Variant report

Variant	esv1832313
Chromosome Location	chr6:149789511-149840750
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1526)
CpG islands
(count:1162)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1526 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:149817948-149817956	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:149838569-149839020	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:149838610-149838954	K562	blood:	n/a	n/a
4	ARID3A	chr6:149815057-149815379	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:149820177-149820586	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:149805810-149806816	HepG2	liver:	n/a	n/a
7	ATF1	chr6:149820324-149820571	K562	blood:	n/a	n/a
8	ATF2	chr6:149802895-149803670	GM12878	blood:	n/a	n/a
9	ATF2	chr6:149815979-149816566	GM12878	blood:	n/a	n/a
10	ATF2	chr6:149792810-149793813	GM12878	blood:	n/a	n/a
11	ATF2	chr6:149805947-149806460	GM12878	blood:	n/a	n/a
12	ATF2	chr6:149789927-149790416	GM12878	blood:	n/a	n/a
13	ATF2	chr6:149817708-149818172	GM12878	blood:	n/a	n/a
14	ATF2	chr6:149794137-149794625	GM12878	blood:	n/a	n/a
15	ATF2	chr6:149802774-149803763	GM12878	blood:	n/a	n/a
16	ATF2	chr6:149789899-149790409	GM12878	blood:	n/a	n/a
17	ATF2	chr6:149805417-149806918	GM12878	blood:	n/a	n/a
18	ATF2	chr6:149794115-149794595	GM12878	blood:	n/a	n/a
19	ATF2	chr6:149792855-149793395	GM12878	blood:	n/a	n/a
20	ATF2	chr6:149815968-149816428	GM12878	blood:	n/a	n/a
21	ATF3	chr6:149818513-149818843	K562	blood:	n/a	n/a
22	BACH1	chr6:149824304-149824307	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr6:149817848-149818115	GM12878	blood:	n/a	n/a
24	BATF	chr6:149805894-149806464	GM12878	blood:	n/a	n/a
25	BATF	chr6:149792984-149793324	GM12878	blood:	n/a	n/a
26	BATF	chr6:149792884-149793330	GM12878	blood:	n/a	n/a
27	BATF	chr6:149816006-149816348	GM12878	blood:	n/a	n/a
28	BATF	chr6:149815909-149816350	GM12878	blood:	n/a	n/a
29	BATF	chr6:149789990-149790354	GM12878	blood:	n/a	n/a
30	BATF	chr6:149819582-149819781	GM12878	blood:	n/a	chr6:149819685-149819696
31	BCL11A	chr6:149803282-149803590	GM12878	blood:	n/a	chr6:149803419-149803432 chr6:149803530-149803539
32	BCL11A	chr6:149805927-149806376	GM12878	blood:	n/a	chr6:149806120-149806129 chr6:149806231-149806240
33	BCL11A	chr6:149816091-149816323	GM12878	blood:	n/a	n/a
34	BCL11A	chr6:149815996-149816341	GM12878	blood:	n/a	n/a
35	BCL11A	chr6:149792950-149793283	GM12878	blood:	n/a	n/a
36	BCL11A	chr6:149792911-149793305	GM12878	blood:	n/a	n/a
37	BCL11A	chr6:149804438-149804679	GM12878	blood:	n/a	n/a
38	BCL11A	chr6:149811131-149811443	GM12878	blood:	n/a	n/a
39	BCL11A	chr6:149789963-149790382	GM12878	blood:	n/a	n/a
40	BCL3	chr6:149817855-149818128	GM12878	blood:	n/a	n/a
41	BCL3	chr6:149794083-149794603	GM12878	blood:	n/a	n/a
42	BCL3	chr6:149789909-149790414	GM12878	blood:	n/a	n/a
43	BCL3	chr6:149803109-149803623	GM12878	blood:	n/a	chr6:149803419-149803432 chr6:149803530-149803539
44	BCL3	chr6:149815979-149816365	GM12878	blood:	n/a	n/a
45	BCL3	chr6:149792891-149793836	GM12878	blood:	n/a	n/a
46	BCLAF1	chr6:149805776-149806379	GM12878	blood:	n/a	chr6:149806120-149806129 chr6:149806231-149806240
47	BCLAF1	chr6:149789876-149790420	GM12878	blood:	n/a	n/a
48	BCLAF1	chr6:149792820-149793613	GM12878	blood:	n/a	n/a
49	BCLAF1	chr6:149806418-149806944	GM12878	blood:	n/a	n/a
50	BCLAF1	chr6:149816002-149816382	GM12878	blood:	n/a	n/a

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:149803206-149803256	NT2-D1	testis:	n/a
2	chr6:149803111-149803161	ovcar-3	ovarian:	n/a
3	chr6:149806635-149806685	GM06990	blood:	n/a
4	chr6:149803206-149803256	NT2-D1	testis:	n/a
5	chr6:149803111-149803161	ovcar-3	ovarian:	n/a
6	chr6:149806635-149806685	GM06990	blood:	n/a
7	chr6:149803087-149803137	AG09319	gingival:	n/a
8	chr6:149806331-149806381	SK-N-SH	brain:	n/a
9	chr6:149813350-149813400	BE2_C	brain:	n/a
10	chr6:149803426-149803476	MCF-7	breast:	n/a
11	chr6:149803087-149803137	NHDF-neo	bronchial:	n/a
12	chr6:149806131-149806181	ProgFib	skin:	n/a
13	chr6:149803444-149803494	H1-hESC	embryonic stem cell:	embryo
14	chr6:149803426-149803476	GM06990	blood:	n/a
15	chr6:149806339-149806389	HCF	heart:	n/a
16	chr6:149806331-149806381	HL-60	blood:	n/a
17	chr6:149806273-149806323	HCPEpiC	choroid plexus:	n/a
18	chr6:149806081-149806131	SK-N-MC	brain:	n/a
19	chr6:149806339-149806389	NB4	blood:	n/a
20	chr6:149805995-149806045	MCF-7	breast:	n/a
21	chr6:149803444-149803494	HRPEpiC	eye:	n/a
22	chr6:149806077-149806127	AG09309	skin:	n/a
23	chr6:149806502-149806552	Hepatocyte	liver:	n/a
24	chr6:149806732-149806782	NH-A	brain:	n/a
25	chr6:149806635-149806685	GM12878	blood:	n/a
26	chr6:149803111-149803161	GM19239	blood:	n/a
27	chr6:149806339-149806389	AG09319	gingival:	n/a
28	chr6:149803087-149803137	ECC-1	luminal epithelium:	n/a
29	chr6:149813417-149813467	HIPEpiC	eye:	n/a
30	chr6:149806273-149806323	HPAEpiC	pulmonary alveolar:	n/a
31	chr6:149806235-149806285	BJ	skin:	n/a
32	chr6:149806131-149806181	MCF-7	breast:	n/a
33	chr6:149806635-149806685	NHDF-neo	bronchial:	n/a
34	chr6:149806077-149806127	SK-N-SH	brain:	n/a
35	chr6:149806081-149806131	SKMC	muscle:	n/a
36	chr6:149806339-149806389	AoSMC	blood vessel:	n/a
37	chr6:149806502-149806552	HCM	heart:	n/a
38	chr6:149803206-149803256	AG04450	lung:	fetal
39	chr6:149803426-149803476	MCF10A-Er-Src	breast:	n/a
40	chr6:149813417-149813467	Jurkat	blood:	n/a
41	chr6:149803087-149803137	HCPEpiC	choroid plexus:	n/a
42	chr6:149803206-149803256	H1-hESC	embryonic stem cell:	embryo
43	chr6:149806235-149806285	HNPCEpiC	eye:	n/a
44	chr6:149806732-149806782	Hepatocyte	liver:	n/a
45	chr6:149806077-149806127	HAEpiC	amniotic membrane:	n/a
46	chr6:149803111-149803161	Hepatocyte	liver:	n/a
47	chr6:149803206-149803256	HRCEpiC	kidney:	n/a
48	chr6:149803444-149803494	HPAEpiC	pulmonary alveolar:	n/a
49	chr6:149803087-149803137	MCF10A-Er-Src	breast:	n/a
50	chr6:149803206-149803256	ProgFib	skin:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:149826630..149828653-chr6:149833596..149836466,2	MCF-7	breast:
2	chr6:149351574..149354764-chr6:149837931..149839815,3	MCF-7	breast:
3	chr6:149827201..149829312-chr6:149829316..149833197,3	K562	blood:
4	chr6:149818918..149821487-chr6:149828653..149831549,2	K562	blood:
5	chr6:149829549..149832059-chr6:149838355..149841591,3	K562	blood:
6	chr6:149821833..149823936-chr6:149826832..149829564,2	K562	blood:
7	chr6:149352653..149356079-chr6:149835245..149838856,4	MCF-7	breast:
8	chr6:149827201..149829312-chr6:149829316..149833197,3	K562	blood:
9	chr6:149763319..149765484-chr6:149839894..149842239,2	MCF-7	breast:
10	chr6:149833219..149834722-chr6:149885011..149886863,2	K562	blood:
11	chr6:149795137..149796969-chr6:149800706..149802832,2	K562	blood:
12	chr6:149821833..149823936-chr6:149826832..149829564,2	K562	blood:
13	chr6:149820594..149823333-chr6:149826797..149829564,2	K562	blood:
14	chr6:149795286..149796796-chr6:149799603..149801991,2	MCF-7	breast:
15	chr6:149806502..149808230-chr6:149808327..149810146,3	MCF-7	breast:
16	chr6:149827622..149830307-chr6:149831697..149834831,3	K562	blood:
17	chr6:149827622..149830307-chr6:149831697..149834831,3	K562	blood:
18	chr6:149806502..149808230-chr6:149808327..149810146,3	MCF-7	breast:
19	chr6:149827523..149830271-chr6:149854343..149857106,2	K562	blood:
20	chr6:149830636..149832927-chr6:149835174..149836889,2	K562	blood:
21	chr6:149637666..149639444-chr6:149793847..149796038,2	K562	blood:
22	chr6:149383326..149385978-chr6:149822230..149824541,2	K562	blood:
23	chr6:149820594..149823333-chr6:149826797..149829564,2	K562	blood:
24	chr6:149792520..149794344-chr6:149794518..149797030,2	K562	blood:
25	chr6:149801342..149802873-chr6:149804387..149807166,3	MCF-7	breast:
26	chr6:149818918..149821487-chr6:149828653..149831549,2	K562	blood:
27	chr6:149785728..149788361-chr6:149790642..149793612,2	K562	blood:
28	chr6:149792520..149794344-chr6:149794518..149797030,2	K562	blood:
29	chr6:149826630..149828653-chr6:149833596..149836466,2	MCF-7	breast:
30	chr6:149795137..149796969-chr6:149800706..149802832,2	K562	blood:
31	chr6:149832205..149836453-chr6:149836476..149839244,4	K562	blood:
32	chr6:149830636..149832927-chr6:149835174..149836889,2	K562	blood:
33	chr6:149798641..149801260-chr6:149810434..149812141,2	K562	blood:
34	chr6:149839863..149841479-chr6:149843925..149845587,2	K562	blood:
35	chr6:149798641..149801260-chr6:149810434..149812141,2	K562	blood:
36	chr6:149812643..149814756-chr6:149815936..149817479,2	K562	blood:
37	chr6:149795286..149796796-chr6:149799603..149801991,2	MCF-7	breast:
38	chr6:149833362..149835926-chr6:149836869..149839457,3	K562	blood:

No data

Variant related genes	Relation type
PPIL4	TF binding region
RNU7-3P	TF binding region
ENSG00000219553	TF binding region
ZC3H12D	TF binding region
PPIL4	CpG island
RNU7-3P	CpG island
ENSG00000219553	CpG island
ZC3H12D	CpG island
ENSG00000131013	chromatin interactions
ENSG00000219553	chromatin interactions
ENSG00000055208	chromatin interactions
ENSG00000252244	chromatin interactions
ENSG00000178199	chromatin interactions
ENSG00000236591	chromatin interactions

Extended variants
information (count: 1849 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1849 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188377946	chr6:149789625-149789626	Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs547372105	chr6:149789650-149789651	Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567506703	chr6:149789692-149789693	Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs370003144	chr6:149789709-149789710	Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529953788	chr6:149789711-149789712	Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375013912	chr6:149789759-149789760	Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548936314	chr6:149789760-149789761	Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs437931	chr6:149789772-149789773	Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs117325528	chr6:149789796-149789797	Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558269997	chr6:149789879-149789880	Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs555228338	chr6:149789899-149789900	Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs193222619	chr6:149789998-149789999	Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs367950351	chr6:149790048-149790049	Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs149242293	chr6:149790085-149790086	Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143417466	chr6:149790111-149790112	Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574356310	chr6:149790135-149790136	Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543367144	chr6:149790141-149790142	Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556175850	chr6:149790227-149790228	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576142305	chr6:149790259-149790260	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545116372	chr6:149790275-149790276	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565038413	chr6:149790312-149790313	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs139004257	chr6:149790315-149790316	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374062646	chr6:149790316-149790317	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs386706939	chr6:149790319-149790320	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184047483	chr6:149790320-149790321	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs368593388	chr6:149790322-149790323	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372110448	chr6:149790324-149790325	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549697900	chr6:149790329-149790330	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs377172441	chr6:149790331-149790332	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568900742	chr6:149790339-149790340	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563825347	chr6:149790357-149790358	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577220336	chr6:149790360-149790361	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187788105	chr6:149790379-149790380	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2789499	chr6:149790393-149790394	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571671119	chr6:149790407-149790408	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534052319	chr6:149790421-149790422	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371517120	chr6:149790454-149790455	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191610481	chr6:149790484-149790485	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs419562	chr6:149790511-149790512	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs536932167	chr6:149790519-149790520	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556938784	chr6:149790542-149790543	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569083754	chr6:149790550-149790551	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576105357	chr6:149790551-149790552	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544942763	chr6:149790612-149790613	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs558277720	chr6:149790652-149790653	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs139663005	chr6:149790666-149790667	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs540796752	chr6:149790669-149790670	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs78500019	chr6:149790691-149790692	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs373349002	chr6:149790761-149790762	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs574330343	chr6:149790772-149790773	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
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
Gastric cancer	17908304	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
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	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
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Cancer	17160897	CNVD
Breast cancer	17417639	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1664 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149776200-149789600	Weak transcription	Fetal Thymus	thymus
2	chr6:149776800-149802000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr6:149780800-149793400	Weak transcription	Primary T cells from cord blood	blood
4	chr6:149781400-149793800	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr6:149782200-149802000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr6:149783200-149802400	Weak transcription	Primary hematopoietic stem cells	blood
7	chr6:149783800-149793400	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
8	chr6:149784400-149789600	Weak transcription	Duodenum Mucosa	Duodenum
9	chr6:149785200-149792800	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
10	chr6:149785800-149789600	Weak transcription	Colon Smooth Muscle	Colon
11	chr6:149785800-149789600	Weak transcription	Rectal Smooth Muscle	rectum
12	chr6:149785800-149793400	Weak transcription	Hela-S3	cervix
13	chr6:149785800-149794600	Weak transcription	Gastric	stomach
14	chr6:149785800-149794800	Weak transcription	Right Atrium	heart
15	chr6:149786000-149794200	Weak transcription	Colonic Mucosa	Colon
16	chr6:149786200-149793400	Weak transcription	Stomach Mucosa	stomach
17	chr6:149786400-149789600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr6:149787000-149790000	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chr6:149787400-149789600	Weak transcription	Fetal Intestine Small	intestine
20	chr6:149787400-149790800	Weak transcription	Lung	lung
21	chr6:149788200-149789600	Enhancers	Primary T cells fromperipheralblood	blood
22	chr6:149788200-149789600	Genic enhancers	Primary T helper cells PMA-I stimulated	--
23	chr6:149788200-149790000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
24	chr6:149788200-149791200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr6:149788200-149792400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr6:149788200-149795200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr6:149788400-149794600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:149788600-149789600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr6:149788600-149790400	Enhancers	Duodenum Smooth Muscle	Duodenum
30	chr6:149788800-149789600	Genic enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr6:149788800-149789800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr6:149788800-149790000	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr6:149788800-149790200	Flanking Active TSS	GM12878-XiMat	blood
34	chr6:149789000-149789600	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr6:149789000-149790600	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr6:149789000-149792800	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr6:149789000-149794400	Weak transcription	Brain Cingulate Gyrus	brain
38	chr6:149789200-149789600	Enhancers	Primary B cells from cord blood	blood
39	chr6:149789200-149793800	Weak transcription	HepG2	liver
40	chr6:149789400-149789800	Weak transcription	Spleen	Spleen
41	chr6:149789400-149790200	Flanking Active TSS	Primary B cells from peripheral blood	blood
42	chr6:149789400-149790200	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr6:149789400-149790200	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
44	chr6:149789400-149790400	Enhancers	Primary T killer memory cells from peripheral blood	blood
45	chr6:149789400-149790400	Enhancers	Stomach Smooth Muscle	stomach
46	chr6:149789400-149806000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr6:149789600-149789800	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
48	chr6:149789600-149789800	Active TSS	Duodenum Mucosa	Duodenum
49	chr6:149789600-149790000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
50	chr6:149789600-149790000	Strong transcription	Fetal Intestine Small	intestine

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