Variant report

Variant	esv3519768
Chromosome Location	chr16:46873184-46960035
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2394)
CpG islands
(count:1588)
Chromatin interactive
region (count:71)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2394 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:46902900-46903015	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:46898391-46898395	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:46887920-46888125	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:46910494-46910903	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:46916320-46916793	HepG2	liver:	n/a	n/a
6	ARID3A	chr16:46953059-46953061	HepG2	liver:	n/a	n/a
7	ARID3A	chr16:46929952-46930302	HepG2	liver:	n/a	n/a
8	ARID3A	chr16:46874238-46874279	HepG2	liver:	n/a	n/a
9	ARID3A	chr16:46891569-46891792	HepG2	liver:	n/a	n/a
10	ARID3A	chr16:46917760-46918018	HepG2	liver:	n/a	n/a
11	ARID3A	chr16:46873889-46873891	HepG2	liver:	n/a	n/a
12	ATF2	chr16:46944867-46945264	GM12878	blood:	n/a	n/a
13	ATF2	chr16:46944800-46945242	GM12878	blood:	n/a	n/a
14	ATF2	chr16:46952764-46953470	GM12878	blood:	n/a	n/a
15	ATF2	chr16:46887845-46888290	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr16:46952992-46953364	GM12878	blood:	n/a	n/a
17	ATF3	chr16:46900247-46900439	HepG2	liver:	n/a	n/a
18	ATF3	chr16:46916480-46916776	HepG2	liver:	n/a	n/a
19	ATF3	chr16:46918014-46918261	K562	blood:	n/a	chr16:46918129-46918138
20	ATF3	chr16:46917722-46918064	K562	blood:	n/a	n/a
21	ATF3	chr16:46917639-46917984	A549	lung:	n/a	n/a
22	ATF3	chr16:46917770-46917975	K562	blood:	n/a	n/a
23	ATF3	chr16:46917665-46918009	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF3	chr16:46950934-46951142	K562	blood:	n/a	n/a
25	BACH1	chr16:46917761-46918204	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr16:46944816-46945256	GM12878	blood:	n/a	n/a
27	BATF	chr16:46944834-46945219	GM12878	blood:	n/a	n/a
28	BATF	chr16:46898306-46898562	GM12878	blood:	n/a	chr16:46898410-46898421
29	BATF	chr16:46925856-46926100	GM12878	blood:	n/a	n/a
30	BATF	chr16:46952732-46953483	GM12878	blood:	n/a	n/a
31	BCL11A	chr16:46944839-46945192	GM12878	blood:	n/a	n/a
32	BCL3	chr16:46910253-46910878	A549	lung:	n/a	n/a
33	BCL3	chr16:46909930-46910196	GM12878	blood:	n/a	n/a
34	BCL3	chr16:46958046-46958259	GM12878	blood:	n/a	n/a
35	BCL3	chr16:46937742-46938104	GM12878	blood:	n/a	n/a
36	BCL3	chr16:46909902-46910107	GM12878	blood:	n/a	n/a
37	BCLAF1	chr16:46917861-46918409	GM12878	blood:	n/a	chr16:46918169-46918182 chr16:46918136-46918144 chr16:46918170-46918183
38	BCLAF1	chr16:46952771-46953443	GM12878	blood:	n/a	n/a
39	BCLAF1	chr16:46952684-46953475	GM12878	blood:	n/a	n/a
40	BCLAF1	chr16:46887770-46888248	GM12878	blood:	n/a	n/a
41	BCLAF1	chr16:46917973-46918280	GM12878	blood:	n/a	chr16:46918169-46918182 chr16:46918136-46918144 chr16:46918170-46918183
42	BCLAF1	chr16:46944839-46945417	GM12878	blood:	n/a	n/a
43	BHLHE40	chr16:46910396-46910782	HepG2	liver:	n/a	n/a
44	BHLHE40	chr16:46910403-46910813	HepG2	liver:	n/a	n/a
45	BHLHE40	chr16:46917933-46918311	GM12878	blood:	n/a	n/a
46	BHLHE40	chr16:46873747-46873775	HepG2	liver:	n/a	n/a
47	BHLHE40	chr16:46917467-46918273	HepG2	liver:	n/a	n/a
48	BHLHE40	chr16:46952896-46953370	GM12878	blood:	n/a	n/a
49	BHLHE40	chr16:46944934-46945163	GM12878	blood:	n/a	n/a
50	BHLHE40	chr16:46917781-46918258	K562	blood:	n/a	n/a

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:46919112-46919162	BJ	skin:	n/a
2	chr16:46919075-46919125	HRCEpiC	kidney:	n/a
3	chr16:46919112-46919162	BJ	skin:	n/a
4	chr16:46919075-46919125	HRCEpiC	kidney:	n/a
5	chr16:46920836-46920886	PFSK-1	brain:	n/a
6	chr16:46918160-46918210	HCPEpiC	choroid plexus:	n/a
7	chr16:46921663-46921713	RPTEC	kidney:	n/a
8	chr16:46878553-46878603	AG10803	skin:	n/a
9	chr16:46918233-46918283	HNPCEpiC	eye:	n/a
10	chr16:46876498-46876548	HUVEC	blood vessel:	n/a
11	chr16:46918233-46918283	HCM	heart:	n/a
12	chr16:46876498-46876548	HCPEpiC	choroid plexus:	n/a
13	chr16:46917888-46917938	T-47D	breast:	n/a
14	chr16:46920836-46920886	SK-N-SH_RA	brain:	n/a
15	chr16:46917888-46917938	PFSK-1	brain:	n/a
16	chr16:46893929-46893979	NHDF-neo	bronchial:	n/a
17	chr16:46919112-46919162	HUVEC	blood vessel:	n/a
18	chr16:46878553-46878603	HRCEpiC	kidney:	n/a
19	chr16:46918233-46918283	AG09309	skin:	n/a
20	chr16:46878164-46878214	MCF-7	breast:	n/a
21	chr16:46915319-46915369	ovcar-3	ovarian:	n/a
22	chr16:46877831-46877881	Caco-2	colon:	n/a
23	chr16:46880518-46880568	NHDF-neo	bronchial:	n/a
24	chr16:46918956-46919006	AG10803	skin:	n/a
25	chr16:46917496-46917546	NHDF-neo	bronchial:	n/a
26	chr16:46881511-46881561	HepG2	liver:	n/a
27	chr16:46873954-46874004	ovcar-3	ovarian:	n/a
28	chr16:46920836-46920886	MCF10A-Er-Src	breast:	n/a
29	chr16:46919075-46919125	T-47D	breast:	n/a
30	chr16:46878164-46878214	PANC-1	pancreas:	n/a
31	chr16:46918160-46918210	CMK	blood:	n/a
32	chr16:46920075-46920125	AG09319	gingival:	n/a
33	chr16:46915319-46915369	HRE	kidney:	n/a
34	chr16:46873954-46874004	RPTEC	kidney:	n/a
35	chr16:46876498-46876548	HPAEpiC	pulmonary alveolar:	n/a
36	chr16:46920075-46920125	ProgFib	skin:	n/a
37	chr16:46918433-46918483	HRCEpiC	kidney:	n/a
38	chr16:46917888-46917938	SK-N-SH_RA	brain:	n/a
39	chr16:46918956-46919006	HRCEpiC	kidney:	n/a
40	chr16:46915319-46915369	GM12878	blood:	n/a
41	chr16:46920836-46920886	MCF-7	breast:	n/a
42	chr16:46918160-46918210	SK-N-SH_RA	brain:	n/a
43	chr16:46915319-46915369	SK-N-SH	brain:	n/a
44	chr16:46920075-46920125	Hela-S3	cervix:	n/a
45	chr16:46918433-46918483	GM12892	blood:	n/a
46	chr16:46943697-46943747	HRCEpiC	kidney:	n/a
47	chr16:46919112-46919162	GM06990	blood:	n/a
48	chr16:46917681-46917731	HCM	heart:	n/a
49	chr16:46920075-46920125	HCPEpiC	choroid plexus:	n/a
50	chr16:46919112-46919162	LNCaP	prostate:	n/a

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:46926124..46928049-chr16:46935227..46936767,2	K562	blood:
2	chr16:46892458..46893278-chr16:46963324..46964061,2	MCF-7	breast:
3	chr16:46912960..46915086-chr16:46924704..46926210,2	K562	blood:
4	chr16:46876960..46879253-chr16:46881282..46882965,2	K562	blood:
5	chr16:46937070..46939899-chr16:46944886..46947118,2	K562	blood:
6	chr16:46887576..46888484-chr16:46942484..46943485,11	K562	blood:
7	chr16:46910161..46915169-chr16:46917028..46920503,6	MCF-7	breast:
8	chr16:46917403..46918059-chr9:134131479..134132405,2	Hela-S3	cervix:
9	chr16:46882446..46885231-chr16:46887367..46889893,2	K562	blood:
10	chr16:46899085..46900954-chr16:46906232..46907925,2	MCF-7	breast:
11	chr16:46923713..46925987-chr16:46943511..46946070,2	MCF-7	breast:
12	chr16:46934207..46935040-chr16:46963392..46964242,3	MCF-7	breast:
13	chr16:46822185..46825488-chr16:46917726..46919426,3	K562	blood:
14	chr16:46891478..46892076-chr16:46942492..46943005,2	K562	blood:
15	chr16:46910895..46914385-chr16:46916188..46919908,3	MCF-7	breast:
16	chr16:46953985..46956976-chr16:46957030..46958598,2	K562	blood:
17	chr16:46912960..46915086-chr16:46924704..46926210,2	K562	blood:
18	chr16:46916414..46917983-chr16:46954082..46956744,2	K562	blood:
19	chr16:46917387..46917972-chr8:38265324..38266247,2	Hela-S3	cervix:
20	chr16:46916956..46921483-chr16:46924468..46930263,8	MCF-7	breast:
21	chr16:46891478..46892076-chr16:46942492..46943005,2	K562	blood:
22	chr16:46887954..46888533-chr16:46963297..46964234,2	MCF-7	breast:
23	chr16:46917956..46920289-chr16:46920497..46924419,3	K562	blood:
24	chr16:46910117..46912387-chr16:46912466..46915411,3	MCF-7	breast:
25	chr16:46722100..46725335-chr16:46890075..46893189,3	K562	blood:
26	chr16:46887627..46888303-chr16:46942315..46943365,3	MCF-7	breast:
27	chr16:46917473..46918075-chr17:77812758..77813708,2	HCT-116	colon:
28	chr16:46926056..46928049-chr16:46934795..46936767,2	K562	blood:
29	chr16:46895641..46897768-chr16:46916063..46918079,2	K562	blood:
30	chr16:46932297..46935211-chr16:46938670..46940478,2	K562	blood:
31	chr16:46706996..46707945-chr16:46942502..46943366,7	K562	blood:
32	chr16:46887576..46888484-chr16:46942484..46943485,11	K562	blood:
33	chr16:46721433..46723160-chr16:46922380..46924051,2	K562	blood:
34	chr16:46910567..46913398-chr16:46926504..46929766,3	MCF-7	breast:
35	chr16:46932297..46935211-chr16:46938670..46940478,2	K562	blood:
36	chr16:46887624..46888459-chr16:46963379..46963903,4	MCF-7	breast:
37	chr16:46887627..46888303-chr16:46942315..46943365,3	MCF-7	breast:
38	chr16:46887422..46888524-chr16:46942474..46943404,10	MCF-7	breast:
39	chr16:46934210..46935361-chr16:46942618..46943358,4	MCF-7	breast:
40	chr16:46892340..46895420-chr16:46933101..46936147,3	MCF-7	breast:
41	chr16:46934210..46935361-chr16:46942618..46943358,4	MCF-7	breast:
42	chr16:46890264..46892011-chr16:46944513..46947246,2	MCF-7	breast:
43	chr16:46951055..46952888-chr16:46955972..46959090,3	K562	blood:
44	chr16:46937070..46939899-chr16:46944886..46947118,2	K562	blood:
45	chr16:46897113..46899445-chr16:46917730..46919526,2	MCF-7	breast:
46	chr16:46899085..46900954-chr16:46906232..46907925,2	MCF-7	breast:
47	chr16:46890264..46892011-chr16:46944513..46947246,2	MCF-7	breast:
48	chr16:46887599..46888547-chr16:47071365..47072310,3	MCF-7	breast:
49	chr16:46933814..46935655-chr16:46950387..46952278,2	MCF-7	breast:
50	chr16:46892340..46895420-chr16:46933101..46936147,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ORC6-5	chr16:46952988-46953903	expRegAs_chr16_5319_+
2	lnc-GPT2-5	chr16:46884911-46885166	NONHSAT142272

No data

Variant related genes	Relation type
GPT2	TF binding region
CKBP1	TF binding region
ENSG00000261725	TF binding region
GPT2	CpG island
CKBP1	CpG island
ENSG00000261725	CpG island
ENSG00000166123	chromatin interactions
ENSG00000140795	chromatin interactions
ENSG00000069329	chromatin interactions
ENSG00000141582	chromatin interactions
ENSG00000260782	chromatin interactions
ENSG00000260889	chromatin interactions
ENSG00000091651	chromatin interactions
ENSG00000261725	chromatin interactions

Extended variants
information (count: 2842 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2842 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539478977	chr16:46873287-46873288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs558106598	chr16:46873315-46873316	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548178233	chr16:46873316-46873317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs538599518	chr16:46873322-46873323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566424992	chr16:46873342-46873343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556943885	chr16:46873350-46873351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533872384	chr16:46873362-46873363	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375325373	chr16:46873389-46873390	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558704284	chr16:46873456-46873457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576993676	chr16:46873498-46873499	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs117664304	chr16:46873569-46873570	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555953823	chr16:46873581-46873582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189564857	chr16:46873669-46873670	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs541799160	chr16:46873740-46873741	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs143191156	chr16:46873756-46873757	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs369136875	chr16:46873764-46873765	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs560238073	chr16:46873814-46873815	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs373391898	chr16:46873832-46873833	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs573569031	chr16:46873891-46873892	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs58355374	chr16:46873911-46873912	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs397801537	chr16:46873917-46873918	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs540596225	chr16:46873955-46873956	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs565594042	chr16:46873987-46873988	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs534878655	chr16:46874071-46874072	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs532562794	chr16:46874089-46874090	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs144560307	chr16:46874122-46874123	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs201466395	chr16:46874131-46874132	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs551160982	chr16:46874143-46874144	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs145855528	chr16:46874174-46874175	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs530177489	chr16:46874175-46874176	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs149016605	chr16:46874217-46874218	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs566563527	chr16:46874227-46874228	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs533817117	chr16:46874239-46874240	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs552162833	chr16:46874423-46874424	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs114491823	chr16:46874428-46874429	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs537603618	chr16:46874437-46874438	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs78550662	chr16:46874527-46874528	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs181832432	chr16:46874531-46874532	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs574583090	chr16:46874534-46874535	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs369239579	chr16:46874541-46874542	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs574733799	chr16:46874548-46874549	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs75408269	chr16:46874571-46874572	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs75797524	chr16:46874600-46874601	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs35338847	chr16:46874623-46874624	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs75145574	chr16:46874665-46874666	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs545496182	chr16:46874669-46874670	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs545798200	chr16:46874675-46874676	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs565398459	chr16:46874729-46874730	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs564067511	chr16:46874776-46874777	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs577466245	chr16:46874786-46874787	Enhancers Weak transcription Flanking Active TSS	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:2422 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:46865600-46878200	Weak transcription	Right Atrium	heart
2	chr16:46873000-46873600	Enhancers	HepG2	liver
3	chr16:46873000-46874800	Enhancers	Liver	Liver
4	chr16:46873600-46874800	Flanking Active TSS	HepG2	liver
5	chr16:46874800-46875400	Enhancers	HepG2	liver
6	chr16:46875400-46880200	Weak transcription	HepG2	liver
7	chr16:46876400-46876600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr16:46876600-46881600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr16:46877600-46878600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr16:46877800-46878000	Enhancers	Primary B cells from cord blood	blood
11	chr16:46877800-46878000	Enhancers	Primary B cells from peripheral blood	blood
12	chr16:46877800-46878000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr16:46877800-46878000	Enhancers	Right Ventricle	heart
14	chr16:46877800-46878000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
15	chr16:46877800-46878000	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
16	chr16:46877800-46878000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
17	chr16:46877800-46878200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
18	chr16:46877800-46878200	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr16:46877800-46878200	ZNF genes & repeats	Spleen	Spleen
20	chr16:46877800-46878600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr16:46878000-46878200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr16:46878000-46878200	Active TSS	Primary neutrophils fromperipheralblood	blood
23	chr16:46878000-46878200	ZNF genes & repeats	Esophagus	oesophagus
24	chr16:46878000-46878200	Bivalent Enhancer	Small Intestine	intestine
25	chr16:46878000-46878200	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
26	chr16:46878000-46878200	Active TSS	Monocytes-CD14+_RO01746	blood
27	chr16:46878000-46878400	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
28	chr16:46878000-46878400	Flanking Active TSS	Primary B cells from peripheral blood	blood
29	chr16:46878000-46878400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr16:46878000-46878400	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr16:46878000-46878400	Active TSS	Colonic Mucosa	Colon
32	chr16:46878000-46878400	Enhancers	Placenta	Placenta
33	chr16:46878000-46878400	Enhancers	Gastric	stomach
34	chr16:46878000-46878400	Flanking Active TSS	Right Ventricle	heart
35	chr16:46878000-46878400	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
36	chr16:46878000-46878600	Flanking Active TSS	Primary B cells from cord blood	blood
37	chr16:46878000-46878600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
38	chr16:46878000-46878600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr16:46878000-46878600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr16:46878000-46878600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr16:46878000-46878600	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr16:46878000-46878600	Bivalent Enhancer	Adipose Nuclei	Adipose
43	chr16:46878000-46878600	Enhancers	Pancreas	Pancrea
44	chr16:46878000-46878800	Bivalent/Poised TSS	Osteobl	bone
45	chr16:46878000-46879000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr16:46878200-46878400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
47	chr16:46878200-46878400	Enhancers	Fetal Heart	heart
48	chr16:46878200-46878400	Enhancers	Right Atrium	heart
49	chr16:46878200-46878400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
50	chr16:46878200-46878400	Enhancers	Spleen	Spleen

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