Variant report

Variant	nsv428148
Chromosome Location	chr6:58137660-58406917
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1402)
CpG islands
(count:2198)
Chromatin interactive
region (count:3)
LncRNA
region (count:35)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1402 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:58287566-58287962	GM12878	blood:	n/a	n/a
2	ATF2	chr6:58226933-58227385	GM12878	blood:	n/a	n/a
3	ATF2	chr6:58312840-58313086	GM12878	blood:	n/a	n/a
4	ATF2	chr6:58225246-58225574	GM12878	blood:	n/a	n/a
5	ATF2	chr6:58226948-58227297	GM12878	blood:	n/a	n/a
6	ATF2	chr6:58287667-58287899	GM12878	blood:	n/a	n/a
7	ATF3	chr6:58142472-58142715	K562	blood:	n/a	n/a
8	ATF3	chr6:58149095-58149601	K562	blood:	n/a	n/a
9	ATF3	chr6:58142478-58142721	A549	lung:	n/a	n/a
10	ATF3	chr6:58141691-58142004	K562	blood:	n/a	n/a
11	BATF	chr6:58225176-58225639	GM12878	blood:	n/a	n/a
12	BATF	chr6:58205099-58205316	GM12878	blood:	n/a	n/a
13	BATF	chr6:58274807-58275130	GM12878	blood:	n/a	chr6:58274977-58274988
14	BATF	chr6:58226995-58227530	GM12878	blood:	n/a	n/a
15	BATF	chr6:58287533-58287892	GM12878	blood:	n/a	n/a
16	BATF	chr6:58159860-58160064	GM12878	blood:	n/a	n/a
17	BATF	chr6:58241206-58241440	GM12878	blood:	n/a	chr6:58241313-58241322 chr6:58241337-58241348
18	BATF	chr6:58312874-58313176	GM12878	blood:	n/a	chr6:58313100-58313108
19	BATF	chr6:58274740-58275182	GM12878	blood:	n/a	chr6:58274977-58274988
20	BATF	chr6:58241654-58241917	GM12878	blood:	n/a	chr6:58241758-58241769
21	BATF	chr6:58226989-58227547	GM12878	blood:	n/a	n/a
22	BATF	chr6:58312874-58313181	GM12878	blood:	n/a	chr6:58313100-58313108
23	BATF	chr6:58192220-58192422	GM12878	blood:	n/a	n/a
24	BATF	chr6:58225149-58225723	GM12878	blood:	n/a	n/a
25	BATF	chr6:58326544-58326859	GM12878	blood:	n/a	n/a
26	BATF	chr6:58241686-58241892	GM12878	blood:	n/a	chr6:58241758-58241769
27	BCL11A	chr6:58312858-58313167	GM12878	blood:	n/a	chr6:58313103-58313112
28	BCL11A	chr6:58205087-58205300	GM12878	blood:	n/a	n/a
29	BCL11A	chr6:58227066-58227268	GM12878	blood:	n/a	n/a
30	BCL11A	chr6:58287570-58287800	GM12878	blood:	n/a	n/a
31	BCL11A	chr6:58245996-58246178	GM12878	blood:	n/a	n/a
32	BCL11A	chr6:58287319-58287843	GM12878	blood:	n/a	n/a
33	BCL11A	chr6:58225136-58225637	GM12878	blood:	n/a	n/a
34	BCL11A	chr6:58226962-58227383	GM12878	blood:	n/a	n/a
35	BCL11A	chr6:58312939-58313153	GM12878	blood:	n/a	chr6:58313103-58313112
36	BCLAF1	chr6:58287548-58287910	GM12878	blood:	n/a	n/a
37	BCLAF1	chr6:58287452-58288025	GM12878	blood:	n/a	n/a
38	BCLAF1	chr6:58312816-58313161	GM12878	blood:	n/a	chr6:58313103-58313112
39	BHLHE40	chr6:58312965-58313069	GM12878	blood:	n/a	n/a
40	CBX3	chr6:58287498-58287998	K562	blood:	n/a	n/a
41	CBX3	chr6:58287493-58287955	K562	blood:	n/a	n/a
42	CCNT2	chr6:58287622-58287859	K562	blood:	n/a	n/a
43	CEBPB	chr6:58167746-58168156	K562	blood:	n/a	chr6:58168013-58168026 chr6:58168014-58168025
44	CEBPB	chr6:58287573-58287962	K562	blood:	n/a	n/a
45	CEBPB	chr6:58167907-58168057	K562	blood:	n/a	chr6:58168013-58168026 chr6:58168014-58168025
46	CEBPB	chr6:58146782-58147007	HepG2	liver:	n/a	n/a
47	CEBPB	chr6:58167855-58168177	HepG2	liver:	n/a	chr6:58168013-58168026 chr6:58168014-58168025
48	CEBPB	chr6:58385936-58386118	IMR90	lung:	n/a	n/a
49	CEBPB	chr6:58357831-58357857	HepG2	liver:	n/a	chr6:58357833-58357844 chr6:58357834-58357845
50	CEBPB	chr6:58287720-58287958	Hela-S3	cervix:	n/a	n/a

(count:2198 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:58263193-58263243	K562	blood:	n/a
2	chr6:58287430-58287480	IMR90	lung:	fetal
3	chr6:58263193-58263243	K562	blood:	n/a
4	chr6:58287430-58287480	IMR90	lung:	fetal
5	chr6:58148485-58148535	HEK293	kidney:	embryo
6	chr6:58148485-58148535	GM19239	blood:	n/a
7	chr6:58287825-58287875	HL-60	blood:	n/a
8	chr6:58399664-58399714	AG04449	skin:	fetal
9	chr6:58180750-58180800	HCT-116	colon:	n/a
10	chr6:58148898-58148948	NH-A	brain:	n/a
11	chr6:58399664-58399714	AG09309	skin:	n/a
12	chr6:58147897-58147947	A549	lung:	n/a
13	chr6:58148485-58148535	Jurkat	blood:	n/a
14	chr6:58180096-58180146	HPAEpiC	pulmonary alveolar:	n/a
15	chr6:58148898-58148948	MCF10A-Er-Src	breast:	n/a
16	chr6:58399664-58399714	Caco-2	colon:	n/a
17	chr6:58399664-58399714	PrEC	prostate:	n/a
18	chr6:58142044-58142094	U87	brain:	n/a
19	chr6:58263122-58263172	RPTEC	kidney:	n/a
20	chr6:58142044-58142094	PrEC	prostate:	n/a
21	chr6:58141890-58141940	BE2_C	brain:	n/a
22	chr6:58289131-58289181	HUVEC	blood vessel:	n/a
23	chr6:58180750-58180800	AG04449	skin:	fetal
24	chr6:58148485-58148535	HNPCEpiC	eye:	n/a
25	chr6:58286735-58286785	K562	blood:	n/a
26	chr6:58259157-58259207	HUVEC	blood vessel:	n/a
27	chr6:58287430-58287480	HCPEpiC	choroid plexus:	n/a
28	chr6:58263122-58263172	PFSK-1	brain:	n/a
29	chr6:58290947-58290997	ECC-1	luminal epithelium:	n/a
30	chr6:58289131-58289181	HPAEpiC	pulmonary alveolar:	n/a
31	chr6:58148898-58148948	GM19239	blood:	n/a
32	chr6:58399793-58399843	HCPEpiC	choroid plexus:	n/a
33	chr6:58147897-58147947	HepG2	liver:	n/a
34	chr6:58287430-58287480	T-47D	breast:	n/a
35	chr6:58147525-58147575	LNCaP	prostate:	n/a
36	chr6:58399793-58399843	A549	lung:	n/a
37	chr6:58147525-58147575	MCF10A-Er-Src	breast:	n/a
38	chr6:58287827-58287877	Hela-S3	cervix:	n/a
39	chr6:58263122-58263172	CMK	blood:	n/a
40	chr6:58147525-58147575	ECC-1	luminal epithelium:	n/a
41	chr6:58263193-58263243	NB4	blood:	n/a
42	chr6:58142044-58142094	GM19239	blood:	n/a
43	chr6:58286735-58286785	GM12878	blood:	n/a
44	chr6:58141890-58141940	HCPEpiC	choroid plexus:	n/a
45	chr6:58287822-58287872	NHBE	bronchial:	n/a
46	chr6:58285006-58285056	HL-60	blood:	n/a
47	chr6:58290947-58290997	Jurkat	blood:	n/a
48	chr6:58263193-58263243	T-47D	breast:	n/a
49	chr6:58148898-58148948	SK-N-MC	brain:	n/a
50	chr6:58287827-58287877	LNCaP	prostate:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:58293670..58295896-chr6:58296442..58298545,2	K562	blood:
2	chr6:58293670..58295896-chr6:58296442..58300027,3	K562	blood:
3	chr5:37379216..37379885-chr6:58287233..58287739,2	Hela-S3	cervix:

(count:35 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAB23-19	chr6:58397998-58399412	NONHSAT113321
2	lnc-RAB23-3	chr6:58272350-58273455	NONHSAT113310
3	lnc-BAG2-4	chr6:58186873-58187271	XLOC_005332
4	lnc-BAG2-6	chr6:58297873-58297934	ENSG00000225096
5	lnc-RAB23-17	chr6:58186881-58187205	NONHSAT113305
6	lnc-BAG2-12	chr6:58294832-58295048	l_3195_chr6:58290605-58295048_testes
7	lnc-RAB23-3	chr6:58234838-58240189	ENSG00000272316.1
8	lnc-RAB23-16	chr6:58182169-58182746	ENSG00000272541.1
9	lnc-RAB23-17	chr6:58192326-58192620	NONHSAT113305
10	lnc-BAG2-12	chr6:58290606-58290988	l_3195_chr6:58290605-58295048_testes
11	lnc-RAB23-3	chr6:58272350-58273455	NONHSAT113311
12	lnc-BAG2-6	chr6:58298372-58298496	ENSG00000225096
13	lnc-RAB23-3	chr6:58287599-58287654	NONHSAT113319
14	lnc-BAG2-5	chr6:58243460-58243544	ENSG00000236143.1
15	lnc-RAB23-3	chr6:58275196-58275417	NONHSAT113318
16	lnc-RAB23-3	chr6:58275636-58276125	NONHSAT113311
17	lnc-RAB23-3	chr6:58287430-58287502	NONHSAT113319
18	lnc-RAB23-3	chr6:58234692-58238642	XLOC_005753
19	lnc-RAB23-4	chr6:58272361-58273455	ENSG00000215190
20	lnc-RAB23-3	chr6:58285306-58285389	NONHSAT113317
21	lnc-RAB23-3	chr6:58287430-58287502	NONHSAT113317
22	lnc-RAB23-3	chr6:58272400-58273455	NONHSAT113318
23	lnc-RAB23-4	chr6:58275151-58276677	ENSG00000215190
24	lnc-RAB23-3	chr6:58287599-58287654	NONHSAT113317
25	lnc-BAG2-4	chr6:58182220-58183029	XLOC_005332
26	lnc-BAG2-6	chr6:58291908-58292021	ENSG00000225096
27	lnc-RAB23-3	chr6:58239194-58239687	XLOC_005753
28	lnc-RAB23-3	chr6:58275087-58275346	NONHSAT113319
29	lnc-RAB23-3	chr6:58275196-58275346	NONHSAT113311
30	lnc-RAB23-3	chr6:58285306-58285389	NONHSAT113319
31	lnc-BAG2-5	chr6:58243374-58243434	ENSG00000236143.1
32	lnc-RAB23-3	chr6:58275196-58275346	NONHSAT113310
33	lnc-RAB23-3	chr6:58276137-58276366	NONHSAT113310
34	lnc-RAB23-3	chr6:58272393-58273455	NONHSAT113317
35	lnc-RAB23-18	chr6:58228887-58229426	ENSG00000271761.1

No data

Variant related genes	Relation type
ENSG00000272316	TF binding region
ENSG00000272541	TF binding region
GUSBP4	TF binding region
LINC00680	TF binding region
POM121L14P	TF binding region
GAPDHP15	TF binding region
ENSG00000271761	TF binding region
ENSG00000216687	TF binding region
ENSG00000225096	TF binding region
ENSG00000272316	CpG island
ENSG00000272541	CpG island
GUSBP4	CpG island
LINC00680	CpG island
POM121L14P	CpG island
GAPDHP15	CpG island
ENSG00000271761	CpG island
ENSG00000216687	CpG island
ENSG00000225096	CpG island
ENSG00000082068	chromatin interactions
ENSG00000214563	chromatin interactions

Extended variants
information (count: 4281 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:4281 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575005295	chr6:58141208-58141209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs535692690	chr6:58141224-58141225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs557199258	chr6:58141245-58141246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183776776	chr6:58141273-58141274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs111445126	chr6:58141352-58141353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs545789051	chr6:58141357-58141358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs112304630	chr6:58141368-58141369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs112370365	chr6:58141372-58141373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564180201	chr6:58141378-58141379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs62412337	chr6:58141427-58141428	Bivalent/Poised TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs375446090	chr6:58141436-58141437	Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540747109	chr6:58141440-58141441	Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs368627485	chr6:58141449-58141450	Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs186965648	chr6:58141463-58141464	Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs367555793	chr6:58141485-58141486	Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370276998	chr6:58141516-58141517	Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs562062052	chr6:58141542-58141543	Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs529862280	chr6:58141553-58141554	Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541671098	chr6:58141569-58141570	Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563530158	chr6:58141573-58141574	Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs373644013	chr6:58141590-58141591	Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs552195297	chr6:58141662-58141663	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs548179871	chr6:58141670-58141671	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs528153281	chr6:58141744-58141745	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs546647530	chr6:58141762-58141763	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs568079323	chr6:58141766-58141767	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs535996737	chr6:58141767-58141768	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs202227447	chr6:58141768-58141769	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs143584179	chr6:58141774-58141775	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs539777049	chr6:58141819-58141820	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs557706314	chr6:58141820-58141821	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs573160441	chr6:58141848-58141849	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs114738914	chr6:58141854-58141855	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs115657434	chr6:58141869-58141870	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs13362721	chr6:58141876-58141877	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	mRNA abundance
36	rs371412677	chr6:58141878-58141879	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs555788154	chr6:58141879-58141880	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs13362752	chr6:58141886-58141887	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs542044279	chr6:58141890-58141891	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs563517594	chr6:58141891-58141892	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs570002623	chr6:58141895-58141896	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs538889782	chr6:58141904-58141905	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs546147590	chr6:58141905-58141906	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs200015566	chr6:58141913-58141914	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs78359853	chr6:58141920-58141921	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs112263870	chr6:58141939-58141940	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs62412338	chr6:58141946-58141947	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs117780823	chr6:58141952-58141953	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs568143105	chr6:58141957-58141958	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs192483975	chr6:58141960-58141961	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Neuroblastoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
Schizophrenia	20967226	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD

Chromatin state (count:1124 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:58141200-58141600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:58141400-58141800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
3	chr6:58141400-58143200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
4	chr6:58141400-58143400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
5	chr6:58141600-58141800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr6:58141600-58141800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr6:58141600-58141800	Bivalent Enhancer	Brain Germinal Matrix	brain
8	chr6:58141600-58141800	Bivalent Enhancer	Placenta	Placenta
9	chr6:58141600-58141800	Bivalent Enhancer	NHDF-Ad	bronchial
10	chr6:58141600-58142000	Bivalent Enhancer	HUVEC	blood vessel
11	chr6:58141600-58142000	Active TSS	K562	blood
12	chr6:58141600-58142200	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
13	chr6:58141600-58142200	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
14	chr6:58141600-58142200	Bivalent Enhancer	Fetal Muscle Leg	muscle
15	chr6:58141600-58142400	Active TSS	H1 Cell Line	embryonic stem cell
16	chr6:58141600-58143000	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr6:58141600-58143000	Active TSS	H9 Cell Line	embryonic stem cell
18	chr6:58141600-58143000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
19	chr6:58141600-58143000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
20	chr6:58141600-58143000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr6:58141600-58143200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
22	chr6:58141600-58143400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
23	chr6:58141800-58142000	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr6:58141800-58142000	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
25	chr6:58141800-58142000	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr6:58141800-58142000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr6:58141800-58142000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr6:58141800-58142000	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
29	chr6:58141800-58142000	Bivalent Enhancer	Fetal Stomach	stomach
30	chr6:58141800-58142000	Bivalent Enhancer	Fetal Thymus	thymus
31	chr6:58141800-58142000	Flanking Bivalent TSS/Enh	NHDF-Ad	bronchial
32	chr6:58141800-58142000	Bivalent Enhancer	NHEK	skin
33	chr6:58141800-58142200	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr6:58141800-58142200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
35	chr6:58141800-58142200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
36	chr6:58141800-58142200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
37	chr6:58141800-58142200	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr6:58141800-58142200	Bivalent Enhancer	Adipose Nuclei	Adipose
39	chr6:58141800-58142200	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
40	chr6:58141800-58142200	Bivalent Enhancer	Esophagus	oesophagus
41	chr6:58141800-58142200	ZNF genes & repeats	Right Atrium	heart
42	chr6:58141800-58142400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr6:58141800-58142600	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr6:58141800-58142600	Enhancers	Pancreas	Pancrea
45	chr6:58141800-58143000	Active TSS	iPS-15b Cell Line	embryonic stem cell
46	chr6:58142000-58142200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr6:58142000-58142200	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr6:58142000-58142200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr6:58142000-58142200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr6:58142000-58142200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin

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