Variant report

Variant	nsv888827
Chromosome Location	chr7:101562674-101650302
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1748)
CpG islands
(count:2263)
Chromatin interactive
region (count:269)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1748 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:101565404-101565727	K562	blood:	n/a	n/a
2	ARID3A	chr7:101618979-101619111	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:101612988-101613093	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:101567667-101567677	K562	blood:	n/a	n/a
5	ARID3A	chr7:101590884-101591548	K562	blood:	n/a	n/a
6	ATF1	chr7:101591203-101591468	K562	blood:	n/a	n/a
7	ATF1	chr7:101565449-101565741	K562	blood:	n/a	n/a
8	ATF2	chr7:101601014-101601433	GM12878	blood:	n/a	n/a
9	ATF2	chr7:101624772-101625788	GM12878	blood:	n/a	n/a
10	ATF2	chr7:101633969-101634812	GM12878	blood:	n/a	n/a
11	ATF2	chr7:101596654-101597159	GM12878	blood:	n/a	n/a
12	ATF2	chr7:101628184-101628802	GM12878	blood:	n/a	n/a
13	ATF2	chr7:101633931-101634825	GM12878	blood:	n/a	n/a
14	ATF2	chr7:101628267-101628688	GM12878	blood:	n/a	n/a
15	ATF2	chr7:101576738-101577444	GM12878	blood:	n/a	n/a
16	ATF2	chr7:101624950-101625759	GM12878	blood:	n/a	n/a
17	ATF2	chr7:101579824-101580758	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr7:101632792-101633565	GM12878	blood:	n/a	n/a
19	ATF2	chr7:101596616-101597200	GM12878	blood:	n/a	n/a
20	ATF2	chr7:101576670-101577467	GM12878	blood:	n/a	n/a
21	ATF3	chr7:101585247-101585714	A549	lung:	n/a	n/a
22	ATF3	chr7:101639638-101639846	K562	blood:	n/a	n/a
23	BACH1	chr7:101584104-101584460	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr7:101585074-101585404	K562	blood:	n/a	n/a
25	BACH1	chr7:101580108-101580464	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr7:101630664-101630794	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr7:101591200-101591541	H1-hESC	embryonic stem cell:	n/a	n/a
28	BATF	chr7:101625154-101625513	GM12878	blood:	n/a	chr7:101625422-101625432
29	BATF	chr7:101634223-101634678	GM12878	blood:	n/a	n/a
30	BATF	chr7:101601103-101601344	GM12878	blood:	n/a	n/a
31	BATF	chr7:101596639-101597052	GM12878	blood:	n/a	n/a
32	BATF	chr7:101596644-101597050	GM12878	blood:	n/a	n/a
33	BATF	chr7:101576845-101577190	GM12878	blood:	n/a	n/a
34	BATF	chr7:101634322-101634547	GM12878	blood:	n/a	n/a
35	BATF	chr7:101628342-101628615	GM12878	blood:	n/a	n/a
36	BATF	chr7:101576807-101577149	GM12878	blood:	n/a	n/a
37	BATF	chr7:101628334-101628672	GM12878	blood:	n/a	n/a
38	BATF	chr7:101626666-101626987	GM12878	blood:	n/a	n/a
39	BATF	chr7:101625043-101625639	GM12878	blood:	n/a	chr7:101625422-101625432
40	BATF	chr7:101597858-101598102	GM12878	blood:	n/a	n/a
41	BCL11A	chr7:101633053-101633481	GM12878	blood:	n/a	n/a
42	BCL11A	chr7:101625024-101625540	GM12878	blood:	n/a	chr7:101625475-101625484
43	BCL11A	chr7:101601087-101601290	GM12878	blood:	n/a	n/a
44	BCL11A	chr7:101628387-101628604	GM12878	blood:	n/a	n/a
45	BCL11A	chr7:101576828-101577255	GM12878	blood:	n/a	n/a
46	BCL11A	chr7:101634158-101634684	GM12878	blood:	n/a	chr7:101634448-101634457
47	BCL11A	chr7:101634172-101634647	GM12878	blood:	n/a	chr7:101634448-101634457
48	BCL11A	chr7:101628337-101628624	GM12878	blood:	n/a	chr7:101628338-101628347
49	BCL11A	chr7:101625103-101625646	GM12878	blood:	n/a	chr7:101625475-101625484
50	BCL3	chr7:101596737-101597104	GM12878	blood:	n/a	n/a

(count:2263 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:101632568-101632618	Jurkat	blood:	n/a
2	chr7:101599518-101599568	Hepatocyte	liver:	n/a
3	chr7:101585659-101585709	NH-A	brain:	n/a
4	chr7:101608014-101608064	SAEC	small airway:	n/a
5	chr7:101632568-101632618	ECC-1	luminal epithelium:	n/a
6	chr7:101630888-101630938	T-47D	breast:	n/a
7	chr7:101632568-101632618	Jurkat	blood:	n/a
8	chr7:101599518-101599568	Hepatocyte	liver:	n/a
9	chr7:101585659-101585709	NH-A	brain:	n/a
10	chr7:101608014-101608064	SAEC	small airway:	n/a
11	chr7:101632568-101632618	ECC-1	luminal epithelium:	n/a
12	chr7:101630888-101630938	T-47D	breast:	n/a
13	chr7:101566857-101566907	GM06990	blood:	n/a
14	chr7:101647464-101647514	HNPCEpiC	eye:	n/a
15	chr7:101615743-101615793	AoSMC	blood vessel:	n/a
16	chr7:101630948-101630998	PrEC	prostate:	n/a
17	chr7:101616020-101616070	T-47D	breast:	n/a
18	chr7:101630620-101630670	SK-N-MC	brain:	n/a
19	chr7:101630546-101630596	HNPCEpiC	eye:	n/a
20	chr7:101596131-101596181	SK-N-SH	brain:	n/a
21	chr7:101566857-101566907	U87	brain:	n/a
22	chr7:101596218-101596268	AoSMC	blood vessel:	n/a
23	chr7:101599518-101599568	GM12891	blood:	n/a
24	chr7:101630620-101630670	GM12878	blood:	n/a
25	chr7:101616020-101616070	BE2_C	brain:	n/a
26	chr7:101596404-101596454	NH-A	brain:	n/a
27	chr7:101599518-101599568	HRCEpiC	kidney:	n/a
28	chr7:101632568-101632618	HPAEpiC	pulmonary alveolar:	n/a
29	chr7:101615743-101615793	PANC-1	pancreas:	n/a
30	chr7:101599518-101599568	RPTEC	kidney:	n/a
31	chr7:101585659-101585709	HAEpiC	amniotic membrane:	n/a
32	chr7:101647464-101647514	HMEC	breast:	n/a
33	chr7:101596140-101596190	HCM	heart:	n/a
34	chr7:101579929-101579979	Caco-2	colon:	n/a
35	chr7:101630650-101630700	SAEC	small airway:	n/a
36	chr7:101647464-101647514	HCPEpiC	choroid plexus:	n/a
37	chr7:101630839-101630889	BE2_C	brain:	n/a
38	chr7:101630546-101630596	SK-N-SH_RA	brain:	n/a
39	chr7:101596140-101596190	HMEC	breast:	n/a
40	chr7:101629430-101629480	ovcar-3	ovarian:	n/a
41	chr7:101599518-101599568	HEEpiC	esophagus:	n/a
42	chr7:101599518-101599568	ECC-1	luminal epithelium:	n/a
43	chr7:101630948-101630998	CMK	blood:	n/a
44	chr7:101630650-101630700	SKMC	muscle:	n/a
45	chr7:101586761-101586811	CMK	blood:	n/a
46	chr7:101647464-101647514	H1-hESC	embryonic stem cell:	embryo
47	chr7:101647464-101647514	ProgFib	skin:	n/a
48	chr7:101571219-101571269	HCF	heart:	n/a
49	chr7:101630888-101630938	HL-60	blood:	n/a
50	chr7:101579003-101579053	HCF	heart:	n/a

(count:269 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr7:101647281..101648020-chr7:101707540..101708409,2	MCF-7	breast:
2	chr7:101554525..101555243-chr7:101647231..101647936,2	MCF-7	breast:
3	chr7:101460014..101461798-chr7:101579155..101581945,2	MCF-7	breast:
4	chr7:101635097..101635843-chr7:101647196..101647966,2	MCF-7	breast:
5	chr7:101630321..101633242-chr7:101633881..101635594,2	K562	blood:
6	chr7:101583272..101586097-chr7:101589522..101591483,2	K562	blood:
7	chr7:101627337..101631221-chr7:101631346..101635612,7	MCF-7	breast:
8	chr7:101497931..101500798-chr7:101614587..101617565,2	MCF-7	breast:
9	chr7:101628172..101630666-chr7:101646616..101649464,3	MCF-7	breast:
10	chr7:101605272..101609533-chr7:101610048..101615596,9	MCF-7	breast:
11	chr7:101588702..101590928-chr7:101591262..101593681,2	MCF-7	breast:
12	chr7:101526412..101529161-chr7:101615489..101617394,2	MCF-7	breast:
13	chr7:101588349..101588849-chr7:101647202..101647807,2	MCF-7	breast:
14	chr7:101616108..101616642-chr7:101957466..101958066,2	MCF-7	breast:
15	chr7:101583272..101586097-chr7:101589522..101591483,2	K562	blood:
16	chr7:101584411..101586887-chr7:101593987..101597254,4	MCF-7	breast:
17	chr7:101563970..101566081-chr7:101566918..101569155,2	K562	blood:
18	chr7:101563970..101566081-chr7:101566918..101569155,2	K562	blood:
19	chr7:101586382..101587949-chr7:101645381..101648210,2	MCF-7	breast:
20	chr7:101627337..101631221-chr7:101631346..101635612,7	MCF-7	breast:
21	chr7:101600575..101602590-chr7:101617429..101619775,2	MCF-7	breast:
22	chr7:101524415..101527254-chr7:101635329..101637588,2	MCF-7	breast:
23	chr7:101570061..101571761-chr7:101572477..101575327,2	K562	blood:
24	chr7:101608777..101611154-chr7:101612762..101615202,2	K562	blood:
25	chr20:52278044..52278974-chr7:101647121..101648013,2	MCF-7	breast:
26	chr7:101459375..101461266-chr7:101618989..101621791,3	MCF-7	breast:
27	chr7:101617978..101621240-chr7:101621803..101623926,3	K562	blood:
28	chr7:101572285..101574199-chr7:101650323..101652421,2	K562	blood:
29	chr7:101596523..101598043-chr7:101600103..101601856,2	K562	blood:
30	chr7:101577286..101579411-chr7:101581063..101582726,2	K562	blood:
31	chr7:101343414..101344257-chr7:101647212..101647964,4	MCF-7	breast:
32	chr7:101525729..101526362-chr7:101588047..101588871,2	MCF-7	breast:
33	chr7:101546954..101549494-chr7:101560538..101563127,2	MCF-7	breast:
34	chr7:101557512..101560612-chr7:101577165..101580347,3	K562	blood:
35	chr7:101583996..101590317-chr7:101598825..101610404,14	MCF-7	breast:
36	chr7:101528031..101528981-chr7:101647157..101648096,6	MCF-7	breast:
37	chr7:101616128..101616927-chr7:101635299..101635807,2	MCF-7	breast:
38	chr7:101568282..101570634-chr7:101582586..101584152,2	MCF-7	breast:
39	chr7:101457373..101459567-chr7:101616573..101618153,2	K562	blood:
40	chr7:101563285..101566884-chr7:101569000..101572598,3	MCF-7	breast:
41	chr7:101615765..101617035-chr7:101647115..101648119,24	MCF-7	breast:
42	chr7:101615283..101617064-chr7:101647091..101648139,67	MCF-7	breast:
43	chr7:101625094..101626938-chr7:101639657..101641295,2	MCF-7	breast:
44	chr7:101457163..101465176-chr7:101645974..101654631,24	MCF-7	breast:
45	chr7:101608777..101611154-chr7:101612762..101615202,2	K562	blood:
46	chr7:101645872..101649176-chr7:101651087..101654410,4	MCF-7	breast:
47	chr7:101631872..101634524-chr7:101635259..101637821,2	MCF-7	breast:
48	chr7:101587675..101589304-chr7:101641856..101645951,3	MCF-7	breast:
49	chr7:101457960..101459591-chr7:101593595..101596073,2	MCF-7	breast:
50	chr7:101459912..101462343-chr7:101596378..101599149,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SH2B2-7	chr7:101603396-101605174	ENSG00000272219.1

No data

Variant related genes	Relation type
ENSG00000272219	TF binding region
CUX1	TF binding region
ENSG00000272219	CpG island
CUX1	CpG island
ENSG00000206652	chromatin interactions
ENSG00000261135	chromatin interactions
ENSG00000272219	chromatin interactions
ENSG00000160999	chromatin interactions
ENSG00000257923	chromatin interactions

Extended variants
information (count: 3240 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:3240 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17407001	chr7:101562674-101562675	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs114409557	chr7:101562675-101562676	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528214207	chr7:101562686-101562687	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs547507112	chr7:101562715-101562716	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187343510	chr7:101562731-101562732	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs371677269	chr7:101562734-101562735	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs73712587	chr7:101562759-101562760	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs548739806	chr7:101562760-101562761	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs191630519	chr7:101562793-101562794	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs537727959	chr7:101562794-101562795	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs200330207	chr7:101562812-101562813	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs141262393	chr7:101562814-101562815	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs576938817	chr7:101562829-101562830	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs534568706	chr7:101562841-101562842	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs184580867	chr7:101562870-101562871	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs574452583	chr7:101562899-101562900	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs187407902	chr7:101562904-101562905	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs563488495	chr7:101562905-101562906	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs546670778	chr7:101562968-101562969	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs575304436	chr7:101562978-101562979	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs565083481	chr7:101562989-101562990	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs192057112	chr7:101562990-101562991	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs564010502	chr7:101563003-101563004	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs150837976	chr7:101563028-101563029	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs541009829	chr7:101563029-101563030	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs201380214	chr7:101563096-101563097	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs138242668	chr7:101563101-101563102	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs530205356	chr7:101563129-101563130	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs548537542	chr7:101563141-101563142	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs114855659	chr7:101563160-101563161	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs185678134	chr7:101563169-101563170	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs115773413	chr7:101563192-101563193	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs571146201	chr7:101563261-101563262	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs190590563	chr7:101563266-101563267	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs181051437	chr7:101563296-101563297	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs184256448	chr7:101563304-101563305	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs568103678	chr7:101563306-101563307	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs537084996	chr7:101563320-101563321	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs372342721	chr7:101563333-101563334	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs11368186	chr7:101563407-101563408	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs398005626	chr7:101563419-101563420	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs535547257	chr7:101563422-101563423	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs556734764	chr7:101563428-101563429	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs368050272	chr7:101563464-101563465	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs7791278	chr7:101563471-101563472	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs188577555	chr7:101563561-101563562	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs567525822	chr7:101563584-101563585	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs557663518	chr7:101563591-101563592	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs181075446	chr7:101563606-101563607	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs374777767	chr7:101563630-101563631	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	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
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Cancer	19907438	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:2991 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101544000-101569800	Weak transcription	HMEC	breast
2	chr7:101544200-101579800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:101555400-101565600	Weak transcription	Stomach Mucosa	stomach
4	chr7:101555400-101567400	Weak transcription	HUVEC	blood vessel
5	chr7:101556000-101572600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr7:101556400-101566800	Weak transcription	NHDF-Ad	bronchial
7	chr7:101557200-101565600	Weak transcription	NH-A	brain
8	chr7:101557400-101566000	Weak transcription	Aorta	Aorta
9	chr7:101557400-101566400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr7:101557400-101573600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr7:101557600-101565800	Weak transcription	Rectal Smooth Muscle	rectum
12	chr7:101557600-101568200	Weak transcription	Brain Anterior Caudate	brain
13	chr7:101557600-101571200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr7:101558000-101564600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
15	chr7:101558000-101565600	Strong transcription	Fetal Intestine Small	intestine
16	chr7:101558000-101567800	Strong transcription	Dnd41	blood
17	chr7:101558000-101570200	Strong transcription	Fetal Stomach	stomach
18	chr7:101558200-101563000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr7:101558200-101563200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:101558200-101563200	Strong transcription	Primary T cells from cord blood	blood
21	chr7:101558200-101563400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr7:101558200-101563400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr7:101558200-101563400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr7:101558200-101563400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr7:101558200-101563400	Strong transcription	Thymus	Thymus
26	chr7:101558200-101564600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr7:101558200-101570400	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr7:101558400-101563200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr7:101558400-101563200	Strong transcription	Lung	lung
30	chr7:101558400-101563400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr7:101558400-101563400	Strong transcription	Rectal Mucosa Donor 29	rectum
32	chr7:101558400-101563400	Strong transcription	Sigmoid Colon	Sigmoid Colon
33	chr7:101558400-101564000	Strong transcription	Primary neutrophils fromperipheralblood	blood
34	chr7:101558400-101565600	Weak transcription	Colon Smooth Muscle	Colon
35	chr7:101558400-101567000	Strong transcription	Primary monocytes fromperipheralblood	blood
36	chr7:101558600-101563200	Strong transcription	Primary hematopoietic stem cells	blood
37	chr7:101558600-101563400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr7:101558600-101564000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr7:101558600-101567000	Weak transcription	Psoas Muscle	Psoas
40	chr7:101558600-101577800	Weak transcription	Brain Angular Gyrus	brain
41	chr7:101558800-101563000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr7:101558800-101563200	Strong transcription	HUES6 Cell Line	embryonic stem cell
43	chr7:101558800-101563200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr7:101558800-101563200	Strong transcription	Spleen	Spleen
45	chr7:101558800-101563400	Strong transcription	Fetal Intestine Large	intestine
46	chr7:101558800-101564400	Strong transcription	Osteobl	bone
47	chr7:101558800-101565000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr7:101559000-101562800	Strong transcription	NHLF	lung
49	chr7:101559000-101563000	Strong transcription	Duodenum Mucosa	Duodenum
50	chr7:101559000-101563000	Strong transcription	Rectal Mucosa Donor 31	rectum

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