Variant report

Variant	nsv983498
Chromosome Location	chr12:32153446-32388092
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3473)
CpG islands
(count:1711)
Chromatin interactive
region (count:117)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3473 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:32200362-32201261	K562	blood:	n/a	n/a
2	ARID3A	chr12:32153228-32153727	K562	blood:	n/a	n/a
3	ARID3A	chr12:32158464-32158892	K562	blood:	n/a	n/a
4	ARID3A	chr12:32259705-32259888	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:32183003-32183359	K562	blood:	n/a	n/a
6	ARID3A	chr12:32213606-32213852	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:32284640-32284932	HepG2	liver:	n/a	n/a
8	ARID3A	chr12:32288688-32289629	HepG2	liver:	n/a	n/a
9	ARID3A	chr12:32213547-32213848	K562	blood:	n/a	n/a
10	ARID3A	chr12:32182766-32182776	K562	blood:	n/a	n/a
11	ARID3A	chr12:32187062-32187394	K562	blood:	n/a	n/a
12	ARID3A	chr12:32260581-32260894	K562	blood:	n/a	n/a
13	ARID3A	chr12:32173938-32174440	K562	blood:	n/a	n/a
14	ARID3A	chr12:32222000-32222367	HepG2	liver:	n/a	n/a
15	ARID3A	chr12:32192858-32193616	K562	blood:	n/a	n/a
16	ARID3A	chr12:32340026-32340324	HepG2	liver:	n/a	n/a
17	ARID3A	chr12:32261459-32261489	K562	blood:	n/a	n/a
18	ARID3A	chr12:32183690-32184712	K562	blood:	n/a	n/a
19	ARID3A	chr12:32207151-32207474	K562	blood:	n/a	n/a
20	ARID3A	chr12:32173008-32173640	K562	blood:	n/a	chr12:32173009-32173025 chr12:32173012-32173028
21	ARID3A	chr12:32204432-32204885	K562	blood:	n/a	n/a
22	ARID3A	chr12:32293830-32294110	HepG2	liver:	n/a	n/a
23	ATF1	chr12:32205355-32205521	K562	blood:	n/a	n/a
24	ATF1	chr12:32184012-32184492	K562	blood:	n/a	n/a
25	ATF1	chr12:32268645-32268952	K562	blood:	n/a	n/a
26	ATF1	chr12:32203036-32203105	K562	blood:	n/a	n/a
27	ATF1	chr12:32173951-32174406	K562	blood:	n/a	n/a
28	ATF1	chr12:32153310-32153625	K562	blood:	n/a	n/a
29	ATF1	chr12:32204425-32204862	K562	blood:	n/a	n/a
30	ATF1	chr12:32273598-32273605	K562	blood:	n/a	n/a
31	ATF1	chr12:32187095-32187402	K562	blood:	n/a	n/a
32	ATF1	chr12:32200324-32201255	K562	blood:	n/a	n/a
33	ATF1	chr12:32158405-32158812	K562	blood:	n/a	n/a
34	ATF2	chr12:32166327-32166733	H1-hESC	embryonic stem cell:	n/a	n/a
35	ATF2	chr12:32169809-32170266	H1-hESC	embryonic stem cell:	n/a	n/a
36	ATF2	chr12:32292706-32293143	H1-hESC	embryonic stem cell:	n/a	n/a
37	ATF2	chr12:32213411-32213812	GM12878	blood:	n/a	n/a
38	ATF2	chr12:32213478-32213885	GM12878	blood:	n/a	n/a
39	ATF2	chr12:32287345-32287885	GM12878	blood:	n/a	n/a
40	ATF2	chr12:32213450-32213857	H1-hESC	embryonic stem cell:	n/a	n/a
41	ATF2	chr12:32292690-32293098	GM12878	blood:	n/a	n/a
42	ATF2	chr12:32291754-32292465	GM12878	blood:	n/a	n/a
43	ATF2	chr12:32166251-32166794	H1-hESC	embryonic stem cell:	n/a	n/a
44	ATF2	chr12:32349459-32350020	GM12878	blood:	n/a	n/a
45	ATF2	chr12:32291665-32292570	GM12878	blood:	n/a	n/a
46	ATF3	chr12:32158396-32158863	K562	blood:	n/a	n/a
47	ATF3	chr12:32204374-32204872	A549	lung:	n/a	n/a
48	ATF3	chr12:32200736-32201209	K562	blood:	n/a	n/a
49	ATF3	chr12:32259460-32259931	K562	blood:	n/a	chr12:32259560-32259569 chr12:32259720-32259729
50	ATF3	chr12:32183911-32184420	K562	blood:	n/a	n/a

(count:1711 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:32331973-32332023	U87	brain:	n/a
2	chr12:32260442-32260492	SK-N-MC	brain:	n/a
3	chr12:32242870-32242920	SK-N-SH_RA	brain:	n/a
4	chr12:32331973-32332023	U87	brain:	n/a
5	chr12:32260442-32260492	SK-N-MC	brain:	n/a
6	chr12:32242870-32242920	SK-N-SH_RA	brain:	n/a
7	chr12:32192489-32192539	HCM	heart:	n/a
8	chr12:32277197-32277247	Caco-2	colon:	n/a
9	chr12:32242870-32242920	HCM	heart:	n/a
10	chr12:32292997-32293047	RPTEC	kidney:	n/a
11	chr12:32309670-32309720	HMEC	breast:	n/a
12	chr12:32260000-32260050	HRPEpiC	eye:	n/a
13	chr12:32331973-32332023	GM12892	blood:	n/a
14	chr12:32271511-32271561	SAEC	small airway:	n/a
15	chr12:32361535-32361585	HPAEpiC	pulmonary alveolar:	n/a
16	chr12:32308125-32308175	SAEC	small airway:	n/a
17	chr12:32260000-32260050	A549	lung:	n/a
18	chr12:32308125-32308175	GM12878	blood:	n/a
19	chr12:32185731-32185781	HepG2	liver:	n/a
20	chr12:32259338-32259388	HCPEpiC	choroid plexus:	n/a
21	chr12:32242870-32242920	Hela-S3	cervix:	n/a
22	chr12:32309670-32309720	SK-N-SH_RA	brain:	n/a
23	chr12:32292997-32293047	MCF10A-Er-Src	breast:	n/a
24	chr12:32255927-32255977	SK-N-MC	brain:	n/a
25	chr12:32260103-32260153	SK-N-MC	brain:	n/a
26	chr12:32309670-32309720	PANC-1	pancreas:	n/a
27	chr12:32292997-32293047	HNPCEpiC	eye:	n/a
28	chr12:32271511-32271561	AoSMC	blood vessel:	n/a
29	chr12:32255927-32255977	A549	lung:	n/a
30	chr12:32259338-32259388	HNPCEpiC	eye:	n/a
31	chr12:32260091-32260141	HEEpiC	esophagus:	n/a
32	chr12:32260000-32260050	GM12891	blood:	n/a
33	chr12:32192489-32192539	NHBE	bronchial:	n/a
34	chr12:32263164-32263214	A549	lung:	n/a
35	chr12:32299085-32299135	HCF	heart:	n/a
36	chr12:32313007-32313057	PrEC	prostate:	n/a
37	chr12:32260376-32260426	HCM	heart:	n/a
38	chr12:32192489-32192539	PFSK-1	brain:	n/a
39	chr12:32259544-32259594	Caco-2	colon:	n/a
40	chr12:32259462-32259512	H1-hESC	embryonic stem cell:	embryo
41	chr12:32260018-32260068	U87	brain:	n/a
42	chr12:32313007-32313057	BE2_C	brain:	n/a
43	chr12:32259338-32259388	PANC-1	pancreas:	n/a
44	chr12:32255927-32255977	HRPEpiC	eye:	n/a
45	chr12:32299085-32299135	ECC-1	luminal epithelium:	n/a
46	chr12:32260103-32260153	PFSK-1	brain:	n/a
47	chr12:32370933-32370983	HIPEpiC	eye:	n/a
48	chr12:32309670-32309720	Jurkat	blood:	n/a
49	chr12:32308125-32308175	HL-60	blood:	n/a
50	chr12:32259338-32259388	Hela-S3	cervix:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:32110978..32112717-chr12:32158767..32160498,2	K562	blood:
2	chr12:32257278..32259683-chr12:32278967..32281640,2	MCF-7	breast:
3	chr12:32303242..32304848-chr12:32309924..32311593,2	K562	blood:
4	chr12:32270760..32273640-chr12:32274008..32276299,2	K562	blood:
5	chr12:32303242..32304848-chr12:32309924..32311593,2	K562	blood:
6	chr12:32259049..32259569-chr8:146052164..146052785,2	NB4	blood:
7	chr12:32116205..32118530-chr12:32174123..32177069,2	K562	blood:
8	chr12:32213222..32214189-chr12:32464699..32465690,4	MCF-7	breast:
9	chr12:32359581..32362497-chr12:32406536..32409461,2	MCF-7	breast:
10	chr12:32228668..32231442-chr12:32233018..32235183,2	K562	blood:
11	chr12:32185942..32189585-chr12:32195326..32198101,3	K562	blood:
12	chr12:32270760..32273640-chr12:32274008..32276299,2	K562	blood:
13	chr12:32330686..32332341-chr12:32334381..32336776,2	MCF-7	breast:
14	chr12:32331886..32334489-chr12:32336141..32338880,2	MCF-7	breast:
15	chr12:32330903..32333479-chr12:32337570..32339472,2	MCF-7	breast:
16	chr12:32193881..32196557-chr12:32221966..32223576,2	MCF-7	breast:
17	chr12:32337947..32340107-chr12:32424491..32426226,2	MCF-7	breast:
18	chr12:32289581..32291718-chr12:32293913..32296070,2	K562	blood:
19	chr12:32175862..32178406-chr12:32179354..32181196,2	K562	blood:
20	chr12:32378528..32381260-chr12:32382291..32384074,2	K562	blood:
21	chr12:32254333..32256394-chr12:32262873..32265545,2	K562	blood:
22	chr12:32257278..32259683-chr12:32278967..32281640,2	MCF-7	breast:
23	chr12:32258248..32259913-chr12:32280000..32281853,2	K562	blood:
24	chr12:32168121..32171020-chr12:32184096..32185622,2	K562	blood:
25	chr12:32282801..32284501-chr12:32289010..32291503,2	K562	blood:
26	chr12:31835175..31835818-chr12:32213320..32214060,2	MCF-7	breast:
27	chr12:32264689..32269066-chr12:32271365..32275666,5	K562	blood:
28	chr12:32254333..32256394-chr12:32262873..32265545,2	K562	blood:
29	chr12:32264689..32269066-chr12:32271365..32275666,5	K562	blood:
30	chr12:32228668..32231442-chr12:32233018..32235183,2	K562	blood:
31	chr12:32227476..32229609-chr12:32237278..32240241,2	K562	blood:
32	chr12:32293794..32295739-chr12:32312256..32314518,2	K562	blood:
33	chr12:32221817..32224949-chr12:32258403..32261337,3	MCF-7	breast:
34	chr12:32260677..32263592-chr12:32286494..32288195,2	MCF-7	breast:
35	chr12:32323730..32326324-chr12:32330475..32332808,2	MCF-7	breast:
36	chr12:32185942..32189585-chr12:32195326..32198101,3	K562	blood:
37	chr12:31477784..31479544-chr12:32254408..32256874,2	K562	blood:
38	chr12:32247038..32249750-chr12:32258395..32261347,2	MCF-7	breast:
39	chr12:32173443..32176016-chr12:32188514..32190413,2	K562	blood:
40	chr1:8084249..8084749-chr12:32303184..32303685,2	Hela-S3	cervix:
41	chr12:32260830..32263543-chr12:32269172..32271594,2	MCF-7	breast:
42	chr12:32303348..32305774-chr12:32310093..32311635,2	K562	blood:
43	chr12:32251948..32253659-chr12:32257584..32260500,2	MCF-7	breast:
44	chr12:32184129..32186800-chr12:32198545..32200849,2	K562	blood:
45	chr12:32266483..32268686-chr12:32270377..32273170,2	MCF-7	breast:
46	chr12:32260830..32263543-chr12:32269172..32271594,2	MCF-7	breast:
47	chr12:32270889..32273201-chr12:32278383..32279888,2	K562	blood:
48	chr12:31880708..31883036-chr12:32258362..32261321,3	K562	blood:
49	chr12:32258502..32261631-chr12:32261998..32266748,8	K562	blood:
50	chr12:32286132..32287839-chr12:32288847..32291147,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BICD1-2	chr12:32204371-32204515	NONHSAT027603
2	lnc-C12orf35-4	chr12:32154358-32155125	NONHSAT027600
3	lnc-C12orf35-7	chr12:32160061-32160369	NONHSAT027602
4	lnc-BICD1-2	chr12:32204070-32204143	NONHSAT027603
5	lnc-H3F3C-9	chr12:32380344-32381088	NONHSAT027607
6	lnc-H3F3C-4	chr12:32257610-32257707	ENSG00000257530.1
7	lnc-H3F3C-8	chr12:32253419-32253669	NONHSAT027605
8	lnc-H3F3C-4	chr12:32257051-32257224	ENSG00000257530.1
9	lnc-C12orf35-6	chr12:32155165-32157256	NONHSAT027601
10	lnc-H3F3C-4	chr12:32260328-32260462	ENSG00000257530.1

No data

Variant related genes	Relation type
ENSG00000258134	TF binding region
ENSG00000257852	TF binding region
ENSG00000257094	TF binding region
ENSG00000271357	TF binding region
BICD1	TF binding region
ENSG00000257530	TF binding region
ENSG00000258134	CpG island
ENSG00000257852	CpG island
ENSG00000257094	CpG island
ENSG00000271357	CpG island
BICD1	CpG island
ENSG00000257530	CpG island
ENSG00000151743	chromatin interactions
ENSG00000258134	chromatin interactions
ENSG00000139146	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000257530	chromatin interactions
ENSG00000151746	chromatin interactions
ENSG00000174718	chromatin interactions

Extended variants
information (count: 9822 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:9822 , 50 per page) page: 1 2 3 4 5 6 7 ... 197

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184121212	chr12:32153453-32153454	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs566222760	chr12:32153501-32153502	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs535219967	chr12:32153541-32153542	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs146646346	chr12:32153602-32153603	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs141198783	chr12:32153618-32153619	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs370508789	chr12:32153645-32153646	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs61553197	chr12:32153646-32153647	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs531047536	chr12:32153659-32153660	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs2594036	chr12:32153661-32153662	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs561003295	chr12:32153670-32153671	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs200118941	chr12:32153682-32153683	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182053734	chr12:32153806-32153807	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554054957	chr12:32153809-32153810	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574158291	chr12:32153810-32153811	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs187156845	chr12:32153828-32153829	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs112914173	chr12:32153876-32153877	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs562835616	chr12:32153878-32153879	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576403794	chr12:32153905-32153906	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs7979317	chr12:32153915-32153916	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs202196542	chr12:32153933-32153934	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs9788276	chr12:32153966-32153967	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs528019122	chr12:32153992-32153993	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs63644860	chr12:32154014-32154015	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs201490443	chr12:32154035-32154036	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs74071822	chr12:32154036-32154037	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs188845437	chr12:32154056-32154057	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs10583078	chr12:32154067-32154068	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs528940329	chr12:32154109-32154110	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs112312706	chr12:32154133-32154134	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs148322540	chr12:32154146-32154147	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537856034	chr12:32154183-32154184	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs575903727	chr12:32154185-32154186	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs77009402	chr12:32154203-32154204	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553991287	chr12:32154220-32154221	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs573894625	chr12:32154241-32154242	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs368497708	chr12:32154263-32154264	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs67535682	chr12:32154308-32154309	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs386761819	chr12:32154310-32154311	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs576319966	chr12:32154312-32154313	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs398076556	chr12:32154320-32154321	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs201418360	chr12:32154321-32154322	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs202148928	chr12:32154322-32154323	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs545378882	chr12:32154331-32154332	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs59579014	chr12:32154334-32154335	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs181303321	chr12:32154390-32154391	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs541359719	chr12:32154402-32154403	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs150430337	chr12:32154405-32154406	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs111283194	chr12:32154440-32154441	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs12302346	chr12:32154445-32154446	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs562594358	chr12:32154451-32154452	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	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
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
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
microdeletion syndrome	16199537	CNVD
Chordoma	18071362	CNVD
Cancer	20164920	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:4124 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:32134800-32155400	Weak transcription	NHDF-Ad	bronchial
2	chr12:32135000-32156000	Weak transcription	Brain Cingulate Gyrus	brain
3	chr12:32135000-32156400	Weak transcription	Gastric	stomach
4	chr12:32136000-32155000	Weak transcription	HSMMtube	muscle
5	chr12:32136200-32155400	Weak transcription	Osteobl	bone
6	chr12:32137200-32158600	Weak transcription	HUVEC	blood vessel
7	chr12:32139200-32153800	Strong transcription	HUES64 Cell Line	embryonic stem cell
8	chr12:32139200-32154400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr12:32139800-32153800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
10	chr12:32139800-32154200	Strong transcription	HUES48 Cell Line	embryonic stem cell
11	chr12:32140200-32156200	Strong transcription	Primary neutrophils fromperipheralblood	blood
12	chr12:32140800-32156600	Strong transcription	Thymus	Thymus
13	chr12:32141400-32154200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr12:32141400-32154800	Strong transcription	Fetal Intestine Large	intestine
15	chr12:32141400-32154800	Strong transcription	Fetal Intestine Small	intestine
16	chr12:32141400-32156200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr12:32141800-32154200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr12:32141800-32155000	Strong transcription	HUES6 Cell Line	embryonic stem cell
19	chr12:32142200-32155800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr12:32142600-32155000	Strong transcription	Liver	Liver
21	chr12:32143000-32154800	Strong transcription	H1 Cell Line	embryonic stem cell
22	chr12:32143000-32154800	Strong transcription	Adipose Nuclei	Adipose
23	chr12:32143200-32154400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr12:32143200-32154400	Strong transcription	Primary T helper cells PMA-I stimulated	--
25	chr12:32143200-32156200	Strong transcription	Primary T cells from cord blood	blood
26	chr12:32143800-32154800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr12:32143800-32158400	Weak transcription	Fetal Heart	heart
28	chr12:32144000-32154400	Strong transcription	Dnd41	blood
29	chr12:32144000-32155600	Weak transcription	Small Intestine	intestine
30	chr12:32144200-32154800	Strong transcription	Primary T cells fromperipheralblood	blood
31	chr12:32144400-32155800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr12:32144600-32154400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
33	chr12:32145000-32154800	Strong transcription	Primary T helper cells fromperipheralblood	blood
34	chr12:32145400-32154800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr12:32145600-32154400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr12:32145800-32154200	Strong transcription	Fetal Stomach	stomach
37	chr12:32145800-32154800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr12:32145800-32154800	Strong transcription	Left Ventricle	heart
39	chr12:32145800-32155600	Weak transcription	Stomach Mucosa	stomach
40	chr12:32146400-32153800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr12:32146600-32154800	Strong transcription	Ovary	ovary
42	chr12:32146800-32154400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr12:32146800-32155000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr12:32147200-32154800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr12:32147200-32154800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr12:32147200-32154800	Strong transcription	Primary T helper naive cells from peripheral blood	blood
47	chr12:32147200-32154800	Strong transcription	Fetal Muscle Leg	muscle
48	chr12:32147200-32154800	Strong transcription	Spleen	Spleen
49	chr12:32148000-32154200	Strong transcription	Primary monocytes fromperipheralblood	blood
50	chr12:32148000-32154800	Strong transcription	Placenta	Placenta

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