Variant report

Variant	esv3369872
Chromosome Location	chr6:4134903-4137401
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:649)
CpG islands
(count:977)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:649 , 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	chr6:4134680-4135751	HepG2	liver:	n/a	chr6:4135064-4135080
2	ATF2	chr6:4136212-4136649	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr6:4136052-4136850	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:4135164-4135738	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr6:4136526-4136755	K562	blood:	n/a	n/a
6	BHLHE40	chr6:4134431-4135779	GM12878	blood:	n/a	n/a
7	BHLHE40	chr6:4136185-4136634	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:4135234-4135791	HepG2	liver:	n/a	n/a
9	BHLHE40	chr6:4135192-4135765	K562	blood:	n/a	n/a
10	BHLHE40	chr6:4136167-4136589	HepG2	liver:	n/a	n/a
11	BHLHE40	chr6:4136164-4136888	K562	blood:	n/a	n/a
12	BHLHE40	chr6:4134279-4134930	K562	blood:	n/a	n/a
13	BRCA1	chr6:4135590-4135779	HepG2	liver:	n/a	n/a
14	BRCA1	chr6:4135339-4135514	GM12878	blood:	n/a	n/a
15	BRCA1	chr6:4136325-4136776	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr6:4134788-4135758	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr6:4135141-4135841	K562	blood:	n/a	n/a
18	CBX3	chr6:4134169-4134920	K562	blood:	n/a	chr6:4134467-4134478
19	CBX3	chr6:4136004-4136710	K562	blood:	n/a	n/a
20	CCNT2	chr6:4136119-4136569	K562	blood:	n/a	n/a
21	CCNT2	chr6:4135251-4135803	K562	blood:	n/a	n/a
22	CEBPB	chr6:4136344-4136603	K562	blood:	n/a	n/a
23	CEBPB	chr6:4136244-4136475	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr6:4134619-4134978	Hela-S3	cervix:	n/a	chr6:4134853-4134864 chr6:4134854-4134865
25	CEBPB	chr6:4136283-4136599	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr6:4134675-4135037	HepG2	liver:	n/a	chr6:4134853-4134864 chr6:4134854-4134865
27	CEBPB	chr6:4134655-4134981	HepG2	liver:	n/a	chr6:4134853-4134864 chr6:4134854-4134865
28	CEBPB	chr6:4134751-4134960	HepG2	liver:	n/a	chr6:4134853-4134864 chr6:4134854-4134865
29	CEBPD	chr6:4135516-4136103	HepG2	liver:	n/a	n/a
30	CEBPD	chr6:4136121-4136577	HepG2	liver:	n/a	n/a
31	CEBPD	chr6:4135377-4135879	K562	blood:	n/a	n/a
32	CEBPD	chr6:4135632-4135896	HepG2	liver:	n/a	n/a
33	CEBPD	chr6:4136132-4136373	HepG2	liver:	n/a	n/a
34	CHD1	chr6:4135585-4135768	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD1	chr6:4134536-4135763	GM12878	blood:	n/a	n/a
36	CHD1	chr6:4134762-4135251	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD1	chr6:4134965-4135843	IMR90	lung:	n/a	n/a
38	CHD1	chr6:4136259-4136388	GM12878	blood:	n/a	n/a
39	CHD2	chr6:4135163-4136550	Hela-S3	cervix:	n/a	chr6:4136253-4136263
40	CHD2	chr6:4136174-4136383	K562	blood:	n/a	chr6:4136253-4136263
41	CHD2	chr6:4135164-4135780	K562	blood:	n/a	n/a
42	CHD2	chr6:4135420-4135730	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr6:4135177-4135502	HepG2	liver:	n/a	n/a
44	CHD2	chr6:4134563-4134909	GM12878	blood:	n/a	n/a
45	CHD2	chr6:4135162-4135772	GM12878	blood:	n/a	n/a
46	CHD2	chr6:4136234-4136434	HepG2	liver:	n/a	chr6:4136253-4136263
47	CHD2	chr6:4136311-4136930	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr6:4136188-4136564	GM12878	blood:	n/a	chr6:4136253-4136263
49	CREB1	chr6:4135080-4136718	K562	blood:	n/a	n/a
50	CREB1	chr6:4135072-4136655	HepG2	liver:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:4135762-4135812	HAEpiC	amniotic membrane:	n/a
2	chr6:4135762-4135812	HAEpiC	amniotic membrane:	n/a
3	chr6:4135757-4135807	A549	lung:	n/a
4	chr6:4135889-4135939	U87	brain:	n/a
5	chr6:4136040-4136090	Jurkat	blood:	n/a
6	chr6:4135877-4135927	ovcar-3	ovarian:	n/a
7	chr6:4135850-4135900	H1-hESC	embryonic stem cell:	embryo
8	chr6:4135862-4135912	HEEpiC	esophagus:	n/a
9	chr6:4135862-4135912	PFSK-1	brain:	n/a
10	chr6:4135575-4135625	NT2-D1	testis:	n/a
11	chr6:4136040-4136090	PFSK-1	brain:	n/a
12	chr6:4136366-4136416	ovcar-3	ovarian:	n/a
13	chr6:4135889-4135939	HNPCEpiC	eye:	n/a
14	chr6:4135762-4135812	HCF	heart:	n/a
15	chr6:4135609-4135659	HRPEpiC	eye:	n/a
16	chr6:4136366-4136416	AG04449	skin:	fetal
17	chr6:4135877-4135927	HCT-116	colon:	n/a
18	chr6:4136196-4136246	H1-hESC	embryonic stem cell:	embryo
19	chr6:4136202-4136252	AG09319	gingival:	n/a
20	chr6:4135844-4135894	Hela-S3	cervix:	n/a
21	chr6:4136196-4136246	PrEC	prostate:	n/a
22	chr6:4136196-4136246	U87	brain:	n/a
23	chr6:4136196-4136246	T-47D	breast:	n/a
24	chr6:4136366-4136416	HRE	kidney:	n/a
25	chr6:4135762-4135812	AG04450	lung:	fetal
26	chr6:4135762-4135812	HMEC	breast:	n/a
27	chr6:4135877-4135927	PrEC	prostate:	n/a
28	chr6:4135757-4135807	GM12891	blood:	n/a
29	chr6:4135889-4135939	GM06990	blood:	n/a
30	chr6:4135844-4135894	HRPEpiC	eye:	n/a
31	chr6:4135850-4135900	HRPEpiC	eye:	n/a
32	chr6:4135862-4135912	LNCaP	prostate:	n/a
33	chr6:4135862-4135912	SK-N-SH_RA	brain:	n/a
34	chr6:4136202-4136252	GM12878	blood:	n/a
35	chr6:4135753-4135803	HRPEpiC	eye:	n/a
36	chr6:4135609-4135659	GM19239	blood:	n/a
37	chr6:4135877-4135927	LNCaP	prostate:	n/a
38	chr6:4135862-4135912	NB4	blood:	n/a
39	chr6:4135762-4135812	HCM	heart:	n/a
40	chr6:4136564-4136614	NHDF-neo	bronchial:	n/a
41	chr6:4136564-4136614	GM12891	blood:	n/a
42	chr6:4135609-4135659	HepG2	liver:	n/a
43	chr6:4135844-4135894	MCF-7	breast:	n/a
44	chr6:4135877-4135927	HRPEpiC	eye:	n/a
45	chr6:4135762-4135812	NB4	blood:	n/a
46	chr6:4135862-4135912	RPTEC	kidney:	n/a
47	chr6:4136366-4136416	NT2-D1	testis:	n/a
48	chr6:4135575-4135625	NB4	blood:	n/a
49	chr6:4135757-4135807	BJ	skin:	n/a
50	chr6:4135753-4135803	ovcar-3	ovarian:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:4016355..4024618-chr6:4131840..4138381,21	K562	blood:
2	chr15:66796710..66797327-chr6:4135519..4136323,2	Hela-S3	cervix:
3	chr6:4056059..4057941-chr6:4133460..4135296,2	K562	blood:
4	chr6:4135400..4136088-chr9:130213299..130213825,2	Hela-S3	cervix:
5	chr6:4017302..4025509-chr6:4131840..4138381,19	K562	blood:
6	chr6:4134858..4135600-chr6:74230356..74231112,2	Hela-S3	cervix:
7	chr5:180672773..180673634-chr6:4135301..4135859,2	Hela-S3	cervix:
8	chr6:4017451..4019157-chr6:4136336..4137878,2	MCF-7	breast:
9	chr6:4135404..4135915-chrX:48937014..48937608,2	Hela-S3	cervix:
10	chr11:288787..289365-chr6:4136018..4136659,2	NB4	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf201-1	chr6:4135657-4135779	ENSG00000254821.1

No data

Variant related genes	Relation type
ENSG00000254821	TF binding region
ENSG00000234817	TF binding region
ECI2	TF binding region
ENSG00000254821	CpG island
ENSG00000234817	CpG island
ECI2	CpG island
ENSG00000148356	chromatin interactions
ENSG00000174444	chromatin interactions
ENSG00000230648	chromatin interactions
ENSG00000272248	chromatin interactions
ENSG00000174442	chromatin interactions
ENSG00000156508	chromatin interactions
ENSG00000197958	chromatin interactions
ENSG00000196998	chromatin interactions
ENSG00000142102	chromatin interactions
ENSG00000112739	chromatin interactions
ENSG00000233937	chromatin interactions
ENSG00000250232	chromatin interactions

Extended variants
information (count: 99 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:99 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559978106	chr6:4134920-4134921	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs532022776	chr6:4134931-4134932	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs545395304	chr6:4134995-4134996	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs566031030	chr6:4135087-4135088	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs3789215	chr6:4135096-4135097	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs188842300	chr6:4135132-4135133	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs557538624	chr6:4135159-4135160	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs530270174	chr6:4135162-4135163	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs547325362	chr6:4135206-4135207	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs35071107	chr6:4135225-4135226	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs147511679	chr6:4135235-4135236	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs539081150	chr6:4135247-4135248	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs45529732	chr6:4135262-4135263	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs569283699	chr6:4135319-4135320	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs538350240	chr6:4135326-4135327	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs3804317	chr6:4135342-4135343	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs574303613	chr6:4135344-4135345	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs62394205	chr6:4135396-4135397	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs540031402	chr6:4135447-4135448	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
20	rs553700065	chr6:4135485-4135486	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
21	rs576707838	chr6:4135488-4135489	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
22	rs545516294	chr6:4135501-4135502	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
23	rs562519220	chr6:4135529-4135530	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
24	rs531180504	chr6:4135552-4135553	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
25	rs377026780	chr6:4135553-4135554	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
26	rs561586478	chr6:4135566-4135567	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
27	rs530357967	chr6:4135615-4135616	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
28	rs534941701	chr6:4135644-4135645	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
29	rs372051217	chr6:4135649-4135650	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
30	rs567200034	chr6:4135650-4135651	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
31	rs532835655	chr6:4135660-4135661	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
32	rs552558012	chr6:4135690-4135691	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
33	rs6910963	chr6:4135716-4135717	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs377382757	chr6:4135728-4135729	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
35	rs6910984	chr6:4135754-4135755	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
36	rs11549819	chr6:4135758-4135759	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
37	rs369145992	chr6:4135765-4135766	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
38	rs28510878	chr6:4135805-4135806	Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs199968749	chr6:4135812-4135813	Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
40	rs563097686	chr6:4135818-4135819	Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
41	rs576594562	chr6:4135822-4135823	Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
42	rs539743313	chr6:4135826-4135827	Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
43	rs374200875	chr6:4135831-4135832	Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
44	rs568312903	chr6:4135837-4135838	Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
45	rs575996598	chr6:4135840-4135841	Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
46	rs193227225	chr6:4135841-4135842	Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
47	rs561812608	chr6:4135874-4135875	Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs572149276	chr6:4135908-4135909	Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs540861129	chr6:4135912-4135913	Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs560680585	chr6:4136055-4136056	Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
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
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	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
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
dysmorphism	22105932	CNVD
psychomotor delay	22105932	CNVD

Chromatin state (count:388 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4133800-4135000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr6:4133800-4135000	Flanking Active TSS	HUVEC	blood vessel
3	chr6:4133800-4136800	Active TSS	H1 Cell Line	embryonic stem cell
4	chr6:4133800-4136800	Active TSS	H9 Cell Line	embryonic stem cell
5	chr6:4134000-4135000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
6	chr6:4134000-4135000	Flanking Active TSS	Brain Germinal Matrix	brain
7	chr6:4134000-4135000	Flanking Active TSS	Duodenum Mucosa	Duodenum
8	chr6:4134000-4135000	Flanking Active TSS	Dnd41	blood
9	chr6:4134000-4135000	Flanking Active TSS	NH-A	brain
10	chr6:4134000-4135200	Flanking Active TSS	Adipose Nuclei	Adipose
11	chr6:4134000-4135600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr6:4134000-4136800	Active TSS	Ovary	ovary
13	chr6:4134000-4136800	Active TSS	Rectal Mucosa Donor 29	rectum
14	chr6:4134200-4135000	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr6:4134200-4135000	Enhancers	Primary B cells from peripheral blood	blood
16	chr6:4134200-4135000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
17	chr6:4134200-4135000	Flanking Active TSS	Brain Angular Gyrus	brain
18	chr6:4134200-4135000	Flanking Active TSS	Brain Cingulate Gyrus	brain
19	chr6:4134200-4135000	Flanking Active TSS	Brain Substantia Nigra	brain
20	chr6:4134200-4135000	Flanking Active TSS	Stomach Smooth Muscle	stomach
21	chr6:4134200-4135000	Flanking Active TSS	HMEC	breast
22	chr6:4134200-4135200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr6:4134200-4135200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr6:4134200-4135200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
25	chr6:4134200-4135400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr6:4134200-4135800	Flanking Active TSS	Primary hematopoietic stem cells	blood
27	chr6:4134200-4136800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr6:4134200-4136800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr6:4134200-4137000	Active TSS	Aorta	Aorta
30	chr6:4134400-4135000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr6:4134400-4135000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
32	chr6:4134400-4135000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
33	chr6:4134400-4135000	Flanking Active TSS	Fetal Lung	lung
34	chr6:4134400-4135000	Enhancers	Lung	lung
35	chr6:4134400-4135400	Flanking Active TSS	Primary T cells from cord blood	blood
36	chr6:4134400-4136600	Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr6:4134400-4136600	Active TSS	iPS-15b Cell Line	embryonic stem cell
38	chr6:4134400-4136600	Active TSS	Fetal Brain Female	brain
39	chr6:4134400-4136600	Active TSS	Hela-S3	cervix
40	chr6:4134400-4136800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr6:4134400-4137000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr6:4134600-4135000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr6:4134600-4135000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
44	chr6:4134600-4135000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
45	chr6:4134600-4135000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
46	chr6:4134600-4135200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr6:4134600-4135200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
48	chr6:4134600-4135200	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr6:4134600-4135200	Weak transcription	Spleen	Spleen
50	chr6:4134600-4135400	Active TSS	Right Atrium	heart

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