Variant report

Variant	nsv462425
Chromosome Location	chr5:117843869-117967472
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:117884442-117884668	HepG2	liver:	n/a	n/a
2	BATF	chr5:117966281-117966527	GM12878	blood:	n/a	chr5:117966409-117966419 chr5:117966408-117966419
3	BHLHE40	chr5:117934828-117934953	GM12878	blood:	n/a	n/a
4	CEBPB	chr5:117898360-117898614	MCF-7	breast:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
5	CEBPB	chr5:117893153-117893464	HepG2	liver:	n/a	chr5:117893294-117893305
6	CEBPB	chr5:117884436-117884805	Hela-S3	cervix:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
7	CEBPB	chr5:117932234-117932584	HepG2	liver:	n/a	n/a
8	CEBPB	chr5:117966977-117967267	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr5:117898314-117898635	A549	lung:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
10	CEBPB	chr5:117898345-117898611	Hela-S3	cervix:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
11	CEBPB	chr5:117898339-117898607	H1-hESC	embryonic stem cell:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
12	CEBPB	chr5:117884333-117884820	HCT-116	colon:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
13	CEBPB	chr5:117884508-117884707	HepG2	liver:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
14	CEBPB	chr5:117884446-117884760	HepG2	liver:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
15	CEBPB	chr5:117932289-117932583	A549	lung:	n/a	n/a
16	CEBPB	chr5:117898330-117898641	IMR90	lung:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
17	CEBPB	chr5:117898380-117898661	K562	blood:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
18	CEBPB	chr5:117898306-117898626	HepG2	liver:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
19	CEBPB	chr5:117884403-117884809	HepG2	liver:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
20	CEBPB	chr5:117884396-117884796	MCF-7	breast:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
21	CEBPB	chr5:117884404-117884771	HCT-116	colon:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
22	CEBPB	chr5:117884538-117884752	A549	lung:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
23	CEBPB	chr5:117884363-117884907	MCF-7	breast:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
24	CEBPB	chr5:117884451-117884780	IMR90	lung:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
25	CEBPB	chr5:117889409-117889983	IMR90	lung:	n/a	chr5:117889970-117889981 chr5:117889559-117889576 chr5:117889970-117889983 chr5:117889970-117889981
26	CEBPD	chr5:117884545-117884701	HepG2	liver:	n/a	chr5:117884575-117884586
27	CTCF	chr5:117928620-117928770	BE2_C	brain:	n/a	n/a
28	CTCF	chr5:117947160-117947310	AG04449	skin:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
29	CTCF	chr5:117947099-117947367	MCF-7	breast:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
30	CTCF	chr5:117928785-117928856	Gliobla	brain:	n/a	chr5:117928819-117928828
31	CTCF	chr5:117928700-117928850	HRE	kidney:	n/a	chr5:117928819-117928828
32	CTCF	chr5:117928820-117928970	GM12872	blood:	n/a	n/a
33	CTCF	chr5:117964862-117964891	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr5:117964760-117964910	AG09319	gingival:	n/a	n/a
35	CTCF	chr5:117942723-117942920	GM12878	blood:	n/a	n/a
36	CTCF	chr5:117947180-117947330	HVMF	connective:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
37	CTCF	chr5:117928740-117928890	GM12866	blood:	n/a	chr5:117928819-117928828
38	CTCF	chr5:117947140-117947290	HEEpiC	esophagus:	n/a	chr5:117947225-117947246 chr5:117947230-117947248
39	CTCF	chr5:117953767-117953787	LNCaP	prostate:	n/a	n/a
40	CTCF	chr5:117947180-117947330	HBMEC	blood vessel:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
41	CTCF	chr5:117928720-117928870	HPF	lung:	n/a	chr5:117928819-117928828
42	CTCF	chr5:117928680-117928830	Hela-S3	cervix:	n/a	chr5:117928819-117928828
43	CTCF	chr5:117947160-117947310	SAEC	small airway:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
44	CTCF	chr5:117947160-117947310	NHDF-neo	bronchial:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
45	CTCF	chr5:117928760-117929010	HA-sp	spinal cord:	n/a	chr5:117928819-117928828
46	CTCF	chr5:117947180-117947330	HFF	foreskin:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
47	CTCF	chr5:117942680-117942830	GM12871	blood:	n/a	n/a
48	CTCF	chr5:117947140-117947290	HAc	cerebellar:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
49	CTCF	chr5:117947140-117947290	K562	blood:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
50	CTCF	chr5:117947160-117947310	HUVEC	blood vessel:	n/a	chr5:117947230-117947248 chr5:117947225-117947246

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:117964718-117964768	BJ	skin:	n/a
2	chr5:117964718-117964768	HEK293	kidney:	embryo
3	chr5:117964718-117964768	HIPEpiC	eye:	n/a
4	chr5:117964718-117964768	Caco-2	colon:	n/a
5	chr5:117964718-117964768	ECC-1	luminal epithelium:	n/a
6	chr5:117964718-117964768	HAEpiC	amniotic membrane:	n/a
7	chr5:117964718-117964768	AG10803	skin:	n/a
8	chr5:117964718-117964768	HCF	heart:	n/a
9	chr5:117964718-117964768	IMR90	lung:	fetal
10	chr5:117964718-117964768	SK-N-MC	brain:	n/a
11	chr5:117964718-117964768	NHBE	bronchial:	n/a
12	chr5:117964718-117964768	H1-hESC	embryonic stem cell:	embryo
13	chr5:117964718-117964768	NH-A	brain:	n/a
14	chr5:117964718-117964768	NHDF-neo	bronchial:	n/a
15	chr5:117964718-117964768	HUVEC	blood vessel:	n/a
16	chr5:117964718-117964768	HCPEpiC	choroid plexus:	n/a
17	chr5:117964718-117964768	MCF-7	breast:	n/a
18	chr5:117964718-117964768	LNCaP	prostate:	n/a
19	chr5:117964718-117964768	HCM	heart:	n/a
20	chr5:117964718-117964768	HMEC	breast:	n/a
21	chr5:117964718-117964768	GM06990	blood:	n/a
22	chr5:117964718-117964768	SKMC	muscle:	n/a
23	chr5:117964718-117964768	HRPEpiC	eye:	n/a
24	chr5:117964718-117964768	SK-N-SH_RA	brain:	n/a
25	chr5:117964718-117964768	Hela-S3	cervix:	n/a
26	chr5:117964718-117964768	U87	brain:	n/a
27	chr5:117964718-117964768	K562	blood:	n/a
28	chr5:117964718-117964768	BE2_C	brain:	n/a
29	chr5:117964718-117964768	GM12892	blood:	n/a
30	chr5:117964718-117964768	GM19239	blood:	n/a
31	chr5:117964718-117964768	ovcar-3	ovarian:	n/a
32	chr5:117964718-117964768	T-47D	breast:	n/a
33	chr5:117964718-117964768	HRE	kidney:	n/a
34	chr5:117964718-117964768	Jurkat	blood:	n/a
35	chr5:117964718-117964768	A549	lung:	n/a
36	chr5:117964718-117964768	PFSK-1	brain:	n/a
37	chr5:117964718-117964768	HepG2	liver:	n/a
38	chr5:117964718-117964768	GM12878	blood:	n/a
39	chr5:117964718-117964768	AG04450	lung:	fetal
40	chr5:117964718-117964768	AoSMC	blood vessel:	n/a
41	chr5:117964718-117964768	GM12891	blood:	n/a
42	chr5:117964718-117964768	PANC-1	pancreas:	n/a
43	chr5:117964718-117964768	AG09319	gingival:	n/a
44	chr5:117964718-117964768	ProgFib	skin:	n/a
45	chr5:117964718-117964768	HRCEpiC	kidney:	n/a
46	chr5:117964718-117964768	AG09309	skin:	n/a
47	chr5:117964718-117964768	SK-N-SH	brain:	n/a
48	chr5:117964718-117964768	NB4	blood:	n/a
49	chr5:117964718-117964768	HCT-116	colon:	n/a
50	chr5:117964718-117964768	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:117853508..117855086-chr5:117856732..117858837,2	K562	blood:
2	chr5:117892457..117896152-chr5:117898946..117902524,3	MCF-7	breast:
3	chr5:117893334..117895634-chr5:117899247..117902608,3	K562	blood:
4	chr5:117930634..117932935-chr5:117933519..117935108,2	MCF-7	breast:
5	chr5:117953386..117954146-chr5:118127518..118128022,2	MCF-7	breast:
6	chr5:117911515..117913042-chr5:117914826..117917481,2	MCF-7	breast:
7	chr5:117947053..117948753-chr5:118127871..118130563,2	MCF-7	breast:
8	chr5:117892457..117896152-chr5:117898946..117902524,3	MCF-7	breast:
9	chr5:117887915..117890272-chr5:117891445..117894908,3	MCF-7	breast:
10	chr5:117923008..117924830-chr5:117927973..117929496,2	MCF-7	breast:
11	chr5:117893334..117895634-chr5:117899247..117902608,3	K562	blood:
12	chr3:161088409..161090897-chr5:117945115..117947573,2	MCF-7	breast:
13	chr5:117946766..117947670-chr5:118127610..118128249,2	MCF-7	breast:
14	chr5:117911515..117913042-chr5:117914826..117917481,2	MCF-7	breast:
15	chr5:117923008..117924830-chr5:117927973..117929496,2	MCF-7	breast:
16	chr5:117853508..117855086-chr5:117856732..117858837,2	K562	blood:
17	chr5:117887915..117890272-chr5:117891445..117894908,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DTWD2-3	chr5:117846583-117846759	NONHSAT103396
2	lnc-DTWD2-3	chr5:117897616-117897826	NONHSAT103403
3	lnc-DMXL1-2	chr5:117912735-117912889	XLOC_004526
4	lnc-DTWD2-3	chr5:117856867-117858541	NR_104610
5	lnc-DTWD2-3	chr5:117857424-117858532	NONHSAT103400
6	lnc-DTWD2-3	chr5:117856867-117858541	XLOC_004965
7	lnc-DTWD2-3	chr5:117846583-117846759	NR_104610
8	lnc-DTWD2-3	chr5:117846583-117846759	XLOC_004965
9	lnc-DTWD2-3	chr5:117897616-117897818	XLOC_004965
10	lnc-DTWD2-3	chr5:117859344-117859509	NR_104610
11	lnc-DTWD2-10	chr5:117887243-117887411	l_3002_chr5:117837955-117925717_heart
12	lnc-DMXL1-2	chr5:117911270-117911381	XLOC_004526
13	lnc-DTWD2-10	chr5:117925515-117925717	l_3002_chr5:117837955-117925717_heart
14	lnc-DTWD2-3	chr5:117858422-117858541	XLOC_004965
15	lnc-DTWD2-3	chr5:117856867-117858541	NONHSAT103396
16	lnc-DTWD2-10	chr5:117918641-117918733	l_3002_chr5:117837955-117925717_heart
17	lnc-DTWD2-3	chr5:117890742-117890834	NONHSAT103403
18	lnc-DTWD2-10	chr5:117874482-117874658	l_3002_chr5:117837955-117925717_heart
19	lnc-DMXL1-1	chr5:117945434-117945572	XLOC_004527
20	lnc-DMXL1-2	chr5:117915349-117915489	XLOC_004526
21	lnc-DMXL1-1	chr5:117931883-117931916	XLOC_004527
22	lnc-DMXL1-1	chr5:117947055-117947122	XLOC_004527
23	lnc-DTWD2-10	chr5:117886321-117886440	l_3002_chr5:117837955-117925717_heart
24	lnc-DTWD2-3	chr5:117897616-117897812	NR_104610
25	lnc-DTWD2-3	chr5:117846583-117846759	XLOC_004965
26	lnc-DMXL1-1	chr5:117949988-117950046	XLOC_004527
27	lnc-DTWD2-3	chr5:117859344-117859509	XLOC_004965
28	lnc-DTWD2-3	chr5:117859344-117859512	XLOC_004965
29	lnc-DTWD2-3	chr5:117859344-117859509	XLOC_004965
30	lnc-DTWD2-3	chr5:117897616-117897812	NONHSAT103396
31	lnc-DTWD2-3	chr5:117897616-117897812	XLOC_004965
32	lnc-DTWD2-3	chr5:117858422-117858541	XLOC_004965
33	lnc-DTWD2-3	chr5:117897616-117897751	XLOC_004965
34	lnc-DMXL1-1	chr5:117963545-117963787	XLOC_004527
35	lnc-DTWD2-3	chr5:117859344-117859509	NONHSAT103396
36	lnc-DTWD2-3	chr5:117863970-117864208	NONHSAT103401
37	lnc-DTWD2-3	chr5:117856867-117857041	NONHSAT103400
38	lnc-DTWD2-10	chr5:117909342-117909743	l_3002_chr5:117837955-117925717_heart
39	lnc-DTWD2-3	chr5:117897616-117897818	XLOC_004965
40	lnc-DMXL1-2	chr5:117916227-117916343	XLOC_004526
41	lnc-DTWD2-3	chr5:117881443-117881844	XLOC_004965
42	lnc-DTWD2-3	chr5:117890742-117890834	XLOC_004965
43	lnc-DTWD2-3	chr5:117881461-117881844	NONHSAT103403
44	lnc-DTWD2-3	chr5:117859424-117859509	NONHSAT103401
45	lnc-DMXL1-2	chr5:117916964-117917019	XLOC_004526
46	lnc-DTWD2-3	chr5:117846583-117846759	NONHSAT103400
47	lnc-DTWD2-3	chr5:117881553-117881844	XLOC_004965
48	lnc-DTWD2-3	chr5:117846583-117846759	XLOC_004965
49	lnc-DTWD2-3	chr5:117888048-117888244	XLOC_004965

Variant related genes	Relation type
ENSG00000249551	TF binding region
ENSG00000249128	TF binding region
ENSG00000250891	TF binding region
ENSG00000249551	CpG island
ENSG00000249128	CpG island
ENSG00000250891	CpG island
ENSG00000196542	chromatin interactions
ENSG00000249128	chromatin interactions
KRAS	miRNA target sites
HOXA5	miRNA target sites
MARS2	miRNA target sites
CELSR3	miRNA target sites
MAT2A	miRNA target sites
SFRS2	miRNA target sites
DHX57	miRNA target sites
MATR3	miRNA target sites
TAX1BP1	miRNA target sites
NR2C2AP	miRNA target sites
DICER1	miRNA target sites
MARK2	miRNA target sites
CEBPD	miRNA target sites
CEBPZ	miRNA target sites
DIABLO	miRNA target sites

Extended variants
information (count: 4944 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:4944 , 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	rs3924079	chr5:117843869-117843870	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs535151681	chr5:117843895-117843896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552594678	chr5:117843958-117843959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs193284199	chr5:117843965-117843966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568459914	chr5:117843970-117843971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537308078	chr5:117844004-117844005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs557639793	chr5:117844042-117844043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577156887	chr5:117844061-117844062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369467231	chr5:117844062-117844063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs4308508	chr5:117844105-117844106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553176197	chr5:117844150-117844151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs572572607	chr5:117844173-117844174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs528456061	chr5:117844182-117844183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541923348	chr5:117844270-117844271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76839228	chr5:117844282-117844283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575198204	chr5:117844290-117844291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371059826	chr5:117844294-117844295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs543918396	chr5:117844304-117844305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371913342	chr5:117844334-117844335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546557931	chr5:117844359-117844360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140534877	chr5:117844381-117844382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533301513	chr5:117844407-117844408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540407822	chr5:117844472-117844473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560411223	chr5:117844488-117844489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs116061682	chr5:117844489-117844490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs116190214	chr5:117844517-117844518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs75758652	chr5:117844557-117844558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557129648	chr5:117844562-117844563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568950228	chr5:117844563-117844564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530932704	chr5:117844596-117844597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550593737	chr5:117844631-117844632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570786833	chr5:117844664-117844665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539763191	chr5:117844676-117844677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs79431323	chr5:117844684-117844685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185651341	chr5:117844696-117844697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12655513	chr5:117844728-117844729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541248698	chr5:117844738-117844739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555436490	chr5:117844751-117844752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs34627397	chr5:117844754-117844755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143644453	chr5:117844765-117844766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148176253	chr5:117844774-117844775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557814389	chr5:117844859-117844860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs13187909	chr5:117844894-117844895	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs142005877	chr5:117844904-117844905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs59615591	chr5:117844926-117844927	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs529090776	chr5:117844927-117844928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542505369	chr5:117844930-117844931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7719824	chr5:117844940-117844941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530935089	chr5:117844943-117844944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550530324	chr5:117844948-117844949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
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
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
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Breast cancer	21509527	CNVD
Autism	22543975	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:321 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:117841200-117859200	Weak transcription	Left Ventricle	heart
2	chr5:117853000-117853200	Enhancers	Esophagus	oesophagus
3	chr5:117854800-117857800	Enhancers	Fetal Heart	heart
4	chr5:117856600-117857000	Enhancers	Right Ventricle	heart
5	chr5:117857800-117861200	Weak transcription	Fetal Heart	heart
6	chr5:117859200-117859400	ZNF genes & repeats	Left Ventricle	heart
7	chr5:117859400-117870200	Weak transcription	Left Ventricle	heart
8	chr5:117860600-117861400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr5:117860800-117861800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr5:117861000-117861400	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr5:117861000-117861600	Enhancers	H9 Cell Line	embryonic stem cell
12	chr5:117861000-117861600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr5:117861200-117861600	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr5:117861200-117861600	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr5:117861200-117861800	Enhancers	Fetal Heart	heart
16	chr5:117861200-117862000	Enhancers	H1 Cell Line	embryonic stem cell
17	chr5:117861200-117863800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr5:117861400-117861800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr5:117861600-117866000	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr5:117861600-117866400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr5:117861800-117862000	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr5:117861800-117863200	Weak transcription	Fetal Heart	heart
23	chr5:117861800-117866400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr5:117862000-117866000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr5:117862800-117863800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr5:117863200-117866600	Enhancers	Fetal Heart	heart
27	chr5:117863400-117863800	Enhancers	Osteobl	bone
28	chr5:117863800-117864200	Enhancers	Right Atrium	heart
29	chr5:117863800-117868200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr5:117864200-117866000	Weak transcription	Right Atrium	heart
31	chr5:117864600-117865600	Enhancers	Fetal Lung	lung
32	chr5:117865200-117865600	Enhancers	Brain Germinal Matrix	brain
33	chr5:117865200-117865800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr5:117865600-117865800	Flanking Active TSS	Fetal Lung	lung
35	chr5:117865800-117866200	Active TSS	Fetal Lung	lung
36	chr5:117866000-117866400	Enhancers	Right Atrium	heart
37	chr5:117866000-117866800	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr5:117866000-117867200	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr5:117866000-117867400	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr5:117866400-117866800	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr5:117866400-117867200	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr5:117866400-117870200	Weak transcription	Right Atrium	heart
43	chr5:117866600-117868600	Weak transcription	Fetal Heart	heart
44	chr5:117868000-117870600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr5:117868200-117869600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr5:117868600-117870400	Enhancers	Fetal Heart	heart
47	chr5:117869400-117870000	Enhancers	Primary hematopoietic stem cells	blood
48	chr5:117870200-117870400	Enhancers	Left Ventricle	heart
49	chr5:117870200-117870400	Enhancers	Right Atrium	heart
50	chr5:117875200-117876000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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