Variant report

Variant	esv3422353
Chromosome Location	chr6:166794787-166797335
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1024)
CpG islands
(count:1650)
Chromatin interactive
region (count:14)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1024 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:166795192-166795590	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:166796328-166797478	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:166795144-166795477	K562	blood:	n/a	n/a
4	ARID3A	chr6:166796573-166796755	K562	blood:	n/a	n/a
5	ATF2	chr6:166795205-166795713	GM12878	blood:	n/a	n/a
6	ATF2	chr6:166796996-166797487	GM12878	blood:	n/a	n/a
7	ATF2	chr6:166796376-166796843	GM12878	blood:	n/a	n/a
8	ATF3	chr6:166796334-166796977	HepG2	liver:	n/a	chr6:166796817-166796825 chr6:166796479-166796499 chr6:166796616-166796625
9	ATF3	chr6:166795332-166795630	K562	blood:	n/a	chr6:166795452-166795461
10	ATF3	chr6:166796274-166796847	GM12878	blood:	n/a	chr6:166796817-166796825 chr6:166796479-166796499 chr6:166796616-166796625
11	ATF3	chr6:166796333-166796743	H1-hESC	embryonic stem cell:	n/a	chr6:166796479-166796499 chr6:166796616-166796625
12	ATF3	chr6:166796271-166797080	K562	blood:	n/a	chr6:166796817-166796825 chr6:166796479-166796499 chr6:166796616-166796625
13	BACH1	chr6:166796586-166797268	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr6:166796971-166797154	K562	blood:	n/a	n/a
15	BACH1	chr6:166795411-166795584	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL3	chr6:166796390-166797220	GM12878	blood:	n/a	chr6:166796612-166796625 chr6:166796995-166797008 chr6:166796621-166796634
17	BCLAF1	chr6:166796980-166797517	GM12878	blood:	n/a	chr6:166796995-166797008
18	BCLAF1	chr6:166796099-166796903	GM12878	blood:	n/a	chr6:166796612-166796625 chr6:166796621-166796634
19	BCLAF1	chr6:166795168-166795681	GM12878	blood:	n/a	chr6:166795474-166795487
20	BCLAF1	chr6:166795172-166795686	GM12878	blood:	n/a	chr6:166795474-166795487
21	BHLHE40	chr6:166796246-166797436	GM12878	blood:	n/a	chr6:166796445-166796461 chr6:166796987-166797003 chr6:166796619-166796635
22	BHLHE40	chr6:166796185-166797343	HepG2	liver:	n/a	chr6:166796445-166796461 chr6:166796987-166797003 chr6:166796619-166796635
23	BHLHE40	chr6:166796078-166797514	K562	blood:	n/a	chr6:166796445-166796461 chr6:166796987-166797003 chr6:166796619-166796635
24	BHLHE40	chr6:166795239-166795687	GM12878	blood:	n/a	n/a
25	BHLHE40	chr6:166795026-166795846	K562	blood:	n/a	n/a
26	BHLHE40	chr6:166795294-166795735	HepG2	liver:	n/a	n/a
27	BRCA1	chr6:166795395-166795778	HepG2	liver:	n/a	n/a
28	BRCA1	chr6:166796652-166796762	HepG2	liver:	n/a	n/a
29	BRCA1	chr6:166796261-166796416	HepG2	liver:	n/a	n/a
30	CBX3	chr6:166796163-166797683	K562	blood:	n/a	n/a
31	CBX3	chr6:166795182-166795715	K562	blood:	n/a	n/a
32	CCNT2	chr6:166795256-166797209	K562	blood:	n/a	chr6:166796616-166796625 chr6:166795492-166795501
33	CEBPB	chr6:166796543-166796821	HepG2	liver:	n/a	n/a
34	CEBPB	chr6:166794880-166795644	GM12878	blood:	n/a	n/a
35	CEBPB	chr6:166797188-166797727	Hela-S3	cervix:	n/a	chr6:166797642-166797653
36	CEBPB	chr6:166796251-166796923	Hela-S3	cervix:	n/a	chr6:166796419-166796427
37	CEBPB	chr6:166795361-166795561	HepG2	liver:	n/a	n/a
38	CEBPB	chr6:166796347-166796891	K562	blood:	n/a	chr6:166796419-166796427
39	CEBPD	chr6:166796537-166796915	HepG2	liver:	n/a	n/a
40	CEBPD	chr6:166796209-166797082	K562	blood:	n/a	n/a
41	CEBPD	chr6:166796204-166796905	HepG2	liver:	n/a	n/a
42	CHD1	chr6:166794902-166795761	IMR90	lung:	n/a	n/a
43	CHD1	chr6:166796189-166796338	GM12878	blood:	n/a	n/a
44	CHD1	chr6:166796680-166797442	GM12878	blood:	n/a	n/a
45	CHD2	chr6:166796313-166797263	K562	blood:	n/a	n/a
46	CHD2	chr6:166796297-166797002	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr6:166796400-166796764	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr6:166795232-166795631	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr6:166795231-166795797	GM12878	blood:	n/a	n/a
50	CHD2	chr6:166796287-166797289	GM12878	blood:	n/a	n/a

(count:1650 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:166797224-166797274	AG04450	lung:	fetal
2	chr6:166796744-166796794	GM06990	blood:	n/a
3	chr6:166796759-166796809	H1-hESC	embryonic stem cell:	embryo
4	chr6:166797224-166797274	AG04450	lung:	fetal
5	chr6:166796744-166796794	GM06990	blood:	n/a
6	chr6:166796759-166796809	H1-hESC	embryonic stem cell:	embryo
7	chr6:166797178-166797228	NT2-D1	testis:	n/a
8	chr6:166796284-166796334	T-47D	breast:	n/a
9	chr6:166797293-166797343	HIPEpiC	eye:	n/a
10	chr6:166797258-166797308	RPTEC	kidney:	n/a
11	chr6:166796386-166796436	MCF10A-Er-Src	breast:	n/a
12	chr6:166797286-166797336	IMR90	lung:	fetal
13	chr6:166796759-166796809	Hela-S3	cervix:	n/a
14	chr6:166796700-166796750	HEEpiC	esophagus:	n/a
15	chr6:166797286-166797336	BJ	skin:	n/a
16	chr6:166796891-166796941	NB4	blood:	n/a
17	chr6:166796706-166796756	HL-60	blood:	n/a
18	chr6:166797260-166797310	AoSMC	blood vessel:	n/a
19	chr6:166797128-166797178	HRE	kidney:	n/a
20	chr6:166797128-166797178	BJ	skin:	n/a
21	chr6:166797293-166797343	HL-60	blood:	n/a
22	chr6:166795816-166795866	ProgFib	skin:	n/a
23	chr6:166797178-166797228	ECC-1	luminal epithelium:	n/a
24	chr6:166796706-166796756	HPAEpiC	pulmonary alveolar:	n/a
25	chr6:166796588-166796638	SK-N-SH	brain:	n/a
26	chr6:166797267-166797317	Hela-S3	cervix:	n/a
27	chr6:166797120-166797170	SK-N-MC	brain:	n/a
28	chr6:166797222-166797272	PANC-1	pancreas:	n/a
29	chr6:166796700-166796750	SAEC	small airway:	n/a
30	chr6:166797300-166797350	HCF	heart:	n/a
31	chr6:166796706-166796756	MCF-7	breast:	n/a
32	chr6:166796579-166796629	HCM	heart:	n/a
33	chr6:166796984-166797034	NT2-D1	testis:	n/a
34	chr6:166796700-166796750	HCPEpiC	choroid plexus:	n/a
35	chr6:166796386-166796436	HUVEC	blood vessel:	n/a
36	chr6:166797258-166797308	LNCaP	prostate:	n/a
37	chr6:166796700-166796750	GM12878	blood:	n/a
38	chr6:166797267-166797317	ovcar-3	ovarian:	n/a
39	chr6:166796752-166796802	HNPCEpiC	eye:	n/a
40	chr6:166796752-166796802	AG04449	skin:	fetal
41	chr6:166797224-166797274	NT2-D1	testis:	n/a
42	chr6:166795816-166795866	HAEpiC	amniotic membrane:	n/a
43	chr6:166796706-166796756	CMK	blood:	n/a
44	chr6:166797293-166797343	RPTEC	kidney:	n/a
45	chr6:166797120-166797170	HNPCEpiC	eye:	n/a
46	chr6:166797125-166797175	BJ	skin:	n/a
47	chr6:166796700-166796750	Jurkat	blood:	n/a
48	chr6:166796891-166796941	NHDF-neo	bronchial:	n/a
49	chr6:166797120-166797170	Hepatocyte	liver:	n/a
50	chr6:166797061-166797111	NT2-D1	testis:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:166744077..166744772-chr6:166795075..166795860,2	MCF-7	breast:
2	chr6:166750705..166753304-chr6:166793796..166795469,2	K562	blood:
3	chr6:166796680..166799689-chr6:166808021..166810118,3	K562	blood:
4	chr6:166754173..166757774-chr6:166795355..166798060,3	MCF-7	breast:
5	chr6:166751804..166757558-chr6:166793969..166799153,5	K562	blood:
6	chr6:166743072..166748840-chr6:166793771..166798653,8	K562	blood:
7	chr6:166726357..166727438-chr6:166794885..166795636,3	K562	blood:
8	chr6:166726860..166727411-chr6:166795185..166795905,2	MCF-7	breast:
9	chr6:166746293..166747904-chr6:166796894..166799021,2	K562	blood:
10	chr6:166743853..166744743-chr6:166794927..166795865,3	K562	blood:
11	chr6:166689127..166689809-chr6:166795241..166795961,2	K562	blood:
12	chr6:166753320..166757958-chr6:166794622..166799153,8	K562	blood:
13	chr6:166383156..166385383-chr6:166793262..166795662,2	K562	blood:
14	chr6:166740985..166743870-chr6:166796738..166798607,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FGFR1OP-2	chr6:166796964-166802453	NONHSAT116046
2	lnc-FGFR1OP-2	chr6:166796677-166798312	ENSG00000261420.1

No data

Variant related genes	Relation type
ENSG00000261420	TF binding region
MPC1	TF binding region
ENSG00000261420	CpG island
MPC1	CpG island
ENSG00000198818	chromatin interactions
ENSG00000233231	chromatin interactions

Extended variants
information (count: 110 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:110 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3734604	chr6:166794853-166794854	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566476276	chr6:166794854-166794855	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs112335590	chr6:166794901-166794902	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs535043858	chr6:166794906-166794907	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs557235961	chr6:166794920-166794921	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs569028119	chr6:166794939-166794940	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs573502787	chr6:166794942-166794943	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs539648255	chr6:166794951-166794952	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs369534684	chr6:166794985-166794986	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs557653861	chr6:166795018-166795019	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs116782338	chr6:166795031-166795032	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs558709588	chr6:166795040-166795041	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs555853078	chr6:166795114-166795115	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs367900079	chr6:166795121-166795122	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs574095596	chr6:166795153-166795154	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs373054126	chr6:166795205-166795206	Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs544585345	chr6:166795308-166795309	Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs563220648	chr6:166795347-166795348	Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs12202703	chr6:166795369-166795370	Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs113131104	chr6:166795446-166795447	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs9766808	chr6:166795599-166795600	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs1569459	chr6:166795621-166795622	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs527830489	chr6:166795624-166795625	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs142225518	chr6:166795625-166795626	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs558340653	chr6:166795668-166795669	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs570836000	chr6:166795692-166795693	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs528878361	chr6:166795704-166795705	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs188974461	chr6:166795725-166795726	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs550284147	chr6:166795739-166795740	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs3778437	chr6:166795768-166795769	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs539343829	chr6:166795817-166795818	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs557979316	chr6:166795823-166795824	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs73265156	chr6:166795836-166795837	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs140962904	chr6:166795850-166795851	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs370189619	chr6:166795856-166795857	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs151209326	chr6:166795876-166795877	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs13193623	chr6:166795894-166795895	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs555914380	chr6:166795961-166795962	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs1546855	chr6:166795986-166795987	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs544649007	chr6:166796012-166796013	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs556272525	chr6:166796022-166796023	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs111488468	chr6:166796033-166796034	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs578227688	chr6:166796038-166796039	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs545377667	chr6:166796039-166796040	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs560797688	chr6:166796042-166796043	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs527894835	chr6:166796088-166796089	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs374420236	chr6:166796106-166796107	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs542782757	chr6:166796124-166796125	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs561473903	chr6:166796138-166796139	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs528941946	chr6:166796161-166796162	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
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
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
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:349 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166774800-166795000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr6:166775800-166794800	Weak transcription	Primary hematopoietic stem cells	blood
3	chr6:166777400-166795400	Weak transcription	Gastric	stomach
4	chr6:166778200-166795000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr6:166778400-166794800	Weak transcription	Fetal Stomach	stomach
6	chr6:166778400-166795000	Weak transcription	Colonic Mucosa	Colon
7	chr6:166779400-166794800	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr6:166779600-166794800	Weak transcription	Fetal Intestine Large	intestine
9	chr6:166780600-166794800	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr6:166780600-166795400	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr6:166782600-166794800	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr6:166782600-166794800	Weak transcription	Fetal Thymus	thymus
13	chr6:166782600-166795000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr6:166783800-166794800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr6:166789000-166794800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr6:166791000-166795200	Weak transcription	Left Ventricle	heart
17	chr6:166792400-166794800	Enhancers	Skeletal Muscle Female	skeletal muscle
18	chr6:166793000-166795400	Weak transcription	Lung	lung
19	chr6:166793200-166794800	Enhancers	Stomach Mucosa	stomach
20	chr6:166793600-166795000	Weak transcription	Aorta	Aorta
21	chr6:166793600-166795000	Weak transcription	Ovary	ovary
22	chr6:166793800-166794800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr6:166793800-166795000	Weak transcription	HUVEC	blood vessel
24	chr6:166794200-166795200	Flanking Active TSS	Liver	Liver
25	chr6:166794400-166794800	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr6:166794400-166794800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr6:166794400-166794800	Enhancers	Fetal Brain Female	brain
28	chr6:166794400-166795000	Flanking Active TSS	Dnd41	blood
29	chr6:166794400-166795200	Enhancers	Fetal Brain Male	brain
30	chr6:166794400-166795400	Weak transcription	Pancreas	Pancrea
31	chr6:166794400-166795600	Active TSS	HepG2	liver
32	chr6:166794400-166796400	Active TSS	Right Atrium	heart
33	chr6:166794400-166797600	Active TSS	GM12878-XiMat	blood
34	chr6:166794400-166797800	Active TSS	ES-I3 Cell Line	embryonic stem cell
35	chr6:166794400-166798000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr6:166794600-166794800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
37	chr6:166794600-166794800	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr6:166794600-166794800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr6:166794600-166794800	Active TSS	Primary B cells from cord blood	blood
40	chr6:166794600-166794800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
41	chr6:166794600-166794800	Enhancers	Primary T helper naive cells from peripheral blood	blood
42	chr6:166794600-166794800	Enhancers	Primary T helper cells PMA-I stimulated	--
43	chr6:166794600-166794800	Enhancers	Primary T helper cells fromperipheralblood	blood
44	chr6:166794600-166794800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr6:166794600-166794800	Flanking Active TSS	Brain Anterior Caudate	brain
46	chr6:166794600-166794800	Enhancers	Brain Hippocampus Middle	brain
47	chr6:166794600-166794800	Flanking Active TSS	Duodenum Mucosa	Duodenum
48	chr6:166794600-166794800	Flanking Active TSS	Fetal Heart	heart
49	chr6:166794600-166794800	Enhancers	Fetal Intestine Small	intestine
50	chr6:166794600-166794800	Enhancers	Fetal Kidney	kidney

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