Variant report

Variant	nsv882201
Chromosome Location	chr5:74787310-74890618
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1634)
CpG islands
(count:1221)
Chromatin interactive
region (count:72)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1634 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:74812604-74812638	K562	blood:	n/a	n/a
2	ARID3A	chr5:74862715-74863894	K562	blood:	n/a	n/a
3	ARID3A	chr5:74814259-74814285	K562	blood:	n/a	n/a
4	ARID3A	chr5:74805985-74806006	K562	blood:	n/a	n/a
5	ARID3A	chr5:74819121-74819443	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:74807447-74807886	HepG2	liver:	n/a	n/a
7	ATF1	chr5:74807363-74807935	K562	blood:	n/a	n/a
8	ATF1	chr5:74862721-74863061	K562	blood:	n/a	n/a
9	ATF1	chr5:74863472-74863878	K562	blood:	n/a	n/a
10	ATF2	chr5:74862440-74863129	GM12878	blood:	n/a	n/a
11	ATF2	chr5:74870688-74871677	GM12878	blood:	n/a	n/a
12	ATF2	chr5:74807091-74808445	GM12878	blood:	n/a	n/a
13	ATF2	chr5:74819875-74820317	GM12878	blood:	n/a	n/a
14	ATF2	chr5:74871087-74871872	GM12878	blood:	n/a	n/a
15	ATF2	chr5:74807353-74807916	GM12878	blood:	n/a	n/a
16	ATF2	chr5:74862437-74863106	GM12878	blood:	n/a	n/a
17	ATF2	chr5:74819795-74820370	GM12878	blood:	n/a	n/a
18	ATF3	chr5:74862524-74863113	K562	blood:	n/a	n/a
19	ATF3	chr5:74807482-74807834	K562	blood:	n/a	n/a
20	ATF3	chr5:74863563-74863848	K562	blood:	n/a	n/a
21	BACH1	chr5:74807586-74808018	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr5:74863648-74863757	K562	blood:	n/a	n/a
23	BACH1	chr5:74889810-74889831	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr5:74862833-74862978	K562	blood:	n/a	chr5:74862884-74862898
25	BATF	chr5:74807602-74807877	GM12878	blood:	n/a	n/a
26	BATF	chr5:74862521-74862990	GM12878	blood:	n/a	n/a
27	BATF	chr5:74819890-74820272	GM12878	blood:	n/a	chr5:74820117-74820127 chr5:74820113-74820123
28	BATF	chr5:74871273-74871606	GM12878	blood:	n/a	n/a
29	BATF	chr5:74862473-74863017	GM12878	blood:	n/a	n/a
30	BATF	chr5:74863505-74863889	GM12878	blood:	n/a	n/a
31	BATF	chr5:74822009-74822205	GM12878	blood:	n/a	n/a
32	BATF	chr5:74864113-74864399	GM12878	blood:	n/a	n/a
33	BATF	chr5:74861931-74862138	GM12878	blood:	n/a	n/a
34	BATF	chr5:74819848-74820276	GM12878	blood:	n/a	chr5:74820117-74820127 chr5:74820113-74820123
35	BATF	chr5:74870977-74871704	GM12878	blood:	n/a	n/a
36	BCL11A	chr5:74862544-74862992	GM12878	blood:	n/a	chr5:74862887-74862896 chr5:74862886-74862895
37	BCL11A	chr5:74862509-74862941	GM12878	blood:	n/a	chr5:74862887-74862896 chr5:74862886-74862895
38	BCL11A	chr5:74819918-74820233	GM12878	blood:	n/a	n/a
39	BCL11A	chr5:74884618-74884817	H1-hESC	embryonic stem cell:	n/a	n/a
40	BCL11A	chr5:74871314-74871654	GM12878	blood:	n/a	chr5:74871486-74871495
41	BCL11A	chr5:74871169-74871684	GM12878	blood:	n/a	chr5:74871486-74871495
42	BCL11A	chr5:74884546-74884904	H1-hESC	embryonic stem cell:	n/a	n/a
43	BCL3	chr5:74807483-74807937	A549	lung:	n/a	n/a
44	BCL3	chr5:74871391-74871690	GM12878	blood:	n/a	chr5:74871486-74871495
45	BCL3	chr5:74807328-74807983	A549	lung:	n/a	chr5:74807373-74807382
46	BCL3	chr5:74861720-74862261	A549	lung:	n/a	n/a
47	BCL3	chr5:74862507-74863055	GM12878	blood:	n/a	chr5:74862887-74862896 chr5:74862886-74862895
48	BCL3	chr5:74862468-74863147	A549	lung:	n/a	chr5:74862887-74862896 chr5:74862886-74862895
49	BCLAF1	chr5:74862535-74862970	GM12878	blood:	n/a	chr5:74862887-74862896 chr5:74862886-74862895
50	BCLAF1	chr5:74870858-74871622	GM12878	blood:	n/a	chr5:74871486-74871495

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:74807829-74807879	SK-N-SH_RA	brain:	n/a
2	chr5:74807829-74807879	SK-N-SH_RA	brain:	n/a
3	chr5:74807937-74807987	SK-N-SH_RA	brain:	n/a
4	chr5:74862702-74862752	HRPEpiC	eye:	n/a
5	chr5:74806661-74806711	AG04449	skin:	fetal
6	chr5:74798138-74798188	NHDF-neo	bronchial:	n/a
7	chr5:74811445-74811495	HIPEpiC	eye:	n/a
8	chr5:74807937-74807987	Caco-2	colon:	n/a
9	chr5:74807973-74808023	NT2-D1	testis:	n/a
10	chr5:74808293-74808343	Hepatocyte	liver:	n/a
11	chr5:74807308-74807358	SAEC	small airway:	n/a
12	chr5:74807829-74807879	SK-N-SH	brain:	n/a
13	chr5:74807535-74807585	Hela-S3	cervix:	n/a
14	chr5:74807542-74807592	HIPEpiC	eye:	n/a
15	chr5:74807689-74807739	HCF	heart:	n/a
16	chr5:74807829-74807879	PFSK-1	brain:	n/a
17	chr5:74806504-74806554	SK-N-SH	brain:	n/a
18	chr5:74833385-74833435	Hepatocyte	liver:	n/a
19	chr5:74807829-74807879	PrEC	prostate:	n/a
20	chr5:74811445-74811495	AG04450	lung:	fetal
21	chr5:74807689-74807739	K562	blood:	n/a
22	chr5:74807829-74807879	NH-A	brain:	n/a
23	chr5:74806504-74806554	ProgFib	skin:	n/a
24	chr5:74798138-74798188	HEEpiC	esophagus:	n/a
25	chr5:74807973-74808023	Caco-2	colon:	n/a
26	chr5:74807829-74807879	NHDF-neo	bronchial:	n/a
27	chr5:74806951-74807001	ovcar-3	ovarian:	n/a
28	chr5:74807542-74807592	ovcar-3	ovarian:	n/a
29	chr5:74806504-74806554	HRPEpiC	eye:	n/a
30	chr5:74808039-74808089	GM12892	blood:	n/a
31	chr5:74807829-74807879	HAEpiC	amniotic membrane:	n/a
32	chr5:74808039-74808089	BJ	skin:	n/a
33	chr5:74807882-74807932	Jurkat	blood:	n/a
34	chr5:74807882-74807932	HPAEpiC	pulmonary alveolar:	n/a
35	chr5:74807308-74807358	PrEC	prostate:	n/a
36	chr5:74798138-74798188	RPTEC	kidney:	n/a
37	chr5:74807689-74807739	SK-N-SH	brain:	n/a
38	chr5:74807937-74807987	ECC-1	luminal epithelium:	n/a
39	chr5:74833385-74833435	Caco-2	colon:	n/a
40	chr5:74807973-74808023	HIPEpiC	eye:	n/a
41	chr5:74798138-74798188	AG09319	gingival:	n/a
42	chr5:74807907-74807957	SK-N-MC	brain:	n/a
43	chr5:74811445-74811495	AG09309	skin:	n/a
44	chr5:74807542-74807592	PFSK-1	brain:	n/a
45	chr5:74807829-74807879	GM19239	blood:	n/a
46	chr5:74807973-74808023	PANC-1	pancreas:	n/a
47	chr5:74798138-74798188	NB4	blood:	n/a
48	chr5:74807689-74807739	SKMC	muscle:	n/a
49	chr5:74807815-74807865	HUVEC	blood vessel:	n/a
50	chr5:74807937-74807987	HRCEpiC	kidney:	n/a

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:74880212..74881196-chr5:74962425..74963375,4	MCF-7	breast:
2	chr5:74757814..74760336-chr5:74803800..74805741,2	MCF-7	breast:
3	chr5:74804574..74807080-chr5:74963425..74964973,2	K562	blood:
4	chr5:74863361..74865877-chr5:74866045..74867591,2	MCF-7	breast:
5	chr5:74852680..74855218-chr5:74864113..74866476,2	K562	blood:
6	chr5:74820287..74822535-chr5:74827846..74830107,2	K562	blood:
7	chr12:57881788..57882314-chr5:74806957..74807584,2	NB4	blood:
8	chr5:74880501..74881472-chr5:74976763..74977639,2	MCF-7	breast:
9	chr5:74885603..74887138-chr5:74892522..74895230,2	K562	blood:
10	chr5:74793165..74795664-chr5:74814824..74817209,2	K562	blood:
11	chr5:74808217..74810593-chr5:74816041..74817596,2	K562	blood:
12	chr5:74773320..74775283-chr5:74785477..74788278,2	K562	blood:
13	chr5:74735651..74738520-chr5:74798535..74800607,2	K562	blood:
14	chr5:74811981..74814673-chr5:74874113..74876597,2	K562	blood:
15	chr5:74840733..74842326-chr5:74845611..74848333,2	K562	blood:
16	chr5:74835008..74837584-chr5:74853567..74856265,2	K562	blood:
17	chr5:74880200..74881111-chr5:74976869..74977697,3	MCF-7	breast:
18	chr5:74790647..74794380-chr5:74795733..74800125,4	K562	blood:
19	chr5:74811101..74813110-chr5:74815287..74817345,2	K562	blood:
20	chr5:74786766..74788653-chr5:74965428..74967574,2	K562	blood:
21	chr5:74808667..74810597-chr5:74818060..74820048,3	K562	blood:
22	chr5:74868580..74871320-chr5:74902166..74903871,2	MCF-7	breast:
23	chr5:74839175..74841677-chr5:74843205..74845206,2	K562	blood:
24	chr5:74819271..74821743-chr5:74831867..74834038,2	MCF-7	breast:
25	chr5:74828971..74830534-chr5:74850595..74852572,2	K562	blood:
26	chr5:74845037..74847535-chr5:74848930..74850561,2	K562	blood:
27	chr5:74839175..74841677-chr5:74843205..74845206,2	K562	blood:
28	chr5:74789576..74794585-chr5:74804962..74807794,4	MCF-7	breast:
29	chr5:74796618..74799716-chr5:74800501..74803148,3	K562	blood:
30	chr5:74790647..74794380-chr5:74795733..74800125,4	K562	blood:
31	chr5:74805731..74808646-chr5:74817149..74819644,4	MCF-7	breast:
32	chr5:74818089..74820423-chr5:74844136..74846157,2	MCF-7	breast:
33	chr5:74799687..74804684-chr5:74805759..74808184,7	MCF-7	breast:
34	chr5:74631501..74634174-chr5:74801829..74803875,2	K562	blood:
35	chr5:74805305..74807843-chr5:74822655..74824255,2	MCF-7	breast:
36	chr5:74881366..74883122-chr5:74885074..74886574,2	K562	blood:
37	chr5:74871511..74873926-chr5:75008368..75010666,2	K562	blood:
38	chr5:74820287..74822535-chr5:74827846..74830107,2	K562	blood:
39	chr5:74815294..74818982-chr5:74820247..74823584,4	K562	blood:
40	chr5:74808667..74810597-chr5:74818060..74820048,3	K562	blood:
41	chr5:74808217..74810593-chr5:74816041..74817596,2	K562	blood:
42	chr5:74796488..74799637-chr5:74801966..74804118,4	MCF-7	breast:
43	chr5:74815294..74818982-chr5:74820247..74823584,4	K562	blood:
44	chr5:74863361..74865877-chr5:74866045..74867591,2	MCF-7	breast:
45	chr5:74630713..74633733-chr5:74805590..74808087,5	MCF-7	breast:
46	chr5:74845037..74847535-chr5:74848930..74850561,2	K562	blood:
47	chr5:74828971..74830534-chr5:74850595..74852572,2	K562	blood:
48	chr5:74806414..74809041-chr5:74824381..74827349,2	K562	blood:
49	chr5:74796642..74799069-chr5:75014421..75017256,2	K562	blood:
50	chr5:74818089..74820423-chr5:74844136..74846157,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	POLK	hsa-miR-30c-5p	chr5:74877682-74877705
2	POLK	hsa-miR-132-3p	chr5:74878186-74878207

Variant related genes	Relation type
POLK	TF binding region
COL4A3BP	TF binding region
RNU7-175P	TF binding region
POLK	CpG island
COL4A3BP	CpG island
RNU7-175P	CpG island
ENSG00000152359	chromatin interactions
ENSG00000248881	chromatin interactions
ENSG00000189159	chromatin interactions
ENSG00000113161	chromatin interactions
ENSG00000122008	chromatin interactions
ENSG00000166986	chromatin interactions
ENSG00000132680	chromatin interactions
ENSG00000113163	chromatin interactions
ENSG00000189045	chromatin interactions
ENSG00000247372	chromatin interactions

Extended variants
information (count: 3619 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:3619 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6896136	chr5:74787310-74787311	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs75922028	chr5:74787324-74787325	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs113977857	chr5:74787338-74787339	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs370383725	chr5:74787346-74787347	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs529546226	chr5:74787366-74787367	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs189818780	chr5:74787396-74787397	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs561553718	chr5:74787405-74787406	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147387298	chr5:74787459-74787460	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs139534797	chr5:74787481-74787482	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs145101334	chr5:74787492-74787493	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532998002	chr5:74787517-74787518	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs549546978	chr5:74787527-74787528	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs543492194	chr5:74787558-74787559	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs144900944	chr5:74787589-74787590	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs28612248	chr5:74787620-74787621	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs148601372	chr5:74787640-74787641	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs565948462	chr5:74787656-74787657	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs534970620	chr5:74787717-74787718	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs181600233	chr5:74787730-74787731	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs578138521	chr5:74787736-74787737	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs184811834	chr5:74787845-74787846	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs557569038	chr5:74787926-74787927	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs371378262	chr5:74787980-74787981	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs541948367	chr5:74788009-74788010	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs189536267	chr5:74788012-74788013	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs182036877	chr5:74788029-74788030	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs71627100	chr5:74788035-74788036	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs185874133	chr5:74788059-74788060	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs527339895	chr5:74788107-74788108	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs375309952	chr5:74788116-74788117	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs189648622	chr5:74788122-74788123	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs181247671	chr5:74788160-74788161	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs186596638	chr5:74788166-74788167	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs549436301	chr5:74788177-74788178	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs79567260	chr5:74788259-74788260	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs151221622	chr5:74788267-74788268	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs190315971	chr5:74788300-74788301	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs140363965	chr5:74788311-74788312	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs535059890	chr5:74788319-74788320	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs551785757	chr5:74788354-74788355	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs555546788	chr5:74788377-74788378	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs4640773	chr5:74788403-74788404	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs182936437	chr5:74788425-74788426	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs185998833	chr5:74788438-74788439	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs541053859	chr5:74788503-74788504	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs117196531	chr5:74788517-74788518	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs536810388	chr5:74788525-74788526	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs200867615	chr5:74788533-74788534	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs183263164	chr5:74788537-74788538	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs188138750	chr5:74788569-74788570	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	22355333	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:3244 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74732000-74787400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr5:74742400-74794200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr5:74760400-74792200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr5:74762200-74805800	Weak transcription	Pancreas	Pancrea
5	chr5:74763200-74787400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr5:74764800-74798600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr5:74765200-74795400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr5:74765200-74804600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr5:74769200-74794000	Weak transcription	Fetal Thymus	thymus
10	chr5:74769400-74794800	Weak transcription	Stomach Mucosa	stomach
11	chr5:74770400-74805200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr5:74771800-74794200	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr5:74773200-74787800	Weak transcription	Ovary	ovary
14	chr5:74775200-74804000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr5:74777000-74794200	Weak transcription	Dnd41	blood
16	chr5:74777200-74787400	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr5:74777400-74797800	Weak transcription	Colonic Mucosa	Colon
18	chr5:74778600-74787600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr5:74778600-74787600	Weak transcription	Lung	lung
20	chr5:74778600-74794200	Weak transcription	Right Ventricle	heart
21	chr5:74778600-74796800	Weak transcription	Esophagus	oesophagus
22	chr5:74778600-74806400	Weak transcription	Gastric	stomach
23	chr5:74778800-74805400	Weak transcription	HMEC	breast
24	chr5:74779000-74804200	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr5:74782200-74795400	Weak transcription	HSMM	muscle
26	chr5:74782600-74805400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr5:74783000-74803000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr5:74783600-74793800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr5:74784000-74787400	Weak transcription	HepG2	liver
30	chr5:74784000-74795400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr5:74784000-74803200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr5:74785200-74792600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr5:74785200-74803800	Weak transcription	Brain Cingulate Gyrus	brain
34	chr5:74785400-74787400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr5:74785400-74794400	Weak transcription	Stomach Smooth Muscle	stomach
36	chr5:74785400-74799000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr5:74785600-74787400	Weak transcription	NHEK	skin
38	chr5:74785600-74788200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr5:74785600-74788400	ZNF genes & repeats	Fetal Lung	lung
40	chr5:74785800-74787400	Weak transcription	Osteobl	bone
41	chr5:74785800-74787800	Strong transcription	Rectal Mucosa Donor 29	rectum
42	chr5:74785800-74788200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr5:74785800-74788400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
44	chr5:74785800-74788600	Strong transcription	Skeletal Muscle Female	skeletal muscle
45	chr5:74785800-74788600	ZNF genes & repeats	GM12878-XiMat	blood
46	chr5:74785800-74805200	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr5:74785800-74806400	Weak transcription	Spleen	Spleen
48	chr5:74786000-74788000	Strong transcription	Liver	Liver
49	chr5:74786000-74788000	Weak transcription	NHDF-Ad	bronchial
50	chr5:74786000-74788200	Strong transcription	Fetal Stomach	stomach

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