Variant report

Variant	nsv527859
Chromosome Location	chr16:76605753-76722500
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:995)
CpG islands
(count:366)
Chromatin interactive
region (count:24)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:995 , 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	chr16:76687350-76687721	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:76684292-76684820	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:76668888-76668938	K562	blood:	n/a	n/a
4	ARID3A	chr16:76608141-76609300	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:76673948-76674099	K562	blood:	n/a	n/a
6	ATF1	chr16:76614425-76614592	K562	blood:	n/a	n/a
7	ATF1	chr16:76668805-76669470	K562	blood:	n/a	n/a
8	ATF1	chr16:76687134-76687664	K562	blood:	n/a	n/a
9	ATF3	chr16:76687346-76687640	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr16:76668818-76669064	K562	blood:	n/a	n/a
11	BACH1	chr16:76703299-76703491	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr16:76610931-76611290	GM12878	blood:	n/a	n/a
13	BATF	chr16:76617930-76618131	GM12878	blood:	n/a	chr16:76618063-76618074
14	BATF	chr16:76610960-76611272	GM12878	blood:	n/a	n/a
15	BATF	chr16:76617883-76618255	GM12878	blood:	n/a	chr16:76618063-76618074
16	BHLHE40	chr16:76608424-76608923	HepG2	liver:	n/a	n/a
17	BHLHE40	chr16:76668642-76669184	K562	blood:	n/a	n/a
18	BHLHE40	chr16:76610846-76611310	GM12878	blood:	n/a	n/a
19	BHLHE40	chr16:76704362-76704737	K562	blood:	n/a	chr16:76704597-76704606
20	CBX3	chr16:76668556-76669332	K562	blood:	n/a	n/a
21	CBX3	chr16:76668672-76669213	K562	blood:	n/a	n/a
22	CCNT2	chr16:76668739-76669178	K562	blood:	n/a	n/a
23	CEBPB	chr16:76640302-76640497	H1-hESC	embryonic stem cell:	n/a	chr16:76640353-76640364
24	CEBPB	chr16:76668970-76669641	K562	blood:	n/a	chr16:76669437-76669448
25	CEBPB	chr16:76687286-76687682	HepG2	liver:	n/a	n/a
26	CEBPB	chr16:76695763-76696093	HepG2	liver:	n/a	n/a
27	CEBPB	chr16:76687308-76687632	K562	blood:	n/a	n/a
28	CEBPB	chr16:76687258-76687706	A549	lung:	n/a	n/a
29	CEBPB	chr16:76687239-76687712	MCF-7	breast:	n/a	n/a
30	CEBPB	chr16:76702300-76702493	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr16:76640219-76640497	Hela-S3	cervix:	n/a	chr16:76640353-76640364
32	CEBPB	chr16:76626178-76626377	H1-hESC	embryonic stem cell:	n/a	chr16:76626265-76626276
33	CEBPB	chr16:76687295-76687707	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr16:76608602-76608974	HepG2	liver:	n/a	n/a
35	CEBPB	chr16:76696611-76696792	HepG2	liver:	n/a	chr16:76696685-76696698 chr16:76696686-76696697 chr16:76696685-76696696
36	CEBPB	chr16:76668991-76669576	K562	blood:	n/a	chr16:76669437-76669448
37	CEBPB	chr16:76710097-76710858	MCF-7	breast:	n/a	n/a
38	CEBPB	chr16:76669283-76669515	K562	blood:	n/a	chr16:76669437-76669448
39	CEBPB	chr16:76640194-76640523	K562	blood:	n/a	chr16:76640353-76640364
40	CEBPB	chr16:76687291-76687702	HepG2	liver:	n/a	n/a
41	CEBPB	chr16:76668375-76668595	HepG2	liver:	n/a	chr16:76668457-76668468
42	CEBPB	chr16:76687359-76687568	HepG2	liver:	n/a	n/a
43	CEBPB	chr16:76626164-76626375	A549	lung:	n/a	chr16:76626265-76626276
44	CEBPB	chr16:76608534-76608982	HepG2	liver:	n/a	n/a
45	CEBPB	chr16:76640227-76640508	A549	lung:	n/a	chr16:76640353-76640364
46	CEBPB	chr16:76640177-76640533	IMR90	lung:	n/a	chr16:76640353-76640364
47	CEBPB	chr16:76687305-76687716	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr16:76687293-76687724	K562	blood:	n/a	n/a
49	CEBPB	chr16:76669262-76669518	HepG2	liver:	n/a	chr16:76669437-76669448
50	CEBPB	chr16:76626105-76626409	HepG2	liver:	n/a	chr16:76626265-76626276

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:76668836-76668886	H1-hESC	embryonic stem cell:	embryo
2	chr16:76666860-76666910	SK-N-SH	brain:	n/a
3	chr16:76670197-76670247	GM12892	blood:	n/a
4	chr16:76668836-76668886	IMR90	lung:	fetal
5	chr16:76669151-76669201	HMEC	breast:	n/a
6	chr16:76665665-76665715	HUVEC	blood vessel:	n/a
7	chr16:76670197-76670247	BE2_C	brain:	n/a
8	chr16:76668836-76668886	A549	lung:	n/a
9	chr16:76708064-76708114	PFSK-1	brain:	n/a
10	chr16:76708064-76708114	A549	lung:	n/a
11	chr16:76668836-76668886	HNPCEpiC	eye:	n/a
12	chr16:76665665-76665715	GM12878	blood:	n/a
13	chr16:76670197-76670247	AoSMC	blood vessel:	n/a
14	chr16:76669151-76669201	AG04449	skin:	fetal
15	chr16:76669151-76669201	HUVEC	blood vessel:	n/a
16	chr16:76670197-76670247	HEK293	kidney:	embryo
17	chr16:76708064-76708114	U87	brain:	n/a
18	chr16:76666860-76666910	HRCEpiC	kidney:	n/a
19	chr16:76668836-76668886	HEEpiC	esophagus:	n/a
20	chr16:76665665-76665715	HRCEpiC	kidney:	n/a
21	chr16:76665665-76665715	MCF10A-Er-Src	breast:	n/a
22	chr16:76708064-76708114	ovcar-3	ovarian:	n/a
23	chr16:76670197-76670247	SK-N-MC	brain:	n/a
24	chr16:76708064-76708114	HRE	kidney:	n/a
25	chr16:76708064-76708114	LNCaP	prostate:	n/a
26	chr16:76665665-76665715	SK-N-SH	brain:	n/a
27	chr16:76670197-76670247	A549	lung:	n/a
28	chr16:76708064-76708114	CMK	blood:	n/a
29	chr16:76708064-76708114	NT2-D1	testis:	n/a
30	chr16:76669151-76669201	RPTEC	kidney:	n/a
31	chr16:76708064-76708114	NB4	blood:	n/a
32	chr16:76669151-76669201	HRE	kidney:	n/a
33	chr16:76670197-76670247	Hepatocyte	liver:	n/a
34	chr16:76665665-76665715	PANC-1	pancreas:	n/a
35	chr16:76668836-76668886	GM12892	blood:	n/a
36	chr16:76668836-76668886	BE2_C	brain:	n/a
37	chr16:76665665-76665715	U87	brain:	n/a
38	chr16:76666860-76666910	Hela-S3	cervix:	n/a
39	chr16:76708064-76708114	K562	blood:	n/a
40	chr16:76670197-76670247	T-47D	breast:	n/a
41	chr16:76708064-76708114	HCF	heart:	n/a
42	chr16:76666860-76666910	PFSK-1	brain:	n/a
43	chr16:76668836-76668886	GM19239	blood:	n/a
44	chr16:76669151-76669201	Hela-S3	cervix:	n/a
45	chr16:76666860-76666910	AG09309	skin:	n/a
46	chr16:76668836-76668886	NT2-D1	testis:	n/a
47	chr16:76669151-76669201	GM06990	blood:	n/a
48	chr16:76669151-76669201	Jurkat	blood:	n/a
49	chr16:76666860-76666910	HPAEpiC	pulmonary alveolar:	n/a
50	chr16:76669151-76669201	MCF10A-Er-Src	breast:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:75835108..75835786-chr16:76687075..76687822,2	MCF-7	breast:
2	chr16:75834944..75835823-chr16:76687371..76688062,3	MCF-7	breast:
3	chr16:76699528..76700343-chr16:77076632..77077627,2	MCF-7	breast:
4	chr16:76312365..76313607-chr16:76673596..76674287,4	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	chr16:76312246..76313469-chr16:76687103..76688657,6	MCF-7	breast:
9	chr16:76669652..76671358-chr16:76701917..76703611,2	K562	blood:
10	chr16:76699516..76700310-chr16:77203606..77204151,2	MCF-7	breast:
11	chr16:76703589..76705752-chr16:76708591..76711050,2	MCF-7	breast:
12	chr16:76679307..76681357-chr16:76683795..76685911,2	MCF-7	breast:
13	chr16:76607256..76609840-chr16:76614807..76617382,2	K562	blood:
14	chr16:76703589..76705752-chr16:76708591..76711050,2	MCF-7	breast:
15	chr16:76665227..76667688-chr16:76668445..76671290,2	K562	blood:
16	chr16:76636023..76638622-chr16:76652291..76654068,2	K562	blood:
17	chr16:76679307..76681357-chr16:76683795..76685911,2	MCF-7	breast:
18	chr16:76687186..76688106-chr16:76857078..76857671,2	MCF-7	breast:
19	chr16:76607256..76609840-chr16:76614807..76617382,2	K562	blood:
20	chr16:76701550..76704283-chr16:76707898..76709517,2	K562	blood:
21	chr16:76701550..76704283-chr16:76707898..76709517,2	K562	blood:
22	chr16:76699506..76700441-chr16:77205329..77206242,3	MCF-7	breast:
23	chr16:76319924..76320753-chr16:76686923..76687617,2	MCF-7	breast:
24	chr16:76687235..76688893-chr16:76692839..76694713,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-58C22.1.1-1	chr16:76689454-76689561	ENSG00000250514
2	lnc-RP11-58C22.1.1-1	chr16:76668895-76669046	ENSG00000250514
3	lnc-RP11-58C22.1.1-1	chr16:76669394-76669520	ENSG00000250514
4	lnc-RP11-58C22.1.1-1	chr16:76690565-76692375	ENSG00000250514

No data

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

Extended variants
information (count: 2532 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2532 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148424920	chr16:76607223-76607224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs556943000	chr16:76607237-76607238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs565145018	chr16:76607247-76607248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs190400098	chr16:76607300-76607301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542089715	chr16:76607312-76607313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs60072161	chr16:76607317-76607318	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs572517701	chr16:76607319-76607320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs541138706	chr16:76607334-76607335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564233808	chr16:76607363-76607364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs533203414	chr16:76607398-76607399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs549745201	chr16:76607413-76607414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs562674923	chr16:76607435-76607436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531651288	chr16:76607530-76607531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548158040	chr16:76607573-76607574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs117288713	chr16:76607588-76607589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs147133171	chr16:76607619-76607620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs7186700	chr16:76607635-76607636	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs570559008	chr16:76607723-76607724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539465181	chr16:76607727-76607728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556177783	chr16:76607732-76607733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs367755814	chr16:76607761-76607762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562081017	chr16:76607790-76607791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs180709737	chr16:76607844-76607845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs536167066	chr16:76607874-76607875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555745575	chr16:76607877-76607878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572641884	chr16:76607886-76607887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs4243125	chr16:76607888-76607889	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs377467317	chr16:76607902-76607903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564270882	chr16:76607933-76607934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs547053971	chr16:76607956-76607957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs577700717	chr16:76607982-76607983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543477244	chr16:76608020-76608021	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs111527568	chr16:76608036-76608037	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs111440034	chr16:76608042-76608043	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs373250601	chr16:76608050-76608051	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs144475458	chr16:76608083-76608084	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs561824161	chr16:76608091-76608092	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs368438306	chr16:76608095-76608096	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs78226841	chr16:76608097-76608098	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs7186989	chr16:76608116-76608117	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs4887868	chr16:76608160-76608161	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs570593186	chr16:76608212-76608213	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs183679788	chr16:76608310-76608311	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs7203365	chr16:76608322-76608323	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs568624972	chr16:76608325-76608326	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs34171899	chr16:76608332-76608333	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs188442700	chr16:76608338-76608339	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs534157124	chr16:76608418-76608419	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs181295644	chr16:76608441-76608442	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs556073426	chr16:76608498-76608499	Enhancers Flanking Active TSS	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:173 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:76607200-76607600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr16:76607400-76608000	Enhancers	HepG2	liver
3	chr16:76608000-76608600	Enhancers	Fetal Intestine Small	intestine
4	chr16:76608000-76608800	Flanking Active TSS	HepG2	liver
5	chr16:76608400-76609400	Enhancers	Fetal Intestine Large	intestine
6	chr16:76608600-76609000	Enhancers	Liver	Liver
7	chr16:76608800-76610000	Enhancers	HepG2	liver
8	chr16:76610000-76610400	Weak transcription	HepG2	liver
9	chr16:76610200-76612200	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr16:76610400-76611200	Enhancers	Fetal Lung	lung
11	chr16:76610400-76611200	Enhancers	HepG2	liver
12	chr16:76610400-76611400	Enhancers	Primary hematopoietic stem cells	blood
13	chr16:76610400-76611800	Enhancers	GM12878-XiMat	blood
14	chr16:76611200-76611800	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr16:76614400-76614600	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr16:76615400-76616200	Enhancers	Brain Germinal Matrix	brain
17	chr16:76616200-76616800	Weak transcription	Brain Germinal Matrix	brain
18	chr16:76616800-76617800	Enhancers	Brain Germinal Matrix	brain
19	chr16:76616800-76618000	Enhancers	Fetal Brain Male	brain
20	chr16:76616800-76618200	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr16:76616800-76618400	Enhancers	Fetal Brain Female	brain
22	chr16:76617000-76617200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr16:76617000-76617200	Enhancers	Brain Angular Gyrus	brain
24	chr16:76617000-76617400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr16:76617000-76618000	Enhancers	Fetal Lung	lung
26	chr16:76617200-76617400	Flanking Active TSS	Brain Angular Gyrus	brain
27	chr16:76617200-76617600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr16:76617200-76617600	Enhancers	Adipose Nuclei	Adipose
29	chr16:76617200-76617600	Enhancers	Fetal Muscle Leg	muscle
30	chr16:76617200-76617600	Enhancers	Fetal Stomach	stomach
31	chr16:76617200-76617800	Active TSS	Brain Anterior Caudate	brain
32	chr16:76617200-76617800	Active TSS	Brain Cingulate Gyrus	brain
33	chr16:76617200-76617800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
34	chr16:76617200-76617800	Active TSS	Pancreatic Islets	Pancreatic Islet
35	chr16:76617200-76618000	Active TSS	Brain Hippocampus Middle	brain
36	chr16:76617200-76618200	Active TSS	Brain Inferior Temporal Lobe	brain
37	chr16:76617200-76618200	Active TSS	Brain Substantia Nigra	brain
38	chr16:76617400-76617800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr16:76617400-76617800	Active TSS	Brain Angular Gyrus	brain
40	chr16:76617600-76618000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr16:76617800-76618200	Active TSS	Brain Germinal Matrix	brain
42	chr16:76617800-76618400	Enhancers	Brain Cingulate Gyrus	brain
43	chr16:76618000-76618200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr16:76618000-76618400	Enhancers	Brain Angular Gyrus	brain
45	chr16:76618000-76621000	Weak transcription	Fetal Lung	lung
46	chr16:76618200-76619600	Enhancers	Brain Germinal Matrix	brain
47	chr16:76618800-76619800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr16:76619600-76620600	Weak transcription	Brain Germinal Matrix	brain
49	chr16:76619800-76621000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr16:76620600-76620800	Enhancers	Brain Germinal Matrix	brain

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