Variant report

Variant	nsv522921
Chromosome Location	chr1:102170295-102876392
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1826)
CpG islands
(count:1162)
Chromatin interactive
region (count:37)
LncRNA
region (count:30)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1826 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:102331101-102331231	K562	blood:	n/a	n/a
2	ATF1	chr1:102831922-102832055	K562	blood:	n/a	n/a
3	ATF1	chr1:102631086-102631200	K562	blood:	n/a	n/a
4	ATF1	chr1:102204864-102205096	K562	blood:	n/a	n/a
5	ATF2	chr1:102743792-102744012	GM12878	blood:	n/a	n/a
6	BACH1	chr1:102311592-102311621	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:102462480-102462684	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr1:102546333-102546406	K562	blood:	n/a	n/a
9	BATF	chr1:102707535-102707855	GM12878	blood:	n/a	chr1:102707709-102707720
10	BATF	chr1:102346026-102346355	GM12878	blood:	n/a	n/a
11	BATF	chr1:102346057-102346369	GM12878	blood:	n/a	n/a
12	BATF	chr1:102478939-102479253	GM12878	blood:	n/a	n/a
13	BATF	chr1:102707530-102707843	GM12878	blood:	n/a	chr1:102707709-102707720
14	BCL11A	chr1:102308712-102308996	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL11A	chr1:102707343-102707835	GM12878	blood:	n/a	n/a
16	BCL11A	chr1:102573095-102573287	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL11A	chr1:102346126-102346353	GM12878	blood:	n/a	n/a
18	BCL11A	chr1:102707463-102707840	GM12878	blood:	n/a	n/a
19	BCL3	chr1:102511094-102511294	GM12878	blood:	n/a	n/a
20	BHLHE40	chr1:102707270-102707856	GM12878	blood:	n/a	n/a
21	CEBPB	chr1:102458849-102459202	Hela-S3	cervix:	n/a	chr1:102458998-102459011 chr1:102458998-102459009
22	CEBPB	chr1:102715452-102715789	IMR90	lung:	n/a	chr1:102715615-102715624 chr1:102715613-102715626 chr1:102715613-102715624 chr1:102715613-102715626 chr1:102715614-102715625 chr1:102715615-102715624 chr1:102715615-102715624 chr1:102715615-102715624
23	CEBPB	chr1:102563427-102563590	A549	lung:	n/a	n/a
24	CEBPB	chr1:102190858-102191192	HepG2	liver:	n/a	chr1:102191019-102191030
25	CEBPB	chr1:102551598-102551862	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr1:102758061-102758332	HepG2	liver:	n/a	chr1:102758175-102758186
27	CEBPB	chr1:102734656-102734961	IMR90	lung:	n/a	n/a
28	CEBPB	chr1:102509452-102509741	HepG2	liver:	n/a	chr1:102509579-102509590 chr1:102509578-102509591
29	CEBPB	chr1:102263266-102263754	MCF-7	breast:	n/a	n/a
30	CEBPB	chr1:102371408-102371417	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr1:102548808-102549090	A549	lung:	n/a	chr1:102548911-102548922
32	CEBPB	chr1:102758137-102758265	A549	lung:	n/a	chr1:102758175-102758186
33	CEBPB	chr1:102513055-102513196	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr1:102447627-102447928	IMR90	lung:	n/a	n/a
35	CEBPB	chr1:102697417-102697780	IMR90	lung:	n/a	chr1:102697602-102697613 chr1:102697750-102697761
36	CEBPB	chr1:102363806-102363953	HepG2	liver:	n/a	n/a
37	CEBPB	chr1:102548861-102549164	Hela-S3	cervix:	n/a	chr1:102548911-102548922
38	CEBPB	chr1:102419807-102420140	IMR90	lung:	n/a	chr1:102419972-102419983
39	CEBPB	chr1:102680866-102681180	HepG2	liver:	n/a	chr1:102681013-102681024
40	CEBPB	chr1:102818974-102819308	HepG2	liver:	n/a	chr1:102819149-102819160
41	CEBPB	chr1:102798140-102798492	HepG2	liver:	n/a	chr1:102798315-102798326
42	CEBPB	chr1:102383891-102384166	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr1:102648586-102648614	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr1:102350238-102350441	Hela-S3	cervix:	n/a	chr1:102350368-102350379
45	CEBPB	chr1:102843548-102843788	IMR90	lung:	n/a	n/a
46	CEBPB	chr1:102536746-102536869	K562	blood:	n/a	n/a
47	CEBPB	chr1:102548842-102549099	H1-hESC	embryonic stem cell:	n/a	chr1:102548911-102548922
48	CEBPB	chr1:102509443-102509716	IMR90	lung:	n/a	chr1:102509579-102509590 chr1:102509578-102509591
49	CEBPB	chr1:102697446-102697771	H1-hESC	embryonic stem cell:	n/a	chr1:102697602-102697613 chr1:102697750-102697761
50	CEBPB	chr1:102697455-102697776	K562	blood:	n/a	chr1:102697602-102697613 chr1:102697750-102697761

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:102462877-102462927	U87	brain:	n/a
2	chr1:102700639-102700689	BE2_C	brain:	n/a
3	chr1:102462855-102462905	HL-60	blood:	n/a
4	chr1:102462877-102462927	U87	brain:	n/a
5	chr1:102700639-102700689	BE2_C	brain:	n/a
6	chr1:102462855-102462905	HL-60	blood:	n/a
7	chr1:102462445-102462495	GM19239	blood:	n/a
8	chr1:102462590-102462640	PFSK-1	brain:	n/a
9	chr1:102263519-102263569	AG04449	skin:	fetal
10	chr1:102312608-102312658	HepG2	liver:	n/a
11	chr1:102462445-102462495	NH-A	brain:	n/a
12	chr1:102462590-102462640	AG09309	skin:	n/a
13	chr1:102462632-102462682	PrEC	prostate:	n/a
14	chr1:102462855-102462905	AG09309	skin:	n/a
15	chr1:102462682-102462732	U87	brain:	n/a
16	chr1:102462682-102462732	BJ	skin:	n/a
17	chr1:102312608-102312658	HCM	heart:	n/a
18	chr1:102627049-102627099	SKMC	muscle:	n/a
19	chr1:102462682-102462732	HCT-116	colon:	n/a
20	chr1:102263519-102263569	HNPCEpiC	eye:	n/a
21	chr1:102462656-102462706	T-47D	breast:	n/a
22	chr1:102308808-102308858	RPTEC	kidney:	n/a
23	chr1:102462175-102462225	HCPEpiC	choroid plexus:	n/a
24	chr1:102312608-102312658	SK-N-SH_RA	brain:	n/a
25	chr1:102700639-102700689	HMEC	breast:	n/a
26	chr1:102462877-102462927	SK-N-MC	brain:	n/a
27	chr1:102462445-102462495	RPTEC	kidney:	n/a
28	chr1:102462632-102462682	AG04450	lung:	fetal
29	chr1:102312671-102312721	SAEC	small airway:	n/a
30	chr1:102462175-102462225	AoSMC	blood vessel:	n/a
31	chr1:102462656-102462706	GM19239	blood:	n/a
32	chr1:102312671-102312721	Caco-2	colon:	n/a
33	chr1:102462445-102462495	ovcar-3	ovarian:	n/a
34	chr1:102263519-102263569	HCT-116	colon:	n/a
35	chr1:102627049-102627099	HCM	heart:	n/a
36	chr1:102462682-102462732	ProgFib	skin:	n/a
37	chr1:102462855-102462905	T-47D	breast:	n/a
38	chr1:102700639-102700689	HIPEpiC	eye:	n/a
39	chr1:102312608-102312658	NHDF-neo	bronchial:	n/a
40	chr1:102462855-102462905	NHDF-neo	bronchial:	n/a
41	chr1:102700608-102700658	BE2_C	brain:	n/a
42	chr1:102263519-102263569	LNCaP	prostate:	n/a
43	chr1:102462877-102462927	H1-hESC	embryonic stem cell:	embryo
44	chr1:102627049-102627099	BE2_C	brain:	n/a
45	chr1:102462682-102462732	MCF-7	breast:	n/a
46	chr1:102462043-102462093	AG09309	skin:	n/a
47	chr1:102263519-102263569	HCF	heart:	n/a
48	chr1:102263519-102263569	AG04450	lung:	fetal
49	chr1:102308808-102308858	HRPEpiC	eye:	n/a
50	chr1:102462632-102462682	HCT-116	colon:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:102240164..102243164-chr12:120728529..120730974,3	MCF-7	breast:
2	chr1:102310233..102312368-chr1:102385841..102387762,2	MCF-7	breast:
3	chr1:102701228..102703682-chr1:102706014..102708929,2	K562	blood:
4	chr1:54418703..54421611-chr1:102613977..102616372,3	MCF-7	breast:
5	chr1:102816532..102818032-chr6:130363143..130365830,2	MCF-7	breast:
6	chr1:102310233..102312368-chr1:102385841..102387762,2	MCF-7	breast:
7	chr1:102199817..102202358-chr1:102206092..102207812,2	K562	blood:
8	chr1:102285335..102286320-chr1:102656866..102657699,4	MCF-7	breast:
9	chr1:102580503..102583097-chr1:102602225..102604313,2	K562	blood:
10	chr1:102264508..102267132-chr1:102269526..102271581,2	K562	blood:
11	chr1:102701228..102703682-chr1:102706014..102708929,2	K562	blood:
12	chr1:102167808..102170688-chr1:102173598..102175511,2	K562	blood:
13	chr1:102241644..102242164-chr12:120729314..120730227,2	MCF-7	breast:
14	chr1:102199817..102202358-chr1:102206092..102207812,2	K562	blood:
15	chr1:102863880..102865440-chr1:102870522..102872481,2	K562	blood:
16	chr1:102451706..102453377-chr1:102456104..102458404,2	K562	blood:
17	chr1:102239600..102242307-chr11:61744597..61746750,2	MCF-7	breast:
18	chr1:102569587..102571901-chr1:102578895..102580582,2	K562	blood:
19	chr1:102285335..102286320-chr1:102656866..102657699,4	MCF-7	breast:
20	chr1:102451706..102453377-chr1:102456104..102458404,2	K562	blood:
21	chr1:102182832..102185107-chr1:102185315..102186982,2	K562	blood:
22	chr1:102434316..102436694-chr1:102437372..102439039,2	K562	blood:
23	chr1:102685538..102686359-chr1:201441216..201441918,2	MCF-7	breast:
24	chr1:102308106..102310001-chr1:102313421..102315280,2	K562	blood:
25	chr1:102459133..102459923-chr1:102657241..102657780,2	MCF-7	breast:
26	chr1:102167808..102170688-chr1:102173598..102175511,2	K562	blood:
27	chr1:102118967..102119744-chr1:102285327..102286064,2	MCF-7	breast:
28	chr1:102863880..102865440-chr1:102870522..102872481,2	K562	blood:
29	chr1:102241664..102242164-chr12:120729395..120729995,2	HCT-116	colon:
30	chr1:102182832..102185107-chr1:102185315..102186982,2	K562	blood:
31	chr1:102308106..102310001-chr1:102313421..102315280,2	K562	blood:
32	chr1:102569587..102571901-chr1:102578895..102580582,2	K562	blood:
33	chr1:102459133..102459923-chr1:102657241..102657780,2	MCF-7	breast:
34	chr1:102580503..102583097-chr1:102602225..102604313,2	K562	blood:
35	chr1:102456863..102457700-chr7:19592037..19592862,2	MCF-7	breast:
36	chr1:102434316..102436694-chr1:102437372..102439039,2	K562	blood:
37	chr1:102264508..102267132-chr1:102269526..102271581,2	K562	blood:

(count:30 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-S1PR1-5	chr1:102571334-102571564	XLOC_000321
2	lnc-OLFM3-1	chr1:102855050-102855186	XLOC_000943
3	lnc-OLFM3-1	chr1:102852918-102852977	XLOC_000943
4	lnc-S1PR1-5	chr1:102569886-102569928	XLOC_000321
5	lnc-OLFM3-1	chr1:102852918-102852977	XLOC_000943
6	lnc-S1PR1-13	chr1:102358661-102359603	NONHSAT004869
7	lnc-OLFM3-3	chr1:102627638-102627774	NONHSAT004870
8	lnc-S1PR1-4	chr1:102189298-102189431	NONHSAT004864
9	lnc-S1PR1-4	chr1:102194827-102195047	NONHSAT004864
10	lnc-OLFM3-3	chr1:102437883-102438141	NONHSAT004870
11	lnc-OLFM3-3	chr1:102548414-102548472	NONHSAT004870
12	lnc-OLFM3-1	chr1:102852761-102852807	XLOC_000943
13	lnc-OLFM3-1	chr1:102854091-102854185	XLOC_000943
14	lnc-OLFM3-1	chr1:102830569-102830793	XLOC_000943
15	lnc-OLFM3-1	chr1:102775825-102775884	XLOC_000943
16	lnc-OLFM3-1	chr1:102775826-102775884	XLOC_000943
17	lnc-OLFM3-1	chr1:102853515-102853765	XLOC_000943
18	lnc-S1PR1-4	chr1:102189298-102189431	ENSG00000226715
19	lnc-OLFM3-3	chr1:102625506-102625565	NONHSAT004870
20	lnc-S1PR1-13	chr1:102358613-102360299	NONHSAT004867
21	lnc-OLFM3-3	chr1:102626679-102626773	NONHSAT004870
22	lnc-S1PR1-13	chr1:102337567-102337661	NONHSAT004867
23	lnc-OLFM3-1	chr1:102665295-102665553	XLOC_000943
24	lnc-OLFM3-1	chr1:102854091-102854120	XLOC_000943
25	lnc-OLFM3-1	chr1:102855050-102855163	XLOC_000943
26	lnc-S1PR1-12	chr1:102348072-102348450	NONHSAT004868
27	lnc-OLFM3-1	chr1:102854091-102854185	XLOC_000943
28	lnc-OLFM3-1	chr1:102852644-102852807	XLOC_000943
29	lnc-S1PR1-4	chr1:102194827-102195170	ENSG00000226715
30	lnc-OLFM3-3	chr1:102625349-102625395	NONHSAT004870

No data

Variant related genes	Relation type
RNU6-965P	TF binding region
OLFM3	TF binding region
ENSG00000233359	TF binding region
ENSG00000183298	TF binding region
DNAJA1P5	TF binding region
RNU6-352P	TF binding region
ENSG00000226715	TF binding region
ENSG00000271277	TF binding region
RNU6-965P	CpG island
OLFM3	CpG island
ENSG00000233359	CpG island
ENSG00000183298	CpG island
DNAJA1P5	CpG island
RNU6-352P	CpG island
ENSG00000226715	CpG island
ENSG00000271277	CpG island
ENSG00000202538	chromatin interactions
C1orf103	miRNA target sites
LNX2	miRNA target sites
MPHOSPH9	miRNA target sites
C10orf26	miRNA target sites
MEST	miRNA target sites
GCET2	miRNA target sites
PRNP	miRNA target sites
SYNE2	miRNA target sites

Extended variants
information (count: 10385 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:10385 , 50 per page) page: 1 2 3 4 5 6 7 ... 208

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11164273	chr1:102170295-102170296	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs147796248	chr1:102170297-102170298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs138916277	chr1:102170321-102170322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs565023393	chr1:102170345-102170346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs1484294	chr1:102170476-102170477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557164173	chr1:102170490-102170491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184463544	chr1:102170502-102170503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542976537	chr1:102170534-102170535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs554918153	chr1:102170550-102170551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs573144874	chr1:102170554-102170555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs540635518	chr1:102170557-102170558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565093860	chr1:102170605-102170606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs533232485	chr1:102170611-102170612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs550313091	chr1:102170652-102170653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs532680332	chr1:102170673-102170674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs72727846	chr1:102170682-102170683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577389586	chr1:102170706-102170707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567130635	chr1:102170719-102170720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs563921297	chr1:102170788-102170789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188907264	chr1:102170793-102170794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs75962631	chr1:102170828-102170829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs139957369	chr1:102170833-102170834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs527936671	chr1:102170834-102170835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546612767	chr1:102170851-102170852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs116679392	chr1:102170852-102170853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs145139735	chr1:102170858-102170859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs182034122	chr1:102170898-102170899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568899371	chr1:102171031-102171032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs536472214	chr1:102171041-102171042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs574800752	chr1:102171044-102171045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs373077362	chr1:102171045-102171046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs554756092	chr1:102171060-102171061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs147920474	chr1:102171118-102171119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs148988765	chr1:102171170-102171171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112619850	chr1:102171190-102171191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs558957611	chr1:102171231-102171232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs78127172	chr1:102171244-102171245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs78518435	chr1:102171245-102171246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs577149888	chr1:102171274-102171275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs544729792	chr1:102171286-102171287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs143811398	chr1:102171294-102171295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs566598768	chr1:102171318-102171319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs148178555	chr1:102171329-102171330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs186077108	chr1:102171347-102171348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs191065866	chr1:102171360-102171361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567940638	chr1:102171414-102171415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543315709	chr1:102171429-102171430	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528021948	chr1:102171472-102171473	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs72986975	chr1:102171498-102171499	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs180735864	chr1:102171540-102171541	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:112)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	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
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
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	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
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Breast cancer	22522925	CNVD
Lung cancer	17086460	CNVD
Gastric cancer	16891809	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:815 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:102169400-102172400	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr1:102169800-102171600	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr1:102170000-102171400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
4	chr1:102170000-102172200	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr1:102170200-102171400	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr1:102170200-102172200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr1:102170200-102172200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr1:102170600-102170800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr1:102171200-102171600	Enhancers	H9 Cell Line	embryonic stem cell
10	chr1:102171200-102172000	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr1:102171200-102172200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr1:102171200-102172800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr1:102171400-102172000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr1:102171600-102171800	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr1:102171800-102172200	Enhancers	H9 Cell Line	embryonic stem cell
16	chr1:102172000-102172200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
17	chr1:102172400-102178000	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr1:102175000-102175200	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr1:102175200-102179000	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr1:102178000-102178200	Enhancers	H9 Cell Line	embryonic stem cell
21	chr1:102178000-102178200	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr1:102178000-102178200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr1:102178200-102178800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
24	chr1:102178400-102178800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
25	chr1:102178400-102180200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr1:102178400-102181000	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr1:102178600-102179000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
28	chr1:102178600-102181200	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr1:102178800-102179000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
30	chr1:102178800-102179200	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr1:102179000-102179400	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr1:102179000-102179800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr1:102179000-102180600	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr1:102179200-102179600	Enhancers	H1 Cell Line	embryonic stem cell
35	chr1:102179200-102179800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
36	chr1:102179400-102179600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
37	chr1:102179600-102180600	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr1:102179800-102180400	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr1:102179800-102181200	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr1:102180400-102180600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
41	chr1:102180600-102180800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
42	chr1:102180600-102180800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
43	chr1:102180800-102181000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr1:102189000-102189400	Active TSS	GM12878-XiMat	blood
45	chr1:102191200-102191400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr1:102191600-102193000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr1:102193000-102193800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr1:102193400-102193600	Bivalent Enhancer	GM12878-XiMat	blood
49	chr1:102193600-102193800	Enhancers	GM12878-XiMat	blood
50	chr1:102193800-102194000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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