Variant report

Variant	esv1845198
Chromosome Location	chr1:71274759-71514969
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1350)
CpG islands
(count:978)
Chromatin interactive
region (count:96)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1350 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:71508903-71509315	K562	blood:	n/a	n/a
2	ARID3A	chr1:71511965-71512135	K562	blood:	n/a	n/a
3	ARID3A	chr1:71510208-71510932	K562	blood:	n/a	n/a
4	ARID3A	chr1:71472265-71472284	K562	blood:	n/a	n/a
5	ARID3A	chr1:71340527-71340612	K562	blood:	n/a	n/a
6	ARID3A	chr1:71332347-71332486	K562	blood:	n/a	n/a
7	ARID3A	chr1:71468699-71468724	K562	blood:	n/a	n/a
8	ARID3A	chr1:71511378-71511609	K562	blood:	n/a	n/a
9	ARID3A	chr1:71343106-71343389	K562	blood:	n/a	n/a
10	ARID3A	chr1:71436198-71436440	K562	blood:	n/a	n/a
11	ARID3A	chr1:71356154-71356634	K562	blood:	n/a	n/a
12	ARID3A	chr1:71460522-71460848	K562	blood:	n/a	n/a
13	ARID3A	chr1:71481128-71481217	K562	blood:	n/a	n/a
14	ATF1	chr1:71445230-71445327	K562	blood:	n/a	n/a
15	ATF1	chr1:71356152-71356426	K562	blood:	n/a	n/a
16	ATF1	chr1:71451500-71451902	K562	blood:	n/a	n/a
17	ATF1	chr1:71343077-71343340	K562	blood:	n/a	n/a
18	ATF1	chr1:71427045-71427515	K562	blood:	n/a	n/a
19	ATF1	chr1:71510574-71510921	K562	blood:	n/a	n/a
20	ATF1	chr1:71375175-71375423	K562	blood:	n/a	n/a
21	ATF3	chr1:71510507-71510912	K562	blood:	n/a	n/a
22	BACH1	chr1:71513504-71513540	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr1:71468156-71468161	K562	blood:	n/a	n/a
24	BACH1	chr1:71377587-71377854	K562	blood:	n/a	n/a
25	BHLHE40	chr1:71427278-71427427	K562	blood:	n/a	n/a
26	BHLHE40	chr1:71485053-71485253	K562	blood:	n/a	n/a
27	BHLHE40	chr1:71480894-71480941	K562	blood:	n/a	n/a
28	BHLHE40	chr1:71287764-71287765	K562	blood:	n/a	n/a
29	BHLHE40	chr1:71436134-71436325	K562	blood:	n/a	n/a
30	BHLHE40	chr1:71465554-71465707	K562	blood:	n/a	n/a
31	BHLHE40	chr1:71362058-71362252	K562	blood:	n/a	n/a
32	BHLHE40	chr1:71501191-71501340	K562	blood:	n/a	n/a
33	BHLHE40	chr1:71510716-71511619	K562	blood:	n/a	n/a
34	BHLHE40	chr1:71512038-71514051	K562	blood:	n/a	chr1:71513319-71513335 chr1:71513322-71513338 chr1:71513407-71513423 chr1:71513352-71513368 chr1:71513419-71513435
35	BRCA1	chr1:71361486-71361517	GM12878	blood:	n/a	n/a
36	CBX3	chr1:71317529-71317793	K562	blood:	n/a	n/a
37	CBX3	chr1:71347391-71347736	K562	blood:	n/a	n/a
38	CBX3	chr1:71512656-71513704	K562	blood:	n/a	n/a
39	CBX3	chr1:71511945-71512532	K562	blood:	n/a	n/a
40	CCNT2	chr1:71510706-71510856	K562	blood:	n/a	n/a
41	CCNT2	chr1:71356056-71356365	K562	blood:	n/a	n/a
42	CCNT2	chr1:71375173-71375436	K562	blood:	n/a	n/a
43	CCNT2	chr1:71511971-71513807	K562	blood:	n/a	chr1:71513534-71513543 chr1:71512342-71512351
44	CCNT2	chr1:71474825-71475012	K562	blood:	n/a	n/a
45	CEBPB	chr1:71340570-71340885	MCF-7	breast:	n/a	n/a
46	CEBPB	chr1:71467330-71467690	HepG2	liver:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
47	CEBPB	chr1:71320980-71321196	H1-hESC	embryonic stem cell:	n/a	chr1:71321073-71321084
48	CEBPB	chr1:71485618-71485862	IMR90	lung:	n/a	chr1:71485756-71485767
49	CEBPB	chr1:71444470-71444536	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr1:71513488-71513954	K562	blood:	n/a	chr1:71513897-71513910

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:71513733-71513783	AG09319	gingival:	n/a
2	chr1:71513726-71513776	PrEC	prostate:	n/a
3	chr1:71513733-71513783	AG09319	gingival:	n/a
4	chr1:71513726-71513776	PrEC	prostate:	n/a
5	chr1:71472738-71472788	GM06990	blood:	n/a
6	chr1:71354374-71354424	PANC-1	pancreas:	n/a
7	chr1:71513726-71513776	SAEC	small airway:	n/a
8	chr1:71512485-71512535	H1-hESC	embryonic stem cell:	embryo
9	chr1:71513494-71513544	SK-N-SH_RA	brain:	n/a
10	chr1:71472738-71472788	HRPEpiC	eye:	n/a
11	chr1:71354374-71354424	U87	brain:	n/a
12	chr1:71512973-71513023	SK-N-SH	brain:	n/a
13	chr1:71514431-71514481	HEEpiC	esophagus:	n/a
14	chr1:71513114-71513164	SK-N-SH	brain:	n/a
15	chr1:71513566-71513616	HRCEpiC	kidney:	n/a
16	chr1:71513726-71513776	ProgFib	skin:	n/a
17	chr1:71514431-71514481	AG04450	lung:	fetal
18	chr1:71513626-71513676	ovcar-3	ovarian:	n/a
19	chr1:71511514-71511564	PFSK-1	brain:	n/a
20	chr1:71511514-71511564	HCM	heart:	n/a
21	chr1:71418388-71418438	NHDF-neo	bronchial:	n/a
22	chr1:71513494-71513544	NT2-D1	testis:	n/a
23	chr1:71512100-71512150	GM06990	blood:	n/a
24	chr1:71513626-71513676	A549	lung:	n/a
25	chr1:71513626-71513676	PrEC	prostate:	n/a
26	chr1:71472738-71472788	NHBE	bronchial:	n/a
27	chr1:71514431-71514481	Hepatocyte	liver:	n/a
28	chr1:71513566-71513616	HCT-116	colon:	n/a
29	chr1:71513494-71513544	HCPEpiC	choroid plexus:	n/a
30	chr1:71513566-71513616	MCF-7	breast:	n/a
31	chr1:71513626-71513676	HPAEpiC	pulmonary alveolar:	n/a
32	chr1:71513114-71513164	AoSMC	blood vessel:	n/a
33	chr1:71512973-71513023	GM12892	blood:	n/a
34	chr1:71513494-71513544	CMK	blood:	n/a
35	chr1:71513789-71513839	PANC-1	pancreas:	n/a
36	chr1:71513733-71513783	BJ	skin:	n/a
37	chr1:71354374-71354424	H1-hESC	embryonic stem cell:	embryo
38	chr1:71513566-71513616	GM12891	blood:	n/a
39	chr1:71512973-71513023	ProgFib	skin:	n/a
40	chr1:71510804-71510854	HRCEpiC	kidney:	n/a
41	chr1:71513733-71513783	K562	blood:	n/a
42	chr1:71510804-71510854	HL-60	blood:	n/a
43	chr1:71513566-71513616	HepG2	liver:	n/a
44	chr1:71513494-71513544	ProgFib	skin:	n/a
45	chr1:71514431-71514481	K562	blood:	n/a
46	chr1:71354374-71354424	HRPEpiC	eye:	n/a
47	chr1:71513726-71513776	MCF-7	breast:	n/a
48	chr1:71513626-71513676	NHDF-neo	bronchial:	n/a
49	chr1:71510804-71510854	SK-N-MC	brain:	n/a
50	chr1:71512100-71512150	HPAEpiC	pulmonary alveolar:	n/a

(count:96 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:71312320..71315164-chr1:71322380..71324396,3	K562	blood:
2	chr1:71372779..71374433-chr1:71377421..71380381,2	K562	blood:
3	chr1:71340625..71342302-chr1:71347493..71349338,2	MCF-7	breast:
4	chr1:71427617..71429337-chr1:71437684..71440303,2	K562	blood:
5	chr1:71210586..71211482-chr1:71361701..71362695,3	MCF-7	breast:
6	chr1:71497365..71498885-chr1:71507254..71510170,2	K562	blood:
7	chr1:71398892..71400673-chr1:71400772..71403313,2	K562	blood:
8	chr1:71423003..71424991-chr1:71446277..71448535,2	K562	blood:
9	chr1:71128661..71130608-chr1:71489552..71491952,2	K562	blood:
10	chr1:70994251..70996830-chr1:71512472..71514167,2	MCF-7	breast:
11	chr1:71509104..71511027-chr1:71511341..71513340,2	MCF-7	breast:
12	chr1:71150765..71151639-chr1:71429287..71429792,2	MCF-7	breast:
13	chr1:71442791..71448002-chr1:71448870..71452211,5	K562	blood:
14	chr1:71499849..71501736-chr1:71503385..71504973,2	K562	blood:
15	chr1:71357369..71360235-chr1:71360695..71362626,2	K562	blood:
16	chr1:71323872..71326494-chr1:71327391..71329274,2	K562	blood:
17	chr1:71510894..71514340-chr1:71523075..71528309,6	K562	blood:
18	chr1:71357369..71360235-chr1:71360695..71362626,2	K562	blood:
19	chr1:71493019..71494900-chr1:71500523..71502505,2	K562	blood:
20	chr1:71484257..71486555-chr1:71489083..71490597,2	MCF-7	breast:
21	chr1:71323872..71326494-chr1:71327391..71329274,2	K562	blood:
22	chr1:71378991..71380997-chr1:71383679..71385899,2	K562	blood:
23	chr1:71442791..71448002-chr1:71448870..71452211,5	K562	blood:
24	chr1:71496393..71498256-chr1:71498283..71500475,2	K562	blood:
25	chr1:71340555..71343191-chr1:71344242..71347755,3	MCF-7	breast:
26	chr1:71347287..71350966-chr1:71352408..71354626,3	K562	blood:
27	chr1:71350292..71353402-chr1:71355074..71357779,3	MCF-7	breast:
28	chr1:71273558..71276293-chr1:71278434..71280516,2	K562	blood:
29	chr1:71473756..71476164-chr1:71480981..71482752,2	K562	blood:
30	chr1:71113661..71115986-chr1:71510232..71513062,3	K562	blood:
31	chr1:71326560..71329237-chr1:71329964..71332164,2	K562	blood:
32	chr1:71499543..71503702-chr1:71511179..71513554,5	K562	blood:
33	chr1:71287392..71290336-chr1:71291277..71292974,2	K562	blood:
34	chr1:71371588..71372088-chr13:111314049..111314743,2	Hela-S3	cervix:
35	chr1:71032636..71034814-chr1:71507461..71509971,2	K562	blood:
36	chr1:71427617..71429337-chr1:71437684..71440303,2	K562	blood:
37	chr1:71484257..71486555-chr1:71489083..71490597,2	MCF-7	breast:
38	chr1:71475910..71477737-chr1:71480653..71482581,2	MCF-7	breast:
39	chr1:71475910..71477737-chr1:71480653..71482581,2	MCF-7	breast:
40	chr1:71002710..71005624-chr1:71510534..71512998,2	K562	blood:
41	chr1:71332208..71332839-chr1:71513027..71513694,2	MCF-7	breast:
42	chr1:71240165..71242218-chr1:71510173..71512188,2	K562	blood:
43	chr1:71374929..71377417-chr1:71518030..71520956,2	K562	blood:
44	chr1:71499849..71501736-chr1:71503385..71504973,2	K562	blood:
45	chr1:71373472..71375942-chr1:71510520..71512137,2	K562	blood:
46	chr1:71498308..71501736-chr1:71503473..71506751,3	K562	blood:
47	chr1:71347287..71350966-chr1:71352408..71354626,3	K562	blood:
48	chr1:71313216..71315164-chr1:71322380..71324396,2	K562	blood:
49	chr1:71361958..71362473-chr1:71515591..71516340,2	MCF-7	breast:
50	chr1:71467023..71468927-chr1:71512007..71514052,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTH-14	chr1:71461328-71461385	l_71_chr1:71319635-71475982_testes
2	lnc-ZRANB2-2	chr1:71472542-71473814	NONHSAT003875
3	lnc-CTH-14	chr1:71475926-71475982	l_71_chr1:71319635-71475982_testes
4	lnc-CTH-14	chr1:71500505-71500572	l_71_chr1:71319635-71475982_testes
5	lnc-PTGER3-5	chr1:71304595-71304798	expReg_chr1_9994_-
6	lnc-PTGER3-6	chr1:71303599-71303905	expReg_chr1_9991_-
7	lnc-CTH-14	chr1:71319636-71319684	l_71_chr1:71319635-71475982_testes
8	lnc-CTH-12	chr1:71430529-71431707	NONHSAT003873
9	lnc-CTH-2	chr1:71304646-71304747	XLOC_000247
10	lnc-CTH-4	chr1:71514538-71514671	ENSG00000235079.1
11	lnc-CTH-12	chr1:71426588-71426941	NONHSAT003873
12	lnc-CTH-14	chr1:71475401-71475924	l_71_chr1:71319635-71475982_testes
13	lnc-CTH-13	chr1:71489933-71490390	NONHSAT003876
14	lnc-CTH-14	chr1:71329935-71329975	l_71_chr1:71319635-71475982_testes
15	lnc-CTH-2	chr1:71304646-71304750	NONHSAT003869
16	lnc-CTH-13	chr1:71489270-71489329	NONHSAT003876
17	lnc-CTH-2	chr1:71303920-71304557	XLOC_000247
18	lnc-CTH-2	chr1:71304482-71304557	NONHSAT003869
19	lnc-CTH-2	chr1:71278981-71279634	NONHSAT003869
20	lnc-CTH-3	chr1:71416584-71417176	ENSG00000235782.1
21	lnc-CTH-3	chr1:71416418-71416476	ENSG00000235782.1
22	lnc-ZRANB2-3	chr1:71471537-71472185	ENSG00000269933.1
23	lnc-CTH-3	chr1:71413062-71413158	ENSG00000235782.1
24	lnc-PTGER3-4	chr1:71305532-71305946	expReg_chr1_9998_-

No data

Variant related genes	Relation type
ZRANB2-AS1	TF binding region
ENSG00000269933	TF binding region
PTGER3	TF binding region
ENSG00000235782	TF binding region
ZRANB2-AS1	CpG island
ENSG00000269933	CpG island
PTGER3	CpG island
ENSG00000235782	CpG island
ENSG00000050628	chromatin interactions
ENSG00000269933	chromatin interactions
ENSG00000132485	chromatin interactions
ENSG00000235782	chromatin interactions
ENSG00000116761	chromatin interactions
ENSG00000235079	chromatin interactions
ENSG00000229956	chromatin interactions
ENSG00000233020	chromatin interactions
SETD8	miRNA target sites

Extended variants
information (count: 7071 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:7071 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1327456	chr1:71274759-71274760	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555317496	chr1:71274880-71274881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575279242	chr1:71274894-71274895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs144445778	chr1:71274931-71274932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183462550	chr1:71274961-71274962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs147827406	chr1:71274969-71274970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs115230774	chr1:71274996-71274997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560157830	chr1:71275048-71275049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs371800271	chr1:71275049-71275050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs202218569	chr1:71275065-71275066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs573758784	chr1:71275079-71275080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs374718087	chr1:71275156-71275157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs2257772	chr1:71275174-71275175	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs563879119	chr1:71275189-71275190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs188722451	chr1:71275214-71275215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs181157756	chr1:71275261-71275262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs562459790	chr1:71275317-71275318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs531343887	chr1:71275358-71275359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs551606769	chr1:71275385-71275386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558232422	chr1:71275407-71275408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs565057519	chr1:71275445-71275446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs578186630	chr1:71275470-71275471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs527450046	chr1:71275542-71275543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs547262633	chr1:71275545-71275546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567149276	chr1:71275586-71275587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576501936	chr1:71275619-71275620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538862513	chr1:71275672-71275673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs114033728	chr1:71275681-71275682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs568870501	chr1:71275740-71275741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs5775031	chr1:71275817-71275818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537853125	chr1:71275844-71275845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs12073070	chr1:71275877-71275878	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs578198725	chr1:71275904-71275905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534542833	chr1:71276004-71276005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs373313324	chr1:71276009-71276010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs554403903	chr1:71276035-71276036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs207460188	chr1:71276119-71276120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs114315907	chr1:71276145-71276146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs116263215	chr1:71276169-71276170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs114318575	chr1:71276187-71276188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs576932456	chr1:71278211-71278212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543325307	chr1:71278235-71278236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs2257934	chr1:71278247-71278248	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs111683508	chr1:71278252-71278253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs10889891	chr1:71278253-71278254	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs572547575	chr1:71278281-71278282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541581966	chr1:71278324-71278325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs561260759	chr1:71278338-71278339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs563526865	chr1:71278342-71278343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs530128869	chr1:71278360-71278361	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
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
Melanoma	17363583	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
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	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
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Cancer	20164920	CNVD
Glioblastoma multiforme	21510904	CNVD
Acute myeloid leukemia	20962326	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:971 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:71274400-71275400	Enhancers	Fetal Brain Male	brain
2	chr1:71274800-71275600	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr1:71274800-71276200	Enhancers	Fetal Brain Female	brain
4	chr1:71278200-71278800	Enhancers	NHDF-Ad	bronchial
5	chr1:71278200-71279000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:71278800-71283600	Weak transcription	NHDF-Ad	bronchial
7	chr1:71279000-71283600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr1:71283400-71286200	Enhancers	Fetal Heart	heart
9	chr1:71283600-71284000	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr1:71283600-71284400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr1:71283600-71284600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr1:71283600-71285200	Enhancers	NHDF-Ad	bronchial
13	chr1:71283600-71286200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr1:71283800-71285000	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr1:71283800-71285200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr1:71283800-71285200	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr1:71284000-71284400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr1:71284400-71284600	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr1:71284600-71285600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr1:71285000-71286000	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr1:71285000-71286400	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr1:71285200-71285600	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr1:71285600-71286400	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr1:71286000-71286200	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr1:71286200-71286400	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr1:71304400-71304600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr1:71304800-71305000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr1:71304800-71305800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr1:71305800-71308400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr1:71305800-71309000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr1:71306200-71307200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr1:71306400-71308400	Enhancers	NHDF-Ad	bronchial
33	chr1:71306800-71307200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr1:71312600-71313000	Enhancers	H1 Cell Line	embryonic stem cell
35	chr1:71312600-71313000	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr1:71312600-71313000	Enhancers	Adipose Nuclei	Adipose
37	chr1:71312600-71313200	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr1:71312600-71313200	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr1:71312600-71313400	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr1:71312600-71313600	Enhancers	Fetal Heart	heart
41	chr1:71326800-71327000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr1:71327000-71328000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr1:71327200-71327400	Enhancers	Adipose Nuclei	Adipose
44	chr1:71327400-71328400	Weak transcription	Adipose Nuclei	Adipose
45	chr1:71327600-71328600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr1:71328000-71330800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr1:71328400-71330400	Enhancers	Adipose Nuclei	Adipose
48	chr1:71328400-71331000	Enhancers	NHDF-Ad	bronchial
49	chr1:71328600-71329000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr1:71329000-71329400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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