Variant report

Variant	esv1850383
Chromosome Location	chr7:102112311-102332802
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:7524)
CpG islands
(count:2079)
Chromatin interactive
region (count:4)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:7524 , 50 per page) page: 1 2 3 4 5 6 7 ... 151

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102212897-102213097	HepG2	liver:	n/a	n/a
2	ATF2	chr7:102153014-102153393	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr7:102213014-102213141	GM12878	blood:	n/a	n/a
4	ATF3	chr7:102312022-102312401	A549	lung:	n/a	chr7:102312144-102312152
5	ATF3	chr7:102213014-102213188	K562	blood:	n/a	n/a
6	ATF3	chr7:102312099-102312242	K562	blood:	n/a	chr7:102312144-102312152
7	BACH1	chr7:102213021-102213172	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr7:102134745-102135058	GM12878	blood:	n/a	n/a
9	BATF	chr7:102118716-102119971	GM12878	blood:	n/a	n/a
10	BATF	chr7:102254253-102254722	GM12878	blood:	n/a	n/a
11	BATF	chr7:102214085-102214343	GM12878	blood:	n/a	n/a
12	BATF	chr7:102211064-102211322	GM12878	blood:	n/a	n/a
13	BATF	chr7:102329824-102330101	GM12878	blood:	n/a	n/a
14	BATF	chr7:102330287-102330744	GM12878	blood:	n/a	n/a
15	BATF	chr7:102211460-102211924	GM12878	blood:	n/a	n/a
16	BATF	chr7:102254118-102255225	GM12878	blood:	n/a	n/a
17	BATF	chr7:102179772-102180041	GM12878	blood:	n/a	n/a
18	BATF	chr7:102313180-102313439	GM12878	blood:	n/a	n/a
19	BATF	chr7:102291963-102292217	GM12878	blood:	n/a	n/a
20	BATF	chr7:102310144-102310402	GM12878	blood:	n/a	n/a
21	BATF	chr7:102148082-102148394	GM12878	blood:	n/a	n/a
22	BATF	chr7:102313151-102313476	GM12878	blood:	n/a	n/a
23	BATF	chr7:102185510-102186196	GM12878	blood:	n/a	n/a
24	BATF	chr7:102187719-102187949	GM12878	blood:	n/a	n/a
25	BATF	chr7:102207398-102207660	GM12878	blood:	n/a	n/a
26	BATF	chr7:102311459-102312701	GM12878	blood:	n/a	n/a
27	BATF	chr7:102233914-102234227	GM12878	blood:	n/a	n/a
28	BATF	chr7:102234392-102234834	GM12878	blood:	n/a	n/a
29	BATF	chr7:102117408-102117666	GM12878	blood:	n/a	n/a
30	BATF	chr7:102212379-102213628	GM12878	blood:	n/a	n/a
31	BATF	chr7:102167226-102167423	GM12878	blood:	n/a	n/a
32	BATF	chr7:102305017-102305524	GM12878	blood:	n/a	n/a
33	BATF	chr7:102120470-102120746	GM12878	blood:	n/a	n/a
34	BATF	chr7:102306478-102306740	GM12878	blood:	n/a	n/a
35	BATF	chr7:102285771-102286300	GM12878	blood:	n/a	chr7:102286082-102286093
36	BATF	chr7:102278828-102279089	GM12878	blood:	n/a	n/a
37	BATF	chr7:102157223-102157674	GM12878	blood:	n/a	n/a
38	BATF	chr7:102257362-102257620	GM12878	blood:	n/a	n/a
39	BATF	chr7:102254763-102255038	GM12878	blood:	n/a	n/a
40	BATF	chr7:102266316-102266513	GM12878	blood:	n/a	n/a
41	BATF	chr7:102252871-102253062	GM12878	blood:	n/a	n/a
42	BATF	chr7:102155784-102156059	GM12878	blood:	n/a	n/a
43	BATF	chr7:102179720-102179981	GM12878	blood:	n/a	n/a
44	BATF	chr7:102155139-102156246	GM12878	blood:	n/a	n/a
45	BATF	chr7:102158383-102158641	GM12878	blood:	n/a	n/a
46	BATF	chr7:102278880-102279149	GM12878	blood:	n/a	n/a
47	BATF	chr7:102205933-102206440	GM12878	blood:	n/a	n/a
48	BATF	chr7:102285752-102286469	GM12878	blood:	n/a	chr7:102286082-102286093
49	BATF	chr7:102192070-102192285	GM12878	blood:	n/a	n/a
50	BATF	chr7:102293584-102293766	GM12878	blood:	n/a	n/a

(count:2079 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102327236-102327286	HMEC	breast:	n/a
2	chr7:102196182-102196232	AG04449	skin:	fetal
3	chr7:102132012-102132062	MCF-7	breast:	n/a
4	chr7:102313389-102313439	HCF	heart:	n/a
5	chr7:102136524-102136574	HRCEpiC	kidney:	n/a
6	chr7:102327236-102327286	HMEC	breast:	n/a
7	chr7:102196182-102196232	AG04449	skin:	fetal
8	chr7:102132012-102132062	MCF-7	breast:	n/a
9	chr7:102313389-102313439	HCF	heart:	n/a
10	chr7:102136524-102136574	HRCEpiC	kidney:	n/a
11	chr7:102113759-102113809	ProgFib	skin:	n/a
12	chr7:102332458-102332508	SK-N-SH_RA	brain:	n/a
13	chr7:102332458-102332508	AG10803	skin:	n/a
14	chr7:102132012-102132062	SK-N-SH_RA	brain:	n/a
15	chr7:102118300-102118350	SK-N-SH_RA	brain:	n/a
16	chr7:102134668-102134718	GM19239	blood:	n/a
17	chr7:102312308-102312358	BE2_C	brain:	n/a
18	chr7:102196182-102196232	HNPCEpiC	eye:	n/a
19	chr7:102327236-102327286	BJ	skin:	n/a
20	chr7:102151231-102151281	SK-N-SH	brain:	n/a
21	chr7:102134668-102134718	BJ	skin:	n/a
22	chr7:102259241-102259291	HCF	heart:	n/a
23	chr7:102196182-102196232	Caco-2	colon:	n/a
24	chr7:102279588-102279638	A549	lung:	n/a
25	chr7:102155527-102155577	GM06990	blood:	n/a
26	chr7:102113759-102113809	HL-60	blood:	n/a
27	chr7:102212892-102212942	HCF	heart:	n/a
28	chr7:102119529-102119579	GM19239	blood:	n/a
29	chr7:102118300-102118350	SKMC	muscle:	n/a
30	chr7:102113759-102113809	GM12878	blood:	n/a
31	chr7:102119529-102119579	H1-hESC	embryonic stem cell:	embryo
32	chr7:102329146-102329196	AG09309	skin:	n/a
33	chr7:102119710-102119760	NHBE	bronchial:	n/a
34	chr7:102155527-102155577	Caco-2	colon:	n/a
35	chr7:102119453-102119503	AG04449	skin:	fetal
36	chr7:102246378-102246428	MCF10A-Er-Src	breast:	n/a
37	chr7:102279588-102279638	H1-hESC	embryonic stem cell:	embryo
38	chr7:102155527-102155577	GM12892	blood:	n/a
39	chr7:102313412-102313462	PANC-1	pancreas:	n/a
40	chr7:102312315-102312365	HCT-116	colon:	n/a
41	chr7:102259241-102259291	HEK293	kidney:	embryo
42	chr7:102119453-102119503	HUVEC	blood vessel:	n/a
43	chr7:102119710-102119760	HL-60	blood:	n/a
44	chr7:102312308-102312358	HEK293	kidney:	embryo
45	chr7:102312318-102312368	HepG2	liver:	n/a
46	chr7:102246378-102246428	CMK	blood:	n/a
47	chr7:102312315-102312365	GM12892	blood:	n/a
48	chr7:102312308-102312358	A549	lung:	n/a
49	chr7:102113508-102113558	HEEpiC	esophagus:	n/a
50	chr7:102136524-102136574	SKMC	muscle:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:102110628..102112535-chr8:144951000..144953117,2	MCF-7	breast:
2	chr7:102110592..102113197-chr7:102117853..102119354,2	MCF-7	breast:
3	chr7:102095105..102097142-chr7:102112791..102114354,2	K562	blood:
4	chr7:102110592..102113197-chr7:102117853..102119354,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POLR2J-1	chr7:102120179-102121095	NONHSAT122510

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RASA4	hsa-miR-335-5p	chr7:102128407-102128431
2	RASA4	hsa-miR-335-5p	chr7:102227581-102227605

Variant related genes	Relation type
ENSG00000270249	TF binding region
RASA4B	TF binding region
ENSG00000272949	TF binding region
ENSG00000205236	TF binding region
POLR2J	TF binding region
ENSG00000228049	TF binding region
ENSG00000238997	TF binding region
UPK3BL	TF binding region
POLR2J2	TF binding region
SPDYE2	TF binding region
ENSG00000271745	TF binding region
RASA4	TF binding region
RASA4DP	TF binding region
POLR2J3	TF binding region
SPDYE2B	TF binding region
ENSG00000256604	TF binding region
ENSG00000238392	TF binding region
ENSG00000270249	CpG island
RASA4B	CpG island
ENSG00000272949	CpG island
ENSG00000205236	CpG island
POLR2J	CpG island
ENSG00000228049	CpG island
ENSG00000238997	CpG island
UPK3BL	CpG island
POLR2J2	CpG island
SPDYE2	CpG island
ENSG00000271745	CpG island
RASA4	CpG island
RASA4DP	CpG island
POLR2J3	CpG island
SPDYE2B	CpG island
ENSG00000256604	CpG island
ENSG00000238392	CpG island
ENSG00000264471	chromatin interactions
ENSG00000227184	chromatin interactions
ENSG00000005075	chromatin interactions

Extended variants
information (count: 2607 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:2607 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545522368	chr7:102112346-102112347	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs139480794	chr7:102112385-102112386	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs528397779	chr7:102112393-102112394	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs4473948	chr7:102112397-102112398	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs561563355	chr7:102112418-102112419	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs184505913	chr7:102112420-102112421	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs577413810	chr7:102112440-102112441	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs76753661	chr7:102112444-102112445	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs574114409	chr7:102112457-102112458	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs75779918	chr7:102112466-102112467	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs541689659	chr7:102112478-102112479	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs562254608	chr7:102112481-102112482	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs189644954	chr7:102112487-102112488	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs553793742	chr7:102112516-102112517	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs544805605	chr7:102112549-102112550	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs535353099	chr7:102112550-102112551	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs572161875	chr7:102112556-102112557	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs553660456	chr7:102112596-102112597	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs575086885	chr7:102112597-102112598	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs375151598	chr7:102112622-102112623	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs535719886	chr7:102112629-102112630	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs77848505	chr7:102112634-102112635	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs199773228	chr7:102112635-102112636	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs545859560	chr7:102112640-102112641	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs6959500	chr7:102112650-102112651	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs560178149	chr7:102112651-102112652	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs192461134	chr7:102112658-102112659	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs146591819	chr7:102112683-102112684	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs527362228	chr7:102112684-102112685	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs561603036	chr7:102112693-102112694	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs376086325	chr7:102112697-102112698	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs370479415	chr7:102112701-102112702	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs146629843	chr7:102112702-102112703	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs540345599	chr7:102112704-102112705	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs113220559	chr7:102112705-102112706	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs141553698	chr7:102112714-102112715	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs147046550	chr7:102112715-102112716	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs372960452	chr7:102112752-102112753	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs111699541	chr7:102112757-102112758	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs376179619	chr7:102112760-102112761	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs545677974	chr7:102112767-102112768	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs189236248	chr7:102112792-102112793	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs113354586	chr7:102112793-102112794	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs552678466	chr7:102112794-102112795	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs570865326	chr7:102112803-102112804	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs377633304	chr7:102112804-102112805	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs528446534	chr7:102112810-102112811	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs532636753	chr7:102112817-102112818	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs180769106	chr7:102112831-102112832	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs371398506	chr7:102112838-102112839	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
Cancer	19907438	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Bipolar disorder	19114987	CNVD
abnormal development	18461090	CNVD

Chromatin state (count:1497 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102106400-102112600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:102106400-102112600	Weak transcription	Aorta	Aorta
3	chr7:102106400-102119400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr7:102106600-102112400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:102106600-102112600	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr7:102106600-102112600	Weak transcription	Ovary	ovary
7	chr7:102106600-102112800	Weak transcription	Psoas Muscle	Psoas
8	chr7:102106600-102112800	Weak transcription	HSMMtube	muscle
9	chr7:102106600-102112800	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr7:102106600-102113200	Weak transcription	Fetal Lung	lung
11	chr7:102106600-102115000	Weak transcription	Primary hematopoietic stem cells	blood
12	chr7:102106600-102119200	Weak transcription	Right Atrium	heart
13	chr7:102106800-102112400	Weak transcription	Brain Substantia Nigra	brain
14	chr7:102106800-102112400	Weak transcription	Left Ventricle	heart
15	chr7:102106800-102112400	Weak transcription	Rectal Smooth Muscle	rectum
16	chr7:102106800-102112600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr7:102106800-102112600	Weak transcription	HSMM	muscle
18	chr7:102106800-102113200	Weak transcription	HMEC	breast
19	chr7:102106800-102113600	Weak transcription	Colon Smooth Muscle	Colon
20	chr7:102106800-102113600	Weak transcription	Hela-S3	cervix
21	chr7:102106800-102114400	Weak transcription	Brain Angular Gyrus	brain
22	chr7:102106800-102114400	Strong transcription	NHLF	lung
23	chr7:102106800-102114600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr7:102106800-102114600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr7:102106800-102116400	Strong transcription	Fetal Stomach	stomach
26	chr7:102106800-102118800	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr7:102106800-102119200	Weak transcription	NHDF-Ad	bronchial
28	chr7:102107400-102116200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr7:102107400-102116200	Strong transcription	Primary neutrophils fromperipheralblood	blood
30	chr7:102107600-102112400	Weak transcription	Primary B cells from cord blood	blood
31	chr7:102107600-102118200	Weak transcription	HUVEC	blood vessel
32	chr7:102107600-102119200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr7:102107600-102120400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr7:102107800-102112400	Strong transcription	Fetal Muscle Trunk	muscle
35	chr7:102107800-102114200	Weak transcription	Fetal Brain Male	brain
36	chr7:102107800-102114400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
37	chr7:102107800-102114400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr7:102107800-102114600	Strong transcription	Primary B cells from peripheral blood	blood
39	chr7:102107800-102114600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr7:102107800-102114800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr7:102107800-102115600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr7:102107800-102116000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr7:102107800-102116400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr7:102107800-102118000	Weak transcription	NH-A	brain
45	chr7:102108000-102112400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr7:102108000-102113600	Strong transcription	Cortex derived primary cultured neurospheres	brain
47	chr7:102108000-102113800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
48	chr7:102108000-102114600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr7:102108000-102114600	Strong transcription	HUES6 Cell Line	embryonic stem cell
50	chr7:102108000-102114600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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