Variant report

Variant	nsv526546
Chromosome Location	chr11:92742186-92851178
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1223)
CpG islands
(count:306)
Chromatin interactive
region (count:13)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1223 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:92787915-92788307	K562	blood:	n/a	n/a
2	ARID3A	chr11:92767231-92767668	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:92788050-92788317	HepG2	liver:	n/a	n/a
4	ATF2	chr11:92849693-92850455	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr11:92849764-92850516	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr11:92798512-92798767	K562	blood:	n/a	n/a
7	ATF3	chr11:92788004-92788604	HCT-116	colon:	n/a	n/a
8	ATF3	chr11:92788028-92788486	A549	lung:	n/a	n/a
9	BACH1	chr11:92822489-92822857	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr11:92814910-92815217	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr11:92838808-92838969	GM12878	blood:	n/a	n/a
12	BATF	chr11:92788020-92788337	GM12878	blood:	n/a	chr11:92788186-92788196 chr11:92788185-92788196
13	BATF	chr11:92788026-92788341	GM12878	blood:	n/a	chr11:92788186-92788196 chr11:92788185-92788196
14	BATF	chr11:92816104-92816405	GM12878	blood:	n/a	chr11:92816273-92816284 chr11:92816294-92816305
15	BCL11A	chr11:92838794-92838964	GM12878	blood:	n/a	n/a
16	BCL3	chr11:92788010-92788344	GM12878	blood:	n/a	chr11:92788067-92788076
17	BCL3	chr11:92787926-92788465	A549	lung:	n/a	chr11:92788067-92788076
18	BDP1	chr11:92792490-92793029	Hela-S3	cervix:	n/a	n/a
19	BHLHE40	chr11:92788152-92788404	K562	blood:	n/a	n/a
20	BHLHE40	chr11:92798092-92798214	K562	blood:	n/a	n/a
21	BRCA1	chr11:92830767-92831305	Hela-S3	cervix:	n/a	n/a
22	BRF1	chr11:92850302-92850860	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr11:92787839-92788641	HCT-116	colon:	n/a	n/a
24	CBX3	chr11:92787904-92788636	HCT-116	colon:	n/a	n/a
25	CCNT2	chr11:92792210-92792631	K562	blood:	n/a	chr11:92792379-92792399
26	CEBPB	chr11:92788079-92788408	HepG2	liver:	n/a	n/a
27	CEBPB	chr11:92788108-92788362	K562	blood:	n/a	n/a
28	CEBPB	chr11:92826220-92826269	HepG2	liver:	n/a	chr11:92826224-92826235
29	CEBPB	chr11:92788016-92788469	IMR90	lung:	n/a	n/a
30	CEBPB	chr11:92746871-92747188	IMR90	lung:	n/a	n/a
31	CEBPB	chr11:92764469-92764937	IMR90	lung:	n/a	n/a
32	CEBPB	chr11:92822604-92822953	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr11:92826183-92826272	IMR90	lung:	n/a	chr11:92826224-92826235
34	CEBPB	chr11:92798483-92798840	K562	blood:	n/a	n/a
35	CEBPB	chr11:92798570-92798737	K562	blood:	n/a	n/a
36	CEBPB	chr11:92788015-92788408	K562	blood:	n/a	n/a
37	CEBPB	chr11:92753294-92753494	HepG2	liver:	n/a	n/a
38	CEBPB	chr11:92788036-92788446	A549	lung:	n/a	n/a
39	CEBPB	chr11:92767173-92767728	HepG2	liver:	n/a	chr11:92767566-92767579 chr11:92767565-92767582
40	CEBPB	chr11:92800620-92800881	HepG2	liver:	n/a	chr11:92800729-92800740
41	CEBPB	chr11:92787921-92788547	A549	lung:	n/a	n/a
42	CEBPB	chr11:92787809-92788655	HCT-116	colon:	n/a	n/a
43	CEBPB	chr11:92788096-92788488	A549	lung:	n/a	n/a
44	CEBPB	chr11:92787852-92788622	HCT-116	colon:	n/a	n/a
45	CEBPB	chr11:92833040-92833374	IMR90	lung:	n/a	n/a
46	CEBPB	chr11:92798488-92798838	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr11:92787969-92788503	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr11:92795956-92796283	IMR90	lung:	n/a	n/a
49	CEBPB	chr11:92798464-92798835	HepG2	liver:	n/a	n/a
50	CEBPB	chr11:92798444-92798748	K562	blood:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:92806448-92806498	Hepatocyte	liver:	n/a
2	chr11:92806448-92806498	Hepatocyte	liver:	n/a
3	chr11:92814421-92814471	HIPEpiC	eye:	n/a
4	chr11:92850491-92850541	AoSMC	blood vessel:	n/a
5	chr11:92787048-92787098	HCF	heart:	n/a
6	chr11:92806448-92806498	AG09309	skin:	n/a
7	chr11:92787048-92787098	HMEC	breast:	n/a
8	chr11:92754025-92754075	AoSMC	blood vessel:	n/a
9	chr11:92787048-92787098	GM06990	blood:	n/a
10	chr11:92814421-92814471	GM06990	blood:	n/a
11	chr11:92814421-92814471	Jurkat	blood:	n/a
12	chr11:92754025-92754075	HRPEpiC	eye:	n/a
13	chr11:92754025-92754075	SK-N-SH	brain:	n/a
14	chr11:92814421-92814471	NB4	blood:	n/a
15	chr11:92754025-92754075	GM06990	blood:	n/a
16	chr11:92814421-92814471	SK-N-SH	brain:	n/a
17	chr11:92787048-92787098	LNCaP	prostate:	n/a
18	chr11:92850491-92850541	HRCEpiC	kidney:	n/a
19	chr11:92787048-92787098	HPAEpiC	pulmonary alveolar:	n/a
20	chr11:92806448-92806498	MCF10A-Er-Src	breast:	n/a
21	chr11:92806448-92806498	AG04450	lung:	fetal
22	chr11:92814421-92814471	NHDF-neo	bronchial:	n/a
23	chr11:92814421-92814471	HRCEpiC	kidney:	n/a
24	chr11:92806448-92806498	BJ	skin:	n/a
25	chr11:92814421-92814471	HCF	heart:	n/a
26	chr11:92787048-92787098	K562	blood:	n/a
27	chr11:92787048-92787098	NHDF-neo	bronchial:	n/a
28	chr11:92754025-92754075	IMR90	lung:	fetal
29	chr11:92806448-92806498	AG09319	gingival:	n/a
30	chr11:92787048-92787098	HCT-116	colon:	n/a
31	chr11:92850491-92850541	AG04449	skin:	fetal
32	chr11:92754025-92754075	MCF10A-Er-Src	breast:	n/a
33	chr11:92806448-92806498	HL-60	blood:	n/a
34	chr11:92754025-92754075	ProgFib	skin:	n/a
35	chr11:92850491-92850541	NT2-D1	testis:	n/a
36	chr11:92850491-92850541	PANC-1	pancreas:	n/a
37	chr11:92787048-92787098	GM19239	blood:	n/a
38	chr11:92754025-92754075	HNPCEpiC	eye:	n/a
39	chr11:92806448-92806498	HAEpiC	amniotic membrane:	n/a
40	chr11:92806448-92806498	HCT-116	colon:	n/a
41	chr11:92754025-92754075	HCPEpiC	choroid plexus:	n/a
42	chr11:92806448-92806498	IMR90	lung:	fetal
43	chr11:92806448-92806498	AoSMC	blood vessel:	n/a
44	chr11:92806448-92806498	T-47D	breast:	n/a
45	chr11:92754025-92754075	A549	lung:	n/a
46	chr11:92787048-92787098	SK-N-SH	brain:	n/a
47	chr11:92754025-92754075	HCM	heart:	n/a
48	chr11:92850491-92850541	Hela-S3	cervix:	n/a
49	chr11:92806448-92806498	H1-hESC	embryonic stem cell:	embryo
50	chr11:92850491-92850541	HCM	heart:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:92741730..92744392-chr11:92756499..92758327,2	K562	blood:
2	chr11:92809585..92811861-chr11:92818184..92821055,2	K562	blood:
3	chr11:92819613..92822569-chr11:92833632..92835784,2	K562	blood:
4	chr11:92749584..92751637-chr11:92755686..92757340,2	K562	blood:
5	chr11:92741730..92744392-chr11:92756499..92758327,2	K562	blood:
6	chr11:92819613..92822569-chr11:92833632..92835784,2	K562	blood:
7	chr11:92762354..92765084-chr11:92765117..92767154,2	MCF-7	breast:
8	chr11:92733468..92735228-chr11:92742109..92743780,2	K562	blood:
9	chr11:92749584..92751637-chr11:92755686..92757340,2	K562	blood:
10	chr11:92762354..92765084-chr11:92765117..92767154,2	MCF-7	breast:
11	chr11:92809585..92811861-chr11:92818184..92821055,2	K562	blood:
12	chr11:92828855..92830678-chr11:92832342..92834792,2	K562	blood:
13	chr11:92828855..92830678-chr11:92832342..92834792,2	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC36A4-4	chr11:92785561-92785993	NONHSAT023637

No data

Variant related genes	Relation type
RPL26P31	TF binding region
RPL26P31	CpG island

Extended variants
information (count: 4171 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:4171 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs956267	chr11:92742186-92742187	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559780240	chr11:92742187-92742188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182979018	chr11:92742193-92742194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551884897	chr11:92742197-92742198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571164164	chr11:92742207-92742208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs143972391	chr11:92742215-92742216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549567112	chr11:92742293-92742294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs370662117	chr11:92742297-92742298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs1396374	chr11:92742322-92742323	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs138574491	chr11:92742340-92742341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs565814449	chr11:92742341-92742342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs377403923	chr11:92742362-92742363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs558174205	chr11:92742383-92742384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs74363484	chr11:92742399-92742400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs78070254	chr11:92742402-92742403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs556012427	chr11:92742406-92742407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs554685497	chr11:92742414-92742415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs7481137	chr11:92742418-92742419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs956268	chr11:92742423-92742424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs574417213	chr11:92742430-92742431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs537590202	chr11:92742473-92742474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs555736217	chr11:92742478-92742479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541246647	chr11:92742487-92742488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs7114120	chr11:92742500-92742501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs117838632	chr11:92742516-92742517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563099514	chr11:92742527-92742528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs545795764	chr11:92742558-92742559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576616337	chr11:92742560-92742561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563689276	chr11:92742589-92742590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs577247808	chr11:92742598-92742599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs563098366	chr11:92742603-92742604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531326287	chr11:92742629-92742630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543076854	chr11:92742637-92742638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561428853	chr11:92742639-92742640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs529113759	chr11:92742653-92742654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545737517	chr11:92742656-92742657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs544888002	chr11:92742689-92742690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547272039	chr11:92742699-92742700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559199266	chr11:92742720-92742721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12785983	chr11:92742731-92742732	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs16918377	chr11:92742769-92742770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548254250	chr11:92742776-92742777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12791982	chr11:92742779-92742780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530542643	chr11:92742799-92742800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528120848	chr11:92742803-92742804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570034074	chr11:92742805-92742806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537427258	chr11:92742828-92742829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555926426	chr11:92742855-92742856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs117865322	chr11:92743008-92743009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs60466262	chr11:92743027-92743028	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	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
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Sudden cardiac death	19188705	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21958427	CNVD
Breast cancer	17133270	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Autism	19546859	CNVD
Fragile x	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	21062444	CNVD
Cancer	21499728	CNVD
Breast cancer	19181860	CNVD
Breast cancer	17603634	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Mantle cell lymphoma	19029149	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD

Chromatin state (count:820 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:92741800-92742600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr11:92742200-92742600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr11:92742600-92746800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr11:92746600-92747000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr11:92746800-92747000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr11:92749200-92751600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr11:92749800-92750000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr11:92750800-92752000	Enhancers	A549	lung
9	chr11:92751000-92751200	Enhancers	NH-A	brain
10	chr11:92751000-92751200	Enhancers	Osteobl	bone
11	chr11:92751000-92751600	Enhancers	HSMM	muscle
12	chr11:92751000-92751800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr11:92751000-92751800	Enhancers	Muscle Satellite Cultured Cells	--
14	chr11:92751200-92751600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr11:92751200-92753400	Enhancers	NHEK	skin
16	chr11:92751200-92754800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr11:92751200-92754800	Enhancers	HMEC	breast
18	chr11:92751400-92751800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr11:92751400-92751800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr11:92751400-92753600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr11:92751400-92754200	Weak transcription	Aorta	Aorta
22	chr11:92751600-92751800	Enhancers	HSMMtube	muscle
23	chr11:92751600-92753000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr11:92751600-92753000	Weak transcription	NH-A	brain
25	chr11:92751600-92753200	Weak transcription	HSMM	muscle
26	chr11:92751600-92753600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr11:92751800-92752000	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr11:92751800-92752800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr11:92751800-92752800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr11:92751800-92752800	Weak transcription	HSMMtube	muscle
31	chr11:92751800-92753000	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr11:92751800-92753200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr11:92752000-92752600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr11:92752000-92753200	Weak transcription	A549	lung
35	chr11:92752600-92755000	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr11:92752800-92753000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr11:92752800-92753600	Enhancers	HSMMtube	muscle
38	chr11:92752800-92753800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr11:92752800-92753800	Enhancers	NHLF	lung
40	chr11:92752800-92754800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr11:92752800-92754800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr11:92752800-92754800	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr11:92752800-92754800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr11:92753000-92753400	Enhancers	NH-A	brain
45	chr11:92753000-92753600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr11:92753000-92753600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr11:92753000-92753600	Enhancers	Muscle Satellite Cultured Cells	--
48	chr11:92753000-92753800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr11:92753000-92755000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr11:92753200-92753400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links