Variant report

Variant	esv3453724
Chromosome Location	chr1:160098374-160136495
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:483)
CpG islands
(count:613)
Chromatin interactive
region (count:24)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:483 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:160117925-160118242	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:160128710-160128754	HepG2	liver:	n/a	n/a
3	ATF1	chr1:160133501-160133802	K562	blood:	n/a	n/a
4	ATF1	chr1:160120205-160120221	K562	blood:	n/a	n/a
5	BATF	chr1:160131821-160132025	GM12878	blood:	n/a	n/a
6	BHLHE40	chr1:160132143-160132299	K562	blood:	n/a	n/a
7	CEBPB	chr1:160120699-160120902	K562	blood:	n/a	chr1:160120849-160120860
8	CEBPB	chr1:160119551-160119828	K562	blood:	n/a	n/a
9	CEBPB	chr1:160132147-160132389	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr1:160132108-160132437	K562	blood:	n/a	n/a
11	CEBPB	chr1:160132220-160132485	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:160132209-160132397	HepG2	liver:	n/a	n/a
13	CEBPB	chr1:160120715-160120923	HepG2	liver:	n/a	chr1:160120849-160120860
14	CEBPB	chr1:160119158-160119911	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr1:160119516-160119883	IMR90	lung:	n/a	n/a
16	CEBPB	chr1:160132110-160132658	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr1:160132115-160132508	ECC-1	luminal epithelium:	n/a	n/a
18	CEBPB	chr1:160132151-160132470	K562	blood:	n/a	n/a
19	CEBPB	chr1:160120801-160120877	IMR90	lung:	n/a	chr1:160120849-160120860
20	CEBPB	chr1:160132089-160132529	MCF-7	breast:	n/a	n/a
21	CEBPD	chr1:160132197-160132424	HepG2	liver:	n/a	n/a
22	CHD2	chr1:160132114-160132416	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr1:160132160-160132310	K562	blood:	n/a	n/a
24	CTCF	chr1:160132011-160132522	K562	blood:	n/a	n/a
25	CTCF	chr1:160133546-160133704	Fibrobl	skin:	n/a	n/a
26	CTCF	chr1:160132240-160132390	NHEK	skin:	n/a	n/a
27	CTCF	chr1:160132200-160132350	HepG2	liver:	n/a	n/a
28	CTCF	chr1:160132122-160132415	GM19238	blood:	n/a	n/a
29	CTCF	chr1:160132180-160132330	GM12865	blood:	n/a	n/a
30	CTCF	chr1:160132063-160132493	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr1:160132200-160132350	GM12867	blood:	n/a	n/a
32	CTCF	chr1:160132140-160132290	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr1:160133560-160133710	AG09309	skin:	n/a	n/a
34	CTCF	chr1:160132160-160132310	GM12874	blood:	n/a	n/a
35	CTCF	chr1:160132102-160132344	A549	lung:	n/a	n/a
36	CTCF	chr1:160132242-160132274	LNCaP	prostate:	n/a	n/a
37	CTCF	chr1:160132080-160132230	HCT-116	colon:	n/a	n/a
38	CTCF	chr1:160132140-160132290	HVMF	connective:	n/a	n/a
39	CTCF	chr1:160132160-160132310	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr1:160105324-160105349	GM10266	blood:	n/a	n/a
41	CTCF	chr1:160132220-160132370	NB4	blood:	n/a	n/a
42	CTCF	chr1:160132167-160132356	GM10248	blood:	n/a	n/a
43	CTCF	chr1:160133560-160133710	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr1:160132200-160132350	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr1:160132160-160132310	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr1:160133540-160133690	AG10803	skin:	n/a	n/a
47	CTCF	chr1:160132180-160132330	HRE	kidney:	n/a	n/a
48	CTCF	chr1:160133429-160133793	A549	lung:	n/a	n/a
49	CTCF	chr1:160133560-160133710	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr1:160132133-160132389	MCF-7	breast:	n/a	n/a

(count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:160112673-160112723	SK-N-SH	brain:	n/a
2	chr1:160121201-160121251	GM19239	blood:	n/a
3	chr1:160121487-160121537	HRE	kidney:	n/a
4	chr1:160112673-160112723	SK-N-SH	brain:	n/a
5	chr1:160121201-160121251	GM19239	blood:	n/a
6	chr1:160121487-160121537	HRE	kidney:	n/a
7	chr1:160121487-160121537	IMR90	lung:	fetal
8	chr1:160098527-160098577	HCPEpiC	choroid plexus:	n/a
9	chr1:160098527-160098577	NH-A	brain:	n/a
10	chr1:160098579-160098629	U87	brain:	n/a
11	chr1:160112673-160112723	Hela-S3	cervix:	n/a
12	chr1:160121412-160121462	HCPEpiC	choroid plexus:	n/a
13	chr1:160121412-160121462	AG04450	lung:	fetal
14	chr1:160098527-160098577	Hepatocyte	liver:	n/a
15	chr1:160098579-160098629	AG10803	skin:	n/a
16	chr1:160135275-160135325	HEEpiC	esophagus:	n/a
17	chr1:160121487-160121537	MCF10A-Er-Src	breast:	n/a
18	chr1:160121412-160121462	Hela-S3	cervix:	n/a
19	chr1:160135527-160135577	HAEpiC	amniotic membrane:	n/a
20	chr1:160135527-160135577	MCF10A-Er-Src	breast:	n/a
21	chr1:160135275-160135325	Caco-2	colon:	n/a
22	chr1:160112673-160112723	HRCEpiC	kidney:	n/a
23	chr1:160112673-160112723	HCPEpiC	choroid plexus:	n/a
24	chr1:160121263-160121313	HCPEpiC	choroid plexus:	n/a
25	chr1:160121487-160121537	SAEC	small airway:	n/a
26	chr1:160135527-160135577	HL-60	blood:	n/a
27	chr1:160121263-160121313	BE2_C	brain:	n/a
28	chr1:160098579-160098629	LNCaP	prostate:	n/a
29	chr1:160121412-160121462	HAEpiC	amniotic membrane:	n/a
30	chr1:160135275-160135325	MCF-7	breast:	n/a
31	chr1:160121263-160121313	ProgFib	skin:	n/a
32	chr1:160121412-160121462	SK-N-SH_RA	brain:	n/a
33	chr1:160121201-160121251	GM12891	blood:	n/a
34	chr1:160135275-160135325	PFSK-1	brain:	n/a
35	chr1:160112673-160112723	SAEC	small airway:	n/a
36	chr1:160098527-160098577	ovcar-3	ovarian:	n/a
37	chr1:160135527-160135577	HCM	heart:	n/a
38	chr1:160112673-160112723	NHBE	bronchial:	n/a
39	chr1:160135275-160135325	NH-A	brain:	n/a
40	chr1:160121487-160121537	HCM	heart:	n/a
41	chr1:160121201-160121251	HRPEpiC	eye:	n/a
42	chr1:160121263-160121313	AoSMC	blood vessel:	n/a
43	chr1:160135275-160135325	CMK	blood:	n/a
44	chr1:160135275-160135325	HAEpiC	amniotic membrane:	n/a
45	chr1:160121412-160121462	LNCaP	prostate:	n/a
46	chr1:160121283-160121333	ProgFib	skin:	n/a
47	chr1:160121263-160121313	HEEpiC	esophagus:	n/a
48	chr1:160112673-160112723	NT2-D1	testis:	n/a
49	chr1:160098579-160098629	GM12892	blood:	n/a
50	chr1:160098579-160098629	GM12891	blood:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:160133173..160136099-chr1:160172374..160174599,2	K562	blood:
2	chr1:160131804..160132724-chr1:160162606..160163404,2	MCF-7	breast:
3	chr1:160098805..160101465-chr1:160105602..160107369,2	K562	blood:
4	chr1:160099410..160101934-chr1:160112290..160114172,2	K562	blood:
5	chr1:160132125..160132726-chr1:160260589..160261287,2	MCF-7	breast:
6	chr1:160132228..160135096-chr1:160135442..160137169,3	K562	blood:
7	chr1:160083301..160085781-chr1:160135957..160137542,2	K562	blood:
8	chr1:160130613..160132686-chr1:160182546..160184780,2	MCF-7	breast:
9	chr1:160112963..160115059-chr1:160116109..160118179,2	K562	blood:
10	chr1:160099410..160101934-chr1:160112290..160114172,2	K562	blood:
11	chr1:160070877..160071401-chr1:160133164..160133996,2	K562	blood:
12	chr1:160103698..160106616-chr1:160108808..160110694,2	K562	blood:
13	chr1:160128612..160131573-chr1:160136132..160138965,2	MCF-7	breast:
14	chr1:160097137..160099642-chr1:160101829..160104164,2	K562	blood:
15	chr1:160131739..160132508-chr1:160221767..160222395,2	K562	blood:
16	chr1:160083469..160085740-chr1:160096653..160098636,2	K562	blood:
17	chr1:160093121..160095812-chr1:160107178..160109878,2	K562	blood:
18	chr1:160104302..160107204-chr1:160107299..160108872,2	MCF-7	breast:
19	chr1:160103698..160106616-chr1:160108808..160110694,2	K562	blood:
20	chr1:160106375..160109177-chr1:160123607..160125337,2	K562	blood:
21	chr1:160070559..160071355-chr1:160131889..160132803,3	K562	blood:
22	chr1:160112963..160115059-chr1:160116109..160118179,2	K562	blood:
23	chr1:160133173..160135864-chr1:160173099..160175487,2	K562	blood:
24	chr1:160130003..160134008-chr1:160228517..160234292,5	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP1A4-1	chr1:160111084-160111567	NONHSAT007042
2	lnc-ATP1A2-1	chr1:160124109-160124456	expReg_chr1_18488_+
3	lnc-ATP1A4-1	chr1:160109749-160109774	NONHSAT007042
4	lnc-ATP1A4-1	chr1:160110441-160110564	NONHSAT007042

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ATP1A2	hsa-miR-122-5p	chr1:160112547-160112565

Variant related genes	Relation type
ATP1A2	TF binding region
ATP1A4	TF binding region
ATP1A2	CpG island
ATP1A4	CpG island
ENSG00000132681	chromatin interactions
ENSG00000162734	chromatin interactions
ENSG00000265381	chromatin interactions
ENSG00000228606	chromatin interactions
ENSG00000018625	chromatin interactions
ENSG00000132716	chromatin interactions

Extended variants
information (count: 1761 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:1761 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551031181	chr1:160098390-160098391	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs372784025	chr1:160098398-160098399	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs376250714	chr1:160098413-160098414	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs368793006	chr1:160098414-160098415	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs371070057	chr1:160098431-160098432	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs142140032	chr1:160098444-160098445	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs140363699	chr1:160098453-160098454	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs121918613	chr1:160098457-160098458	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs180827585	chr1:160098462-160098463	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs55741021	chr1:160098516-160098517	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs138766432	chr1:160098528-160098529	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs1063125	chr1:160098543-160098544	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs572467842	chr1:160098546-160098547	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs61734526	chr1:160098549-160098550	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs121918620	chr1:160098551-160098552	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs374374188	chr1:160098552-160098553	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs28934002	chr1:160098557-160098558	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs137878081	chr1:160098580-160098581	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs547954866	chr1:160098627-160098628	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs372185438	chr1:160098644-160098645	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
21	rs200681048	chr1:160098654-160098655	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
22	rs367946782	chr1:160098668-160098669	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
23	rs566242283	chr1:160098681-160098682	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
24	rs189922200	chr1:160098688-160098689	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
25	rs558237808	chr1:160098696-160098697	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
26	rs576516174	chr1:160098697-160098698	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
27	rs371640186	chr1:160098738-160098739	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
28	rs373704478	chr1:160098740-160098741	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
29	rs200130188	chr1:160098741-160098742	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs182959335	chr1:160098759-160098760	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
31	rs77319999	chr1:160098779-160098780	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
32	rs377054439	chr1:160098791-160098792	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
33	rs121918618	chr1:160098797-160098798	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
34	rs138696612	chr1:160098803-160098804	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
35	rs142309356	chr1:160098804-160098805	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
36	rs139499540	chr1:160098815-160098816	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs370111257	chr1:160098841-160098842	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs374067427	chr1:160098850-160098851	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs542189014	chr1:160098892-160098893	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs373294271	chr1:160098898-160098899	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs544710713	chr1:160098904-160098905	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs375905731	chr1:160098916-160098917	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs201570970	chr1:160098927-160098928	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs397801520	chr1:160098928-160098929	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs17846711	chr1:160098929-160098930	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs530469412	chr1:160098930-160098931	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs545633334	chr1:160098946-160098947	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs201515950	chr1:160099010-160099011	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs373024075	chr1:160099016-160099017	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs562278306	chr1:160099057-160099058	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21045282	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Follicular lymphoma	18703704	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	19602461	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:483 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:160088000-160146200	Weak transcription	Spleen	Spleen
2	chr1:160088800-160107400	Weak transcription	Fetal Brain Female	brain
3	chr1:160090200-160104600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr1:160090600-160112600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr1:160092400-160112200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
6	chr1:160092800-160100800	Strong transcription	Fetal Stomach	stomach
7	chr1:160093000-160098600	Enhancers	Placenta	Placenta
8	chr1:160093600-160099800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr1:160093800-160098400	Enhancers	HepG2	liver
10	chr1:160093800-160101200	Strong transcription	HUES64 Cell Line	embryonic stem cell
11	chr1:160093800-160101800	Weak transcription	Gastric	stomach
12	chr1:160093800-160106600	Strong transcription	Cortex derived primary cultured neurospheres	brain
13	chr1:160094000-160112000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr1:160094600-160100800	Enhancers	HSMM	muscle
15	chr1:160094800-160110200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
16	chr1:160095000-160099400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:160095000-160103200	Strong transcription	HUES48 Cell Line	embryonic stem cell
18	chr1:160095400-160098600	Weak transcription	Fetal Heart	heart
19	chr1:160095400-160108200	Strong transcription	HUES6 Cell Line	embryonic stem cell
20	chr1:160096000-160098800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr1:160097000-160100000	Genic enhancers	Brain Substantia Nigra	brain
22	chr1:160097000-160101400	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
23	chr1:160097000-160109800	Strong transcription	H1 Cell Line	embryonic stem cell
24	chr1:160097200-160098400	Genic enhancers	Brain Hippocampus Middle	brain
25	chr1:160097200-160098600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr1:160097200-160099200	Enhancers	Adipose Nuclei	Adipose
27	chr1:160097200-160099600	Enhancers	Brain Angular Gyrus	brain
28	chr1:160097200-160099800	Strong transcription	Aorta	Aorta
29	chr1:160097200-160100000	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr1:160097200-160100200	Transcr. at gene 5' and 3'	Skeletal Muscle Female	skeletal muscle
31	chr1:160097200-160100800	Strong transcription	ES-I3 Cell Line	embryonic stem cell
32	chr1:160097200-160100800	Genic enhancers	Left Ventricle	heart
33	chr1:160097200-160101400	Strong transcription	H9 Cell Line	embryonic stem cell
34	chr1:160097200-160103400	Enhancers	Psoas Muscle	Psoas
35	chr1:160097200-160103400	Enhancers	Right Atrium	heart
36	chr1:160097200-160112200	Weak transcription	Brain Germinal Matrix	brain
37	chr1:160097400-160098400	Genic enhancers	Colon Smooth Muscle	Colon
38	chr1:160097400-160098600	Genic enhancers	Fetal Muscle Trunk	muscle
39	chr1:160097400-160098800	Enhancers	A549	lung
40	chr1:160097400-160099000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr1:160097400-160099000	Enhancers	Muscle Satellite Cultured Cells	--
42	chr1:160097400-160099600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr1:160097400-160100600	Genic enhancers	Fetal Muscle Leg	muscle
44	chr1:160097400-160100600	Strong transcription	Ovary	ovary
45	chr1:160097400-160101400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
46	chr1:160097400-160101600	Weak transcription	Pancreas	Pancrea
47	chr1:160097400-160104800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr1:160097400-160107600	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr1:160097600-160098400	Enhancers	Osteobl	bone
50	chr1:160097600-160098600	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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