Variant report

Variant	nsv542439
Chromosome Location	chr15:76762161-77196336
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2057)
CpG islands
(count:976)
Chromatin interactive
region (count:76)
LncRNA
region (count:3)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:2057 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:76825612-76826689	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:77187500-77187518	K562	blood:	n/a	n/a
3	ARID3A	chr15:77195600-77196035	K562	blood:	n/a	n/a
4	ARID3A	chr15:76865111-76865365	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:77097607-77097795	K562	blood:	n/a	n/a
6	ARID3A	chr15:77195604-77196037	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:76935433-76935442	HepG2	liver:	n/a	n/a
8	ARID3A	chr15:76806361-76807005	HepG2	liver:	n/a	n/a
9	ARID3A	chr15:77133205-77133582	HepG2	liver:	n/a	chr15:77133207-77133223
10	ATF1	chr15:77195821-77195946	K562	blood:	n/a	n/a
11	ATF1	chr15:77116459-77116462	K562	blood:	n/a	n/a
12	ATF1	chr15:77191152-77191234	K562	blood:	n/a	n/a
13	ATF2	chr15:76867545-76868188	GM12878	blood:	n/a	n/a
14	ATF2	chr15:77003703-77004047	GM12878	blood:	n/a	n/a
15	ATF2	chr15:76867574-76868256	GM12878	blood:	n/a	n/a
16	ATF2	chr15:77157766-77158219	GM12878	blood:	n/a	n/a
17	ATF2	chr15:77003716-77004122	GM12878	blood:	n/a	n/a
18	BACH1	chr15:77097486-77097858	K562	blood:	n/a	n/a
19	BACH1	chr15:77092170-77092438	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr15:77097576-77097776	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr15:77157833-77158450	GM12878	blood:	n/a	chr15:77158232-77158242
22	BATF	chr15:76996436-76996655	GM12878	blood:	n/a	n/a
23	BATF	chr15:77195741-77195995	GM12878	blood:	n/a	n/a
24	BATF	chr15:76996451-76996676	GM12878	blood:	n/a	n/a
25	BATF	chr15:76867629-76868083	GM12878	blood:	n/a	n/a
26	BATF	chr15:76946672-76946896	GM12878	blood:	n/a	n/a
27	BATF	chr15:76946679-76946925	GM12878	blood:	n/a	n/a
28	BATF	chr15:76867553-76868299	GM12878	blood:	n/a	n/a
29	BATF	chr15:76907151-76907359	GM12878	blood:	n/a	n/a
30	BATF	chr15:77157842-77158213	GM12878	blood:	n/a	n/a
31	BATF	chr15:76868780-76869125	GM12878	blood:	n/a	n/a
32	BATF	chr15:76907137-76907384	GM12878	blood:	n/a	n/a
33	BCL11A	chr15:76867646-76868017	GM12878	blood:	n/a	n/a
34	BCL11A	chr15:76946684-76946864	GM12878	blood:	n/a	n/a
35	BCL11A	chr15:76867571-76868071	GM12878	blood:	n/a	n/a
36	BCL11A	chr15:77157831-77158218	GM12878	blood:	n/a	n/a
37	BCL11A	chr15:77003618-77004150	GM12878	blood:	n/a	n/a
38	BCL11A	chr15:77003630-77004113	GM12878	blood:	n/a	n/a
39	BCL3	chr15:76867594-76868106	GM12878	blood:	n/a	n/a
40	BCL3	chr15:76825763-76826141	GM12878	blood:	n/a	n/a
41	BCL3	chr15:76867671-76868118	GM12878	blood:	n/a	n/a
42	BCL3	chr15:76825735-76826094	GM12878	blood:	n/a	n/a
43	BCLAF1	chr15:77003650-77004026	GM12878	blood:	n/a	n/a
44	BCLAF1	chr15:76867603-76868092	GM12878	blood:	n/a	n/a
45	BCLAF1	chr15:76867350-76868205	GM12878	blood:	n/a	n/a
46	BCLAF1	chr15:77157731-77158205	GM12878	blood:	n/a	n/a
47	BHLHE40	chr15:76946680-76946809	GM12878	blood:	n/a	n/a
48	BHLHE40	chr15:76867676-76868010	GM12878	blood:	n/a	n/a
49	BHLHE40	chr15:77003580-77004137	GM12878	blood:	n/a	n/a
50	BRCA1	chr15:77159107-77159375	Hela-S3	cervix:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:77095150-77095200	AG09309	skin:	n/a
2	chr15:77191652-77191702	HL-60	blood:	n/a
3	chr15:77177353-77177403	BJ	skin:	n/a
4	chr15:77168444-77168494	HIPEpiC	eye:	n/a
5	chr15:77158041-77158091	HIPEpiC	eye:	n/a
6	chr15:77095150-77095200	GM06990	blood:	n/a
7	chr15:77168028-77168078	HIPEpiC	eye:	n/a
8	chr15:77191652-77191702	BJ	skin:	n/a
9	chr15:77154861-77154911	HCPEpiC	choroid plexus:	n/a
10	chr15:77158041-77158091	HCF	heart:	n/a
11	chr15:77155635-77155685	GM12891	blood:	n/a
12	chr15:77155635-77155685	HMEC	breast:	n/a
13	chr15:77168028-77168078	GM06990	blood:	n/a
14	chr15:77177353-77177403	RPTEC	kidney:	n/a
15	chr15:77168444-77168494	SKMC	muscle:	n/a
16	chr15:77168444-77168494	GM12892	blood:	n/a
17	chr15:77155635-77155685	HAEpiC	amniotic membrane:	n/a
18	chr15:77154253-77154303	SKMC	muscle:	n/a
19	chr15:77158041-77158091	HEEpiC	esophagus:	n/a
20	chr15:77134243-77134293	NB4	blood:	n/a
21	chr15:76901065-76901115	BJ	skin:	n/a
22	chr15:77154861-77154911	IMR90	lung:	fetal
23	chr15:77154861-77154911	GM12892	blood:	n/a
24	chr15:77177353-77177403	HepG2	liver:	n/a
25	chr15:77154253-77154303	HepG2	liver:	n/a
26	chr15:77168444-77168494	ECC-1	luminal epithelium:	n/a
27	chr15:76868964-76869014	K562	blood:	n/a
28	chr15:77154861-77154911	HMEC	breast:	n/a
29	chr15:77085390-77085440	AG09309	skin:	n/a
30	chr15:77155635-77155685	Caco-2	colon:	n/a
31	chr15:77154253-77154303	CMK	blood:	n/a
32	chr15:76868964-76869014	MCF10A-Er-Src	breast:	n/a
33	chr15:77155635-77155685	HPAEpiC	pulmonary alveolar:	n/a
34	chr15:77176239-77176289	SK-N-SH_RA	brain:	n/a
35	chr15:77095150-77095200	HNPCEpiC	eye:	n/a
36	chr15:77168028-77168078	AG04449	skin:	fetal
37	chr15:77154861-77154911	LNCaP	prostate:	n/a
38	chr15:77155428-77155478	NT2-D1	testis:	n/a
39	chr15:77134243-77134293	PFSK-1	brain:	n/a
40	chr15:77085390-77085440	HMEC	breast:	n/a
41	chr15:77191652-77191702	AG04450	lung:	fetal
42	chr15:77175742-77175792	HCM	heart:	n/a
43	chr15:77168444-77168494	HCF	heart:	n/a
44	chr15:77134243-77134293	GM19239	blood:	n/a
45	chr15:77176239-77176289	HEEpiC	esophagus:	n/a
46	chr15:77168028-77168078	AG10803	skin:	n/a
47	chr15:77168444-77168494	GM06990	blood:	n/a
48	chr15:76868964-76869014	PrEC	prostate:	n/a
49	chr15:77155635-77155685	HRPEpiC	eye:	n/a
50	chr15:77095150-77095200	U87	brain:	n/a

(count:76 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:77195051..77197848-chr15:77221697..77224553,2	MCF-7	breast:
2	chr15:76997314..76998845-chr15:77007470..77009179,2	MCF-7	breast:
3	chr15:76969596..76972550-chr15:76979737..76981959,2	MCF-7	breast:
4	chr15:76959064..76961382-chr15:76964223..76965946,2	MCF-7	breast:
5	chr15:76969596..76972550-chr15:76979737..76981959,2	MCF-7	breast:
6	chr15:76810534..76813037-chr15:76815373..76817326,2	MCF-7	breast:
7	chr15:76855877..76857707-chr15:76866696..76869240,2	MCF-7	breast:
8	chr15:76934737..76935336-chr15:77133237..77133799,2	MCF-7	breast:
9	chr15:76810534..76813037-chr15:76815373..76817326,2	MCF-7	breast:
10	chr15:77051074..77052943-chr15:77058188..77061067,2	K562	blood:
11	chr15:77051074..77052943-chr15:77058188..77061067,2	K562	blood:
12	chr15:76482840..76483720-chr15:77132911..77133894,4	MCF-7	breast:
13	chr15:76803456..76806308-chr15:77131835..77134067,2	MCF-7	breast:
14	chr15:76439768..76440654-chr15:77152468..77153214,2	K562	blood:
15	chr15:77195708..77198409-chr15:77360659..77363583,2	K562	blood:
16	chr11:60896554..60897446-chr15:76806259..76806955,2	MCF-7	breast:
17	chr15:76978559..76980160-chr15:76982250..76984451,2	MCF-7	breast:
18	chr15:77196182..77198169-chr15:77222869..77226186,3	K562	blood:
19	chr15:76855877..76857707-chr15:76866696..76869240,2	MCF-7	breast:
20	chr15:76821101..76824629-chr15:76825214..76826999,4	K562	blood:
21	chr15:76789083..76790896-chr15:76806122..76808106,2	MCF-7	breast:
22	chr15:77188777..77191809-chr15:77196421..77199146,3	K562	blood:
23	chr15:77024348..77024882-chr15:77132939..77133789,2	MCF-7	breast:
24	chr15:77196194..77198493-chr15:77235491..77237833,2	K562	blood:
25	chr15:76482009..76484403-chr15:77035735..77037455,2	MCF-7	breast:
26	chr15:77119804..77122749-chr15:77124403..77126200,2	K562	blood:
27	chr15:76934897..76935640-chr15:77158999..77159764,3	MCF-7	breast:
28	chr15:76493051..76495991-chr15:76813493..76815400,2	MCF-7	breast:
29	chr15:76812872..76815537-chr15:76817323..76820278,2	MCF-7	breast:
30	chr15:77192531..77194476-chr15:77194873..77197873,3	K562	blood:
31	chr15:76967596..76970375-chr15:76976896..76979262,2	K562	blood:
32	chr15:76978559..76980160-chr15:76982250..76984451,2	MCF-7	breast:
33	chr15:77017797..77020777-chr8:43093705..43096561,2	K562	blood:
34	chr15:77164850..77168974-chr15:77171197..77173807,3	K562	blood:
35	chr15:77151146..77154145-chr15:77195611..77198369,2	MCF-7	breast:
36	chr15:77122706..77125362-chr15:77130709..77133578,2	K562	blood:
37	chr15:76812872..76815537-chr15:76817323..76820278,2	MCF-7	breast:
38	chr15:77083317..77084988-chr15:77087176..77089675,2	K562	blood:
39	chr15:76997314..76998845-chr15:77007470..77009179,2	MCF-7	breast:
40	chr15:77083317..77084988-chr15:77087176..77089675,2	K562	blood:
41	chr15:77044758..77046845-chr15:77050241..77052508,2	MCF-7	breast:
42	chr15:77194744..77199863-chr15:77220881..77225601,7	MCF-7	breast:
43	chr15:77085685..77088111-chr15:77091340..77093808,2	K562	blood:
44	chr15:77052021..77055015-chr15:77055082..77056903,3	K562	blood:
45	chr15:76934737..76935336-chr15:77133237..77133799,2	MCF-7	breast:
46	chr15:77196272..77198559-chr15:77223364..77225357,2	K562	blood:
47	chr15:77024348..77024882-chr15:77132939..77133789,2	MCF-7	breast:
48	chr15:77092193..77094695-chr15:77097938..77099629,2	K562	blood:
49	chr15:76789083..76790896-chr15:76806122..76808106,2	MCF-7	breast:
50	chr15:77119804..77122749-chr15:77124403..77126200,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ETFA-5	chr15:76833537-76833934	NONHSAT047406
2	lnc-ISL2-4	chr15:76764440-76764706	NONHSAT047405
3	lnc-RCN2-1	chr15:77028982-77029321	NONHSAT047408

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3713	chr15:76878988-76879007	MIMAT0018164

No data

Variant related genes	Relation type
ENSG00000261232	TF binding region
SCAPER	TF binding region
RN7SKP217	TF binding region
MIR3713	TF binding region
ENSG00000261232	CpG island
SCAPER	CpG island
RN7SKP217	CpG island
MIR3713	CpG island
ENSG00000269951	chromatin interactions
ENSG00000140382	chromatin interactions
ENSG00000266449	chromatin interactions
ENSG00000169758	chromatin interactions
ENSG00000117906	chromatin interactions
ENSG00000140391	chromatin interactions
ENSG00000140386	chromatin interactions

Extended variants
information (count: 15192 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:15192 , 50 per page) page: 1 2 3 4 5 6 7 ... 304

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182808293	chr15:76762214-76762215	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs557877183	chr15:76762237-76762238	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs79232464	chr15:76762247-76762248	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs11341310	chr15:76762280-76762281	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs398027989	chr15:76762286-76762287	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs503483	chr15:76762291-76762292	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs148170755	chr15:76762326-76762327	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs187233814	chr15:76762342-76762343	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs141614429	chr15:76762359-76762360	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs150516930	chr15:76762407-76762408	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs375840429	chr15:76762469-76762470	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs115746968	chr15:76762515-76762516	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs73442176	chr15:76762516-76762517	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs532199610	chr15:76762525-76762526	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538529044	chr15:76762536-76762537	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192215259	chr15:76762544-76762545	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138445691	chr15:76762568-76762569	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535841150	chr15:76762573-76762574	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs369291626	chr15:76762590-76762591	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs141689208	chr15:76762717-76762718	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184496851	chr15:76762718-76762719	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558688456	chr15:76762721-76762722	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146214781	chr15:76762766-76762767	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139263196	chr15:76762787-76762788	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188620727	chr15:76762794-76762795	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554307573	chr15:76762801-76762802	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs114675990	chr15:76762825-76762826	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs157780	chr15:76762855-76762856	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs578111409	chr15:76762884-76762885	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs193297954	chr15:76762888-76762889	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs184253272	chr15:76762917-76762918	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs144106313	chr15:76762919-76762920	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs565606452	chr15:76762960-76762961	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs532545448	chr15:76762965-76762966	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs11635463	chr15:76762986-76762987	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs565426302	chr15:76763055-76763056	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs529748074	chr15:76763056-76763057	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs189060658	chr15:76763060-76763061	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs569570604	chr15:76763088-76763089	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs537314121	chr15:76763111-76763112	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs157781	chr15:76763118-76763119	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs144114924	chr15:76763126-76763127	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs76057589	chr15:76763228-76763229	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs553214416	chr15:76763229-76763230	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs185860	chr15:76763248-76763249	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs377720693	chr15:76763256-76763257	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs543167167	chr15:76763306-76763307	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs554915373	chr15:76763318-76763319	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs115586791	chr15:76763336-76763337	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs200080389	chr15:76763361-76763362	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:4270 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76711600-76767200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr15:76720800-76763600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr15:76725800-76812600	Weak transcription	Left Ventricle	heart
4	chr15:76742800-76762400	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr15:76750400-76763800	Weak transcription	Placenta	Placenta
6	chr15:76753200-76762800	Weak transcription	Esophagus	oesophagus
7	chr15:76753800-76764400	Weak transcription	Fetal Intestine Large	intestine
8	chr15:76754000-76764400	Weak transcription	Brain Hippocampus Middle	brain
9	chr15:76754200-76763600	Weak transcription	Pancreas	Pancrea
10	chr15:76754400-76763600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr15:76754800-76764400	Weak transcription	Fetal Muscle Trunk	muscle
12	chr15:76755600-76764600	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr15:76757800-76765200	Weak transcription	Aorta	Aorta
14	chr15:76758400-76765600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr15:76758600-76762400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr15:76758800-76764400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr15:76758800-76765000	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr15:76758800-76765200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr15:76759200-76762600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr15:76759200-76763800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr15:76759200-76764400	Weak transcription	Psoas Muscle	Psoas
22	chr15:76759400-76762600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr15:76759400-76763600	Strong transcription	Liver	Liver
24	chr15:76759400-76764400	Weak transcription	Fetal Muscle Leg	muscle
25	chr15:76759800-76762800	Weak transcription	Duodenum Mucosa	Duodenum
26	chr15:76759800-76763400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr15:76759800-76770400	Weak transcription	Colon Smooth Muscle	Colon
28	chr15:76760000-76762400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr15:76760000-76772600	Weak transcription	GM12878-XiMat	blood
30	chr15:76760400-76773800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr15:76760600-76763000	Weak transcription	Right Ventricle	heart
32	chr15:76760600-76764200	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr15:76760800-76763000	Strong transcription	Primary B cells from cord blood	blood
34	chr15:76760800-76763000	Strong transcription	Duodenum Smooth Muscle	Duodenum
35	chr15:76760800-76763400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr15:76760800-76763400	Weak transcription	Brain Angular Gyrus	brain
37	chr15:76760800-76764200	Strong transcription	Primary T helper cells fromperipheralblood	blood
38	chr15:76761000-76763200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr15:76761000-76763400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr15:76761000-76763600	Strong transcription	Primary T cells fromperipheralblood	blood
41	chr15:76761200-76762800	Strong transcription	Rectal Mucosa Donor 29	rectum
42	chr15:76761200-76762800	Strong transcription	Stomach Smooth Muscle	stomach
43	chr15:76761200-76762800	Strong transcription	Monocytes-CD14+_RO01746	blood
44	chr15:76761200-76763400	Strong transcription	Primary B cells from peripheral blood	blood
45	chr15:76761200-76764800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr15:76761400-76762800	Weak transcription	Small Intestine	intestine
47	chr15:76761400-76763600	Weak transcription	Brain Anterior Caudate	brain
48	chr15:76761400-76765400	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr15:76761600-76763200	Strong transcription	Adipose Nuclei	Adipose
50	chr15:76761800-76762800	Strong transcription	Dnd41	blood

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