Variant report

Variant	esv3363743
Chromosome Location	chr6:13486598-13489146
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:640)
CpG islands
(count:793)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:640 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:13487615-13487775	HepG2	liver:	n/a	n/a
2	BACH1	chr6:13487322-13487860	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr6:13486528-13486759	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr6:13487425-13487979	GM12878	blood:	n/a	chr6:13487731-13487744 chr6:13487728-13487741
5	BHLHE40	chr6:13488435-13488864	HepG2	liver:	n/a	chr6:13488677-13488693 chr6:13488523-13488539 chr6:13488692-13488701 chr6:13488692-13488701
6	BHLHE40	chr6:13488361-13488901	GM12878	blood:	n/a	chr6:13488677-13488693 chr6:13488523-13488539 chr6:13488692-13488701 chr6:13488692-13488701
7	BHLHE40	chr6:13486953-13487214	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:13485785-13487912	K562	blood:	n/a	chr6:13486336-13486352 chr6:13487437-13487453 chr6:13487232-13487248
9	CBX3	chr6:13487452-13487949	K562	blood:	n/a	n/a
10	CBX3	chr6:13486781-13487276	K562	blood:	n/a	n/a
11	CBX3	chr6:13486083-13486758	K562	blood:	n/a	n/a
12	CCNT2	chr6:13488663-13488807	K562	blood:	n/a	n/a
13	CCNT2	chr6:13486483-13486682	K562	blood:	n/a	n/a
14	CCNT2	chr6:13486929-13488181	K562	blood:	n/a	n/a
15	CEBPB	chr6:13488186-13488555	K562	blood:	n/a	n/a
16	CEBPB	chr6:13486936-13487242	K562	blood:	n/a	n/a
17	CEBPB	chr6:13488222-13488530	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr6:13487601-13487962	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr6:13488219-13488589	HepG2	liver:	n/a	n/a
20	CEBPB	chr6:13486154-13487272	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr6:13488216-13488572	IMR90	lung:	n/a	n/a
22	CEBPB	chr6:13486929-13487220	IMR90	lung:	n/a	n/a
23	CEBPB	chr6:13488217-13488597	K562	blood:	n/a	n/a
24	CEBPB	chr6:13488214-13488567	HepG2	liver:	n/a	n/a
25	CEBPB	chr6:13488103-13488550	A549	lung:	n/a	n/a
26	CEBPB	chr6:13488171-13488589	A549	lung:	n/a	n/a
27	CEBPB	chr6:13488145-13488606	MCF-7	breast:	n/a	n/a
28	CEBPB	chr6:13488223-13488553	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr6:13487529-13487578	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD1	chr6:13485653-13487078	GM12878	blood:	n/a	n/a
31	CHD2	chr6:13487545-13487965	K562	blood:	n/a	n/a
32	CHD2	chr6:13486965-13487165	K562	blood:	n/a	n/a
33	CHD2	chr6:13486187-13488238	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr6:13486273-13486697	K562	blood:	n/a	n/a
35	CHD2	chr6:13487684-13487873	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr6:13487527-13487880	HepG2	liver:	n/a	n/a
37	CHD2	chr6:13486173-13486687	GM12878	blood:	n/a	n/a
38	CHD2	chr6:13487678-13488232	GM12878	blood:	n/a	n/a
39	CHD2	chr6:13486967-13487197	GM12878	blood:	n/a	n/a
40	CHD2	chr6:13487051-13487125	HepG2	liver:	n/a	n/a
41	CREB1	chr6:13487598-13488055	A549	lung:	n/a	n/a
42	CREB1	chr6:13486907-13487199	A549	lung:	n/a	n/a
43	CTCF	chr6:13487540-13487690	HPF	lung:	n/a	chr6:13487667-13487680
44	CTCF	chr6:13487540-13487690	GM12869	blood:	n/a	chr6:13487667-13487680
45	CTCF	chr6:13486900-13487050	GM12878	blood:	n/a	n/a
46	CTCF	chr6:13487580-13487730	HEEpiC	esophagus:	n/a	chr6:13487667-13487680
47	CTCF	chr6:13487560-13487710	BE2_C	brain:	n/a	chr6:13487667-13487680
48	CTCF	chr6:13487020-13487170	GM12864	blood:	n/a	n/a
49	CTCF	chr6:13487520-13487670	WI-38	lung:	n/a	n/a
50	CTCF	chr6:13487620-13487770	A549	lung:	n/a	chr6:13487667-13487680

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:13487662-13487712	HIPEpiC	eye:	n/a
2	chr6:13487018-13487068	GM12891	blood:	n/a
3	chr6:13487668-13487718	HAEpiC	amniotic membrane:	n/a
4	chr6:13487879-13487929	HAEpiC	amniotic membrane:	n/a
5	chr6:13487863-13487913	PFSK-1	brain:	n/a
6	chr6:13488404-13488454	LNCaP	prostate:	n/a
7	chr6:13486608-13486658	GM12892	blood:	n/a
8	chr6:13487662-13487712	GM12878	blood:	n/a
9	chr6:13487863-13487913	ECC-1	luminal epithelium:	n/a
10	chr6:13486599-13486649	HUVEC	blood vessel:	n/a
11	chr6:13486608-13486658	HCM	heart:	n/a
12	chr6:13487018-13487068	IMR90	lung:	fetal
13	chr6:13487863-13487913	SK-N-SH_RA	brain:	n/a
14	chr6:13487879-13487929	PANC-1	pancreas:	n/a
15	chr6:13487863-13487913	AG09319	gingival:	n/a
16	chr6:13487018-13487068	GM12878	blood:	n/a
17	chr6:13488404-13488454	CMK	blood:	n/a
18	chr6:13488404-13488454	MCF10A-Er-Src	breast:	n/a
19	chr6:13487863-13487913	HCM	heart:	n/a
20	chr6:13486933-13486983	LNCaP	prostate:	n/a
21	chr6:13487883-13487933	NB4	blood:	n/a
22	chr6:13488404-13488454	HIPEpiC	eye:	n/a
23	chr6:13487883-13487933	HL-60	blood:	n/a
24	chr6:13486933-13486983	AG04449	skin:	fetal
25	chr6:13487863-13487913	CMK	blood:	n/a
26	chr6:13488167-13488217	HepG2	liver:	n/a
27	chr6:13487668-13487718	HMEC	breast:	n/a
28	chr6:13487863-13487913	HL-60	blood:	n/a
29	chr6:13487863-13487913	IMR90	lung:	fetal
30	chr6:13487662-13487712	GM12891	blood:	n/a
31	chr6:13486599-13486649	GM06990	blood:	n/a
32	chr6:13486599-13486649	AG09309	skin:	n/a
33	chr6:13486933-13486983	AoSMC	blood vessel:	n/a
34	chr6:13487903-13487953	BE2_C	brain:	n/a
35	chr6:13487903-13487953	SAEC	small airway:	n/a
36	chr6:13486933-13486983	HL-60	blood:	n/a
37	chr6:13488257-13488307	HNPCEpiC	eye:	n/a
38	chr6:13486933-13486983	SK-N-SH_RA	brain:	n/a
39	chr6:13486608-13486658	BE2_C	brain:	n/a
40	chr6:13486933-13486983	Hepatocyte	liver:	n/a
41	chr6:13488167-13488217	NHDF-neo	bronchial:	n/a
42	chr6:13486608-13486658	PANC-1	pancreas:	n/a
43	chr6:13487668-13487718	HepG2	liver:	n/a
44	chr6:13486599-13486649	GM12892	blood:	n/a
45	chr6:13487903-13487953	MCF10A-Er-Src	breast:	n/a
46	chr6:13488404-13488454	A549	lung:	n/a
47	chr6:13488167-13488217	CMK	blood:	n/a
48	chr6:13488167-13488217	HRPEpiC	eye:	n/a
49	chr6:13486933-13486983	NHDF-neo	bronchial:	n/a
50	chr6:13488167-13488217	GM12892	blood:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:13406818..13408886-chr6:13483840..13488220,5	MCF-7	breast:
2	chr6:13273285..13276286-chr6:13486162..13489029,4	K562	blood:
3	chr6:13471062..13472931-chr6:13486374..13489089,2	MCF-7	breast:
4	chr6:13484664..13490672-chr6:13572714..13577234,9	K562	blood:
5	chr6:13273285..13276286-chr6:13486162..13489029,3	K562	blood:
6	chr6:13325999..13330365-chr6:13484429..13488653,6	MCF-7	breast:
7	chr6:13486736..13489619-chr6:13614070..13616875,2	MCF-7	breast:
8	chr6:13486147..13488786-chr6:13613803..13616517,3	K562	blood:
9	chr6:13326316..13328538-chr6:13485562..13488530,2	MCF-7	breast:
10	chr6:13465251..13472690-chr6:13481619..13489131,10	K562	blood:
11	chr6:13484642..13487748-chr6:13572714..13576594,3	K562	blood:
12	chr6:13489026..13490564-chr6:13494155..13495687,2	K562	blood:
13	chr6:13484393..13490113-chr6:13572102..13578017,14	MCF-7	breast:
14	chr6:13488196..13489716-chr6:13537164..13538771,2	MCF-7	breast:
15	chr6:13408139..13410381-chr6:13486541..13489029,3	MCF-7	breast:
16	chr6:13486545..13489203-chr6:13612282..13616748,6	MCF-7	breast:
17	chr6:13485388..13489511-chr6:13572660..13577514,13	MCF-7	breast:
18	chr6:13328740..13330326-chr6:13487032..13488615,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000187461	TF binding region
GFOD1	TF binding region
ENSG00000187461	CpG island
GFOD1	CpG island
ENSG00000215022	chromatin interactions
ENSG00000261071	chromatin interactions
ENSG00000225921	chromatin interactions
ENSG00000145990	chromatin interactions
ENSG00000145979	chromatin interactions
ENSG00000124523	chromatin interactions

Extended variants
information (count: 82 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:82 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534864608	chr6:13486638-13486639	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs114976037	chr6:13486639-13486640	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs574822203	chr6:13486646-13486647	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs537322169	chr6:13486647-13486648	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs113737912	chr6:13486657-13486658	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs576789094	chr6:13486670-13486671	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs545441491	chr6:13486671-13486672	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs112913968	chr6:13486702-13486703	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs370271749	chr6:13486730-13486731	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs542051363	chr6:13486792-13486793	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs561922307	chr6:13486801-13486802	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs530980347	chr6:13486805-13486806	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs373410864	chr6:13486814-13486815	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs111276733	chr6:13486819-13486820	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs148309873	chr6:13486822-13486823	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs533368418	chr6:13486837-13486838	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs546677549	chr6:13486840-13486841	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs375888928	chr6:13486856-13486857	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs367719585	chr6:13486885-13486886	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs371504912	chr6:13486886-13486887	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs116041625	chr6:13486934-13486935	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs148842953	chr6:13486952-13486953	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs112233421	chr6:13486976-13486977	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs142356137	chr6:13487043-13487044	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs144880953	chr6:13487075-13487076	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs148284020	chr6:13487080-13487081	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs80189999	chr6:13487087-13487088	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs62385806	chr6:13487174-13487175	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs536811899	chr6:13487202-13487203	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs9382141	chr6:13487231-13487232	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs374786643	chr6:13487236-13487237	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs112397920	chr6:13487274-13487275	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs570652446	chr6:13487297-13487298	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs539459700	chr6:13487336-13487337	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs549568711	chr6:13487402-13487403	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs550572532	chr6:13487408-13487409	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs62385807	chr6:13487458-13487459	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs62385808	chr6:13487463-13487464	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs982391	chr6:13487552-13487553	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs114234739	chr6:13487594-13487595	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs2494773	chr6:13487631-13487632	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs76456719	chr6:13487647-13487648	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs564848591	chr6:13487686-13487687	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs533450884	chr6:13487692-13487693	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs147024123	chr6:13487776-13487777	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs529277531	chr6:13487786-13487787	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs549515272	chr6:13487806-13487807	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs371250969	chr6:13487882-13487883	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs569333507	chr6:13487903-13487904	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs12202450	chr6:13487931-13487932	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
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
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
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
abnormal development	18461090	CNVD
Cancer	16790693	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:425 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:13483200-13488800	Active TSS	Right Atrium	heart
2	chr6:13483400-13487600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr6:13484200-13488600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr6:13484600-13487200	Flanking Active TSS	Liver	Liver
5	chr6:13484600-13488400	Active TSS	GM12878-XiMat	blood
6	chr6:13484800-13487200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
7	chr6:13484800-13488400	Active TSS	Right Ventricle	heart
8	chr6:13485000-13486600	Active TSS	Colonic Mucosa	Colon
9	chr6:13485000-13488800	Active TSS	Brain Angular Gyrus	brain
10	chr6:13485000-13489600	Active TSS	Rectal Smooth Muscle	rectum
11	chr6:13485200-13488200	Active TSS	Stomach Smooth Muscle	stomach
12	chr6:13485200-13488200	Active TSS	NHLF	lung
13	chr6:13485200-13488600	Active TSS	Left Ventricle	heart
14	chr6:13485200-13488600	Active TSS	A549	lung
15	chr6:13485200-13488800	Active TSS	Brain Anterior Caudate	brain
16	chr6:13485200-13488800	Active TSS	Psoas Muscle	Psoas
17	chr6:13485400-13487200	Flanking Active TSS	Primary T cells from cord blood	blood
18	chr6:13485400-13487200	Active TSS	Fetal Brain Male	brain
19	chr6:13485400-13487600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
20	chr6:13485400-13488600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr6:13485400-13488600	Active TSS	NHDF-Ad	bronchial
22	chr6:13485600-13486800	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
23	chr6:13485600-13487000	Bivalent/Poised TSS	Fetal Intestine Large	intestine
24	chr6:13485600-13488200	Active TSS	Placenta Amnion	Placenta Amnion
25	chr6:13485600-13488200	Active TSS	HSMMtube	muscle
26	chr6:13485600-13488600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
27	chr6:13485600-13488600	Active TSS	Esophagus	oesophagus
28	chr6:13485600-13488600	Active TSS	Lung	lung
29	chr6:13485600-13488800	Flanking Active TSS	Primary B cells from cord blood	blood
30	chr6:13485600-13488800	Active TSS	Duodenum Smooth Muscle	Duodenum
31	chr6:13485600-13489000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr6:13485800-13486600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
33	chr6:13485800-13486800	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr6:13485800-13487000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
35	chr6:13485800-13487200	Flanking Active TSS	Placenta	Placenta
36	chr6:13485800-13487400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
37	chr6:13485800-13487400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
38	chr6:13485800-13488600	Active TSS	Ovary	ovary
39	chr6:13486000-13486600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr6:13486000-13486600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr6:13486000-13486800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr6:13486000-13486800	Active TSS	HepG2	liver
43	chr6:13486000-13487000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr6:13486000-13487000	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr6:13486000-13487000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr6:13486000-13487200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
47	chr6:13486000-13487200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
48	chr6:13486000-13487400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
49	chr6:13486000-13487400	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
50	chr6:13486000-13487600	Active TSS	Fetal Heart	heart

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