Variant report

Variant	nsv873071
Chromosome Location	chr1:197079671-197187605
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2064)
CpG islands
(count:1769)
Chromatin interactive
region (count:129)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:2064 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:197168611-197169006	K562	blood:	n/a	n/a
2	ARID3A	chr1:197170259-197171301	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:197112143-197112170	K562	blood:	n/a	n/a
4	ARID3A	chr1:197142850-197143703	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:197169385-197169814	K562	blood:	n/a	n/a
6	ARID3A	chr1:197170530-197171305	K562	blood:	n/a	n/a
7	ARID3A	chr1:197115676-197116328	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:197115609-197116380	K562	blood:	n/a	n/a
9	ARID3A	chr1:197148161-197148543	K562	blood:	n/a	n/a
10	ATF1	chr1:197115660-197116278	K562	blood:	n/a	n/a
11	ATF1	chr1:197170194-197170835	K562	blood:	n/a	n/a
12	ATF1	chr1:197182375-197182561	K562	blood:	n/a	n/a
13	ATF2	chr1:197170121-197170977	GM12878	blood:	n/a	n/a
14	ATF2	chr1:197115869-197116225	GM12878	blood:	n/a	n/a
15	ATF2	chr1:197115463-197116052	GM12878	blood:	n/a	n/a
16	ATF2	chr1:197170452-197170871	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr1:197170451-197171192	GM12878	blood:	n/a	n/a
18	ATF2	chr1:197170462-197170888	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr1:197170398-197170985	A549	lung:	n/a	n/a
20	ATF3	chr1:197170234-197170693	K562	blood:	n/a	n/a
21	ATF3	chr1:197170407-197170931	A549	lung:	n/a	n/a
22	BACH1	chr1:197148085-197148442	K562	blood:	n/a	n/a
23	BACH1	chr1:197115545-197115832	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr1:197170609-197170882	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr1:197169652-197169753	K562	blood:	n/a	n/a
26	BACH1	chr1:197109159-197109190	K562	blood:	n/a	n/a
27	BACH1	chr1:197162983-197163017	K562	blood:	n/a	n/a
28	BACH1	chr1:197115244-197115303	H1-hESC	embryonic stem cell:	n/a	n/a
29	BATF	chr1:197148116-197148453	GM12878	blood:	n/a	chr1:197148311-197148322
30	BATF	chr1:197170495-197170792	GM12878	blood:	n/a	n/a
31	BCL11A	chr1:197098823-197099125	H1-hESC	embryonic stem cell:	n/a	n/a
32	BCL3	chr1:197170442-197170998	A549	lung:	n/a	chr1:197170526-197170539 chr1:197170492-197170501
33	BCLAF1	chr1:197170501-197170980	GM12878	blood:	n/a	chr1:197170526-197170539
34	BCLAF1	chr1:197169892-197170481	GM12878	blood:	n/a	chr1:197170369-197170382 chr1:197170427-197170436
35	BCLAF1	chr1:197170474-197170940	GM12878	blood:	n/a	chr1:197170526-197170539 chr1:197170492-197170501
36	BHLHE40	chr1:197170090-197170951	K562	blood:	n/a	chr1:197170374-197170390
37	BHLHE40	chr1:197166826-197167245	K562	blood:	n/a	n/a
38	BHLHE40	chr1:197170008-197170942	GM12878	blood:	n/a	chr1:197170374-197170390
39	BHLHE40	chr1:197170221-197170867	HepG2	liver:	n/a	chr1:197170374-197170390
40	BHLHE40	chr1:197128733-197128735	K562	blood:	n/a	n/a
41	BHLHE40	chr1:197111610-197111637	GM12878	blood:	n/a	n/a
42	BHLHE40	chr1:197150951-197151527	GM12878	blood:	n/a	n/a
43	BHLHE40	chr1:197114605-197114608	GM12878	blood:	n/a	n/a
44	BHLHE40	chr1:197169772-197169789	K562	blood:	n/a	n/a
45	BHLHE40	chr1:197115209-197116304	K562	blood:	n/a	n/a
46	BHLHE40	chr1:197115678-197116228	GM12878	blood:	n/a	n/a
47	BRCA1	chr1:197115668-197116391	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr1:197170530-197170852	HepG2	liver:	n/a	n/a
49	BRCA1	chr1:197169515-197171411	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr1:197115767-197115897	GM12878	blood:	n/a	n/a

(count:1769 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:197169700-197169750	HCPEpiC	choroid plexus:	n/a
2	chr1:197099113-197099163	SKMC	muscle:	n/a
3	chr1:197115927-197115977	BJ	skin:	n/a
4	chr1:197099113-197099163	SK-N-SH_RA	brain:	n/a
5	chr1:197149498-197149548	H1-hESC	embryonic stem cell:	embryo
6	chr1:197116622-197116672	Hepatocyte	liver:	n/a
7	chr1:197170891-197170941	Hela-S3	cervix:	n/a
8	chr1:197170372-197170422	IMR90	lung:	fetal
9	chr1:197168091-197168141	ECC-1	luminal epithelium:	n/a
10	chr1:197115812-197115862	SAEC	small airway:	n/a
11	chr1:197169700-197169750	PFSK-1	brain:	n/a
12	chr1:197115927-197115977	SK-N-MC	brain:	n/a
13	chr1:197173499-197173549	CMK	blood:	n/a
14	chr1:197115545-197115595	HCF	heart:	n/a
15	chr1:197168091-197168141	HL-60	blood:	n/a
16	chr1:197115755-197115805	GM06990	blood:	n/a
17	chr1:197170599-197170649	Caco-2	colon:	n/a
18	chr1:197149498-197149548	SK-N-SH_RA	brain:	n/a
19	chr1:197170599-197170649	HUVEC	blood vessel:	n/a
20	chr1:197099113-197099163	HCM	heart:	n/a
21	chr1:197115894-197115944	K562	blood:	n/a
22	chr1:197115504-197115554	GM12891	blood:	n/a
23	chr1:197170891-197170941	HEK293	kidney:	embryo
24	chr1:197168091-197168141	CMK	blood:	n/a
25	chr1:197115405-197115455	AG09319	gingival:	n/a
26	chr1:197115755-197115805	AG09319	gingival:	n/a
27	chr1:197115894-197115944	T-47D	breast:	n/a
28	chr1:197169700-197169750	HEEpiC	esophagus:	n/a
29	chr1:197170891-197170941	NHBE	bronchial:	n/a
30	chr1:197099113-197099163	HUVEC	blood vessel:	n/a
31	chr1:197115841-197115891	SK-N-SH_RA	brain:	n/a
32	chr1:197115834-197115884	HUVEC	blood vessel:	n/a
33	chr1:197115545-197115595	HMEC	breast:	n/a
34	chr1:197168091-197168141	PrEC	prostate:	n/a
35	chr1:197169957-197170007	T-47D	breast:	n/a
36	chr1:197099113-197099163	ovcar-3	ovarian:	n/a
37	chr1:197115964-197116014	HCF	heart:	n/a
38	chr1:197124878-197124928	MCF10A-Er-Src	breast:	n/a
39	chr1:197115504-197115554	HCT-116	colon:	n/a
40	chr1:197169700-197169750	HCM	heart:	n/a
41	chr1:197115964-197116014	SAEC	small airway:	n/a
42	chr1:197173499-197173549	HRCEpiC	kidney:	n/a
43	chr1:197169700-197169750	AG09309	skin:	n/a
44	chr1:197169957-197170007	RPTEC	kidney:	n/a
45	chr1:197115958-197116008	CMK	blood:	n/a
46	chr1:197099113-197099163	PrEC	prostate:	n/a
47	chr1:197116190-197116240	BJ	skin:	n/a
48	chr1:197170372-197170422	HL-60	blood:	n/a
49	chr1:197115927-197115977	SK-N-SH	brain:	n/a
50	chr1:197170372-197170422	SK-N-MC	brain:	n/a

(count:129 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:197100050..197103962-chr1:197110434..197115621,7	K562	blood:
2	chr1:197092500..197094237-chr1:197110834..197113696,2	K562	blood:
3	chr1:197102908..197105277-chr1:197113696..197116665,2	MCF-7	breast:
4	chr1:197086007..197089050-chr1:197097882..197101609,3	K562	blood:
5	chr1:197118116..197120208-chr1:197163140..197165149,2	MCF-7	breast:
6	chr1:197089752..197091362-chr1:197102516..197104850,2	K562	blood:
7	chr1:197142224..197144891-chr1:197148016..197149647,2	K562	blood:
8	chr1:193072582..193075085-chr1:197113385..197115206,2	K562	blood:
9	chr1:197159273..197161304-chr1:197164955..197167252,3	K562	blood:
10	chr1:197093674..197095835-chr1:197097163..197099418,3	K562	blood:
11	chr1:197093048..197099045-chr1:197107378..197117076,12	K562	blood:
12	chr1:197165132..197167397-chr1:197181290..197183417,2	K562	blood:
13	chr1:197126302..197127851-chr1:197131460..197133305,2	K562	blood:
14	chr1:197082888..197084637-chr1:197110135..197112878,2	K562	blood:
15	chr1:197112460..197117731-chr1:197129268..197134426,6	K562	blood:
16	chr1:197147159..197149078-chr1:197192241..197194774,2	MCF-7	breast:
17	chr1:197130853..197132396-chr1:197133681..197135184,2	MCF-7	breast:
18	chr1:197134959..197137671-chr1:197138755..197140780,2	K562	blood:
19	chr1:197153884..197156331-chr1:197167263..197169035,2	K562	blood:
20	chr1:197167660..197168424-chr7:117707343..117708112,2	MCF-7	breast:
21	chr1:197149136..197149963-chr1:197303278..197304212,2	MCF-7	breast:
22	chr1:197115985..197117514-chr1:197120837..197122642,2	MCF-7	breast:
23	chr1:197169953..197172580-chr1:197177266..197179766,2	K562	blood:
24	chr1:197121011..197127851-chr1:197128597..197135190,9	K562	blood:
25	chr1:197114016..197115684-chr1:197163598..197165339,2	K562	blood:
26	chr1:197114016..197117152-chr1:197163839..197167436,4	K562	blood:
27	chr1:197063964..197065535-chr1:197110090..197112434,2	K562	blood:
28	chr1:197108980..197111975-chr1:197160260..197161833,2	K562	blood:
29	chr1:197121011..197127851-chr1:197128597..197135190,9	K562	blood:
30	chr1:197068919..197071341-chr1:197120763..197122532,2	K562	blood:
31	chr1:197159273..197161304-chr1:197164955..197167252,3	K562	blood:
32	chr1:197098436..197100309-chr1:197101264..197103559,2	K562	blood:
33	chr1:197161517..197163826-chr1:197164890..197167674,2	K562	blood:
34	chr1:197154600..197157025-chr1:197162185..197164324,3	K562	blood:
35	chr1:197117346..197120287-chr1:197339485..197341167,2	K562	blood:
36	chr1:197102908..197105277-chr1:197113696..197116665,2	MCF-7	breast:
37	chr1:197086007..197087668-chr1:197097835..197099382,2	K562	blood:
38	chr1:197090506..197092545-chr1:197093003..197095180,2	MCF-7	breast:
39	chr1:197149215..197150102-chr1:197326053..197326779,3	MCF-7	breast:
40	chr1:197152680..197155309-chr1:197165847..197169413,3	MCF-7	breast:
41	chr1:197130853..197132396-chr1:197133681..197135184,2	MCF-7	breast:
42	chr1:197128463..197130578-chr1:197135579..197137702,2	K562	blood:
43	chr1:197157362..197159719-chr1:197168800..197171686,3	K562	blood:
44	chr1:197086992..197089260-chr1:197103012..197104578,2	K562	blood:
45	chr1:197185992..197188090-chr1:197191988..197194131,2	K562	blood:
46	chr1:197149241..197150078-chr1:197325625..197326699,7	K562	blood:
47	chr1:197170029..197170798-chr6:31496172..31496731,2	HCT-116	colon:
48	chr1:197142224..197144891-chr1:197148016..197149647,2	K562	blood:
49	chr1:197169410..197171188-chr1:197190699..197192659,2	MCF-7	breast:
50	chr1:197126302..197127851-chr1:197131460..197133305,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASPM-1	chr1:197134241-197136321	ucscGeneNc_uc001guz_1
2	lnc-ASPM-1	chr1:197172978-197173181	NONHSAT008615
3	lnc-ASPM-1	chr1:197135770-197136321	NONHSAT008615
4	lnc-CFHR5-2	chr1:197170771-197172215	NONHSAT008616
5	lnc-ASPM-1	chr1:197136163-197136321	NONHSAT008612
6	lnc-ZBTB41-2	chr1:197107878-197108437	NONHSAT008613
7	lnc-ASPM-1	chr1:197172978-197173181	ucscGeneNc_uc001guz_1
8	lnc-ASPM-1	chr1:197172978-197173162	NONHSAT008612

No data

(count:7 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	ZBTB41	hsa-miR-374b-5p	chr1:197126457-197126479
2	ZBTB41	hsa-miR-93-5p	chr1:197127045-197127065
3	ZBTB41	hsa-miR-93-5p	chr1:197127238-197127232
4	ZBTB41	hsa-miR-93-5p	chr1:197127232-197127255
5	ZBTB41	hsa-miR-374b-5p	chr1:197126567-197126589
6	ZBTB41	hsa-miR-93-5p	chr1:197127051-197127045
7	ZBTB41	hsa-miR-374b-5p	chr1:197126423-197126443

Variant related genes	Relation type
ENSG00000235748	TF binding region
ZBTB41	TF binding region
CRB1	TF binding region
ENSG00000237861	TF binding region
ASPM	TF binding region
ENSG00000235748	CpG island
ZBTB41	CpG island
CRB1	CpG island
ENSG00000237861	CpG island
ASPM	CpG island
ENSG00000237861	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000140299	chromatin interactions
ENSG00000066279	chromatin interactions
ENSG00000177888	chromatin interactions
ENSG00000235748	chromatin interactions
ENSG00000197903	chromatin interactions
ENSG00000134376	chromatin interactions
ENSG00000184825	chromatin interactions
ENSG00000204511	chromatin interactions
ENSG00000023572	chromatin interactions
ENSG00000259884	chromatin interactions

Extended variants
information (count: 3916 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:3916 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2026429	chr1:197079671-197079672	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571233484	chr1:197079729-197079730	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs539342600	chr1:197079741-197079742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs377717042	chr1:197079758-197079759	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554463101	chr1:197079759-197079760	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs149947341	chr1:197079806-197079807	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145097943	chr1:197079818-197079819	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148922450	chr1:197079825-197079826	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs576478513	chr1:197079853-197079854	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs543872858	chr1:197079885-197079886	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558686763	chr1:197079972-197079973	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373298130	chr1:197079977-197079978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs576787450	chr1:197079984-197079985	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12723094	chr1:197079986-197079987	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs544943311	chr1:197080008-197080009	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10922166	chr1:197080036-197080037	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs182136625	chr1:197080143-197080144	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112099740	chr1:197080144-197080145	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187218519	chr1:197080191-197080192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571994196	chr1:197080193-197080194	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10801590	chr1:197080203-197080204	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs531327330	chr1:197080257-197080258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191642426	chr1:197080271-197080272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs114765484	chr1:197080349-197080350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs554365990	chr1:197080358-197080359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564881226	chr1:197080404-197080405	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532133107	chr1:197080438-197080439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576108155	chr1:197080439-197080440	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs117223332	chr1:197080460-197080461	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs75003874	chr1:197080461-197080462	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575226177	chr1:197080471-197080472	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548524565	chr1:197080478-197080479	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183551935	chr1:197080480-197080481	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537160239	chr1:197080598-197080599	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558618446	chr1:197080670-197080671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs576874179	chr1:197080702-197080703	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142411116	chr1:197080759-197080760	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79222044	chr1:197080767-197080768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185577882	chr1:197080854-197080855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542879262	chr1:197080858-197080859	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560927768	chr1:197080884-197080885	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs118076793	chr1:197080975-197080976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146636250	chr1:197081022-197081023	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564967784	chr1:197081037-197081038	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544701226	chr1:197081077-197081078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532169846	chr1:197081152-197081153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs116115588	chr1:197081188-197081189	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112253975	chr1:197081207-197081208	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147919005	chr1:197081242-197081243	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141753962	chr1:197081251-197081252	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Glioblastoma multiforme	21080181	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
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Mental retardation	21062444	CNVD
Liver carcinoma	19366792	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20962326	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2920 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:197052200-197083600	Weak transcription	Fetal Stomach	stomach
2	chr1:197052200-197106600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:197052200-197114200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr1:197054200-197113600	Weak transcription	Fetal Kidney	kidney
5	chr1:197055000-197114200	Weak transcription	Primary B cells from cord blood	blood
6	chr1:197066600-197083600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr1:197067000-197092200	Weak transcription	Fetal Intestine Large	intestine
8	chr1:197070600-197100000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr1:197070800-197085400	Weak transcription	Osteobl	bone
10	chr1:197071000-197084400	Weak transcription	Fetal Heart	heart
11	chr1:197071000-197105400	Strong transcription	Dnd41	blood
12	chr1:197071400-197095800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr1:197071800-197104600	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr1:197072600-197087400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr1:197072600-197104600	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr1:197072600-197107400	Weak transcription	Fetal Intestine Small	intestine
17	chr1:197073000-197104000	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr1:197073000-197115000	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr1:197073600-197098400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr1:197073800-197083400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr1:197073800-197085200	Weak transcription	GM12878-XiMat	blood
22	chr1:197073800-197091400	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr1:197074000-197080000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr1:197074000-197085400	Weak transcription	HepG2	liver
25	chr1:197074000-197115000	Weak transcription	Fetal Brain Male	brain
26	chr1:197074200-197085000	Weak transcription	NHDF-Ad	bronchial
27	chr1:197074200-197091400	Weak transcription	NHEK	skin
28	chr1:197074200-197102000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr1:197074800-197082200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
30	chr1:197076200-197094000	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr1:197076400-197080400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr1:197076400-197081200	Weak transcription	Thymus	Thymus
33	chr1:197076400-197085200	Weak transcription	NH-A	brain
34	chr1:197076400-197096400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr1:197076600-197081600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr1:197076600-197084200	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr1:197076600-197085200	Weak transcription	HMEC	breast
38	chr1:197076800-197081800	Weak transcription	Primary hematopoietic stem cells	blood
39	chr1:197077000-197080400	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr1:197077000-197085400	Weak transcription	K562	blood
41	chr1:197077000-197114200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr1:197077200-197082000	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr1:197077200-197083400	Weak transcription	Fetal Muscle Leg	muscle
44	chr1:197077200-197083800	Weak transcription	Fetal Muscle Trunk	muscle
45	chr1:197077200-197090800	Weak transcription	NHLF	lung
46	chr1:197077400-197083000	Weak transcription	Fetal Lung	lung
47	chr1:197077600-197083600	Weak transcription	HUVEC	blood vessel
48	chr1:197077800-197083600	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr1:197077800-197083600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr1:197077800-197084400	Weak transcription	HSMM	muscle

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