Variant report

Variant	nsv1049011
Chromosome Location	chr16:12655176-12672143
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:425)
CpG islands
(count:671)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:425 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:12667681-12668060	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:12664201-12664286	HepG2	liver:	n/a	n/a
3	ATF2	chr16:12666972-12667661	GM12878	blood:	n/a	n/a
4	ATF2	chr16:12666927-12667980	GM12878	blood:	n/a	n/a
5	BACH1	chr16:12667697-12667939	K562	blood:	n/a	n/a
6	BATF	chr16:12667208-12667587	GM12878	blood:	n/a	n/a
7	BCL3	chr16:12667189-12667642	GM12878	blood:	n/a	n/a
8	BCL3	chr16:12667035-12667697	GM12878	blood:	n/a	n/a
9	BCLAF1	chr16:12667037-12667943	GM12878	blood:	n/a	n/a
10	BCLAF1	chr16:12666973-12667572	GM12878	blood:	n/a	n/a
11	BHLHE40	chr16:12667748-12667970	K562	blood:	n/a	n/a
12	BHLHE40	chr16:12664073-12664400	HepG2	liver:	n/a	n/a
13	BHLHE40	chr16:12667237-12667896	GM12878	blood:	n/a	n/a
14	CEBPB	chr16:12667136-12667964	GM12878	blood:	n/a	n/a
15	CEBPB	chr16:12664077-12664393	HepG2	liver:	n/a	n/a
16	CEBPB	chr16:12664070-12664394	HepG2	liver:	n/a	n/a
17	CEBPB	chr16:12670389-12670529	K562	blood:	n/a	chr16:12670481-12670492
18	CEBPB	chr16:12670322-12670610	HepG2	liver:	n/a	chr16:12670481-12670492
19	CEBPB	chr16:12662622-12662650	K562	blood:	n/a	n/a
20	CHD2	chr16:12670921-12670923	HepG2	liver:	n/a	n/a
21	CHD2	chr16:12667782-12667927	HepG2	liver:	n/a	n/a
22	CTCF	chr16:12667800-12667950	A549	lung:	n/a	n/a
23	CTCF	chr16:12667740-12667890	GM12870	blood:	n/a	n/a
24	CTCF	chr16:12667760-12667910	Caco-2	colon:	n/a	n/a
25	CTCF	chr16:12667720-12667870	BE2_C	brain:	n/a	n/a
26	CTCF	chr16:12667740-12667890	GM12869	blood:	n/a	n/a
27	CTCF	chr16:12667669-12667956	GM19238	blood:	n/a	n/a
28	CTCF	chr16:12667720-12667870	HFF-Myc	foreskin:	n/a	n/a
29	CTCF	chr16:12667467-12667589	ProgFib	skin:	n/a	n/a
30	CTCF	chr16:12667687-12667691	Kidney_OC	kidney:	n/a	n/a
31	CTCF	chr16:12667720-12667870	HAc	cerebellar:	n/a	n/a
32	CTCF	chr16:12667678-12667960	HepG2	liver:	n/a	n/a
33	CTCF	chr16:12667680-12667830	GM06990	blood:	n/a	n/a
34	CTCF	chr16:12667760-12667910	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr16:12667720-12667936	MCF-7	breast:	n/a	n/a
36	CTCF	chr16:12667760-12667910	MCF-7	breast:	n/a	n/a
37	CTCF	chr16:12667707-12667950	MCF-7	breast:	n/a	n/a
38	CTCF	chr16:12667740-12667890	SAEC	small airway:	n/a	n/a
39	CTCF	chr16:12667740-12667890	HEK293	kidney:	n/a	n/a
40	CTCF	chr16:12667360-12667510	GM12873	blood:	n/a	n/a
41	CTCF	chr16:12667800-12667950	GM06990	blood:	n/a	n/a
42	CTCF	chr16:12667820-12667970	NHEK	skin:	n/a	n/a
43	CTCF	chr16:12667760-12667910	HCFaa	heart:	n/a	n/a
44	CTCF	chr16:12667760-12667910	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr16:12667703-12667948	A549	lung:	n/a	n/a
46	CTCF	chr16:12667573-12667644	LNCaP	prostate:	n/a	n/a
47	CTCF	chr16:12667760-12667910	HEK293	kidney:	n/a	n/a
48	CTCF	chr16:12667780-12667930	K562	blood:	n/a	n/a
49	CTCF	chr16:12667693-12667954	MCF-7	breast:	n/a	n/a
50	CTCF	chr16:12667701-12667940	ProgFib	skin:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:12664318-12664368	CMK	blood:	n/a
2	chr16:12657151-12657201	SAEC	small airway:	n/a
3	chr16:12662474-12662524	AG09319	gingival:	n/a
4	chr16:12667646-12667696	GM19239	blood:	n/a
5	chr16:12662659-12662709	NB4	blood:	n/a
6	chr16:12662659-12662709	LNCaP	prostate:	n/a
7	chr16:12662474-12662524	ovcar-3	ovarian:	n/a
8	chr16:12662474-12662524	U87	brain:	n/a
9	chr16:12667646-12667696	HRPEpiC	eye:	n/a
10	chr16:12656958-12657008	Caco-2	colon:	n/a
11	chr16:12657151-12657201	AG09319	gingival:	n/a
12	chr16:12661268-12661318	AG10803	skin:	n/a
13	chr16:12667646-12667696	U87	brain:	n/a
14	chr16:12664318-12664368	U87	brain:	n/a
15	chr16:12664318-12664368	HCF	heart:	n/a
16	chr16:12662474-12662524	HepG2	liver:	n/a
17	chr16:12661268-12661318	Jurkat	blood:	n/a
18	chr16:12662581-12662631	Caco-2	colon:	n/a
19	chr16:12659137-12659187	HUVEC	blood vessel:	n/a
20	chr16:12662659-12662709	GM19239	blood:	n/a
21	chr16:12662474-12662524	SKMC	muscle:	n/a
22	chr16:12661268-12661318	HL-60	blood:	n/a
23	chr16:12665018-12665068	RPTEC	kidney:	n/a
24	chr16:12662374-12662424	BE2_C	brain:	n/a
25	chr16:12664318-12664368	RPTEC	kidney:	n/a
26	chr16:12662581-12662631	NH-A	brain:	n/a
27	chr16:12657151-12657201	NH-A	brain:	n/a
28	chr16:12659137-12659187	Hela-S3	cervix:	n/a
29	chr16:12665018-12665068	NT2-D1	testis:	n/a
30	chr16:12662474-12662524	SAEC	small airway:	n/a
31	chr16:12661268-12661318	AG09319	gingival:	n/a
32	chr16:12662581-12662631	SK-N-MC	brain:	n/a
33	chr16:12667646-12667696	GM12878	blood:	n/a
34	chr16:12662659-12662709	GM12878	blood:	n/a
35	chr16:12657151-12657201	GM12891	blood:	n/a
36	chr16:12667646-12667696	NHBE	bronchial:	n/a
37	chr16:12659137-12659187	HEEpiC	esophagus:	n/a
38	chr16:12657151-12657201	Hepatocyte	liver:	n/a
39	chr16:12656958-12657008	AG09319	gingival:	n/a
40	chr16:12661268-12661318	BJ	skin:	n/a
41	chr16:12657151-12657201	LNCaP	prostate:	n/a
42	chr16:12656958-12657008	ovcar-3	ovarian:	n/a
43	chr16:12657151-12657201	HUVEC	blood vessel:	n/a
44	chr16:12665018-12665068	PFSK-1	brain:	n/a
45	chr16:12656958-12657008	HCT-116	colon:	n/a
46	chr16:12662659-12662709	HL-60	blood:	n/a
47	chr16:12662374-12662424	HIPEpiC	eye:	n/a
48	chr16:12664318-12664368	Caco-2	colon:	n/a
49	chr16:12662581-12662631	RPTEC	kidney:	n/a
50	chr16:12659137-12659187	H1-hESC	embryonic stem cell:	embryo

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:12667518..12668062-chr16:12712002..12712507,2	MCF-7	breast:
2	chr16:12667422..12668391-chr16:12912804..12913870,6	MCF-7	breast:
3	chr16:12667303..12668256-chr16:12994641..12995560,2	MCF-7	breast:
4	chr16:12667763..12668530-chr16:12912908..12913815,2	MCF-7	breast:
5	chr16:12664367..12666728-chr16:12670658..12673027,2	K562	blood:
6	chr16:12667378..12668264-chr16:12909027..12909976,6	MCF-7	breast:
7	chr16:12656706..12658781-chr16:12659071..12661791,2	MCF-7	breast:
8	chr16:12434411..12435246-chr16:12667446..12668002,2	MCF-7	breast:
9	chr16:12667311..12668307-chr16:12912660..12913925,10	K562	blood:
10	chr16:12667441..12668160-chr16:12908986..12909620,2	K562	blood:
11	chr16:12666208..12667949-chr16:12909884..12912499,2	K562	blood:
12	chr16:12548883..12549752-chr16:12667238..12668263,4	MCF-7	breast:
13	chr16:12651809..12653725-chr16:12657374..12659013,2	MCF-7	breast:
14	chr16:12664367..12666728-chr16:12670658..12673027,2	K562	blood:
15	chr16:12667431..12668234-chr16:12930367..12931210,2	MCF-7	breast:
16	chr16:12656706..12658781-chr16:12659071..12661791,2	MCF-7	breast:
17	chr16:12667239..12668915-chr16:12896290..12899009,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000259876	TF binding region
ENSG00000259876	CpG island
ENSG00000237515	chromatin interactions
ENSG00000103381	chromatin interactions

Extended variants
information (count: 2793 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:2793 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11075096	chr16:12655176-12655177	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536085142	chr16:12655180-12655181	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555166007	chr16:12655188-12655189	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188824190	chr16:12655194-12655195	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577004927	chr16:12655201-12655202	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546012745	chr16:12655203-12655204	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534282522	chr16:12655205-12655206	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376485373	chr16:12655209-12655210	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577978832	chr16:12655221-12655222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs141703515	chr16:12655225-12655226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150350979	chr16:12655230-12655231	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs12925894	chr16:12655233-12655234	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs542856621	chr16:12655235-12655236	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs180858767	chr16:12655236-12655237	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs572514325	chr16:12655240-12655241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs541035986	chr16:12655241-12655242	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs12925384	chr16:12655245-12655246	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs533187437	chr16:12655254-12655255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138072286	chr16:12655258-12655259	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185116763	chr16:12655265-12655266	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs373223796	chr16:12655279-12655280	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529419381	chr16:12655284-12655285	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs375928309	chr16:12655288-12655289	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565605183	chr16:12655296-12655297	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534737130	chr16:12655299-12655300	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189876805	chr16:12655339-12655340	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571248044	chr16:12655344-12655345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537085850	chr16:12655347-12655348	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs370497959	chr16:12655349-12655350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183910420	chr16:12655353-12655354	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573884944	chr16:12655358-12655359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375708418	chr16:12655359-12655360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs75026380	chr16:12655360-12655361	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553151270	chr16:12655364-12655365	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572979464	chr16:12655368-12655369	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs117074658	chr16:12655369-12655370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564278945	chr16:12655372-12655373	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564401566	chr16:12655388-12655389	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577610006	chr16:12655390-12655391	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543413803	chr16:12655391-12655392	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs13338085	chr16:12655402-12655403	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs187299608	chr16:12655406-12655407	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375502907	chr16:12655407-12655408	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533158694	chr16:12655417-12655418	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549283843	chr16:12655418-12655419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368747943	chr16:12655421-12655422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs559875769	chr16:12655428-12655429	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372381789	chr16:12655430-12655431	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551493599	chr16:12655434-12655435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12924625	chr16:12655437-12655438	Weak transcription Strong transcription	n/a	n/a	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:272 , 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	chr16:12632800-12663800	Weak transcription	Aorta	Aorta
3	chr16:12639400-12659000	Weak transcription	Lung	lung
4	chr16:12641200-12667000	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr16:12642000-12662200	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr16:12643000-12659200	Weak transcription	Placenta	Placenta
7	chr16:12645200-12661600	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr16:12646000-12655400	Weak transcription	Gastric	stomach
9	chr16:12646000-12659000	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr16:12646000-12661000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr16:12646200-12659800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr16:12646200-12660000	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr16:12646400-12659400	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr16:12646400-12660800	Weak transcription	Thymus	Thymus
15	chr16:12647400-12658800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr16:12647400-12662200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr16:12647400-12665200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr16:12647600-12661600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr16:12648000-12662200	Weak transcription	Fetal Stomach	stomach
20	chr16:12648400-12668800	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr16:12648800-12659200	Weak transcription	Esophagus	oesophagus
22	chr16:12649000-12658600	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr16:12649800-12662200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr16:12652200-12660200	Strong transcription	Primary B cells from cord blood	blood
25	chr16:12652200-12669200	Weak transcription	Brain Cingulate Gyrus	brain
26	chr16:12652400-12658200	Strong transcription	Primary B cells from peripheral blood	blood
27	chr16:12652400-12666400	Weak transcription	Brain Anterior Caudate	brain
28	chr16:12652600-12665800	Weak transcription	Brain Angular Gyrus	brain
29	chr16:12652600-12672200	Weak transcription	Right Ventricle	heart
30	chr16:12652800-12663400	Weak transcription	Brain Substantia Nigra	brain
31	chr16:12653200-12659200	Weak transcription	Adipose Nuclei	Adipose
32	chr16:12653200-12662200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr16:12653200-12667600	Weak transcription	Brain Hippocampus Middle	brain
34	chr16:12653200-12669200	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr16:12653400-12659800	Weak transcription	Ovary	ovary
36	chr16:12653600-12659000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr16:12653600-12662400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr16:12653600-12662600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr16:12653600-12663200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr16:12653800-12662600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr16:12653800-12665800	Weak transcription	NHDF-Ad	bronchial
42	chr16:12654400-12655400	Strong transcription	GM12878-XiMat	blood
43	chr16:12654400-12655600	Strong transcription	Stomach Smooth Muscle	stomach
44	chr16:12654800-12659600	Strong transcription	Primary T cells from cord blood	blood
45	chr16:12655000-12656000	Strong transcription	Spleen	Spleen
46	chr16:12655400-12655800	Weak transcription	GM12878-XiMat	blood
47	chr16:12655400-12656000	Strong transcription	Gastric	stomach
48	chr16:12655600-12659000	Weak transcription	Stomach Smooth Muscle	stomach
49	chr16:12655800-12656600	ZNF genes & repeats	GM12878-XiMat	blood
50	chr16:12656000-12661600	Weak transcription	Spleen	Spleen

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