Variant report

Variant	esv3448080
Chromosome Location	chr11:48187996-48289788
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	chr11:48194471-48194702	HepG2	liver:	n/a	n/a
2	ATF3	chr11:48194364-48194613	K562	blood:	n/a	n/a
3	ATF3	chr11:48194480-48194676	K562	blood:	n/a	n/a
4	BHLHE40	chr11:48194470-48194703	GM12878	blood:	n/a	n/a
5	BRCA1	chr11:48194532-48194633	GM12878	blood:	n/a	n/a
6	BRCA1	chr11:48194475-48194742	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr11:48235490-48235559	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr11:48232351-48232666	K562	blood:	n/a	chr11:48232504-48232515
9	CEBPB	chr11:48194408-48194759	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr11:48232368-48232629	A549	lung:	n/a	chr11:48232504-48232515
11	CEBPB	chr11:48232346-48232660	IMR90	lung:	n/a	chr11:48232504-48232515
12	CEBPB	chr11:48232372-48232647	Hela-S3	cervix:	n/a	chr11:48232504-48232515
13	CEBPB	chr11:48232376-48232660	HepG2	liver:	n/a	chr11:48232504-48232515
14	CHD1	chr11:48194544-48194553	GM12878	blood:	n/a	n/a
15	CHD2	chr11:48212930-48213130	K562	blood:	n/a	n/a
16	CHD2	chr11:48194572-48194700	HepG2	liver:	n/a	n/a
17	CHD2	chr11:48199898-48199928	Hela-S3	cervix:	n/a	n/a
18	CREB1	chr11:48194478-48194746	A549	lung:	n/a	n/a
19	CTCF	chr11:48231680-48231830	HepG2	liver:	n/a	n/a
20	CTCF	chr11:48194409-48194724	Spleen_OC	spleen:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
21	CTCF	chr11:48194520-48194670	K562	blood:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
22	CTCF	chr11:48206096-48206241	GM12878	blood:	n/a	chr11:48206171-48206192
23	CTCF	chr11:48231700-48231850	GM12866	blood:	n/a	n/a
24	CTCF	chr11:48194500-48194650	GM12874	blood:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
25	CTCF	chr11:48194422-48194736	MCF-7	breast:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194723-48194736 chr11:48194575-48194588 chr11:48194573-48194589
26	CTCF	chr11:48194540-48194690	HMF	breast:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
27	CTCF	chr11:48231700-48231850	GM12872	blood:	n/a	n/a
28	CTCF	chr11:48231640-48231790	NHLF	lung:	n/a	n/a
29	CTCF	chr11:48231635-48231854	K562	blood:	n/a	n/a
30	CTCF	chr11:48194361-48194801	GM12878	blood:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194723-48194736 chr11:48194575-48194588 chr11:48194573-48194589
31	CTCF	chr11:48194432-48194721	LNCaP	prostate:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
32	CTCF	chr11:48236663-48236678	MCF-7	breast:	n/a	n/a
33	CTCF	chr11:48231700-48231850	HCFaa	heart:	n/a	n/a
34	CTCF	chr11:48194480-48194630	WI-38	lung:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
35	CTCF	chr11:48194427-48194735	MCF-7	breast:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
36	CTCF	chr11:48206180-48206330	HCT-116	colon:	n/a	n/a
37	CTCF	chr11:48206116-48206263	MCF-7	breast:	n/a	chr11:48206171-48206192
38	CTCF	chr11:48194480-48194630	SAEC	small airway:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
39	CTCF	chr11:48231700-48231850	GM12873	blood:	n/a	n/a
40	CTCF	chr11:48194872-48194930	GM19238	blood:	n/a	n/a
41	CTCF	chr11:48194403-48194736	GM12878	blood:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194723-48194736 chr11:48194575-48194588 chr11:48194573-48194589
42	CTCF	chr11:48231452-48231970	A549	lung:	n/a	n/a
43	CTCF	chr11:48206120-48206270	GM12871	blood:	n/a	chr11:48206171-48206192
44	CTCF	chr11:48194540-48194690	A549	lung:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
45	CTCF	chr11:48206109-48206267	MCF-7	breast:	n/a	chr11:48206171-48206192
46	CTCF	chr11:48231720-48231870	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr11:48194480-48194630	GM12868	blood:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
48	CTCF	chr11:48231720-48231870	BJ	skin:	n/a	n/a
49	CTCF	chr11:48192440-48192590	BJ	skin:	n/a	n/a
50	CTCF	chr11:48231764-48231822	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48285200-48285250	BE2_C	brain:	n/a
2	chr11:48237353-48237403	Jurkat	blood:	n/a
3	chr11:48284249-48284299	HEK293	kidney:	embryo
4	chr11:48285200-48285250	BE2_C	brain:	n/a
5	chr11:48237353-48237403	Jurkat	blood:	n/a
6	chr11:48284249-48284299	HEK293	kidney:	embryo
7	chr11:48238724-48238774	HRCEpiC	kidney:	n/a
8	chr11:48237358-48237408	HL-60	blood:	n/a
9	chr11:48237358-48237408	HNPCEpiC	eye:	n/a
10	chr11:48237353-48237403	AG09319	gingival:	n/a
11	chr11:48284249-48284299	PrEC	prostate:	n/a
12	chr11:48238724-48238774	ECC-1	luminal epithelium:	n/a
13	chr11:48238296-48238346	PFSK-1	brain:	n/a
14	chr11:48238296-48238346	BJ	skin:	n/a
15	chr11:48238724-48238774	SK-N-MC	brain:	n/a
16	chr11:48191068-48191118	HNPCEpiC	eye:	n/a
17	chr11:48191068-48191118	Jurkat	blood:	n/a
18	chr11:48191068-48191118	SKMC	muscle:	n/a
19	chr11:48285821-48285871	PANC-1	pancreas:	n/a
20	chr11:48285821-48285871	Hela-S3	cervix:	n/a
21	chr11:48237358-48237408	SK-N-MC	brain:	n/a
22	chr11:48284249-48284299	SAEC	small airway:	n/a
23	chr11:48191068-48191118	PrEC	prostate:	n/a
24	chr11:48285200-48285250	GM12891	blood:	n/a
25	chr11:48238296-48238346	SK-N-SH	brain:	n/a
26	chr11:48191068-48191118	HEK293	kidney:	embryo
27	chr11:48238724-48238774	CMK	blood:	n/a
28	chr11:48284249-48284299	AG09309	skin:	n/a
29	chr11:48266856-48266906	Jurkat	blood:	n/a
30	chr11:48191068-48191118	NB4	blood:	n/a
31	chr11:48285200-48285250	GM12892	blood:	n/a
32	chr11:48284249-48284299	HRPEpiC	eye:	n/a
33	chr11:48266856-48266906	HPAEpiC	pulmonary alveolar:	n/a
34	chr11:48237358-48237408	HAEpiC	amniotic membrane:	n/a
35	chr11:48285821-48285871	CMK	blood:	n/a
36	chr11:48285821-48285871	SK-N-SH_RA	brain:	n/a
37	chr11:48285200-48285250	BJ	skin:	n/a
38	chr11:48284249-48284299	HPAEpiC	pulmonary alveolar:	n/a
39	chr11:48285200-48285250	HCM	heart:	n/a
40	chr11:48285821-48285871	GM12892	blood:	n/a
41	chr11:48266856-48266906	U87	brain:	n/a
42	chr11:48266856-48266906	AG04450	lung:	fetal
43	chr11:48238724-48238774	GM19239	blood:	n/a
44	chr11:48238296-48238346	NHBE	bronchial:	n/a
45	chr11:48285821-48285871	ovcar-3	ovarian:	n/a
46	chr11:48285200-48285250	NT2-D1	testis:	n/a
47	chr11:48237353-48237403	SKMC	muscle:	n/a
48	chr11:48285821-48285871	AoSMC	blood vessel:	n/a
49	chr11:48266856-48266906	MCF10A-Er-Src	breast:	n/a
50	chr11:48266856-48266906	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:48194206..48195039-chr11:49190936..49191807,2	MCF-7	breast:
2	chr11:48205861..48206473-chr11:48233802..48234494,2	MCF-7	breast:
3	chr11:48193798..48195313-chr11:48231364..48232253,10	MCF-7	breast:
4	chr11:48205861..48206473-chr11:48233802..48234494,2	MCF-7	breast:
5	chr11:48205381..48206618-chr11:48231139..48232409,4	MCF-7	breast:
6	chr11:48234220..48234962-chr11:48329425..48329937,2	MCF-7	breast:
7	chr11:48193798..48195313-chr11:48231364..48232253,10	MCF-7	breast:
8	chr11:48205381..48206618-chr11:48231139..48232409,4	MCF-7	breast:
9	chr11:48194137..48195015-chr11:48231499..48232341,4	MCF-7	breast:
10	chr11:48194137..48195015-chr11:48231499..48232341,4	MCF-7	breast:

No.	miRNA target gene	miRNA name	Chromosome Location
1	PTPRJ	hsa-miR-155-5p	chr11:48190351-48190373
2	PTPRJ	hsa-miR-155-5p	chr11:48190367-48190373
3	PTPRJ	hsa-miR-16-5p	chr11:48190236-48190242
4	PTPRJ	hsa-miR-16-5p	chr11:48190225-48190243
5	PTPRJ	hsa-miR-26b-5p	chr11:48190233-48190256
6	PTPRJ	hsa-miR-328-3p	chr11:48191725-48191748
7	PTPRJ	hsa-miR-124-3p	chr11:48189431-48189437
8	PTPRJ	hsa-miR-124-3p	chr11:48189418-48189438

Variant related genes	Relation type
OR4X2	TF binding region
OR4B2P	TF binding region
OR4X1	TF binding region
OR4B1	TF binding region
OR4X2	CpG island
OR4B2P	CpG island
OR4X1	CpG island
OR4B1	CpG island

Extended variants
information (count: 1185 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1185 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553004368	chr11:48188013-48188014	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs181480506	chr11:48188022-48188023	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544581847	chr11:48188054-48188055	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186169852	chr11:48188089-48188090	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571706363	chr11:48188156-48188157	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs191790078	chr11:48188157-48188158	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs112482541	chr11:48188158-48188159	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs561423952	chr11:48188180-48188181	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs530283932	chr11:48188230-48188231	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs540488366	chr11:48188260-48188261	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs560622486	chr11:48188263-48188264	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs532684511	chr11:48188289-48188290	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs552603999	chr11:48188295-48188296	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs555100713	chr11:48188297-48188298	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143634239	chr11:48188315-48188316	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs541964650	chr11:48188357-48188358	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs117979538	chr11:48188392-48188393	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550804980	chr11:48188403-48188404	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs117379429	chr11:48188439-48188440	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs536431359	chr11:48188470-48188471	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs557839774	chr11:48188521-48188522	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs546505641	chr11:48188533-48188534	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs577279429	chr11:48188609-48188610	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184082078	chr11:48188621-48188622	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373473662	chr11:48188622-48188623	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs148117873	chr11:48188647-48188648	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs141878277	chr11:48188673-48188674	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs555207493	chr11:48188677-48188678	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs372519671	chr11:48188712-48188713	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs371633411	chr11:48188717-48188718	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11039556	chr11:48188748-48188749	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs540802430	chr11:48188773-48188774	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs369579079	chr11:48188806-48188807	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188934138	chr11:48188844-48188845	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs139396147	chr11:48188855-48188856	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577409423	chr11:48188859-48188860	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs199803858	chr11:48188871-48188872	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs12809012	chr11:48188872-48188873	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs371796701	chr11:48188875-48188876	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs35920791	chr11:48188908-48188909	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs200505007	chr11:48188909-48188910	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs375419721	chr11:48188953-48188954	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs191012650	chr11:48188965-48188966	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs529989420	chr11:48188979-48188980	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs73452004	chr11:48188980-48188981	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs542898958	chr11:48189000-48189001	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559529578	chr11:48189026-48189027	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs538447514	chr11:48189074-48189075	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs139911163	chr11:48189077-48189078	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs79113573	chr11:48189082-48189083	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Breast cancer	21990379	CNVD
Acute myeloid leukemia	20729466	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:526 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48131600-48191600	Weak transcription	Small Intestine	intestine
2	chr11:48138200-48192600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr11:48149800-48190600	Weak transcription	Right Ventricle	heart
4	chr11:48151400-48191600	Weak transcription	Stomach Mucosa	stomach
5	chr11:48156400-48191400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr11:48163400-48192400	Weak transcription	Colon Smooth Muscle	Colon
7	chr11:48173000-48188200	Weak transcription	Brain Germinal Matrix	brain
8	chr11:48174000-48190800	Strong transcription	Liver	Liver
9	chr11:48175200-48191200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr11:48175400-48192400	Strong transcription	Primary neutrophils fromperipheralblood	blood
11	chr11:48175600-48188000	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr11:48175600-48188200	Weak transcription	Fetal Heart	heart
13	chr11:48175600-48191000	Strong transcription	Primary T cells fromperipheralblood	blood
14	chr11:48175800-48190800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr11:48175800-48190800	Weak transcription	HSMMtube	muscle
16	chr11:48175800-48191600	Weak transcription	Rectal Smooth Muscle	rectum
17	chr11:48176000-48190800	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr11:48176000-48194600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr11:48176200-48191000	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr11:48176200-48191200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr11:48176200-48192000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr11:48176400-48189000	Strong transcription	Primary T cells from cord blood	blood
23	chr11:48176400-48189200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr11:48176600-48188600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr11:48176600-48190600	Strong transcription	Primary monocytes fromperipheralblood	blood
26	chr11:48176600-48191800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr11:48177000-48190400	Weak transcription	Fetal Muscle Trunk	muscle
28	chr11:48177400-48188400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr11:48177600-48191000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr11:48177600-48191000	Weak transcription	Fetal Kidney	kidney
31	chr11:48177600-48191200	Strong transcription	Primary B cells from peripheral blood	blood
32	chr11:48177600-48191400	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr11:48178000-48188600	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr11:48178000-48191200	Strong transcription	Primary B cells from cord blood	blood
35	chr11:48178200-48190800	Weak transcription	Skeletal Muscle Female	skeletal muscle
36	chr11:48179200-48190800	Weak transcription	Left Ventricle	heart
37	chr11:48179200-48193200	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr11:48179400-48191000	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr11:48179400-48192200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr11:48183400-48191000	Strong transcription	Primary T helper cells PMA-I stimulated	--
41	chr11:48184000-48189200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
42	chr11:48184000-48189800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr11:48184000-48190000	Strong transcription	Sigmoid Colon	Sigmoid Colon
44	chr11:48184000-48191600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr11:48184200-48190800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr11:48184200-48191000	Strong transcription	Rectal Mucosa Donor 29	rectum
47	chr11:48184400-48190600	Weak transcription	NHLF	lung
48	chr11:48184400-48191200	Weak transcription	Ovary	ovary
49	chr11:48184400-48191200	Weak transcription	HUVEC	blood vessel
50	chr11:48184600-48190600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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