Variant report

Variant	esv2758105
Chromosome Location	chr7:16272822-16527390
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2458)
CpG islands
(count:2626)
Chromatin interactive
region (count:244)
LncRNA
region (count:34)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2458 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:16299083-16299409	K562	blood:	n/a	n/a
2	ARID3A	chr7:16471884-16472097	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:16461163-16461514	K562	blood:	n/a	n/a
4	ARID3A	chr7:16461914-16463016	K562	blood:	n/a	chr7:16462172-16462188
5	ARID3A	chr7:16395882-16396058	K562	blood:	n/a	n/a
6	ARID3A	chr7:16524530-16524826	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:16511670-16511947	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:16308350-16309290	K562	blood:	n/a	n/a
9	ARID3A	chr7:16299684-16300431	K562	blood:	n/a	n/a
10	ARID3A	chr7:16358762-16358838	K562	blood:	n/a	n/a
11	ARID3A	chr7:16514797-16514866	K562	blood:	n/a	n/a
12	ARID3A	chr7:16300636-16301991	K562	blood:	n/a	n/a
13	ARID3A	chr7:16459362-16459750	K562	blood:	n/a	n/a
14	ARID3A	chr7:16457669-16457783	K562	blood:	n/a	n/a
15	ARID3A	chr7:16460094-16460425	K562	blood:	n/a	n/a
16	ARID3A	chr7:16473205-16473834	K562	blood:	n/a	n/a
17	ARID3A	chr7:16316566-16316667	K562	blood:	n/a	n/a
18	ARID3A	chr7:16505139-16505775	K562	blood:	n/a	n/a
19	ARID3A	chr7:16315775-16315950	K562	blood:	n/a	n/a
20	ARID3A	chr7:16302411-16302607	K562	blood:	n/a	n/a
21	ARID3A	chr7:16307063-16308041	K562	blood:	n/a	n/a
22	ARID3A	chr7:16304739-16305925	K562	blood:	n/a	n/a
23	ARID3A	chr7:16495363-16495428	K562	blood:	n/a	n/a
24	ARID3A	chr7:16439551-16439741	HepG2	liver:	n/a	n/a
25	ARID3A	chr7:16503037-16504167	K562	blood:	n/a	n/a
26	ARID3A	chr7:16456572-16456868	K562	blood:	n/a	n/a
27	ARID3A	chr7:16460669-16460758	K562	blood:	n/a	n/a
28	ARID3A	chr7:16471381-16472335	K562	blood:	n/a	n/a
29	ATF1	chr7:16524430-16524691	K562	blood:	n/a	n/a
30	ATF1	chr7:16304760-16305221	K562	blood:	n/a	n/a
31	ATF1	chr7:16301437-16301703	K562	blood:	n/a	n/a
32	ATF1	chr7:16429321-16429351	K562	blood:	n/a	n/a
33	ATF1	chr7:16468387-16468718	K562	blood:	n/a	n/a
34	ATF1	chr7:16505212-16505815	K562	blood:	n/a	n/a
35	ATF1	chr7:16456591-16456804	K562	blood:	n/a	n/a
36	ATF1	chr7:16308377-16309311	K562	blood:	n/a	n/a
37	ATF1	chr7:16300049-16300351	K562	blood:	n/a	n/a
38	ATF1	chr7:16471797-16472094	K562	blood:	n/a	n/a
39	ATF1	chr7:16462512-16463042	K562	blood:	n/a	n/a
40	ATF1	chr7:16387453-16387736	K562	blood:	n/a	n/a
41	ATF1	chr7:16385921-16386215	K562	blood:	n/a	n/a
42	ATF1	chr7:16451661-16451777	K562	blood:	n/a	n/a
43	ATF1	chr7:16416812-16417091	K562	blood:	n/a	n/a
44	ATF3	chr7:16308269-16309108	K562	blood:	n/a	n/a
45	BACH1	chr7:16316614-16316635	K562	blood:	n/a	n/a
46	BACH1	chr7:16441300-16441318	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr7:16328920-16329240	K562	blood:	n/a	n/a
48	BACH1	chr7:16458567-16458702	K562	blood:	n/a	n/a
49	BACH1	chr7:16471974-16472143	H1-hESC	embryonic stem cell:	n/a	n/a
50	BATF	chr7:16390376-16390578	GM12878	blood:	n/a	chr7:16390477-16390488

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:16437376-16437426	BE2_C	brain:	n/a
2	chr7:16524513-16524563	IMR90	lung:	fetal
3	chr7:16502585-16502635	NT2-D1	testis:	n/a
4	chr7:16437376-16437426	BE2_C	brain:	n/a
5	chr7:16524513-16524563	IMR90	lung:	fetal
6	chr7:16502585-16502635	NT2-D1	testis:	n/a
7	chr7:16501619-16501669	AG04450	lung:	fetal
8	chr7:16438128-16438178	PrEC	prostate:	n/a
9	chr7:16438022-16438072	BJ	skin:	n/a
10	chr7:16460435-16460485	AG04450	lung:	fetal
11	chr7:16511803-16511853	U87	brain:	n/a
12	chr7:16505592-16505642	Hepatocyte	liver:	n/a
13	chr7:16464635-16464685	NH-A	brain:	n/a
14	chr7:16436951-16437001	HL-60	blood:	n/a
15	chr7:16460965-16461015	IMR90	lung:	fetal
16	chr7:16505409-16505459	HUVEC	blood vessel:	n/a
17	chr7:16438316-16438366	SK-N-SH_RA	brain:	n/a
18	chr7:16438316-16438366	BJ	skin:	n/a
19	chr7:16524513-16524563	HPAEpiC	pulmonary alveolar:	n/a
20	chr7:16464635-16464685	MCF10A-Er-Src	breast:	n/a
21	chr7:16439993-16440043	HCT-116	colon:	n/a
22	chr7:16461062-16461112	HEEpiC	esophagus:	n/a
23	chr7:16505664-16505714	H1-hESC	embryonic stem cell:	embryo
24	chr7:16505592-16505642	T-47D	breast:	n/a
25	chr7:16438465-16438515	HepG2	liver:	n/a
26	chr7:16459464-16459514	GM19239	blood:	n/a
27	chr7:16438022-16438072	HNPCEpiC	eye:	n/a
28	chr7:16438022-16438072	AoSMC	blood vessel:	n/a
29	chr7:16438128-16438178	HCT-116	colon:	n/a
30	chr7:16462463-16462513	Hela-S3	cervix:	n/a
31	chr7:16505409-16505459	HCM	heart:	n/a
32	chr7:16505409-16505459	HAEpiC	amniotic membrane:	n/a
33	chr7:16460435-16460485	ovcar-3	ovarian:	n/a
34	chr7:16461244-16461294	MCF10A-Er-Src	breast:	n/a
35	chr7:16461077-16461127	U87	brain:	n/a
36	chr7:16438394-16438444	RPTEC	kidney:	n/a
37	chr7:16437298-16437348	H1-hESC	embryonic stem cell:	embryo
38	chr7:16505592-16505642	GM12892	blood:	n/a
39	chr7:16505409-16505459	NHBE	bronchial:	n/a
40	chr7:16436998-16437048	GM12892	blood:	n/a
41	chr7:16506262-16506312	AoSMC	blood vessel:	n/a
42	chr7:16436951-16437001	AG04450	lung:	fetal
43	chr7:16438022-16438072	ECC-1	luminal epithelium:	n/a
44	chr7:16502585-16502635	SKMC	muscle:	n/a
45	chr7:16438394-16438444	A549	lung:	n/a
46	chr7:16505409-16505459	AoSMC	blood vessel:	n/a
47	chr7:16437447-16437497	NHDF-neo	bronchial:	n/a
48	chr7:16439165-16439215	Hela-S3	cervix:	n/a
49	chr7:16461244-16461294	H1-hESC	embryonic stem cell:	embryo
50	chr7:16506521-16506571	AG10803	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:16319990..16321943-chr7:16331962..16333549,2	K562	blood:
2	chr7:16471379..16473974-chr7:16493852..16495378,2	K562	blood:
3	chr7:16322591..16325161-chr7:16326295..16328787,3	K562	blood:
4	chr7:16423814..16426314-chr7:16443888..16446431,2	K562	blood:
5	chr7:16475707..16477810-chr7:16493923..16496726,2	K562	blood:
6	chr7:16431599..16434211-chr7:16436454..16438200,2	K562	blood:
7	chr7:12753228..12755385-chr7:16301600..16303385,2	K562	blood:
8	chr7:16301478..16303849-chr7:16518183..16519712,2	K562	blood:
9	chr7:16285409..16288180-chr7:16295653..16298089,2	K562	blood:
10	chr7:16374992..16378303-chr7:16378786..16381334,3	K562	blood:
11	chr7:16473934..16476388-chr7:16667166..16670049,2	K562	blood:
12	chr7:16437189..16440785-chr7:16463112..16464821,3	MCF-7	breast:
13	chr7:16444286..16446056-chr7:16454023..16455999,2	K562	blood:
14	chr7:16274806..16276431-chr7:16298235..16300903,2	K562	blood:
15	chr7:16451377..16453700-chr7:16455359..16457041,2	MCF-7	breast:
16	chr7:16332474..16335082-chr7:16341108..16343730,3	K562	blood:
17	chr7:16317326..16322342-chr7:16324212..16328939,6	K562	blood:
18	chr7:16358608..16360256-chr7:16374793..16376621,2	K562	blood:
19	chr7:16478161..16480424-chr7:16488951..16492232,3	K562	blood:
20	chr7:16375946..16378002-chr7:16389862..16391543,2	MCF-7	breast:
21	chr7:16338494..16340742-chr7:16343830..16346096,2	K562	blood:
22	chr7:16467203..16469517-chr7:16495684..16498438,2	K562	blood:
23	chr7:16438588..16440667-chr7:16440672..16442750,2	K562	blood:
24	chr7:16431022..16434211-chr7:16436122..16439402,3	K562	blood:
25	chr7:16429864..16431992-chr7:16432066..16434396,2	K562	blood:
26	chr7:16444286..16446056-chr7:16454023..16455999,2	K562	blood:
27	chr7:16307417..16309237-chr7:16685352..16687215,2	K562	blood:
28	chr7:16335409..16337001-chr7:16354047..16355950,2	K562	blood:
29	chr7:16343653..16345575-chr7:16349935..16352190,3	K562	blood:
30	chr7:16467203..16469517-chr7:16495684..16498438,2	K562	blood:
31	chr7:16473484..16474112-chr7:16604373..16605315,2	MCF-7	breast:
32	chr7:16404670..16406505-chr7:16408648..16410407,2	MCF-7	breast:
33	chr7:16343653..16345575-chr7:16349935..16352190,3	K562	blood:
34	chr7:16277063..16278675-chr7:16280781..16282945,2	K562	blood:
35	chr7:16165242..16168046-chr7:16300329..16302056,2	K562	blood:
36	chr7:16338494..16340742-chr7:16343830..16346096,2	K562	blood:
37	chr7:16471379..16473974-chr7:16493852..16495378,2	K562	blood:
38	chr7:16355252..16356944-chr7:16359954..16363461,3	K562	blood:
39	chr7:16441360..16443090-chr7:16448119..16450606,2	K562	blood:
40	chr7:16329621..16333476-chr7:16335490..16337666,4	K562	blood:
41	chr7:16277063..16278861-chr7:16280781..16282424,2	K562	blood:
42	chr7:16272248..16275452-chr7:16305157..16308165,4	K562	blood:
43	chr7:16349823..16352454-chr7:16353444..16355930,3	K562	blood:
44	chr7:16424852..16427430-chr7:16453245..16455678,2	K562	blood:
45	chr7:16451524..16456332-chr7:16459501..16462581,7	MCF-7	breast:
46	chr7:16482403..16486501-chr7:16489191..16492629,4	K562	blood:
47	chr7:16277063..16278861-chr7:16280781..16282424,2	K562	blood:
48	chr7:16382268..16383861-chr7:16437645..16440357,2	K562	blood:
49	chr7:16329621..16333476-chr7:16335490..16337666,4	K562	blood:
50	chr7:16301506..16303412-chr7:20253971..20256529,2	K562	blood:

(count:34 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC006035.2-1	chr7:16310630-16310643	NONHSAT119294
2	lnc-AC006035.2-1	chr7:16308874-16309215	ENSG00000241044
3	lnc-AC006035.2-1	chr7:16305852-16305936	NONHSAT119296
4	lnc-AC006035.2-1	chr7:16305852-16305936	NONHSAT119292
5	lnc-AC006035.2-1	chr7:16305852-16305936	ENSG00000229688
6	lnc-AC006035.2-1	chr7:16276934-16277038	ENSG00000229688
7	lnc-AC006035.2-1	chr7:16308482-16310229	NONHSAT119292
8	lnc-AC006035.2-1	chr7:16276934-16277038	NONHSAT119294
9	lnc-AC006035.2-1	chr7:16287510-16287714	ENSG00000229688.3
10	lnc-AC006035.2-1	chr7:16305852-16305936	NONHSAT119295
11	lnc-AC006035.2-1	chr7:16276934-16277035	NONHSAT119295
12	lnc-AC006035.2-1	chr7:16301524-16301721	NONHSAT119293
13	lnc-AC006035.2-1	chr7:16308482-16309502	NONHSAT119295
14	lnc-AC006035.2-1	chr7:16276934-16277031	ENSG00000229688.3
15	lnc-AC006035.2-1	chr7:16288360-16288362	NONHSAT119294
16	lnc-AC006035.2-1	chr7:16308482-16310229	NONHSAT119294
17	lnc-AC006035.2-1	chr7:16301527-16301721	NONHSAT119294
18	lnc-AC006035.2-1	chr7:16276934-16277035	ENSG00000229688.3
19	lnc-AC006035.2-1	chr7:16308482-16310229	ENSG00000229688
20	lnc-AC006035.2-1	chr7:16276934-16277038	NONHSAT119293
21	lnc-AC006035.2-1	chr7:16275527-16275604	NONHSAT119292
22	lnc-AC006035.2-1	chr7:16276934-16276977	NONHSAT119292
23	lnc-AC006035.2-1	chr7:16308482-16309502	NONHSAT119296
24	lnc-AC006035.2-1	chr7:16275007-16276752	ucscGeneNc_uc003stf_2
25	lnc-AC006035.2-1	chr7:16275527-16275604	ENSG00000229688
26	lnc-AC006035.2-1	chr7:16308482-16310229	NONHSAT119293
27	lnc-AC006035.2-1	chr7:16301524-16301721	ENSG00000229688
28	lnc-AC006035.2-1	chr7:16305852-16305936	NONHSAT119294
29	lnc-AC006035.2-1	chr7:16305852-16305936	ENSG00000229688
30	lnc-AC006035.2-1	chr7:16275527-16275604	NONHSAT119295
31	lnc-AC006035.2-1	chr7:16310142-16310229	ENSG00000241044
32	lnc-AC006035.2-1	chr7:16308482-16308872	ENSG00000229688
33	lnc-AC006035.2-1	chr7:16305852-16305936	NONHSAT119293
34	lnc-AC006035.2-1	chr7:16276934-16276977	ENSG00000229688

No data

Variant related genes	Relation type
ENSG00000272537	TF binding region
ISPD-AS1	TF binding region
ISPD	TF binding region
SOSTDC1	TF binding region
ENSG00000272537	CpG island
ISPD-AS1	CpG island
ISPD	CpG island
SOSTDC1	CpG island
ENSG00000106537	chromatin interactions
ENSG00000272537	chromatin interactions
ENSG00000229688	chromatin interactions
ENSG00000236778	chromatin interactions
ENSG00000136261	chromatin interactions
ENSG00000214960	chromatin interactions
ENSG00000106524	chromatin interactions
ENSG00000102786	chromatin interactions
ENSG00000171243	chromatin interactions
ENSG00000127870	chromatin interactions
GLTP	miRNA target sites
HAS3	miRNA target sites
LMLN	miRNA target sites
DIS3L	miRNA target sites
RSRC2	miRNA target sites
SEC63	miRNA target sites
TTC8	miRNA target sites
CDKN1B	miRNA target sites

Extended variants
information (count: 10687 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:10687 , 50 per page) page: 1 2 3 4 5 6 7 ... 214

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541697623	chr7:16272837-16272838	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs1295175	chr7:16272850-16272851	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs559419181	chr7:16272866-16272867	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs535735886	chr7:16272878-16272879	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs1295174	chr7:16272913-16272914	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs541699541	chr7:16272925-16272926	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs565865328	chr7:16272935-16272936	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs530980824	chr7:16272948-16272949	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs552727615	chr7:16272963-16272964	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs11978407	chr7:16272972-16272973	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs528523304	chr7:16273021-16273022	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs547267627	chr7:16273049-16273050	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs536492655	chr7:16273051-16273052	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs536153127	chr7:16273090-16273091	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs555085688	chr7:16273124-16273125	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs371522730	chr7:16273164-16273165	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs185483820	chr7:16273220-16273221	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs190788104	chr7:16273233-16273234	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs141160480	chr7:16273287-16273288	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs180819784	chr7:16273297-16273298	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs374424283	chr7:16273337-16273338	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs143433954	chr7:16273341-16273342	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs147973519	chr7:16273342-16273343	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs184884615	chr7:16273380-16273381	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs188186637	chr7:16273464-16273465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181069309	chr7:16273556-16273557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186649794	chr7:16273609-16273610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564616322	chr7:16273617-16273618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191493164	chr7:16273640-16273641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs546636449	chr7:16273663-16273664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs562115143	chr7:16273667-16273668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547184423	chr7:16273676-16273677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183822449	chr7:16273691-16273692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564161024	chr7:16273721-16273722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569091720	chr7:16273742-16273743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs539212288	chr7:16273765-16273766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539675307	chr7:16273797-16273798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551855837	chr7:16273804-16273805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558247327	chr7:16273829-16273830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532877746	chr7:16273853-16273854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187173346	chr7:16273865-16273866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs73291476	chr7:16273874-16273875	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs534726804	chr7:16273916-16273917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552649484	chr7:16273931-16273932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs574395351	chr7:16273935-16273936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150102874	chr7:16273961-16273962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557320500	chr7:16273963-16273964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192102894	chr7:16273996-16273997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574036739	chr7:16274064-16274065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576639972	chr7:16274071-16274072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	19805367	CNVD
Autism	20808228	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1870 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16250200-16275800	Weak transcription	Pancreas	Pancrea
2	chr7:16270800-16273400	ZNF genes & repeats	K562	blood
3	chr7:16271200-16273200	Weak transcription	Fetal Lung	lung
4	chr7:16272200-16276600	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr7:16272200-16276800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr7:16272800-16273000	Enhancers	Primary T cells from cord blood	blood
7	chr7:16273000-16274200	Weak transcription	Primary T cells from cord blood	blood
8	chr7:16273200-16273400	Enhancers	Fetal Lung	lung
9	chr7:16273400-16274200	Weak transcription	Fetal Lung	lung
10	chr7:16273400-16274200	Weak transcription	K562	blood
11	chr7:16274200-16274800	Enhancers	Primary T cells from cord blood	blood
12	chr7:16274200-16274800	Enhancers	NHEK	skin
13	chr7:16274200-16275000	Enhancers	Fetal Lung	lung
14	chr7:16274200-16275600	Enhancers	Fetal Heart	heart
15	chr7:16274200-16275600	Enhancers	K562	blood
16	chr7:16274400-16275200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr7:16275000-16304400	Weak transcription	Fetal Lung	lung
18	chr7:16275200-16275800	Enhancers	Fetal Brain Female	brain
19	chr7:16276400-16276800	Enhancers	Fetal Brain Male	brain
20	chr7:16276800-16277200	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr7:16277200-16278400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr7:16278600-16278800	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr7:16280200-16289400	Weak transcription	Left Ventricle	heart
24	chr7:16284800-16287600	Weak transcription	Ovary	ovary
25	chr7:16286200-16287600	Enhancers	Brain Substantia Nigra	brain
26	chr7:16286400-16288600	Weak transcription	Fetal Stomach	stomach
27	chr7:16286600-16287000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr7:16286600-16287200	Enhancers	Brain Cingulate Gyrus	brain
29	chr7:16286800-16287400	Enhancers	Brain Hippocampus Middle	brain
30	chr7:16286800-16295800	Weak transcription	Stomach Smooth Muscle	stomach
31	chr7:16287600-16287800	ZNF genes & repeats	Ovary	ovary
32	chr7:16287800-16288000	Weak transcription	Ovary	ovary
33	chr7:16287800-16289200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr7:16288000-16291800	Weak transcription	Gastric	stomach
35	chr7:16288600-16289200	ZNF genes & repeats	Fetal Stomach	stomach
36	chr7:16289200-16296600	Weak transcription	Fetal Stomach	stomach
37	chr7:16291200-16293800	Weak transcription	Fetal Kidney	kidney
38	chr7:16295600-16296600	Weak transcription	K562	blood
39	chr7:16295800-16296000	ZNF genes & repeats	Stomach Smooth Muscle	stomach
40	chr7:16296200-16299600	Weak transcription	Fetal Heart	heart
41	chr7:16296600-16296800	Enhancers	Fetal Stomach	stomach
42	chr7:16296600-16297000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr7:16296600-16298000	Genic enhancers	K562	blood
44	chr7:16296800-16297400	Weak transcription	Fetal Stomach	stomach
45	chr7:16297000-16299000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr7:16297400-16297600	Enhancers	Fetal Stomach	stomach
47	chr7:16297600-16297800	Weak transcription	Fetal Stomach	stomach
48	chr7:16298000-16298600	Weak transcription	K562	blood
49	chr7:16298600-16300000	Enhancers	K562	blood
50	chr7:16299600-16300200	Enhancers	Fetal Heart	heart

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