Variant report

Variant	esv3336787
Chromosome Location	chr6:147829109-147831307
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:211)
CpG islands
(count:610)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:211 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr6:147828493-147829666	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr6:147829901-147830079	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr6:147831064-147831358	K562	blood:	n/a	n/a
4	CCNT2	chr6:147830210-147830266	K562	blood:	n/a	n/a
5	CCNT2	chr6:147829098-147829308	K562	blood:	n/a	n/a
6	CCNT2	chr6:147829509-147829850	K562	blood:	n/a	chr6:147829712-147829721
7	CHD1	chr6:147830668-147830686	H1-hESC	embryonic stem cell:	n/a	n/a
8	CREB1	chr6:147829372-147829888	A549	lung:	n/a	n/a
9	CTBP2	chr6:147829088-147830660	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr6:147830192-147830508	IMR90	lung:	n/a	n/a
11	CTCF	chr6:147829200-147829350	GM12869	blood:	n/a	n/a
12	CTCF	chr6:147830340-147830490	GM12871	blood:	n/a	n/a
13	CTCF	chr6:147829759-147829829	Kidney_OC	kidney:	n/a	n/a
14	CTCF	chr6:147830300-147830450	AG04449	skin:	n/a	n/a
15	CTCF	chr6:147830280-147830430	NHLF	lung:	n/a	n/a
16	CTCF	chr6:147830330-147830421	NHEK	skin:	n/a	n/a
17	CTCF	chr6:147830280-147830430	Caco-2	colon:	n/a	n/a
18	CTCF	chr6:147830324-147830467	K562	blood:	n/a	n/a
19	CTCF	chr6:147830380-147830530	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr6:147829280-147829430	NHDF-neo	bronchial:	n/a	chr6:147829346-147829359
21	CTCF	chr6:147829400-147829550	HEK293	kidney:	n/a	n/a
22	CTCF	chr6:147830405-147830407	A549	lung:	n/a	n/a
23	CTCF	chr6:147830306-147830383	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr6:147829240-147829390	HRPEpiC	eye:	n/a	chr6:147829346-147829359
25	CTCF	chr6:147829780-147829930	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr6:147830277-147830304	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr6:147830220-147830370	AG09309	skin:	n/a	n/a
28	CTCF	chr6:147830220-147830370	AG09319	gingival:	n/a	n/a
29	CTCF	chr6:147829420-147829570	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr6:147829320-147829570	K562	blood:	n/a	chr6:147829346-147829359
31	CTCF	chr6:147829080-147829230	RPTEC	kidney:	n/a	n/a
32	CTCF	chr6:147829100-147829250	GM12866	blood:	n/a	n/a
33	CTCF	chr6:147829160-147829310	HMEC	breast:	n/a	n/a
34	CTCF	chr6:147830340-147830490	AG04449	skin:	n/a	n/a
35	CTCF	chr6:147829280-147829430	HBMEC	blood vessel:	n/a	chr6:147829346-147829359
36	CTCF	chr6:147830300-147830450	AG04450	lung:	n/a	n/a
37	CTCF	chr6:147829280-147829430	AG09319	gingival:	n/a	chr6:147829346-147829359
38	CTCF	chr6:147830376-147830403	A549	lung:	n/a	n/a
39	CTCF	chr6:147829020-147829170	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr6:147829420-147829570	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr6:147829400-147829550	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr6:147830240-147830512	GM19238	blood:	n/a	n/a
43	CTCF	chr6:147830410-147830411	A549	lung:	n/a	n/a
44	CTCF	chr6:147829280-147829570	AG04449	skin:	n/a	chr6:147829346-147829359
45	CTCF	chr6:147830480-147830630	BJ	skin:	n/a	n/a
46	CTCF	chr6:147829240-147829390	GM12867	blood:	n/a	chr6:147829346-147829359
47	CTCF	chr6:147830220-147830370	NHEK	skin:	n/a	n/a
48	CTCF	chr6:147829440-147829590	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr6:147830460-147830610	HAc	cerebellar:	n/a	n/a
50	CTCF	chr6:147829220-147829370	HMF	breast:	n/a	chr6:147829346-147829359

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:147830046-147830096	NB4	blood:	n/a
2	chr6:147830561-147830611	SAEC	small airway:	n/a
3	chr6:147829913-147829963	NB4	blood:	n/a
4	chr6:147830046-147830096	GM12892	blood:	n/a
5	chr6:147830172-147830222	ProgFib	skin:	n/a
6	chr6:147830025-147830075	NH-A	brain:	n/a
7	chr6:147829408-147829458	PFSK-1	brain:	n/a
8	chr6:147830172-147830222	GM19239	blood:	n/a
9	chr6:147830055-147830105	SK-N-SH	brain:	n/a
10	chr6:147829913-147829963	HRCEpiC	kidney:	n/a
11	chr6:147829408-147829458	Jurkat	blood:	n/a
12	chr6:147829801-147829851	NHBE	bronchial:	n/a
13	chr6:147829799-147829849	GM19239	blood:	n/a
14	chr6:147830043-147830093	GM06990	blood:	n/a
15	chr6:147829408-147829458	RPTEC	kidney:	n/a
16	chr6:147830043-147830093	AG09319	gingival:	n/a
17	chr6:147829801-147829851	BE2_C	brain:	n/a
18	chr6:147829799-147829849	GM12891	blood:	n/a
19	chr6:147829801-147829851	HRCEpiC	kidney:	n/a
20	chr6:147830055-147830105	BE2_C	brain:	n/a
21	chr6:147829799-147829849	IMR90	lung:	fetal
22	chr6:147830561-147830611	HAEpiC	amniotic membrane:	n/a
23	chr6:147830046-147830096	GM19239	blood:	n/a
24	chr6:147829913-147829963	BJ	skin:	n/a
25	chr6:147830055-147830105	AG09309	skin:	n/a
26	chr6:147829799-147829849	AG09319	gingival:	n/a
27	chr6:147830172-147830222	Hela-S3	cervix:	n/a
28	chr6:147829913-147829963	ovcar-3	ovarian:	n/a
29	chr6:147829799-147829849	MCF10A-Er-Src	breast:	n/a
30	chr6:147830172-147830222	K562	blood:	n/a
31	chr6:147830025-147830075	HCPEpiC	choroid plexus:	n/a
32	chr6:147830172-147830222	BJ	skin:	n/a
33	chr6:147830046-147830096	H1-hESC	embryonic stem cell:	embryo
34	chr6:147830172-147830222	PFSK-1	brain:	n/a
35	chr6:147830172-147830222	AG09309	skin:	n/a
36	chr6:147830025-147830075	GM06990	blood:	n/a
37	chr6:147830043-147830093	RPTEC	kidney:	n/a
38	chr6:147830172-147830222	Caco-2	colon:	n/a
39	chr6:147830055-147830105	PANC-1	pancreas:	n/a
40	chr6:147829801-147829851	HUVEC	blood vessel:	n/a
41	chr6:147829913-147829963	HAEpiC	amniotic membrane:	n/a
42	chr6:147830561-147830611	MCF10A-Er-Src	breast:	n/a
43	chr6:147830025-147830075	HIPEpiC	eye:	n/a
44	chr6:147829801-147829851	HAEpiC	amniotic membrane:	n/a
45	chr6:147829801-147829851	SAEC	small airway:	n/a
46	chr6:147830043-147830093	SK-N-SH	brain:	n/a
47	chr6:147829799-147829849	GM06990	blood:	n/a
48	chr6:147830046-147830096	HIPEpiC	eye:	n/a
49	chr6:147830025-147830075	AoSMC	blood vessel:	n/a
50	chr6:147830025-147830075	CMK	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:147830521..147832164-chr6:147833225..147837282,3	K562	blood:

No data

Variant related genes	Relation type
SAMD5	TF binding region
SAMD5	CpG island

Extended variants
information (count: 95 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:95 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539035457	chr6:147829122-147829123	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs558953944	chr6:147829137-147829138	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs572436526	chr6:147829164-147829165	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs541549692	chr6:147829269-147829270	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs113076303	chr6:147829284-147829285	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs183074908	chr6:147829320-147829321	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs573802826	chr6:147829329-147829330	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs55866133	chr6:147829529-147829530	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs55792163	chr6:147829532-147829533	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs534648235	chr6:147829596-147829597	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs542479613	chr6:147829637-147829638	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs112150638	chr6:147829640-147829641	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs116980459	chr6:147829670-147829671	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs35009077	chr6:147829684-147829685	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs544604200	chr6:147829709-147829710	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs564937487	chr6:147829718-147829719	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs561045748	chr6:147829734-147829735	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs527372510	chr6:147829749-147829750	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs375131400	chr6:147829765-147829766	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs547489407	chr6:147829769-147829770	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs533667951	chr6:147829804-147829805	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs567722358	chr6:147829828-147829829	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs530324785	chr6:147829840-147829841	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs73020122	chr6:147829844-147829845	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs570360212	chr6:147829848-147829849	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs73578573	chr6:147829895-147829896	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs370573324	chr6:147829919-147829920	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs76970923	chr6:147829928-147829929	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs373742632	chr6:147829988-147829989	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs555062315	chr6:147830007-147830008	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs191603443	chr6:147830023-147830024	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs369486241	chr6:147830026-147830027	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs200392173	chr6:147830065-147830066	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs367585597	chr6:147830072-147830073	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs66812182	chr6:147830073-147830074	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs544938806	chr6:147830089-147830090	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs373110663	chr6:147830105-147830106	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
38	rs376324781	chr6:147830126-147830127	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs564695962	chr6:147830130-147830131	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs199651315	chr6:147830131-147830132	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs373282999	chr6:147830172-147830173	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs147569487	chr6:147830188-147830189	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs13202878	chr6:147830195-147830196	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs372741951	chr6:147830208-147830209	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
45	rs71547193	chr6:147830212-147830213	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs200703854	chr6:147830219-147830220	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs140318247	chr6:147830224-147830225	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs200871958	chr6:147830280-147830281	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs145237793	chr6:147830292-147830293	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs142462155	chr6:147830303-147830304	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Zellweger syndrome	21572526	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
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
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147827800-147829200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
2	chr6:147827800-147829200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
3	chr6:147827800-147829200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
4	chr6:147827800-147829600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:147827800-147829600	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
6	chr6:147827800-147830200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
7	chr6:147827800-147830800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
8	chr6:147827800-147831800	Active TSS	Pancreatic Islets	Pancreatic Islet
9	chr6:147827800-147834000	Active TSS	Breast Myoepithelial Primary Cells	Breast
10	chr6:147828000-147829200	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
11	chr6:147828000-147829200	Flanking Active TSS	Colonic Mucosa	Colon
12	chr6:147828000-147829400	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr6:147828000-147829400	Enhancers	Fetal Heart	heart
14	chr6:147828000-147829400	Flanking Bivalent TSS/Enh	Placenta	Placenta
15	chr6:147828000-147829400	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
16	chr6:147828000-147829600	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
17	chr6:147828000-147829600	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
18	chr6:147828000-147829600	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
19	chr6:147828000-147829600	Flanking Bivalent TSS/Enh	HepG2	liver
20	chr6:147828000-147830200	Flanking Active TSS	Liver	Liver
21	chr6:147828000-147830400	Active TSS	A549	lung
22	chr6:147828000-147830800	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
23	chr6:147828000-147831000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
24	chr6:147828000-147831200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
25	chr6:147828000-147831200	Active TSS	Aorta	Aorta
26	chr6:147828200-147830000	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
27	chr6:147828200-147830000	Active TSS	Small Intestine	intestine
28	chr6:147828200-147830600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
29	chr6:147828400-147829400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr6:147828400-147829800	Bivalent Enhancer	Fetal Brain Male	brain
31	chr6:147828400-147830200	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr6:147828400-147830200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr6:147828400-147830400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr6:147828400-147830400	Active TSS	Gastric	stomach
35	chr6:147828400-147831200	Active TSS	Right Atrium	heart
36	chr6:147828400-147832400	Active TSS	Fetal Kidney	kidney
37	chr6:147828600-147829200	Enhancers	Primary B cells from cord blood	blood
38	chr6:147828600-147829400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr6:147828600-147829400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr6:147828600-147829400	Bivalent/Poised TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr6:147828600-147830200	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr6:147828600-147830400	Active TSS	NHDF-Ad	bronchial
43	chr6:147828600-147830600	Active TSS	Fetal Lung	lung
44	chr6:147828600-147830800	Active TSS	Brain Angular Gyrus	brain
45	chr6:147828600-147831000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
46	chr6:147828600-147831600	Active TSS	HSMM	muscle
47	chr6:147828600-147832000	Active TSS	Fetal Intestine Large	intestine
48	chr6:147828600-147832000	Active TSS	Rectal Mucosa Donor 31	rectum
49	chr6:147828600-147832200	Active TSS	HSMMtube	muscle
50	chr6:147828800-147829200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell

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