Variant report

Variant	esv3437533
Chromosome Location	chr6:56819343-56820491
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:56819983-56820269	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:56819871-56820412	K562	blood:	n/a	n/a
3	ATF2	chr6:56819977-56820719	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr6:56819919-56821092	GM12878	blood:	n/a	n/a
5	ATF2	chr6:56820294-56820697	GM12878	blood:	n/a	n/a
6	ATF2	chr6:56819836-56820432	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr6:56819767-56820311	K562	blood:	n/a	chr6:56819820-56819829 chr6:56819932-56819941
8	ATF3	chr6:56819728-56820242	K562	blood:	n/a	chr6:56819820-56819829 chr6:56819932-56819941
9	ATF3	chr6:56819392-56819722	K562	blood:	n/a	chr6:56819516-56819525
10	BACH1	chr6:56818233-56820972	H1-hESC	embryonic stem cell:	n/a	chr6:56819593-56819607 chr6:56818672-56818686
11	BACH1	chr6:56819418-56819736	K562	blood:	n/a	chr6:56819593-56819607
12	BATF	chr6:56820373-56820898	GM12878	blood:	n/a	chr6:56820511-56820521
13	BCL3	chr6:56819927-56820328	GM12878	blood:	n/a	chr6:56820001-56820014 chr6:56820313-56820322
14	BCL3	chr6:56819954-56820443	A549	lung:	n/a	chr6:56820001-56820014 chr6:56820313-56820322
15	BCLAF1	chr6:56820479-56821024	GM12878	blood:	n/a	chr6:56820510-56820519
16	BCLAF1	chr6:56819882-56821005	GM12878	blood:	n/a	chr6:56820510-56820519 chr6:56819882-56819891 chr6:56820001-56820014 chr6:56820313-56820322 chr6:56819885-56819894
17	BCLAF1	chr6:56819863-56820348	GM12878	blood:	n/a	chr6:56819877-56819890 chr6:56819880-56819893 chr6:56819882-56819891 chr6:56820001-56820014 chr6:56820313-56820322 chr6:56819885-56819894
18	BHLHE40	chr6:56819271-56820988	GM12878	blood:	n/a	chr6:56819836-56819852 chr6:56819844-56819860 chr6:56819850-56819866 chr6:56819771-56819787
19	BHLHE40	chr6:56819251-56820292	HepG2	liver:	n/a	chr6:56819836-56819852 chr6:56819844-56819860 chr6:56819850-56819866 chr6:56819771-56819787
20	BHLHE40	chr6:56819202-56820978	K562	blood:	n/a	chr6:56819836-56819852 chr6:56819844-56819860 chr6:56819850-56819866 chr6:56819771-56819787
21	BRCA1	chr6:56819972-56820319	HepG2	liver:	n/a	n/a
22	BRCA1	chr6:56820000-56820621	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr6:56819972-56820280	K562	blood:	n/a	n/a
24	CBX3	chr6:56819851-56820510	K562	blood:	n/a	n/a
25	CCNT2	chr6:56818752-56820369	K562	blood:	n/a	n/a
26	CEBPB	chr6:56820375-56820995	MCF-7	breast:	n/a	n/a
27	CEBPB	chr6:56820443-56820930	K562	blood:	n/a	n/a
28	CEBPB	chr6:56820431-56820914	K562	blood:	n/a	n/a
29	CEBPB	chr6:56820468-56820936	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:56819899-56820929	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr6:56819799-56820931	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr6:56819866-56819947	K562	blood:	n/a	n/a
33	CEBPB	chr6:56820346-56821087	GM12878	blood:	n/a	n/a
34	CEBPB	chr6:56819901-56820883	IMR90	lung:	n/a	n/a
35	CEBPB	chr6:56820480-56820912	A549	lung:	n/a	n/a
36	CHD1	chr6:56818955-56819466	GM12878	blood:	n/a	n/a
37	CHD1	chr6:56820402-56820952	GM12878	blood:	n/a	n/a
38	CHD1	chr6:56819139-56819433	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr6:56820050-56820464	K562	blood:	n/a	n/a
40	CHD2	chr6:56818414-56819460	GM12878	blood:	n/a	n/a
41	CHD2	chr6:56819190-56820887	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr6:56819985-56820438	GM12878	blood:	n/a	n/a
43	CHD2	chr6:56820000-56820341	HepG2	liver:	n/a	n/a
44	CHD2	chr6:56819969-56820965	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr6:56819264-56820550	K562	blood:	n/a	chr6:56819901-56819914
46	CREB1	chr6:56819244-56820384	A549	lung:	n/a	chr6:56819901-56819914
47	CREB1	chr6:56818922-56820539	H1-hESC	embryonic stem cell:	n/a	chr6:56819901-56819914
48	CREB1	chr6:56819182-56821037	HepG2	liver:	n/a	chr6:56819901-56819914
49	CREB1	chr6:56820026-56820269	A549	lung:	n/a	n/a
50	CREB1	chr6:56819158-56820470	GM12878	blood:	n/a	chr6:56819901-56819914

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:56820286-56820336	HCM	heart:	n/a
2	chr6:56820286-56820336	HCM	heart:	n/a
3	chr6:56819432-56819482	SK-N-SH	brain:	n/a
4	chr6:56819432-56819482	GM12892	blood:	n/a
5	chr6:56819432-56819482	ovcar-3	ovarian:	n/a
6	chr6:56819623-56819673	H1-hESC	embryonic stem cell:	embryo
7	chr6:56819298-56819348	AG09309	skin:	n/a
8	chr6:56819623-56819673	NHBE	bronchial:	n/a
9	chr6:56819429-56819479	T-47D	breast:	n/a
10	chr6:56819429-56819479	NH-A	brain:	n/a
11	chr6:56819912-56819962	Hela-S3	cervix:	n/a
12	chr6:56819429-56819479	HEEpiC	esophagus:	n/a
13	chr6:56819615-56819665	Hela-S3	cervix:	n/a
14	chr6:56820087-56820137	AG09309	skin:	n/a
15	chr6:56819612-56819662	HEEpiC	esophagus:	n/a
16	chr6:56819615-56819665	U87	brain:	n/a
17	chr6:56820386-56820436	HRPEpiC	eye:	n/a
18	chr6:56820386-56820436	HIPEpiC	eye:	n/a
19	chr6:56819615-56819665	HL-60	blood:	n/a
20	chr6:56820286-56820336	BE2_C	brain:	n/a
21	chr6:56820087-56820137	U87	brain:	n/a
22	chr6:56820087-56820137	HepG2	liver:	n/a
23	chr6:56819432-56819482	Caco-2	colon:	n/a
24	chr6:56819615-56819665	MCF-7	breast:	n/a
25	chr6:56820286-56820336	Jurkat	blood:	n/a
26	chr6:56819429-56819479	AG10803	skin:	n/a
27	chr6:56819432-56819482	AG09319	gingival:	n/a
28	chr6:56819615-56819665	HEK293	kidney:	embryo
29	chr6:56820286-56820336	AG10803	skin:	n/a
30	chr6:56820386-56820436	NH-A	brain:	n/a
31	chr6:56819623-56819673	MCF-7	breast:	n/a
32	chr6:56819612-56819662	SK-N-MC	brain:	n/a
33	chr6:56819615-56819665	NHDF-neo	bronchial:	n/a
34	chr6:56819615-56819665	HCPEpiC	choroid plexus:	n/a
35	chr6:56820286-56820336	HUVEC	blood vessel:	n/a
36	chr6:56819429-56819479	HUVEC	blood vessel:	n/a
37	chr6:56820386-56820436	HRE	kidney:	n/a
38	chr6:56819912-56819962	HCM	heart:	n/a
39	chr6:56819612-56819662	AG10803	skin:	n/a
40	chr6:56819623-56819673	SK-N-SH_RA	brain:	n/a
41	chr6:56819298-56819348	ProgFib	skin:	n/a
42	chr6:56819612-56819662	NH-A	brain:	n/a
43	chr6:56819912-56819962	IMR90	lung:	fetal
44	chr6:56819432-56819482	PFSK-1	brain:	n/a
45	chr6:56819429-56819479	ovcar-3	ovarian:	n/a
46	chr6:56819298-56819348	U87	brain:	n/a
47	chr6:56819912-56819962	Hepatocyte	liver:	n/a
48	chr6:56819623-56819673	GM12878	blood:	n/a
49	chr6:56820386-56820436	ovcar-3	ovarian:	n/a
50	chr6:56820286-56820336	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:56819605..56821184-chr6:57037443..57039145,2	K562	blood:
2	chr6:56819190..56819889-chr8:141520799..141521484,2	Hela-S3	cervix:
3	chr6:56809927..56811973-chr6:56817461..56820564,4	MCF-7	breast:
4	chr10:101380540..101381425-chr6:56819022..56819785,2	NB4	blood:
5	chr6:56818533..56822842-chr6:56954657..56959004,6	K562	blood:
6	chr6:56816669..56821714-chr6:56908406..56912975,10	K562	blood:
7	chr6:56817813..56820711-chr6:56965881..56967844,2	K562	blood:
8	chr6:56817242..56820030-chr9:96215701..96218251,2	MCF-7	breast:
9	chr6:56818015..56821855-chr6:57180367..57183028,4	K562	blood:
10	chr6:56818562..56821573-chr6:56964600..56969072,4	K562	blood:
11	chr3:53925577..53926163-chr6:56819278..56819811,2	Hela-S3	cervix:
12	chr6:56767464..56768319-chr6:56820397..56821373,5	MCF-7	breast:
13	chr6:56820267..56822074-chr6:56879367..56881411,2	K562	blood:
14	chr6:56817930..56821539-chr6:56909452..56912838,6	K562	blood:
15	chr6:56714424..56718313-chr6:56818301..56821248,4	MCF-7	breast:
16	chr6:56817510..56820425-chr6:57182215..57184592,2	K562	blood:
17	chr6:56820330..56821970-chr6:56922226..56924549,2	MCF-7	breast:
18	chr6:56818167..56820292-chr6:57177596..57182762,4	MCF-7	breast:
19	chr6:56818718..56821144-chr6:56954189..56956169,2	MCF-7	breast:
20	chr6:56716516..56717082-chr6:56820161..56820759,2	MCF-7	breast:
21	chr6:56818586..56820160-chr6:56954804..56956394,2	K562	blood:
22	chr6:56817882..56819972-chr6:57035811..57037517,2	K562	blood:
23	chr6:56820475..56822704-chr6:56829156..56832250,3	MCF-7	breast:

Variant related genes	Relation type
BEND6	TF binding region
DST	TF binding region
BEND6	CpG island
DST	CpG island
ENSG00000146143	chromatin interactions
ENSG00000226803	chromatin interactions
ENSG00000151914	chromatin interactions
ENSG00000200224	chromatin interactions
ENSG00000113811	chromatin interactions
ENSG00000112200	chromatin interactions
ENSG00000188938	chromatin interactions
ENSG00000112208	chromatin interactions
ENSG00000168116	chromatin interactions
ENSG00000104472	chromatin interactions
ENSG00000260475	chromatin interactions

Extended variants
information (count: 32 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:32 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555749699	chr6:56819380-56819381	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
2	rs13219655	chr6:56819412-56819413	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
3	rs568067794	chr6:56819470-56819471	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
4	rs535057053	chr6:56819486-56819487	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
5	rs557026817	chr6:56819564-56819565	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
6	rs575033955	chr6:56819582-56819583	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
7	rs539146286	chr6:56819584-56819585	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
8	rs557561290	chr6:56819724-56819725	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
9	rs572688845	chr6:56819757-56819758	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
10	rs540538892	chr6:56819779-56819780	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
11	rs561807560	chr6:56819809-56819810	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
12	rs573982192	chr6:56819899-56819900	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
13	rs544240118	chr6:56819918-56819919	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
14	rs562861910	chr6:56819919-56819920	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs533493489	chr6:56820007-56820008	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
16	rs551888601	chr6:56820045-56820046	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs560684233	chr6:56820051-56820052	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs527853229	chr6:56820104-56820105	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs549652450	chr6:56820143-56820144	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs12154043	chr6:56820163-56820164	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs13193465	chr6:56820248-56820249	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs550206687	chr6:56820288-56820289	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs568316444	chr6:56820299-56820300	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs565304072	chr6:56820305-56820306	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs568493913	chr6:56820320-56820321	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs539183677	chr6:56820346-56820347	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs557400257	chr6:56820347-56820348	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs114324793	chr6:56820359-56820360	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs145259774	chr6:56820394-56820395	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs13193800	chr6:56820405-56820406	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs571167156	chr6:56820409-56820410	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs527345067	chr6:56820480-56820481	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Osteosarcoma	16790693	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
Lung cancer	18438408	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Neurocytoma	17123091	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Neuroblastoma	19686582	CNVD
Neuroblastoma	17289879	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	16912164	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD

Chromatin state (count:259 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:56817000-56820600	Active TSS	NHLF	lung
2	chr6:56817800-56819400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
3	chr6:56817800-56821200	Active TSS	NHDF-Ad	bronchial
4	chr6:56818000-56820400	Active TSS	Muscle Satellite Cultured Cells	--
5	chr6:56818000-56820600	Active TSS	Colon Smooth Muscle	Colon
6	chr6:56818000-56821000	Active TSS	HSMM	muscle
7	chr6:56818000-56821200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr6:56818000-56821400	Active TSS	Pancreatic Islets	Pancreatic Islet
9	chr6:56818200-56819400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
10	chr6:56818200-56819400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
11	chr6:56818200-56819400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr6:56818200-56819400	Flanking Active TSS	Placenta	Placenta
13	chr6:56818200-56819400	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
14	chr6:56818200-56819400	Active TSS	Right Atrium	heart
15	chr6:56818200-56819400	Flanking Active TSS	HUVEC	blood vessel
16	chr6:56818200-56820200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr6:56818200-56820200	Bivalent/Poised TSS	Rectal Mucosa Donor 31	rectum
18	chr6:56818200-56820400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
19	chr6:56818200-56820400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr6:56818200-56820800	Active TSS	Breast Myoepithelial Primary Cells	Breast
21	chr6:56818200-56820800	Active TSS	Aorta	Aorta
22	chr6:56818200-56821000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr6:56818200-56821000	Bivalent/Poised TSS	Fetal Kidney	kidney
24	chr6:56818200-56821000	Active TSS	Rectal Smooth Muscle	rectum
25	chr6:56818200-56821000	Active TSS	A549	lung
26	chr6:56818400-56819400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
27	chr6:56818400-56819400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
28	chr6:56818400-56819400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
29	chr6:56818400-56819400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
30	chr6:56818400-56819400	Flanking Bivalent TSS/Enh	Primary B cells from cord blood	blood
31	chr6:56818400-56819400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
32	chr6:56818400-56819400	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
33	chr6:56818400-56819400	Flanking Bivalent TSS/Enh	Liver	Liver
34	chr6:56818400-56819400	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
35	chr6:56818400-56819400	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
36	chr6:56818400-56819600	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
37	chr6:56818400-56820400	Active TSS	HSMMtube	muscle
38	chr6:56818400-56820600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr6:56818400-56820600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr6:56818400-56820600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr6:56818400-56820600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
42	chr6:56818400-56820800	Active TSS	Ovary	ovary
43	chr6:56818400-56820800	Active TSS	Psoas Muscle	Psoas
44	chr6:56818400-56821000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr6:56818400-56821000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr6:56818400-56821000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr6:56818400-56821000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr6:56818400-56821000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr6:56818400-56821000	Active TSS	GM12878-XiMat	blood
50	chr6:56818400-56821000	Active TSS	Osteobl	bone

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