Variant report

Variant	nsv4813
Chromosome Location	chr5:42157598-42202029
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:55)
CpG islands
(count:244)
Chromatin interactive
region (count:3)
LncRNA
region (count:43)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:55 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr5:42182922-42183030	MCF-7	breast:	n/a	n/a
2	CTCF	chr5:42180340-42180490	GM06990	blood:	n/a	n/a
3	CTCF	chr5:42182840-42182990	HPF	lung:	n/a	n/a
4	CTCF	chr5:42180280-42180430	GM12866	blood:	n/a	n/a
5	CTCF	chr5:42180260-42180410	HepG2	liver:	n/a	n/a
6	CTCF	chr5:42182940-42183090	Caco-2	colon:	n/a	n/a
7	CTCF	chr5:42180220-42180370	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr5:42182911-42182996	MCF-7	breast:	n/a	n/a
9	CTCF	chr5:42180200-42180350	GM06990	blood:	n/a	n/a
10	CTCF	chr5:42182932-42182983	LNCaP	prostate:	n/a	n/a
11	E2F4	chr5:42185650-42185769	MCF10A-Er-Src	breast:	n/a	chr5:42185744-42185753
12	EP300	chr5:42195812-42196365	T-47D	breast:	n/a	n/a
13	FAM48A	chr5:42165128-42165281	GM12878	blood:	n/a	n/a
14	FAM48A	chr5:42185055-42185233	GM12878	blood:	n/a	n/a
15	FAM48A	chr5:42188448-42188543	GM12878	blood:	n/a	n/a
16	FOS	chr5:42157365-42157708	MCF10A-Er-Src	breast:	n/a	chr5:42157534-42157544 chr5:42157535-42157544 chr5:42157536-42157543 chr5:42157535-42157543
17	FOS	chr5:42157355-42157713	MCF10A-Er-Src	breast:	n/a	chr5:42157534-42157544 chr5:42157535-42157544 chr5:42157536-42157543 chr5:42157535-42157543
18	FOS	chr5:42157366-42157727	MCF10A-Er-Src	breast:	n/a	chr5:42157534-42157544 chr5:42157535-42157544 chr5:42157536-42157543 chr5:42157535-42157543
19	FOS	chr5:42157386-42157689	MCF10A-Er-Src	breast:	n/a	chr5:42157534-42157544 chr5:42157535-42157544 chr5:42157536-42157543 chr5:42157535-42157543
20	FOXA1	chr5:42195924-42196399	T-47D	breast:	n/a	n/a
21	FOXA1	chr5:42170404-42170720	T-47D	breast:	n/a	n/a
22	FOXA1	chr5:42170374-42170715	T-47D	breast:	n/a	n/a
23	FOXA1	chr5:42195973-42196294	T-47D	breast:	n/a	n/a
24	FOXA2	chr5:42179113-42179552	A549	lung:	n/a	n/a
25	GATA3	chr5:42170376-42170762	T-47D	breast:	n/a	n/a
26	GATA3	chr5:42170345-42170789	T-47D	breast:	n/a	n/a
27	GATA3	chr5:42168278-42168606	T-47D	breast:	n/a	n/a
28	GATA3	chr5:42195923-42196330	T-47D	breast:	n/a	n/a
29	GATA3	chr5:42195933-42196358	T-47D	breast:	n/a	n/a
30	JUND	chr5:42195890-42196421	T-47D	breast:	n/a	n/a
31	JUND	chr5:42200123-42200597	HepG2	liver:	n/a	n/a
32	MAFF	chr5:42158617-42158733	HepG2	liver:	n/a	chr5:42158661-42158679
33	MAFK	chr5:42164558-42164700	HepG2	liver:	n/a	n/a
34	MAFK	chr5:42158572-42158749	HepG2	liver:	n/a	chr5:42158663-42158678
35	MAFK	chr5:42158561-42158809	HepG2	liver:	n/a	chr5:42158663-42158678
36	MAFK	chr5:42188857-42189109	HepG2	liver:	n/a	chr5:42188981-42189001 chr5:42188989-42189003
37	MAZ	chr5:42170499-42170513	HepG2	liver:	n/a	n/a
38	MYC	chr5:42157393-42157638	MCF10A-Er-Src	breast:	n/a	chr5:42157534-42157543 chr5:42157535-42157544
39	MYC	chr5:42157467-42157681	MCF10A-Er-Src	breast:	n/a	chr5:42157534-42157543 chr5:42157535-42157544
40	POLR2A	chr5:42194970-42195002	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr5:42190375-42190708	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr5:42160223-42160393	ProgFib	skin:	n/a	n/a
43	POLR2A	chr5:42167869-42168134	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr5:42169589-42169639	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr5:42182853-42182936	A549	lung:	n/a	n/a
46	POLR2A	chr5:42183450-42183853	H1-neurons	neurons:	n/a	n/a
47	POLR2A	chr5:42196483-42196536	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr5:42192933-42192962	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr5:42183478-42183902	H1-neurons	neurons:	n/a	n/a
50	POLR2A	chr5:42199831-42199886	MCF10A-Er-Src	breast:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:42175438-42175488	SK-N-MC	brain:	n/a
2	chr5:42176806-42176856	HRPEpiC	eye:	n/a
3	chr5:42175438-42175488	H1-hESC	embryonic stem cell:	embryo
4	chr5:42176806-42176856	GM12892	blood:	n/a
5	chr5:42175438-42175488	SK-N-SH_RA	brain:	n/a
6	chr5:42175368-42175418	HIPEpiC	eye:	n/a
7	chr5:42176454-42176504	SAEC	small airway:	n/a
8	chr5:42175438-42175488	HEK293	kidney:	embryo
9	chr5:42175368-42175418	GM19239	blood:	n/a
10	chr5:42175368-42175418	Hela-S3	cervix:	n/a
11	chr5:42175438-42175488	HRPEpiC	eye:	n/a
12	chr5:42175368-42175418	SK-N-MC	brain:	n/a
13	chr5:42175368-42175418	AG10803	skin:	n/a
14	chr5:42176454-42176504	U87	brain:	n/a
15	chr5:42175368-42175418	NHDF-neo	bronchial:	n/a
16	chr5:42176454-42176504	SK-N-SH	brain:	n/a
17	chr5:42175368-42175418	U87	brain:	n/a
18	chr5:42176806-42176856	HIPEpiC	eye:	n/a
19	chr5:42176454-42176504	HIPEpiC	eye:	n/a
20	chr5:42176806-42176856	HUVEC	blood vessel:	n/a
21	chr5:42176806-42176856	LNCaP	prostate:	n/a
22	chr5:42175438-42175488	GM12891	blood:	n/a
23	chr5:42176806-42176856	AG04450	lung:	fetal
24	chr5:42175438-42175488	AG09309	skin:	n/a
25	chr5:42175368-42175418	HUVEC	blood vessel:	n/a
26	chr5:42175438-42175488	HEEpiC	esophagus:	n/a
27	chr5:42175368-42175418	BJ	skin:	n/a
28	chr5:42176806-42176856	IMR90	lung:	fetal
29	chr5:42175438-42175488	HMEC	breast:	n/a
30	chr5:42175438-42175488	HIPEpiC	eye:	n/a
31	chr5:42176806-42176856	HCM	heart:	n/a
32	chr5:42176454-42176504	ovcar-3	ovarian:	n/a
33	chr5:42176454-42176504	AoSMC	blood vessel:	n/a
34	chr5:42176454-42176504	BJ	skin:	n/a
35	chr5:42176454-42176504	Jurkat	blood:	n/a
36	chr5:42176454-42176504	Hela-S3	cervix:	n/a
37	chr5:42176806-42176856	SK-N-SH	brain:	n/a
38	chr5:42175368-42175418	HPAEpiC	pulmonary alveolar:	n/a
39	chr5:42176454-42176504	CMK	blood:	n/a
40	chr5:42176806-42176856	K562	blood:	n/a
41	chr5:42175368-42175418	SAEC	small airway:	n/a
42	chr5:42176454-42176504	MCF-7	breast:	n/a
43	chr5:42176806-42176856	HNPCEpiC	eye:	n/a
44	chr5:42175438-42175488	HPAEpiC	pulmonary alveolar:	n/a
45	chr5:42175368-42175418	GM06990	blood:	n/a
46	chr5:42175368-42175418	AoSMC	blood vessel:	n/a
47	chr5:42175368-42175418	HCPEpiC	choroid plexus:	n/a
48	chr5:42176806-42176856	NHDF-neo	bronchial:	n/a
49	chr5:42175368-42175418	HCT-116	colon:	n/a
50	chr5:42176806-42176856	AG10803	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:42164889..42166959-chr5:42173984..42175632,2	K562	blood:
2	chr5:42164889..42166959-chr5:42173984..42175632,2	K562	blood:
3	chr5:42182671..42183209-chr7:83415074..83415902,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OXCT1-1	chr5:42159439-42159548	XLOC_004800
2	lnc-OXCT1-1	chr5:42159439-42159548	NR_104635
3	lnc-OXCT1-1	chr5:42159129-42159155	NR_104636
4	lnc-OXCT1-1	chr5:42159129-42159155	XLOC_004800
5	lnc-OXCT1-1	chr5:42159439-42159548	ENSG00000248519
6	lnc-OXCT1-1	chr5:42159129-42159155	XLOC_004800
7	lnc-FBXO4-1	chr5:42157823-42157966	NONHSAT101190
8	lnc-OXCT1-1	chr5:42175255-42175444	XLOC_004800
9	lnc-OXCT1-1	chr5:42159439-42159548	XLOC_004800
10	lnc-OXCT1-1	chr5:42159127-42159155	XLOC_004800
11	lnc-FBXO4-1	chr5:42168564-42168689	NONHSAT101190
12	lnc-OXCT1-1	chr5:42175255-42175447	NR_104636
13	lnc-OXCT1-1	chr5:42159127-42159155	XLOC_004800
14	lnc-OXCT1-1	chr5:42168565-42168689	NR_104635
15	lnc-OXCT1-1	chr5:42175255-42175444	XLOC_004800
16	lnc-FBXO4-1	chr5:42159327-42159548	NONHSAT101190
17	lnc-OXCT1-1	chr5:42168565-42168689	ENSG00000248519
18	lnc-OXCT1-1	chr5:42159439-42159548	XLOC_004800
19	lnc-OXCT1-2	chr5:42195196-42195305	ucscGeneNc_uc003jms_1
20	lnc-OXCT1-2	chr5:42191692-42193270	ucscGeneNc_uc003jms_1
21	lnc-OXCT1-1	chr5:42168565-42168689	XLOC_004800
22	lnc-FBXO4-1	chr5:42157824-42157966	XLOC_004360
23	lnc-OXCT1-1	chr5:42175255-42175444	XLOC_004800
24	lnc-OXCT1-1	chr5:42168565-42168689	XLOC_004800
25	lnc-OXCT1-1	chr5:42159129-42159155	XLOC_004800
26	lnc-OXCT1-1	chr5:42159439-42159548	NR_104636
27	lnc-FBXO4-1	chr5:42159126-42159155	NONHSAT101190
28	lnc-OXCT1-1	chr5:42159439-42159548	XLOC_004800
29	lnc-OXCT1-1	chr5:42159439-42159548	XLOC_004800
30	lnc-OXCT1-1	chr5:42175255-42175444	XLOC_004800
31	lnc-OXCT1-1	chr5:42159439-42159548	XLOC_004800
32	lnc-OXCT1-1	chr5:42159439-42159548	XLOC_004800
33	lnc-FBXO4-1	chr5:42175254-42175444	NONHSAT101190
34	lnc-OXCT1-1	chr5:42175255-42175447	NR_104635
35	lnc-OXCT1-1	chr5:42168565-42168689	XLOC_004800
36	lnc-GHR-1	chr5:42188368-42191625	ENSG00000260786.1
37	lnc-OXCT1-1	chr5:42168565-42168678	XLOC_004800
38	lnc-OXCT1-1	chr5:42175255-42175356	ENSG00000248519
39	lnc-OXCT1-1	chr5:42175255-42175366	XLOC_004800
40	lnc-OXCT1-1	chr5:42159439-42159548	XLOC_004800
41	lnc-OXCT1-1	chr5:42175255-42175366	XLOC_004800
42	lnc-OXCT1-1	chr5:42159129-42159155	XLOC_004800
43	lnc-OXCT1-1	chr5:42175255-42175275	XLOC_004800

No data

Variant related genes	Relation type
ENSG00000260786	TF binding region
ENSG00000260786	CpG island
FBLIM1	miRNA target sites
VN1R1	miRNA target sites
BIRC6	miRNA target sites
HADH	miRNA target sites
PHLPP2	miRNA target sites
MDFIC	miRNA target sites
FNDC3B	miRNA target sites
BLCAP	miRNA target sites
FAM171B	miRNA target sites
SERPINB9	miRNA target sites
CLIP3	miRNA target sites
BIRC5	miRNA target sites
ZC3H12C	miRNA target sites
FCHO2	miRNA target sites
ALCAM	miRNA target sites

Extended variants
information (count: 569 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:569 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554599758	chr5:42157644-42157645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs4957204	chr5:42157649-42157650	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs550781122	chr5:42157709-42157710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192143204	chr5:42157802-42157803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185179847	chr5:42157843-42157844	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs115956917	chr5:42157858-42157859	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs190467784	chr5:42157882-42157883	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs561175107	chr5:42157913-42157914	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs182175492	chr5:42157918-42157919	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs531063694	chr5:42157925-42157926	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs550730358	chr5:42157943-42157944	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs78599417	chr5:42157962-42157963	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs62370484	chr5:42157980-42157981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560939224	chr5:42158014-42158015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs147743944	chr5:42158028-42158029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs547091085	chr5:42158055-42158056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185961337	chr5:42158071-42158072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538835309	chr5:42158073-42158074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548725335	chr5:42158170-42158171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550453355	chr5:42158191-42158192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148391507	chr5:42158192-42158193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs142359934	chr5:42158199-42158200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs569218569	chr5:42158205-42158206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs148804251	chr5:42158238-42158239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534172606	chr5:42158256-42158257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs386687616	chr5:42158275-42158276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs554637415	chr5:42158301-42158302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs528031582	chr5:42158307-42158308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs572856552	chr5:42158319-42158320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs75514903	chr5:42158353-42158354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs142501974	chr5:42158411-42158412	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531252089	chr5:42158418-42158419	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576825604	chr5:42158504-42158505	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113748721	chr5:42158517-42158518	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs140729953	chr5:42158523-42158524	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs371081567	chr5:42158587-42158588	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375603948	chr5:42158588-42158589	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575574533	chr5:42158599-42158600	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs144633139	chr5:42158611-42158612	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561217525	chr5:42158640-42158641	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs528480473	chr5:42158657-42158658	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs146707584	chr5:42158739-42158740	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs188055055	chr5:42158794-42158795	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs532495005	chr5:42158827-42158828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs550790266	chr5:42158833-42158834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs552435177	chr5:42158851-42158852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs73080081	chr5:42158873-42158874	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs536575689	chr5:42158886-42158887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs548526416	chr5:42158922-42158923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569381676	chr5:42158934-42158935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
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
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
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
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	22286061	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	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Hepatocellular carcinoma	18929564	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:42152600-42158400	Weak transcription	Adipose Nuclei	Adipose
2	chr5:42153400-42158400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr5:42156400-42157600	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr5:42156600-42157600	Enhancers	Fetal Heart	heart
5	chr5:42156800-42157600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr5:42157200-42157600	Enhancers	NHEK	skin
7	chr5:42157600-42158000	Weak transcription	Fetal Heart	heart
8	chr5:42158000-42159000	Enhancers	Fetal Heart	heart
9	chr5:42158400-42158600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr5:42158400-42158800	Strong transcription	Adipose Nuclei	Adipose
11	chr5:42158800-42161000	Weak transcription	Adipose Nuclei	Adipose
12	chr5:42168200-42168800	Enhancers	H1 Cell Line	embryonic stem cell
13	chr5:42168400-42168800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr5:42168400-42168800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr5:42168400-42168800	Enhancers	Esophagus	oesophagus
16	chr5:42168400-42169000	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr5:42168400-42169200	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr5:42168600-42169200	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr5:42173800-42175200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr5:42173800-42175400	Active TSS	Adipose Nuclei	Adipose
21	chr5:42175200-42175400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr5:42175200-42176400	Enhancers	Ovary	ovary
23	chr5:42175400-42175800	Weak transcription	Adipose Nuclei	Adipose
24	chr5:42175400-42177000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr5:42175800-42177000	Enhancers	Adipose Nuclei	Adipose
26	chr5:42177400-42177800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
27	chr5:42182800-42183000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr5:42189800-42190200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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