Variant report

Variant	esv2761649
Chromosome Location	chr1:119840645-119925936
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1356)
CpG islands
(count:855)
Chromatin interactive
region (count:34)
LncRNA
region (count:36)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1356 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:119888144-119888445	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:119917049-119917085	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:119881299-119881701	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:119883823-119884517	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:119870092-119870925	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:119903943-119904138	HepG2	liver:	n/a	n/a
7	ATF1	chr1:119894597-119894901	K562	blood:	n/a	n/a
8	ATF1	chr1:119872747-119872985	K562	blood:	n/a	n/a
9	ATF2	chr1:119883483-119883881	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr1:119866082-119866696	GM12878	blood:	n/a	n/a
11	ATF2	chr1:119861053-119861613	GM12878	blood:	n/a	n/a
12	ATF2	chr1:119890293-119890922	GM12878	blood:	n/a	n/a
13	ATF2	chr1:119866094-119866708	GM12878	blood:	n/a	n/a
14	ATF2	chr1:119861034-119861596	GM12878	blood:	n/a	n/a
15	ATF2	chr1:119890380-119890938	GM12878	blood:	n/a	n/a
16	ATF3	chr1:119861506-119861677	K562	blood:	n/a	n/a
17	BACH1	chr1:119883484-119883848	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr1:119890363-119890780	GM12878	blood:	n/a	n/a
19	BATF	chr1:119890463-119890928	GM12878	blood:	n/a	n/a
20	BATF	chr1:119866185-119866610	GM12878	blood:	n/a	n/a
21	BATF	chr1:119866206-119866587	GM12878	blood:	n/a	n/a
22	BATF	chr1:119861178-119861706	GM12878	blood:	n/a	n/a
23	BATF	chr1:119861057-119861558	GM12878	blood:	n/a	n/a
24	BCL11A	chr1:119866152-119866607	GM12878	blood:	n/a	n/a
25	BCL11A	chr1:119890371-119890929	GM12878	blood:	n/a	n/a
26	BCL11A	chr1:119866191-119866610	GM12878	blood:	n/a	n/a
27	BCL11A	chr1:119890397-119890774	GM12878	blood:	n/a	n/a
28	BCL3	chr1:119866185-119866589	GM12878	blood:	n/a	n/a
29	BCL3	chr1:119890460-119890872	GM12878	blood:	n/a	n/a
30	BCLAF1	chr1:119861057-119861587	GM12878	blood:	n/a	n/a
31	BCLAF1	chr1:119866168-119866647	GM12878	blood:	n/a	n/a
32	BCLAF1	chr1:119866192-119866633	GM12878	blood:	n/a	n/a
33	BHLHE40	chr1:119869692-119870837	HepG2	liver:	n/a	n/a
34	BHLHE40	chr1:119883984-119884447	HepG2	liver:	n/a	n/a
35	BHLHE40	chr1:119866193-119867155	GM12878	blood:	n/a	n/a
36	BHLHE40	chr1:119859563-119859695	K562	blood:	n/a	n/a
37	BHLHE40	chr1:119890448-119891138	GM12878	blood:	n/a	n/a
38	BHLHE40	chr1:119870106-119870786	GM12878	blood:	n/a	n/a
39	BRCA1	chr1:119862365-119862387	GM12878	blood:	n/a	n/a
40	CEBPB	chr1:119861438-119861712	Hela-S3	cervix:	n/a	chr1:119861595-119861606
41	CEBPB	chr1:119882900-119882914	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr1:119922919-119923192	HepG2	liver:	n/a	chr1:119923045-119923056
43	CEBPB	chr1:119916969-119917571	A549	lung:	n/a	n/a
44	CEBPB	chr1:119916991-119917442	A549	lung:	n/a	n/a
45	CEBPB	chr1:119903884-119904163	HepG2	liver:	n/a	chr1:119904066-119904078
46	CEBPB	chr1:119859611-119860034	K562	blood:	n/a	n/a
47	CEBPB	chr1:119854750-119854950	A549	lung:	n/a	chr1:119854760-119854771 chr1:119854831-119854848 chr1:119854758-119854771 chr1:119854834-119854847 chr1:119854836-119854847 chr1:119854760-119854771
48	CEBPB	chr1:119884082-119884436	HepG2	liver:	n/a	n/a
49	CEBPB	chr1:119922993-119923102	HepG2	liver:	n/a	chr1:119923045-119923056
50	CEBPB	chr1:119870528-119870689	HepG2	liver:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:119869897-119869947	GM12891	blood:	n/a
2	chr1:119869897-119869947	GM12891	blood:	n/a
3	chr1:119870478-119870528	U87	brain:	n/a
4	chr1:119870287-119870337	IMR90	lung:	fetal
5	chr1:119910574-119910624	K562	blood:	n/a
6	chr1:119860821-119860871	GM12878	blood:	n/a
7	chr1:119911000-119911050	PFSK-1	brain:	n/a
8	chr1:119870339-119870389	SK-N-SH	brain:	n/a
9	chr1:119874251-119874301	AoSMC	blood vessel:	n/a
10	chr1:119910574-119910624	ECC-1	luminal epithelium:	n/a
11	chr1:119870287-119870337	GM19239	blood:	n/a
12	chr1:119870339-119870389	LNCaP	prostate:	n/a
13	chr1:119914432-119914482	MCF-7	breast:	n/a
14	chr1:119870802-119870852	MCF-7	breast:	n/a
15	chr1:119910205-119910255	NB4	blood:	n/a
16	chr1:119870287-119870337	HRCEpiC	kidney:	n/a
17	chr1:119910670-119910720	GM19239	blood:	n/a
18	chr1:119870339-119870389	NH-A	brain:	n/a
19	chr1:119869897-119869947	IMR90	lung:	fetal
20	chr1:119870339-119870389	NHBE	bronchial:	n/a
21	chr1:119870339-119870389	HRCEpiC	kidney:	n/a
22	chr1:119870287-119870337	HUVEC	blood vessel:	n/a
23	chr1:119910574-119910624	SAEC	small airway:	n/a
24	chr1:119870339-119870389	HEK293	kidney:	embryo
25	chr1:119910574-119910624	ovcar-3	ovarian:	n/a
26	chr1:119870478-119870528	HRCEpiC	kidney:	n/a
27	chr1:119911000-119911050	HCF	heart:	n/a
28	chr1:119869897-119869947	HCT-116	colon:	n/a
29	chr1:119870478-119870528	RPTEC	kidney:	n/a
30	chr1:119911000-119911050	Jurkat	blood:	n/a
31	chr1:119911000-119911050	A549	lung:	n/a
32	chr1:119869897-119869947	ProgFib	skin:	n/a
33	chr1:119870339-119870389	SK-N-SH_RA	brain:	n/a
34	chr1:119914432-119914482	HAEpiC	amniotic membrane:	n/a
35	chr1:119866618-119866668	PANC-1	pancreas:	n/a
36	chr1:119870802-119870852	HEEpiC	esophagus:	n/a
37	chr1:119870287-119870337	HAEpiC	amniotic membrane:	n/a
38	chr1:119860821-119860871	HL-60	blood:	n/a
39	chr1:119914432-119914482	GM12891	blood:	n/a
40	chr1:119870339-119870389	ECC-1	luminal epithelium:	n/a
41	chr1:119910205-119910255	CMK	blood:	n/a
42	chr1:119914432-119914482	A549	lung:	n/a
43	chr1:119874251-119874301	HRE	kidney:	n/a
44	chr1:119870802-119870852	RPTEC	kidney:	n/a
45	chr1:119911000-119911050	HCM	heart:	n/a
46	chr1:119910205-119910255	IMR90	lung:	fetal
47	chr1:119910574-119910624	NHBE	bronchial:	n/a
48	chr1:119911480-119911530	HEEpiC	esophagus:	n/a
49	chr1:119869897-119869947	NH-A	brain:	n/a
50	chr1:119870287-119870337	HRPEpiC	eye:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:119828739..119830086-chr1:119909537..119910745,9	MCF-7	breast:
2	chr1:119894771..119896375-chr1:119898314..119900462,2	MCF-7	breast:
3	chr1:119913437..119915978-chr1:119926365..119928542,2	K562	blood:
4	chr1:119839247..119840828-chr1:119842873..119844537,2	K562	blood:
5	chr1:119843544..119846464-chr1:119854842..119856473,2	MCF-7	breast:
6	chr1:119830769..119833666-chr1:119908545..119910106,2	MCF-7	breast:
7	chr1:119875573..119878427-chr1:119879294..119881488,2	K562	blood:
8	chr1:119828910..119830613-chr1:119909189..119910809,25	MCF-7	breast:
9	chr1:118694047..118694604-chr1:119909841..119910884,3	K562	blood:
10	chr1:119839973..119842420-chr1:119853333..119855352,2	MCF-7	breast:
11	chr1:119844182..119846397-chr1:119863723..119866323,2	K562	blood:
12	chr1:119914912..119915700-chr1:120154301..120154847,3	MCF-7	breast:
13	chr1:119857728..119859280-chr1:119859990..119862431,2	MCF-7	breast:
14	chr1:119861894..119863890-chr1:119865436..119868489,3	MCF-7	breast:
15	chr1:119681886..119684418-chr1:119920647..119923183,2	K562	blood:
16	chr1:119874569..119876262-chr1:119880980..119883218,2	MCF-7	breast:
17	chr1:119839973..119842420-chr1:119853333..119855352,2	MCF-7	breast:
18	chr1:119910930..119912615-chr1:119914552..119916368,2	K562	blood:
19	chr1:119839247..119840828-chr1:119842873..119844537,2	K562	blood:
20	chr1:119829167..119829733-chr1:119859168..119859936,2	MCF-7	breast:
21	chr1:119915031..119915964-chr1:119992237..119993475,3	MCF-7	breast:
22	chr1:119859568..119860444-chr1:119908558..119909246,2	K562	blood:
23	chr1:119844182..119846397-chr1:119863723..119866323,2	K562	blood:
24	chr1:119859568..119860444-chr1:119908558..119909246,2	K562	blood:
25	chr1:119915016..119915722-chr1:120059055..120059910,2	MCF-7	breast:
26	chr1:119857728..119859280-chr1:119859990..119862431,2	MCF-7	breast:
27	chr1:119874569..119876262-chr1:119880980..119883218,2	MCF-7	breast:
28	chr1:119894771..119896375-chr1:119898314..119900462,2	MCF-7	breast:
29	chr1:119843544..119846464-chr1:119854842..119856473,2	MCF-7	breast:
30	chr1:119875573..119878427-chr1:119879294..119881488,2	K562	blood:
31	chr1:119861894..119863890-chr1:119865436..119868489,3	MCF-7	breast:
32	chr1:119836003..119837992-chr1:119839451..119841888,2	K562	blood:
33	chr1:119818904..119819557-chr1:119910123..119910771,2	MCF-7	breast:
34	chr1:119869695..119871890-chr1:119874910..119876484,2	MCF-7	breast:

(count:36 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WARS2-2	chr1:119859984-119860550	NONHSAT005550
2	lnc-WARS2-6	chr1:119921802-119921918	NONHSAT005565
3	lnc-HAO2-1	chr1:119870798-119870910	NONHSAT005553
4	lnc-HAO2-3	chr1:119896204-119896598	NONHSAT005561
5	lnc-WARS2-6	chr1:119921802-119921918	NONHSAT005563
6	lnc-WARS2-1	chr1:119860894-119860947	XLOC_000984
7	lnc-HSD3B2-2	chr1:119911569-119911631	ENSG00000230921.1
8	lnc-HAO2-1	chr1:119871331-119871412	NONHSAT005556
9	lnc-HSD3B2-2	chr1:119912707-119912954	ENSG00000230921.1
10	lnc-WARS2-5	chr1:119886750-119886980	NONHSAT005559
11	lnc-HAO2-1	chr1:119871367-119871412	XLOC_000370
12	lnc-WARS2-6	chr1:119912622-119912733	NONHSAT005565
13	lnc-HAO2-1	chr1:119897040-119897156	ENSG00000232650
14	lnc-HAO2-1	chr1:119871366-119871412	NONHSAT005553
15	lnc-WARS2-2	chr1:119869508-119869762	XLOC_000983
16	lnc-HSD3B2-2	chr1:119912707-119912953	NR_046780
17	lnc-WARS2-2	chr1:119870430-119870538	XLOC_000983
18	lnc-HAO2-1	chr1:119898614-119898805	ENSG00000232650
19	lnc-WARS2-6	chr1:119903224-119903317	NONHSAT005563
20	lnc-HAO2-3	chr1:119897168-119897341	NONHSAT005561
21	lnc-WARS2-2	chr1:119869586-119869926	XLOC_000983
22	lnc-HAO2-1	chr1:119870799-119870910	XLOC_000370
23	lnc-WARS2-6	chr1:119899025-119899176	NONHSAT005563
24	lnc-WARS2-1	chr1:119860048-119860550	XLOC_000984
25	lnc-WARS2-5	chr1:119885424-119885975	NONHSAT005560
26	lnc-HAO2-1	chr1:119872963-119873671	NONHSAT005553
27	lnc-HAO2-1	chr1:119897040-119897156	NONHSAT005556
28	lnc-HSD3B2-2	chr1:119911569-119911631	NR_046780
29	lnc-HAO2-1	chr1:119871367-119871412	ENSG00000232650
30	lnc-HAO2-1	chr1:119904741-119904997	NONHSAT005556
31	lnc-HAO2-1	chr1:119870875-119870910	ENSG00000232650
32	lnc-WARS2-5	chr1:119885424-119885975	NONHSAT005559
33	lnc-WARS2-5	chr1:119886980-119887075	NONHSAT005560
34	lnc-WARS2-5	chr1:119886750-119886843	NONHSAT005560
35	lnc-WARS2-2	chr1:119869586-119869966	NONHSAT005550
36	lnc-HAO2-1	chr1:119873155-119873438	XLOC_000370

No data

Variant related genes	Relation type
HAO2	TF binding region
RNU1-75P	TF binding region
HAO2-IT1	TF binding region
ENSG00000227712	TF binding region
ENSG00000232650	TF binding region
HAO2	CpG island
RNU1-75P	CpG island
HAO2-IT1	CpG island
ENSG00000227712	CpG island
ENSG00000232650	CpG island
ENSG00000231365	chromatin interactions
ENSG00000232650	chromatin interactions
ENSG00000116874	chromatin interactions
ENSG00000227712	chromatin interactions
ENSG00000116882	chromatin interactions
ENSG00000230921	chromatin interactions
LITAF	miRNA target sites

Extended variants
information (count: 3012 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:3012 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6428814	chr1:119840645-119840646	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs587746055	chr1:119840711-119840712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs74911865	chr1:119840728-119840729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186681336	chr1:119840735-119840736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs147227922	chr1:119840738-119840739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs148687406	chr1:119840744-119840745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs142189921	chr1:119840797-119840798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs191043860	chr1:119840803-119840804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150758670	chr1:119840815-119840816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs368137517	chr1:119840816-119840817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs587599753	chr1:119840848-119840849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs587675559	chr1:119840860-119840861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs139310819	chr1:119840878-119840879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182808016	chr1:119840903-119840904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs144258128	chr1:119840904-119840905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs587613622	chr1:119840937-119840938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs373590170	chr1:119840940-119840941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs587687425	chr1:119840976-119840977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs74997348	chr1:119840986-119840987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188226841	chr1:119840992-119840993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs116429620	chr1:119840994-119840995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs61082270	chr1:119841022-119841023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs79292317	chr1:119841023-119841024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs112044878	chr1:119841025-119841026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs397981503	chr1:119841041-119841042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs587773021	chr1:119841070-119841071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs587647422	chr1:119841105-119841106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs587688275	chr1:119841185-119841186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs587760921	chr1:119841211-119841212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs587642247	chr1:119841229-119841230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs374974219	chr1:119841234-119841235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs587720454	chr1:119841284-119841285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs587599851	chr1:119841296-119841297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs587650852	chr1:119841300-119841301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs587708251	chr1:119841418-119841419	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs587606184	chr1:119841533-119841534	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs1418023	chr1:119841593-119841594	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs587739199	chr1:119841609-119841610	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs192760555	chr1:119841623-119841624	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs587689046	chr1:119841634-119841635	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs587768105	chr1:119841721-119841722	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs587641956	chr1:119841754-119841755	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs146553999	chr1:119841800-119841801	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs587730093	chr1:119841837-119841838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs587630190	chr1:119841838-119841839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs116179341	chr1:119841871-119841872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs587765273	chr1:119841921-119841922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs587634916	chr1:119841970-119841971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141249509	chr1:119841995-119841996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs587755531	chr1:119842004-119842005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Aetanephric adenomas	20802469	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Systemic lupus erythematosus	21956041	CNVD
Breast cancer	21804112	CNVD
Mental retardation	21062444	CNVD
Myelofibrosis	22110671	CNVD
Emphysema	19352772	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
Follicular lymphoma	18703704	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:965 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:119837000-119846200	Weak transcription	Liver	Liver
2	chr1:119837200-119841200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:119837200-119841400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:119837800-119840800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr1:119837800-119841000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr1:119838000-119841000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr1:119838200-119840800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr1:119838200-119846000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr1:119838200-119846200	Weak transcription	HepG2	liver
10	chr1:119838400-119846200	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr1:119840600-119841600	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr1:119840600-119841800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr1:119840600-119842000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr1:119840800-119841000	Enhancers	Primary T killer memory cells from peripheral blood	blood
15	chr1:119840800-119842000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
16	chr1:119841000-119841400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr1:119841000-119841800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr1:119841200-119841400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
19	chr1:119841200-119841600	Enhancers	NH-A	brain
20	chr1:119841200-119842000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr1:119841200-119842000	Enhancers	HMEC	breast
22	chr1:119841400-119841600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr1:119841400-119841800	Enhancers	Primary T killer memory cells from peripheral blood	blood
24	chr1:119841400-119841800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:119841600-119841800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
26	chr1:119844000-119844400	Enhancers	Fetal Muscle Leg	muscle
27	chr1:119844000-119846800	Enhancers	Fetal Brain Male	brain
28	chr1:119844400-119846000	Weak transcription	Fetal Muscle Leg	muscle
29	chr1:119845600-119846400	Enhancers	H9 Cell Line	embryonic stem cell
30	chr1:119845600-119846400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr1:119845600-119846800	Enhancers	NHDF-Ad	bronchial
32	chr1:119845600-119847400	Enhancers	Fetal Muscle Trunk	muscle
33	chr1:119845800-119846600	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr1:119845800-119846600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:119846000-119846200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
36	chr1:119846000-119846600	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr1:119846000-119846800	Enhancers	Fetal Muscle Leg	muscle
38	chr1:119846000-119847000	Enhancers	Fetal Stomach	stomach
39	chr1:119846200-119846600	Enhancers	H1 Cell Line	embryonic stem cell
40	chr1:119846200-119846600	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr1:119846200-119846800	Enhancers	Colon Smooth Muscle	Colon
42	chr1:119846200-119846800	Enhancers	HepG2	liver
43	chr1:119846200-119847200	Enhancers	Liver	Liver
44	chr1:119846400-119846600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr1:119846400-119846800	Enhancers	Rectal Mucosa Donor 29	rectum
46	chr1:119846400-119846800	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr1:119846400-119847000	Enhancers	Fetal Lung	lung
48	chr1:119846600-119846800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr1:119846600-119846800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr1:119846600-119846800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin

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