Variant report

Variant	nsv878038
Chromosome Location	chr3:178924867-178962897
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:220)
CpG islands
(count:122)
Chromatin interactive
region (count:24)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:220 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:178954452-178954841	K562	blood:	n/a	n/a
2	ATF1	chr3:178950953-178951045	K562	blood:	n/a	n/a
3	ATF1	chr3:178954531-178954856	K562	blood:	n/a	n/a
4	ATF3	chr3:178933277-178933584	K562	blood:	n/a	n/a
5	CBX3	chr3:178945168-178945500	HCT-116	colon:	n/a	n/a
6	CCNT2	chr3:178954482-178954890	K562	blood:	n/a	n/a
7	CEBPB	chr3:178945251-178945450	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr3:178951995-178952405	K562	blood:	n/a	chr3:178952238-178952249
9	CEBPB	chr3:178944915-178945634	HCT-116	colon:	n/a	n/a
10	CEBPB	chr3:178945038-178945627	HCT-116	colon:	n/a	n/a
11	CEBPB	chr3:178933378-178933567	A549	lung:	n/a	chr3:178933429-178933440
12	CEBPB	chr3:178933329-178933585	IMR90	lung:	n/a	chr3:178933429-178933440
13	CEBPB	chr3:178952122-178952266	HepG2	liver:	n/a	chr3:178952238-178952249
14	CEBPB	chr3:178936575-178937116	K562	blood:	n/a	chr3:178936655-178936668
15	CEBPB	chr3:178944072-178944265	K562	blood:	n/a	chr3:178944212-178944225 chr3:178944212-178944223 chr3:178944212-178944225
16	CEBPB	chr3:178952091-178952392	H1-hESC	embryonic stem cell:	n/a	chr3:178952238-178952249
17	CEBPB	chr3:178933224-178933585	HepG2	liver:	n/a	chr3:178933429-178933440
18	CEBPB	chr3:178933205-178933620	K562	blood:	n/a	chr3:178933429-178933440
19	CEBPB	chr3:178933223-178933758	Hela-S3	cervix:	n/a	chr3:178933429-178933440
20	CEBPB	chr3:178936924-178936992	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr3:178952047-178952419	IMR90	lung:	n/a	chr3:178952238-178952249
22	CEBPB	chr3:178936763-178937119	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr3:178936577-178937153	IMR90	lung:	n/a	chr3:178936655-178936668
24	CEBPB	chr3:178952057-178952413	HepG2	liver:	n/a	chr3:178952238-178952249
25	CEBPB	chr3:178952055-178952380	Hela-S3	cervix:	n/a	chr3:178952238-178952249
26	CEBPB	chr3:178933253-178933523	K562	blood:	n/a	chr3:178933429-178933440
27	CEBPB	chr3:178952052-178952426	K562	blood:	n/a	chr3:178952238-178952249
28	CEBPB	chr3:178933340-178933580	K562	blood:	n/a	chr3:178933429-178933440
29	CEBPB	chr3:178952090-178952341	A549	lung:	n/a	chr3:178952238-178952249
30	CEBPB	chr3:178952019-178952405	ECC-1	luminal epithelium:	n/a	chr3:178952238-178952249
31	CEBPB	chr3:178952113-178952308	K562	blood:	n/a	chr3:178952238-178952249
32	CEBPB	chr3:178936909-178937138	HepG2	liver:	n/a	n/a
33	CTCF	chr3:178940380-178940530	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr3:178932940-178933090	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr3:178940380-178940530	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr3:178932720-178932870	HAc	cerebellar:	n/a	n/a
37	CTCF	chr3:178933822-178933851	GM10248	blood:	n/a	n/a
38	CTCF	chr3:178940380-178940530	AG10803	skin:	n/a	n/a
39	CTCF	chr3:178932867-178932963	GM12878	blood:	n/a	n/a
40	CTCF	chr3:178932849-178932953	K562	blood:	n/a	n/a
41	CTCF	chr3:178932820-178932970	AG09319	gingival:	n/a	n/a
42	CTCF	chr3:178932826-178932989	MCF-7	breast:	n/a	n/a
43	CTCF	chr3:178932720-178932870	HMEC	breast:	n/a	n/a
44	CTCF	chr3:178940380-178940530	AG04450	lung:	n/a	n/a
45	CTCF	chr3:178932860-178933010	MCF-7	breast:	n/a	n/a
46	CTCF	chr3:178932845-178932919	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chr3:178932800-178932950	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr3:178932820-178932970	GM12865	blood:	n/a	n/a
49	CTCF	chr3:178940360-178940510	AG10803	skin:	n/a	n/a
50	CTCF	chr3:178940440-178940590	HMF	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:178961439-178961489	HCPEpiC	choroid plexus:	n/a
2	chr3:178961439-178961489	NH-A	brain:	n/a
3	chr3:178961439-178961489	HL-60	blood:	n/a
4	chr3:178961439-178961489	SK-N-SH_RA	brain:	n/a
5	chr3:178961439-178961489	HEK293	kidney:	embryo
6	chr3:178961439-178961489	Caco-2	colon:	n/a
7	chr3:178961439-178961489	HRPEpiC	eye:	n/a
8	chr3:178961439-178961489	HRCEpiC	kidney:	n/a
9	chr3:178961439-178961489	HPAEpiC	pulmonary alveolar:	n/a
10	chr3:178961439-178961489	LNCaP	prostate:	n/a
11	chr3:178961439-178961489	HEEpiC	esophagus:	n/a
12	chr3:178960688-178960738	GM12891	blood:	n/a
13	chr3:178960688-178960738	RPTEC	kidney:	n/a
14	chr3:178961439-178961489	ovcar-3	ovarian:	n/a
15	chr3:178960688-178960738	HEK293	kidney:	embryo
16	chr3:178961439-178961489	AG09319	gingival:	n/a
17	chr3:178960688-178960738	PANC-1	pancreas:	n/a
18	chr3:178961439-178961489	GM12891	blood:	n/a
19	chr3:178961439-178961489	SAEC	small airway:	n/a
20	chr3:178960688-178960738	AG10803	skin:	n/a
21	chr3:178961439-178961489	SK-N-SH	brain:	n/a
22	chr3:178960688-178960738	MCF-7	breast:	n/a
23	chr3:178961439-178961489	AG09309	skin:	n/a
24	chr3:178960688-178960738	AG09319	gingival:	n/a
25	chr3:178961439-178961489	U87	brain:	n/a
26	chr3:178960688-178960738	GM06990	blood:	n/a
27	chr3:178961439-178961489	AG04450	lung:	fetal
28	chr3:178960688-178960738	SK-N-SH	brain:	n/a
29	chr3:178960688-178960738	GM12878	blood:	n/a
30	chr3:178961439-178961489	H1-hESC	embryonic stem cell:	embryo
31	chr3:178961439-178961489	Hela-S3	cervix:	n/a
32	chr3:178960688-178960738	HPAEpiC	pulmonary alveolar:	n/a
33	chr3:178961439-178961489	NT2-D1	testis:	n/a
34	chr3:178960688-178960738	MCF10A-Er-Src	breast:	n/a
35	chr3:178960688-178960738	AoSMC	blood vessel:	n/a
36	chr3:178960688-178960738	HepG2	liver:	n/a
37	chr3:178960688-178960738	GM12892	blood:	n/a
38	chr3:178961439-178961489	RPTEC	kidney:	n/a
39	chr3:178961439-178961489	IMR90	lung:	fetal
40	chr3:178961439-178961489	NHBE	bronchial:	n/a
41	chr3:178961439-178961489	CMK	blood:	n/a
42	chr3:178960688-178960738	A549	lung:	n/a
43	chr3:178960688-178960738	HIPEpiC	eye:	n/a
44	chr3:178960688-178960738	Jurkat	blood:	n/a
45	chr3:178960688-178960738	SK-N-MC	brain:	n/a
46	chr3:178961439-178961489	GM12878	blood:	n/a
47	chr3:178960688-178960738	CMK	blood:	n/a
48	chr3:178961439-178961489	MCF10A-Er-Src	breast:	n/a
49	chr3:178961439-178961489	PrEC	prostate:	n/a
50	chr3:178960688-178960738	NHDF-neo	bronchial:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:178951996..178954548-chr3:178958414..178959970,2	K562	blood:
2	chr3:178961430..178967225-chr3:178967360..178970302,5	K562	blood:
3	chr3:178946686..178948186-chr8:146053818..146055345,2	MCF-7	breast:
4	chr3:178945435..178949746-chr3:178950084..178953844,5	K562	blood:
5	chr3:178896594..178898172-chr3:178937850..178940381,2	MCF-7	breast:
6	chr3:178936118..178938279-chr3:178940553..178942291,2	K562	blood:
7	chr3:178945786..178948159-chr3:178949089..178951584,2	K562	blood:
8	chr3:178961495..178963231-chr3:178964563..178967338,2	K562	blood:
9	chr3:178945435..178949746-chr3:178950084..178953844,5	K562	blood:
10	chr3:178945786..178948159-chr3:178949089..178951584,2	K562	blood:
11	chr3:178865043..178866778-chr3:178924785..178927041,2	MCF-7	breast:
12	chr3:178953311..178955072-chr3:178966973..178969868,2	K562	blood:
13	chr3:178943942..178946700-chr3:178952979..178954820,2	MCF-7	breast:
14	chr3:178918266..178919818-chr3:178962428..178965232,2	MCF-7	breast:
15	chr3:178884097..178886726-chr3:178940111..178942496,2	K562	blood:
16	chr3:178951419..178954730-chr3:178963879..178966667,3	K562	blood:
17	chr3:178865100..178867630-chr3:178921872..178925209,3	K562	blood:
18	chr3:178943942..178946700-chr3:178952979..178954820,2	MCF-7	breast:
19	chr3:178961023..178967533-chr3:178968774..178973213,9	K562	blood:
20	chr3:178961566..178964034-chr3:178975468..178977653,2	MCF-7	breast:
21	chr3:178944054..178944911-chr3:184425621..184426330,2	MCF-7	breast:
22	chr3:178951996..178954548-chr3:178958414..178959970,2	K562	blood:
23	chr3:178865795..178867355-chr3:178932431..178934661,2	MCF-7	breast:
24	chr3:178957491..178960489-chr3:179038933..179040932,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNMB3-1	chr3:178957530-178957852	NONHSAT093389
2	lnc-KCNMB3-1	chr3:178960921-178961077	NONHSAT093389
3	lnc-ZNF639-4	chr3:178953578-178955289	NONHSAT093388
4	lnc-KCNMB3-2	chr3:178954479-178955163	ENSG00000272700.1

No data

(count:2 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PIK3CA	hsa-miR-148b-3p	chr3:178952181-178952202
2	PIK3CA	hsa-miR-17-5p	chr3:178952320-178952342

Variant related genes	Relation type
PIK3CA	TF binding region
KCNMB3	TF binding region
ENSG00000272700	TF binding region
PIK3CA	CpG island
KCNMB3	CpG island
ENSG00000272700	CpG island
ENSG00000121864	chromatin interactions
ENSG00000171121	chromatin interactions
ENSG00000121879	chromatin interactions
ENSG00000147789	chromatin interactions
ENSG00000229102	chromatin interactions

Extended variants
information (count: 1318 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1318 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4854957	chr3:178924867-178924868	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs547270905	chr3:178924879-178924880	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs566076127	chr3:178924897-178924898	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs6765953	chr3:178924950-178924951	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs13099856	chr3:178925016-178925017	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs6803219	chr3:178925022-178925023	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs546517033	chr3:178925023-178925024	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs535548091	chr3:178925029-178925030	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs192778883	chr3:178925123-178925124	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs555173485	chr3:178925147-178925148	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs575102240	chr3:178925177-178925178	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs534429266	chr3:178925179-178925180	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs6790724	chr3:178925224-178925225	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs369018161	chr3:178925234-178925235	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs554444034	chr3:178925254-178925255	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs138941473	chr3:178925322-178925323	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs201256283	chr3:178925325-178925326	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs199590857	chr3:178925326-178925327	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs200702343	chr3:178925327-178925328	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs397991767	chr3:178925329-178925330	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs183864605	chr3:178925335-178925336	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs199712520	chr3:178925338-178925339	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs188248368	chr3:178925358-178925359	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs6791153	chr3:178925374-178925375	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs567509282	chr3:178925388-178925389	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs111420326	chr3:178925445-178925446	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs541933010	chr3:178925452-178925453	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs577787562	chr3:178925466-178925467	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs577005060	chr3:178925479-178925480	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs527464110	chr3:178925489-178925490	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs547324455	chr3:178925520-178925521	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs9826115	chr3:178925550-178925551	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs533087107	chr3:178925551-178925552	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs536067765	chr3:178925560-178925561	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs57113337	chr3:178925562-178925563	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs569691090	chr3:178925628-178925629	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs75971907	chr3:178925665-178925666	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs7638323	chr3:178925677-178925678	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs73187276	chr3:178925736-178925737	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs534382287	chr3:178925761-178925762	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs191105052	chr3:178925770-178925771	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs558962881	chr3:178925771-178925772	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs150431540	chr3:178925809-178925810	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs138285956	chr3:178925821-178925822	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs530028936	chr3:178925853-178925854	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs183588318	chr3:178925907-178925908	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs528035348	chr3:178925923-178925924	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs190564941	chr3:178925961-178925962	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs111795256	chr3:178925966-178925967	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs146106026	chr3:178926032-178926033	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Anaplastic thyroid cancer	17989125	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Ovarian cancer	18208621	CNVD
Thyroid cancer	17317825	CNVD
Thyroid cancer	17989125	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	21806811	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	19653912	CNVD
Endometrial cancer	19261849	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Prostate cancer	18632612	CNVD
Autism	20685689	CNVD
Human papillomavirus	17975027	CNVD
Adenocarcinoma	18757405	CNVD
Lung cancer	18757405	CNVD
Squamous cell cancer	18757405	CNVD
small cell lung cancer	18757405	CNVD

Chromatin state (count:873 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:178899200-178951800	Weak transcription	K562	blood
2	chr3:178900000-178929800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr3:178906400-178962400	Weak transcription	HepG2	liver
4	chr3:178909000-178931400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr3:178909000-178947000	Weak transcription	Ovary	ovary
6	chr3:178909400-178925400	Weak transcription	Aorta	Aorta
7	chr3:178911200-178953400	Weak transcription	Gastric	stomach
8	chr3:178912400-178978600	Weak transcription	Right Ventricle	heart
9	chr3:178912600-178947800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr3:178913000-178925000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr3:178913000-178925400	Weak transcription	Pancreas	Pancrea
12	chr3:178913000-178930800	Weak transcription	Left Ventricle	heart
13	chr3:178913000-178948200	Weak transcription	Psoas Muscle	Psoas
14	chr3:178913200-178945200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr3:178913200-178947000	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr3:178913200-178947000	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr3:178913800-178954000	Weak transcription	Fetal Heart	heart
18	chr3:178913800-178969000	Weak transcription	Small Intestine	intestine
19	chr3:178914000-178928200	Weak transcription	Brain Hippocampus Middle	brain
20	chr3:178914200-178928000	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr3:178914200-178928000	Weak transcription	Brain Substantia Nigra	brain
22	chr3:178914200-178928200	Weak transcription	Brain Anterior Caudate	brain
23	chr3:178914600-178945200	Weak transcription	HMEC	breast
24	chr3:178914800-178926400	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr3:178914800-178927200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr3:178914800-178927800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr3:178914800-178928000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr3:178914800-178928000	Weak transcription	Colon Smooth Muscle	Colon
29	chr3:178914800-178928000	Weak transcription	Osteobl	bone
30	chr3:178914800-178928200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr3:178914800-178933400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr3:178914800-178941400	Weak transcription	GM12878-XiMat	blood
33	chr3:178914800-178942800	Weak transcription	NH-A	brain
34	chr3:178914800-178948000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr3:178914800-178972800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr3:178915400-178929400	Weak transcription	HSMMtube	muscle
37	chr3:178915400-178931000	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr3:178915400-178946000	Weak transcription	Stomach Mucosa	stomach
39	chr3:178915400-178947000	Weak transcription	NHDF-Ad	bronchial
40	chr3:178915600-178947600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr3:178915800-178965200	Weak transcription	Hela-S3	cervix
42	chr3:178916600-178925800	Strong transcription	Monocytes-CD14+_RO01746	blood
43	chr3:178916600-178926400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr3:178916600-178932600	Strong transcription	Primary monocytes fromperipheralblood	blood
45	chr3:178916800-178930000	Strong transcription	Primary B cells from cord blood	blood
46	chr3:178917200-178932200	Strong transcription	Primary T helper cells fromperipheralblood	blood
47	chr3:178917400-178932600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr3:178917400-178932600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr3:178917400-178948400	Weak transcription	Esophagus	oesophagus
50	chr3:178917600-178930000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood

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