Variant report

Variant	esv2422366
Chromosome Location	chr12:31071959-31276836
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3160)
CpG islands
(count:2692)
Chromatin interactive
region (count:50)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3160 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:31227121-31227652	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:31205625-31205628	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:31226612-31226780	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:31227278-31227505	K562	blood:	n/a	n/a
5	ATF1	chr12:31219201-31219422	K562	blood:	n/a	n/a
6	ATF1	chr12:31267437-31267611	K562	blood:	n/a	n/a
7	ATF1	chr12:31230204-31230267	K562	blood:	n/a	n/a
8	ATF2	chr12:31270089-31270375	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr12:31226662-31226898	K562	blood:	n/a	n/a
10	BACH1	chr12:31182528-31182802	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr12:31226535-31226812	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr12:31270094-31270475	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr12:31200617-31200912	GM12878	blood:	n/a	chr12:31200777-31200788
14	BATF	chr12:31204619-31204884	GM12878	blood:	n/a	n/a
15	BATF	chr12:31233393-31233591	GM12878	blood:	n/a	n/a
16	BATF	chr12:31228050-31228506	GM12878	blood:	n/a	chr12:31228339-31228347
17	BATF	chr12:31200609-31200914	GM12878	blood:	n/a	chr12:31200777-31200788
18	BATF	chr12:31226544-31227607	GM12878	blood:	n/a	n/a
19	BATF	chr12:31227825-31228526	GM12878	blood:	n/a	chr12:31228339-31228347
20	BATF	chr12:31233397-31233563	GM12878	blood:	n/a	n/a
21	BATF	chr12:31253312-31253563	GM12878	blood:	n/a	n/a
22	BCL11A	chr12:31227413-31227974	GM12878	blood:	n/a	chr12:31227476-31227485 chr12:31227507-31227514
23	BCL11A	chr12:31227467-31227641	GM12878	blood:	n/a	chr12:31227476-31227485 chr12:31227507-31227514
24	BCL11A	chr12:31133143-31133385	GM12878	blood:	n/a	n/a
25	BCL11A	chr12:31226719-31227117	GM12878	blood:	n/a	chr12:31226785-31226794 chr12:31227056-31227065
26	BCL11A	chr12:31228004-31228492	GM12878	blood:	n/a	n/a
27	BCL11A	chr12:31228135-31228506	GM12878	blood:	n/a	n/a
28	BCL11A	chr12:31226764-31227047	GM12878	blood:	n/a	chr12:31226785-31226794
29	BCL3	chr12:31236203-31236417	GM12878	blood:	n/a	n/a
30	BCL3	chr12:31236196-31236433	GM12878	blood:	n/a	n/a
31	BHLHE40	chr12:31203581-31203781	K562	blood:	n/a	n/a
32	BHLHE40	chr12:31253866-31254071	GM12878	blood:	n/a	n/a
33	BHLHE40	chr12:31252507-31252676	GM12878	blood:	n/a	n/a
34	BHLHE40	chr12:31143178-31143220	A549	lung:	n/a	n/a
35	BHLHE40	chr12:31227096-31227339	K562	blood:	n/a	chr12:31227176-31227192
36	BHLHE40	chr12:31165039-31165126	K562	blood:	n/a	n/a
37	BHLHE40	chr12:31270127-31270331	GM12878	blood:	n/a	n/a
38	BHLHE40	chr12:31227101-31227187	GM12878	blood:	n/a	n/a
39	BHLHE40	chr12:31226599-31226889	GM12878	blood:	n/a	n/a
40	BHLHE40	chr12:31219222-31219531	K562	blood:	n/a	n/a
41	BHLHE40	chr12:31138858-31138979	K562	blood:	n/a	n/a
42	BHLHE40	chr12:31253434-31253625	GM12878	blood:	n/a	n/a
43	BHLHE40	chr12:31204659-31204964	GM12878	blood:	n/a	n/a
44	BHLHE40	chr12:31226533-31226888	K562	blood:	n/a	n/a
45	BHLHE40	chr12:31270186-31270438	K562	blood:	n/a	n/a
46	BRCA1	chr12:31270178-31270208	GM12878	blood:	n/a	n/a
47	BRCA1	chr12:31226555-31227323	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr12:31226630-31226830	GM12878	blood:	n/a	n/a
49	CBX3	chr12:31224793-31225171	K562	blood:	n/a	n/a
50	CBX3	chr12:31219097-31219592	K562	blood:	n/a	n/a

(count:2692 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:31257362-31257412	AG09309	skin:	n/a
2	chr12:31272119-31272169	MCF-7	breast:	n/a
3	chr12:31254007-31254057	RPTEC	kidney:	n/a
4	chr12:31226441-31226491	BE2_C	brain:	n/a
5	chr12:31156691-31156741	HUVEC	blood vessel:	n/a
6	chr12:31226801-31226851	ECC-1	luminal epithelium:	n/a
7	chr12:31254036-31254086	HNPCEpiC	eye:	n/a
8	chr12:31130225-31130275	HEEpiC	esophagus:	n/a
9	chr12:31257362-31257412	AG09309	skin:	n/a
10	chr12:31272119-31272169	MCF-7	breast:	n/a
11	chr12:31254007-31254057	RPTEC	kidney:	n/a
12	chr12:31226441-31226491	BE2_C	brain:	n/a
13	chr12:31156691-31156741	HUVEC	blood vessel:	n/a
14	chr12:31226801-31226851	ECC-1	luminal epithelium:	n/a
15	chr12:31254036-31254086	HNPCEpiC	eye:	n/a
16	chr12:31130225-31130275	HEEpiC	esophagus:	n/a
17	chr12:31138958-31139008	AG09319	gingival:	n/a
18	chr12:31226718-31226768	ECC-1	luminal epithelium:	n/a
19	chr12:31079583-31079633	HEK293	kidney:	embryo
20	chr12:31226801-31226851	RPTEC	kidney:	n/a
21	chr12:31226536-31226586	HepG2	liver:	n/a
22	chr12:31226606-31226656	U87	brain:	n/a
23	chr12:31080052-31080102	AoSMC	blood vessel:	n/a
24	chr12:31227271-31227321	IMR90	lung:	fetal
25	chr12:31138958-31139008	AG10803	skin:	n/a
26	chr12:31226606-31226656	AG04449	skin:	fetal
27	chr12:31256838-31256888	HIPEpiC	eye:	n/a
28	chr12:31272865-31272915	PrEC	prostate:	n/a
29	chr12:31227271-31227321	PFSK-1	brain:	n/a
30	chr12:31226536-31226586	PANC-1	pancreas:	n/a
31	chr12:31079694-31079744	HepG2	liver:	n/a
32	chr12:31226714-31226764	HEEpiC	esophagus:	n/a
33	chr12:31230936-31230986	HMEC	breast:	n/a
34	chr12:31226441-31226491	AG09319	gingival:	n/a
35	chr12:31226441-31226491	HRPEpiC	eye:	n/a
36	chr12:31271783-31271833	HCF	heart:	n/a
37	chr12:31189289-31189339	SK-N-SH	brain:	n/a
38	chr12:31078790-31078840	NB4	blood:	n/a
39	chr12:31226801-31226851	GM19239	blood:	n/a
40	chr12:31272119-31272169	BJ	skin:	n/a
41	chr12:31241496-31241546	T-47D	breast:	n/a
42	chr12:31226718-31226768	HCPEpiC	choroid plexus:	n/a
43	chr12:31233201-31233251	GM06990	blood:	n/a
44	chr12:31226718-31226768	K562	blood:	n/a
45	chr12:31230936-31230986	AG09309	skin:	n/a
46	chr12:31257362-31257412	ProgFib	skin:	n/a
47	chr12:31227271-31227321	GM06990	blood:	n/a
48	chr12:31149418-31149468	ECC-1	luminal epithelium:	n/a
49	chr12:31255279-31255329	HMEC	breast:	n/a
50	chr12:31226825-31226875	MCF10A-Er-Src	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:31173555..31175653-chr12:31188660..31191059,2	MCF-7	breast:
2	chr12:31070913..31073527-chr12:31081618..31083991,3	MCF-7	breast:
3	chr12:31112508..31114318-chr12:31114721..31117661,2	K562	blood:
4	chr12:31121879..31124648-chr12:31129528..31132087,2	K562	blood:
5	chr12:30999859..31000781-chr12:31142534..31143349,2	K562	blood:
6	chr12:31108040..31110070-chr12:31110418..31112146,2	K562	blood:
7	chr12:31190011..31191899-chr12:31193367..31195134,2	K562	blood:
8	chr12:31121879..31124648-chr12:31129528..31132087,2	K562	blood:
9	chr12:31159465..31161712-chr12:31163343..31166025,2	K562	blood:
10	chr12:31118639..31119261-chr12:31138195..31139078,2	MCF-7	breast:
11	chr12:31122020..31124643-chr12:31127496..31129096,2	K562	blood:
12	chr12:31082310..31084451-chr12:31104159..31107270,3	MCF-7	breast:
13	chr12:31191870..31193698-chr12:31194648..31196462,2	K562	blood:
14	chr12:9620489..9621323-chr12:31206721..31207493,2	MCF-7	breast:
15	chr12:31070913..31073527-chr12:31081618..31083991,3	MCF-7	breast:
16	chr12:31048548..31050529-chr12:31126004..31127624,2	MCF-7	breast:
17	chr12:9436173..9436735-chr12:31226434..31227168,3	Hela-S3	cervix:
18	chr12:31116301..31118839-chr12:31122102..31125851,3	K562	blood:
19	chr12:31082310..31084451-chr12:31104159..31107270,3	MCF-7	breast:
20	chr12:31122291..31124648-chr12:31129528..31132132,2	K562	blood:
21	chr12:9620209..9621328-chr12:31206996..31207808,4	MCF-7	breast:
22	chr12:31226738..31227630-chr20:47894738..47895520,2	Hela-S3	cervix:
23	chr12:31116301..31118839-chr12:31122102..31125851,3	K562	blood:
24	chr12:31004147..31004726-chr12:31088536..31089374,2	MCF-7	breast:
25	chr12:31086101..31088564-chr12:31089320..31090867,2	K562	blood:
26	chr12:31105834..31108432-chr12:31108761..31111175,2	K562	blood:
27	chr12:31118586..31119188-chr12:31138566..31139432,2	MCF-7	breast:
28	chr12:31122291..31124648-chr12:31129528..31132132,2	K562	blood:
29	chr12:31191870..31193698-chr12:31194648..31196462,2	K562	blood:
30	chr12:31108040..31110070-chr12:31110418..31112146,2	K562	blood:
31	chr12:31063874..31066002-chr12:31083561..31086374,2	MCF-7	breast:
32	chr12:31190011..31191899-chr12:31193367..31195134,2	K562	blood:
33	chr12:31113324..31114881-chr12:31120140..31121725,2	K562	blood:
34	chr12:31122020..31124643-chr12:31127496..31129096,2	K562	blood:
35	chr12:31149175..31150805-chr12:31151820..31154429,2	K562	blood:
36	chr12:31112508..31114318-chr12:31114721..31117661,2	K562	blood:
37	chr12:31114199..31115183-chr12:31138028..31138949,2	MCF-7	breast:
38	chr12:31149175..31150805-chr12:31151820..31154429,2	K562	blood:
39	chr12:31114199..31115183-chr12:31138028..31138949,2	MCF-7	breast:
40	chr12:31118586..31119188-chr12:31138566..31139432,2	MCF-7	breast:
41	chr12:31113324..31114881-chr12:31120140..31121725,2	K562	blood:
42	chr12:31068113..31070208-chr12:31087806..31090681,2	K562	blood:
43	chr12:31226022..31227620-chr12:31260408..31262678,2	MCF-7	breast:
44	chr12:31086101..31088564-chr12:31089320..31090867,2	K562	blood:
45	chr12:31269688..31270486-chr12:31404974..31405959,2	K562	blood:
46	chr12:31105834..31108432-chr12:31108761..31111175,2	K562	blood:
47	chr12:31003713..31004456-chr12:31138363..31139354,3	MCF-7	breast:
48	chr12:31118639..31119261-chr12:31138195..31139078,2	MCF-7	breast:
49	chr12:31173555..31175653-chr12:31188660..31191059,2	MCF-7	breast:
50	chr12:9435913..9436700-chr12:31226425..31227148,3	HCT-116	colon:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM60A-6	chr12:31269291-31269403	NONHSAT140066
2	lnc-CAPRIN2-5	chr12:31073397-31074125	NONHSAT027523
3	lnc-FAM60A-1	chr12:31203850-31204329	ENSG00000245614
4	lnc-FAM60A-7	chr12:31267330-31267397	NONHSAT027538
5	lnc-FAM60A-7	chr12:31265915-31266017	NONHSAT027538
6	lnc-FAM60A-6	chr12:31270354-31270558	NONHSAT140066
7	lnc-CAPRIN2-6	chr12:31104861-31104971	ucscGeneNc_uc001rjq_1
8	lnc-CAPRIN2-5	chr12:31076691-31076831	NONHSAT027523
9	lnc-FAM60A-7	chr12:31264627-31264743	NONHSAT027538
10	lnc-CAPRIN2-6	chr12:31117396-31117961	ucscGeneNc_uc001rjq_1
11	lnc-FAM60A-1	chr12:31213594-31213684	ENSG00000245614

No data

Variant related genes	Relation type
DDX11-AS1	TF binding region
ENSG00000226472	TF binding region
ENSG00000177359	TF binding region
ENSG00000270926	TF binding region
ENSG00000212533	TF binding region
ENSG00000256984	TF binding region
TSPAN11	TF binding region
DDX11	TF binding region
DDX11-AS1	CpG island
ENSG00000226472	CpG island
ENSG00000177359	CpG island
ENSG00000270926	CpG island
ENSG00000212533	CpG island
ENSG00000256984	CpG island
TSPAN11	CpG island
DDX11	CpG island
ENSG00000177410	chromatin interactions
ENSG00000256984	chromatin interactions
ENSG00000013573	chromatin interactions
ENSG00000243517	chromatin interactions
ENSG00000111788	chromatin interactions
ENSG00000209042	chromatin interactions
ENSG00000245614	chromatin interactions
ENSG00000124201	chromatin interactions
TBC1D9	miRNA target sites
ANKRD29	miRNA target sites

Extended variants
information (count: 8672 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:8672 , 50 per page) page: 1 2 3 4 5 6 7 ... 174

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143656913	chr12:31073426-31073427	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs12422710	chr12:31073449-31073450	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs202017459	chr12:31073451-31073452	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs557525208	chr12:31073493-31073494	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs566270374	chr12:31073526-31073527	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs533625138	chr12:31073549-31073550	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs555096505	chr12:31073585-31073586	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs569964794	chr12:31073608-31073609	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs137989918	chr12:31073622-31073623	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs545856111	chr12:31073645-31073646	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs543825741	chr12:31073670-31073671	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs557641738	chr12:31073704-31073705	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs575959540	chr12:31073765-31073766	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs139252981	chr12:31073771-31073772	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs564664425	chr12:31073796-31073797	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs556019264	chr12:31073862-31073863	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs181160050	chr12:31073889-31073890	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs186180771	chr12:31074000-31074001	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs113892856	chr12:31075649-31075650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs375058943	chr12:31075650-31075651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs113011709	chr12:31075656-31075657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs146336863	chr12:31075657-31075658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192954725	chr12:31075662-31075663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs549635123	chr12:31075670-31075671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs12809886	chr12:31075689-31075690	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs373221430	chr12:31075717-31075718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs182780527	chr12:31075730-31075731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547372328	chr12:31075768-31075769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs186686964	chr12:31075785-31075786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs11614203	chr12:31075850-31075851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs373508683	chr12:31075855-31075856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530326954	chr12:31075883-31075884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs534210064	chr12:31075925-31075926	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs113556722	chr12:31075926-31075927	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs112749377	chr12:31075927-31075928	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs397829526	chr12:31075930-31075931	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs555954205	chr12:31075947-31075948	Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
38	rs113394760	chr12:31075956-31075957	Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs567785618	chr12:31075985-31075986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs538400650	chr12:31076022-31076023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556246337	chr12:31076116-31076117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs569899765	chr12:31076122-31076123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs371626719	chr12:31076136-31076137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs150274526	chr12:31076140-31076141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs58212085	chr12:31076166-31076167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs78440219	chr12:31076274-31076275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs138691836	chr12:31076312-31076313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs191438337	chr12:31076326-31076327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs531424164	chr12:31076327-31076328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs183614184	chr12:31076345-31076346	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
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
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
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Williams Syndrome	20824207	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3437 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31075600-31076400	Enhancers	Right Atrium	heart
2	chr12:31076000-31076600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr12:31076200-31076400	Enhancers	Left Ventricle	heart
4	chr12:31076400-31079000	Weak transcription	Right Atrium	heart
5	chr12:31076600-31078800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr12:31077800-31079000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:31077800-31079000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr12:31078000-31078600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
9	chr12:31078000-31079000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
10	chr12:31078200-31079000	Bivalent Enhancer	Fetal Muscle Leg	muscle
11	chr12:31078400-31078600	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
12	chr12:31078400-31078600	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr12:31078400-31078600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
14	chr12:31078400-31078600	Enhancers	Brain Anterior Caudate	brain
15	chr12:31078400-31078600	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
16	chr12:31078400-31078800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr12:31078400-31078800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
18	chr12:31078400-31079000	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr12:31078400-31079000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
20	chr12:31078400-31079200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
21	chr12:31078400-31080000	Enhancers	Fetal Heart	heart
22	chr12:31078600-31078800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
23	chr12:31078600-31078800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
24	chr12:31078600-31078800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr12:31078600-31078800	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr12:31078600-31078800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
27	chr12:31078600-31078800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
28	chr12:31078600-31078800	Enhancers	Brain Cingulate Gyrus	brain
29	chr12:31078600-31078800	Enhancers	Brain Germinal Matrix	brain
30	chr12:31078600-31078800	Enhancers	Fetal Brain Female	brain
31	chr12:31078600-31078800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
32	chr12:31078600-31078800	Bivalent/Poised TSS	Hela-S3	cervix
33	chr12:31078600-31079000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr12:31078600-31079000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr12:31078600-31079000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr12:31078600-31079000	Bivalent Enhancer	Brain Anterior Caudate	brain
37	chr12:31078600-31079000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
38	chr12:31078600-31079000	Bivalent Enhancer	Fetal Stomach	stomach
39	chr12:31078600-31079200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr12:31078600-31079200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
41	chr12:31078600-31079200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
42	chr12:31078600-31079200	Enhancers	Left Ventricle	heart
43	chr12:31078600-31079200	Enhancers	Lung	lung
44	chr12:31078800-31079000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
45	chr12:31078800-31079000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
46	chr12:31078800-31079000	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
47	chr12:31078800-31079000	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr12:31078800-31079000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr12:31078800-31079000	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr12:31078800-31079000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin

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