Variant report

Variant	nsv1040622
Chromosome Location	chr12:85502226-85693132
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	ATF2	chr12:85673925-85674351	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr12:85674234-85674859	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr12:85673890-85674445	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr12:85672070-85672089	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr12:85674051-85674416	A549	lung:	n/a	chr12:85674286-85674302
6	BHLHE40	chr12:85674086-85674392	HepG2	liver:	n/a	chr12:85674286-85674302
7	BRCA1	chr12:85674532-85675298	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr12:85673812-85674196	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr12:85673932-85674153	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr12:85659173-85659496	IMR90	lung:	n/a	chr12:85659315-85659326
11	CEBPB	chr12:85686734-85687014	K562	blood:	n/a	chr12:85686874-85686883 chr12:85686874-85686883 chr12:85686872-85686885 chr12:85686872-85686883 chr12:85686874-85686883 chr12:85686872-85686885 chr12:85686872-85686885 chr12:85686874-85686885 chr12:85686874-85686885 chr12:85686874-85686883
12	CEBPB	chr12:85652282-85652436	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr12:85641358-85641697	Hela-S3	cervix:	n/a	chr12:85641501-85641513
14	CEBPB	chr12:85551145-85551452	A549	lung:	n/a	n/a
15	CEBPB	chr12:85653520-85653539	Hela-S3	cervix:	n/a	chr12:85653520-85653529
16	CEBPB	chr12:85536088-85536377	HepG2	liver:	n/a	chr12:85536185-85536196
17	CEBPB	chr12:85619290-85619582	IMR90	lung:	n/a	chr12:85619428-85619439
18	CEBPB	chr12:85647607-85648083	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr12:85686722-85687025	Hela-S3	cervix:	n/a	chr12:85686874-85686883 chr12:85686874-85686883 chr12:85686872-85686885 chr12:85686872-85686883 chr12:85686874-85686883 chr12:85686872-85686885 chr12:85686872-85686885 chr12:85686874-85686885 chr12:85686874-85686885 chr12:85686874-85686883
20	CEBPB	chr12:85659294-85659415	K562	blood:	n/a	chr12:85659315-85659326
21	CEBPB	chr12:85686698-85687011	HepG2	liver:	n/a	chr12:85686874-85686883 chr12:85686874-85686883 chr12:85686872-85686885 chr12:85686872-85686883 chr12:85686874-85686883 chr12:85686872-85686885 chr12:85686872-85686885 chr12:85686874-85686885 chr12:85686874-85686885 chr12:85686874-85686883
22	CEBPB	chr12:85657771-85657832	A549	lung:	n/a	n/a
23	CEBPB	chr12:85666453-85666732	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr12:85659239-85659501	A549	lung:	n/a	chr12:85659315-85659326
25	CEBPB	chr12:85619295-85619549	A549	lung:	n/a	chr12:85619428-85619439
26	CEBPB	chr12:85688019-85688136	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr12:85659161-85659499	HepG2	liver:	n/a	chr12:85659315-85659326
28	CEBPB	chr12:85686742-85686942	A549	lung:	n/a	chr12:85686874-85686883 chr12:85686874-85686883 chr12:85686872-85686885 chr12:85686872-85686883 chr12:85686874-85686883 chr12:85686872-85686885 chr12:85686872-85686885 chr12:85686874-85686885 chr12:85686874-85686885 chr12:85686874-85686883
29	CEBPB	chr12:85674187-85674666	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr12:85657681-85657860	K562	blood:	n/a	n/a
31	CEBPB	chr12:85673583-85675940	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr12:85666449-85666664	HepG2	liver:	n/a	n/a
33	CEBPB	chr12:85637235-85637436	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr12:85619275-85619599	HepG2	liver:	n/a	chr12:85619428-85619439
35	CEBPB	chr12:85536096-85536348	A549	lung:	n/a	chr12:85536185-85536196
36	CEBPB	chr12:85599606-85599840	A549	lung:	n/a	n/a
37	CEBPB	chr12:85671689-85671797	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD1	chr12:85674004-85674385	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD1	chr12:85673361-85673574	H1-hESC	embryonic stem cell:	n/a	chr12:85673513-85673523
40	CHD2	chr12:85647638-85648104	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr12:85672170-85672308	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr12:85673863-85674704	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr12:85673372-85675289	Hela-S3	cervix:	n/a	chr12:85673513-85673523
44	CREB1	chr12:85674176-85674475	A549	lung:	n/a	n/a
45	CREB1	chr12:85673779-85674985	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr12:85674483-85674811	A549	lung:	n/a	n/a
47	CREB1	chr12:85673876-85674778	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTBP2	chr12:85671727-85674564	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTBP2	chr12:85667099-85667756	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr12:85562317-85562433	GM10248	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:85677430-85677480	LNCaP	prostate:	n/a
2	chr12:85674531-85674581	GM12878	blood:	n/a
3	chr12:85677430-85677480	LNCaP	prostate:	n/a
4	chr12:85674531-85674581	GM12878	blood:	n/a
5	chr12:85673884-85673934	K562	blood:	n/a
6	chr12:85673884-85673934	ECC-1	luminal epithelium:	n/a
7	chr12:85673860-85673910	NB4	blood:	n/a
8	chr12:85673915-85673965	AG04450	lung:	fetal
9	chr12:85667353-85667403	HRE	kidney:	n/a
10	chr12:85671892-85671942	PFSK-1	brain:	n/a
11	chr12:85674140-85674190	HCM	heart:	n/a
12	chr12:85667451-85667501	AG04450	lung:	fetal
13	chr12:85671892-85671942	BJ	skin:	n/a
14	chr12:85674296-85674346	HMEC	breast:	n/a
15	chr12:85673860-85673910	NHBE	bronchial:	n/a
16	chr12:85674022-85674072	GM19239	blood:	n/a
17	chr12:85674694-85674744	K562	blood:	n/a
18	chr12:85671892-85671942	HPAEpiC	pulmonary alveolar:	n/a
19	chr12:85677430-85677480	HNPCEpiC	eye:	n/a
20	chr12:85674458-85674508	SK-N-SH	brain:	n/a
21	chr12:85671892-85671942	ProgFib	skin:	n/a
22	chr12:85674694-85674744	HIPEpiC	eye:	n/a
23	chr12:85667616-85667666	SK-N-SH	brain:	n/a
24	chr12:85673270-85673320	IMR90	lung:	fetal
25	chr12:85674022-85674072	GM12878	blood:	n/a
26	chr12:85674531-85674581	HEEpiC	esophagus:	n/a
27	chr12:85673347-85673397	HL-60	blood:	n/a
28	chr12:85673221-85673271	U87	brain:	n/a
29	chr12:85674458-85674508	NHDF-neo	bronchial:	n/a
30	chr12:85671811-85671861	ECC-1	luminal epithelium:	n/a
31	chr12:85671811-85671861	SK-N-MC	brain:	n/a
32	chr12:85674140-85674190	ovcar-3	ovarian:	n/a
33	chr12:85672285-85672335	HIPEpiC	eye:	n/a
34	chr12:85673200-85673250	NT2-D1	testis:	n/a
35	chr12:85667353-85667403	HPAEpiC	pulmonary alveolar:	n/a
36	chr12:85674694-85674744	Hela-S3	cervix:	n/a
37	chr12:85673860-85673910	HNPCEpiC	eye:	n/a
38	chr12:85673347-85673397	NH-A	brain:	n/a
39	chr12:85674022-85674072	HCPEpiC	choroid plexus:	n/a
40	chr12:85673884-85673934	Hepatocyte	liver:	n/a
41	chr12:85673200-85673250	HUVEC	blood vessel:	n/a
42	chr12:85674458-85674508	ovcar-3	ovarian:	n/a
43	chr12:85673270-85673320	HAEpiC	amniotic membrane:	n/a
44	chr12:85671976-85672026	RPTEC	kidney:	n/a
45	chr12:85671811-85671861	HCM	heart:	n/a
46	chr12:85673221-85673271	AG04449	skin:	fetal
47	chr12:85674296-85674346	HUVEC	blood vessel:	n/a
48	chr12:85672623-85672673	BJ	skin:	n/a
49	chr12:85673860-85673910	HPAEpiC	pulmonary alveolar:	n/a
50	chr12:85673221-85673271	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:85673978..85677049-chr12:85677580..85680082,3	MCF-7	breast:
2	chr12:85550574..85552513-chr12:85557330..85559057,2	MCF-7	breast:
3	chr12:85549075..85550214-chr12:85841829..85842800,6	MCF-7	breast:
4	chr12:85535998..85538330-chr12:85580098..85581911,2	K562	blood:
5	chr12:85535998..85538330-chr12:85580098..85581911,2	K562	blood:
6	chr12:85549387..85549978-chr12:85835659..85836204,2	MCF-7	breast:
7	chr12:85500330..85501960-chr12:85504219..85505982,2	K562	blood:
8	chr12:85625880..85629090-chr12:85630770..85633051,3	K562	blood:
9	chr12:85625880..85629090-chr12:85630770..85633051,3	K562	blood:
10	chr12:85673978..85677049-chr12:85677580..85680082,3	MCF-7	breast:
11	chr12:85550574..85552513-chr12:85557330..85559057,2	MCF-7	breast:
12	chr12:85688551..85691285-chr12:85694636..85697474,2	MCF-7	breast:
13	chr12:85549530..85550247-chr12:86266080..86266618,2	MCF-7	breast:
14	chr1:11968120..11968947-chr12:85674873..85675678,2	Hela-S3	cervix:
15	chr12:85673846..85674381-chr15:59664602..59665102,2	Hela-S3	cervix:
16	chr12:85496315..85499030-chr12:85506456..85509353,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRIQ1-3	chr12:85657322-85658235	ENSG00000269916.1

Variant related genes	Relation type
ALX1	TF binding region
ENSG00000269916	TF binding region
LRRIQ1	TF binding region
ALX1	CpG island
ENSG00000269916	CpG island
LRRIQ1	CpG island
ENSG00000157470	chromatin interactions
ENSG00000157483	chromatin interactions
ENSG00000199347	chromatin interactions

Extended variants
information (count: 2407 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2407 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377663639	chr12:85511811-85511812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs186820302	chr12:85511889-85511890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs112420919	chr12:85511923-85511924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs200571818	chr12:85511979-85511980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs576890901	chr12:85511983-85511984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560844299	chr12:85512002-85512003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs531357682	chr12:85512007-85512008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369062670	chr12:85512039-85512040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs34556983	chr12:85512045-85512046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs75460496	chr12:85512075-85512076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191753261	chr12:85512093-85512094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs553801372	chr12:85512097-85512098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs182519275	chr12:85512103-85512104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539599612	chr12:85512194-85512195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs149482351	chr12:85512195-85512196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533432636	chr12:85527808-85527809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549386499	chr12:85527825-85527826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1690835	chr12:85527897-85527898	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs566828805	chr12:85527989-85527990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs146662917	chr12:85527995-85527996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs190287046	chr12:85528025-85528026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140307166	chr12:85528051-85528052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs577817848	chr12:85528143-85528144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181250599	chr12:85528224-85528225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs185892355	chr12:85528281-85528282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188203720	chr12:85528308-85528309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs539138363	chr12:85528375-85528376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553787664	chr12:85528385-85528386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs7137906	chr12:85528393-85528394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs571970282	chr12:85528456-85528457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs542249546	chr12:85528475-85528476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs180996103	chr12:85528508-85528509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560986073	chr12:85528516-85528517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs575711839	chr12:85528520-85528521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543149802	chr12:85528523-85528524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs371807273	chr12:85528551-85528552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185381536	chr12:85528565-85528566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533369574	chr12:85528566-85528567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559805161	chr12:85531419-85531420	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs77919111	chr12:85531432-85531433	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs547978745	chr12:85531456-85531457	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs144760886	chr12:85531457-85531458	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs544729553	chr12:85531465-85531466	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs530697779	chr12:85531503-85531504	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs79726589	chr12:85531581-85531582	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs369626012	chr12:85531607-85531608	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs373547571	chr12:85531653-85531654	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs61740224	chr12:85531684-85531685	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs370228797	chr12:85531699-85531700	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs77956957	chr12:85531701-85531702	Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:577 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:85511800-85512200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr12:85527800-85528200	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr12:85527800-85528400	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr12:85527800-85528400	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr12:85528000-85528600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr12:85531400-85531800	Active TSS	Fetal Kidney	kidney
7	chr12:85547800-85550000	Active TSS	Fetal Kidney	kidney
8	chr12:85549200-85549400	Enhancers	Hela-S3	cervix
9	chr12:85549400-85549800	Flanking Active TSS	Hela-S3	cervix
10	chr12:85549800-85550400	Enhancers	Hela-S3	cervix
11	chr12:85550000-85551400	Active TSS	A549	lung
12	chr12:85550400-85550600	Weak transcription	Hela-S3	cervix
13	chr12:85550600-85551200	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr12:85550600-85551200	Enhancers	HUVEC	blood vessel
15	chr12:85550600-85551600	Active TSS	Hela-S3	cervix
16	chr12:85550800-85551800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr12:85551600-85557200	Weak transcription	Hela-S3	cervix
18	chr12:85557200-85557400	Enhancers	Hela-S3	cervix
19	chr12:85557400-85557800	Weak transcription	Hela-S3	cervix
20	chr12:85557800-85558400	Enhancers	Hela-S3	cervix
21	chr12:85560200-85573000	Weak transcription	Fetal Kidney	kidney
22	chr12:85568800-85569200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:85571200-85571600	Enhancers	HUVEC	blood vessel
24	chr12:85571600-85571800	Enhancers	Hela-S3	cervix
25	chr12:85571600-85573000	Weak transcription	HUVEC	blood vessel
26	chr12:85572000-85573200	Weak transcription	Hela-S3	cervix
27	chr12:85573000-85573600	Enhancers	A549	lung
28	chr12:85573000-85573800	Enhancers	Fetal Kidney	kidney
29	chr12:85573000-85574800	Enhancers	HUVEC	blood vessel
30	chr12:85573200-85574600	Enhancers	Hela-S3	cervix
31	chr12:85573400-85574000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr12:85573400-85574000	Enhancers	Fetal Lung	lung
33	chr12:85573400-85574000	Enhancers	NH-A	brain
34	chr12:85573400-85574200	Enhancers	Muscle Satellite Cultured Cells	--
35	chr12:85573600-85574000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr12:85573600-85574000	Flanking Active TSS	A549	lung
37	chr12:85573800-85577400	Weak transcription	Fetal Kidney	kidney
38	chr12:85574000-85574200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr12:85574000-85574400	Enhancers	A549	lung
40	chr12:85574000-85576400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr12:85574400-85576200	Weak transcription	A549	lung
42	chr12:85574600-85582200	Weak transcription	Hela-S3	cervix
43	chr12:85574800-85582200	Weak transcription	HUVEC	blood vessel
44	chr12:85576200-85576400	Enhancers	A549	lung
45	chr12:85576400-85576600	Flanking Active TSS	A549	lung
46	chr12:85576400-85576800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr12:85576600-85577000	Active TSS	A549	lung
48	chr12:85577000-85580000	Weak transcription	A549	lung
49	chr12:85577400-85577800	Enhancers	Fetal Kidney	kidney
50	chr12:85580000-85580600	Enhancers	A549	lung

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