873-58424073	H1-hESC	embryonic stem cell:	n/a	chr11:58423993-58424004
29	CEBPB	chr11:58423905-58424118	ECC-1	luminal epithelium:	n/a	chr11:58423993-58424004
30	CHD2	chr11:58414489-58415227	GM12878	blood:	n/a	n/a
31	CREB1	chr11:58421581-58421878	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr11:58421460-58421897	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr11:58421560-58421710	SAEC	small airway:	n/a	chr11:58421645-58421661 chr11:58421647-58421660 chr11:58421644-58421662 chr11:58421646-58421667
34	CTCF	chr11:58421600-58421750	GM12869	blood:	n/a	chr11:58421645-58421661 chr11:58421647-58421660 chr11:58421644-58421662 chr11:58421646-58421667
35	CTCF	chr11:58414620-58414770	GM06990	blood:	n/a	n/a
36	CTCF	chr11:58421560-58421710	HPF	lung:	n/a	chr11:58421645-58421661 chr11:58421647-58421660 chr11:58421644-58421662 chr11:58421646-58421667
37	CTCF	chr11:58421580-58421730	GM12875	blood:	n/a	chr11:58421645-58421661 chr11:58421647-58421660 chr11:58421644-58421662 chr11:58421646-58421667
38	CTCF	chr11:58421281-58421397	GM20000	blood:	n/a	n/a
39	CTCF	chr11:58421515-58421828	GM12891	blood:	n/a	chr11:58421645-58421661 chr11:58421647-58421660 chr11:58421644-58421662 chr11:58421646-58421667
40	CTCF	chr11:58420920-58421070	HPF	lung:	n/a	n/a
41	CTCF	chr11:58414620-58414770	GM12878	blood:	n/a	n/a
42	CTCF	chr11:58421580-58421730	SK-N-SH_RA	brain:	n/a	chr11:58421645-58421661 chr11:58421647-58421660 chr11:58421644-58421662 chr11:58421646-58421667
43	CTCF	chr11:58421120-58421270	NHLF	lung:	n/a	n/a
44	CTCF	chr11:58421327-58421804	Kidney_OC	kidney:	n/a	chr11:58421645-58421661 chr11:58421647-58421660 chr11:58421644-58421662 chr11:58421646-58421667
45	CTCF	chr11:58421546-58421764	HepG2	liver:	n/a	chr11:58421645-58421661 chr11:58421647-58421660 chr11:58421644-58421662 chr11:58421646-58421667
46	CTCF	chr11:58421580-58421730	Caco-2	colon:	n/a	chr11:58421645-58421661 chr11:58421647-58421660 chr11:58421644-58421662 chr11:58421646-58421667
47	CTCF	chr11:58414453-58414915	GM12878	blood:	n/a	n/a
48	CTCF	chr11:58421600-58421750	GM12874	blood:	n/a	chr11:58421645-58421661 chr11:58421647-58421660 chr11:58421644-58421662 chr11:58421646-58421667
49	CTCF	chr11:58426240-58426390	GM12873	blood:	n/a	n/a
50	CTCF	chr11:58421510-58421825	A549	lung:	n/a	chr11:58421645-58421661 chr11:58421647-58421660 chr11:58421644-58421662 chr11:58421646-58421667

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58420680-58420730	HepG2	liver:	n/a
2	chr11:58420680-58420730	HepG2	liver:	n/a
3	chr11:58420680-58420730	HCPEpiC	choroid plexus:	n/a
4	chr11:58420680-58420730	SK-N-MC	brain:	n/a
5	chr11:58420680-58420730	K562	blood:	n/a
6	chr11:58420680-58420730	SK-N-SH_RA	brain:	n/a
7	chr11:58420680-58420730	HAEpiC	amniotic membrane:	n/a
8	chr11:58420680-58420730	HRPEpiC	eye:	n/a
9	chr11:58420680-58420730	AG04450	lung:	fetal
10	chr11:58420680-58420730	GM06990	blood:	n/a
11	chr11:58420680-58420730	BE2_C	brain:	n/a
12	chr11:58420680-58420730	NB4	blood:	n/a
13	chr11:58420680-58420730	GM12892	blood:	n/a
14	chr11:58420680-58420730	HNPCEpiC	eye:	n/a
15	chr11:58420680-58420730	AG09309	skin:	n/a
16	chr11:58420680-58420730	SAEC	small airway:	n/a
17	chr11:58420680-58420730	CMK	blood:	n/a
18	chr11:58420680-58420730	T-47D	breast:	n/a
19	chr11:58420680-58420730	HEEpiC	esophagus:	n/a
20	chr11:58420680-58420730	MCF-7	breast:	n/a
21	chr11:58420680-58420730	NT2-D1	testis:	n/a
22	chr11:58420680-58420730	LNCaP	prostate:	n/a
23	chr11:58420680-58420730	HIPEpiC	eye:	n/a
24	chr11:58420680-58420730	AoSMC	blood vessel:	n/a
25	chr11:58420680-58420730	NHDF-neo	bronchial:	n/a
26	chr11:58420680-58420730	ECC-1	luminal epithelium:	n/a
27	chr11:58420680-58420730	SKMC	muscle:	n/a
28	chr11:58420680-58420730	GM19239	blood:	n/a
29	chr11:58420680-58420730	HCF	heart:	n/a
30	chr11:58420680-58420730	U87	brain:	n/a
31	chr11:58420680-58420730	HPAEpiC	pulmonary alveolar:	n/a
32	chr11:58420680-58420730	HEK293	kidney:	embryo
33	chr11:58420680-58420730	GM12891	blood:	n/a
34	chr11:58420680-58420730	NH-A	brain:	n/a
35	chr11:58420680-58420730	PrEC	prostate:	n/a
36	chr11:58420680-58420730	Hepatocyte	liver:	n/a
37	chr11:58420680-58420730	NHBE	bronchial:	n/a
38	chr11:58420680-58420730	HMEC	breast:	n/a
39	chr11:58420680-58420730	A549	lung:	n/a
40	chr11:58420680-58420730	AG04449	skin:	fetal
41	chr11:58420680-58420730	HUVEC	blood vessel:	n/a
42	chr11:58420680-58420730	AG10803	skin:	n/a
43	chr11:58420680-58420730	HL-60	blood:	n/a
44	chr11:58420680-58420730	HRCEpiC	kidney:	n/a
45	chr11:58420680-58420730	ovcar-3	ovarian:	n/a
46	chr11:58420680-58420730	H1-hESC	embryonic stem cell:	embryo
47	chr11:58420680-58420730	GM12878	blood:	n/a
48	chr11:58420680-58420730	SK-N-SH	brain:	n/a
49	chr11:58420680-58420730	MCF10A-Er-Src	breast:	n/a
50	chr11:58420680-58420730	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:58421175..58421959-chr11:58555571..58556541,3	MCF-7	breast:
2	chr11:58345323..58347198-chr11:58413010..58415739,2	K562	blood:
3	chr11:58344369..58347020-chr11:58402658..58405186,3	K562	blood:
4	chr11:58402930..58405768-chr11:58406418..58410060,3	K562	blood:
5	chr11:58402145..58403700-chr11:58406157..58408220,2	K562	blood:
6	chr11:58408491..58410275-chr11:58912566..58915086,2	K562	blood:
7	chr11:58421165..58421796-chr11:58687413..58688096,2	MCF-7	breast:
8	chr11:58420893..58422551-chr11:58555581..58556580,16	K562	blood:
9	chr11:58342748..58344272-chr11:58413170..58414792,2	K562	blood:
10	chr11:58343949..58346815-chr11:58430372..58432698,2	K562	blood:
11	chr11:58344813..58346955-chr11:58405857..58408185,2	MCF-7	breast:
12	chr11:58385876..58387982-chr11:58406021..58408836,2	MCF-7	breast:
13	chr11:58397520..58400716-chr11:58402056..58406653,5	K562	blood:
14	chr11:58405749..58408727-chr11:58417141..58419096,2	K562	blood:
15	chr11:58421187..58422454-chr11:58442760..58443739,3	MCF-7	breast:
16	chr11:58421221..58422040-chr11:58442879..58443634,3	MCF-7	breast:
17	chr11:58405749..58408727-chr11:58417141..58419096,2	K562	blood:
18	chr11:58396664..58398524-chr11:58408556..58410829,2	K562	blood:
19	chr11:58402930..58405768-chr11:58406418..58410060,3	K562	blood:
20	chr11:58346089..58348099-chr11:58414530..58417041,2	MCF-7	breast:
21	chr11:58420038..58422147-chr11:58426346..58428518,2	K562	blood:
22	chr11:58420038..58422147-chr11:58426346..58428518,2	K562	blood:

Variant related genes	Relation type
ENSG00000265783	TF binding region
ENSG00000265783	CpG island
ENSG00000110031	chromatin interactions
ENSG00000255073	chromatin interactions
ENSG00000186660	chromatin interactions

Extended variants
information (count: 1026 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:1026 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2298608	chr11:58404467-58404468	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs2298607	chr11:58404499-58404500	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs370546804	chr11:58404526-58404527	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs545690240	chr11:58404539-58404540	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs565089367	chr11:58404576-58404577	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs192161954	chr11:58404589-58404590	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs547847782	chr11:58404624-58404625	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs76831077	chr11:58404648-58404649	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs2154631	chr11:58404733-58404734	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs548519936	chr11:58404762-58404763	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs184377313	chr11:58404902-58404903	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs187232024	chr11:58404908-58404909	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs552517074	chr11:58404973-58404974	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs570999642	chr11:58405023-58405024	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs377691139	chr11:58405044-58405045	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs534452568	chr11:58405054-58405055	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs553093737	chr11:58405056-58405057	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs375745001	chr11:58405103-58405104	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs143204047	chr11:58405107-58405108	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs535444389	chr11:58405108-58405109	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs556955162	chr11:58405109-58405110	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs192613905	chr11:58405129-58405130	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs546051233	chr11:58405131-58405132	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs138920887	chr11:58405176-58405177	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs375555197	chr11:58405210-58405211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370369123	chr11:58405225-58405226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113248970	chr11:58405250-58405251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201619408	chr11:58405251-58405252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs77772291	chr11:58405263-58405264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201585456	chr11:58405265-58405266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572980707	chr11:58405280-58405281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs143054948	chr11:58405293-58405294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541210283	chr11:58405312-58405313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374172972	chr11:58405316-58405317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530091314	chr11:58405321-58405322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184592881	chr11:58405344-58405345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563313430	chr11:58405347-58405348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557908309	chr11:58405351-58405352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547852812	chr11:58405359-58405360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189116997	chr11:58405382-58405383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2509928	chr11:58405458-58405459	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs570997006	chr11:58405513-58405514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543525918	chr11:58405619-58405620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs114854332	chr11:58405646-58405647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547167099	chr11:58405665-58405666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12799215	chr11:58405674-58405675	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs34152962	chr11:58405716-58405717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs535509112	chr11:58405758-58405759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182566882	chr11:58405774-58405775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568813912	chr11:58405801-58405802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:204 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58392000-58406000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr11:58393000-58407200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr11:58393200-58407000	Weak transcription	Thymus	Thymus
4	chr11:58393800-58406200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr11:58393800-58407800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr11:58394000-58407200	Weak transcription	Left Ventricle	heart
7	chr11:58394000-58407800	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr11:58394600-58407200	Weak transcription	Primary T cells from cord blood	blood
9	chr11:58394600-58407200	Weak transcription	Primary hematopoietic stem cells	blood
10	chr11:58394800-58407000	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr11:58394800-58408200	Weak transcription	Duodenum Mucosa	Duodenum
12	chr11:58395200-58407000	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr11:58395200-58407000	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr11:58395600-58407200	Weak transcription	Dnd41	blood
15	chr11:58395800-58407800	Weak transcription	Fetal Thymus	thymus
16	chr11:58396200-58407000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr11:58402400-58407800	Weak transcription	Fetal Intestine Small	intestine
18	chr11:58403600-58407200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr11:58404400-58408000	Weak transcription	Ovary	ovary
20	chr11:58404800-58405200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr11:58405200-58407800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr11:58406000-58406200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr11:58406000-58407600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr11:58406000-58410200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr11:58406200-58408200	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr11:58406200-58411200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr11:58406200-58413000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr11:58406600-58409200	Enhancers	Brain Hippocampus Middle	brain
29	chr11:58406800-58409000	Enhancers	Primary T helper naive cells from peripheral blood	blood
30	chr11:58407000-58407200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr11:58407000-58407400	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr11:58407000-58408200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr11:58407000-58408400	Enhancers	Brain Anterior Caudate	brain
34	chr11:58407000-58408800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr11:58407000-58408800	Enhancers	Brain Angular Gyrus	brain
36	chr11:58407000-58408800	Enhancers	Thymus	Thymus
37	chr11:58407000-58409000	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr11:58407000-58409000	Enhancers	Primary T cells fromperipheralblood	blood
39	chr11:58407000-58409000	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr11:58407000-58409000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
41	chr11:58407000-58409000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr11:58407000-58409200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr11:58407200-58407800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr11:58407200-58408400	Enhancers	Primary T cells from cord blood	blood
45	chr11:58407200-58408600	Enhancers	Left Ventricle	heart
46	chr11:58407200-58408600	Enhancers	Lung	lung
47	chr11:58407200-58408800	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr11:58407200-58408800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chr11:58407200-58408800	Enhancers	Primary T killer memory cells from peripheral blood	blood
50	chr11:58407200-58408800	Enhancers	Sigmoid Colon	Sigmoid Colon

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