Variant report

Variant	nsv1023953
Chromosome Location	chr5:75831037-75913784
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1533)
CpG islands
(count:366)
Chromatin interactive
region (count:44)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1533 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:75840098-75840519	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:75842649-75843062	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:75832805-75833764	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:75878262-75878267	K562	blood:	n/a	n/a
5	ARID3A	chr5:75838744-75839045	K562	blood:	n/a	n/a
6	ARID3A	chr5:75879112-75879647	K562	blood:	n/a	n/a
7	ARID3A	chr5:75840176-75840537	K562	blood:	n/a	n/a
8	ARID3A	chr5:75894704-75894734	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:75879372-75879648	HepG2	liver:	n/a	n/a
10	ATF1	chr5:75904695-75905158	K562	blood:	n/a	n/a
11	ATF1	chr5:75852689-75853049	K562	blood:	n/a	n/a
12	ATF1	chr5:75838766-75839534	K562	blood:	n/a	n/a
13	ATF1	chr5:75831344-75831612	K562	blood:	n/a	n/a
14	ATF1	chr5:75840185-75840485	K562	blood:	n/a	n/a
15	ATF2	chr5:75843116-75843713	GM12878	blood:	n/a	n/a
16	ATF2	chr5:75852537-75853136	GM12878	blood:	n/a	n/a
17	ATF2	chr5:75904511-75905102	GM12878	blood:	n/a	n/a
18	ATF2	chr5:75904575-75905156	GM12878	blood:	n/a	n/a
19	ATF2	chr5:75838932-75839432	GM12878	blood:	n/a	n/a
20	ATF2	chr5:75840097-75840472	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr5:75852601-75853040	GM12878	blood:	n/a	n/a
22	ATF2	chr5:75842225-75843735	GM12878	blood:	n/a	n/a
23	ATF2	chr5:75877922-75878580	GM12878	blood:	n/a	n/a
24	ATF2	chr5:75877962-75878487	GM12878	blood:	n/a	n/a
25	ATF2	chr5:75885636-75886289	GM12878	blood:	n/a	n/a
26	ATF2	chr5:75885854-75886295	GM12878	blood:	n/a	n/a
27	BATF	chr5:75885837-75886185	GM12878	blood:	n/a	chr5:75886008-75886019 chr5:75886009-75886019
28	BATF	chr5:75843287-75843575	GM12878	blood:	n/a	n/a
29	BATF	chr5:75885818-75886149	GM12878	blood:	n/a	chr5:75886008-75886019 chr5:75886009-75886019
30	BATF	chr5:75878063-75878435	GM12878	blood:	n/a	n/a
31	BATF	chr5:75878120-75878359	GM12878	blood:	n/a	n/a
32	BATF	chr5:75843274-75843642	GM12878	blood:	n/a	n/a
33	BCL11A	chr5:75878053-75878407	GM12878	blood:	n/a	n/a
34	BCL11A	chr5:75878060-75878454	GM12878	blood:	n/a	n/a
35	BCL3	chr5:75878087-75878399	GM12878	blood:	n/a	n/a
36	BCLAF1	chr5:75877985-75878556	GM12878	blood:	n/a	n/a
37	BCLAF1	chr5:75885718-75886254	GM12878	blood:	n/a	chr5:75886011-75886020
38	BCLAF1	chr5:75842536-75843685	GM12878	blood:	n/a	chr5:75843310-75843319
39	BCLAF1	chr5:75852559-75853097	GM12878	blood:	n/a	n/a
40	BHLHE40	chr5:75832927-75832932	K562	blood:	n/a	n/a
41	BHLHE40	chr5:75879352-75879536	GM12878	blood:	n/a	n/a
42	BHLHE40	chr5:75877874-75878590	GM12878	blood:	n/a	n/a
43	BHLHE40	chr5:75839001-75839405	GM12878	blood:	n/a	n/a
44	BHLHE40	chr5:75839322-75839547	K562	blood:	n/a	n/a
45	BHLHE40	chr5:75904800-75905088	K562	blood:	n/a	n/a
46	BHLHE40	chr5:75842244-75843807	GM12878	blood:	n/a	n/a
47	BHLHE40	chr5:75885807-75886280	GM12878	blood:	n/a	n/a
48	BHLHE40	chr5:75840305-75840403	K562	blood:	n/a	n/a
49	BHLHE40	chr5:75878083-75878443	K562	blood:	n/a	n/a
50	BHLHE40	chr5:75897312-75897624	K562	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:75903700-75903750	GM12892	blood:	n/a
2	chr5:75903700-75903750	K562	blood:	n/a
3	chr5:75903397-75903447	AG04449	skin:	fetal
4	chr5:75878300-75878350	ECC-1	luminal epithelium:	n/a
5	chr5:75838704-75838754	Hela-S3	cervix:	n/a
6	chr5:75903397-75903447	CMK	blood:	n/a
7	chr5:75903700-75903750	NH-A	brain:	n/a
8	chr5:75903397-75903447	AoSMC	blood vessel:	n/a
9	chr5:75903700-75903750	ECC-1	luminal epithelium:	n/a
10	chr5:75903397-75903447	BE2_C	brain:	n/a
11	chr5:75831679-75831729	AG10803	skin:	n/a
12	chr5:75838704-75838754	SK-N-MC	brain:	n/a
13	chr5:75903700-75903750	MCF10A-Er-Src	breast:	n/a
14	chr5:75903700-75903750	IMR90	lung:	fetal
15	chr5:75903397-75903447	HEK293	kidney:	embryo
16	chr5:75838704-75838754	U87	brain:	n/a
17	chr5:75838704-75838754	GM12892	blood:	n/a
18	chr5:75831679-75831729	SK-N-SH	brain:	n/a
19	chr5:75831679-75831729	ECC-1	luminal epithelium:	n/a
20	chr5:75912664-75912714	AoSMC	blood vessel:	n/a
21	chr5:75912664-75912714	RPTEC	kidney:	n/a
22	chr5:75838704-75838754	HCT-116	colon:	n/a
23	chr5:75878300-75878350	A549	lung:	n/a
24	chr5:75878300-75878350	HIPEpiC	eye:	n/a
25	chr5:75838704-75838754	Hepatocyte	liver:	n/a
26	chr5:75903700-75903750	GM19239	blood:	n/a
27	chr5:75838704-75838754	ProgFib	skin:	n/a
28	chr5:75903700-75903750	SKMC	muscle:	n/a
29	chr5:75912664-75912714	BJ	skin:	n/a
30	chr5:75878300-75878350	IMR90	lung:	fetal
31	chr5:75912664-75912714	HNPCEpiC	eye:	n/a
32	chr5:75831679-75831729	MCF-7	breast:	n/a
33	chr5:75903397-75903447	HL-60	blood:	n/a
34	chr5:75878300-75878350	HCM	heart:	n/a
35	chr5:75903700-75903750	A549	lung:	n/a
36	chr5:75903397-75903447	SKMC	muscle:	n/a
37	chr5:75838704-75838754	SK-N-SH_RA	brain:	n/a
38	chr5:75903700-75903750	NT2-D1	testis:	n/a
39	chr5:75878300-75878350	Jurkat	blood:	n/a
40	chr5:75878300-75878350	HepG2	liver:	n/a
41	chr5:75878300-75878350	BJ	skin:	n/a
42	chr5:75903397-75903447	HNPCEpiC	eye:	n/a
43	chr5:75878300-75878350	HPAEpiC	pulmonary alveolar:	n/a
44	chr5:75912664-75912714	Jurkat	blood:	n/a
45	chr5:75912664-75912714	NH-A	brain:	n/a
46	chr5:75831679-75831729	U87	brain:	n/a
47	chr5:75878300-75878350	K562	blood:	n/a
48	chr5:75838704-75838754	PrEC	prostate:	n/a
49	chr5:75878300-75878350	HMEC	breast:	n/a
50	chr5:75903397-75903447	PANC-1	pancreas:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:75633886..75634436-chr5:75839825..75840735,2	K562	blood:
2	chr5:75897979..75898810-chr5:75937080..75938018,3	K562	blood:
3	chr5:75897247..75898569-chr5:75937033..75938017,10	MCF-7	breast:
4	chr5:75858031..75860083-chr5:75863526..75866442,2	K562	blood:
5	chr5:75906449..75908343-chr5:75910406..75912617,2	K562	blood:
6	chr5:75906209..75908634-chr5:75909482..75912617,3	K562	blood:
7	chr5:75878372..75880301-chr5:75883948..75885454,2	K562	blood:
8	chr5:75896963..75898061-chr5:76070096..76071180,9	MCF-7	breast:
9	chr5:75873843..75876744-chr5:75876856..75878367,2	K562	blood:
10	chr5:75897714..75898323-chr5:75934762..75935296,2	MCF-7	breast:
11	chr5:75910340..75912765-chr5:75915221..75917269,3	K562	blood:
12	chr5:75633417..75634381-chr5:75839891..75840630,3	MCF-7	breast:
13	chr5:75898209..75899288-chr5:76070136..76071088,4	MCF-7	breast:
14	chr5:75199631..75200148-chr5:75897260..75897978,2	K562	blood:
15	chr5:75896964..75897974-chr5:75936696..75938042,13	K562	blood:
16	chr5:75849302..75851121-chr5:75858658..75860638,2	K562	blood:
17	chr5:75906449..75908343-chr5:75910406..75912617,2	K562	blood:
18	chr5:75896999..75898252-chr5:76070091..76071474,10	K562	blood:
19	chr5:75873843..75876744-chr5:75876856..75878367,2	K562	blood:
20	chr5:75897975..75898494-chr5:75937296..75938025,2	MCF-7	breast:
21	chr5:75896478..75897915-chr5:75936605..75938172,9	MCF-7	breast:
22	chr5:75698517..75699563-chr5:75839811..75840781,6	MCF-7	breast:
23	chr5:75633485..75634409-chr5:75878986..75879511,2	K562	blood:
24	chr5:75854326..75856350-chr5:75859586..75862495,2	K562	blood:
25	chr5:75897144..75897771-chr5:103707251..103707772,2	MCF-7	breast:
26	chr5:75854326..75856350-chr5:75859586..75862495,2	K562	blood:
27	chr5:75699529..75700200-chr5:75878922..75879530,2	K562	blood:
28	chr5:75628819..75631136-chr5:75840007..75842103,2	K562	blood:
29	chr5:75906209..75908634-chr5:75909482..75912617,3	K562	blood:
30	chr5:75899087..75901579-chr5:75954997..75956885,2	K562	blood:
31	chr5:75901625..75904371-chr5:75985828..75988323,2	MCF-7	breast:
32	chr5:75858031..75860083-chr5:75863526..75866442,2	K562	blood:
33	chr5:75899104..75902387-chr5:75903056..75906871,6	K562	blood:
34	chr5:75698659..75699503-chr5:75839829..75840376,2	K562	blood:
35	chr5:75826263..75829016-chr5:75865983..75867633,2	K562	blood:
36	chr5:75633462..75634419-chr5:75839412..75840924,7	MCF-7	breast:
37	chr5:75849302..75851121-chr5:75858658..75860638,2	K562	blood:
38	chr5:75699826..75701586-chr5:75896000..75897576,2	K562	blood:
39	chr5:75861596..75864384-chr5:75866146..75868439,3	K562	blood:
40	chr5:75878372..75880301-chr5:75883948..75885454,2	K562	blood:
41	chr5:75897329..75897974-chr5:132288926..132289426,2	MCF-7	breast:
42	chr5:75824972..75827134-chr5:75830080..75833927,3	K562	blood:
43	chr5:75897438..75897959-chr5:76070126..76070803,2	MCF-7	breast:
44	chr5:75861596..75864384-chr5:75866146..75868439,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-F2RL2-1	chr5:75904685-75904795	ENSG00000249713.1
2	lnc-F2RL2-1	chr5:75902433-75903909	ENSG00000249713.1

No data

Variant related genes	Relation type
IQGAP2	TF binding region
ENSG00000249713	TF binding region
IQGAP2	CpG island
ENSG00000249713	CpG island
ENSG00000249713	chromatin interactions
ENSG00000145703	chromatin interactions

Extended variants
information (count: 3171 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:3171 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7707801	chr5:75831037-75831038	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144436497	chr5:75831113-75831114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs115352191	chr5:75831133-75831134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs76187345	chr5:75831152-75831153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs558710209	chr5:75831159-75831160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557650356	chr5:75831160-75831161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs567527588	chr5:75831202-75831203	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs536651799	chr5:75831244-75831245	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553466876	chr5:75831297-75831298	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112529803	chr5:75831325-75831326	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183314132	chr5:75831368-75831369	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187754247	chr5:75831371-75831372	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs114607123	chr5:75831405-75831406	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs575117892	chr5:75831567-75831568	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs544162921	chr5:75831647-75831648	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543316905	chr5:75831655-75831656	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557398909	chr5:75831736-75831737	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192584766	chr5:75831746-75831747	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146197484	chr5:75831795-75831796	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs371300745	chr5:75831797-75831798	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs369314932	chr5:75831801-75831802	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs183612780	chr5:75831804-75831805	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542224151	chr5:75831811-75831812	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs189495173	chr5:75831812-75831813	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs528152268	chr5:75831841-75831842	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs142254272	chr5:75831849-75831850	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs17748061	chr5:75831856-75831857	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111792923	chr5:75831861-75831862	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs545584812	chr5:75831890-75831891	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550948666	chr5:75831919-75831920	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs577801984	chr5:75831994-75831995	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs545114415	chr5:75831997-75831998	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs536989209	chr5:75832018-75832019	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs529954975	chr5:75832084-75832085	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs547016350	chr5:75832162-75832163	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566897653	chr5:75832187-75832188	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs539117102	chr5:75832193-75832194	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs553954739	chr5:75832240-75832241	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559022907	chr5:75832243-75832244	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs577734272	chr5:75832313-75832314	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs540147760	chr5:75832321-75832322	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs537251787	chr5:75832323-75832324	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs192683755	chr5:75832382-75832383	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs573589086	chr5:75832401-75832402	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs57694731	chr5:75832438-75832439	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs185075642	chr5:75832454-75832455	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs575988764	chr5:75832479-75832480	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572521357	chr5:75832483-75832484	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs559906894	chr5:75832522-75832523	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs10054114	chr5:75832526-75832527	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:87)

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
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
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	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
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
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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1628 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75806800-75834200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr5:75806800-75839200	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr5:75820200-75832600	Weak transcription	Fetal Intestine Small	intestine
4	chr5:75822200-75831200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr5:75822200-75831200	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr5:75823000-75838400	Weak transcription	Primary T cells from cord blood	blood
7	chr5:75823400-75832000	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr5:75824000-75831200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr5:75824000-75831400	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr5:75824200-75834400	Weak transcription	Fetal Thymus	thymus
11	chr5:75825800-75831400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr5:75826600-75834800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr5:75826800-75833000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr5:75826800-75834000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr5:75826800-75834600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr5:75826800-75840000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr5:75827000-75835000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr5:75827600-75834200	Weak transcription	Primary hematopoietic stem cells	blood
19	chr5:75828400-75834000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr5:75828600-75833800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr5:75828600-75839000	Weak transcription	Lung	lung
22	chr5:75828800-75831400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr5:75829000-75831400	Weak transcription	Liver	Liver
24	chr5:75829000-75832600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr5:75829000-75836200	Weak transcription	K562	blood
26	chr5:75829000-75838000	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr5:75829200-75833600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr5:75829800-75831400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr5:75829800-75832800	Enhancers	HepG2	liver
30	chr5:75830000-75831400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr5:75830000-75831800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr5:75830000-75841600	Enhancers	Stomach Mucosa	stomach
33	chr5:75830200-75833200	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr5:75830400-75832400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr5:75830400-75833400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
36	chr5:75830800-75831600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr5:75830800-75831600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr5:75830800-75831600	Enhancers	Pancreas	Pancrea
39	chr5:75830800-75832200	Enhancers	H1 Cell Line	embryonic stem cell
40	chr5:75830800-75832200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr5:75831000-75831400	Weak transcription	Gastric	stomach
42	chr5:75831000-75831600	Enhancers	Placenta	Placenta
43	chr5:75831000-75831800	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr5:75831000-75831800	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr5:75831000-75832600	Weak transcription	Duodenum Mucosa	Duodenum
46	chr5:75831200-75831600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr5:75831200-75831800	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr5:75831200-75831800	Strong transcription	Primary monocytes fromperipheralblood	blood
49	chr5:75831200-75832000	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr5:75831400-75831600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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