Variant report

Variant	esv3498689
Chromosome Location	chr22:29763576-29812598
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1296)
CpG islands
(count:1039)
Chromatin interactive
region (count:69)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1296 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:29778868-29779190	K562	blood:	n/a	n/a
2	ARID3A	chr22:29784494-29784815	K562	blood:	n/a	n/a
3	ARID3A	chr22:29790955-29791320	HepG2	liver:	n/a	n/a
4	ARID3A	chr22:29784598-29784803	HepG2	liver:	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	ATF2	chr22:29765407-29765735	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr22:29765433-29765705	H1-hESC	embryonic stem cell:	n/a	chr22:29765575-29765589
9	BATF	chr22:29808804-29809035	GM12878	blood:	n/a	n/a
10	BATF	chr22:29810856-29811337	GM12878	blood:	n/a	n/a
11	BATF	chr22:29763694-29763993	GM12878	blood:	n/a	chr22:29763867-29763878
12	BCL11A	chr22:29801979-29802220	GM12878	blood:	n/a	n/a
13	BCL3	chr22:29784461-29785020	GM12878	blood:	n/a	chr22:29784573-29784582 chr22:29784685-29784698 chr22:29784546-29784555
14	BCLAF1	chr22:29781657-29782228	GM12878	blood:	n/a	chr22:29781963-29781972
15	BCLAF1	chr22:29784167-29784915	GM12878	blood:	n/a	chr22:29784573-29784582 chr22:29784685-29784698 chr22:29784546-29784555
16	BCLAF1	chr22:29784355-29784799	GM12878	blood:	n/a	chr22:29784573-29784582 chr22:29784685-29784698 chr22:29784546-29784555
17	BHLHE40	chr22:29765504-29765531	HepG2	liver:	n/a	n/a
18	BHLHE40	chr22:29783782-29784846	GM12878	blood:	n/a	chr22:29784290-29784306
19	BHLHE40	chr22:29784305-29784732	HepG2	liver:	n/a	n/a
20	BHLHE40	chr22:29810866-29811343	GM12878	blood:	n/a	n/a
21	BHLHE40	chr22:29807666-29807691	GM12878	blood:	n/a	n/a
22	BHLHE40	chr22:29783767-29784854	K562	blood:	n/a	chr22:29784290-29784306
23	BHLHE40	chr22:29779081-29779149	K562	blood:	n/a	n/a
24	BRCA1	chr22:29784309-29784324	HepG2	liver:	n/a	n/a
25	BRCA1	chr22:29784487-29784668	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr22:29791082-29791132	HepG2	liver:	n/a	n/a
27	CBX3	chr22:29784370-29784766	K562	blood:	n/a	n/a
28	CCNT2	chr22:29784213-29784825	K562	blood:	n/a	n/a
29	CCNT2	chr22:29778935-29779230	K562	blood:	n/a	n/a
30	CEBPB	chr22:29805054-29805264	MCF-7	breast:	n/a	chr22:29805152-29805163
31	CEBPB	chr22:29804956-29805312	K562	blood:	n/a	chr22:29805152-29805163
32	CEBPB	chr22:29765427-29765877	A549	lung:	n/a	n/a
33	CEBPB	chr22:29771539-29771762	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr22:29771521-29771829	MCF-7	breast:	n/a	n/a
35	CEBPB	chr22:29773811-29774403	MCF-7	breast:	n/a	n/a
36	CEBPB	chr22:29771466-29771819	IMR90	lung:	n/a	n/a
37	CEBPB	chr22:29765380-29765923	K562	blood:	n/a	n/a
38	CEBPB	chr22:29805051-29805224	K562	blood:	n/a	chr22:29805152-29805163
39	CEBPB	chr22:29765351-29765917	IMR90	lung:	n/a	n/a
40	CEBPB	chr22:29773211-29773460	MCF-7	breast:	n/a	n/a
41	CEBPB	chr22:29771588-29771690	A549	lung:	n/a	n/a
42	CEBPB	chr22:29765357-29765938	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr22:29784560-29784804	K562	blood:	n/a	n/a
44	CEBPB	chr22:29765707-29765808	HepG2	liver:	n/a	n/a
45	CEBPB	chr22:29784541-29784752	HepG2	liver:	n/a	n/a
46	CEBPB	chr22:29804972-29805323	K562	blood:	n/a	chr22:29805152-29805163
47	CEBPB	chr22:29791176-29791249	K562	blood:	n/a	n/a
48	CEBPB	chr22:29765292-29765790	ECC-1	luminal epithelium:	n/a	n/a
49	CEBPB	chr22:29765399-29765731	K562	blood:	n/a	n/a
50	CEBPB	chr22:29784634-29784925	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:29784441-29784491	AG10803	skin:	n/a
2	chr22:29784697-29784747	PANC-1	pancreas:	n/a
3	chr22:29784441-29784491	AG10803	skin:	n/a
4	chr22:29784697-29784747	PANC-1	pancreas:	n/a
5	chr22:29784237-29784287	PFSK-1	brain:	n/a
6	chr22:29784671-29784721	AG04450	lung:	fetal
7	chr22:29784624-29784674	A549	lung:	n/a
8	chr22:29783861-29783911	HNPCEpiC	eye:	n/a
9	chr22:29784644-29784694	HPAEpiC	pulmonary alveolar:	n/a
10	chr22:29784694-29784744	AG09309	skin:	n/a
11	chr22:29785355-29785405	HEK293	kidney:	embryo
12	chr22:29783861-29783911	NHBE	bronchial:	n/a
13	chr22:29784692-29784742	AG09309	skin:	n/a
14	chr22:29784237-29784287	AoSMC	blood vessel:	n/a
15	chr22:29783861-29783911	GM06990	blood:	n/a
16	chr22:29784671-29784721	GM12891	blood:	n/a
17	chr22:29784441-29784491	NHBE	bronchial:	n/a
18	chr22:29784624-29784674	ECC-1	luminal epithelium:	n/a
19	chr22:29784692-29784742	HPAEpiC	pulmonary alveolar:	n/a
20	chr22:29784694-29784744	AG04449	skin:	fetal
21	chr22:29784237-29784287	NHDF-neo	bronchial:	n/a
22	chr22:29784692-29784742	MCF10A-Er-Src	breast:	n/a
23	chr22:29784697-29784747	BJ	skin:	n/a
24	chr22:29784778-29784828	HCPEpiC	choroid plexus:	n/a
25	chr22:29784644-29784694	GM12892	blood:	n/a
26	chr22:29781841-29781891	CMK	blood:	n/a
27	chr22:29784697-29784747	AG04450	lung:	fetal
28	chr22:29784237-29784287	HMEC	breast:	n/a
29	chr22:29784778-29784828	ECC-1	luminal epithelium:	n/a
30	chr22:29784624-29784674	HRE	kidney:	n/a
31	chr22:29784697-29784747	AG04449	skin:	fetal
32	chr22:29784813-29784863	IMR90	lung:	fetal
33	chr22:29784436-29784486	Jurkat	blood:	n/a
34	chr22:29784692-29784742	HNPCEpiC	eye:	n/a
35	chr22:29784671-29784721	HNPCEpiC	eye:	n/a
36	chr22:29784671-29784721	HCM	heart:	n/a
37	chr22:29781841-29781891	HEEpiC	esophagus:	n/a
38	chr22:29784694-29784744	PFSK-1	brain:	n/a
39	chr22:29784813-29784863	Hela-S3	cervix:	n/a
40	chr22:29784624-29784674	K562	blood:	n/a
41	chr22:29784644-29784694	LNCaP	prostate:	n/a
42	chr22:29784237-29784287	HRE	kidney:	n/a
43	chr22:29787625-29787675	NHDF-neo	bronchial:	n/a
44	chr22:29784624-29784674	HCT-116	colon:	n/a
45	chr22:29781841-29781891	PFSK-1	brain:	n/a
46	chr22:29784441-29784491	GM12891	blood:	n/a
47	chr22:29785355-29785405	ECC-1	luminal epithelium:	n/a
48	chr22:29784671-29784721	AG09309	skin:	n/a
49	chr22:29784644-29784694	HepG2	liver:	n/a
50	chr22:29784671-29784721	NB4	blood:	n/a

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr22:29780907..29784157-chr22:29912302..29916422,4	MCF-7	breast:
2	chr22:29774091..29774727-chr22:29781651..29782814,5	MCF-7	breast:
3	chr22:29771983..29774340-chr22:29774881..29776429,2	K562	blood:
4	chr22:29712026..29714411-chr22:29782149..29784555,3	K562	blood:
5	chr22:29780492..29782846-chr22:29865528..29867159,2	MCF-7	breast:
6	chr22:29786384..29789088-chr22:29790926..29793690,2	K562	blood:
7	chr22:29787252..29790791-chr22:29920718..29924086,3	MCF-7	breast:
8	chr22:29760830..29763484-chr22:29765100..29766942,2	K562	blood:
9	chr22:29704896..29707829-chr22:29780262..29782390,2	MCF-7	breast:
10	chr22:29775197..29780621-chr22:29782246..29785885,8	K562	blood:
11	chr22:29209443..29210342-chr22:29781715..29782736,4	MCF-7	breast:
12	chr22:29774141..29774748-chr22:29913157..29913945,3	MCF-7	breast:
13	chr22:29704102..29706466-chr22:29771552..29773376,2	MCF-7	breast:
14	chr22:29781890..29782717-chr22:29913055..29913918,8	MCF-7	breast:
15	chr22:29790656..29791686-chr22:29920171..29921137,10	MCF-7	breast:
16	chr22:29790720..29791562-chr22:29920209..29921282,4	MCF-7	breast:
17	chr22:29792125..29793668-chr22:29802474..29805006,2	K562	blood:
18	chr22:29801402..29803143-chr22:32549344..32551299,2	K562	blood:
19	chr22:29784630..29786169-chr22:29786224..29787893,2	K562	blood:
20	chr22:29770782..29772689-chr22:29780811..29782872,2	K562	blood:
21	chr22:29771666..29773871-chr22:29789734..29792185,2	MCF-7	breast:
22	chr22:29771731..29774347-chr22:29784237..29785863,2	MCF-7	breast:
23	chr22:29786384..29789088-chr22:29790926..29793690,2	K562	blood:
24	chr22:29774109..29774727-chr22:29781778..29782854,8	MCF-7	breast:
25	chr22:29771898..29775582-chr22:29781742..29783845,4	MCF-7	breast:
26	chr22:29781864..29782673-chr22:29877575..29878342,2	MCF-7	breast:
27	chr22:29771666..29773871-chr22:29789734..29792185,2	MCF-7	breast:
28	chr22:29774091..29774727-chr22:29781651..29782814,5	MCF-7	breast:
29	chr22:29708527..29710108-chr22:29782946..29784507,2	K562	blood:
30	chr22:29784630..29786169-chr22:29786224..29787893,2	K562	blood:
31	chr22:29791047..29793663-chr22:29794223..29797120,2	MCF-7	breast:
32	chr22:29773835..29774566-chr22:29913414..29914007,2	MCF-7	breast:
33	chr22:29784558..29786360-chr22:29786552..29791390,4	MCF-7	breast:
34	chr22:29771898..29775582-chr22:29781742..29783845,4	MCF-7	breast:
35	chr22:29778467..29780035-chr22:29782839..29784624,2	MCF-7	breast:
36	chr22:29770398..29771976-chr22:29778753..29780431,2	K562	blood:
37	chr22:29792125..29793668-chr22:29802474..29805006,2	K562	blood:
38	chr22:29777011..29779930-chr22:29821335..29822984,2	K562	blood:
39	chr22:29739232..29740930-chr22:29780922..29783404,2	MCF-7	breast:
40	chr22:29781675..29783812-chr22:29788035..29790235,2	MCF-7	breast:
41	chr22:29792519..29794058-chr22:29864789..29867115,2	MCF-7	breast:
42	chr22:29782601..29785697-chr22:29975164..29978533,5	MCF-7	breast:
43	chr22:29781310..29782787-chr22:29913055..29914130,15	MCF-7	breast:
44	chr22:29783197..29785326-chr22:29874558..29877420,2	MCF-7	breast:
45	chr22:29764682..29767147-chr22:29767285..29770224,2	MCF-7	breast:
46	chr22:29774954..29777707-chr22:29779123..29781815,2	K562	blood:
47	chr22:29783150..29785946-chr22:29944649..29946343,2	MCF-7	breast:
48	chr22:29664123..29665985-chr22:29772545..29774915,2	MCF-7	breast:
49	chr22:29781675..29783812-chr22:29788035..29790235,2	MCF-7	breast:
50	chr22:29794482..29794991-chr22:29913162..29914018,2	MCF-7	breast:

No data

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

Extended variants
information (count: 1487 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1487 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55829919	chr22:29763586-29763587	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs5763167	chr22:29763607-29763608	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs397832698	chr22:29763655-29763656	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs11703979	chr22:29763677-29763678	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs434287	chr22:29763733-29763734	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs145991559	chr22:29763760-29763761	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs565170842	chr22:29763761-29763762	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs184408818	chr22:29763798-29763799	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs544216029	chr22:29763813-29763814	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs560687004	chr22:29763900-29763901	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs547961907	chr22:29763905-29763906	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs114247226	chr22:29763922-29763923	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs139523682	chr22:29763979-29763980	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs117488182	chr22:29763980-29763981	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs149688672	chr22:29764001-29764002	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs7286220	chr22:29764004-29764005	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs539901226	chr22:29764057-29764058	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs79487870	chr22:29764087-29764088	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569810196	chr22:29764097-29764098	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs530744691	chr22:29764128-29764129	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs560435708	chr22:29764148-29764149	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144457179	chr22:29764178-29764179	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189430419	chr22:29764226-29764227	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs560861101	chr22:29764428-29764429	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141319385	chr22:29764468-29764469	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552659047	chr22:29764504-29764505	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs148401875	chr22:29764583-29764584	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532338307	chr22:29764596-29764597	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs554894246	chr22:29764618-29764619	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542817282	chr22:29764687-29764688	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181237687	chr22:29764697-29764698	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs3044030	chr22:29764702-29764703	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs397836413	chr22:29764706-29764707	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543802139	chr22:29764730-29764731	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376102714	chr22:29764745-29764746	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561549462	chr22:29764746-29764747	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559203010	chr22:29764813-29764814	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs577316478	chr22:29764823-29764824	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs738903	chr22:29764836-29764837	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs531480803	chr22:29764896-29764897	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs530243747	chr22:29764922-29764923	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs148054188	chr22:29764930-29764931	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs542292028	chr22:29764969-29764970	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs145704136	chr22:29764975-29764976	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs530726928	chr22:29765042-29765043	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs147747312	chr22:29765075-29765076	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs542003116	chr22:29765101-29765102	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs142588278	chr22:29765102-29765103	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs528089838	chr22:29765114-29765115	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs144842227	chr22:29765120-29765121	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 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:1990 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29723000-29765000	Strong transcription	Primary T helper cells fromperipheralblood	blood
2	chr22:29741000-29782800	Weak transcription	Hela-S3	cervix
3	chr22:29745000-29765200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr22:29750600-29765200	Weak transcription	NHDF-Ad	bronchial
5	chr22:29750600-29766800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr22:29750800-29764400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr22:29753000-29777600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr22:29754600-29770400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr22:29754800-29765200	Weak transcription	HSMM	muscle
10	chr22:29755000-29765200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr22:29755000-29772200	Weak transcription	Aorta	Aorta
12	chr22:29755000-29783800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr22:29755200-29765000	Weak transcription	NH-A	brain
14	chr22:29755200-29773800	Weak transcription	Stomach Mucosa	stomach
15	chr22:29755200-29781000	Weak transcription	Fetal Brain Male	brain
16	chr22:29755200-29782800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr22:29755400-29764600	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr22:29755400-29765400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr22:29755400-29783600	Weak transcription	Fetal Kidney	kidney
20	chr22:29755600-29763800	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr22:29755600-29763800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr22:29755600-29771400	Weak transcription	Psoas Muscle	Psoas
23	chr22:29755600-29778600	Weak transcription	Fetal Lung	lung
24	chr22:29755800-29776600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr22:29756000-29764000	Weak transcription	Brain Substantia Nigra	brain
26	chr22:29756000-29764200	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr22:29756000-29764400	Weak transcription	Brain Angular Gyrus	brain
28	chr22:29756000-29764400	Weak transcription	NHEK	skin
29	chr22:29756000-29764600	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr22:29756000-29764600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr22:29756000-29764600	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr22:29756000-29765200	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr22:29756000-29765200	Weak transcription	HepG2	liver
34	chr22:29756000-29765200	Weak transcription	Osteobl	bone
35	chr22:29756000-29765400	Weak transcription	A549	lung
36	chr22:29756000-29766400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr22:29756000-29766400	Weak transcription	Stomach Smooth Muscle	stomach
38	chr22:29756000-29766600	Weak transcription	Pancreas	Pancrea
39	chr22:29756000-29769000	Weak transcription	Gastric	stomach
40	chr22:29756000-29771400	Weak transcription	Esophagus	oesophagus
41	chr22:29756000-29771400	Weak transcription	HMEC	breast
42	chr22:29756000-29771800	Weak transcription	NHLF	lung
43	chr22:29756000-29772200	Weak transcription	Right Atrium	heart
44	chr22:29756000-29776200	Weak transcription	Small Intestine	intestine
45	chr22:29756000-29779800	Weak transcription	Brain Germinal Matrix	brain
46	chr22:29756000-29783600	Weak transcription	Right Ventricle	heart
47	chr22:29756000-29783800	Weak transcription	Ovary	ovary
48	chr22:29756200-29764600	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr22:29756200-29764600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr22:29756200-29764800	Weak transcription	Rectal Smooth Muscle	rectum

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