Variant report

Variant	esv3414588
Chromosome Location	chr16:12068301-12070249
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:342)
CpG islands
(count:122)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:342 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:12070205-12070509	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:12069643-12069843	K562	blood:	n/a	n/a
3	ATF2	chr16:12070090-12070379	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr16:12070121-12070372	GM12878	blood:	n/a	n/a
5	ATF3	chr16:12069564-12069800	K562	blood:	n/a	n/a
6	BACH1	chr16:12069756-12069801	K562	blood:	n/a	n/a
7	BCLAF1	chr16:12070137-12070721	GM12878	blood:	n/a	chr16:12070697-12070710
8	BHLHE40	chr16:12069759-12070608	K562	blood:	n/a	n/a
9	BRCA1	chr16:12070238-12070626	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr16:12070247-12070523	HepG2	liver:	n/a	n/a
11	CBX3	chr16:12069642-12069962	K562	blood:	n/a	n/a
12	CBX3	chr16:12070040-12070649	K562	blood:	n/a	n/a
13	CEBPB	chr16:12069580-12070770	Hela-S3	cervix:	n/a	n/a
14	CEBPD	chr16:12070158-12070850	HepG2	liver:	n/a	n/a
15	CHD2	chr16:12070249-12070656	HepG2	liver:	n/a	n/a
16	CHD2	chr16:12069658-12069974	Hela-S3	cervix:	n/a	n/a
17	CHD2	chr16:12069790-12070535	K562	blood:	n/a	n/a
18	CHD2	chr16:12070175-12070649	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr16:12070160-12070769	A549	lung:	n/a	n/a
20	CREB1	chr16:12070218-12070741	GM12878	blood:	n/a	n/a
21	CREB1	chr16:12069781-12071025	HepG2	liver:	n/a	n/a
22	CTCF	chr16:12070240-12070390	SK-N-SH_RA	brain:	n/a	n/a
23	E2F6	chr16:12070074-12070611	A549	lung:	n/a	chr16:12070300-12070312 chr16:12070514-12070523 chr16:12070301-12070308 chr16:12070301-12070308 chr16:12070301-12070308
24	EGR1	chr16:12070114-12070707	ECC-1	luminal epithelium:	n/a	chr16:12070513-12070523
25	EGR1	chr16:12070142-12070705	MCF-7	breast:	n/a	chr16:12070513-12070523
26	EGR1	chr16:12070058-12070592	K562	blood:	n/a	chr16:12070513-12070523
27	EGR1	chr16:12070080-12070558	K562	blood:	n/a	chr16:12070513-12070523
28	ELF1	chr16:12070150-12070713	MCF-7	breast:	n/a	n/a
29	ELF1	chr16:12070129-12070694	MCF-7	breast:	n/a	n/a
30	ELF1	chr16:12070209-12070679	HepG2	liver:	n/a	n/a
31	ELF1	chr16:12069943-12071133	GM12878	blood:	n/a	chr16:12070737-12070749
32	ELF1	chr16:12070060-12070758	HepG2	liver:	n/a	chr16:12070737-12070749
33	ELF1	chr16:12070157-12070835	GM12878	blood:	n/a	chr16:12070737-12070749
34	ELK1	chr16:12069776-12069896	Hela-S3	cervix:	n/a	n/a
35	ELK1	chr16:12070230-12070802	K562	blood:	n/a	n/a
36	EP300	chr16:12069595-12069853	K562	blood:	n/a	n/a
37	EP300	chr16:12070202-12070579	HepG2	liver:	n/a	chr16:12070291-12070305
38	ETS1	chr16:12070230-12070677	K562	blood:	n/a	chr16:12070512-12070523
39	FOS	chr16:12069560-12069908	MCF10A-Er-Src	breast:	n/a	chr16:12069729-12069740 chr16:12069682-12069693
40	FOS	chr16:12069558-12069884	MCF10A-Er-Src	breast:	n/a	chr16:12069729-12069740 chr16:12069682-12069693
41	FOS	chr16:12069559-12069911	MCF10A-Er-Src	breast:	n/a	chr16:12069729-12069740 chr16:12069682-12069693
42	FOS	chr16:12069551-12069888	MCF10A-Er-Src	breast:	n/a	chr16:12069729-12069740 chr16:12069682-12069693
43	FOS	chr16:12069545-12069899	HUVEC	blood vessel:	n/a	chr16:12069729-12069740 chr16:12069682-12069693
44	FOSL1	chr16:12069580-12069902	K562	blood:	n/a	chr16:12069729-12069740
45	FOSL1	chr16:12069541-12069840	K562	blood:	n/a	chr16:12069729-12069740
46	FOSL2	chr16:12069505-12069925	HepG2	liver:	n/a	n/a
47	FOSL2	chr16:12069587-12069836	A549	lung:	n/a	n/a
48	FOSL2	chr16:12069582-12070066	SK-N-SH	brain:	n/a	n/a
49	FOSL2	chr16:12069545-12070262	A549	lung:	n/a	n/a
50	FOSL2	chr16:12069597-12070000	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:12070223-12070273	Jurkat	blood:	n/a
2	chr16:12069782-12069832	K562	blood:	n/a
3	chr16:12070223-12070273	HCPEpiC	choroid plexus:	n/a
4	chr16:12070223-12070273	HL-60	blood:	n/a
5	chr16:12069782-12069832	Caco-2	colon:	n/a
6	chr16:12070223-12070273	HIPEpiC	eye:	n/a
7	chr16:12070223-12070273	SKMC	muscle:	n/a
8	chr16:12069782-12069832	HCPEpiC	choroid plexus:	n/a
9	chr16:12070223-12070273	SK-N-MC	brain:	n/a
10	chr16:12070223-12070273	HRPEpiC	eye:	n/a
11	chr16:12070223-12070273	HepG2	liver:	n/a
12	chr16:12069782-12069832	BE2_C	brain:	n/a
13	chr16:12070223-12070273	CMK	blood:	n/a
14	chr16:12069782-12069832	NT2-D1	testis:	n/a
15	chr16:12069782-12069832	PANC-1	pancreas:	n/a
16	chr16:12069782-12069832	SK-N-MC	brain:	n/a
17	chr16:12070223-12070273	Hela-S3	cervix:	n/a
18	chr16:12069782-12069832	IMR90	lung:	fetal
19	chr16:12070223-12070273	AG09309	skin:	n/a
20	chr16:12069782-12069832	PFSK-1	brain:	n/a
21	chr16:12070223-12070273	RPTEC	kidney:	n/a
22	chr16:12070223-12070273	T-47D	breast:	n/a
23	chr16:12069782-12069832	Jurkat	blood:	n/a
24	chr16:12070223-12070273	NHDF-neo	bronchial:	n/a
25	chr16:12070223-12070273	Caco-2	colon:	n/a
26	chr16:12070223-12070273	HEEpiC	esophagus:	n/a
27	chr16:12070223-12070273	HUVEC	blood vessel:	n/a
28	chr16:12070223-12070273	GM06990	blood:	n/a
29	chr16:12069782-12069832	HMEC	breast:	n/a
30	chr16:12070223-12070273	HCF	heart:	n/a
31	chr16:12070223-12070273	PFSK-1	brain:	n/a
32	chr16:12070223-12070273	AoSMC	blood vessel:	n/a
33	chr16:12069782-12069832	H1-hESC	embryonic stem cell:	embryo
34	chr16:12070223-12070273	PANC-1	pancreas:	n/a
35	chr16:12070223-12070273	GM12891	blood:	n/a
36	chr16:12070223-12070273	ECC-1	luminal epithelium:	n/a
37	chr16:12069782-12069832	MCF10A-Er-Src	breast:	n/a
38	chr16:12070223-12070273	NT2-D1	testis:	n/a
39	chr16:12069782-12069832	AoSMC	blood vessel:	n/a
40	chr16:12069782-12069832	GM12878	blood:	n/a
41	chr16:12069782-12069832	Hela-S3	cervix:	n/a
42	chr16:12069782-12069832	HCF	heart:	n/a
43	chr16:12069782-12069832	HL-60	blood:	n/a
44	chr16:12069782-12069832	GM12892	blood:	n/a
45	chr16:12070223-12070273	MCF-7	breast:	n/a
46	chr16:12069782-12069832	GM06990	blood:	n/a
47	chr16:12070223-12070273	GM19239	blood:	n/a
48	chr16:12069782-12069832	A549	lung:	n/a
49	chr16:12069782-12069832	HIPEpiC	eye:	n/a
50	chr16:12069782-12069832	HNPCEpiC	eye:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:12006532..12011371-chr16:12068460..12073371,6	K562	blood:
2	chr16:12068621..12072204-chr16:12129850..12134239,5	MCF-7	breast:
3	chr16:12069955..12070873-chr2:55277200..55277711,2	Hela-S3	cervix:
4	chr16:12065230..12068702-chr16:12068954..12072616,4	MCF-7	breast:
5	chr12:57118643..57119257-chr16:12069612..12070224,2	Hela-S3	cervix:
6	chr15:70389855..70390480-chr16:12070045..12070666,2	Hela-S3	cervix:
7	chr16:12062509..12065114-chr16:12069207..12070961,2	MCF-7	breast:
8	chr16:12007711..12010113-chr16:12069770..12071913,2	MCF-7	breast:
9	chr16:12068975..12070484-chr16:12084406..12086978,2	K562	blood:
10	chr16:12006809..12011472-chr16:12069677..12072698,7	MCF-7	breast:
11	chr16:12058363..12061770-chr16:12069205..12072370,4	MCF-7	breast:
12	chr16:12069629..12072468-chr16:12173207..12175470,2	MCF-7	breast:
13	chr16:12063141..12068645-chr16:12069062..12072358,5	K562	blood:
14	chr16:12065745..12068664-chr16:12070251..12071956,2	K562	blood:

No data

Variant related genes	Relation type
SNX29	TF binding region
SNX29	CpG island
ENSG00000048462	chromatin interactions
ENSG00000115310	chromatin interactions
ENSG00000234719	chromatin interactions
ENSG00000048471	chromatin interactions
ENSG00000241641	chromatin interactions
ENSG00000196531	chromatin interactions
ENSG00000140332	chromatin interactions
ENSG00000103342	chromatin interactions
ENSG00000266163	chromatin interactions
ENSG00000260224	chromatin interactions
ENSG00000260488	chromatin interactions

Extended variants
information (count: 111 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:111 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143447136	chr16:12068305-12068306	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs563168312	chr16:12068306-12068307	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs529108325	chr16:12068318-12068319	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs548853806	chr16:12068323-12068324	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs147973291	chr16:12068329-12068330	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs58631586	chr16:12068337-12068338	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs191748617	chr16:12068352-12068353	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs575847268	chr16:12068367-12068368	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs75532411	chr16:12068379-12068380	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs570821385	chr16:12068384-12068385	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs539942188	chr16:12068393-12068394	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs550350643	chr16:12068433-12068434	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs113108305	chr16:12068458-12068459	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs570272354	chr16:12068479-12068480	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs536096813	chr16:12068496-12068497	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs556092293	chr16:12068517-12068518	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs184338581	chr16:12068525-12068526	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs532870878	chr16:12068528-12068529	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs557752050	chr16:12068567-12068568	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs78985081	chr16:12068574-12068575	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs559433827	chr16:12068625-12068626	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs543119860	chr16:12068657-12068658	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs556700554	chr16:12068668-12068669	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs12930665	chr16:12068707-12068708	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs542438729	chr16:12068712-12068713	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs189484312	chr16:12068735-12068736	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs559368786	chr16:12068748-12068749	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs138702711	chr16:12068768-12068769	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs368865303	chr16:12068771-12068772	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs420203	chr16:12068788-12068789	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs376635281	chr16:12068857-12068858	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs62037670	chr16:12068869-12068870	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs533423852	chr16:12068873-12068874	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs188203641	chr16:12068925-12068926	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs570210920	chr16:12068956-12068957	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs67790570	chr16:12068969-12068970	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs549633636	chr16:12068970-12068971	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs530752557	chr16:12068988-12068989	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs71139568	chr16:12069002-12069003	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs192463337	chr16:12069003-12069004	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs374203380	chr16:12069023-12069024	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs376657502	chr16:12069024-12069025	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs566210757	chr16:12069067-12069068	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs549837592	chr16:12069090-12069091	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs376054792	chr16:12069116-12069117	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs535351567	chr16:12069123-12069124	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs138816062	chr16:12069147-12069148	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs571233986	chr16:12069166-12069167	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs12051197	chr16:12069171-12069172	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs556614500	chr16:12069183-12069184	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	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
Breast cancer	21858162	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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:377 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12052200-12069600	Weak transcription	Primary T cells from cord blood	blood
2	chr16:12054600-12069400	Weak transcription	Stomach Smooth Muscle	stomach
3	chr16:12056800-12069400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr16:12058800-12069400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr16:12059000-12069400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr16:12059000-12069400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr16:12059000-12069400	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr16:12059200-12069400	Weak transcription	Adipose Nuclei	Adipose
9	chr16:12059400-12069400	Weak transcription	Brain Cingulate Gyrus	brain
10	chr16:12059400-12069400	Weak transcription	NHEK	skin
11	chr16:12059400-12069600	Weak transcription	Brain Anterior Caudate	brain
12	chr16:12059400-12069600	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr16:12059400-12069600	Weak transcription	Brain Substantia Nigra	brain
14	chr16:12059400-12069600	Weak transcription	HSMMtube	muscle
15	chr16:12059600-12069400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr16:12059600-12069600	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr16:12059800-12069600	Weak transcription	Fetal Thymus	thymus
18	chr16:12061600-12069400	Weak transcription	Pancreas	Pancrea
19	chr16:12061800-12069200	Weak transcription	K562	blood
20	chr16:12061800-12069600	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr16:12063600-12069400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr16:12064200-12069600	Weak transcription	Colonic Mucosa	Colon
23	chr16:12064400-12068800	Strong transcription	Fetal Stomach	stomach
24	chr16:12064800-12068400	Strong transcription	Thymus	Thymus
25	chr16:12065000-12069600	Weak transcription	Spleen	Spleen
26	chr16:12065200-12068600	Strong transcription	Primary B cells from peripheral blood	blood
27	chr16:12065200-12069600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr16:12065400-12068400	Strong transcription	Fetal Intestine Small	intestine
29	chr16:12065400-12069400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr16:12065600-12069400	Weak transcription	Primary B cells from cord blood	blood
31	chr16:12065800-12068400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr16:12065800-12069400	Weak transcription	Colon Smooth Muscle	Colon
33	chr16:12065800-12069600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr16:12066000-12069400	Weak transcription	Brain Germinal Matrix	brain
35	chr16:12066200-12069200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr16:12066200-12069200	Weak transcription	Placenta	Placenta
37	chr16:12066200-12069400	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr16:12066200-12069400	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr16:12066200-12069400	Weak transcription	GM12878-XiMat	blood
40	chr16:12066400-12069400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr16:12066400-12069400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr16:12066400-12069400	Weak transcription	Fetal Brain Female	brain
43	chr16:12066400-12069600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr16:12066400-12069600	Weak transcription	Fetal Intestine Large	intestine
45	chr16:12066400-12069600	Weak transcription	Ovary	ovary
46	chr16:12066400-12069600	Weak transcription	Stomach Mucosa	stomach
47	chr16:12066400-12069800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr16:12066600-12069200	Weak transcription	Liver	Liver
49	chr16:12066800-12069400	Weak transcription	Primary T helper cells PMA-I stimulated	--
50	chr16:12066800-12069600	Weak transcription	Esophagus	oesophagus

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