Variant report

Variant	nsv905349
Chromosome Location	chr16:12408750-12445863
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:695)
CpG islands
(count:244)
Chromatin interactive
region (count:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:695 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:12413001-12413168	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:12409154-12409881	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:12435377-12435548	HepG2	liver:	n/a	n/a
4	ATF2	chr16:12416866-12417337	GM12878	blood:	n/a	n/a
5	ATF2	chr16:12416881-12417410	GM12878	blood:	n/a	n/a
6	BATF	chr16:12416598-12417218	GM12878	blood:	n/a	chr16:12417152-12417162
7	BATF	chr16:12416598-12417287	GM12878	blood:	n/a	chr16:12417152-12417162
8	BCL11A	chr16:12416596-12417208	GM12878	blood:	n/a	n/a
9	BCL11A	chr16:12416522-12417258	GM12878	blood:	n/a	n/a
10	BCL3	chr16:12416893-12417263	GM12878	blood:	n/a	n/a
11	BCLAF1	chr16:12416895-12417228	GM12878	blood:	n/a	n/a
12	BHLHE40	chr16:12434295-12434610	HepG2	liver:	n/a	n/a
13	BHLHE40	chr16:12409285-12409752	HepG2	liver:	n/a	n/a
14	BHLHE40	chr16:12435349-12435740	HepG2	liver:	n/a	n/a
15	BHLHE40	chr16:12416963-12417204	GM12878	blood:	n/a	n/a
16	BHLHE40	chr16:12411300-12411631	GM12878	blood:	n/a	n/a
17	BHLHE40	chr16:12442556-12442849	GM12878	blood:	n/a	n/a
18	BHLHE40	chr16:12443836-12444154	K562	blood:	n/a	n/a
19	BRCA1	chr16:12415204-12415356	HepG2	liver:	n/a	n/a
20	CBX3	chr16:12435118-12436344	HCT-116	colon:	n/a	n/a
21	CEBPB	chr16:12409508-12409650	A549	lung:	n/a	n/a
22	CEBPB	chr16:12416859-12417153	GM12878	blood:	n/a	n/a
23	CEBPB	chr16:12409462-12409756	HepG2	liver:	n/a	n/a
24	CEBPB	chr16:12414143-12414652	IMR90	lung:	n/a	n/a
25	CEBPB	chr16:12435361-12435579	HepG2	liver:	n/a	n/a
26	CEBPB	chr16:12433687-12434238	IMR90	lung:	n/a	n/a
27	CEBPB	chr16:12415251-12415474	HepG2	liver:	n/a	n/a
28	CEBPB	chr16:12435268-12435616	IMR90	lung:	n/a	n/a
29	CEBPB	chr16:12434288-12434632	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr16:12416611-12417377	GM12878	blood:	n/a	n/a
31	CHD1	chr16:12413960-12414942	IMR90	lung:	n/a	n/a
32	CHD2	chr16:12434342-12434600	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr16:12435490-12435652	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr16:12409457-12409586	GM12878	blood:	n/a	n/a
35	CHD2	chr16:12412268-12412332	HepG2	liver:	n/a	n/a
36	CHD2	chr16:12411249-12411634	GM12878	blood:	n/a	n/a
37	CREB1	chr16:12416944-12417331	GM12878	blood:	n/a	n/a
38	CTCF	chr16:12434380-12434530	A549	lung:	n/a	n/a
39	CTCF	chr16:12435472-12435572	MCF-7	breast:	n/a	n/a
40	CTCF	chr16:12434329-12434567	GM10266	blood:	n/a	n/a
41	CTCF	chr16:12444900-12445050	HepG2	liver:	n/a	n/a
42	CTCF	chr16:12444940-12445090	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr16:12434360-12434510	GM12869	blood:	n/a	n/a
44	CTCF	chr16:12434400-12434550	GM12872	blood:	n/a	n/a
45	CTCF	chr16:12434380-12434530	HepG2	liver:	n/a	n/a
46	CTCF	chr16:12434280-12434430	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr16:12434380-12434530	NHLF	lung:	n/a	n/a
48	CTCF	chr16:12434265-12434613	A549	lung:	n/a	n/a
49	CTCF	chr16:12434380-12434530	NB4	blood:	n/a	n/a
50	CTCF	chr16:12434322-12434600	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:12434580-12434630	MCF10A-Er-Src	breast:	n/a
2	chr16:12442738-12442788	HMEC	breast:	n/a
3	chr16:12411139-12411189	HEK293	kidney:	embryo
4	chr16:12442738-12442788	HepG2	liver:	n/a
5	chr16:12411139-12411189	AG09309	skin:	n/a
6	chr16:12414821-12414871	HRCEpiC	kidney:	n/a
7	chr16:12442738-12442788	NH-A	brain:	n/a
8	chr16:12442738-12442788	PFSK-1	brain:	n/a
9	chr16:12442738-12442788	A549	lung:	n/a
10	chr16:12411139-12411189	SK-N-MC	brain:	n/a
11	chr16:12414821-12414871	AG09309	skin:	n/a
12	chr16:12442738-12442788	SKMC	muscle:	n/a
13	chr16:12434580-12434630	NT2-D1	testis:	n/a
14	chr16:12442738-12442788	HPAEpiC	pulmonary alveolar:	n/a
15	chr16:12414821-12414871	Hepatocyte	liver:	n/a
16	chr16:12442738-12442788	AG04449	skin:	fetal
17	chr16:12411139-12411189	SAEC	small airway:	n/a
18	chr16:12442738-12442788	IMR90	lung:	fetal
19	chr16:12434580-12434630	SK-N-MC	brain:	n/a
20	chr16:12414821-12414871	SKMC	muscle:	n/a
21	chr16:12434580-12434630	PFSK-1	brain:	n/a
22	chr16:12414821-12414871	SK-N-SH_RA	brain:	n/a
23	chr16:12414821-12414871	CMK	blood:	n/a
24	chr16:12442738-12442788	AoSMC	blood vessel:	n/a
25	chr16:12434580-12434630	BJ	skin:	n/a
26	chr16:12411139-12411189	HRCEpiC	kidney:	n/a
27	chr16:12442738-12442788	MCF10A-Er-Src	breast:	n/a
28	chr16:12434580-12434630	HCPEpiC	choroid plexus:	n/a
29	chr16:12434580-12434630	HAEpiC	amniotic membrane:	n/a
30	chr16:12414821-12414871	HCPEpiC	choroid plexus:	n/a
31	chr16:12411139-12411189	GM19239	blood:	n/a
32	chr16:12411139-12411189	HRPEpiC	eye:	n/a
33	chr16:12434580-12434630	GM12892	blood:	n/a
34	chr16:12434580-12434630	AG04449	skin:	fetal
35	chr16:12411139-12411189	GM12891	blood:	n/a
36	chr16:12411139-12411189	HCM	heart:	n/a
37	chr16:12411139-12411189	BJ	skin:	n/a
38	chr16:12434580-12434630	Hepatocyte	liver:	n/a
39	chr16:12442738-12442788	AG09309	skin:	n/a
40	chr16:12442738-12442788	ProgFib	skin:	n/a
41	chr16:12442738-12442788	HEEpiC	esophagus:	n/a
42	chr16:12442738-12442788	HUVEC	blood vessel:	n/a
43	chr16:12414821-12414871	U87	brain:	n/a
44	chr16:12414821-12414871	GM12891	blood:	n/a
45	chr16:12414821-12414871	GM12878	blood:	n/a
46	chr16:12411139-12411189	AG09319	gingival:	n/a
47	chr16:12414821-12414871	ECC-1	luminal epithelium:	n/a
48	chr16:12442738-12442788	SAEC	small airway:	n/a
49	chr16:12442738-12442788	AG04450	lung:	fetal
50	chr16:12414821-12414871	HNPCEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr16:12426103..12428836-chr16:12432217..12434096,4	K562	blood:
2	chr16:12434411..12435246-chr16:12667446..12668002,2	MCF-7	breast:
3	chr16:12434031..12434617-chr16:12912936..12913439,2	K562	blood:
4	chr16:12433483..12435044-chr16:12435490..12437605,2	K562	blood:
5	chr16:12434404..12435162-chr16:12548365..12549293,2	MCF-7	breast:
6	chr16:12426504..12430184-chr16:12432340..12435917,5	K562	blood:
7	chr16:12405145..12407568-chr16:12414371..12416056,2	MCF-7	breast:
8	chr16:12384757..12387424-chr16:12410690..12412315,2	MCF-7	breast:
9	chr16:12415388..12417131-chr16:12421455..12424382,2	MCF-7	breast:
10	chr16:12388084..12390009-chr16:12417985..12420361,2	MCF-7	breast:
11	chr16:12407586..12410005-chr16:12412153..12414940,2	K562	blood:
12	chr16:12434035..12434594-chr16:12912889..12913804,2	MCF-7	breast:
13	chr16:12407586..12410005-chr16:12412153..12414940,2	K562	blood:
14	chr16:12433483..12435044-chr16:12435490..12437605,2	K562	blood:
15	chr16:12426103..12428836-chr16:12432217..12434096,4	K562	blood:
16	chr16:12434163..12434889-chr16:12562200..12562981,2	MCF-7	breast:
17	chr16:12412998..12415794-chr16:12417822..12420522,2	MCF-7	breast:
18	chr16:12426504..12430184-chr16:12432340..12435917,5	K562	blood:
19	chr16:12415388..12417131-chr16:12421455..12424382,2	MCF-7	breast:
20	chr16:12404079..12406298-chr16:12408481..12410395,2	K562	blood:
21	chr16:12412998..12415794-chr16:12417822..12420522,2	MCF-7	breast:

No data

Variant related genes	Relation type
SNX29	TF binding region
SNX29	CpG island

Extended variants
information (count: 1894 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1894 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs209853	chr16:12408750-12408751	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs113358621	chr16:12408759-12408760	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs192543648	chr16:12408774-12408775	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147631555	chr16:12408787-12408788	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559213812	chr16:12408815-12408816	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs72786351	chr16:12408821-12408822	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs184982486	chr16:12408855-12408856	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs571372357	chr16:12408878-12408879	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs537363043	chr16:12408886-12408887	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs550856133	chr16:12408924-12408925	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs567549620	chr16:12408950-12408951	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs16959190	chr16:12408951-12408952	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs209852	chr16:12408964-12408965	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs572486966	chr16:12408969-12408970	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs552795677	chr16:12408994-12408995	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs187485751	chr16:12409010-12409011	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs143001964	chr16:12409019-12409020	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs578104029	chr16:12409059-12409060	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs376814409	chr16:12409065-12409066	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs191420709	chr16:12409075-12409076	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs184625906	chr16:12409079-12409080	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs148192350	chr16:12409142-12409143	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs113532706	chr16:12409144-12409145	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559293199	chr16:12409189-12409190	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189513402	chr16:12409190-12409191	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs551425878	chr16:12409191-12409192	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs565790803	chr16:12409201-12409202	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs181900288	chr16:12409207-12409208	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs141171171	chr16:12409221-12409222	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs184982169	chr16:12409229-12409230	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs567611229	chr16:12409261-12409262	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs190323143	chr16:12409325-12409326	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs549118340	chr16:12409347-12409348	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs566019202	chr16:12409351-12409352	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs555950394	chr16:12409364-12409365	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs209851	chr16:12409392-12409393	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs76064938	chr16:12409420-12409421	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181152144	chr16:12409426-12409427	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs371335055	chr16:12409430-12409431	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs376069953	chr16:12409472-12409473	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs186699421	chr16:12409480-12409481	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536324788	chr16:12409486-12409487	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs574038886	chr16:12409487-12409488	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs542874778	chr16:12409530-12409531	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs556021303	chr16:12409544-12409545	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs552713009	chr16:12409586-12409587	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs189749990	chr16:12409590-12409591	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs544661866	chr16:12409643-12409644	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs565017759	chr16:12409654-12409655	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs114792807	chr16:12409673-12409674	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	17603634	CNVD
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Lung cancer	18438408	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22102821	CNVD
Autism	22495311	CNVD
idiopathic generalized epilepsy	19843651	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Intellectual disability	22102821	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelofibrosis	22110671	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Prostate cancer	18632612	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lujan-Fryns syndrom	21521776	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	19786961	CNVD
Mental retardation	19786961	CNVD
Schizophrenia	19786961	CNVD
Mental retardation	19951919	CNVD
Autism	18791038	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Malignant germ cell tumour	17285132	CNVD
Autism	17480035	CNVD
Schizophrenia	19955444	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:773 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12359800-12418000	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr16:12371400-12456800	Weak transcription	Aorta	Aorta
3	chr16:12373400-12414200	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr16:12374200-12417200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr16:12384400-12409000	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr16:12385800-12410800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr16:12395000-12409200	Weak transcription	Liver	Liver
8	chr16:12395400-12413800	Weak transcription	Left Ventricle	heart
9	chr16:12395600-12409400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr16:12395600-12417200	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr16:12396000-12414800	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr16:12396200-12414000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr16:12396800-12416400	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr16:12401200-12409000	Weak transcription	Brain Germinal Matrix	brain
15	chr16:12404000-12414800	Weak transcription	Thymus	Thymus
16	chr16:12404200-12427400	Weak transcription	Primary T cells from cord blood	blood
17	chr16:12404600-12413400	Weak transcription	Fetal Heart	heart
18	chr16:12405200-12411800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr16:12405600-12409000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr16:12405600-12409400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr16:12405600-12409800	Weak transcription	Ovary	ovary
22	chr16:12405600-12410400	Weak transcription	Esophagus	oesophagus
23	chr16:12405600-12412800	Weak transcription	Fetal Muscle Trunk	muscle
24	chr16:12405600-12413200	Weak transcription	Right Ventricle	heart
25	chr16:12405600-12426400	Weak transcription	Lung	lung
26	chr16:12405600-12442400	Weak transcription	Spleen	Spleen
27	chr16:12405800-12409000	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr16:12405800-12413200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr16:12405800-12417800	Weak transcription	Adipose Nuclei	Adipose
30	chr16:12406200-12413200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr16:12406600-12409000	Weak transcription	Fetal Brain Female	brain
32	chr16:12406600-12409200	Weak transcription	Fetal Brain Male	brain
33	chr16:12407200-12409000	Enhancers	HepG2	liver
34	chr16:12407400-12410800	Enhancers	Primary B cells from peripheral blood	blood
35	chr16:12407400-12412200	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr16:12407800-12410200	Enhancers	Gastric	stomach
37	chr16:12407800-12411600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr16:12407800-12412800	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr16:12408000-12409400	Enhancers	Brain Cingulate Gyrus	brain
40	chr16:12408000-12409400	Enhancers	Stomach Smooth Muscle	stomach
41	chr16:12408000-12409600	Enhancers	Fetal Stomach	stomach
42	chr16:12408000-12411800	Enhancers	NHEK	skin
43	chr16:12408200-12408800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr16:12408200-12409000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr16:12408200-12409000	Enhancers	HSMM	muscle
46	chr16:12408200-12409400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr16:12408200-12409400	Enhancers	HSMMtube	muscle
48	chr16:12408200-12409600	Enhancers	H1 Cell Line	embryonic stem cell
49	chr16:12408200-12409800	Weak transcription	Right Atrium	heart
50	chr16:12408200-12410000	Enhancers	Fetal Intestine Large	intestine

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