Variant report

Variant	nsv1006065
Chromosome Location	chr3:112147080-112276983
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1663)
CpG islands
(count:305)
Chromatin interactive
region (count:51)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1663 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:112250371-112250382	K562	blood:	n/a	n/a
2	ARID3A	chr3:112250194-112250459	HepG2	liver:	n/a	n/a
3	ATF2	chr3:112258495-112259308	GM12878	blood:	n/a	n/a
4	ATF2	chr3:112202984-112203674	GM12878	blood:	n/a	n/a
5	ATF2	chr3:112208326-112210333	GM12878	blood:	n/a	n/a
6	ATF2	chr3:112201412-112201996	GM12878	blood:	n/a	n/a
7	ATF2	chr3:112178586-112180203	GM12878	blood:	n/a	n/a
8	ATF2	chr3:112181801-112183834	GM12878	blood:	n/a	n/a
9	ATF2	chr3:112233216-112233958	GM12878	blood:	n/a	n/a
10	ATF2	chr3:112174606-112175451	GM12878	blood:	n/a	n/a
11	ATF2	chr3:112174716-112175428	GM12878	blood:	n/a	n/a
12	ATF2	chr3:112208191-112210297	GM12878	blood:	n/a	n/a
13	ATF2	chr3:112237760-112238685	GM12878	blood:	n/a	n/a
14	ATF2	chr3:112191977-112192593	GM12878	blood:	n/a	n/a
15	ATF2	chr3:112182945-112183787	GM12878	blood:	n/a	n/a
16	ATF2	chr3:112217882-112218686	GM12878	blood:	n/a	n/a
17	ATF2	chr3:112217577-112218762	GM12878	blood:	n/a	n/a
18	ATF2	chr3:112258649-112259179	GM12878	blood:	n/a	n/a
19	ATF2	chr3:112181963-112182703	GM12878	blood:	n/a	n/a
20	ATF2	chr3:112178323-112180365	GM12878	blood:	n/a	n/a
21	ATF2	chr3:112233307-112233940	GM12878	blood:	n/a	n/a
22	BATF	chr3:112233387-112233955	GM12878	blood:	n/a	n/a
23	BATF	chr3:112179396-112179832	GM12878	blood:	n/a	chr3:112179585-112179594
24	BATF	chr3:112222377-112222753	GM12878	blood:	n/a	n/a
25	BATF	chr3:112233345-112233906	GM12878	blood:	n/a	n/a
26	BATF	chr3:112179289-112179926	GM12878	blood:	n/a	chr3:112179889-112179899 chr3:112179585-112179594
27	BATF	chr3:112178649-112178996	GM12878	blood:	n/a	n/a
28	BATF	chr3:112183149-112183504	GM12878	blood:	n/a	n/a
29	BATF	chr3:112208785-112209113	GM12878	blood:	n/a	n/a
30	BATF	chr3:112208739-112209174	GM12878	blood:	n/a	n/a
31	BATF	chr3:112258695-112259018	GM12878	blood:	n/a	n/a
32	BATF	chr3:112183210-112183468	GM12878	blood:	n/a	n/a
33	BATF	chr3:112180623-112180947	GM12878	blood:	n/a	chr3:112180796-112180807
34	BCL11A	chr3:112192183-112192464	GM12878	blood:	n/a	n/a
35	BCL11A	chr3:112179271-112179712	GM12878	blood:	n/a	chr3:112179524-112179533
36	BCL11A	chr3:112179330-112179886	GM12878	blood:	n/a	chr3:112179524-112179533
37	BCL11A	chr3:112208757-112209201	GM12878	blood:	n/a	n/a
38	BCL11A	chr3:112233466-112233775	GM12878	blood:	n/a	n/a
39	BCL11A	chr3:112178672-112178956	GM12878	blood:	n/a	n/a
40	BCL11A	chr3:112233338-112233797	GM12878	blood:	n/a	n/a
41	BCL11A	chr3:112183088-112183485	GM12878	blood:	n/a	n/a
42	BCL3	chr3:112208669-112209195	GM12878	blood:	n/a	n/a
43	BCL3	chr3:112208660-112209498	GM12878	blood:	n/a	n/a
44	BCL3	chr3:112233334-112233931	GM12878	blood:	n/a	n/a
45	BCL3	chr3:112183082-112183515	GM12878	blood:	n/a	n/a
46	BCL3	chr3:112245548-112245831	GM12878	blood:	n/a	n/a
47	BCL3	chr3:112178509-112180324	GM12878	blood:	n/a	chr3:112179524-112179533
48	BCL3	chr3:112174642-112175427	GM12878	blood:	n/a	n/a
49	BCL3	chr3:112179382-112180021	GM12878	blood:	n/a	chr3:112179524-112179533
50	BCL3	chr3:112181977-112182583	GM12878	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:112276088-112276138	GM12892	blood:	n/a
2	chr3:112184271-112184321	HEK293	kidney:	embryo
3	chr3:112218761-112218811	SK-N-SH	brain:	n/a
4	chr3:112276088-112276138	HNPCEpiC	eye:	n/a
5	chr3:112184271-112184321	HCT-116	colon:	n/a
6	chr3:112184271-112184321	PrEC	prostate:	n/a
7	chr3:112218510-112218560	SAEC	small airway:	n/a
8	chr3:112218510-112218560	IMR90	lung:	fetal
9	chr3:112276088-112276138	GM19239	blood:	n/a
10	chr3:112218761-112218811	AG09309	skin:	n/a
11	chr3:112276088-112276138	AG09319	gingival:	n/a
12	chr3:112218761-112218811	HL-60	blood:	n/a
13	chr3:112218510-112218560	GM12878	blood:	n/a
14	chr3:112218510-112218560	BE2_C	brain:	n/a
15	chr3:112276088-112276138	GM06990	blood:	n/a
16	chr3:112218510-112218560	HEEpiC	esophagus:	n/a
17	chr3:112184271-112184321	HPAEpiC	pulmonary alveolar:	n/a
18	chr3:112217973-112218023	MCF-7	breast:	n/a
19	chr3:112218761-112218811	HAEpiC	amniotic membrane:	n/a
20	chr3:112217973-112218023	PrEC	prostate:	n/a
21	chr3:112276088-112276138	MCF-7	breast:	n/a
22	chr3:112218510-112218560	GM19239	blood:	n/a
23	chr3:112184271-112184321	HCM	heart:	n/a
24	chr3:112218510-112218560	HCF	heart:	n/a
25	chr3:112184271-112184321	HMEC	breast:	n/a
26	chr3:112218761-112218811	NHBE	bronchial:	n/a
27	chr3:112218510-112218560	ProgFib	skin:	n/a
28	chr3:112184271-112184321	GM12878	blood:	n/a
29	chr3:112218510-112218560	Caco-2	colon:	n/a
30	chr3:112218510-112218560	Hela-S3	cervix:	n/a
31	chr3:112217973-112218023	AG09309	skin:	n/a
32	chr3:112276088-112276138	ECC-1	luminal epithelium:	n/a
33	chr3:112218510-112218560	K562	blood:	n/a
34	chr3:112217973-112218023	BE2_C	brain:	n/a
35	chr3:112217973-112218023	Hela-S3	cervix:	n/a
36	chr3:112218510-112218560	HRCEpiC	kidney:	n/a
37	chr3:112218510-112218560	U87	brain:	n/a
38	chr3:112218761-112218811	HRPEpiC	eye:	n/a
39	chr3:112184271-112184321	HRE	kidney:	n/a
40	chr3:112276088-112276138	HepG2	liver:	n/a
41	chr3:112218761-112218811	A549	lung:	n/a
42	chr3:112184271-112184321	HNPCEpiC	eye:	n/a
43	chr3:112276088-112276138	T-47D	breast:	n/a
44	chr3:112217973-112218023	NT2-D1	testis:	n/a
45	chr3:112218761-112218811	Caco-2	colon:	n/a
46	chr3:112276088-112276138	SKMC	muscle:	n/a
47	chr3:112276088-112276138	Jurkat	blood:	n/a
48	chr3:112218761-112218811	GM06990	blood:	n/a
49	chr3:112276088-112276138	HEEpiC	esophagus:	n/a
50	chr3:112276088-112276138	MCF10A-Er-Src	breast:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:112045750..112047025-chr3:112237531..112238950,15	MCF-7	breast:
2	chr3:111830661..111831289-chr3:112238353..112238915,2	K562	blood:
3	chr3:112259312..112262688-chr3:112264103..112268109,5	MCF-7	breast:
4	chr3:112011899..112013194-chr3:112237762..112239193,5	MCF-7	breast:
5	chr3:112255414..112258114-chr3:112258815..112260452,2	MCF-7	breast:
6	chr3:112257894..112260182-chr3:112261876..112264065,2	K562	blood:
7	chr3:111855697..111856656-chr3:112238008..112238836,2	K562	blood:
8	chr3:112259312..112262688-chr3:112264103..112268109,5	MCF-7	breast:
9	chr17:58220578..58221151-chr3:112183496..112184268,2	MCF-7	breast:
10	chr3:112253284..112253915-chr3:126107853..126108632,2	MCF-7	breast:
11	chr3:112255866..112257509-chr3:112258178..112260464,2	K562	blood:
12	chr3:112046007..112046874-chr3:112156015..112156737,3	MCF-7	breast:
13	chr3:112253490..112256363-chr3:112279039..112281187,3	K562	blood:
14	chr3:112267679..112269481-chr3:112276502..112278431,2	MCF-7	breast:
15	chr3:112257894..112260182-chr3:112261876..112264065,2	K562	blood:
16	chr3:112267679..112269481-chr3:112276502..112278431,2	MCF-7	breast:
17	chr3:112011976..112013367-chr3:112237943..112239384,10	MCF-7	breast:
18	chr3:112045925..112046858-chr3:112237972..112238492,2	K562	blood:
19	chr3:112272255..112274870-chr3:112277581..112280165,3	K562	blood:
20	chr3:112267834..112269856-chr3:112273355..112275580,2	MCF-7	breast:
21	chr3:112257611..112259171-chr3:112300442..112301943,2	K562	blood:
22	chr3:112052345..112054034-chr3:112155349..112157049,2	MCF-7	breast:
23	chr3:112274013..112276880-chr3:112736926..112739647,2	MCF-7	breast:
24	chr3:111830414..111830964-chr3:112156344..112156927,2	MCF-7	breast:
25	chr3:112271839..112274196-chr3:112276069..112278465,2	K562	blood:
26	chr3:112268324..112269882-chr3:112359880..112361529,2	MCF-7	breast:
27	chr3:112267834..112269856-chr3:112273355..112275580,2	MCF-7	breast:
28	chr3:112045532..112046934-chr3:112156222..112157470,7	MCF-7	breast:
29	chr3:111830383..111831315-chr3:112250332..112250864,2	K562	blood:
30	chr3:112270443..112273330-chr3:112277844..112281278,5	MCF-7	breast:
31	chr3:112250901..112252598-chr3:112279157..112281596,2	MCF-7	breast:
32	chr3:112262046..112263985-chr3:112278635..112280484,2	K562	blood:
33	chr3:112270877..112274678-chr3:112278992..112281610,4	MCF-7	breast:
34	chr3:111856051..111856906-chr3:112237978..112238501,2	MCF-7	breast:
35	chr3:112274879..112277454-chr3:112278984..112281643,2	K562	blood:
36	chr3:112030207..112032434-chr3:112262315..112264380,2	K562	blood:
37	chr3:112263776..112266083-chr3:112359451..112361414,2	MCF-7	breast:
38	chr3:112189206..112190998-chr3:112191867..112193876,2	K562	blood:
39	chr3:112257078..112259281-chr3:112279236..112282506,3	MCF-7	breast:
40	chr3:112273986..112276332-chr3:112279376..112281873,3	MCF-7	breast:
41	chr11:65325880..65326380-chr3:112226218..112226735,2	Hela-S3	cervix:
42	chr3:111815832..111818403-chr3:112276886..112278586,2	MCF-7	breast:
43	chr3:112272044..112274714-chr3:112358450..112360286,2	MCF-7	breast:
44	chr3:112046305..112046882-chr3:112237913..112238884,3	MCF-7	breast:
45	chr3:112271839..112274196-chr3:112276069..112278465,2	K562	blood:
46	chr3:112215809..112217939-chr3:112219323..112221326,2	K562	blood:
47	chr3:112012262..112013019-chr3:112156556..112157096,2	MCF-7	breast:
48	chr3:112215809..112217939-chr3:112219323..112221326,2	K562	blood:
49	chr3:112276557..112278101-chr3:112358499..112360515,2	MCF-7	breast:
50	chr3:112265548..112268745-chr3:112278905..112281998,3	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATG3-3	chr3:112184773-112185230	NONHSAT091179
2	lnc-SLC35A5-2	chr3:112273149-112273439	expReg_chr3_7492_+
3	lnc-BTLA-4	chr3:112179309-112179627	NONHSAT091178
4	lnc-ATG3-3	chr3:112188819-112189300	NONHSAT091180
5	lnc-ATG3-1	chr3:112244395-112246989	NONHSAT091182
6	lnc-BTLA-4	chr3:112148802-112149477	NONHSAT091178
7	lnc-BTLA-4	chr3:112178630-112179297	NONHSAT091178
8	lnc-ATG3-3	chr3:112188819-112188869	NONHSAT091179
9	lnc-ATG3-3	chr3:112188605-112188651	NONHSAT091179
10	lnc-ATG3-3	chr3:112188603-112188651	NONHSAT091180

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ATG3	hsa-miR-155-5p	chr3:112251414-112251436

Variant related genes	Relation type
SLC35A5	TF binding region
ATG3	TF binding region
BTLA	TF binding region
OR7E100P	TF binding region
SLC35A5	CpG island
ATG3	CpG island
BTLA	CpG island
OR7E100P	CpG island
ENSG00000163608	chromatin interactions
ENSG00000091986	chromatin interactions
ENSG00000172139	chromatin interactions
ENSG00000138459	chromatin interactions
ENSG00000240057	chromatin interactions
ENSG00000186265	chromatin interactions
ENSG00000144848	chromatin interactions
CHUK	miRNA target sites

Extended variants
information (count: 4810 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:4810 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534002649	chr3:112147110-112147111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs72954452	chr3:112147151-112147152	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs573449805	chr3:112147185-112147186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149291783	chr3:112147209-112147210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562178844	chr3:112147210-112147211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs555682871	chr3:112147221-112147222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs183911257	chr3:112147225-112147226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs544531367	chr3:112147240-112147241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs575145170	chr3:112147259-112147260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs377541733	chr3:112147270-112147271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs58164505	chr3:112147271-112147272	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs75292779	chr3:112147331-112147332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs376230906	chr3:112147339-112147340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs1586508	chr3:112147356-112147357	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs75366149	chr3:112147369-112147370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs79803365	chr3:112147376-112147377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs115492914	chr3:112147418-112147419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs569250284	chr3:112147426-112147427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs955212	chr3:112147428-112147429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs572804111	chr3:112147468-112147469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs111839401	chr3:112147499-112147500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs955213	chr3:112147501-112147502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs34045258	chr3:112147548-112147549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551347566	chr3:112147561-112147562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188648293	chr3:112147568-112147569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs180820612	chr3:112147574-112147575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553961283	chr3:112147582-112147583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573386412	chr3:112147596-112147597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs74677872	chr3:112147598-112147599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540128945	chr3:112147609-112147610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555842403	chr3:112147644-112147645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs575590889	chr3:112147679-112147680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs74562885	chr3:112147681-112147682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs184521844	chr3:112147752-112147753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs578216531	chr3:112147761-112147762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs529465130	chr3:112147779-112147780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs528866891	chr3:112147782-112147783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs189501489	chr3:112147796-112147797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs59429955	chr3:112147803-112147804	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs529535675	chr3:112147815-112147816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543099161	chr3:112147854-112147855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562982084	chr3:112147863-112147864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530287919	chr3:112147877-112147878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs77965972	chr3:112147882-112147883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs571429957	chr3:112147890-112147891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs527617800	chr3:112147893-112147894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs56735831	chr3:112147945-112147946	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs374517828	chr3:112147956-112147957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs181936187	chr3:112147960-112147961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs536050861	chr3:112148032-112148033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Basal cell lymphoma	21115979	CNVD
Attention deficit hyperactivity disorder	22180640	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2105 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112137000-112150400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:112137200-112147200	Weak transcription	Placenta	Placenta
3	chr3:112144400-112150400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr3:112145400-112151000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr3:112145600-112150400	Weak transcription	GM12878-XiMat	blood
6	chr3:112145600-112150600	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr3:112145600-112150800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr3:112146200-112149800	Weak transcription	Primary B cells from cord blood	blood
9	chr3:112147200-112147400	Enhancers	Placenta	Placenta
10	chr3:112147200-112147600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr3:112147200-112147800	Enhancers	Sigmoid Colon	Sigmoid Colon
12	chr3:112147400-112148200	Enhancers	Fetal Intestine Large	intestine
13	chr3:112147600-112150600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr3:112147800-112148400	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr3:112150400-112150600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
16	chr3:112150400-112152800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
17	chr3:112150600-112150800	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr3:112150600-112150800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr3:112150800-112151800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
20	chr3:112150800-112152200	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr3:112151000-112151800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
22	chr3:112151800-112156000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr3:112151800-112156600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr3:112152000-112153400	Enhancers	Primary T helper cells PMA-I stimulated	--
25	chr3:112153400-112154200	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr3:112154200-112154400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr3:112154200-112154800	Enhancers	Primary T helper cells PMA-I stimulated	--
28	chr3:112154400-112154600	Enhancers	Primary B cells from peripheral blood	blood
29	chr3:112154400-112154600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
30	chr3:112154400-112154600	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr3:112154400-112154600	Enhancers	Sigmoid Colon	Sigmoid Colon
32	chr3:112154600-112155600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr3:112154600-112155800	Weak transcription	Primary B cells from peripheral blood	blood
34	chr3:112154800-112155400	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr3:112154800-112156000	Weak transcription	Primary T helper cells fromperipheralblood	blood
36	chr3:112155000-112156200	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr3:112155400-112156600	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr3:112155600-112156600	Enhancers	Placenta	Placenta
39	chr3:112155600-112157000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
40	chr3:112155600-112157000	ZNF genes & repeats	GM12878-XiMat	blood
41	chr3:112155800-112156600	Enhancers	Primary B cells from peripheral blood	blood
42	chr3:112155800-112156800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
43	chr3:112155800-112156800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
44	chr3:112155800-112157000	Enhancers	Primary T cells fromperipheralblood	blood
45	chr3:112155800-112157000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
46	chr3:112156000-112156400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr3:112156000-112156400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr3:112156000-112156600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
49	chr3:112156000-112156600	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr3:112156000-112156600	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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