Variant report

Variant	nsv588882
Chromosome Location	chr22:29767925-29807855
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:972)
CpG islands
(count:1037)
Chromatin interactive
region (count:68)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:972 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:29790955-29791320	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:29784494-29784815	K562	blood:	n/a	n/a
3	ARID3A	chr22:29784598-29784803	HepG2	liver:	n/a	n/a
4	ARID3A	chr22:29778868-29779190	K562	blood:	n/a	n/a
5	ATF1	chr22:29797555-29797746	K562	blood:	n/a	n/a
6	ATF2	chr22:29784482-29784966	GM12878	blood:	n/a	n/a
7	BCL11A	chr22:29801979-29802220	GM12878	blood:	n/a	n/a
8	BCL3	chr22:29784461-29785020	GM12878	blood:	n/a	chr22:29784573-29784582 chr22:29784685-29784698 chr22:29784546-29784555
9	BCLAF1	chr22:29784355-29784799	GM12878	blood:	n/a	chr22:29784573-29784582 chr22:29784685-29784698 chr22:29784546-29784555
10	BCLAF1	chr22:29781657-29782228	GM12878	blood:	n/a	chr22:29781963-29781972
11	BCLAF1	chr22:29784167-29784915	GM12878	blood:	n/a	chr22:29784573-29784582 chr22:29784685-29784698 chr22:29784546-29784555
12	BHLHE40	chr22:29783767-29784854	K562	blood:	n/a	chr22:29784290-29784306
13	BHLHE40	chr22:29807666-29807691	GM12878	blood:	n/a	n/a
14	BHLHE40	chr22:29784305-29784732	HepG2	liver:	n/a	n/a
15	BHLHE40	chr22:29783782-29784846	GM12878	blood:	n/a	chr22:29784290-29784306
16	BHLHE40	chr22:29779081-29779149	K562	blood:	n/a	n/a
17	BRCA1	chr22:29784309-29784324	HepG2	liver:	n/a	n/a
18	BRCA1	chr22:29784487-29784668	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr22:29791082-29791132	HepG2	liver:	n/a	n/a
20	CBX3	chr22:29784370-29784766	K562	blood:	n/a	n/a
21	CCNT2	chr22:29778935-29779230	K562	blood:	n/a	n/a
22	CCNT2	chr22:29784213-29784825	K562	blood:	n/a	n/a
23	CEBPB	chr22:29804956-29805312	K562	blood:	n/a	chr22:29805152-29805163
24	CEBPB	chr22:29773811-29774403	MCF-7	breast:	n/a	n/a
25	CEBPB	chr22:29771478-29771805	K562	blood:	n/a	n/a
26	CEBPB	chr22:29773211-29773460	MCF-7	breast:	n/a	n/a
27	CEBPB	chr22:29784634-29784925	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr22:29805089-29805202	IMR90	lung:	n/a	chr22:29805152-29805163
29	CEBPB	chr22:29784432-29784838	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr22:29791176-29791249	K562	blood:	n/a	n/a
31	CEBPB	chr22:29805000-29805273	HepG2	liver:	n/a	chr22:29805152-29805163
32	CEBPB	chr22:29784541-29784752	HepG2	liver:	n/a	n/a
33	CEBPB	chr22:29771466-29771819	IMR90	lung:	n/a	n/a
34	CEBPB	chr22:29805051-29805224	K562	blood:	n/a	chr22:29805152-29805163
35	CEBPB	chr22:29773807-29774448	MCF-7	breast:	n/a	n/a
36	CEBPB	chr22:29781370-29781510	HepG2	liver:	n/a	n/a
37	CEBPB	chr22:29771521-29771829	MCF-7	breast:	n/a	n/a
38	CEBPB	chr22:29771539-29771762	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr22:29805054-29805264	MCF-7	breast:	n/a	chr22:29805152-29805163
40	CEBPB	chr22:29784560-29784804	K562	blood:	n/a	n/a
41	CEBPB	chr22:29804972-29805323	K562	blood:	n/a	chr22:29805152-29805163
42	CEBPB	chr22:29771588-29771690	A549	lung:	n/a	n/a
43	CEBPD	chr22:29778931-29779287	K562	blood:	n/a	n/a
44	CEBPD	chr22:29784249-29784577	HepG2	liver:	n/a	n/a
45	CHD1	chr22:29784047-29784690	GM12878	blood:	n/a	chr22:29784363-29784373
46	CHD2	chr22:29790975-29791296	GM12878	blood:	n/a	n/a
47	CHD2	chr22:29784311-29784747	Hela-S3	cervix:	n/a	chr22:29784363-29784373
48	CHD2	chr22:29784755-29784887	HepG2	liver:	n/a	n/a
49	CHD2	chr22:29783991-29784944	GM12878	blood:	n/a	chr22:29784363-29784373
50	CHD2	chr22:29791078-29791089	HepG2	liver:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:29783861-29783911	NHDF-neo	bronchial:	n/a
2	chr22:29787625-29787675	T-47D	breast:	n/a
3	chr22:29784697-29784747	MCF10A-Er-Src	breast:	n/a
4	chr22:29778415-29778465	NH-A	brain:	n/a
5	chr22:29784436-29784486	HepG2	liver:	n/a
6	chr22:29787625-29787675	AG04449	skin:	fetal
7	chr22:29782753-29782803	NHDF-neo	bronchial:	n/a
8	chr22:29784778-29784828	H1-hESC	embryonic stem cell:	embryo
9	chr22:29782753-29782803	GM19239	blood:	n/a
10	chr22:29785355-29785405	Hepatocyte	liver:	n/a
11	chr22:29784441-29784491	SK-N-SH	brain:	n/a
12	chr22:29781841-29781891	AG04450	lung:	fetal
13	chr22:29784441-29784491	HPAEpiC	pulmonary alveolar:	n/a
14	chr22:29781841-29781891	SK-N-MC	brain:	n/a
15	chr22:29785355-29785405	HCF	heart:	n/a
16	chr22:29784694-29784744	AG09309	skin:	n/a
17	chr22:29784441-29784491	MCF10A-Er-Src	breast:	n/a
18	chr22:29782753-29782803	AG04450	lung:	fetal
19	chr22:29784644-29784694	ovcar-3	ovarian:	n/a
20	chr22:29784644-29784694	AG04450	lung:	fetal
21	chr22:29784697-29784747	HEEpiC	esophagus:	n/a
22	chr22:29787625-29787675	MCF-7	breast:	n/a
23	chr22:29782753-29782803	CMK	blood:	n/a
24	chr22:29784237-29784287	T-47D	breast:	n/a
25	chr22:29778415-29778465	ProgFib	skin:	n/a
26	chr22:29784237-29784287	HCT-116	colon:	n/a
27	chr22:29784671-29784721	HEEpiC	esophagus:	n/a
28	chr22:29784671-29784721	HL-60	blood:	n/a
29	chr22:29785355-29785405	ovcar-3	ovarian:	n/a
30	chr22:29784813-29784863	AG04449	skin:	fetal
31	chr22:29778415-29778465	CMK	blood:	n/a
32	chr22:29785355-29785405	BJ	skin:	n/a
33	chr22:29784237-29784287	ECC-1	luminal epithelium:	n/a
34	chr22:29784671-29784721	AG04449	skin:	fetal
35	chr22:29784813-29784863	HepG2	liver:	n/a
36	chr22:29784697-29784747	U87	brain:	n/a
37	chr22:29784697-29784747	K562	blood:	n/a
38	chr22:29784436-29784486	HEEpiC	esophagus:	n/a
39	chr22:29784694-29784744	MCF10A-Er-Src	breast:	n/a
40	chr22:29784671-29784721	ProgFib	skin:	n/a
41	chr22:29784778-29784828	HEEpiC	esophagus:	n/a
42	chr22:29784778-29784828	NT2-D1	testis:	n/a
43	chr22:29787625-29787675	HepG2	liver:	n/a
44	chr22:29781841-29781891	Jurkat	blood:	n/a
45	chr22:29787625-29787675	A549	lung:	n/a
46	chr22:29784624-29784674	AoSMC	blood vessel:	n/a
47	chr22:29783861-29783911	IMR90	lung:	fetal
48	chr22:29778415-29778465	HepG2	liver:	n/a
49	chr22:29784813-29784863	U87	brain:	n/a
50	chr22:29784813-29784863	HMEC	breast:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr22:29771898..29775582-chr22:29781742..29783845,4	MCF-7	breast:
2	chr22:29771666..29773871-chr22:29789734..29792185,2	MCF-7	breast:
3	chr22:29781864..29782673-chr22:29877575..29878342,2	MCF-7	breast:
4	chr22:29776140..29778611-chr22:29995991..29998407,2	K562	blood:
5	chr22:29790720..29791562-chr22:29920209..29921282,4	MCF-7	breast:
6	chr22:29712026..29714411-chr22:29782149..29784555,3	K562	blood:
7	chr22:29702455..29704377-chr22:29769522..29771265,2	MCF-7	breast:
8	chr22:29781310..29782787-chr22:29913055..29914130,15	MCF-7	breast:
9	chr22:29771731..29774347-chr22:29784237..29785863,2	MCF-7	breast:
10	chr22:29775197..29780621-chr22:29782246..29785885,8	K562	blood:
11	chr22:29794548..29795126-chr22:29913333..29914116,2	MCF-7	breast:
12	chr22:29664123..29665985-chr22:29772545..29774915,2	MCF-7	breast:
13	chr22:29762328..29763973-chr22:29771513..29774228,2	MCF-7	breast:
14	chr22:29704896..29707829-chr22:29780262..29782390,2	MCF-7	breast:
15	chr22:29774109..29774727-chr22:29781778..29782854,8	MCF-7	breast:
16	chr22:29780907..29784157-chr22:29912302..29916422,4	MCF-7	breast:
17	chr22:29791047..29793663-chr22:29794223..29797120,2	MCF-7	breast:
18	chr22:29774141..29774748-chr22:29913157..29913945,3	MCF-7	breast:
19	chr22:29783150..29785946-chr22:29944649..29946343,2	MCF-7	breast:
20	chr22:29782601..29785697-chr22:29975164..29978533,5	MCF-7	breast:
21	chr22:29774091..29774727-chr22:29781651..29782814,5	MCF-7	breast:
22	chr22:29781890..29782717-chr22:29913055..29913918,8	MCF-7	breast:
23	chr22:29774091..29774727-chr22:29781651..29782814,5	MCF-7	breast:
24	chr22:29792519..29794058-chr22:29864789..29867115,2	MCF-7	breast:
25	chr22:29770398..29771976-chr22:29778753..29780431,2	K562	blood:
26	chr22:29739232..29740930-chr22:29780922..29783404,2	MCF-7	breast:
27	chr22:29701440..29703925-chr22:29779026..29781003,2	MCF-7	breast:
28	chr22:29708527..29710108-chr22:29782946..29784507,2	K562	blood:
29	chr22:29774109..29774727-chr22:29781778..29782854,8	MCF-7	breast:
30	chr22:29792125..29793668-chr22:29802474..29805006,2	K562	blood:
31	chr22:29704102..29706466-chr22:29771552..29773376,2	MCF-7	breast:
32	chr22:29771898..29775582-chr22:29781742..29783845,4	MCF-7	breast:
33	chr22:29792125..29793668-chr22:29802474..29805006,2	K562	blood:
34	chr22:29781329..29782720-chr22:29913118..29914020,4	MCF-7	breast:
35	chr22:29737136..29739598-chr22:29772687..29775574,2	MCF-7	breast:
36	chr22:29778467..29780035-chr22:29782839..29784624,2	MCF-7	breast:
37	chr22:29794482..29794991-chr22:29913162..29914018,2	MCF-7	breast:
38	chr22:29774954..29777707-chr22:29779123..29781815,2	K562	blood:
39	chr22:29774954..29777707-chr22:29779123..29781815,2	K562	blood:
40	chr22:29771733..29774744-chr22:29774993..29776760,3	MCF-7	breast:
41	chr22:29771983..29774340-chr22:29774881..29776429,2	K562	blood:
42	chr22:29701804..29704290-chr22:29781998..29785634,5	MCF-7	breast:
43	chr22:29777011..29779930-chr22:29821335..29822984,2	K562	blood:
44	chr22:29784558..29786360-chr22:29786552..29791390,4	MCF-7	breast:
45	chr22:29770782..29772689-chr22:29780811..29782872,2	K562	blood:
46	chr22:29790656..29791686-chr22:29920171..29921137,10	MCF-7	breast:
47	chr22:29781578..29782726-chr22:29877337..29878344,7	MCF-7	breast:
48	chr22:29209443..29210342-chr22:29781715..29782736,4	MCF-7	breast:
49	chr22:29781675..29783812-chr22:29788035..29790235,2	MCF-7	breast:
50	chr22:29784630..29786169-chr22:29786224..29787893,2	K562	blood:

No data

Variant related genes	Relation type
AP1B1	TF binding region
AP1B1	CpG island
ENSG00000184117	chromatin interactions
ENSG00000100280	chromatin interactions
ENSG00000185340	chromatin interactions
ENSG00000273216	chromatin interactions
ENSG00000100263	chromatin interactions
ENSG00000100296	chromatin interactions
ENSG00000182944	chromatin interactions
ENSG00000100285	chromatin interactions

Extended variants
information (count: 1146 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1146 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2267136	chr22:29767925-29767926	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs186913248	chr22:29767971-29767972	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs560309155	chr22:29768029-29768030	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs202227201	chr22:29768122-29768123	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs75709960	chr22:29768243-29768244	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs541715496	chr22:29768281-29768282	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs191712549	chr22:29768282-29768283	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs572937952	chr22:29768290-29768291	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs542728832	chr22:29768293-29768294	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs562348347	chr22:29768305-29768306	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs35028553	chr22:29768308-29768309	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs183276834	chr22:29768325-29768326	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs188141507	chr22:29768384-29768385	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs114193023	chr22:29768390-29768391	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs533173604	chr22:29768426-29768427	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs695265	chr22:29768430-29768431	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs542066467	chr22:29768474-29768475	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs566509398	chr22:29768503-29768504	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs534064336	chr22:29768539-29768540	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs561949126	chr22:29768653-29768654	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs191127429	chr22:29768654-29768655	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs567454721	chr22:29768714-29768715	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs548399642	chr22:29768756-29768757	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs537601532	chr22:29768876-29768877	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs556433722	chr22:29768905-29768906	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs535949131	chr22:29768931-29768932	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs577977400	chr22:29768958-29768959	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs561371471	chr22:29768995-29768996	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs545300352	chr22:29768996-29768997	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs182216117	chr22:29769053-29769054	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs5763171	chr22:29769089-29769090	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs187641506	chr22:29769136-29769137	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs149647749	chr22:29769137-29769138	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs560775789	chr22:29769211-29769212	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs574188149	chr22:29769253-29769254	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs544445566	chr22:29769254-29769255	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs546725538	chr22:29769258-29769259	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs563220517	chr22:29769260-29769261	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs75449622	chr22:29769275-29769276	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs79816048	chr22:29769277-29769278	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs112999495	chr22:29769280-29769281	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs5752903	chr22:29769306-29769307	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs551645344	chr22:29769329-29769330	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs560158137	chr22:29769338-29769339	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs371216390	chr22:29769361-29769362	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs192558613	chr22:29769452-29769453	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs185686578	chr22:29769497-29769498	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs567617792	chr22:29769514-29769515	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs116929602	chr22:29769529-29769530	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs549737592	chr22:29769582-29769583	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	21251322	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
abnormal development	18461090	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	17322880	CNVD
Breast cancer	20409316	CNVD
Neurofibromatosis type 2	19566914	CNVD
Autism	19384346	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1487 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29741000-29782800	Weak transcription	Hela-S3	cervix
2	chr22:29753000-29777600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr22:29754600-29770400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr22:29755000-29772200	Weak transcription	Aorta	Aorta
5	chr22:29755000-29783800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr22:29755200-29773800	Weak transcription	Stomach Mucosa	stomach
7	chr22:29755200-29781000	Weak transcription	Fetal Brain Male	brain
8	chr22:29755200-29782800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr22:29755400-29783600	Weak transcription	Fetal Kidney	kidney
10	chr22:29755600-29771400	Weak transcription	Psoas Muscle	Psoas
11	chr22:29755600-29778600	Weak transcription	Fetal Lung	lung
12	chr22:29755800-29776600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr22:29756000-29769000	Weak transcription	Gastric	stomach
14	chr22:29756000-29771400	Weak transcription	Esophagus	oesophagus
15	chr22:29756000-29771400	Weak transcription	HMEC	breast
16	chr22:29756000-29771800	Weak transcription	NHLF	lung
17	chr22:29756000-29772200	Weak transcription	Right Atrium	heart
18	chr22:29756000-29776200	Weak transcription	Small Intestine	intestine
19	chr22:29756000-29779800	Weak transcription	Brain Germinal Matrix	brain
20	chr22:29756000-29783600	Weak transcription	Right Ventricle	heart
21	chr22:29756000-29783800	Weak transcription	Ovary	ovary
22	chr22:29756200-29779200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr22:29756400-29770400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr22:29756400-29772200	Weak transcription	Fetal Heart	heart
25	chr22:29756400-29782600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr22:29758200-29771800	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr22:29758200-29777000	Weak transcription	Colonic Mucosa	Colon
28	chr22:29761600-29768600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr22:29762600-29771400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr22:29762800-29768400	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr22:29762800-29770800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr22:29762800-29771800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr22:29762800-29777200	Weak transcription	Fetal Brain Female	brain
34	chr22:29764000-29769200	Strong transcription	Fetal Intestine Small	intestine
35	chr22:29764200-29771400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr22:29764600-29768200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr22:29765200-29769600	Genic enhancers	Primary B cells from peripheral blood	blood
38	chr22:29765400-29768000	Strong transcription	Primary T cells from cord blood	blood
39	chr22:29765400-29776000	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr22:29765400-29782600	Weak transcription	Colon Smooth Muscle	Colon
41	chr22:29765400-29783600	Weak transcription	Rectal Smooth Muscle	rectum
42	chr22:29765600-29771000	Weak transcription	Placenta Amnion	Placenta Amnion
43	chr22:29765600-29771400	Weak transcription	HepG2	liver
44	chr22:29765600-29775800	Weak transcription	HUVEC	blood vessel
45	chr22:29765600-29783600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr22:29765600-29783600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr22:29765800-29771400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr22:29765800-29771400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr22:29765800-29771600	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr22:29765800-29771800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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