Variant report

Variant	nsv557456
Chromosome Location	chr12:10532326-10698255
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1414)
CpG islands
(count:977)
Chromatin interactive
region (count:21)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1414 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:10536954-10536986	K562	blood:	n/a	n/a
2	ARID3A	chr12:10562084-10562332	K562	blood:	n/a	n/a
3	ARID3A	chr12:10548121-10548681	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:10653777-10653877	K562	blood:	n/a	n/a
5	ARID3A	chr12:10563882-10564383	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:10592356-10592503	HepG2	liver:	n/a	n/a
7	ATF1	chr12:10562095-10562363	K562	blood:	n/a	n/a
8	ATF2	chr12:10695883-10696624	GM12878	blood:	n/a	n/a
9	ATF2	chr12:10544776-10545621	GM12878	blood:	n/a	n/a
10	ATF2	chr12:10693152-10694036	GM12878	blood:	n/a	n/a
11	ATF2	chr12:10695894-10696491	GM12878	blood:	n/a	n/a
12	ATF2	chr12:10693081-10694102	GM12878	blood:	n/a	n/a
13	ATF2	chr12:10547858-10548386	GM12878	blood:	n/a	n/a
14	BATF	chr12:10696061-10696446	GM12878	blood:	n/a	n/a
15	BATF	chr12:10641882-10642185	GM12878	blood:	n/a	chr12:10642014-10642025
16	BATF	chr12:10693300-10693868	GM12878	blood:	n/a	chr12:10693650-10693661
17	BATF	chr12:10583308-10583579	GM12878	blood:	n/a	chr12:10583461-10583472
18	BATF	chr12:10598779-10599011	GM12878	blood:	n/a	chr12:10598893-10598904
19	BATF	chr12:10641906-10642182	GM12878	blood:	n/a	chr12:10642014-10642025
20	BATF	chr12:10696036-10696487	GM12878	blood:	n/a	n/a
21	BATF	chr12:10693317-10693939	GM12878	blood:	n/a	chr12:10693650-10693661
22	BCL11A	chr12:10696199-10696390	GM12878	blood:	n/a	n/a
23	BCL11A	chr12:10693354-10693625	GM12878	blood:	n/a	n/a
24	BCL11A	chr12:10547793-10548282	GM12878	blood:	n/a	n/a
25	BCL11A	chr12:10696076-10696426	GM12878	blood:	n/a	n/a
26	BCL11A	chr12:10544909-10545281	GM12878	blood:	n/a	n/a
27	BCL11A	chr12:10544925-10545336	GM12878	blood:	n/a	n/a
28	BCL11A	chr12:10547875-10548349	GM12878	blood:	n/a	n/a
29	BCL11A	chr12:10583293-10583483	GM12878	blood:	n/a	n/a
30	BCL11A	chr12:10671811-10671985	GM12878	blood:	n/a	n/a
31	BCL11A	chr12:10598783-10598965	GM12878	blood:	n/a	n/a
32	BCL11A	chr12:10693310-10693858	GM12878	blood:	n/a	n/a
33	BCL3	chr12:10693210-10693959	GM12878	blood:	n/a	n/a
34	BCL3	chr12:10592167-10592607	A549	lung:	n/a	n/a
35	BCL3	chr12:10696031-10696586	GM12878	blood:	n/a	n/a
36	BCL3	chr12:10695995-10696628	GM12878	blood:	n/a	n/a
37	BCL3	chr12:10693360-10693849	GM12878	blood:	n/a	n/a
38	BCLAF1	chr12:10547846-10548369	GM12878	blood:	n/a	n/a
39	BCLAF1	chr12:10693241-10693808	GM12878	blood:	n/a	n/a
40	BCLAF1	chr12:10544936-10545515	GM12878	blood:	n/a	chr12:10545490-10545499
41	BCLAF1	chr12:10544894-10545448	GM12878	blood:	n/a	n/a
42	BCLAF1	chr12:10696071-10696445	GM12878	blood:	n/a	n/a
43	BCLAF1	chr12:10693217-10694044	GM12878	blood:	n/a	n/a
44	BHLHE40	chr12:10562058-10562261	K562	blood:	n/a	n/a
45	BHLHE40	chr12:10559410-10559764	GM12878	blood:	n/a	n/a
46	BHLHE40	chr12:10547847-10548665	GM12878	blood:	n/a	n/a
47	BHLHE40	chr12:10693305-10693679	GM12878	blood:	n/a	n/a
48	BHLHE40	chr12:10559427-10559772	K562	blood:	n/a	n/a
49	BRCA1	chr12:10562044-10562186	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr12:10574950-10575149	Hela-S3	cervix:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10560602-10560652	HPAEpiC	pulmonary alveolar:	n/a
2	chr12:10560602-10560652	HPAEpiC	pulmonary alveolar:	n/a
3	chr12:10545083-10545133	HRE	kidney:	n/a
4	chr12:10586130-10586180	RPTEC	kidney:	n/a
5	chr12:10658281-10658331	SKMC	muscle:	n/a
6	chr12:10586130-10586180	AG09309	skin:	n/a
7	chr12:10607364-10607414	HIPEpiC	eye:	n/a
8	chr12:10586130-10586180	BJ	skin:	n/a
9	chr12:10586130-10586180	SAEC	small airway:	n/a
10	chr12:10605936-10605986	NH-A	brain:	n/a
11	chr12:10658539-10658589	HRPEpiC	eye:	n/a
12	chr12:10570179-10570229	BE2_C	brain:	n/a
13	chr12:10560602-10560652	HUVEC	blood vessel:	n/a
14	chr12:10560602-10560652	BE2_C	brain:	n/a
15	chr12:10658425-10658475	SAEC	small airway:	n/a
16	chr12:10607364-10607414	SKMC	muscle:	n/a
17	chr12:10544636-10544686	HRE	kidney:	n/a
18	chr12:10605936-10605986	GM12891	blood:	n/a
19	chr12:10544636-10544686	NHDF-neo	bronchial:	n/a
20	chr12:10599740-10599790	MCF-7	breast:	n/a
21	chr12:10607364-10607414	HL-60	blood:	n/a
22	chr12:10570179-10570229	Caco-2	colon:	n/a
23	chr12:10605936-10605986	GM19239	blood:	n/a
24	chr12:10544636-10544686	CMK	blood:	n/a
25	chr12:10543073-10543123	HCM	heart:	n/a
26	chr12:10658539-10658589	PrEC	prostate:	n/a
27	chr12:10605936-10605986	HCF	heart:	n/a
28	chr12:10607538-10607588	A549	lung:	n/a
29	chr12:10608067-10608117	Caco-2	colon:	n/a
30	chr12:10545083-10545133	T-47D	breast:	n/a
31	chr12:10583355-10583405	GM12891	blood:	n/a
32	chr12:10599740-10599790	HCM	heart:	n/a
33	chr12:10599740-10599790	HCF	heart:	n/a
34	chr12:10658425-10658475	HCF	heart:	n/a
35	chr12:10588483-10588533	NH-A	brain:	n/a
36	chr12:10545083-10545133	HepG2	liver:	n/a
37	chr12:10543073-10543123	HCPEpiC	choroid plexus:	n/a
38	chr12:10586130-10586180	HRCEpiC	kidney:	n/a
39	chr12:10583355-10583405	K562	blood:	n/a
40	chr12:10599740-10599790	HRPEpiC	eye:	n/a
41	chr12:10586130-10586180	HAEpiC	amniotic membrane:	n/a
42	chr12:10560602-10560652	HRPEpiC	eye:	n/a
43	chr12:10544636-10544686	IMR90	lung:	fetal
44	chr12:10607538-10607588	BJ	skin:	n/a
45	chr12:10543073-10543123	MCF-7	breast:	n/a
46	chr12:10608067-10608117	HCM	heart:	n/a
47	chr12:10599740-10599790	ECC-1	luminal epithelium:	n/a
48	chr12:10544636-10544686	AG10803	skin:	n/a
49	chr12:10658539-10658589	GM12878	blood:	n/a
50	chr12:10658539-10658589	NT2-D1	testis:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:10484099..10484956-chr12:10652861..10653779,2	MCF-7	breast:
2	chr12:10572017..10574193-chr12:10588542..10590731,2	MCF-7	breast:
3	chr12:10534850..10537741-chr12:10540764..10542364,2	MCF-7	breast:
4	chr1:28974955..28975586-chr12:10563608..10564342,2	Hela-S3	cervix:
5	chr12:10516092..10519058-chr12:10537972..10540241,2	K562	blood:
6	chr12:10693047..10695502-chr12:10698886..10701191,2	K562	blood:
7	chr12:10388252..10388816-chr12:10653557..10654233,2	MCF-7	breast:
8	chr12:10561211..10561774-chr17:76182659..76183234,2	Hela-S3	cervix:
9	chr12:10547736..10550018-chr12:10555798..10557891,2	MCF-7	breast:
10	chr12:10604438..10606172-chr12:10606795..10608691,2	K562	blood:
11	chr12:10548044..10548696-chr9:117267865..117268396,2	Hela-S3	cervix:
12	chr12:10527378..10530229-chr12:10546803..10548399,2	K562	blood:
13	chr12:10572017..10574193-chr12:10588542..10590731,2	MCF-7	breast:
14	chr12:10559960..10560793-chrX:131351678..131352452,2	Hela-S3	cervix:
15	chr12:10604438..10606172-chr12:10606795..10608691,2	K562	blood:
16	chr12:10536735..10538905-chr12:10543028..10545121,2	MCF-7	breast:
17	chr12:10547736..10550018-chr12:10555798..10557891,2	MCF-7	breast:
18	chr12:10554334..10554872-chr16:81477760..81478703,2	Hela-S3	cervix:
19	chr12:10537029..10538774-chr12:10541549..10544546,2	K562	blood:
20	chr12:10563346..10565218-chr12:11316267..11318781,2	K562	blood:
21	chr12:10514090..10517702-chr12:10563594..10568036,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF2S3L.1-6	chr12:10601202-10602083	l_610_chr12:10597245-10602083_whiteBloodCell
2	lnc-KLRD1-1	chr12:10532301-10532435	ENSG00000245648
3	lnc-KLRD1-1	chr12:10548778-10551105	ENSG00000245648
4	lnc-EIF2S3L.1-6	chr12:10597246-10597382	l_610_chr12:10597245-10602083_whiteBloodCell

No data

Variant related genes	Relation type
ENSG00000180574	TF binding region
KLRC2	TF binding region
KLRC3	TF binding region
KLRK1	TF binding region
KLRC4	TF binding region
KLRC1	TF binding region
KLRC4-KLRK1	TF binding region
ENSG00000255641	TF binding region
ENSG00000180574	CpG island
KLRC2	CpG island
KLRC3	CpG island
KLRK1	CpG island
KLRC4	CpG island
KLRC1	CpG island
KLRC4-KLRK1	CpG island
ENSG00000255641	CpG island
ENSG00000205809	chromatin interactions
ENSG00000167900	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000123728	chromatin interactions
ENSG00000134545	chromatin interactions
ENSG00000205810	chromatin interactions
ENSG00000245648	chromatin interactions
ENSG00000255641	chromatin interactions
ENSG00000213809	chromatin interactions
ESR1	miRNA target sites

Extended variants
information (count: 4862 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:4862 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2255336	chr12:10532326-10532327	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs377167821	chr12:10532337-10532338	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
3	rs141717786	chr12:10532344-10532345	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
4	rs557219486	chr12:10532362-10532363	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
5	rs200989597	chr12:10532363-10532364	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
6	rs564026526	chr12:10532378-10532379	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
7	rs545769255	chr12:10532380-10532381	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
8	rs552976948	chr12:10532411-10532412	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs572990230	chr12:10532412-10532413	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs367583023	chr12:10532413-10532414	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs200500085	chr12:10532415-10532416	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs2617151	chr12:10532434-10532435	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs373759060	chr12:10532441-10532442	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs530311026	chr12:10532491-10532492	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs543799908	chr12:10532496-10532497	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs74060366	chr12:10532527-10532528	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs571120580	chr12:10532580-10532581	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs557740175	chr12:10532595-10532596	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs532426550	chr12:10532611-10532612	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187171226	chr12:10532629-10532630	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs113940077	chr12:10532642-10532643	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs75909190	chr12:10532647-10532648	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs375835537	chr12:10532649-10532650	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559290214	chr12:10532702-10532703	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs528576079	chr12:10532704-10532705	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs2733849	chr12:10532722-10532723	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs372760111	chr12:10532728-10532729	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs548231651	chr12:10532757-10532758	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs150646988	chr12:10532761-10532762	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372907203	chr12:10532776-10532777	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs192816482	chr12:10532783-10532784	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs550635374	chr12:10532789-10532790	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184427692	chr12:10532809-10532810	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539320008	chr12:10532814-10532815	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs2733848	chr12:10532833-10532834	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs572828004	chr12:10532854-10532855	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs535589857	chr12:10532855-10532856	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs555490246	chr12:10532863-10532864	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs574965803	chr12:10532866-10532867	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs189308252	chr12:10532879-10532880	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs563706345	chr12:10532885-10532886	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs535507945	chr12:10532886-10532887	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs577484533	chr12:10532910-10532911	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546049529	chr12:10532916-10532917	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192245233	chr12:10532944-10532945	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs149782374	chr12:10532953-10532954	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs371216346	chr12:10532960-10532961	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs185020117	chr12:10532963-10532964	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs12826560	chr12:10532965-10532966	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs2859569	chr12:10532990-10532991	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	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
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:777 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10518400-10537000	Weak transcription	Left Ventricle	heart
2	chr12:10519600-10534800	Weak transcription	Fetal Stomach	stomach
3	chr12:10519600-10547800	Weak transcription	Colon Smooth Muscle	Colon
4	chr12:10521800-10534600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr12:10522400-10534000	Weak transcription	Thymus	Thymus
6	chr12:10523000-10536000	Weak transcription	Ovary	ovary
7	chr12:10525400-10547200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr12:10525600-10533200	Weak transcription	Fetal Intestine Large	intestine
9	chr12:10525600-10534600	Weak transcription	Pancreas	Pancrea
10	chr12:10525800-10534400	Weak transcription	Spleen	Spleen
11	chr12:10527200-10534400	Weak transcription	Brain Substantia Nigra	brain
12	chr12:10527400-10533000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr12:10527400-10533000	Weak transcription	Primary T cells from cord blood	blood
14	chr12:10527400-10533200	Weak transcription	Fetal Intestine Small	intestine
15	chr12:10527400-10534400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr12:10527600-10538600	Weak transcription	Brain Hippocampus Middle	brain
17	chr12:10528600-10533000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr12:10528800-10533000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr12:10528800-10533000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr12:10529800-10533000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr12:10531000-10533200	Weak transcription	Hela-S3	cervix
22	chr12:10531200-10544400	Weak transcription	Primary B cells from peripheral blood	blood
23	chr12:10531400-10533200	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr12:10531600-10533000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
25	chr12:10531800-10533000	Weak transcription	NHEK	skin
26	chr12:10531800-10534400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr12:10532000-10532400	Transcr. at gene 5' and 3'	Primary T killer naive cells fromperipheralblood	blood
28	chr12:10532000-10532600	Strong transcription	Primary T cells fromperipheralblood	blood
29	chr12:10532000-10533000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr12:10532000-10534600	Strong transcription	Primary B cells from cord blood	blood
31	chr12:10532200-10532400	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr12:10532400-10532800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr12:10532400-10533400	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr12:10532600-10533000	Genic enhancers	Primary T cells fromperipheralblood	blood
35	chr12:10532800-10533600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr12:10533000-10533200	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
37	chr12:10533000-10533400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
38	chr12:10533000-10533800	Strong transcription	Primary T cells from cord blood	blood
39	chr12:10533000-10533800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr12:10533000-10533800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr12:10533000-10534000	Transcr. at gene 5' and 3'	Primary T cells fromperipheralblood	blood
42	chr12:10533000-10534600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr12:10533000-10534600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr12:10533000-10534800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr12:10533000-10534800	Strong transcription	NHEK	skin
46	chr12:10533200-10533600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
47	chr12:10533200-10533600	Transcr. at gene 5' and 3'	Primary T helper naive cells from peripheral blood	blood
48	chr12:10533200-10533800	Strong transcription	Fetal Intestine Large	intestine
49	chr12:10533200-10533800	Strong transcription	Fetal Intestine Small	intestine
50	chr12:10533200-10534800	Genic enhancers	Hela-S3	cervix

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