Variant report

Variant	nsv897330
Chromosome Location	chr11:48168664-48850587
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2457)
CpG islands
(count:1282)
Chromatin interactive
region (count:21)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:2457 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

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	ARID3A	chr11:48600198-48600306	K562	blood:	n/a	n/a
3	ATF1	chr11:48845364-48845733	K562	blood:	n/a	n/a
4	ATF1	chr11:48796111-48796444	K562	blood:	n/a	n/a
5	ATF1	chr11:48849264-48849333	K562	blood:	n/a	n/a
6	ATF1	chr11:48292484-48292679	K562	blood:	n/a	n/a
7	ATF1	chr11:48356437-48356637	K562	blood:	n/a	n/a
8	ATF3	chr11:48194364-48194613	K562	blood:	n/a	n/a
9	ATF3	chr11:48845439-48845653	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr11:48194480-48194676	K562	blood:	n/a	n/a
11	BACH1	chr11:48356973-48356986	K562	blood:	n/a	n/a
12	BACH1	chr11:48814467-48814498	K562	blood:	n/a	n/a
13	BATF	chr11:48817733-48818014	GM12878	blood:	n/a	n/a
14	BATF	chr11:48810099-48810738	GM12878	blood:	n/a	n/a
15	BATF	chr11:48776572-48776725	GM12878	blood:	n/a	n/a
16	BATF	chr11:48805015-48805320	GM12878	blood:	n/a	n/a
17	BATF	chr11:48844664-48844887	GM12878	blood:	n/a	n/a
18	BATF	chr11:48775367-48775560	GM12878	blood:	n/a	n/a
19	BATF	chr11:48834403-48834545	GM12878	blood:	n/a	n/a
20	BATF	chr11:48844232-48844479	GM12878	blood:	n/a	n/a
21	BATF	chr11:48828245-48828541	GM12878	blood:	n/a	n/a
22	BATF	chr11:48842846-48843034	GM12878	blood:	n/a	n/a
23	BATF	chr11:48741581-48741798	GM12878	blood:	n/a	n/a
24	BATF	chr11:48844167-48844436	GM12878	blood:	n/a	n/a
25	BATF	chr11:48810174-48810367	GM12878	blood:	n/a	n/a
26	BATF	chr11:48834286-48834608	GM12878	blood:	n/a	n/a
27	BATF	chr11:48831050-48831447	GM12878	blood:	n/a	n/a
28	BATF	chr11:48776576-48776723	GM12878	blood:	n/a	n/a
29	BATF	chr11:48775372-48775512	GM12878	blood:	n/a	n/a
30	BATF	chr11:48810469-48810756	GM12878	blood:	n/a	n/a
31	BATF	chr11:48828245-48828584	GM12878	blood:	n/a	n/a
32	BATF	chr11:48804986-48805223	GM12878	blood:	n/a	n/a
33	BATF	chr11:48839569-48839852	GM12878	blood:	n/a	n/a
34	BCL11A	chr11:48776528-48776717	GM12878	blood:	n/a	n/a
35	BCL11A	chr11:48844230-48844427	GM12878	blood:	n/a	n/a
36	BCL11A	chr11:48843199-48843455	GM12878	blood:	n/a	n/a
37	BCL11A	chr11:48810484-48810738	GM12878	blood:	n/a	n/a
38	BCL11A	chr11:48817821-48818049	GM12878	blood:	n/a	n/a
39	BCL11A	chr11:48804969-48805215	GM12878	blood:	n/a	n/a
40	BCL11A	chr11:48831065-48831468	GM12878	blood:	n/a	n/a
41	BCL11A	chr11:48844176-48844483	GM12878	blood:	n/a	n/a
42	BCL11A	chr11:48845411-48845640	GM12878	blood:	n/a	n/a
43	BCL11A	chr11:48834409-48834539	GM12878	blood:	n/a	n/a
44	BCL11A	chr11:48810204-48810361	GM12878	blood:	n/a	n/a
45	BCL11A	chr11:48845478-48845589	H1-hESC	embryonic stem cell:	n/a	n/a
46	BCL11A	chr11:48810501-48810790	GM12878	blood:	n/a	n/a
47	BCL11A	chr11:48844631-48844885	GM12878	blood:	n/a	n/a
48	BCL11A	chr11:48776564-48776735	GM12878	blood:	n/a	n/a
49	BCL11A	chr11:48834381-48834593	GM12878	blood:	n/a	n/a
50	BCL11A	chr11:48810132-48810472	GM12878	blood:	n/a	n/a

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48374446-48374496	HCM	heart:	n/a
2	chr11:48374446-48374496	HCM	heart:	n/a
3	chr11:48284249-48284299	NHBE	bronchial:	n/a
4	chr11:48238724-48238774	AG04450	lung:	fetal
5	chr11:48191068-48191118	GM12891	blood:	n/a
6	chr11:48191068-48191118	NB4	blood:	n/a
7	chr11:48237353-48237403	HCPEpiC	choroid plexus:	n/a
8	chr11:48345815-48345865	HIPEpiC	eye:	n/a
9	chr11:48185069-48185119	U87	brain:	n/a
10	chr11:48266856-48266906	SAEC	small airway:	n/a
11	chr11:48345815-48345865	GM12892	blood:	n/a
12	chr11:48237358-48237408	GM19239	blood:	n/a
13	chr11:48374446-48374496	AG09319	gingival:	n/a
14	chr11:48510647-48510697	AG10803	skin:	n/a
15	chr11:48238724-48238774	A549	lung:	n/a
16	chr11:48509488-48509538	GM12891	blood:	n/a
17	chr11:48238724-48238774	HEEpiC	esophagus:	n/a
18	chr11:48327164-48327214	GM06990	blood:	n/a
19	chr11:48345815-48345865	HRE	kidney:	n/a
20	chr11:48328132-48328182	MCF10A-Er-Src	breast:	n/a
21	chr11:48285200-48285250	HMEC	breast:	n/a
22	chr11:48510647-48510697	NHBE	bronchial:	n/a
23	chr11:48326388-48326438	GM12878	blood:	n/a
24	chr11:48237358-48237408	HRCEpiC	kidney:	n/a
25	chr11:48326388-48326438	ECC-1	luminal epithelium:	n/a
26	chr11:48374446-48374496	Jurkat	blood:	n/a
27	chr11:48345361-48345411	Jurkat	blood:	n/a
28	chr11:48345815-48345865	GM12891	blood:	n/a
29	chr11:48238296-48238346	PANC-1	pancreas:	n/a
30	chr11:48367974-48368024	CMK	blood:	n/a
31	chr11:48185069-48185119	NHBE	bronchial:	n/a
32	chr11:48185069-48185119	HEK293	kidney:	embryo
33	chr11:48328132-48328182	HCPEpiC	choroid plexus:	n/a
34	chr11:48238296-48238346	HCM	heart:	n/a
35	chr11:48266856-48266906	HL-60	blood:	n/a
36	chr11:48509778-48509828	PFSK-1	brain:	n/a
37	chr11:48510647-48510697	AG09319	gingival:	n/a
38	chr11:48509778-48509828	HCPEpiC	choroid plexus:	n/a
39	chr11:48326388-48326438	HCPEpiC	choroid plexus:	n/a
40	chr11:48185069-48185119	BJ	skin:	n/a
41	chr11:48285821-48285871	A549	lung:	n/a
42	chr11:48327164-48327214	PFSK-1	brain:	n/a
43	chr11:48238296-48238346	GM12878	blood:	n/a
44	chr11:48266856-48266906	HRPEpiC	eye:	n/a
45	chr11:48238296-48238346	HRCEpiC	kidney:	n/a
46	chr11:48266856-48266906	ovcar-3	ovarian:	n/a
47	chr11:48327164-48327214	H1-hESC	embryonic stem cell:	embryo
48	chr11:48345361-48345411	ECC-1	luminal epithelium:	n/a
49	chr11:48191068-48191118	LNCaP	prostate:	n/a
50	chr11:48509778-48509828	T-47D	breast:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:48366878..48368914-chr11:48372533..48375413,2	MCF-7	breast:
2	chr11:48194137..48195015-chr11:48231499..48232341,4	MCF-7	breast:
3	chr11:48175475..48177463-chr11:48181716..48184556,2	MCF-7	breast:
4	chr11:48194137..48195015-chr11:48231499..48232341,4	MCF-7	breast:
5	chr11:48234220..48234962-chr11:48329425..48329937,2	MCF-7	breast:
6	chr11:48194206..48195039-chr11:49190936..49191807,2	MCF-7	breast:
7	chr11:48193798..48195313-chr11:48231364..48232253,10	MCF-7	breast:
8	chr11:48205861..48206473-chr11:48233802..48234494,2	MCF-7	breast:
9	chr11:48205381..48206618-chr11:48231139..48232409,4	MCF-7	breast:
10	chr11:48175475..48177463-chr11:48181716..48184556,2	MCF-7	breast:
11	chr11:48234220..48234962-chr11:48329425..48329937,2	MCF-7	breast:
12	chr11:48478071..48478587-chr11:49191267..49191777,2	MCF-7	breast:
13	chr11:48167809..48169447-chr6:82621853..82624317,2	MCF-7	breast:
14	chr11:48292794..48294613-chr11:48297509..48299435,2	K562	blood:
15	chr11:48205861..48206473-chr11:48233802..48234494,2	MCF-7	breast:
16	chr11:48361908..48364233-chr11:48365831..48368223,2	MCF-7	breast:
17	chr11:48292794..48294613-chr11:48297509..48299435,2	K562	blood:
18	chr11:48811378..48811898-chr8:46850618..46851141,2	MCF-7	breast:
19	chr11:48193798..48195313-chr11:48231364..48232253,10	MCF-7	breast:
20	chr11:48361908..48364233-chr11:48365831..48368223,2	MCF-7	breast:
21	chr11:48205381..48206618-chr11:48231139..48232409,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4C5-1	chr11:48507915-48508377	NONHSAT021297

No data

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

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

Variant related genes	Relation type
OR4C9P	TF binding region
OR4C5	TF binding region
OR4C4P	TF binding region
OR4C10P	TF binding region
OR4A47	TF binding region
OR4C2P	TF binding region
OR4X2	TF binding region
OR4A41P	TF binding region
OR4A40P	TF binding region
OR4A46P	TF binding region
OR4B2P	TF binding region
OR4A44P	TF binding region
OR4A45P	TF binding region
OR4A48P	TF binding region
OR4X1	TF binding region
OR4R1P	TF binding region
OR4C3	TF binding region
OR4S1	TF binding region
OR4A42P	TF binding region
OR4B1	TF binding region
OR4A43P	TF binding region
OR4C9P	CpG island
OR4C5	CpG island
OR4C4P	CpG island
OR4C10P	CpG island
OR4A47	CpG island
OR4C2P	CpG island
OR4X2	CpG island
OR4A41P	CpG island
OR4A40P	CpG island
OR4A46P	CpG island
OR4B2P	CpG island
OR4A44P	CpG island
OR4A45P	CpG island
OR4A48P	CpG island
OR4X1	CpG island
OR4R1P	CpG island
OR4C3	CpG island
OR4S1	CpG island
OR4A42P	CpG island
OR4B1	CpG island
OR4A43P	CpG island
ENSG00000197161	chromatin interactions

Extended variants
information (count: 16882 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:16882 , 50 per page) page: 1 2 3 4 5 6 7 ... 338

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3741410	chr11:48168664-48168665	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs572760363	chr11:48168671-48168672	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141696977	chr11:48168673-48168674	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs571249761	chr11:48168674-48168675	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558380359	chr11:48168683-48168684	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370894330	chr11:48168687-48168688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs374489131	chr11:48168723-48168724	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150110008	chr11:48168731-48168732	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574879463	chr11:48168763-48168764	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138451880	chr11:48168764-48168765	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs142960080	chr11:48168765-48168766	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs369508895	chr11:48168795-48168796	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529387957	chr11:48168797-48168798	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369234784	chr11:48168894-48168895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542577617	chr11:48168910-48168911	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76315518	chr11:48168916-48168917	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191631365	chr11:48168917-48168918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182163497	chr11:48168941-48168942	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187098128	chr11:48168954-48168955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533103614	chr11:48168963-48168964	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs531735334	chr11:48168982-48168983	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549731944	chr11:48169035-48169036	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs569700551	chr11:48169055-48169056	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs576597258	chr11:48169069-48169070	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537608261	chr11:48169070-48169071	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535230425	chr11:48169079-48169080	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs548976450	chr11:48169097-48169098	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs191012058	chr11:48169115-48169116	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564908563	chr11:48169212-48169213	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs555580747	chr11:48169251-48169252	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs182085625	chr11:48169267-48169268	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537622339	chr11:48169298-48169299	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557286218	chr11:48169309-48169310	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs4752905	chr11:48169312-48169313	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs542762102	chr11:48169323-48169324	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs559315823	chr11:48169329-48169330	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs76178567	chr11:48169416-48169417	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530747637	chr11:48169519-48169520	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186724474	chr11:48169537-48169538	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545008372	chr11:48169544-48169545	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550450158	chr11:48169545-48169546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189917828	chr11:48169553-48169554	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533094846	chr11:48169585-48169586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549934516	chr11:48169613-48169614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146109915	chr11:48169649-48169650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528977911	chr11:48169663-48169664	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549137831	chr11:48169676-48169677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs10742834	chr11:48169717-48169718	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs534550640	chr11:48169787-48169788	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551418277	chr11:48169909-48169910	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Ovarian clear cell carcinoma	21343371	CNVD
Medulloblastoma	21163964	CNVD
early-passage human iPS cells	21368824	CNVD
Intellectual disability	22045946	CNVD

Chromatin state (count:1592 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

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	chr11:48138200-48192600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr11:48139600-48172200	Strong transcription	Primary monocytes fromperipheralblood	blood
6	chr11:48144000-48175200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr11:48145600-48175600	Weak transcription	Fetal Brain Male	brain
8	chr11:48145800-48184200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr11:48146400-48175400	Weak transcription	Fetal Heart	heart
10	chr11:48149800-48174600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr11:48149800-48190600	Weak transcription	Right Ventricle	heart
12	chr11:48151400-48191600	Weak transcription	Stomach Mucosa	stomach
13	chr11:48151600-48174400	Strong transcription	Primary neutrophils fromperipheralblood	blood
14	chr11:48152000-48175400	Weak transcription	K562	blood
15	chr11:48156200-48173000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr11:48156400-48191400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr11:48157400-48170800	Strong transcription	Fetal Stomach	stomach
18	chr11:48157400-48172800	Strong transcription	Primary T cells from cord blood	blood
19	chr11:48157400-48172800	Strong transcription	Fetal Intestine Small	intestine
20	chr11:48157400-48173200	Strong transcription	Liver	Liver
21	chr11:48157400-48173600	Strong transcription	Primary B cells from peripheral blood	blood
22	chr11:48157600-48169800	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr11:48157600-48173400	Strong transcription	Primary B cells from cord blood	blood
24	chr11:48157600-48173800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr11:48159000-48169800	Strong transcription	Spleen	Spleen
26	chr11:48159000-48171800	Weak transcription	Left Ventricle	heart
27	chr11:48161400-48172200	Weak transcription	Brain Germinal Matrix	brain
28	chr11:48162000-48174400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr11:48163400-48172000	Weak transcription	Fetal Muscle Trunk	muscle
30	chr11:48163400-48172200	Weak transcription	Esophagus	oesophagus
31	chr11:48163400-48173000	Strong transcription	Primary T helper cells fromperipheralblood	blood
32	chr11:48163400-48173000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr11:48163400-48174400	Weak transcription	HSMMtube	muscle
34	chr11:48163400-48175200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr11:48163400-48192400	Weak transcription	Colon Smooth Muscle	Colon
36	chr11:48163800-48173000	Strong transcription	Primary T helper cells PMA-I stimulated	--
37	chr11:48163800-48174400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr11:48164000-48169000	Strong transcription	Sigmoid Colon	Sigmoid Colon
39	chr11:48164000-48169400	Strong transcription	Lung	lung
40	chr11:48164000-48173000	Strong transcription	Primary T cells fromperipheralblood	blood
41	chr11:48164000-48173200	Strong transcription	Fetal Intestine Large	intestine
42	chr11:48164000-48173400	Strong transcription	A549	lung
43	chr11:48164200-48169200	Strong transcription	Placenta	Placenta
44	chr11:48164200-48169200	Strong transcription	Stomach Smooth Muscle	stomach
45	chr11:48164200-48169400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr11:48164200-48169400	Strong transcription	Cortex derived primary cultured neurospheres	brain
47	chr11:48164200-48169400	Strong transcription	Adipose Nuclei	Adipose
48	chr11:48164200-48169400	Strong transcription	Brain Angular Gyrus	brain
49	chr11:48164200-48169400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr11:48164200-48169400	Strong transcription	Pancreatic Islets	Pancreatic Islet

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