Variant report

Variant	nsv429774
Chromosome Location	chr7:70294296-70357061
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:764)
CpG islands
(count:427)
Chromatin interactive
region (count:20)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:764 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:70295432-70295731	HepG2	liver:	n/a	n/a
2	ATF2	chr7:70321901-70322317	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr7:70294118-70294578	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:70322821-70323622	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr7:70314522-70315080	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr7:70314491-70315160	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr7:70355291-70355733	GM12878	blood:	n/a	n/a
8	BACH1	chr7:70323194-70323394	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:70294211-70294569	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr7:70294231-70294607	GM12878	blood:	n/a	n/a
11	BATF	chr7:70294291-70294547	GM12878	blood:	n/a	n/a
12	BHLHE40	chr7:70346608-70346813	K562	blood:	n/a	n/a
13	BHLHE40	chr7:70295491-70295711	HepG2	liver:	n/a	n/a
14	BHLHE40	chr7:70294189-70294529	K562	blood:	n/a	n/a
15	BHLHE40	chr7:70349178-70349357	K562	blood:	n/a	n/a
16	BHLHE40	chr7:70294194-70294616	GM12878	blood:	n/a	n/a
17	BRCA1	chr7:70294156-70294507	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr7:70299440-70299798	HepG2	liver:	n/a	chr7:70299603-70299614
19	CEBPB	chr7:70299453-70299778	A549	lung:	n/a	chr7:70299603-70299614
20	CEBPB	chr7:70295428-70295714	HepG2	liver:	n/a	chr7:70295552-70295563
21	CEBPB	chr7:70349310-70349766	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr7:70299455-70299763	K562	blood:	n/a	chr7:70299603-70299614
23	CEBPB	chr7:70311011-70311153	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr7:70294654-70294840	HepG2	liver:	n/a	n/a
25	CEBPB	chr7:70294172-70294801	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr7:70295315-70295710	HepG2	liver:	n/a	chr7:70295552-70295563
27	CEBPB	chr7:70299422-70299775	IMR90	lung:	n/a	chr7:70299603-70299614
28	CEBPB	chr7:70299414-70299733	MCF-7	breast:	n/a	chr7:70299603-70299614
29	CEBPB	chr7:70314283-70314959	H1-hESC	embryonic stem cell:	n/a	chr7:70314674-70314686
30	CEBPB	chr7:70295452-70295643	HepG2	liver:	n/a	chr7:70295552-70295563
31	CEBPB	chr7:70299521-70299730	H1-hESC	embryonic stem cell:	n/a	chr7:70299603-70299614
32	CEBPB	chr7:70347542-70347743	HepG2	liver:	n/a	chr7:70347648-70347659
33	CEBPD	chr7:70295350-70295592	HepG2	liver:	n/a	n/a
34	CHD2	chr7:70323263-70323459	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr7:70314201-70315062	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr7:70294218-70294410	HepG2	liver:	n/a	chr7:70294263-70294270
37	CHD2	chr7:70294198-70294398	K562	blood:	n/a	chr7:70294263-70294270
38	CHD2	chr7:70294154-70294772	H1-hESC	embryonic stem cell:	n/a	chr7:70294263-70294270
39	CTBP2	chr7:70349262-70350113	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr7:70322020-70322170	HEK293	kidney:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
41	CTCF	chr7:70321992-70322160	A549	lung:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
42	CTCF	chr7:70320900-70321050	WI-38	lung:	n/a	n/a
43	CTCF	chr7:70294700-70294850	GM12864	blood:	n/a	n/a
44	CTCF	chr7:70321660-70321810	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr7:70322440-70322590	GM12874	blood:	n/a	n/a
46	CTCF	chr7:70320540-70320690	MCF-7	breast:	n/a	n/a
47	CTCF	chr7:70294220-70294370	GM12874	blood:	n/a	chr7:70294310-70294326 chr7:70294311-70294332 chr7:70294309-70294327
48	CTCF	chr7:70321600-70321750	NB4	blood:	n/a	n/a
49	CTCF	chr7:70321923-70322300	K562	blood:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
50	CTCF	chr7:70294187-70294490	ECC-1	luminal epithelium:	n/a	chr7:70294310-70294326 chr7:70294311-70294332 chr7:70294309-70294327

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:70311321-70311371	GM12891	blood:	n/a
2	chr7:70311321-70311371	U87	brain:	n/a
3	chr7:70311532-70311582	HL-60	blood:	n/a
4	chr7:70294511-70294561	PANC-1	pancreas:	n/a
5	chr7:70294511-70294561	HEK293	kidney:	embryo
6	chr7:70294264-70294314	U87	brain:	n/a
7	chr7:70294264-70294314	GM12891	blood:	n/a
8	chr7:70311532-70311582	K562	blood:	n/a
9	chr7:70311532-70311582	HNPCEpiC	eye:	n/a
10	chr7:70311435-70311485	SK-N-SH	brain:	n/a
11	chr7:70311532-70311582	Jurkat	blood:	n/a
12	chr7:70322401-70322451	HRE	kidney:	n/a
13	chr7:70294511-70294561	HCT-116	colon:	n/a
14	chr7:70294264-70294314	GM12878	blood:	n/a
15	chr7:70322401-70322451	SK-N-MC	brain:	n/a
16	chr7:70294264-70294314	Caco-2	colon:	n/a
17	chr7:70294525-70294575	HMEC	breast:	n/a
18	chr7:70322401-70322451	Hela-S3	cervix:	n/a
19	chr7:70294525-70294575	BJ	skin:	n/a
20	chr7:70294264-70294314	GM06990	blood:	n/a
21	chr7:70322401-70322451	HNPCEpiC	eye:	n/a
22	chr7:70294525-70294575	GM12892	blood:	n/a
23	chr7:70311532-70311582	HRCEpiC	kidney:	n/a
24	chr7:70311321-70311371	Hepatocyte	liver:	n/a
25	chr7:70294264-70294314	SAEC	small airway:	n/a
26	chr7:70294264-70294314	T-47D	breast:	n/a
27	chr7:70311532-70311582	GM19239	blood:	n/a
28	chr7:70311532-70311582	RPTEC	kidney:	n/a
29	chr7:70311435-70311485	U87	brain:	n/a
30	chr7:70311532-70311582	Caco-2	colon:	n/a
31	chr7:70311532-70311582	AG09309	skin:	n/a
32	chr7:70294525-70294575	HCT-116	colon:	n/a
33	chr7:70311532-70311582	Hela-S3	cervix:	n/a
34	chr7:70294264-70294314	CMK	blood:	n/a
35	chr7:70294511-70294561	AoSMC	blood vessel:	n/a
36	chr7:70294511-70294561	ProgFib	skin:	n/a
37	chr7:70294525-70294575	HRE	kidney:	n/a
38	chr7:70294264-70294314	NB4	blood:	n/a
39	chr7:70311435-70311485	PFSK-1	brain:	n/a
40	chr7:70322401-70322451	HepG2	liver:	n/a
41	chr7:70311532-70311582	HCT-116	colon:	n/a
42	chr7:70294511-70294561	SK-N-SH	brain:	n/a
43	chr7:70294525-70294575	SKMC	muscle:	n/a
44	chr7:70294525-70294575	U87	brain:	n/a
45	chr7:70294264-70294314	AG09319	gingival:	n/a
46	chr7:70294525-70294575	Caco-2	colon:	n/a
47	chr7:70294264-70294314	PrEC	prostate:	n/a
48	chr7:70311435-70311485	SAEC	small airway:	n/a
49	chr7:70294511-70294561	HEEpiC	esophagus:	n/a
50	chr7:70311435-70311485	AG09309	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:70294183..70294797-chr7:71197949..71198693,3	MCF-7	breast:
2	chr7:70321684..70322394-chr7:70659915..70660431,2	MCF-7	breast:
3	chr7:70321617..70322562-chr7:70976561..70977221,2	MCF-7	breast:
4	chr7:70321665..70322892-chr7:71197945..71198934,7	MCF-7	breast:
5	chr7:70321651..70322570-chr7:71197952..71198877,7	K562	blood:
6	chr7:70321682..70322568-chr7:71200885..71201597,2	K562	blood:
7	chr7:70294046..70294810-chr7:70321629..70322145,2	MCF-7	breast:
8	chr7:70295507..70296249-chr7:71198004..71198896,2	MCF-7	breast:
9	chr7:70321514..70322440-chr7:71198003..71198947,6	MCF-7	breast:
10	chr7:70309809..70312680-chr7:70313436..70316301,3	K562	blood:
11	chr5:126205511..126206011-chr7:70301812..70302369,2	MCF-7	breast:
12	chr7:70293870..70294792-chr7:71200529..71201300,6	MCF-7	breast:
13	chr7:70294117..70295302-chr7:71197788..71199575,6	MCF-7	breast:
14	chr7:70294046..70294810-chr7:70321629..70322145,2	MCF-7	breast:
15	chr7:70316123..70316992-chr7:71197861..71198674,2	K562	blood:
16	chr7:70309809..70312680-chr7:70313436..70316301,3	K562	blood:
17	chr7:70319996..70320657-chr7:71198026..71198561,2	MCF-7	breast:
18	chr7:70320133..70320969-chr7:71200768..71201606,2	MCF-7	breast:
19	chr7:70293845..70294790-chr7:71197836..71198902,6	K562	blood:
20	chr7:70321614..70322798-chr7:71200589..71201582,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AUTS2-3	chr7:70302724-70302999	NONHSAT121342

No data

Variant related genes	Relation type
ENSG00000236978	TF binding region
ENSG00000236978	CpG island

Extended variants
information (count: 2374 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2374 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17142075	chr7:70294296-70294297	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs534953301	chr7:70294299-70294300	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs537128696	chr7:70294303-70294304	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs76278677	chr7:70294304-70294305	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs548104368	chr7:70294305-70294306	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs563735683	chr7:70294306-70294307	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs531058680	chr7:70294308-70294309	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs10245302	chr7:70294323-70294324	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs542119443	chr7:70294337-70294338	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs542795121	chr7:70294366-70294367	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs62459597	chr7:70294421-70294422	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs534720108	chr7:70294491-70294492	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs547227384	chr7:70294567-70294568	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs568682892	chr7:70294580-70294581	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs113940316	chr7:70294602-70294603	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs531688806	chr7:70294608-70294609	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs372412617	chr7:70294609-70294610	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs548699648	chr7:70294701-70294702	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs545002416	chr7:70294717-70294718	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs566912552	chr7:70294718-70294719	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs565089775	chr7:70294788-70294789	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs557166972	chr7:70294820-70294821	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575710094	chr7:70294831-70294832	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184828484	chr7:70294834-70294835	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs527793754	chr7:70294848-70294849	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571954641	chr7:70294940-70294941	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558119944	chr7:70294947-70294948	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189440870	chr7:70295000-70295001	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs145019716	chr7:70295001-70295002	Enhancers Bivalent Enhancer Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs9691642	chr7:70295022-70295023	Enhancers Bivalent Enhancer Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs559567935	chr7:70295078-70295079	Enhancers Bivalent Enhancer Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs574657398	chr7:70295085-70295086	Enhancers Bivalent Enhancer Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs542027821	chr7:70295100-70295101	Enhancers Bivalent Enhancer Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs563498284	chr7:70295139-70295140	Enhancers Bivalent Enhancer Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs182074913	chr7:70295212-70295213	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566745914	chr7:70295235-70295236	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146783640	chr7:70295250-70295251	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115467202	chr7:70295294-70295295	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529144393	chr7:70295325-70295326	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536236602	chr7:70295334-70295335	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549199186	chr7:70295345-70295346	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546695626	chr7:70295358-70295359	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs111772949	chr7:70295383-70295384	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535801649	chr7:70295407-70295408	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs1106222	chr7:70295438-70295439	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs569149030	chr7:70295460-70295461	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs539653438	chr7:70295483-70295484	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs558182921	chr7:70295516-70295517	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs537900563	chr7:70295534-70295535	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs372921751	chr7:70295591-70295592	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	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
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16461572	CNVD
Acute monocytic leukemia	16498392	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18765545	CNVD
Chordoma	18071362	CNVD
Williams Syndrome	20824207	CNVD
Dyslexia	22102821	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70291600-70294400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:70294000-70294400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
3	chr7:70294000-70294400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr7:70294000-70294400	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr7:70294000-70294400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
6	chr7:70294000-70294400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
7	chr7:70294000-70294400	Enhancers	Brain Angular Gyrus	brain
8	chr7:70294000-70294400	Active TSS	Brain Anterior Caudate	brain
9	chr7:70294000-70294400	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
10	chr7:70294000-70294400	Enhancers	Fetal Brain Male	brain
11	chr7:70294000-70294400	Enhancers	Fetal Muscle Trunk	muscle
12	chr7:70294000-70294400	Bivalent Enhancer	Fetal Muscle Leg	muscle
13	chr7:70294000-70294400	Bivalent Enhancer	Fetal Stomach	stomach
14	chr7:70294000-70294400	Enhancers	GM12878-XiMat	blood
15	chr7:70294000-70294400	Enhancers	HSMM	muscle
16	chr7:70294000-70294600	Enhancers	HMEC	breast
17	chr7:70294000-70294800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr7:70294000-70295200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
19	chr7:70294000-70296400	Enhancers	Liver	Liver
20	chr7:70294200-70294400	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr7:70294200-70294400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr7:70294200-70294400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr7:70294200-70294400	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr7:70294200-70294400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr7:70294200-70294400	Enhancers	Primary hematopoietic stem cells	blood
26	chr7:70294200-70294400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr7:70294200-70294400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr7:70294200-70294400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr7:70294200-70294400	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr7:70294200-70294400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr7:70294200-70294400	Active TSS	Brain Hippocampus Middle	brain
32	chr7:70294200-70294400	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr7:70294200-70294400	Enhancers	Brain Substantia Nigra	brain
34	chr7:70294200-70294400	Enhancers	Fetal Brain Female	brain
35	chr7:70294200-70294400	Enhancers	Ovary	ovary
36	chr7:70294200-70294400	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
37	chr7:70294200-70294400	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
38	chr7:70294200-70294400	Flanking Active TSS	Dnd41	blood
39	chr7:70294200-70294400	Enhancers	NH-A	brain
40	chr7:70294200-70294600	Flanking Active TSS	Primary T cells from cord blood	blood
41	chr7:70294200-70294600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
42	chr7:70294200-70294600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr7:70294200-70295000	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr7:70294200-70295000	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr7:70294200-70295000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr7:70294400-70294600	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr7:70294400-70294600	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr7:70294400-70294600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
49	chr7:70294400-70294600	Bivalent/Poised TSS	Primary B cells from cord blood	blood
50	chr7:70294400-70294600	Flanking Active TSS	Primary B cells from peripheral blood	blood

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