Variant report

Variant	nsv1022032
Chromosome Location	chr5:75785106-75914003
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1919)
CpG islands
(count:553)
Chromatin interactive
region (count:60)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1919 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:75840176-75840537	K562	blood:	n/a	n/a
2	ARID3A	chr5:75840098-75840519	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	chr5:75789147-75789935	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:75823377-75823925	K562	blood:	n/a	n/a
7	ARID3A	chr5:75818296-75818721	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:75786915-75787126	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:75817778-75817942	HepG2	liver:	n/a	n/a
10	ARID3A	chr5:75879372-75879648	HepG2	liver:	n/a	n/a
11	ARID3A	chr5:75879112-75879647	K562	blood:	n/a	n/a
12	ARID3A	chr5:75838744-75839045	K562	blood:	n/a	n/a
13	ARID3A	chr5:75894704-75894734	HepG2	liver:	n/a	n/a
14	ARID3A	chr5:75842649-75843062	HepG2	liver:	n/a	n/a
15	ATF1	chr5:75823469-75823927	K562	blood:	n/a	n/a
16	ATF1	chr5:75831344-75831612	K562	blood:	n/a	n/a
17	ATF1	chr5:75794062-75794159	K562	blood:	n/a	n/a
18	ATF1	chr5:75838766-75839534	K562	blood:	n/a	n/a
19	ATF1	chr5:75852689-75853049	K562	blood:	n/a	n/a
20	ATF1	chr5:75840185-75840485	K562	blood:	n/a	n/a
21	ATF1	chr5:75904695-75905158	K562	blood:	n/a	n/a
22	ATF2	chr5:75904575-75905156	GM12878	blood:	n/a	n/a
23	ATF2	chr5:75877962-75878487	GM12878	blood:	n/a	n/a
24	ATF2	chr5:75852601-75853040	GM12878	blood:	n/a	n/a
25	ATF2	chr5:75885636-75886289	GM12878	blood:	n/a	n/a
26	ATF2	chr5:75842225-75843735	GM12878	blood:	n/a	n/a
27	ATF2	chr5:75816935-75817430	GM12878	blood:	n/a	chr5:75817177-75817188
28	ATF2	chr5:75795230-75795845	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr5:75816937-75817495	GM12878	blood:	n/a	chr5:75817177-75817188
30	ATF2	chr5:75840097-75840472	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr5:75852537-75853136	GM12878	blood:	n/a	n/a
32	ATF2	chr5:75843116-75843713	GM12878	blood:	n/a	n/a
33	ATF2	chr5:75904511-75905102	GM12878	blood:	n/a	n/a
34	ATF2	chr5:75838932-75839432	GM12878	blood:	n/a	n/a
35	ATF2	chr5:75877922-75878580	GM12878	blood:	n/a	n/a
36	ATF2	chr5:75885854-75886295	GM12878	blood:	n/a	n/a
37	ATF3	chr5:75823590-75823923	K562	blood:	n/a	chr5:75823798-75823811
38	ATF3	chr5:75823709-75823953	HCT-116	colon:	n/a	chr5:75823798-75823811
39	BATF	chr5:75878063-75878435	GM12878	blood:	n/a	n/a
40	BATF	chr5:75843287-75843575	GM12878	blood:	n/a	n/a
41	BATF	chr5:75878120-75878359	GM12878	blood:	n/a	n/a
42	BATF	chr5:75885837-75886185	GM12878	blood:	n/a	chr5:75886008-75886019 chr5:75886009-75886019
43	BATF	chr5:75843274-75843642	GM12878	blood:	n/a	n/a
44	BATF	chr5:75885818-75886149	GM12878	blood:	n/a	chr5:75886008-75886019 chr5:75886009-75886019
45	BCL11A	chr5:75878053-75878407	GM12878	blood:	n/a	n/a
46	BCL11A	chr5:75878060-75878454	GM12878	blood:	n/a	n/a
47	BCL3	chr5:75878087-75878399	GM12878	blood:	n/a	n/a
48	BCLAF1	chr5:75842536-75843685	GM12878	blood:	n/a	chr5:75843310-75843319
49	BCLAF1	chr5:75877985-75878556	GM12878	blood:	n/a	n/a
50	BCLAF1	chr5:75885718-75886254	GM12878	blood:	n/a	chr5:75886011-75886020

(count:553 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:75810564-75810614	ECC-1	luminal epithelium:	n/a
2	chr5:75820852-75820902	AG10803	skin:	n/a
3	chr5:75878300-75878350	HL-60	blood:	n/a
4	chr5:75903700-75903750	RPTEC	kidney:	n/a
5	chr5:75810564-75810614	ECC-1	luminal epithelium:	n/a
6	chr5:75820852-75820902	AG10803	skin:	n/a
7	chr5:75878300-75878350	HL-60	blood:	n/a
8	chr5:75903700-75903750	RPTEC	kidney:	n/a
9	chr5:75794475-75794525	HCPEpiC	choroid plexus:	n/a
10	chr5:75903700-75903750	K562	blood:	n/a
11	chr5:75903397-75903447	HCF	heart:	n/a
12	chr5:75831679-75831729	NB4	blood:	n/a
13	chr5:75810564-75810614	PFSK-1	brain:	n/a
14	chr5:75838704-75838754	SAEC	small airway:	n/a
15	chr5:75878300-75878350	HRPEpiC	eye:	n/a
16	chr5:75831679-75831729	HL-60	blood:	n/a
17	chr5:75903397-75903447	SK-N-MC	brain:	n/a
18	chr5:75820852-75820902	ovcar-3	ovarian:	n/a
19	chr5:75810564-75810614	SK-N-MC	brain:	n/a
20	chr5:75903700-75903750	AG09309	skin:	n/a
21	chr5:75878300-75878350	HepG2	liver:	n/a
22	chr5:75838704-75838754	HCPEpiC	choroid plexus:	n/a
23	chr5:75831679-75831729	HRCEpiC	kidney:	n/a
24	chr5:75903397-75903447	HIPEpiC	eye:	n/a
25	chr5:75878300-75878350	Hela-S3	cervix:	n/a
26	chr5:75831679-75831729	BJ	skin:	n/a
27	chr5:75878300-75878350	GM12878	blood:	n/a
28	chr5:75903700-75903750	HCF	heart:	n/a
29	chr5:75878300-75878350	GM19239	blood:	n/a
30	chr5:75794475-75794525	PrEC	prostate:	n/a
31	chr5:75903700-75903750	HRPEpiC	eye:	n/a
32	chr5:75820852-75820902	HCT-116	colon:	n/a
33	chr5:75831679-75831729	HCT-116	colon:	n/a
34	chr5:75838704-75838754	HCF	heart:	n/a
35	chr5:75903700-75903750	HCM	heart:	n/a
36	chr5:75810564-75810614	T-47D	breast:	n/a
37	chr5:75912664-75912714	H1-hESC	embryonic stem cell:	embryo
38	chr5:75903700-75903750	LNCaP	prostate:	n/a
39	chr5:75794475-75794525	U87	brain:	n/a
40	chr5:75903397-75903447	A549	lung:	n/a
41	chr5:75912664-75912714	HCF	heart:	n/a
42	chr5:75903700-75903750	HIPEpiC	eye:	n/a
43	chr5:75903397-75903447	HUVEC	blood vessel:	n/a
44	chr5:75912664-75912714	GM06990	blood:	n/a
45	chr5:75838704-75838754	HRPEpiC	eye:	n/a
46	chr5:75794475-75794525	GM12892	blood:	n/a
47	chr5:75810564-75810614	U87	brain:	n/a
48	chr5:75831679-75831729	HEEpiC	esophagus:	n/a
49	chr5:75810564-75810614	NHBE	bronchial:	n/a
50	chr5:75912664-75912714	HRE	kidney:	n/a

(count:60 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:75795227..75796824-chr5:75800531..75803295,2	K562	blood:
2	chr5:75897144..75897771-chr5:103707251..103707772,2	MCF-7	breast:
3	chr5:75633417..75634381-chr5:75839891..75840630,3	MCF-7	breast:
4	chr5:75858031..75860083-chr5:75863526..75866442,2	K562	blood:
5	chr5:75849302..75851121-chr5:75858658..75860638,2	K562	blood:
6	chr5:75897979..75898810-chr5:75937080..75938018,3	K562	blood:
7	chr5:75698517..75699563-chr5:75839811..75840781,6	MCF-7	breast:
8	chr5:75795227..75796824-chr5:75800531..75803295,2	K562	blood:
9	chr5:75199631..75200148-chr5:75897260..75897978,2	K562	blood:
10	chr5:75861596..75864384-chr5:75866146..75868439,3	K562	blood:
11	chr5:75897329..75897974-chr5:132288926..132289426,2	MCF-7	breast:
12	chr5:75824401..75825972-chr5:75826826..75829137,2	MCF-7	breast:
13	chr5:75633886..75634436-chr5:75839825..75840735,2	K562	blood:
14	chr5:75785398..75787925-chr5:75797888..75800417,2	K562	blood:
15	chr5:75878372..75880301-chr5:75883948..75885454,2	K562	blood:
16	chr5:75698659..75699503-chr5:75839829..75840376,2	K562	blood:
17	chr5:75873843..75876744-chr5:75876856..75878367,2	K562	blood:
18	chr5:75899104..75902387-chr5:75903056..75906871,6	K562	blood:
19	chr5:75899087..75901579-chr5:75954997..75956885,2	K562	blood:
20	chr5:75910340..75912765-chr5:75915221..75917269,3	K562	blood:
21	chr5:75816896..75819004-chr5:75820235..75822172,2	K562	blood:
22	chr5:75897247..75898569-chr5:75937033..75938017,10	MCF-7	breast:
23	chr5:75633462..75634419-chr5:75839412..75840924,7	MCF-7	breast:
24	chr5:75824972..75827134-chr5:75830080..75833927,3	K562	blood:
25	chr5:75628819..75631136-chr5:75840007..75842103,2	K562	blood:
26	chr5:75784025..75785696-chr5:75819227..75820918,2	K562	blood:
27	chr5:75906449..75908343-chr5:75910406..75912617,2	K562	blood:
28	chr5:75878372..75880301-chr5:75883948..75885454,2	K562	blood:
29	chr5:75906449..75908343-chr5:75910406..75912617,2	K562	blood:
30	chr5:75897975..75898494-chr5:75937296..75938025,2	MCF-7	breast:
31	chr5:75906209..75908634-chr5:75909482..75912617,3	K562	blood:
32	chr5:75906209..75908634-chr5:75909482..75912617,3	K562	blood:
33	chr5:75897438..75897959-chr5:76070126..76070803,2	MCF-7	breast:
34	chr5:75813206..75815347-chr5:75817807..75820110,2	K562	blood:
35	chr5:75824972..75827134-chr5:75830080..75833927,3	K562	blood:
36	chr5:75861596..75864384-chr5:75866146..75868439,3	K562	blood:
37	chr5:75896999..75898252-chr5:76070091..76071474,10	K562	blood:
38	chr5:75896964..75897974-chr5:75936696..75938042,13	K562	blood:
39	chr5:75816896..75819004-chr5:75820235..75822172,2	K562	blood:
40	chr5:75826263..75829016-chr5:75865983..75867633,2	K562	blood:
41	chr5:75784025..75785696-chr5:75819227..75820918,2	K562	blood:
42	chr5:75858031..75860083-chr5:75863526..75866442,2	K562	blood:
43	chr5:75896478..75897915-chr5:75936605..75938172,9	MCF-7	breast:
44	chr5:75826263..75829016-chr5:75865983..75867633,2	K562	blood:
45	chr5:75898209..75899288-chr5:76070136..76071088,4	MCF-7	breast:
46	chr5:75813206..75815347-chr5:75817807..75820110,2	K562	blood:
47	chr5:75804818..75806552-chr5:75817322..75819919,2	MCF-7	breast:
48	chr5:75901625..75904371-chr5:75985828..75988323,2	MCF-7	breast:
49	chr5:75873843..75876744-chr5:75876856..75878367,2	K562	blood:
50	chr5:75896963..75898061-chr5:76070096..76071180,9	MCF-7	breast:

(count:3 , 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
3	lnc-SV2C-4	chr5:75806265-75806591	NONHSAT102239

No data

Variant related genes	Relation type
ENSG00000249713	TF binding region
IQGAP2	TF binding region
ENSG00000250574	TF binding region
ENSG00000249713	CpG island
IQGAP2	CpG island
ENSG00000250574	CpG island
ENSG00000145703	chromatin interactions
ENSG00000250574	chromatin interactions
ENSG00000249713	chromatin interactions

Extended variants
information (count: 4943 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:4943 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13172341	chr5:75785106-75785107	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs112831325	chr5:75785111-75785112	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs538703451	chr5:75785135-75785136	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs558999228	chr5:75785149-75785150	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs115374806	chr5:75785167-75785168	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs368958199	chr5:75785179-75785180	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs183599602	chr5:75785226-75785227	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs144240408	chr5:75785261-75785262	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs13154264	chr5:75785264-75785265	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs376014241	chr5:75785271-75785272	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs528239717	chr5:75785280-75785281	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs188329088	chr5:75785282-75785283	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs13158404	chr5:75785296-75785297	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs529346232	chr5:75785318-75785319	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs572796054	chr5:75785397-75785398	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544721234	chr5:75785459-75785460	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564979206	chr5:75785521-75785522	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs10035371	chr5:75785535-75785536	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs566398137	chr5:75785539-75785540	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550734740	chr5:75785572-75785573	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs181251996	chr5:75785599-75785600	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530283398	chr5:75785666-75785667	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs567847649	chr5:75785715-75785716	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs185894234	chr5:75785740-75785741	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs546886416	chr5:75785748-75785749	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535023479	chr5:75785815-75785816	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs10035441	chr5:75785818-75785819	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs539007643	chr5:75785839-75785840	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs140219320	chr5:75785857-75785858	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs74368525	chr5:75785942-75785943	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571752964	chr5:75785964-75785965	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs150236786	chr5:75785965-75785966	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557150698	chr5:75785966-75785967	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs573886733	chr5:75786010-75786011	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs536500906	chr5:75786011-75786012	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553296064	chr5:75786027-75786028	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs138898395	chr5:75786073-75786074	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191760305	chr5:75786142-75786143	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs6884352	chr5:75786150-75786151	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs556374514	chr5:75786183-75786184	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs575264919	chr5:75786213-75786214	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs148994725	chr5:75786245-75786246	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs35453582	chr5:75786300-75786301	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs113257939	chr5:75786301-75786302	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs560695769	chr5:75786345-75786346	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs7724382	chr5:75786349-75786350	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs181859488	chr5:75786365-75786366	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs575627552	chr5:75786373-75786374	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs145893644	chr5:75786383-75786384	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs7711417	chr5:75786404-75786405	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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:2626 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75769600-75816600	Weak transcription	Primary B cells from cord blood	blood
2	chr5:75775000-75785800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr5:75775600-75787600	Weak transcription	Gastric	stomach
4	chr5:75776200-75785800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr5:75776200-75787600	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr5:75776200-75801000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr5:75776400-75791200	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr5:75776400-75800200	Weak transcription	Primary T cells from cord blood	blood
9	chr5:75776800-75791000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr5:75778000-75785800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr5:75778400-75793200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr5:75779200-75785600	Weak transcription	Brain Germinal Matrix	brain
13	chr5:75780200-75786200	Weak transcription	Fetal Intestine Small	intestine
14	chr5:75780200-75786200	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr5:75780200-75787400	Weak transcription	Placenta	Placenta
16	chr5:75780400-75788000	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr5:75780800-75786800	Weak transcription	Primary hematopoietic stem cells	blood
18	chr5:75780800-75793400	Weak transcription	Small Intestine	intestine
19	chr5:75781000-75786000	Weak transcription	Duodenum Mucosa	Duodenum
20	chr5:75781000-75787400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr5:75781200-75786200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr5:75781600-75785800	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr5:75781600-75786000	Weak transcription	Primary T helper cells fromperipheralblood	blood
24	chr5:75781600-75786200	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr5:75781600-75787600	Weak transcription	Colonic Mucosa	Colon
26	chr5:75782600-75786000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr5:75782800-75785800	Weak transcription	Stomach Mucosa	stomach
28	chr5:75783400-75785600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr5:75783400-75785600	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr5:75783400-75785800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
31	chr5:75783400-75786200	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr5:75783400-75786600	Enhancers	H1 Cell Line	embryonic stem cell
33	chr5:75783600-75785600	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr5:75783600-75785600	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr5:75783800-75785800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
36	chr5:75783800-75787400	Weak transcription	Pancreas	Pancrea
37	chr5:75783800-75788200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr5:75783800-75788800	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr5:75784000-75785600	Weak transcription	Fetal Lung	lung
40	chr5:75784000-75786600	Weak transcription	Liver	Liver
41	chr5:75784000-75788800	Weak transcription	K562	blood
42	chr5:75784000-75791600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr5:75784200-75789200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr5:75784400-75789400	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr5:75784400-75789800	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr5:75784600-75785600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr5:75784600-75785800	Enhancers	H9 Cell Line	embryonic stem cell
48	chr5:75784600-75785800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr5:75784600-75786600	Weak transcription	Fetal Stomach	stomach
50	chr5:75784600-75788600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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