Variant report

Variant	nsv1047295
Chromosome Location	chr11:48159630-48388686
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1175)
CpG islands
(count:1224)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:1175 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

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	ATF1	chr11:48356437-48356637	K562	blood:	n/a	n/a
3	ATF1	chr11:48292484-48292679	K562	blood:	n/a	n/a
4	ATF3	chr11:48194480-48194676	K562	blood:	n/a	n/a
5	ATF3	chr11:48194364-48194613	K562	blood:	n/a	n/a
6	BACH1	chr11:48356973-48356986	K562	blood:	n/a	n/a
7	BHLHE40	chr11:48194470-48194703	GM12878	blood:	n/a	n/a
8	BRCA1	chr11:48361931-48361935	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr11:48329323-48329679	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr11:48194475-48194742	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr11:48235490-48235559	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr11:48194532-48194633	GM12878	blood:	n/a	n/a
13	CBX3	chr11:48329320-48329744	HCT-116	colon:	n/a	n/a
14	CBX3	chr11:48175001-48175304	K562	blood:	n/a	n/a
15	CEBPB	chr11:48232372-48232647	Hela-S3	cervix:	n/a	chr11:48232504-48232515
16	CEBPB	chr11:48171761-48172146	ECC-1	luminal epithelium:	n/a	n/a
17	CEBPB	chr11:48161560-48161749	HepG2	liver:	n/a	chr11:48161642-48161653
18	CEBPB	chr11:48340990-48341301	A549	lung:	n/a	n/a
19	CEBPB	chr11:48376639-48376671	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr11:48232376-48232660	HepG2	liver:	n/a	chr11:48232504-48232515
21	CEBPB	chr11:48161501-48161776	Hela-S3	cervix:	n/a	chr11:48161642-48161653
22	CEBPB	chr11:48171833-48172148	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr11:48171812-48172128	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPB	chr11:48232351-48232666	K562	blood:	n/a	chr11:48232504-48232515
25	CEBPB	chr11:48232368-48232629	A549	lung:	n/a	chr11:48232504-48232515
26	CEBPB	chr11:48367044-48367318	HepG2	liver:	n/a	n/a
27	CEBPB	chr11:48374701-48375094	Hela-S3	cervix:	n/a	chr11:48374900-48374913
28	CEBPB	chr11:48367027-48367324	HCT-116	colon:	n/a	n/a
29	CEBPB	chr11:48170213-48170393	A549	lung:	n/a	n/a
30	CEBPB	chr11:48232346-48232660	IMR90	lung:	n/a	chr11:48232504-48232515
31	CEBPB	chr11:48186415-48186684	A549	lung:	n/a	n/a
32	CEBPB	chr11:48161530-48161773	A549	lung:	n/a	chr11:48161642-48161653
33	CEBPB	chr11:48332469-48332671	HepG2	liver:	n/a	chr11:48332598-48332609
34	CEBPB	chr11:48161546-48161713	K562	blood:	n/a	chr11:48161642-48161653
35	CEBPB	chr11:48186361-48186787	MCF-7	breast:	n/a	n/a
36	CEBPB	chr11:48161558-48161771	H1-hESC	embryonic stem cell:	n/a	chr11:48161642-48161653
37	CEBPB	chr11:48367014-48367428	HCT-116	colon:	n/a	n/a
38	CEBPB	chr11:48171823-48172149	IMR90	lung:	n/a	n/a
39	CEBPB	chr11:48194408-48194759	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr11:48161481-48161783	IMR90	lung:	n/a	chr11:48161642-48161653
41	CEBPB	chr11:48186338-48186812	MCF-7	breast:	n/a	n/a
42	CEBPB	chr11:48367001-48367415	Hela-S3	cervix:	n/a	n/a
43	CEBPZ	chr11:48360331-48360376	HepG2	liver:	n/a	n/a
44	CHD1	chr11:48194544-48194553	GM12878	blood:	n/a	n/a
45	CHD2	chr11:48166761-48166787	HepG2	liver:	n/a	n/a
46	CHD2	chr11:48194572-48194700	HepG2	liver:	n/a	n/a
47	CHD2	chr11:48212930-48213130	K562	blood:	n/a	n/a
48	CHD2	chr11:48199898-48199928	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr11:48377806-48377814	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr11:48344566-48344658	K562	blood:	n/a	n/a

(count:1224 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48345815-48345865	PANC-1	pancreas:	n/a
2	chr11:48285821-48285871	HRPEpiC	eye:	n/a
3	chr11:48285200-48285250	AG10803	skin:	n/a
4	chr11:48285821-48285871	Hela-S3	cervix:	n/a
5	chr11:48345815-48345865	PANC-1	pancreas:	n/a
6	chr11:48285821-48285871	HRPEpiC	eye:	n/a
7	chr11:48285200-48285250	AG10803	skin:	n/a
8	chr11:48285821-48285871	Hela-S3	cervix:	n/a
9	chr11:48266856-48266906	PFSK-1	brain:	n/a
10	chr11:48345361-48345411	A549	lung:	n/a
11	chr11:48327164-48327214	GM12878	blood:	n/a
12	chr11:48345815-48345865	NHBE	bronchial:	n/a
13	chr11:48238724-48238774	SAEC	small airway:	n/a
14	chr11:48345361-48345411	GM06990	blood:	n/a
15	chr11:48367974-48368024	HepG2	liver:	n/a
16	chr11:48191068-48191118	MCF10A-Er-Src	breast:	n/a
17	chr11:48328132-48328182	HRPEpiC	eye:	n/a
18	chr11:48161380-48161430	HL-60	blood:	n/a
19	chr11:48238296-48238346	Hela-S3	cervix:	n/a
20	chr11:48345361-48345411	SK-N-SH	brain:	n/a
21	chr11:48367974-48368024	HUVEC	blood vessel:	n/a
22	chr11:48345815-48345865	CMK	blood:	n/a
23	chr11:48161861-48161911	NH-A	brain:	n/a
24	chr11:48161380-48161430	BJ	skin:	n/a
25	chr11:48284249-48284299	PFSK-1	brain:	n/a
26	chr11:48266856-48266906	SAEC	small airway:	n/a
27	chr11:48285200-48285250	HEEpiC	esophagus:	n/a
28	chr11:48374446-48374496	RPTEC	kidney:	n/a
29	chr11:48345815-48345865	A549	lung:	n/a
30	chr11:48285200-48285250	GM06990	blood:	n/a
31	chr11:48346680-48346730	HRE	kidney:	n/a
32	chr11:48237353-48237403	AG10803	skin:	n/a
33	chr11:48237353-48237403	HEEpiC	esophagus:	n/a
34	chr11:48238724-48238774	HRE	kidney:	n/a
35	chr11:48326388-48326438	SK-N-SH_RA	brain:	n/a
36	chr11:48346680-48346730	HEK293	kidney:	embryo
37	chr11:48374446-48374496	T-47D	breast:	n/a
38	chr11:48237358-48237408	A549	lung:	n/a
39	chr11:48326388-48326438	BE2_C	brain:	n/a
40	chr11:48345361-48345411	RPTEC	kidney:	n/a
41	chr11:48191068-48191118	AG04449	skin:	fetal
42	chr11:48237358-48237408	AG04450	lung:	fetal
43	chr11:48284249-48284299	ECC-1	luminal epithelium:	n/a
44	chr11:48345361-48345411	HepG2	liver:	n/a
45	chr11:48185069-48185119	HAEpiC	amniotic membrane:	n/a
46	chr11:48326388-48326438	BJ	skin:	n/a
47	chr11:48238724-48238774	GM19239	blood:	n/a
48	chr11:48161861-48161911	NHBE	bronchial:	n/a
49	chr11:48345815-48345865	HEEpiC	esophagus:	n/a
50	chr11:48345361-48345411	HEEpiC	esophagus:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:48234220..48234962-chr11:48329425..48329937,2	MCF-7	breast:
2	chr11:48193798..48195313-chr11:48231364..48232253,10	MCF-7	breast:
3	chr11:48147718..48152937-chr11:48156132..48159658,5	MCF-7	breast:
4	chr11:48162891..48165104-chr11:48166215..48167785,2	K562	blood:
5	chr11:48205861..48206473-chr11:48233802..48234494,2	MCF-7	breast:
6	chr11:48205381..48206618-chr11:48231139..48232409,4	MCF-7	breast:
7	chr11:48361908..48364233-chr11:48365831..48368223,2	MCF-7	breast:
8	chr11:48167809..48169447-chr6:82621853..82624317,2	MCF-7	breast:
9	chr11:48205861..48206473-chr11:48233802..48234494,2	MCF-7	breast:
10	chr11:48292794..48294613-chr11:48297509..48299435,2	K562	blood:
11	chr11:48193798..48195313-chr11:48231364..48232253,10	MCF-7	breast:
12	chr11:48175475..48177463-chr11:48181716..48184556,2	MCF-7	breast:
13	chr11:47857319..47859657-chr11:48158646..48160993,2	K562	blood:
14	chr11:48366878..48368914-chr11:48372533..48375413,2	MCF-7	breast:
15	chr11:48234220..48234962-chr11:48329425..48329937,2	MCF-7	breast:
16	chr11:48000629..48003536-chr11:48164616..48166215,2	K562	blood:
17	chr11:48194137..48195015-chr11:48231499..48232341,4	MCF-7	breast:
18	chr11:48194206..48195039-chr11:49190936..49191807,2	MCF-7	breast:
19	chr11:48194137..48195015-chr11:48231499..48232341,4	MCF-7	breast:
20	chr11:48205381..48206618-chr11:48231139..48232409,4	MCF-7	breast:
21	chr11:48175475..48177463-chr11:48181716..48184556,2	MCF-7	breast:
22	chr11:48361908..48364233-chr11:48365831..48368223,2	MCF-7	breast:
23	chr11:48292794..48294613-chr11:48297509..48299435,2	K562	blood:

No data

(count:8 , 50 per page) page: 1

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

Variant related genes	Relation type
OR4X2	TF binding region
OR4B2P	TF binding region
OR4X1	TF binding region
PTPRJ	TF binding region
OR4C5	TF binding region
OR4C4P	TF binding region
OR4C3	TF binding region
OR4S1	TF binding region
OR4B1	TF binding region
OR4X2	CpG island
OR4B2P	CpG island
OR4X1	CpG island
PTPRJ	CpG island
OR4C5	CpG island
OR4C4P	CpG island
OR4C3	CpG island
OR4S1	CpG island
OR4B1	CpG island
ENSG00000197161	chromatin interactions
ENSG00000149177	chromatin interactions

Extended variants
information (count: 6500 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:6500 , 50 per page) page: 1 2 3 4 5 6 7 ... 130

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549071351	chr11:48159661-48159662	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs80026812	chr11:48159703-48159704	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145763924	chr11:48159713-48159714	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs190490578	chr11:48159818-48159819	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs116502206	chr11:48159901-48159902	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373691770	chr11:48159902-48159903	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs555962919	chr11:48159973-48159974	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs576022786	chr11:48159984-48159985	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535571847	chr11:48159990-48159991	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555042854	chr11:48159992-48159993	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs557498879	chr11:48160016-48160017	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs376654098	chr11:48160100-48160101	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs111404321	chr11:48160106-48160107	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs541735816	chr11:48160117-48160118	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs370208880	chr11:48160180-48160181	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs577551818	chr11:48160240-48160241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs558450046	chr11:48160304-48160305	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs113408284	chr11:48160306-48160307	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538025448	chr11:48160338-48160339	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182207612	chr11:48160358-48160359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs12273137	chr11:48160426-48160427	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs10734564	chr11:48160429-48160430	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs543156521	chr11:48160514-48160515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115962516	chr11:48160548-48160549	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185893728	chr11:48160564-48160565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551366817	chr11:48160591-48160592	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113253936	chr11:48160609-48160610	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs12273331	chr11:48160610-48160611	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs542821688	chr11:48160620-48160621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs76460130	chr11:48160621-48160622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535195284	chr11:48160625-48160626	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555479017	chr11:48160650-48160651	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189208569	chr11:48160679-48160680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559492364	chr11:48160686-48160687	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534550471	chr11:48160689-48160690	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs371060380	chr11:48160694-48160695	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs76575368	chr11:48160695-48160696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs578240915	chr11:48160700-48160701	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544159603	chr11:48160701-48160702	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573485632	chr11:48160721-48160722	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113004194	chr11:48160965-48160966	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs377444976	chr11:48160982-48160983	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs557249353	chr11:48160997-48160998	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs375648458	chr11:48161005-48161006	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs368633740	chr11:48161021-48161022	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs574219155	chr11:48161040-48161041	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs542865256	chr11:48161045-48161046	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs138339280	chr11:48161049-48161050	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs374727162	chr11:48161061-48161062	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559753032	chr11:48161066-48161067	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:1667 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48131600-48191600	Weak transcription	Small Intestine	intestine
2	chr11:48137000-48172000	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr11:48137000-48175200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr11:48137200-48161000	Weak transcription	NHDF-Ad	bronchial
5	chr11:48138200-48192600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr11:48139600-48172200	Strong transcription	Primary monocytes fromperipheralblood	blood
7	chr11:48141200-48162800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr11:48141200-48163200	Strong transcription	Fetal Intestine Large	intestine
9	chr11:48143200-48164200	Weak transcription	Ovary	ovary
10	chr11:48144000-48175200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr11:48145600-48175600	Weak transcription	Fetal Brain Male	brain
12	chr11:48145800-48184200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr11:48146400-48160200	Weak transcription	Esophagus	oesophagus
14	chr11:48146400-48175400	Weak transcription	Fetal Heart	heart
15	chr11:48146800-48160800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr11:48147000-48166400	Weak transcription	Fetal Thymus	thymus
17	chr11:48147400-48160800	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr11:48149800-48160200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr11:48149800-48161000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr11:48149800-48161000	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr11:48149800-48161200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr11:48149800-48174600	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr11:48149800-48190600	Weak transcription	Right Ventricle	heart
24	chr11:48150000-48161000	Weak transcription	Fetal Muscle Trunk	muscle
25	chr11:48150400-48161200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr11:48151200-48164400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr11:48151400-48163000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
28	chr11:48151400-48191600	Weak transcription	Stomach Mucosa	stomach
29	chr11:48151600-48160600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr11:48151600-48161000	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr11:48151600-48164200	Weak transcription	NHLF	lung
32	chr11:48151600-48174400	Strong transcription	Primary neutrophils fromperipheralblood	blood
33	chr11:48152000-48161000	Weak transcription	Aorta	Aorta
34	chr11:48152000-48165600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr11:48152000-48175400	Weak transcription	K562	blood
36	chr11:48152200-48160800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr11:48152200-48160800	Weak transcription	Rectal Smooth Muscle	rectum
38	chr11:48152200-48161000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr11:48152200-48161200	Weak transcription	Fetal Muscle Leg	muscle
40	chr11:48152200-48164400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr11:48152400-48160400	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr11:48153400-48160600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr11:48153400-48164400	Weak transcription	Fetal Lung	lung
44	chr11:48153400-48166200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr11:48155000-48162200	Strong transcription	Cortex derived primary cultured neurospheres	brain
46	chr11:48155400-48160800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr11:48156000-48164400	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr11:48156200-48173000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr11:48156400-48160800	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr11:48156400-48161200	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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