Variant report

Variant	nsv558877
Chromosome Location	chr12:51690751-51733951
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:592)
CpG islands
(count:977)
Chromatin interactive
region (count:64)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:592 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:51729914-51729925	K562	blood:	n/a	n/a
2	ARID3A	chr12:51720510-51720934	K562	blood:	n/a	n/a
3	ARID3A	chr12:51714725-51715166	K562	blood:	n/a	n/a
4	ARID3A	chr12:51712319-51712572	K562	blood:	n/a	n/a
5	ATF1	chr12:51720465-51720878	K562	blood:	n/a	n/a
6	ATF2	chr12:51714629-51715214	GM12878	blood:	n/a	n/a
7	ATF2	chr12:51720370-51720948	GM12878	blood:	n/a	n/a
8	BACH1	chr12:51720624-51720970	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr12:51720521-51720953	K562	blood:	n/a	n/a
10	BCLAF1	chr12:51720403-51721047	GM12878	blood:	n/a	chr12:51720643-51720652
11	BCLAF1	chr12:51714360-51714950	GM12878	blood:	n/a	chr12:51714693-51714702 chr12:51714932-51714941
12	BCLAF1	chr12:51717646-51718225	GM12878	blood:	n/a	n/a
13	BHLHE40	chr12:51714766-51715088	K562	blood:	n/a	n/a
14	BHLHE40	chr12:51717713-51718108	GM12878	blood:	n/a	n/a
15	BHLHE40	chr12:51720362-51720921	K562	blood:	n/a	n/a
16	BHLHE40	chr12:51714326-51714366	K562	blood:	n/a	n/a
17	CBX3	chr12:51714408-51715186	K562	blood:	n/a	chr12:51714841-51714852
18	CBX3	chr12:51720458-51721020	K562	blood:	n/a	n/a
19	CCNT2	chr12:51712271-51712540	K562	blood:	n/a	n/a
20	CCNT2	chr12:51720532-51721185	K562	blood:	n/a	n/a
21	CCNT2	chr12:51714698-51715133	K562	blood:	n/a	n/a
22	CEBPB	chr12:51720901-51721056	HepG2	liver:	n/a	chr12:51720985-51720996
23	CEBPB	chr12:51720590-51721090	K562	blood:	n/a	chr12:51720757-51720768 chr12:51720985-51720996
24	CEBPB	chr12:51720832-51721145	HepG2	liver:	n/a	chr12:51720985-51720996
25	CEBPB	chr12:51712566-51713142	MCF-7	breast:	n/a	n/a
26	CEBPB	chr12:51720735-51721189	A549	lung:	n/a	chr12:51720757-51720768 chr12:51720985-51720996
27	CEBPB	chr12:51729826-51730026	K562	blood:	n/a	n/a
28	CEBPB	chr12:51700222-51700477	K562	blood:	n/a	chr12:51700361-51700372
29	CEBPB	chr12:51718713-51719252	MCF-7	breast:	n/a	chr12:51718946-51718957
30	CEBPB	chr12:51720610-51721162	IMR90	lung:	n/a	chr12:51720757-51720768 chr12:51720985-51720996
31	CEBPB	chr12:51723521-51723889	K562	blood:	n/a	n/a
32	CEBPB	chr12:51712671-51713004	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr12:51720598-51721266	ECC-1	luminal epithelium:	n/a	chr12:51720757-51720768 chr12:51720985-51720996
34	CEBPB	chr12:51720653-51721190	HCT-116	colon:	n/a	chr12:51720757-51720768 chr12:51720985-51720996
35	CEBPB	chr12:51720720-51721251	MCF-7	breast:	n/a	chr12:51720757-51720768 chr12:51720985-51720996
36	CEBPB	chr12:51720634-51721148	A549	lung:	n/a	chr12:51720757-51720768 chr12:51720985-51720996
37	CEBPB	chr12:51700355-51700438	HepG2	liver:	n/a	chr12:51700361-51700372
38	CEBPB	chr12:51720457-51721312	A549	lung:	n/a	chr12:51720757-51720768 chr12:51720985-51720996
39	CEBPB	chr12:51720565-51721205	Hela-S3	cervix:	n/a	chr12:51720757-51720768 chr12:51720985-51720996
40	CEBPB	chr12:51720617-51721223	MCF-7	breast:	n/a	chr12:51720757-51720768 chr12:51720985-51720996
41	CEBPB	chr12:51713981-51714013	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr12:51723546-51723845	K562	blood:	n/a	n/a
43	CEBPB	chr12:51720502-51721202	K562	blood:	n/a	chr12:51720757-51720768 chr12:51720985-51720996
44	CEBPB	chr12:51712760-51712977	K562	blood:	n/a	n/a
45	CEBPB	chr12:51720700-51721162	ECC-1	luminal epithelium:	n/a	chr12:51720757-51720768 chr12:51720985-51720996
46	CEBPB	chr12:51718760-51719194	MCF-7	breast:	n/a	chr12:51718946-51718957
47	CEBPB	chr12:51713903-51714094	A549	lung:	n/a	n/a
48	CEBPB	chr12:51712592-51713052	MCF-7	breast:	n/a	n/a
49	CEBPB	chr12:51714886-51715237	K562	blood:	n/a	n/a
50	CEBPB	chr12:51720823-51721134	H1-hESC	embryonic stem cell:	n/a	chr12:51720985-51720996

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:51713220-51713270	AG09309	skin:	n/a
2	chr12:51713220-51713270	AG09309	skin:	n/a
3	chr12:51718108-51718158	GM06990	blood:	n/a
4	chr12:51718310-51718360	Jurkat	blood:	n/a
5	chr12:51717960-51718010	HAEpiC	amniotic membrane:	n/a
6	chr12:51718108-51718158	AG10803	skin:	n/a
7	chr12:51718355-51718405	Jurkat	blood:	n/a
8	chr12:51713220-51713270	HPAEpiC	pulmonary alveolar:	n/a
9	chr12:51718011-51718061	NB4	blood:	n/a
10	chr12:51718011-51718061	T-47D	breast:	n/a
11	chr12:51718088-51718138	GM06990	blood:	n/a
12	chr12:51701979-51702029	HIPEpiC	eye:	n/a
13	chr12:51718108-51718158	T-47D	breast:	n/a
14	chr12:51717674-51717724	IMR90	lung:	fetal
15	chr12:51718112-51718162	HRE	kidney:	n/a
16	chr12:51717865-51717915	H1-hESC	embryonic stem cell:	embryo
17	chr12:51701979-51702029	NT2-D1	testis:	n/a
18	chr12:51717865-51717915	AG10803	skin:	n/a
19	chr12:51720755-51720805	ProgFib	skin:	n/a
20	chr12:51717960-51718010	HNPCEpiC	eye:	n/a
21	chr12:51717960-51718010	GM12892	blood:	n/a
22	chr12:51718251-51718301	HRPEpiC	eye:	n/a
23	chr12:51715252-51715302	NHBE	bronchial:	n/a
24	chr12:51717960-51718010	H1-hESC	embryonic stem cell:	embryo
25	chr12:51717978-51718028	A549	lung:	n/a
26	chr12:51720755-51720805	HL-60	blood:	n/a
27	chr12:51715252-51715302	HCPEpiC	choroid plexus:	n/a
28	chr12:51718355-51718405	AG10803	skin:	n/a
29	chr12:51718088-51718138	U87	brain:	n/a
30	chr12:51718251-51718301	Caco-2	colon:	n/a
31	chr12:51718355-51718405	AG09319	gingival:	n/a
32	chr12:51701979-51702029	HRCEpiC	kidney:	n/a
33	chr12:51718112-51718162	Caco-2	colon:	n/a
34	chr12:51717978-51718028	ECC-1	luminal epithelium:	n/a
35	chr12:51717674-51717724	SK-N-SH_RA	brain:	n/a
36	chr12:51718310-51718360	LNCaP	prostate:	n/a
37	chr12:51722300-51722350	PFSK-1	brain:	n/a
38	chr12:51717978-51718028	H1-hESC	embryonic stem cell:	embryo
39	chr12:51718251-51718301	MCF-7	breast:	n/a
40	chr12:51718251-51718301	GM06990	blood:	n/a
41	chr12:51717865-51717915	T-47D	breast:	n/a
42	chr12:51718355-51718405	HCPEpiC	choroid plexus:	n/a
43	chr12:51718310-51718360	A549	lung:	n/a
44	chr12:51717978-51718028	AG09319	gingival:	n/a
45	chr12:51715252-51715302	GM12892	blood:	n/a
46	chr12:51718251-51718301	HCF	heart:	n/a
47	chr12:51717674-51717724	ProgFib	skin:	n/a
48	chr12:51717865-51717915	HEK293	kidney:	embryo
49	chr12:51717978-51718028	ovcar-3	ovarian:	n/a
50	chr12:51718251-51718301	IMR90	lung:	fetal

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:51696998..51699958-chr12:51701711..51703812,2	K562	blood:
2	chr12:51729334..51731458-chr12:51738258..51740598,2	K562	blood:
3	chr12:51719185..51720763-chr12:51721819..51723856,2	MCF-7	breast:
4	chr12:51712171..51715020-chr12:51716929..51719322,2	MCF-7	breast:
5	chr12:51726670..51729630-chr12:51730629..51732198,2	K562	blood:
6	chr12:51726670..51729630-chr12:51730629..51732198,2	K562	blood:
7	chr12:51662740..51664596-chr12:51691397..51693911,2	MCF-7	breast:
8	chr12:51476882..51478669-chr12:51732135..51734824,2	K562	blood:
9	chr12:51631606..51634068-chr12:51733691..51737462,4	K562	blood:
10	chr12:51715545..51717672-chr12:51739386..51741358,2	K562	blood:
11	chr12:51658184..51660274-chr12:51733778..51735476,2	MCF-7	breast:
12	chr12:51438469..51440828-chr12:51713413..51715859,2	K562	blood:
13	chr12:51662477..51664063-chr12:51717292..51718857,2	MCF-7	breast:
14	chr12:51712710..51716828-chr12:51719754..51724043,5	K562	blood:
15	chr12:51715738..51718672-chr12:51724028..51726868,2	MCF-7	breast:
16	chr12:51632383..51635139-chr12:51689169..51690990,2	K562	blood:
17	chr12:51712710..51714894-chr12:51720855..51723845,2	K562	blood:
18	chr12:51637545..51639615-chr12:51692458..51694056,2	MCF-7	breast:
19	chr12:51475962..51477532-chr12:51714487..51716389,2	K562	blood:
20	chr12:51702787..51706135-chr12:51715860..51718375,3	K562	blood:
21	chr12:51694624..51697203-chr12:51700162..51702400,2	MCF-7	breast:
22	chr12:51662029..51664846-chr12:51687985..51690771,3	MCF-7	breast:
23	chr12:51661913..51666807-chr12:51714627..51721165,8	MCF-7	breast:
24	chr12:51701016..51703258-chr12:51704233..51707521,3	MCF-7	breast:
25	chr12:51712710..51716828-chr12:51719754..51724043,5	K562	blood:
26	chr12:51685363..51688079-chr12:51689486..51691141,2	K562	blood:
27	chr12:51566806..51568529-chr12:51720798..51723312,2	K562	blood:
28	chr12:51661276..51664134-chr12:51700484..51702022,2	MCF-7	breast:
29	chr12:51710356..51713645-chr12:51720668..51723733,3	MCF-7	breast:
30	chr12:51662774..51665391-chr12:51722763..51725080,2	MCF-7	breast:
31	chr12:51663552..51665090-chr12:51718894..51721818,2	MCF-7	breast:
32	chr12:51662595..51665038-chr12:51711097..51713316,2	K562	blood:
33	chr12:51686282..51687950-chr12:51722730..51724837,2	MCF-7	breast:
34	chr12:51610324..51613201-chr12:51733720..51736973,4	K562	blood:
35	chr12:51417902..51420501-chr12:51719275..51722211,2	K562	blood:
36	chr12:51719185..51720763-chr12:51721819..51723856,2	MCF-7	breast:
37	chr12:51661063..51664468-chr12:51732483..51736872,6	MCF-7	breast:
38	chr12:51710356..51713645-chr12:51720668..51723733,3	MCF-7	breast:
39	chr12:51661930..51666177-chr12:51732145..51735624,5	MCF-7	breast:
40	chr12:51732471..51736842-chr12:51740584..51742945,3	MCF-7	breast:
41	chr12:51633168..51635077-chr12:51718759..51720463,2	MCF-7	breast:
42	chr12:51686041..51688079-chr12:51689117..51691141,2	K562	blood:
43	chr12:51712004..51713863-chr12:51716596..51718189,2	K562	blood:
44	chr12:51724277..51726294-chr12:51726344..51728218,2	MCF-7	breast:
45	chr12:51661800..51664432-chr12:51720431..51722225,2	K562	blood:
46	chr12:51714696..51717509-chr12:51745471..51747033,2	MCF-7	breast:
47	chr12:51696998..51699958-chr12:51701711..51703812,2	K562	blood:
48	chr12:51694624..51697203-chr12:51700162..51702400,2	MCF-7	breast:
49	chr12:51632967..51634708-chr12:51718961..51721755,2	K562	blood:
50	chr12:51662271..51665038-chr12:51711816..51714647,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DAZAP2-5	chr12:51692952-51693261	expReg_chr12_4580_+
2	lnc-CELA1-1	chr12:51716369-51717042	NONHSAT028255
3	lnc-CELA1-1	chr12:51717806-51717869	NONHSAT028255
4	lnc-DAZAP2-6	chr12:51705285-51705526	expReg_chr12_4589_+

No data

Variant related genes	Relation type
BIN2	TF binding region
BIN2	CpG island
ENSG00000110925	chromatin interactions
ENSG00000110911	chromatin interactions
ENSG00000139610	chromatin interactions
ENSG00000184271	chromatin interactions
ENSG00000183283	chromatin interactions
ENSG00000170545	chromatin interactions
ENSG00000110934	chromatin interactions
ENSG00000135457	chromatin interactions
ENSG00000123268	chromatin interactions

Extended variants
information (count: 1698 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1698 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2288367	chr12:51690751-51690752	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs571602022	chr12:51690801-51690802	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs186095299	chr12:51690808-51690809	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs375904054	chr12:51690837-51690838	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs551006604	chr12:51690839-51690840	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs200001519	chr12:51690848-51690849	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs111723252	chr12:51690865-51690866	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs555892885	chr12:51690927-51690928	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs201208876	chr12:51690951-51690952	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs572570940	chr12:51690979-51690980	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs541253132	chr12:51691023-51691024	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564427361	chr12:51691045-51691046	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190904428	chr12:51691071-51691072	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538366798	chr12:51691072-51691073	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs563537564	chr12:51691081-51691082	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529348159	chr12:51691088-51691089	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs140864171	chr12:51691090-51691091	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs369744351	chr12:51691101-51691102	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs3782468	chr12:51691127-51691128	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571147611	chr12:51691128-51691129	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs184082568	chr12:51691129-51691130	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs138774035	chr12:51691137-51691138	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs386762971	chr12:51691148-51691149	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs3782469	chr12:51691149-51691150	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537344648	chr12:51691150-51691151	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs550509375	chr12:51691162-51691163	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549171781	chr12:51691187-51691188	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs34375896	chr12:51691188-51691189	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs553501608	chr12:51691207-51691208	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs137911994	chr12:51691225-51691226	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552768191	chr12:51691237-51691238	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572925163	chr12:51691244-51691245	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564628720	chr12:51691252-51691253	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372906714	chr12:51691258-51691259	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557978931	chr12:51691265-51691266	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368222919	chr12:51691266-51691267	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577871062	chr12:51691300-51691301	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543718629	chr12:51691306-51691307	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375588984	chr12:51691307-51691308	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572029235	chr12:51691313-51691314	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs7134625	chr12:51691413-51691414	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs573974557	chr12:51691420-51691421	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs543036570	chr12:51691422-51691423	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs554583216	chr12:51691430-51691431	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs556844740	chr12:51691461-51691462	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs149486714	chr12:51691465-51691466	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs528644075	chr12:51691467-51691468	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs144321166	chr12:51691508-51691509	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs565083548	chr12:51691517-51691518	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs186926558	chr12:51691520-51691521	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21509527	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	20409316	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Intracranial arachnoid cysts	20187927	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1107 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:51664600-51692800	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr12:51673800-51697600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr12:51674000-51698400	Strong transcription	Fetal Thymus	thymus
4	chr12:51674000-51701400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr12:51674200-51704000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr12:51674400-51698400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr12:51674400-51698600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr12:51674400-51698800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr12:51674400-51700600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr12:51676800-51691000	Weak transcription	Placenta	Placenta
11	chr12:51678000-51697600	Weak transcription	Adipose Nuclei	Adipose
12	chr12:51678800-51693000	Weak transcription	Duodenum Mucosa	Duodenum
13	chr12:51680600-51701600	Weak transcription	Small Intestine	intestine
14	chr12:51681200-51696600	Strong transcription	Primary T cells fromperipheralblood	blood
15	chr12:51681800-51714200	Weak transcription	Gastric	stomach
16	chr12:51683600-51693000	Weak transcription	Spleen	Spleen
17	chr12:51685800-51697600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr12:51686200-51702800	Weak transcription	Colonic Mucosa	Colon
19	chr12:51686600-51698800	Strong transcription	Primary B cells from peripheral blood	blood
20	chr12:51686800-51692800	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr12:51686800-51698600	Strong transcription	Primary T cells from cord blood	blood
22	chr12:51686800-51701200	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr12:51687000-51703800	Strong transcription	Primary neutrophils fromperipheralblood	blood
24	chr12:51687000-51707400	Strong transcription	Primary monocytes fromperipheralblood	blood
25	chr12:51687200-51696800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr12:51687200-51697200	Strong transcription	Primary T helper naive cells from peripheral blood	blood
27	chr12:51687800-51697200	Strong transcription	Primary T helper cells fromperipheralblood	blood
28	chr12:51687800-51700000	Strong transcription	Monocytes-CD14+_RO01746	blood
29	chr12:51687800-51708000	Strong transcription	Thymus	Thymus
30	chr12:51688000-51690800	Weak transcription	K562	blood
31	chr12:51688000-51698400	Strong transcription	Primary T helper cells PMA-I stimulated	--
32	chr12:51688800-51696800	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr12:51689200-51691600	Strong transcription	Primary B cells from cord blood	blood
34	chr12:51689400-51691600	Strong transcription	GM12878-XiMat	blood
35	chr12:51689400-51691800	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
36	chr12:51689600-51691200	Strong transcription	Primary T killer memory cells from peripheral blood	blood
37	chr12:51689600-51696000	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr12:51690000-51693000	Weak transcription	Primary hematopoietic stem cells	blood
39	chr12:51690400-51691000	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr12:51690800-51691200	Enhancers	K562	blood
41	chr12:51691000-51692800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr12:51691000-51696800	Strong transcription	Placenta	Placenta
43	chr12:51691200-51692800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr12:51691200-51694200	Weak transcription	K562	blood
45	chr12:51691600-51693000	Weak transcription	Primary B cells from cord blood	blood
46	chr12:51691600-51693000	Weak transcription	GM12878-XiMat	blood
47	chr12:51691800-51692600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
48	chr12:51691800-51702200	Weak transcription	Rectal Smooth Muscle	rectum
49	chr12:51692600-51698200	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr12:51692800-51693400	Strong transcription	Sigmoid Colon	Sigmoid Colon

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