Variant report

Variant	nsv439
Chromosome Location	chr11:93135936-93171682
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	ATF1	chr11:93140996-93141323	K562	blood:	n/a	n/a
2	ATF3	chr11:93141005-93141334	K562	blood:	n/a	n/a
3	CEBPB	chr11:93140968-93141291	K562	blood:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
4	CEBPB	chr11:93140988-93141325	H1-hESC	embryonic stem cell:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
5	CEBPB	chr11:93146378-93146499	K562	blood:	n/a	n/a
6	CEBPB	chr11:93140980-93141347	IMR90	lung:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
7	CEBPB	chr11:93140969-93141354	HepG2	liver:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
8	CEBPB	chr11:93146382-93146537	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr11:93140982-93141344	A549	lung:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
10	CEBPB	chr11:93140958-93141353	Hela-S3	cervix:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
11	CEBPB	chr11:93145425-93145556	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr11:93141014-93141258	HepG2	liver:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
13	CEBPB	chr11:93140968-93141348	K562	blood:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
14	CEBPB	chr11:93140940-93141345	HCT-116	colon:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
15	CEBPB	chr11:93140924-93141389	A549	lung:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
16	CEBPB	chr11:93140894-93141393	K562	blood:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
17	CEBPB	chr11:93141045-93141317	ECC-1	luminal epithelium:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
18	CEBPB	chr11:93140897-93141476	HCT-116	colon:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
19	CTCF	chr11:93153020-93153065	GM10248	blood:	n/a	n/a
20	CTCF	chr11:93164880-93165030	HA-sp	spinal cord:	n/a	n/a
21	CTCF	chr11:93153008-93153097	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr11:93161820-93161970	AG04450	lung:	n/a	n/a
23	CTCF	chr11:93161800-93161950	NHDF-neo	bronchial:	n/a	n/a
24	CTCF	chr11:93150442-93150502	GM13976	blood:	n/a	n/a
25	E2F4	chr11:93137300-93137492	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr11:93171676-93171818	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr11:93141003-93141303	MCF10A-Er-Src	breast:	n/a	n/a
28	EGR1	chr11:93141132-93141341	K562	blood:	n/a	chr11:93141235-93141248 chr11:93141234-93141249
29	EGR1	chr11:93141099-93141328	K562	blood:	n/a	chr11:93141235-93141248 chr11:93141234-93141249
30	EP300	chr11:93141013-93141299	Hela-S3	cervix:	n/a	chr11:93141159-93141173 chr11:93141140-93141154
31	EP300	chr11:93140926-93141303	K562	blood:	n/a	chr11:93141159-93141173 chr11:93141140-93141154
32	FAM48A	chr11:93161780-93161991	GM12878	blood:	n/a	n/a
33	FOS	chr11:93140989-93141337	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr11:93140982-93141346	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr11:93140976-93141333	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr11:93140976-93141342	MCF10A-Er-Src	breast:	n/a	n/a
37	FOXA2	chr11:93159915-93160295	A549	lung:	n/a	n/a
38	FOXA2	chr11:93154308-93154786	A549	lung:	n/a	n/a
39	FOXA2	chr11:93154228-93154961	A549	lung:	n/a	n/a
40	JUN	chr11:93169950-93169975	H1-hESC	embryonic stem cell:	n/a	n/a
41	JUN	chr11:93161814-93162049	K562	blood:	n/a	n/a
42	JUN	chr11:93141080-93141306	HepG2	liver:	n/a	chr11:93141159-93141172
43	JUND	chr11:93137233-93137302	H1-hESC	embryonic stem cell:	n/a	n/a
44	JUND	chr11:93141002-93141332	HepG2	liver:	n/a	n/a
45	JUND	chr11:93140982-93141348	K562	blood:	n/a	n/a
46	KAP1	chr11:93145828-93146215	K562	blood:	n/a	n/a
47	MAFF	chr11:93144901-93145218	K562	blood:	n/a	chr11:93145052-93145070
48	MAFF	chr11:93144904-93145236	HepG2	liver:	n/a	chr11:93145052-93145070
49	MAFF	chr11:93139363-93139622	K562	blood:	n/a	n/a
50	MAFK	chr11:93144889-93145230	HepG2	liver:	n/a	chr11:93145057-93145068 chr11:93145053-93145068

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:93143810-93143860	HL-60	blood:	n/a
2	chr11:93143810-93143860	A549	lung:	n/a
3	chr11:93143810-93143860	GM06990	blood:	n/a
4	chr11:93143810-93143860	BJ	skin:	n/a
5	chr11:93143810-93143860	SKMC	muscle:	n/a
6	chr11:93143810-93143860	HRCEpiC	kidney:	n/a
7	chr11:93143810-93143860	HNPCEpiC	eye:	n/a
8	chr11:93143810-93143860	ovcar-3	ovarian:	n/a
9	chr11:93143810-93143860	PANC-1	pancreas:	n/a
10	chr11:93143810-93143860	SK-N-MC	brain:	n/a
11	chr11:93143810-93143860	GM12892	blood:	n/a
12	chr11:93143810-93143860	AG04450	lung:	fetal
13	chr11:93143810-93143860	HCF	heart:	n/a
14	chr11:93143810-93143860	HCM	heart:	n/a
15	chr11:93143810-93143860	NHDF-neo	bronchial:	n/a
16	chr11:93143810-93143860	T-47D	breast:	n/a
17	chr11:93143810-93143860	K562	blood:	n/a
18	chr11:93143810-93143860	Caco-2	colon:	n/a
19	chr11:93143810-93143860	MCF-7	breast:	n/a
20	chr11:93143810-93143860	HIPEpiC	eye:	n/a
21	chr11:93143810-93143860	GM19239	blood:	n/a
22	chr11:93143810-93143860	AG04449	skin:	fetal
23	chr11:93143810-93143860	HEEpiC	esophagus:	n/a
24	chr11:93143810-93143860	ECC-1	luminal epithelium:	n/a
25	chr11:93143810-93143860	ProgFib	skin:	n/a
26	chr11:93143810-93143860	AG10803	skin:	n/a
27	chr11:93143810-93143860	HepG2	liver:	n/a
28	chr11:93143810-93143860	SK-N-SH	brain:	n/a
29	chr11:93143810-93143860	PFSK-1	brain:	n/a
30	chr11:93143810-93143860	AoSMC	blood vessel:	n/a
31	chr11:93143810-93143860	HCT-116	colon:	n/a
32	chr11:93143810-93143860	SAEC	small airway:	n/a
33	chr11:93143810-93143860	HMEC	breast:	n/a
34	chr11:93143810-93143860	PrEC	prostate:	n/a
35	chr11:93143810-93143860	HEK293	kidney:	embryo
36	chr11:93143810-93143860	GM12891	blood:	n/a
37	chr11:93143810-93143860	HRE	kidney:	n/a
38	chr11:93143810-93143860	NT2-D1	testis:	n/a
39	chr11:93143810-93143860	HUVEC	blood vessel:	n/a
40	chr11:93143810-93143860	AG09319	gingival:	n/a
41	chr11:93143810-93143860	U87	brain:	n/a
42	chr11:93143810-93143860	LNCaP	prostate:	n/a
43	chr11:93143810-93143860	H1-hESC	embryonic stem cell:	embryo
44	chr11:93143810-93143860	NHBE	bronchial:	n/a
45	chr11:93143810-93143860	IMR90	lung:	fetal
46	chr11:93143810-93143860	HRPEpiC	eye:	n/a
47	chr11:93143810-93143860	MCF10A-Er-Src	breast:	n/a
48	chr11:93143810-93143860	NH-A	brain:	n/a
49	chr11:93143810-93143860	BE2_C	brain:	n/a
50	chr11:93143810-93143860	SK-N-SH_RA	brain:	n/a

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

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

Extended variants
information (count: 474 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543654504	chr11:93135942-93135943	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs190787550	chr11:93135959-93135960	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs183340290	chr11:93135971-93135972	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs77744211	chr11:93135979-93135980	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs141246783	chr11:93135999-93136000	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs560097795	chr11:93136073-93136074	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs527553867	chr11:93136087-93136088	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs552440239	chr11:93136125-93136126	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs564271927	chr11:93136182-93136183	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs531510745	chr11:93136219-93136220	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs370595867	chr11:93136247-93136248	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs548835972	chr11:93136262-93136263	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs117675379	chr11:93136277-93136278	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs568529264	chr11:93136315-93136316	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs535972623	chr11:93136316-93136317	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs146950670	chr11:93136404-93136405	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs2605574	chr11:93136444-93136445	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs367823257	chr11:93136491-93136492	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs549394386	chr11:93136539-93136540	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs186413191	chr11:93136541-93136542	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs117190620	chr11:93136705-93136706	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs59350684	chr11:93136785-93136786	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs137913564	chr11:93136928-93136929	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs576700093	chr11:93137054-93137055	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs190422547	chr11:93137076-93137077	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs537214975	chr11:93137100-93137101	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs112008954	chr11:93137150-93137151	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs35132273	chr11:93137154-93137155	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs555563568	chr11:93137382-93137383	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs574148013	chr11:93137389-93137390	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs541537582	chr11:93137408-93137409	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs140665848	chr11:93137448-93137449	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs572005895	chr11:93137457-93137458	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs371635351	chr11:93137459-93137460	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs2260769	chr11:93137475-93137476	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs564387858	chr11:93137499-93137500	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs573116489	chr11:93137501-93137502	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs531652928	chr11:93137505-93137506	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs549971669	chr11:93137526-93137527	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs561865366	chr11:93137551-93137552	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs529365017	chr11:93137553-93137554	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs183060998	chr11:93137676-93137677	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs566087558	chr11:93137699-93137700	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs533338077	chr11:93137721-93137722	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs551500736	chr11:93137766-93137767	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs540639965	chr11:93137785-93137786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570171667	chr11:93137879-93137880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs569986779	chr11:93137892-93137893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs537352390	chr11:93138046-93138047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs551380985	chr11:93138058-93138059	Weak transcription Enhancers	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93126800-93145200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:93137200-93137400	Enhancers	Left Ventricle	heart
3	chr11:93137200-93137600	Active TSS	Pancreatic Islets	Pancreatic Islet
4	chr11:93137600-93139000	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr11:93139000-93145200	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr11:93140000-93144800	Weak transcription	Psoas Muscle	Psoas
7	chr11:93143400-93143800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr11:93143400-93144400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr11:93143400-93144400	Enhancers	H1 Cell Line	embryonic stem cell
10	chr11:93143400-93144600	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr11:93143400-93145400	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr11:93143400-93145600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr11:93143600-93144200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:93143600-93144400	Enhancers	H9 Cell Line	embryonic stem cell
15	chr11:93143600-93144400	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr11:93143600-93144800	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr11:93143600-93145200	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr11:93143800-93144000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr11:93143800-93145000	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr11:93143800-93145400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr11:93144000-93144200	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr11:93144000-93145400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr11:93144200-93144400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr11:93144200-93145200	Enhancers	Muscle Satellite Cultured Cells	--
25	chr11:93144400-93145200	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr11:93145200-93145400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr11:93145200-93145400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
28	chr11:93152400-93152800	Enhancers	H9 Cell Line	embryonic stem cell
29	chr11:93161600-93162200	Enhancers	Dnd41	blood
30	chr11:93165600-93166000	Enhancers	GM12878-XiMat	blood

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