Variant report

Variant	nsv827386
Chromosome Location	chr15:75161362-75166473
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:627)
CpG islands
(count:488)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:627 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:75165416-75165717	HepG2	liver:	n/a	n/a
2	ATF1	chr15:75165221-75166124	K562	blood:	n/a	n/a
3	ATF2	chr15:75164927-75166133	GM12878	blood:	n/a	n/a
4	ATF2	chr15:75161787-75162930	GM12878	blood:	n/a	n/a
5	ATF2	chr15:75165117-75165757	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr15:75161825-75163020	GM12878	blood:	n/a	n/a
7	ATF3	chr15:75165780-75166374	A549	lung:	n/a	n/a
8	ATF3	chr15:75165512-75165742	K562	blood:	n/a	n/a
9	BACH1	chr15:75165764-75165964	K562	blood:	n/a	n/a
10	BACH1	chr15:75165424-75165595	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr15:75165518-75165767	GM12878	blood:	n/a	n/a
12	BATF	chr15:75162352-75162822	GM12878	blood:	n/a	chr15:75162591-75162600
13	BATF	chr15:75162099-75162861	GM12878	blood:	n/a	chr15:75162591-75162600
14	BCL11A	chr15:75162256-75162728	GM12878	blood:	n/a	n/a
15	BCL11A	chr15:75162238-75163092	GM12878	blood:	n/a	n/a
16	BCL3	chr15:75162299-75162798	GM12878	blood:	n/a	n/a
17	BCL3	chr15:75164975-75165739	A549	lung:	n/a	chr15:75165680-75165689
18	BCLAF1	chr15:75162019-75162844	GM12878	blood:	n/a	n/a
19	BCLAF1	chr15:75161744-75163302	GM12878	blood:	n/a	n/a
20	BCLAF1	chr15:75165284-75165742	GM12878	blood:	n/a	chr15:75165680-75165689
21	BHLHE40	chr15:75162064-75162780	GM12878	blood:	n/a	n/a
22	BHLHE40	chr15:75165200-75165629	K562	blood:	n/a	chr15:75165475-75165491
23	BHLHE40	chr15:75165255-75165749	GM12878	blood:	n/a	chr15:75165475-75165491
24	BHLHE40	chr15:75165955-75166155	K562	blood:	n/a	n/a
25	BRCA1	chr15:75165326-75165657	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr15:75165173-75165706	HepG2	liver:	n/a	n/a
27	CBX3	chr15:75165269-75165753	K562	blood:	n/a	n/a
28	CCNT2	chr15:75165342-75165749	K562	blood:	n/a	n/a
29	CEBPB	chr15:75166354-75166568	HepG2	liver:	n/a	chr15:75166416-75166427
30	CEBPB	chr15:75165298-75165592	K562	blood:	n/a	n/a
31	CEBPB	chr15:75166182-75166530	K562	blood:	n/a	chr15:75166416-75166427
32	CEBPB	chr15:75162157-75163309	GM12878	blood:	n/a	n/a
33	CEBPB	chr15:75162357-75162765	GM12878	blood:	n/a	n/a
34	CEBPB	chr15:75166390-75166482	H1-hESC	embryonic stem cell:	n/a	chr15:75166416-75166427
35	CEBPB	chr15:75165260-75165687	Hela-S3	cervix:	n/a	n/a
36	CEBPD	chr15:75165279-75165979	HepG2	liver:	n/a	n/a
37	CHD1	chr15:75165897-75166079	GM12878	blood:	n/a	n/a
38	CHD1	chr15:75164776-75165493	GM12878	blood:	n/a	n/a
39	CHD1	chr15:75162105-75163430	GM12878	blood:	n/a	n/a
40	CHD2	chr15:75165145-75165704	GM12878	blood:	n/a	n/a
41	CHD2	chr15:75165142-75165990	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr15:75165200-75165746	K562	blood:	n/a	n/a
43	CHD2	chr15:75162217-75162862	GM12878	blood:	n/a	n/a
44	CHD2	chr15:75165341-75165697	HepG2	liver:	n/a	n/a
45	CHD2	chr15:75165196-75165775	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr15:75165973-75165979	GM12878	blood:	n/a	n/a
47	CREB1	chr15:75165027-75166253	HepG2	liver:	n/a	n/a
48	CREB1	chr15:75165177-75165987	K562	blood:	n/a	n/a
49	CREB1	chr15:75165025-75166084	GM12878	blood:	n/a	n/a
50	CREB1	chr15:75165125-75165978	HepG2	liver:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:75166202-75166252	HRE	kidney:	n/a
2	chr15:75165438-75165488	AG09309	skin:	n/a
3	chr15:75162173-75162223	HMEC	breast:	n/a
4	chr15:75162173-75162223	HIPEpiC	eye:	n/a
5	chr15:75165624-75165674	HRPEpiC	eye:	n/a
6	chr15:75166202-75166252	GM12892	blood:	n/a
7	chr15:75165624-75165674	HCT-116	colon:	n/a
8	chr15:75165624-75165674	ProgFib	skin:	n/a
9	chr15:75165642-75165692	HUVEC	blood vessel:	n/a
10	chr15:75162173-75162223	SAEC	small airway:	n/a
11	chr15:75165624-75165674	GM19239	blood:	n/a
12	chr15:75165821-75165871	A549	lung:	n/a
13	chr15:75165642-75165692	SK-N-SH	brain:	n/a
14	chr15:75165896-75165946	AoSMC	blood vessel:	n/a
15	chr15:75165821-75165871	Hela-S3	cervix:	n/a
16	chr15:75165338-75165388	BJ	skin:	n/a
17	chr15:75165624-75165674	GM12891	blood:	n/a
18	chr15:75162173-75162223	HCT-116	colon:	n/a
19	chr15:75165624-75165674	Jurkat	blood:	n/a
20	chr15:75165338-75165388	HRCEpiC	kidney:	n/a
21	chr15:75165642-75165692	Jurkat	blood:	n/a
22	chr15:75166202-75166252	LNCaP	prostate:	n/a
23	chr15:75165821-75165871	U87	brain:	n/a
24	chr15:75165438-75165488	U87	brain:	n/a
25	chr15:75162173-75162223	SK-N-SH	brain:	n/a
26	chr15:75162173-75162223	MCF10A-Er-Src	breast:	n/a
27	chr15:75162173-75162223	NHBE	bronchial:	n/a
28	chr15:75165338-75165388	HUVEC	blood vessel:	n/a
29	chr15:75165338-75165388	A549	lung:	n/a
30	chr15:75166202-75166252	SK-N-MC	brain:	n/a
31	chr15:75166202-75166252	AG04449	skin:	fetal
32	chr15:75165438-75165488	Caco-2	colon:	n/a
33	chr15:75165642-75165692	Hela-S3	cervix:	n/a
34	chr15:75165338-75165388	HCM	heart:	n/a
35	chr15:75165624-75165674	Hela-S3	cervix:	n/a
36	chr15:75165624-75165674	HL-60	blood:	n/a
37	chr15:75165438-75165488	AG04450	lung:	fetal
38	chr15:75165642-75165692	AG04449	skin:	fetal
39	chr15:75165896-75165946	AG10803	skin:	n/a
40	chr15:75165896-75165946	MCF10A-Er-Src	breast:	n/a
41	chr15:75165438-75165488	HEK293	kidney:	embryo
42	chr15:75165642-75165692	GM12891	blood:	n/a
43	chr15:75166202-75166252	RPTEC	kidney:	n/a
44	chr15:75165821-75165871	Caco-2	colon:	n/a
45	chr15:75165624-75165674	PrEC	prostate:	n/a
46	chr15:75165896-75165946	ovcar-3	ovarian:	n/a
47	chr15:75162173-75162223	GM12892	blood:	n/a
48	chr15:75165438-75165488	HUVEC	blood vessel:	n/a
49	chr15:75165642-75165692	LNCaP	prostate:	n/a
50	chr15:75165438-75165488	NHBE	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr15:75161914..75167776-chr15:75191644..75199761,13	MCF-7	breast:
2	chr15:75163277..75165219-chr15:75166368..75168466,2	MCF-7	breast:
3	chr15:75163901..75170368-chr15:75180139..75184021,10	K562	blood:
4	chr15:75160386..75162406-chr15:75181750..75183774,2	MCF-7	breast:
5	chr15:75110223..75112810-chr15:75165268..75167627,2	MCF-7	breast:
6	chr15:75162469..75167536-chr15:75180880..75184902,6	K562	blood:
7	chr15:75129767..75136088-chr15:75163908..75167881,8	K562	blood:
8	chr15:75136180..75138079-chr15:75161900..75164141,2	K562	blood:
9	chr15:75158451..75161193-chr15:75161527..75164480,2	MCF-7	breast:
10	chr15:75164573..75166914-chr15:75228746..75230664,2	K562	blood:
11	chr15:75163277..75165219-chr15:75166368..75168466,2	MCF-7	breast:
12	chr15:75161949..75163457-chr15:75228815..75230977,2	MCF-7	breast:
13	chr15:75166310..75168984-chr15:75177329..75180043,2	MCF-7	breast:
14	chr15:75164429..75167842-chr15:75196018..75198435,3	K562	blood:
15	chr15:75163342..75166719-chr15:75180364..75184673,7	MCF-7	breast:
16	chr15:75157220..75162664-chr15:75181204..75183708,6	MCF-7	breast:
17	chr15:75073135..75075746-chr15:75163972..75165852,2	K562	blood:
18	chr15:75163351..75167012-chr15:75180238..75185061,13	MCF-7	breast:
19	chr1:249199798..249200453-chr15:75165136..75165714,2	Hela-S3	cervix:
20	chr15:75132063..75136088-chr15:75165447..75167881,5	K562	blood:
21	chr15:75163746..75165751-chr15:75191304..75195509,4	K562	blood:
22	chr15:75163895..75166026-chr15:75315159..75317542,2	MCF-7	breast:
23	chr15:75134049..75139648-chr15:75161531..75167020,13	MCF-7	breast:
24	chr15:75152352..75156342-chr15:75158618..75163297,4	K562	blood:

No data

Variant related genes	Relation type
SCAMP2	TF binding region
SCAMP2	CpG island
ENSG00000178802	chromatin interactions
ENSG00000260483	chromatin interactions
ENSG00000140474	chromatin interactions
ENSG00000140506	chromatin interactions
ENSG00000178761	chromatin interactions
ENSG00000138621	chromatin interactions
ENSG00000185220	chromatin interactions
ENSG00000103653	chromatin interactions
ENSG00000178741	chromatin interactions
ENSG00000260824	chromatin interactions

Extended variants
information (count: 188 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:188 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371522854	chr15:75161363-75161364	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs540116496	chr15:75161384-75161385	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs78551075	chr15:75161412-75161413	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs539379508	chr15:75161418-75161419	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs558451244	chr15:75161433-75161434	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs567173834	chr15:75161480-75161481	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs534360070	chr15:75161487-75161488	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs188857322	chr15:75161490-75161491	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs192548270	chr15:75161508-75161509	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs574062274	chr15:75161515-75161516	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs184853848	chr15:75161521-75161522	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs556513327	chr15:75161660-75161661	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs577919720	chr15:75161678-75161679	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs150267702	chr15:75161720-75161721	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs12101507	chr15:75161758-75161759	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs572818064	chr15:75161870-75161871	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs540023473	chr15:75161902-75161903	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs555019138	chr15:75161974-75161975	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs528978194	chr15:75162025-75162026	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs574843130	chr15:75162117-75162118	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs550443046	chr15:75162128-75162129	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs188933656	chr15:75162137-75162138	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs532745585	chr15:75162165-75162166	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs560425493	chr15:75162173-75162174	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs145881802	chr15:75162198-75162199	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs148823599	chr15:75162253-75162254	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs192221644	chr15:75162525-75162526	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs556919050	chr15:75162532-75162533	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs549576134	chr15:75162556-75162557	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs184828416	chr15:75162558-75162559	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs78749825	chr15:75162593-75162594	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs556338068	chr15:75162650-75162651	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs545717527	chr15:75162724-75162725	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs729263	chr15:75162751-75162752	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs538613969	chr15:75162771-75162772	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs553784117	chr15:75162772-75162773	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs189647779	chr15:75162786-75162787	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs540184147	chr15:75162830-75162831	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs180772632	chr15:75162840-75162841	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs560776084	chr15:75162870-75162871	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs573712170	chr15:75162878-75162879	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs369195379	chr15:75162887-75162888	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs544397598	chr15:75162890-75162891	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs562416013	chr15:75162892-75162893	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs533073002	chr15:75162904-75162905	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs184363888	chr15:75162949-75162950	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs560216088	chr15:75162956-75162957	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs572468587	chr15:75162975-75162976	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs531347039	chr15:75162995-75162996	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs143449927	chr15:75163004-75163005	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	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
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Epilepsy	22083797	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	18438408	CNVD

Chromatin state (count:824 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:75136200-75161800	Weak transcription	Fetal Kidney	kidney
2	chr15:75136600-75163000	Weak transcription	Fetal Brain Male	brain
3	chr15:75137000-75164800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr15:75143600-75163000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr15:75146000-75164800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr15:75146200-75163200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr15:75146400-75161800	Weak transcription	Fetal Lung	lung
8	chr15:75146400-75163200	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr15:75146600-75163000	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr15:75146600-75164600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr15:75147000-75164800	Weak transcription	Ovary	ovary
12	chr15:75147200-75164800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr15:75150400-75161800	Weak transcription	Aorta	Aorta
14	chr15:75151200-75161800	Weak transcription	Brain Angular Gyrus	brain
15	chr15:75151800-75161800	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr15:75152200-75162200	Weak transcription	Brain Cingulate Gyrus	brain
17	chr15:75152400-75161800	Weak transcription	Brain Hippocampus Middle	brain
18	chr15:75153600-75162200	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chr15:75155000-75162000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
20	chr15:75155800-75164400	Genic enhancers	Fetal Intestine Small	intestine
21	chr15:75156000-75164800	Enhancers	Fetal Intestine Large	intestine
22	chr15:75156600-75163800	Enhancers	Stomach Mucosa	stomach
23	chr15:75156800-75163600	Enhancers	Right Ventricle	heart
24	chr15:75157000-75163000	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr15:75157600-75161800	Enhancers	Colonic Mucosa	Colon
26	chr15:75157800-75162000	Enhancers	Adipose Nuclei	Adipose
27	chr15:75157800-75164600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr15:75158000-75161800	Enhancers	Fetal Heart	heart
29	chr15:75158000-75165000	Enhancers	Spleen	Spleen
30	chr15:75158200-75162200	Enhancers	HepG2	liver
31	chr15:75158200-75164600	Enhancers	Pancreas	Pancrea
32	chr15:75158200-75165000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr15:75158400-75161600	Enhancers	Psoas Muscle	Psoas
34	chr15:75158400-75164800	Enhancers	Liver	Liver
35	chr15:75158600-75162000	Genic enhancers	Fetal Muscle Leg	muscle
36	chr15:75158600-75162000	Enhancers	Right Atrium	heart
37	chr15:75158600-75163800	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr15:75158800-75162000	Weak transcription	NHLF	lung
39	chr15:75159000-75161400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr15:75159000-75161800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr15:75159000-75161800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr15:75159000-75161800	Weak transcription	NH-A	brain
43	chr15:75159000-75164600	Weak transcription	Osteobl	bone
44	chr15:75159200-75161400	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr15:75159200-75161800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr15:75159200-75161800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr15:75159200-75162200	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr15:75159200-75164000	Enhancers	Small Intestine	intestine
49	chr15:75159200-75164800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
50	chr15:75159400-75161600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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