Variant report

Variant	nsv831119
Chromosome Location	chr7:124714009-124890119
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:446)
CpG islands
(count:306)
Chromatin interactive
region (count:27)
LncRNA
region (count:49)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:446 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:124738399-124738950	GM12878	blood:	n/a	n/a
2	BACH1	chr7:124767606-124767626	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr7:124738517-124738718	GM12878	blood:	n/a	chr7:124738608-124738619 chr7:124738609-124738619
4	BATF	chr7:124738440-124738777	GM12878	blood:	n/a	chr7:124738608-124738619 chr7:124738609-124738619
5	BATF	chr7:124795049-124795303	GM12878	blood:	n/a	n/a
6	BCL11A	chr7:124776492-124776702	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr7:124738474-124738831	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:124724253-124724254	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:124759668-124759931	GM12878	blood:	n/a	n/a
10	CCNT2	chr7:124745648-124745845	K562	blood:	n/a	n/a
11	CCNT2	chr7:124797085-124797285	K562	blood:	n/a	n/a
12	CCNT2	chr7:124813780-124813862	K562	blood:	n/a	n/a
13	CEBPB	chr7:124859344-124859624	A549	lung:	n/a	chr7:124859444-124859455
14	CEBPB	chr7:124799503-124799797	K562	blood:	n/a	chr7:124799654-124799665
15	CEBPB	chr7:124859302-124859629	IMR90	lung:	n/a	chr7:124859444-124859455
16	CEBPB	chr7:124859288-124859542	HepG2	liver:	n/a	chr7:124859444-124859455
17	CEBPB	chr7:124776394-124776676	H1-hESC	embryonic stem cell:	n/a	chr7:124776499-124776511
18	CEBPB	chr7:124776349-124776719	ECC-1	luminal epithelium:	n/a	chr7:124776499-124776511
19	CEBPB	chr7:124760863-124761132	IMR90	lung:	n/a	chr7:124760971-124760984 chr7:124760971-124760984 chr7:124760973-124760984
20	CEBPB	chr7:124777249-124777684	ECC-1	luminal epithelium:	n/a	chr7:124777420-124777431 chr7:124777418-124777431
21	CEBPB	chr7:124799625-124799735	A549	lung:	n/a	chr7:124799654-124799665
22	CEBPB	chr7:124777183-124777689	HCT-116	colon:	n/a	chr7:124777420-124777431 chr7:124777418-124777431
23	CEBPB	chr7:124851598-124851805	A549	lung:	n/a	n/a
24	CEBPB	chr7:124722882-124722994	A549	lung:	n/a	chr7:124722952-124722961
25	CEBPB	chr7:124752861-124753197	IMR90	lung:	n/a	n/a
26	CEBPB	chr7:124859395-124859595	K562	blood:	n/a	chr7:124859444-124859455
27	CEBPB	chr7:124776400-124777639	Hela-S3	cervix:	n/a	chr7:124777420-124777431 chr7:124777418-124777431 chr7:124776499-124776511
28	CEBPB	chr7:124752836-124753259	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr7:124776367-124776746	ECC-1	luminal epithelium:	n/a	chr7:124776499-124776511
30	CEBPB	chr7:124777143-124777571	HCT-116	colon:	n/a	chr7:124777420-124777431 chr7:124777418-124777431
31	CEBPB	chr7:124752875-124753279	HCT-116	colon:	n/a	n/a
32	CEBPB	chr7:124777316-124777605	ECC-1	luminal epithelium:	n/a	chr7:124777420-124777431 chr7:124777418-124777431
33	CEBPB	chr7:124799504-124799828	HepG2	liver:	n/a	chr7:124799654-124799665
34	CHD2	chr7:124759811-124759940	GM12878	blood:	n/a	n/a
35	CHD2	chr7:124776507-124776673	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr7:124874094-124874143	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr7:124874080-124874230	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr7:124728080-124728230	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr7:124847960-124848110	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr7:124849146-124849185	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr7:124874000-124874150	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr7:124734728-124734771	K562	blood:	n/a	n/a
43	CTCF	chr7:124816581-124816659	Fibrobl	skin:	n/a	n/a
44	CTCF	chr7:124847840-124847990	MCF-7	breast:	n/a	n/a
45	CTCF	chr7:124813780-124813930	BJ	skin:	n/a	n/a
46	CTCF	chr7:124847974-124848046	MCF-7	breast:	n/a	n/a
47	CTCF	chr7:124742634-124742707	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr7:124847960-124848110	NHEK	skin:	n/a	n/a
49	CTCF	chr7:124741968-124742016	Lung_OC	lung:	n/a	n/a
50	CTCF	chr7:124882938-124882965	LNCaP	prostate:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:124765425-124765475	HL-60	blood:	n/a
2	chr7:124765425-124765475	HL-60	blood:	n/a
3	chr7:124765471-124765521	PrEC	prostate:	n/a
4	chr7:124765450-124765500	SKMC	muscle:	n/a
5	chr7:124765450-124765500	NH-A	brain:	n/a
6	chr7:124821737-124821787	H1-hESC	embryonic stem cell:	embryo
7	chr7:124765425-124765475	MCF10A-Er-Src	breast:	n/a
8	chr7:124765450-124765500	PANC-1	pancreas:	n/a
9	chr7:124821777-124821827	CMK	blood:	n/a
10	chr7:124821777-124821827	HAEpiC	amniotic membrane:	n/a
11	chr7:124821737-124821787	GM12892	blood:	n/a
12	chr7:124821777-124821827	GM12891	blood:	n/a
13	chr7:124765450-124765500	GM12892	blood:	n/a
14	chr7:124821737-124821787	ovcar-3	ovarian:	n/a
15	chr7:124765425-124765475	Caco-2	colon:	n/a
16	chr7:124765471-124765521	SK-N-SH	brain:	n/a
17	chr7:124821777-124821827	K562	blood:	n/a
18	chr7:124765471-124765521	HCF	heart:	n/a
19	chr7:124821777-124821827	NHBE	bronchial:	n/a
20	chr7:124765425-124765475	CMK	blood:	n/a
21	chr7:124765450-124765500	GM19239	blood:	n/a
22	chr7:124765471-124765521	HNPCEpiC	eye:	n/a
23	chr7:124821777-124821827	SK-N-SH_RA	brain:	n/a
24	chr7:124821737-124821787	NT2-D1	testis:	n/a
25	chr7:124821777-124821827	A549	lung:	n/a
26	chr7:124821737-124821787	RPTEC	kidney:	n/a
27	chr7:124821777-124821827	HNPCEpiC	eye:	n/a
28	chr7:124765425-124765475	AoSMC	blood vessel:	n/a
29	chr7:124765471-124765521	HCT-116	colon:	n/a
30	chr7:124821777-124821827	NH-A	brain:	n/a
31	chr7:124765450-124765500	H1-hESC	embryonic stem cell:	embryo
32	chr7:124765425-124765475	HNPCEpiC	eye:	n/a
33	chr7:124821777-124821827	HRCEpiC	kidney:	n/a
34	chr7:124765425-124765475	NHBE	bronchial:	n/a
35	chr7:124765425-124765475	GM19239	blood:	n/a
36	chr7:124821777-124821827	SAEC	small airway:	n/a
37	chr7:124765425-124765475	GM12892	blood:	n/a
38	chr7:124765450-124765500	HRE	kidney:	n/a
39	chr7:124765471-124765521	NHBE	bronchial:	n/a
40	chr7:124765471-124765521	GM19239	blood:	n/a
41	chr7:124765471-124765521	Jurkat	blood:	n/a
42	chr7:124765450-124765500	HRPEpiC	eye:	n/a
43	chr7:124765450-124765500	BJ	skin:	n/a
44	chr7:124821777-124821827	MCF-7	breast:	n/a
45	chr7:124765471-124765521	PFSK-1	brain:	n/a
46	chr7:124821737-124821787	ECC-1	luminal epithelium:	n/a
47	chr7:124765450-124765500	NT2-D1	testis:	n/a
48	chr7:124821777-124821827	MCF10A-Er-Src	breast:	n/a
49	chr7:124821777-124821827	AG09309	skin:	n/a
50	chr7:124821777-124821827	AG04449	skin:	fetal

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:124885290..124887904-chr7:124890626..124892616,2	MCF-7	breast:
2	chr7:124816634..124819440-chr7:124929772..124932344,2	K562	blood:
3	chr7:124794532..124796895-chr7:124797728..124800589,2	K562	blood:
4	chr7:124768386..124770245-chr7:124771796..124774751,2	MCF-7	breast:
5	chr7:124720373..124721901-chr7:124740400..124743244,2	K562	blood:
6	chr7:124728103..124730281-chr7:124737035..124739420,2	K562	blood:
7	chr7:124728103..124730281-chr7:124737035..124739420,2	K562	blood:
8	chr7:124715890..124718550-chr7:124819406..124822329,2	MCF-7	breast:
9	chr7:124735275..124737095-chr7:124743479..124745063,2	K562	blood:
10	chr7:124701246..124703610-chr7:124820642..124822320,2	MCF-7	breast:
11	chr7:124820580..124823044-chr7:124838776..124840487,2	MCF-7	breast:
12	chr7:124738749..124741628-chr7:124743456..124745788,2	K562	blood:
13	chr7:124855825..124857755-chr7:124906299..124909207,2	MCF-7	breast:
14	chr7:124820580..124823044-chr7:124838776..124840487,2	MCF-7	breast:
15	chr7:124783039..124785786-chr7:124787614..124790434,2	MCF-7	breast:
16	chr7:124708792..124711418-chr7:124715743..124718371,2	K562	blood:
17	chr7:124735275..124737095-chr7:124743479..124745063,2	K562	blood:
18	chr4:125278115..125279744-chr7:124830556..124832056,2	MCF-7	breast:
19	chr7:124783039..124785786-chr7:124787614..124790434,2	MCF-7	breast:
20	chr7:124720373..124721901-chr7:124740400..124743244,2	K562	blood:
21	chr7:124878093..124880264-chr7:124889805..124892447,2	MCF-7	breast:
22	chr7:124715890..124718550-chr7:124819406..124822329,2	MCF-7	breast:
23	chr7:124846681..124848535-chr7:125206338..125208006,2	K562	blood:
24	chr7:124794532..124796895-chr7:124797728..124800589,2	K562	blood:
25	chr7:124878093..124880264-chr7:124889805..124892447,2	MCF-7	breast:
26	chr7:124738749..124741628-chr7:124743456..124745788,2	K562	blood:
27	chr7:124768386..124770245-chr7:124771796..124774751,2	MCF-7	breast:

(count:49 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPAM1-4	chr7:124739458-124739567	ENSG00000224897
2	lnc-SPAM1-4	chr7:124778627-124778715	NONHSAT123098
3	lnc-SPAM1-4	chr7:124729744-124729830	ENSG00000224897
4	lnc-SPAM1-4	chr7:124729744-124729830	ENSG00000224897
5	lnc-SPAM1-5	chr7:124824623-124824667	ENSG00000237764.2
6	lnc-POT1-4	chr7:124800028-124800601	NONHSAT123100
7	lnc-SPAM1-4	chr7:124720766-124720867	ENSG00000224897
8	lnc-SPAM1-4	chr7:124756928-124757082	NONHSAT123098
9	lnc-SPAM1-4	chr7:124742014-124742104	ENSG00000224897
10	lnc-SPAM1-4	chr7:124756928-124757082	ENSG00000224897
11	lnc-SPAM1-4	chr7:124765879-124765961	ENSG00000224897
12	lnc-SPAM1-4	chr7:124758683-124758776	ENSG00000224897
13	lnc-SPAM1-4	chr7:124763035-124763129	ENSG00000224897
14	lnc-SPAM1-5	chr7:124835002-124835138	NONHSAT123102
15	lnc-SPAM1-5	chr7:124812272-124812288	ENSG00000237764.2
16	lnc-SPAM1-4	chr7:124765879-124766031	ENSG00000224897
17	lnc-SPAM1-4	chr7:124761696-124761897	ENSG00000224897
18	lnc-SPAM1-4	chr7:124739410-124739567	NONHSAT123098
19	lnc-POT1-1	chr7:124793517-124793665	XLOC_006593
20	lnc-SPAM1-4	chr7:124765879-124766031	ENSG00000224897
21	lnc-SPAM1-5	chr7:124824623-124824667	NR_110188
22	lnc-POT1-2	chr7:124886398-124886584	ENSG00000219445
23	lnc-POT1-1	chr7:124791380-124791830	XLOC_006593
24	lnc-SPAM1-4	chr7:124793540-124793621	ENSG00000224897
25	lnc-POT1-2	chr7:124890034-124890111	NR_110183
26	lnc-SPAM1-5	chr7:124835002-124835138	ENSG00000237764.2
27	lnc-POT1-2	chr7:124870580-124870614	NONHSAT123104
28	lnc-POT1-2	chr7:124870622-124870895	NONHSAT123104
29	lnc-POT1-2	chr7:124890034-124890111	ENSG00000219445
30	lnc-POT1-2	chr7:124869633-124870895	ENSG00000219445
31	lnc-SPAM1-4	chr7:124778627-124778713	ENSG00000224897
32	lnc-POT1-2	chr7:124869633-124870895	NR_110183
33	lnc-SPAM1-5	chr7:124826098-124826546	NONHSAT123102
34	lnc-SPAM1-5	chr7:124826098-124826546	NR_110188
35	lnc-SPAM1-4	chr7:124782769-124784620	ENSG00000224897
36	lnc-POT1-2	chr7:124888355-124888495	NR_110183
37	lnc-POT1-2	chr7:124888355-124888495	ENSG00000219445
38	lnc-SPAM1-5	chr7:124826098-124826546	ENSG00000237764.2
39	lnc-SPAM1-4	chr7:124778627-124778713	ENSG00000224897
40	lnc-SPAM1-4	chr7:124817698-124819369	ENSG00000224897
41	lnc-SPAM1-5	chr7:124824624-124824667	NONHSAT123102
42	lnc-SPAM1-4	chr7:124782769-124785288	ENSG00000224897
43	lnc-SPAM1-5	chr7:124835002-124835138	NR_110188
44	lnc-POT1-2	chr7:124888355-124888495	NONHSAT123104
45	lnc-SPAM1-4	chr7:124756928-124757082	ENSG00000224897
46	lnc-SPAM1-4	chr7:124765879-124766031	NONHSAT123098
47	lnc-SPAM1-4	chr7:124778627-124778713	ENSG00000224897
48	lnc-POT1-2	chr7:124890034-124890111	NONHSAT123104
49	lnc-SPAM1-4	chr7:124720766-124720867	ENSG00000224897

No data

Variant related genes	Relation type
ENSG00000205898	TF binding region
ENSG00000224899	TF binding region
ENSG00000237764	TF binding region
ENSG00000205898	CpG island
ENSG00000224899	CpG island
ENSG00000237764	CpG island
ZNF776	miRNA target sites
ARHGAP19	miRNA target sites
PITX1	miRNA target sites
ELAC2	miRNA target sites
GTF2A2	miRNA target sites
PHF10	miRNA target sites
CDKN2AIP	miRNA target sites
ZNF238	miRNA target sites
HIBADH	miRNA target sites
ILF2	miRNA target sites
E2F3	miRNA target sites
NUDT15	miRNA target sites
CREBZF	miRNA target sites
YIPF5	miRNA target sites
MYO5C	miRNA target sites
NOTCH1	miRNA target sites
MCL1	miRNA target sites
ENC1	miRNA target sites
ING3	miRNA target sites
ISM2	miRNA target sites
SOCS6	miRNA target sites
XYLT2	miRNA target sites

Extended variants
information (count: 4613 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:4613 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10253197	chr7:124714602-124714603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs12670265	chr7:124714606-124714607	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs533746403	chr7:124714615-124714616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs574628425	chr7:124714715-124714716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185127439	chr7:124720803-124720804	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs559002531	chr7:124720824-124720825	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs191217284	chr7:124720865-124720866	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs552545017	chr7:124723600-124723601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574177523	chr7:124723637-124723638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561725000	chr7:124723683-124723684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527724703	chr7:124723770-124723771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201635141	chr7:124723814-124723815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375376234	chr7:124723873-124723874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs386717503	chr7:124723894-124723895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200004720	chr7:124723901-124723902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556734582	chr7:124723905-124723906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200617757	chr7:124723906-124723907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75111010	chr7:124723908-124723909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569170535	chr7:124723930-124723931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570373689	chr7:124723967-124723968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs111237375	chr7:124723993-124723994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35873213	chr7:124724047-124724048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369579084	chr7:124724050-124724051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549682169	chr7:124724066-124724067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs117362831	chr7:124724076-124724077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs148224594	chr7:124724082-124724083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs549129957	chr7:124724093-124724094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562049924	chr7:124724117-124724118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554426997	chr7:124724202-124724203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534648390	chr7:124724251-124724252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs141143213	chr7:124724305-124724306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs150726635	chr7:124724323-124724324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs66852389	chr7:124724348-124724349	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs533625388	chr7:124724356-124724357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556463371	chr7:124724372-124724373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs578039065	chr7:124724419-124724420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs545422953	chr7:124724452-124724453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs561885549	chr7:124724453-124724454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs553811115	chr7:124724467-124724468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs572218151	chr7:124724489-124724490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs139199422	chr7:124724506-124724507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs80145443	chr7:124724519-124724520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs202154405	chr7:124724566-124724567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs564161738	chr7:124724599-124724600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs189097674	chr7:124724603-124724604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs79542630	chr7:124724709-124724710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs563320083	chr7:124724737-124724738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574031089	chr7:124724822-124724823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs181278823	chr7:124724899-124724900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs59342385	chr7:124724900-124724901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	21635232	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	22522925	CNVD
Autism	20858243	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:124714600-124714800	Enhancers	Placenta Amnion	Placenta Amnion
2	chr7:124723600-124728400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:124724200-124727800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr7:124724400-124724600	Enhancers	Brain Inferior Temporal Lobe	brain
5	chr7:124724400-124725800	Enhancers	Brain Substantia Nigra	brain
6	chr7:124724600-124725600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr7:124725600-124726000	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr7:124725800-124726200	Enhancers	Brain Cingulate Gyrus	brain
9	chr7:124727800-124728600	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr7:124728000-124728600	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr7:124728200-124728400	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr7:124728200-124728600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
13	chr7:124728200-124729200	Enhancers	Fetal Heart	heart
14	chr7:124728200-124729800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr7:124728400-124730000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr7:124728400-124730000	Enhancers	NHEK	skin
17	chr7:124728600-124730800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr7:124728600-124731200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr7:124729000-124731200	Enhancers	HMEC	breast
20	chr7:124729400-124729800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr7:124729800-124730800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr7:124729800-124730800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr7:124730000-124730400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr7:124730000-124730400	Weak transcription	NHEK	skin
25	chr7:124730000-124731600	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr7:124730400-124731000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr7:124730400-124731000	Enhancers	NHEK	skin
28	chr7:124730800-124731000	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr7:124730800-124731000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr7:124730800-124731200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr7:124731200-124732200	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr7:124731600-124732000	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr7:124732000-124732200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr7:124732200-124734600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr7:124734000-124734600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr7:124734600-124735000	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr7:124734600-124735000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr7:124734600-124735200	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr7:124734600-124735200	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr7:124734800-124735200	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr7:124734800-124735200	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr7:124738400-124739000	Enhancers	Fetal Heart	heart
43	chr7:124738800-124739800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr7:124739600-124740000	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr7:124739800-124776000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr7:124756000-124756800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr7:124756600-124756800	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr7:124756600-124757000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:124756800-124758400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr7:124757000-124758000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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