Variant report

Variant	esv3326694
Chromosome Location	chr7:5795518-5852599
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1182)
CpG islands
(count:1405)
Chromatin interactive
region (count:38)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1182 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:5821215-5821617	K562	blood:	n/a	n/a
2	ARID3A	chr7:5807434-5807806	HepG2	liver:	n/a	chr7:5807779-5807795
3	ARID3A	chr7:5795066-5795627	K562	blood:	n/a	n/a
4	ARID3A	chr7:5813469-5813783	K562	blood:	n/a	n/a
5	ARID3A	chr7:5821223-5821516	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:5837477-5837688	K562	blood:	n/a	n/a
7	ARID3A	chr7:5826122-5826510	K562	blood:	n/a	n/a
8	ATF1	chr7:5795291-5795600	K562	blood:	n/a	n/a
9	ATF1	chr7:5826182-5826466	K562	blood:	n/a	n/a
10	ATF1	chr7:5837427-5837729	K562	blood:	n/a	n/a
11	ATF1	chr7:5821130-5821587	K562	blood:	n/a	n/a
12	ATF2	chr7:5821065-5821572	GM12878	blood:	n/a	n/a
13	ATF2	chr7:5821109-5821583	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr7:5821082-5821515	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr7:5813323-5813726	K562	blood:	n/a	chr7:5813565-5813579
16	ATF3	chr7:5826108-5826365	K562	blood:	n/a	n/a
17	ATF3	chr7:5821176-5821637	A549	lung:	n/a	n/a
18	ATF3	chr7:5826145-5826345	K562	blood:	n/a	n/a
19	ATF3	chr7:5821109-5821676	A549	lung:	n/a	n/a
20	ATF3	chr7:5821100-5821451	K562	blood:	n/a	n/a
21	BACH1	chr7:5821155-5821414	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr7:5795391-5795591	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr7:5810847-5810938	K562	blood:	n/a	n/a
24	BACH1	chr7:5795215-5795679	K562	blood:	n/a	n/a
25	BCL3	chr7:5821019-5821639	A549	lung:	n/a	chr7:5821285-5821298 chr7:5821316-5821324
26	BCL3	chr7:5821185-5821680	A549	lung:	n/a	chr7:5821285-5821298 chr7:5821316-5821324
27	BCLAF1	chr7:5821091-5821689	K562	blood:	n/a	chr7:5821285-5821298 chr7:5821316-5821324
28	BCLAF1	chr7:5821070-5821753	GM12878	blood:	n/a	chr7:5821285-5821298 chr7:5821316-5821324
29	BCLAF1	chr7:5821069-5821672	K562	blood:	n/a	chr7:5821285-5821298 chr7:5821316-5821324
30	BCLAF1	chr7:5821040-5821673	GM12878	blood:	n/a	chr7:5821285-5821298 chr7:5821316-5821324
31	BHLHE40	chr7:5830403-5830547	A549	lung:	n/a	n/a
32	BHLHE40	chr7:5817625-5817897	GM12878	blood:	n/a	n/a
33	BHLHE40	chr7:5821157-5821452	HepG2	liver:	n/a	n/a
34	BHLHE40	chr7:5795306-5795596	K562	blood:	n/a	n/a
35	BHLHE40	chr7:5820771-5820774	K562	blood:	n/a	n/a
36	BHLHE40	chr7:5826102-5826422	K562	blood:	n/a	n/a
37	BHLHE40	chr7:5821124-5821604	K562	blood:	n/a	chr7:5821155-5821171
38	BHLHE40	chr7:5821108-5821597	GM12878	blood:	n/a	chr7:5821155-5821171
39	BRCA1	chr7:5821213-5821484	HepG2	liver:	n/a	n/a
40	BRCA1	chr7:5821222-5821465	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr7:5820533-5820584	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr7:5813381-5813721	Hela-S3	cervix:	n/a	n/a
43	CBX3	chr7:5813239-5813778	K562	blood:	n/a	n/a
44	CBX3	chr7:5821114-5821700	K562	blood:	n/a	n/a
45	CBX3	chr7:5820938-5821793	HCT-116	colon:	n/a	n/a
46	CBX3	chr7:5821041-5822095	K562	blood:	n/a	n/a
47	CBX3	chr7:5825939-5826501	K562	blood:	n/a	n/a
48	CBX3	chr7:5813109-5813866	HCT-116	colon:	n/a	n/a
49	CBX3	chr7:5821023-5821768	HCT-116	colon:	n/a	n/a
50	CCNT2	chr7:5795407-5795596	K562	blood:	n/a	n/a

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5821227-5821277	HAEpiC	amniotic membrane:	n/a
2	chr7:5821596-5821646	HL-60	blood:	n/a
3	chr7:5821227-5821277	HAEpiC	amniotic membrane:	n/a
4	chr7:5821596-5821646	HL-60	blood:	n/a
5	chr7:5821313-5821363	GM12892	blood:	n/a
6	chr7:5812747-5812797	HEEpiC	esophagus:	n/a
7	chr7:5821297-5821347	HRPEpiC	eye:	n/a
8	chr7:5822206-5822256	HRCEpiC	kidney:	n/a
9	chr7:5834292-5834342	HNPCEpiC	eye:	n/a
10	chr7:5812747-5812797	AG04449	skin:	fetal
11	chr7:5821500-5821550	BE2_C	brain:	n/a
12	chr7:5821500-5821550	Hepatocyte	liver:	n/a
13	chr7:5825437-5825487	ProgFib	skin:	n/a
14	chr7:5821294-5821344	HRE	kidney:	n/a
15	chr7:5821313-5821363	HPAEpiC	pulmonary alveolar:	n/a
16	chr7:5821307-5821357	AG09319	gingival:	n/a
17	chr7:5812747-5812797	HCF	heart:	n/a
18	chr7:5834372-5834422	IMR90	lung:	fetal
19	chr7:5833383-5833433	NB4	blood:	n/a
20	chr7:5825437-5825487	GM19239	blood:	n/a
21	chr7:5821307-5821357	H1-hESC	embryonic stem cell:	embryo
22	chr7:5834292-5834342	CMK	blood:	n/a
23	chr7:5833383-5833433	ProgFib	skin:	n/a
24	chr7:5822206-5822256	HEEpiC	esophagus:	n/a
25	chr7:5821313-5821363	ovcar-3	ovarian:	n/a
26	chr7:5821320-5821370	GM12892	blood:	n/a
27	chr7:5821500-5821550	IMR90	lung:	fetal
28	chr7:5821294-5821344	SK-N-MC	brain:	n/a
29	chr7:5806497-5806547	HIPEpiC	eye:	n/a
30	chr7:5821320-5821370	SK-N-SH_RA	brain:	n/a
31	chr7:5821305-5821355	HL-60	blood:	n/a
32	chr7:5821307-5821357	AG10803	skin:	n/a
33	chr7:5820542-5820592	HCF	heart:	n/a
34	chr7:5833275-5833325	HCT-116	colon:	n/a
35	chr7:5834292-5834342	HCM	heart:	n/a
36	chr7:5833444-5833494	GM12878	blood:	n/a
37	chr7:5821305-5821355	GM19239	blood:	n/a
38	chr7:5812747-5812797	HL-60	blood:	n/a
39	chr7:5834292-5834342	NH-A	brain:	n/a
40	chr7:5821500-5821550	AG09319	gingival:	n/a
41	chr7:5833383-5833433	GM06990	blood:	n/a
42	chr7:5821500-5821550	PFSK-1	brain:	n/a
43	chr7:5833383-5833433	AG04450	lung:	fetal
44	chr7:5834425-5834475	Jurkat	blood:	n/a
45	chr7:5819198-5819248	Jurkat	blood:	n/a
46	chr7:5821320-5821370	ovcar-3	ovarian:	n/a
47	chr7:5825437-5825487	HRE	kidney:	n/a
48	chr7:5821099-5821149	HCF	heart:	n/a
49	chr7:5834292-5834342	HMEC	breast:	n/a
50	chr7:5834425-5834475	PrEC	prostate:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:5813104..5816450-chr7:5816759..5819412,5	MCF-7	breast:
2	chr7:5790125..5792090-chr7:5812066..5813881,3	K562	blood:
3	chr7:5805613..5808202-chr7:5812244..5816146,3	K562	blood:
4	chr7:5812370..5815650-chr7:5819494..5823462,5	K562	blood:
5	chr7:5013311..5013911-chr7:5820908..5821412,3	HCT-116	colon:
6	chr7:5012931..5013720-chr7:5820910..5821674,3	MCF-7	breast:
7	chr7:5811498..5815650-chr7:5819399..5823462,6	K562	blood:
8	chr7:5012695..5014428-chr7:5820890..5822170,10	MCF-7	breast:
9	chr6:74233083..74233652-chr7:5820678..5821633,2	Hela-S3	cervix:
10	chr7:5792453..5794631-chr7:5795297..5797484,2	K562	blood:
11	chr7:5802352..5803887-chr7:5805406..5807643,2	MCF-7	breast:
12	chr7:5198471..5200829-chr7:5846767..5848341,2	MCF-7	breast:
13	chr7:5805613..5808202-chr7:5813571..5816146,2	K562	blood:
14	chr7:5805043..5806822-chr7:5811285..5813063,2	MCF-7	breast:
15	chr7:5798985..5801479-chr7:5819651..5822590,2	MCF-7	breast:
16	chr7:5569817..5572389-chr7:5795762..5797317,2	K562	blood:
17	chr7:5782625..5785209-chr7:5794939..5796627,2	K562	blood:
18	chr7:5012217..5014206-chr7:5819722..5821650,2	MCF-7	breast:
19	chr7:5813104..5816450-chr7:5816759..5819412,5	MCF-7	breast:
20	chr7:5798985..5801479-chr7:5819651..5822590,2	MCF-7	breast:
21	chr7:5794825..5797015-chr7:5812858..5815077,2	K562	blood:
22	chr7:5804467..5808977-chr7:5818984..5822702,6	MCF-7	breast:
23	chr7:5794825..5797015-chr7:5812858..5815077,2	K562	blood:
24	chr7:5805043..5806822-chr7:5811285..5813063,2	MCF-7	breast:
25	chr7:5013565..5014445-chr7:5820432..5821785,4	K562	blood:
26	chr7:5810649..5812378-chr7:5816522..5818185,2	K562	blood:
27	chr7:5805613..5808202-chr7:5813571..5816146,2	K562	blood:
28	chr7:5816356..5819327-chr7:5819768..5821296,2	MCF-7	breast:
29	chr7:5012944..5014466-chr7:5819776..5821589,2	MCF-7	breast:
30	chr7:5805613..5808202-chr7:5812244..5816146,3	K562	blood:
31	chr7:5195253..5196797-chr7:5849975..5851503,2	MCF-7	breast:
32	chr7:5810649..5812378-chr7:5816522..5818185,2	K562	blood:
33	chr7:5814291..5819419-chr7:5819714..5822624,8	MCF-7	breast:
34	chr7:5802352..5803887-chr7:5805406..5807643,2	MCF-7	breast:
35	chr7:5012284..5014483-chr7:5819277..5821280,2	K562	blood:
36	chr7:5795115..5796838-chr7:5800518..5802402,2	K562	blood:
37	chr7:5013249..5014674-chr7:5819932..5821408,8	Hela-S3	cervix:
38	chr7:5012983..5015694-chr7:5819277..5821133,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OCM-1	chr7:5850593-5850617	NONHSAT118937
2	lnc-OCM-1	chr7:5834113-5834518	XLOC_005976
3	lnc-RSPH10B-2	chr7:5817118-5817259	NONHSAT118935
4	lnc-RSPH10B-2	chr7:5806526-5806570	NONHSAT118935
5	lnc-OCM-1	chr7:5834113-5834518	XLOC_005976
6	lnc-RSPH10B-2	chr7:5819616-5819899	NONHSAT118936
7	lnc-RSPH10B-2	chr7:5800719-5800769	NONHSAT118935
8	lnc-RSPH10B-2	chr7:5817157-5817259	NONHSAT118936
9	lnc-OCM-1	chr7:5850594-5850617	XLOC_005976
10	lnc-RSPH10B-2	chr7:5819616-5819923	NONHSAT118935
11	lnc-OCM-1	chr7:5834112-5834518	NONHSAT118937

No data

Variant related genes	Relation type
RNF216	TF binding region
RNF216	CpG island
ENSG00000011275	chromatin interactions
ENSG00000229862	chromatin interactions
ENSG00000156508	chromatin interactions
ENSG00000075624	chromatin interactions
ENSG00000196204	chromatin interactions
NR3C1	miRNA target sites

Extended variants
information (count: 3194 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3194 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564018794	chr7:5795543-5795544	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs75064103	chr7:5795573-5795574	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs72564340	chr7:5795610-5795611	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs35288893	chr7:5795611-5795612	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs371692506	chr7:5795612-5795613	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs200949911	chr7:5795637-5795638	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs543221962	chr7:5795650-5795651	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs551730020	chr7:5795675-5795676	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs529413452	chr7:5795682-5795683	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs547859856	chr7:5795690-5795691	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs565971031	chr7:5795697-5795698	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs533336313	chr7:5795699-5795700	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs546031648	chr7:5795703-5795704	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs111676958	chr7:5795727-5795728	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs570379939	chr7:5795738-5795739	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs537701363	chr7:5795739-5795740	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs370109940	chr7:5795744-5795745	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs376251541	chr7:5795751-5795752	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs576148029	chr7:5795767-5795768	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs144141253	chr7:5795772-5795773	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs186478425	chr7:5795830-5795831	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs4720639	chr7:5795891-5795892	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs553815267	chr7:5795893-5795894	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs189398542	chr7:5795906-5795907	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs539068852	chr7:5795927-5795928	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs117547683	chr7:5795939-5795940	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs537770516	chr7:5795962-5795963	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs575933253	chr7:5795973-5795974	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs146343316	chr7:5795999-5796000	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs547402355	chr7:5796000-5796001	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs564820542	chr7:5796022-5796023	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs561774769	chr7:5796028-5796029	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs375382980	chr7:5796038-5796039	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs573761958	chr7:5796055-5796056	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs574104046	chr7:5796135-5796136	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs541191898	chr7:5796186-5796187	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs4724722	chr7:5796227-5796228	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs139067537	chr7:5796228-5796229	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs375634424	chr7:5796287-5796288	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs551810513	chr7:5796296-5796297	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs563628075	chr7:5796311-5796312	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs528743598	chr7:5796352-5796353	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs578065444	chr7:5796390-5796391	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs567798110	chr7:5796415-5796416	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs34267282	chr7:5796446-5796447	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs535198797	chr7:5796465-5796466	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs546851356	chr7:5796468-5796469	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs545182921	chr7:5796472-5796473	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs181759038	chr7:5796479-5796480	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs13237895	chr7:5796486-5796487	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:80)

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
Urothelial carcinoma	21177765	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
Multiple myeloma	17550852	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	21346763	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1410 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5762000-5820400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:5768800-5798200	Weak transcription	Colonic Mucosa	Colon
3	chr7:5774200-5800600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr7:5781400-5799600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr7:5781400-5816800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:5783600-5798200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr7:5784000-5819600	Weak transcription	Fetal Heart	heart
8	chr7:5784200-5798000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr7:5785200-5807000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr7:5786000-5798000	Weak transcription	Fetal Brain Male	brain
11	chr7:5790400-5800600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr7:5790400-5804600	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr7:5790800-5798200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr7:5790800-5798200	Weak transcription	Esophagus	oesophagus
15	chr7:5790800-5820400	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr7:5791000-5796200	Weak transcription	Ovary	ovary
17	chr7:5791000-5796400	Weak transcription	Fetal Intestine Small	intestine
18	chr7:5791000-5797200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr7:5791200-5798000	Weak transcription	Aorta	Aorta
20	chr7:5791400-5798200	Weak transcription	Fetal Brain Female	brain
21	chr7:5791400-5798200	Weak transcription	NHLF	lung
22	chr7:5792400-5797800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr7:5792400-5798200	Weak transcription	Brain Germinal Matrix	brain
24	chr7:5792600-5795600	Weak transcription	Fetal Intestine Large	intestine
25	chr7:5792600-5796200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr7:5792600-5796600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr7:5792600-5797200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr7:5792600-5798000	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr7:5792600-5798000	Weak transcription	Thymus	Thymus
30	chr7:5792600-5798200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr7:5792600-5798200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr7:5792600-5798200	Weak transcription	NH-A	brain
33	chr7:5792600-5798600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr7:5792600-5816600	Weak transcription	Right Ventricle	heart
35	chr7:5792800-5795800	Weak transcription	Fetal Muscle Leg	muscle
36	chr7:5792800-5796200	Weak transcription	Primary T cells from cord blood	blood
37	chr7:5792800-5796200	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr7:5792800-5796400	Weak transcription	GM12878-XiMat	blood
39	chr7:5792800-5796400	Weak transcription	NHEK	skin
40	chr7:5792800-5796600	Weak transcription	Liver	Liver
41	chr7:5792800-5796800	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr7:5792800-5796800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr7:5792800-5796800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr7:5792800-5796800	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr7:5792800-5797000	Weak transcription	Fetal Lung	lung
46	chr7:5792800-5797200	Weak transcription	Osteobl	bone
47	chr7:5792800-5797400	Weak transcription	Fetal Stomach	stomach
48	chr7:5792800-5797800	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr7:5792800-5798000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr7:5792800-5798000	Weak transcription	HepG2	liver

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