Variant report

Variant	nsv984259
Chromosome Location	chr16:12092609-12104575
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	chr16:12104500-12104540	K562	blood:	n/a	n/a
2	ARID3A	chr16:12096327-12096556	K562	blood:	n/a	n/a
3	ATF1	chr16:12096247-12096752	K562	blood:	n/a	n/a
4	ATF3	chr16:12104302-12104598	K562	blood:	n/a	n/a
5	ATF3	chr16:12096266-12096532	K562	blood:	n/a	n/a
6	BHLHE40	chr16:12096312-12096824	K562	blood:	n/a	chr16:12096528-12096544 chr16:12096522-12096538
7	CEBPB	chr16:12098159-12098359	Hela-S3	cervix:	n/a	chr16:12098261-12098272
8	CEBPB	chr16:12095879-12095971	K562	blood:	n/a	n/a
9	CEBPB	chr16:12093678-12093802	HepG2	liver:	n/a	n/a
10	CREB1	chr16:12096171-12096787	K562	blood:	n/a	n/a
11	CREB1	chr16:12096182-12096751	K562	blood:	n/a	n/a
12	CTCF	chr16:12096452-12096665	K562	blood:	n/a	chr16:12096529-12096542
13	CUX1	chr16:12096336-12096906	K562	blood:	n/a	n/a
14	CUX1	chr16:12092759-12092833	GM12878	blood:	n/a	n/a
15	E2F4	chr16:12096259-12096459	MCF10A-Er-Src	breast:	n/a	n/a
16	EBF1	chr16:12104556-12104926	GM12878	blood:	n/a	chr16:12104737-12104748
17	EBF1	chr16:12092603-12092969	GM12878	blood:	n/a	chr16:12092790-12092801
18	EBF1	chr16:12092601-12092908	GM12878	blood:	n/a	chr16:12092790-12092801
19	EBF1	chr16:12104572-12104849	GM12878	blood:	n/a	chr16:12104737-12104748
20	EBF1	chr16:12092573-12092928	GM12878	blood:	n/a	chr16:12092790-12092801
21	ELF1	chr16:12096311-12096743	K562	blood:	n/a	n/a
22	EP300	chr16:12096354-12096737	K562	blood:	n/a	chr16:12096378-12096387 chr16:12096377-12096386
23	ESR1	chr16:12093231-12093661	ECC-1	luminal epithelium:	n/a	n/a
24	ESR1	chr16:12093249-12093690	ECC-1	luminal epithelium:	n/a	n/a
25	ESR1	chr16:12093398-12093624	ECC-1	luminal epithelium:	n/a	n/a
26	ESR1	chr16:12093330-12093619	ECC-1	luminal epithelium:	n/a	n/a
27	FOS	chr16:12096230-12096536	MCF10A-Er-Src	breast:	n/a	chr16:12096378-12096386 chr16:12096377-12096386 chr16:12096377-12096387 chr16:12096378-12096385 chr16:12096378-12096387
28	FOS	chr16:12096230-12096551	MCF10A-Er-Src	breast:	n/a	chr16:12096378-12096386 chr16:12096377-12096386 chr16:12096377-12096387 chr16:12096378-12096385 chr16:12096378-12096387
29	FOS	chr16:12096217-12096558	MCF10A-Er-Src	breast:	n/a	chr16:12096378-12096386 chr16:12096377-12096386 chr16:12096377-12096387 chr16:12096378-12096385 chr16:12096378-12096387
30	FOS	chr16:12096227-12096587	MCF10A-Er-Src	breast:	n/a	chr16:12096378-12096386 chr16:12096377-12096386 chr16:12096377-12096387 chr16:12096378-12096385 chr16:12096378-12096387
31	FOSL1	chr16:12096180-12096618	K562	blood:	n/a	chr16:12096378-12096386 chr16:12096377-12096386 chr16:12096377-12096387 chr16:12096378-12096385 chr16:12096378-12096387
32	FOSL2	chr16:12104241-12104577	HepG2	liver:	n/a	n/a
33	FOSL2	chr16:12096251-12096656	SK-N-SH	brain:	n/a	chr16:12096378-12096386 chr16:12096377-12096386 chr16:12096377-12096387 chr16:12096378-12096385 chr16:12096378-12096387
34	GABPA	chr16:12096326-12096671	K562	blood:	n/a	n/a
35	GATA2	chr16:12096317-12096723	K562	blood:	n/a	chr16:12096519-12096526 chr16:12096631-12096638 chr16:12096629-12096638 chr16:12096629-12096639
36	GATA3	chr16:12099638-12099742	SH-SY5Y	brain:	n/a	n/a
37	JUN	chr16:12096211-12096729	K562	blood:	n/a	chr16:12096378-12096386 chr16:12096377-12096386 chr16:12096377-12096387 chr16:12096378-12096385 chr16:12096378-12096387
38	JUN	chr16:12104313-12104513	K562	blood:	n/a	n/a
39	JUN	chr16:12096225-12096557	K562	blood:	n/a	chr16:12096378-12096386 chr16:12096377-12096386 chr16:12096377-12096387 chr16:12096378-12096385 chr16:12096378-12096387
40	JUN	chr16:12096173-12096930	K562	blood:	n/a	chr16:12096378-12096386 chr16:12096377-12096386 chr16:12096377-12096387 chr16:12096378-12096385 chr16:12096378-12096387
41	JUN	chr16:12104303-12105167	K562	blood:	n/a	n/a
42	JUND	chr16:12104339-12104469	H1-hESC	embryonic stem cell:	n/a	n/a
43	JUND	chr16:12096271-12096540	HepG2	liver:	n/a	chr16:12096378-12096386 chr16:12096377-12096386 chr16:12096377-12096387 chr16:12096378-12096385 chr16:12096376-12096387 chr16:12096378-12096387
44	JUND	chr16:12098218-12098234	K562	blood:	n/a	n/a
45	JUND	chr16:12104328-12104489	H1-hESC	embryonic stem cell:	n/a	n/a
46	JUND	chr16:12104256-12104608	K562	blood:	n/a	n/a
47	JUND	chr16:12096201-12096763	K562	blood:	n/a	chr16:12096378-12096386 chr16:12096377-12096386 chr16:12096377-12096387 chr16:12096378-12096385 chr16:12096376-12096387 chr16:12096378-12096387
48	KAP1	chr16:12096297-12096793	U2OS	brain:	n/a	chr16:12096376-12096385
49	MAFF	chr16:12097229-12097396	HepG2	liver:	n/a	n/a
50	MAFK	chr16:12097238-12097419	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:12096923-12096973	Jurkat	blood:	n/a
2	chr16:12096923-12096973	HRCEpiC	kidney:	n/a
3	chr16:12096923-12096973	RPTEC	kidney:	n/a
4	chr16:12096947-12096997	HepG2	liver:	n/a
5	chr16:12096947-12096997	H1-hESC	embryonic stem cell:	embryo
6	chr16:12096947-12096997	HL-60	blood:	n/a
7	chr16:12096923-12096973	HUVEC	blood vessel:	n/a
8	chr16:12096923-12096973	HRE	kidney:	n/a
9	chr16:12096947-12096997	Jurkat	blood:	n/a
10	chr16:12096923-12096973	K562	blood:	n/a
11	chr16:12096947-12096997	CMK	blood:	n/a
12	chr16:12096923-12096973	HCM	heart:	n/a
13	chr16:12096923-12096973	CMK	blood:	n/a
14	chr16:12096923-12096973	NB4	blood:	n/a
15	chr16:12096947-12096997	GM12892	blood:	n/a
16	chr16:12096923-12096973	HAEpiC	amniotic membrane:	n/a
17	chr16:12096947-12096997	SKMC	muscle:	n/a
18	chr16:12096947-12096997	PrEC	prostate:	n/a
19	chr16:12096923-12096973	Hela-S3	cervix:	n/a
20	chr16:12096947-12096997	HCPEpiC	choroid plexus:	n/a
21	chr16:12096947-12096997	MCF-7	breast:	n/a
22	chr16:12096947-12096997	HAEpiC	amniotic membrane:	n/a
23	chr16:12096923-12096973	AG04449	skin:	fetal
24	chr16:12096947-12096997	AG10803	skin:	n/a
25	chr16:12096947-12096997	LNCaP	prostate:	n/a
26	chr16:12096923-12096973	HRPEpiC	eye:	n/a
27	chr16:12096947-12096997	MCF10A-Er-Src	breast:	n/a
28	chr16:12096923-12096973	HEK293	kidney:	embryo
29	chr16:12096947-12096997	ECC-1	luminal epithelium:	n/a
30	chr16:12096923-12096973	SKMC	muscle:	n/a
31	chr16:12096947-12096997	IMR90	lung:	fetal
32	chr16:12096923-12096973	T-47D	breast:	n/a
33	chr16:12096947-12096997	ProgFib	skin:	n/a
34	chr16:12096923-12096973	HepG2	liver:	n/a
35	chr16:12096947-12096997	PANC-1	pancreas:	n/a
36	chr16:12096923-12096973	AG09309	skin:	n/a
37	chr16:12096923-12096973	A549	lung:	n/a
38	chr16:12096947-12096997	NB4	blood:	n/a
39	chr16:12096947-12096997	NHBE	bronchial:	n/a
40	chr16:12096923-12096973	GM06990	blood:	n/a
41	chr16:12096947-12096997	AoSMC	blood vessel:	n/a
42	chr16:12096923-12096973	NHDF-neo	bronchial:	n/a
43	chr16:12096947-12096997	NH-A	brain:	n/a
44	chr16:12096947-12096997	T-47D	breast:	n/a
45	chr16:12096923-12096973	HMEC	breast:	n/a
46	chr16:12096923-12096973	HCT-116	colon:	n/a
47	chr16:12096947-12096997	GM06990	blood:	n/a
48	chr16:12096947-12096997	HRPEpiC	eye:	n/a
49	chr16:12096947-12096997	GM19239	blood:	n/a
50	chr16:12096923-12096973	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:12104065..12105673-chr16:12116123..12118604,2	MCF-7	breast:
2	chr16:12090531..12092530-chr16:12098658..12100809,2	K562	blood:
3	chr16:12070747..12072341-chr16:12096319..12098894,2	MCF-7	breast:

Variant related genes	Relation type
SNX29	TF binding region
SNX29	CpG island
ENSG00000260488	chromatin interactions

Extended variants
information (count: 590 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:590 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542142040	chr16:12092618-12092619	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs554646832	chr16:12092699-12092700	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs369136242	chr16:12092700-12092701	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs139870379	chr16:12092701-12092702	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs373103450	chr16:12092703-12092704	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs373055040	chr16:12092705-12092706	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs147535913	chr16:12092725-12092726	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs560580400	chr16:12092736-12092737	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs543996537	chr16:12092742-12092743	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs542754728	chr16:12092743-12092744	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs532702737	chr16:12092750-12092751	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs550654576	chr16:12092769-12092770	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs546439640	chr16:12092773-12092774	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs113424285	chr16:12092777-12092778	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs563138549	chr16:12092799-12092800	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs10163386	chr16:12092814-12092815	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs548889803	chr16:12092816-12092817	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs140130468	chr16:12092868-12092869	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs546065616	chr16:12092886-12092887	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs536008292	chr16:12092985-12092986	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs527322379	chr16:12093009-12093010	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs8052542	chr16:12093023-12093024	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs3743592	chr16:12093024-12093025	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs191267497	chr16:12093027-12093028	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs183179954	chr16:12093028-12093029	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535380384	chr16:12093042-12093043	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs187855683	chr16:12093049-12093050	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs574700124	chr16:12093060-12093061	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs373550109	chr16:12093091-12093092	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534198370	chr16:12093096-12093097	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs377673253	chr16:12093108-12093109	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs371463158	chr16:12093114-12093115	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs368155593	chr16:12093117-12093118	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs377154975	chr16:12093134-12093135	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554283188	chr16:12093212-12093213	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577433093	chr16:12093225-12093226	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs566380515	chr16:12093248-12093249	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs369590890	chr16:12093257-12093258	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs377431909	chr16:12093272-12093273	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs538512411	chr16:12093284-12093285	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs370905996	chr16:12093323-12093324	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs192432830	chr16:12093347-12093348	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs558450300	chr16:12093355-12093356	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs183668020	chr16:12093367-12093368	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs562415644	chr16:12093380-12093381	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs373542733	chr16:12093385-12093386	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs4461090	chr16:12093388-12093389	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs563772943	chr16:12093408-12093409	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs528792452	chr16:12093426-12093427	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs2865102	chr16:12093439-12093440	Weak transcription Strong transcription Enhancers	TF binding region	1 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:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12071400-12130800	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr16:12071800-12140200	Weak transcription	Fetal Intestine Small	intestine
3	chr16:12072000-12093600	Weak transcription	Fetal Stomach	stomach
4	chr16:12072200-12093800	Weak transcription	Thymus	Thymus
5	chr16:12072200-12096600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr16:12072200-12102600	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr16:12072400-12096400	Weak transcription	Ovary	ovary
8	chr16:12072400-12104400	Weak transcription	NHLF	lung
9	chr16:12072600-12094000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr16:12072600-12094000	Weak transcription	Stomach Smooth Muscle	stomach
11	chr16:12072600-12099000	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr16:12072800-12102800	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr16:12079600-12109600	Weak transcription	Gastric	stomach
14	chr16:12080200-12093800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr16:12082000-12093000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr16:12083400-12102800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr16:12085400-12118200	Weak transcription	Esophagus	oesophagus
18	chr16:12086800-12096600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr16:12087400-12092800	Genic enhancers	Primary B cells from peripheral blood	blood
20	chr16:12088200-12100800	Weak transcription	Fetal Brain Female	brain
21	chr16:12088600-12093800	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr16:12088600-12098200	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr16:12088600-12104200	Weak transcription	Right Ventricle	heart
24	chr16:12088600-12109200	Weak transcription	Fetal Kidney	kidney
25	chr16:12088600-12110000	Weak transcription	NH-A	brain
26	chr16:12088800-12094400	Weak transcription	Duodenum Mucosa	Duodenum
27	chr16:12088800-12096400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr16:12088800-12096400	Weak transcription	Right Atrium	heart
29	chr16:12088800-12098600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr16:12088800-12106600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr16:12088800-12108200	Weak transcription	Fetal Muscle Trunk	muscle
32	chr16:12088800-12115400	Weak transcription	Placenta	Placenta
33	chr16:12089000-12093200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr16:12089000-12093800	Weak transcription	Brain Anterior Caudate	brain
35	chr16:12089000-12093800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr16:12089000-12093800	Weak transcription	Lung	lung
37	chr16:12089000-12094000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr16:12089000-12094400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr16:12089000-12094400	Weak transcription	Left Ventricle	heart
40	chr16:12089000-12094600	Weak transcription	Brain Angular Gyrus	brain
41	chr16:12089000-12099800	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr16:12089000-12104400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr16:12089400-12093400	Weak transcription	Brain Cingulate Gyrus	brain
44	chr16:12089400-12103000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr16:12090200-12094200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr16:12090600-12093200	Weak transcription	Adipose Nuclei	Adipose
47	chr16:12090800-12093800	Weak transcription	Aorta	Aorta
48	chr16:12090800-12093800	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr16:12090800-12096400	Weak transcription	Primary hematopoietic stem cells	blood
50	chr16:12091000-12093400	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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