Variant report

Variant	nsv898967
Chromosome Location	chr12:31858031-31899475
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1940)
CpG islands
(count:916)
Chromatin interactive
region (count:60)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1940 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:31867921-31869074	K562	blood:	n/a	n/a
2	ARID3A	chr12:31867437-31867929	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:31885731-31886428	K562	blood:	n/a	n/a
4	ARID3A	chr12:31881925-31882635	K562	blood:	n/a	n/a
5	ARID3A	chr12:31884744-31885249	K562	blood:	n/a	n/a
6	ARID3A	chr12:31881277-31882558	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:31886709-31887110	K562	blood:	n/a	n/a
8	ARID3A	chr12:31885745-31886049	HepG2	liver:	n/a	n/a
9	ARID3A	chr12:31889472-31889784	K562	blood:	n/a	n/a
10	ATF1	chr12:31890405-31890713	K562	blood:	n/a	n/a
11	ATF1	chr12:31881774-31882463	K562	blood:	n/a	n/a
12	ATF1	chr12:31886679-31886984	K562	blood:	n/a	n/a
13	ATF1	chr12:31884800-31885188	K562	blood:	n/a	n/a
14	ATF1	chr12:31885812-31886142	K562	blood:	n/a	n/a
15	ATF1	chr12:31871666-31871919	K562	blood:	n/a	n/a
16	ATF1	chr12:31868139-31868530	K562	blood:	n/a	n/a
17	ATF1	chr12:31876520-31876732	K562	blood:	n/a	n/a
18	ATF1	chr12:31889406-31889741	K562	blood:	n/a	n/a
19	ATF2	chr12:31881803-31882263	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr12:31886626-31886922	GM12878	blood:	n/a	n/a
21	ATF2	chr12:31885888-31886507	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr12:31885832-31886530	GM12878	blood:	n/a	n/a
23	ATF2	chr12:31881809-31882417	GM12878	blood:	n/a	n/a
24	ATF2	chr12:31881386-31882387	GM12878	blood:	n/a	n/a
25	ATF2	chr12:31886015-31886514	GM12878	blood:	n/a	n/a
26	ATF2	chr12:31874889-31875464	GM12878	blood:	n/a	n/a
27	ATF2	chr12:31885789-31886430	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr12:31874713-31875488	GM12878	blood:	n/a	n/a
29	ATF2	chr12:31881812-31882271	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr12:31868121-31868730	GM12878	blood:	n/a	n/a
31	ATF2	chr12:31889393-31889776	GM12878	blood:	n/a	n/a
32	ATF3	chr12:31881120-31881630	GM12878	blood:	n/a	n/a
33	ATF3	chr12:31881809-31882490	A549	lung:	n/a	chr12:31882044-31882052 chr12:31882043-31882054 chr12:31882042-31882053 chr12:31882044-31882051 chr12:31882043-31882051 chr12:31882040-31882055
34	ATF3	chr12:31881331-31881494	K562	blood:	n/a	n/a
35	ATF3	chr12:31881803-31882700	A549	lung:	n/a	chr12:31882044-31882052 chr12:31882043-31882054 chr12:31882042-31882053 chr12:31882044-31882051 chr12:31882043-31882051 chr12:31882040-31882055
36	ATF3	chr12:31885713-31886363	A549	lung:	n/a	n/a
37	ATF3	chr12:31885816-31886291	K562	blood:	n/a	n/a
38	ATF3	chr12:31868100-31868586	K562	blood:	n/a	n/a
39	ATF3	chr12:31886623-31887038	K562	blood:	n/a	n/a
40	BACH1	chr12:31885798-31886420	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr12:31886720-31886969	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr12:31885753-31886212	K562	blood:	n/a	n/a
43	BACH1	chr12:31886753-31886971	K562	blood:	n/a	n/a
44	BACH1	chr12:31881898-31882337	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr12:31883780-31884181	K562	blood:	n/a	n/a
46	BACH1	chr12:31882637-31882951	K562	blood:	n/a	n/a
47	BACH1	chr12:31893659-31894032	K562	blood:	n/a	n/a
48	BATF	chr12:31876445-31876707	GM12878	blood:	n/a	n/a
49	BATF	chr12:31874979-31875373	GM12878	blood:	n/a	n/a
50	BATF	chr12:31881803-31882098	GM12878	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:31884655-31884705	NH-A	brain:	n/a
2	chr12:31884655-31884705	NH-A	brain:	n/a
3	chr12:31882290-31882340	HepG2	liver:	n/a
4	chr12:31882280-31882330	HCF	heart:	n/a
5	chr12:31879426-31879476	AG04449	skin:	fetal
6	chr12:31882280-31882330	HCT-116	colon:	n/a
7	chr12:31882203-31882253	HepG2	liver:	n/a
8	chr12:31881951-31882001	NH-A	brain:	n/a
9	chr12:31881433-31881483	HepG2	liver:	n/a
10	chr12:31882596-31882646	HEK293	kidney:	embryo
11	chr12:31881778-31881828	HCT-116	colon:	n/a
12	chr12:31879426-31879476	Hepatocyte	liver:	n/a
13	chr12:31882282-31882332	HCF	heart:	n/a
14	chr12:31882421-31882471	NHBE	bronchial:	n/a
15	chr12:31882280-31882330	LNCaP	prostate:	n/a
16	chr12:31881433-31881483	AG09309	skin:	n/a
17	chr12:31882282-31882332	ECC-1	luminal epithelium:	n/a
18	chr12:31882290-31882340	ProgFib	skin:	n/a
19	chr12:31882421-31882471	GM12891	blood:	n/a
20	chr12:31882596-31882646	BJ	skin:	n/a
21	chr12:31882203-31882253	A549	lung:	n/a
22	chr12:31881433-31881483	U87	brain:	n/a
23	chr12:31882203-31882253	HAEpiC	amniotic membrane:	n/a
24	chr12:31883115-31883165	GM19239	blood:	n/a
25	chr12:31879426-31879476	AG09309	skin:	n/a
26	chr12:31879426-31879476	NHBE	bronchial:	n/a
27	chr12:31882596-31882646	AoSMC	blood vessel:	n/a
28	chr12:31881951-31882001	BE2_C	brain:	n/a
29	chr12:31881969-31882019	NH-A	brain:	n/a
30	chr12:31882089-31882139	K562	blood:	n/a
31	chr12:31883115-31883165	HMEC	breast:	n/a
32	chr12:31883115-31883165	GM12878	blood:	n/a
33	chr12:31882280-31882330	K562	blood:	n/a
34	chr12:31884655-31884705	HL-60	blood:	n/a
35	chr12:31884655-31884705	HMEC	breast:	n/a
36	chr12:31882280-31882330	ECC-1	luminal epithelium:	n/a
37	chr12:31879426-31879476	NT2-D1	testis:	n/a
38	chr12:31879426-31879476	HepG2	liver:	n/a
39	chr12:31882280-31882330	HRE	kidney:	n/a
40	chr12:31881433-31881483	NHBE	bronchial:	n/a
41	chr12:31882282-31882332	Hela-S3	cervix:	n/a
42	chr12:31882596-31882646	HCPEpiC	choroid plexus:	n/a
43	chr12:31881433-31881483	IMR90	lung:	fetal
44	chr12:31882280-31882330	HepG2	liver:	n/a
45	chr12:31882198-31882248	GM12892	blood:	n/a
46	chr12:31882290-31882340	HEK293	kidney:	embryo
47	chr12:31883115-31883165	HRCEpiC	kidney:	n/a
48	chr12:31881951-31882001	HL-60	blood:	n/a
49	chr12:31882203-31882253	AG09319	gingival:	n/a
50	chr12:31883115-31883165	HPAEpiC	pulmonary alveolar:	n/a

(count:60 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:31867508..31869786-chr12:31900848..31903323,2	K562	blood:
2	chr12:31880235..31884620-chr12:31906466..31910642,5	K562	blood:
3	chr11:62609120..62609942-chr12:31881240..31881895,2	Hela-S3	cervix:
4	chr12:31867098..31869695-chr12:31872689..31874325,2	MCF-7	breast:
5	chr12:31863317..31864932-chr12:31883835..31885754,2	K562	blood:
6	chr12:31890191..31892449-chr12:31894562..31897405,2	K562	blood:
7	chr12:31880350..31888706-chr12:31898122..31903847,15	K562	blood:
8	chr12:31882430..31883133-chr8:134584326..134584942,2	Hela-S3	cervix:
9	chr12:31896972..31898999-chr12:31900743..31902454,2	K562	blood:
10	chr12:31861423..31863642-chr12:31880479..31882083,2	MCF-7	breast:
11	chr12:31477737..31479382-chr12:31879609..31881760,2	MCF-7	breast:
12	chr12:31883178..31885919-chr12:31902028..31904052,3	K562	blood:
13	chr12:31889555..31891560-chr12:31894005..31895879,2	MCF-7	breast:
14	chr12:31868001..31870341-chr12:32112733..32115276,2	K562	blood:
15	chr12:31810792..31812576-chr12:31866206..31867920,2	K562	blood:
16	chr12:31890682..31895418-chr12:31897600..31900050,5	K562	blood:
17	chr12:31839479..31841877-chr12:31870440..31872048,2	MCF-7	breast:
18	chr12:31880350..31888706-chr12:31898122..31903847,15	K562	blood:
19	chr12:31889555..31891560-chr12:31894005..31895879,2	MCF-7	breast:
20	chr12:31882281..31884282-chr12:32455901..32458701,2	K562	blood:
21	chr12:31881018..31881659-chr15:93443139..93444027,3	Hela-S3	cervix:
22	chr12:31882162..31882742-chr8:125551065..125551799,2	Hela-S3	cervix:
23	chr12:31880190..31881947-chr12:31893722..31895247,2	K562	blood:
24	chr12:31881243..31883910-chr12:32111522..32113326,3	MCF-7	breast:
25	chr12:31885987..31887663-chr12:31893396..31895350,2	K562	blood:
26	chr12:31882882..31884422-chr12:31893426..31895408,2	K562	blood:
27	chr12:31885885..31887666-chr12:31889660..31891228,2	MCF-7	breast:
28	chr12:31866804..31870237-chr12:31900678..31903673,4	K562	blood:
29	chr12:31882068..31882792-chr14:75593054..75593701,2	Hela-S3	cervix:
30	chr12:31810441..31812153-chr12:31879361..31881376,2	K562	blood:
31	chr12:31477256..31480149-chr12:31881924..31883474,2	K562	blood:
32	chr12:31811076..31814149-chr12:31866420..31869336,3	K562	blood:
33	chr12:31885987..31887663-chr12:31893396..31895350,2	K562	blood:
34	chr12:31812410..31814271-chr12:31879800..31882059,2	MCF-7	breast:
35	chr12:31882882..31884422-chr12:31893426..31895408,2	K562	blood:
36	chr12:31886667..31888400-chr12:31898421..31901414,2	K562	blood:
37	chr12:31880708..31883036-chr12:32258362..32261321,3	K562	blood:
38	chr12:31884351..31886609-chr12:31902358..31904418,2	MCF-7	breast:
39	chr11:34126691..34127308-chr12:31881453..31882172,2	Hela-S3	cervix:
40	chr12:31872900..31875719-chr15:72766354..72768356,2	MCF-7	breast:
41	chr12:31878745..31882142-chr12:32111934..32114509,3	K562	blood:
42	chr12:31477256..31479632-chr12:31880019..31883424,4	K562	blood:
43	chr12:31863317..31864932-chr12:31883835..31885754,2	K562	blood:
44	chr12:31890682..31895418-chr12:31897600..31900050,5	K562	blood:
45	chr12:31879460..31881406-chr12:31997211..31999546,2	K562	blood:
46	chr12:31885898..31889640-chr12:32111582..32115997,5	K562	blood:
47	chr12:31860661..31864274-chr12:31866939..31870536,4	K562	blood:
48	chr12:31885818..31888336-chr12:32049032..32051077,2	K562	blood:
49	chr12:31881279..31883605-chr12:31884352..31886662,3	MCF-7	breast:
50	chr12:31878269..31883010-chr12:31884108..31887220,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-METTL20-8	chr12:31882249-31884462	NONHSAT027572

No data

Variant related genes	Relation type
AMN1	TF binding region
ENSG00000266482	TF binding region
AMN1	CpG island
ENSG00000266482	CpG island
ENSG00000135372	chromatin interactions
ENSG00000256987	chromatin interactions
ENSG00000147684	chromatin interactions
ENSG00000119638	chromatin interactions
ENSG00000147687	chromatin interactions
ENSG00000151743	chromatin interactions
ENSG00000256843	chromatin interactions
ENSG00000223722	chromatin interactions
ENSG00000151746	chromatin interactions
ENSG00000139160	chromatin interactions
ENSG00000244436	chromatin interactions
ENSG00000166233	chromatin interactions
ENSG00000174718	chromatin interactions
ENSG00000257530	chromatin interactions
ENSG00000173575	chromatin interactions
ENSG00000139146	chromatin interactions
ENSG00000261423	chromatin interactions
ENSG00000133316	chromatin interactions

Extended variants
information (count: 1505 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1505 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11051540	chr12:31858031-31858032	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530379810	chr12:31858060-31858061	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs74085164	chr12:31858089-31858090	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs573943130	chr12:31858120-31858121	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370070300	chr12:31858153-31858154	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs36117515	chr12:31858227-31858228	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs562843519	chr12:31858235-31858236	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147514095	chr12:31858267-31858268	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs186420403	chr12:31858302-31858303	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs36021805	chr12:31858378-31858379	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs543799623	chr12:31858425-31858426	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs114493077	chr12:31858434-31858435	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs78638639	chr12:31858435-31858436	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs142874266	chr12:31858473-31858474	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs527883079	chr12:31858489-31858490	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs35188085	chr12:31858589-31858590	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs547543657	chr12:31858632-31858633	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567633612	chr12:31858750-31858751	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536518630	chr12:31858783-31858784	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs370962819	chr12:31858809-31858810	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs34841509	chr12:31858846-31858847	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs568791989	chr12:31858852-31858853	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537835650	chr12:31858865-31858866	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs557617091	chr12:31858968-31858969	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs546859584	chr12:31858969-31858970	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs111791140	chr12:31858972-31858973	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs150973989	chr12:31858973-31858974	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs61591448	chr12:31858985-31858986	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs574006483	chr12:31858998-31858999	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560418210	chr12:31859013-31859014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542972306	chr12:31859018-31859019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562756563	chr12:31859043-31859044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576398994	chr12:31859044-31859045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145708260	chr12:31859078-31859079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190821437	chr12:31859106-31859107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs4619231	chr12:31859111-31859112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs1965289	chr12:31859138-31859139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs111563071	chr12:31859139-31859140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565243232	chr12:31859163-31859164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370490344	chr12:31859207-31859208	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs527750495	chr12:31859210-31859211	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs143483769	chr12:31859240-31859241	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs541246252	chr12:31859241-31859242	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs140040900	chr12:31859246-31859247	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs3032986	chr12:31859270-31859271	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs183151748	chr12:31859298-31859299	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs572196112	chr12:31859342-31859343	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs545882893	chr12:31859347-31859348	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs550098766	chr12:31859350-31859351	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs570323474	chr12:31859413-31859414	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1734 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31822600-31862000	Weak transcription	Rectal Smooth Muscle	rectum
2	chr12:31822600-31874200	Weak transcription	Right Ventricle	heart
3	chr12:31827000-31871800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr12:31835600-31860200	Weak transcription	Fetal Kidney	kidney
5	chr12:31837000-31859400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr12:31837200-31860400	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr12:31837200-31865000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr12:31838600-31881000	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr12:31839800-31871800	Weak transcription	Gastric	stomach
10	chr12:31840200-31858200	Weak transcription	Duodenum Mucosa	Duodenum
11	chr12:31840200-31859600	Weak transcription	Primary hematopoietic stem cells	blood
12	chr12:31840200-31861800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr12:31841200-31860400	Weak transcription	Fetal Muscle Leg	muscle
14	chr12:31841600-31860200	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr12:31841600-31870000	Weak transcription	Pancreas	Pancrea
16	chr12:31842000-31860200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr12:31844600-31871800	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr12:31845600-31860400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr12:31846400-31860200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr12:31846400-31860200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr12:31846400-31862400	Weak transcription	Aorta	Aorta
22	chr12:31846400-31871800	Weak transcription	Lung	lung
23	chr12:31846600-31860200	Weak transcription	Fetal Lung	lung
24	chr12:31847800-31860200	Weak transcription	Fetal Intestine Small	intestine
25	chr12:31847800-31860400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr12:31848200-31859600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr12:31848800-31860200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr12:31849000-31880000	Weak transcription	Psoas Muscle	Psoas
29	chr12:31849200-31860200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr12:31849600-31860800	Weak transcription	Colon Smooth Muscle	Colon
31	chr12:31850800-31867600	Weak transcription	Brain Substantia Nigra	brain
32	chr12:31851000-31860200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr12:31851000-31880800	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr12:31851600-31860800	Weak transcription	Liver	Liver
35	chr12:31851600-31863200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
36	chr12:31852800-31859200	Weak transcription	Fetal Stomach	stomach
37	chr12:31852800-31860200	Weak transcription	Brain Germinal Matrix	brain
38	chr12:31852800-31861800	Weak transcription	Left Ventricle	heart
39	chr12:31852800-31871000	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr12:31852800-31879600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr12:31853000-31859400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr12:31853000-31859600	Weak transcription	Fetal Brain Female	brain
43	chr12:31853000-31860000	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr12:31853000-31860200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr12:31853000-31860200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr12:31853000-31860200	Weak transcription	Primary T cells from cord blood	blood
47	chr12:31853000-31860200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr12:31853000-31860200	Weak transcription	Dnd41	blood
49	chr12:31853000-31867200	Weak transcription	Brain Anterior Caudate	brain
50	chr12:31853200-31860200	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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