Variant report

Variant	nsv539170
Chromosome Location	chr7:145606069-145910049
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1550)
CpG islands
(count:1342)
Chromatin interactive
region (count:95)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1550 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:145750569-145750925	K562	blood:	n/a	n/a
2	ARID3A	chr7:145787264-145787483	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:145787152-145787489	K562	blood:	n/a	n/a
4	ARID3A	chr7:145772258-145772458	K562	blood:	n/a	n/a
5	ARID3A	chr7:145755180-145755400	K562	blood:	n/a	n/a
6	ARID3A	chr7:145652488-145652580	K562	blood:	n/a	n/a
7	ARID3A	chr7:145878136-145878188	K562	blood:	n/a	n/a
8	ARID3A	chr7:145677810-145677911	K562	blood:	n/a	n/a
9	ARID3A	chr7:145703778-145703907	K562	blood:	n/a	n/a
10	ATF1	chr7:145775000-145775187	K562	blood:	n/a	n/a
11	ATF1	chr7:145728285-145728287	K562	blood:	n/a	n/a
12	ATF1	chr7:145717949-145718148	K562	blood:	n/a	n/a
13	ATF1	chr7:145699648-145699984	K562	blood:	n/a	n/a
14	ATF1	chr7:145750609-145750997	K562	blood:	n/a	n/a
15	ATF3	chr7:145716456-145716610	K562	blood:	n/a	n/a
16	ATF3	chr7:145750662-145750929	K562	blood:	n/a	n/a
17	ATF3	chr7:145683356-145683677	K562	blood:	n/a	n/a
18	BACH1	chr7:145845611-145845615	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr7:145686566-145686880	K562	blood:	n/a	n/a
20	BACH1	chr7:145727177-145727179	K562	blood:	n/a	n/a
21	BACH1	chr7:145642174-145642233	K562	blood:	n/a	n/a
22	BACH1	chr7:145750738-145750913	K562	blood:	n/a	n/a
23	BACH1	chr7:145812851-145813178	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr7:145842137-145842377	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr7:145813392-145814179	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr7:145694357-145694559	GM12878	blood:	n/a	n/a
27	BATF	chr7:145694359-145694555	GM12878	blood:	n/a	n/a
28	BCL11A	chr7:145694365-145694584	GM12878	blood:	n/a	n/a
29	BCL11A	chr7:145694347-145694680	GM12878	blood:	n/a	n/a
30	BHLHE40	chr7:145616543-145616610	K562	blood:	n/a	n/a
31	BHLHE40	chr7:145699653-145700059	K562	blood:	n/a	n/a
32	BHLHE40	chr7:145660449-145660549	K562	blood:	n/a	n/a
33	BHLHE40	chr7:145755118-145755377	K562	blood:	n/a	n/a
34	BHLHE40	chr7:145694345-145694571	HepG2	liver:	n/a	n/a
35	BHLHE40	chr7:145683463-145683590	K562	blood:	n/a	n/a
36	BHLHE40	chr7:145750584-145750950	K562	blood:	n/a	n/a
37	BHLHE40	chr7:145699695-145700051	GM12878	blood:	n/a	n/a
38	BHLHE40	chr7:145621411-145621433	K562	blood:	n/a	n/a
39	BHLHE40	chr7:145824603-145824809	K562	blood:	n/a	chr7:145824732-145824741 chr7:145824733-145824742 chr7:145824732-145824741
40	BHLHE40	chr7:145793673-145793674	K562	blood:	n/a	n/a
41	BHLHE40	chr7:145812888-145813075	K562	blood:	n/a	n/a
42	BHLHE40	chr7:145719613-145719737	K562	blood:	n/a	n/a
43	BRCA1	chr7:145787246-145787465	H1-hESC	embryonic stem cell:	n/a	chr7:145787445-145787452
44	BRCA1	chr7:145887640-145887719	GM12878	blood:	n/a	n/a
45	CBX3	chr7:145750559-145750949	K562	blood:	n/a	n/a
46	CBX3	chr7:145812871-145813165	K562	blood:	n/a	n/a
47	CBX3	chr7:145888550-145888786	K562	blood:	n/a	n/a
48	CBX3	chr7:145812824-145813236	K562	blood:	n/a	n/a
49	CBX3	chr7:145716048-145716747	K562	blood:	n/a	n/a
50	CBX3	chr7:145888491-145888877	K562	blood:	n/a	n/a

(count:1342 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:145813437-145813487	Hepatocyte	liver:	n/a
2	chr7:145813413-145813463	HRE	kidney:	n/a
3	chr7:145814152-145814202	NHBE	bronchial:	n/a
4	chr7:145716614-145716664	K562	blood:	n/a
5	chr7:145813915-145813965	MCF-7	breast:	n/a
6	chr7:145812871-145812921	MCF10A-Er-Src	breast:	n/a
7	chr7:145875026-145875076	LNCaP	prostate:	n/a
8	chr7:145716614-145716664	NHBE	bronchial:	n/a
9	chr7:145814152-145814202	Jurkat	blood:	n/a
10	chr7:145813494-145813544	GM12878	blood:	n/a
11	chr7:145689965-145690015	SKMC	muscle:	n/a
12	chr7:145813008-145813058	NT2-D1	testis:	n/a
13	chr7:145716504-145716554	HAEpiC	amniotic membrane:	n/a
14	chr7:145813008-145813058	HCF	heart:	n/a
15	chr7:145689965-145690015	IMR90	lung:	fetal
16	chr7:145740788-145740838	H1-hESC	embryonic stem cell:	embryo
17	chr7:145813437-145813487	PrEC	prostate:	n/a
18	chr7:145812842-145812892	HRCEpiC	kidney:	n/a
19	chr7:145813421-145813471	SKMC	muscle:	n/a
20	chr7:145813915-145813965	NT2-D1	testis:	n/a
21	chr7:145814003-145814053	H1-hESC	embryonic stem cell:	embryo
22	chr7:145813946-145813996	NHDF-neo	bronchial:	n/a
23	chr7:145813437-145813487	HUVEC	blood vessel:	n/a
24	chr7:145813432-145813482	AG09319	gingival:	n/a
25	chr7:145813439-145813489	HAEpiC	amniotic membrane:	n/a
26	chr7:145875026-145875076	PANC-1	pancreas:	n/a
27	chr7:145813413-145813463	HEK293	kidney:	embryo
28	chr7:145812842-145812892	AG09309	skin:	n/a
29	chr7:145812871-145812921	T-47D	breast:	n/a
30	chr7:145813439-145813489	HCF	heart:	n/a
31	chr7:145812842-145812892	PrEC	prostate:	n/a
32	chr7:145813494-145813544	MCF10A-Er-Src	breast:	n/a
33	chr7:145813494-145813544	NT2-D1	testis:	n/a
34	chr7:145813421-145813471	HEEpiC	esophagus:	n/a
35	chr7:145716504-145716554	PrEC	prostate:	n/a
36	chr7:145740788-145740838	SK-N-SH_RA	brain:	n/a
37	chr7:145814003-145814053	T-47D	breast:	n/a
38	chr7:145813946-145813996	SK-N-SH	brain:	n/a
39	chr7:145813432-145813482	BJ	skin:	n/a
40	chr7:145875026-145875076	HL-60	blood:	n/a
41	chr7:145813915-145813965	HPAEpiC	pulmonary alveolar:	n/a
42	chr7:145813946-145813996	AG10803	skin:	n/a
43	chr7:145814152-145814202	AG04449	skin:	fetal
44	chr7:145689965-145690015	HCF	heart:	n/a
45	chr7:145814306-145814356	A549	lung:	n/a
46	chr7:145740788-145740838	HepG2	liver:	n/a
47	chr7:145716614-145716664	AG09309	skin:	n/a
48	chr7:145813421-145813471	NH-A	brain:	n/a
49	chr7:145875026-145875076	HEK293	kidney:	embryo
50	chr7:145813915-145813965	AoSMC	blood vessel:	n/a

(count:95 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:145684833..145687404-chr7:145706239..145708972,2	K562	blood:
2	chr7:145879679..145882297-chr7:145885152..145887234,2	K562	blood:
3	chr7:145721579..145724410-chr7:145727561..145729692,3	K562	blood:
4	chr7:145774442..145776114-chr7:145776448..145779399,2	K562	blood:
5	chr7:145870161..145872926-chr7:145874663..145877386,2	K562	blood:
6	chr7:145806708..145809039-chr7:145812340..145814652,2	K562	blood:
7	chr7:145782097..145783756-chr7:145785466..145787437,2	K562	blood:
8	chr7:145872793..145874958-chr7:145879839..145881542,2	K562	blood:
9	chr7:145765986..145768873-chr7:145770171..145772250,2	K562	blood:
10	chr7:145693446..145695856-chr7:145705246..145708235,3	K562	blood:
11	chr7:145680328..145682466-chr7:145758892..145760742,2	K562	blood:
12	chr7:145684833..145687404-chr7:145706239..145708972,2	K562	blood:
13	chr7:145679343..145681995-chr7:145683818..145685327,2	K562	blood:
14	chr7:145715314..145718621-chr7:145718754..145721889,3	K562	blood:
15	chr7:145757899..145760042-chr7:145772123..145774268,2	K562	blood:
16	chr7:145706930..145710318-chr7:145716575..145718700,3	K562	blood:
17	chr7:145614214..145615977-chr7:145619608..145621998,3	K562	blood:
18	chr7:145757899..145760042-chr7:145772123..145774268,2	K562	blood:
19	chr7:145620799..145623095-chr7:145631387..145633696,2	K562	blood:
20	chr7:145697305..145699991-chr7:145700087..145702652,2	K562	blood:
21	chr7:145640094..145641820-chr7:145645010..145646727,2	K562	blood:
22	chr7:145633292..145636880-chr7:145639535..145641924,3	K562	blood:
23	chr7:145870161..145872926-chr7:145874663..145877386,2	K562	blood:
24	chr7:145620799..145622783-chr7:145631883..145633696,2	K562	blood:
25	chr7:145879679..145882297-chr7:145885152..145887234,2	K562	blood:
26	chr7:145872793..145874958-chr7:145879839..145881542,2	K562	blood:
27	chr7:145716150..145718502-chr7:145724762..145727451,3	K562	blood:
28	chr7:145771822..145774419-chr7:145775630..145778255,2	K562	blood:
29	chr7:145765986..145768873-chr7:145770171..145772250,2	K562	blood:
30	chr7:145774442..145776114-chr7:145776448..145779399,2	K562	blood:
31	chr7:145706930..145710318-chr7:145716575..145718700,3	K562	blood:
32	chr7:145638170..145640134-chr7:145641870..145644599,2	K562	blood:
33	chr7:145688129..145689794-chr7:145691841..145693343,2	K562	blood:
34	chr7:145691152..145693851-chr7:145700419..145703123,2	K562	blood:
35	chr7:145709801..145711953-chr7:145718759..145720900,2	K562	blood:
36	chr7:145747031..145750592-chr7:145750800..145754125,3	K562	blood:
37	chr7:145349967..145350847-chr7:145786768..145787358,3	MCF-7	breast:
38	chr7:145794339..145796121-chr7:145802069..145803645,2	K562	blood:
39	chr7:144712868..144713384-chr7:145787231..145787880,2	MCF-7	breast:
40	chr7:145697305..145699991-chr7:145700087..145702652,2	K562	blood:
41	chr7:145704641..145707485-chr7:145707900..145710506,2	K562	blood:
42	chr7:145640094..145641820-chr7:145645010..145646727,2	K562	blood:
43	chr7:145614214..145615977-chr7:145619608..145621998,3	K562	blood:
44	chr7:144551617..144552520-chr7:145786903..145787735,4	MCF-7	breast:
45	chr7:145696018..145698429-chr7:145703495..145706180,2	K562	blood:
46	chr7:145728196..145729845-chr7:145732878..145734449,2	K562	blood:
47	chr7:145749911..145752197-chr7:145756067..145758121,2	K562	blood:
48	chr7:145749911..145752197-chr7:145756067..145758121,2	K562	blood:
49	chr7:145805690..145807503-chr7:145809091..145811939,2	K562	blood:
50	chr7:145696018..145698429-chr7:145703495..145706180,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNTNAP2-2	chr7:145793180-145793471	NONHSAT123946
2	lnc-CNTNAP2-3	chr7:145747717-145747809	NONHSAT123945
3	lnc-CNTNAP2-3	chr7:145777121-145777289	NONHSAT123945
4	lnc-CNTNAP2-4	chr7:145747160-145747457	NONHSAT123944

No data

Variant related genes	Relation type
CNTNAP2	TF binding region
RN7SL207P	TF binding region
CNTNAP2	CpG island
RN7SL207P	CpG island
ENSG00000264018	chromatin interactions
ENSG00000174469	chromatin interactions

Extended variants
information (count: 5502 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:5502 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115039469	chr7:145606125-145606126	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186482150	chr7:145606161-145606162	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140055632	chr7:145606162-145606163	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545257721	chr7:145606173-145606174	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371402782	chr7:145606176-145606177	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs372374134	chr7:145606181-145606182	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs116678671	chr7:145606187-145606188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530906761	chr7:145606229-145606230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191501738	chr7:145606269-145606270	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs567433239	chr7:145606275-145606276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528424600	chr7:145606323-145606324	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546613066	chr7:145606333-145606334	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs116450873	chr7:145606403-145606404	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538956623	chr7:145606438-145606439	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534542864	chr7:145606442-145606443	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs569076875	chr7:145606444-145606445	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182423802	chr7:145606496-145606497	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs144010686	chr7:145606553-145606554	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs6965379	chr7:145606555-145606556	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs73738409	chr7:145606562-145606563	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs139107882	chr7:145606586-145606587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12703749	chr7:145606593-145606594	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs34456612	chr7:145606601-145606602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs528495761	chr7:145606639-145606640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs545730649	chr7:145606653-145606654	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73460964	chr7:145606712-145606713	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs531095198	chr7:145606745-145606746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542819253	chr7:145606753-145606754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561019910	chr7:145606806-145606807	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149875665	chr7:145606816-145606817	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546572065	chr7:145606840-145606841	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565102672	chr7:145606847-145606848	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571640574	chr7:145606866-145606867	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567394213	chr7:145606896-145606897	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144871247	chr7:145606904-145606905	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73460965	chr7:145606939-145606940	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs569065111	chr7:145607002-145607003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536404437	chr7:145607021-145607022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs73460969	chr7:145607036-145607037	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs185112845	chr7:145607107-145607108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533903696	chr7:145607114-145607115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190707621	chr7:145607127-145607128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576813668	chr7:145607132-145607133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs34421931	chr7:145607153-145607154	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4726775	chr7:145607158-145607159	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs557588818	chr7:145607166-145607167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73460971	chr7:145607185-145607186	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs542780595	chr7:145607187-145607188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73460973	chr7:145607243-145607244	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs546891752	chr7:145607262-145607263	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
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
Wilms tumour	21544195	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
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pancreatitis	21956041	CNVD
Acute myeloid leukemia	16864856	CNVD
Gastric cancer	16891809	CNVD
Lung cancer	17086460	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20808228	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	20718829	CNVD
Neuropsychiatric disorder	21827697	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Autism	20964600	CNVD
Epilepsy	17646849	CNVD
Mental retardation	19896112	CNVD
Autism	20531469	CNVD

Chromatin state (count:523 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:145598000-145614000	Weak transcription	K562	blood
2	chr7:145605400-145606800	Enhancers	Primary B cells from cord blood	blood
3	chr7:145606800-145607000	Flanking Active TSS	Primary B cells from cord blood	blood
4	chr7:145606800-145608000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr7:145607000-145607200	Enhancers	Primary B cells from cord blood	blood
6	chr7:145607000-145607400	Enhancers	Primary B cells from peripheral blood	blood
7	chr7:145607000-145608000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr7:145607200-145607400	Flanking Active TSS	Primary B cells from cord blood	blood
9	chr7:145607400-145608000	Enhancers	Primary B cells from cord blood	blood
10	chr7:145614000-145614200	Strong transcription	K562	blood
11	chr7:145614200-145617200	Weak transcription	K562	blood
12	chr7:145617200-145617800	ZNF genes & repeats	K562	blood
13	chr7:145617800-145621000	Weak transcription	K562	blood
14	chr7:145619200-145619600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr7:145621000-145621400	ZNF genes & repeats	K562	blood
16	chr7:145621400-145623600	Weak transcription	K562	blood
17	chr7:145623600-145624200	ZNF genes & repeats	K562	blood
18	chr7:145624200-145632400	Weak transcription	K562	blood
19	chr7:145626200-145627000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr7:145629000-145629600	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr7:145629200-145630000	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr7:145629400-145630000	Enhancers	H1 Cell Line	embryonic stem cell
23	chr7:145629400-145630000	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr7:145629400-145630000	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr7:145629400-145630000	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr7:145629400-145630200	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr7:145629800-145630200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr7:145630000-145634800	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr7:145630000-145634800	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr7:145630000-145635000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr7:145634600-145635000	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr7:145634800-145635200	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr7:145634800-145635200	ZNF genes & repeats	K562	blood
34	chr7:145634800-145635400	Enhancers	H1 Cell Line	embryonic stem cell
35	chr7:145634800-145635400	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr7:145635000-145635200	Enhancers	H9 Cell Line	embryonic stem cell
37	chr7:145635000-145635400	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr7:145635000-145635400	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr7:145635000-145635400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr7:145635000-145635600	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr7:145635200-145635600	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr7:145640200-145640400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr7:145640600-145640800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:145648200-145648600	Enhancers	Fetal Lung	lung
45	chr7:145648600-145649600	Weak transcription	Fetal Lung	lung
46	chr7:145649600-145649800	Enhancers	Fetal Lung	lung
47	chr7:145654400-145655000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr7:145658000-145660800	Weak transcription	K562	blood
49	chr7:145676800-145682600	Weak transcription	K562	blood
50	chr7:145679000-145679600	Enhancers	Brain Cingulate Gyrus	brain

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