Variant report

Variant	nsv882197
Chromosome Location	chr5:74692776-74946455
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2666)
CpG islands
(count:2199)
Chromatin interactive
region (count:121)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2666 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:74734777-74734829	K562	blood:	n/a	n/a
2	ARID3A	chr5:74862715-74863894	K562	blood:	n/a	n/a
3	ARID3A	chr5:74701386-74701433	K562	blood:	n/a	n/a
4	ARID3A	chr5:74814259-74814285	K562	blood:	n/a	n/a
5	ARID3A	chr5:74906446-74906556	K562	blood:	n/a	n/a
6	ARID3A	chr5:74807447-74807886	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:74805985-74806006	K562	blood:	n/a	n/a
8	ARID3A	chr5:74912064-74912380	K562	blood:	n/a	n/a
9	ARID3A	chr5:74812604-74812638	K562	blood:	n/a	n/a
10	ARID3A	chr5:74904794-74905021	K562	blood:	n/a	n/a
11	ARID3A	chr5:74819121-74819443	HepG2	liver:	n/a	n/a
12	ARID3A	chr5:74916424-74916742	HepG2	liver:	n/a	n/a
13	ARID3A	chr5:74913152-74913154	K562	blood:	n/a	n/a
14	ARID3A	chr5:74915925-74916471	K562	blood:	n/a	n/a
15	ARID3A	chr5:74903955-74904149	K562	blood:	n/a	n/a
16	ATF1	chr5:74807363-74807935	K562	blood:	n/a	n/a
17	ATF1	chr5:74863472-74863878	K562	blood:	n/a	n/a
18	ATF1	chr5:74862721-74863061	K562	blood:	n/a	n/a
19	ATF1	chr5:74769475-74769581	K562	blood:	n/a	n/a
20	ATF1	chr5:74912163-74912344	K562	blood:	n/a	n/a
21	ATF2	chr5:74819875-74820317	GM12878	blood:	n/a	n/a
22	ATF2	chr5:74871087-74871872	GM12878	blood:	n/a	n/a
23	ATF2	chr5:74807091-74808445	GM12878	blood:	n/a	n/a
24	ATF2	chr5:74807353-74807916	GM12878	blood:	n/a	n/a
25	ATF2	chr5:74944406-74945026	GM12878	blood:	n/a	n/a
26	ATF2	chr5:74870688-74871677	GM12878	blood:	n/a	n/a
27	ATF2	chr5:74862440-74863129	GM12878	blood:	n/a	n/a
28	ATF2	chr5:74862437-74863106	GM12878	blood:	n/a	n/a
29	ATF2	chr5:74819795-74820370	GM12878	blood:	n/a	n/a
30	ATF3	chr5:74862524-74863113	K562	blood:	n/a	n/a
31	ATF3	chr5:74863563-74863848	K562	blood:	n/a	n/a
32	ATF3	chr5:74807482-74807834	K562	blood:	n/a	n/a
33	ATF3	chr5:74944630-74944858	K562	blood:	n/a	n/a
34	BACH1	chr5:74889810-74889831	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr5:74907812-74907884	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr5:74807586-74808018	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr5:74863648-74863757	K562	blood:	n/a	n/a
38	BACH1	chr5:74862833-74862978	K562	blood:	n/a	chr5:74862884-74862898
39	BATF	chr5:74861931-74862138	GM12878	blood:	n/a	n/a
40	BATF	chr5:74862473-74863017	GM12878	blood:	n/a	n/a
41	BATF	chr5:74862521-74862990	GM12878	blood:	n/a	n/a
42	BATF	chr5:74769789-74770085	GM12878	blood:	n/a	n/a
43	BATF	chr5:74870977-74871704	GM12878	blood:	n/a	n/a
44	BATF	chr5:74807602-74807877	GM12878	blood:	n/a	n/a
45	BATF	chr5:74871273-74871606	GM12878	blood:	n/a	n/a
46	BATF	chr5:74944597-74944931	GM12878	blood:	n/a	chr5:74944774-74944785 chr5:74944775-74944785
47	BATF	chr5:74776944-74777150	GM12878	blood:	n/a	chr5:74777074-74777085
48	BATF	chr5:74819848-74820276	GM12878	blood:	n/a	chr5:74820117-74820127 chr5:74820113-74820123
49	BATF	chr5:74822009-74822205	GM12878	blood:	n/a	n/a
50	BATF	chr5:74864113-74864399	GM12878	blood:	n/a	n/a

(count:2199 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:74807907-74807957	GM06990	blood:	n/a
2	chr5:74908170-74908220	SK-N-MC	brain:	n/a
3	chr5:74811445-74811495	HRPEpiC	eye:	n/a
4	chr5:74807907-74807957	GM06990	blood:	n/a
5	chr5:74908170-74908220	SK-N-MC	brain:	n/a
6	chr5:74811445-74811495	HRPEpiC	eye:	n/a
7	chr5:74910129-74910179	T-47D	breast:	n/a
8	chr5:74762295-74762345	HUVEC	blood vessel:	n/a
9	chr5:74811445-74811495	HNPCEpiC	eye:	n/a
10	chr5:74807882-74807932	K562	blood:	n/a
11	chr5:74862702-74862752	BJ	skin:	n/a
12	chr5:74907694-74907744	U87	brain:	n/a
13	chr5:74898460-74898510	MCF10A-Er-Src	breast:	n/a
14	chr5:74862702-74862752	HepG2	liver:	n/a
15	chr5:74807308-74807358	NT2-D1	testis:	n/a
16	chr5:74807973-74808023	HCPEpiC	choroid plexus:	n/a
17	chr5:74806951-74807001	SAEC	small airway:	n/a
18	chr5:74798138-74798188	U87	brain:	n/a
19	chr5:74907124-74907174	HRE	kidney:	n/a
20	chr5:74807308-74807358	HIPEpiC	eye:	n/a
21	chr5:74806951-74807001	HepG2	liver:	n/a
22	chr5:74913041-74913091	NH-A	brain:	n/a
23	chr5:74862702-74862752	PFSK-1	brain:	n/a
24	chr5:74908125-74908175	ovcar-3	ovarian:	n/a
25	chr5:74807829-74807879	LNCaP	prostate:	n/a
26	chr5:74913041-74913091	RPTEC	kidney:	n/a
27	chr5:74806504-74806554	GM12878	blood:	n/a
28	chr5:74808051-74808101	HMEC	breast:	n/a
29	chr5:74707372-74707422	NHBE	bronchial:	n/a
30	chr5:74907694-74907744	Hela-S3	cervix:	n/a
31	chr5:74808293-74808343	HPAEpiC	pulmonary alveolar:	n/a
32	chr5:74808051-74808101	LNCaP	prostate:	n/a
33	chr5:74811445-74811495	NHBE	bronchial:	n/a
34	chr5:74807815-74807865	LNCaP	prostate:	n/a
35	chr5:74862702-74862752	SK-N-SH	brain:	n/a
36	chr5:74807973-74808023	HAEpiC	amniotic membrane:	n/a
37	chr5:74772303-74772353	AG09319	gingival:	n/a
38	chr5:74908125-74908175	HCM	heart:	n/a
39	chr5:74807542-74807592	SK-N-MC	brain:	n/a
40	chr5:74907592-74907642	HepG2	liver:	n/a
41	chr5:74798138-74798188	HepG2	liver:	n/a
42	chr5:74806661-74806711	Jurkat	blood:	n/a
43	chr5:74807542-74807592	HCF	heart:	n/a
44	chr5:74908170-74908220	HCT-116	colon:	n/a
45	chr5:74913041-74913091	Hepatocyte	liver:	n/a
46	chr5:74908170-74908220	MCF10A-Er-Src	breast:	n/a
47	chr5:74833385-74833435	AoSMC	blood vessel:	n/a
48	chr5:74907592-74907642	PANC-1	pancreas:	n/a
49	chr5:74907287-74907337	AoSMC	blood vessel:	n/a
50	chr5:74833385-74833435	HCT-116	colon:	n/a

(count:121 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:74889870..74892388-chr5:74899059..74901805,3	K562	blood:
2	chr5:74889934..74892388-chr5:74899059..74901805,2	K562	blood:
3	chr5:74770863..74773429-chr5:74777117..74779848,3	MCF-7	breast:
4	chr5:74915137..74917681-chr5:74948612..74950531,2	K562	blood:
5	chr5:74806025..74808781-chr5:74906137..74908952,2	MCF-7	breast:
6	chr5:74804046..74805995-chr5:74976601..74978123,2	K562	blood:
7	chr5:74868580..74871320-chr5:74902166..74903871,2	MCF-7	breast:
8	chr5:74756440..74758113-chr5:75010084..75012046,2	K562	blood:
9	chr5:74722161..74724280-chr5:74725505..74728463,2	K562	blood:
10	chr5:74735651..74738520-chr5:74798535..74800607,2	K562	blood:
11	chr5:74728841..74731298-chr5:74732916..74734821,2	MCF-7	breast:
12	chr5:74801840..74804392-chr5:74804791..74808072,5	K562	blood:
13	chr1:155904008..155904889-chr5:74806958..74807496,2	Hela-S3	cervix:
14	chr5:74880212..74881196-chr5:74962425..74963375,4	MCF-7	breast:
15	chr5:74735651..74738520-chr5:74798535..74800607,2	K562	blood:
16	chr5:74840733..74842326-chr5:74845611..74848333,2	K562	blood:
17	chr5:74757814..74760336-chr5:74803800..74805741,2	MCF-7	breast:
18	chr5:74885603..74887138-chr5:74892522..74895230,2	K562	blood:
19	chr5:74932832..74935591-chr5:74937414..74939380,2	MCF-7	breast:
20	chr5:74815294..74818982-chr5:74820247..74823584,4	K562	blood:
21	chr5:74805305..74807843-chr5:74822655..74824255,2	MCF-7	breast:
22	chr5:74770863..74773429-chr5:74777117..74779848,3	MCF-7	breast:
23	chr5:74880080..74881244-chr5:74962362..74964218,14	MCF-7	breast:
24	chr5:74796618..74799716-chr5:74800501..74803148,3	K562	blood:
25	chr5:74773320..74775283-chr5:74785477..74788278,2	K562	blood:
26	chr5:74753229..74754839-chr5:74755148..74758107,2	K562	blood:
27	chr10:15412992..15413653-chr5:74896234..74896879,2	MCF-7	breast:
28	chr3:167116749..167117659-chr5:74876077..74876717,2	MCF-7	breast:
29	chr5:74863361..74865877-chr5:74866045..74867591,2	MCF-7	breast:
30	chr5:74793165..74795664-chr5:74814824..74817209,2	K562	blood:
31	chr5:74805731..74808646-chr5:74817149..74819644,4	MCF-7	breast:
32	chr5:74819271..74821743-chr5:74831867..74834038,2	MCF-7	breast:
33	chr5:74775852..74778323-chr5:74787473..74789396,2	K562	blood:
34	chr5:74805960..74807609-chr5:74862131..74863821,2	K562	blood:
35	chr5:74835008..74837584-chr5:74853567..74856265,2	K562	blood:
36	chr5:74808667..74810597-chr5:74818060..74820048,3	K562	blood:
37	chr5:74828971..74830534-chr5:74850595..74852572,2	K562	blood:
38	chr5:74717369..74719270-chr5:74723978..74725689,2	K562	blood:
39	chr5:74773320..74775283-chr5:74785477..74788278,2	K562	blood:
40	chr5:74871511..74873926-chr5:75008368..75010666,2	K562	blood:
41	chr5:74796488..74799637-chr5:74801966..74804118,4	MCF-7	breast:
42	chr5:74811981..74814673-chr5:74874113..74876597,2	K562	blood:
43	chr5:74835008..74837584-chr5:74853567..74856265,2	K562	blood:
44	chr5:74786766..74788653-chr5:74965428..74967574,2	K562	blood:
45	chr5:74806025..74808781-chr5:74906137..74908952,2	MCF-7	breast:
46	chr5:74905446..74908420-chr5:74909324..74911813,2	MCF-7	breast:
47	chr5:74711691..74714209-chr5:74716587..74718777,2	K562	blood:
48	chr5:74757814..74760336-chr5:74803800..74805741,2	MCF-7	breast:
49	chr5:74932832..74935591-chr5:74937414..74939380,2	MCF-7	breast:
50	chr5:74912858..74914560-chr5:74917246..74919606,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POC5-4	chr5:74907076-74907508	NONHSAT102214
2	lnc-POC5-1	chr5:74894307-74894806	ENSG00000248881.1
3	lnc-ANKDD1B-3	chr5:74893242-74893614	NONHSAT102210
4	lnc-POC5-1	chr5:74894952-74895205	ENSG00000248881.1
5	lnc-ANKDD1B-3	chr5:74892939-74893003	NONHSAT102209
6	lnc-ANKDD1B-3	chr5:74893759-74893813	NONHSAT102210
7	lnc-ANKDD1B-1	chr5:74902446-74902775	XLOC_004431
8	lnc-POLK-1	chr5:74931137-74931707	NONHSAT102215
9	lnc-ANKDD1B-4	chr5:74943057-74943408	ucscGeneNc_uc010izt_1
10	lnc-ANKDD1B-3	chr5:74893572-74893865	NONHSAT102209
11	lnc-ANKDD1B-2	chr5:74904642-74905808	ENSG00000272040.1
12	lnc-POC5-4	chr5:74907701-74908056	NONHSAT102214
13	lnc-ANKDD1B-1	chr5:74906143-74906582	XLOC_004431

No data

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

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

Variant related genes	Relation type
POLK	TF binding region
ENSG00000272040	TF binding region
COL4A3BP	TF binding region
ANKDD1B	TF binding region
ENSG00000248881	TF binding region
RNU7-175P	TF binding region
POLK	CpG island
ENSG00000272040	CpG island
COL4A3BP	CpG island
ANKDD1B	CpG island
ENSG00000248881	CpG island
RNU7-175P	CpG island
ENSG00000189045	chromatin interactions
ENSG00000113163	chromatin interactions
ENSG00000189159	chromatin interactions
ENSG00000248881	chromatin interactions
ENSG00000148468	chromatin interactions
ENSG00000152359	chromatin interactions
ENSG00000122008	chromatin interactions
ENSG00000247372	chromatin interactions
ENSG00000113161	chromatin interactions
ENSG00000132680	chromatin interactions
ENSG00000166986	chromatin interactions

Extended variants
information (count: 9031 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:9031 , 50 per page) page: 1 2 3 4 5 6 7 ... 181

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6453133	chr5:74692776-74692777	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs114253542	chr5:74692810-74692811	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs538261866	chr5:74692888-74692889	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182012623	chr5:74692902-74692903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537587156	chr5:74692936-74692937	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568875813	chr5:74692987-74692988	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537919363	chr5:74692988-74692989	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs543192984	chr5:74693002-74693003	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs149128547	chr5:74693048-74693049	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186292788	chr5:74693160-74693161	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559838709	chr5:74693196-74693197	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2739108	chr5:74693197-74693198	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs116409442	chr5:74693208-74693209	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs143397100	chr5:74693209-74693210	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577018380	chr5:74693285-74693286	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545884464	chr5:74693287-74693288	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs114154597	chr5:74693299-74693300	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576480455	chr5:74693397-74693398	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs111984786	chr5:74693420-74693421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191123968	chr5:74693421-74693422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs141549057	chr5:74693438-74693439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541594125	chr5:74693444-74693445	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564779192	chr5:74693453-74693454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182139640	chr5:74693467-74693468	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551909383	chr5:74693472-74693473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185248101	chr5:74693481-74693482	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs13354109	chr5:74693546-74693547	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs547922051	chr5:74693559-74693560	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567811502	chr5:74693560-74693561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533741412	chr5:74693611-74693612	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191137789	chr5:74693628-74693629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569751976	chr5:74693646-74693647	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570668746	chr5:74693679-74693680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs373045750	chr5:74693696-74693697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539689828	chr5:74693714-74693715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567450427	chr5:74693744-74693745	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556160316	chr5:74693757-74693758	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376575641	chr5:74693839-74693840	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375650246	chr5:74693864-74693865	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542243910	chr5:74693894-74693895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182984282	chr5:74693912-74693913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373969230	chr5:74693992-74693993	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188413147	chr5:74694027-74694028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541660826	chr5:74694045-74694046	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571209260	chr5:74694060-74694061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564675296	chr5:74694091-74694092	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373714924	chr5:74694128-74694129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549157710	chr5:74694149-74694150	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377572730	chr5:74694182-74694183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115126105	chr5:74694257-74694258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Pancreatic cancer	17952125	CNVD
Obesity	20935630	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:6259 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74656400-74725600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr5:74656600-74694800	Weak transcription	Brain Angular Gyrus	brain
3	chr5:74656800-74731400	Weak transcription	Rectal Smooth Muscle	rectum
4	chr5:74657800-74708000	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr5:74659800-74720600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr5:74660000-74722800	Weak transcription	Fetal Heart	heart
7	chr5:74660200-74707800	Weak transcription	Stomach Mucosa	stomach
8	chr5:74665000-74703000	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr5:74667000-74723200	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr5:74667200-74693600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr5:74670800-74709400	Weak transcription	Pancreas	Pancrea
12	chr5:74670800-74720600	Weak transcription	Right Ventricle	heart
13	chr5:74670800-74731400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr5:74671000-74722800	Weak transcription	Hela-S3	cervix
15	chr5:74674400-74761400	Weak transcription	Esophagus	oesophagus
16	chr5:74675400-74694800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr5:74675400-74699600	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr5:74675400-74720800	Weak transcription	Small Intestine	intestine
19	chr5:74676200-74695000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr5:74676200-74721000	Weak transcription	Brain Hippocampus Middle	brain
21	chr5:74677000-74701000	Weak transcription	A549	lung
22	chr5:74677400-74722800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr5:74677600-74693600	Weak transcription	Colon Smooth Muscle	Colon
24	chr5:74677600-74709200	Weak transcription	Gastric	stomach
25	chr5:74677600-74734200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr5:74677800-74694800	Weak transcription	Fetal Kidney	kidney
27	chr5:74677800-74695200	Weak transcription	Brain Anterior Caudate	brain
28	chr5:74677800-74721000	Weak transcription	NH-A	brain
29	chr5:74677800-74725000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr5:74677800-74731400	Weak transcription	Aorta	Aorta
31	chr5:74678000-74708000	Weak transcription	NHLF	lung
32	chr5:74678000-74720600	Weak transcription	Colonic Mucosa	Colon
33	chr5:74678000-74730800	Weak transcription	Psoas Muscle	Psoas
34	chr5:74680600-74721000	Weak transcription	HMEC	breast
35	chr5:74680800-74694800	Weak transcription	Stomach Smooth Muscle	stomach
36	chr5:74680800-74722600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr5:74681000-74723200	Weak transcription	HUVEC	blood vessel
38	chr5:74681400-74694800	Weak transcription	Placenta	Placenta
39	chr5:74681400-74718400	Weak transcription	Brain Germinal Matrix	brain
40	chr5:74681600-74694800	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr5:74681600-74695000	Weak transcription	Brain Substantia Nigra	brain
42	chr5:74681800-74720600	Weak transcription	Fetal Brain Male	brain
43	chr5:74682000-74695000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr5:74682000-74699000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr5:74682000-74708000	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr5:74682200-74694200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr5:74682200-74705000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr5:74683200-74698600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr5:74683800-74695000	Weak transcription	Fetal Brain Female	brain
50	chr5:74684000-74693200	Weak transcription	Brain Cingulate Gyrus	brain

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