Variant report

Variant	nsv904270
Chromosome Location	chr15:59140329-59238415
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1944)
CpG islands
(count:1711)
Chromatin interactive
region (count:132)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1944 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:59225679-59226514	K562	blood:	n/a	n/a
2	ARID3A	chr15:59225611-59226373	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:59156691-59157389	HepG2	liver:	n/a	n/a
4	ATF1	chr15:59210516-59210796	K562	blood:	n/a	n/a
5	ATF1	chr15:59158433-59158785	K562	blood:	n/a	n/a
6	ATF2	chr15:59221857-59222528	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr15:59225938-59226467	GM12878	blood:	n/a	n/a
8	ATF2	chr15:59225549-59225918	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr15:59158413-59158831	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr15:59225430-59225867	GM12878	blood:	n/a	n/a
11	ATF2	chr15:59222138-59222506	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr15:59225455-59226570	GM12878	blood:	n/a	n/a
13	ATF2	chr15:59225517-59226327	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr15:59225320-59226545	A549	lung:	n/a	chr15:59226077-59226086
15	ATF3	chr15:59225706-59226100	K562	blood:	n/a	chr15:59226077-59226086
16	ATF3	chr15:59225681-59226319	K562	blood:	n/a	chr15:59226077-59226086
17	ATF3	chr15:59225429-59226288	A549	lung:	n/a	chr15:59226077-59226086
18	BACH1	chr15:59226069-59226459	K562	blood:	n/a	n/a
19	BACH1	chr15:59156865-59157214	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr15:59225662-59226378	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr15:59230017-59230208	GM12878	blood:	n/a	n/a
22	BATF	chr15:59230005-59230215	GM12878	blood:	n/a	n/a
23	BCL3	chr15:59167563-59168150	A549	lung:	n/a	n/a
24	BCL3	chr15:59158379-59158846	A549	lung:	n/a	n/a
25	BCL3	chr15:59168519-59168937	A549	lung:	n/a	n/a
26	BCL3	chr15:59225378-59226563	A549	lung:	n/a	chr15:59226076-59226085 chr15:59225502-59225515
27	BCL3	chr15:59225432-59226697	A549	lung:	n/a	chr15:59226076-59226085 chr15:59225502-59225515
28	BCLAF1	chr15:59225317-59226499	GM12878	blood:	n/a	chr15:59226076-59226085 chr15:59225502-59225515
29	BCLAF1	chr15:59224987-59226560	GM12878	blood:	n/a	chr15:59226076-59226085 chr15:59225502-59225515 chr15:59225307-59225320 chr15:59225307-59225320
30	BCLAF1	chr15:59225383-59226414	K562	blood:	n/a	chr15:59226076-59226085 chr15:59225502-59225515
31	BCLAF1	chr15:59225482-59226373	K562	blood:	n/a	chr15:59226076-59226085 chr15:59225502-59225515
32	BHLHE40	chr15:59156764-59157975	HepG2	liver:	n/a	n/a
33	BHLHE40	chr15:59158552-59158660	K562	blood:	n/a	n/a
34	BHLHE40	chr15:59225106-59226471	GM12878	blood:	n/a	chr15:59225307-59225323 chr15:59225507-59225523 chr15:59225974-59225990
35	BHLHE40	chr15:59225561-59226572	HepG2	liver:	n/a	chr15:59225974-59225990
36	BHLHE40	chr15:59209405-59209434	K562	blood:	n/a	n/a
37	BHLHE40	chr15:59225217-59226640	K562	blood:	n/a	chr15:59225307-59225323 chr15:59225507-59225523 chr15:59225974-59225990
38	BHLHE40	chr15:59172501-59172713	GM12878	blood:	n/a	n/a
39	BRCA1	chr15:59226061-59226408	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr15:59225766-59225781	GM12878	blood:	n/a	n/a
41	BRCA1	chr15:59225583-59225819	H1-hESC	embryonic stem cell:	n/a	n/a
42	BRCA1	chr15:59225637-59226328	HepG2	liver:	n/a	n/a
43	BRCA1	chr15:59158404-59158783	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr15:59225561-59226513	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr15:59156807-59157289	HepG2	liver:	n/a	n/a
46	CBX3	chr15:59158338-59158849	HCT-116	colon:	n/a	n/a
47	CBX3	chr15:59158322-59158859	K562	blood:	n/a	n/a
48	CBX3	chr15:59211487-59211884	K562	blood:	n/a	n/a
49	CBX3	chr15:59158467-59158820	K562	blood:	n/a	n/a
50	CBX3	chr15:59225554-59226639	K562	blood:	n/a	n/a

(count:1711 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:59226299-59226349	HAEpiC	amniotic membrane:	n/a
2	chr15:59226205-59226255	MCF10A-Er-Src	breast:	n/a
3	chr15:59225898-59225948	HNPCEpiC	eye:	n/a
4	chr15:59226299-59226349	HAEpiC	amniotic membrane:	n/a
5	chr15:59226205-59226255	MCF10A-Er-Src	breast:	n/a
6	chr15:59225898-59225948	HNPCEpiC	eye:	n/a
7	chr15:59226409-59226459	SAEC	small airway:	n/a
8	chr15:59179234-59179284	RPTEC	kidney:	n/a
9	chr15:59225898-59225948	HL-60	blood:	n/a
10	chr15:59179239-59179289	SAEC	small airway:	n/a
11	chr15:59157075-59157125	K562	blood:	n/a
12	chr15:59225166-59225216	MCF-7	breast:	n/a
13	chr15:59157123-59157173	Hepatocyte	liver:	n/a
14	chr15:59179239-59179289	HIPEpiC	eye:	n/a
15	chr15:59154450-59154500	PrEC	prostate:	n/a
16	chr15:59226205-59226255	RPTEC	kidney:	n/a
17	chr15:59179584-59179634	GM12892	blood:	n/a
18	chr15:59226509-59226559	NHDF-neo	bronchial:	n/a
19	chr15:59226299-59226349	NB4	blood:	n/a
20	chr15:59154450-59154500	HL-60	blood:	n/a
21	chr15:59225898-59225948	T-47D	breast:	n/a
22	chr15:59179239-59179289	SK-N-SH_RA	brain:	n/a
23	chr15:59225903-59225953	MCF-7	breast:	n/a
24	chr15:59225813-59225863	CMK	blood:	n/a
25	chr15:59225166-59225216	SK-N-SH	brain:	n/a
26	chr15:59179234-59179284	AG09319	gingival:	n/a
27	chr15:59146882-59146932	HepG2	liver:	n/a
28	chr15:59225861-59225911	AG04449	skin:	fetal
29	chr15:59225898-59225948	MCF10A-Er-Src	breast:	n/a
30	chr15:59156878-59156928	AG10803	skin:	n/a
31	chr15:59171928-59171978	CMK	blood:	n/a
32	chr15:59226509-59226559	SKMC	muscle:	n/a
33	chr15:59226509-59226559	GM12891	blood:	n/a
34	chr15:59179584-59179634	MCF-7	breast:	n/a
35	chr15:59226205-59226255	AG04449	skin:	fetal
36	chr15:59157523-59157573	PANC-1	pancreas:	n/a
37	chr15:59179584-59179634	AG04449	skin:	fetal
38	chr15:59179239-59179289	Hela-S3	cervix:	n/a
39	chr15:59226509-59226559	SK-N-SH_RA	brain:	n/a
40	chr15:59171928-59171978	GM06990	blood:	n/a
41	chr15:59226205-59226255	BJ	skin:	n/a
42	chr15:59179234-59179284	GM12892	blood:	n/a
43	chr15:59157123-59157173	AG10803	skin:	n/a
44	chr15:59225658-59225708	NT2-D1	testis:	n/a
45	chr15:59225861-59225911	NH-A	brain:	n/a
46	chr15:59157857-59157907	HRE	kidney:	n/a
47	chr15:59146882-59146932	GM19239	blood:	n/a
48	chr15:59225861-59225911	HAEpiC	amniotic membrane:	n/a
49	chr15:59179239-59179289	K562	blood:	n/a
50	chr15:59156878-59156928	HUVEC	blood vessel:	n/a

(count:132 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:59165302..59167186-chr15:59171743..59174191,2	MCF-7	breast:
2	chr15:59211698..59213211-chr15:59216846..59218373,2	K562	blood:
3	chr15:59169108..59171726-chr15:59174874..59180386,5	K562	blood:
4	chr15:59188873..59192935-chr15:59224019..59226745,3	MCF-7	breast:
5	chr15:59202197..59204009-chr15:59224221..59225773,2	K562	blood:
6	chr15:59204944..59209018-chr15:59223573..59227454,4	K562	blood:
7	chr15:59162668..59165557-chr15:59167625..59170277,3	K562	blood:
8	chr15:59227418..59230634-chr15:59231791..59235343,3	K562	blood:
9	chr15:59150203..59152122-chr4:10117805..10120287,2	MCF-7	breast:
10	chr15:59167284..59169096-chr15:59170311..59173301,2	K562	blood:
11	chr15:59185300..59188168-chr15:59204704..59206498,2	K562	blood:
12	chr15:59220368..59223224-chr15:59377778..59380612,2	K562	blood:
13	chr15:59194271..59195983-chr15:59200756..59202760,2	K562	blood:
14	chr15:59225681..59226564-chr7:72971674..72972371,2	Hela-S3	cervix:
15	chr15:59225573..59226390-chr16:74734014..74734956,2	Hela-S3	cervix:
16	chr15:59158172..59158742-chr20:25371320..25372132,2	HCT-116	colon:
17	chr15:59040867..59044243-chr15:59224539..59228117,4	K562	blood:
18	chr15:59202509..59204413-chr15:59224273..59227251,2	K562	blood:
19	chr1:181057576..181058245-chr15:59225965..59226855,2	HCT-116	colon:
20	chr15:59184668..59186750-chr15:59215804..59218388,2	K562	blood:
21	chr15:59225042..59225969-chr3:111804939..111805795,2	Hela-S3	cervix:
22	chr15:59211354..59213234-chr15:59223328..59226412,3	MCF-7	breast:
23	chr15:59040418..59042472-chr15:59216479..59218851,2	K562	blood:
24	chr15:59169081..59172963-chr15:59222560..59227013,5	K562	blood:
25	chr15:59208848..59211308-chr15:59211819..59213462,3	K562	blood:
26	chr15:59168045..59172125-chr15:59189388..59193241,4	K562	blood:
27	chr15:59224605..59227198-chr15:59227629..59230492,2	MCF-7	breast:
28	chr15:59150365..59151946-chr15:59158006..59159550,2	K562	blood:
29	chr15:59198637..59200258-chr15:59218606..59220770,2	K562	blood:
30	chr15:59173863..59177301-chr15:59223266..59225843,3	K562	blood:
31	chr15:59146076..59151361-chr15:59223071..59227542,5	MCF-7	breast:
32	chr15:59061037..59064884-chr15:59224205..59227723,8	K562	blood:
33	chr15:44828640..44829478-chr15:59225791..59226422,2	Hela-S3	cervix:
34	chr15:59198637..59200258-chr15:59218606..59220770,2	K562	blood:
35	chr15:59202614..59206575-chr15:59224317..59226928,5	MCF-7	breast:
36	chr15:59204944..59209018-chr15:59223573..59227454,4	K562	blood:
37	chr15:59212424..59217333-chr15:59223129..59226870,5	MCF-7	breast:
38	chr15:59171523..59173361-chr15:59197628..59200554,2	K562	blood:
39	chr15:59223805..59226728-chr15:59396182..59398979,2	MCF-7	breast:
40	chr15:59188873..59192935-chr15:59224019..59226745,3	MCF-7	breast:
41	chr15:59062764..59064503-chr15:59191462..59194303,2	K562	blood:
42	chr15:59211698..59213211-chr15:59216846..59218373,2	K562	blood:
43	chr15:59194271..59195983-chr15:59200756..59202760,2	K562	blood:
44	chr15:59169557..59171872-chr15:59175822..59177559,2	K562	blood:
45	chr15:59225147..59225809-chr17:76164621..76165184,2	Hela-S3	cervix:
46	chr15:59204944..59207520-chr15:59224526..59227454,2	K562	blood:
47	chr15:59225391..59225969-chr21:38338855..38339364,2	Hela-S3	cervix:
48	chr15:59144722..59148208-chr15:59148286..59151538,5	K562	blood:
49	chr15:59200337..59203296-chr15:59205002..59207680,2	K562	blood:
50	chr15:59061870..59064465-chr15:59224425..59227494,5	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM10-8	chr15:59193167-59193486	NONHSAT044141
2	lnc-RNF111-2	chr15:59152982-59154096	NONHSAT044134
3	lnc-FAM63B-3	chr15:59161858-59162333	NONHSAT044135
4	lnc-SLTM-2	chr15:59219077-59219556	ENSG00000247934
5	lnc-SLTM-2	chr15:59211128-59211697	ENSG00000247934
6	lnc-ADAM10-8	chr15:59204762-59205000	NONHSAT044141
7	lnc-RNF111-3	chr15:59149733-59149750	NONHSAT044131
8	lnc-RNF111-3	chr15:59148026-59149425	NONHSAT044131

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SLTM	hsa-miR-186-5p	chr15:59172081-59172102
2	FAM63B	hsa-miR-124-3p	chr15:59148311-59148330

Variant related genes	Relation type
ZNF444P1	TF binding region
ENSG00000259353	TF binding region
SLTM	TF binding region
ENSG00000242747	TF binding region
RNF111	TF binding region
ENSG00000225798	TF binding region
ZNF444P1	CpG island
ENSG00000259353	CpG island
SLTM	CpG island
ENSG00000242747	CpG island
RNF111	CpG island
ENSG00000225798	CpG island
ENSG00000179933	chromatin interactions
ENSG00000168395	chromatin interactions
ENSG00000100997	chromatin interactions
ENSG00000114529	chromatin interactions
ENSG00000162496	chromatin interactions
ENSG00000259943	chromatin interactions
ENSG00000100401	chromatin interactions
ENSG00000182934	chromatin interactions
ENSG00000137776	chromatin interactions
ENSG00000127314	chromatin interactions
ENSG00000166012	chromatin interactions
ENSG00000084073	chromatin interactions
ENSG00000111678	chromatin interactions
ENSG00000100813	chromatin interactions
ENSG00000272173	chromatin interactions
ENSG00000106635	chromatin interactions
ENSG00000157456	chromatin interactions
ENSG00000168003	chromatin interactions
ENSG00000259353	chromatin interactions
ENSG00000245975	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000171522	chromatin interactions
ENSG00000128272	chromatin interactions
ENSG00000269792	chromatin interactions
ENSG00000104131	chromatin interactions
ENSG00000204256	chromatin interactions
ENSG00000182919	chromatin interactions
ENSG00000118515	chromatin interactions
ENSG00000108639	chromatin interactions
ENSG00000136861	chromatin interactions
ENSG00000259738	chromatin interactions
ENSG00000238923	chromatin interactions
ENSG00000255717	chromatin interactions
ENSG00000157450	chromatin interactions
ENSG00000179523	chromatin interactions
ENSG00000196689	chromatin interactions
ENSG00000128923	chromatin interactions
ENSG00000085274	chromatin interactions
ENSG00000159267	chromatin interactions
ENSG00000197956	chromatin interactions
ENSG00000137845	chromatin interactions
ENSG00000110074	chromatin interactions
ENSG00000162783	chromatin interactions
ENSG00000126070	chromatin interactions
ENSG00000188483	chromatin interactions
ENSG00000168404	chromatin interactions

Extended variants
information (count: 3731 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:3731 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4775096	chr15:59140329-59140330	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs148709874	chr15:59140336-59140337	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558087172	chr15:59140415-59140416	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576432910	chr15:59140418-59140419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543850010	chr15:59140419-59140420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569963805	chr15:59140437-59140438	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs76514889	chr15:59140458-59140459	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541631591	chr15:59140475-59140476	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs376505962	chr15:59140539-59140540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373252934	chr15:59140568-59140569	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562181647	chr15:59140582-59140583	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs527553558	chr15:59140661-59140662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs118107890	chr15:59140664-59140665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs142359441	chr15:59140670-59140671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531729786	chr15:59140709-59140710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs550236486	chr15:59140724-59140725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs372926100	chr15:59140786-59140787	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs67438612	chr15:59140793-59140794	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs4775097	chr15:59140801-59140802	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs535963439	chr15:59140802-59140803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368955858	chr15:59140814-59140815	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs151270452	chr15:59140818-59140819	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs347111	chr15:59140828-59140829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183700317	chr15:59140899-59140900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs4774312	chr15:59140924-59140925	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs147085482	chr15:59140926-59140927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566974531	chr15:59140927-59140928	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs147708670	chr15:59140938-59140939	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555762577	chr15:59140940-59140941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575954635	chr15:59140949-59140950	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535987712	chr15:59140991-59140992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs142640909	chr15:59141000-59141001	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186885869	chr15:59141022-59141023	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112068235	chr15:59141024-59141025	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560043362	chr15:59141035-59141036	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs59631822	chr15:59141142-59141143	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs546062761	chr15:59141143-59141144	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564360141	chr15:59141183-59141184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544864897	chr15:59141229-59141230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531667391	chr15:59141284-59141285	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs191618449	chr15:59141302-59141303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377513194	chr15:59141333-59141334	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529326651	chr15:59141358-59141359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184998941	chr15:59141367-59141368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369503590	chr15:59141383-59141384	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564230333	chr15:59141415-59141416	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556091566	chr15:59141427-59141428	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs793572	chr15:59141468-59141469	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs551592964	chr15:59141472-59141473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569992299	chr15:59141473-59141474	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
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
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Lung cancer	19238632	CNVD
Non-small cell lung cancer	19255323	CNVD
Non-small cell lung cancer	18509184	CNVD
head and neck squamous cell carcinoma	19318576	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3103 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:59064600-59145600	Weak transcription	Gastric	stomach
2	chr15:59065800-59142800	Weak transcription	Aorta	Aorta
3	chr15:59067000-59157800	Weak transcription	Hela-S3	cervix
4	chr15:59077800-59153600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr15:59090200-59156600	Weak transcription	Small Intestine	intestine
6	chr15:59095200-59156800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr15:59103600-59148800	Weak transcription	A549	lung
8	chr15:59103800-59157000	Weak transcription	Psoas Muscle	Psoas
9	chr15:59104000-59146600	Weak transcription	NH-A	brain
10	chr15:59104000-59148400	Weak transcription	Rectal Smooth Muscle	rectum
11	chr15:59104000-59157000	Weak transcription	Esophagus	oesophagus
12	chr15:59104000-59157200	Weak transcription	NHLF	lung
13	chr15:59106000-59156800	Weak transcription	Lung	lung
14	chr15:59106200-59156800	Weak transcription	Ovary	ovary
15	chr15:59106200-59157000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr15:59106600-59146400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr15:59106600-59157000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr15:59106800-59144600	Weak transcription	HSMMtube	muscle
19	chr15:59106800-59156400	Weak transcription	Fetal Kidney	kidney
20	chr15:59107200-59142000	Weak transcription	Brain Germinal Matrix	brain
21	chr15:59107200-59147600	Weak transcription	Osteobl	bone
22	chr15:59111800-59159600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr15:59112000-59147800	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr15:59115000-59146800	Weak transcription	HepG2	liver
25	chr15:59119400-59144000	Weak transcription	Fetal Brain Female	brain
26	chr15:59119600-59149600	Weak transcription	Dnd41	blood
27	chr15:59120000-59169000	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr15:59122000-59156400	Weak transcription	Fetal Heart	heart
29	chr15:59122200-59141600	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr15:59126000-59156600	Weak transcription	Right Ventricle	heart
31	chr15:59126200-59141800	Weak transcription	Stomach Smooth Muscle	stomach
32	chr15:59126200-59157000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr15:59126800-59144800	Weak transcription	Stomach Mucosa	stomach
34	chr15:59126800-59151200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr15:59127200-59141400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr15:59127200-59150400	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr15:59127200-59156600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr15:59129800-59140800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr15:59129800-59143800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr15:59130000-59148400	Weak transcription	Colon Smooth Muscle	Colon
41	chr15:59132600-59146800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr15:59132800-59149600	Weak transcription	HUVEC	blood vessel
43	chr15:59135600-59146600	Weak transcription	K562	blood
44	chr15:59136000-59151800	Weak transcription	GM12878-XiMat	blood
45	chr15:59137200-59156800	Weak transcription	Spleen	Spleen
46	chr15:59137400-59140600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr15:59137400-59140800	Strong transcription	NHEK	skin
48	chr15:59137400-59141200	Strong transcription	Placenta	Placenta
49	chr15:59137400-59142600	Strong transcription	Primary neutrophils fromperipheralblood	blood
50	chr15:59137400-59145800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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