Variant report

Variant	esv3437839
Chromosome Location	chr1:63152564-63156062
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:619)
CpG islands
(count:427)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:619 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:63153903-63154123	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:63155138-63157154	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:63153014-63153399	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:63155854-63156261	K562	blood:	n/a	n/a
5	ATF1	chr1:63155923-63156556	K562	blood:	n/a	n/a
6	ATF2	chr1:63153966-63154538	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr1:63155903-63156411	K562	blood:	n/a	n/a
8	BCLAF1	chr1:63155871-63156403	K562	blood:	n/a	n/a
9	BCLAF1	chr1:63153932-63154386	GM12878	blood:	n/a	n/a
10	BCLAF1	chr1:63153878-63154436	GM12878	blood:	n/a	chr1:63154385-63154394
11	BHLHE40	chr1:63153813-63154292	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:63153099-63153368	K562	blood:	n/a	n/a
13	BHLHE40	chr1:63155883-63156310	K562	blood:	n/a	n/a
14	BHLHE40	chr1:63156016-63157064	HepG2	liver:	n/a	n/a
15	BHLHE40	chr1:63153877-63154737	K562	blood:	n/a	chr1:63154459-63154475
16	BRCA1	chr1:63154179-63154584	HepG2	liver:	n/a	n/a
17	BRCA1	chr1:63154082-63154258	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr1:63153325-63153360	GM12878	blood:	n/a	n/a
19	CBX3	chr1:63153800-63154660	HCT-116	colon:	n/a	n/a
20	CBX3	chr1:63153967-63154417	K562	blood:	n/a	n/a
21	CBX3	chr1:63155878-63156440	K562	blood:	n/a	n/a
22	CCNT2	chr1:63153123-63154453	K562	blood:	n/a	n/a
23	CCNT2	chr1:63155851-63156363	K562	blood:	n/a	chr1:63156120-63156140
24	CEBPB	chr1:63153984-63154309	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr1:63155991-63156521	HepG2	liver:	n/a	n/a
26	CEBPB	chr1:63155108-63155663	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr1:63154065-63154379	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr1:63155222-63155745	HepG2	liver:	n/a	n/a
29	CEBPB	chr1:63155276-63155565	HepG2	liver:	n/a	n/a
30	CEBPB	chr1:63155987-63156330	K562	blood:	n/a	n/a
31	CEBPB	chr1:63154929-63155605	HCT-116	colon:	n/a	n/a
32	CEBPB	chr1:63154977-63155730	IMR90	lung:	n/a	n/a
33	CEBPB	chr1:63155869-63156332	K562	blood:	n/a	n/a
34	CEBPB	chr1:63155945-63156494	IMR90	lung:	n/a	n/a
35	CEBPD	chr1:63155746-63156414	K562	blood:	n/a	n/a
36	CEBPD	chr1:63153093-63153521	HepG2	liver:	n/a	n/a
37	CEBPD	chr1:63155819-63156386	K562	blood:	n/a	n/a
38	CHD1	chr1:63153221-63153359	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD1	chr1:63153931-63154855	IMR90	lung:	n/a	n/a
40	CHD1	chr1:63153645-63154366	GM12878	blood:	n/a	n/a
41	CHD1	chr1:63153928-63154604	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr1:63153018-63153218	HepG2	liver:	n/a	n/a
43	CHD2	chr1:63155138-63155565	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr1:63154015-63154519	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr1:63153847-63154504	GM12878	blood:	n/a	n/a
46	CHD2	chr1:63154087-63154264	HepG2	liver:	n/a	n/a
47	CHD2	chr1:63153238-63154628	Hela-S3	cervix:	n/a	n/a
48	CREB1	chr1:63153897-63154384	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr1:63153100-63154478	HepG2	liver:	n/a	n/a
50	CREB1	chr1:63153827-63154230	A549	lung:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:63154287-63154337	NHBE	bronchial:	n/a
2	chr1:63154584-63154634	AG04449	skin:	fetal
3	chr1:63154320-63154370	HRPEpiC	eye:	n/a
4	chr1:63154668-63154718	U87	brain:	n/a
5	chr1:63154465-63154515	BJ	skin:	n/a
6	chr1:63153194-63153244	HL-60	blood:	n/a
7	chr1:63153804-63153854	Jurkat	blood:	n/a
8	chr1:63154584-63154634	GM12878	blood:	n/a
9	chr1:63153194-63153244	NH-A	brain:	n/a
10	chr1:63154465-63154515	Caco-2	colon:	n/a
11	chr1:63154668-63154718	GM12891	blood:	n/a
12	chr1:63154668-63154718	NT2-D1	testis:	n/a
13	chr1:63154320-63154370	AG04450	lung:	fetal
14	chr1:63154465-63154515	HAEpiC	amniotic membrane:	n/a
15	chr1:63154320-63154370	Jurkat	blood:	n/a
16	chr1:63154668-63154718	GM06990	blood:	n/a
17	chr1:63153194-63153244	ProgFib	skin:	n/a
18	chr1:63154287-63154337	K562	blood:	n/a
19	chr1:63154584-63154634	BJ	skin:	n/a
20	chr1:63154668-63154718	GM12892	blood:	n/a
21	chr1:63154287-63154337	NT2-D1	testis:	n/a
22	chr1:63154320-63154370	LNCaP	prostate:	n/a
23	chr1:63153194-63153244	GM12878	blood:	n/a
24	chr1:63153194-63153244	K562	blood:	n/a
25	chr1:63153804-63153854	SK-N-SH_RA	brain:	n/a
26	chr1:63154287-63154337	AG09319	gingival:	n/a
27	chr1:63154465-63154515	GM12878	blood:	n/a
28	chr1:63153194-63153244	PANC-1	pancreas:	n/a
29	chr1:63154668-63154718	H1-hESC	embryonic stem cell:	embryo
30	chr1:63153194-63153244	HepG2	liver:	n/a
31	chr1:63154320-63154370	K562	blood:	n/a
32	chr1:63153194-63153244	T-47D	breast:	n/a
33	chr1:63154584-63154634	H1-hESC	embryonic stem cell:	embryo
34	chr1:63154465-63154515	SKMC	muscle:	n/a
35	chr1:63153804-63153854	HIPEpiC	eye:	n/a
36	chr1:63154465-63154515	HepG2	liver:	n/a
37	chr1:63154668-63154718	AG04449	skin:	fetal
38	chr1:63154584-63154634	Caco-2	colon:	n/a
39	chr1:63154287-63154337	NH-A	brain:	n/a
40	chr1:63153194-63153244	NHDF-neo	bronchial:	n/a
41	chr1:63154287-63154337	SAEC	small airway:	n/a
42	chr1:63154465-63154515	ProgFib	skin:	n/a
43	chr1:63154287-63154337	HNPCEpiC	eye:	n/a
44	chr1:63154584-63154634	HepG2	liver:	n/a
45	chr1:63153804-63153854	HRPEpiC	eye:	n/a
46	chr1:63153194-63153244	Caco-2	colon:	n/a
47	chr1:63154584-63154634	HRCEpiC	kidney:	n/a
48	chr1:63154584-63154634	Hepatocyte	liver:	n/a
49	chr1:63153804-63153854	A549	lung:	n/a
50	chr1:63154584-63154634	K562	blood:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:63146913..63149001-chr1:63152180..63153818,3	MCF-7	breast:
2	chr1:63141617..63143983-chr1:63151351..63153918,2	MCF-7	breast:
3	chr1:63151590..63154458-chr1:63248689..63250715,2	K562	blood:
4	chr1:63144223..63146231-chr1:63150074..63152820,2	K562	blood:
5	chr1:63151590..63154458-chr1:63248689..63251365,3	K562	blood:

No data

Variant related genes	Relation type
DOCK7	TF binding region
ENSG00000235545	TF binding region
DOCK7	CpG island
ENSG00000235545	CpG island
ENSG00000125703	chromatin interactions

Extended variants
information (count: 129 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:129 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140139002	chr1:63152591-63152592	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs572571452	chr1:63152606-63152607	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs145671324	chr1:63152623-63152624	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs544864071	chr1:63152636-63152637	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs147717050	chr1:63152643-63152644	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs531765915	chr1:63152652-63152653	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs117649068	chr1:63152654-63152655	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs189728246	chr1:63152665-63152666	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs528088598	chr1:63152676-63152677	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs562809252	chr1:63152702-63152703	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs533082974	chr1:63152705-63152706	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs546660777	chr1:63152742-63152743	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs149204310	chr1:63152797-63152798	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs78947002	chr1:63152799-63152800	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs559733781	chr1:63152819-63152820	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs373832165	chr1:63152826-63152827	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs111615209	chr1:63152829-63152830	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs367586154	chr1:63152906-63152907	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs369914786	chr1:63153010-63153011	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs180858516	chr1:63153041-63153042	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs186145962	chr1:63153077-63153078	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs377045587	chr1:63153113-63153114	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs548699810	chr1:63153117-63153118	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs567020542	chr1:63153119-63153120	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs190853497	chr1:63153157-63153158	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs555750330	chr1:63153170-63153171	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs373277402	chr1:63153176-63153177	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs68148663	chr1:63153200-63153201	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs56280080	chr1:63153202-63153203	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs367723878	chr1:63153214-63153215	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs536140925	chr1:63153216-63153217	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs571177230	chr1:63153226-63153227	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs538985801	chr1:63153233-63153234	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs113689968	chr1:63153242-63153243	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs369635664	chr1:63153256-63153257	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs79386202	chr1:63153287-63153288	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs374082932	chr1:63153371-63153372	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs191366065	chr1:63153405-63153406	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs536831182	chr1:63153426-63153427	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs554942905	chr1:63153468-63153469	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs555146724	chr1:63153500-63153501	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs576599965	chr1:63153532-63153533	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs543893779	chr1:63153538-63153539	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs540603845	chr1:63153543-63153544	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs565279036	chr1:63153587-63153588	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs577138677	chr1:63153624-63153625	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs545011691	chr1:63153658-63153659	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs560377179	chr1:63153677-63153678	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs372600235	chr1:63153739-63153740	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs527542313	chr1:63153832-63153833	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Breast cancer	16620391	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
CNS Malformation Syndrome	17530927	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	20459617	CNVD
Endometrioid adenocarcinoma	16974079	CNVD

Chromatin state (count:566 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:63113600-63152800	Weak transcription	Primary B cells from cord blood	blood
2	chr1:63138000-63153000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:63141400-63152600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr1:63143000-63153000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr1:63147600-63152600	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr1:63148200-63152600	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr1:63148400-63152600	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr1:63148600-63153000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr1:63148800-63152800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr1:63148800-63152800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr1:63149000-63152800	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr1:63149000-63152800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr1:63149600-63152600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr1:63150000-63153000	Enhancers	Liver	Liver
15	chr1:63150200-63152800	Enhancers	Adipose Nuclei	Adipose
16	chr1:63150200-63152800	Enhancers	Fetal Brain Male	brain
17	chr1:63150200-63153000	Enhancers	Fetal Lung	lung
18	chr1:63150600-63152800	Enhancers	Stomach Mucosa	stomach
19	chr1:63150800-63152600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr1:63150800-63152600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr1:63150800-63152600	Enhancers	Duodenum Mucosa	Duodenum
22	chr1:63150800-63152600	Enhancers	Fetal Intestine Small	intestine
23	chr1:63150800-63152600	Enhancers	HMEC	breast
24	chr1:63150800-63152800	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr1:63150800-63152800	Enhancers	K562	blood
26	chr1:63150800-63153000	Enhancers	Fetal Heart	heart
27	chr1:63151000-63152600	Enhancers	Fetal Intestine Large	intestine
28	chr1:63151000-63153000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr1:63151200-63152800	Enhancers	HUVEC	blood vessel
30	chr1:63151200-63153000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr1:63151400-63153000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr1:63151400-63153000	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr1:63151600-63152600	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr1:63151600-63152600	Weak transcription	Right Atrium	heart
35	chr1:63151600-63152800	Weak transcription	Primary T helper cells fromperipheralblood	blood
36	chr1:63151600-63152800	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr1:63151600-63153000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr1:63151600-63153000	Weak transcription	Aorta	Aorta
39	chr1:63151600-63153000	Weak transcription	Gastric	stomach
40	chr1:63151600-63153000	Weak transcription	Pancreas	Pancrea
41	chr1:63151600-63153000	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr1:63151600-63153000	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr1:63151600-63153200	Weak transcription	Esophagus	oesophagus
44	chr1:63151600-63153200	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr1:63151600-63153200	Weak transcription	Spleen	Spleen
46	chr1:63151800-63152600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr1:63151800-63152800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr1:63151800-63152800	Enhancers	HSMM	muscle
49	chr1:63151800-63153000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr1:63151800-63153000	Weak transcription	Ovary	ovary

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