Variant report

Variant	nsv832391
Chromosome Location	chr12:44394137-44552555
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	chr12:44409177-44409526	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:44409240-44409513	K562	blood:	n/a	n/a
3	ATF1	chr12:44475362-44475482	K562	blood:	n/a	n/a
4	ATF2	chr12:44415159-44415890	GM12878	blood:	n/a	n/a
5	ATF2	chr12:44551120-44551571	GM12878	blood:	n/a	n/a
6	ATF2	chr12:44415220-44415807	GM12878	blood:	n/a	n/a
7	BACH1	chr12:44528706-44528743	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr12:44415233-44415762	GM12878	blood:	n/a	n/a
9	BCL11A	chr12:44415197-44415792	GM12878	blood:	n/a	n/a
10	BCLAF1	chr12:44409134-44409543	GM12878	blood:	n/a	n/a
11	BCLAF1	chr12:44415154-44415809	GM12878	blood:	n/a	n/a
12	BHLHE40	chr12:44415165-44415754	GM12878	blood:	n/a	n/a
13	BRCA1	chr12:44396336-44396349	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr12:44533947-44533972	GM12878	blood:	n/a	n/a
15	BRCA1	chr12:44447296-44448017	Hela-S3	cervix:	n/a	chr12:44447702-44447709
16	BRCA1	chr12:44394238-44394440	HepG2	liver:	n/a	n/a
17	CEBPB	chr12:44520590-44520987	IMR90	lung:	n/a	chr12:44520806-44520815 chr12:44520806-44520815 chr12:44520806-44520815 chr12:44520804-44520817 chr12:44520804-44520815
18	CEBPB	chr12:44511047-44511491	Hela-S3	cervix:	n/a	chr12:44511255-44511266
19	CEBPB	chr12:44511211-44511359	HepG2	liver:	n/a	chr12:44511255-44511266
20	CEBPB	chr12:44495261-44495682	IMR90	lung:	n/a	chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495448-44495459
21	CEBPB	chr12:44495264-44495647	HepG2	liver:	n/a	chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495448-44495459
22	CEBPB	chr12:44511200-44511256	K562	blood:	n/a	n/a
23	CEBPB	chr12:44520672-44520994	K562	blood:	n/a	chr12:44520806-44520815 chr12:44520806-44520815 chr12:44520806-44520815 chr12:44520804-44520817 chr12:44520804-44520815
24	CEBPB	chr12:44447204-44448444	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr12:44447719-44447744	A549	lung:	n/a	n/a
26	CEBPB	chr12:44446384-44446675	HepG2	liver:	n/a	n/a
27	CEBPB	chr12:44495264-44495616	H1-hESC	embryonic stem cell:	n/a	chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495448-44495459
28	CEBPB	chr12:44520618-44520991	HepG2	liver:	n/a	chr12:44520806-44520815 chr12:44520806-44520815 chr12:44520806-44520815 chr12:44520804-44520817 chr12:44520804-44520815
29	CEBPB	chr12:44520592-44521017	ECC-1	luminal epithelium:	n/a	chr12:44520806-44520815 chr12:44520806-44520815 chr12:44520806-44520815 chr12:44520804-44520817 chr12:44520804-44520815
30	CEBPB	chr12:44446477-44446595	HepG2	liver:	n/a	n/a
31	CEBPB	chr12:44495263-44495643	Hela-S3	cervix:	n/a	chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495448-44495459
32	CEBPB	chr12:44520623-44520995	Hela-S3	cervix:	n/a	chr12:44520806-44520815 chr12:44520806-44520815 chr12:44520806-44520815 chr12:44520804-44520817 chr12:44520804-44520815
33	CEBPB	chr12:44547805-44548105	IMR90	lung:	n/a	chr12:44547960-44547973
34	CEBPB	chr12:44520609-44521046	ECC-1	luminal epithelium:	n/a	chr12:44520806-44520815 chr12:44520806-44520815 chr12:44520806-44520815 chr12:44520804-44520817 chr12:44520804-44520815
35	CEBPB	chr12:44520630-44520990	A549	lung:	n/a	chr12:44520806-44520815 chr12:44520806-44520815 chr12:44520806-44520815 chr12:44520804-44520817 chr12:44520804-44520815
36	CEBPB	chr12:44495261-44495642	A549	lung:	n/a	chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495448-44495459
37	CEBPB	chr12:44495275-44495682	ECC-1	luminal epithelium:	n/a	chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495448-44495459
38	CEBPB	chr12:44495263-44495633	K562	blood:	n/a	chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495448-44495459
39	CEBPB	chr12:44520628-44520993	H1-hESC	embryonic stem cell:	n/a	chr12:44520806-44520815 chr12:44520806-44520815 chr12:44520806-44520815 chr12:44520804-44520817 chr12:44520804-44520815
40	CEBPB	chr12:44521624-44521887	HepG2	liver:	n/a	chr12:44521735-44521746
41	CEBPB	chr12:44445292-44445293	K562	blood:	n/a	n/a
42	CEBPB	chr12:44495260-44495590	A549	lung:	n/a	chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495448-44495459
43	CEBPB	chr12:44495233-44495696	A549	lung:	n/a	chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495448-44495459
44	CEBPB	chr12:44495215-44495706	ECC-1	luminal epithelium:	n/a	chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495448-44495459
45	CEBPB	chr12:44520584-44521027	A549	lung:	n/a	chr12:44520806-44520815 chr12:44520806-44520815 chr12:44520806-44520815 chr12:44520804-44520817 chr12:44520804-44520815
46	CEBPB	chr12:44472158-44472347	A549	lung:	n/a	n/a
47	CEBPB	chr12:44495288-44495653	MCF-7	breast:	n/a	chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495450-44495459 chr12:44495448-44495459
48	CHD2	chr12:44464637-44464647	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr12:44447389-44447906	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr12:44398140-44398290	HCPEpiC	choroid plexus:	n/a	chr12:44398269-44398282 chr12:44398267-44398285

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:44410498-44410548	BE2_C	brain:	n/a
2	chr12:44413094-44413144	HRCEpiC	kidney:	n/a
3	chr12:44421638-44421688	CMK	blood:	n/a
4	chr12:44410498-44410548	HIPEpiC	eye:	n/a
5	chr12:44413094-44413144	HMEC	breast:	n/a
6	chr12:44421638-44421688	NH-A	brain:	n/a
7	chr12:44421638-44421688	HIPEpiC	eye:	n/a
8	chr12:44413094-44413144	HAEpiC	amniotic membrane:	n/a
9	chr12:44413094-44413144	AG09309	skin:	n/a
10	chr12:44410498-44410548	AG04450	lung:	fetal
11	chr12:44421638-44421688	HEK293	kidney:	embryo
12	chr12:44413094-44413144	GM12892	blood:	n/a
13	chr12:44413094-44413144	A549	lung:	n/a
14	chr12:44410498-44410548	SKMC	muscle:	n/a
15	chr12:44421638-44421688	AG04449	skin:	fetal
16	chr12:44410498-44410548	Jurkat	blood:	n/a
17	chr12:44421638-44421688	RPTEC	kidney:	n/a
18	chr12:44413094-44413144	T-47D	breast:	n/a
19	chr12:44421638-44421688	SK-N-SH_RA	brain:	n/a
20	chr12:44410498-44410548	HUVEC	blood vessel:	n/a
21	chr12:44410498-44410548	HMEC	breast:	n/a
22	chr12:44421638-44421688	GM19239	blood:	n/a
23	chr12:44410498-44410548	PrEC	prostate:	n/a
24	chr12:44410498-44410548	GM06990	blood:	n/a
25	chr12:44410498-44410548	HCM	heart:	n/a
26	chr12:44410498-44410548	H1-hESC	embryonic stem cell:	embryo
27	chr12:44421638-44421688	AG09319	gingival:	n/a
28	chr12:44421638-44421688	HRPEpiC	eye:	n/a
29	chr12:44421638-44421688	AG10803	skin:	n/a
30	chr12:44410498-44410548	BJ	skin:	n/a
31	chr12:44421638-44421688	ProgFib	skin:	n/a
32	chr12:44413094-44413144	AG04449	skin:	fetal
33	chr12:44410498-44410548	HRPEpiC	eye:	n/a
34	chr12:44410498-44410548	PANC-1	pancreas:	n/a
35	chr12:44410498-44410548	AG09319	gingival:	n/a
36	chr12:44421638-44421688	GM12891	blood:	n/a
37	chr12:44413094-44413144	Hela-S3	cervix:	n/a
38	chr12:44413094-44413144	GM12878	blood:	n/a
39	chr12:44413094-44413144	SK-N-SH_RA	brain:	n/a
40	chr12:44413094-44413144	BE2_C	brain:	n/a
41	chr12:44413094-44413144	H1-hESC	embryonic stem cell:	embryo
42	chr12:44410498-44410548	Caco-2	colon:	n/a
43	chr12:44413094-44413144	HPAEpiC	pulmonary alveolar:	n/a
44	chr12:44413094-44413144	HEEpiC	esophagus:	n/a
45	chr12:44410498-44410548	K562	blood:	n/a
46	chr12:44421638-44421688	HCT-116	colon:	n/a
47	chr12:44421638-44421688	LNCaP	prostate:	n/a
48	chr12:44421638-44421688	K562	blood:	n/a
49	chr12:44421638-44421688	PFSK-1	brain:	n/a
50	chr12:44410498-44410548	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:44446827..44449468-chr12:44449634..44452541,2	K562	blood:
2	chr12:44408858..44409800-chr12:45267480..45268238,2	MCF-7	breast:
3	chr12:44464953..44466951-chr12:44469834..44471344,2	MCF-7	breast:
4	chr12:44450654..44453609-chr12:44454497..44456502,2	K562	blood:
5	chr12:44550647..44552515-chr12:44553138..44554864,2	MCF-7	breast:
6	chr12:44409231..44409847-chr12:45324739..45325375,2	MCF-7	breast:
7	chr12:44393933..44394766-chr12:45324489..45325458,2	MCF-7	breast:
8	chr12:44464525..44467032-chr12:44467847..44469939,2	K562	blood:
9	chr12:44393907..44394577-chr12:45342454..45343052,2	MCF-7	breast:
10	chr12:44446827..44449468-chr12:44449634..44452541,2	K562	blood:
11	chr12:44450654..44453609-chr12:44454497..44456502,2	K562	blood:
12	chr12:44433437..44434185-chr7:139305396..139306017,2	MCF-7	breast:
13	chr12:44464525..44467032-chr12:44467847..44469939,2	K562	blood:
14	chr12:44397809..44398404-chrX:134418432..134418932,2	MCF-7	breast:
15	chr12:44464953..44466951-chr12:44469834..44471344,2	MCF-7	breast:
16	chr12:43184139..43186103-chr12:44487352..44490285,2	K562	blood:
17	chr12:44396911..44397707-chr12:45324896..45325406,2	MCF-7	breast:
18	chr12:44385802..44388469-chr12:44397794..44400628,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TWF1-1	chr12:44402423-44403946	NONHSAT027810

Variant related genes	Relation type
TMEM117	TF binding region
ENSG00000258212	TF binding region
TMEM117	CpG island
ENSG00000258212	CpG island

Extended variants
information (count: 5439 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:5439 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73286255	chr12:44394175-44394176	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs12301507	chr12:44394202-44394203	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs78936216	chr12:44394322-44394323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs142230054	chr12:44394341-44394342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555987248	chr12:44394375-44394376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs151211334	chr12:44394376-44394377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73087620	chr12:44394399-44394400	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs140447985	chr12:44394419-44394420	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs149982868	chr12:44394430-44394431	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs12320155	chr12:44394433-44394434	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs565087527	chr12:44394434-44394435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577512894	chr12:44394437-44394438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562902910	chr12:44394451-44394452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544914894	chr12:44394465-44394466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181621134	chr12:44394488-44394489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs530296947	chr12:44394489-44394490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542415700	chr12:44394505-44394506	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146589682	chr12:44394525-44394526	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs141286008	chr12:44394584-44394585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369380045	chr12:44394604-44394605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570347362	chr12:44394653-44394654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs531541043	chr12:44394699-44394700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs376425843	chr12:44394703-44394704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs549648880	chr12:44394786-44394787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs11182369	chr12:44394840-44394841	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs535287283	chr12:44394842-44394843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553511659	chr12:44394853-44394854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566960966	chr12:44394862-44394863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551931469	chr12:44394883-44394884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11182370	chr12:44394889-44394890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374304724	chr12:44394890-44394891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577156108	chr12:44394913-44394914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs11182371	chr12:44394939-44394940	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs556920482	chr12:44394956-44394957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs74084793	chr12:44394974-44394975	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs377747230	chr12:44394992-44394993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539844549	chr12:44395015-44395016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527751399	chr12:44395049-44395050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560432173	chr12:44395146-44395147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186625246	chr12:44395159-44395160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs11182372	chr12:44395170-44395171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545571471	chr12:44395175-44395176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564142456	chr12:44395201-44395202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549562489	chr12:44395208-44395209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567707551	chr12:44395244-44395245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs116092432	chr12:44395262-44395263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549336672	chr12:44395264-44395265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568025424	chr12:44395343-44395344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138971669	chr12:44395356-44395357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547617622	chr12:44395362-44395363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	20164919	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	19039135	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:476 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:44361400-44401400	Weak transcription	Aorta	Aorta
2	chr12:44383200-44402400	Weak transcription	HSMMtube	muscle
3	chr12:44384400-44399600	Weak transcription	Fetal Intestine Small	intestine
4	chr12:44386800-44394400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr12:44387400-44399200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr12:44387600-44399400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr12:44390000-44394400	Weak transcription	HepG2	liver
8	chr12:44390800-44439200	Weak transcription	Esophagus	oesophagus
9	chr12:44393800-44394200	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr12:44394000-44394600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr12:44394400-44394600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr12:44394400-44394800	Enhancers	HepG2	liver
13	chr12:44394400-44394800	Enhancers	HMEC	breast
14	chr12:44394400-44394800	Enhancers	NHEK	skin
15	chr12:44394600-44400000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr12:44394600-44403200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr12:44394800-44399000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr12:44394800-44401800	Weak transcription	HMEC	breast
19	chr12:44395000-44401400	Weak transcription	Fetal Intestine Large	intestine
20	chr12:44397000-44399400	Weak transcription	Ovary	ovary
21	chr12:44397200-44398000	Enhancers	NHDF-Ad	bronchial
22	chr12:44397200-44398400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr12:44397400-44398200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr12:44397600-44397800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr12:44397600-44398200	Enhancers	Osteobl	bone
26	chr12:44397800-44398000	Enhancers	HSMM	muscle
27	chr12:44398000-44402400	Weak transcription	HSMM	muscle
28	chr12:44399200-44400200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr12:44399200-44401800	Weak transcription	Duodenum Mucosa	Duodenum
30	chr12:44399400-44399600	ZNF genes & repeats	Ovary	ovary
31	chr12:44399400-44399800	Weak transcription	Psoas Muscle	Psoas
32	chr12:44399400-44401000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr12:44399600-44400000	ZNF genes & repeats	Fetal Intestine Small	intestine
34	chr12:44400000-44400200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr12:44400200-44401400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr12:44400200-44401800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr12:44401000-44401400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr12:44401400-44402000	ZNF genes & repeats	Aorta	Aorta
39	chr12:44401400-44403600	ZNF genes & repeats	Fetal Intestine Large	intestine
40	chr12:44401400-44403800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr12:44401400-44404000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr12:44401600-44403400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
43	chr12:44401800-44402600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr12:44401800-44403000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
45	chr12:44401800-44403200	ZNF genes & repeats	HMEC	breast
46	chr12:44402000-44432200	Weak transcription	Aorta	Aorta
47	chr12:44402400-44402800	ZNF genes & repeats	HSMMtube	muscle
48	chr12:44402400-44403000	ZNF genes & repeats	HSMM	muscle
49	chr12:44402600-44403600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr12:44402800-44403800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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