Variant report

Variant	nsv1020006
Chromosome Location	chr7:110915339-111066647
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:937)
CpG islands
(count:61)
Chromatin interactive
region (count:117)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(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	chr7:110953154-110953413	K562	blood:	n/a	n/a
2	ARID3A	chr7:110969611-110970170	K562	blood:	n/a	n/a
3	ARID3A	chr7:110966486-110967469	K562	blood:	n/a	n/a
4	ARID3A	chr7:110968691-110969273	K562	blood:	n/a	n/a
5	ARID3A	chr7:111024781-111024793	K562	blood:	n/a	n/a
6	ARID3A	chr7:110946747-110946768	K562	blood:	n/a	n/a
7	ARID3A	chr7:110997534-110997571	K562	blood:	n/a	n/a
8	ARID3A	chr7:111008626-111008764	K562	blood:	n/a	n/a
9	ARID3A	chr7:111021038-111021344	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:111064774-111065198	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:110968080-110968421	K562	blood:	n/a	n/a
12	ARID3A	chr7:110967767-110967878	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	ATF2	chr7:111053704-111054218	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr7:110935269-110935465	K562	blood:	n/a	n/a
17	BATF	chr7:110960156-110960503	GM12878	blood:	n/a	n/a
18	BATF	chr7:111029015-111029334	GM12878	blood:	n/a	n/a
19	BATF	chr7:110992517-110992735	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:111029036-111029324	GM12878	blood:	n/a	n/a
21	BHLHE40	chr7:110964357-110964616	GM12878	blood:	n/a	n/a
22	CBX3	chr7:110983007-110983449	K562	blood:	n/a	n/a
23	CBX3	chr7:110983037-110983415	K562	blood:	n/a	n/a
24	CBX3	chr7:110969313-110970175	K562	blood:	n/a	n/a
25	CBX3	chr7:111051022-111051426	K562	blood:	n/a	n/a
26	CCNT2	chr7:110941498-110941584	K562	blood:	n/a	n/a
27	CCNT2	chr7:110953302-110953502	K562	blood:	n/a	n/a
28	CEBPB	chr7:110926298-110926561	A549	lung:	n/a	n/a
29	CEBPB	chr7:111051675-111051855	HepG2	liver:	n/a	chr7:111051705-111051716
30	CEBPB	chr7:111004390-111004910	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr7:111000171-111000608	IMR90	lung:	n/a	n/a
32	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
33	CEBPB	chr7:111004360-111004835	A549	lung:	n/a	n/a
34	CEBPB	chr7:111004430-111004833	A549	lung:	n/a	n/a
35	CEBPB	chr7:111051577-111051787	K562	blood:	n/a	chr7:111051705-111051716
36	CEBPB	chr7:110952998-110953331	HepG2	liver:	n/a	chr7:110953149-110953162 chr7:110953149-110953160
37	CEBPB	chr7:111002722-111002977	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr7:111012012-111012259	HepG2	liver:	n/a	chr7:111012124-111012137 chr7:111012124-111012135
39	CEBPB	chr7:111033045-111033376	ECC-1	luminal epithelium:	n/a	n/a
40	CEBPB	chr7:110953010-110953338	Hela-S3	cervix:	n/a	chr7:110953149-110953162 chr7:110953149-110953160
41	CEBPB	chr7:110952985-110953363	A549	lung:	n/a	chr7:110953149-110953162 chr7:110953149-110953160
42	CEBPB	chr7:111004404-111004934	IMR90	lung:	n/a	n/a
43	CEBPB	chr7:110944027-110944028	K562	blood:	n/a	n/a
44	CEBPB	chr7:110953014-110953336	IMR90	lung:	n/a	chr7:110953149-110953162 chr7:110953149-110953160
45	CEBPB	chr7:111003647-111003648	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr7:111059906-111060145	K562	blood:	n/a	n/a
47	CEBPB	chr7:111033008-111033349	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr7:111004463-111004919	HCT-116	colon:	n/a	n/a
49	CEBPB	chr7:111004511-111004739	K562	blood:	n/a	n/a
50	CEBPB	chr7:110952993-110953313	H1-hESC	embryonic stem cell:	n/a	chr7:110953149-110953162 chr7:110953149-110953160

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:111033064-111033114	HUVEC	blood vessel:	n/a
2	chr7:111033064-111033114	NT2-D1	testis:	n/a
3	chr7:111033064-111033114	HepG2	liver:	n/a
4	chr7:111033064-111033114	HAEpiC	amniotic membrane:	n/a
5	chr7:111033064-111033114	H1-hESC	embryonic stem cell:	embryo
6	chr7:111033064-111033114	HPAEpiC	pulmonary alveolar:	n/a
7	chr7:111033064-111033114	BJ	skin:	n/a
8	chr7:111033064-111033114	AG10803	skin:	n/a
9	chr7:111033064-111033114	SAEC	small airway:	n/a
10	chr7:111033064-111033114	CMK	blood:	n/a
11	chr7:111033064-111033114	HMEC	breast:	n/a
12	chr7:111033064-111033114	Jurkat	blood:	n/a
13	chr7:111033064-111033114	NHBE	bronchial:	n/a
14	chr7:111033064-111033114	SK-N-SH	brain:	n/a
15	chr7:111033064-111033114	ECC-1	luminal epithelium:	n/a
16	chr7:111033064-111033114	AG04450	lung:	fetal
17	chr7:111033064-111033114	HCF	heart:	n/a
18	chr7:111033064-111033114	GM19239	blood:	n/a
19	chr7:111033064-111033114	HRE	kidney:	n/a
20	chr7:111033064-111033114	GM12891	blood:	n/a
21	chr7:111033064-111033114	Hela-S3	cervix:	n/a
22	chr7:111033064-111033114	SK-N-MC	brain:	n/a
23	chr7:111033064-111033114	PFSK-1	brain:	n/a
24	chr7:111033064-111033114	A549	lung:	n/a
25	chr7:111033064-111033114	PrEC	prostate:	n/a
26	chr7:111033064-111033114	SKMC	muscle:	n/a
27	chr7:111033064-111033114	HNPCEpiC	eye:	n/a
28	chr7:111033064-111033114	HRCEpiC	kidney:	n/a
29	chr7:111033064-111033114	ProgFib	skin:	n/a
30	chr7:111033064-111033114	HCM	heart:	n/a
31	chr7:111033064-111033114	Caco-2	colon:	n/a
32	chr7:111033064-111033114	HEEpiC	esophagus:	n/a
33	chr7:111033064-111033114	HCPEpiC	choroid plexus:	n/a
34	chr7:111033064-111033114	NH-A	brain:	n/a
35	chr7:111033064-111033114	NB4	blood:	n/a
36	chr7:111033064-111033114	HIPEpiC	eye:	n/a
37	chr7:111033064-111033114	MCF10A-Er-Src	breast:	n/a
38	chr7:111033064-111033114	RPTEC	kidney:	n/a
39	chr7:111033064-111033114	HRPEpiC	eye:	n/a
40	chr7:111033064-111033114	GM12892	blood:	n/a
41	chr7:111033064-111033114	AG09309	skin:	n/a
42	chr7:111033064-111033114	AG09319	gingival:	n/a
43	chr7:111033064-111033114	AoSMC	blood vessel:	n/a
44	chr7:111033064-111033114	GM06990	blood:	n/a
45	chr7:111033064-111033114	ovcar-3	ovarian:	n/a
46	chr7:111033064-111033114	MCF-7	breast:	n/a
47	chr7:111033064-111033114	PANC-1	pancreas:	n/a
48	chr7:111033064-111033114	IMR90	lung:	fetal
49	chr7:111033064-111033114	AG04449	skin:	fetal
50	chr7:111033064-111033114	HEK293	kidney:	embryo

(count:117 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:110953570..110955733-chr7:111376151..111377847,2	MCF-7	breast:
2	chr7:110958175..110962470-chr7:110967524..110970471,4	K562	blood:
3	chr7:110934094..110935861-chr7:110939196..110941083,3	K562	blood:
4	chr7:110994535..110996072-chr7:110997457..110999303,2	K562	blood:
5	chr7:110977304..110981066-chr7:110982767..110987604,6	K562	blood:
6	chr7:111014312..111015875-chr7:111016018..111018954,2	MCF-7	breast:
7	chr7:110955341..110956918-chr7:110957234..110959729,2	K562	blood:
8	chr7:110941905..110944454-chr7:110944620..110946786,2	K562	blood:
9	chr7:110968689..110972135-chr7:110972915..110976641,3	K562	blood:
10	chr7:110969852..110970371-chr7:111126745..111127278,2	K562	blood:
11	chr7:111001961..111006807-chr7:111013802..111016795,4	K562	blood:
12	chr7:110941905..110944454-chr7:110944620..110946786,2	K562	blood:
13	chr7:110958175..110961174-chr7:110967524..110969443,2	K562	blood:
14	chr7:111043409..111046006-chr7:111053282..111056029,3	K562	blood:
15	chr7:111018357..111021397-chr7:111023712..111026997,4	K562	blood:
16	chr7:110977304..110981066-chr7:110982767..110987604,6	K562	blood:
17	chr7:110924432..110929578-chr7:110932859..110937635,6	K562	blood:
18	chr7:110935982..110938365-chr7:110942817..110944691,2	K562	blood:
19	chr7:110929795..110932437-chr7:110933207..110936083,3	K562	blood:
20	chr7:110948192..110950310-chr7:110952497..110954721,2	K562	blood:
21	chr7:110919285..110921892-chr7:110924129..110926222,2	K562	blood:
22	chr7:111027546..111029195-chr7:111032815..111035330,2	K562	blood:
23	chr7:111025105..111026879-chr7:111027995..111029881,2	K562	blood:
24	chr7:111050112..111052168-chr7:111053965..111056674,3	K562	blood:
25	chr5:125812513..125813255-chr7:110998210..110998982,2	MCF-7	breast:
26	chr7:110994535..110996072-chr7:110997457..110999303,2	K562	blood:
27	chr7:110970635..110973843-chr7:110975141..110978905,5	K562	blood:
28	chr7:111008511..111011324-chr7:111012744..111015031,2	K562	blood:
29	chr7:110958175..110961174-chr7:110967524..110969443,2	K562	blood:
30	chr7:111018357..111021397-chr7:111023712..111026997,4	K562	blood:
31	chr7:110919285..110921892-chr7:110924129..110926222,2	K562	blood:
32	chr7:111031028..111033164-chr7:111033658..111035591,2	K562	blood:
33	chr7:110973996..110977417-chr7:110978130..110980823,3	K562	blood:
34	chr7:110924432..110926999-chr7:110933691..110937635,4	K562	blood:
35	chr7:110946449..110947994-chr7:110949688..110952187,2	K562	blood:
36	chr7:110969454..110970228-chr7:111375556..111376647,3	MCF-7	breast:
37	chr7:110997175..111000339-chr7:111001551..111003490,3	K562	blood:
38	chr7:110973996..110977417-chr7:110978130..110980823,3	K562	blood:
39	chr7:111030301..111032703-chr7:111035909..111038064,2	K562	blood:
40	chr17:41463788..41465299-chr7:111034758..111036259,2	K562	blood:
41	chr7:110959334..110960882-chr7:110965813..110967484,2	K562	blood:
42	chr7:110729634..110730189-chr7:110952732..110953606,2	MCF-7	breast:
43	chr7:111033619..111035253-chr7:111039961..111041629,2	K562	blood:
44	chr7:110970635..110973843-chr7:110975141..110978905,5	K562	blood:
45	chr7:110989989..110992007-chr7:110993979..110995982,2	K562	blood:
46	chr7:111003207..111005251-chr7:111008050..111010228,2	K562	blood:
47	chr7:110989989..110992007-chr7:110993979..110995982,2	K562	blood:
48	chr7:110922885..110927148-chr7:110927337..110932171,6	K562	blood:
49	chr7:110946449..110947994-chr7:110949688..110952187,2	K562	blood:
50	chr7:110946954..110949529-chr7:111129446..111130953,2	MCF-7	breast:

No data

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

Extended variants
information (count: 5029 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:5029 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs37743	chr7:110915339-110915340	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537030418	chr7:110915354-110915355	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs528393521	chr7:110915364-110915365	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs115147468	chr7:110915386-110915387	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs573766958	chr7:110915387-110915388	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs144563273	chr7:110915441-110915442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184454778	chr7:110915495-110915496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs578125739	chr7:110915512-110915513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545323611	chr7:110915579-110915580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563997786	chr7:110915581-110915582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187849507	chr7:110915632-110915633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543422231	chr7:110915650-110915651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs561689171	chr7:110915670-110915671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs191911671	chr7:110915755-110915756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs372969912	chr7:110915757-110915758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs184005757	chr7:110915795-110915796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs111367597	chr7:110915801-110915802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112869033	chr7:110915827-110915828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551319019	chr7:110915831-110915832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556912644	chr7:110915874-110915875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569909009	chr7:110915887-110915888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs530733145	chr7:110915957-110915958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548928108	chr7:110916029-110916030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368016126	chr7:110916045-110916046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs116736966	chr7:110916060-110916061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534747304	chr7:110916081-110916082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs150924641	chr7:110916136-110916137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571688958	chr7:110916138-110916139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539208709	chr7:110916172-110916173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs557300701	chr7:110916229-110916230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575387650	chr7:110916241-110916242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575980792	chr7:110916256-110916257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189073475	chr7:110916257-110916258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537853175	chr7:110916271-110916272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555363632	chr7:110916272-110916273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs141965535	chr7:110916291-110916292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541076083	chr7:110916303-110916304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs371453449	chr7:110916313-110916314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532910845	chr7:110916329-110916330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545158231	chr7:110916330-110916331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560603603	chr7:110916393-110916394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144887830	chr7:110916463-110916464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373821561	chr7:110916499-110916500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528087731	chr7:110916528-110916529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548868287	chr7:110916544-110916545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs55697907	chr7:110916586-110916587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73422068	chr7:110916602-110916603	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs181506033	chr7:110916607-110916608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185743831	chr7:110916624-110916625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113503198	chr7:110916629-110916630	Weak transcription	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
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
Autism	20841430	CNVD

Chromatin state (count:624 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110905000-110917400	Weak transcription	Psoas Muscle	Psoas
2	chr7:110905000-110926200	Weak transcription	Aorta	Aorta
3	chr7:110911600-110926800	Weak transcription	Primary T cells from cord blood	blood
4	chr7:110914400-110915400	Enhancers	Brain Germinal Matrix	brain
5	chr7:110914400-110915400	Enhancers	Fetal Brain Female	brain
6	chr7:110914400-110915400	Enhancers	HSMMtube	muscle
7	chr7:110914400-110915600	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr7:110914400-110915800	Enhancers	Brain Anterior Caudate	brain
9	chr7:110914600-110915400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr7:110914600-110915400	Enhancers	Adipose Nuclei	Adipose
11	chr7:110914600-110915800	Enhancers	Fetal Heart	heart
12	chr7:110914800-110915400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr7:110915000-110915400	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr7:110915000-110915400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr7:110915000-110915400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr7:110915000-110915400	Flanking Active TSS	Brain Cingulate Gyrus	brain
17	chr7:110915000-110915400	Enhancers	Fetal Lung	lung
18	chr7:110915000-110917000	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr7:110915200-110915400	Enhancers	Ovary	ovary
20	chr7:110915200-110915400	Enhancers	NHLF	lung
21	chr7:110915200-110915600	Enhancers	NH-A	brain
22	chr7:110915400-110926800	Weak transcription	Ovary	ovary
23	chr7:110915800-110929800	Weak transcription	Fetal Heart	heart
24	chr7:110917000-110917600	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr7:110917000-110917600	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr7:110917400-110917800	Enhancers	Psoas Muscle	Psoas
27	chr7:110920400-110923400	Weak transcription	K562	blood
28	chr7:110923400-110923600	ZNF genes & repeats	K562	blood
29	chr7:110923600-110924800	Weak transcription	K562	blood
30	chr7:110924400-110931000	Weak transcription	Fetal Lung	lung
31	chr7:110926800-110927000	Enhancers	Ovary	ovary
32	chr7:110929800-110931200	Enhancers	Fetal Heart	heart
33	chr7:110929800-110931600	Enhancers	HSMMtube	muscle
34	chr7:110930400-110931400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr7:110930600-110931400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr7:110930600-110931400	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr7:110930600-110931400	Enhancers	Psoas Muscle	Psoas
38	chr7:110930600-110932800	Enhancers	Adipose Nuclei	Adipose
39	chr7:110931000-110931200	Enhancers	Fetal Lung	lung
40	chr7:110931000-110931800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr7:110931000-110931800	Enhancers	Colon Smooth Muscle	Colon
42	chr7:110931000-110933200	Enhancers	Brain Germinal Matrix	brain
43	chr7:110931200-110932000	Weak transcription	Fetal Lung	lung
44	chr7:110931200-110932800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr7:110931200-110932800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr7:110931400-110932800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr7:110931400-110938200	Weak transcription	Psoas Muscle	Psoas
48	chr7:110931600-110932400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr7:110931600-110932600	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr7:110931800-110932200	Weak transcription	Colon Smooth Muscle	Colon

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