Variant report

Variant	esv2830314
Chromosome Location	chr1:45430218-45455285
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:689)
CpG islands
(count:855)
Chromatin interactive
region (count:54)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:689 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:45436007-45436055	K562	blood:	n/a	n/a
2	ARID3A	chr1:45452136-45452589	K562	blood:	n/a	n/a
3	ARID3A	chr1:45452131-45452488	HepG2	liver:	n/a	n/a
4	ATF1	chr1:45452100-45452567	K562	blood:	n/a	n/a
5	ATF2	chr1:45452105-45452622	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr1:45451998-45452561	GM12878	blood:	n/a	n/a
7	ATF2	chr1:45452055-45452538	GM12878	blood:	n/a	n/a
8	ATF2	chr1:45451925-45452539	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr1:45452157-45452590	K562	blood:	n/a	chr1:45452413-45452422
10	BACH1	chr1:45452301-45452545	K562	blood:	n/a	n/a
11	BATF	chr1:45452199-45452478	GM12878	blood:	n/a	n/a
12	BCL3	chr1:45452048-45452683	A549	lung:	n/a	n/a
13	BCL3	chr1:45451893-45452656	A549	lung:	n/a	n/a
14	BCLAF1	chr1:45451981-45452606	GM12878	blood:	n/a	n/a
15	BCLAF1	chr1:45451980-45452634	GM12878	blood:	n/a	n/a
16	BHLHE40	chr1:45448822-45448902	GM12878	blood:	n/a	n/a
17	BHLHE40	chr1:45452260-45452571	A549	lung:	n/a	n/a
18	BHLHE40	chr1:45452965-45453069	K562	blood:	n/a	n/a
19	BHLHE40	chr1:45433806-45434309	K562	blood:	n/a	n/a
20	BHLHE40	chr1:45451943-45452706	K562	blood:	n/a	n/a
21	BHLHE40	chr1:45452066-45452607	GM12878	blood:	n/a	n/a
22	BHLHE40	chr1:45451463-45451676	K562	blood:	n/a	n/a
23	BHLHE40	chr1:45451982-45452624	HepG2	liver:	n/a	n/a
24	BRCA1	chr1:45452231-45452525	HepG2	liver:	n/a	n/a
25	BRCA1	chr1:45433850-45434133	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr1:45452001-45452700	HCT-116	colon:	n/a	n/a
27	CBX3	chr1:45451824-45452695	K562	blood:	n/a	n/a
28	CBX3	chr1:45452017-45452657	K562	blood:	n/a	n/a
29	CCNT2	chr1:45434223-45434410	K562	blood:	n/a	n/a
30	CCNT2	chr1:45452011-45452558	K562	blood:	n/a	chr1:45452413-45452422
31	CEBPB	chr1:45438507-45438778	K562	blood:	n/a	chr1:45438663-45438674
32	CEBPB	chr1:45448953-45449048	Hela-S3	cervix:	n/a	chr1:45448993-45449004
33	CEBPB	chr1:45438660-45438678	H1-hESC	embryonic stem cell:	n/a	chr1:45438663-45438674
34	CEBPB	chr1:45434463-45434548	IMR90	lung:	n/a	chr1:45434519-45434530
35	CEBPB	chr1:45439403-45439707	IMR90	lung:	n/a	chr1:45439560-45439571
36	CEBPB	chr1:45441689-45441883	IMR90	lung:	n/a	n/a
37	CEBPB	chr1:45438557-45438782	A549	lung:	n/a	chr1:45438663-45438674
38	CEBPB	chr1:45451964-45452444	HepG2	liver:	n/a	n/a
39	CEBPB	chr1:45439420-45439694	HepG2	liver:	n/a	chr1:45439560-45439571
40	CEBPB	chr1:45451865-45451866	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr1:45451821-45452460	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr1:45434343-45434710	K562	blood:	n/a	chr1:45434519-45434530
43	CEBPB	chr1:45438536-45438782	IMR90	lung:	n/a	chr1:45438663-45438674
44	CEBPB	chr1:45451812-45452546	K562	blood:	n/a	n/a
45	CEBPB	chr1:45434509-45434597	HepG2	liver:	n/a	chr1:45434519-45434530
46	CEBPB	chr1:45451965-45452613	GM12878	blood:	n/a	n/a
47	CEBPB	chr1:45441707-45441890	A549	lung:	n/a	n/a
48	CEBPB	chr1:45439480-45439646	A549	lung:	n/a	chr1:45439560-45439571
49	CEBPB	chr1:45439471-45439697	K562	blood:	n/a	chr1:45439560-45439571
50	CEBPB	chr1:45451925-45452468	ECC-1	luminal epithelium:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:45449830-45449880	PrEC	prostate:	n/a
2	chr1:45449830-45449880	PrEC	prostate:	n/a
3	chr1:45453003-45453053	GM06990	blood:	n/a
4	chr1:45454424-45454474	ProgFib	skin:	n/a
5	chr1:45452605-45452655	T-47D	breast:	n/a
6	chr1:45454343-45454393	HCT-116	colon:	n/a
7	chr1:45454343-45454393	HRPEpiC	eye:	n/a
8	chr1:45452580-45452630	Hela-S3	cervix:	n/a
9	chr1:45452319-45452369	SK-N-MC	brain:	n/a
10	chr1:45454424-45454474	HCT-116	colon:	n/a
11	chr1:45454424-45454474	SK-N-MC	brain:	n/a
12	chr1:45452509-45452559	SAEC	small airway:	n/a
13	chr1:45451736-45451786	NB4	blood:	n/a
14	chr1:45451992-45452042	RPTEC	kidney:	n/a
15	chr1:45454343-45454393	HMEC	breast:	n/a
16	chr1:45452521-45452571	PANC-1	pancreas:	n/a
17	chr1:45449830-45449880	MCF10A-Er-Src	breast:	n/a
18	chr1:45449830-45449880	BE2_C	brain:	n/a
19	chr1:45452509-45452559	HCT-116	colon:	n/a
20	chr1:45451736-45451786	NHDF-neo	bronchial:	n/a
21	chr1:45451736-45451786	SAEC	small airway:	n/a
22	chr1:45451736-45451786	HEK293	kidney:	embryo
23	chr1:45452240-45452290	SK-N-MC	brain:	n/a
24	chr1:45451992-45452042	BJ	skin:	n/a
25	chr1:45452319-45452369	CMK	blood:	n/a
26	chr1:45453003-45453053	HCPEpiC	choroid plexus:	n/a
27	chr1:45452605-45452655	RPTEC	kidney:	n/a
28	chr1:45452240-45452290	A549	lung:	n/a
29	chr1:45452509-45452559	BE2_C	brain:	n/a
30	chr1:45452319-45452369	GM19239	blood:	n/a
31	chr1:45452521-45452571	SK-N-SH_RA	brain:	n/a
32	chr1:45454370-45454420	PANC-1	pancreas:	n/a
33	chr1:45453003-45453053	MCF10A-Er-Src	breast:	n/a
34	chr1:45452521-45452571	A549	lung:	n/a
35	chr1:45452319-45452369	Caco-2	colon:	n/a
36	chr1:45454343-45454393	NB4	blood:	n/a
37	chr1:45452509-45452559	AG04450	lung:	fetal
38	chr1:45454424-45454474	ECC-1	luminal epithelium:	n/a
39	chr1:45454370-45454420	AoSMC	blood vessel:	n/a
40	chr1:45452166-45452216	GM12891	blood:	n/a
41	chr1:45452509-45452559	ProgFib	skin:	n/a
42	chr1:45449830-45449880	HUVEC	blood vessel:	n/a
43	chr1:45454424-45454474	AG04449	skin:	fetal
44	chr1:45454424-45454474	NB4	blood:	n/a
45	chr1:45452240-45452290	SAEC	small airway:	n/a
46	chr1:45452240-45452290	HRPEpiC	eye:	n/a
47	chr1:45454343-45454393	NH-A	brain:	n/a
48	chr1:45453003-45453053	NH-A	brain:	n/a
49	chr1:45452521-45452571	AG04449	skin:	fetal
50	chr1:45454370-45454420	AG04450	lung:	fetal

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:45452472..45454113-chr1:45457671..45459951,2	K562	blood:
2	chr1:45430652..45433311-chr1:45435078..45437709,3	K562	blood:
3	chr1:45284581..45287931-chr1:45452240..45453906,3	MCF-7	breast:
4	chr1:45452263..45453960-chr1:45454277..45456496,2	K562	blood:
5	chr1:45450629..45452184-chr1:45572673..45575146,2	K562	blood:
6	chr1:45445644..45447946-chr1:45746715..45748640,2	K562	blood:
7	chr1:45273964..45275771-chr1:45451640..45453619,2	K562	blood:
8	chr1:45424939..45427483-chr1:45450541..45452158,2	K562	blood:
9	chr1:45449901..45454181-chr1:45475970..45480540,16	K562	blood:
10	chr1:45245416..45248456-chr1:45442657..45444544,3	K562	blood:
11	chr1:45450947..45453129-chr1:45770139..45772507,2	K562	blood:
12	chr1:45284059..45286396-chr1:45450000..45452623,4	MCF-7	breast:
13	chr1:45194988..45198272-chr1:45451491..45453905,3	K562	blood:
14	chr1:45430590..45432812-chr1:45438899..45441605,2	K562	blood:
15	chr1:45444980..45449241-chr1:45450734..45453463,5	MCF-7	breast:
16	chr1:45452234..45453881-chr1:45454230..45457935,4	K562	blood:
17	chr1:45443941..45446548-chr1:45450111..45452073,2	K562	blood:
18	chr1:45428206..45430987-chr1:45432704..45434653,2	K562	blood:
19	chr1:45452234..45453881-chr1:45454230..45457935,4	K562	blood:
20	chr1:45444590..45447316-chr1:45478691..45480340,2	K562	blood:
21	chr1:45428206..45430987-chr1:45432704..45434653,2	K562	blood:
22	chr1:45240606..45242978-chr1:45452437..45454075,2	K562	blood:
23	chr1:45447308..45449249-chr1:45476981..45478639,2	K562	blood:
24	chr1:45436208..45437832-chr1:45438280..45440463,2	K562	blood:
25	chr1:45186345..45187927-chr1:45443599..45445522,2	K562	blood:
26	chr1:45239905..45242727-chr1:45449975..45452356,2	K562	blood:
27	chr1:45452263..45453960-chr1:45454277..45456496,2	K562	blood:
28	chr1:45273709..45275495-chr1:45442746..45445462,2	K562	blood:
29	chr1:45441142..45443966-chr1:45451667..45454449,3	K562	blood:
30	chr1:45282334..45285552-chr1:45442428..45444971,3	K562	blood:
31	chr1:45284052..45287183-chr1:45440779..45443928,3	K562	blood:
32	chr1:45430652..45433311-chr1:45435408..45437709,2	K562	blood:
33	chr1:45451300..45453679-chr1:45476530..45479236,3	MCF-7	breast:
34	chr1:45430590..45432812-chr1:45438899..45441605,2	K562	blood:
35	chr1:45427848..45431686-chr1:45448944..45451154,3	K562	blood:
36	chr1:45186384..45188891-chr1:45454101..45455749,3	K562	blood:
37	chr1:45450854..45457330-chr1:45465047..45472849,14	K562	blood:
38	chr1:45427848..45431686-chr1:45448944..45451154,3	K562	blood:
39	chr1:45442231..45443785-chr1:45444690..45447265,2	MCF-7	breast:
40	chr1:45430590..45432812-chr1:45438899..45441605,3	K562	blood:
41	chr1:45446769..45450642-chr1:45450825..45453643,3	K562	blood:
42	chr1:45430652..45433311-chr1:45435078..45437709,3	K562	blood:
43	chr1:45283589..45286724-chr1:45434878..45437346,4	K562	blood:
44	chr1:45443941..45446548-chr1:45450111..45452073,2	K562	blood:
45	chr1:45300154..45301812-chr1:45433774..45435407,2	K562	blood:
46	chr1:45271433..45273539-chr1:45450490..45453055,2	K562	blood:
47	chr1:45283976..45287622-chr1:45450715..45458034,11	K562	blood:
48	chr1:45436208..45437832-chr1:45438280..45440463,2	K562	blood:
49	chr1:45442231..45443785-chr1:45444690..45447265,2	MCF-7	breast:
50	chr1:45451325..45453836-chr1:45473269..45474967,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF2B3-1	chr1:45454377-45457506	NONHSAT002914
2	lnc-UROD-1	chr1:45444991-45445276	l_49_chr1:45444990-45456130_testes

No data

Variant related genes	Relation type
ENSG00000232369	TF binding region
EIF2B3	TF binding region
ENSG00000232369	CpG island
EIF2B3	CpG island
ENSG00000142937	chromatin interactions
ENSG00000222009	chromatin interactions
ENSG00000126088	chromatin interactions
ENSG00000162415	chromatin interactions
ENSG00000126107	chromatin interactions
ENSG00000070785	chromatin interactions
ENSG00000200913	chromatin interactions
ENSG00000225721	chromatin interactions
ENSG00000188396	chromatin interactions
ENSG00000264294	chromatin interactions
ENSG00000199377	chromatin interactions
ENSG00000232369	chromatin interactions
ENSG00000268949	chromatin interactions
ENSG00000234093	chromatin interactions
ENSG00000202444	chromatin interactions
ENSG00000200169	chromatin interactions

Extended variants
information (count: 949 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:949 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11211059	chr1:45430218-45430219	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs60253555	chr1:45430229-45430230	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs561082469	chr1:45430242-45430243	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs529786920	chr1:45430341-45430342	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs150537202	chr1:45430364-45430365	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs569509605	chr1:45430494-45430495	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs532173088	chr1:45430549-45430550	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374224037	chr1:45430565-45430566	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs371381626	chr1:45430586-45430587	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs574031928	chr1:45430602-45430603	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs571933802	chr1:45430603-45430604	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs534109502	chr1:45430681-45430682	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs139542455	chr1:45430693-45430694	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs567539090	chr1:45430741-45430742	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs536307992	chr1:45430743-45430744	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs556660592	chr1:45430751-45430752	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs576358175	chr1:45430776-45430777	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149717206	chr1:45430808-45430809	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558558269	chr1:45430848-45430849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376212505	chr1:45430901-45430902	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs72676587	chr1:45430947-45430948	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs34973587	chr1:45430961-45430962	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs370216591	chr1:45430980-45430981	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs76381075	chr1:45431131-45431132	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112335754	chr1:45431163-45431164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs376473873	chr1:45431164-45431165	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs12753406	chr1:45431178-45431179	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs559912686	chr1:45431183-45431184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs181108200	chr1:45431186-45431187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145303949	chr1:45431280-45431281	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563443290	chr1:45431301-45431302	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373128773	chr1:45431306-45431307	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs386366856	chr1:45431307-45431308	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556332762	chr1:45431404-45431405	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs58263876	chr1:45431414-45431415	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs559099697	chr1:45431428-45431429	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs148929316	chr1:45431443-45431444	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576090966	chr1:45431475-45431476	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547696106	chr1:45431590-45431591	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10218751	chr1:45431591-45431592	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs7519454	chr1:45431617-45431618	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs186117149	chr1:45431618-45431619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570166812	chr1:45431644-45431645	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs546354	chr1:45431664-45431665	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs558884065	chr1:45431691-45431692	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572474480	chr1:45431744-45431745	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191016665	chr1:45431835-45431836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554943034	chr1:45431837-45431838	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574679463	chr1:45431870-45431871	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs640743	chr1:45431883-45431884	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	17603634	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
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
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
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
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
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	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
Uveal melanoma	20484589	CNVD
Ovarian cancer	22174824	CNVD
Muscle-eye-brain disease	21572526	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20680643	CNVD
Colorectal cancer	19287155	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1003 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:45389200-45450200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr1:45391200-45438400	Weak transcription	Dnd41	blood
3	chr1:45391200-45439800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr1:45391400-45437200	Weak transcription	Fetal Thymus	thymus
5	chr1:45392400-45433800	Weak transcription	Primary hematopoietic stem cells	blood
6	chr1:45392800-45443200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr1:45397800-45435800	Weak transcription	Primary B cells from cord blood	blood
8	chr1:45407600-45438400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr1:45412000-45440000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr1:45412800-45441000	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr1:45413200-45436200	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr1:45413400-45437800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr1:45413400-45439600	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr1:45413400-45439800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:45413400-45441400	Weak transcription	Brain Anterior Caudate	brain
16	chr1:45413600-45441400	Weak transcription	Colon Smooth Muscle	Colon
17	chr1:45413600-45442800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr1:45413800-45433800	Weak transcription	NH-A	brain
19	chr1:45413800-45437600	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr1:45413800-45438400	Weak transcription	Right Ventricle	heart
21	chr1:45413800-45439800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr1:45413800-45441600	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr1:45414000-45435600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr1:45414000-45436200	Weak transcription	Ovary	ovary
25	chr1:45414000-45438400	Weak transcription	Stomach Smooth Muscle	stomach
26	chr1:45414000-45439400	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr1:45414000-45439600	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr1:45414000-45440000	Weak transcription	Brain Angular Gyrus	brain
29	chr1:45414000-45440000	Weak transcription	Fetal Lung	lung
30	chr1:45414000-45441000	Weak transcription	Fetal Kidney	kidney
31	chr1:45414000-45441600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr1:45414000-45443200	Weak transcription	Pancreas	Pancrea
33	chr1:45414000-45450800	Weak transcription	Rectal Smooth Muscle	rectum
34	chr1:45414000-45451000	Weak transcription	Spleen	Spleen
35	chr1:45414200-45433800	Weak transcription	HSMM	muscle
36	chr1:45414200-45433800	Weak transcription	HUVEC	blood vessel
37	chr1:45414200-45443000	Weak transcription	Gastric	stomach
38	chr1:45415000-45437200	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr1:45415400-45438600	Weak transcription	Skeletal Muscle Male	skeletal muscle
40	chr1:45415600-45440400	Weak transcription	Fetal Brain Female	brain
41	chr1:45416600-45443600	Weak transcription	Psoas Muscle	Psoas
42	chr1:45417600-45442000	Weak transcription	Placenta	Placenta
43	chr1:45421000-45450800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr1:45421400-45443400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
45	chr1:45422000-45441400	Weak transcription	Esophagus	oesophagus
46	chr1:45423400-45433800	Weak transcription	Hela-S3	cervix
47	chr1:45423400-45439600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr1:45423600-45441400	Weak transcription	NHLF	lung
49	chr1:45423800-45433800	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr1:45424000-45435600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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