Variant report

Variant	nsv588878
Chromosome Location	chr22:28248840-28314113
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1309)
CpG islands
(count:244)
Chromatin interactive
region (count:60)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:1309 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:28309038-28309269	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:28282418-28282880	HepG2	liver:	n/a	n/a
3	ARID3A	chr22:28266094-28267208	HepG2	liver:	n/a	n/a
4	ARID3A	chr22:28276878-28277134	HepG2	liver:	n/a	n/a
5	ARID3A	chr22:28275978-28276275	HepG2	liver:	n/a	n/a
6	ARID3A	chr22:28309003-28309742	K562	blood:	n/a	n/a
7	ATF1	chr22:28309119-28309617	K562	blood:	n/a	n/a
8	ATF2	chr22:28291531-28292128	GM12878	blood:	n/a	n/a
9	ATF2	chr22:28292137-28292757	GM12878	blood:	n/a	n/a
10	ATF2	chr22:28291457-28292035	GM12878	blood:	n/a	n/a
11	ATF3	chr22:28282322-28282648	K562	blood:	n/a	chr22:28282452-28282467 chr22:28282452-28282465
12	BATF	chr22:28292226-28292595	GM12878	blood:	n/a	n/a
13	BATF	chr22:28291626-28292009	GM12878	blood:	n/a	n/a
14	BATF	chr22:28292157-28292605	GM12878	blood:	n/a	n/a
15	BATF	chr22:28291526-28292006	GM12878	blood:	n/a	n/a
16	BCL11A	chr22:28292260-28292610	GM12878	blood:	n/a	n/a
17	BCL11A	chr22:28273612-28273818	GM12878	blood:	n/a	n/a
18	BCL11A	chr22:28291598-28291955	GM12878	blood:	n/a	n/a
19	BCL11A	chr22:28292237-28292521	GM12878	blood:	n/a	n/a
20	BCL11A	chr22:28291655-28291924	GM12878	blood:	n/a	n/a
21	BCLAF1	chr22:28291999-28292659	GM12878	blood:	n/a	n/a
22	BHLHE40	chr22:28299850-28300263	GM12878	blood:	n/a	n/a
23	BHLHE40	chr22:28291353-28292650	GM12878	blood:	n/a	n/a
24	BHLHE40	chr22:28264914-28265236	GM12878	blood:	n/a	n/a
25	BRCA1	chr22:28261906-28263780	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr22:28306764-28306776	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr22:28292663-28292673	GM12878	blood:	n/a	n/a
28	CCNT2	chr22:28309133-28309692	K562	blood:	n/a	n/a
29	CCNT2	chr22:28307425-28307624	K562	blood:	n/a	n/a
30	CEBPB	chr22:28282070-28282766	IMR90	lung:	n/a	n/a
31	CEBPB	chr22:28249466-28249800	K562	blood:	n/a	n/a
32	CEBPB	chr22:28249479-28249808	A549	lung:	n/a	n/a
33	CEBPB	chr22:28249456-28249826	IMR90	lung:	n/a	n/a
34	CEBPB	chr22:28309052-28309566	K562	blood:	n/a	n/a
35	CEBPB	chr22:28262029-28262501	A549	lung:	n/a	chr22:28262218-28262231
36	CEBPB	chr22:28262016-28263097	IMR90	lung:	n/a	chr22:28262900-28262909 chr22:28262218-28262231 chr22:28262899-28262910 chr22:28262900-28262909
37	CEBPB	chr22:28262691-28263102	A549	lung:	n/a	chr22:28262900-28262909 chr22:28262899-28262910 chr22:28262900-28262909
38	CEBPB	chr22:28261961-28263516	Hela-S3	cervix:	n/a	chr22:28262900-28262909 chr22:28262218-28262231 chr22:28262899-28262910 chr22:28262900-28262909
39	CEBPB	chr22:28262679-28263024	HepG2	liver:	n/a	chr22:28262900-28262909 chr22:28262899-28262910 chr22:28262900-28262909
40	CEBPB	chr22:28262751-28263055	H1-hESC	embryonic stem cell:	n/a	chr22:28262900-28262909 chr22:28262899-28262910 chr22:28262900-28262909
41	CEBPB	chr22:28250791-28250980	HepG2	liver:	n/a	n/a
42	CEBPB	chr22:28262778-28262952	HepG2	liver:	n/a	chr22:28262900-28262909 chr22:28262899-28262910 chr22:28262900-28262909
43	CEBPB	chr22:28249510-28249774	MCF-7	breast:	n/a	n/a
44	CEBPB	chr22:28262693-28263098	HepG2	liver:	n/a	chr22:28262900-28262909 chr22:28262899-28262910 chr22:28262900-28262909
45	CEBPB	chr22:28255179-28255690	MCF-7	breast:	n/a	n/a
46	CEBPB	chr22:28256628-28256859	HepG2	liver:	n/a	chr22:28256738-28256750 chr22:28256712-28256723
47	CEBPB	chr22:28249585-28249786	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr22:28288080-28288442	HepG2	liver:	n/a	chr22:28288248-28288261 chr22:28288249-28288260
49	CEBPB	chr22:28255310-28255556	IMR90	lung:	n/a	n/a
50	CEBPB	chr22:28265836-28266170	IMR90	lung:	n/a	chr22:28266007-28266018

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:28249567-28249617	HMEC	breast:	n/a
2	chr22:28311714-28311764	CMK	blood:	n/a
3	chr22:28311714-28311764	BJ	skin:	n/a
4	chr22:28249567-28249617	GM12878	blood:	n/a
5	chr22:28280411-28280461	PrEC	prostate:	n/a
6	chr22:28311714-28311764	HRPEpiC	eye:	n/a
7	chr22:28311714-28311764	HCT-116	colon:	n/a
8	chr22:28280411-28280461	HMEC	breast:	n/a
9	chr22:28249567-28249617	PANC-1	pancreas:	n/a
10	chr22:28280359-28280409	T-47D	breast:	n/a
11	chr22:28280411-28280461	HL-60	blood:	n/a
12	chr22:28280411-28280461	PFSK-1	brain:	n/a
13	chr22:28280359-28280409	NT2-D1	testis:	n/a
14	chr22:28311714-28311764	AoSMC	blood vessel:	n/a
15	chr22:28280411-28280461	RPTEC	kidney:	n/a
16	chr22:28311714-28311764	T-47D	breast:	n/a
17	chr22:28311714-28311764	HUVEC	blood vessel:	n/a
18	chr22:28280359-28280409	HPAEpiC	pulmonary alveolar:	n/a
19	chr22:28311714-28311764	RPTEC	kidney:	n/a
20	chr22:28311714-28311764	HL-60	blood:	n/a
21	chr22:28311714-28311764	SK-N-SH_RA	brain:	n/a
22	chr22:28280411-28280461	NH-A	brain:	n/a
23	chr22:28249567-28249617	H1-hESC	embryonic stem cell:	embryo
24	chr22:28249567-28249617	HCT-116	colon:	n/a
25	chr22:28249567-28249617	LNCaP	prostate:	n/a
26	chr22:28249567-28249617	PrEC	prostate:	n/a
27	chr22:28311714-28311764	NH-A	brain:	n/a
28	chr22:28280411-28280461	ProgFib	skin:	n/a
29	chr22:28280359-28280409	U87	brain:	n/a
30	chr22:28280411-28280461	HNPCEpiC	eye:	n/a
31	chr22:28311714-28311764	HEEpiC	esophagus:	n/a
32	chr22:28249567-28249617	HPAEpiC	pulmonary alveolar:	n/a
33	chr22:28249567-28249617	GM19239	blood:	n/a
34	chr22:28280411-28280461	GM06990	blood:	n/a
35	chr22:28280359-28280409	HMEC	breast:	n/a
36	chr22:28280359-28280409	AG09309	skin:	n/a
37	chr22:28249567-28249617	PFSK-1	brain:	n/a
38	chr22:28280411-28280461	SK-N-SH	brain:	n/a
39	chr22:28280359-28280409	ECC-1	luminal epithelium:	n/a
40	chr22:28280359-28280409	GM12878	blood:	n/a
41	chr22:28249567-28249617	SK-N-SH_RA	brain:	n/a
42	chr22:28311714-28311764	ProgFib	skin:	n/a
43	chr22:28280411-28280461	AG10803	skin:	n/a
44	chr22:28249567-28249617	HIPEpiC	eye:	n/a
45	chr22:28249567-28249617	IMR90	lung:	fetal
46	chr22:28280359-28280409	CMK	blood:	n/a
47	chr22:28280411-28280461	HRPEpiC	eye:	n/a
48	chr22:28249567-28249617	GM12892	blood:	n/a
49	chr22:28311714-28311764	NHBE	bronchial:	n/a
50	chr22:28280411-28280461	A549	lung:	n/a

(count:60 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr22:28295028..28296560-chr22:28302255..28303933,2	K562	blood:
2	chr22:28296490..28297994-chr22:28315052..28317693,3	MCF-7	breast:
3	chr22:28288104..28290281-chr22:28296485..28298916,2	K562	blood:
4	chr22:28296920..28299668-chr22:28312010..28313621,2	K562	blood:
5	chr22:28278686..28280659-chr22:28281964..28283752,2	K562	blood:
6	chr22:28282458..28285409-chr22:28313416..28316132,4	MCF-7	breast:
7	chr22:28283009..28285381-chr22:28406270..28408539,2	MCF-7	breast:
8	chr22:28287234..28287912-chr22:28405296..28405956,2	MCF-7	breast:
9	chr22:28282285..28283174-chr22:28386700..28387606,3	K562	blood:
10	chr22:28277423..28279775-chr22:28284286..28285949,2	MCF-7	breast:
11	chr22:28296920..28299668-chr22:28312010..28313621,2	K562	blood:
12	chr22:28282292..28283627-chr22:28405010..28406031,9	MCF-7	breast:
13	chr22:28272869..28275526-chr22:28276490..28279131,2	K562	blood:
14	chr22:28296852..28298965-chr22:28300379..28302947,2	K562	blood:
15	chr22:28262052..28264776-chr22:28281551..28284390,2	MCF-7	breast:
16	chr22:28303429..28305158-chr22:28305808..28308439,2	K562	blood:
17	chr22:28301560..28304524-chr22:28307675..28309326,2	MCF-7	breast:
18	chr22:28253925..28256869-chr22:28259144..28262465,3	K562	blood:
19	chr22:28277423..28279775-chr22:28284286..28285949,2	MCF-7	breast:
20	chr22:28279841..28281808-chr22:28384681..28387461,2	K562	blood:
21	chr22:28288104..28290281-chr22:28295657..28298916,3	K562	blood:
22	chr22:28308235..28310167-chr22:28310580..28312213,2	MCF-7	breast:
23	chr22:28302387..28305058-chr22:28313431..28315998,3	MCF-7	breast:
24	chr22:28308235..28310167-chr22:28310580..28312213,2	MCF-7	breast:
25	chr22:28284462..28287110-chr22:28306843..28308571,2	K562	blood:
26	chr22:28305823..28310839-chr22:28313322..28318569,8	MCF-7	breast:
27	chr22:28284462..28287110-chr22:28306843..28308571,2	K562	blood:
28	chr22:28278788..28281432-chr22:28313283..28315949,2	MCF-7	breast:
29	chr22:28295306..28297742-chr22:28307525..28310849,3	MCF-7	breast:
30	chr22:28246691..28248368-chr22:28250166..28251740,2	K562	blood:
31	chr22:28276614..28277411-chr22:28398597..28399104,2	MCF-7	breast:
32	chr22:28272869..28275526-chr22:28276490..28279131,2	K562	blood:
33	chr22:28262052..28264776-chr22:28281551..28284390,2	MCF-7	breast:
34	chr22:28288104..28290281-chr22:28295657..28298916,3	K562	blood:
35	chr22:28296852..28298965-chr22:28300379..28302947,2	K562	blood:
36	chr22:28248595..28250412-chr22:28253357..28255056,2	K562	blood:
37	chr22:28309477..28311651-chr22:28318341..28320072,2	K562	blood:
38	chr22:28302292..28303953-chr22:28313832..28316495,2	MCF-7	breast:
39	chr22:28283637..28286512-chr22:28293366..28294906,2	MCF-7	breast:
40	chr22:28276059..28277066-chr22:28405009..28405550,3	K562	blood:
41	chr22:28287078..28287897-chr22:28332995..28334074,3	MCF-7	breast:
42	chr22:27801863..27802520-chr22:28276059..28277086,3	MCF-7	breast:
43	chr22:28282181..28282812-chr22:28405106..28405979,3	MCF-7	breast:
44	chr22:28282766..28284835-chr22:28303057..28305816,2	MCF-7	breast:
45	chr22:28279056..28281403-chr22:28286781..28288906,2	K562	blood:
46	chr22:28295306..28297742-chr22:28307525..28310849,3	MCF-7	breast:
47	chr22:28295028..28296560-chr22:28302255..28303933,2	K562	blood:
48	chr22:28278686..28280659-chr22:28281964..28283752,2	K562	blood:
49	chr22:28288104..28290281-chr22:28296485..28298916,2	K562	blood:
50	chr22:28248595..28250412-chr22:28253357..28255056,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MN1-8	chr22:28276022-28277106	NONHSAT084602

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	PITPNB	hsa-miR-181a-5p	chr22:28249073-28249095
2	PITPNB	hsa-miR-215-5p	chr22:28250829-28250823
3	PITPNB	hsa-miR-181a-5p	chr22:28250269-28250262
4	PITPNB	hsa-miR-193b-3p	chr22:28248989-28249009
5	PITPNB	hsa-miR-181a-5p	chr22:28248948-28248941
6	PITPNB	hsa-miR-192-5p	chr22:28250829-28250823

Variant related genes	Relation type
TTC28-AS1	TF binding region
PITPNB	TF binding region
TTC28-AS1	CpG island
PITPNB	CpG island
ENSG00000100154	chromatin interactions
ENSG00000180957	chromatin interactions
ENSG00000264073	chromatin interactions
ENSG00000235954	chromatin interactions

Extended variants
information (count: 2103 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2103 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116714418	chr22:28248840-28248841	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs200535513	chr22:28249076-28249077	Weak transcription Strong transcription Genic enhancers	miRNA target site	1 gene(s)	Overlapped CNVs	n/a
3	rs377157648	chr22:28249101-28249102	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs199651842	chr22:28249592-28249593	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs368262276	chr22:28249681-28249682	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373582751	chr22:28249864-28249865	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs202169708	chr22:28249923-28249924	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs138650673	chr22:28249930-28249931	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs116481815	chr22:28250172-28250173	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200320101	chr22:28250226-28250227	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs201980063	chr22:28250320-28250321	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs200221740	chr22:28250321-28250322	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs9625341	chr22:28250369-28250370	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs9625342	chr22:28250399-28250400	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs373113614	chr22:28250504-28250505	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs115485592	chr22:28250810-28250811	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs200533083	chr22:28250933-28250934	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs551652743	chr22:28251006-28251007	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs111616372	chr22:28251008-28251009	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs111939615	chr22:28251153-28251154	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs145330658	chr22:28251158-28251159	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs373863136	chr22:28251178-28251179	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs202075029	chr22:28251182-28251183	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs73880342	chr22:28251260-28251261	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571409794	chr22:28251311-28251312	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs370757704	chr22:28251444-28251445	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs114960948	chr22:28251512-28251513	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111890777	chr22:28251572-28251573	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs5762386	chr22:28251684-28251685	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs200377706	chr22:28251708-28251709	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs376274343	chr22:28251730-28251731	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs115981934	chr22:28251843-28251844	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs113973389	chr22:28251886-28251887	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534004693	chr22:28251906-28251907	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs115714187	chr22:28252040-28252041	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs111882246	chr22:28252044-28252045	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs116674916	chr22:28252047-28252048	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs368240323	chr22:28252217-28252218	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs375442648	chr22:28252272-28252273	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs553656689	chr22:28252438-28252439	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573756069	chr22:28252514-28252515	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs200505470	chr22:28252551-28252552	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs114939048	chr22:28252565-28252566	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs116178225	chr22:28252687-28252688	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs200780655	chr22:28252690-28252691	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs202068440	chr22:28252765-28252766	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs536386967	chr22:28252780-28252781	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs367907679	chr22:28252952-28252953	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs372514022	chr22:28253198-28253199	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs199872809	chr22:28253225-28253226	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Breast cancer	21509527	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
Breast cancer	21785460	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
Ovine squamous-cell carcinoma	17599052	CNVD
Cat eye syndrome	16708226	CNVD
Olfactory neuroblastoma	18408657	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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD

Chromatin state (count:3437 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:28238800-28255200	Weak transcription	Stomach Mucosa	stomach
2	chr22:28239200-28259400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr22:28239600-28250800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr22:28240400-28254800	Strong transcription	Primary T cells from cord blood	blood
5	chr22:28240800-28258400	Strong transcription	Thymus	Thymus
6	chr22:28241200-28249600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr22:28241400-28257800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr22:28241400-28261600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr22:28241600-28258000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr22:28242000-28253400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr22:28242000-28259400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr22:28242200-28249400	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr22:28242200-28259000	Strong transcription	Primary T cells fromperipheralblood	blood
14	chr22:28242200-28259400	Strong transcription	Primary T helper cells PMA-I stimulated	--
15	chr22:28242400-28263200	Strong transcription	GM12878-XiMat	blood
16	chr22:28242600-28249400	Strong transcription	HSMM	muscle
17	chr22:28242600-28249600	Strong transcription	Primary neutrophils fromperipheralblood	blood
18	chr22:28242600-28249600	Strong transcription	Muscle Satellite Cultured Cells	--
19	chr22:28242600-28258200	Strong transcription	Rectal Mucosa Donor 29	rectum
20	chr22:28242600-28259200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
21	chr22:28242600-28259400	Strong transcription	NHEK	skin
22	chr22:28242800-28255200	Strong transcription	Duodenum Mucosa	Duodenum
23	chr22:28242800-28259400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr22:28243200-28256400	Strong transcription	Primary B cells from cord blood	blood
25	chr22:28243800-28256200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr22:28243800-28259600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr22:28243800-28274000	Strong transcription	Dnd41	blood
28	chr22:28244000-28249400	Strong transcription	Primary monocytes fromperipheralblood	blood
29	chr22:28244000-28261800	Strong transcription	HMEC	breast
30	chr22:28244000-28263600	Strong transcription	Primary T helper cells fromperipheralblood	blood
31	chr22:28244200-28254200	Strong transcription	A549	lung
32	chr22:28244200-28264200	Strong transcription	Primary B cells from peripheral blood	blood
33	chr22:28245000-28249800	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr22:28245400-28250000	Strong transcription	Fetal Intestine Large	intestine
35	chr22:28245400-28255000	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr22:28245800-28249600	Strong transcription	Colonic Mucosa	Colon
37	chr22:28246000-28249000	Strong transcription	Brain Inferior Temporal Lobe	brain
38	chr22:28246000-28252000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr22:28246200-28254000	Strong transcription	Sigmoid Colon	Sigmoid Colon
40	chr22:28246400-28249400	Strong transcription	NHLF	lung
41	chr22:28246400-28249600	Strong transcription	Osteobl	bone
42	chr22:28246400-28254400	Strong transcription	Rectal Mucosa Donor 31	rectum
43	chr22:28246400-28255000	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr22:28246400-28259400	Strong transcription	Placenta	Placenta
45	chr22:28246600-28249000	Strong transcription	Stomach Smooth Muscle	stomach
46	chr22:28246600-28249200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr22:28246600-28249400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr22:28246600-28249600	Strong transcription	Brain Anterior Caudate	brain
49	chr22:28246600-28249800	Strong transcription	Brain Angular Gyrus	brain
50	chr22:28246600-28249800	Strong transcription	Esophagus	oesophagus

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