Variant report

Variant	nsv1026991
Chromosome Location	chr5:180077614-180229093
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1737)
CpG islands
(count:2141)
Chromatin interactive
region (count:94)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1737 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:180212570-180213141	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr5:180144959-180145359	GM12878	blood:	n/a	n/a
3	ATF2	chr5:180212679-180213244	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr5:180145061-180145379	GM12878	blood:	n/a	chr5:180145207-180145218
5	BATF	chr5:180145040-180145312	GM12878	blood:	n/a	chr5:180145207-180145218
6	BATF	chr5:180169789-180169977	GM12878	blood:	n/a	n/a
7	BATF	chr5:180097198-180097443	GM12878	blood:	n/a	n/a
8	BCL11A	chr5:180145100-180145299	GM12878	blood:	n/a	chr5:180145235-180145244
9	BCL11A	chr5:180085399-180085773	GM12878	blood:	n/a	n/a
10	BCL11A	chr5:180145000-180145348	GM12878	blood:	n/a	chr5:180145235-180145244
11	BCL3	chr5:180097085-180097491	GM12878	blood:	n/a	n/a
12	BCL3	chr5:180229004-180229979	A549	lung:	n/a	chr5:180229768-180229781
13	CBX3	chr5:180208965-180209392	K562	blood:	n/a	n/a
14	CBX3	chr5:180198766-180199290	K562	blood:	n/a	n/a
15	CBX3	chr5:180215613-180215981	K562	blood:	n/a	n/a
16	CBX3	chr5:180208858-180209504	K562	blood:	n/a	n/a
17	CBX3	chr5:180127492-180127736	K562	blood:	n/a	n/a
18	CBX3	chr5:180198844-180199194	K562	blood:	n/a	n/a
19	CEBPB	chr5:180208882-180209430	K562	blood:	n/a	n/a
20	CEBPB	chr5:180229018-180229879	HCT-116	colon:	n/a	chr5:180229202-180229214
21	CEBPB	chr5:180229075-180229803	A549	lung:	n/a	chr5:180229202-180229214
22	CEBPB	chr5:180209005-180209250	K562	blood:	n/a	n/a
23	CEBPB	chr5:180131341-180131657	K562	blood:	n/a	n/a
24	CEBPD	chr5:180131384-180131803	K562	blood:	n/a	n/a
25	CEBPD	chr5:180208777-180209303	K562	blood:	n/a	n/a
26	CEBPD	chr5:180208780-180209396	K562	blood:	n/a	n/a
27	CREB1	chr5:180144836-180145451	GM12878	blood:	n/a	n/a
28	CREB1	chr5:180144917-180145413	GM12878	blood:	n/a	n/a
29	CTCF	chr5:180146205-180146324	Fibrobl	skin:	n/a	n/a
30	CTCF	chr5:180146180-180146285	GM19240	blood:	n/a	n/a
31	CTCF	chr5:180226320-180226470	SAEC	small airway:	n/a	n/a
32	CTCF	chr5:180146520-180146670	HRE	kidney:	n/a	n/a
33	CTCF	chr5:180145360-180145510	GM12874	blood:	n/a	n/a
34	CTCF	chr5:180217238-180217265	HepG2	liver:	n/a	chr5:180217245-180217258 chr5:180217242-180217260
35	CTCF	chr5:180145880-180146030	NHEK	skin:	n/a	n/a
36	CTCF	chr5:180227360-180227510	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr5:180211620-180211770	GM12873	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
38	CTCF	chr5:180226380-180226530	HCT-116	colon:	n/a	n/a
39	CTCF	chr5:180107591-180107909	K562	blood:	n/a	n/a
40	CTCF	chr5:180145840-180145990	GM12873	blood:	n/a	n/a
41	CTCF	chr5:180227680-180227830	HAc	cerebellar:	n/a	n/a
42	CTCF	chr5:180227620-180227770	HPF	lung:	n/a	n/a
43	CTCF	chr5:180097598-180097855	ProgFib	skin:	n/a	chr5:180097737-180097755 chr5:180097732-180097753
44	CTCF	chr5:180100420-180100570	K562	blood:	n/a	chr5:180100461-180100470 chr5:180100458-180100476 chr5:180100461-180100474
45	CTCF	chr5:180227540-180227690	GM12873	blood:	n/a	n/a
46	CTCF	chr5:180211620-180211770	AG04450	lung:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
47	CTCF	chr5:180159424-180159582	K562	blood:	n/a	n/a
48	CTCF	chr5:180145800-180145950	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr5:180145666-180146117	MCF-7	breast:	n/a	n/a
50	CTCF	chr5:180145665-180146176	MCF-7	breast:	n/a	n/a

(count:2141 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:180219412-180219462	CMK	blood:	n/a
2	chr5:180099956-180100006	A549	lung:	n/a
3	chr5:180085446-180085496	AG09319	gingival:	n/a
4	chr5:180218509-180218559	AG04449	skin:	fetal
5	chr5:180111966-180112016	CMK	blood:	n/a
6	chr5:180111800-180111850	A549	lung:	n/a
7	chr5:180219412-180219462	CMK	blood:	n/a
8	chr5:180099956-180100006	A549	lung:	n/a
9	chr5:180085446-180085496	AG09319	gingival:	n/a
10	chr5:180218509-180218559	AG04449	skin:	fetal
11	chr5:180111966-180112016	CMK	blood:	n/a
12	chr5:180111800-180111850	A549	lung:	n/a
13	chr5:180167965-180168015	HL-60	blood:	n/a
14	chr5:180100701-180100751	SK-N-MC	brain:	n/a
15	chr5:180116385-180116435	ProgFib	skin:	n/a
16	chr5:180219412-180219462	SK-N-SH_RA	brain:	n/a
17	chr5:180219707-180219757	HNPCEpiC	eye:	n/a
18	chr5:180219707-180219757	GM12891	blood:	n/a
19	chr5:180112929-180112979	U87	brain:	n/a
20	chr5:180219008-180219058	HAEpiC	amniotic membrane:	n/a
21	chr5:180111800-180111850	AG09319	gingival:	n/a
22	chr5:180111966-180112016	PANC-1	pancreas:	n/a
23	chr5:180097910-180097960	Caco-2	colon:	n/a
24	chr5:180085446-180085496	NHBE	bronchial:	n/a
25	chr5:180229067-180229117	T-47D	breast:	n/a
26	chr5:180227299-180227349	HCPEpiC	choroid plexus:	n/a
27	chr5:180218509-180218559	SK-N-MC	brain:	n/a
28	chr5:180111800-180111850	AG04450	lung:	fetal
29	chr5:180217700-180217750	AoSMC	blood vessel:	n/a
30	chr5:180220005-180220055	HCF	heart:	n/a
31	chr5:180213189-180213239	SAEC	small airway:	n/a
32	chr5:180101281-180101331	HRE	kidney:	n/a
33	chr5:180213189-180213239	A549	lung:	n/a
34	chr5:180111966-180112016	AG09319	gingival:	n/a
35	chr5:180166492-180166542	HCM	heart:	n/a
36	chr5:180111966-180112016	GM12891	blood:	n/a
37	chr5:180100963-180101013	ECC-1	luminal epithelium:	n/a
38	chr5:180113361-180113411	Jurkat	blood:	n/a
39	chr5:180085446-180085496	GM12891	blood:	n/a
40	chr5:180085924-180085974	HRPEpiC	eye:	n/a
41	chr5:180103241-180103291	Hela-S3	cervix:	n/a
42	chr5:180218509-180218559	PrEC	prostate:	n/a
43	chr5:180218509-180218559	HL-60	blood:	n/a
44	chr5:180167566-180167616	SK-N-SH	brain:	n/a
45	chr5:180111800-180111850	NH-A	brain:	n/a
46	chr5:180101440-180101490	Hela-S3	cervix:	n/a
47	chr5:180101143-180101193	GM06990	blood:	n/a
48	chr5:180111800-180111850	AoSMC	blood vessel:	n/a
49	chr5:180101143-180101193	SAEC	small airway:	n/a
50	chr5:180111966-180112016	GM12878	blood:	n/a

(count:94 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:180158275..180159905-chr5:180163258..180165205,2	K562	blood:
2	chr5:180048663..180050730-chr5:180113911..180116171,2	K562	blood:
3	chr5:180094037..180096535-chr5:180099976..180102790,2	K562	blood:
4	chr5:180207628..180210924-chr5:180228309..180230947,5	MCF-7	breast:
5	chr5:180094037..180096535-chr5:180099976..180102790,2	K562	blood:
6	chr5:180217957..180220948-chr5:180429295..180431970,2	K562	blood:
7	chr5:180224924..180227171-chr5:180287379..180289877,3	MCF-7	breast:
8	chr5:180217067..180219759-chr5:180269419..180271439,2	K562	blood:
9	chr5:180092442..180094516-chr5:180097000..180098654,2	K562	blood:
10	chr5:180227369..180230069-chr5:180671459..180674771,3	MCF-7	breast:
11	chr5:180208930..180211085-chr5:180226767..180229407,2	K562	blood:
12	chr5:180136617..180138276-chr5:180153652..180155749,2	K562	blood:
13	chr5:179718120..179720283-chr5:180227933..180230146,2	MCF-7	breast:
14	chr5:180171538..180174150-chr5:180179388..180180987,2	K562	blood:
15	chr5:180032730..180033573-chr5:180097208..180098138,2	MCF-7	breast:
16	chr5:180209019..180210957-chr5:180453882..180456380,2	K562	blood:
17	chr3:18286488..18287319-chr5:180097543..180098157,2	MCF-7	breast:
18	chr5:180227912..180229802-chr5:180527459..180529455,2	K562	blood:
19	chr5:180083705..180084315-chr6:10033064..10033612,2	MCF-7	breast:
20	chr5:180211375..180212214-chr5:180226180..180226854,2	MCF-7	breast:
21	chr5:180219008..180221127-chr5:180221660..180224233,2	MCF-7	breast:
22	chr5:180147687..180149481-chr5:180151717..180153867,2	K562	blood:
23	chr5:180130605..180132994-chr5:180134010..180136773,2	MCF-7	breast:
24	chr5:180168086..180169925-chr5:180190599..180192805,2	K562	blood:
25	chr5:40835246..40835914-chr5:180228933..180229470,2	Hela-S3	cervix:
26	chr5:180038293..180038846-chr5:180097248..180097778,2	K562	blood:
27	chr5:180091768..180093922-chr5:180095583..180097208,2	K562	blood:
28	chr5:180147687..180149481-chr5:180151717..180153867,2	K562	blood:
29	chr5:180226030..180229620-chr5:180255411..180258955,4	K562	blood:
30	chr5:179919075..179921338-chr5:180210769..180213087,2	MCF-7	breast:
31	chr5:180210430..180214631-chr5:180286463..180290673,6	MCF-7	breast:
32	chr5:180168086..180169925-chr5:180190599..180192805,2	K562	blood:
33	chr5:180172009..180174376-chr5:180240608..180243076,2	MCF-7	breast:
34	chr5:180211375..180212214-chr5:180226180..180226854,2	MCF-7	breast:
35	chr5:180211640..180213961-chr5:180214094..180219248,5	K562	blood:
36	chr5:180221672..180224385-chr5:180256701..180259508,2	K562	blood:
37	chr5:180022631..180025317-chr5:180096101..180098291,2	MCF-7	breast:
38	chr5:180202113..180204208-chr5:180208493..180210882,2	K562	blood:
39	chr5:180212092..180214294-chr5:180453988..180456472,2	K562	blood:
40	chr5:180210073..180212750-chr5:180649135..180651698,2	MCF-7	breast:
41	chr5:180216327..180219256-chr5:180485099..180486798,2	K562	blood:
42	chr5:180208930..180211085-chr5:180226767..180229407,2	K562	blood:
43	chr5:180228019..180233439-chr5:180285963..180289843,10	MCF-7	breast:
44	chr5:180113673..180116367-chr5:180119581..180121156,3	K562	blood:
45	chr5:180211185..180212156-chr5:180225940..180226892,9	MCF-7	breast:
46	chr5:180211185..180212156-chr5:180225940..180226892,9	MCF-7	breast:
47	chr5:180153993..180156519-chr5:180159947..180161759,2	K562	blood:
48	chr5:180076787..180079357-chr5:180092252..180095157,2	K562	blood:
49	chr5:180226982..180228709-chr5:180280762..180282451,2	K562	blood:
50	chr5:180202321..180205166-chr5:180643152..180645917,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP62-3	chr5:180222406-180222875	NONHSAT105809
2	lnc-CNOT6-3	chr5:180111766-180111906	XLOC_004682
3	lnc-BTNL8-8	chr5:180190563-180190835	ucscGeneNc_uc003mmk_2
4	lnc-FLT4-1	chr5:180098892-180099598	NONHSAT105695
5	lnc-OR2Y1-1	chr5:180155280-180155484	expReg_chr5_11028_-
6	lnc-BTNL8-8	chr5:180192279-180192466	ucscGeneNc_uc003mmk_2
7	lnc-CNOT6-3	chr5:180112648-180113546	NONHSAT105706
8	lnc-OR2Y1-2	chr5:180189565-180191201	ucscGeneNc_uc003mmj_1
9	lnc-BTNL8-8	chr5:180193918-180195284	ucscGeneNc_uc003mmk_2
10	lnc-CNOT6-3	chr5:180111765-180111906	NONHSAT105706
11	lnc-CNOT6-3	chr5:180112649-180113546	XLOC_004682
12	lnc-ZFP62-3	chr5:180222430-180222875	NONHSAT105810

No data

Variant related genes	Relation type
FLT4	TF binding region
OR2AI1P	TF binding region
RNU1-17P	TF binding region
ENSG00000260841	TF binding region
ENSG00000248717	TF binding region
OR2Y1	TF binding region
ENSG00000251352	TF binding region
FLT4	CpG island
OR2AI1P	CpG island
RNU1-17P	CpG island
ENSG00000260841	CpG island
ENSG00000248717	CpG island
OR2Y1	CpG island
ENSG00000251352	CpG island
ENSG00000146063	chromatin interactions
ENSG00000145592	chromatin interactions
ENSG00000214295	chromatin interactions
ENSG00000196670	chromatin interactions
ENSG00000264732	chromatin interactions
ENSG00000236791	chromatin interactions
ENSG00000233937	chromatin interactions
ENSG00000050748	chromatin interactions
ENSG00000260841	chromatin interactions
ENSG00000081791	chromatin interactions
ENSG00000264549	chromatin interactions
ENSG00000146054	chromatin interactions
ENSG00000204628	chromatin interactions
ENSG00000037280	chromatin interactions
ENSG00000268397	chromatin interactions
ENSG00000131446	chromatin interactions
ENSG00000245060	chromatin interactions
ENSG00000248514	chromatin interactions
ENSG00000199892	chromatin interactions
ENSG00000248367	chromatin interactions

Extended variants
information (count: 4302 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:4302 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551101030	chr5:180077622-180077623	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs3806860	chr5:180077708-180077709	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs577984374	chr5:180077760-180077761	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs543873781	chr5:180077801-180077802	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs115086722	chr5:180077874-180077875	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs556761038	chr5:180077922-180077923	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs150926061	chr5:180077927-180077928	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs549415275	chr5:180077940-180077941	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs78750164	chr5:180078434-180078435	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs144903531	chr5:180078447-180078448	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs542650552	chr5:180078449-180078450	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs560401923	chr5:180078452-180078453	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs559825845	chr5:180078490-180078491	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs528561419	chr5:180078504-180078505	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs138724091	chr5:180078513-180078514	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs565107187	chr5:180078532-180078533	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs531114945	chr5:180078548-180078549	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs13187322	chr5:180078549-180078550	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs112258362	chr5:180078574-180078575	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs528930292	chr5:180078581-180078582	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs548682748	chr5:180078600-180078601	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs79324086	chr5:180079228-180079229	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs6889643	chr5:180079230-180079231	Inactive region	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs372137452	chr5:180085605-180085606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs113675834	chr5:180085618-180085619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs149414228	chr5:180085621-180085622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs372646960	chr5:180085629-180085630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs113223352	chr5:180085636-180085637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs376409470	chr5:180085637-180085638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369935850	chr5:180085645-180085646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs200897302	chr5:180085653-180085654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs201490362	chr5:180085658-180085659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs377366783	chr5:180085661-180085662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs566488153	chr5:180085662-180085663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs199892579	chr5:180085669-180085670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs200970404	chr5:180085693-180085694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs201820941	chr5:180085698-180085699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs377603473	chr5:180085701-180085702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs370258424	chr5:180085709-180085710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs374973766	chr5:180085722-180085723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs368468004	chr5:180085725-180085726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs372860988	chr5:180085733-180085734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs538639730	chr5:180085741-180085742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs374178884	chr5:180085743-180085744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs368489091	chr5:180085749-180085750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs113258998	chr5:180085759-180085760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs372138774	chr5:180085765-180085766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs201070502	chr5:180085770-180085771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs376099397	chr5:180085773-180085774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs113950347	chr5:180085778-180085779	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Autism	22543975	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	17440070	CNVD
Schizophrenia	21346763	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1895 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:180075800-180077800	Bivalent/Poised TSS	Primary T cells from cord blood	blood
2	chr5:180077400-180077800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
3	chr5:180077400-180077800	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
4	chr5:180077400-180077800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr5:180077400-180078000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
6	chr5:180077400-180078000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
7	chr5:180077600-180077800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
8	chr5:180077600-180077800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
9	chr5:180077600-180077800	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
10	chr5:180077600-180077800	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr5:180077600-180077800	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr5:180077600-180077800	Bivalent/Poised TSS	Fetal Brain Male	brain
13	chr5:180077600-180077800	Bivalent Enhancer	Dnd41	blood
14	chr5:180078400-180078600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
15	chr5:180085600-180085800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr5:180085800-180086000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr5:180085800-180086000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr5:180085800-180086000	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
19	chr5:180085800-180086000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr5:180085800-180086000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr5:180085800-180086000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr5:180085800-180086000	Bivalent Enhancer	Brain Germinal Matrix	brain
23	chr5:180085800-180086000	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
24	chr5:180085800-180086000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
25	chr5:180085800-180086000	Bivalent Enhancer	Fetal Brain Male	brain
26	chr5:180085800-180086000	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
27	chr5:180085800-180086000	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
28	chr5:180085800-180086200	Active TSS	H9 Cell Line	embryonic stem cell
29	chr5:180085800-180086200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
30	chr5:180085800-180086200	Active TSS	iPS-15b Cell Line	embryonic stem cell
31	chr5:180085800-180086200	Active TSS	iPS-18 Cell Line	embryonic stem cell
32	chr5:180085800-180086200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr5:180085800-180086200	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
34	chr5:180085800-180086200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
35	chr5:180085800-180086200	Bivalent/Poised TSS	Primary T cells from cord blood	blood
36	chr5:180085800-180086200	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr5:180085800-180086200	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
38	chr5:180085800-180086200	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
39	chr5:180085800-180086200	Bivalent Enhancer	Spleen	Spleen
40	chr5:180085800-180086600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
41	chr5:180085800-180086600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
42	chr5:180085800-180086600	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr5:180085800-180086600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
44	chr5:180085800-180086600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
45	chr5:180085800-180086600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
46	chr5:180085800-180086600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
47	chr5:180086000-180086200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr5:180086000-180086200	Bivalent/Poised TSS	Brain Germinal Matrix	brain
49	chr5:180086000-180086200	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
50	chr5:180086000-180086400	Bivalent/Poised TSS	HSMM	muscle

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