Variant report

Variant	nsv1028759
Chromosome Location	chr5:112300490-112358514
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1365)
CpG islands
(count:977)
Chromatin interactive
region (count:67)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:1365 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:112331599-112332110	K562	blood:	n/a	n/a
2	ARID3A	chr5:112311741-112312466	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:112314010-112314936	K562	blood:	n/a	n/a
4	ARID3A	chr5:112314122-112315087	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:112356054-112356887	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:112305141-112305502	K562	blood:	n/a	n/a
7	ARID3A	chr5:112315420-112315798	K562	blood:	n/a	n/a
8	ARID3A	chr5:112338145-112338444	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:112309657-112309842	K562	blood:	n/a	n/a
10	ARID3A	chr5:112304331-112304845	HepG2	liver:	n/a	n/a
11	ATF1	chr5:112315379-112315733	K562	blood:	n/a	n/a
12	ATF1	chr5:112314616-112314856	K562	blood:	n/a	n/a
13	ATF2	chr5:112304969-112305601	GM12878	blood:	n/a	n/a
14	ATF2	chr5:112314466-112314881	GM12878	blood:	n/a	n/a
15	ATF2	chr5:112311910-112312892	GM12878	blood:	n/a	n/a
16	ATF2	chr5:112305065-112305600	GM12878	blood:	n/a	n/a
17	ATF2	chr5:112312179-112312635	GM12878	blood:	n/a	n/a
18	ATF3	chr5:112314539-112314910	K562	blood:	n/a	n/a
19	BACH1	chr5:112305173-112305398	K562	blood:	n/a	n/a
20	BACH1	chr5:112312635-112313210	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr5:112305142-112305350	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr5:112305082-112305568	GM12878	blood:	n/a	chr5:112305283-112305294
23	BATF	chr5:112312377-112312647	GM12878	blood:	n/a	n/a
24	BATF	chr5:112305110-112305495	GM12878	blood:	n/a	chr5:112305283-112305294
25	BATF	chr5:112301602-112301889	GM12878	blood:	n/a	chr5:112301778-112301789
26	BCL11A	chr5:112305189-112305477	GM12878	blood:	n/a	n/a
27	BCL11A	chr5:112305092-112305622	GM12878	blood:	n/a	n/a
28	BCL3	chr5:112311902-112312813	A549	lung:	n/a	chr5:112312160-112312169
29	BCL3	chr5:112312003-112312786	A549	lung:	n/a	chr5:112312160-112312169
30	BCLAF1	chr5:112331668-112332141	GM12878	blood:	n/a	chr5:112332017-112332026
31	BCLAF1	chr5:112305092-112305684	GM12878	blood:	n/a	n/a
32	BCLAF1	chr5:112311838-112312959	GM12878	blood:	n/a	chr5:112312160-112312169 chr5:112312855-112312868
33	BHLHE40	chr5:112313263-112313613	K562	blood:	n/a	n/a
34	BHLHE40	chr5:112311458-112312697	K562	blood:	n/a	n/a
35	BHLHE40	chr5:112305117-112305526	GM12878	blood:	n/a	n/a
36	BHLHE40	chr5:112309562-112310034	K562	blood:	n/a	n/a
37	BHLHE40	chr5:112358408-112358807	GM12878	blood:	n/a	n/a
38	BHLHE40	chr5:112305124-112305788	K562	blood:	n/a	n/a
39	BHLHE40	chr5:112312029-112312924	GM12878	blood:	n/a	chr5:112312792-112312808
40	BRCA1	chr5:112312618-112312679	H1-hESC	embryonic stem cell:	n/a	n/a
41	BRCA1	chr5:112313084-112313085	GM12878	blood:	n/a	n/a
42	BRCA1	chr5:112311894-112312263	H1-hESC	embryonic stem cell:	n/a	n/a
43	BRCA1	chr5:112312604-112312685	GM12878	blood:	n/a	n/a
44	BRCA1	chr5:112312073-112312262	HepG2	liver:	n/a	n/a
45	CBX3	chr5:112309476-112309969	K562	blood:	n/a	n/a
46	CBX3	chr5:112356118-112356899	HCT-116	colon:	n/a	n/a
47	CBX3	chr5:112305067-112305889	K562	blood:	n/a	n/a
48	CBX3	chr5:112311850-112312679	K562	blood:	n/a	n/a
49	CBX3	chr5:112356072-112356997	HCT-116	colon:	n/a	n/a
50	CBX3	chr5:112311680-112312959	K562	blood:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:112312643-112312693	ECC-1	luminal epithelium:	n/a
2	chr5:112312643-112312693	ECC-1	luminal epithelium:	n/a
3	chr5:112312951-112313001	HL-60	blood:	n/a
4	chr5:112320495-112320545	NHBE	bronchial:	n/a
5	chr5:112312254-112312304	SK-N-MC	brain:	n/a
6	chr5:112356289-112356339	U87	brain:	n/a
7	chr5:112312254-112312304	HUVEC	blood vessel:	n/a
8	chr5:112312254-112312304	A549	lung:	n/a
9	chr5:112312497-112312547	NT2-D1	testis:	n/a
10	chr5:112312497-112312547	NH-A	brain:	n/a
11	chr5:112356289-112356339	BJ	skin:	n/a
12	chr5:112320495-112320545	HPAEpiC	pulmonary alveolar:	n/a
13	chr5:112305407-112305457	HCF	heart:	n/a
14	chr5:112312957-112313007	ovcar-3	ovarian:	n/a
15	chr5:112312406-112312456	GM12892	blood:	n/a
16	chr5:112312497-112312547	AG04449	skin:	fetal
17	chr5:112312951-112313001	AG09309	skin:	n/a
18	chr5:112312406-112312456	GM19239	blood:	n/a
19	chr5:112312093-112312143	Jurkat	blood:	n/a
20	chr5:112309167-112309217	SAEC	small airway:	n/a
21	chr5:112312254-112312304	GM12892	blood:	n/a
22	chr5:112312164-112312214	K562	blood:	n/a
23	chr5:112312232-112312282	HCF	heart:	n/a
24	chr5:112320495-112320545	GM06990	blood:	n/a
25	chr5:112312164-112312214	BJ	skin:	n/a
26	chr5:112312232-112312282	GM12891	blood:	n/a
27	chr5:112312164-112312214	GM06990	blood:	n/a
28	chr5:112312093-112312143	PFSK-1	brain:	n/a
29	chr5:112312232-112312282	Hela-S3	cervix:	n/a
30	chr5:112305407-112305457	H1-hESC	embryonic stem cell:	embryo
31	chr5:112332984-112333034	AoSMC	blood vessel:	n/a
32	chr5:112312254-112312304	MCF10A-Er-Src	breast:	n/a
33	chr5:112312643-112312693	IMR90	lung:	fetal
34	chr5:112305407-112305457	HUVEC	blood vessel:	n/a
35	chr5:112312232-112312282	NHDF-neo	bronchial:	n/a
36	chr5:112332984-112333034	ProgFib	skin:	n/a
37	chr5:112320495-112320545	ProgFib	skin:	n/a
38	chr5:112312232-112312282	PANC-1	pancreas:	n/a
39	chr5:112312643-112312693	HRE	kidney:	n/a
40	chr5:112312254-112312304	SKMC	muscle:	n/a
41	chr5:112312497-112312547	HPAEpiC	pulmonary alveolar:	n/a
42	chr5:112356289-112356339	ovcar-3	ovarian:	n/a
43	chr5:112312254-112312304	BJ	skin:	n/a
44	chr5:112315632-112315682	H1-hESC	embryonic stem cell:	embryo
45	chr5:112312406-112312456	AG09319	gingival:	n/a
46	chr5:112312093-112312143	NHBE	bronchial:	n/a
47	chr5:112309167-112309217	ovcar-3	ovarian:	n/a
48	chr5:112312643-112312693	MCF10A-Er-Src	breast:	n/a
49	chr5:112312643-112312693	SK-N-SH_RA	brain:	n/a
50	chr5:112312406-112312456	IMR90	lung:	fetal

(count:67 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:112295383..112297610-chr5:112302677..112305586,2	K562	blood:
2	chr5:112311145..112314018-chr5:112314616..112318663,4	MCF-7	breast:
3	chr5:112312174..112316217-chr5:112322371..112325036,3	K562	blood:
4	chr5:112305819..112307438-chr5:112325134..112326776,2	K562	blood:
5	chr5:112293295..112296045-chr5:112298149..112301329,3	MCF-7	breast:
6	chr17:8286009..8286509-chr5:112311786..112312581,2	NB4	blood:
7	chr22:29196449..29197081-chr5:112312184..112312841,2	HCT-116	colon:
8	chr5:112299891..112302551-chr5:112304057..112307148,4	K562	blood:
9	chr5:89770106..89771750-chr5:112311690..112313641,2	K562	blood:
10	chr5:112202949..112204762-chr5:112314290..112317071,2	MCF-7	breast:
11	chr5:112304286..112307784-chr5:112309316..112313122,5	MCF-7	breast:
12	chr5:112238408..112240377-chr5:112318483..112320645,2	K562	blood:
13	chr5:112325917..112328748-chr5:112331994..112335756,3	K562	blood:
14	chr5:112255338..112258184-chr5:112308831..112311561,3	MCF-7	breast:
15	chr5:112330272..112333699-chr5:112335984..112338498,3	K562	blood:
16	chr5:112308899..112310478-chr5:112310482..112312099,2	MCF-7	breast:
17	chr5:112313991..112316155-chr5:112326453..112328052,2	K562	blood:
18	chr5:112310720..112312332-chr5:112321502..112323309,2	MCF-7	breast:
19	chr5:112312383..112314551-chr5:112314826..112319334,4	MCF-7	breast:
20	chr5:112328300..112329801-chr5:112353472..112355961,2	MCF-7	breast:
21	chr5:112331454..112332350-chr5:112714388..112714930,2	K562	blood:
22	chr5:112305819..112307438-chr5:112325134..112326776,2	K562	blood:
23	chr5:112349384..112350972-chr5:112360644..112363312,2	MCF-7	breast:
24	chr5:112255914..112262078-chr5:112308752..112315375,16	MCF-7	breast:
25	chr5:112197171..112198752-chr5:112310924..112312714,2	MCF-7	breast:
26	chr5:112306796..112308962-chr5:112312352..112314828,2	MCF-7	breast:
27	chr5:112299891..112302551-chr5:112304057..112307148,4	K562	blood:
28	chr5:112346718..112348969-chr5:112352127..112354346,2	MCF-7	breast:
29	chr5:112314675..112316382-chr5:112352070..112354061,2	K562	blood:
30	chr5:112312686..112316155-chr5:112325860..112328052,3	K562	blood:
31	chr5:112331438..112332505-chr5:112665779..112666817,4	MCF-7	breast:
32	chr5:112312686..112316155-chr5:112325860..112328052,3	K562	blood:
33	chr5:112255892..112258052-chr5:112329081..112331628,2	MCF-7	breast:
34	chr5:112356556..112358824-chr5:112361701..112363317,2	K562	blood:
35	chr5:112296171..112299064-chr5:112312877..112315865,3	K562	blood:
36	chr5:112325066..112326678-chr5:112327871..112329666,2	K562	blood:
37	chr5:112255746..112257849-chr5:112312359..112314246,3	MCF-7	breast:
38	chr5:112249716..112252598-chr5:112302249..112303940,2	MCF-7	breast:
39	chr5:112255209..112259355-chr5:112310614..112316433,9	K562	blood:
40	chr5:112291720..112294004-chr5:112309905..112311791,2	MCF-7	breast:
41	chr5:112312938..112314772-chr5:112369842..112371988,2	K562	blood:
42	chr5:112324079..112326587-chr5:112329747..112331307,2	K562	blood:
43	chr5:112308899..112310478-chr5:112310482..112312099,2	MCF-7	breast:
44	chr5:112312385..112315007-chr5:112318753..112321264,2	MCF-7	breast:
45	chr5:112195538..112198310-chr5:112312375..112313895,2	K562	blood:
46	chr5:112256092..112257666-chr5:112304099..112305751,2	MCF-7	breast:
47	chr5:112317791..112320092-chr5:112860829..112862554,2	K562	blood:
48	chr5:112314675..112316382-chr5:112352070..112354061,2	K562	blood:
49	chr5:112303578..112305254-chr5:112311850..112314177,2	MCF-7	breast:
50	chr5:112346718..112348969-chr5:112352127..112354346,2	MCF-7	breast:

No data

(count:8 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	DCP2	hsa-miR-148b-3p	chr5:112351276-112351282
2	DCP2	hsa-miR-92a-3p	chr5:112349543-112349549
3	DCP2	hsa-miR-148b-3p	chr5:112355072-112355078
4	DCP2	hsa-miR-128-3p	chr5:112351278-112351284
5	DCP2	hsa-miR-148b-3p	chr5:112349344-112349350
6	MCC	hsa-miR-26b-5p	chr5:112358130-112358124
7	DCP2	hsa-miR-128-3p	chr5:112351766-112351773
8	DCP2	hsa-miR-148b-3p	chr5:112351764-112351770

Variant related genes	Relation type
DCP2	TF binding region
DCP2	CpG island
ENSG00000100219	chromatin interactions
ENSG00000212643	chromatin interactions
ENSG00000161970	chromatin interactions
ENSG00000263809	chromatin interactions
ENSG00000226471	chromatin interactions
ENSG00000273254	chromatin interactions
ENSG00000272869	chromatin interactions
ENSG00000176055	chromatin interactions
ENSG00000129625	chromatin interactions
ENSG00000156256	chromatin interactions
ENSG00000153037	chromatin interactions
ENSG00000113356	chromatin interactions
ENSG00000172795	chromatin interactions

Extended variants
information (count: 2798 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2798 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191992691	chr5:112300526-112300527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs528836995	chr5:112300539-112300540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs143296791	chr5:112300605-112300606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs13360667	chr5:112300621-112300622	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs370399200	chr5:112300622-112300623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs74921423	chr5:112300626-112300627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535165666	chr5:112300637-112300638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557039021	chr5:112300672-112300673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs148318205	chr5:112300710-112300711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539056266	chr5:112300719-112300720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529364773	chr5:112300750-112300751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182688047	chr5:112300761-112300762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572797638	chr5:112300763-112300764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs112193231	chr5:112300765-112300766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187045193	chr5:112300775-112300776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543669141	chr5:112300796-112300797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573796576	chr5:112300801-112300802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs147097876	chr5:112300804-112300805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533691078	chr5:112300805-112300806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563778956	chr5:112300812-112300813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371429677	chr5:112300814-112300815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546212776	chr5:112300820-112300821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551818288	chr5:112300831-112300832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs114445653	chr5:112300845-112300846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528777659	chr5:112300897-112300898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547286046	chr5:112300917-112300918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376085643	chr5:112300940-112300941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138471049	chr5:112300945-112300946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113187152	chr5:112300947-112300948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550363365	chr5:112300967-112300968	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs567026687	chr5:112300994-112300995	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs576328725	chr5:112300999-112301000	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs539193619	chr5:112301004-112301005	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs150680808	chr5:112301027-112301028	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs6869064	chr5:112301031-112301032	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs74294438	chr5:112301042-112301043	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs555656644	chr5:112301060-112301061	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs1625623	chr5:112301096-112301097	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs577797134	chr5:112301127-112301128	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs199857998	chr5:112301258-112301259	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs200956906	chr5:112301289-112301290	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs60531715	chr5:112301290-112301291	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs556440624	chr5:112301312-112301313	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs73789266	chr5:112301316-112301317	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs546349867	chr5:112301328-112301329	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs564436838	chr5:112301332-112301333	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs573209618	chr5:112301357-112301358	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs17135222	chr5:112301362-112301363	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs562411790	chr5:112301383-112301384	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs78513642	chr5:112301472-112301473	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
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
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Myelofibrosis	22110671	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Colorectal cancer	21297112	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Sezary syndrome	18413736	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2080 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:112294000-112311800	Weak transcription	Right Atrium	heart
2	chr5:112294800-112304400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr5:112295200-112304400	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr5:112297000-112304400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr5:112298200-112311800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr5:112300000-112301600	Weak transcription	HepG2	liver
7	chr5:112300000-112305200	Weak transcription	NH-A	brain
8	chr5:112300000-112305600	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr5:112300000-112307000	Weak transcription	Primary B cells from peripheral blood	blood
10	chr5:112300200-112303200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr5:112300200-112303800	Weak transcription	A549	lung
12	chr5:112300200-112305000	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr5:112300200-112305000	Weak transcription	Hela-S3	cervix
14	chr5:112300200-112305000	Weak transcription	HUVEC	blood vessel
15	chr5:112300200-112305000	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr5:112300200-112311400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr5:112300400-112302000	Weak transcription	Placenta	Placenta
18	chr5:112300400-112303600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr5:112300400-112303600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr5:112300400-112303800	Weak transcription	K562	blood
21	chr5:112300400-112304200	Weak transcription	GM12878-XiMat	blood
22	chr5:112300400-112304600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr5:112300400-112305200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr5:112301600-112301800	Enhancers	HepG2	liver
25	chr5:112301800-112302200	Weak transcription	HepG2	liver
26	chr5:112302000-112306200	Enhancers	Placenta	Placenta
27	chr5:112302200-112303800	Enhancers	HepG2	liver
28	chr5:112302400-112302600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr5:112302600-112305200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr5:112303200-112304000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr5:112303600-112305600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr5:112303600-112305800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr5:112303800-112304600	Flanking Active TSS	A549	lung
34	chr5:112303800-112304600	Flanking Active TSS	HepG2	liver
35	chr5:112303800-112305200	Enhancers	K562	blood
36	chr5:112303800-112305800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr5:112304000-112304800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr5:112304200-112304400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr5:112304200-112305400	Enhancers	GM12878-XiMat	blood
40	chr5:112304200-112305600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr5:112304200-112305600	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr5:112304200-112305600	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr5:112304200-112306000	Enhancers	H1 Cell Line	embryonic stem cell
44	chr5:112304400-112305200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr5:112304400-112305600	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr5:112304400-112305800	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr5:112304400-112309400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr5:112304600-112305000	Enhancers	A549	lung
49	chr5:112304600-112305600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr5:112304600-112305600	Enhancers	HUES48 Cell Line	embryonic stem cell

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