Variant report

Variant	esv2750979
Chromosome Location	chr11:107566557-107624198
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:594)
CpG islands
(count:1161)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:594 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:107611660-107612010	K562	blood:	n/a	n/a
2	ATF1	chr11:107611621-107612014	K562	blood:	n/a	n/a
3	BCLAF1	chr11:107611758-107612134	GM12878	blood:	n/a	n/a
4	BCLAF1	chr11:107611617-107612062	GM12878	blood:	n/a	n/a
5	BHLHE40	chr11:107611713-107611932	K562	blood:	n/a	n/a
6	BHLHE40	chr11:107611683-107612272	GM12878	blood:	n/a	n/a
7	BRCA1	chr11:107611863-107611999	GM12878	blood:	n/a	n/a
8	CBX3	chr11:107611711-107612054	K562	blood:	n/a	n/a
9	CBX3	chr11:107566702-107567329	HCT-116	colon:	n/a	n/a
10	CBX3	chr11:107566660-107567358	HCT-116	colon:	n/a	n/a
11	CEBPB	chr11:107575807-107576208	A549	lung:	n/a	chr11:107576020-107576031 chr11:107576018-107576031 chr11:107576015-107576032
12	CEBPB	chr11:107575797-107576195	Hela-S3	cervix:	n/a	chr11:107576020-107576031 chr11:107576018-107576031 chr11:107576015-107576032
13	CEBPB	chr11:107566832-107567243	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr11:107590352-107590718	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr11:107575623-107576218	A549	lung:	n/a	chr11:107576020-107576031 chr11:107576018-107576031 chr11:107576015-107576032
16	CEBPB	chr11:107590473-107590616	K562	blood:	n/a	n/a
17	CEBPB	chr11:107611754-107611981	K562	blood:	n/a	n/a
18	CEBPB	chr11:107575834-107576166	A549	lung:	n/a	chr11:107576020-107576031 chr11:107576018-107576031 chr11:107576015-107576032
19	CEBPB	chr11:107590385-107590675	IMR90	lung:	n/a	n/a
20	CEBPB	chr11:107575740-107576211	IMR90	lung:	n/a	chr11:107576020-107576031 chr11:107576018-107576031 chr11:107576015-107576032
21	CEBPB	chr11:107581149-107581285	K562	blood:	n/a	n/a
22	CEBPB	chr11:107578515-107579018	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr11:107566649-107567344	HCT-116	colon:	n/a	n/a
24	CEBPB	chr11:107611669-107612000	K562	blood:	n/a	n/a
25	CEBPB	chr11:107566805-107567263	IMR90	lung:	n/a	n/a
26	CHD1	chr11:107611648-107612196	IMR90	lung:	n/a	n/a
27	CHD1	chr11:107611804-107612012	GM12878	blood:	n/a	n/a
28	CTCF	chr11:107611760-107611910	AG09309	skin:	n/a	n/a
29	CTCF	chr11:107611820-107611970	HCM	heart:	n/a	n/a
30	CTCF	chr11:107611800-107611950	HMF	breast:	n/a	n/a
31	CTCF	chr11:107615120-107615270	HMF	breast:	n/a	n/a
32	CTCF	chr11:107611760-107611910	GM12864	blood:	n/a	n/a
33	CTCF	chr11:107611800-107611950	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr11:107615180-107615330	HEK293	kidney:	n/a	n/a
35	CTCF	chr11:107611780-107611930	HA-sp	spinal cord:	n/a	n/a
36	CTCF	chr11:107611760-107611910	K562	blood:	n/a	n/a
37	CTCF	chr11:107615060-107615210	K562	blood:	n/a	n/a
38	CTCF	chr11:107615160-107615310	GM12864	blood:	n/a	n/a
39	CTCF	chr11:107611800-107611950	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr11:107615180-107615330	Caco-2	colon:	n/a	n/a
41	CTCF	chr11:107611820-107611970	NB4	blood:	n/a	n/a
42	CTCF	chr11:107611822-107611968	GM19240	blood:	n/a	n/a
43	CTCF	chr11:107612113-107612120	GM12891	blood:	n/a	n/a
44	CTCF	chr11:107615080-107615230	SAEC	small airway:	n/a	n/a
45	CTCF	chr11:107611820-107611970	RPTEC	kidney:	n/a	n/a
46	CTCF	chr11:107611840-107611990	GM12864	blood:	n/a	n/a
47	CTCF	chr11:107611853-107611949	Fibrobl	skin:	n/a	n/a
48	CTCF	chr11:107611780-107611930	GM12872	blood:	n/a	n/a
49	CTCF	chr11:107611636-107612006	K562	blood:	n/a	n/a
50	CTCF	chr11:107611780-107611930	GM12801	blood:	n/a	n/a

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:107582884-107582934	SK-N-SH_RA	brain:	n/a
2	chr11:107582818-107582868	A549	lung:	n/a
3	chr11:107582884-107582934	SK-N-SH_RA	brain:	n/a
4	chr11:107582818-107582868	A549	lung:	n/a
5	chr11:107583339-107583389	HRCEpiC	kidney:	n/a
6	chr11:107582876-107582926	ovcar-3	ovarian:	n/a
7	chr11:107570881-107570931	ProgFib	skin:	n/a
8	chr11:107583406-107583456	HPAEpiC	pulmonary alveolar:	n/a
9	chr11:107579390-107579440	GM06990	blood:	n/a
10	chr11:107621307-107621357	HCF	heart:	n/a
11	chr11:107579390-107579440	AG04449	skin:	fetal
12	chr11:107621307-107621357	GM12891	blood:	n/a
13	chr11:107579390-107579440	HEEpiC	esophagus:	n/a
14	chr11:107621307-107621357	NB4	blood:	n/a
15	chr11:107582876-107582926	GM12892	blood:	n/a
16	chr11:107621307-107621357	ECC-1	luminal epithelium:	n/a
17	chr11:107575901-107575951	HRE	kidney:	n/a
18	chr11:107582876-107582926	CMK	blood:	n/a
19	chr11:107582804-107582854	U87	brain:	n/a
20	chr11:107582818-107582868	HCF	heart:	n/a
21	chr11:107578640-107578690	MCF10A-Er-Src	breast:	n/a
22	chr11:107574836-107574886	HL-60	blood:	n/a
23	chr11:107582818-107582868	MCF-7	breast:	n/a
24	chr11:107582734-107582784	MCF10A-Er-Src	breast:	n/a
25	chr11:107578640-107578690	SK-N-MC	brain:	n/a
26	chr11:107570881-107570931	AG09309	skin:	n/a
27	chr11:107575901-107575951	HAEpiC	amniotic membrane:	n/a
28	chr11:107579390-107579440	BE2_C	brain:	n/a
29	chr11:107621204-107621254	HAEpiC	amniotic membrane:	n/a
30	chr11:107582734-107582784	ECC-1	luminal epithelium:	n/a
31	chr11:107583339-107583389	CMK	blood:	n/a
32	chr11:107583406-107583456	CMK	blood:	n/a
33	chr11:107570881-107570931	HCM	heart:	n/a
34	chr11:107621204-107621254	CMK	blood:	n/a
35	chr11:107579390-107579440	AG04450	lung:	fetal
36	chr11:107574836-107574886	NH-A	brain:	n/a
37	chr11:107582884-107582934	GM19239	blood:	n/a
38	chr11:107567020-107567070	HRCEpiC	kidney:	n/a
39	chr11:107578640-107578690	PrEC	prostate:	n/a
40	chr11:107582884-107582934	NB4	blood:	n/a
41	chr11:107621204-107621254	U87	brain:	n/a
42	chr11:107575901-107575951	U87	brain:	n/a
43	chr11:107582884-107582934	GM12878	blood:	n/a
44	chr11:107582804-107582854	Hepatocyte	liver:	n/a
45	chr11:107582876-107582926	AG04450	lung:	fetal
46	chr11:107582818-107582868	AG09319	gingival:	n/a
47	chr11:107575901-107575951	NB4	blood:	n/a
48	chr11:107621204-107621254	AG09319	gingival:	n/a
49	chr11:107582804-107582854	MCF-7	breast:	n/a
50	chr11:107574836-107574886	HPAEpiC	pulmonary alveolar:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:107581160..107581699-chr2:20677885..20678629,2	MCF-7	breast:
2	chr11:107623853..107625487-chr11:107628696..107631031,2	K562	blood:
3	chr11:107568027..107570324-chr11:107571232..107574133,2	K562	blood:
4	chr11:107596819..107597459-chr11:124725059..124725764,2	MCF-7	breast:
5	chr11:107614634..107615702-chr11:107641448..107642000,3	MCF-7	breast:
6	chr11:107436309..107438020-chr11:107596616..107599192,2	K562	blood:
7	chr11:107591458..107593748-chr11:107595284..107597502,2	K562	blood:
8	chr11:107611768..107612356-chr11:107641576..107642546,2	MCF-7	breast:
9	chr11:107579136..107581936-chr11:107582041..107586270,3	K562	blood:
10	chr11:107611355..107612284-chr11:107768737..107769652,4	MCF-7	breast:
11	chr11:107591458..107593748-chr11:107595284..107597502,2	K562	blood:
12	chr11:107611439..107612355-chr11:107641879..107642586,3	K562	blood:
13	chr11:107568027..107570324-chr11:107571232..107574133,2	K562	blood:
14	chr11:107579372..107581674-chr11:107582041..107583758,2	K562	blood:
15	chr11:107435305..107437870-chr11:107574680..107577639,2	K562	blood:

No data

Variant related genes	Relation type
SLN	TF binding region
ENSG00000268602	TF binding region
ENSG00000254702	TF binding region
SLN	CpG island
ENSG00000268602	CpG island
ENSG00000254702	CpG island
ENSG00000268602	chromatin interactions
ENSG00000170290	chromatin interactions
ENSG00000137760	chromatin interactions

Extended variants
information (count: 1720 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1720 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10890753	chr11:107566557-107566558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs556367321	chr11:107566570-107566571	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564741362	chr11:107566573-107566574	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs597872	chr11:107566585-107566586	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs559375001	chr11:107566599-107566600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs368181312	chr11:107566604-107566605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs540984857	chr11:107566620-107566621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559584579	chr11:107566634-107566635	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs597465	chr11:107566637-107566638	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs548167351	chr11:107566639-107566640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs569810891	chr11:107566647-107566648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539107745	chr11:107566648-107566649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552270981	chr11:107566686-107566687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571068596	chr11:107566765-107566766	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535202916	chr11:107566808-107566809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368886949	chr11:107566820-107566821	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538381599	chr11:107566846-107566847	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146965991	chr11:107566876-107566877	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs535519780	chr11:107566918-107566919	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147772622	chr11:107566954-107566955	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs60291066	chr11:107567020-107567021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs66971078	chr11:107567021-107567022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112799371	chr11:107567025-107567026	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575194006	chr11:107567064-107567065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142587833	chr11:107567140-107567141	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186168671	chr11:107567179-107567180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576999749	chr11:107567225-107567226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541199169	chr11:107567280-107567281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11212330	chr11:107567288-107567289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143371048	chr11:107567305-107567306	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs112255556	chr11:107567333-107567334	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113046113	chr11:107567339-107567340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188715237	chr11:107567360-107567361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560635461	chr11:107567362-107567363	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs148379770	chr11:107567364-107567365	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181494350	chr11:107567374-107567375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552333752	chr11:107567411-107567412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs564184698	chr11:107567413-107567414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs11365615	chr11:107567415-107567416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149200666	chr11:107567423-107567424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs17107335	chr11:107567457-107567458	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs547160518	chr11:107567500-107567501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs568520195	chr11:107567536-107567537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs12362924	chr11:107567544-107567545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs550835015	chr11:107567597-107567598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs542813288	chr11:107567674-107567675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs115887459	chr11:107567706-107567707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs12223802	chr11:107567717-107567718	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs492661	chr11:107567754-107567755	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs374299344	chr11:107567757-107567758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	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
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Obesity	19966786	CNVD
Renal cell carcinoma	21668985	CNVD
Cancer	20164920	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21993859	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:443 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:107561200-107566800	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr11:107562400-107566600	Weak transcription	NHDF-Ad	bronchial
3	chr11:107562400-107566800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr11:107562400-107570200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr11:107562600-107566600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr11:107562600-107566600	Weak transcription	A549	lung
7	chr11:107562600-107567200	Weak transcription	Fetal Muscle Leg	muscle
8	chr11:107562600-107567200	Weak transcription	HSMMtube	muscle
9	chr11:107562600-107567600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr11:107565600-107566600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr11:107566200-107567200	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr11:107566200-107567400	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr11:107566200-107567800	Enhancers	HUVEC	blood vessel
14	chr11:107566200-107568000	Enhancers	Muscle Satellite Cultured Cells	--
15	chr11:107566200-107568000	Enhancers	NH-A	brain
16	chr11:107566200-107568000	Enhancers	NHLF	lung
17	chr11:107566200-107568400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr11:107566400-107567400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr11:107566400-107567600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr11:107566400-107567800	Enhancers	Placenta Amnion	Placenta Amnion
21	chr11:107566400-107567800	Enhancers	Osteobl	bone
22	chr11:107566400-107568000	Enhancers	HSMM	muscle
23	chr11:107566400-107569000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr11:107566600-107567000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr11:107566600-107567200	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr11:107566600-107567600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr11:107566600-107567800	Enhancers	A549	lung
28	chr11:107566600-107567800	Enhancers	HMEC	breast
29	chr11:107566600-107567800	Enhancers	NHDF-Ad	bronchial
30	chr11:107566600-107567800	Enhancers	NHEK	skin
31	chr11:107566600-107568200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr11:107566600-107568200	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr11:107566600-107568600	Enhancers	Psoas Muscle	Psoas
34	chr11:107566800-107567800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr11:107566800-107568200	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr11:107567000-107571800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr11:107567200-107567600	Enhancers	Adipose Nuclei	Adipose
38	chr11:107567200-107567800	Enhancers	Fetal Muscle Leg	muscle
39	chr11:107567200-107568600	Enhancers	HSMMtube	muscle
40	chr11:107567200-107571600	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr11:107567200-107571600	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr11:107567400-107568200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr11:107567400-107570400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr11:107567600-107568400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr11:107567800-107570200	Weak transcription	Fetal Muscle Leg	muscle
46	chr11:107567800-107573000	Weak transcription	A549	lung
47	chr11:107567800-107573000	Weak transcription	NHDF-Ad	bronchial
48	chr11:107568000-107573200	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr11:107568000-107574800	Weak transcription	NH-A	brain
50	chr11:107568000-107575000	Weak transcription	HSMM	muscle

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