Variant report

Variant	nsv1018031
Chromosome Location	chr5:177655010-177746378
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2131)
CpG islands
(count:2323)
Chromatin interactive
region (count:112)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2131 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:177710357-177711424	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:177711067-177711470	K562	blood:	n/a	n/a
3	ARID3A	chr5:177658303-177658558	K562	blood:	n/a	n/a
4	ARID3A	chr5:177707033-177707311	HepG2	liver:	n/a	n/a
5	ATF2	chr5:177662015-177662614	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr5:177663731-177664017	K562	blood:	n/a	n/a
7	ATF3	chr5:177658255-177658574	K562	blood:	n/a	n/a
8	BACH1	chr5:177707055-177707255	K562	blood:	n/a	n/a
9	BACH1	chr5:177711109-177711430	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr5:177658981-177659154	K562	blood:	n/a	n/a
11	BACH1	chr5:177659303-177660211	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr5:177660141-177660312	K562	blood:	n/a	n/a
13	BATF	chr5:177666372-177666910	GM12878	blood:	n/a	n/a
14	BCL11A	chr5:177666388-177666934	GM12878	blood:	n/a	n/a
15	BHLHE40	chr5:177706227-177706368	K562	blood:	n/a	chr5:177706263-177706279
16	BHLHE40	chr5:177706958-177707403	HepG2	liver:	n/a	n/a
17	BHLHE40	chr5:177706952-177707347	K562	blood:	n/a	n/a
18	BHLHE40	chr5:177658902-177660468	K562	blood:	n/a	chr5:177659901-177659917
19	BHLHE40	chr5:177710571-177710897	HepG2	liver:	n/a	n/a
20	BHLHE40	chr5:177693987-177694158	K562	blood:	n/a	chr5:177694037-177694046 chr5:177694039-177694048 chr5:177694036-177694049 chr5:177694038-177694047 chr5:177694038-177694047
21	BHLHE40	chr5:177711076-177711282	K562	blood:	n/a	n/a
22	BHLHE40	chr5:177683800-177684182	K562	blood:	n/a	n/a
23	BHLHE40	chr5:177659243-177660128	HepG2	liver:	n/a	chr5:177659901-177659917
24	BHLHE40	chr5:177706971-177707322	GM12878	blood:	n/a	n/a
25	BHLHE40	chr5:177682382-177682671	K562	blood:	n/a	n/a
26	BHLHE40	chr5:177659237-177659880	GM12878	blood:	n/a	n/a
27	BHLHE40	chr5:177663448-177664079	K562	blood:	n/a	n/a
28	BHLHE40	chr5:177661787-177662611	K562	blood:	n/a	n/a
29	BHLHE40	chr5:177663708-177663985	GM12878	blood:	n/a	n/a
30	BHLHE40	chr5:177739816-177740223	K562	blood:	n/a	n/a
31	BHLHE40	chr5:177658248-177658493	K562	blood:	n/a	n/a
32	BRCA1	chr5:177662236-177662384	GM12878	blood:	n/a	n/a
33	BRCA1	chr5:177706982-177707288	HepG2	liver:	n/a	n/a
34	BRCA1	chr5:177662109-177662420	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr5:177707011-177707315	H1-hESC	embryonic stem cell:	n/a	n/a
36	BRCA1	chr5:177659209-177660020	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr5:177706965-177707294	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr5:177662132-177662544	H1-hESC	embryonic stem cell:	n/a	n/a
39	BRCA1	chr5:177659175-177659241	HepG2	liver:	n/a	n/a
40	BRCA1	chr5:177676940-177677091	GM12878	blood:	n/a	n/a
41	BRCA1	chr5:177711097-177711413	H1-hESC	embryonic stem cell:	n/a	n/a
42	BRCA1	chr5:177662057-177662301	HepG2	liver:	n/a	n/a
43	CBX3	chr5:177702811-177703140	K562	blood:	n/a	n/a
44	CBX3	chr5:177706868-177707236	K562	blood:	n/a	n/a
45	CBX3	chr5:177661893-177662621	K562	blood:	n/a	n/a
46	CBX3	chr5:177710986-177711408	K562	blood:	n/a	n/a
47	CBX3	chr5:177702851-177703084	K562	blood:	n/a	n/a
48	CBX3	chr5:177711042-177711391	K562	blood:	n/a	n/a
49	CBX3	chr5:177658924-177659313	K562	blood:	n/a	n/a
50	CBX3	chr5:177663620-177664042	K562	blood:	n/a	n/a

(count:2323 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:177708528-177708578	PANC-1	pancreas:	n/a
2	chr5:177713841-177713891	K562	blood:	n/a
3	chr5:177657311-177657361	PrEC	prostate:	n/a
4	chr5:177707101-177707151	PFSK-1	brain:	n/a
5	chr5:177708304-177708354	NT2-D1	testis:	n/a
6	chr5:177708528-177708578	PANC-1	pancreas:	n/a
7	chr5:177713841-177713891	K562	blood:	n/a
8	chr5:177657311-177657361	PrEC	prostate:	n/a
9	chr5:177707101-177707151	PFSK-1	brain:	n/a
10	chr5:177708304-177708354	NT2-D1	testis:	n/a
11	chr5:177728612-177728662	Hela-S3	cervix:	n/a
12	chr5:177660305-177660355	NHBE	bronchial:	n/a
13	chr5:177740069-177740119	HRCEpiC	kidney:	n/a
14	chr5:177659971-177660021	ovcar-3	ovarian:	n/a
15	chr5:177658991-177659041	NHBE	bronchial:	n/a
16	chr5:177697400-177697450	AG09319	gingival:	n/a
17	chr5:177657311-177657361	MCF10A-Er-Src	breast:	n/a
18	chr5:177657311-177657361	SK-N-MC	brain:	n/a
19	chr5:177734534-177734584	AG09309	skin:	n/a
20	chr5:177708457-177708507	Jurkat	blood:	n/a
21	chr5:177659229-177659279	GM19239	blood:	n/a
22	chr5:177707036-177707086	HRCEpiC	kidney:	n/a
23	chr5:177729089-177729139	MCF-7	breast:	n/a
24	chr5:177660036-177660086	NHDF-neo	bronchial:	n/a
25	chr5:177707226-177707276	PrEC	prostate:	n/a
26	chr5:177708457-177708507	AG09319	gingival:	n/a
27	chr5:177707101-177707151	HIPEpiC	eye:	n/a
28	chr5:177660036-177660086	HCT-116	colon:	n/a
29	chr5:177708304-177708354	MCF-7	breast:	n/a
30	chr5:177697477-177697527	HEK293	kidney:	embryo
31	chr5:177740069-177740119	SK-N-SH_RA	brain:	n/a
32	chr5:177660351-177660401	HUVEC	blood vessel:	n/a
33	chr5:177659919-177659969	NHDF-neo	bronchial:	n/a
34	chr5:177730633-177730683	Hepatocyte	liver:	n/a
35	chr5:177660305-177660355	HL-60	blood:	n/a
36	chr5:177708457-177708507	ECC-1	luminal epithelium:	n/a
37	chr5:177732295-177732345	NB4	blood:	n/a
38	chr5:177740217-177740267	PrEC	prostate:	n/a
39	chr5:177697647-177697697	HCM	heart:	n/a
40	chr5:177725929-177725979	RPTEC	kidney:	n/a
41	chr5:177740217-177740267	AG10803	skin:	n/a
42	chr5:177659229-177659279	AG09319	gingival:	n/a
43	chr5:177662552-177662602	BE2_C	brain:	n/a
44	chr5:177697400-177697450	GM19239	blood:	n/a
45	chr5:177662552-177662602	HRCEpiC	kidney:	n/a
46	chr5:177660351-177660401	HCM	heart:	n/a
47	chr5:177697669-177697719	Hepatocyte	liver:	n/a
48	chr5:177708304-177708354	ECC-1	luminal epithelium:	n/a
49	chr5:177725929-177725979	ovcar-3	ovarian:	n/a
50	chr5:177740106-177740156	SK-N-SH_RA	brain:	n/a

(count:112 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:177706726..177707270-chr5:178157310..178157911,2	MCF-7	breast:
2	chr5:177673184..177676409-chr5:177679568..177684017,5	K562	blood:
3	chr5:177706712..177707519-chr5:178016864..178017694,3	MCF-7	breast:
4	chr5:177019232..177020994-chr5:177656791..177659399,2	K562	blood:
5	chr5:177666998..177669633-chr5:177705585..177707860,2	MCF-7	breast:
6	chr5:177675640..177677996-chr5:177730945..177733479,2	K562	blood:
7	chr5:177671586..177674457-chr5:177675153..177677148,2	MCF-7	breast:
8	chr5:177661743..177662668-chr5:178266372..178266966,2	K562	blood:
9	chr5:177705531..177707369-chr5:177709194..177711179,2	K562	blood:
10	chr5:177688646..177691134-chr5:177692615..177694812,2	MCF-7	breast:
11	chr5:177710809..177711655-chr5:177978098..177978611,2	MCF-7	breast:
12	chr5:177662161..177662775-chr5:177732667..177733658,2	MCF-7	breast:
13	chr5:177708522..177710701-chr5:178921263..178923252,2	K562	blood:
14	chr5:177631158..177632989-chr5:177704368..177706626,2	MCF-7	breast:
15	chr5:177675640..177677996-chr5:177730945..177733479,2	K562	blood:
16	chr5:177714990..177717211-chr5:177717437..177719265,2	MCF-7	breast:
17	chr5:177666154..177668382-chr5:177684774..177687012,2	MCF-7	breast:
18	chr5:177682472..177686138-chr5:177686968..177690671,4	K562	blood:
19	chr5:177680211..177682699-chr5:177684964..177686597,2	K562	blood:
20	chr5:177710796..177711682-chr5:178266072..178266614,2	K562	blood:
21	chr5:177661877..177662434-chr5:177700931..177701850,2	MCF-7	breast:
22	chr5:177698904..177700407-chr5:177706155..177707702,2	K562	blood:
23	chr5:177711262..177713126-chr5:177716170..177718163,3	K562	blood:
24	chr5:177722976..177725589-chr5:177728477..177731343,2	MCF-7	breast:
25	chr5:177732771..177735579-chr5:177738101..177740737,3	K562	blood:
26	chr5:177659189..177660088-chr5:178017540..178018315,2	K562	blood:
27	chr5:177637291..177640571-chr5:177674983..177676979,3	K562	blood:
28	chr5:177543150..177544003-chr5:177676886..177677587,2	MCF-7	breast:
29	chr5:177658397..177661582-chr5:177665181..177668920,4	MCF-7	breast:
30	chr5:177723976..177725542-chr5:178052631..178055035,2	K562	blood:
31	chr5:177673184..177676409-chr5:177679568..177684017,5	K562	blood:
32	chr5:177711262..177713126-chr5:177716170..177718163,3	K562	blood:
33	chr5:177662114..177662778-chr5:178017450..178018023,2	MCF-7	breast:
34	chr5:177706927..177707599-chr5:177977871..177978610,3	MCF-7	breast:
35	chr5:177664686..177666446-chr5:177667061..177669063,2	MCF-7	breast:
36	chr5:177688646..177691134-chr5:177692615..177694812,2	MCF-7	breast:
37	chr5:177674663..177677489-chr5:177694652..177697569,3	K562	blood:
38	chr5:177705017..177707369-chr5:177709194..177712378,3	K562	blood:
39	chr5:177712048..177714602-chr5:177804410..177806425,2	MCF-7	breast:
40	chr5:177658492..177661017-chr5:177701580..177703752,2	MCF-7	breast:
41	chr5:177661196..177662135-chr5:178266134..178266915,2	MCF-7	breast:
42	chr5:177662161..177662775-chr5:177732667..177733658,2	MCF-7	breast:
43	chr5:177731199..177733626-chr5:177734789..177737506,2	MCF-7	breast:
44	chr5:177663150..177665160-chr5:178157825..178159335,2	MCF-7	breast:
45	chr5:177712144..177714829-chr5:177719190..177721304,2	MCF-7	breast:
46	chr5:177706663..177708953-chr5:178261165..178263624,2	MCF-7	breast:
47	chr5:177671586..177674457-chr5:177675153..177677148,2	MCF-7	breast:
48	chr5:177706637..177707790-chr5:178017212..178018303,12	K562	blood:
49	chr5:177659087..177660769-chr5:178052015..178054177,2	K562	blood:
50	chr5:177663359..177666352-chr5:177692543..177695366,2	K562	blood:

No data

Variant related genes	Relation type
PHYKPL	TF binding region
PHYKPL	CpG island
ENSG00000050767	chromatin interactions
ENSG00000244234	chromatin interactions
ENSG00000242341	chromatin interactions
ENSG00000169131	chromatin interactions
ENSG00000197451	chromatin interactions
ENSG00000241878	chromatin interactions
ENSG00000113240	chromatin interactions
ENSG00000175309	chromatin interactions
ENSG00000184840	chromatin interactions
ENSG00000182718	chromatin interactions

Extended variants
information (count: 4303 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:4303 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186392879	chr5:177655028-177655029	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs542432437	chr5:177655083-177655084	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs190999969	chr5:177655105-177655106	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs571376319	chr5:177655158-177655159	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs576055801	chr5:177655191-177655192	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs11738131	chr5:177655194-177655195	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs182768871	chr5:177655208-177655209	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs535536540	chr5:177655211-177655212	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs573664479	chr5:177655272-177655273	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs143448352	chr5:177655273-177655274	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs199519924	chr5:177655288-177655289	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs146125073	chr5:177655313-177655314	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs138895762	chr5:177655320-177655321	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs565020473	chr5:177655323-177655324	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs10074929	chr5:177655332-177655333	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs531803215	chr5:177655349-177655350	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs187799488	chr5:177655408-177655409	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs376290336	chr5:177655490-177655491	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs549983011	chr5:177655508-177655509	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs11740356	chr5:177655512-177655513	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs529238235	chr5:177655516-177655517	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs544248895	chr5:177655581-177655582	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs149330363	chr5:177655612-177655613	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs565993942	chr5:177655644-177655645	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs539762480	chr5:177655647-177655648	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs6881230	chr5:177655692-177655693	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs561639540	chr5:177655699-177655700	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs570131376	chr5:177655703-177655704	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs191165679	chr5:177655730-177655731	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs183414478	chr5:177655732-177655733	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs532319860	chr5:177655741-177655742	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs534552588	chr5:177655832-177655833	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs553011981	chr5:177655839-177655840	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs187411383	chr5:177655840-177655841	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs79355194	chr5:177655845-177655846	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs368170749	chr5:177655863-177655864	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs563628632	chr5:177655876-177655877	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs144523715	chr5:177655901-177655902	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs192165755	chr5:177655907-177655908	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs2913865	chr5:177655932-177655933	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs529347551	chr5:177655970-177655971	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs184717670	chr5:177655973-177655974	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs559346035	chr5:177656001-177656002	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs188135029	chr5:177656037-177656038	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs2913864	chr5:177656083-177656084	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs61473059	chr5:177656090-177656091	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs192706265	chr5:177656091-177656092	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs561377000	chr5:177656105-177656106	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs55725801	chr5:177656124-177656125	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs554434593	chr5:177656125-177656126	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	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
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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1778 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177635800-177657000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr5:177639400-177657600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr5:177640400-177655600	Weak transcription	Right Atrium	heart
4	chr5:177643400-177656400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr5:177643600-177655200	Weak transcription	Stomach Mucosa	stomach
6	chr5:177645400-177656800	Strong transcription	Primary B cells from peripheral blood	blood
7	chr5:177645400-177656800	Strong transcription	Dnd41	blood
8	chr5:177646200-177657000	Weak transcription	Fetal Brain Male	brain
9	chr5:177646600-177657400	Strong transcription	Thymus	Thymus
10	chr5:177646800-177658000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr5:177647800-177657000	Strong transcription	Brain Germinal Matrix	brain
12	chr5:177648000-177656000	Strong transcription	Placenta Amnion	Placenta Amnion
13	chr5:177648000-177656800	Strong transcription	Primary B cells from cord blood	blood
14	chr5:177648000-177658000	Strong transcription	Fetal Thymus	thymus
15	chr5:177648200-177657000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr5:177648200-177657000	Strong transcription	NHLF	lung
17	chr5:177648200-177657400	Strong transcription	Fetal Brain Female	brain
18	chr5:177648200-177657800	Genic enhancers	Fetal Intestine Large	intestine
19	chr5:177648600-177656400	Strong transcription	GM12878-XiMat	blood
20	chr5:177648600-177658000	Strong transcription	Spleen	Spleen
21	chr5:177649000-177657400	Strong transcription	Primary T cells from cord blood	blood
22	chr5:177649400-177655200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr5:177649400-177655600	Strong transcription	Primary neutrophils fromperipheralblood	blood
24	chr5:177649400-177657000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr5:177649400-177657200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr5:177649400-177657200	Strong transcription	Monocytes-CD14+_RO01746	blood
27	chr5:177649600-177657800	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr5:177650200-177656600	Weak transcription	Brain Angular Gyrus	brain
29	chr5:177650600-177655400	Weak transcription	HUVEC	blood vessel
30	chr5:177651000-177657000	Strong transcription	Brain Inferior Temporal Lobe	brain
31	chr5:177651200-177656200	Strong transcription	Lung	lung
32	chr5:177651400-177655600	Strong transcription	Adipose Nuclei	Adipose
33	chr5:177651400-177658000	Genic enhancers	Primary T cells fromperipheralblood	blood
34	chr5:177651600-177657800	Strong transcription	Fetal Muscle Leg	muscle
35	chr5:177651600-177658000	Strong transcription	HUES6 Cell Line	embryonic stem cell
36	chr5:177651600-177658000	Strong transcription	Cortex derived primary cultured neurospheres	brain
37	chr5:177651800-177656800	Strong transcription	Fetal Muscle Trunk	muscle
38	chr5:177651800-177657000	Strong transcription	Right Ventricle	heart
39	chr5:177651800-177658000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr5:177652000-177655400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr5:177652000-177657000	Strong transcription	Muscle Satellite Cultured Cells	--
42	chr5:177652000-177657000	Strong transcription	Placenta	Placenta
43	chr5:177652000-177658000	Strong transcription	HUES64 Cell Line	embryonic stem cell
44	chr5:177652000-177658000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
45	chr5:177652000-177658200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr5:177652200-177657600	Genic enhancers	Liver	Liver
47	chr5:177652400-177655400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr5:177652800-177658200	Strong transcription	HUES48 Cell Line	embryonic stem cell
49	chr5:177653600-177657000	Strong transcription	Duodenum Smooth Muscle	Duodenum
50	chr5:177653600-177657600	Genic enhancers	Duodenum Mucosa	Duodenum

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