Variant report

Variant	nsv904138
Chromosome Location	chr15:43268970-43414673
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:934)
CpG islands
(count:794)
Chromatin interactive
region (count:88)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:934 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:43387449-43387830	K562	blood:	n/a	n/a
2	ARID3A	chr15:43397648-43398773	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:43397368-43397887	K562	blood:	n/a	n/a
4	ARID3A	chr15:43398251-43398659	K562	blood:	n/a	n/a
5	ARID3A	chr15:43386853-43387247	K562	blood:	n/a	n/a
6	ARID3A	chr15:43414527-43414775	K562	blood:	n/a	n/a
7	ARID3A	chr15:43388218-43388264	HepG2	liver:	n/a	n/a
8	ATF1	chr15:43387460-43387755	K562	blood:	n/a	n/a
9	ATF1	chr15:43386875-43387161	K562	blood:	n/a	n/a
10	ATF1	chr15:43398151-43398528	K562	blood:	n/a	n/a
11	ATF2	chr15:43397682-43398573	GM12878	blood:	n/a	n/a
12	ATF2	chr15:43397991-43398451	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr15:43378722-43379113	GM12878	blood:	n/a	n/a
14	ATF3	chr15:43398117-43398486	HepG2	liver:	n/a	n/a
15	ATF3	chr15:43398097-43398441	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr15:43398126-43398472	K562	blood:	n/a	n/a
17	BACH1	chr15:43397593-43397889	K562	blood:	n/a	n/a
18	BACH1	chr15:43300070-43300234	K562	blood:	n/a	n/a
19	BATF	chr15:43378759-43379062	GM12878	blood:	n/a	n/a
20	BATF	chr15:43359977-43360156	GM12878	blood:	n/a	n/a
21	BATF	chr15:43317398-43317616	GM12878	blood:	n/a	chr15:43317546-43317557
22	BATF	chr15:43359931-43360160	GM12878	blood:	n/a	n/a
23	BATF	chr15:43378535-43379134	GM12878	blood:	n/a	n/a
24	BATF	chr15:43317425-43317631	GM12878	blood:	n/a	chr15:43317546-43317557
25	BATF	chr15:43388203-43388457	GM12878	blood:	n/a	n/a
26	BCL11A	chr15:43368163-43368349	GM12878	blood:	n/a	n/a
27	BCLAF1	chr15:43397552-43398686	GM12878	blood:	n/a	n/a
28	BCLAF1	chr15:43397997-43398637	GM12878	blood:	n/a	n/a
29	BHLHE40	chr15:43397805-43398668	GM12878	blood:	n/a	n/a
30	BHLHE40	chr15:43397656-43398507	K562	blood:	n/a	n/a
31	BHLHE40	chr15:43271357-43271588	HepG2	liver:	n/a	n/a
32	BHLHE40	chr15:43382873-43382875	GM12878	blood:	n/a	n/a
33	BRCA1	chr15:43398031-43398634	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr15:43396304-43396666	Hela-S3	cervix:	n/a	n/a
35	CBX3	chr15:43399955-43400320	K562	blood:	n/a	n/a
36	CBX3	chr15:43397993-43398585	K562	blood:	n/a	n/a
37	CCNT2	chr15:43386885-43387085	K562	blood:	n/a	n/a
38	CCNT2	chr15:43398119-43398840	K562	blood:	n/a	n/a
39	CEBPB	chr15:43391414-43391809	K562	blood:	n/a	chr15:43391596-43391609 chr15:43391598-43391607 chr15:43391596-43391607 chr15:43391598-43391607 chr15:43391598-43391607
40	CEBPB	chr15:43339371-43339585	HepG2	liver:	n/a	chr15:43339452-43339463
41	CEBPB	chr15:43395906-43396582	Hela-S3	cervix:	n/a	chr15:43396333-43396346 chr15:43396335-43396346 chr15:43396314-43396325 chr15:43396312-43396323 chr15:43396314-43396323 chr15:43396312-43396325
42	CEBPB	chr15:43286806-43287085	IMR90	lung:	n/a	n/a
43	CEBPB	chr15:43396101-43396528	MCF-7	breast:	n/a	chr15:43396333-43396346 chr15:43396335-43396346 chr15:43396314-43396325 chr15:43396312-43396323 chr15:43396314-43396323 chr15:43396312-43396325
44	CEBPB	chr15:43374726-43375076	IMR90	lung:	n/a	chr15:43374901-43374912
45	CEBPB	chr15:43361465-43361481	K562	blood:	n/a	n/a
46	CEBPB	chr15:43414590-43415017	IMR90	lung:	n/a	chr15:43414834-43414845 chr15:43414833-43414846
47	CEBPB	chr15:43360281-43360994	K562	blood:	n/a	n/a
48	CEBPB	chr15:43414614-43414973	K562	blood:	n/a	chr15:43414834-43414845 chr15:43414833-43414846
49	CEBPB	chr15:43360346-43360517	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr15:43413364-43413686	K562	blood:	n/a	chr15:43413524-43413535

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43398346-43398396	Jurkat	blood:	n/a
2	chr15:43398346-43398396	Jurkat	blood:	n/a
3	chr15:43398338-43398388	GM12891	blood:	n/a
4	chr15:43398101-43398151	AG10803	skin:	n/a
5	chr15:43398101-43398151	Hela-S3	cervix:	n/a
6	chr15:43399625-43399675	HPAEpiC	pulmonary alveolar:	n/a
7	chr15:43398173-43398223	SKMC	muscle:	n/a
8	chr15:43398302-43398352	NT2-D1	testis:	n/a
9	chr15:43398826-43398876	HIPEpiC	eye:	n/a
10	chr15:43398435-43398485	GM12878	blood:	n/a
11	chr15:43399625-43399675	PFSK-1	brain:	n/a
12	chr15:43398435-43398485	NHBE	bronchial:	n/a
13	chr15:43398826-43398876	ProgFib	skin:	n/a
14	chr15:43398270-43398320	MCF10A-Er-Src	breast:	n/a
15	chr15:43387679-43387729	GM19239	blood:	n/a
16	chr15:43398173-43398223	PFSK-1	brain:	n/a
17	chr15:43399625-43399675	HCM	heart:	n/a
18	chr15:43398435-43398485	PrEC	prostate:	n/a
19	chr15:43398435-43398485	A549	lung:	n/a
20	chr15:43399625-43399675	GM12892	blood:	n/a
21	chr15:43398338-43398388	ECC-1	luminal epithelium:	n/a
22	chr15:43398270-43398320	Hela-S3	cervix:	n/a
23	chr15:43398302-43398352	GM12891	blood:	n/a
24	chr15:43398365-43398415	HIPEpiC	eye:	n/a
25	chr15:43398101-43398151	HRE	kidney:	n/a
26	chr15:43398302-43398352	PrEC	prostate:	n/a
27	chr15:43398826-43398876	HRPEpiC	eye:	n/a
28	chr15:43398338-43398388	K562	blood:	n/a
29	chr15:43398581-43398631	AG10803	skin:	n/a
30	chr15:43387679-43387729	SK-N-SH_RA	brain:	n/a
31	chr15:43297145-43297195	PANC-1	pancreas:	n/a
32	chr15:43398173-43398223	BE2_C	brain:	n/a
33	chr15:43398581-43398631	HCPEpiC	choroid plexus:	n/a
34	chr15:43398173-43398223	ovcar-3	ovarian:	n/a
35	chr15:43387679-43387729	NHDF-neo	bronchial:	n/a
36	chr15:43399625-43399675	LNCaP	prostate:	n/a
37	chr15:43398826-43398876	HEK293	kidney:	embryo
38	chr15:43398346-43398396	CMK	blood:	n/a
39	chr15:43398826-43398876	GM06990	blood:	n/a
40	chr15:43398346-43398396	HCT-116	colon:	n/a
41	chr15:43398435-43398485	HPAEpiC	pulmonary alveolar:	n/a
42	chr15:43398270-43398320	RPTEC	kidney:	n/a
43	chr15:43398826-43398876	MCF10A-Er-Src	breast:	n/a
44	chr15:43398826-43398876	PFSK-1	brain:	n/a
45	chr15:43398435-43398485	RPTEC	kidney:	n/a
46	chr15:43398338-43398388	HL-60	blood:	n/a
47	chr15:43398101-43398151	Jurkat	blood:	n/a
48	chr15:43398302-43398352	MCF10A-Er-Src	breast:	n/a
49	chr15:43398101-43398151	PrEC	prostate:	n/a
50	chr15:43398302-43398352	AG04450	lung:	fetal

(count:88 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:43397688..43398582-chr8:41909391..41910087,2	Hela-S3	cervix:
2	chr15:43397022..43400041-chr15:43403163..43407004,5	K562	blood:
3	chr15:43278687..43281856-chr15:43291013..43293652,3	K562	blood:
4	chr15:43397794..43398667-chr16:1755602..1756312,2	Hela-S3	cervix:
5	chr15:43385287..43387946-chr15:43396303..43398701,2	K562	blood:
6	chr15:43336054..43338771-chr15:43342997..43344575,2	MCF-7	breast:
7	chr15:43375936..43379231-chr15:43382227..43385005,3	K562	blood:
8	chr15:43368519..43371458-chr15:43478469..43480102,2	K562	blood:
9	chr15:43339146..43340895-chr15:43431393..43434266,2	K562	blood:
10	chr15:43379754..43382277-chr15:43415120..43416972,2	K562	blood:
11	chr15:43392028..43394734-chr15:43397894..43400122,2	MCF-7	breast:
12	chr15:43388815..43390634-chr15:43391926..43394516,2	K562	blood:
13	chr15:43380437..43382771-chr15:43396547..43398200,2	K562	blood:
14	chr15:43360392..43362682-chr15:43423469..43425924,2	K562	blood:
15	chr15:43278687..43281856-chr15:43291013..43293652,3	K562	blood:
16	chr15:43306847..43311067-chr15:43312226..43316473,3	K562	blood:
17	chr15:43292761..43295218-chr15:43297989..43300121,2	K562	blood:
18	chr15:43383221..43388610-chr15:43389653..43393489,4	K562	blood:
19	chr15:43387616..43389532-chr15:43477126..43479053,2	K562	blood:
20	chr15:43346995..43348533-chr15:43350036..43351977,2	K562	blood:
21	chr15:43274336..43276326-chr15:43276849..43278909,2	K562	blood:
22	chr15:43395932..43399418-chr15:43425897..43428585,4	K562	blood:
23	chr15:43406517..43409330-chr15:43424584..43426379,2	MCF-7	breast:
24	chr15:43325373..43328292-chr15:43334536..43336063,2	K562	blood:
25	chr15:43282136..43285343-chr15:43291276..43293438,3	K562	blood:
26	chr15:43397435..43400079-chr15:43619938..43624138,3	K562	blood:
27	chr15:43409363..43412996-chr15:43414014..43416433,4	K562	blood:
28	chr15:43392059..43394941-chr15:43396768..43399559,3	K562	blood:
29	chr15:43388815..43390634-chr15:43391926..43394516,2	K562	blood:
30	chr1:156698639..156699343-chr15:43397712..43398533,2	Hela-S3	cervix:
31	chr15:43356222..43358202-chr15:43362263..43364733,2	MCF-7	breast:
32	chr15:43337776..43340565-chr15:43396734..43398497,2	K562	blood:
33	chr15:43380437..43382771-chr15:43396547..43398200,2	K562	blood:
34	chr15:43413837..43416869-chr15:43476770..43480897,4	K562	blood:
35	chr15:43390055..43391666-chr15:43396242..43397765,2	MCF-7	breast:
36	chr15:43383221..43388610-chr15:43389653..43393489,4	K562	blood:
37	chr15:43397983..43399514-chr15:43421683..43423629,2	K562	blood:
38	chr15:43414412..43417295-chr15:43437126..43440064,2	K562	blood:
39	chr15:43389228..43391104-chr15:43396856..43399270,2	K562	blood:
40	chr15:43283018..43285343-chr15:43291276..43293330,3	K562	blood:
41	chr15:43375936..43379231-chr15:43382227..43385005,3	K562	blood:
42	chr15:43283254..43285115-chr15:43286974..43289576,2	K562	blood:
43	chr15:43412581..43417001-chr15:43422670..43429913,10	K562	blood:
44	chr15:43383221..43385892-chr15:43389653..43392510,3	K562	blood:
45	chr15:43396979..43399675-chr15:43425245..43427228,2	MCF-7	breast:
46	chr1:145382743..145383443-chr15:43397728..43398383,2	Hela-S3	cervix:
47	chr15:43402075..43404958-chr15:43407508..43410226,3	K562	blood:
48	chr15:43285221..43287358-chr15:43299885..43302016,2	K562	blood:
49	chr15:43285221..43287358-chr15:43299885..43302016,2	K562	blood:
50	chr15:43360121..43362777-chr15:43399326..43401275,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EPB42-2	chr15:43398666-43398735	NONHSAT042053
2	lnc-EPB42-2	chr15:43398423-43398493	NONHSAT042053
3	lnc-EPB42-2	chr15:43401117-43401168	NONHSAT042053

No data

Variant related genes	Relation type
UBR1	TF binding region
RPS3AP47	TF binding region
TMEM62	TF binding region
UBR1	CpG island
RPS3AP47	CpG island
TMEM62	CpG island
ENSG00000138834	chromatin interactions
ENSG00000168806	chromatin interactions
ENSG00000166946	chromatin interactions
ENSG00000143303	chromatin interactions
ENSG00000205871	chromatin interactions
ENSG00000137842	chromatin interactions
ENSG00000067369	chromatin interactions
ENSG00000159459	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000260928	chromatin interactions
ENSG00000083168	chromatin interactions
ENSG00000099875	chromatin interactions
ENSG00000261687	chromatin interactions
ENSG00000168803	chromatin interactions

Extended variants
information (count: 5034 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:5034 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4375634	chr15:43268970-43268971	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs35242751	chr15:43268992-43268993	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140972409	chr15:43268993-43268994	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs4375635	chr15:43269014-43269015	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200749394	chr15:43269027-43269028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs149778120	chr15:43269032-43269033	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368739715	chr15:43269055-43269056	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs186148655	chr15:43269080-43269081	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371411777	chr15:43269093-43269094	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs149531184	chr15:43269102-43269103	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573532739	chr15:43269124-43269125	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs114229411	chr15:43269131-43269132	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558421140	chr15:43269156-43269157	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190904681	chr15:43269181-43269182	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182750841	chr15:43269189-43269190	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573815046	chr15:43269192-43269193	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544833082	chr15:43269211-43269212	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564723320	chr15:43269237-43269238	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575185603	chr15:43269244-43269245	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544076034	chr15:43269251-43269252	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563537622	chr15:43269268-43269269	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144062661	chr15:43269402-43269403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs35911194	chr15:43269424-43269425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs140469954	chr15:43269437-43269438	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559823874	chr15:43269461-43269462	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs528578026	chr15:43269510-43269511	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552017189	chr15:43269578-43269579	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs59550447	chr15:43269622-43269623	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528500766	chr15:43269695-43269696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373786682	chr15:43269716-43269717	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs571841219	chr15:43269821-43269822	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537743974	chr15:43269872-43269873	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs551213289	chr15:43269874-43269875	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs199730160	chr15:43269880-43269881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201655415	chr15:43269881-43269882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74009231	chr15:43269888-43269889	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs78144092	chr15:43269897-43269898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs62020702	chr15:43269899-43269900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147284877	chr15:43269914-43269915	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188633051	chr15:43269918-43269919	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566596561	chr15:43269967-43269968	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544054828	chr15:43269979-43269980	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114733898	chr15:43269991-43269992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200055321	chr15:43270048-43270049	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575050354	chr15:43270084-43270085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7175979	chr15:43270122-43270123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546603068	chr15:43270131-43270132	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375684584	chr15:43270144-43270145	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs34183082	chr15:43270157-43270158	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554893737	chr15:43270172-43270173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Cancer	20164919	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Intellectual disability	21811512	CNVD

Chromatin state (count:4467 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43232000-43362800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr15:43241200-43269800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr15:43241600-43271000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr15:43241600-43271800	Strong transcription	Primary T helper cells fromperipheralblood	blood
5	chr15:43241800-43270800	Strong transcription	Primary T cells fromperipheralblood	blood
6	chr15:43242200-43270800	Strong transcription	Primary T helper cells PMA-I stimulated	--
7	chr15:43244000-43276400	Weak transcription	Psoas Muscle	Psoas
8	chr15:43248000-43320600	Weak transcription	Stomach Mucosa	stomach
9	chr15:43249600-43283200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr15:43251400-43269800	Strong transcription	Fetal Thymus	thymus
11	chr15:43252400-43298400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr15:43252800-43295800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr15:43255200-43278800	Weak transcription	Esophagus	oesophagus
14	chr15:43258800-43277600	Weak transcription	Colonic Mucosa	Colon
15	chr15:43260200-43270600	Strong transcription	Rectal Mucosa Donor 29	rectum
16	chr15:43260200-43270800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr15:43260600-43270400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr15:43260600-43270400	Strong transcription	Duodenum Smooth Muscle	Duodenum
19	chr15:43260600-43270800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr15:43260600-43271000	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr15:43260600-43271800	Strong transcription	Adipose Nuclei	Adipose
22	chr15:43261000-43277000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr15:43261800-43270800	Strong transcription	Primary T cells from cord blood	blood
24	chr15:43262400-43269600	Strong transcription	Brain Inferior Temporal Lobe	brain
25	chr15:43262400-43269800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr15:43262400-43276800	Strong transcription	Primary B cells from peripheral blood	blood
27	chr15:43262600-43269400	Strong transcription	Placenta Amnion	Placenta Amnion
28	chr15:43262600-43269600	Strong transcription	Fetal Intestine Large	intestine
29	chr15:43262600-43269800	Strong transcription	Placenta	Placenta
30	chr15:43262600-43269800	Strong transcription	Skeletal Muscle Male	skeletal muscle
31	chr15:43262600-43270400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr15:43262600-43270600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr15:43262600-43270600	Strong transcription	Stomach Smooth Muscle	stomach
34	chr15:43262600-43270800	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr15:43262600-43270800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr15:43262600-43270800	Strong transcription	Rectal Mucosa Donor 31	rectum
37	chr15:43262600-43270800	Strong transcription	Osteobl	bone
38	chr15:43262600-43271000	Strong transcription	HSMM	muscle
39	chr15:43262600-43271200	Strong transcription	Skeletal Muscle Female	skeletal muscle
40	chr15:43262600-43272200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr15:43262600-43292000	Strong transcription	Fetal Muscle Trunk	muscle
42	chr15:43262800-43270800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr15:43263000-43269800	Strong transcription	Left Ventricle	heart
44	chr15:43263000-43270400	Strong transcription	Primary B cells from cord blood	blood
45	chr15:43263200-43270800	Strong transcription	Muscle Satellite Cultured Cells	--
46	chr15:43263400-43284000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr15:43264000-43269600	Strong transcription	HSMMtube	muscle
48	chr15:43264000-43269800	Strong transcription	Sigmoid Colon	Sigmoid Colon
49	chr15:43264000-43283000	Strong transcription	Primary monocytes fromperipheralblood	blood
50	chr15:43264200-43269600	Strong transcription	Brain Germinal Matrix	brain

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