Variant report

Variant	nsv539101
Chromosome Location	chr7:120836198-120881658
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:204)
CpG islands
(count:61)
Chromatin interactive
region (count:41)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:204 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:120869574-120869602	K562	blood:	n/a	n/a
2	BHLHE40	chr7:120851610-120851680	K562	blood:	n/a	n/a
3	BRCA1	chr7:120844643-120844790	Hela-S3	cervix:	n/a	n/a
4	CCNT2	chr7:120851534-120851936	K562	blood:	n/a	n/a
5	CCNT2	chr7:120868852-120868936	K562	blood:	n/a	n/a
6	CCNT2	chr7:120850727-120850917	K562	blood:	n/a	n/a
7	CEBPB	chr7:120842726-120842982	K562	blood:	n/a	n/a
8	CEBPB	chr7:120844737-120845132	Hela-S3	cervix:	n/a	chr7:120844976-120844987 chr7:120844976-120844987
9	CEBPB	chr7:120842695-120842983	IMR90	lung:	n/a	n/a
10	CEBPB	chr7:120844891-120845145	K562	blood:	n/a	chr7:120844976-120844987 chr7:120844976-120844987
11	CHD2	chr7:120872208-120872397	K562	blood:	n/a	n/a
12	CTCF	chr7:120871880-120872030	GM12873	blood:	n/a	n/a
13	CTCF	chr7:120870240-120870390	RPTEC	kidney:	n/a	n/a
14	CTCF	chr7:120842421-120842490	K562	blood:	n/a	n/a
15	CTCF	chr7:120842380-120842530	NHEK	skin:	n/a	n/a
16	CTCF	chr7:120878160-120878310	K562	blood:	n/a	n/a
17	CTCF	chr7:120842408-120842494	ProgFib	skin:	n/a	n/a
18	CTCF	chr7:120842340-120842490	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr7:120842315-120842522	K562	blood:	n/a	n/a
20	CTCF	chr7:120842410-120842476	Gliobla	brain:	n/a	n/a
21	CTCF	chr7:120842405-120842496	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr7:120842440-120842590	HMF	breast:	n/a	n/a
23	CTCF	chr7:120842360-120842510	HEK293	kidney:	n/a	n/a
24	CTCF	chr7:120843040-120843190	WERI-Rb-1	eye:	n/a	chr7:120843130-120843151 chr7:120843128-120843146 chr7:120843131-120843140
25	CTCF	chr7:120842200-120842350	HRPEpiC	eye:	n/a	n/a
26	CTCF	chr7:120842280-120842430	HMEC	breast:	n/a	n/a
27	CTCF	chr7:120872027-120872136	Hela-S3	cervix:	n/a	chr7:120872078-120872091 chr7:120872075-120872093
28	CTCF	chr7:120842360-120842510	K562	blood:	n/a	n/a
29	CTCF	chr7:120873937-120874020	GM12878	blood:	n/a	n/a
30	CTCF	chr7:120842400-120842550	HMF	breast:	n/a	n/a
31	CTCF	chr7:120860260-120860410	HAc	cerebellar:	n/a	n/a
32	CTCF	chr7:120843061-120843219	Medullo	brain:	n/a	chr7:120843130-120843151 chr7:120843128-120843146 chr7:120843131-120843140
33	CTCF	chr7:120872049-120872135	MCF-7	breast:	n/a	chr7:120872078-120872091 chr7:120872075-120872093
34	CTCF	chr7:120850327-120850418	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr7:120872020-120872170	HEK293	kidney:	n/a	chr7:120872078-120872091 chr7:120872075-120872093
36	CTCF	chr7:120877980-120878130	HA-sp	spinal cord:	n/a	n/a
37	CTCF	chr7:120872052-120872069	GM10266	blood:	n/a	n/a
38	E2F4	chr7:120843184-120843384	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr7:120858926-120858997	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr7:120871718-120872065	MCF10A-Er-Src	breast:	n/a	n/a
41	ELK1	chr7:120846029-120846039	K562	blood:	n/a	n/a
42	EP300	chr7:120844626-120844991	SK-N-SH_RA	brain:	n/a	n/a
43	EP300	chr7:120844566-120845016	SK-N-SH_RA	brain:	n/a	n/a
44	FAM48A	chr7:120852010-120852190	GM12878	blood:	n/a	n/a
45	FOS	chr7:120842713-120843162	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr7:120842742-120843132	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr7:120844759-120845054	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr7:120844698-120845160	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr7:120842750-120843107	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr7:120842791-120843015	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:120852287-120852337	AG09319	gingival:	n/a
2	chr7:120852287-120852337	BJ	skin:	n/a
3	chr7:120852287-120852337	HEEpiC	esophagus:	n/a
4	chr7:120852287-120852337	AoSMC	blood vessel:	n/a
5	chr7:120852287-120852337	ovcar-3	ovarian:	n/a
6	chr7:120852287-120852337	PFSK-1	brain:	n/a
7	chr7:120852287-120852337	PrEC	prostate:	n/a
8	chr7:120852287-120852337	SKMC	muscle:	n/a
9	chr7:120852287-120852337	AG04450	lung:	fetal
10	chr7:120852287-120852337	Caco-2	colon:	n/a
11	chr7:120852287-120852337	GM19239	blood:	n/a
12	chr7:120852287-120852337	HCT-116	colon:	n/a
13	chr7:120852287-120852337	HUVEC	blood vessel:	n/a
14	chr7:120852287-120852337	RPTEC	kidney:	n/a
15	chr7:120852287-120852337	AG09309	skin:	n/a
16	chr7:120852287-120852337	A549	lung:	n/a
17	chr7:120852287-120852337	LNCaP	prostate:	n/a
18	chr7:120852287-120852337	SK-N-SH	brain:	n/a
19	chr7:120852287-120852337	NHDF-neo	bronchial:	n/a
20	chr7:120852287-120852337	HIPEpiC	eye:	n/a
21	chr7:120852287-120852337	AG04449	skin:	fetal
22	chr7:120852287-120852337	AG10803	skin:	n/a
23	chr7:120852287-120852337	BE2_C	brain:	n/a
24	chr7:120852287-120852337	GM12891	blood:	n/a
25	chr7:120852287-120852337	HNPCEpiC	eye:	n/a
26	chr7:120852287-120852337	GM06990	blood:	n/a
27	chr7:120852287-120852337	NB4	blood:	n/a
28	chr7:120852287-120852337	MCF-7	breast:	n/a
29	chr7:120852287-120852337	CMK	blood:	n/a
30	chr7:120852287-120852337	HMEC	breast:	n/a
31	chr7:120852287-120852337	HRE	kidney:	n/a
32	chr7:120852287-120852337	K562	blood:	n/a
33	chr7:120852287-120852337	GM12892	blood:	n/a
34	chr7:120852287-120852337	SAEC	small airway:	n/a
35	chr7:120852287-120852337	NHBE	bronchial:	n/a
36	chr7:120852287-120852337	HL-60	blood:	n/a
37	chr7:120852287-120852337	NH-A	brain:	n/a
38	chr7:120852287-120852337	MCF10A-Er-Src	breast:	n/a
39	chr7:120852287-120852337	ECC-1	luminal epithelium:	n/a
40	chr7:120852287-120852337	HPAEpiC	pulmonary alveolar:	n/a
41	chr7:120852287-120852337	HCPEpiC	choroid plexus:	n/a
42	chr7:120852287-120852337	GM12878	blood:	n/a
43	chr7:120852287-120852337	U87	brain:	n/a
44	chr7:120852287-120852337	SK-N-MC	brain:	n/a
45	chr7:120852287-120852337	SK-N-SH_RA	brain:	n/a
46	chr7:120852287-120852337	HCM	heart:	n/a
47	chr7:120852287-120852337	HCF	heart:	n/a
48	chr7:120852287-120852337	PANC-1	pancreas:	n/a
49	chr7:120852287-120852337	NT2-D1	testis:	n/a
50	chr7:120852287-120852337	HRCEpiC	kidney:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:120849619..120853631-chr7:120859182..120861121,3	K562	blood:
2	chr7:120849619..120853631-chr7:120859182..120861121,3	K562	blood:
3	chr7:120842227..120844085-chr7:120858166..120859847,2	K562	blood:
4	chr7:120853643..120855944-chr7:120855960..120858802,3	K562	blood:
5	chr7:120879517..120881994-chr7:120882337..120885417,3	K562	blood:
6	chr7:120865025..120867701-chr7:120877950..120880426,2	K562	blood:
7	chr7:120811226..120812887-chr7:120837406..120839127,2	K562	blood:
8	chr7:120832993..120835198-chr7:120838379..120841275,3	K562	blood:
9	chr7:120842227..120844085-chr7:120858166..120859847,2	K562	blood:
10	chr7:120836283..120838682-chr7:120872699..120875576,2	K562	blood:
11	chr7:120841468..120846547-chr7:120846758..120854034,8	K562	blood:
12	chr7:120853643..120855944-chr7:120855960..120858802,3	K562	blood:
13	chr7:120854329..120856810-chr7:120876127..120877752,2	K562	blood:
14	chr7:120848908..120852746-chr7:120854048..120856854,5	K562	blood:
15	chr7:120865025..120867701-chr7:120877950..120880426,2	K562	blood:
16	chr7:120868481..120870338-chr7:120872297..120875239,2	K562	blood:
17	chr7:120878568..120880747-chr7:120916933..120919501,2	K562	blood:
18	chr7:120855438..120857964-chr7:120860983..120863737,2	K562	blood:
19	chr7:120836253..120841319-chr7:120841811..120848062,9	K562	blood:
20	chr7:120848400..120850146-chr7:120867197..120869985,2	K562	blood:
21	chr7:120854329..120856810-chr7:120876127..120877752,2	K562	blood:
22	chr7:120865059..120868027-chr7:120873539..120876045,2	K562	blood:
23	chr7:120865059..120868027-chr7:120873539..120876045,2	K562	blood:
24	chr7:120836253..120841319-chr7:120841811..120848062,9	K562	blood:
25	chr7:120836283..120838682-chr7:120872699..120875576,2	K562	blood:
26	chr7:120858530..120860172-chr7:120865997..120868025,2	K562	blood:
27	chr7:120831876..120833803-chr7:120835458..120837128,2	K562	blood:
28	chr7:120841468..120846547-chr7:120846758..120854034,8	K562	blood:
29	chr7:120819870..120822812-chr7:120840045..120842182,2	K562	blood:
30	chr7:120867657..120869346-chr7:120882060..120884535,2	K562	blood:
31	chr7:120848908..120852746-chr7:120854048..120856854,5	K562	blood:
32	chr7:120873011..120874844-chr7:120878339..120881386,3	K562	blood:
33	chr7:120856242..120858668-chr7:120894112..120895725,2	K562	blood:
34	chr7:120868481..120870338-chr7:120872297..120875239,2	K562	blood:
35	chr7:120855438..120857964-chr7:120860983..120863737,2	K562	blood:
36	chr7:120858530..120860172-chr7:120865997..120868025,2	K562	blood:
37	chr7:120873011..120874844-chr7:120878339..120881386,3	K562	blood:
38	chr7:120833230..120836102-chr7:120842125..120844509,2	K562	blood:
39	chr7:120848400..120850146-chr7:120867197..120869985,2	K562	blood:
40	chr7:120870734..120873223-chr7:120882275..120885118,2	K562	blood:
41	chr7:120879517..120881082-chr7:120883141..120886021,2	K562	blood:

No data

Variant related genes	Relation type
RNU6-517P	TF binding region
RNU6-517P	CpG island
ENSG00000207090	chromatin interactions

Extended variants
information (count: 1547 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1547 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112811374	chr7:120836212-120836213	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs150090426	chr7:120836222-120836223	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537283713	chr7:120836380-120836381	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs138356499	chr7:120836402-120836403	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs7808138	chr7:120836416-120836417	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs567886824	chr7:120836469-120836470	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs142777998	chr7:120836505-120836506	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs147375756	chr7:120836530-120836531	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs575670304	chr7:120836546-120836547	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs117697420	chr7:120836567-120836568	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs183622013	chr7:120836641-120836642	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529142039	chr7:120836643-120836644	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs542556642	chr7:120836673-120836674	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559265613	chr7:120836700-120836701	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs3735469	chr7:120836712-120836713	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs553413889	chr7:120836770-120836771	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551187135	chr7:120836796-120836797	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370230711	chr7:120836804-120836805	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs375815731	chr7:120836808-120836809	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs143605756	chr7:120836856-120836857	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs79429606	chr7:120836868-120836869	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188678901	chr7:120836879-120836880	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550509354	chr7:120836947-120836948	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567152311	chr7:120837037-120837038	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191951614	chr7:120837131-120837132	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375155809	chr7:120837171-120837172	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs57229057	chr7:120837173-120837174	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs67306888	chr7:120837190-120837191	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573228635	chr7:120837205-120837206	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545416579	chr7:120837232-120837233	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547303606	chr7:120837338-120837339	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs567200245	chr7:120837357-120837358	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs539207390	chr7:120837492-120837493	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs73215398	chr7:120837613-120837614	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs369421844	chr7:120837665-120837666	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs117086320	chr7:120837676-120837677	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs184147553	chr7:120837683-120837684	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs150495845	chr7:120837688-120837689	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs373722731	chr7:120837694-120837695	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs574734632	chr7:120837710-120837711	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs543280349	chr7:120837711-120837712	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs559197583	chr7:120837715-120837716	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs572820216	chr7:120837733-120837734	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs544768857	chr7:120837762-120837763	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs148694007	chr7:120837776-120837777	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs142196288	chr7:120837886-120837887	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs550399906	chr7:120837921-120837922	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs561078177	chr7:120837957-120837958	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs6944198	chr7:120837959-120837960	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs546640376	chr7:120837974-120837975	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	21115979	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:120819200-120861000	Strong transcription	K562	blood
2	chr7:120823600-120874800	Weak transcription	NHLF	lung
3	chr7:120833200-120838400	Weak transcription	HSMM	muscle
4	chr7:120833600-120846200	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr7:120834000-120838400	Weak transcription	Primary B cells from peripheral blood	blood
6	chr7:120835600-120837800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr7:120835600-120839400	Enhancers	Skeletal Muscle Male	skeletal muscle
8	chr7:120835800-120836200	Enhancers	Ovary	ovary
9	chr7:120835800-120836400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr7:120835800-120836400	Enhancers	HSMMtube	muscle
11	chr7:120835800-120836600	Enhancers	Aorta	Aorta
12	chr7:120835800-120836800	Enhancers	Skeletal Muscle Female	skeletal muscle
13	chr7:120835800-120836800	Enhancers	Osteobl	bone
14	chr7:120835800-120837000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr7:120835800-120837000	Enhancers	Psoas Muscle	Psoas
16	chr7:120835800-120837600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr7:120836000-120836400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr7:120836000-120836400	Enhancers	Right Atrium	heart
19	chr7:120836000-120836400	Enhancers	Right Ventricle	heart
20	chr7:120836000-120836600	Enhancers	Left Ventricle	heart
21	chr7:120836000-120836800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr7:120836000-120836800	Enhancers	Adipose Nuclei	Adipose
23	chr7:120836000-120836800	Enhancers	Fetal Heart	heart
24	chr7:120836000-120836800	Enhancers	NHDF-Ad	bronchial
25	chr7:120836200-120836400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr7:120836200-120836400	Enhancers	Colon Smooth Muscle	Colon
27	chr7:120836200-120836600	Enhancers	NH-A	brain
28	chr7:120836200-120836800	Enhancers	Fetal Muscle Leg	muscle
29	chr7:120836200-120837600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr7:120836200-120851400	Weak transcription	Ovary	ovary
31	chr7:120836400-120836600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr7:120836400-120836800	Enhancers	Brain Germinal Matrix	brain
33	chr7:120836400-120838400	Weak transcription	Right Atrium	heart
34	chr7:120836400-120844600	Weak transcription	HSMMtube	muscle
35	chr7:120836400-120851400	Weak transcription	Colon Smooth Muscle	Colon
36	chr7:120836400-120851600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr7:120836400-120851600	Weak transcription	Right Ventricle	heart
38	chr7:120836400-120851600	Weak transcription	Stomach Smooth Muscle	stomach
39	chr7:120836600-120836800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr7:120836600-120837600	Weak transcription	Left Ventricle	heart
41	chr7:120836600-120841400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr7:120836600-120842200	Weak transcription	Aorta	Aorta
43	chr7:120836600-120851400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr7:120836800-120837200	Weak transcription	Fetal Heart	heart
45	chr7:120836800-120837200	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr7:120836800-120838600	Weak transcription	Fetal Muscle Leg	muscle
47	chr7:120836800-120858200	Weak transcription	Adipose Nuclei	Adipose
48	chr7:120837000-120837400	Weak transcription	Psoas Muscle	Psoas
49	chr7:120837000-120837800	Enhancers	Fetal Brain Male	brain
50	chr7:120837200-120838600	Enhancers	Fetal Heart	heart

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