Variant report

Variant	nsv1034208
Chromosome Location	chr5:42119128-42290759
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:282)
CpG islands
(count:244)
Chromatin interactive
region (count:20)
LncRNA
region (count:62)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:282 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr5:42230928-42231280	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr5:42278871-42278878	H1-hESC	embryonic stem cell:	n/a	n/a
3	CBX3	chr5:42149496-42149748	K562	blood:	n/a	n/a
4	CBX3	chr5:42149458-42149761	K562	blood:	n/a	n/a
5	CCNT2	chr5:42271507-42271707	K562	blood:	n/a	n/a
6	CEBPB	chr5:42252397-42252791	IMR90	lung:	n/a	chr5:42252570-42252581 chr5:42252605-42252616
7	CEBPB	chr5:42252431-42252754	A549	lung:	n/a	chr5:42252570-42252581 chr5:42252605-42252616
8	CEBPB	chr5:42146883-42147119	IMR90	lung:	n/a	chr5:42147025-42147038 chr5:42147027-42147038
9	CEBPB	chr5:42252456-42252692	H1-hESC	embryonic stem cell:	n/a	chr5:42252570-42252581 chr5:42252605-42252616
10	CEBPB	chr5:42252419-42252717	K562	blood:	n/a	chr5:42252570-42252581 chr5:42252605-42252616
11	CEBPB	chr5:42252442-42252717	Hela-S3	cervix:	n/a	chr5:42252570-42252581 chr5:42252605-42252616
12	CEBPB	chr5:42274650-42274863	HepG2	liver:	n/a	chr5:42274759-42274770
13	CEBPB	chr5:42236337-42236376	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr5:42146958-42147053	K562	blood:	n/a	chr5:42147025-42147038 chr5:42147027-42147038
15	CEBPB	chr5:42284731-42285003	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr5:42252388-42252769	HepG2	liver:	n/a	chr5:42252570-42252581 chr5:42252605-42252616
17	CTCF	chr5:42263120-42263270	HEK293	kidney:	n/a	n/a
18	CTCF	chr5:42180220-42180370	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr5:42182940-42183090	Caco-2	colon:	n/a	n/a
20	CTCF	chr5:42228460-42228610	NHEK	skin:	n/a	n/a
21	CTCF	chr5:42262763-42262833	Medullo	brain:	n/a	n/a
22	CTCF	chr5:42182840-42182990	HPF	lung:	n/a	n/a
23	CTCF	chr5:42228531-42228534	ProgFib	skin:	n/a	n/a
24	CTCF	chr5:42180340-42180490	GM06990	blood:	n/a	n/a
25	CTCF	chr5:42228483-42228551	HepG2	liver:	n/a	n/a
26	CTCF	chr5:42182911-42182996	MCF-7	breast:	n/a	n/a
27	CTCF	chr5:42228340-42228490	MCF-7	breast:	n/a	n/a
28	CTCF	chr5:42182922-42183030	MCF-7	breast:	n/a	n/a
29	CTCF	chr5:42180280-42180430	GM12866	blood:	n/a	n/a
30	CTCF	chr5:42123210-42123305	MCF-7	breast:	n/a	n/a
31	CTCF	chr5:42123320-42123470	MCF-7	breast:	n/a	n/a
32	CTCF	chr5:42228420-42228570	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr5:42228480-42228630	AG09319	gingival:	n/a	n/a
34	CTCF	chr5:42180260-42180410	HepG2	liver:	n/a	n/a
35	CTCF	chr5:42228431-42228654	LNCaP	prostate:	n/a	n/a
36	CTCF	chr5:42228440-42228590	HCFaa	heart:	n/a	n/a
37	CTCF	chr5:42228440-42228590	HMF	breast:	n/a	n/a
38	CTCF	chr5:42228400-42228550	HMEC	breast:	n/a	n/a
39	CTCF	chr5:42228503-42228590	NHEK	skin:	n/a	n/a
40	CTCF	chr5:42228474-42228580	GM12878	blood:	n/a	n/a
41	CTCF	chr5:42247957-42248038	GM20000	blood:	n/a	n/a
42	CTCF	chr5:42228440-42228590	GM06990	blood:	n/a	n/a
43	CTCF	chr5:42228440-42228590	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr5:42228420-42228570	HPF	lung:	n/a	n/a
45	CTCF	chr5:42228460-42228625	MCF-7	breast:	n/a	n/a
46	CTCF	chr5:42228480-42228630	GM12878	blood:	n/a	n/a
47	CTCF	chr5:42182932-42182983	LNCaP	prostate:	n/a	n/a
48	CTCF	chr5:42228428-42228483	Lung_OC	lung:	n/a	n/a
49	CTCF	chr5:42228460-42228610	MCF-7	breast:	n/a	n/a
50	CTCF	chr5:42228420-42228570	HMF	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:42175438-42175488	MCF10A-Er-Src	breast:	n/a
2	chr5:42176806-42176856	GM12891	blood:	n/a
3	chr5:42176454-42176504	LNCaP	prostate:	n/a
4	chr5:42176806-42176856	NT2-D1	testis:	n/a
5	chr5:42175368-42175418	HRCEpiC	kidney:	n/a
6	chr5:42176454-42176504	K562	blood:	n/a
7	chr5:42175438-42175488	AG09309	skin:	n/a
8	chr5:42176806-42176856	ECC-1	luminal epithelium:	n/a
9	chr5:42176806-42176856	HRPEpiC	eye:	n/a
10	chr5:42176806-42176856	PFSK-1	brain:	n/a
11	chr5:42176454-42176504	HIPEpiC	eye:	n/a
12	chr5:42175438-42175488	AG10803	skin:	n/a
13	chr5:42176454-42176504	Jurkat	blood:	n/a
14	chr5:42176454-42176504	AG10803	skin:	n/a
15	chr5:42176806-42176856	HUVEC	blood vessel:	n/a
16	chr5:42176454-42176504	GM12878	blood:	n/a
17	chr5:42175368-42175418	HRPEpiC	eye:	n/a
18	chr5:42176806-42176856	HEEpiC	esophagus:	n/a
19	chr5:42176806-42176856	MCF10A-Er-Src	breast:	n/a
20	chr5:42176454-42176504	PFSK-1	brain:	n/a
21	chr5:42175368-42175418	NH-A	brain:	n/a
22	chr5:42176806-42176856	HPAEpiC	pulmonary alveolar:	n/a
23	chr5:42176806-42176856	NHBE	bronchial:	n/a
24	chr5:42175438-42175488	SK-N-MC	brain:	n/a
25	chr5:42175368-42175418	IMR90	lung:	fetal
26	chr5:42176806-42176856	GM12878	blood:	n/a
27	chr5:42176454-42176504	HEEpiC	esophagus:	n/a
28	chr5:42176454-42176504	SK-N-SH_RA	brain:	n/a
29	chr5:42176806-42176856	HMEC	breast:	n/a
30	chr5:42175438-42175488	H1-hESC	embryonic stem cell:	embryo
31	chr5:42175368-42175418	T-47D	breast:	n/a
32	chr5:42175368-42175418	HepG2	liver:	n/a
33	chr5:42175368-42175418	PFSK-1	brain:	n/a
34	chr5:42175368-42175418	CMK	blood:	n/a
35	chr5:42176454-42176504	Caco-2	colon:	n/a
36	chr5:42175438-42175488	T-47D	breast:	n/a
37	chr5:42175368-42175418	GM19239	blood:	n/a
38	chr5:42176806-42176856	PANC-1	pancreas:	n/a
39	chr5:42175368-42175418	GM06990	blood:	n/a
40	chr5:42175368-42175418	HEK293	kidney:	embryo
41	chr5:42175438-42175488	A549	lung:	n/a
42	chr5:42175438-42175488	HL-60	blood:	n/a
43	chr5:42176806-42176856	SAEC	small airway:	n/a
44	chr5:42176454-42176504	U87	brain:	n/a
45	chr5:42175438-42175488	SK-N-SH	brain:	n/a
46	chr5:42175368-42175418	GM12891	blood:	n/a
47	chr5:42176806-42176856	HNPCEpiC	eye:	n/a
48	chr5:42176454-42176504	ProgFib	skin:	n/a
49	chr5:42176454-42176504	GM12892	blood:	n/a
50	chr5:42176806-42176856	NB4	blood:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:42127815..42129414-chr5:42135015..42137366,2	K562	blood:
2	chr5:42228294..42229001-chr5:42656539..42657726,4	MCF-7	breast:
3	chr5:42213251..42214932-chr5:42220476..42222558,2	K562	blood:
4	chr5:42228076..42228879-chr5:42636463..42637129,2	MCF-7	breast:
5	chr5:42122185..42124242-chr5:42127395..42129833,2	MCF-7	breast:
6	chr5:42122185..42124242-chr5:42127395..42129833,2	MCF-7	breast:
7	chr5:42127815..42129414-chr5:42135015..42137366,2	K562	blood:
8	chr5:42272147..42275776-chr5:42281474..42285473,4	K562	blood:
9	chr5:42275847..42277398-chr5:42279299..42281970,2	K562	blood:
10	chr5:42182671..42183209-chr7:83415074..83415902,2	MCF-7	breast:
11	chr5:42272928..42275449-chr5:42293817..42296582,2	K562	blood:
12	chr16:75656853..75657363-chr5:42260815..42261315,2	MCF-7	breast:
13	chr5:42272928..42275449-chr5:42292455..42296582,3	K562	blood:
14	chr5:42108690..42109427-chr5:42127456..42127968,2	MCF-7	breast:
15	chr5:42164889..42166959-chr5:42173984..42175632,2	K562	blood:
16	chr5:42272147..42275776-chr5:42281474..42285473,4	K562	blood:
17	chr5:42164889..42166959-chr5:42173984..42175632,2	K562	blood:
18	chr5:42228431..42229012-chr5:42583047..42583600,3	MCF-7	breast:
19	chr5:42213251..42214932-chr5:42220476..42222558,2	K562	blood:
20	chr5:42275847..42277398-chr5:42279299..42281970,2	K562	blood:

(count:62 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OXCT1-1	chr5:42154409-42157513	XLOC_004800
2	lnc-OXCT1-1	chr5:42159439-42159548	XLOC_004800
3	lnc-OXCT1-1	chr5:42159129-42159155	NR_104636
4	lnc-OXCT1-1	chr5:42175255-42175444	XLOC_004800
5	lnc-OXCT1-1	chr5:42159439-42159548	XLOC_004800
6	lnc-OXCT1-2	chr5:42191692-42193270	ucscGeneNc_uc003jms_1
7	lnc-FBXO4-1	chr5:42175254-42175444	NONHSAT101190
8	lnc-OXCT1-1	chr5:42175255-42175356	ENSG00000248519
9	lnc-OXCT1-1	chr5:42175255-42175444	XLOC_004800
10	lnc-OXCT1-1	chr5:42159439-42159548	XLOC_004800
11	lnc-OXCT1-1	chr5:42175255-42175366	XLOC_004800
12	lnc-OXCT1-1	chr5:42159439-42159548	NR_104636
13	lnc-OXCT1-1	chr5:42159439-42159548	XLOC_004800
14	lnc-OXCT1-1	chr5:42155935-42157513	NR_104635
15	lnc-OXCT1-1	chr5:42159127-42159155	XLOC_004800
16	lnc-OXCT1-1	chr5:42168565-42168689	ENSG00000248519
17	lnc-FBXO4-1	chr5:42157823-42157966	NONHSAT101190
18	lnc-OXCT1-1	chr5:42153043-42153776	XLOC_004800
19	lnc-OXCT1-1	chr5:42157044-42157513	XLOC_004800
20	lnc-OXCT1-1	chr5:42157044-42157513	XLOC_004800
21	lnc-OXCT1-1	chr5:42153753-42153776	XLOC_004800
22	lnc-OXCT1-1	chr5:42159129-42159155	XLOC_004800
23	lnc-OXCT1-1	chr5:42175255-42175275	XLOC_004800
24	lnc-OXCT1-1	chr5:42159129-42159155	XLOC_004800
25	lnc-OXCT1-1	chr5:42159127-42159155	XLOC_004800
26	lnc-OXCT1-1	chr5:42156651-42157513	XLOC_004800
27	lnc-OXCT1-1	chr5:42159439-42159548	XLOC_004800
28	lnc-OXCT1-1	chr5:42175255-42175444	XLOC_004800
29	lnc-OXCT1-1	chr5:42155935-42157513	NR_104636
30	lnc-OXCT1-1	chr5:42168565-42168689	XLOC_004800
31	lnc-OXCT1-2	chr5:42211012-42211113	ucscGeneNc_uc003jms_1
32	lnc-FBXO4-1	chr5:42159126-42159155	NONHSAT101190
33	lnc-OXCT1-1	chr5:42168565-42168678	XLOC_004800
34	lnc-OXCT1-1	chr5:42153043-42153776	XLOC_004800
35	lnc-OXCT1-1	chr5:42168565-42168689	NR_104635
36	lnc-FBXO4-1	chr5:42153042-42153776	NONHSAT101190
37	lnc-OXCT1-1	chr5:42159439-42159548	XLOC_004800
38	lnc-OXCT1-1	chr5:42168565-42168689	XLOC_004800
39	lnc-OXCT1-1	chr5:42159129-42159155	XLOC_004800
40	lnc-OXCT1-1	chr5:42159439-42159548	XLOC_004800
41	lnc-OXCT1-1	chr5:42159439-42159548	XLOC_004800
42	lnc-GHR-1	chr5:42188368-42191625	ENSG00000260786.1
43	lnc-FBXO4-1	chr5:42157824-42157966	XLOC_004360
44	lnc-OXCT1-2	chr5:42195196-42195305	ucscGeneNc_uc003jms_1
45	lnc-OXCT1-1	chr5:42155935-42157513	ENSG00000248519
46	lnc-FBXO4-1	chr5:42154408-42157540	NONHSAT101190
47	lnc-OXCT1-1	chr5:42157034-42157513	XLOC_004800
48	lnc-OXCT1-1	chr5:42159439-42159548	NR_104635
49	lnc-FBXO4-1	chr5:42159327-42159548	NONHSAT101190
50	lnc-OXCT1-1	chr5:42153043-42153776	XLOC_004800

No data

Variant related genes	Relation type
ENSG00000260786	TF binding region
ENSG00000260786	CpG island
ENSG00000065457	chromatin interactions
CLIP3	miRNA target sites
PHLPP2	miRNA target sites
FAM171A1	miRNA target sites
ZC3H12C	miRNA target sites
FAM171B	miRNA target sites
BIRC6	miRNA target sites
ELMOD2	miRNA target sites
TPD52L2	miRNA target sites
FCHO2	miRNA target sites
BLCAP	miRNA target sites
VN1R1	miRNA target sites
BIRC5	miRNA target sites
G2E3	miRNA target sites
FNDC3B	miRNA target sites
MDFIC	miRNA target sites
HADH	miRNA target sites
SERPINB9	miRNA target sites
GFPT2	miRNA target sites
ELOVL2	miRNA target sites
SNTA1	miRNA target sites
BIN3	miRNA target sites
FBLIM1	miRNA target sites
ALCAM	miRNA target sites

Extended variants
information (count: 2624 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:2624 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574482487	chr5:42119412-42119413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs192039916	chr5:42119471-42119472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184469016	chr5:42119491-42119492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572156195	chr5:42119505-42119506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545948419	chr5:42119513-42119514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs931230	chr5:42119514-42119515	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs143894513	chr5:42119533-42119534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189301032	chr5:42119580-42119581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192498135	chr5:42119582-42119583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539706526	chr5:42119614-42119615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs115755201	chr5:42119618-42119619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565744977	chr5:42119670-42119671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs931231	chr5:42119671-42119672	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs534148848	chr5:42119675-42119676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs275044	chr5:42119728-42119729	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs570693517	chr5:42119730-42119731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs184133600	chr5:42119762-42119763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs556435993	chr5:42119763-42119764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs557626434	chr5:42119790-42119791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs147278185	chr5:42119794-42119795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs140871727	chr5:42119798-42119799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs553990915	chr5:42119843-42119844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189513766	chr5:42119855-42119856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs543393301	chr5:42119856-42119857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs78183444	chr5:42119879-42119880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576297188	chr5:42119921-42119922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs543789376	chr5:42119943-42119944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561918730	chr5:42119970-42119971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs12332782	chr5:42119990-42119991	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs190281163	chr5:42123022-42123023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11744111	chr5:42123035-42123036	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs554299801	chr5:42123080-42123081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs566451105	chr5:42123108-42123109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs143836452	chr5:42123124-42123125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112905266	chr5:42123197-42123198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs182713281	chr5:42123200-42123201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs4626371	chr5:42123212-42123213	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs561263778	chr5:42123221-42123222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs545582960	chr5:42123233-42123234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557707836	chr5:42123280-42123281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs187400411	chr5:42123304-42123305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs375726130	chr5:42123323-42123324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs193029372	chr5:42123437-42123438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs185770622	chr5:42123440-42123441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs77124355	chr5:42123464-42123465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs532875530	chr5:42123499-42123500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs528483016	chr5:42123511-42123512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs72748699	chr5:42123546-42123547	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs116227369	chr5:42123549-42123550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs532193171	chr5:42123566-42123567	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Hepatocellular carcinoma	18929564	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:42119400-42120000	Enhancers	Brain Germinal Matrix	brain
2	chr5:42123000-42123600	Enhancers	Adipose Nuclei	Adipose
3	chr5:42131200-42131600	Enhancers	H1 Cell Line	embryonic stem cell
4	chr5:42131200-42132400	Enhancers	Fetal Muscle Trunk	muscle
5	chr5:42131200-42132400	Enhancers	Fetal Muscle Leg	muscle
6	chr5:42131400-42131800	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr5:42149000-42149800	ZNF genes & repeats	Liver	Liver
8	chr5:42149000-42150000	ZNF genes & repeats	Adipose Nuclei	Adipose
9	chr5:42149200-42150400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr5:42149400-42150200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
11	chr5:42152200-42152600	Enhancers	Adipose Nuclei	Adipose
12	chr5:42152200-42152800	Enhancers	Fetal Heart	heart
13	chr5:42152600-42158400	Weak transcription	Adipose Nuclei	Adipose
14	chr5:42152800-42156600	Weak transcription	Fetal Heart	heart
15	chr5:42153000-42153400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr5:42153400-42158400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr5:42156400-42157600	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr5:42156600-42157600	Enhancers	Fetal Heart	heart
19	chr5:42156800-42157400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr5:42156800-42157400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr5:42156800-42157600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr5:42157200-42157600	Enhancers	NHEK	skin
23	chr5:42157600-42158000	Weak transcription	Fetal Heart	heart
24	chr5:42158000-42159000	Enhancers	Fetal Heart	heart
25	chr5:42158400-42158600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr5:42158400-42158800	Strong transcription	Adipose Nuclei	Adipose
27	chr5:42158800-42161000	Weak transcription	Adipose Nuclei	Adipose
28	chr5:42168200-42168800	Enhancers	H1 Cell Line	embryonic stem cell
29	chr5:42168400-42168800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr5:42168400-42168800	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr5:42168400-42168800	Enhancers	Esophagus	oesophagus
32	chr5:42168400-42169000	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr5:42168400-42169200	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr5:42168600-42169200	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr5:42173800-42175200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr5:42173800-42175400	Active TSS	Adipose Nuclei	Adipose
37	chr5:42175200-42175400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr5:42175200-42176400	Enhancers	Ovary	ovary
39	chr5:42175400-42175800	Weak transcription	Adipose Nuclei	Adipose
40	chr5:42175400-42177000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr5:42175800-42177000	Enhancers	Adipose Nuclei	Adipose
42	chr5:42177400-42177800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
43	chr5:42182800-42183000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr5:42189800-42190200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr5:42218000-42218200	Enhancers	Adipose Nuclei	Adipose
46	chr5:42218200-42218800	Weak transcription	Adipose Nuclei	Adipose
47	chr5:42218200-42219400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr5:42218600-42219400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr5:42218600-42219400	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr5:42218800-42219400	Enhancers	Adipose Nuclei	Adipose

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