Variant report

Variant	nsv1034649
Chromosome Location	chr7:110879251-111060773
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1052)
CpG islands
(count:183)
Chromatin interactive
region (count:129)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1052 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:110967767-110967878	K562	blood:	n/a	n/a
2	ARID3A	chr7:110953154-110953413	K562	blood:	n/a	n/a
3	ARID3A	chr7:110968080-110968421	K562	blood:	n/a	n/a
4	ARID3A	chr7:110946747-110946768	K562	blood:	n/a	n/a
5	ARID3A	chr7:110969611-110970170	K562	blood:	n/a	n/a
6	ARID3A	chr7:111021038-111021344	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:110895612-110896118	K562	blood:	n/a	n/a
8	ARID3A	chr7:111024781-111024793	K562	blood:	n/a	n/a
9	ARID3A	chr7:110968691-110969273	K562	blood:	n/a	n/a
10	ARID3A	chr7:110966486-110967469	K562	blood:	n/a	n/a
11	ARID3A	chr7:110997534-110997571	K562	blood:	n/a	n/a
12	ARID3A	chr7:111008626-111008764	K562	blood:	n/a	n/a
13	ATF1	chr7:111054516-111054769	K562	blood:	n/a	n/a
14	ATF1	chr7:111012802-111012930	K562	blood:	n/a	n/a
15	ATF1	chr7:110895660-110895855	K562	blood:	n/a	n/a
16	ATF1	chr7:110889894-110890092	K562	blood:	n/a	n/a
17	ATF2	chr7:111053704-111054218	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr7:110935269-110935465	K562	blood:	n/a	n/a
19	BATF	chr7:110960156-110960503	GM12878	blood:	n/a	n/a
20	BATF	chr7:111029015-111029334	GM12878	blood:	n/a	n/a
21	BATF	chr7:110992517-110992735	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:111029036-111029324	GM12878	blood:	n/a	n/a
23	BHLHE40	chr7:110913546-110913742	K562	blood:	n/a	n/a
24	BHLHE40	chr7:110964357-110964616	GM12878	blood:	n/a	n/a
25	CBX3	chr7:110983007-110983449	K562	blood:	n/a	n/a
26	CBX3	chr7:110969313-110970175	K562	blood:	n/a	n/a
27	CBX3	chr7:110910820-110911290	K562	blood:	n/a	n/a
28	CBX3	chr7:110983037-110983415	K562	blood:	n/a	n/a
29	CBX3	chr7:111051022-111051426	K562	blood:	n/a	n/a
30	CCNT2	chr7:110953302-110953502	K562	blood:	n/a	n/a
31	CCNT2	chr7:110896464-110896592	K562	blood:	n/a	n/a
32	CCNT2	chr7:110895712-110896018	K562	blood:	n/a	n/a
33	CCNT2	chr7:110941498-110941584	K562	blood:	n/a	n/a
34	CEBPB	chr7:111012015-111012233	Hela-S3	cervix:	n/a	chr7:111012124-111012137 chr7:111012124-111012135
35	CEBPB	chr7:111000057-111000344	A549	lung:	n/a	n/a
36	CEBPB	chr7:110953014-110953336	IMR90	lung:	n/a	chr7:110953149-110953162 chr7:110953149-110953160
37	CEBPB	chr7:110900063-110900420	HepG2	liver:	n/a	n/a
38	CEBPB	chr7:111051675-111051855	HepG2	liver:	n/a	chr7:111051705-111051716
39	CEBPB	chr7:111000028-111000516	HepG2	liver:	n/a	n/a
40	CEBPB	chr7:111053686-111053711	A549	lung:	n/a	n/a
41	CEBPB	chr7:111004492-111004784	A549	lung:	n/a	n/a
42	CEBPB	chr7:110952998-110953331	HepG2	liver:	n/a	chr7:110953149-110953162 chr7:110953149-110953160
43	CEBPB	chr7:110944027-110944028	K562	blood:	n/a	n/a
44	CEBPB	chr7:110906606-110907154	ECC-1	luminal epithelium:	n/a	chr7:110906880-110906891
45	CEBPB	chr7:111019342-111019579	HepG2	liver:	n/a	chr7:111019423-111019434 chr7:111019422-111019435 chr7:111019501-111019512 chr7:111019422-111019435 chr7:111019513-111019526 chr7:111019422-111019435
46	CEBPB	chr7:110953082-110953239	K562	blood:	n/a	chr7:110953149-110953162 chr7:110953149-110953160
47	CEBPB	chr7:111012012-111012259	HepG2	liver:	n/a	chr7:111012124-111012137 chr7:111012124-111012135
48	CEBPB	chr7:111004409-111004885	MCF-7	breast:	n/a	n/a
49	CEBPB	chr7:111033024-111033260	K562	blood:	n/a	n/a
50	CEBPB	chr7:110952993-110953347	ECC-1	luminal epithelium:	n/a	chr7:110953149-110953162 chr7:110953149-110953160

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:111033064-111033114	MCF10A-Er-Src	breast:	n/a
2	chr7:110906785-110906835	HIPEpiC	eye:	n/a
3	chr7:110879415-110879465	LNCaP	prostate:	n/a
4	chr7:110906785-110906835	SK-N-SH_RA	brain:	n/a
5	chr7:110879415-110879465	ovcar-3	ovarian:	n/a
6	chr7:111033064-111033114	Hepatocyte	liver:	n/a
7	chr7:111033064-111033114	K562	blood:	n/a
8	chr7:110906785-110906835	PANC-1	pancreas:	n/a
9	chr7:110906785-110906835	NH-A	brain:	n/a
10	chr7:110906785-110906835	GM12892	blood:	n/a
11	chr7:111033064-111033114	HPAEpiC	pulmonary alveolar:	n/a
12	chr7:110906785-110906835	BJ	skin:	n/a
13	chr7:111033064-111033114	PANC-1	pancreas:	n/a
14	chr7:110906785-110906835	NHBE	bronchial:	n/a
15	chr7:110906785-110906835	HNPCEpiC	eye:	n/a
16	chr7:110879415-110879465	HCT-116	colon:	n/a
17	chr7:111033064-111033114	HRE	kidney:	n/a
18	chr7:110879415-110879465	HRE	kidney:	n/a
19	chr7:111033064-111033114	H1-hESC	embryonic stem cell:	embryo
20	chr7:111033064-111033114	NB4	blood:	n/a
21	chr7:110879415-110879465	GM12892	blood:	n/a
22	chr7:110906785-110906835	U87	brain:	n/a
23	chr7:111033064-111033114	AoSMC	blood vessel:	n/a
24	chr7:110906785-110906835	HL-60	blood:	n/a
25	chr7:110906785-110906835	GM06990	blood:	n/a
26	chr7:110906785-110906835	HCF	heart:	n/a
27	chr7:110879415-110879465	K562	blood:	n/a
28	chr7:110879415-110879465	NH-A	brain:	n/a
29	chr7:110879415-110879465	GM19239	blood:	n/a
30	chr7:111033064-111033114	A549	lung:	n/a
31	chr7:111033064-111033114	BJ	skin:	n/a
32	chr7:111033064-111033114	ECC-1	luminal epithelium:	n/a
33	chr7:110879415-110879465	CMK	blood:	n/a
34	chr7:110879415-110879465	NB4	blood:	n/a
35	chr7:110879415-110879465	HL-60	blood:	n/a
36	chr7:110879415-110879465	HCPEpiC	choroid plexus:	n/a
37	chr7:110879415-110879465	BJ	skin:	n/a
38	chr7:110879415-110879465	SKMC	muscle:	n/a
39	chr7:111033064-111033114	ovcar-3	ovarian:	n/a
40	chr7:111033064-111033114	HEK293	kidney:	embryo
41	chr7:110879415-110879465	GM12891	blood:	n/a
42	chr7:110906785-110906835	HAEpiC	amniotic membrane:	n/a
43	chr7:111033064-111033114	SK-N-SH_RA	brain:	n/a
44	chr7:110906785-110906835	HCPEpiC	choroid plexus:	n/a
45	chr7:111033064-111033114	HCF	heart:	n/a
46	chr7:110879415-110879465	HEEpiC	esophagus:	n/a
47	chr7:110879415-110879465	A549	lung:	n/a
48	chr7:110906785-110906835	GM19239	blood:	n/a
49	chr7:111033064-111033114	HCT-116	colon:	n/a
50	chr7:110906785-110906835	AG09309	skin:	n/a

(count:129 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:111008511..111011324-chr7:111012744..111015031,2	K562	blood:
2	chr7:110970635..110973843-chr7:110975141..110978905,5	K562	blood:
3	chr7:110958175..110962470-chr7:110967524..110970471,4	K562	blood:
4	chr7:111018295..111020688-chr7:111021531..111024788,3	MCF-7	breast:
5	chr7:110994535..110996072-chr7:110997457..110999303,2	K562	blood:
6	chr7:110962569..110964668-chr7:110968085..110971412,3	K562	blood:
7	chr7:110978869..110982048-chr7:110982767..110985792,3	K562	blood:
8	chr7:110994957..110999323-chr7:111001198..111006593,6	K562	blood:
9	chr7:110975357..110976070-chr7:111125914..111126817,2	K562	blood:
10	chr7:111020866..111024340-chr7:111025481..111028509,4	MCF-7	breast:
11	chr7:110973996..110977417-chr7:110978130..110980823,3	K562	blood:
12	chr7:110958175..110961174-chr7:110967524..110969443,2	K562	blood:
13	chr7:110929795..110932437-chr7:110933207..110936083,3	K562	blood:
14	chr7:110924808..110925532-chr7:111126328..111127072,2	MCF-7	breast:
15	chr7:110904002..110906677-chr7:110908987..110911839,2	K562	blood:
16	chr7:110962126..110964268-chr7:110964422..110967257,2	K562	blood:
17	chr7:110959106..110960834-chr7:110964696..110967313,2	K562	blood:
18	chr17:41463788..41465299-chr7:111034758..111036259,2	K562	blood:
19	chr7:110901387..110901887-chr9:130159518..130160059,2	Hela-S3	cervix:
20	chr7:111013152..111016122-chr7:111032306..111034572,2	K562	blood:
21	chr7:111050112..111052168-chr7:111053965..111056674,3	K562	blood:
22	chr7:110946494..110948605-chr7:110949688..110952299,2	K562	blood:
23	chr7:110924432..110929578-chr7:110932859..110937635,6	K562	blood:
24	chr12:108200986..108203742-chr7:111052172..111055145,3	MCF-7	breast:
25	chr7:110946449..110947994-chr7:110949688..110952187,2	K562	blood:
26	chr7:110964713..110967341-chr7:110967524..110969143,2	K562	blood:
27	chr7:110953570..110955733-chr7:111376151..111377847,2	MCF-7	breast:
28	chr7:110901427..110902958-chr7:110904579..110907166,2	MCF-7	breast:
29	chr7:110935982..110938365-chr7:110942817..110944691,2	K562	blood:
30	chr7:110907955..110909675-chr7:110912861..110914751,2	K562	blood:
31	chr7:110962569..110964668-chr7:110968085..110971412,3	K562	blood:
32	chr7:110994957..110999323-chr7:111001198..111006593,6	K562	blood:
33	chr7:110901427..110902958-chr7:110904579..110907166,2	MCF-7	breast:
34	chr7:110946494..110948605-chr7:110949688..110952299,2	K562	blood:
35	chr7:110935982..110938365-chr7:110942817..110944691,2	K562	blood:
36	chr7:111033619..111035253-chr7:111039961..111041629,2	K562	blood:
37	chr7:110963413..110966213-chr7:110967085..110969024,2	K562	blood:
38	chr7:110924432..110929578-chr7:110932859..110937635,6	K562	blood:
39	chr7:110934094..110935861-chr7:110939196..110941083,3	K562	blood:
40	chr7:110946188..110948736-chr7:111369766..111372546,2	K562	blood:
41	chr7:110941321..110943443-chr7:111373654..111375242,2	K562	blood:
42	chr7:111025105..111026879-chr7:111027995..111029881,2	K562	blood:
43	chr7:111018295..111020688-chr7:111021531..111024788,3	MCF-7	breast:
44	chr7:110919285..110921892-chr7:110924129..110926222,2	K562	blood:
45	chr7:110973996..110977417-chr7:110978130..110980823,3	K562	blood:
46	chr7:110946954..110949529-chr7:111129446..111130953,2	MCF-7	breast:
47	chr7:111003207..111005251-chr7:111008050..111010228,2	K562	blood:
48	chr7:110959334..110960882-chr7:110965813..110967484,2	K562	blood:
49	chr7:110991909..110993941-chr7:110997470..110999246,2	K562	blood:
50	chr7:110958175..110962470-chr7:110967524..110970471,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DOCK4-7	chr7:110902289-110902553	expReg_chr7_8342_-

No data

Variant related genes	Relation type
ENSG00000227948	TF binding region
ENSG00000243621	TF binding region
IMMP2L	TF binding region
ENSG00000227948	CpG island
ENSG00000243621	CpG island
IMMP2L	CpG island
ENSG00000227948	chromatin interactions
ENSG00000136856	chromatin interactions
ENSG00000184903	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000243621	chromatin interactions

Extended variants
information (count: 5986 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:5986 , 50 per page) page: 1 2 3 4 5 6 7 ... 120

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs37715	chr7:110879251-110879252	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs188187328	chr7:110879264-110879265	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs571368809	chr7:110879323-110879324	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs538399333	chr7:110879346-110879347	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557107057	chr7:110879391-110879392	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs575380924	chr7:110879399-110879400	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577017259	chr7:110879401-110879402	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs554781648	chr7:110879409-110879410	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs536524225	chr7:110879416-110879417	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs554460138	chr7:110879423-110879424	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs150243942	chr7:110879433-110879434	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs114910975	chr7:110879436-110879437	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs138910558	chr7:110879446-110879447	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs577258850	chr7:110879454-110879455	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs111568989	chr7:110879458-110879459	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs191929175	chr7:110879460-110879461	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs563077767	chr7:110879487-110879488	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs37716	chr7:110879514-110879515	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs184013147	chr7:110879594-110879595	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs560776295	chr7:110879607-110879608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112862177	chr7:110879621-110879622	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546615570	chr7:110879649-110879650	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs571301516	chr7:110879664-110879665	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370965548	chr7:110879669-110879670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs145717476	chr7:110879672-110879673	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550428847	chr7:110879681-110879682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543914391	chr7:110879714-110879715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569003251	chr7:110879741-110879742	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374487148	chr7:110879751-110879752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138174272	chr7:110879774-110879775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs37717	chr7:110879776-110879777	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs572800016	chr7:110879808-110879809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534990304	chr7:110879823-110879824	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533874498	chr7:110879835-110879836	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558513300	chr7:110879857-110879858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112390943	chr7:110879902-110879903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs189095908	chr7:110879934-110879935	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs113488895	chr7:110879982-110879983	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs574935542	chr7:110880030-110880031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181619549	chr7:110880039-110880040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs560714958	chr7:110880047-110880048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs111281050	chr7:110880079-110880080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs112855877	chr7:110880088-110880089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs75580077	chr7:110880095-110880096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs200018252	chr7:110880101-110880102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs532032027	chr7:110880125-110880126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs371210216	chr7:110880151-110880152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs371602347	chr7:110880163-110880164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs73420096	chr7:110880223-110880224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs527238903	chr7:110880226-110880227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
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
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
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	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
Autism	19401682	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	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Breast cancer	21509527	CNVD
Schizophrenia	23813976	CNVD
Autism	20531469	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:807 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110873200-110879600	Weak transcription	K562	blood
2	chr7:110878000-110880000	Enhancers	Fetal Lung	lung
3	chr7:110878200-110879600	Active TSS	Pancreatic Islets	Pancreatic Islet
4	chr7:110878200-110881000	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr7:110878600-110879400	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr7:110878600-110879400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr7:110878600-110879400	Flanking Active TSS	Adipose Nuclei	Adipose
8	chr7:110878600-110879400	Active TSS	Brain Substantia Nigra	brain
9	chr7:110878600-110879400	Active TSS	Duodenum Smooth Muscle	Duodenum
10	chr7:110878600-110879400	Active TSS	Right Atrium	heart
11	chr7:110878600-110879400	Flanking Active TSS	HUVEC	blood vessel
12	chr7:110878600-110879600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr7:110878600-110879600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr7:110878600-110879800	Enhancers	Liver	Liver
15	chr7:110878600-110880000	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr7:110878800-110879400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr7:110878800-110879400	Active TSS	Brain Hippocampus Middle	brain
18	chr7:110878800-110879400	Active TSS	Ovary	ovary
19	chr7:110878800-110879400	Active TSS	Rectal Mucosa Donor 29	rectum
20	chr7:110878800-110879400	Active TSS	NHDF-Ad	bronchial
21	chr7:110878800-110879400	Active TSS	Osteobl	bone
22	chr7:110878800-110879600	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr7:110878800-110879600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr7:110879000-110879400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
25	chr7:110879000-110879400	Active TSS	Breast Myoepithelial Primary Cells	Breast
26	chr7:110879000-110879400	Active TSS	Brain Angular Gyrus	brain
27	chr7:110879000-110879400	Weak transcription	Brain Germinal Matrix	brain
28	chr7:110879000-110879400	Active TSS	Rectal Smooth Muscle	rectum
29	chr7:110879000-110880800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr7:110879200-110879400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr7:110879200-110879400	Active TSS	Brain Anterior Caudate	brain
32	chr7:110879200-110879400	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr7:110879200-110879400	Active TSS	A549	lung
34	chr7:110879200-110879400	Flanking Active TSS	NHLF	lung
35	chr7:110879200-110879600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr7:110879200-110879600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr7:110879200-110879600	Enhancers	Colon Smooth Muscle	Colon
38	chr7:110879200-110880200	Enhancers	Brain Cingulate Gyrus	brain
39	chr7:110879200-110882200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr7:110879200-110882400	Weak transcription	Aorta	Aorta
41	chr7:110879400-110879600	Enhancers	HUVEC	blood vessel
42	chr7:110879400-110879600	Enhancers	Osteobl	bone
43	chr7:110879400-110879800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr7:110879400-110879800	Enhancers	Brain Anterior Caudate	brain
45	chr7:110879400-110880000	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr7:110879400-110880000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr7:110879400-110880000	Enhancers	Adipose Nuclei	Adipose
48	chr7:110879400-110880200	Enhancers	Brain Angular Gyrus	brain
49	chr7:110879400-110880200	Enhancers	Brain Substantia Nigra	brain
50	chr7:110879400-110881200	Enhancers	Brain Germinal Matrix	brain

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