Variant report

Variant	nsv608072
Chromosome Location	chr7:106718347-106753248
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:370)
CpG islands
(count:122)
Chromatin interactive
region (count:31)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:370 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:106750473-106750655	K562	blood:	n/a	n/a
2	ARID3A	chr7:106720940-106721360	K562	blood:	n/a	n/a
3	ARID3A	chr7:106744032-106744181	K562	blood:	n/a	n/a
4	ARID3A	chr7:106718750-106720391	K562	blood:	n/a	n/a
5	ARID3A	chr7:106730129-106730427	K562	blood:	n/a	n/a
6	ARID3A	chr7:106741159-106741579	K562	blood:	n/a	n/a
7	ARID3A	chr7:106740529-106740821	K562	blood:	n/a	n/a
8	ATF1	chr7:106732605-106732798	K562	blood:	n/a	n/a
9	ATF1	chr7:106721012-106721318	K562	blood:	n/a	n/a
10	ATF1	chr7:106719343-106720292	K562	blood:	n/a	n/a
11	ATF1	chr7:106750362-106750662	K562	blood:	n/a	n/a
12	ATF1	chr7:106741385-106741536	K562	blood:	n/a	n/a
13	ATF1	chr7:106743858-106744272	K562	blood:	n/a	n/a
14	ATF1	chr7:106730190-106730452	K562	blood:	n/a	n/a
15	BHLHE40	chr7:106718846-106718879	K562	blood:	n/a	n/a
16	BHLHE40	chr7:106744070-106744089	K562	blood:	n/a	n/a
17	BHLHE40	chr7:106750421-106750621	K562	blood:	n/a	n/a
18	BHLHE40	chr7:106719840-106720470	K562	blood:	n/a	n/a
19	CBX3	chr7:106750286-106750796	K562	blood:	n/a	n/a
20	CBX3	chr7:106750177-106750836	K562	blood:	n/a	n/a
21	CBX3	chr7:106739573-106740006	K562	blood:	n/a	n/a
22	CBX3	chr7:106743711-106744314	K562	blood:	n/a	n/a
23	CBX3	chr7:106718522-106720646	K562	blood:	n/a	n/a
24	CBX3	chr7:106739495-106740173	K562	blood:	n/a	n/a
25	CBX3	chr7:106752273-106752693	K562	blood:	n/a	n/a
26	CBX3	chr7:106740203-106741882	K562	blood:	n/a	n/a
27	CBX3	chr7:106749385-106750168	K562	blood:	n/a	n/a
28	CCNT2	chr7:106730181-106730390	K562	blood:	n/a	n/a
29	CCNT2	chr7:106741350-106741607	K562	blood:	n/a	n/a
30	CCNT2	chr7:106750655-106750725	K562	blood:	n/a	n/a
31	CCNT2	chr7:106719271-106720327	K562	blood:	n/a	chr7:106719507-106719516
32	CEBPB	chr7:106726271-106726497	K562	blood:	n/a	chr7:106726358-106726369
33	CEBPB	chr7:106726234-106726462	HepG2	liver:	n/a	chr7:106726358-106726369
34	CEBPB	chr7:106726238-106726506	A549	lung:	n/a	chr7:106726358-106726369
35	CEBPB	chr7:106719574-106720358	K562	blood:	n/a	n/a
36	CEBPB	chr7:106740536-106740895	K562	blood:	n/a	n/a
37	CEBPB	chr7:106746187-106746366	K562	blood:	n/a	n/a
38	CEBPB	chr7:106718594-106719936	K562	blood:	n/a	chr7:106719442-106719459 chr7:106719125-106719138
39	CEBPB	chr7:106740580-106740880	K562	blood:	n/a	n/a
40	CEBPB	chr7:106718436-106719555	K562	blood:	n/a	chr7:106719442-106719459 chr7:106719125-106719138
41	CEBPB	chr7:106752474-106752706	K562	blood:	n/a	n/a
42	CEBPB	chr7:106718611-106719111	HCT-116	colon:	n/a	n/a
43	CEBPD	chr7:106741116-106741765	K562	blood:	n/a	n/a
44	CEBPD	chr7:106718994-106720340	K562	blood:	n/a	n/a
45	CHD2	chr7:106743927-106744002	K562	blood:	n/a	n/a
46	CHD2	chr7:106750375-106750673	K562	blood:	n/a	n/a
47	CREB1	chr7:106743803-106744439	K562	blood:	n/a	n/a
48	CREB1	chr7:106743958-106744179	GM12878	blood:	n/a	n/a
49	CTCF	chr7:106750424-106750585	K562	blood:	n/a	n/a
50	CTCF	chr7:106718740-106718890	SK-N-SH_RA	brain:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:106751055-106751105	GM12878	blood:	n/a
2	chr7:106730486-106730536	BJ	skin:	n/a
3	chr7:106730486-106730536	SAEC	small airway:	n/a
4	chr7:106730486-106730536	HL-60	blood:	n/a
5	chr7:106751055-106751105	GM06990	blood:	n/a
6	chr7:106751055-106751105	AG04449	skin:	fetal
7	chr7:106730486-106730536	ovcar-3	ovarian:	n/a
8	chr7:106730486-106730536	HCM	heart:	n/a
9	chr7:106730486-106730536	HCF	heart:	n/a
10	chr7:106730486-106730536	HEK293	kidney:	embryo
11	chr7:106751055-106751105	RPTEC	kidney:	n/a
12	chr7:106751055-106751105	HEEpiC	esophagus:	n/a
13	chr7:106730486-106730536	HNPCEpiC	eye:	n/a
14	chr7:106751055-106751105	LNCaP	prostate:	n/a
15	chr7:106730486-106730536	GM12892	blood:	n/a
16	chr7:106751055-106751105	NH-A	brain:	n/a
17	chr7:106730486-106730536	HepG2	liver:	n/a
18	chr7:106730486-106730536	HRCEpiC	kidney:	n/a
19	chr7:106730486-106730536	MCF10A-Er-Src	breast:	n/a
20	chr7:106730486-106730536	T-47D	breast:	n/a
21	chr7:106751055-106751105	GM19239	blood:	n/a
22	chr7:106730486-106730536	Hepatocyte	liver:	n/a
23	chr7:106751055-106751105	HRCEpiC	kidney:	n/a
24	chr7:106730486-106730536	NT2-D1	testis:	n/a
25	chr7:106751055-106751105	HL-60	blood:	n/a
26	chr7:106751055-106751105	SK-N-SH_RA	brain:	n/a
27	chr7:106751055-106751105	HEK293	kidney:	embryo
28	chr7:106751055-106751105	Jurkat	blood:	n/a
29	chr7:106751055-106751105	HRPEpiC	eye:	n/a
30	chr7:106730486-106730536	NH-A	brain:	n/a
31	chr7:106751055-106751105	AG09309	skin:	n/a
32	chr7:106751055-106751105	HMEC	breast:	n/a
33	chr7:106751055-106751105	GM12892	blood:	n/a
34	chr7:106730486-106730536	NHBE	bronchial:	n/a
35	chr7:106751055-106751105	BJ	skin:	n/a
36	chr7:106730486-106730536	U87	brain:	n/a
37	chr7:106730486-106730536	NB4	blood:	n/a
38	chr7:106730486-106730536	H1-hESC	embryonic stem cell:	embryo
39	chr7:106730486-106730536	PrEC	prostate:	n/a
40	chr7:106730486-106730536	Jurkat	blood:	n/a
41	chr7:106730486-106730536	HMEC	breast:	n/a
42	chr7:106730486-106730536	SK-N-SH_RA	brain:	n/a
43	chr7:106730486-106730536	AG09319	gingival:	n/a
44	chr7:106751055-106751105	AG09319	gingival:	n/a
45	chr7:106730486-106730536	AG10803	skin:	n/a
46	chr7:106730486-106730536	HRE	kidney:	n/a
47	chr7:106730486-106730536	HCT-116	colon:	n/a
48	chr7:106751055-106751105	AoSMC	blood vessel:	n/a
49	chr7:106730486-106730536	HUVEC	blood vessel:	n/a
50	chr7:106751055-106751105	BE2_C	brain:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:106748010..106751921-chr7:106752496..106755574,4	K562	blood:
2	chr7:106586197..106587750-chr7:106745864..106748117,2	MCF-7	breast:
3	chr7:106741436..106746909-chr7:106747521..106753328,9	K562	blood:
4	chr7:106666230..106669183-chr7:106749968..106751976,2	K562	blood:
5	chr7:106744290..106747255-chr7:106747787..106750851,4	K562	blood:
6	chr7:106421019..106423387-chr7:106739356..106741392,2	K562	blood:
7	chr7:106740731..106742473-chr7:106742481..106744526,2	K562	blood:
8	chr7:106748482..106750486-chr7:106755215..106757859,2	K562	blood:
9	chr7:106646100..106649101-chr7:106740481..106744411,5	K562	blood:
10	chr7:106717699..106720289-chr7:106745636..106748104,2	K562	blood:
11	chr7:106745573..106748544-chr7:106750453..106753053,3	MCF-7	breast:
12	chr7:106684901..106686809-chr7:106742213..106744522,2	K562	blood:
13	chr7:106741436..106746909-chr7:106747521..106753328,9	K562	blood:
14	chr7:106744290..106747255-chr7:106747787..106750851,4	K562	blood:
15	chr7:106743520..106747466-chr7:106753735..106757334,5	K562	blood:
16	chr7:106684108..106687627-chr7:106750603..106753634,3	K562	blood:
17	chr7:106729487..106732696-chr7:106740924..106743417,3	K562	blood:
18	chr7:106750972..106752817-chr7:106755862..106758071,2	K562	blood:
19	chr7:106678495..106681311-chr7:106741541..106744451,2	K562	blood:
20	chr7:106716669..106718547-chr7:106773467..106775452,2	K562	blood:
21	chr7:106235623..106237461-chr7:106724037..106726160,2	K562	blood:
22	chr7:106745573..106748544-chr7:106750453..106753053,3	MCF-7	breast:
23	chr7:106627271..106629858-chr7:106719833..106721746,2	K562	blood:
24	chr7:106617391..106619356-chr7:106752500..106754196,2	K562	blood:
25	chr7:106751220..106753946-chr7:106786479..106788942,2	K562	blood:
26	chr7:106740395..106742534-chr7:106758353..106760020,2	MCF-7	breast:
27	chr7:106728783..106730823-chr7:106808194..106810345,2	K562	blood:
28	chr7:106554583..106556503-chr7:106724936..106727740,2	K562	blood:
29	chr7:106740731..106742473-chr7:106742481..106744526,2	K562	blood:
30	chr7:106748010..106751921-chr7:106752496..106755574,4	K562	blood:
31	chr7:106748482..106752472-chr7:106755862..106758984,6	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COG5-2	chr7:106718212-106718683	ENSG00000243193.2

No data

Variant related genes	Relation type
ENSG00000243193	TF binding region
PRKAR2B	TF binding region
ENSG00000243193	CpG island
PRKAR2B	CpG island
ENSG00000251978	chromatin interactions
ENSG00000005249	chromatin interactions
ENSG00000243193	chromatin interactions
ENSG00000105856	chromatin interactions

Extended variants
information (count: 1309 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1309 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10235601	chr7:106718347-106718348	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs376331709	chr7:106718367-106718368	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs542969613	chr7:106718368-106718369	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs562827266	chr7:106718455-106718456	Weak transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs112953061	chr7:106718508-106718509	Weak transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs185468240	chr7:106718516-106718517	Weak transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs565079529	chr7:106718522-106718523	Weak transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs10279179	chr7:106718529-106718530	Weak transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs114292340	chr7:106718547-106718548	Weak transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs144208450	chr7:106718552-106718553	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs566571504	chr7:106718553-106718554	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs537267854	chr7:106718563-106718564	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs527824231	chr7:106718576-106718577	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs549330115	chr7:106718587-106718588	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs115515328	chr7:106718601-106718602	Enhancers Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs111296898	chr7:106718615-106718616	Enhancers Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs66861003	chr7:106718646-106718647	Enhancers Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs537884311	chr7:106718656-106718657	Enhancers Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs398005751	chr7:106718662-106718663	Enhancers Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs75777274	chr7:106718663-106718664	Enhancers Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs188191912	chr7:106718796-106718797	Enhancers Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs2536506	chr7:106718844-106718845	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs561607834	chr7:106718864-106718865	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs192933312	chr7:106718891-106718892	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs553798521	chr7:106719008-106719009	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs150347697	chr7:106719010-106719011	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs73723710	chr7:106719039-106719040	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs556487203	chr7:106719054-106719055	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs576319113	chr7:106719102-106719103	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs145022619	chr7:106719202-106719203	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs564938711	chr7:106719236-106719237	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs527656968	chr7:106719368-106719369	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs368743874	chr7:106719374-106719375	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs541181083	chr7:106719378-106719379	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs142252794	chr7:106719389-106719390	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs17340577	chr7:106719413-106719414	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs554105281	chr7:106719513-106719514	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs549194930	chr7:106719515-106719516	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs569212400	chr7:106719527-106719528	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs117837967	chr7:106719533-106719534	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs2299419	chr7:106719536-106719537	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs184613985	chr7:106719552-106719553	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs375122348	chr7:106719586-106719587	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs146081794	chr7:106719598-106719599	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs557419392	chr7:106719602-106719603	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs576008719	chr7:106719615-106719616	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs138937430	chr7:106719622-106719623	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs142671754	chr7:106719651-106719652	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs576182444	chr7:106719727-106719728	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs562416140	chr7:106719761-106719762	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
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
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
Breast cancer	21858162	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Melanoma	17363583	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:297 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:106706400-106718600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:106706400-106720000	Weak transcription	Spleen	Spleen
3	chr7:106706800-106719200	Weak transcription	Fetal Brain Male	brain
4	chr7:106708800-106718600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr7:106710200-106720000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr7:106712200-106719000	Weak transcription	Brain Anterior Caudate	brain
7	chr7:106716000-106721400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr7:106716000-106721400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr7:106716800-106718400	Flanking Active TSS	HUVEC	blood vessel
10	chr7:106717600-106722600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr7:106717800-106721200	Enhancers	Adipose Nuclei	Adipose
12	chr7:106718000-106718400	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr7:106718000-106720800	Enhancers	Left Ventricle	heart
14	chr7:106718000-106730600	Weak transcription	Fetal Brain Female	brain
15	chr7:106718200-106718800	Genic enhancers	K562	blood
16	chr7:106718200-106720000	Weak transcription	Primary hematopoietic stem cells	blood
17	chr7:106718400-106718800	Enhancers	HUVEC	blood vessel
18	chr7:106718400-106719400	Enhancers	Fetal Muscle Leg	muscle
19	chr7:106718400-106719800	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr7:106718600-106718800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr7:106718600-106719200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr7:106718600-106721000	Enhancers	Fetal Heart	heart
23	chr7:106718800-106719000	Enhancers	Gastric	stomach
24	chr7:106718800-106719400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr7:106718800-106719400	Enhancers	A549	lung
26	chr7:106718800-106720000	Flanking Active TSS	HUVEC	blood vessel
27	chr7:106718800-106720400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr7:106718800-106720600	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr7:106718800-106720800	Enhancers	Lung	lung
30	chr7:106718800-106721200	Transcr. at gene 5' and 3'	K562	blood
31	chr7:106718800-106727800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr7:106719000-106719200	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr7:106719000-106719400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr7:106719000-106719400	Enhancers	Brain Anterior Caudate	brain
35	chr7:106719000-106719800	Enhancers	Brain Germinal Matrix	brain
36	chr7:106719000-106720800	Weak transcription	Gastric	stomach
37	chr7:106719000-106721200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr7:106719200-106719400	Enhancers	Brain Substantia Nigra	brain
39	chr7:106719200-106719400	Enhancers	Fetal Brain Male	brain
40	chr7:106719200-106719400	Enhancers	Fetal Stomach	stomach
41	chr7:106719200-106719600	Enhancers	Ovary	ovary
42	chr7:106719200-106719800	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr7:106719200-106720800	Enhancers	Right Ventricle	heart
44	chr7:106719400-106719600	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr7:106719400-106720000	Weak transcription	Fetal Stomach	stomach
46	chr7:106719400-106720200	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr7:106719400-106720400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr7:106719400-106720400	Weak transcription	Fetal Muscle Leg	muscle
49	chr7:106719400-106720600	Weak transcription	Brain Substantia Nigra	brain
50	chr7:106719400-106723800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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