Variant report

Variant	nsv1041733
Chromosome Location	chr12:32247427-32312547
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1560)
CpG islands
(count:1221)
Chromatin interactive
region (count:49)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1560 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:32284640-32284932	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:32259705-32259888	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:32261459-32261489	K562	blood:	n/a	n/a
4	ARID3A	chr12:32260581-32260894	K562	blood:	n/a	n/a
5	ARID3A	chr12:32288688-32289629	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:32293830-32294110	HepG2	liver:	n/a	n/a
7	ATF1	chr12:32273598-32273605	K562	blood:	n/a	n/a
8	ATF1	chr12:32268645-32268952	K562	blood:	n/a	n/a
9	ATF2	chr12:32292690-32293098	GM12878	blood:	n/a	n/a
10	ATF2	chr12:32287345-32287885	GM12878	blood:	n/a	n/a
11	ATF2	chr12:32292706-32293143	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr12:32291754-32292465	GM12878	blood:	n/a	n/a
13	ATF2	chr12:32291665-32292570	GM12878	blood:	n/a	n/a
14	ATF3	chr12:32259460-32259931	K562	blood:	n/a	chr12:32259560-32259569 chr12:32259720-32259729
15	BACH1	chr12:32273308-32273757	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr12:32263997-32264250	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr12:32259289-32260021	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr12:32299183-32299595	GM12878	blood:	n/a	n/a
19	BATF	chr12:32292015-32292310	GM12878	blood:	n/a	n/a
20	BATF	chr12:32299229-32299485	GM12878	blood:	n/a	n/a
21	BATF	chr12:32291949-32292283	GM12878	blood:	n/a	n/a
22	BATF	chr12:32287432-32287765	GM12878	blood:	n/a	n/a
23	BATF	chr12:32287405-32287816	GM12878	blood:	n/a	n/a
24	BCL11A	chr12:32291882-32292363	GM12878	blood:	n/a	chr12:32292146-32292155
25	BCL11A	chr12:32273449-32273737	H1-hESC	embryonic stem cell:	n/a	chr12:32273476-32273485
26	BCL11A	chr12:32273515-32273725	H1-hESC	embryonic stem cell:	n/a	n/a
27	BCL11A	chr12:32292017-32292219	GM12878	blood:	n/a	chr12:32292146-32292155
28	BCL3	chr12:32259595-32260532	A549	lung:	n/a	chr12:32259946-32259959 chr12:32259690-32259699 chr12:32259939-32259952 chr12:32259952-32259965 chr12:32259948-32259961
29	BCL3	chr12:32291970-32292385	GM12878	blood:	n/a	chr12:32292146-32292155
30	BCLAF1	chr12:32291936-32292503	GM12878	blood:	n/a	chr12:32292146-32292155
31	BCLAF1	chr12:32287335-32287915	GM12878	blood:	n/a	n/a
32	BCLAF1	chr12:32259283-32259958	GM12878	blood:	n/a	chr12:32259690-32259699 chr12:32259552-32259561 chr12:32259939-32259952
33	BCLAF1	chr12:32299002-32299526	GM12878	blood:	n/a	n/a
34	BCLAF1	chr12:32291865-32293224	GM12878	blood:	n/a	chr12:32292146-32292155
35	BHLHE40	chr12:32291923-32292385	GM12878	blood:	n/a	n/a
36	BHLHE40	chr12:32260621-32260743	GM12878	blood:	n/a	n/a
37	BHLHE40	chr12:32299218-32299398	GM12878	blood:	n/a	n/a
38	BHLHE40	chr12:32257567-32257753	K562	blood:	n/a	n/a
39	BHLHE40	chr12:32259497-32260130	K562	blood:	n/a	chr12:32259515-32259531 chr12:32259946-32259962 chr12:32259951-32259967 chr12:32259788-32259804 chr12:32259945-32259961
40	BHLHE40	chr12:32308882-32309027	K562	blood:	n/a	n/a
41	BRCA1	chr12:32259617-32260086	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr12:32259461-32259921	HepG2	liver:	n/a	n/a
43	CBX3	chr12:32259339-32260140	K562	blood:	n/a	n/a
44	CBX3	chr12:32268386-32269225	HCT-116	colon:	n/a	n/a
45	CCNT2	chr12:32263204-32263404	K562	blood:	n/a	n/a
46	CCNT2	chr12:32273450-32273638	K562	blood:	n/a	n/a
47	CCNT2	chr12:32259388-32260157	K562	blood:	n/a	chr12:32259720-32259729
48	CCNT2	chr12:32260677-32260970	K562	blood:	n/a	n/a
49	CEBPB	chr12:32259716-32259784	K562	blood:	n/a	n/a
50	CEBPB	chr12:32284640-32284914	HepG2	liver:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:32260103-32260153	PANC-1	pancreas:	n/a
2	chr12:32260103-32260153	PANC-1	pancreas:	n/a
3	chr12:32260376-32260426	ProgFib	skin:	n/a
4	chr12:32255927-32255977	Hela-S3	cervix:	n/a
5	chr12:32277197-32277247	HCPEpiC	choroid plexus:	n/a
6	chr12:32263164-32263214	AG10803	skin:	n/a
7	chr12:32255927-32255977	PANC-1	pancreas:	n/a
8	chr12:32259462-32259512	Hela-S3	cervix:	n/a
9	chr12:32260442-32260492	U87	brain:	n/a
10	chr12:32258877-32258927	HRCEpiC	kidney:	n/a
11	chr12:32263164-32263214	HL-60	blood:	n/a
12	chr12:32260376-32260426	GM12892	blood:	n/a
13	chr12:32259462-32259512	BJ	skin:	n/a
14	chr12:32308125-32308175	ECC-1	luminal epithelium:	n/a
15	chr12:32271511-32271561	AG09309	skin:	n/a
16	chr12:32277197-32277247	SK-N-MC	brain:	n/a
17	chr12:32260376-32260426	AG04450	lung:	fetal
18	chr12:32292997-32293047	MCF10A-Er-Src	breast:	n/a
19	chr12:32277197-32277247	HCT-116	colon:	n/a
20	chr12:32260000-32260050	AG09309	skin:	n/a
21	chr12:32259544-32259594	HPAEpiC	pulmonary alveolar:	n/a
22	chr12:32255927-32255977	HPAEpiC	pulmonary alveolar:	n/a
23	chr12:32292997-32293047	SAEC	small airway:	n/a
24	chr12:32287236-32287286	AG09319	gingival:	n/a
25	chr12:32260376-32260426	NHBE	bronchial:	n/a
26	chr12:32259462-32259512	GM12892	blood:	n/a
27	chr12:32259544-32259594	Caco-2	colon:	n/a
28	chr12:32259544-32259594	U87	brain:	n/a
29	chr12:32255927-32255977	HCF	heart:	n/a
30	chr12:32299085-32299135	CMK	blood:	n/a
31	chr12:32260018-32260068	AG10803	skin:	n/a
32	chr12:32258877-32258927	BE2_C	brain:	n/a
33	chr12:32260376-32260426	HEK293	kidney:	embryo
34	chr12:32309670-32309720	HL-60	blood:	n/a
35	chr12:32260442-32260492	GM19239	blood:	n/a
36	chr12:32271511-32271561	H1-hESC	embryonic stem cell:	embryo
37	chr12:32308125-32308175	SAEC	small airway:	n/a
38	chr12:32260091-32260141	AG09309	skin:	n/a
39	chr12:32299085-32299135	SAEC	small airway:	n/a
40	chr12:32263164-32263214	SKMC	muscle:	n/a
41	chr12:32277197-32277247	HRPEpiC	eye:	n/a
42	chr12:32260442-32260492	GM12891	blood:	n/a
43	chr12:32308125-32308175	NB4	blood:	n/a
44	chr12:32259703-32259753	T-47D	breast:	n/a
45	chr12:32260091-32260141	LNCaP	prostate:	n/a
46	chr12:32259544-32259594	HUVEC	blood vessel:	n/a
47	chr12:32260091-32260141	GM19239	blood:	n/a
48	chr12:32260442-32260492	BJ	skin:	n/a
49	chr12:32277197-32277247	NHDF-neo	bronchial:	n/a
50	chr12:32260000-32260050	SKMC	muscle:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:32266483..32268686-chr12:32270377..32273170,2	MCF-7	breast:
2	chr12:32282801..32284501-chr12:32289010..32291503,2	K562	blood:
3	chr12:32303242..32304848-chr12:32309924..32311593,2	K562	blood:
4	chr12:32286132..32287839-chr12:32288847..32291147,2	K562	blood:
5	chr12:32293794..32295739-chr12:32312256..32314518,2	K562	blood:
6	chr12:32251948..32253659-chr12:32257584..32260500,2	MCF-7	breast:
7	chr12:32289581..32291718-chr12:32293913..32296070,2	K562	blood:
8	chr12:32255421..32257599-chr12:32259211..32261141,2	MCF-7	breast:
9	chr12:32258502..32261631-chr12:32261998..32266748,8	K562	blood:
10	chr12:32246977..32248862-chr12:32261358..32263191,2	K562	blood:
11	chr12:32311735..32314628-chr17:57918387..57920948,2	MCF-7	breast:
12	chr12:32260676..32263344-chr12:32452464..32455287,2	MCF-7	breast:
13	chr12:32257278..32259683-chr12:32278967..32281640,2	MCF-7	breast:
14	chr12:32258139..32262130-chr12:32264296..32270162,5	K562	blood:
15	chr12:32260830..32263543-chr12:32269172..32271594,2	MCF-7	breast:
16	chr12:32264689..32269066-chr12:32271365..32275666,5	K562	blood:
17	chr12:32247038..32249750-chr12:32258395..32261347,2	MCF-7	breast:
18	chr12:32246977..32248862-chr12:32261358..32263191,2	K562	blood:
19	chr12:32308162..32310894-chr12:32324401..32326618,2	MCF-7	breast:
20	chr12:32303242..32304848-chr12:32309924..32311593,2	K562	blood:
21	chr12:32293794..32295739-chr12:32312256..32314518,2	K562	blood:
22	chr12:32303348..32305774-chr12:32310093..32311635,2	K562	blood:
23	chr12:32260677..32263592-chr12:32286494..32288195,2	MCF-7	breast:
24	chr12:32270889..32273201-chr12:32278383..32279888,2	K562	blood:
25	chr12:32258248..32259913-chr12:32280000..32281853,2	K562	blood:
26	chr12:32286132..32287839-chr12:32288847..32291147,2	K562	blood:
27	chr12:32259049..32259569-chr8:146052164..146052785,2	NB4	blood:
28	chr12:32270760..32273640-chr12:32274008..32276299,2	K562	blood:
29	chr12:32254333..32256394-chr12:32262873..32265545,2	K562	blood:
30	chr12:32260830..32263543-chr12:32269172..32271594,2	MCF-7	breast:
31	chr12:32266483..32268686-chr12:32270377..32273170,2	MCF-7	breast:
32	chr12:32260649..32262291-chr12:32271936..32273601,2	MCF-7	breast:
33	chr12:32254187..32255875-chr12:32258802..32261694,2	K562	blood:
34	chr12:31477784..31479544-chr12:32254408..32256874,2	K562	blood:
35	chr12:32260649..32262291-chr12:32271936..32273601,2	MCF-7	breast:
36	chr12:32258933..32260496-chr12:32285593..32287517,2	MCF-7	breast:
37	chr12:31880708..31883036-chr12:32258362..32261321,3	K562	blood:
38	chr1:8084249..8084749-chr12:32303184..32303685,2	Hela-S3	cervix:
39	chr12:32303348..32305774-chr12:32310093..32311635,2	K562	blood:
40	chr12:32258592..32261102-chr12:32271397..32273435,2	MCF-7	breast:
41	chr12:32254333..32256394-chr12:32262873..32265545,2	K562	blood:
42	chr12:32270889..32273201-chr12:32278383..32279888,2	K562	blood:
43	chr12:32282801..32284501-chr12:32289010..32291503,2	K562	blood:
44	chr12:32289581..32291718-chr12:32293913..32296070,2	K562	blood:
45	chr12:32261687..32264441-chr12:32470359..32472104,2	MCF-7	breast:
46	chr12:32257278..32259683-chr12:32278967..32281640,2	MCF-7	breast:
47	chr12:32270760..32273640-chr12:32274008..32276299,2	K562	blood:
48	chr12:32260677..32263592-chr12:32286494..32288195,2	MCF-7	breast:
49	chr12:32264689..32269066-chr12:32271365..32275666,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-H3F3C-4	chr12:32257051-32257224	ENSG00000257530.1
2	lnc-H3F3C-4	chr12:32257610-32257707	ENSG00000257530.1
3	lnc-H3F3C-8	chr12:32253419-32253669	NONHSAT027605
4	lnc-H3F3C-4	chr12:32260328-32260462	ENSG00000257530.1

No data

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

Extended variants
information (count: 2636 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2636 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558732022	chr12:32247432-32247433	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs73308369	chr12:32247477-32247478	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs535421454	chr12:32247502-32247503	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs626254	chr12:32247530-32247531	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs625819	chr12:32247628-32247629	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs625806	chr12:32247638-32247639	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs189523717	chr12:32247648-32247649	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs78401797	chr12:32247652-32247653	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs140331291	chr12:32247684-32247685	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs180768272	chr12:32247685-32247686	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs539958637	chr12:32247688-32247689	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs531509493	chr12:32247693-32247694	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs551560762	chr12:32247694-32247695	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs186448411	chr12:32247700-32247701	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs527757755	chr12:32247705-32247706	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs547889141	chr12:32247727-32247728	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs73308371	chr12:32247756-32247757	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs189308594	chr12:32247770-32247771	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs681525	chr12:32247808-32247809	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs181735815	chr12:32247824-32247825	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs681412	chr12:32247885-32247886	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs664672	chr12:32247889-32247890	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs149952486	chr12:32247896-32247897	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs538956322	chr12:32247905-32247906	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs2460872	chr12:32247918-32247919	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs112294022	chr12:32247947-32247948	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs680975	chr12:32247974-32247975	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs186967000	chr12:32247975-32247976	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs534918291	chr12:32248172-32248173	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs61662064	chr12:32248174-32248175	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs191303121	chr12:32248177-32248178	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs145143246	chr12:32248189-32248190	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs57927254	chr12:32248233-32248234	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs576367255	chr12:32248266-32248267	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs545343820	chr12:32248317-32248318	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs183220628	chr12:32248366-32248367	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs186206527	chr12:32248435-32248436	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs527466756	chr12:32248436-32248437	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs4001796	chr12:32248437-32248438	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs367823586	chr12:32248438-32248439	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs3983577	chr12:32248456-32248457	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs36017540	chr12:32248457-32248458	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs541266189	chr12:32248464-32248465	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs114539162	chr12:32248536-32248537	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs530141822	chr12:32248598-32248599	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs149031255	chr12:32248643-32248644	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs565910550	chr12:32248649-32248650	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs528144452	chr12:32248651-32248652	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs115328262	chr12:32248687-32248688	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs376910906	chr12:32248696-32248697	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Myelofibrosis	22110671	CNVD
microdeletion syndrome	16199537	CNVD
Chordoma	18071362	CNVD
Cancer	20164920	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2222 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:32230000-32259200	Weak transcription	Right Atrium	heart
2	chr12:32243000-32253400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr12:32243400-32250000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr12:32243400-32253400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr12:32247400-32248600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr12:32248600-32249000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr12:32249000-32250800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr12:32249600-32250000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr12:32249800-32250400	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr12:32250000-32250200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr12:32250000-32250400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr12:32250600-32258600	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr12:32250800-32251400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr12:32251000-32251400	Enhancers	HUVEC	blood vessel
15	chr12:32252200-32252400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr12:32252200-32252400	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr12:32252200-32252400	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr12:32252200-32252800	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr12:32252400-32252600	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr12:32252400-32253400	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr12:32252400-32253400	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr12:32252400-32253400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr12:32252600-32258400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr12:32252800-32253200	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr12:32253200-32253800	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr12:32253400-32253800	Enhancers	H1 Cell Line	embryonic stem cell
27	chr12:32253400-32253800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr12:32253400-32254200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr12:32253400-32254200	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr12:32253400-32254200	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr12:32253400-32254200	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr12:32253400-32254400	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr12:32253400-32254400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr12:32253800-32254000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr12:32253800-32257400	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr12:32253800-32258400	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr12:32253800-32258800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr12:32254000-32259000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr12:32254200-32257400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr12:32254200-32258400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr12:32254200-32258600	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr12:32254400-32257400	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr12:32254400-32257400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr12:32255000-32255200	Enhancers	NHDF-Ad	bronchial
45	chr12:32255200-32259000	Weak transcription	NHDF-Ad	bronchial
46	chr12:32257000-32258800	Weak transcription	HUVEC	blood vessel
47	chr12:32257200-32257800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr12:32257200-32257800	Enhancers	K562	blood
49	chr12:32257200-32258000	Enhancers	Fetal Heart	heart
50	chr12:32257400-32257600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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