Variant report

Variant	nsv608344
Chromosome Location	chr7:124703756-124805279
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:277)
CpG islands
(count:183)
Chromatin interactive
region (count:25)
LncRNA
region (count:27)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:277 , 50 per page) page: 1 2 3 4 5 6

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	chr7:124795049-124795303	GM12878	blood:	n/a	n/a
5	BATF	chr7:124738440-124738777	GM12878	blood:	n/a	chr7:124738608-124738619 chr7:124738609-124738619
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	chr7:124797085-124797285	K562	blood:	n/a	n/a
11	CCNT2	chr7:124745648-124745845	K562	blood:	n/a	n/a
12	CEBPB	chr7:124799503-124799797	K562	blood:	n/a	chr7:124799654-124799665
13	CEBPB	chr7:124776367-124776746	ECC-1	luminal epithelium:	n/a	chr7:124776499-124776511
14	CEBPB	chr7:124777249-124777684	ECC-1	luminal epithelium:	n/a	chr7:124777420-124777431 chr7:124777418-124777431
15	CEBPB	chr7:124777183-124777689	HCT-116	colon:	n/a	chr7:124777420-124777431 chr7:124777418-124777431
16	CEBPB	chr7:124705655-124705974	K562	blood:	n/a	chr7:124705807-124705818
17	CEBPB	chr7:124760863-124761132	IMR90	lung:	n/a	chr7:124760971-124760984 chr7:124760971-124760984 chr7:124760973-124760984
18	CEBPB	chr7:124777143-124777571	HCT-116	colon:	n/a	chr7:124777420-124777431 chr7:124777418-124777431
19	CEBPB	chr7:124752875-124753279	HCT-116	colon:	n/a	n/a
20	CEBPB	chr7:124777316-124777605	ECC-1	luminal epithelium:	n/a	chr7:124777420-124777431 chr7:124777418-124777431
21	CEBPB	chr7:124705649-124705960	A549	lung:	n/a	chr7:124705807-124705818
22	CEBPB	chr7:124705644-124705956	IMR90	lung:	n/a	chr7:124705807-124705818
23	CEBPB	chr7:124722882-124722994	A549	lung:	n/a	chr7:124722952-124722961
24	CEBPB	chr7:124776394-124776676	H1-hESC	embryonic stem cell:	n/a	chr7:124776499-124776511
25	CEBPB	chr7:124705636-124705969	HepG2	liver:	n/a	chr7:124705807-124705818
26	CEBPB	chr7:124799504-124799828	HepG2	liver:	n/a	chr7:124799654-124799665
27	CEBPB	chr7:124776400-124777639	Hela-S3	cervix:	n/a	chr7:124777420-124777431 chr7:124777418-124777431 chr7:124776499-124776511
28	CEBPB	chr7:124752861-124753197	IMR90	lung:	n/a	n/a
29	CEBPB	chr7:124799625-124799735	A549	lung:	n/a	chr7:124799654-124799665
30	CEBPB	chr7:124752836-124753259	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr7:124776349-124776719	ECC-1	luminal epithelium:	n/a	chr7:124776499-124776511
32	CHD2	chr7:124759811-124759940	GM12878	blood:	n/a	n/a
33	CHD2	chr7:124776507-124776673	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr7:124798560-124798710	GM06990	blood:	n/a	n/a
35	CTCF	chr7:124742593-124742684	GM13977	blood:	n/a	n/a
36	CTCF	chr7:124728080-124728230	HRPEpiC	eye:	n/a	n/a
37	CTCF	chr7:124803445-124803486	MCF-7	breast:	n/a	n/a
38	CTCF	chr7:124750332-124750364	LNCaP	prostate:	n/a	n/a
39	CTCF	chr7:124734728-124734771	K562	blood:	n/a	n/a
40	CTCF	chr7:124748796-124748829	GM13976	blood:	n/a	n/a
41	CTCF	chr7:124742634-124742707	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr7:124741968-124742016	Lung_OC	lung:	n/a	n/a
43	E2F4	chr7:124789430-124789525	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr7:124766691-124766751	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr7:124712689-124712748	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr7:124760021-124760214	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr7:124776356-124776683	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr7:124777221-124777543	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr7:124720258-124720452	MCF10A-Er-Src	breast:	n/a	n/a
50	EBF1	chr7:124738542-124739016	GM12878	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:124765450-124765500	NH-A	brain:	n/a
2	chr7:124765450-124765500	PrEC	prostate:	n/a
3	chr7:124765425-124765475	SK-N-SH	brain:	n/a
4	chr7:124765450-124765500	T-47D	breast:	n/a
5	chr7:124765450-124765500	GM19239	blood:	n/a
6	chr7:124765471-124765521	Hela-S3	cervix:	n/a
7	chr7:124765450-124765500	Caco-2	colon:	n/a
8	chr7:124765471-124765521	NH-A	brain:	n/a
9	chr7:124765471-124765521	AG04449	skin:	fetal
10	chr7:124765450-124765500	NHBE	bronchial:	n/a
11	chr7:124765450-124765500	U87	brain:	n/a
12	chr7:124765450-124765500	HEEpiC	esophagus:	n/a
13	chr7:124765425-124765475	Jurkat	blood:	n/a
14	chr7:124765450-124765500	HCPEpiC	choroid plexus:	n/a
15	chr7:124765425-124765475	HCM	heart:	n/a
16	chr7:124765425-124765475	ProgFib	skin:	n/a
17	chr7:124765450-124765500	NHDF-neo	bronchial:	n/a
18	chr7:124765450-124765500	NB4	blood:	n/a
19	chr7:124765471-124765521	SK-N-SH	brain:	n/a
20	chr7:124765450-124765500	CMK	blood:	n/a
21	chr7:124765425-124765475	BE2_C	brain:	n/a
22	chr7:124765450-124765500	Jurkat	blood:	n/a
23	chr7:124765425-124765475	LNCaP	prostate:	n/a
24	chr7:124765450-124765500	AG04449	skin:	fetal
25	chr7:124765471-124765521	AG09309	skin:	n/a
26	chr7:124765450-124765500	MCF10A-Er-Src	breast:	n/a
27	chr7:124765425-124765475	U87	brain:	n/a
28	chr7:124765471-124765521	HMEC	breast:	n/a
29	chr7:124765471-124765521	Caco-2	colon:	n/a
30	chr7:124765425-124765475	HPAEpiC	pulmonary alveolar:	n/a
31	chr7:124765471-124765521	PrEC	prostate:	n/a
32	chr7:124765425-124765475	AG10803	skin:	n/a
33	chr7:124765450-124765500	HCM	heart:	n/a
34	chr7:124765425-124765475	Hela-S3	cervix:	n/a
35	chr7:124765425-124765475	AoSMC	blood vessel:	n/a
36	chr7:124765450-124765500	HIPEpiC	eye:	n/a
37	chr7:124765471-124765521	AoSMC	blood vessel:	n/a
38	chr7:124765425-124765475	SAEC	small airway:	n/a
39	chr7:124765471-124765521	HNPCEpiC	eye:	n/a
40	chr7:124765450-124765500	HepG2	liver:	n/a
41	chr7:124765450-124765500	HCF	heart:	n/a
42	chr7:124765471-124765521	GM12878	blood:	n/a
43	chr7:124765471-124765521	NT2-D1	testis:	n/a
44	chr7:124765450-124765500	LNCaP	prostate:	n/a
45	chr7:124765425-124765475	NB4	blood:	n/a
46	chr7:124765471-124765521	Hepatocyte	liver:	n/a
47	chr7:124765425-124765475	GM19239	blood:	n/a
48	chr7:124765450-124765500	BE2_C	brain:	n/a
49	chr7:124765471-124765521	ECC-1	luminal epithelium:	n/a
50	chr7:124765450-124765500	SAEC	small airway:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:124728103..124730281-chr7:124737035..124739420,2	K562	blood:
2	chr7:124794532..124796895-chr7:124797728..124800589,2	K562	blood:
3	chr7:124738749..124741628-chr7:124743456..124745788,2	K562	blood:
4	chr7:124697959..124699891-chr7:124704188..124706087,2	K562	blood:
5	chr7:124794532..124796895-chr7:124797728..124800589,2	K562	blood:
6	chr7:124704352..124706297-chr7:124709672..124711396,2	K562	blood:
7	chr7:124735275..124737095-chr7:124743479..124745063,2	K562	blood:
8	chr7:124704352..124706297-chr7:124709672..124711396,2	K562	blood:
9	chr7:124704797..124707787-chr7:124709672..124712293,2	K562	blood:
10	chr7:124704797..124707787-chr7:124709672..124712293,2	K562	blood:
11	chr7:124768386..124770245-chr7:124771796..124774751,2	MCF-7	breast:
12	chr7:124738749..124741628-chr7:124743456..124745788,2	K562	blood:
13	chr7:124783039..124785786-chr7:124787614..124790434,2	MCF-7	breast:
14	chr7:124735275..124737095-chr7:124743479..124745063,2	K562	blood:
15	chr7:124715890..124718550-chr7:124819406..124822329,2	MCF-7	breast:
16	chr7:124783039..124785786-chr7:124787614..124790434,2	MCF-7	breast:
17	chr7:124768386..124770245-chr7:124771796..124774751,2	MCF-7	breast:
18	chr7:124709051..124711137-chr7:124712296..124713913,2	K562	blood:
19	chr7:124611698..124614462-chr7:124706318..124708451,2	K562	blood:
20	chr7:124720373..124721901-chr7:124740400..124743244,2	K562	blood:
21	chr7:124709051..124711137-chr7:124712296..124713913,2	K562	blood:
22	chr7:124720373..124721901-chr7:124740400..124743244,2	K562	blood:
23	chr7:124728103..124730281-chr7:124737035..124739420,2	K562	blood:
24	chr7:124708792..124711418-chr7:124715743..124718371,2	K562	blood:
25	chr7:124708792..124711418-chr7:124715743..124718371,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPAM1-4	chr7:124782769-124785288	ENSG00000224897
2	lnc-POT1-4	chr7:124800028-124800601	NONHSAT123100
3	lnc-SPAM1-4	chr7:124742014-124742104	ENSG00000224897
4	lnc-SPAM1-4	chr7:124756928-124757082	NONHSAT123098
5	lnc-SPAM1-4	chr7:124778627-124778713	ENSG00000224897
6	lnc-SPAM1-4	chr7:124758683-124758776	ENSG00000224897
7	lnc-SPAM1-4	chr7:124739458-124739567	ENSG00000224897
8	lnc-POT1-1	chr7:124791380-124791830	XLOC_006593
9	lnc-SPAM1-4	chr7:124763035-124763129	ENSG00000224897
10	lnc-SPAM1-4	chr7:124778627-124778713	ENSG00000224897
11	lnc-SPAM1-4	chr7:124756928-124757082	ENSG00000224897
12	lnc-SPAM1-4	chr7:124756928-124757082	ENSG00000224897
13	lnc-SPAM1-4	chr7:124765879-124766031	ENSG00000224897
14	lnc-SPAM1-4	chr7:124761696-124761897	ENSG00000224897
15	lnc-SPAM1-4	chr7:124778627-124778715	NONHSAT123098
16	lnc-SPAM1-4	chr7:124720766-124720867	ENSG00000224897
17	lnc-SPAM1-4	chr7:124729744-124729830	ENSG00000224897
18	lnc-SPAM1-4	chr7:124782769-124784620	ENSG00000224897
19	lnc-SPAM1-4	chr7:124729744-124729830	ENSG00000224897
20	lnc-SPAM1-4	chr7:124765879-124765961	ENSG00000224897
21	lnc-SPAM1-4	chr7:124765879-124766031	ENSG00000224897
22	lnc-POT1-1	chr7:124793517-124793665	XLOC_006593
23	lnc-SPAM1-4	chr7:124793540-124793621	ENSG00000224897
24	lnc-SPAM1-4	chr7:124778627-124778713	ENSG00000224897
25	lnc-SPAM1-4	chr7:124720766-124720867	ENSG00000224897
26	lnc-SPAM1-4	chr7:124765879-124766031	NONHSAT123098
27	lnc-SPAM1-4	chr7:124739410-124739567	NONHSAT123098

No data

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

Extended variants
information (count: 2660 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2660 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13226395	chr7:124703756-124703757	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs138216767	chr7:124703774-124703775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184024796	chr7:124703802-124703803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187364317	chr7:124703811-124703812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs536364605	chr7:124703815-124703816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563758000	chr7:124703904-124703905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552960489	chr7:124703969-124703970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548491618	chr7:124703982-124703983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs79076281	chr7:124704051-124704052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541676953	chr7:124704056-124704057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564661700	chr7:124704100-124704101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs116319244	chr7:124704101-124704102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs142133191	chr7:124704103-124704104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563549921	chr7:124704116-124704117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529301273	chr7:124704130-124704131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549087110	chr7:124704153-124704154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs79947217	chr7:124704162-124704163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76561820	chr7:124704164-124704165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs559663576	chr7:124704190-124704191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191762136	chr7:124704192-124704193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73225498	chr7:124704197-124704198	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs139964051	chr7:124704217-124704218	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
23	rs547735371	chr7:124704219-124704220	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
24	rs372834778	chr7:124704235-124704236	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
25	rs377693331	chr7:124704237-124704238	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
26	rs142364545	chr7:124704254-124704255	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
27	rs111773076	chr7:124704279-124704280	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
28	rs6973166	chr7:124704294-124704295	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
29	rs141916504	chr7:124704305-124704306	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
30	rs567474251	chr7:124704314-124704315	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
31	rs6976746	chr7:124704315-124704316	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
32	rs182785028	chr7:124704386-124704387	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
33	rs187434036	chr7:124704404-124704405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191519585	chr7:124704452-124704453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs527553787	chr7:124704453-124704454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538284350	chr7:124704475-124704476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547586632	chr7:124704476-124704477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558425656	chr7:124704493-124704494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570580944	chr7:124704503-124704504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs112759525	chr7:124704544-124704545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs35490255	chr7:124704546-124704547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111941999	chr7:124704547-124704548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs578152921	chr7:124704605-124704606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs68032029	chr7:124704630-124704631	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs557103598	chr7:124704646-124704647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs2929321	chr7:124704680-124704681	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs150612647	chr7:124704699-124704700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551111955	chr7:124704732-124704733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528480792	chr7:124704737-124704738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545110693	chr7:124704849-124704850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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

Chromatin state (count:133 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:124702200-124706600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:124702200-124712200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr7:124704200-124704400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chr7:124704200-124704400	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
5	chr7:124710400-124711000	Enhancers	Fetal Intestine Large	intestine
6	chr7:124712200-124712600	Enhancers	Placenta Amnion	Placenta Amnion
7	chr7:124714600-124714800	Enhancers	Placenta Amnion	Placenta Amnion
8	chr7:124723600-124728400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr7:124724200-124727800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr7:124724400-124724600	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr7:124724400-124725800	Enhancers	Brain Substantia Nigra	brain
12	chr7:124724600-124725600	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr7:124725600-124726000	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr7:124725800-124726200	Enhancers	Brain Cingulate Gyrus	brain
15	chr7:124727800-124728600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr7:124728000-124728600	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr7:124728200-124728400	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr7:124728200-124728600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr7:124728200-124729200	Enhancers	Fetal Heart	heart
20	chr7:124728200-124729800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr7:124728400-124730000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr7:124728400-124730000	Enhancers	NHEK	skin
23	chr7:124728600-124730800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
24	chr7:124728600-124731200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr7:124729000-124731200	Enhancers	HMEC	breast
26	chr7:124729400-124729800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr7:124729800-124730800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr7:124729800-124730800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr7:124730000-124730400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr7:124730000-124730400	Weak transcription	NHEK	skin
31	chr7:124730000-124731600	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr7:124730400-124731000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr7:124730400-124731000	Enhancers	NHEK	skin
34	chr7:124730800-124731000	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr7:124730800-124731000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr7:124730800-124731200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr7:124731200-124732200	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr7:124731600-124732000	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr7:124732000-124732200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
40	chr7:124732200-124734600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr7:124734000-124734600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr7:124734600-124735000	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr7:124734600-124735000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr7:124734600-124735200	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr7:124734600-124735200	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr7:124734800-124735200	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr7:124734800-124735200	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr7:124738400-124739000	Enhancers	Fetal Heart	heart
49	chr7:124738800-124739800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr7:124739600-124740000	Enhancers	Breast Myoepithelial Primary Cells	Breast

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