Variant report

Variant	nsv888989
Chromosome Location	chr7:110898122-111092478
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1179)
CpG islands
(count:244)
Chromatin interactive
region (count:141)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1179 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:111008626-111008764	K562	blood:	n/a	n/a
2	ARID3A	chr7:110997534-110997571	K562	blood:	n/a	n/a
3	ARID3A	chr7:110953154-110953413	K562	blood:	n/a	n/a
4	ARID3A	chr7:111077670-111079453	K562	blood:	n/a	chr7:111078420-111078436 chr7:111078560-111078576
5	ARID3A	chr7:111064774-111065198	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:111024781-111024793	K562	blood:	n/a	n/a
7	ARID3A	chr7:110969611-110970170	K562	blood:	n/a	n/a
8	ARID3A	chr7:111021038-111021344	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:110946747-110946768	K562	blood:	n/a	n/a
10	ARID3A	chr7:110966486-110967469	K562	blood:	n/a	n/a
11	ARID3A	chr7:110968080-110968421	K562	blood:	n/a	n/a
12	ARID3A	chr7:110968691-110969273	K562	blood:	n/a	n/a
13	ARID3A	chr7:110967767-110967878	K562	blood:	n/a	n/a
14	ATF1	chr7:111054516-111054769	K562	blood:	n/a	n/a
15	ATF1	chr7:111078600-111078973	K562	blood:	n/a	n/a
16	ATF1	chr7:111012802-111012930	K562	blood:	n/a	n/a
17	ATF2	chr7:111053704-111054218	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr7:111078506-111078989	K562	blood:	n/a	n/a
19	BACH1	chr7:110935269-110935465	K562	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	BATF	chr7:110960156-110960503	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:111029036-111029324	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:110913546-110913742	K562	blood:	n/a	n/a
25	BHLHE40	chr7:110964357-110964616	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:111078559-111079458	K562	blood:	n/a	n/a
27	CBX3	chr7:110983007-110983449	K562	blood:	n/a	n/a
28	CBX3	chr7:110969313-110970175	K562	blood:	n/a	n/a
29	CBX3	chr7:111078458-111079603	K562	blood:	n/a	n/a
30	CBX3	chr7:111051022-111051426	K562	blood:	n/a	n/a
31	CBX3	chr7:110983037-110983415	K562	blood:	n/a	n/a
32	CBX3	chr7:111076674-111077685	K562	blood:	n/a	n/a
33	CBX3	chr7:111079900-111081343	K562	blood:	n/a	n/a
34	CBX3	chr7:111074271-111074726	K562	blood:	n/a	n/a
35	CBX3	chr7:111073025-111074149	K562	blood:	n/a	n/a
36	CBX3	chr7:110910820-110911290	K562	blood:	n/a	n/a
37	CBX3	chr7:111090809-111091116	K562	blood:	n/a	n/a
38	CCNT2	chr7:111078445-111079337	K562	blood:	n/a	n/a
39	CCNT2	chr7:110941498-110941584	K562	blood:	n/a	n/a
40	CCNT2	chr7:110953302-110953502	K562	blood:	n/a	n/a
41	CEBPB	chr7:110952965-110953316	MCF-7	breast:	n/a	chr7:110953149-110953162 chr7:110953149-110953160
42	CEBPB	chr7:110899999-110900422	K562	blood:	n/a	n/a
43	CEBPB	chr7:111002722-111002977	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr7:110944027-110944028	K562	blood:	n/a	n/a
45	CEBPB	chr7:111004478-111004846	MCF-7	breast:	n/a	n/a
46	CEBPB	chr7:110953010-110953338	Hela-S3	cervix:	n/a	chr7:110953149-110953162 chr7:110953149-110953160
47	CEBPB	chr7:110953068-110953334	A549	lung:	n/a	chr7:110953149-110953162 chr7:110953149-110953160
48	CEBPB	chr7:111000057-111000344	A549	lung:	n/a	n/a
49	CEBPB	chr7:111012012-111012259	HepG2	liver:	n/a	chr7:111012124-111012137 chr7:111012124-111012135
50	CEBPB	chr7:111033045-111033376	ECC-1	luminal epithelium:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:111086055-111086105	SK-N-SH_RA	brain:	n/a
2	chr7:111033064-111033114	SKMC	muscle:	n/a
3	chr7:111086055-111086105	HepG2	liver:	n/a
4	chr7:111086055-111086105	MCF-7	breast:	n/a
5	chr7:110906785-110906835	GM06990	blood:	n/a
6	chr7:111079100-111079150	HNPCEpiC	eye:	n/a
7	chr7:111033064-111033114	HepG2	liver:	n/a
8	chr7:111079100-111079150	AG10803	skin:	n/a
9	chr7:111079100-111079150	BJ	skin:	n/a
10	chr7:110906785-110906835	NHDF-neo	bronchial:	n/a
11	chr7:111033064-111033114	HAEpiC	amniotic membrane:	n/a
12	chr7:110906785-110906835	HRCEpiC	kidney:	n/a
13	chr7:110906785-110906835	HCF	heart:	n/a
14	chr7:111079100-111079150	HIPEpiC	eye:	n/a
15	chr7:111033064-111033114	NT2-D1	testis:	n/a
16	chr7:111079100-111079150	NHDF-neo	bronchial:	n/a
17	chr7:110906785-110906835	A549	lung:	n/a
18	chr7:111086055-111086105	HCM	heart:	n/a
19	chr7:111086055-111086105	GM12878	blood:	n/a
20	chr7:110906785-110906835	GM12891	blood:	n/a
21	chr7:111086055-111086105	GM12891	blood:	n/a
22	chr7:111033064-111033114	HRE	kidney:	n/a
23	chr7:110906785-110906835	CMK	blood:	n/a
24	chr7:111086055-111086105	HRPEpiC	eye:	n/a
25	chr7:111086055-111086105	T-47D	breast:	n/a
26	chr7:111086055-111086105	PANC-1	pancreas:	n/a
27	chr7:111033064-111033114	SK-N-SH	brain:	n/a
28	chr7:111033064-111033114	NHBE	bronchial:	n/a
29	chr7:111079100-111079150	HRPEpiC	eye:	n/a
30	chr7:111079100-111079150	NH-A	brain:	n/a
31	chr7:110906785-110906835	PANC-1	pancreas:	n/a
32	chr7:111079100-111079150	PFSK-1	brain:	n/a
33	chr7:111079100-111079150	PANC-1	pancreas:	n/a
34	chr7:110906785-110906835	MCF10A-Er-Src	breast:	n/a
35	chr7:111033064-111033114	K562	blood:	n/a
36	chr7:110906785-110906835	GM19239	blood:	n/a
37	chr7:110906785-110906835	PFSK-1	brain:	n/a
38	chr7:111086055-111086105	SAEC	small airway:	n/a
39	chr7:111079100-111079150	HEK293	kidney:	embryo
40	chr7:111086055-111086105	HL-60	blood:	n/a
41	chr7:111086055-111086105	HUVEC	blood vessel:	n/a
42	chr7:111033064-111033114	HCPEpiC	choroid plexus:	n/a
43	chr7:111033064-111033114	GM19239	blood:	n/a
44	chr7:110906785-110906835	LNCaP	prostate:	n/a
45	chr7:111079100-111079150	Jurkat	blood:	n/a
46	chr7:110906785-110906835	HPAEpiC	pulmonary alveolar:	n/a
47	chr7:111033064-111033114	AoSMC	blood vessel:	n/a
48	chr7:111079100-111079150	CMK	blood:	n/a
49	chr7:111079100-111079150	GM06990	blood:	n/a
50	chr7:111033064-111033114	HIPEpiC	eye:	n/a

(count:141 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:110997175..111000339-chr7:111001551..111003490,3	K562	blood:
2	chr7:110946494..110948605-chr7:110949688..110952299,2	K562	blood:
3	chr7:110962569..110964668-chr7:110968085..110971412,3	K562	blood:
4	chr12:108202177..108204461-chr7:111052206..111055078,3	MCF-7	breast:
5	chr7:111018357..111021397-chr7:111023712..111026997,4	K562	blood:
6	chr7:110958175..110962470-chr7:110967524..110970471,4	K562	blood:
7	chr7:110922885..110927148-chr7:110927337..110932171,6	K562	blood:
8	chr7:111020866..111024340-chr7:111025481..111028509,4	MCF-7	breast:
9	chr7:110991909..110993941-chr7:110997470..110999246,2	K562	blood:
10	chr7:110969503..110970311-chr7:111375483..111376413,3	K562	blood:
11	chr7:110977304..110981066-chr7:110982767..110987604,6	K562	blood:
12	chr7:110934094..110935861-chr7:110939196..110941083,3	K562	blood:
13	chr7:110989989..110992007-chr7:110993979..110995982,2	K562	blood:
14	chr12:108200986..108203742-chr7:111052172..111055145,3	MCF-7	breast:
15	chr7:111014312..111015875-chr7:111016018..111018954,2	MCF-7	breast:
16	chr7:110964713..110967341-chr7:110967524..110969143,2	K562	blood:
17	chr5:125812513..125813255-chr7:110998210..110998982,2	MCF-7	breast:
18	chr7:110924808..110925532-chr7:111126328..111127072,2	MCF-7	breast:
19	chr7:110968689..110972135-chr7:110972915..110976641,3	K562	blood:
20	chr7:110958175..110961174-chr7:110967524..110969443,2	K562	blood:
21	chr7:111018295..111020688-chr7:111021531..111024788,3	MCF-7	breast:
22	chr7:111001961..111006807-chr7:111013802..111016795,4	K562	blood:
23	chr7:111079252..111081356-chr7:111081507..111084110,2	K562	blood:
24	chr7:110962126..110964268-chr7:110964422..110967257,2	K562	blood:
25	chr7:111070056..111074231-chr7:111075733..111078781,4	K562	blood:
26	chr7:111013152..111016122-chr7:111032306..111034572,2	K562	blood:
27	chr7:110989989..110992007-chr7:110993979..110995982,2	K562	blood:
28	chr7:110901427..110902958-chr7:110904579..110907166,2	MCF-7	breast:
29	chr7:111017537..111020347-chr7:111082285..111084321,2	K562	blood:
30	chr7:111043409..111046006-chr7:111053282..111056029,3	K562	blood:
31	chr7:111012849..111014530-chr7:111019458..111021313,2	K562	blood:
32	chr7:110994957..110999323-chr7:111001198..111006593,6	K562	blood:
33	chr7:110973996..110977417-chr7:110978130..110980823,3	K562	blood:
34	chr7:110924432..110929578-chr7:110932859..110937635,6	K562	blood:
35	chr7:110959106..110960834-chr7:110964696..110967313,2	K562	blood:
36	chr7:111079252..111081356-chr7:111081507..111084110,2	K562	blood:
37	chr7:110924432..110926999-chr7:110933691..110937635,4	K562	blood:
38	chr7:110941321..110943443-chr7:111373654..111375242,2	K562	blood:
39	chr7:110904002..110906677-chr7:110908987..110911839,2	K562	blood:
40	chr7:110907955..110909675-chr7:110912861..110914751,2	K562	blood:
41	chr7:110975357..110976070-chr7:111125914..111126817,2	K562	blood:
42	chr7:110994957..110999323-chr7:111001198..111006593,6	K562	blood:
43	chr7:110946188..110948736-chr7:111369766..111372546,2	K562	blood:
44	chr7:110946449..110947994-chr7:110949688..110952187,2	K562	blood:
45	chr7:111070056..111074231-chr7:111075733..111078781,4	K562	blood:
46	chr7:111020866..111024340-chr7:111025481..111028509,4	MCF-7	breast:
47	chr7:110910606..110912820-chr7:110916912..110919074,2	K562	blood:
48	chr7:111008511..111011324-chr7:111012744..111015031,2	K562	blood:
49	chr7:110969600..110972534-chr7:111078171..111081389,3	K562	blood:
50	chr7:110929795..110932437-chr7:110933207..110936083,3	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
IMMP2L	TF binding region
ENSG00000243621	TF binding region
ENSG00000227948	CpG island
IMMP2L	CpG island
ENSG00000243621	CpG island
ENSG00000184903	chromatin interactions
ENSG00000243621	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000227948	chromatin interactions
ENSG00000136856	chromatin interactions

Extended variants
information (count: 6578 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:6578 , 50 per page) page: 1 2 3 4 5 6 7 ... 132

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10487307	chr7:110898122-110898123	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553177979	chr7:110898134-110898135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560395593	chr7:110898204-110898205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs527631659	chr7:110898205-110898206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552592005	chr7:110898259-110898260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs28829	chr7:110898279-110898280	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs531810232	chr7:110898345-110898346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574441929	chr7:110898498-110898499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374250383	chr7:110898594-110898595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550311681	chr7:110898608-110898609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568627822	chr7:110898620-110898621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs10244829	chr7:110898628-110898629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554116330	chr7:110898746-110898747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376293636	chr7:110898760-110898761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566353093	chr7:110898800-110898801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs370458821	chr7:110898808-110898809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553831857	chr7:110898846-110898847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143031446	chr7:110898855-110898856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs13240464	chr7:110898915-110898916	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
20	rs113321187	chr7:110898921-110898922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs555844533	chr7:110898940-110898941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184010045	chr7:110898945-110898946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540969833	chr7:110898999-110899000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542000815	chr7:110899003-110899004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560126771	chr7:110899051-110899052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374761119	chr7:110899064-110899065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140108535	chr7:110899076-110899077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs34973771	chr7:110899083-110899084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189087267	chr7:110899174-110899175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564436831	chr7:110899181-110899182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs143788737	chr7:110899202-110899203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112882248	chr7:110899209-110899210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs550250773	chr7:110899246-110899247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568537376	chr7:110899252-110899253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570238194	chr7:110899286-110899287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529408235	chr7:110899353-110899354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181510747	chr7:110899387-110899388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185611291	chr7:110899449-110899450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539709907	chr7:110899459-110899460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558038117	chr7:110899475-110899476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190771968	chr7:110899479-110899480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs150889785	chr7:110899566-110899567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs139293767	chr7:110899613-110899614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs2109298	chr7:110899634-110899635	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs557035154	chr7:110899638-110899639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs111949695	chr7:110899711-110899712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201330845	chr7:110899713-110899714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs142290446	chr7:110899722-110899723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs3052105	chr7:110899726-110899727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548534380	chr7:110899728-110899729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Autism	20841430	CNVD

Chromatin state (count:840 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110882600-110903800	Weak transcription	Aorta	Aorta
2	chr7:110893600-110914800	Weak transcription	Pancreas	Pancrea
3	chr7:110896200-110903600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr7:110901200-110903800	Enhancers	Osteobl	bone
5	chr7:110901200-110908200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr7:110901600-110904000	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr7:110901800-110902000	Enhancers	Muscle Satellite Cultured Cells	--
8	chr7:110901800-110902800	Enhancers	HepG2	liver
9	chr7:110902000-110902600	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr7:110902400-110902800	Enhancers	A549	lung
11	chr7:110902400-110903000	Enhancers	Psoas Muscle	Psoas
12	chr7:110902600-110902800	Enhancers	Muscle Satellite Cultured Cells	--
13	chr7:110902800-110903600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr7:110902800-110905200	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr7:110902800-110905800	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr7:110902800-110906600	Weak transcription	HepG2	liver
17	chr7:110902800-110912000	Weak transcription	A549	lung
18	chr7:110903000-110904600	Weak transcription	Psoas Muscle	Psoas
19	chr7:110903400-110907600	Enhancers	Fetal Lung	lung
20	chr7:110903600-110903800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr7:110903600-110903800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr7:110903600-110904000	Enhancers	Adipose Nuclei	Adipose
23	chr7:110903600-110904800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr7:110903800-110904000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr7:110903800-110904000	Enhancers	Aorta	Aorta
26	chr7:110903800-110904600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr7:110903800-110905200	Weak transcription	Osteobl	bone
28	chr7:110903800-110906000	Enhancers	Skeletal Muscle Male	skeletal muscle
29	chr7:110903800-110908400	Enhancers	HSMMtube	muscle
30	chr7:110904000-110904200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr7:110904000-110904400	Weak transcription	Adipose Nuclei	Adipose
32	chr7:110904000-110904400	Weak transcription	Aorta	Aorta
33	chr7:110904000-110906200	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr7:110904200-110905000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr7:110904400-110905000	Enhancers	Aorta	Aorta
36	chr7:110904400-110905600	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr7:110904400-110907400	Enhancers	Adipose Nuclei	Adipose
38	chr7:110904600-110904800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr7:110904600-110905000	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr7:110904600-110905000	Enhancers	Psoas Muscle	Psoas
41	chr7:110904600-110905800	Enhancers	Fetal Brain Female	brain
42	chr7:110904600-110906000	Enhancers	Fetal Brain Male	brain
43	chr7:110904600-110907000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr7:110904600-110907600	Enhancers	Placenta	Placenta
45	chr7:110904800-110905000	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr7:110904800-110905200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr7:110904800-110905400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr7:110905000-110905600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr7:110905000-110905600	Enhancers	HSMM	muscle
50	chr7:110905000-110906600	Weak transcription	HUES6 Cell Line	embryonic stem cell

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