Variant report

Variant	esv1827709
Chromosome Location	chr7:99353500-99440051
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:937)
CpG islands
(count:794)
Chromatin interactive
region (count:53)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:937 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:99370143-99370615	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:99429327-99429685	K562	blood:	n/a	n/a
3	ARID3A	chr7:99404545-99405000	K562	blood:	n/a	n/a
4	ARID3A	chr7:99392404-99393206	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:99430754-99431796	K562	blood:	n/a	n/a
6	ARID3A	chr7:99419549-99419766	K562	blood:	n/a	n/a
7	ARID3A	chr7:99426820-99427600	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:99424875-99425944	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:99434104-99434299	K562	blood:	n/a	n/a
10	ARID3A	chr7:99404110-99404262	K562	blood:	n/a	n/a
11	ARID3A	chr7:99432732-99433168	K562	blood:	n/a	n/a
12	ARID3A	chr7:99429291-99429572	HepG2	liver:	n/a	n/a
13	ARID3A	chr7:99364310-99364654	K562	blood:	n/a	n/a
14	ATF1	chr7:99430854-99431444	K562	blood:	n/a	n/a
15	ATF1	chr7:99432770-99433199	K562	blood:	n/a	n/a
16	ATF1	chr7:99404571-99404887	K562	blood:	n/a	n/a
17	ATF2	chr7:99365248-99365724	GM12878	blood:	n/a	n/a
18	ATF2	chr7:99365148-99365713	GM12878	blood:	n/a	n/a
19	ATF3	chr7:99430791-99431355	K562	blood:	n/a	n/a
20	ATF3	chr7:99432723-99433146	K562	blood:	n/a	n/a
21	BACH1	chr7:99432990-99433289	K562	blood:	n/a	n/a
22	BACH1	chr7:99405302-99405480	K562	blood:	n/a	n/a
23	BATF	chr7:99365239-99365549	GM12878	blood:	n/a	n/a
24	BATF	chr7:99365247-99365623	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:99365231-99365629	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:99392437-99393170	HepG2	liver:	n/a	chr7:99392859-99392872 chr7:99392861-99392870 chr7:99392860-99392869 chr7:99392862-99392871 chr7:99392861-99392870 chr7:99392855-99392876
27	BHLHE40	chr7:99366245-99366383	GM12878	blood:	n/a	n/a
28	BHLHE40	chr7:99392731-99393041	HepG2	liver:	n/a	chr7:99392859-99392872 chr7:99392861-99392870 chr7:99392860-99392869 chr7:99392862-99392871 chr7:99392861-99392870 chr7:99392855-99392876
29	BHLHE40	chr7:99430853-99431475	K562	blood:	n/a	n/a
30	BHLHE40	chr7:99432169-99432206	K562	blood:	n/a	n/a
31	BHLHE40	chr7:99360674-99360886	K562	blood:	n/a	n/a
32	BHLHE40	chr7:99432803-99433190	K562	blood:	n/a	n/a
33	BHLHE40	chr7:99427790-99428048	HepG2	liver:	n/a	n/a
34	BHLHE40	chr7:99424742-99425120	HepG2	liver:	n/a	n/a
35	BHLHE40	chr7:99404583-99404761	K562	blood:	n/a	n/a
36	BHLHE40	chr7:99365355-99365633	GM12878	blood:	n/a	n/a
37	BHLHE40	chr7:99392763-99393031	K562	blood:	n/a	chr7:99392859-99392872 chr7:99392861-99392870 chr7:99392860-99392869 chr7:99392862-99392871 chr7:99392861-99392870 chr7:99392855-99392876
38	BHLHE40	chr7:99429304-99429544	K562	blood:	n/a	n/a
39	CBX3	chr7:99404465-99404987	K562	blood:	n/a	n/a
40	CBX3	chr7:99360292-99360970	K562	blood:	n/a	n/a
41	CBX3	chr7:99430760-99431645	K562	blood:	n/a	n/a
42	CBX3	chr7:99432638-99434132	K562	blood:	n/a	n/a
43	CBX3	chr7:99403139-99403596	K562	blood:	n/a	n/a
44	CBX3	chr7:99403227-99403610	K562	blood:	n/a	n/a
45	CCNT2	chr7:99392757-99392906	K562	blood:	n/a	n/a
46	CCNT2	chr7:99419544-99419637	K562	blood:	n/a	n/a
47	CCNT2	chr7:99432819-99433141	K562	blood:	n/a	n/a
48	CCNT2	chr7:99429506-99429551	K562	blood:	n/a	n/a
49	CCNT2	chr7:99434289-99434393	K562	blood:	n/a	n/a
50	CCNT2	chr7:99404687-99404891	K562	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99425577-99425627	AG09319	gingival:	n/a
2	chr7:99425577-99425627	AG09319	gingival:	n/a
3	chr7:99425577-99425627	MCF-7	breast:	n/a
4	chr7:99425193-99425243	HCT-116	colon:	n/a
5	chr7:99376495-99376545	HCT-116	colon:	n/a
6	chr7:99437259-99437309	HCT-116	colon:	n/a
7	chr7:99382370-99382420	HEEpiC	esophagus:	n/a
8	chr7:99383155-99383205	HEEpiC	esophagus:	n/a
9	chr7:99355204-99355254	SK-N-MC	brain:	n/a
10	chr7:99383155-99383205	HRPEpiC	eye:	n/a
11	chr7:99355204-99355254	CMK	blood:	n/a
12	chr7:99383155-99383205	SK-N-MC	brain:	n/a
13	chr7:99424203-99424253	AG04449	skin:	fetal
14	chr7:99425614-99425664	HEEpiC	esophagus:	n/a
15	chr7:99383224-99383274	HCPEpiC	choroid plexus:	n/a
16	chr7:99425193-99425243	NT2-D1	testis:	n/a
17	chr7:99437259-99437309	GM19239	blood:	n/a
18	chr7:99355204-99355254	AoSMC	blood vessel:	n/a
19	chr7:99425614-99425664	A549	lung:	n/a
20	chr7:99425577-99425627	AG09309	skin:	n/a
21	chr7:99425577-99425627	Hela-S3	cervix:	n/a
22	chr7:99425614-99425664	MCF-7	breast:	n/a
23	chr7:99383224-99383274	HCM	heart:	n/a
24	chr7:99382370-99382420	AG04449	skin:	fetal
25	chr7:99425614-99425664	HRE	kidney:	n/a
26	chr7:99424203-99424253	PrEC	prostate:	n/a
27	chr7:99382370-99382420	HCT-116	colon:	n/a
28	chr7:99424203-99424253	NT2-D1	testis:	n/a
29	chr7:99355204-99355254	ovcar-3	ovarian:	n/a
30	chr7:99392865-99392915	AG09319	gingival:	n/a
31	chr7:99437259-99437309	BJ	skin:	n/a
32	chr7:99392865-99392915	MCF10A-Er-Src	breast:	n/a
33	chr7:99355204-99355254	A549	lung:	n/a
34	chr7:99383224-99383274	HepG2	liver:	n/a
35	chr7:99425193-99425243	MCF-7	breast:	n/a
36	chr7:99391506-99391556	HCM	heart:	n/a
37	chr7:99437259-99437309	ProgFib	skin:	n/a
38	chr7:99391506-99391556	PANC-1	pancreas:	n/a
39	chr7:99425614-99425664	CMK	blood:	n/a
40	chr7:99392865-99392915	Hela-S3	cervix:	n/a
41	chr7:99382370-99382420	BE2_C	brain:	n/a
42	chr7:99355204-99355254	HMEC	breast:	n/a
43	chr7:99425193-99425243	HEK293	kidney:	embryo
44	chr7:99437259-99437309	HRCEpiC	kidney:	n/a
45	chr7:99383224-99383274	HNPCEpiC	eye:	n/a
46	chr7:99425577-99425627	NB4	blood:	n/a
47	chr7:99391506-99391556	ovcar-3	ovarian:	n/a
48	chr7:99355204-99355254	GM19239	blood:	n/a
49	chr7:99425193-99425243	BE2_C	brain:	n/a
50	chr7:99382086-99382136	HCT-116	colon:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:99434310..99436769-chr7:99443746..99446761,3	K562	blood:
2	chr7:99355786..99358236-chr7:99360607..99362683,2	K562	blood:
3	chr7:99412647..99414218-chr7:99422343..99425321,2	K562	blood:
4	chr7:99427241..99429654-chr7:99429801..99432501,3	K562	blood:
5	chr7:99374500..99377711-chr7:99378798..99381871,3	MCF-7	breast:
6	chr7:99433750..99434429-chr7:113008535..113009149,2	MCF-7	breast:
7	chr7:99415648..99420194-chr7:99515880..99518686,4	MCF-7	breast:
8	chr7:99389616..99391219-chr7:99413108..99414812,2	K562	blood:
9	chr7:99318007..99319564-chr7:99439691..99441723,2	K562	blood:
10	chr7:99358230..99360940-chr7:99460072..99462897,2	K562	blood:
11	chr17:41438232..41439081-chr7:99390219..99391187,2	Hela-S3	cervix:
12	chr7:99434310..99436769-chr7:99443746..99446718,2	K562	blood:
13	chr7:99380939..99382491-chr7:99384838..99386622,2	K562	blood:
14	chr7:99412647..99414834-chr7:99418684..99423843,4	K562	blood:
15	chr7:99412647..99414834-chr7:99418684..99423843,4	K562	blood:
16	chr7:99432826..99435527-chr7:99436007..99438743,2	K562	blood:
17	chr7:99389428..99391803-chr7:99419733..99421498,2	MCF-7	breast:
18	chr7:99423210..99426949-chr7:99431563..99434644,4	K562	blood:
19	chr7:99348892..99351554-chr7:99353145..99355344,2	MCF-7	breast:
20	chr7:99427440..99433214-chr7:99433946..99436669,7	K562	blood:
21	chr7:99438226..99440315-chr7:99455557..99458209,2	MCF-7	breast:
22	chr7:99364077..99366983-chr7:99367660..99369579,3	K562	blood:
23	chr7:99389616..99391219-chr7:99413108..99414812,2	K562	blood:
24	chr7:99436167..99437949-chr7:99514061..99515612,2	MCF-7	breast:
25	chr7:99374500..99377711-chr7:99378798..99381871,3	MCF-7	breast:
26	chr7:99418069..99420911-chr7:99424832..99427207,2	MCF-7	breast:
27	chr7:99429881..99432803-chr7:99433485..99436669,5	K562	blood:
28	chr1:115645039..115645569-chr7:99419573..99420093,2	MCF-7	breast:
29	chr7:99429881..99432803-chr7:99433485..99436669,5	K562	blood:
30	chr7:99036409..99038760-chr7:99436644..99439361,2	MCF-7	breast:
31	chr7:99415454..99416963-chr7:99419228..99420818,2	K562	blood:
32	chr7:99427440..99433214-chr7:99433946..99436669,7	K562	blood:
33	chr7:99148029..99149878-chr7:99432203..99434942,2	MCF-7	breast:
34	chr7:99123163..99123910-chr7:99435300..99436219,3	MCF-7	breast:
35	chr7:99213826..99215884-chr7:99424650..99426774,2	MCF-7	breast:
36	chr7:99213374..99216034-chr7:99427343..99429224,2	MCF-7	breast:
37	chr7:99425105..99426708-chr7:99428229..99429979,2	MCF-7	breast:
38	chr7:99395302..99397097-chr7:99400248..99401808,2	K562	blood:
39	chr7:99355786..99358236-chr7:99360607..99362683,2	K562	blood:
40	chr7:99395302..99397097-chr7:99400248..99401808,2	K562	blood:
41	chr7:99217535..99219333-chr7:99417446..99419082,2	K562	blood:
42	chr7:99224377..99226344-chr7:99414554..99417105,2	K562	blood:
43	chr7:99415454..99416963-chr7:99419228..99420818,2	K562	blood:
44	chr7:99427241..99429654-chr7:99429801..99432501,3	K562	blood:
45	chr7:99389428..99391803-chr7:99419733..99421498,2	MCF-7	breast:
46	chr7:99422031..99424143-chr7:99425107..99427446,2	K562	blood:
47	chr7:99422341..99424566-chr7:99425014..99427812,3	K562	blood:
48	chr7:99228963..99230026-chr7:99435320..99436119,4	MCF-7	breast:
49	chr7:99432826..99435527-chr7:99436007..99438743,2	K562	blood:
50	chr7:99418450..99421323-chr7:99421994..99426269,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP3A43-3	chr7:99434942-99435122	l_3456_chr7:99433239-99444356_testes
2	lnc-CYP3A43-6	chr7:99364166-99364515	ENSG00000273407.1
3	lnc-CYP3A43-3	chr7:99433240-99433345	l_3456_chr7:99433239-99444356_testes
4	lnc-CYP3A43-3	chr7:99433366-99433482	l_3456_chr7:99433239-99444356_testes

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CYP3A4	hsa-miR-27b-3p	chr7:99355142-99355162

Variant related genes	Relation type
CYP3A4	TF binding region
ENSG00000273407	TF binding region
ENSG00000261511	TF binding region
CYP3A43	TF binding region
CYP3A4	CpG island
ENSG00000273407	CpG island
ENSG00000261511	CpG island
CYP3A43	CpG island
ENSG00000197037	chromatin interactions
ENSG00000273407	chromatin interactions
ENSG00000160917	chromatin interactions
ENSG00000261511	chromatin interactions
ENSG00000160870	chromatin interactions
ENSG00000160868	chromatin interactions
ENSG00000146833	chromatin interactions
ENSG00000021461	chromatin interactions
ENSG00000106246	chromatin interactions
ENSG00000221909	chromatin interactions

Extended variants
information (count: 2698 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:2698 , 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	rs59836234	chr7:99353549-99353550	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs529933269	chr7:99353563-99353564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186116636	chr7:99353581-99353582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569974727	chr7:99353642-99353643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs376228449	chr7:99353668-99353669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537043061	chr7:99353714-99353715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551928204	chr7:99353722-99353723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570515369	chr7:99353738-99353739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534450858	chr7:99353740-99353741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571804889	chr7:99353781-99353782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553055095	chr7:99353816-99353817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574658379	chr7:99353830-99353831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530793207	chr7:99353925-99353926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535663060	chr7:99353975-99353976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557187156	chr7:99354000-99354001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368444125	chr7:99354010-99354011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139909079	chr7:99354016-99354017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564357477	chr7:99354037-99354038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573265025	chr7:99354059-99354060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs572143437	chr7:99354080-99354081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540337468	chr7:99354113-99354114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12333983	chr7:99354114-99354115	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs191136137	chr7:99354138-99354139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548405730	chr7:99354154-99354155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563567018	chr7:99354228-99354229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557624994	chr7:99354241-99354242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs28988609	chr7:99354252-99354253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs28988608	chr7:99354295-99354296	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs28988607	chr7:99354299-99354300	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs547127695	chr7:99354365-99354366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs143510426	chr7:99354406-99354407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs146754704	chr7:99354425-99354426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546338197	chr7:99354465-99354466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs181586830	chr7:99354585-99354586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535650826	chr7:99354601-99354602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185997841	chr7:99354611-99354612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575516082	chr7:99354616-99354617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs367576049	chr7:99354630-99354631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558444773	chr7:99354634-99354635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs28988606	chr7:99354661-99354662	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs562115782	chr7:99354745-99354746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs28371763	chr7:99354808-99354809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534020143	chr7:99354908-99354909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs34469568	chr7:99354937-99354938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs117070162	chr7:99354947-99354948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs28969391	chr7:99354989-99354990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs33972239	chr7:99354990-99354991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371661164	chr7:99355038-99355039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs369197496	chr7:99355072-99355073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs28988604	chr7:99355073-99355074	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	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
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164919	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:575 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99350000-99355400	Weak transcription	Liver	Liver
2	chr7:99350800-99354200	Weak transcription	Esophagus	oesophagus
3	chr7:99350800-99357600	Weak transcription	Fetal Intestine Small	intestine
4	chr7:99350800-99359800	Weak transcription	Fetal Lung	lung
5	chr7:99350800-99369800	Weak transcription	Pancreas	Pancrea
6	chr7:99351000-99364000	Weak transcription	Duodenum Mucosa	Duodenum
7	chr7:99352800-99355600	Weak transcription	Aorta	Aorta
8	chr7:99354200-99354400	Enhancers	Esophagus	oesophagus
9	chr7:99355400-99365800	Strong transcription	Liver	Liver
10	chr7:99357400-99358400	Enhancers	HepG2	liver
11	chr7:99357600-99358400	Enhancers	Fetal Intestine Small	intestine
12	chr7:99357800-99358200	Enhancers	Fetal Intestine Large	intestine
13	chr7:99358000-99358200	Enhancers	K562	blood
14	chr7:99358200-99359800	Weak transcription	K562	blood
15	chr7:99358400-99360400	Weak transcription	Fetal Intestine Small	intestine
16	chr7:99359600-99360200	Active TSS	Sigmoid Colon	Sigmoid Colon
17	chr7:99359600-99361600	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr7:99359600-99361600	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr7:99359600-99362000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr7:99359800-99360400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr7:99359800-99360400	Enhancers	K562	blood
22	chr7:99359800-99360600	Enhancers	Fetal Lung	lung
23	chr7:99359800-99361400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr7:99359800-99361400	Enhancers	HMEC	breast
25	chr7:99360000-99360400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr7:99360000-99360600	Enhancers	NHEK	skin
27	chr7:99360000-99361000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr7:99360000-99361600	Enhancers	Muscle Satellite Cultured Cells	--
29	chr7:99360000-99361600	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr7:99360200-99360400	Enhancers	Hela-S3	cervix
31	chr7:99360400-99360600	Enhancers	Fetal Intestine Small	intestine
32	chr7:99360400-99360800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr7:99360400-99360800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr7:99360400-99360800	Enhancers	Fetal Muscle Leg	muscle
35	chr7:99360400-99360800	Enhancers	Placenta Amnion	Placenta Amnion
36	chr7:99360400-99360800	Flanking Active TSS	Hela-S3	cervix
37	chr7:99360400-99361000	Enhancers	HSMMtube	muscle
38	chr7:99360400-99361000	Flanking Active TSS	K562	blood
39	chr7:99360400-99361000	Enhancers	Osteobl	bone
40	chr7:99360400-99361200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr7:99360400-99361200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr7:99360400-99361400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr7:99360400-99361400	Enhancers	HSMM	muscle
44	chr7:99360400-99361400	Enhancers	NH-A	brain
45	chr7:99360400-99361600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr7:99360400-99361600	Enhancers	Stomach Mucosa	stomach
47	chr7:99360600-99360800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr7:99360600-99360800	Flanking Active TSS	Fetal Lung	lung
49	chr7:99360600-99361000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr7:99360600-99361000	Flanking Active TSS	NHEK	skin

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