Variant report

Variant	nsv880535
Chromosome Location	chr5:27376682-27706007
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1407)
CpG islands
(count:489)
Chromatin interactive
region (count:43)
LncRNA
region (count:45)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1407 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:27471950-27472762	HepG2	liver:	n/a	n/a
2	ATF1	chr5:27428887-27428920	K562	blood:	n/a	n/a
3	ATF1	chr5:27558936-27558964	K562	blood:	n/a	n/a
4	ATF2	chr5:27472335-27472849	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr5:27480439-27480694	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr5:27472100-27472589	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr5:27652535-27652935	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr5:27652689-27652930	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr5:27556668-27556706	K562	blood:	n/a	n/a
10	BACH1	chr5:27472602-27472610	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr5:27661991-27662055	K562	blood:	n/a	n/a
12	BHLHE40	chr5:27390071-27390112	K562	blood:	n/a	n/a
13	BHLHE40	chr5:27523477-27524035	K562	blood:	n/a	n/a
14	BHLHE40	chr5:27619787-27619798	GM12878	blood:	n/a	n/a
15	BHLHE40	chr5:27523586-27524110	HepG2	liver:	n/a	n/a
16	BHLHE40	chr5:27473142-27473831	HepG2	liver:	n/a	n/a
17	BHLHE40	chr5:27473140-27473798	GM12878	blood:	n/a	n/a
18	BHLHE40	chr5:27473085-27473935	K562	blood:	n/a	n/a
19	BHLHE40	chr5:27472077-27472614	GM12878	blood:	n/a	n/a
20	BHLHE40	chr5:27473428-27473653	HepG2	liver:	n/a	n/a
21	BHLHE40	chr5:27473412-27473860	A549	lung:	n/a	n/a
22	BRCA1	chr5:27702297-27703320	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr5:27573051-27573067	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr5:27690611-27690620	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr5:27403373-27403840	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr5:27472043-27473952	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr5:27448587-27448827	HepG2	liver:	n/a	chr5:27448671-27448682
28	CEBPB	chr5:27652664-27653021	HepG2	liver:	n/a	chr5:27652846-27652857
29	CEBPB	chr5:27496435-27496760	HepG2	liver:	n/a	chr5:27496587-27496600 chr5:27496589-27496598 chr5:27496589-27496600 chr5:27496587-27496600 chr5:27496587-27496598
30	CEBPB	chr5:27376600-27376800	A549	lung:	n/a	chr5:27376717-27376728
31	CEBPB	chr5:27488786-27488986	HepG2	liver:	n/a	chr5:27488807-27488820 chr5:27488848-27488857 chr5:27488846-27488857 chr5:27488809-27488820 chr5:27488809-27488820 chr5:27488807-27488818 chr5:27488807-27488820
32	CEBPB	chr5:27554835-27555111	IMR90	lung:	n/a	chr5:27554975-27554986
33	CEBPB	chr5:27611376-27611664	A549	lung:	n/a	chr5:27611459-27611470 chr5:27611545-27611556
34	CEBPB	chr5:27702080-27703426	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr5:27402580-27402860	HepG2	liver:	n/a	chr5:27402684-27402697 chr5:27402755-27402766
36	CEBPB	chr5:27541950-27542182	HepG2	liver:	n/a	chr5:27541959-27541970 chr5:27541996-27542007
37	CEBPB	chr5:27674174-27674519	Hela-S3	cervix:	n/a	chr5:27674346-27674355 chr5:27674346-27674355 chr5:27674344-27674357 chr5:27674346-27674355
38	CEBPB	chr5:27674171-27674520	HepG2	liver:	n/a	chr5:27674346-27674355 chr5:27674346-27674355 chr5:27674344-27674357 chr5:27674346-27674355
39	CEBPB	chr5:27704950-27705251	A549	lung:	n/a	chr5:27705070-27705081
40	CEBPB	chr5:27704941-27705258	Hela-S3	cervix:	n/a	chr5:27705070-27705081
41	CEBPB	chr5:27496418-27496770	IMR90	lung:	n/a	chr5:27496587-27496600 chr5:27496589-27496598 chr5:27496589-27496600 chr5:27496587-27496600 chr5:27496587-27496598
42	CEBPB	chr5:27402961-27403754	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr5:27390828-27391122	IMR90	lung:	n/a	n/a
44	CEBPB	chr5:27531759-27531985	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr5:27510117-27510388	Hela-S3	cervix:	n/a	chr5:27510236-27510247
46	CEBPB	chr5:27556395-27556606	A549	lung:	n/a	chr5:27556450-27556461
47	CEBPB	chr5:27472147-27472690	HepG2	liver:	n/a	n/a
48	CEBPB	chr5:27652624-27653031	H1-hESC	embryonic stem cell:	n/a	chr5:27652846-27652857
49	CEBPB	chr5:27472163-27473883	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr5:27496448-27496745	Hela-S3	cervix:	n/a	chr5:27496587-27496600 chr5:27496589-27496598 chr5:27496589-27496600 chr5:27496587-27496600 chr5:27496587-27496598

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:27523974-27524024	AG09309	skin:	n/a
2	chr5:27523974-27524024	AG09309	skin:	n/a
3	chr5:27472542-27472592	A549	lung:	n/a
4	chr5:27472029-27472079	HPAEpiC	pulmonary alveolar:	n/a
5	chr5:27523909-27523959	HEK293	kidney:	embryo
6	chr5:27472520-27472570	NH-A	brain:	n/a
7	chr5:27387958-27388008	BE2_C	brain:	n/a
8	chr5:27523974-27524024	Caco-2	colon:	n/a
9	chr5:27472029-27472079	MCF-7	breast:	n/a
10	chr5:27387958-27388008	GM12892	blood:	n/a
11	chr5:27532684-27532734	PFSK-1	brain:	n/a
12	chr5:27472029-27472079	GM12892	blood:	n/a
13	chr5:27387958-27388008	GM19239	blood:	n/a
14	chr5:27472520-27472570	HCM	heart:	n/a
15	chr5:27438836-27438886	HUVEC	blood vessel:	n/a
16	chr5:27472029-27472079	Hela-S3	cervix:	n/a
17	chr5:27523974-27524024	SAEC	small airway:	n/a
18	chr5:27387958-27388008	HRCEpiC	kidney:	n/a
19	chr5:27532684-27532734	NT2-D1	testis:	n/a
20	chr5:27523974-27524024	MCF-7	breast:	n/a
21	chr5:27523909-27523959	HUVEC	blood vessel:	n/a
22	chr5:27438836-27438886	HEK293	kidney:	embryo
23	chr5:27472542-27472592	AG04449	skin:	fetal
24	chr5:27523974-27524024	BE2_C	brain:	n/a
25	chr5:27523909-27523959	HL-60	blood:	n/a
26	chr5:27523909-27523959	HRE	kidney:	n/a
27	chr5:27472029-27472079	A549	lung:	n/a
28	chr5:27387958-27388008	SK-N-SH	brain:	n/a
29	chr5:27472029-27472079	CMK	blood:	n/a
30	chr5:27523909-27523959	MCF10A-Er-Src	breast:	n/a
31	chr5:27523974-27524024	ProgFib	skin:	n/a
32	chr5:27472542-27472592	BJ	skin:	n/a
33	chr5:27523974-27524024	HNPCEpiC	eye:	n/a
34	chr5:27387958-27388008	U87	brain:	n/a
35	chr5:27532684-27532734	NH-A	brain:	n/a
36	chr5:27387958-27388008	HUVEC	blood vessel:	n/a
37	chr5:27523974-27524024	SKMC	muscle:	n/a
38	chr5:27438836-27438886	HRE	kidney:	n/a
39	chr5:27532684-27532734	GM19239	blood:	n/a
40	chr5:27523974-27524024	GM06990	blood:	n/a
41	chr5:27387958-27388008	AG04450	lung:	fetal
42	chr5:27472029-27472079	K562	blood:	n/a
43	chr5:27438836-27438886	AoSMC	blood vessel:	n/a
44	chr5:27472029-27472079	MCF10A-Er-Src	breast:	n/a
45	chr5:27472542-27472592	HEEpiC	esophagus:	n/a
46	chr5:27523974-27524024	HepG2	liver:	n/a
47	chr5:27472520-27472570	AG04449	skin:	fetal
48	chr5:27438836-27438886	HepG2	liver:	n/a
49	chr5:27523974-27524024	NT2-D1	testis:	n/a
50	chr5:27472029-27472079	SKMC	muscle:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:27386479..27389149-chr5:27394969..27398145,3	K562	blood:
2	chr5:27410717..27413698-chr5:27423274..27425658,2	K562	blood:
3	chr5:27483953..27485836-chr5:27487380..27490659,3	K562	blood:
4	chr10:69644380..69644911-chr5:27472591..27473140,2	Hela-S3	cervix:
5	chr5:27415884..27418944-chr5:27423264..27427119,3	K562	blood:
6	chr5:27483953..27486391-chr5:27488039..27490659,3	K562	blood:
7	chr5:27619372..27621025-chr5:27624606..27626826,2	K562	blood:
8	chr5:27606222..27608157-chr5:27609171..27611817,2	MCF-7	breast:
9	chr5:27384539..27388630-chr5:27389237..27391656,3	K562	blood:
10	chr5:27384451..27386814-chr5:27398781..27400428,2	K562	blood:
11	chr5:27422999..27425291-chr5:27429898..27432218,2	K562	blood:
12	chr5:27483953..27486391-chr5:27488039..27490659,3	K562	blood:
13	chr5:27386479..27389149-chr5:27394969..27398145,3	K562	blood:
14	chr5:27441556..27444509-chr5:27447634..27449803,2	K562	blood:
15	chr19:45907739..45908484-chr5:27472364..27473126,2	Hela-S3	cervix:
16	chr5:27356861..27358465-chr5:27382622..27384445,2	K562	blood:
17	chr5:27530537..27533471-chr5:27821180..27823240,2	K562	blood:
18	chr5:27619372..27621025-chr5:27624606..27626826,2	K562	blood:
19	chr5:27384539..27388630-chr5:27389237..27391656,3	K562	blood:
20	chr5:27465898..27467546-chr5:27470324..27472509,2	K562	blood:
21	chr5:27410717..27413698-chr5:27423274..27425658,2	K562	blood:
22	chr5:27441556..27444509-chr5:27447634..27449803,2	K562	blood:
23	chr5:27483622..27485658-chr5:27500054..27501684,2	K562	blood:
24	chr5:27415884..27418944-chr5:27423264..27427119,3	K562	blood:
25	chr5:27286321..27288328-chr5:27551307..27553852,2	MCF-7	breast:
26	chr5:27560772..27563762-chr5:27570947..27572476,2	MCF-7	breast:
27	chr5:27606222..27608157-chr5:27609171..27611817,2	MCF-7	breast:
28	chr3:133852407..133853154-chr5:27377165..27378018,2	MCF-7	breast:
29	chr5:27470415..27473388-chr5:27486185..27488435,2	K562	blood:
30	chr5:27467308..27469302-chr5:27473283..27475423,2	K562	blood:
31	chr5:27662645..27663246-chr6:2453687..2454350,2	MCF-7	breast:
32	chr5:27367781..27370478-chr5:27378982..27381299,2	MCF-7	breast:
33	chr5:27483953..27485836-chr5:27487380..27490659,3	K562	blood:
34	chr13:92004278..92006382-chr5:27545617..27547117,2	K562	blood:
35	chr5:27467308..27469302-chr5:27473283..27475423,2	K562	blood:
36	chr5:27384451..27386814-chr5:27398781..27400428,2	K562	blood:
37	chr5:27600351..27602569-chr5:27603495..27605126,2	K562	blood:
38	chr5:27560772..27563762-chr5:27570947..27572476,2	MCF-7	breast:
39	chr5:27483622..27485658-chr5:27500054..27501684,2	K562	blood:
40	chr5:27703201..27705490-chr5:27706279..27707941,2	MCF-7	breast:
41	chr5:27466020..27468393-chr5:27470324..27473144,3	K562	blood:
42	chr5:27422999..27425291-chr5:27429898..27432218,2	K562	blood:
43	chr5:27600351..27602569-chr5:27603495..27605126,2	K562	blood:

(count:45 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C5orf17-13	chr5:27497127-27497768	NONHSAT100808
2	lnc-C5orf17-8	chr5:27472418-27472626	XLOC_004323
3	lnc-C5orf17-8	chr5:27485033-27485136	ENSG00000250337
4	lnc-CDH9-2	chr5:27406639-27406877	XLOC_004761
5	lnc-CDH9-2	chr5:27412720-27412796	XLOC_004761
6	lnc-C5orf17-9	chr5:27574964-27575000	XLOC_004324
7	lnc-C5orf17-14	chr5:27511399-27511559	ucscGeneNc_uc003jgv_1
8	lnc-C5orf17-8	chr5:27494342-27494425	ENSG00000250337
9	lnc-C5orf17-14	chr5:27508148-27508383	ucscGeneNc_uc003jgv_1
10	lnc-CDH9-2	chr5:27412713-27412796	XLOC_004761
11	lnc-C5orf17-8	chr5:27476194-27477201	XLOC_004323
12	lnc-CDH9-2	chr5:27406639-27406877	XLOC_004761
13	lnc-CDH9-2	chr5:27412713-27412768	XLOC_004761
14	lnc-CDH9-2	chr5:27413322-27413758	XLOC_004761
15	lnc-CDH9-2	chr5:27436260-27436518	XLOC_004761
16	lnc-C5orf17-8	chr5:27472414-27472626	ENSG00000250337
17	lnc-C5orf17-8	chr5:27485033-27487999	XLOC_004323
18	lnc-C5orf17-8	chr5:27496056-27496274	XLOC_004323
19	lnc-C5orf17-8	chr5:27475642-27475802	XLOC_004323
20	lnc-C5orf17-8	chr5:27477746-27477908	ENSG00000250337
21	lnc-C5orf17-8	chr5:27485033-27485136	ENSG00000250337
22	lnc-CDH9-2	chr5:27409693-27409751	XLOC_004761
23	lnc-C5orf17-8	chr5:27475642-27475802	ENSG00000250337
24	lnc-CDH9-2	chr5:27423608-27423708	XLOC_004761
25	lnc-C5orf17-8	chr5:27494420-27494442	XLOC_004323
26	lnc-C5orf17-8	chr5:27472414-27472626	ENSG00000250337
27	lnc-CDH9-2	chr5:27406639-27406877	XLOC_004761
28	lnc-C5orf17-8	chr5:27475642-27475802	ENSG00000250337
29	lnc-C5orf17-14	chr5:27520790-27521692	ucscGeneNc_uc003jgv_1
30	lnc-CDH9-2	chr5:27413322-27413758	XLOC_004761
31	lnc-CDH9-9	chr5:27446084-27446144	l_2893_chr5:27442393-27446144_testes
32	lnc-C5orf17-8	chr5:27489389-27489493	ENSG00000250337
33	lnc-CDH9-2	chr5:27410327-27410387	XLOC_004761
34	lnc-CDH9-2	chr5:27406640-27406877	XLOC_004761
35	lnc-C5orf17-8	chr5:27494226-27494425	ENSG00000250337
36	lnc-C5orf17-8	chr5:27475642-27475802	ENSG00000250337
37	lnc-CDH9-9	chr5:27448470-27448525	l_2893_chr5:27442393-27446144_testes
38	lnc-C5orf17-9	chr5:27570754-27570955	XLOC_004324
39	lnc-CDH9-2	chr5:27428267-27428320	XLOC_004761
40	lnc-CDH9-9	chr5:27442394-27442634	l_2893_chr5:27442393-27446144_testes
41	lnc-C5orf17-8	chr5:27494342-27494425	ENSG00000250337
42	lnc-C5orf17-8	chr5:27476833-27477908	XLOC_004323
43	lnc-C5orf17-8	chr5:27489389-27489493	ENSG00000250337
44	lnc-C5orf17-8	chr5:27472414-27472626	ENSG00000250337
45	lnc-CDH9-2	chr5:27412775-27412796	XLOC_004761

No data

Variant related genes	Relation type
LINC01021	TF binding region
ENSG00000248490	TF binding region
LINC01021	CpG island
ENSG00000248490	CpG island
ENSG00000250337	chromatin interactions
ENSG00000104881	chromatin interactions
ENSG00000096717	chromatin interactions
CHEK1	miRNA target sites
RANBP10	miRNA target sites
TERF2	miRNA target sites
KRAS	miRNA target sites
YWHAQ	miRNA target sites
CKAP5	miRNA target sites
PTPN22	miRNA target sites
BTAF1	miRNA target sites
SIRT1	miRNA target sites
NUDT12	miRNA target sites
BCL2	miRNA target sites
SYNJ1	miRNA target sites
SCCPDH	miRNA target sites

Extended variants
information (count: 4033 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4033 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs57760953	chr5:27377811-27377812	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs374937523	chr5:27377822-27377823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191327421	chr5:27377824-27377825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149399326	chr5:27377853-27377854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183794108	chr5:27377855-27377856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs576180543	chr5:27377903-27377904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188624449	chr5:27377926-27377927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs543605606	chr5:27377927-27377928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565274477	chr5:27377935-27377936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs547403831	chr5:27377953-27377954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs115448616	chr5:27377964-27377965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541052005	chr5:27378005-27378006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs200573043	chr5:27378032-27378033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs143785581	chr5:27378054-27378055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529130456	chr5:27378083-27378084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs193247738	chr5:27378103-27378104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185659575	chr5:27378122-27378123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148007035	chr5:27378127-27378128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs372131142	chr5:27378148-27378149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs530773408	chr5:27378156-27378157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs552391176	chr5:27378171-27378172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190172283	chr5:27378188-27378189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs182728	chr5:27378197-27378198	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs547783480	chr5:27378217-27378218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs565894388	chr5:27378239-27378240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73747005	chr5:27378256-27378257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs181587682	chr5:27378257-27378258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs6872538	chr5:27378322-27378323	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs141658233	chr5:27378336-27378337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs368756934	chr5:27378373-27378374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs142665444	chr5:27387029-27387030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs550601103	chr5:27387079-27387080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs144821624	chr5:27387087-27387088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs16896750	chr5:27387088-27387089	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs114992933	chr5:27387176-27387177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs181568624	chr5:27387223-27387224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs9293266	chr5:27387253-27387254	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs555116440	chr5:27387261-27387262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs386686560	chr5:27387294-27387295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147918656	chr5:27387296-27387297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs139028117	chr5:27387300-27387301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs141766196	chr5:27387312-27387313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs146949189	chr5:27387337-27387338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs558092333	chr5:27387375-27387376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs10058813	chr5:27387385-27387386	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs528548296	chr5:27387395-27387396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs540842970	chr5:27387405-27387406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs562220255	chr5:27387408-27387409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs148014441	chr5:27387459-27387460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs373249043	chr5:27387466-27387467	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	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
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	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
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18194544	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Compulsive disorder	18923513	CNVD
Epilepsy	18923513	CNVD
Prader-willi syndrome	18923513	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:335 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:27377800-27378400	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr5:27378000-27378400	Enhancers	Placenta Amnion	Placenta Amnion
3	chr5:27387000-27389200	Enhancers	HepG2	liver
4	chr5:27387400-27388200	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr5:27387600-27388000	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr5:27387600-27388200	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr5:27387600-27388200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr5:27387600-27388200	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr5:27387600-27388200	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr5:27387600-27388800	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr5:27388200-27389800	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr5:27388600-27389800	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr5:27388800-27389800	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr5:27389200-27389600	Weak transcription	HepG2	liver
15	chr5:27389600-27390000	Enhancers	HepG2	liver
16	chr5:27389800-27390000	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr5:27389800-27390200	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr5:27392000-27393400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr5:27392400-27393600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr5:27402600-27404200	Active TSS	A549	lung
21	chr5:27403000-27403200	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr5:27403000-27403200	Enhancers	Hela-S3	cervix
23	chr5:27403200-27403800	Active TSS	Hela-S3	cervix
24	chr5:27403200-27404000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr5:27403400-27403800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr5:27403400-27403800	Active TSS	Fetal Muscle Leg	muscle
27	chr5:27403400-27404000	Active TSS	HMEC	breast
28	chr5:27403400-27404000	Active TSS	Osteobl	bone
29	chr5:27403400-27404200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr5:27403600-27404000	Active TSS	Pancreatic Islets	Pancreatic Islet
31	chr5:27410400-27411000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr5:27417800-27418200	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr5:27434000-27435200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr5:27434200-27435200	Enhancers	NHEK	skin
35	chr5:27435000-27435200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr5:27435000-27435400	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr5:27435000-27435400	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr5:27435000-27435600	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr5:27435200-27436200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr5:27436200-27436600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr5:27436400-27436600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr5:27436800-27449400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr5:27442800-27443200	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr5:27446600-27449200	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr5:27447600-27448400	ZNF genes & repeats	Spleen	Spleen
46	chr5:27450600-27451200	Enhancers	Fetal Heart	heart
47	chr5:27450800-27451000	Active TSS	Pancreatic Islets	Pancreatic Islet
48	chr5:27450800-27451200	Enhancers	Rectal Smooth Muscle	rectum
49	chr5:27450800-27451400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr5:27451000-27451400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet

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