Variant report

Variant	nsv886726
Chromosome Location	chr6:141428255-141764919
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1307)
CpG islands
(count:305)
Chromatin interactive
region (count:39)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1307 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:141586969-141587287	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:141702263-141702688	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:141647618-141647926	HepG2	liver:	n/a	n/a
4	ATF1	chr6:141612636-141612753	K562	blood:	n/a	n/a
5	ATF2	chr6:141702222-141702676	GM12878	blood:	n/a	n/a
6	ATF2	chr6:141709759-141710160	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr6:141474627-141475071	GM12878	blood:	n/a	n/a
8	ATF2	chr6:141702298-141702702	GM12878	blood:	n/a	n/a
9	ATF3	chr6:141647541-141647917	A549	lung:	n/a	n/a
10	BACH1	chr6:141441909-141442156	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr6:141586960-141586966	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr6:141702264-141702585	GM12878	blood:	n/a	chr6:141702436-141702447
13	BATF	chr6:141625060-141625335	GM12878	blood:	n/a	n/a
14	BATF	chr6:141474651-141475037	GM12878	blood:	n/a	n/a
15	BATF	chr6:141428710-141429022	GM12878	blood:	n/a	chr6:141428864-141428875
16	BATF	chr6:141702232-141702646	GM12878	blood:	n/a	chr6:141702436-141702447
17	BATF	chr6:141647651-141647932	GM12878	blood:	n/a	chr6:141647803-141647814
18	BCL11A	chr6:141474772-141475048	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL11A	chr6:141702248-141702564	GM12878	blood:	n/a	chr6:141702430-141702439 chr6:141702440-141702449 chr6:141702439-141702448
20	BCL11A	chr6:141702335-141702575	GM12878	blood:	n/a	chr6:141702430-141702439 chr6:141702440-141702449 chr6:141702439-141702448
21	BCL11A	chr6:141474759-141475057	GM12878	blood:	n/a	n/a
22	BCL11A	chr6:141709759-141710112	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCL11A	chr6:141474827-141475050	H1-hESC	embryonic stem cell:	n/a	n/a
24	BCL3	chr6:141702321-141702647	GM12878	blood:	n/a	chr6:141702430-141702439 chr6:141702440-141702449 chr6:141702439-141702448
25	BCL3	chr6:141647588-141647832	GM12878	blood:	n/a	n/a
26	BCL3	chr6:141647553-141647910	GM12878	blood:	n/a	n/a
27	BCLAF1	chr6:141702322-141702563	GM12878	blood:	n/a	chr6:141702430-141702439 chr6:141702440-141702449 chr6:141702439-141702448
28	BHLHE40	chr6:141702358-141702623	GM12878	blood:	n/a	n/a
29	BRCA1	chr6:141647463-141648010	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr6:141630527-141630762	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr6:141516590-141516647	HepG2	liver:	n/a	n/a
32	CBX3	chr6:141647435-141648087	HCT-116	colon:	n/a	n/a
33	CBX3	chr6:141742585-141742940	HCT-116	colon:	n/a	n/a
34	CBX3	chr6:141647419-141648088	HCT-116	colon:	n/a	n/a
35	CBX3	chr6:141428603-141429239	HCT-116	colon:	n/a	n/a
36	CCNT2	chr6:141438727-141438866	K562	blood:	n/a	n/a
37	CCNT2	chr6:141546232-141546292	K562	blood:	n/a	n/a
38	CEBPB	chr6:141622933-141623251	HepG2	liver:	n/a	chr6:141622957-141622968
39	CEBPB	chr6:141742530-141742887	IMR90	lung:	n/a	n/a
40	CEBPB	chr6:141742602-141742871	A549	lung:	n/a	n/a
41	CEBPB	chr6:141431059-141431333	HepG2	liver:	n/a	chr6:141431189-141431200
42	CEBPB	chr6:141470508-141470777	HepG2	liver:	n/a	chr6:141470635-141470646
43	CEBPB	chr6:141746014-141746310	HepG2	liver:	n/a	chr6:141746166-141746177
44	CEBPB	chr6:141760039-141760303	HepG2	liver:	n/a	chr6:141760191-141760202
45	CEBPB	chr6:141622937-141623281	IMR90	lung:	n/a	chr6:141622957-141622968
46	CEBPB	chr6:141711121-141711395	H1-hESC	embryonic stem cell:	n/a	chr6:141711246-141711257 chr6:141711244-141711255 chr6:141711244-141711257 chr6:141711244-141711257 chr6:141711244-141711257
47	CEBPB	chr6:141632391-141632610	HepG2	liver:	n/a	n/a
48	CEBPB	chr6:141722290-141722536	HepG2	liver:	n/a	chr6:141722379-141722390
49	CEBPB	chr6:141452308-141452536	HepG2	liver:	n/a	chr6:141452387-141452398
50	CEBPB	chr6:141647427-141648015	Hela-S3	cervix:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:141603542-141603592	AG04449	skin:	fetal
2	chr6:141520754-141520804	AG09309	skin:	n/a
3	chr6:141473527-141473577	H1-hESC	embryonic stem cell:	embryo
4	chr6:141520754-141520804	IMR90	lung:	fetal
5	chr6:141473527-141473577	AG09319	gingival:	n/a
6	chr6:141520754-141520804	HPAEpiC	pulmonary alveolar:	n/a
7	chr6:141473527-141473577	A549	lung:	n/a
8	chr6:141603542-141603592	LNCaP	prostate:	n/a
9	chr6:141643325-141643375	ECC-1	luminal epithelium:	n/a
10	chr6:141486137-141486187	SK-N-SH_RA	brain:	n/a
11	chr6:141603542-141603592	AoSMC	blood vessel:	n/a
12	chr6:141603542-141603592	NT2-D1	testis:	n/a
13	chr6:141603542-141603592	Hela-S3	cervix:	n/a
14	chr6:141486137-141486187	HCT-116	colon:	n/a
15	chr6:141486137-141486187	HPAEpiC	pulmonary alveolar:	n/a
16	chr6:141643325-141643375	PrEC	prostate:	n/a
17	chr6:141520754-141520804	HepG2	liver:	n/a
18	chr6:141603542-141603592	NH-A	brain:	n/a
19	chr6:141643325-141643375	ProgFib	skin:	n/a
20	chr6:141520754-141520804	HIPEpiC	eye:	n/a
21	chr6:141643325-141643375	PFSK-1	brain:	n/a
22	chr6:141603542-141603592	HRE	kidney:	n/a
23	chr6:141473527-141473577	HNPCEpiC	eye:	n/a
24	chr6:141603542-141603592	RPTEC	kidney:	n/a
25	chr6:141643325-141643375	GM06990	blood:	n/a
26	chr6:141520754-141520804	MCF-7	breast:	n/a
27	chr6:141486137-141486187	K562	blood:	n/a
28	chr6:141643325-141643375	HRCEpiC	kidney:	n/a
29	chr6:141520754-141520804	HCT-116	colon:	n/a
30	chr6:141603542-141603592	CMK	blood:	n/a
31	chr6:141520754-141520804	HMEC	breast:	n/a
32	chr6:141643325-141643375	PANC-1	pancreas:	n/a
33	chr6:141643325-141643375	ovcar-3	ovarian:	n/a
34	chr6:141486137-141486187	HEK293	kidney:	embryo
35	chr6:141520754-141520804	AoSMC	blood vessel:	n/a
36	chr6:141603542-141603592	MCF10A-Er-Src	breast:	n/a
37	chr6:141603542-141603592	ECC-1	luminal epithelium:	n/a
38	chr6:141486137-141486187	Hela-S3	cervix:	n/a
39	chr6:141520754-141520804	T-47D	breast:	n/a
40	chr6:141486137-141486187	H1-hESC	embryonic stem cell:	embryo
41	chr6:141486137-141486187	NH-A	brain:	n/a
42	chr6:141643325-141643375	HEK293	kidney:	embryo
43	chr6:141520754-141520804	GM06990	blood:	n/a
44	chr6:141520754-141520804	PrEC	prostate:	n/a
45	chr6:141486137-141486187	HRCEpiC	kidney:	n/a
46	chr6:141520754-141520804	NHBE	bronchial:	n/a
47	chr6:141643325-141643375	AG09319	gingival:	n/a
48	chr6:141603542-141603592	AG04450	lung:	fetal
49	chr6:141643325-141643375	Hela-S3	cervix:	n/a
50	chr6:141520754-141520804	NH-A	brain:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:141557548..141559369-chr6:141561478..141563521,2	K562	blood:
2	chr6:141724021..141726766-chr6:141733635..141735399,2	K562	blood:
3	chr6:141466947..141468620-chr6:141486006..141488236,2	K562	blood:
4	chr6:141535806..141537434-chr6:141539065..141540907,2	K562	blood:
5	chr10:79621997..79624207-chr6:141528494..141531301,2	MCF-7	breast:
6	chr6:141557548..141559369-chr6:141561478..141563521,2	K562	blood:
7	chr6:141607703..141609358-chr6:141615352..141617178,2	K562	blood:
8	chr6:141630271..141631033-chr6:141883682..141884206,2	MCF-7	breast:
9	chr6:141630409..141632111-chr6:141635351..141637298,2	MCF-7	breast:
10	chr6:141368847..141371211-chr6:141441776..141443428,2	K562	blood:
11	chr6:141565815..141567855-chr6:141569717..141571593,2	MCF-7	breast:
12	chr6:141737292..141738838-chr6:141741938..141743477,2	MCF-7	breast:
13	chr6:141723648..141725230-chr6:141726285..141728524,2	K562	blood:
14	chr6:141724021..141726766-chr6:141733635..141735399,2	K562	blood:
15	chr6:141474693..141476532-chr6:141479215..141481575,2	MCF-7	breast:
16	chr6:141737292..141738838-chr6:141741938..141743477,2	MCF-7	breast:
17	chr6:141606885..141609429-chr6:141611912..141614017,2	MCF-7	breast:
18	chr6:141630179..141631093-chr6:141883723..141884605,3	MCF-7	breast:
19	chr6:141602459..141604737-chr6:141622065..141624728,2	K562	blood:
20	chr6:141457381..141459115-chr6:141461082..141463007,2	MCF-7	breast:
21	chr6:141723648..141725230-chr6:141726285..141728524,2	K562	blood:
22	chr6:141569154..141570819-chr6:141571531..141574122,2	K562	blood:
23	chr6:141607703..141609358-chr6:141615352..141617178,2	K562	blood:
24	chr6:141565815..141567855-chr6:141569717..141571593,2	MCF-7	breast:
25	chr6:141606885..141609429-chr6:141611912..141614017,2	MCF-7	breast:
26	chr6:141466947..141468620-chr6:141486006..141488236,2	K562	blood:
27	chr6:141450586..141452410-chr6:141456165..141457885,2	K562	blood:
28	chr6:141569154..141570819-chr6:141571531..141574122,2	K562	blood:
29	chr6:141557220..141559048-chr6:141561478..141563410,2	K562	blood:
30	chr6:141670532..141672796-chr6:141769039..141771621,2	K562	blood:
31	chr6:141450586..141452410-chr6:141456165..141457885,2	K562	blood:
32	chr6:141563813..141566176-chr6:141569270..141571804,2	K562	blood:
33	chr6:141630409..141632111-chr6:141635351..141637298,2	MCF-7	breast:
34	chr6:141535806..141537434-chr6:141539065..141540907,2	K562	blood:
35	chr6:141474693..141476532-chr6:141479215..141481575,2	MCF-7	breast:
36	chr6:141602459..141604737-chr6:141622065..141624728,2	K562	blood:
37	chr6:141557220..141559048-chr6:141561478..141563410,2	K562	blood:
38	chr6:141563813..141566176-chr6:141569270..141571804,2	K562	blood:
39	chr6:141457381..141459115-chr6:141461082..141463007,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GJE1-3	chr6:141724525-141724626	NONHSAT115292
2	lnc-GJE1-3	chr6:141724593-141724626	NONHSAT115293
3	lnc-GJE1-3	chr6:141724525-141724626	NONHSAT115291
4	lnc-GJE1-3	chr6:141724684-141725047	NONHSAT115293
5	lnc-GJE1-3	chr6:141742782-141743070	NONHSAT115294
6	lnc-GJE1-3	chr6:141724707-141725475	NONHSAT115292
7	lnc-GJE1-3	chr6:141724707-141725411	NONHSAT115291
8	lnc-GJE1-3	chr6:141724707-141724930	XLOC_005486
9	lnc-GJE1-3	chr6:141724594-141724626	XLOC_005486

No data

Variant related genes	Relation type
ENSG00000259828	TF binding region
ENSG00000259828	CpG island
WIPF1	miRNA target sites
FBLIM1	miRNA target sites

Extended variants
information (count: 7935 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:7935 , 50 per page) page: 1 2 3 4 5 6 7 ... 159

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9389870	chr6:141428255-141428256	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs375148732	chr6:141428273-141428274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567427325	chr6:141428355-141428356	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147397708	chr6:141428363-141428364	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12055475	chr6:141428384-141428385	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs557141665	chr6:141428419-141428420	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150246890	chr6:141428439-141428440	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs373526506	chr6:141428465-141428466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs559712994	chr6:141428472-141428473	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184528170	chr6:141428477-141428478	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573167115	chr6:141428538-141428539	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs540243721	chr6:141428579-141428580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561622033	chr6:141428591-141428592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs139310613	chr6:141428592-141428593	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112440152	chr6:141428619-141428620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556806178	chr6:141428625-141428626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs528280332	chr6:141428638-141428639	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs377538680	chr6:141428639-141428640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs35357746	chr6:141428697-141428698	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562590440	chr6:141428723-141428724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs141879686	chr6:141428738-141428739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs551946693	chr6:141428744-141428745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560451612	chr6:141428758-141428759	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189048659	chr6:141428771-141428772	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73583328	chr6:141428851-141428852	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs548966650	chr6:141428983-141428984	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575402355	chr6:141429039-141429040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539930391	chr6:141429123-141429124	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567293673	chr6:141429144-141429145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181412872	chr6:141429157-141429158	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550040505	chr6:141429207-141429208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571691562	chr6:141429233-141429234	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539295701	chr6:141429277-141429278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs557944805	chr6:141429287-141429288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573179371	chr6:141429304-141429305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534053184	chr6:141429317-141429318	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555420427	chr6:141429321-141429322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573592064	chr6:141429326-141429327	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs34549050	chr6:141429327-141429328	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113177925	chr6:141429344-141429345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562488376	chr6:141429360-141429361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186324819	chr6:141429414-141429415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs4896517	chr6:141429434-141429435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs570054151	chr6:141429538-141429539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs62431546	chr6:141429540-141429541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs190830984	chr6:141429555-141429556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs145289217	chr6:141429558-141429559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs564087699	chr6:141429607-141429608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs560264505	chr6:141429713-141429714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs527999815	chr6:141429731-141429732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Breast cancer	21364760	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute monocytic leukemia	16498392	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
craniofacial dysmorphism	21918468	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD

Chromatin state (count:1027 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:141424800-141428400	Weak transcription	HUVEC	blood vessel
2	chr6:141424800-141431600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr6:141425000-141431600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr6:141426400-141428400	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr6:141426400-141429000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr6:141426400-141429000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr6:141426600-141428400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr6:141427000-141428800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr6:141427000-141428800	Weak transcription	Spleen	Spleen
10	chr6:141427000-141429200	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr6:141427000-141429600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr6:141427000-141431600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr6:141427200-141428400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr6:141427200-141428400	Weak transcription	HMEC	breast
15	chr6:141427200-141428600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr6:141427200-141428800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr6:141427200-141428800	Weak transcription	NHDF-Ad	bronchial
18	chr6:141427200-141429000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr6:141427200-141429000	Weak transcription	NH-A	brain
20	chr6:141427200-141429400	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr6:141427200-141432800	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr6:141427400-141428600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
23	chr6:141427600-141432600	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr6:141427600-141432800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr6:141428000-141428400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:141428000-141431600	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr6:141428200-141428400	Enhancers	Placenta Amnion	Placenta Amnion
28	chr6:141428200-141429400	Enhancers	NHEK	skin
29	chr6:141428400-141428800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr6:141428400-141428800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr6:141428400-141429000	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr6:141428400-141429400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr6:141428400-141429400	Enhancers	HMEC	breast
34	chr6:141428400-141429800	Enhancers	HUVEC	blood vessel
35	chr6:141428400-141431600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr6:141428600-141428800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr6:141428600-141429000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr6:141428600-141429200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr6:141428600-141429400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr6:141428800-141429000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr6:141428800-141429000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr6:141428800-141429000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr6:141428800-141429000	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr6:141428800-141429000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr6:141428800-141429000	Enhancers	Muscle Satellite Cultured Cells	--
46	chr6:141428800-141429200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr6:141428800-141429200	Enhancers	Spleen	Spleen
48	chr6:141428800-141429200	Enhancers	NHDF-Ad	bronchial
49	chr6:141429000-141429400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr6:141429000-141429400	Enhancers	NH-A	brain

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