Variant report

Variant	esv2762916
Chromosome Location	chr11:72147875-72160112
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	chr11:72157943-72158351	K562	blood:	n/a	n/a
2	ARID3A	chr11:72157941-72158357	HepG2	liver:	n/a	n/a
3	ATF1	chr11:72155913-72155914	K562	blood:	n/a	n/a
4	ATF1	chr11:72158067-72158243	K562	blood:	n/a	n/a
5	BACH1	chr11:72156523-72156824	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr11:72147766-72147993	GM12878	blood:	n/a	n/a
7	BHLHE40	chr11:72148839-72149049	HepG2	liver:	n/a	n/a
8	BHLHE40	chr11:72158069-72158517	K562	blood:	n/a	n/a
9	CBX3	chr11:72151125-72151669	HCT-116	colon:	n/a	n/a
10	CCNT2	chr11:72153132-72153200	K562	blood:	n/a	n/a
11	CEBPB	chr11:72154238-72154334	Hela-S3	cervix:	n/a	chr11:72154263-72154274 chr11:72154261-72154274
12	CEBPB	chr11:72154138-72154357	HepG2	liver:	n/a	chr11:72154263-72154274 chr11:72154261-72154274
13	CEBPB	chr11:72154109-72154431	IMR90	lung:	n/a	chr11:72154263-72154274 chr11:72154261-72154274
14	CEBPB	chr11:72151200-72151466	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr11:72154152-72154364	A549	lung:	n/a	chr11:72154263-72154274 chr11:72154261-72154274
16	CEBPD	chr11:72152872-72153253	K562	blood:	n/a	n/a
17	CTCF	chr11:72158540-72158690	WI-38	lung:	n/a	n/a
18	CTCF	chr11:72160040-72160190	AG04449	skin:	n/a	chr11:72160135-72160148 chr11:72160133-72160151 chr11:72160139-72160148
19	CTCF	chr11:72158000-72158150	HAc	cerebellar:	n/a	n/a
20	CTCF	chr11:72160080-72160230	MCF-7	breast:	n/a	chr11:72160135-72160148 chr11:72160133-72160151 chr11:72160139-72160148
21	CTCF	chr11:72158057-72158327	MCF-7	breast:	n/a	chr11:72158171-72158192
22	CTCF	chr11:72158071-72158293	GM10266	blood:	n/a	chr11:72158171-72158192
23	CTCF	chr11:72151240-72151390	AG10803	skin:	n/a	n/a
24	CTCF	chr11:72158080-72158230	HBMEC	blood vessel:	n/a	chr11:72158171-72158192
25	CTCF	chr11:72158408-72158567	GM19238	blood:	n/a	n/a
26	CTCF	chr11:72158100-72158250	HA-sp	spinal cord:	n/a	chr11:72158171-72158192
27	CTCF	chr11:72157973-72158307	SK-N-SH_RA	brain:	n/a	chr11:72158171-72158192
28	CTCF	chr11:72158100-72158250	RPTEC	kidney:	n/a	chr11:72158171-72158192
29	CTCF	chr11:72158120-72158270	SAEC	small airway:	n/a	chr11:72158171-72158192
30	CTCF	chr11:72158400-72158550	GM12870	blood:	n/a	n/a
31	CTCF	chr11:72158080-72158230	HPAF	blood vessel:	n/a	chr11:72158171-72158192
32	CTCF	chr11:72151200-72151350	AG04449	skin:	n/a	n/a
33	CTCF	chr11:72158060-72158210	GM12868	blood:	n/a	chr11:72158171-72158192
34	CTCF	chr11:72160013-72160281	K562	blood:	n/a	chr11:72160135-72160148 chr11:72160133-72160151 chr11:72160139-72160148
35	CTCF	chr11:72151220-72151370	HCFaa	heart:	n/a	n/a
36	CTCF	chr11:72158140-72158290	GM12874	blood:	n/a	chr11:72158171-72158192
37	CTCF	chr11:72158120-72158270	GM12866	blood:	n/a	chr11:72158171-72158192
38	CTCF	chr11:72158100-72158250	HPF	lung:	n/a	chr11:72158171-72158192
39	CTCF	chr11:72158160-72158310	HVMF	connective:	n/a	chr11:72158171-72158192
40	CTCF	chr11:72158140-72158290	GM12873	blood:	n/a	chr11:72158171-72158192
41	CTCF	chr11:72158080-72158230	GM12864	blood:	n/a	chr11:72158171-72158192
42	CTCF	chr11:72158967-72159000	GM10266	blood:	n/a	n/a
43	CTCF	chr11:72158140-72158290	GM12869	blood:	n/a	chr11:72158171-72158192
44	CTCF	chr11:72158100-72158250	NHDF-neo	bronchial:	n/a	chr11:72158171-72158192
45	CTCF	chr11:72158100-72158250	SAEC	small airway:	n/a	chr11:72158171-72158192
46	CTCF	chr11:72158105-72158254	ProgFib	skin:	n/a	chr11:72158171-72158192
47	CTCF	chr11:72158120-72158270	GM12865	blood:	n/a	chr11:72158171-72158192
48	CTCF	chr11:72158080-72158230	AG09319	gingival:	n/a	chr11:72158171-72158192
49	CTCF	chr11:72158071-72158293	GM10248	blood:	n/a	chr11:72158171-72158192
50	CTCF	chr11:72158026-72158027	Medullo	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:72148947-72148997	CMK	blood:	n/a
2	chr11:72148947-72148997	ECC-1	luminal epithelium:	n/a
3	chr11:72148947-72148997	HRE	kidney:	n/a
4	chr11:72148947-72148997	HAEpiC	amniotic membrane:	n/a
5	chr11:72148947-72148997	GM12892	blood:	n/a
6	chr11:72148947-72148997	U87	brain:	n/a
7	chr11:72148947-72148997	HEEpiC	esophagus:	n/a
8	chr11:72148947-72148997	NT2-D1	testis:	n/a
9	chr11:72148947-72148997	HepG2	liver:	n/a
10	chr11:72148947-72148997	AG04449	skin:	fetal
11	chr11:72148947-72148997	K562	blood:	n/a
12	chr11:72148947-72148997	SKMC	muscle:	n/a
13	chr11:72148947-72148997	PANC-1	pancreas:	n/a
14	chr11:72148947-72148997	AG04450	lung:	fetal
15	chr11:72148947-72148997	Caco-2	colon:	n/a
16	chr11:72148947-72148997	HPAEpiC	pulmonary alveolar:	n/a
17	chr11:72148947-72148997	HRPEpiC	eye:	n/a
18	chr11:72148947-72148997	NHDF-neo	bronchial:	n/a
19	chr11:72148947-72148997	NB4	blood:	n/a
20	chr11:72148947-72148997	HIPEpiC	eye:	n/a
21	chr11:72148947-72148997	NHBE	bronchial:	n/a
22	chr11:72148947-72148997	GM19239	blood:	n/a
23	chr11:72148947-72148997	IMR90	lung:	fetal
24	chr11:72148947-72148997	HUVEC	blood vessel:	n/a
25	chr11:72148947-72148997	GM06990	blood:	n/a
26	chr11:72148947-72148997	MCF10A-Er-Src	breast:	n/a
27	chr11:72148947-72148997	HMEC	breast:	n/a
28	chr11:72148947-72148997	GM12891	blood:	n/a
29	chr11:72148947-72148997	H1-hESC	embryonic stem cell:	embryo
30	chr11:72148947-72148997	Hepatocyte	liver:	n/a
31	chr11:72148947-72148997	HRCEpiC	kidney:	n/a
32	chr11:72148947-72148997	SK-N-MC	brain:	n/a
33	chr11:72148947-72148997	T-47D	breast:	n/a
34	chr11:72148947-72148997	Hela-S3	cervix:	n/a
35	chr11:72148947-72148997	AG09309	skin:	n/a
36	chr11:72148947-72148997	HNPCEpiC	eye:	n/a
37	chr11:72148947-72148997	ProgFib	skin:	n/a
38	chr11:72148947-72148997	HCT-116	colon:	n/a
39	chr11:72148947-72148997	PrEC	prostate:	n/a
40	chr11:72148947-72148997	SK-N-SH_RA	brain:	n/a
41	chr11:72148947-72148997	AoSMC	blood vessel:	n/a
42	chr11:72148947-72148997	HCM	heart:	n/a
43	chr11:72148947-72148997	HCPEpiC	choroid plexus:	n/a
44	chr11:72148947-72148997	MCF-7	breast:	n/a
45	chr11:72148947-72148997	NH-A	brain:	n/a
46	chr11:72148947-72148997	AG09319	gingival:	n/a
47	chr11:72148947-72148997	RPTEC	kidney:	n/a
48	chr11:72148947-72148997	HL-60	blood:	n/a
49	chr11:72148947-72148997	PFSK-1	brain:	n/a
50	chr11:72148947-72148997	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr11:71812827..71814983-chr11:72157130..72160023,3	MCF-7	breast:
2	chr11:72144882..72145842-chr11:72157717..72158559,5	MCF-7	breast:
3	chr11:72145271..72146910-chr11:72154563..72157956,3	MCF-7	breast:
4	chr11:72141748..72142617-chr11:72158017..72158572,2	MCF-7	breast:
5	chr11:72138473..72140807-chr11:72156234..72158136,2	MCF-7	breast:
6	chr11:72150961..72153899-chr11:72155415..72157907,2	MCF-7	breast:
7	chr11:72144928..72145593-chr11:72157728..72158661,3	K562	blood:
8	chr11:72150565..72152924-chr11:72165968..72167789,2	K562	blood:
9	chr11:72144772..72145877-chr11:72157260..72158587,8	MCF-7	breast:
10	chr11:72157990..72159779-chr11:72162354..72164537,2	K562	blood:
11	chr11:72159747..72162636-chr11:72268105..72269694,2	K562	blood:
12	chr11:72150961..72153899-chr11:72155415..72157907,2	MCF-7	breast:

Variant related genes	Relation type
CLPB	TF binding region
CLPB	CpG island
ENSG00000149357	chromatin interactions
ENSG00000162129	chromatin interactions

Extended variants
information (count: 423 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:423 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11235499	chr11:72147875-72147876	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs117758103	chr11:72147876-72147877	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs549483998	chr11:72147877-72147878	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs568026273	chr11:72147885-72147886	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs542240968	chr11:72147887-72147888	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs555298058	chr11:72147909-72147910	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs529761130	chr11:72147955-72147956	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs563514276	chr11:72147956-72147957	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs567173680	chr11:72148030-72148031	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs530592006	chr11:72148042-72148043	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs376047197	chr11:72148043-72148044	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs534347691	chr11:72148084-72148085	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs559208876	chr11:72148116-72148117	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs552666980	chr11:72148120-72148121	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs577237124	chr11:72148147-72148148	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs187222203	chr11:72148149-72148150	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs562208198	chr11:72148195-72148196	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs565809121	chr11:72148217-72148218	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs574769791	chr11:72148226-72148227	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs4475949	chr11:72148244-72148245	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs146698684	chr11:72148269-72148270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs371259531	chr11:72148316-72148317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545561712	chr11:72148343-72148344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs564328579	chr11:72148365-72148366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs531433863	chr11:72148369-72148370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs4488227	chr11:72148384-72148385	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs568415286	chr11:72148413-72148414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs34246182	chr11:72148459-72148460	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs550967253	chr11:72148474-72148475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs144873006	chr11:72148484-72148485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs180766028	chr11:72148586-72148587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs534516346	chr11:72148649-72148650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs559318454	chr11:72148653-72148654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149031106	chr11:72148682-72148683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs538098939	chr11:72148685-72148686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs11826227	chr11:72148686-72148687	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs574841402	chr11:72148740-72148741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs535420423	chr11:72148828-72148829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs374999970	chr11:72148948-72148949	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs569465427	chr11:72148979-72148980	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs117905439	chr11:72148985-72148986	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs185234944	chr11:72149015-72149016	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs564259208	chr11:72149053-72149054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs576182122	chr11:72149072-72149073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543255668	chr11:72149133-72149134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs111413032	chr11:72149236-72149237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs151320605	chr11:72149270-72149271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547386247	chr11:72149295-72149296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559367326	chr11:72149334-72149335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190390113	chr11:72149367-72149368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Acute myeloid leukemia	20729466	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
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	19153074	CNVD
Schizophrenia	21346763	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Acute myeloid leukemia	21251322	CNVD

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:72145600-72149600	Weak transcription	NHDF-Ad	bronchial
2	chr11:72145600-72150200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:72145600-72152000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr11:72145600-72152600	Weak transcription	Right Atrium	heart
5	chr11:72145800-72148800	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr11:72145800-72149000	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr11:72145800-72149600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr11:72145800-72150200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr11:72145800-72150200	Weak transcription	HMEC	breast
10	chr11:72145800-72150400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr11:72146000-72149200	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr11:72146000-72150200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr11:72146000-72150200	Weak transcription	Adipose Nuclei	Adipose
14	chr11:72146000-72152000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr11:72146200-72150600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr11:72146600-72148000	Weak transcription	Fetal Muscle Trunk	muscle
17	chr11:72146800-72151200	Weak transcription	Placenta	Placenta
18	chr11:72147000-72148000	Enhancers	GM12878-XiMat	blood
19	chr11:72147600-72148200	Enhancers	Primary B cells from cord blood	blood
20	chr11:72148000-72148200	Enhancers	Fetal Muscle Trunk	muscle
21	chr11:72148200-72150200	Weak transcription	Fetal Muscle Trunk	muscle
22	chr11:72148200-72150800	Weak transcription	Primary B cells from cord blood	blood
23	chr11:72148800-72150400	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr11:72149000-72150400	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr11:72149200-72150200	Weak transcription	Primary neutrophils fromperipheralblood	blood
26	chr11:72149600-72150600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr11:72149600-72150600	Enhancers	NHDF-Ad	bronchial
28	chr11:72150200-72151000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr11:72150200-72151200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr11:72150200-72151600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr11:72150200-72151600	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr11:72150200-72151600	Enhancers	Muscle Satellite Cultured Cells	--
33	chr11:72150200-72151600	Enhancers	HMEC	breast
34	chr11:72150200-72151600	Enhancers	NHEK	skin
35	chr11:72150200-72152200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr11:72150200-72153000	Enhancers	Adipose Nuclei	Adipose
37	chr11:72150400-72150600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr11:72150400-72150800	Enhancers	Hela-S3	cervix
39	chr11:72150400-72151400	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr11:72150400-72151400	Enhancers	Osteobl	bone
41	chr11:72150400-72154800	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr11:72150600-72151400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr11:72150600-72151600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr11:72150600-72152400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr11:72150800-72151000	Enhancers	Primary B cells from cord blood	blood
46	chr11:72150800-72151600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr11:72150800-72151600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr11:72150800-72158000	Weak transcription	Hela-S3	cervix
49	chr11:72151000-72151400	Weak transcription	Primary B cells from cord blood	blood
50	chr11:72151000-72151600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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