Variant report

Variant	esv1831215
Chromosome Location	chr16:46907546-46962858
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1655)
CpG islands
(count:1099)
Chromatin interactive
region (count:54)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1655 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:46953059-46953061	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:46929952-46930302	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:46910494-46910903	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:46916320-46916793	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:46917760-46918018	HepG2	liver:	n/a	n/a
6	ATF2	chr16:46952764-46953470	GM12878	blood:	n/a	n/a
7	ATF2	chr16:46944800-46945242	GM12878	blood:	n/a	n/a
8	ATF2	chr16:46944867-46945264	GM12878	blood:	n/a	n/a
9	ATF2	chr16:46952992-46953364	GM12878	blood:	n/a	n/a
10	ATF3	chr16:46918014-46918261	K562	blood:	n/a	chr16:46918129-46918138
11	ATF3	chr16:46917665-46918009	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr16:46917770-46917975	K562	blood:	n/a	n/a
13	ATF3	chr16:46917722-46918064	K562	blood:	n/a	n/a
14	ATF3	chr16:46917639-46917984	A549	lung:	n/a	n/a
15	ATF3	chr16:46950934-46951142	K562	blood:	n/a	n/a
16	ATF3	chr16:46916480-46916776	HepG2	liver:	n/a	n/a
17	BACH1	chr16:46917761-46918204	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr16:46925856-46926100	GM12878	blood:	n/a	n/a
19	BATF	chr16:46944834-46945219	GM12878	blood:	n/a	n/a
20	BATF	chr16:46944816-46945256	GM12878	blood:	n/a	n/a
21	BATF	chr16:46952732-46953483	GM12878	blood:	n/a	n/a
22	BCL11A	chr16:46944839-46945192	GM12878	blood:	n/a	n/a
23	BCL3	chr16:46910253-46910878	A549	lung:	n/a	n/a
24	BCL3	chr16:46958046-46958259	GM12878	blood:	n/a	n/a
25	BCL3	chr16:46937742-46938104	GM12878	blood:	n/a	n/a
26	BCL3	chr16:46909930-46910196	GM12878	blood:	n/a	n/a
27	BCL3	chr16:46909902-46910107	GM12878	blood:	n/a	n/a
28	BCLAF1	chr16:46952684-46953475	GM12878	blood:	n/a	n/a
29	BCLAF1	chr16:46917973-46918280	GM12878	blood:	n/a	chr16:46918169-46918182 chr16:46918136-46918144 chr16:46918170-46918183
30	BCLAF1	chr16:46952771-46953443	GM12878	blood:	n/a	n/a
31	BCLAF1	chr16:46917861-46918409	GM12878	blood:	n/a	chr16:46918169-46918182 chr16:46918136-46918144 chr16:46918170-46918183
32	BCLAF1	chr16:46944839-46945417	GM12878	blood:	n/a	n/a
33	BHLHE40	chr16:46917781-46918258	K562	blood:	n/a	n/a
34	BHLHE40	chr16:46910396-46910782	HepG2	liver:	n/a	n/a
35	BHLHE40	chr16:46917467-46918273	HepG2	liver:	n/a	n/a
36	BHLHE40	chr16:46944934-46945163	GM12878	blood:	n/a	n/a
37	BHLHE40	chr16:46917933-46918311	GM12878	blood:	n/a	n/a
38	BHLHE40	chr16:46952896-46953370	GM12878	blood:	n/a	n/a
39	BHLHE40	chr16:46910403-46910813	HepG2	liver:	n/a	n/a
40	BHLHE40	chr16:46910485-46910724	HepG2	liver:	n/a	n/a
41	BHLHE40	chr16:46916438-46916763	HepG2	liver:	n/a	n/a
42	BRCA1	chr16:46917983-46918177	Hela-S3	cervix:	n/a	n/a
43	CBX3	chr16:46917687-46918227	K562	blood:	n/a	n/a
44	CCNT2	chr16:46917551-46918774	K562	blood:	n/a	chr16:46918022-46918031
45	CEBPB	chr16:46917705-46918076	K562	blood:	n/a	n/a
46	CEBPB	chr16:46910386-46910967	HepG2	liver:	n/a	n/a
47	CEBPB	chr16:46929928-46930326	HepG2	liver:	n/a	n/a
48	CEBPB	chr16:46922933-46923139	HepG2	liver:	n/a	chr16:46922994-46923005
49	CEBPB	chr16:46917686-46918398	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr16:46952766-46953079	HepG2	liver:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:46918160-46918210	HEK293	kidney:	embryo
2	chr16:46918160-46918210	HEK293	kidney:	embryo
3	chr16:46917681-46917731	HRE	kidney:	n/a
4	chr16:46918233-46918283	ovcar-3	ovarian:	n/a
5	chr16:46919075-46919125	ECC-1	luminal epithelium:	n/a
6	chr16:46918956-46919006	HRCEpiC	kidney:	n/a
7	chr16:46921663-46921713	HUVEC	blood vessel:	n/a
8	chr16:46919021-46919071	H1-hESC	embryonic stem cell:	embryo
9	chr16:46917681-46917731	HAEpiC	amniotic membrane:	n/a
10	chr16:46920075-46920125	SKMC	muscle:	n/a
11	chr16:46920836-46920886	SK-N-MC	brain:	n/a
12	chr16:46917681-46917731	AG10803	skin:	n/a
13	chr16:46921663-46921713	HRCEpiC	kidney:	n/a
14	chr16:46918956-46919006	Jurkat	blood:	n/a
15	chr16:46919021-46919071	HCT-116	colon:	n/a
16	chr16:46917681-46917731	HMEC	breast:	n/a
17	chr16:46942061-46942111	T-47D	breast:	n/a
18	chr16:46920836-46920886	HPAEpiC	pulmonary alveolar:	n/a
19	chr16:46921663-46921713	HL-60	blood:	n/a
20	chr16:46917496-46917546	HEK293	kidney:	embryo
21	chr16:46942061-46942111	LNCaP	prostate:	n/a
22	chr16:46920836-46920886	U87	brain:	n/a
23	chr16:46921663-46921713	HAEpiC	amniotic membrane:	n/a
24	chr16:46915319-46915369	H1-hESC	embryonic stem cell:	embryo
25	chr16:46917496-46917546	AG09319	gingival:	n/a
26	chr16:46919021-46919071	HEK293	kidney:	embryo
27	chr16:46918956-46919006	BE2_C	brain:	n/a
28	chr16:46915319-46915369	AG09319	gingival:	n/a
29	chr16:46919021-46919071	AG09319	gingival:	n/a
30	chr16:46918956-46919006	BJ	skin:	n/a
31	chr16:46917496-46917546	Hela-S3	cervix:	n/a
32	chr16:46919021-46919071	SKMC	muscle:	n/a
33	chr16:46919112-46919162	HNPCEpiC	eye:	n/a
34	chr16:46917496-46917546	CMK	blood:	n/a
35	chr16:46919112-46919162	MCF10A-Er-Src	breast:	n/a
36	chr16:46919194-46919244	MCF-7	breast:	n/a
37	chr16:46943697-46943747	PANC-1	pancreas:	n/a
38	chr16:46918160-46918210	NB4	blood:	n/a
39	chr16:46918160-46918210	BJ	skin:	n/a
40	chr16:46942061-46942111	U87	brain:	n/a
41	chr16:46943697-46943747	K562	blood:	n/a
42	chr16:46917883-46917933	AG04450	lung:	fetal
43	chr16:46943697-46943747	Jurkat	blood:	n/a
44	chr16:46915319-46915369	Caco-2	colon:	n/a
45	chr16:46917681-46917731	NT2-D1	testis:	n/a
46	chr16:46915319-46915369	CMK	blood:	n/a
47	chr16:46918233-46918283	GM06990	blood:	n/a
48	chr16:46917883-46917933	GM12891	blood:	n/a
49	chr16:46918233-46918283	ProgFib	skin:	n/a
50	chr16:46920075-46920125	Jurkat	blood:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:46892340..46895420-chr16:46933101..46936147,3	MCF-7	breast:
2	chr16:46923713..46925987-chr16:46943511..46946070,2	MCF-7	breast:
3	chr16:46887422..46888524-chr16:46942474..46943404,10	MCF-7	breast:
4	chr16:46887576..46888484-chr16:46942484..46943485,11	K562	blood:
5	chr16:46822185..46825488-chr16:46917726..46919426,3	K562	blood:
6	chr16:46934210..46935361-chr16:46942618..46943358,4	MCF-7	breast:
7	chr16:46912960..46915086-chr16:46924704..46926210,2	K562	blood:
8	chr16:46926056..46928049-chr16:46934795..46936767,2	K562	blood:
9	chr16:46887627..46888303-chr16:46942315..46943365,3	MCF-7	breast:
10	chr16:46916007..46917928-chr16:46919979..46921962,2	MCF-7	breast:
11	chr16:46706996..46707945-chr16:46942502..46943366,7	K562	blood:
12	chr16:46910567..46913398-chr16:46926504..46929766,3	MCF-7	breast:
13	chr16:46917473..46918075-chr17:77812758..77813708,2	HCT-116	colon:
14	chr16:46958303..46960272-chr16:46962691..46966438,3	MCF-7	breast:
15	chr16:46916414..46917983-chr16:46954082..46956744,2	K562	blood:
16	chr16:46916414..46917983-chr16:46954082..46956744,2	K562	blood:
17	chr16:46910117..46912387-chr16:46912466..46915411,3	MCF-7	breast:
18	chr16:46936280..46939899-chr16:46944603..46947118,3	K562	blood:
19	chr16:46953985..46956976-chr16:46957030..46958598,2	K562	blood:
20	chr16:46923713..46925987-chr16:46943511..46946070,2	MCF-7	breast:
21	chr16:46898009..46901625-chr16:46916085..46918224,4	MCF-7	breast:
22	chr16:46958303..46960272-chr16:46962691..46966438,3	MCF-7	breast:
23	chr16:46916007..46917928-chr16:46919979..46921962,2	MCF-7	breast:
24	chr16:46910117..46912387-chr16:46912466..46915411,3	MCF-7	breast:
25	chr16:46916956..46921483-chr16:46924468..46930263,8	MCF-7	breast:
26	chr16:46937070..46939899-chr16:46944886..46947118,2	K562	blood:
27	chr16:46912960..46915086-chr16:46924704..46926210,2	K562	blood:
28	chr16:46934207..46935040-chr16:46963392..46964242,3	MCF-7	breast:
29	chr16:46933814..46935655-chr16:46950387..46952278,2	MCF-7	breast:
30	chr16:46932297..46935211-chr16:46938670..46940478,2	K562	blood:
31	chr16:46932297..46935211-chr16:46938670..46940478,2	K562	blood:
32	chr16:46899085..46900954-chr16:46906232..46907925,2	MCF-7	breast:
33	chr16:46888367..46890662-chr16:46962617..46964242,2	MCF-7	breast:
34	chr16:46961874..46965878-chr16:47005417..47009744,4	K562	blood:
35	chr16:46926124..46928049-chr16:46935227..46936767,2	K562	blood:
36	chr16:46721433..46723160-chr16:46922380..46924051,2	K562	blood:
37	chr16:46918394..46919947-chr16:46922095..46923663,2	MCF-7	breast:
38	chr16:46895641..46897768-chr16:46916063..46918079,2	K562	blood:
39	chr16:46891478..46892076-chr16:46942492..46943005,2	K562	blood:
40	chr16:46934210..46935361-chr16:46942618..46943358,4	MCF-7	breast:
41	chr16:46910161..46915169-chr16:46917028..46920503,6	MCF-7	breast:
42	chr16:46926056..46928049-chr16:46934795..46936767,2	K562	blood:
43	chr16:46910567..46913398-chr16:46926504..46929766,3	MCF-7	breast:
44	chr16:46910895..46914385-chr16:46916188..46919908,3	MCF-7	breast:
45	chr16:46926124..46928049-chr16:46935227..46936767,2	K562	blood:
46	chr16:46951055..46952888-chr16:46955972..46959090,3	K562	blood:
47	chr16:46917403..46918059-chr9:134131479..134132405,2	Hela-S3	cervix:
48	chr16:46917387..46917972-chr8:38265324..38266247,2	Hela-S3	cervix:
49	chr16:46933814..46935655-chr16:46950387..46952278,2	MCF-7	breast:
50	chr16:46917956..46920289-chr16:46920497..46924419,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ORC6-5	chr16:46952988-46953903	expRegAs_chr16_5319_+

No data

Variant related genes	Relation type
GPT2	TF binding region
GPT2	CpG island
ENSG00000261173	chromatin interactions
ENSG00000141582	chromatin interactions
ENSG00000260782	chromatin interactions
ENSG00000091651	chromatin interactions
ENSG00000069345	chromatin interactions
ENSG00000166123	chromatin interactions
ENSG00000069329	chromatin interactions
ENSG00000140795	chromatin interactions

Extended variants
information (count: 1858 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1858 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544134226	chr16:46907601-46907602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs562780651	chr16:46907602-46907603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs76732841	chr16:46907603-46907604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs34355777	chr16:46907627-46907628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs71134511	chr16:46907629-46907630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs398029252	chr16:46907630-46907631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs529906464	chr16:46907655-46907656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542093377	chr16:46907665-46907666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs560269831	chr16:46907676-46907677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs185218776	chr16:46907678-46907679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552264189	chr16:46907684-46907685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs35297862	chr16:46907694-46907695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs13332595	chr16:46907719-46907720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs563897716	chr16:46907761-46907762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs190823450	chr16:46907820-46907821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550949042	chr16:46907826-46907827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs183379925	chr16:46907831-46907832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs536144880	chr16:46907885-46907886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548400911	chr16:46907915-46907916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566741179	chr16:46907950-46907951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533394895	chr16:46907962-46907963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188532545	chr16:46907975-46907976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs146874017	chr16:46908001-46908002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577126851	chr16:46908010-46908011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs538278680	chr16:46908118-46908119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs556495576	chr16:46908155-46908156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373712459	chr16:46908159-46908160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs373909703	chr16:46908261-46908262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs113539387	chr16:46908265-46908266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs200568398	chr16:46908303-46908304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs570775796	chr16:46908309-46908310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs377761870	chr16:46908332-46908333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560353822	chr16:46908368-46908369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs572227377	chr16:46908442-46908443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs545533059	chr16:46908466-46908467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs145896573	chr16:46908496-46908497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371297883	chr16:46908616-46908617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs576392515	chr16:46908649-46908650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs192925894	chr16:46908742-46908743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs138378612	chr16:46908780-46908781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs142970236	chr16:46908792-46908793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs183085448	chr16:46908796-46908797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs548495639	chr16:46908848-46908849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546821589	chr16:46908850-46908851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs372606205	chr16:46908982-46908983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs566679272	chr16:46908984-46908985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs568300645	chr16:46909028-46909029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534417414	chr16:46909039-46909040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs552381529	chr16:46909041-46909042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570972835	chr16:46909073-46909074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	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
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Renal cell carcinoma	18765545	CNVD
Sudden cardiac death	19188705	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2100 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:46888400-46913400	Weak transcription	Esophagus	oesophagus
2	chr16:46898800-46909200	Weak transcription	Pancreas	Pancrea
3	chr16:46898800-46910200	Enhancers	HepG2	liver
4	chr16:46903200-46911200	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr16:46904600-46910200	Weak transcription	Stomach Mucosa	stomach
6	chr16:46905600-46914400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr16:46907000-46907600	Enhancers	HSMMtube	muscle
8	chr16:46909200-46910000	Enhancers	Pancreas	Pancrea
9	chr16:46909800-46911000	Enhancers	Fetal Lung	lung
10	chr16:46909800-46911600	Enhancers	Liver	Liver
11	chr16:46910000-46910400	Enhancers	A549	lung
12	chr16:46910000-46910600	Enhancers	Ovary	ovary
13	chr16:46910000-46910800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr16:46910000-46910800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr16:46910000-46911200	Weak transcription	Pancreas	Pancrea
16	chr16:46910200-46910600	Enhancers	Adipose Nuclei	Adipose
17	chr16:46910200-46910800	Flanking Active TSS	HepG2	liver
18	chr16:46910200-46911600	Enhancers	Stomach Mucosa	stomach
19	chr16:46910400-46910800	Enhancers	Fetal Kidney	kidney
20	chr16:46910400-46910800	Flanking Active TSS	A549	lung
21	chr16:46910600-46910800	Enhancers	Sigmoid Colon	Sigmoid Colon
22	chr16:46910600-46916000	Weak transcription	Adipose Nuclei	Adipose
23	chr16:46910800-46911800	Enhancers	A549	lung
24	chr16:46910800-46912600	Enhancers	HepG2	liver
25	chr16:46911200-46911400	Enhancers	Pancreas	Pancrea
26	chr16:46911200-46913600	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr16:46911200-46914200	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr16:46911400-46911600	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr16:46911400-46911800	Weak transcription	Pancreas	Pancrea
30	chr16:46911600-46912400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
31	chr16:46911600-46912800	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr16:46911600-46915600	Weak transcription	Liver	Liver
33	chr16:46911600-46916600	Weak transcription	Stomach Mucosa	stomach
34	chr16:46911800-46912000	Enhancers	Pancreas	Pancrea
35	chr16:46912000-46912200	Enhancers	Primary B cells from cord blood	blood
36	chr16:46912000-46912600	Enhancers	HUVEC	blood vessel
37	chr16:46912000-46913000	Weak transcription	Pancreas	Pancrea
38	chr16:46912400-46912600	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr16:46912600-46912800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
40	chr16:46912600-46913000	Weak transcription	HepG2	liver
41	chr16:46912800-46914400	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr16:46913000-46913200	Enhancers	Fetal Kidney	kidney
43	chr16:46913000-46915000	Enhancers	Pancreas	Pancrea
44	chr16:46913000-46916000	Enhancers	HepG2	liver
45	chr16:46913400-46913600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr16:46913400-46913600	Enhancers	Esophagus	oesophagus
47	chr16:46913400-46913800	Enhancers	NHEK	skin
48	chr16:46913400-46914000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr16:46913400-46915600	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr16:46913600-46914000	Enhancers	iPS-20b Cell Line	embryonic stem cell

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