Variant report

Variant	nsv1032548
Chromosome Location	chr5:96565121-97046804
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1946)
CpG islands
(count:612)
Chromatin interactive
region (count:44)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1946 , 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	chr5:96632846-96633044	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:96869893-96870174	HepG2	liver:	n/a	n/a
3	ATF1	chr5:96925354-96925372	K562	blood:	n/a	n/a
4	ATF1	chr5:96566806-96567076	K562	blood:	n/a	n/a
5	ATF2	chr5:96736132-96736743	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr5:96883636-96884569	GM12878	blood:	n/a	n/a
7	ATF2	chr5:96736083-96736724	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr5:96691322-96691778	GM12878	blood:	n/a	n/a
9	ATF2	chr5:96883703-96884520	GM12878	blood:	n/a	n/a
10	BACH1	chr5:96861461-96861877	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr5:96600161-96600267	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr5:96885956-96886136	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr5:96883695-96884539	GM12878	blood:	n/a	chr5:96884341-96884350
14	BATF	chr5:96713332-96713631	GM12878	blood:	n/a	n/a
15	BATF	chr5:96883741-96884022	GM12878	blood:	n/a	n/a
16	BATF	chr5:96872418-96872668	GM12878	blood:	n/a	chr5:96872552-96872563
17	BATF	chr5:96884044-96884526	GM12878	blood:	n/a	chr5:96884341-96884350
18	BATF	chr5:96872429-96872695	GM12878	blood:	n/a	chr5:96872552-96872563
19	BCL11A	chr5:96736252-96736517	H1-hESC	embryonic stem cell:	n/a	n/a
20	BCL11A	chr5:96884015-96884504	GM12878	blood:	n/a	n/a
21	BCL11A	chr5:96713335-96713673	GM12878	blood:	n/a	n/a
22	BCL11A	chr5:96736211-96736597	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCL11A	chr5:96884033-96884506	GM12878	blood:	n/a	n/a
24	BCL11A	chr5:96883801-96884003	GM12878	blood:	n/a	chr5:96883828-96883837
25	BCL3	chr5:96928285-96928637	GM12878	blood:	n/a	n/a
26	BCL3	chr5:96831847-96832152	GM12878	blood:	n/a	n/a
27	BCLAF1	chr5:96691310-96691873	GM12878	blood:	n/a	n/a
28	BCLAF1	chr5:96632712-96633177	GM12878	blood:	n/a	n/a
29	BHLHE40	chr5:96691380-96691821	GM12878	blood:	n/a	n/a
30	BHLHE40	chr5:96830650-96830767	GM12878	blood:	n/a	n/a
31	BHLHE40	chr5:96883684-96884500	GM12878	blood:	n/a	n/a
32	BHLHE40	chr5:96869825-96870150	GM12878	blood:	n/a	n/a
33	BRCA1	chr5:96675145-96675188	GM12878	blood:	n/a	n/a
34	BRCA1	chr5:96761275-96761538	H1-hESC	embryonic stem cell:	n/a	n/a
35	CBX3	chr5:96632687-96633278	HCT-116	colon:	n/a	n/a
36	CCNT2	chr5:96691691-96691850	K562	blood:	n/a	n/a
37	CCNT2	chr5:96633727-96633849	K562	blood:	n/a	n/a
38	CEBPB	chr5:96728466-96728767	HepG2	liver:	n/a	chr5:96728592-96728603
39	CEBPB	chr5:96658415-96658662	A549	lung:	n/a	chr5:96658532-96658543
40	CEBPB	chr5:96566703-96567118	Hela-S3	cervix:	n/a	chr5:96566892-96566903 chr5:96566891-96566902
41	CEBPB	chr5:96566558-96567266	A549	lung:	n/a	chr5:96566892-96566903 chr5:96566891-96566902
42	CEBPB	chr5:96566678-96567133	K562	blood:	n/a	chr5:96566892-96566903 chr5:96566891-96566902
43	CEBPB	chr5:96566801-96567023	HepG2	liver:	n/a	chr5:96566892-96566903 chr5:96566891-96566902
44	CEBPB	chr5:96827337-96827579	HepG2	liver:	n/a	chr5:96827480-96827491 chr5:96827469-96827480
45	CEBPB	chr5:96869837-96870355	MCF-7	breast:	n/a	chr5:96870105-96870116
46	CEBPB	chr5:96616391-96616638	HepG2	liver:	n/a	chr5:96616500-96616511
47	CEBPB	chr5:96566591-96567178	K562	blood:	n/a	chr5:96566892-96566903 chr5:96566891-96566902
48	CEBPB	chr5:96566758-96567015	HepG2	liver:	n/a	chr5:96566892-96566903 chr5:96566891-96566902
49	CEBPB	chr5:96566656-96567179	MCF-7	breast:	n/a	chr5:96566892-96566903 chr5:96566891-96566902
50	CEBPB	chr5:96984266-96984278	K562	blood:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:96845117-96845167	HL-60	blood:	n/a
2	chr5:96742935-96742985	Jurkat	blood:	n/a
3	chr5:96845117-96845167	HL-60	blood:	n/a
4	chr5:96742935-96742985	Jurkat	blood:	n/a
5	chr5:96747223-96747273	SAEC	small airway:	n/a
6	chr5:96743054-96743104	RPTEC	kidney:	n/a
7	chr5:96845117-96845167	HPAEpiC	pulmonary alveolar:	n/a
8	chr5:96845117-96845167	HRE	kidney:	n/a
9	chr5:96742935-96742985	NT2-D1	testis:	n/a
10	chr5:96845117-96845167	Hepatocyte	liver:	n/a
11	chr5:96789385-96789435	HRCEpiC	kidney:	n/a
12	chr5:96742935-96742985	HRCEpiC	kidney:	n/a
13	chr5:96915770-96915820	BE2_C	brain:	n/a
14	chr5:96890257-96890307	ProgFib	skin:	n/a
15	chr5:96747223-96747273	HepG2	liver:	n/a
16	chr5:96855476-96855526	PANC-1	pancreas:	n/a
17	chr5:96881859-96881909	AoSMC	blood vessel:	n/a
18	chr5:96742935-96742985	PANC-1	pancreas:	n/a
19	chr5:96743054-96743104	IMR90	lung:	fetal
20	chr5:96876834-96876884	Hela-S3	cervix:	n/a
21	chr5:96881859-96881909	AG10803	skin:	n/a
22	chr5:96890257-96890307	GM19239	blood:	n/a
23	chr5:96789385-96789435	MCF-7	breast:	n/a
24	chr5:96881859-96881909	HCF	heart:	n/a
25	chr5:96855476-96855526	SK-N-MC	brain:	n/a
26	chr5:96881859-96881909	HUVEC	blood vessel:	n/a
27	chr5:96876834-96876884	AG04449	skin:	fetal
28	chr5:96742935-96742985	MCF10A-Er-Src	breast:	n/a
29	chr5:96876834-96876884	AG10803	skin:	n/a
30	chr5:96845117-96845167	GM06990	blood:	n/a
31	chr5:96743054-96743104	Hepatocyte	liver:	n/a
32	chr5:96881859-96881909	U87	brain:	n/a
33	chr5:96915770-96915820	HRCEpiC	kidney:	n/a
34	chr5:96855476-96855526	LNCaP	prostate:	n/a
35	chr5:96876834-96876884	HIPEpiC	eye:	n/a
36	chr5:96876834-96876884	RPTEC	kidney:	n/a
37	chr5:96881859-96881909	HNPCEpiC	eye:	n/a
38	chr5:96845117-96845167	SK-N-MC	brain:	n/a
39	chr5:96845117-96845167	NHDF-neo	bronchial:	n/a
40	chr5:96747223-96747273	HPAEpiC	pulmonary alveolar:	n/a
41	chr5:96881859-96881909	SAEC	small airway:	n/a
42	chr5:96876834-96876884	NT2-D1	testis:	n/a
43	chr5:96915770-96915820	U87	brain:	n/a
44	chr5:96876834-96876884	SAEC	small airway:	n/a
45	chr5:96845117-96845167	ProgFib	skin:	n/a
46	chr5:96881859-96881909	Hepatocyte	liver:	n/a
47	chr5:96743054-96743104	GM06990	blood:	n/a
48	chr5:96789385-96789435	PrEC	prostate:	n/a
49	chr5:96915770-96915820	AG10803	skin:	n/a
50	chr5:96855476-96855526	AG09309	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:96566532..96567370-chr5:96632847..96633430,3	MCF-7	breast:
2	chr5:96687334..96689961-chr5:96691050..96693898,2	MCF-7	breast:
3	chr5:96987103..96987619-chr5:97253568..97254119,2	MCF-7	breast:
4	chr5:96711348..96714233-chr5:96714673..96716999,2	MCF-7	breast:
5	chr5:96566460..96567205-chr5:96869494..96870442,2	MCF-7	breast:
6	chr17:41380186..41382311-chr5:96695804..96697321,3	MCF-7	breast:
7	chr5:96898495..96900851-chr5:96905056..96906917,2	K562	blood:
8	chr5:96720114..96721922-chr5:96728191..96729748,2	MCF-7	breast:
9	chr5:96632616..96633407-chr5:96869853..96870506,3	MCF-7	breast:
10	chr5:96566532..96567370-chr5:96632847..96633430,3	MCF-7	breast:
11	chr17:41380182..41383606-chr5:96695801..96698822,3	K562	blood:
12	chr17:41398650..41400853-chr5:96695801..96698804,5	K562	blood:
13	chr5:96706066..96707837-chr5:96722435..96724433,2	K562	blood:
14	chr5:96865281..96867677-chr5:96867921..96869530,2	K562	blood:
15	chr5:96902855..96905560-chr5:96907320..96909656,2	K562	blood:
16	chr5:96656999..96658653-chr5:96658674..96662108,3	K562	blood:
17	chr5:96757244..96760010-chr5:96764877..96766486,2	MCF-7	breast:
18	chr17:41398860..41401971-chr5:96695801..96698802,6	K562	blood:
19	chr5:96735260..96736761-chr7:31786509..31788468,2	MCF-7	breast:
20	chr5:96632479..96633406-chr5:96869339..96870359,6	MCF-7	breast:
21	chr17:41380182..41383629-chr5:96695802..96698822,5	K562	blood:
22	chr5:96706066..96707837-chr5:96722435..96724433,2	K562	blood:
23	chr5:96632616..96633407-chr5:96869853..96870506,3	MCF-7	breast:
24	chr5:96898495..96900851-chr5:96905056..96906917,2	K562	blood:
25	chr5:96720114..96721922-chr5:96728191..96729748,2	MCF-7	breast:
26	chr5:96632479..96633406-chr5:96869339..96870359,6	MCF-7	breast:
27	chr17:41398605..41400432-chr5:96695803..96698802,4	MCF-7	breast:
28	chr5:96687334..96689961-chr5:96691050..96693898,2	MCF-7	breast:
29	chr5:97027188..97030158-chr5:97031253..97033564,2	K562	blood:
30	chr17:41463734..41465366-chr5:96695802..96697324,2	MCF-7	breast:
31	chr5:96656999..96658653-chr5:96658674..96662108,3	K562	blood:
32	chr17:41464548..41466257-chr5:96697324..96698824,2	MCF-7	breast:
33	chr5:96518180..96520707-chr5:96752048..96753718,2	K562	blood:
34	chr5:96865281..96867677-chr5:96867921..96869530,2	K562	blood:
35	chr3:73159507..73161444-chr5:96697302..96698824,2	K562	blood:
36	chr5:96757244..96760010-chr5:96764877..96766486,2	MCF-7	breast:
37	chr5:96869180..96869850-chr5:98103055..98104021,2	MCF-7	breast:
38	chr5:97027188..97030158-chr5:97031253..97033564,2	K562	blood:
39	chr5:96711348..96714233-chr5:96714673..96716999,2	MCF-7	breast:
40	chr5:96902855..96905560-chr5:96907320..96909656,2	K562	blood:
41	chr5:96697302..96697824-chr5:146587593..146588113,2	Hela-S3	cervix:
42	chr5:96566460..96567205-chr5:96869494..96870442,2	MCF-7	breast:
43	chr17:41462273..41467084-chr5:96695804..96698803,5	K562	blood:
44	chr5:96695823..96698804-chr6:142366314..142367822,2	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RIOK2-3	chr5:96785062-96785445	NONHSAT102929
2	lnc-CTD-2215E18.1.1-2	chr5:96856933-96856994	XLOC_004483
3	lnc-CTD-2215E18.1.1-1	chr5:96767448-96767604	ENSG00000251513.1
4	lnc-CTD-2215E18.1.1-2	chr5:97004255-97004366	XLOC_004483
5	lnc-CTD-2215E18.1.1-2	chr5:97004254-97004366	NONHSAT102931
6	lnc-CTD-2215E18.1.1-2	chr5:96840400-96840496	NR_105028
7	lnc-CTD-2215E18.1.1-2	chr5:96840400-96840496	XLOC_004483
8	lnc-CTD-2215E18.1.1-2	chr5:96856933-96856994	NR_105028
9	lnc-RIOK2-4	chr5:96786031-96786319	NONHSAT102930
10	lnc-CTD-2215E18.1.1-2	chr5:96840399-96840496	NONHSAT102931
11	lnc-CTD-2215E18.1.1-2	chr5:96856932-96856994	NONHSAT102931
12	lnc-CTD-2215E18.1.1-1	chr5:96772257-96772921	ENSG00000251513.1
13	lnc-CTD-2215E18.1.1-2	chr5:97006298-97006750	XLOC_004483
14	lnc-CTD-2215E18.1.1-5	chr5:96704480-96706125	NONHSAT102928
15	lnc-CTD-2215E18.1.1-2	chr5:97006298-97006755	NR_105028
16	lnc-CTD-2215E18.1.1-2	chr5:97004255-97004366	NR_105028
17	lnc-CTD-2215E18.1.1-2	chr5:97006297-97006750	NONHSAT102931

No data

Variant related genes	Relation type
ENSG00000251054	TF binding region
ENSG00000249977	TF binding region
ENSG00000249761	TF binding region
ENSG00000248931	TF binding region
ENSG00000250331	TF binding region
YTHDF1P1	TF binding region
ENSG00000251054	CpG island
ENSG00000249977	CpG island
ENSG00000249761	CpG island
ENSG00000248931	CpG island
ENSG00000250331	CpG island
YTHDF1P1	CpG island
ENSG00000223247	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000058729	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000251513	chromatin interactions

Extended variants
information (count: 9768 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:9768 , 50 per page) page: 1 2 3 4 5 6 7 ... 196

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552573485	chr5:96565154-96565155	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs570770285	chr5:96565187-96565188	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs79982524	chr5:96565189-96565190	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs374510576	chr5:96565207-96565208	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs17630655	chr5:96565280-96565281	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs539474200	chr5:96565288-96565289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs553103646	chr5:96565335-96565336	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs183457828	chr5:96565404-96565405	Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs151205501	chr5:96565445-96565446	Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs36112485	chr5:96565458-96565459	Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs575967841	chr5:96565477-96565478	Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs533663018	chr5:96565484-96565485	Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs140277696	chr5:96565486-96565487	Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs541604733	chr5:96565515-96565516	Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs544241097	chr5:96565516-96565517	Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs562629895	chr5:96565518-96565519	Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs150022587	chr5:96565558-96565559	Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs541999161	chr5:96565581-96565582	Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs188230489	chr5:96565683-96565684	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs114498233	chr5:96565707-96565708	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs552371735	chr5:96565738-96565739	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs112430354	chr5:96565794-96565795	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs564630094	chr5:96565801-96565802	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs531606693	chr5:96565837-96565838	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs550191169	chr5:96565916-96565917	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs568376925	chr5:96565933-96565934	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs555190226	chr5:96565990-96565991	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs529548761	chr5:96566034-96566035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs146574836	chr5:96566055-96566056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs34462198	chr5:96566123-96566124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs397772339	chr5:96566124-96566125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs565948935	chr5:96566138-96566139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375549958	chr5:96566204-96566205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs141228473	chr5:96566238-96566239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144939721	chr5:96566253-96566254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570566187	chr5:96566257-96566258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537402309	chr5:96566268-96566269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181064005	chr5:96566276-96566277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs574753864	chr5:96566366-96566367	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs542158665	chr5:96566378-96566379	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs554140272	chr5:96566439-96566440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572245911	chr5:96566443-96566444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546028281	chr5:96566467-96566468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564417266	chr5:96566478-96566479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532913543	chr5:96566480-96566481	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs35453421	chr5:96566488-96566489	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs368000528	chr5:96566493-96566494	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs531844382	chr5:96566515-96566516	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs71654361	chr5:96566516-96566517	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs7729001	chr5:96566588-96566589	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:86)

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
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
Merkel cell carcinoma	19020549	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
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	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
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19036926	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:999 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96554400-96565400	Weak transcription	Primary B cells from peripheral blood	blood
2	chr5:96562400-96565400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:96564800-96565200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr5:96565000-96565200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr5:96565000-96565600	Enhancers	Placenta Amnion	Placenta Amnion
6	chr5:96565000-96566000	Enhancers	NHDF-Ad	bronchial
7	chr5:96565200-96565400	Enhancers	HUVEC	blood vessel
8	chr5:96565200-96566000	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr5:96565200-96566200	Enhancers	Fetal Heart	heart
10	chr5:96565400-96565600	Enhancers	Primary B cells from peripheral blood	blood
11	chr5:96565400-96565800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr5:96565400-96565800	Flanking Active TSS	HUVEC	blood vessel
13	chr5:96565400-96566000	Enhancers	Fetal Lung	lung
14	chr5:96565400-96566000	Active TSS	Right Atrium	heart
15	chr5:96565600-96566000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr5:96565600-96571200	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr5:96565800-96566000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr5:96565800-96566000	Enhancers	HUVEC	blood vessel
19	chr5:96566000-96567000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr5:96566000-96567000	Weak transcription	NHDF-Ad	bronchial
21	chr5:96566600-96567200	Enhancers	Liver	Liver
22	chr5:96566800-96567200	Active TSS	Brain Angular Gyrus	brain
23	chr5:96566800-96567200	Enhancers	Colon Smooth Muscle	Colon
24	chr5:96566800-96567400	Enhancers	Dnd41	blood
25	chr5:96567000-96567200	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr5:96567000-96567200	Enhancers	Brain Anterior Caudate	brain
27	chr5:96567000-96567200	Enhancers	Brain Cingulate Gyrus	brain
28	chr5:96567000-96567200	Enhancers	NHDF-Ad	bronchial
29	chr5:96567000-96567400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr5:96567000-96567400	Enhancers	Brain Hippocampus Middle	brain
31	chr5:96567000-96567400	Enhancers	Brain Substantia Nigra	brain
32	chr5:96576600-96585200	Weak transcription	Dnd41	blood
33	chr5:96577000-96577600	Enhancers	Stomach Smooth Muscle	stomach
34	chr5:96577000-96578000	Enhancers	Brain Anterior Caudate	brain
35	chr5:96577200-96577400	Enhancers	Brain Angular Gyrus	brain
36	chr5:96577200-96577600	Enhancers	Brain Substantia Nigra	brain
37	chr5:96577200-96577800	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr5:96577200-96579400	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr5:96577200-96579400	Enhancers	Brain Hippocampus Middle	brain
40	chr5:96577400-96579000	Weak transcription	Brain Angular Gyrus	brain
41	chr5:96577600-96578000	Active TSS	Brain Substantia Nigra	brain
42	chr5:96577600-96579000	Weak transcription	Stomach Smooth Muscle	stomach
43	chr5:96577600-96579600	Enhancers	Rectal Smooth Muscle	rectum
44	chr5:96577800-96579000	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr5:96578000-96579000	Weak transcription	Brain Anterior Caudate	brain
46	chr5:96578000-96579400	Enhancers	Brain Substantia Nigra	brain
47	chr5:96578200-96578400	Enhancers	Fetal Muscle Leg	muscle
48	chr5:96578400-96579600	Weak transcription	Fetal Muscle Leg	muscle
49	chr5:96579000-96579200	Enhancers	Brain Anterior Caudate	brain
50	chr5:96579000-96579200	Enhancers	Brain Inferior Temporal Lobe	brain

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