Variant report

Variant	esv1801565
Chromosome Location	chr5:14671030-14684471
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:221)
CpG islands
(count:183)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:221 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:14675812-14676457	GM12878	blood:	n/a	n/a
2	ATF2	chr5:14678482-14679313	GM12878	blood:	n/a	n/a
3	ATF2	chr5:14675748-14676761	GM12878	blood:	n/a	n/a
4	ATF2	chr5:14671356-14672009	GM12878	blood:	n/a	n/a
5	ATF2	chr5:14678629-14679322	GM12878	blood:	n/a	n/a
6	ATF2	chr5:14671229-14671954	GM12878	blood:	n/a	n/a
7	BACH1	chr5:14676446-14676702	K562	blood:	n/a	n/a
8	BATF	chr5:14678940-14679401	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:14676110-14676600	GM12878	blood:	n/a	n/a
10	BCLAF1	chr5:14675804-14676981	GM12878	blood:	n/a	n/a
11	BHLHE40	chr5:14676473-14676831	K562	blood:	n/a	n/a
12	BHLHE40	chr5:14671655-14671942	GM12878	blood:	n/a	n/a
13	BHLHE40	chr5:14676122-14676473	GM12878	blood:	n/a	n/a
14	BHLHE40	chr5:14679010-14679061	GM12878	blood:	n/a	n/a
15	CBX3	chr5:14675849-14676867	K562	blood:	n/a	n/a
16	CCNT2	chr5:14675917-14676117	K562	blood:	n/a	n/a
17	CEBPB	chr5:14674982-14674991	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr5:14679012-14679260	HepG2	liver:	n/a	chr5:14679095-14679106
19	CEBPB	chr5:14678952-14679261	K562	blood:	n/a	chr5:14679095-14679106
20	CEBPB	chr5:14678770-14679387	GM12878	blood:	n/a	chr5:14679095-14679106
21	CHD1	chr5:14671831-14672102	GM12878	blood:	n/a	n/a
22	CHD2	chr5:14676693-14676798	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr5:14676066-14676758	GM12878	blood:	n/a	n/a
24	CHD2	chr5:14676523-14676858	K562	blood:	n/a	n/a
25	CREB1	chr5:14678450-14679458	GM12878	blood:	n/a	n/a
26	CREB1	chr5:14678728-14679387	GM12878	blood:	n/a	n/a
27	CTCF	chr5:14672780-14672930	GM12871	blood:	n/a	n/a
28	CUX1	chr5:14678891-14678998	GM12878	blood:	n/a	n/a
29	E2F4	chr5:14676571-14676791	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr5:14676098-14676393	GM12878	blood:	n/a	n/a
31	E2F6	chr5:14676099-14676348	K562	blood:	n/a	chr5:14676236-14676247
32	E2F6	chr5:14676034-14676568	H1-hESC	embryonic stem cell:	n/a	chr5:14676236-14676247
33	E2F6	chr5:14676067-14676919	K562	blood:	n/a	chr5:14676236-14676247
34	E2F6	chr5:14676033-14676348	H1-hESC	embryonic stem cell:	n/a	chr5:14676236-14676247
35	E2F6	chr5:14676060-14676397	K562	blood:	n/a	chr5:14676236-14676247
36	EBF1	chr5:14671591-14671865	GM12878	blood:	n/a	n/a
37	EBF1	chr5:14676287-14676675	GM12878	blood:	n/a	n/a
38	EBF1	chr5:14676164-14676791	GM12878	blood:	n/a	n/a
39	ELK1	chr5:14675485-14675655	GM12878	blood:	n/a	n/a
40	ELK1	chr5:14671393-14671654	GM12878	blood:	n/a	n/a
41	EP300	chr5:14683912-14684548	SK-N-SH_RA	brain:	n/a	n/a
42	EP300	chr5:14675917-14676758	GM12878	blood:	n/a	chr5:14675929-14675943
43	EP300	chr5:14675931-14676791	K562	blood:	n/a	n/a
44	EP300	chr5:14679113-14679148	GM12878	blood:	n/a	n/a
45	EP300	chr5:14676052-14676238	SK-N-SH_RA	brain:	n/a	n/a
46	EP300	chr5:14684108-14684537	SK-N-SH_RA	brain:	n/a	n/a
47	EP300	chr5:14671555-14671855	GM12878	blood:	n/a	n/a
48	EP300	chr5:14675975-14676544	GM12878	blood:	n/a	n/a
49	EP300	chr5:14679013-14679261	GM12878	blood:	n/a	n/a
50	EP300	chr5:14678971-14679076	GM12878	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:14673322-14673372	HAEpiC	amniotic membrane:	n/a
2	chr5:14673322-14673372	LNCaP	prostate:	n/a
3	chr5:14683126-14683176	Hepatocyte	liver:	n/a
4	chr5:14673322-14673372	Hela-S3	cervix:	n/a
5	chr5:14673322-14673372	AG09309	skin:	n/a
6	chr5:14676460-14676510	GM12878	blood:	n/a
7	chr5:14676460-14676510	HMEC	breast:	n/a
8	chr5:14683126-14683176	HRPEpiC	eye:	n/a
9	chr5:14676460-14676510	NH-A	brain:	n/a
10	chr5:14683126-14683176	AG09309	skin:	n/a
11	chr5:14673322-14673372	T-47D	breast:	n/a
12	chr5:14676460-14676510	GM19239	blood:	n/a
13	chr5:14683126-14683176	GM12878	blood:	n/a
14	chr5:14673322-14673372	ProgFib	skin:	n/a
15	chr5:14676460-14676510	SAEC	small airway:	n/a
16	chr5:14683126-14683176	NHBE	bronchial:	n/a
17	chr5:14673322-14673372	HepG2	liver:	n/a
18	chr5:14673322-14673372	ovcar-3	ovarian:	n/a
19	chr5:14683126-14683176	HL-60	blood:	n/a
20	chr5:14673322-14673372	AG09319	gingival:	n/a
21	chr5:14683126-14683176	Hela-S3	cervix:	n/a
22	chr5:14673322-14673372	HEK293	kidney:	embryo
23	chr5:14676460-14676510	K562	blood:	n/a
24	chr5:14676460-14676510	NT2-D1	testis:	n/a
25	chr5:14676460-14676510	A549	lung:	n/a
26	chr5:14676460-14676510	AoSMC	blood vessel:	n/a
27	chr5:14673322-14673372	SK-N-MC	brain:	n/a
28	chr5:14683126-14683176	HCF	heart:	n/a
29	chr5:14683126-14683176	GM06990	blood:	n/a
30	chr5:14676460-14676510	HIPEpiC	eye:	n/a
31	chr5:14676460-14676510	NB4	blood:	n/a
32	chr5:14676460-14676510	H1-hESC	embryonic stem cell:	embryo
33	chr5:14676460-14676510	ProgFib	skin:	n/a
34	chr5:14683126-14683176	GM12891	blood:	n/a
35	chr5:14676460-14676510	SK-N-MC	brain:	n/a
36	chr5:14683126-14683176	ovcar-3	ovarian:	n/a
37	chr5:14683126-14683176	NB4	blood:	n/a
38	chr5:14676460-14676510	HL-60	blood:	n/a
39	chr5:14683126-14683176	SK-N-SH_RA	brain:	n/a
40	chr5:14673322-14673372	HCPEpiC	choroid plexus:	n/a
41	chr5:14676460-14676510	IMR90	lung:	fetal
42	chr5:14683126-14683176	MCF-7	breast:	n/a
43	chr5:14676460-14676510	GM06990	blood:	n/a
44	chr5:14673322-14673372	ECC-1	luminal epithelium:	n/a
45	chr5:14676460-14676510	Caco-2	colon:	n/a
46	chr5:14673322-14673372	BJ	skin:	n/a
47	chr5:14676460-14676510	RPTEC	kidney:	n/a
48	chr5:14673322-14673372	HMEC	breast:	n/a
49	chr5:14673322-14673372	NT2-D1	testis:	n/a
50	chr5:14673322-14673372	PFSK-1	brain:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:14668622..14671046-chr5:14674810..14676511,2	K562	blood:
2	chr5:14670223..14672828-chr5:14683390..14686379,2	K562	blood:
3	chr5:14666399..14668895-chr5:14676273..14677945,2	MCF-7	breast:
4	chr5:14673734..14676543-chr5:14682799..14684871,2	K562	blood:
5	chr5:14680121..14683231-chr5:14683255..14687909,6	K562	blood:
6	chr5:14663431..14670152-chr5:14672054..14680588,17	K562	blood:
7	chr5:14673734..14676543-chr5:14682799..14684871,2	K562	blood:
8	chr5:14674501..14677095-chr5:14686339..14688159,2	K562	blood:
9	chr5:14662258..14667508-chr5:14670830..14674480,6	MCF-7	breast:
10	chr5:14667600..14670326-chr5:14676712..14678274,2	K562	blood:
11	chr5:14664681..14666885-chr5:14683408..14685365,2	MCF-7	breast:
12	chr5:14663912..14667514-chr5:14673583..14676166,6	K562	blood:
13	chr5:14675013..14677117-chr5:14685914..14688282,2	MCF-7	breast:
14	chr5:14670223..14672828-chr5:14683390..14686379,2	K562	blood:
15	chr5:14448785..14450697-chr5:14676194..14678624,2	MCF-7	breast:
16	chr5:14673939..14676437-chr5:14678453..14680700,3	K562	blood:
17	chr5:14672451..14674258-chr5:14675048..14677621,3	K562	blood:
18	chr5:14663911..14666053-chr5:14679468..14682192,2	MCF-7	breast:
19	chr5:14683758..14686068-chr5:14687921..14690777,3	K562	blood:
20	chr5:14663385..14665837-chr5:14671199..14673342,3	K562	blood:
21	chr5:14668622..14671046-chr5:14674810..14676511,2	K562	blood:
22	chr5:14671524..14673260-chr5:14708223..14710525,2	MCF-7	breast:
23	chr5:14672451..14674258-chr5:14675048..14677621,3	K562	blood:
24	chr5:14680587..14682687-chr5:14683791..14686120,3	K562	blood:

No data

Variant related genes	Relation type
FAM105B	TF binding region
FAM105B	CpG island
ENSG00000154124	chromatin interactions
ENSG00000261360	chromatin interactions

Extended variants
information (count: 497 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:497 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs31923	chr5:14671030-14671031	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs144734997	chr5:14671068-14671069	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs546317378	chr5:14671109-14671110	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs564711621	chr5:14671110-14671111	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs189587921	chr5:14671132-14671133	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs550060652	chr5:14671136-14671137	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs562429954	chr5:14671142-14671143	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs529529615	chr5:14671221-14671222	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs547025502	chr5:14671248-14671249	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs565317076	chr5:14671398-14671399	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs527552884	chr5:14671407-14671408	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs200312937	chr5:14671410-14671411	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs181638172	chr5:14671502-14671503	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs186935683	chr5:14671520-14671521	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs569368112	chr5:14671548-14671549	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs138675721	chr5:14671549-14671550	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs57921966	chr5:14671556-14671557	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs192274967	chr5:14671558-14671559	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs546587365	chr5:14671578-14671579	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs372739632	chr5:14671591-14671592	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs573895147	chr5:14671630-14671631	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs114720260	chr5:14671655-14671656	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs141292557	chr5:14671656-14671657	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs554234336	chr5:14671685-14671686	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs531500312	chr5:14671741-14671742	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs182005179	chr5:14671758-14671759	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs546180201	chr5:14671824-14671825	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs541248431	chr5:14671878-14671879	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs558286922	chr5:14671881-14671882	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs369787172	chr5:14672022-14672023	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs576431461	chr5:14672030-14672031	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs150742789	chr5:14672065-14672066	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs185251472	chr5:14672066-14672067	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs529622200	chr5:14672103-14672104	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs541325142	chr5:14672119-14672120	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs558962676	chr5:14672144-14672145	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs139113339	chr5:14672174-14672175	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs550912597	chr5:14672181-14672182	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs115714619	chr5:14672191-14672192	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs199862555	chr5:14672225-14672226	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs149452680	chr5:14672258-14672259	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs189702461	chr5:14672323-14672324	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs567325477	chr5:14672368-14672369	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs147146425	chr5:14672415-14672416	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs543056473	chr5:14672457-14672458	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs140990929	chr5:14672474-14672475	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs568311014	chr5:14672476-14672477	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs539864675	chr5:14672530-14672531	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs558152030	chr5:14672537-14672538	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs576517918	chr5:14672545-14672546	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Cervical squamous cell carcinoma	21590768	CNVD
abnormal development	18461090	CNVD
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Myelofibrosis	22110671	CNVD
Cri-du chat syndrome	16773131	CNVD
Cryptorchidism	21048976	CNVD
Glioblastoma multiforme	22286061	CNVD
Cervical cancer	16585170	CNVD
Mental retardation	16773131	CNVD
Non-small cell lung cancer	21829676	CNVD
Cri-du chat syndrome	22470819	CNVD
sporadic birth defects	19047251	CNVD
Breast cancer	21364760	CNVD
Non-small cell lung cancer	17643093	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	18940311	CNVD
Central neurocytomas	17123091	CNVD
Mental retardation	17847001	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	19546859	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Williams Syndrome	20824207	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21611746	CNVD

Chromatin state (count:912 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:14665600-14676600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:14666200-14672200	Weak transcription	Aorta	Aorta
3	chr5:14666400-14671200	Weak transcription	Brain Angular Gyrus	brain
4	chr5:14666400-14672200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:14666400-14673200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr5:14666400-14673200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr5:14666400-14674200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chr5:14666400-14675600	Weak transcription	Placenta	Placenta
9	chr5:14666400-14678200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr5:14666400-14681600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr5:14666400-14688200	Weak transcription	Ovary	ovary
12	chr5:14666600-14672000	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr5:14666600-14672200	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr5:14666600-14688200	Weak transcription	Brain Germinal Matrix	brain
15	chr5:14666800-14671200	Weak transcription	Rectal Smooth Muscle	rectum
16	chr5:14666800-14671400	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr5:14666800-14671600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr5:14666800-14671600	Weak transcription	NHDF-Ad	bronchial
19	chr5:14666800-14672000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr5:14666800-14672000	Weak transcription	HSMM	muscle
21	chr5:14666800-14672200	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr5:14666800-14675600	Weak transcription	NHLF	lung
23	chr5:14666800-14675800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr5:14667000-14671200	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr5:14667000-14671200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr5:14667000-14671200	Weak transcription	Brain Hippocampus Middle	brain
27	chr5:14667000-14671600	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr5:14667000-14672200	Weak transcription	Brain Substantia Nigra	brain
29	chr5:14667000-14672400	Weak transcription	Brain Anterior Caudate	brain
30	chr5:14667000-14672400	Weak transcription	HSMMtube	muscle
31	chr5:14667000-14675600	Weak transcription	Thymus	Thymus
32	chr5:14667000-14676600	Weak transcription	Fetal Kidney	kidney
33	chr5:14667000-14680000	Weak transcription	Fetal Brain Female	brain
34	chr5:14667000-14681200	Weak transcription	Brain Cingulate Gyrus	brain
35	chr5:14667000-14690400	Weak transcription	Fetal Brain Male	brain
36	chr5:14667200-14672000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr5:14667200-14672600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr5:14667400-14676600	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr5:14668200-14672200	Weak transcription	Gastric	stomach
40	chr5:14668200-14672200	Weak transcription	Lung	lung
41	chr5:14668200-14672200	Weak transcription	Stomach Smooth Muscle	stomach
42	chr5:14668200-14672600	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr5:14668200-14674200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr5:14668400-14671200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr5:14668400-14671200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr5:14668600-14671200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
47	chr5:14668600-14671200	Enhancers	Primary T killer memory cells from peripheral blood	blood
48	chr5:14668600-14672000	Weak transcription	Colonic Mucosa	Colon
49	chr5:14668600-14672000	Weak transcription	Pancreas	Pancrea
50	chr5:14668600-14672200	Enhancers	Primary T regulatory cells fromperipheralblood	blood

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