Variant report

Variant	nsv462198
Chromosome Location	chr5:59969015-60116613
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2024)
CpG islands
(count:1588)
Chromatin interactive
region (count:107)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2024 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:59983691-59984581	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:59999797-60000151	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:59996034-59996038	K562	blood:	n/a	n/a
4	ARID3A	chr5:59973261-59974501	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:59967702-59969417	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:59995305-59996360	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:59981629-59981926	K562	blood:	n/a	n/a
8	ARID3A	chr5:60106314-60106972	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:60116461-60117150	K562	blood:	n/a	n/a
10	ATF1	chr5:60098191-60098391	K562	blood:	n/a	n/a
11	ATF1	chr5:60116465-60117242	K562	blood:	n/a	n/a
12	ATF1	chr5:60105880-60106051	K562	blood:	n/a	n/a
13	ATF1	chr5:59983879-59984499	K562	blood:	n/a	n/a
14	ATF1	chr5:59995447-59996702	K562	blood:	n/a	n/a
15	ATF1	chr5:59981612-59982022	K562	blood:	n/a	n/a
16	ATF1	chr5:60018170-60018424	K562	blood:	n/a	n/a
17	ATF2	chr5:59995349-59996155	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr5:59995701-59996325	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr5:59995674-59996236	GM12878	blood:	n/a	n/a
20	ATF3	chr5:60106451-60106930	A549	lung:	n/a	chr5:60106679-60106693
21	ATF3	chr5:59981576-59981954	K562	blood:	n/a	n/a
22	ATF3	chr5:59995819-59996207	K562	blood:	n/a	chr5:59996023-59996043 chr5:59996035-59996046
23	BACH1	chr5:59969317-59969517	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr5:59995416-59996305	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr5:60057199-60057512	GM12878	blood:	n/a	n/a
26	BATF	chr5:60034434-60034644	GM12878	blood:	n/a	n/a
27	BATF	chr5:59973533-59973760	GM12878	blood:	n/a	chr5:59973657-59973668
28	BATF	chr5:59973491-59973835	GM12878	blood:	n/a	chr5:59973657-59973668
29	BATF	chr5:59984140-59984343	GM12878	blood:	n/a	chr5:59984260-59984271
30	BATF	chr5:59984076-59984379	GM12878	blood:	n/a	chr5:59984260-59984271
31	BATF	chr5:60057258-60057503	GM12878	blood:	n/a	n/a
32	BATF	chr5:60034409-60034644	GM12878	blood:	n/a	n/a
33	BCL11A	chr5:60057285-60057534	GM12878	blood:	n/a	n/a
34	BCL11A	chr5:60057304-60057451	GM12878	blood:	n/a	n/a
35	BCL3	chr5:59995402-59996329	A549	lung:	n/a	chr5:59995938-59995951 chr5:59995934-59995947 chr5:59996005-59996018 chr5:59995768-59995781 chr5:59995966-59995979
36	BCL3	chr5:60106438-60107052	A549	lung:	n/a	n/a
37	BCLAF1	chr5:59995291-59996358	GM12878	blood:	n/a	chr5:59995938-59995951 chr5:59995934-59995947 chr5:59996005-59996018 chr5:59995768-59995781 chr5:59995966-59995979
38	BCLAF1	chr5:59995423-59996324	GM12878	blood:	n/a	chr5:59995938-59995951 chr5:59995934-59995947 chr5:59996005-59996018 chr5:59995768-59995781 chr5:59995966-59995979
39	BHLHE40	chr5:60093321-60093343	K562	blood:	n/a	n/a
40	BHLHE40	chr5:59995711-59996635	GM12878	blood:	n/a	chr5:59995940-59995956 chr5:59995931-59995947
41	BHLHE40	chr5:59973687-59973838	K562	blood:	n/a	n/a
42	BHLHE40	chr5:59981769-59981936	K562	blood:	n/a	n/a
43	BHLHE40	chr5:59984818-59984850	K562	blood:	n/a	n/a
44	BHLHE40	chr5:60057704-60057885	HepG2	liver:	n/a	n/a
45	BHLHE40	chr5:60116487-60117300	K562	blood:	n/a	n/a
46	BHLHE40	chr5:59990190-59990374	K562	blood:	n/a	n/a
47	BHLHE40	chr5:59995469-59997496	K562	blood:	n/a	chr5:59995940-59995956 chr5:59995931-59995947
48	BHLHE40	chr5:60057135-60057471	HepG2	liver:	n/a	n/a
49	BHLHE40	chr5:60061785-60061831	K562	blood:	n/a	n/a
50	BHLHE40	chr5:59968578-59969094	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:60050299-60050349	ovcar-3	ovarian:	n/a
2	chr5:59995354-59995404	PFSK-1	brain:	n/a
3	chr5:60050299-60050349	ovcar-3	ovarian:	n/a
4	chr5:59995354-59995404	PFSK-1	brain:	n/a
5	chr5:59995837-59995887	PFSK-1	brain:	n/a
6	chr5:59996328-59996378	HEK293	kidney:	embryo
7	chr5:59996455-59996505	HIPEpiC	eye:	n/a
8	chr5:59996025-59996075	SAEC	small airway:	n/a
9	chr5:59995433-59995483	GM19239	blood:	n/a
10	chr5:60073995-60074045	SK-N-SH	brain:	n/a
11	chr5:59971556-59971606	IMR90	lung:	fetal
12	chr5:60073995-60074045	ProgFib	skin:	n/a
13	chr5:59996115-59996165	HCPEpiC	choroid plexus:	n/a
14	chr5:60073995-60074045	NB4	blood:	n/a
15	chr5:59999842-59999892	GM06990	blood:	n/a
16	chr5:60073995-60074045	HIPEpiC	eye:	n/a
17	chr5:59996028-59996078	RPTEC	kidney:	n/a
18	chr5:59995354-59995404	HUVEC	blood vessel:	n/a
19	chr5:60040736-60040786	AG04450	lung:	fetal
20	chr5:59999842-59999892	GM12878	blood:	n/a
21	chr5:60039414-60039464	HNPCEpiC	eye:	n/a
22	chr5:59996115-59996165	HEK293	kidney:	embryo
23	chr5:59996120-59996170	IMR90	lung:	fetal
24	chr5:60073995-60074045	HCM	heart:	n/a
25	chr5:60039729-60039779	LNCaP	prostate:	n/a
26	chr5:59995715-59995765	H1-hESC	embryonic stem cell:	embryo
27	chr5:60073995-60074045	HL-60	blood:	n/a
28	chr5:59995433-59995483	CMK	blood:	n/a
29	chr5:59996105-59996155	AG10803	skin:	n/a
30	chr5:60038293-60038343	IMR90	lung:	fetal
31	chr5:59996421-59996471	PFSK-1	brain:	n/a
32	chr5:60039648-60039698	HPAEpiC	pulmonary alveolar:	n/a
33	chr5:59995433-59995483	HMEC	breast:	n/a
34	chr5:59996105-59996155	GM19239	blood:	n/a
35	chr5:59995433-59995483	GM06990	blood:	n/a
36	chr5:60059120-60059170	SK-N-SH_RA	brain:	n/a
37	chr5:59996066-59996116	HRE	kidney:	n/a
38	chr5:60059120-60059170	HUVEC	blood vessel:	n/a
39	chr5:59995354-59995404	ProgFib	skin:	n/a
40	chr5:59996240-59996290	NHDF-neo	bronchial:	n/a
41	chr5:60039648-60039698	HIPEpiC	eye:	n/a
42	chr5:60073995-60074045	AoSMC	blood vessel:	n/a
43	chr5:59995433-59995483	HEK293	kidney:	embryo
44	chr5:60039819-60039869	AG04449	skin:	fetal
45	chr5:59995433-59995483	PFSK-1	brain:	n/a
46	chr5:59996455-59996505	SAEC	small airway:	n/a
47	chr5:60039648-60039698	HRE	kidney:	n/a
48	chr5:59996066-59996116	IMR90	lung:	fetal
49	chr5:59996240-59996290	Jurkat	blood:	n/a
50	chr5:59999842-59999892	ProgFib	skin:	n/a

(count:107 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:59978724..59981449-chr5:59990551..59993454,2	K562	blood:
2	chr5:59986799..59989085-chr5:59989251..59992450,3	MCF-7	breast:
3	chr5:60115551..60118264-chr5:60126347..60128654,2	MCF-7	breast:
4	chr5:59969188..59971651-chr5:59973747..59976121,2	K562	blood:
5	chr5:59974424..59976131-chr5:59981029..59983580,2	MCF-7	breast:
6	chr5:60091814..60093851-chr5:60098024..60100657,2	K562	blood:
7	chr5:59982146..59984136-chr5:59984712..59987342,2	K562	blood:
8	chr5:60100541..60102761-chr5:60130219..60132557,2	K562	blood:
9	chr5:59973247..59973801-chr5:60224508..60225118,3	K562	blood:
10	chr5:60054901..60056742-chr5:60065532..60068314,2	K562	blood:
11	chr5:59970171..59972111-chr5:59972117..59973629,2	K562	blood:
12	chr5:59973507..59975333-chr5:60177921..60180223,2	MCF-7	breast:
13	chr5:60042570..60044385-chr5:60079016..60080838,2	K562	blood:
14	chr5:59995886..59998322-chr5:60239584..60242446,2	MCF-7	breast:
15	chr5:60042570..60044385-chr5:60079016..60080838,2	K562	blood:
16	chr5:59995106..59997535-chr5:60240120..60242292,3	K562	blood:
17	chr5:60050521..60052217-chr5:60052630..60054560,2	MCF-7	breast:
18	chr5:59994766..59997434-chr5:59998869..60000673,3	MCF-7	breast:
19	chr5:59973332..59975337-chr5:60224481..60226392,2	MCF-7	breast:
20	chr5:59981919..59984018-chr5:59995398..59997534,3	K562	blood:
21	chr5:59979528..59981743-chr5:60138984..60140817,2	K562	blood:
22	chr5:59968567..59969123-chr5:59981115..59981698,2	MCF-7	breast:
23	chr5:59982948..59985839-chr5:59989149..59990796,3	K562	blood:
24	chr5:59976157..59978303-chr5:59980094..59983522,3	K562	blood:
25	chr5:60091814..60093851-chr5:60098024..60100657,2	K562	blood:
26	chr5:59982146..59984136-chr5:59984712..59987342,2	K562	blood:
27	chr5:60089577..60091620-chr5:60092032..60093773,2	K562	blood:
28	chr5:59996423..59998684-chr5:60001090..60003995,3	MCF-7	breast:
29	chr5:59968567..59969123-chr5:59981115..59981698,2	MCF-7	breast:
30	chr5:59994459..59997012-chr5:59999943..60002207,3	K562	blood:
31	chr5:60098668..60100244-chr5:60103216..60104950,2	K562	blood:
32	chr5:59968561..59971245-chr5:59997935..60000093,2	MCF-7	breast:
33	chr5:60104371..60107157-chr5:60107584..60109673,3	MCF-7	breast:
34	chr5:59994210..59996553-chr5:60627404..60629725,2	MCF-7	breast:
35	chr5:59981395..59986593-chr5:59993706..59998197,7	K562	blood:
36	chr5:59974003..59976839-chr5:59984985..59987067,2	K562	blood:
37	chr5:59933171..59934818-chr5:59991480..59994360,2	K562	blood:
38	chr5:59976157..59978303-chr5:59980094..59983522,3	K562	blood:
39	chr5:59990643..59992382-chr5:60006988..60008746,2	K562	blood:
40	chr5:59974810..59977712-chr5:59994412..59996094,2	K562	blood:
41	chr5:60087441..60089276-chr5:60089305..60090863,2	MCF-7	breast:
42	chr5:60017651..60020271-chr5:60037416..60040413,2	MCF-7	breast:
43	chr5:59982948..59985839-chr5:59989149..59990796,3	K562	blood:
44	chr5:60017651..60020271-chr5:60037416..60040413,2	MCF-7	breast:
45	chr5:60098668..60100244-chr5:60103216..60104950,2	K562	blood:
46	chr5:59978724..59981449-chr5:59990551..59993454,2	K562	blood:
47	chr5:59998145..60001535-chr5:60003151..60006329,3	K562	blood:
48	chr5:60096040..60098650-chr5:60101682..60104091,2	K562	blood:
49	chr5:60082437..60084997-chr5:60089364..60092082,2	MCF-7	breast:
50	chr5:59982671..59990838-chr5:59991133..59997951,12	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ELOVL7	hsa-miR-21-5p	chr5:60049832-60049858
2	ELOVL7	hsa-miR-21-5p	chr5:60048157-60048175

Variant related genes	Relation type
DEPDC1B	TF binding region
KRT8P31	TF binding region
ELOVL7	TF binding region
DEPDC1B	CpG island
KRT8P31	CpG island
ELOVL7	CpG island
ENSG00000250148	chromatin interactions
ENSG00000188725	chromatin interactions
ENSG00000251279	chromatin interactions
ENSG00000164181	chromatin interactions
ENSG00000130449	chromatin interactions
ENSG00000164182	chromatin interactions
ENSG00000166348	chromatin interactions
ENSG00000049167	chromatin interactions
ENSG00000268584	chromatin interactions
ENSG00000035499	chromatin interactions

Extended variants
information (count: 4695 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:4695 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12517174	chr5:59969015-59969016	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs563267103	chr5:59969023-59969024	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142371338	chr5:59969051-59969052	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs146382077	chr5:59969092-59969093	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370838061	chr5:59969117-59969118	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188615695	chr5:59969157-59969158	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148048796	chr5:59969185-59969186	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548703679	chr5:59969201-59969202	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545295697	chr5:59969220-59969221	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs181062671	chr5:59969239-59969240	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537456176	chr5:59969290-59969291	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs550964484	chr5:59969313-59969314	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs570741726	chr5:59969401-59969402	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs185102568	chr5:59969423-59969424	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs553387883	chr5:59969431-59969432	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs376192338	chr5:59969467-59969468	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs112251929	chr5:59969537-59969538	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs535615700	chr5:59969564-59969565	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs373853322	chr5:59969584-59969585	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs189606051	chr5:59969595-59969596	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs554474574	chr5:59969596-59969597	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs367717317	chr5:59969625-59969626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs543093512	chr5:59969649-59969650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs118130756	chr5:59969704-59969705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs75665684	chr5:59969705-59969706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552131116	chr5:59969778-59969779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs77246392	chr5:59969784-59969785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs570376341	chr5:59969965-59969966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs559335763	chr5:59969995-59969996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs528303077	chr5:59970009-59970010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs144770684	chr5:59970067-59970068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs180797552	chr5:59970129-59970130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs562185256	chr5:59970202-59970203	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs141800931	chr5:59970203-59970204	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs367907116	chr5:59970398-59970399	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs34184927	chr5:59970511-59970512	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs570872877	chr5:59970531-59970532	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs539405018	chr5:59970581-59970582	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs372482728	chr5:59970619-59970620	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs569301207	chr5:59970628-59970629	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs549819545	chr5:59970658-59970659	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs567020910	chr5:59970667-59970668	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs116033676	chr5:59970690-59970691	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs187579249	chr5:59970705-59970706	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs368499529	chr5:59970771-59970772	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs573682312	chr5:59970914-59970915	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs544381340	chr5:59970922-59970923	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs555571892	chr5:59970945-59970946	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs79730084	chr5:59970992-59970993	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs575414747	chr5:59970995-59970996	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	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
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	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
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Bipolar disorder	19114987	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	21272361	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Contiguous gene syndrome	19525295	CNVD

Chromatin state (count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59933600-59981000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr5:59943400-59977000	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr5:59954000-59980200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr5:59954600-59969200	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr5:59956800-59981800	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr5:59957000-59977000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr5:59960000-59970600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr5:59962400-59970800	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr5:59962600-59969200	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr5:59962600-59969400	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr5:59962600-59970200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr5:59962600-59977000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr5:59962600-59980000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr5:59962600-59980800	Weak transcription	Fetal Thymus	thymus
15	chr5:59962600-59981000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr5:59962600-59981600	Weak transcription	Fetal Muscle Leg	muscle
17	chr5:59962600-59985600	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr5:59962600-59986800	Weak transcription	Fetal Stomach	stomach
19	chr5:59962600-59990000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr5:59962800-59974000	Weak transcription	Dnd41	blood
21	chr5:59962800-59976600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr5:59962800-59978600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr5:59962800-59978800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr5:59964600-59974600	Enhancers	Fetal Intestine Large	intestine
25	chr5:59964800-59974200	Enhancers	Fetal Intestine Small	intestine
26	chr5:59966000-59988800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr5:59966200-59970400	Enhancers	Stomach Mucosa	stomach
28	chr5:59967000-59970200	Enhancers	Rectal Mucosa Donor 29	rectum
29	chr5:59967400-59969600	Enhancers	Liver	Liver
30	chr5:59967400-59970800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr5:59967400-59981800	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr5:59967800-59969800	Enhancers	K562	blood
33	chr5:59968000-59970400	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr5:59968000-59972400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr5:59968000-59978800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr5:59968000-59981800	Weak transcription	Thymus	Thymus
37	chr5:59968400-59969800	Enhancers	Fetal Kidney	kidney
38	chr5:59968600-59969400	Enhancers	A549	lung
39	chr5:59968600-59969400	Strong transcription	GM12878-XiMat	blood
40	chr5:59968600-59969600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
41	chr5:59968600-59970000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr5:59968600-59970000	Enhancers	Fetal Brain Male	brain
43	chr5:59968800-59969400	Enhancers	Pancreas	Pancrea
44	chr5:59968800-59969600	Enhancers	Fetal Lung	lung
45	chr5:59968800-59969800	Enhancers	Fetal Brain Female	brain
46	chr5:59968800-59969800	Enhancers	Placenta	Placenta
47	chr5:59968800-59970600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr5:59969000-59969200	Weak transcription	Primary hematopoietic stem cells	blood
49	chr5:59969000-59969400	Enhancers	Small Intestine	intestine
50	chr5:59969000-59969400	Flanking Active TSS	HepG2	liver

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