Variant report

Variant	esv2754441
Chromosome Location	chr12:46590364-46605239
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:421)
CpG islands
(count:183)
Chromatin interactive
region (count:51)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:421 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:46603345-46604468	GM12878	blood:	n/a	n/a
2	ATF2	chr12:46601182-46601882	GM12878	blood:	n/a	n/a
3	ATF2	chr12:46603315-46604175	GM12878	blood:	n/a	n/a
4	ATF2	chr12:46601240-46602016	GM12878	blood:	n/a	n/a
5	BATF	chr12:46603655-46604350	GM12878	blood:	n/a	n/a
6	BATF	chr12:46601331-46601693	GM12878	blood:	n/a	chr12:46601435-46601444 chr12:46601529-46601538
7	BATF	chr12:46603662-46603989	GM12878	blood:	n/a	n/a
8	BCL11A	chr12:46603684-46604068	GM12878	blood:	n/a	n/a
9	BCL11A	chr12:46603647-46604123	GM12878	blood:	n/a	n/a
10	BCL11A	chr12:46601402-46601734	GM12878	blood:	n/a	chr12:46601701-46601710
11	BCL3	chr12:46603623-46604103	GM12878	blood:	n/a	n/a
12	BCL3	chr12:46601344-46601738	GM12878	blood:	n/a	chr12:46601701-46601710
13	BCLAF1	chr12:46601288-46601876	GM12878	blood:	n/a	chr12:46601701-46601710
14	BCLAF1	chr12:46603623-46604226	GM12878	blood:	n/a	n/a
15	BHLHE40	chr12:46603340-46604258	GM12878	blood:	n/a	n/a
16	BHLHE40	chr12:46601427-46601702	GM12878	blood:	n/a	n/a
17	BRCA1	chr12:46601329-46601344	GM12878	blood:	n/a	n/a
18	CEBPB	chr12:46591648-46591909	HepG2	liver:	n/a	n/a
19	CEBPB	chr12:46603369-46604829	GM12878	blood:	n/a	n/a
20	CHD1	chr12:46603799-46604260	GM12878	blood:	n/a	n/a
21	CHD2	chr12:46603679-46604310	GM12878	blood:	n/a	n/a
22	CHD2	chr12:46603233-46603331	GM12878	blood:	n/a	n/a
23	CTCF	chr12:46599200-46599350	HPAF	blood vessel:	n/a	chr12:46599246-46599254
24	CTCF	chr12:46599211-46599345	Hela-S3	cervix:	n/a	chr12:46599246-46599254
25	CTCF	chr12:46599120-46599270	AG09319	gingival:	n/a	chr12:46599246-46599254
26	CTCF	chr12:46599241-46599279	LNCaP	prostate:	n/a	chr12:46599246-46599254
27	CTCF	chr12:46600480-46600630	MCF-7	breast:	n/a	n/a
28	CTCF	chr12:46599180-46599330	HMF	breast:	n/a	chr12:46599246-46599254
29	CTCF	chr12:46599080-46599230	HCM	heart:	n/a	n/a
30	CTCF	chr12:46599178-46599326	Spleen_OC	spleen:	n/a	chr12:46599246-46599254
31	CTCF	chr12:46599120-46599270	NHDF-neo	bronchial:	n/a	chr12:46599246-46599254
32	CTCF	chr12:46601355-46601422	GM12878	blood:	n/a	n/a
33	CTCF	chr12:46599101-46599350	GM12878	blood:	n/a	chr12:46599246-46599254
34	CTCF	chr12:46599246-46599294	LNCaP	prostate:	n/a	chr12:46599246-46599254
35	CTCF	chr12:46599217-46599269	Lung_OC	lung:	n/a	chr12:46599246-46599254
36	CTCF	chr12:46599166-46599366	K562	blood:	n/a	chr12:46599246-46599254
37	CTCF	chr12:46595340-46595490	GM12867	blood:	n/a	n/a
38	CTCF	chr12:46594520-46594670	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr12:46599140-46599290	HPAF	blood vessel:	n/a	chr12:46599246-46599254
40	CTCF	chr12:46599200-46599350	NHDF-neo	bronchial:	n/a	chr12:46599246-46599254
41	CTCF	chr12:46603980-46604130	MCF-7	breast:	n/a	n/a
42	CTCF	chr12:46604060-46604210	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr12:46599100-46599250	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr12:46599212-46599305	HUVEC	blood vessel:	n/a	chr12:46599246-46599254
45	CUX1	chr12:46603529-46604327	GM12878	blood:	n/a	n/a
46	CUX1	chr12:46601537-46601824	GM12878	blood:	n/a	n/a
47	E2F4	chr12:46594028-46594161	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr12:46602586-46602610	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr12:46603875-46604012	MCF10A-Er-Src	breast:	n/a	n/a
50	EBF1	chr12:46603695-46604118	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:46599923-46599973	HPAEpiC	pulmonary alveolar:	n/a
2	chr12:46599935-46599985	HNPCEpiC	eye:	n/a
3	chr12:46599925-46599975	U87	brain:	n/a
4	chr12:46599925-46599975	HIPEpiC	eye:	n/a
5	chr12:46599935-46599985	GM12878	blood:	n/a
6	chr12:46599935-46599985	HRPEpiC	eye:	n/a
7	chr12:46599923-46599973	LNCaP	prostate:	n/a
8	chr12:46599925-46599975	Caco-2	colon:	n/a
9	chr12:46599925-46599975	GM06990	blood:	n/a
10	chr12:46599923-46599973	HUVEC	blood vessel:	n/a
11	chr12:46599925-46599975	CMK	blood:	n/a
12	chr12:46599925-46599975	SK-N-SH_RA	brain:	n/a
13	chr12:46599935-46599985	HL-60	blood:	n/a
14	chr12:46599925-46599975	HRCEpiC	kidney:	n/a
15	chr12:46599923-46599973	HMEC	breast:	n/a
16	chr12:46599935-46599985	HCM	heart:	n/a
17	chr12:46599925-46599975	IMR90	lung:	fetal
18	chr12:46599925-46599975	Jurkat	blood:	n/a
19	chr12:46599935-46599985	GM12892	blood:	n/a
20	chr12:46599935-46599985	SK-N-SH_RA	brain:	n/a
21	chr12:46599935-46599985	Jurkat	blood:	n/a
22	chr12:46599923-46599973	Jurkat	blood:	n/a
23	chr12:46599923-46599973	HCM	heart:	n/a
24	chr12:46599923-46599973	Hepatocyte	liver:	n/a
25	chr12:46599925-46599975	NHDF-neo	bronchial:	n/a
26	chr12:46599925-46599975	ECC-1	luminal epithelium:	n/a
27	chr12:46599925-46599975	PANC-1	pancreas:	n/a
28	chr12:46599925-46599975	MCF-7	breast:	n/a
29	chr12:46599925-46599975	K562	blood:	n/a
30	chr12:46599925-46599975	AG09309	skin:	n/a
31	chr12:46599923-46599973	GM12891	blood:	n/a
32	chr12:46599925-46599975	HCM	heart:	n/a
33	chr12:46599935-46599985	RPTEC	kidney:	n/a
34	chr12:46599923-46599973	NHBE	bronchial:	n/a
35	chr12:46599923-46599973	AG10803	skin:	n/a
36	chr12:46599923-46599973	GM12878	blood:	n/a
37	chr12:46599925-46599975	ProgFib	skin:	n/a
38	chr12:46599925-46599975	GM12891	blood:	n/a
39	chr12:46599925-46599975	GM12878	blood:	n/a
40	chr12:46599923-46599973	T-47D	breast:	n/a
41	chr12:46599923-46599973	HRCEpiC	kidney:	n/a
42	chr12:46599935-46599985	HMEC	breast:	n/a
43	chr12:46599923-46599973	HIPEpiC	eye:	n/a
44	chr12:46599923-46599973	NHDF-neo	bronchial:	n/a
45	chr12:46599923-46599973	SK-N-SH	brain:	n/a
46	chr12:46599935-46599985	HAEpiC	amniotic membrane:	n/a
47	chr12:46599925-46599975	SKMC	muscle:	n/a
48	chr12:46599935-46599985	PrEC	prostate:	n/a
49	chr12:46599925-46599975	Hepatocyte	liver:	n/a
50	chr12:46599935-46599985	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr12:46603552..46605159-chr12:46765085..46767410,2	MCF-7	breast:
2	chr12:46599272..46601027-chr12:46763701..46766006,2	MCF-7	breast:
3	chr12:46594018..46595589-chr12:46607085..46608611,2	K562	blood:
4	chr12:46598140..46600634-chr12:46609725..46611307,2	MCF-7	breast:
5	chr12:46590374..46592807-chr12:46594598..46596416,2	K562	blood:
6	chr12:46590374..46592185-chr12:46593694..46596416,2	K562	blood:
7	chr12:46595062..46596035-chr12:46887567..46888241,2	MCF-7	breast:
8	chr12:46601918..46605358-chr12:46605865..46610216,5	MCF-7	breast:
9	chr12:46603045..46606011-chr12:46660345..46662347,2	K562	blood:
10	chr12:46596914..46598959-chr12:46645342..46648225,2	K562	blood:
11	chr12:46595398..46597588-chr12:46598013..46599672,2	MCF-7	breast:
12	chr12:46598504..46606384-chr12:46660159..46664661,13	MCF-7	breast:
13	chr12:46595584..46597824-chr12:46604968..46606668,2	K562	blood:
14	chr12:46593719..46596069-chr12:46598625..46601594,2	K562	blood:
15	chr12:46573159..46574150-chr12:46595090..46595990,8	MCF-7	breast:
16	chr12:46545467..46546982-chr12:46599241..46601124,2	MCF-7	breast:
17	chr12:46381552..46382503-chr12:46595173..46595922,2	MCF-7	breast:
18	chr12:46597858..46599601-chr12:46614567..46617452,2	MCF-7	breast:
19	chr12:46602512..46604164-chr12:46658365..46660117,2	MCF-7	breast:
20	chr12:46604867..46608116-chr12:46608247..46612042,4	K562	blood:
21	chr12:46598258..46600271-chr12:46600295..46602398,2	MCF-7	breast:
22	chr12:46595247..46598167-chr12:46765008..46767085,2	MCF-7	breast:
23	chr12:46593741..46596593-chr12:46600786..46603136,2	MCF-7	breast:
24	chr12:46384067..46386455-chr12:46596129..46598262,2	MCF-7	breast:
25	chr12:46593719..46596069-chr12:46598625..46601594,2	K562	blood:
26	chr12:46588334..46590648-chr12:46661672..46663800,3	K562	blood:
27	chr12:46571164..46575821-chr12:46593446..46599247,7	MCF-7	breast:
28	chr12:46601000..46609556-chr12:46658880..46665180,16	MCF-7	breast:
29	chr12:46598997..46599629-chr12:47069182..47070047,2	MCF-7	breast:
30	chr12:46593439..46596072-chr12:46660692..46663699,3	MCF-7	breast:
31	chr12:46573159..46574036-chr12:46595074..46595990,6	MCF-7	breast:
32	chr12:46593902..46597897-chr12:46605177..46609280,4	MCF-7	breast:
33	chr12:46595398..46597588-chr12:46598013..46599672,2	MCF-7	breast:
34	chr12:46604571..46607564-chr12:46643958..46646763,2	MCF-7	breast:
35	chr12:46595186..46598496-chr12:46654294..46656727,3	MCF-7	breast:
36	chr12:46588900..46591153-chr12:46593120..46595375,3	MCF-7	breast:
37	chr12:46593741..46596593-chr12:46600786..46603136,2	MCF-7	breast:
38	chr12:46600082..46602843-chr20:56269478..56271257,2	MCF-7	breast:
39	chr12:46595584..46597824-chr12:46604968..46606668,2	K562	blood:
40	chr12:46593049..46595554-chr12:46612027..46614436,2	MCF-7	breast:
41	chr12:46580626..46582409-chr12:46594371..46596470,2	K562	blood:
42	chr12:46588900..46591153-chr12:46593120..46595375,3	MCF-7	breast:
43	chr12:46593182..46595515-chr12:46654279..46656070,2	MCF-7	breast:
44	chr12:46553848..46555931-chr12:46593507..46596350,2	MCF-7	breast:
45	chr12:46598258..46600271-chr12:46600295..46602398,2	MCF-7	breast:
46	chr12:46517497..46520022-chr12:46601556..46603233,2	MCF-7	breast:
47	chr12:46590494..46598595-chr12:46658954..46664180,10	MCF-7	breast:
48	chr12:46592017..46594239-chr12:46595617..46598192,2	MCF-7	breast:
49	chr12:46593902..46597897-chr12:46605177..46609280,4	MCF-7	breast:
50	chr12:46592017..46594239-chr12:46595617..46598192,2	MCF-7	breast:

No data

Variant related genes	Relation type
SLC38A1	TF binding region
SLC38A1	CpG island
ENSG00000258096	chromatin interactions
ENSG00000139218	chromatin interactions
ENSG00000111371	chromatin interactions
ENSG00000134294	chromatin interactions

Extended variants
information (count: 593 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:593 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7956629	chr12:46590364-46590365	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs145076485	chr12:46590495-46590496	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs572583454	chr12:46590607-46590608	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs376461876	chr12:46590619-46590620	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs187099964	chr12:46590622-46590623	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs557948272	chr12:46590673-46590674	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs577878915	chr12:46590730-46590731	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs543749492	chr12:46590776-46590777	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs562143668	chr12:46590862-46590863	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs575983738	chr12:46590895-46590896	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs527806946	chr12:46590937-46590938	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs147629171	chr12:46590983-46590984	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs561595868	chr12:46590990-46590991	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs12313010	chr12:46590995-46590996	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs117695260	chr12:46590999-46591000	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs532019543	chr12:46591012-46591013	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs564282424	chr12:46591033-46591034	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs562316156	chr12:46591035-46591036	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs142288842	chr12:46591038-46591039	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs12299972	chr12:46591047-46591048	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs191864748	chr12:46591063-46591064	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs549372467	chr12:46591068-46591069	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs566009566	chr12:46591069-46591070	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs534794042	chr12:46591100-46591101	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs375672594	chr12:46591143-46591144	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs557924414	chr12:46591163-46591164	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs577866744	chr12:46591195-46591196	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs537327935	chr12:46591196-46591197	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs11609449	chr12:46591221-46591222	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
30	rs574292372	chr12:46591222-46591223	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs184514965	chr12:46591291-46591292	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs6582621	chr12:46591337-46591338	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs147818061	chr12:46591370-46591371	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs541167842	chr12:46591377-46591378	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs377472399	chr12:46591391-46591392	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs564268294	chr12:46591467-46591468	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs368999478	chr12:46591526-46591527	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs372380276	chr12:46591540-46591541	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs267603472	chr12:46591572-46591573	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs201058166	chr12:46591583-46591584	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs189219749	chr12:46591593-46591594	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs140333362	chr12:46591624-46591625	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs115280791	chr12:46591630-46591631	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs373274606	chr12:46591674-46591675	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs547970163	chr12:46591678-46591679	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs113926825	chr12:46591680-46591681	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs199678692	chr12:46591681-46591682	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs370697142	chr12:46591688-46591689	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs373413303	chr12:46591699-46591700	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs377483452	chr12:46591765-46591766	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
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
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
T-cell prolymphocytic leukemia	17713554	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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Gastric cancer	18160780	CNVD
Myelofibrosis	22110671	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
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21542898	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:609 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:46579000-46594200	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr12:46581600-46603200	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr12:46582200-46603200	Weak transcription	Small Intestine	intestine
4	chr12:46583600-46591800	Weak transcription	Liver	Liver
5	chr12:46585000-46592400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
6	chr12:46585200-46592800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr12:46585200-46593000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
8	chr12:46585400-46590600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr12:46585400-46591800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr12:46585400-46592800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
11	chr12:46586000-46592600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
12	chr12:46586200-46590800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
13	chr12:46586800-46595400	Strong transcription	Placenta	Placenta
14	chr12:46587000-46593000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
15	chr12:46587200-46590600	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr12:46587200-46591000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
17	chr12:46587400-46590400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
18	chr12:46587400-46602000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr12:46587400-46602000	Strong transcription	Muscle Satellite Cultured Cells	--
20	chr12:46587400-46603000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr12:46587800-46601400	Strong transcription	HSMMtube	muscle
22	chr12:46588000-46590600	ZNF genes & repeats	Fetal Intestine Small	intestine
23	chr12:46588000-46590800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
24	chr12:46588000-46593800	Strong transcription	Fetal Muscle Leg	muscle
25	chr12:46588000-46598600	Strong transcription	Primary B cells from peripheral blood	blood
26	chr12:46588000-46603000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr12:46588200-46591000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
28	chr12:46588200-46593000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr12:46588200-46598600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr12:46588200-46598800	Strong transcription	Primary T helper cells PMA-I stimulated	--
31	chr12:46588200-46598800	Strong transcription	Primary T helper cells fromperipheralblood	blood
32	chr12:46588200-46601200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr12:46588200-46601400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr12:46588200-46602200	Strong transcription	HUVEC	blood vessel
35	chr12:46588400-46590600	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr12:46588400-46592200	Strong transcription	Placenta Amnion	Placenta Amnion
37	chr12:46588400-46592800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr12:46588400-46593000	Strong transcription	Skeletal Muscle Male	skeletal muscle
39	chr12:46588400-46593000	Strong transcription	Stomach Smooth Muscle	stomach
40	chr12:46588400-46593800	Strong transcription	Fetal Intestine Large	intestine
41	chr12:46588400-46594200	Strong transcription	Primary T killer memory cells from peripheral blood	blood
42	chr12:46588400-46599800	Strong transcription	Primary T cells from cord blood	blood
43	chr12:46588400-46600400	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr12:46588400-46601400	Strong transcription	Rectal Mucosa Donor 29	rectum
45	chr12:46588400-46602200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr12:46588400-46602400	Strong transcription	HMEC	breast
47	chr12:46588600-46590800	Strong transcription	Brain Inferior Temporal Lobe	brain
48	chr12:46588600-46591200	Strong transcription	Fetal Heart	heart
49	chr12:46588600-46591200	ZNF genes & repeats	K562	blood
50	chr12:46588600-46592600	ZNF genes & repeats	GM12878-XiMat	blood

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