Variant report

Variant	nsv833288
Chromosome Location	chr16:76621358-76785197
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:985)
CpG islands
(count:367)
Chromatin interactive
region (count:32)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:985 , 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	chr16:76684292-76684820	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:76673948-76674099	K562	blood:	n/a	n/a
3	ARID3A	chr16:76687350-76687721	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:76668888-76668938	K562	blood:	n/a	n/a
5	ATF1	chr16:76687134-76687664	K562	blood:	n/a	n/a
6	ATF1	chr16:76668805-76669470	K562	blood:	n/a	n/a
7	ATF3	chr16:76668818-76669064	K562	blood:	n/a	n/a
8	ATF3	chr16:76687346-76687640	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr16:76703299-76703491	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr16:76668642-76669184	K562	blood:	n/a	n/a
11	BHLHE40	chr16:76704362-76704737	K562	blood:	n/a	chr16:76704597-76704606
12	CBX3	chr16:76668556-76669332	K562	blood:	n/a	n/a
13	CBX3	chr16:76668672-76669213	K562	blood:	n/a	n/a
14	CCNT2	chr16:76668739-76669178	K562	blood:	n/a	n/a
15	CEBPB	chr16:76669262-76669518	HepG2	liver:	n/a	chr16:76669437-76669448
16	CEBPB	chr16:76640227-76640508	A549	lung:	n/a	chr16:76640353-76640364
17	CEBPB	chr16:76714462-76714734	HepG2	liver:	n/a	chr16:76714617-76714628 chr16:76714616-76714629
18	CEBPB	chr16:76734138-76734455	HepG2	liver:	n/a	n/a
19	CEBPB	chr16:76734178-76734430	IMR90	lung:	n/a	n/a
20	CEBPB	chr16:76668991-76669576	K562	blood:	n/a	chr16:76669437-76669448
21	CEBPB	chr16:76782214-76782511	A549	lung:	n/a	chr16:76782369-76782380
22	CEBPB	chr16:76777703-76778010	IMR90	lung:	n/a	chr16:76777865-76777876
23	CEBPB	chr16:76696611-76696792	HepG2	liver:	n/a	chr16:76696685-76696698 chr16:76696686-76696697 chr16:76696685-76696696
24	CEBPB	chr16:76687305-76687716	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr16:76756458-76756533	K562	blood:	n/a	chr16:76756489-76756502 chr16:76756490-76756501
26	CEBPB	chr16:76710226-76710819	MCF-7	breast:	n/a	n/a
27	CEBPB	chr16:76626178-76626377	H1-hESC	embryonic stem cell:	n/a	chr16:76626265-76626276
28	CEBPB	chr16:76710451-76710670	HepG2	liver:	n/a	n/a
29	CEBPB	chr16:76687200-76687807	A549	lung:	n/a	n/a
30	CEBPB	chr16:76626105-76626409	HepG2	liver:	n/a	chr16:76626265-76626276
31	CEBPB	chr16:76687239-76687712	MCF-7	breast:	n/a	n/a
32	CEBPB	chr16:76640219-76640497	Hela-S3	cervix:	n/a	chr16:76640353-76640364
33	CEBPB	chr16:76668970-76669641	K562	blood:	n/a	chr16:76669437-76669448
34	CEBPB	chr16:76687258-76687706	A549	lung:	n/a	n/a
35	CEBPB	chr16:76687171-76687709	MCF-7	breast:	n/a	n/a
36	CEBPB	chr16:76687308-76687632	K562	blood:	n/a	n/a
37	CEBPB	chr16:76756351-76756650	IMR90	lung:	n/a	chr16:76756489-76756502 chr16:76756490-76756501 chr16:76756620-76756631
38	CEBPB	chr16:76734183-76734406	K562	blood:	n/a	n/a
39	CEBPB	chr16:76687293-76687724	K562	blood:	n/a	n/a
40	CEBPB	chr16:76698299-76698542	HepG2	liver:	n/a	n/a
41	CEBPB	chr16:76687392-76687580	K562	blood:	n/a	n/a
42	CEBPB	chr16:76640177-76640533	IMR90	lung:	n/a	chr16:76640353-76640364
43	CEBPB	chr16:76777705-76778043	HepG2	liver:	n/a	chr16:76777865-76777876
44	CEBPB	chr16:76687359-76687568	HepG2	liver:	n/a	n/a
45	CEBPB	chr16:76666721-76666977	HepG2	liver:	n/a	n/a
46	CEBPB	chr16:76640177-76640534	HepG2	liver:	n/a	chr16:76640353-76640364
47	CEBPB	chr16:76782215-76782526	IMR90	lung:	n/a	chr16:76782369-76782380
48	CEBPB	chr16:76687295-76687707	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr16:76687366-76687695	HepG2	liver:	n/a	n/a
50	CEBPB	chr16:76687286-76687682	HepG2	liver:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:76708064-76708114	HCT-116	colon:	n/a
2	chr16:76708064-76708114	HCT-116	colon:	n/a
3	chr16:76669151-76669201	NT2-D1	testis:	n/a
4	chr16:76669151-76669201	HEK293	kidney:	embryo
5	chr16:76708064-76708114	HEEpiC	esophagus:	n/a
6	chr16:76665665-76665715	MCF10A-Er-Src	breast:	n/a
7	chr16:76665665-76665715	GM12892	blood:	n/a
8	chr16:76708064-76708114	MCF10A-Er-Src	breast:	n/a
9	chr16:76666860-76666910	PANC-1	pancreas:	n/a
10	chr16:76669151-76669201	PFSK-1	brain:	n/a
11	chr16:76669151-76669201	NHBE	bronchial:	n/a
12	chr16:76665665-76665715	NB4	blood:	n/a
13	chr16:76668836-76668886	MCF-7	breast:	n/a
14	chr16:76666860-76666910	HRE	kidney:	n/a
15	chr16:76665665-76665715	CMK	blood:	n/a
16	chr16:76666860-76666910	PFSK-1	brain:	n/a
17	chr16:76708064-76708114	AG10803	skin:	n/a
18	chr16:76668836-76668886	Caco-2	colon:	n/a
19	chr16:76665665-76665715	AoSMC	blood vessel:	n/a
20	chr16:76669151-76669201	HRE	kidney:	n/a
21	chr16:76666860-76666910	GM06990	blood:	n/a
22	chr16:76668836-76668886	GM12892	blood:	n/a
23	chr16:76666860-76666910	HCF	heart:	n/a
24	chr16:76669151-76669201	HUVEC	blood vessel:	n/a
25	chr16:76669151-76669201	LNCaP	prostate:	n/a
26	chr16:76669151-76669201	HCT-116	colon:	n/a
27	chr16:76708064-76708114	AG04449	skin:	fetal
28	chr16:76670197-76670247	HRCEpiC	kidney:	n/a
29	chr16:76669151-76669201	HRCEpiC	kidney:	n/a
30	chr16:76708064-76708114	SK-N-SH	brain:	n/a
31	chr16:76708064-76708114	AG09309	skin:	n/a
32	chr16:76665665-76665715	HRE	kidney:	n/a
33	chr16:76665665-76665715	NHDF-neo	bronchial:	n/a
34	chr16:76670197-76670247	GM12891	blood:	n/a
35	chr16:76708064-76708114	HNPCEpiC	eye:	n/a
36	chr16:76668836-76668886	RPTEC	kidney:	n/a
37	chr16:76668836-76668886	HCF	heart:	n/a
38	chr16:76665665-76665715	HL-60	blood:	n/a
39	chr16:76668836-76668886	A549	lung:	n/a
40	chr16:76708064-76708114	ECC-1	luminal epithelium:	n/a
41	chr16:76665665-76665715	AG09309	skin:	n/a
42	chr16:76708064-76708114	IMR90	lung:	fetal
43	chr16:76668836-76668886	AG09319	gingival:	n/a
44	chr16:76666860-76666910	SKMC	muscle:	n/a
45	chr16:76670197-76670247	HAEpiC	amniotic membrane:	n/a
46	chr16:76708064-76708114	MCF-7	breast:	n/a
47	chr16:76670197-76670247	SKMC	muscle:	n/a
48	chr16:76668836-76668886	NH-A	brain:	n/a
49	chr16:76669151-76669201	GM12891	blood:	n/a
50	chr16:76669151-76669201	AoSMC	blood vessel:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:76741499..76743675-chr16:76746368..76748815,2	K562	blood:
2	chr16:76699528..76700343-chr16:77076632..77077627,2	MCF-7	breast:
3	chr16:76699506..76700441-chr16:77205329..77206242,3	MCF-7	breast:
4	chr16:76784883..76787638-chr16:76787899..76789936,2	MCF-7	breast:
5	chr16:76669652..76671358-chr16:76701917..76703611,2	K562	blood:
6	chr16:76687235..76688893-chr16:76692839..76694713,2	K562	blood:
7	chr16:76636023..76638622-chr16:76652291..76654068,2	K562	blood:
8	chr16:75835108..75835786-chr16:76687075..76687822,2	MCF-7	breast:
9	chr16:76319924..76320753-chr16:76686923..76687617,2	MCF-7	breast:
10	chr16:76773881..76775450-chr16:76881262..76882791,2	MCF-7	breast:
11	chr16:76703589..76705752-chr16:76708591..76711050,2	MCF-7	breast:
12	chr16:76747877..76750802-chr16:76754682..76756382,2	K562	blood:
13	chr16:76679307..76681357-chr16:76683795..76685911,2	MCF-7	breast:
14	chr16:76312365..76313607-chr16:76673596..76674287,4	MCF-7	breast:
15	chr16:76636023..76638622-chr16:76652291..76654068,2	K562	blood:
16	chr16:76747877..76750802-chr16:76754682..76756382,2	K562	blood:
17	chr16:76687235..76688893-chr16:76692839..76694713,2	K562	blood:
18	chr16:75834944..75835823-chr16:76687371..76688062,3	MCF-7	breast:
19	chr16:76701550..76704283-chr16:76707898..76709517,2	K562	blood:
20	chr16:76665227..76667688-chr16:76668445..76671290,2	K562	blood:
21	chr16:76669652..76671358-chr16:76701917..76703611,2	K562	blood:
22	chr16:76699516..76700310-chr16:77203606..77204151,2	MCF-7	breast:
23	chr16:76756661..76759781-chr16:76761311..76764642,3	K562	blood:
24	chr16:76687186..76688106-chr16:76857078..76857671,2	MCF-7	breast:
25	chr16:76741969..76744727-chr16:76747101..76748627,2	K562	blood:
26	chr16:76756661..76759781-chr16:76761311..76764642,3	K562	blood:
27	chr16:76741969..76744727-chr16:76747101..76748627,2	K562	blood:
28	chr16:76741499..76743675-chr16:76746368..76748815,2	K562	blood:
29	chr16:76701550..76704283-chr16:76707898..76709517,2	K562	blood:
30	chr16:76703589..76705752-chr16:76708591..76711050,2	MCF-7	breast:
31	chr16:76679307..76681357-chr16:76683795..76685911,2	MCF-7	breast:
32	chr16:76312246..76313469-chr16:76687103..76688657,6	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-58C22.1.1-2	chr16:76737141-76737172	XLOC_011792
2	lnc-RP11-58C22.1.1-1	chr16:76690565-76692375	ENSG00000250514
3	lnc-RP11-58C22.1.1-1	chr16:76669394-76669520	ENSG00000250514
4	lnc-RP11-58C22.1.1-1	chr16:76689454-76689561	ENSG00000250514
5	lnc-RP11-58C22.1.1-2	chr16:76733678-76734033	XLOC_011792
6	lnc-RP11-58C22.1.1-4	chr16:76770239-76770376	ENSG00000259995.1
7	lnc-RP11-58C22.1.1-1	chr16:76668895-76669046	ENSG00000250514

No data

Variant related genes	Relation type
ENSG00000259995	TF binding region
ENSG00000250514	TF binding region
ENSG00000259995	CpG island
ENSG00000250514	CpG island
ENSG00000250514	chromatin interactions
CDKN1A	miRNA target sites
SPRYD3	miRNA target sites
DDX3Y	miRNA target sites
CDV3	miRNA target sites

Extended variants
information (count: 2626 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2626 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144236255	chr16:76621364-76621365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs530680435	chr16:76621394-76621395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs72801246	chr16:76621397-76621398	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs113415888	chr16:76629209-76629210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543523299	chr16:76629220-76629221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78770612	chr16:76629271-76629272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541829084	chr16:76629287-76629288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs183813230	chr16:76629325-76629326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs72801252	chr16:76629356-76629357	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs547677007	chr16:76629367-76629368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs540491741	chr16:76629448-76629449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs559801357	chr16:76629462-76629463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs373887332	chr16:76629508-76629509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs34767380	chr16:76629513-76629514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs117673488	chr16:76629518-76629519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs528479080	chr16:76629523-76629524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374666509	chr16:76629597-76629598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528266336	chr16:76629606-76629607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548747551	chr16:76629657-76629658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs7201297	chr16:76629660-76629661	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs7185429	chr16:76629678-76629679	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs550897964	chr16:76629685-76629686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs140869182	chr16:76629693-76629694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs377240283	chr16:76629696-76629697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs535550615	chr16:76629712-76629713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs570999396	chr16:76629725-76629726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs368643447	chr16:76629732-76629733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs72801255	chr16:76629806-76629807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534128137	chr16:76629815-76629816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs117819802	chr16:76629855-76629856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547260010	chr16:76629922-76629923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs73628498	chr16:76629932-76629933	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs566161465	chr16:76629933-76629934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs189882704	chr16:76629958-76629959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181526139	chr16:76629963-76629964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs555079997	chr16:76629976-76629977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs541518087	chr16:76629993-76629994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs187056276	chr16:76630012-76630013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs571706479	chr16:76630035-76630036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs190307632	chr16:76630062-76630063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs34164649	chr16:76630063-76630064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576508198	chr16:76630068-76630069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs550836613	chr16:76630083-76630084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs74784904	chr16:76630149-76630150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs533412927	chr16:76630155-76630156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs537897124	chr16:76630181-76630182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs557688571	chr16:76630221-76630222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs550372080	chr16:76630314-76630315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs563686000	chr16:76630334-76630335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs182036794	chr16:76630335-76630336	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Lung cancer	24585490	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Neuroblastoma	18923524	CNVD
Cancer	20164920	CNVD
Cancer	20581869	CNVD

Chromatin state (count:146 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:76621000-76621400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr16:76629200-76630400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr16:76629600-76630000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr16:76645600-76645800	Enhancers	Placenta Amnion	Placenta Amnion
5	chr16:76646400-76647400	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr16:76647200-76650000	Enhancers	Brain Germinal Matrix	brain
7	chr16:76647400-76647800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr16:76647400-76647800	Enhancers	Placenta Amnion	Placenta Amnion
9	chr16:76647600-76648800	Enhancers	Brain Substantia Nigra	brain
10	chr16:76647800-76648200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr16:76647800-76649000	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr16:76647800-76649400	Enhancers	Fetal Brain Female	brain
13	chr16:76648000-76648600	Enhancers	Brain Hippocampus Middle	brain
14	chr16:76648000-76649200	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr16:76648000-76649800	Enhancers	Fetal Brain Male	brain
16	chr16:76648000-76650000	Enhancers	Fetal Lung	lung
17	chr16:76648200-76649000	Enhancers	Brain Cingulate Gyrus	brain
18	chr16:76648200-76649000	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr16:76648200-76649200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr16:76648400-76649000	Enhancers	Brain Angular Gyrus	brain
21	chr16:76648400-76649200	Enhancers	Fetal Stomach	stomach
22	chr16:76649000-76649200	Enhancers	Placenta Amnion	Placenta Amnion
23	chr16:76649200-76650000	Weak transcription	Fetal Stomach	stomach
24	chr16:76650000-76650200	Enhancers	Fetal Stomach	stomach
25	chr16:76653600-76653800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr16:76653600-76653800	Enhancers	Pancreas	Pancrea
27	chr16:76653800-76654000	ZNF genes & repeats	Pancreas	Pancrea
28	chr16:76656000-76659000	Enhancers	Fetal Lung	lung
29	chr16:76657000-76657600	Enhancers	Fetal Brain Male	brain
30	chr16:76657200-76657800	Enhancers	Fetal Brain Female	brain
31	chr16:76660400-76660800	Enhancers	K562	blood
32	chr16:76668600-76668800	Enhancers	Pancreas	Pancrea
33	chr16:76668600-76669800	Active TSS	K562	blood
34	chr16:76668800-76669200	Active TSS	Gastric	stomach
35	chr16:76668800-76669200	Flanking Active TSS	Pancreas	Pancrea
36	chr16:76669000-76669400	Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr16:76669000-76669400	Active TSS	Duodenum Mucosa	Duodenum
38	chr16:76673400-76674600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr16:76673600-76674000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
40	chr16:76673800-76674400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr16:76684400-76685200	Flanking Active TSS	A549	lung
42	chr16:76684600-76685200	Enhancers	HepG2	liver
43	chr16:76685200-76685400	Enhancers	A549	lung
44	chr16:76686600-76687000	Enhancers	Fetal Brain Male	brain
45	chr16:76687200-76687800	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr16:76687200-76688000	Enhancers	Brain Substantia Nigra	brain
47	chr16:76687200-76688200	Enhancers	Fetal Lung	lung
48	chr16:76687600-76688200	Enhancers	Brain Hippocampus Middle	brain
49	chr16:76687600-76689600	Enhancers	Brain Germinal Matrix	brain
50	chr16:76688200-76690600	Weak transcription	Fetal Lung	lung

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