Variant report

Variant	nsv532181
Chromosome Location	chr7:122291571-122684719
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2191)
CpG islands
(count:2570)
Chromatin interactive
region (count:93)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2191 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:122525653-122525930	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:122467950-122468098	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:122526484-122526694	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:122527046-122527681	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:122488996-122489769	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:122335758-122336328	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:122431984-122432331	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:122318366-122318564	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:122523982-122524287	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:122318792-122318991	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:122443416-122443772	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:122319336-122320305	HepG2	liver:	n/a	n/a
13	ARID3A	chr7:122397065-122397362	HepG2	liver:	n/a	n/a
14	ATF1	chr7:122328801-122328997	K562	blood:	n/a	n/a
15	ATF1	chr7:122641820-122641853	K562	blood:	n/a	n/a
16	ATF2	chr7:122319207-122319730	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr7:122319232-122319766	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr7:122526369-122527153	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr7:122410986-122410996	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr7:122328816-122328949	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr7:122387043-122387275	GM12878	blood:	n/a	n/a
22	BATF	chr7:122387086-122387293	GM12878	blood:	n/a	n/a
23	BATF	chr7:122365495-122365692	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:122319283-122319597	H1-hESC	embryonic stem cell:	n/a	n/a
25	BCL11A	chr7:122319337-122319622	H1-hESC	embryonic stem cell:	n/a	n/a
26	BCL11A	chr7:122386981-122387296	GM12878	blood:	n/a	n/a
27	BCL11A	chr7:122407372-122407682	H1-hESC	embryonic stem cell:	n/a	n/a
28	BCL11A	chr7:122407461-122407732	H1-hESC	embryonic stem cell:	n/a	n/a
29	BCL11A	chr7:122386912-122387429	GM12878	blood:	n/a	n/a
30	BCL3	chr7:122680639-122680893	GM12878	blood:	n/a	n/a
31	BHLHE40	chr7:122542886-122543077	K562	blood:	n/a	n/a
32	BHLHE40	chr7:122526507-122526841	GM12878	blood:	n/a	chr7:122526577-122526593 chr7:122526691-122526707
33	BHLHE40	chr7:122319382-122319714	HepG2	liver:	n/a	n/a
34	BHLHE40	chr7:122527388-122527560	K562	blood:	n/a	n/a
35	BHLHE40	chr7:122409003-122409090	GM12878	blood:	n/a	n/a
36	BHLHE40	chr7:122361311-122361406	HepG2	liver:	n/a	n/a
37	BHLHE40	chr7:122582848-122583160	HepG2	liver:	n/a	n/a
38	BHLHE40	chr7:122350118-122350420	GM12878	blood:	n/a	n/a
39	BHLHE40	chr7:122387024-122387362	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:122526388-122527567	HepG2	liver:	n/a	chr7:122526436-122526452 chr7:122526444-122526460 chr7:122526577-122526593 chr7:122526691-122526707 chr7:122526477-122526493
41	BHLHE40	chr7:122542972-122542982	GM12878	blood:	n/a	n/a
42	BRCA1	chr7:122525959-122526099	H1-hESC	embryonic stem cell:	n/a	n/a
43	BRCA1	chr7:122527461-122527525	HepG2	liver:	n/a	n/a
44	BRCA1	chr7:122526307-122526425	HepG2	liver:	n/a	n/a
45	BRCA1	chr7:122502710-122502723	H1-hESC	embryonic stem cell:	n/a	n/a
46	BRCA1	chr7:122525662-122525812	HepG2	liver:	n/a	n/a
47	BRCA1	chr7:122526469-122526507	Hela-S3	cervix:	n/a	n/a
48	CBX3	chr7:122591086-122591476	HCT-116	colon:	n/a	n/a
49	CBX3	chr7:122661673-122661996	HCT-116	colon:	n/a	n/a
50	CBX3	chr7:122615297-122615758	HCT-116	colon:	n/a	n/a

(count:2570 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:122527522-122527572	PANC-1	pancreas:	n/a
2	chr7:122321539-122321589	HCM	heart:	n/a
3	chr7:122343409-122343459	HRPEpiC	eye:	n/a
4	chr7:122526408-122526458	Hepatocyte	liver:	n/a
5	chr7:122635026-122635076	PANC-1	pancreas:	n/a
6	chr7:122526940-122526990	K562	blood:	n/a
7	chr7:122326807-122326857	HIPEpiC	eye:	n/a
8	chr7:122526408-122526458	HEK293	kidney:	embryo
9	chr7:122527522-122527572	PANC-1	pancreas:	n/a
10	chr7:122321539-122321589	HCM	heart:	n/a
11	chr7:122343409-122343459	HRPEpiC	eye:	n/a
12	chr7:122526408-122526458	Hepatocyte	liver:	n/a
13	chr7:122635026-122635076	PANC-1	pancreas:	n/a
14	chr7:122526940-122526990	K562	blood:	n/a
15	chr7:122326807-122326857	HIPEpiC	eye:	n/a
16	chr7:122526408-122526458	HEK293	kidney:	embryo
17	chr7:122321539-122321589	SK-N-MC	brain:	n/a
18	chr7:122338579-122338629	K562	blood:	n/a
19	chr7:122525974-122526024	HIPEpiC	eye:	n/a
20	chr7:122635026-122635076	MCF-7	breast:	n/a
21	chr7:122388911-122388961	Hela-S3	cervix:	n/a
22	chr7:122526843-122526893	AG04450	lung:	fetal
23	chr7:122526824-122526874	GM12878	blood:	n/a
24	chr7:122635522-122635572	HIPEpiC	eye:	n/a
25	chr7:122338579-122338629	IMR90	lung:	fetal
26	chr7:122526834-122526884	AG09309	skin:	n/a
27	chr7:122488330-122488380	ovcar-3	ovarian:	n/a
28	chr7:122527351-122527401	HRPEpiC	eye:	n/a
29	chr7:122553875-122553925	PANC-1	pancreas:	n/a
30	chr7:122384836-122384886	T-47D	breast:	n/a
31	chr7:122343409-122343459	NB4	blood:	n/a
32	chr7:122526824-122526874	U87	brain:	n/a
33	chr7:122384836-122384886	HNPCEpiC	eye:	n/a
34	chr7:122529707-122529757	HCM	heart:	n/a
35	chr7:122527351-122527401	GM19239	blood:	n/a
36	chr7:122443513-122443563	HIPEpiC	eye:	n/a
37	chr7:122526572-122526622	HRCEpiC	kidney:	n/a
38	chr7:122342889-122342939	NH-A	brain:	n/a
39	chr7:122384836-122384886	Hela-S3	cervix:	n/a
40	chr7:122343409-122343459	LNCaP	prostate:	n/a
41	chr7:122527472-122527522	CMK	blood:	n/a
42	chr7:122553915-122553965	GM12891	blood:	n/a
43	chr7:122526033-122526083	RPTEC	kidney:	n/a
44	chr7:122526834-122526884	NH-A	brain:	n/a
45	chr7:122338579-122338629	HEEpiC	esophagus:	n/a
46	chr7:122342889-122342939	ovcar-3	ovarian:	n/a
47	chr7:122527499-122527549	GM12892	blood:	n/a
48	chr7:122527522-122527572	NB4	blood:	n/a
49	chr7:122326807-122326857	H1-hESC	embryonic stem cell:	embryo
50	chr7:122527437-122527487	HEEpiC	esophagus:	n/a

(count:93 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:122443541..122445086-chr7:122446749..122448778,2	K562	blood:
2	chr7:122443505..122444148-chr7:122788638..122789513,2	MCF-7	breast:
3	chr7:122561098..122562829-chr7:122564886..122567563,2	K562	blood:
4	chr7:122473493..122475814-chr7:122480570..122483503,2	MCF-7	breast:
5	chr7:122473493..122475814-chr7:122480570..122483503,2	MCF-7	breast:
6	chr7:122473308..122475619-chr7:122484474..122486171,2	MCF-7	breast:
7	chr7:122482166..122484643-chr7:122531331..122532997,2	MCF-7	breast:
8	chr7:122630874..122632395-chr7:122639111..122641768,2	K562	blood:
9	chr7:122443038..122444017-chr7:122710508..122711379,2	MCF-7	breast:
10	chr7:122368871..122371613-chr7:122375877..122379228,3	MCF-7	breast:
11	chr7:122487239..122489689-chr7:122524785..122526755,2	MCF-7	breast:
12	chr7:122484466..122486591-chr7:122487501..122489020,2	MCF-7	breast:
13	chr7:122384641..122386460-chr7:122390684..122392862,2	K562	blood:
14	chr7:122597821..122600156-chr7:122601223..122603863,2	K562	blood:
15	chr7:122527428..122528069-chr7:122694498..122695060,2	MCF-7	breast:
16	chr7:122471973..122475729-chr7:122484629..122488935,3	MCF-7	breast:
17	chr7:122225953..122228862-chr7:122376425..122378624,2	K562	blood:
18	chr14:24748707..24751147-chr7:122509604..122511809,2	MCF-7	breast:
19	chr7:122468419..122470374-chr7:122473380..122475782,2	MCF-7	breast:
20	chr7:122483143..122485209-chr7:122487221..122489725,2	MCF-7	breast:
21	chr7:122597821..122600156-chr7:122601223..122603863,2	K562	blood:
22	chr7:122443541..122445086-chr7:122446749..122448778,2	K562	blood:
23	chr7:122484005..122486884-chr7:122524580..122527500,2	MCF-7	breast:
24	chr7:122659402..122661138-chr7:122672194..122673932,2	K562	blood:
25	chr7:122382528..122384037-chr7:122398742..122400591,2	K562	blood:
26	chr7:122678727..122680227-chr7:122869020..122871591,2	K562	blood:
27	chr7:122484843..122489106-chr7:122489595..122492470,4	MCF-7	breast:
28	chr7:122468419..122470374-chr7:122473380..122475782,2	MCF-7	breast:
29	chr7:122659402..122661138-chr7:122672194..122673932,2	K562	blood:
30	chr7:122293297..122295809-chr7:122299127..122301217,2	MCF-7	breast:
31	chr7:122427597..122429988-chr7:122525727..122527279,2	MCF-7	breast:
32	chr7:122556884..122558896-chr7:122561512..122564135,2	K562	blood:
33	chr7:122379171..122379744-chr7:122390634..122391405,2	MCF-7	breast:
34	chr7:122521246..122525169-chr7:122525278..122528321,3	MCF-7	breast:
35	chr7:122450452..122452718-chr7:122483355..122485678,2	MCF-7	breast:
36	chr17:57920427..57922384-chr7:122390814..122393151,2	MCF-7	breast:
37	chr7:122379171..122379744-chr7:122390634..122391405,2	MCF-7	breast:
38	chr7:122296179..122297714-chr7:122297804..122300438,2	MCF-7	breast:
39	chr7:121982082..121984768-chr7:122414729..122417554,2	K562	blood:
40	chr7:122293297..122295809-chr7:122299127..122301217,2	MCF-7	breast:
41	chr7:122473308..122475619-chr7:122484474..122486171,2	MCF-7	breast:
42	chr7:122441614..122445923-chr7:122446621..122449236,4	MCF-7	breast:
43	chr7:122544561..122547077-chr7:122568138..122570128,2	K562	blood:
44	chr7:122542099..122544437-chr7:122545966..122548062,2	K562	blood:
45	chr7:122483143..122485209-chr7:122487221..122489725,2	MCF-7	breast:
46	chr7:122544561..122547077-chr7:122568138..122570128,2	K562	blood:
47	chr7:122449452..122451074-chr7:122524570..122526706,2	MCF-7	breast:
48	chr7:122469925..122472134-chr7:122472549..122474182,2	MCF-7	breast:
49	chr7:122536518..122537575-chr7:122710662..122711391,3	MCF-7	breast:
50	chr7:122556884..122558896-chr7:122561512..122564135,2	K562	blood:

No data

Variant related genes	Relation type
RNF148	TF binding region
RPS26P31	TF binding region
ENSG00000227573	TF binding region
CADPS2	TF binding region
TAS2R16	TF binding region
ENSG00000225795	TF binding region
RNF133	TF binding region
RNF148	CpG island
RPS26P31	CpG island
ENSG00000227573	CpG island
CADPS2	CpG island
TAS2R16	CpG island
ENSG00000225795	CpG island
RNF133	CpG island
ENSG00000188050	chromatin interactions
ENSG00000227573	chromatin interactions
ENSG00000223595	chromatin interactions
ENSG00000081803	chromatin interactions

Extended variants
information (count: 11855 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:11855 , 50 per page) page: 1 2 3 4 5 6 7 ... 238

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10257593	chr7:122291609-122291610	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563846317	chr7:122291647-122291648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529628392	chr7:122291677-122291678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115740169	chr7:122291691-122291692	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs75047633	chr7:122291714-122291715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2471189	chr7:122291720-122291721	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs148093846	chr7:122291742-122291743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs111596787	chr7:122291758-122291759	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs141984804	chr7:122291760-122291761	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537264788	chr7:122291784-122291785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150696257	chr7:122291793-122291794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs62482255	chr7:122291829-122291830	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs536596529	chr7:122291837-122291838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs140106790	chr7:122291843-122291844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143797238	chr7:122291871-122291872	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188240959	chr7:122291880-122291881	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs180684525	chr7:122291903-122291904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577684004	chr7:122291988-122291989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565835037	chr7:122291992-122291993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146377532	chr7:122291997-122291998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563937019	chr7:122292023-122292024	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113946600	chr7:122292036-122292037	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs377506422	chr7:122292039-122292040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs78146910	chr7:122292046-122292047	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs548199883	chr7:122292062-122292063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs528093542	chr7:122292136-122292137	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149912701	chr7:122292163-122292164	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569829491	chr7:122292282-122292283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs148185064	chr7:122292289-122292290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs144879203	chr7:122292305-122292306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs201036877	chr7:122292306-122292307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530663750	chr7:122292311-122292312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184804578	chr7:122292318-122292319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567495146	chr7:122292321-122292322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs370719855	chr7:122292323-122292324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs559071105	chr7:122292325-122292326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs189808006	chr7:122292401-122292402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs546877052	chr7:122292477-122292478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs570990025	chr7:122292551-122292552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181894889	chr7:122292571-122292572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs33997607	chr7:122292629-122292630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534715451	chr7:122292726-122292727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs149037522	chr7:122292764-122292765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs577594994	chr7:122292765-122292766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs537600307	chr7:122292782-122292783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs576996684	chr7:122292794-122292795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs557163695	chr7:122292826-122292827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186872624	chr7:122292849-122292850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556563932	chr7:122292850-122292851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576425898	chr7:122292851-122292852	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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	21922591	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
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute monocytic leukemia	16498392	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1844 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:122288400-122293000	Weak transcription	Small Intestine	intestine
2	chr7:122289000-122292800	Weak transcription	Stomach Mucosa	stomach
3	chr7:122289600-122293000	Weak transcription	Gastric	stomach
4	chr7:122289600-122293000	Weak transcription	Pancreas	Pancrea
5	chr7:122291400-122291800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr7:122291400-122292000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:122291400-122292000	Enhancers	Muscle Satellite Cultured Cells	--
8	chr7:122292000-122292200	Enhancers	Esophagus	oesophagus
9	chr7:122292000-122292200	Enhancers	Lung	lung
10	chr7:122292000-122293800	Enhancers	HUVEC	blood vessel
11	chr7:122292200-122293000	Weak transcription	Esophagus	oesophagus
12	chr7:122292200-122293000	Weak transcription	Lung	lung
13	chr7:122292800-122293200	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr7:122292800-122293800	Enhancers	Stomach Mucosa	stomach
15	chr7:122293000-122293200	Enhancers	Small Intestine	intestine
16	chr7:122293000-122293400	Enhancers	H1 Cell Line	embryonic stem cell
17	chr7:122293000-122293400	Enhancers	H9 Cell Line	embryonic stem cell
18	chr7:122293000-122293400	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr7:122293000-122293400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr7:122293000-122293400	Enhancers	Esophagus	oesophagus
21	chr7:122293000-122293400	Enhancers	Gastric	stomach
22	chr7:122293000-122293400	Enhancers	Pancreas	Pancrea
23	chr7:122293000-122293600	Enhancers	Left Ventricle	heart
24	chr7:122293000-122293600	Enhancers	Lung	lung
25	chr7:122293000-122294000	Enhancers	Fetal Lung	lung
26	chr7:122293400-122294400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr7:122293600-122318600	Weak transcription	Lung	lung
28	chr7:122294000-122314400	Weak transcription	Fetal Lung	lung
29	chr7:122294400-122294600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr7:122301200-122301400	Enhancers	Gastric	stomach
31	chr7:122301400-122315200	Weak transcription	Gastric	stomach
32	chr7:122304800-122305400	Enhancers	Pancreas	Pancrea
33	chr7:122305400-122312600	Weak transcription	Pancreas	Pancrea
34	chr7:122306800-122307000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr7:122306800-122308000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr7:122307000-122308200	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr7:122307000-122308400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr7:122307000-122313800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr7:122307600-122307800	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr7:122307600-122308000	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr7:122307600-122308200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr7:122307600-122308200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr7:122308000-122308200	Enhancers	H9 Cell Line	embryonic stem cell
44	chr7:122308000-122308200	Enhancers	Left Ventricle	heart
45	chr7:122308000-122311400	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr7:122308200-122311400	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr7:122308200-122311600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr7:122308200-122316600	Weak transcription	Left Ventricle	heart
49	chr7:122308400-122314400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr7:122308600-122309000	Enhancers	Placenta Amnion	Placenta Amnion

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