Variant report

Variant	nsv530989
Chromosome Location	chr7:6176729-6438197
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5485)
CpG islands
(count:7094)
Chromatin interactive
region (count:252)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:5485 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:6413828-6414114	K562	blood:	n/a	n/a
2	ARID3A	chr7:6388543-6388891	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:6267859-6269106	K562	blood:	n/a	n/a
4	ARID3A	chr7:6310412-6310591	K562	blood:	n/a	n/a
5	ARID3A	chr7:6344971-6345277	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:6260839-6261320	K562	blood:	n/a	n/a
7	ARID3A	chr7:6388618-6388920	K562	blood:	n/a	n/a
8	ARID3A	chr7:6324006-6324164	K562	blood:	n/a	n/a
9	ARID3A	chr7:6403396-6403567	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:6413730-6413956	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:6318463-6318530	K562	blood:	n/a	n/a
12	ARID3A	chr7:6288375-6288526	K562	blood:	n/a	n/a
13	ARID3A	chr7:6346192-6346528	HepG2	liver:	n/a	n/a
14	ARID3A	chr7:6416501-6416845	HepG2	liver:	n/a	n/a
15	ARID3A	chr7:6310929-6311260	K562	blood:	n/a	n/a
16	ARID3A	chr7:6277511-6278342	HepG2	liver:	n/a	n/a
17	ARID3A	chr7:6424825-6425475	HepG2	liver:	n/a	n/a
18	ARID3A	chr7:6432227-6433385	K562	blood:	n/a	n/a
19	ATF1	chr7:6432902-6433406	K562	blood:	n/a	n/a
20	ATF1	chr7:6260898-6261370	K562	blood:	n/a	n/a
21	ATF1	chr7:6273690-6273874	K562	blood:	n/a	n/a
22	ATF1	chr7:6268544-6269141	K562	blood:	n/a	n/a
23	ATF1	chr7:6388405-6388876	K562	blood:	n/a	n/a
24	ATF1	chr7:6425094-6425398	K562	blood:	n/a	n/a
25	ATF2	chr7:6220664-6221194	GM12878	blood:	n/a	n/a
26	ATF2	chr7:6274038-6274616	GM12878	blood:	n/a	n/a
27	ATF2	chr7:6425006-6425405	GM12878	blood:	n/a	n/a
28	ATF2	chr7:6298428-6298920	GM12878	blood:	n/a	n/a
29	ATF2	chr7:6273884-6274488	GM12878	blood:	n/a	n/a
30	ATF2	chr7:6220717-6221092	GM12878	blood:	n/a	n/a
31	ATF2	chr7:6289620-6290650	GM12878	blood:	n/a	n/a
32	ATF2	chr7:6413103-6413408	GM12878	blood:	n/a	n/a
33	ATF2	chr7:6388437-6388937	H1-hESC	embryonic stem cell:	n/a	chr7:6388596-6388607
34	ATF2	chr7:6201433-6201909	GM12878	blood:	n/a	n/a
35	ATF2	chr7:6296034-6297248	GM12878	blood:	n/a	n/a
36	ATF2	chr7:6388529-6388924	GM12878	blood:	n/a	chr7:6388596-6388607
37	ATF2	chr7:6388420-6388909	GM12878	blood:	n/a	chr7:6388596-6388607
38	ATF2	chr7:6388443-6388988	H1-hESC	embryonic stem cell:	n/a	chr7:6388596-6388607
39	ATF2	chr7:6413747-6414139	GM12878	blood:	n/a	n/a
40	ATF2	chr7:6260931-6261248	GM12878	blood:	n/a	n/a
41	ATF2	chr7:6289625-6290574	GM12878	blood:	n/a	n/a
42	ATF2	chr7:6298381-6298972	GM12878	blood:	n/a	n/a
43	ATF2	chr7:6296134-6297204	GM12878	blood:	n/a	n/a
44	ATF3	chr7:6424947-6425510	A549	lung:	n/a	n/a
45	ATF3	chr7:6312145-6312488	H1-hESC	embryonic stem cell:	n/a	chr7:6312296-6312316 chr7:6312307-6312327 chr7:6312307-6312316
46	ATF3	chr7:6388456-6389065	K562	blood:	n/a	chr7:6388594-6388609 chr7:6388598-6388605 chr7:6388595-6388608 chr7:6388595-6388606 chr7:6388595-6388608 chr7:6388596-6388607 chr7:6388598-6388606 chr7:6388596-6388607
47	ATF3	chr7:6424925-6425559	HCT-116	colon:	n/a	n/a
48	ATF3	chr7:6388397-6388976	HepG2	liver:	n/a	chr7:6388594-6388609 chr7:6388598-6388605 chr7:6388595-6388608 chr7:6388595-6388606 chr7:6388595-6388608 chr7:6388596-6388607 chr7:6388598-6388606 chr7:6388596-6388607
49	ATF3	chr7:6260900-6261277	K562	blood:	n/a	n/a
50	ATF3	chr7:6388356-6388835	K562	blood:	n/a	chr7:6388594-6388609 chr7:6388598-6388605 chr7:6388595-6388608 chr7:6388595-6388606 chr7:6388595-6388608 chr7:6388596-6388607 chr7:6388598-6388606 chr7:6388596-6388607

(count:7094 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6413861-6413911	Hepatocyte	liver:	n/a
2	chr7:6312217-6312267	ProgFib	skin:	n/a
3	chr7:6197576-6197626	SK-N-MC	brain:	n/a
4	chr7:6208213-6208263	PFSK-1	brain:	n/a
5	chr7:6197890-6197940	LNCaP	prostate:	n/a
6	chr7:6210667-6210717	BJ	skin:	n/a
7	chr7:6208128-6208178	HRCEpiC	kidney:	n/a
8	chr7:6204269-6204319	CMK	blood:	n/a
9	chr7:6413877-6413927	BE2_C	brain:	n/a
10	chr7:6211730-6211780	HRE	kidney:	n/a
11	chr7:6193786-6193836	HRPEpiC	eye:	n/a
12	chr7:6203389-6203439	SK-N-MC	brain:	n/a
13	chr7:6199980-6200030	ovcar-3	ovarian:	n/a
14	chr7:6204983-6205033	CMK	blood:	n/a
15	chr7:6414708-6414758	H1-hESC	embryonic stem cell:	embryo
16	chr7:6389919-6389969	ECC-1	luminal epithelium:	n/a
17	chr7:6200116-6200166	PrEC	prostate:	n/a
18	chr7:6312217-6312267	AG09319	gingival:	n/a
19	chr7:6413861-6413911	Hepatocyte	liver:	n/a
20	chr7:6312217-6312267	ProgFib	skin:	n/a
21	chr7:6197576-6197626	SK-N-MC	brain:	n/a
22	chr7:6208213-6208263	PFSK-1	brain:	n/a
23	chr7:6197890-6197940	LNCaP	prostate:	n/a
24	chr7:6210667-6210717	BJ	skin:	n/a
25	chr7:6208128-6208178	HRCEpiC	kidney:	n/a
26	chr7:6204269-6204319	CMK	blood:	n/a
27	chr7:6413877-6413927	BE2_C	brain:	n/a
28	chr7:6211730-6211780	HRE	kidney:	n/a
29	chr7:6193786-6193836	HRPEpiC	eye:	n/a
30	chr7:6203389-6203439	SK-N-MC	brain:	n/a
31	chr7:6199980-6200030	ovcar-3	ovarian:	n/a
32	chr7:6204983-6205033	CMK	blood:	n/a
33	chr7:6414708-6414758	H1-hESC	embryonic stem cell:	embryo
34	chr7:6389919-6389969	ECC-1	luminal epithelium:	n/a
35	chr7:6200116-6200166	PrEC	prostate:	n/a
36	chr7:6312217-6312267	AG09319	gingival:	n/a
37	chr7:6198004-6198054	HRCEpiC	kidney:	n/a
38	chr7:6297970-6298020	MCF-7	breast:	n/a
39	chr7:6286149-6286199	HL-60	blood:	n/a
40	chr7:6238486-6238536	MCF-7	breast:	n/a
41	chr7:6197514-6197564	HNPCEpiC	eye:	n/a
42	chr7:6310773-6310823	AG09319	gingival:	n/a
43	chr7:6188723-6188773	SK-N-MC	brain:	n/a
44	chr7:6205492-6205542	AG10803	skin:	n/a
45	chr7:6313058-6313108	AG10803	skin:	n/a
46	chr7:6208213-6208263	GM19239	blood:	n/a
47	chr7:6412718-6412768	MCF-7	breast:	n/a
48	chr7:6200116-6200166	Jurkat	blood:	n/a
49	chr7:6414202-6414252	PFSK-1	brain:	n/a
50	chr7:6200140-6200190	MCF-7	breast:	n/a

(count:252 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr7:6280841..6283108-chr7:6294501..6296406,2	K562	blood:
2	chr7:6216897..6219662-chr7:6222027..6224471,2	MCF-7	breast:
3	chr7:6199039..6200525-chr7:6362284..6363316,17	MCF-7	breast:
4	chr7:6199470..6202116-chr7:6204941..6208439,5	K562	blood:
5	chr7:6412561..6415167-chr8:145131174..145134036,2	MCF-7	breast:
6	chr7:6047922..6050389-chr7:6388573..6391369,3	K562	blood:
7	chr7:6289334..6292556-chr7:6296327..6298930,3	K562	blood:
8	chr7:6295108..6297565-chr7:6362435..6365344,2	MCF-7	breast:
9	chr7:6402943..6405122-chr7:6514612..6517402,2	K562	blood:
10	chr7:6425290..6426951-chr7:6443487..6445552,2	MCF-7	breast:
11	chr7:6280841..6283704-chr7:6294906..6297324,2	K562	blood:
12	chr7:6310402..6314489-chr7:6314854..6318602,7	K562	blood:
13	chr7:6413015..6417903-chr7:6435938..6439469,5	MCF-7	breast:
14	chr7:6286204..6288303-chr7:6297783..6299306,2	K562	blood:
15	chr7:6415178..6416975-chr7:6426266..6428182,2	MCF-7	breast:
16	chr7:6143046..6145933-chr7:6364932..6367512,2	K562	blood:
17	chr7:6362326..6363972-chr7:6370986..6373639,2	MCF-7	breast:
18	chr7:6311447..6314640-chr7:6315943..6318631,5	K562	blood:
19	chr7:6218147..6221120-chr7:6228782..6230937,2	K562	blood:
20	chr7:6307491..6309134-chr7:6317243..6319734,2	K562	blood:
21	chr7:6238671..6240280-chr7:6246179..6247952,2	K562	blood:
22	chr7:6297786..6300256-chr7:6301628..6303560,2	K562	blood:
23	chr7:6290547..6293891-chr7:6295729..6298569,3	MCF-7	breast:
24	chr7:6362339..6362861-chr7:6969838..6970665,2	K562	blood:
25	chr7:6231008..6235144-chr7:6239773..6243041,3	K562	blood:
26	chr7:6295146..6297854-chr7:6301609..6304566,2	MCF-7	breast:
27	chr7:6386514..6388780-chr7:6439968..6442713,2	MCF-7	breast:
28	chr7:6387247..6388755-chr7:6413232..6415374,2	MCF-7	breast:
29	chr7:6298757..6301475-chr7:6305303..6307556,2	MCF-7	breast:
30	chr7:6218606..6220870-chr7:6221608..6224253,2	K562	blood:
31	chr7:6198247..6199856-chr7:6202022..6204046,2	MCF-7	breast:
32	chr7:6290547..6293891-chr7:6295729..6298569,3	MCF-7	breast:
33	chr7:6412666..6416399-chr7:6429961..6432840,4	MCF-7	breast:
34	chr7:6297786..6300256-chr7:6301628..6303560,2	K562	blood:
35	chr7:6176618..6179246-chr7:6186332..6188449,2	MCF-7	breast:
36	chr7:6424186..6426386-chr7:6428771..6430313,2	K562	blood:
37	chr7:6195894..6198040-chr7:6361741..6363493,2	MCF-7	breast:
38	chr7:6277710..6280661-chr7:6288834..6290468,2	K562	blood:
39	chr7:6199470..6202116-chr7:6204941..6208439,5	K562	blood:
40	chr7:6194593..6196125-chr7:6200629..6202167,2	K562	blood:
41	chr7:6310796..6312409-chr7:6348084..6350532,2	K562	blood:
42	chr7:6283219..6284762-chr7:6288057..6290958,2	MCF-7	breast:
43	chr7:6194450..6196699-chr7:6202081..6204089,2	MCF-7	breast:
44	chr7:6138619..6141275-chr7:6177878..6179542,2	K562	blood:
45	chr7:6204442..6207336-chr7:6209471..6212385,2	MCF-7	breast:
46	chr7:6379408..6381446-chr7:6384710..6386481,2	MCF-7	breast:
47	chr7:6420289..6422847-chr7:6423300..6426069,2	K562	blood:
48	chr7:6198247..6199856-chr7:6202022..6204046,2	MCF-7	breast:
49	chr7:6274798..6277671-chr7:6281292..6283536,4	K562	blood:
50	chr7:6049082..6051960-chr7:6388689..6390680,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAC1-2	chr7:6369092-6369444	NONHSAT118994
2	lnc-EIF2AK1-3	chr7:6212362-6212706	NONHSAT118988
3	lnc-EIF2AK1-3	chr7:6210757-6210945	NONHSAT118988
4	lnc-RAC1-1	chr7:6405329-6405671	expReg_chr7_541_+
5	lnc-RAC1-2	chr7:6370213-6370871	NONHSAT118994
6	lnc-CYTH3-2	chr7:6336984-6337416	NONHSAT118993

No data

(count:6 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	USP42	hsa-miR-16-5p	chr7:6200429-6200451
2	CYTH3	hsa-miR-320a	chr7:6202808-6202802
3	USP42	hsa-miR-320a	chr7:6200204-6200226
4	USP42	hsa-miR-103a-3p	chr7:6199382-6199388
5	USP42	hsa-miR-103a-3p	chr7:6200427-6200450
6	USP42	hsa-miR-16-5p	chr7:6199383-6199389

Variant related genes	Relation type
FAM220A	TF binding region
ENSG00000238534	TF binding region
RAC1	TF binding region
ENSG00000202273	TF binding region
CYTH3	TF binding region
FAM220A	CpG island
ENSG00000238534	CpG island
RAC1	CpG island
ENSG00000202273	CpG island
CYTH3	CpG island
ENSG00000178896	chromatin interactions
ENSG00000231704	chromatin interactions
ENSG00000178397	chromatin interactions
ENSG00000165338	chromatin interactions
ENSG00000106305	chromatin interactions
ENSG00000008256	chromatin interactions
ENSG00000136240	chromatin interactions
ENSG00000106346	chromatin interactions
ENSG00000183808	chromatin interactions
ENSG00000164535	chromatin interactions
ENSG00000269781	chromatin interactions
ENSG00000086232	chromatin interactions
ENSG00000100949	chromatin interactions
ENSG00000253848	chromatin interactions
ENSG00000136238	chromatin interactions
ENSG00000238534	chromatin interactions
ENSG00000167645	chromatin interactions
ENSG00000122512	chromatin interactions

Extended variants
information (count: 13371 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:13371 , 50 per page) page: 1 2 3 4 5 6 7 ... 268

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10226743	chr7:6176787-6176788	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532522017	chr7:6176816-6176817	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs180703163	chr7:6176819-6176820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184980412	chr7:6176822-6176823	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530370986	chr7:6176863-6176864	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs548538909	chr7:6176895-6176896	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566786152	chr7:6176987-6176988	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs10257181	chr7:6176998-6176999	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs146316042	chr7:6177081-6177082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs189359951	chr7:6177117-6177118	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs377555571	chr7:6177121-6177122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538799992	chr7:6177128-6177129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370027954	chr7:6177186-6177187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs199663739	chr7:6177225-6177226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148531501	chr7:6177233-6177234	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs370581737	chr7:6177236-6177237	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576916485	chr7:6177248-6177249	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564875578	chr7:6177250-6177251	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536183481	chr7:6177353-6177354	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554536010	chr7:6177374-6177375	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572716694	chr7:6177375-6177376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539844064	chr7:6177377-6177378	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558189055	chr7:6177380-6177381	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576569569	chr7:6177414-6177415	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544396650	chr7:6177425-6177426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544278122	chr7:6177455-6177456	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562964791	chr7:6177462-6177463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530402647	chr7:6177473-6177474	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372690806	chr7:6177501-6177502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373020846	chr7:6177512-6177513	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376216271	chr7:6177523-6177524	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs13241729	chr7:6177524-6177525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371415361	chr7:6177535-6177536	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs181705885	chr7:6177583-6177584	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552615505	chr7:6177584-6177585	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564565799	chr7:6177608-6177609	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531888276	chr7:6177634-6177635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550774414	chr7:6177688-6177689	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs568993207	chr7:6177714-6177715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12671407	chr7:6177733-6177734	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs528749439	chr7:6177746-6177747	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186710034	chr7:6177813-6177814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150641357	chr7:6177835-6177836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566767719	chr7:6177907-6177908	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533535112	chr7:6177927-6177928	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191612170	chr7:6177940-6177941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540143620	chr7:6177947-6177948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78520727	chr7:6178017-6178018	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs181286342	chr7:6178042-6178043	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs537580375	chr7:6178074-6178075	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	17426248	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioblastoma multiforme	21525872	CNVD
early-passage human iPS cells	21368824	CNVD
Gastric cancer	22014070	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ependymoma	20639864	CNVD
Autism	20685689	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD

Chromatin state (count:8695 , 50 per page) page: 1 2 3 4 5 6 7 ... 174

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6145600-6186000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:6145600-6186400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:6146800-6218200	Weak transcription	Stomach Mucosa	stomach
4	chr7:6157400-6179000	Weak transcription	Fetal Brain Male	brain
5	chr7:6157400-6188400	Weak transcription	Psoas Muscle	Psoas
6	chr7:6157400-6189400	Weak transcription	Fetal Heart	heart
7	chr7:6159600-6178200	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr7:6160600-6201800	Strong transcription	Fetal Thymus	thymus
9	chr7:6161400-6178200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr7:6161400-6180200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr7:6161400-6183800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr7:6161400-6199600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr7:6161400-6202200	Strong transcription	Primary T cells fromperipheralblood	blood
14	chr7:6161600-6179200	Weak transcription	Right Ventricle	heart
15	chr7:6161600-6185200	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr7:6161600-6192000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr7:6161800-6183800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr7:6162000-6176800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr7:6162000-6178400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr7:6162000-6178400	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr7:6162000-6179000	Weak transcription	Colon Smooth Muscle	Colon
22	chr7:6162000-6179400	Weak transcription	HMEC	breast
23	chr7:6162800-6179000	Weak transcription	Brain Hippocampus Middle	brain
24	chr7:6163000-6185000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr7:6164000-6192400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr7:6164200-6199400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr7:6166600-6177200	Strong transcription	Adipose Nuclei	Adipose
28	chr7:6167200-6177200	Strong transcription	Fetal Muscle Leg	muscle
29	chr7:6167400-6205600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr7:6168200-6182600	Weak transcription	HUVEC	blood vessel
31	chr7:6168800-6176800	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr7:6168800-6178200	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr7:6168800-6178800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr7:6168800-6179200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr7:6168800-6179200	Weak transcription	Aorta	Aorta
36	chr7:6168800-6184800	Weak transcription	Small Intestine	intestine
37	chr7:6169800-6178600	Weak transcription	NHEK	skin
38	chr7:6170000-6178600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr7:6170000-6183400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr7:6170400-6178000	Weak transcription	Hela-S3	cervix
41	chr7:6170400-6178200	Weak transcription	NHLF	lung
42	chr7:6170400-6178600	Weak transcription	NH-A	brain
43	chr7:6170600-6178200	Weak transcription	Esophagus	oesophagus
44	chr7:6170600-6178200	Weak transcription	HSMMtube	muscle
45	chr7:6170600-6178800	Weak transcription	Ovary	ovary
46	chr7:6170600-6182400	Weak transcription	K562	blood
47	chr7:6170800-6178200	Weak transcription	Gastric	stomach
48	chr7:6170800-6178200	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr7:6170800-6178400	Weak transcription	Rectal Smooth Muscle	rectum
50	chr7:6171000-6178200	Weak transcription	Colonic Mucosa	Colon

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