Variant report

Variant	nsv555941
Chromosome Location	chr11:93129893-93181050
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	chr11:93177876-93178052	K562	blood:	n/a	n/a
2	ATF1	chr11:93177783-93178116	K562	blood:	n/a	n/a
3	ATF1	chr11:93140996-93141323	K562	blood:	n/a	n/a
4	ATF2	chr11:93177783-93178113	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr11:93177865-93178028	K562	blood:	n/a	n/a
6	ATF3	chr11:93141005-93141334	K562	blood:	n/a	n/a
7	BACH1	chr11:93177912-93178101	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr11:93177965-93178062	K562	blood:	n/a	n/a
9	CBX3	chr11:93177801-93178166	K562	blood:	n/a	n/a
10	CEBPB	chr11:93140969-93141354	HepG2	liver:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
11	CEBPB	chr11:93140968-93141291	K562	blood:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
12	CEBPB	chr11:93140982-93141344	A549	lung:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
13	CEBPB	chr11:93140940-93141345	HCT-116	colon:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
14	CEBPB	chr11:93140968-93141348	K562	blood:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
15	CEBPB	chr11:93141014-93141258	HepG2	liver:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
16	CEBPB	chr11:93141045-93141317	ECC-1	luminal epithelium:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
17	CEBPB	chr11:93140980-93141347	IMR90	lung:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
18	CEBPB	chr11:93140988-93141325	H1-hESC	embryonic stem cell:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
19	CEBPB	chr11:93140924-93141389	A549	lung:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
20	CEBPB	chr11:93177871-93178346	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr11:93146378-93146499	K562	blood:	n/a	n/a
22	CEBPB	chr11:93146382-93146537	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr11:93140958-93141353	Hela-S3	cervix:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
24	CEBPB	chr11:93145425-93145556	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr11:93140894-93141393	K562	blood:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
26	CEBPB	chr11:93140897-93141476	HCT-116	colon:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
27	CHD2	chr11:93177785-93178074	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr11:93177779-93178230	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr11:93177751-93178183	K562	blood:	n/a	n/a
30	CREB1	chr11:93177727-93178137	K562	blood:	n/a	n/a
31	CREB1	chr11:93177691-93178270	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr11:93164880-93165030	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr11:93161800-93161950	NHDF-neo	bronchial:	n/a	n/a
34	CTCF	chr11:93153020-93153065	GM10248	blood:	n/a	n/a
35	CTCF	chr11:93177580-93177730	HepG2	liver:	n/a	n/a
36	CTCF	chr11:93133720-93133870	GM06990	blood:	n/a	n/a
37	CTCF	chr11:93150442-93150502	GM13976	blood:	n/a	n/a
38	CTCF	chr11:93153008-93153097	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr11:93161820-93161970	AG04450	lung:	n/a	n/a
40	CTCF	chr11:93177820-93177970	HepG2	liver:	n/a	n/a
41	E2F4	chr11:93137300-93137492	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr11:93141003-93141303	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr11:93171676-93171818	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr11:93134550-93134655	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr11:93178006-93178134	MCF10A-Er-Src	breast:	n/a	n/a
46	EGR1	chr11:93141132-93141341	K562	blood:	n/a	chr11:93141235-93141248 chr11:93141234-93141249
47	EGR1	chr11:93141099-93141328	K562	blood:	n/a	chr11:93141235-93141248 chr11:93141234-93141249
48	EGR1	chr11:93177787-93178188	K562	blood:	n/a	n/a
49	EGR1	chr11:93177768-93178080	H1-hESC	embryonic stem cell:	n/a	n/a
50	EGR1	chr11:93177837-93178146	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:93143810-93143860	AG04449	skin:	fetal
2	chr11:93143810-93143860	HPAEpiC	pulmonary alveolar:	n/a
3	chr11:93143810-93143860	HRCEpiC	kidney:	n/a
4	chr11:93143810-93143860	A549	lung:	n/a
5	chr11:93143810-93143860	MCF10A-Er-Src	breast:	n/a
6	chr11:93143810-93143860	HMEC	breast:	n/a
7	chr11:93143810-93143860	T-47D	breast:	n/a
8	chr11:93143810-93143860	Hepatocyte	liver:	n/a
9	chr11:93143810-93143860	GM12878	blood:	n/a
10	chr11:93143810-93143860	HCPEpiC	choroid plexus:	n/a
11	chr11:93143810-93143860	HEEpiC	esophagus:	n/a
12	chr11:93143810-93143860	K562	blood:	n/a
13	chr11:93143810-93143860	SKMC	muscle:	n/a
14	chr11:93143810-93143860	HUVEC	blood vessel:	n/a
15	chr11:93143810-93143860	NHBE	bronchial:	n/a
16	chr11:93143810-93143860	LNCaP	prostate:	n/a
17	chr11:93143810-93143860	HAEpiC	amniotic membrane:	n/a
18	chr11:93143810-93143860	SAEC	small airway:	n/a
19	chr11:93143810-93143860	AoSMC	blood vessel:	n/a
20	chr11:93143810-93143860	ProgFib	skin:	n/a
21	chr11:93143810-93143860	AG09319	gingival:	n/a
22	chr11:93143810-93143860	GM06990	blood:	n/a
23	chr11:93143810-93143860	HIPEpiC	eye:	n/a
24	chr11:93143810-93143860	GM12891	blood:	n/a
25	chr11:93143810-93143860	PrEC	prostate:	n/a
26	chr11:93143810-93143860	HL-60	blood:	n/a
27	chr11:93143810-93143860	AG09309	skin:	n/a
28	chr11:93143810-93143860	NB4	blood:	n/a
29	chr11:93143810-93143860	AG04450	lung:	fetal
30	chr11:93143810-93143860	HRPEpiC	eye:	n/a
31	chr11:93143810-93143860	HepG2	liver:	n/a
32	chr11:93143810-93143860	HCM	heart:	n/a
33	chr11:93143810-93143860	HCT-116	colon:	n/a
34	chr11:93143810-93143860	NT2-D1	testis:	n/a
35	chr11:93143810-93143860	SK-N-SH	brain:	n/a
36	chr11:93143810-93143860	GM19239	blood:	n/a
37	chr11:93143810-93143860	HRE	kidney:	n/a
38	chr11:93143810-93143860	BJ	skin:	n/a
39	chr11:93143810-93143860	PFSK-1	brain:	n/a
40	chr11:93143810-93143860	Jurkat	blood:	n/a
41	chr11:93143810-93143860	PANC-1	pancreas:	n/a
42	chr11:93143810-93143860	RPTEC	kidney:	n/a
43	chr11:93143810-93143860	NHDF-neo	bronchial:	n/a
44	chr11:93143810-93143860	BE2_C	brain:	n/a
45	chr11:93143810-93143860	MCF-7	breast:	n/a
46	chr11:93143810-93143860	Hela-S3	cervix:	n/a
47	chr11:93143810-93143860	HCF	heart:	n/a
48	chr11:93143810-93143860	AG10803	skin:	n/a
49	chr11:93143810-93143860	CMK	blood:	n/a
50	chr11:93143810-93143860	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type
1	chr11:93139427..93141896-chr11:93145102..93147867,3	K562	blood:
2	chr11:93139427..93141388-chr11:93145450..93147867,2	K562	blood:
3	chr11:93135720..93137774-chr11:93142733..93145703,2	K562	blood:

Variant related genes	Relation type
ENSG00000221565	TF binding region
CCDC67	TF binding region
ENSG00000221565	CpG island
CCDC67	CpG island
ENSG00000221565	chromatin interactions
ENSG00000165325	chromatin interactions

Extended variants
information (count: 708 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:708 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11020303	chr11:93129893-93129894	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs185612370	chr11:93129905-93129906	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141968325	chr11:93129920-93129921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs367607491	chr11:93129952-93129953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535008484	chr11:93129964-93129965	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553102699	chr11:93130034-93130035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs578128959	chr11:93130053-93130054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs376502497	chr11:93130116-93130117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs59652277	chr11:93130151-93130152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs75624352	chr11:93130152-93130153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs57942067	chr11:93130157-93130158	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs11020304	chr11:93130266-93130267	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs150661036	chr11:93130272-93130273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs551121912	chr11:93130328-93130329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs190562175	chr11:93130376-93130377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs573954483	chr11:93130403-93130404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs16918890	chr11:93130411-93130412	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs559726367	chr11:93130498-93130499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533697300	chr11:93130563-93130564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs1004417	chr11:93130568-93130569	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs544905543	chr11:93130580-93130581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140095244	chr11:93130705-93130706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs181555299	chr11:93130712-93130713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs114754477	chr11:93130755-93130756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567324706	chr11:93130802-93130803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs143659059	chr11:93130804-93130805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs12290334	chr11:93130873-93130874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs190052858	chr11:93130917-93130918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs371100548	chr11:93130955-93130956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs571891142	chr11:93131025-93131026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs374497248	chr11:93131027-93131028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs539200673	chr11:93131065-93131066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs12284477	chr11:93131066-93131067	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs146793672	chr11:93131068-93131069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs111581864	chr11:93131070-93131071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs114790689	chr11:93131087-93131088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573670727	chr11:93131188-93131189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs78420064	chr11:93131195-93131196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185172158	chr11:93131204-93131205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs190967289	chr11:93131234-93131235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs545156354	chr11:93131324-93131325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182680889	chr11:93131350-93131351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs11020305	chr11:93131465-93131466	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs11020306	chr11:93131533-93131534	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs35317680	chr11:93131567-93131568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs561084206	chr11:93131621-93131622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs11020307	chr11:93131632-93131633	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs11020308	chr11:93131667-93131668	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs571893012	chr11:93131757-93131758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs532709731	chr11:93131825-93131826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
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
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
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	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
Mantle cell lymphoma	19029149	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93121000-93130200	Weak transcription	K562	blood
2	chr11:93126400-93130000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr11:93126800-93145200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr11:93128400-93130600	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr11:93128400-93130600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr11:93128400-93130600	Weak transcription	Fetal Heart	heart
7	chr11:93129200-93130400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr11:93129400-93130000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr11:93129400-93130000	Enhancers	NHEK	skin
10	chr11:93129600-93130000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr11:93129600-93130000	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr11:93129600-93130000	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr11:93129600-93130000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr11:93129600-93130000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr11:93129600-93130000	Enhancers	Osteobl	bone
16	chr11:93129600-93130200	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr11:93129800-93130000	Enhancers	H9 Cell Line	embryonic stem cell
18	chr11:93129800-93130000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr11:93129800-93130000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr11:93129800-93130000	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr11:93129800-93130400	Enhancers	NH-A	brain
22	chr11:93130600-93130800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr11:93130600-93130800	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr11:93130600-93131800	Enhancers	Fetal Heart	heart
25	chr11:93137200-93137400	Enhancers	Left Ventricle	heart
26	chr11:93137200-93137600	Active TSS	Pancreatic Islets	Pancreatic Islet
27	chr11:93137600-93139000	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr11:93139000-93145200	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr11:93140000-93144800	Weak transcription	Psoas Muscle	Psoas
30	chr11:93143400-93143800	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr11:93143400-93144400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr11:93143400-93144400	Enhancers	H1 Cell Line	embryonic stem cell
33	chr11:93143400-93144600	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr11:93143400-93145400	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr11:93143400-93145600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr11:93143600-93144200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr11:93143600-93144400	Enhancers	H9 Cell Line	embryonic stem cell
38	chr11:93143600-93144400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr11:93143600-93144800	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr11:93143600-93145200	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr11:93143800-93144000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
42	chr11:93143800-93145000	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr11:93143800-93145400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr11:93144000-93144200	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr11:93144000-93145400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr11:93144200-93144400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
47	chr11:93144200-93145200	Enhancers	Muscle Satellite Cultured Cells	--
48	chr11:93144400-93145200	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr11:93145200-93145400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr11:93145200-93145400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet

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