Variant report

Variant	nsv437802
Chromosome Location	chr16:12667076-12708294
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:972)
CpG islands
(count:61)
Chromatin interactive
region (count:21)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:972 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:12704032-12704253	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:12682648-12682749	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:12707160-12707764	K562	blood:	n/a	n/a
4	ARID3A	chr16:12684292-12684594	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:12706308-12708260	HepG2	liver:	n/a	n/a
6	ARID3A	chr16:12667681-12668060	HepG2	liver:	n/a	n/a
7	ATF1	chr16:12704812-12705249	K562	blood:	n/a	n/a
8	ATF1	chr16:12706396-12706792	K562	blood:	n/a	n/a
9	ATF1	chr16:12707276-12707833	K562	blood:	n/a	n/a
10	ATF1	chr16:12678409-12678811	K562	blood:	n/a	n/a
11	ATF1	chr16:12692604-12692867	K562	blood:	n/a	n/a
12	ATF2	chr16:12706985-12707963	GM12878	blood:	n/a	n/a
13	ATF2	chr16:12666972-12667661	GM12878	blood:	n/a	n/a
14	ATF2	chr16:12707009-12707939	GM12878	blood:	n/a	n/a
15	ATF2	chr16:12666927-12667980	GM12878	blood:	n/a	n/a
16	ATF3	chr16:12707409-12708140	A549	lung:	n/a	n/a
17	ATF3	chr16:12707553-12707788	K562	blood:	n/a	n/a
18	ATF3	chr16:12707532-12707884	K562	blood:	n/a	n/a
19	ATF3	chr16:12707254-12707910	A549	lung:	n/a	n/a
20	BACH1	chr16:12707365-12707905	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr16:12707531-12707771	K562	blood:	n/a	n/a
22	BACH1	chr16:12667697-12667939	K562	blood:	n/a	n/a
23	BATF	chr16:12667208-12667587	GM12878	blood:	n/a	n/a
24	BATF	chr16:12707513-12707826	GM12878	blood:	n/a	chr16:12707702-12707713
25	BATF	chr16:12707465-12707911	GM12878	blood:	n/a	chr16:12707702-12707713
26	BCL11A	chr16:12707487-12707794	GM12878	blood:	n/a	n/a
27	BCL11A	chr16:12707382-12707866	GM12878	blood:	n/a	n/a
28	BCL3	chr16:12667035-12667697	GM12878	blood:	n/a	n/a
29	BCL3	chr16:12667189-12667642	GM12878	blood:	n/a	n/a
30	BCL3	chr16:12707490-12707825	GM12878	blood:	n/a	n/a
31	BCL3	chr16:12707079-12708023	A549	lung:	n/a	n/a
32	BCL3	chr16:12674715-12674922	GM12878	blood:	n/a	chr16:12674840-12674849
33	BCL3	chr16:12707023-12707991	A549	lung:	n/a	n/a
34	BCL3	chr16:12707411-12707905	GM12878	blood:	n/a	n/a
35	BCLAF1	chr16:12666973-12667572	GM12878	blood:	n/a	n/a
36	BCLAF1	chr16:12667037-12667943	GM12878	blood:	n/a	n/a
37	BCLAF1	chr16:12707246-12707930	GM12878	blood:	n/a	n/a
38	BHLHE40	chr16:12707450-12707858	HepG2	liver:	n/a	n/a
39	BHLHE40	chr16:12704952-12705132	K562	blood:	n/a	n/a
40	BHLHE40	chr16:12707308-12708223	K562	blood:	n/a	n/a
41	BHLHE40	chr16:12706410-12706828	HepG2	liver:	n/a	n/a
42	BHLHE40	chr16:12706481-12706681	A549	lung:	n/a	n/a
43	BHLHE40	chr16:12707464-12707820	HepG2	liver:	n/a	n/a
44	BHLHE40	chr16:12707185-12708266	HepG2	liver:	n/a	n/a
45	BHLHE40	chr16:12678441-12678725	HepG2	liver:	n/a	n/a
46	BHLHE40	chr16:12667237-12667896	GM12878	blood:	n/a	n/a
47	BHLHE40	chr16:12706445-12706812	K562	blood:	n/a	n/a
48	BHLHE40	chr16:12674662-12674994	GM12878	blood:	n/a	n/a
49	BHLHE40	chr16:12707133-12707889	GM12878	blood:	n/a	n/a
50	BHLHE40	chr16:12706196-12706208	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:12667646-12667696	AG04450	lung:	fetal
2	chr16:12667646-12667696	IMR90	lung:	fetal
3	chr16:12667646-12667696	A549	lung:	n/a
4	chr16:12667646-12667696	HL-60	blood:	n/a
5	chr16:12667646-12667696	CMK	blood:	n/a
6	chr16:12667646-12667696	GM19239	blood:	n/a
7	chr16:12667646-12667696	MCF-7	breast:	n/a
8	chr16:12667646-12667696	HNPCEpiC	eye:	n/a
9	chr16:12667646-12667696	AG10803	skin:	n/a
10	chr16:12667646-12667696	GM12878	blood:	n/a
11	chr16:12667646-12667696	HRCEpiC	kidney:	n/a
12	chr16:12667646-12667696	K562	blood:	n/a
13	chr16:12667646-12667696	RPTEC	kidney:	n/a
14	chr16:12667646-12667696	AG04449	skin:	fetal
15	chr16:12667646-12667696	SK-N-MC	brain:	n/a
16	chr16:12667646-12667696	T-47D	breast:	n/a
17	chr16:12667646-12667696	NH-A	brain:	n/a
18	chr16:12667646-12667696	HPAEpiC	pulmonary alveolar:	n/a
19	chr16:12667646-12667696	Hela-S3	cervix:	n/a
20	chr16:12667646-12667696	HUVEC	blood vessel:	n/a
21	chr16:12667646-12667696	Hepatocyte	liver:	n/a
22	chr16:12667646-12667696	SK-N-SH_RA	brain:	n/a
23	chr16:12667646-12667696	PANC-1	pancreas:	n/a
24	chr16:12667646-12667696	Jurkat	blood:	n/a
25	chr16:12667646-12667696	SAEC	small airway:	n/a
26	chr16:12667646-12667696	HMEC	breast:	n/a
27	chr16:12667646-12667696	HAEpiC	amniotic membrane:	n/a
28	chr16:12667646-12667696	HCT-116	colon:	n/a
29	chr16:12667646-12667696	AG09309	skin:	n/a
30	chr16:12667646-12667696	HEK293	kidney:	embryo
31	chr16:12667646-12667696	HIPEpiC	eye:	n/a
32	chr16:12667646-12667696	ProgFib	skin:	n/a
33	chr16:12667646-12667696	GM12892	blood:	n/a
34	chr16:12667646-12667696	NB4	blood:	n/a
35	chr16:12667646-12667696	NHBE	bronchial:	n/a
36	chr16:12667646-12667696	HepG2	liver:	n/a
37	chr16:12667646-12667696	NT2-D1	testis:	n/a
38	chr16:12667646-12667696	HCPEpiC	choroid plexus:	n/a
39	chr16:12667646-12667696	PrEC	prostate:	n/a
40	chr16:12667646-12667696	HEEpiC	esophagus:	n/a
41	chr16:12667646-12667696	Caco-2	colon:	n/a
42	chr16:12667646-12667696	AoSMC	blood vessel:	n/a
43	chr16:12667646-12667696	AG09319	gingival:	n/a
44	chr16:12667646-12667696	HCF	heart:	n/a
45	chr16:12667646-12667696	BE2_C	brain:	n/a
46	chr16:12667646-12667696	U87	brain:	n/a
47	chr16:12667646-12667696	SKMC	muscle:	n/a
48	chr16:12667646-12667696	ovcar-3	ovarian:	n/a
49	chr16:12667646-12667696	PFSK-1	brain:	n/a
50	chr16:12667646-12667696	HRE	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr16:12666208..12667949-chr16:12909884..12912499,2	K562	blood:
2	chr16:12707551..12710268-chr16:12710403..12713580,3	K562	blood:
3	chr16:12548883..12549752-chr16:12667238..12668263,4	MCF-7	breast:
4	chr16:12667441..12668160-chr16:12908986..12909620,2	K562	blood:
5	chr16:12667763..12668530-chr16:12912908..12913815,2	MCF-7	breast:
6	chr16:12664367..12666728-chr16:12670658..12673027,2	K562	blood:
7	chr16:12667422..12668391-chr16:12912804..12913870,6	MCF-7	breast:
8	chr16:12695664..12697663-chr16:12702091..12704953,2	MCF-7	breast:
9	chr16:12667311..12668307-chr16:12912660..12913925,10	K562	blood:
10	chr13:55145343..55147455-chr16:12696633..12698151,2	MCF-7	breast:
11	chr16:12667518..12668062-chr16:12712002..12712507,2	MCF-7	breast:
12	chr16:12434411..12435246-chr16:12667446..12668002,2	MCF-7	breast:
13	chr16:12667378..12668264-chr16:12909027..12909976,6	MCF-7	breast:
14	chr16:12705693..12707355-chr16:12894687..12897390,2	K562	blood:
15	chr16:12675875..12678223-chr16:12683631..12685864,2	MCF-7	breast:
16	chr16:12705362..12710268-chr16:12710311..12712475,5	K562	blood:
17	chr16:12667303..12668256-chr16:12994641..12995560,2	MCF-7	breast:
18	chr16:12667431..12668234-chr16:12930367..12931210,2	MCF-7	breast:
19	chr16:12675875..12678223-chr16:12683631..12685864,2	MCF-7	breast:
20	chr16:12705693..12708514-chr16:12893374..12897390,4	K562	blood:
21	chr16:12667239..12668915-chr16:12896290..12899009,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CPPED1-2	chr16:12704595-12704901	ENSG00000259899.1

No data

Variant related genes	Relation type
ENSG00000259899	TF binding region
ENSG00000259899	CpG island
ENSG00000103381	chromatin interactions
ENSG00000259899	chromatin interactions
ENSG00000237515	chromatin interactions

Extended variants
information (count: 4500 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:4500 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10609	chr16:12667076-12667077	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs535031517	chr16:12667096-12667097	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs34084585	chr16:12667098-12667099	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs533251552	chr16:12667102-12667103	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs184636638	chr16:12667107-12667108	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs189035746	chr16:12667111-12667112	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs573674186	chr16:12667114-12667115	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs542340378	chr16:12667116-12667117	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs181675488	chr16:12667122-12667123	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs528052161	chr16:12667134-12667135	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs12477	chr16:12667136-12667137	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs574272478	chr16:12667160-12667161	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs565148281	chr16:12667196-12667197	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs186398163	chr16:12667202-12667203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs550749691	chr16:12667218-12667219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs139414541	chr16:12667231-12667232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs78175785	chr16:12667232-12667233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs3803613	chr16:12667237-12667238	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs543206040	chr16:12667249-12667250	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs142319322	chr16:12667260-12667261	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs556732419	chr16:12667261-12667262	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs189675689	chr16:12667262-12667263	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs11542103	chr16:12667267-12667268	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs537388299	chr16:12667269-12667270	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs557505670	chr16:12667273-12667274	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs573863387	chr16:12667281-12667282	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs375349417	chr16:12667285-12667286	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs569644681	chr16:12667288-12667289	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs545249320	chr16:12667298-12667299	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs150513122	chr16:12667299-12667300	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs558977464	chr16:12667301-12667302	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs181273297	chr16:12667304-12667305	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs543604165	chr16:12667305-12667306	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs564776531	chr16:12667307-12667308	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs530812457	chr16:12667317-12667318	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs369149120	chr16:12667324-12667325	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs139480078	chr16:12667325-12667326	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs185484535	chr16:12667333-12667334	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs11640862	chr16:12667334-12667335	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs546819646	chr16:12667338-12667339	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs149692295	chr16:12667339-12667340	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs528634290	chr16:12667345-12667346	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs551746167	chr16:12667357-12667358	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs549014068	chr16:12667362-12667363	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs377693516	chr16:12667365-12667366	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs3803614	chr16:12667366-12667367	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs557344313	chr16:12667373-12667374	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs540942180	chr16:12667386-12667387	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs374064322	chr16:12667392-12667393	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs3169267	chr16:12667393-12667394	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:69)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Prostate cancer	18632612	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	21858162	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	17847001	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:251 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12613000-12670800	Weak transcription	Pancreas	Pancrea
2	chr16:12648400-12668800	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr16:12652200-12669200	Weak transcription	Brain Cingulate Gyrus	brain
4	chr16:12652600-12672200	Weak transcription	Right Ventricle	heart
5	chr16:12653200-12667600	Weak transcription	Brain Hippocampus Middle	brain
6	chr16:12653200-12669200	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr16:12661200-12667400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr16:12661400-12668200	Weak transcription	Duodenum Mucosa	Duodenum
9	chr16:12661800-12667200	Weak transcription	HSMMtube	muscle
10	chr16:12661800-12667600	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr16:12661800-12670400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr16:12662000-12667400	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr16:12662000-12667400	Weak transcription	Primary hematopoietic stem cells	blood
14	chr16:12662000-12667600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr16:12662800-12672000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr16:12663000-12669200	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr16:12663800-12667400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr16:12664000-12667200	Weak transcription	Fetal Muscle Leg	muscle
19	chr16:12664000-12670600	Weak transcription	Gastric	stomach
20	chr16:12664200-12667600	Weak transcription	Fetal Stomach	stomach
21	chr16:12664200-12668200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr16:12664200-12669400	Weak transcription	Brain Substantia Nigra	brain
23	chr16:12664400-12668600	Weak transcription	Esophagus	oesophagus
24	chr16:12664600-12667400	Weak transcription	Adipose Nuclei	Adipose
25	chr16:12664600-12667800	Weak transcription	Primary T cells from cord blood	blood
26	chr16:12664600-12667800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr16:12664600-12668000	Weak transcription	Fetal Intestine Small	intestine
28	chr16:12664600-12668800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr16:12664600-12669200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr16:12664600-12670600	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr16:12665000-12667800	Weak transcription	HepG2	liver
32	chr16:12665000-12669200	Weak transcription	Aorta	Aorta
33	chr16:12665000-12670600	Weak transcription	Spleen	Spleen
34	chr16:12665200-12669000	Weak transcription	Stomach Smooth Muscle	stomach
35	chr16:12665400-12667800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr16:12665400-12668600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr16:12665600-12668800	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr16:12665800-12668400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr16:12666400-12668000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
40	chr16:12666400-12668200	Enhancers	Primary B cells from peripheral blood	blood
41	chr16:12666600-12667200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
42	chr16:12666800-12668400	Enhancers	Primary B cells from cord blood	blood
43	chr16:12667000-12667200	Enhancers	Placenta	Placenta
44	chr16:12667000-12667400	Enhancers	GM12878-XiMat	blood
45	chr16:12667000-12667800	Enhancers	Fetal Thymus	thymus
46	chr16:12667200-12667600	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr16:12667400-12667600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
48	chr16:12667400-12667600	Flanking Active TSS	GM12878-XiMat	blood
49	chr16:12667400-12667800	Enhancers	Primary T cells fromperipheralblood	blood
50	chr16:12667400-12667800	Enhancers	Primary hematopoietic stem cells	blood

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