Variant report

Variant	esv32940
Chromosome Location	chr10:51051718-51488059
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:51052979-51053503	HepG2	liver:	n/a	n/a
2	BATF	chr10:51370987-51371657	GM12878	blood:	n/a	n/a
3	BATF	chr10:51252451-51252642	GM12878	blood:	n/a	n/a
4	BATF	chr10:51256641-51256857	GM12878	blood:	n/a	chr10:51256767-51256778
5	BATF	chr10:51377417-51377859	GM12878	blood:	n/a	n/a
6	BATF	chr10:51377468-51377823	GM12878	blood:	n/a	n/a
7	BCL11A	chr10:51371149-51371328	GM12878	blood:	n/a	n/a
8	BCL11A	chr10:51377445-51377837	GM12878	blood:	n/a	n/a
9	BCL11A	chr10:51477990-51478142	GM12878	blood:	n/a	n/a
10	BCL11A	chr10:51371338-51371706	GM12878	blood:	n/a	n/a
11	BCL3	chr10:51052818-51053497	A549	lung:	n/a	n/a
12	BHLHE40	chr10:51370779-51370981	HepG2	liver:	n/a	n/a
13	BHLHE40	chr10:51202040-51202312	HepG2	liver:	n/a	n/a
14	CBX3	chr10:51103941-51104320	K562	blood:	n/a	n/a
15	CBX3	chr10:51371133-51371579	K562	blood:	n/a	n/a
16	CBX3	chr10:51370429-51371746	K562	blood:	n/a	n/a
17	CBX3	chr10:51103987-51104280	K562	blood:	n/a	n/a
18	CBX3	chr10:51325757-51326010	K562	blood:	n/a	n/a
19	CBX3	chr10:51325714-51325957	K562	blood:	n/a	n/a
20	CEBPB	chr10:51362034-51362409	IMR90	lung:	n/a	n/a
21	CEBPB	chr10:51052837-51053681	MCF-7	breast:	n/a	chr10:51053042-51053053
22	CEBPB	chr10:51108511-51108719	Hela-S3	cervix:	n/a	chr10:51108616-51108627 chr10:51108616-51108625 chr10:51108616-51108625 chr10:51108614-51108627 chr10:51108616-51108625 chr10:51108614-51108625 chr10:51108616-51108625
23	CEBPB	chr10:51108501-51108786	HepG2	liver:	n/a	chr10:51108616-51108627 chr10:51108616-51108625 chr10:51108616-51108625 chr10:51108614-51108627 chr10:51108616-51108625 chr10:51108614-51108625 chr10:51108616-51108625
24	CEBPB	chr10:51120223-51120576	HepG2	liver:	n/a	chr10:51120380-51120391 chr10:51120380-51120393
25	CEBPB	chr10:51362046-51362409	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr10:51052874-51053601	A549	lung:	n/a	chr10:51053042-51053053
27	CEBPB	chr10:51120250-51120795	IMR90	lung:	n/a	chr10:51120380-51120391 chr10:51120380-51120393
28	CEBPB	chr10:51052922-51053392	K562	blood:	n/a	chr10:51053042-51053053
29	CEBPB	chr10:51052841-51053559	A549	lung:	n/a	chr10:51053042-51053053
30	CEBPB	chr10:51052828-51053595	Hela-S3	cervix:	n/a	chr10:51053042-51053053
31	CEBPB	chr10:51052750-51053623	MCF-7	breast:	n/a	chr10:51053042-51053053
32	CEBPB	chr10:51125670-51125962	IMR90	lung:	n/a	n/a
33	CEBPB	chr10:51108499-51108691	H1-hESC	embryonic stem cell:	n/a	chr10:51108616-51108627 chr10:51108616-51108625 chr10:51108616-51108625 chr10:51108614-51108627 chr10:51108616-51108625 chr10:51108614-51108625 chr10:51108616-51108625
34	CEBPB	chr10:51060119-51060498	Hela-S3	cervix:	n/a	chr10:51060224-51060237
35	CEBPB	chr10:51091883-51092329	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr10:51120363-51120697	Hela-S3	cervix:	n/a	chr10:51120380-51120391 chr10:51120380-51120393
37	CEBPB	chr10:51120215-51120790	A549	lung:	n/a	chr10:51120380-51120391 chr10:51120380-51120393
38	CEBPB	chr10:51397664-51397920	K562	blood:	n/a	n/a
39	CEBPB	chr10:51052751-51053591	A549	lung:	n/a	chr10:51053042-51053053
40	CEBPB	chr10:51108445-51108786	IMR90	lung:	n/a	chr10:51108616-51108627 chr10:51108616-51108625 chr10:51108616-51108625 chr10:51108614-51108627 chr10:51108616-51108625 chr10:51108614-51108625 chr10:51108616-51108625
41	CEBPB	chr10:51108460-51108786	A549	lung:	n/a	chr10:51108616-51108627 chr10:51108616-51108625 chr10:51108616-51108625 chr10:51108614-51108627 chr10:51108616-51108625 chr10:51108614-51108625 chr10:51108616-51108625
42	CEBPB	chr10:51120363-51120417	H1-hESC	embryonic stem cell:	n/a	chr10:51120380-51120391 chr10:51120380-51120393
43	CEBPB	chr10:51108439-51108789	K562	blood:	n/a	chr10:51108616-51108627 chr10:51108616-51108625 chr10:51108616-51108625 chr10:51108614-51108627 chr10:51108616-51108625 chr10:51108614-51108625 chr10:51108616-51108625
44	CEBPB	chr10:51052790-51053553	IMR90	lung:	n/a	chr10:51053042-51053053
45	CEBPB	chr10:51052895-51053556	HepG2	liver:	n/a	chr10:51053042-51053053
46	CEBPB	chr10:51120227-51120517	K562	blood:	n/a	chr10:51120380-51120391 chr10:51120380-51120393
47	CEBPD	chr10:51371138-51371633	K562	blood:	n/a	n/a
48	CEBPD	chr10:51262731-51263098	K562	blood:	n/a	n/a
49	CTCF	chr10:51288997-51289061	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chr10:51382461-51382702	HUVEC	blood vessel:	n/a	chr10:51382599-51382617 chr10:51382600-51382616 chr10:51382602-51382615 chr10:51382601-51382622

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:51463156-51463206	PANC-1	pancreas:	n/a
2	chr10:51222923-51222973	U87	brain:	n/a
3	chr10:51374253-51374303	H1-hESC	embryonic stem cell:	embryo
4	chr10:51487635-51487685	Jurkat	blood:	n/a
5	chr10:51463156-51463206	PANC-1	pancreas:	n/a
6	chr10:51222923-51222973	U87	brain:	n/a
7	chr10:51374253-51374303	H1-hESC	embryonic stem cell:	embryo
8	chr10:51487635-51487685	Jurkat	blood:	n/a
9	chr10:51374253-51374303	HCPEpiC	choroid plexus:	n/a
10	chr10:51225001-51225051	HRE	kidney:	n/a
11	chr10:51463156-51463206	PFSK-1	brain:	n/a
12	chr10:51465444-51465494	HAEpiC	amniotic membrane:	n/a
13	chr10:51225001-51225051	LNCaP	prostate:	n/a
14	chr10:51371691-51371741	Caco-2	colon:	n/a
15	chr10:51371709-51371759	HMEC	breast:	n/a
16	chr10:51371691-51371741	GM19239	blood:	n/a
17	chr10:51468217-51468267	HCM	heart:	n/a
18	chr10:51487558-51487608	Jurkat	blood:	n/a
19	chr10:51374253-51374303	ProgFib	skin:	n/a
20	chr10:51361773-51361823	HCM	heart:	n/a
21	chr10:51461855-51461905	IMR90	lung:	fetal
22	chr10:51224358-51224408	LNCaP	prostate:	n/a
23	chr10:51487759-51487809	U87	brain:	n/a
24	chr10:51371691-51371741	HMEC	breast:	n/a
25	chr10:51252461-51252511	HCF	heart:	n/a
26	chr10:51225028-51225078	HCM	heart:	n/a
27	chr10:51463156-51463206	U87	brain:	n/a
28	chr10:51465444-51465494	SK-N-MC	brain:	n/a
29	chr10:51487558-51487608	HUVEC	blood vessel:	n/a
30	chr10:51222923-51222973	HCM	heart:	n/a
31	chr10:51264883-51264933	CMK	blood:	n/a
32	chr10:51371707-51371757	Jurkat	blood:	n/a
33	chr10:51371707-51371757	ovcar-3	ovarian:	n/a
34	chr10:51487558-51487608	AoSMC	blood vessel:	n/a
35	chr10:51487635-51487685	HNPCEpiC	eye:	n/a
36	chr10:51371691-51371741	GM12891	blood:	n/a
37	chr10:51487635-51487685	AoSMC	blood vessel:	n/a
38	chr10:51361773-51361823	K562	blood:	n/a
39	chr10:51224358-51224408	ovcar-3	ovarian:	n/a
40	chr10:51487635-51487685	Hela-S3	cervix:	n/a
41	chr10:51487759-51487809	GM12878	blood:	n/a
42	chr10:51225001-51225051	ovcar-3	ovarian:	n/a
43	chr10:51461855-51461905	ProgFib	skin:	n/a
44	chr10:51468217-51468267	AoSMC	blood vessel:	n/a
45	chr10:51461855-51461905	SK-N-SH	brain:	n/a
46	chr10:51461855-51461905	HIPEpiC	eye:	n/a
47	chr10:51225028-51225078	NHBE	bronchial:	n/a
48	chr10:51371707-51371757	A549	lung:	n/a
49	chr10:51487759-51487809	AG04449	skin:	fetal
50	chr10:51371709-51371759	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:47652879..47654869-chr10:51487976..51491279,3	MCF-7	breast:
2	chr10:51487738..51490469-chr10:51490768..51492273,2	MCF-7	breast:
3	chr10:47654274..47658037-chr10:51487059..51489810,4	K562	blood:
4	chr10:47652235..47655869-chr10:51487775..51491801,8	MCF-7	breast:
5	chr10:51045976..51047972-chr10:51051417..51053268,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PARG-1	chr10:51227131-51227153	NONHSAT013326
2	lnc-MSMB-2	chr10:51383526-51383726	NONHSAT013336
3	lnc-TIMM23B-2	chr10:51339438-51339770	NONHSAT013334
4	lnc-AGAP8-1	chr10:51216277-51216406	ENSG00000214986
5	lnc-AGAP8-2	chr10:51253787-51253968	ENSG00000244393.2
6	lnc-AGAP8-3	chr10:51211725-51212022	NONHSAT013324
7	lnc-AGAP8-2	chr10:51262049-51262426	ENSG00000244393.2
8	lnc-AGAP8-1	chr10:51214507-51214698	ENSG00000214986
9	lnc-PARG-1	chr10:51230459-51230849	NONHSAT013326
10	lnc-PARG-2	chr10:51240583-51240744	NONHSAT013327
11	lnc-FAM21D-1	chr10:51117659-51117988	NONHSAT013322
12	lnc-PARG-2	chr10:51243388-51243565	NONHSAT013327

Variant related genes	Relation type
FAM25D	TF binding region
AGAP8	TF binding region
ENSG00000230166	TF binding region
TIMM23B	TF binding region
ENSG00000225784	TF binding region
AGAP7	TF binding region
ENSG00000244393	TF binding region
PARG	TF binding region
ENSG00000270568	TF binding region
ENSG00000236787	TF binding region
FAM21D	TF binding region
RNA5SP316	TF binding region
ENSG00000272225	TF binding region
ENSG00000223182	TF binding region
FAM25D	CpG island
AGAP8	CpG island
ENSG00000230166	CpG island
TIMM23B	CpG island
ENSG00000225784	CpG island
AGAP7	CpG island
ENSG00000244393	CpG island
PARG	CpG island
ENSG00000270568	CpG island
ENSG00000236787	CpG island
FAM21D	CpG island
RNA5SP316	CpG island
ENSG00000272225	CpG island
ENSG00000223182	CpG island
ENSG00000259942	chromatin interactions
ENSG00000198250	chromatin interactions

Extended variants
information (count: 2987 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2987 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546951352	chr10:51051770-51051771	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs571827899	chr10:51051832-51051833	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs189797925	chr10:51051895-51051896	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs74419923	chr10:51051904-51051905	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs566798774	chr10:51051938-51051939	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs77308968	chr10:51051939-51051940	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs372668936	chr10:51051955-51051956	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs77133568	chr10:51051964-51051965	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs546245883	chr10:51051977-51051978	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs555011831	chr10:51052100-51052101	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573226471	chr10:51052123-51052124	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs540540856	chr10:51052145-51052146	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181442897	chr10:51052153-51052154	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200728222	chr10:51052195-51052196	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536463109	chr10:51052306-51052307	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs370751637	chr10:51052326-51052327	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371235416	chr10:51052361-51052362	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577000076	chr10:51052385-51052386	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs2579034	chr10:51052394-51052395	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs562285598	chr10:51052411-51052412	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs370193237	chr10:51052422-51052423	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs576730470	chr10:51052434-51052435	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541479987	chr10:51052435-51052436	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs141848014	chr10:51052464-51052465	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs375284684	chr10:51052485-51052486	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs184889555	chr10:51052497-51052498	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs565418683	chr10:51052498-51052499	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532787121	chr10:51052512-51052513	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs551185682	chr10:51052570-51052571	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs569433150	chr10:51052572-51052573	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs536745371	chr10:51052584-51052585	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs548672761	chr10:51052665-51052666	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs34659290	chr10:51052669-51052670	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs397771985	chr10:51052683-51052684	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs146257607	chr10:51052728-51052729	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs533922871	chr10:51052779-51052780	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs538043059	chr10:51052824-51052825	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs35155139	chr10:51052851-51052852	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs189001777	chr10:51052867-51052868	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs180995349	chr10:51052930-51052931	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs538105968	chr10:51052931-51052932	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs572734977	chr10:51052964-51052965	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs74347975	chr10:51052977-51052978	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs556045816	chr10:51053045-51053046	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs574267274	chr10:51053061-51053062	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs78499364	chr10:51053104-51053105	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs372029779	chr10:51053108-51053109	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs368659018	chr10:51053143-51053144	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs186178375	chr10:51053165-51053166	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs572035936	chr10:51053171-51053172	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Schizophrenia	23813976	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	21948486	CNVD
cleft palate	21948486	CNVD
Encephalopathy	21948486	CNVD
Lung cancer	18438408	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
speech delay	21948486	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
XY gonadal dysgenesis	20685758	CNVD
Colorectal cancer	21645411	CNVD
Lung adenocarcinoma	21935476	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:776 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:51019800-51053400	Weak transcription	Small Intestine	intestine
2	chr10:51024000-51052800	Weak transcription	NHLF	lung
3	chr10:51024200-51053200	Weak transcription	Fetal Brain Male	brain
4	chr10:51024600-51054800	Weak transcription	Fetal Heart	heart
5	chr10:51028200-51053000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr10:51028200-51054600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr10:51028400-51053000	Weak transcription	Colonic Mucosa	Colon
8	chr10:51028400-51055000	Weak transcription	Spleen	Spleen
9	chr10:51028400-51056200	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr10:51031000-51053200	Weak transcription	Rectal Smooth Muscle	rectum
11	chr10:51033200-51052000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr10:51038200-51052000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr10:51038800-51052000	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr10:51039800-51052800	Weak transcription	NHDF-Ad	bronchial
15	chr10:51040000-51051800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr10:51040000-51053400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr10:51040400-51053200	Weak transcription	Brain Hippocampus Middle	brain
18	chr10:51040400-51053200	Weak transcription	Esophagus	oesophagus
19	chr10:51040600-51052000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr10:51040600-51053000	Weak transcription	Brain Substantia Nigra	brain
21	chr10:51040600-51053000	Weak transcription	Gastric	stomach
22	chr10:51040600-51053200	Weak transcription	Brain Angular Gyrus	brain
23	chr10:51040600-51053200	Weak transcription	Brain Cingulate Gyrus	brain
24	chr10:51040600-51053400	Weak transcription	Brain Anterior Caudate	brain
25	chr10:51040600-51053400	Weak transcription	Pancreas	Pancrea
26	chr10:51040800-51053200	Weak transcription	Colon Smooth Muscle	Colon
27	chr10:51041000-51053200	Weak transcription	Aorta	Aorta
28	chr10:51041000-51054000	Weak transcription	Thymus	Thymus
29	chr10:51041000-51055000	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr10:51042400-51051800	Strong transcription	Primary monocytes fromperipheralblood	blood
31	chr10:51043200-51052000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr10:51043400-51052000	Strong transcription	Primary B cells from peripheral blood	blood
33	chr10:51043600-51051800	Strong transcription	Stomach Smooth Muscle	stomach
34	chr10:51043600-51052000	Strong transcription	Primary T cells fromperipheralblood	blood
35	chr10:51043600-51052200	Strong transcription	Primary T helper cells fromperipheralblood	blood
36	chr10:51043600-51053200	Weak transcription	Stomach Mucosa	stomach
37	chr10:51043800-51052200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
38	chr10:51043800-51052200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr10:51044200-51052800	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr10:51044400-51053600	Strong transcription	HUES48 Cell Line	embryonic stem cell
41	chr10:51044600-51051800	Strong transcription	Duodenum Smooth Muscle	Duodenum
42	chr10:51044800-51051800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr10:51044800-51052200	Strong transcription	Primary T helper cells PMA-I stimulated	--
44	chr10:51045000-51052000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr10:51045000-51053600	Strong transcription	HUES64 Cell Line	embryonic stem cell
46	chr10:51045200-51052000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr10:51045600-51052000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr10:51045600-51052200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr10:51045800-51052000	Strong transcription	Cortex derived primary cultured neurospheres	brain
50	chr10:51045800-51052000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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