Variant report

Variant	nsv517553
Chromosome Location	chr15:42970899-43023482
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:739)
CpG islands
(count:306)
Chromatin interactive
region (count:42)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:739 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:43008561-43008586	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:43000560-43000618	K562	blood:	n/a	n/a
3	ATF2	chr15:42972346-42972581	GM12878	blood:	n/a	n/a
4	BACH1	chr15:42999321-42999521	K562	blood:	n/a	n/a
5	BATF	chr15:42972290-42972588	GM12878	blood:	n/a	chr15:42972447-42972458 chr15:42972338-42972347
6	BATF	chr15:42972238-42972646	GM12878	blood:	n/a	chr15:42972447-42972458 chr15:42972338-42972347
7	CBX3	chr15:42980028-42980218	K562	blood:	n/a	n/a
8	CBX3	chr15:42979985-42980297	K562	blood:	n/a	n/a
9	CEBPB	chr15:42991266-42991507	A549	lung:	n/a	chr15:42991439-42991450
10	CEBPB	chr15:42991244-42991562	K562	blood:	n/a	chr15:42991439-42991450
11	CEBPB	chr15:42991253-42991568	IMR90	lung:	n/a	chr15:42991439-42991450
12	CEBPB	chr15:42971652-42971803	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr15:42991282-42991562	HepG2	liver:	n/a	chr15:42991439-42991450
14	CEBPB	chr15:42978418-42978648	HepG2	liver:	n/a	n/a
15	CEBPB	chr15:42991299-42991445	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr15:42996684-42996880	A549	lung:	n/a	n/a
17	CEBPB	chr15:43013259-43013503	HepG2	liver:	n/a	n/a
18	CEBPB	chr15:43006909-43007151	IMR90	lung:	n/a	chr15:43007037-43007048
19	CEBPB	chr15:43006914-43007205	HepG2	liver:	n/a	chr15:43007037-43007048
20	CHD2	chr15:43018354-43018365	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr15:42996700-42996850	HMEC	breast:	n/a	n/a
22	CTCF	chr15:42972360-42972510	HEEpiC	esophagus:	n/a	n/a
23	CTCF	chr15:42996720-42996870	BE2_C	brain:	n/a	n/a
24	CTCF	chr15:42996462-42997104	HCT-116	colon:	n/a	n/a
25	CTCF	chr15:43015340-43015490	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr15:42996720-42996870	NHEK	skin:	n/a	n/a
27	CTCF	chr15:42996700-42996850	GM12864	blood:	n/a	n/a
28	CTCF	chr15:42996680-42996830	RPTEC	kidney:	n/a	n/a
29	CTCF	chr15:42996384-42997364	SK-N-SH	brain:	n/a	n/a
30	CTCF	chr15:43015344-43015586	LNCaP	prostate:	n/a	n/a
31	CTCF	chr15:42996570-42996985	IMR90	lung:	n/a	n/a
32	CTCF	chr15:43015340-43015490	GM12864	blood:	n/a	n/a
33	CTCF	chr15:43015260-43015410	GM12867	blood:	n/a	n/a
34	CTCF	chr15:43011866-43011921	LNCaP	prostate:	n/a	n/a
35	CTCF	chr15:43018360-43018510	HRPEpiC	eye:	n/a	chr15:43018481-43018490
36	CTCF	chr15:42996740-42996890	AG04450	lung:	n/a	n/a
37	CTCF	chr15:42996523-42996961	T-47D	breast:	n/a	n/a
38	CTCF	chr15:42972360-42972510	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr15:42996580-42996980	HepG2	liver:	n/a	n/a
40	CTCF	chr15:43015320-43015470	HL-60	blood:	n/a	n/a
41	CTCF	chr15:42996650-42996890	GM10266	blood:	n/a	n/a
42	CTCF	chr15:43015360-43015510	MCF-7	breast:	n/a	n/a
43	CTCF	chr15:42996653-42996899	A549	lung:	n/a	n/a
44	CTCF	chr15:42996631-42996924	Pancreas_OC	pancreas:	n/a	n/a
45	CTCF	chr15:42996700-42996850	GM12865	blood:	n/a	n/a
46	CTCF	chr15:42996700-42996850	AG09309	skin:	n/a	n/a
47	CTCF	chr15:43015220-43015370	HCM	heart:	n/a	n/a
48	CTCF	chr15:43015480-43015630	HCM	heart:	n/a	n/a
49	CTCF	chr15:42996692-42996916	MCF-7	breast:	n/a	n/a
50	CTCF	chr15:43015400-43015550	GM12873	blood:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43012152-43012202	HCF	heart:	n/a
2	chr15:43012152-43012202	HCF	heart:	n/a
3	chr15:43016527-43016577	GM19239	blood:	n/a
4	chr15:43021976-43022026	SKMC	muscle:	n/a
5	chr15:43008690-43008740	MCF-7	breast:	n/a
6	chr15:43012152-43012202	Hepatocyte	liver:	n/a
7	chr15:43016527-43016577	ProgFib	skin:	n/a
8	chr15:43008690-43008740	GM12891	blood:	n/a
9	chr15:43008690-43008740	HMEC	breast:	n/a
10	chr15:43022829-43022879	PFSK-1	brain:	n/a
11	chr15:43016527-43016577	PFSK-1	brain:	n/a
12	chr15:43008690-43008740	HCF	heart:	n/a
13	chr15:43008690-43008740	AG10803	skin:	n/a
14	chr15:43021976-43022026	A549	lung:	n/a
15	chr15:43008690-43008740	NHBE	bronchial:	n/a
16	chr15:43012152-43012202	AG04449	skin:	fetal
17	chr15:43016527-43016577	GM06990	blood:	n/a
18	chr15:43012152-43012202	Hela-S3	cervix:	n/a
19	chr15:43008690-43008740	Jurkat	blood:	n/a
20	chr15:43016527-43016577	HepG2	liver:	n/a
21	chr15:43021976-43022026	SAEC	small airway:	n/a
22	chr15:43008690-43008740	RPTEC	kidney:	n/a
23	chr15:43016527-43016577	HIPEpiC	eye:	n/a
24	chr15:43022829-43022879	AG10803	skin:	n/a
25	chr15:43008690-43008740	PrEC	prostate:	n/a
26	chr15:43022829-43022879	HCT-116	colon:	n/a
27	chr15:43021976-43022026	NT2-D1	testis:	n/a
28	chr15:43021976-43022026	GM06990	blood:	n/a
29	chr15:43008690-43008740	HNPCEpiC	eye:	n/a
30	chr15:43021976-43022026	ovcar-3	ovarian:	n/a
31	chr15:43016527-43016577	NHDF-neo	bronchial:	n/a
32	chr15:43022829-43022879	GM19239	blood:	n/a
33	chr15:43012152-43012202	LNCaP	prostate:	n/a
34	chr15:43022829-43022879	BJ	skin:	n/a
35	chr15:43016527-43016577	Hepatocyte	liver:	n/a
36	chr15:43022829-43022879	ovcar-3	ovarian:	n/a
37	chr15:43008690-43008740	BJ	skin:	n/a
38	chr15:43021976-43022026	SK-N-SH	brain:	n/a
39	chr15:43016527-43016577	HRE	kidney:	n/a
40	chr15:43021976-43022026	K562	blood:	n/a
41	chr15:43022829-43022879	SK-N-MC	brain:	n/a
42	chr15:43016527-43016577	LNCaP	prostate:	n/a
43	chr15:43016527-43016577	AG09309	skin:	n/a
44	chr15:43016527-43016577	PrEC	prostate:	n/a
45	chr15:43012152-43012202	A549	lung:	n/a
46	chr15:43008690-43008740	Caco-2	colon:	n/a
47	chr15:43021976-43022026	HUVEC	blood vessel:	n/a
48	chr15:43021976-43022026	BJ	skin:	n/a
49	chr15:43021976-43022026	AG09319	gingival:	n/a
50	chr15:43012152-43012202	SK-N-SH	brain:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:42964822..42967725-chr15:42973994..42976246,3	K562	blood:
2	chr15:42972332..42975595-chr15:42981286..42984253,3	K562	blood:
3	chr15:43014319..43018768-chr15:43027782..43030873,5	MCF-7	breast:
4	chr15:43014717..43017348-chr15:43028002..43029875,2	MCF-7	breast:
5	chr15:42996508..42997091-chr15:43015306..43015832,2	MCF-7	breast:
6	chr15:43004420..43008133-chr15:43008696..43011545,3	K562	blood:
7	chr15:42972306..42975288-chr15:42982753..42985416,2	K562	blood:
8	chr15:43010972..43017152-chr15:43019499..43025146,7	MCF-7	breast:
9	chr15:43004420..43008133-chr15:43008696..43011545,3	K562	blood:
10	chr15:42985508..42988057-chr15:43016423..43018014,2	K562	blood:
11	chr15:43023409..43026970-chr15:43028555..43030726,4	MCF-7	breast:
12	chr15:42980964..42982902-chr15:42984306..42986135,2	K562	blood:
13	chr15:43015023..43015967-chr15:43218682..43219556,3	MCF-7	breast:
14	chr15:42964822..42967725-chr15:42973994..42976246,2	K562	blood:
15	chr15:42983549..42985784-chr15:42989459..42991340,2	K562	blood:
16	chr15:43005044..43007388-chr15:43020446..43022660,2	K562	blood:
17	chr15:43005044..43007388-chr15:43020446..43022660,2	K562	blood:
18	chr15:42996644..42997222-chr15:43014554..43015613,3	MCF-7	breast:
19	chr15:42972306..42975288-chr15:42982753..42985416,2	K562	blood:
20	chr15:42996321..42997267-chr15:43577508..43578431,6	K562	blood:
21	chr15:43007397..43009798-chr15:43011681..43013458,2	MCF-7	breast:
22	chr15:42996313..42997182-chr15:43218578..43219161,2	MCF-7	breast:
23	chr15:42996508..42997091-chr15:43015306..43015832,2	MCF-7	breast:
24	chr15:42996634..42997289-chr15:43496048..43497151,3	MCF-7	breast:
25	chr15:43002992..43005620-chr15:43005783..43008129,2	K562	blood:
26	chr15:43019448..43022159-chr15:43025632..43028520,2	MCF-7	breast:
27	chr15:42983652..42985690-chr15:42986702..42989327,2	K562	blood:
28	chr15:42957477..42963934-chr15:42964860..42973083,9	K562	blood:
29	chr15:42983652..42985690-chr15:42986702..42989327,2	K562	blood:
30	chr15:42996644..42997222-chr15:43014554..43015613,3	MCF-7	breast:
31	chr15:43011390..43013542-chr15:43022490..43025034,3	K562	blood:
32	chr15:42983549..42985784-chr15:42989459..42991340,2	K562	blood:
33	chr15:42969516..42971199-chr15:42979000..42981438,2	MCF-7	breast:
34	chr15:43020195..43022907-chr15:43026273..43029275,3	MCF-7	breast:
35	chr15:43011244..43015007-chr15:43016381..43019349,5	K562	blood:
36	chr15:42996049..42999040-chr15:43025539..43027255,2	K562	blood:
37	chr15:42967308..42970278-chr15:42981149..42982877,2	K562	blood:
38	chr15:43007694..43010580-chr15:43015984..43019053,4	K562	blood:
39	chr15:43010693..43013698-chr15:43016416..43019349,5	K562	blood:
40	chr15:43007397..43009798-chr15:43011681..43013458,2	MCF-7	breast:
41	chr15:43002992..43005620-chr15:43005783..43008129,2	K562	blood:
42	chr15:42969516..42971199-chr15:42979000..42981438,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CDAN1	hsa-miR-34a-5p	chr15:43016541-43016566

Variant related genes	Relation type
STARD9	TF binding region
ENSG00000239025	TF binding region
CDAN1	TF binding region
STARD9	CpG island
ENSG00000239025	CpG island
CDAN1	CpG island
ENSG00000159433	chromatin interactions
ENSG00000140326	chromatin interactions

Extended variants
information (count: 2292 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2292 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12914570	chr15:42970899-42970900	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs142982376	chr15:42970998-42970999	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs571516103	chr15:42971013-42971014	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs541002345	chr15:42971034-42971035	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs368910118	chr15:42971094-42971095	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs142373995	chr15:42971150-42971151	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs189502218	chr15:42971151-42971152	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs16957037	chr15:42971188-42971189	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs181506969	chr15:42971266-42971267	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs143677353	chr15:42971296-42971297	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs185998838	chr15:42971310-42971311	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs572948171	chr15:42971312-42971313	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs545143032	chr15:42971323-42971324	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs558746876	chr15:42971415-42971416	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs12323990	chr15:42971515-42971516	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs577625321	chr15:42971519-42971520	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs544175764	chr15:42971579-42971580	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs191334483	chr15:42971583-42971584	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs7163030	chr15:42971620-42971621	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs542979258	chr15:42971648-42971649	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs559336456	chr15:42971654-42971655	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs183094452	chr15:42971690-42971691	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs551464299	chr15:42971732-42971733	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs560360250	chr15:42971747-42971748	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs527497690	chr15:42971751-42971752	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs75782255	chr15:42971760-42971761	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs185948399	chr15:42971765-42971766	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs531172718	chr15:42971804-42971805	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs150696104	chr15:42971838-42971839	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs140113581	chr15:42971890-42971891	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs542927420	chr15:42971913-42971914	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs546587046	chr15:42971931-42971932	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs190820260	chr15:42972022-42972023	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs113397507	chr15:42972033-42972034	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs142166951	chr15:42972084-42972085	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs558732473	chr15:42972122-42972123	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs575337117	chr15:42972128-42972129	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs146206454	chr15:42972140-42972141	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs529269398	chr15:42972145-42972146	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs114641497	chr15:42972198-42972199	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs574640812	chr15:42972264-42972265	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs35859208	chr15:42972303-42972304	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs34678707	chr15:42972345-42972346	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs74352881	chr15:42972364-42972365	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs559275672	chr15:42972496-42972497	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs572945099	chr15:42972498-42972499	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs545086800	chr15:42972524-42972525	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs562750032	chr15:42972530-42972531	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs565071183	chr15:42972574-42972575	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs530988461	chr15:42972626-42972627	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1026 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42908800-43015000	Weak transcription	Fetal Kidney	kidney
2	chr15:42928200-42973600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr15:42928200-42974000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr15:42942800-42973600	Weak transcription	Psoas Muscle	Psoas
5	chr15:42945200-42973400	Weak transcription	Thymus	Thymus
6	chr15:42949800-42999200	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr15:42950400-42990200	Strong transcription	Fetal Stomach	stomach
8	chr15:42951000-42995000	Strong transcription	Fetal Muscle Trunk	muscle
9	chr15:42952200-42973400	Weak transcription	Gastric	stomach
10	chr15:42952600-42979000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr15:42952600-42995600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr15:42952800-42996000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr15:42953400-42992200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr15:42954200-42973600	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr15:42954400-42976200	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr15:42954600-42986200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr15:42954800-42983000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
18	chr15:42955000-42990200	Strong transcription	Fetal Muscle Leg	muscle
19	chr15:42955200-42974000	Weak transcription	Esophagus	oesophagus
20	chr15:42956000-42976400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr15:42956800-42973600	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr15:42957000-42976200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr15:42960000-42973400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr15:42960000-42981800	Strong transcription	Primary T cells from cord blood	blood
25	chr15:42960200-42973800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr15:42961000-42977600	Weak transcription	Small Intestine	intestine
27	chr15:42961200-42973800	Weak transcription	Fetal Thymus	thymus
28	chr15:42961200-42989200	Strong transcription	Ovary	ovary
29	chr15:42961400-42990800	Strong transcription	Colon Smooth Muscle	Colon
30	chr15:42961600-42989200	Weak transcription	Pancreas	Pancrea
31	chr15:42961800-42975000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr15:42962000-42974000	Weak transcription	HSMMtube	muscle
33	chr15:42963800-42976200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr15:42964200-42982400	Weak transcription	A549	lung
35	chr15:42964600-42972200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr15:42964600-42972800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr15:42964600-42979200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr15:42965000-42982200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr15:42966000-42972400	Strong transcription	Placenta	Placenta
40	chr15:42966000-42992800	Strong transcription	Duodenum Smooth Muscle	Duodenum
41	chr15:42966200-42972000	Strong transcription	Lung	lung
42	chr15:42966200-42972200	Strong transcription	Cortex derived primary cultured neurospheres	brain
43	chr15:42966400-42978400	Weak transcription	Dnd41	blood
44	chr15:42966400-42988400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr15:42966400-42988600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr15:42966600-42972200	Strong transcription	Rectal Smooth Muscle	rectum
47	chr15:42966600-42979400	Strong transcription	Spleen	Spleen
48	chr15:42966600-42979800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr15:42966600-42982400	Strong transcription	Fetal Brain Female	brain
50	chr15:42966600-42982800	Strong transcription	Primary hematopoietic stem cells	blood

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