Variant report

Variant	nsv882195
Chromosome Location	chr5:74678937-74896798
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2256)
CpG islands
(count:1467)
Chromatin interactive
region (count:99)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2256 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:74814259-74814285	K562	blood:	n/a	n/a
2	ARID3A	chr5:74805985-74806006	K562	blood:	n/a	n/a
3	ARID3A	chr5:74701386-74701433	K562	blood:	n/a	n/a
4	ARID3A	chr5:74862715-74863894	K562	blood:	n/a	n/a
5	ARID3A	chr5:74812604-74812638	K562	blood:	n/a	n/a
6	ARID3A	chr5:74734777-74734829	K562	blood:	n/a	n/a
7	ARID3A	chr5:74819121-74819443	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:74807447-74807886	HepG2	liver:	n/a	n/a
9	ATF1	chr5:74807363-74807935	K562	blood:	n/a	n/a
10	ATF1	chr5:74863472-74863878	K562	blood:	n/a	n/a
11	ATF1	chr5:74862721-74863061	K562	blood:	n/a	n/a
12	ATF1	chr5:74769475-74769581	K562	blood:	n/a	n/a
13	ATF2	chr5:74862437-74863106	GM12878	blood:	n/a	n/a
14	ATF2	chr5:74871087-74871872	GM12878	blood:	n/a	n/a
15	ATF2	chr5:74819795-74820370	GM12878	blood:	n/a	n/a
16	ATF2	chr5:74819875-74820317	GM12878	blood:	n/a	n/a
17	ATF2	chr5:74862440-74863129	GM12878	blood:	n/a	n/a
18	ATF2	chr5:74807091-74808445	GM12878	blood:	n/a	n/a
19	ATF2	chr5:74870688-74871677	GM12878	blood:	n/a	n/a
20	ATF2	chr5:74807353-74807916	GM12878	blood:	n/a	n/a
21	ATF3	chr5:74862524-74863113	K562	blood:	n/a	n/a
22	ATF3	chr5:74863563-74863848	K562	blood:	n/a	n/a
23	ATF3	chr5:74807482-74807834	K562	blood:	n/a	n/a
24	BACH1	chr5:74862833-74862978	K562	blood:	n/a	chr5:74862884-74862898
25	BACH1	chr5:74807586-74808018	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr5:74863648-74863757	K562	blood:	n/a	n/a
27	BACH1	chr5:74889810-74889831	H1-hESC	embryonic stem cell:	n/a	n/a
28	BATF	chr5:74819848-74820276	GM12878	blood:	n/a	chr5:74820117-74820127 chr5:74820113-74820123
29	BATF	chr5:74862521-74862990	GM12878	blood:	n/a	n/a
30	BATF	chr5:74822009-74822205	GM12878	blood:	n/a	n/a
31	BATF	chr5:74861931-74862138	GM12878	blood:	n/a	n/a
32	BATF	chr5:74870977-74871704	GM12878	blood:	n/a	n/a
33	BATF	chr5:74769789-74770085	GM12878	blood:	n/a	n/a
34	BATF	chr5:74863505-74863889	GM12878	blood:	n/a	n/a
35	BATF	chr5:74862473-74863017	GM12878	blood:	n/a	n/a
36	BATF	chr5:74864113-74864399	GM12878	blood:	n/a	n/a
37	BATF	chr5:74807602-74807877	GM12878	blood:	n/a	n/a
38	BATF	chr5:74776944-74777150	GM12878	blood:	n/a	chr5:74777074-74777085
39	BATF	chr5:74871273-74871606	GM12878	blood:	n/a	n/a
40	BATF	chr5:74819890-74820272	GM12878	blood:	n/a	chr5:74820117-74820127 chr5:74820113-74820123
41	BCL11A	chr5:74884618-74884817	H1-hESC	embryonic stem cell:	n/a	n/a
42	BCL11A	chr5:74862544-74862992	GM12878	blood:	n/a	chr5:74862887-74862896 chr5:74862886-74862895
43	BCL11A	chr5:74769916-74770118	GM12878	blood:	n/a	n/a
44	BCL11A	chr5:74871314-74871654	GM12878	blood:	n/a	chr5:74871486-74871495
45	BCL11A	chr5:74769815-74770102	GM12878	blood:	n/a	n/a
46	BCL11A	chr5:74776943-74777142	GM12878	blood:	n/a	n/a
47	BCL11A	chr5:74871169-74871684	GM12878	blood:	n/a	chr5:74871486-74871495
48	BCL11A	chr5:74862509-74862941	GM12878	blood:	n/a	chr5:74862887-74862896 chr5:74862886-74862895
49	BCL11A	chr5:74819918-74820233	GM12878	blood:	n/a	n/a
50	BCL11A	chr5:74884546-74884904	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:74808039-74808089	HCF	heart:	n/a
2	chr5:74806504-74806554	GM12878	blood:	n/a
3	chr5:74807689-74807739	MCF10A-Er-Src	breast:	n/a
4	chr5:74808039-74808089	HCF	heart:	n/a
5	chr5:74806504-74806554	GM12878	blood:	n/a
6	chr5:74807689-74807739	MCF10A-Er-Src	breast:	n/a
7	chr5:74807308-74807358	NT2-D1	testis:	n/a
8	chr5:74707372-74707422	HPAEpiC	pulmonary alveolar:	n/a
9	chr5:74806661-74806711	HRE	kidney:	n/a
10	chr5:74807973-74808023	NT2-D1	testis:	n/a
11	chr5:74807882-74807932	ProgFib	skin:	n/a
12	chr5:74762295-74762345	AG10803	skin:	n/a
13	chr5:74808039-74808089	ProgFib	skin:	n/a
14	chr5:74807907-74807957	HIPEpiC	eye:	n/a
15	chr5:74806661-74806711	MCF-7	breast:	n/a
16	chr5:74772303-74772353	GM06990	blood:	n/a
17	chr5:74807907-74807957	MCF10A-Er-Src	breast:	n/a
18	chr5:74807535-74807585	HPAEpiC	pulmonary alveolar:	n/a
19	chr5:74778002-74778052	GM19239	blood:	n/a
20	chr5:74811445-74811495	HRE	kidney:	n/a
21	chr5:74807542-74807592	H1-hESC	embryonic stem cell:	embryo
22	chr5:74772303-74772353	NH-A	brain:	n/a
23	chr5:74811445-74811495	HMEC	breast:	n/a
24	chr5:74806504-74806554	ovcar-3	ovarian:	n/a
25	chr5:74798138-74798188	CMK	blood:	n/a
26	chr5:74778002-74778052	HRCEpiC	kidney:	n/a
27	chr5:74807815-74807865	HEK293	kidney:	embryo
28	chr5:74808039-74808089	ECC-1	luminal epithelium:	n/a
29	chr5:74807907-74807957	BE2_C	brain:	n/a
30	chr5:74807829-74807879	PFSK-1	brain:	n/a
31	chr5:74808039-74808089	NT2-D1	testis:	n/a
32	chr5:74762295-74762345	SK-N-SH	brain:	n/a
33	chr5:74807689-74807739	HCM	heart:	n/a
34	chr5:74808293-74808343	SK-N-MC	brain:	n/a
35	chr5:74778002-74778052	HPAEpiC	pulmonary alveolar:	n/a
36	chr5:74762295-74762345	PANC-1	pancreas:	n/a
37	chr5:74806661-74806711	GM19239	blood:	n/a
38	chr5:74806661-74806711	H1-hESC	embryonic stem cell:	embryo
39	chr5:74778002-74778052	T-47D	breast:	n/a
40	chr5:74807542-74807592	ProgFib	skin:	n/a
41	chr5:74807829-74807879	BE2_C	brain:	n/a
42	chr5:74807689-74807739	GM12891	blood:	n/a
43	chr5:74833385-74833435	PrEC	prostate:	n/a
44	chr5:74762295-74762345	CMK	blood:	n/a
45	chr5:74778002-74778052	Hela-S3	cervix:	n/a
46	chr5:74807689-74807739	SAEC	small airway:	n/a
47	chr5:74798138-74798188	HMEC	breast:	n/a
48	chr5:74807542-74807592	GM12892	blood:	n/a
49	chr5:74806951-74807001	ovcar-3	ovarian:	n/a
50	chr5:74807973-74808023	GM12891	blood:	n/a

(count:99 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:74630713..74633733-chr5:74805590..74808087,5	MCF-7	breast:
2	chr5:74775852..74778323-chr5:74787473..74789396,2	K562	blood:
3	chr5:74796488..74799637-chr5:74801966..74804118,4	MCF-7	breast:
4	chr5:74840733..74842326-chr5:74845611..74848333,2	K562	blood:
5	chr5:74880080..74881244-chr5:74962362..74964218,14	MCF-7	breast:
6	chr5:74808217..74810593-chr5:74816041..74817596,2	K562	blood:
7	chr5:74880212..74881196-chr5:74962425..74963375,4	MCF-7	breast:
8	chr5:74735651..74738520-chr5:74798535..74800607,2	K562	blood:
9	chr5:74789576..74794585-chr5:74804962..74807794,4	MCF-7	breast:
10	chr5:74881366..74883122-chr5:74885074..74886574,2	K562	blood:
11	chr5:74717369..74719270-chr5:74723978..74725689,2	K562	blood:
12	chr5:74735651..74738520-chr5:74798535..74800607,2	K562	blood:
13	chr5:74863361..74865877-chr5:74866045..74867591,2	MCF-7	breast:
14	chr5:74704826..74707671-chr5:74805831..74807766,2	MCF-7	breast:
15	chr5:74880200..74881111-chr5:74976869..74977697,3	MCF-7	breast:
16	chr5:74885603..74887138-chr5:74892522..74895230,2	K562	blood:
17	chr5:74845037..74847535-chr5:74848930..74850561,2	K562	blood:
18	chr5:74889934..74892388-chr5:74899059..74901805,2	K562	blood:
19	chr5:74835008..74837584-chr5:74853567..74856265,2	K562	blood:
20	chr5:74806025..74808781-chr5:74906137..74908952,2	MCF-7	breast:
21	chr10:15412992..15413653-chr5:74896234..74896879,2	MCF-7	breast:
22	chr5:74790647..74794380-chr5:74795733..74800125,4	K562	blood:
23	chr5:74811101..74813110-chr5:74815287..74817345,2	K562	blood:
24	chr5:74799687..74804684-chr5:74805759..74808184,7	MCF-7	breast:
25	chr5:74871511..74873926-chr5:75008368..75010666,2	K562	blood:
26	chr5:74852680..74855218-chr5:74864113..74866476,2	K562	blood:
27	chr5:74818089..74820423-chr5:74844136..74846157,2	MCF-7	breast:
28	chr5:74864380..74866848-chr5:75012223..75014112,2	K562	blood:
29	chr5:74753229..74754839-chr5:74755148..74758107,2	K562	blood:
30	chr5:74748747..74750601-chr5:74806790..74808643,2	MCF-7	breast:
31	chr5:74786766..74788653-chr5:74965428..74967574,2	K562	blood:
32	chr5:74728841..74731298-chr5:74732916..74734821,2	MCF-7	breast:
33	chr17:73150112..73150644-chr5:74807014..74807870,2	Hela-S3	cervix:
34	chr5:74808667..74810597-chr5:74818060..74820048,3	K562	blood:
35	chr5:74868580..74871320-chr5:74902166..74903871,2	MCF-7	breast:
36	chr3:167116749..167117659-chr5:74876077..74876717,2	MCF-7	breast:
37	chr5:74722161..74724280-chr5:74725505..74728463,2	K562	blood:
38	chr5:74801840..74804392-chr5:74804791..74808072,5	K562	blood:
39	chr5:74845037..74847535-chr5:74848930..74850561,2	K562	blood:
40	chr5:74757814..74760336-chr5:74803800..74805741,2	MCF-7	breast:
41	chr5:74796618..74799716-chr5:74800501..74803148,3	K562	blood:
42	chr5:74712709..74715090-chr5:74716587..74719083,2	K562	blood:
43	chr5:74757814..74760336-chr5:74803800..74805741,2	MCF-7	breast:
44	chr5:74835008..74837584-chr5:74853567..74856265,2	K562	blood:
45	chr5:74688554..74690802-chr5:74806794..74808772,2	MCF-7	breast:
46	chr5:74770863..74773429-chr5:74777117..74779848,3	MCF-7	breast:
47	chr5:74880501..74881472-chr5:74976763..74977639,2	MCF-7	breast:
48	chr5:74756440..74758113-chr5:75010084..75012046,2	K562	blood:
49	chr5:74790647..74794380-chr5:74795733..74800125,4	K562	blood:
50	chr5:74820287..74822535-chr5:74827846..74830107,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKDD1B-3	chr5:74893572-74893865	NONHSAT102209
2	lnc-ANKDD1B-3	chr5:74892939-74893003	NONHSAT102209
3	lnc-ANKDD1B-3	chr5:74893242-74893614	NONHSAT102210
4	lnc-ANKDD1B-3	chr5:74893759-74893813	NONHSAT102210
5	lnc-POC5-1	chr5:74894952-74895205	ENSG00000248881.1
6	lnc-POC5-1	chr5:74894307-74894806	ENSG00000248881.1

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
COL4A3BP	TF binding region
ENSG00000248881	TF binding region
RNU7-175P	TF binding region
POLK	CpG island
COL4A3BP	CpG island
ENSG00000248881	CpG island
RNU7-175P	CpG island
ENSG00000113163	chromatin interactions
ENSG00000248881	chromatin interactions
ENSG00000122008	chromatin interactions
ENSG00000247372	chromatin interactions
ENSG00000189045	chromatin interactions
ENSG00000132680	chromatin interactions
ENSG00000189159	chromatin interactions
ENSG00000148468	chromatin interactions
ENSG00000152359	chromatin interactions
ENSG00000113161	chromatin interactions
ENSG00000166986	chromatin interactions

Extended variants
information (count: 7867 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:7867 , 50 per page) page: 1 2 3 4 5 6 7 ... 158

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3761742	chr5:74678937-74678938	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs534249273	chr5:74678952-74678953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs575344252	chr5:74678956-74678957	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574847887	chr5:74678958-74678959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs368059392	chr5:74678970-74678971	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561011969	chr5:74678986-74678987	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs574439060	chr5:74679015-74679016	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113542648	chr5:74679025-74679026	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138045856	chr5:74679055-74679056	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532460221	chr5:74679237-74679238	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs371486865	chr5:74679313-74679314	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192563220	chr5:74679342-74679343	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562429431	chr5:74679344-74679345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531627287	chr5:74679372-74679373	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112917186	chr5:74679418-74679419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189358657	chr5:74679419-74679420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112893891	chr5:74679454-74679455	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143691750	chr5:74679527-74679528	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs375288782	chr5:74679528-74679529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs3840121	chr5:74679529-74679530	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140975836	chr5:74679566-74679567	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574601709	chr5:74679592-74679593	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540022021	chr5:74679594-74679595	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556922751	chr5:74679667-74679668	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs192504191	chr5:74679852-74679853	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs537880327	chr5:74679964-74679965	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs554226658	chr5:74679984-74679985	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs574479288	chr5:74680031-74680032	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs3931913	chr5:74680053-74680054	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs184843410	chr5:74680073-74680074	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs553949173	chr5:74680122-74680123	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs576663015	chr5:74680158-74680159	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs545574228	chr5:74680160-74680161	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs111608410	chr5:74680162-74680163	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs150432390	chr5:74680172-74680173	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs77856529	chr5:74680231-74680232	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs541822326	chr5:74680256-74680257	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs561904540	chr5:74680260-74680261	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs527798737	chr5:74680363-74680364	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs547608441	chr5:74680393-74680394	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs189594226	chr5:74680419-74680420	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs377098641	chr5:74680431-74680432	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs150256072	chr5:74680438-74680439	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs566172166	chr5:74680448-74680449	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs139096937	chr5:74680490-74680491	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs550387427	chr5:74680518-74680519	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs181517235	chr5:74680556-74680557	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs570372641	chr5:74680637-74680638	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs35250114	chr5:74680657-74680658	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs4389673	chr5:74680658-74680659	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	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:5539 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74656400-74687200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr5:74656400-74725600	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr5:74656600-74694800	Weak transcription	Brain Angular Gyrus	brain
4	chr5:74656800-74731400	Weak transcription	Rectal Smooth Muscle	rectum
5	chr5:74657800-74708000	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr5:74659800-74684800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr5:74659800-74720600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr5:74660000-74722800	Weak transcription	Fetal Heart	heart
9	chr5:74660200-74707800	Weak transcription	Stomach Mucosa	stomach
10	chr5:74661800-74683600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr5:74665000-74703000	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr5:74667000-74723200	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr5:74667200-74688200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr5:74667200-74693600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr5:74667600-74687600	Strong transcription	Primary neutrophils fromperipheralblood	blood
16	chr5:74668000-74688400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr5:74668200-74686200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr5:74668400-74685600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr5:74668600-74681600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
20	chr5:74668600-74686800	Strong transcription	Primary T helper cells fromperipheralblood	blood
21	chr5:74668600-74687200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr5:74668600-74687600	Strong transcription	Adipose Nuclei	Adipose
23	chr5:74668600-74687600	Strong transcription	Fetal Lung	lung
24	chr5:74668600-74691200	Strong transcription	Liver	Liver
25	chr5:74668800-74685800	Strong transcription	Primary B cells from peripheral blood	blood
26	chr5:74669600-74681400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr5:74670800-74709400	Weak transcription	Pancreas	Pancrea
28	chr5:74670800-74720600	Weak transcription	Right Ventricle	heart
29	chr5:74670800-74731400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr5:74671000-74686000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr5:74671000-74722800	Weak transcription	Hela-S3	cervix
32	chr5:74671600-74686000	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr5:74671800-74684200	Strong transcription	Primary hematopoietic stem cells	blood
34	chr5:74672000-74682000	Strong transcription	Primary B cells from cord blood	blood
35	chr5:74672200-74687000	Strong transcription	Rectal Mucosa Donor 31	rectum
36	chr5:74673000-74682400	Strong transcription	HUES48 Cell Line	embryonic stem cell
37	chr5:74673200-74682600	Strong transcription	HUES64 Cell Line	embryonic stem cell
38	chr5:74673200-74685200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr5:74673200-74685800	Strong transcription	HUES6 Cell Line	embryonic stem cell
40	chr5:74673200-74685800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr5:74673200-74685800	Strong transcription	Dnd41	blood
42	chr5:74673200-74686000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr5:74673400-74682200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
44	chr5:74673400-74685800	Strong transcription	Rectal Mucosa Donor 29	rectum
45	chr5:74673400-74686000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr5:74673600-74681400	Strong transcription	Placenta	Placenta
47	chr5:74673600-74681600	Strong transcription	Duodenum Mucosa	Duodenum
48	chr5:74674400-74688000	Weak transcription	NHEK	skin
49	chr5:74674400-74761400	Weak transcription	Esophagus	oesophagus
50	chr5:74674800-74679000	Strong transcription	HSMM	muscle

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