Variant report

Variant	nsv830148
Chromosome Location	chr1:71310366-71483932
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:918)
CpG islands
(count:184)
Chromatin interactive
region (count:54)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:71481128-71481217	K562	blood:	n/a	n/a
2	ARID3A	chr1:71343106-71343389	K562	blood:	n/a	n/a
3	ARID3A	chr1:71436198-71436440	K562	blood:	n/a	n/a
4	ARID3A	chr1:71356154-71356634	K562	blood:	n/a	n/a
5	ARID3A	chr1:71472265-71472284	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	chr1:71460522-71460848	K562	blood:	n/a	n/a
9	ARID3A	chr1:71340527-71340612	K562	blood:	n/a	n/a
10	ATF1	chr1:71343077-71343340	K562	blood:	n/a	n/a
11	ATF1	chr1:71375175-71375423	K562	blood:	n/a	n/a
12	ATF1	chr1:71356152-71356426	K562	blood:	n/a	n/a
13	ATF1	chr1:71427045-71427515	K562	blood:	n/a	n/a
14	ATF1	chr1:71451500-71451902	K562	blood:	n/a	n/a
15	ATF1	chr1:71445230-71445327	K562	blood:	n/a	n/a
16	BACH1	chr1:71377587-71377854	K562	blood:	n/a	n/a
17	BACH1	chr1:71468156-71468161	K562	blood:	n/a	n/a
18	BHLHE40	chr1:71480894-71480941	K562	blood:	n/a	n/a
19	BHLHE40	chr1:71362058-71362252	K562	blood:	n/a	n/a
20	BHLHE40	chr1:71427278-71427427	K562	blood:	n/a	n/a
21	BHLHE40	chr1:71465554-71465707	K562	blood:	n/a	n/a
22	BHLHE40	chr1:71436134-71436325	K562	blood:	n/a	n/a
23	BRCA1	chr1:71361486-71361517	GM12878	blood:	n/a	n/a
24	CBX3	chr1:71347391-71347736	K562	blood:	n/a	n/a
25	CBX3	chr1:71317529-71317793	K562	blood:	n/a	n/a
26	CCNT2	chr1:71474825-71475012	K562	blood:	n/a	n/a
27	CCNT2	chr1:71356056-71356365	K562	blood:	n/a	n/a
28	CCNT2	chr1:71375173-71375436	K562	blood:	n/a	n/a
29	CEBPB	chr1:71423305-71423526	K562	blood:	n/a	n/a
30	CEBPB	chr1:71467358-71467677	IMR90	lung:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
31	CEBPB	chr1:71320980-71321196	H1-hESC	embryonic stem cell:	n/a	chr1:71321073-71321084
32	CEBPB	chr1:71320905-71321259	K562	blood:	n/a	chr1:71321073-71321084
33	CEBPB	chr1:71467330-71467690	HepG2	liver:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
34	CEBPB	chr1:71374950-71375457	K562	blood:	n/a	chr1:71375115-71375126 chr1:71375116-71375125 chr1:71375114-71375125
35	CEBPB	chr1:71314640-71314816	HepG2	liver:	n/a	n/a
36	CEBPB	chr1:71375018-71375229	A549	lung:	n/a	chr1:71375115-71375126 chr1:71375116-71375125 chr1:71375114-71375125
37	CEBPB	chr1:71483442-71483555	IMR90	lung:	n/a	n/a
38	CEBPB	chr1:71366879-71367147	HepG2	liver:	n/a	chr1:71367020-71367031 chr1:71367021-71367032 chr1:71367020-71367033
39	CEBPB	chr1:71423310-71423611	IMR90	lung:	n/a	n/a
40	CEBPB	chr1:71353601-71353934	K562	blood:	n/a	chr1:71353861-71353872
41	CEBPB	chr1:71340570-71340885	MCF-7	breast:	n/a	n/a
42	CEBPB	chr1:71329111-71329418	HepG2	liver:	n/a	n/a
43	CEBPB	chr1:71467389-71467679	H1-hESC	embryonic stem cell:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
44	CEBPB	chr1:71375115-71375469	K562	blood:	n/a	chr1:71375115-71375126 chr1:71375116-71375125
45	CEBPB	chr1:71477312-71477504	HepG2	liver:	n/a	chr1:71477360-71477371
46	CEBPB	chr1:71470760-71470839	HepG2	liver:	n/a	chr1:71470810-71470821
47	CEBPB	chr1:71458240-71458524	HepG2	liver:	n/a	chr1:71458394-71458405 chr1:71458394-71458407
48	CEBPB	chr1:71353618-71354024	H1-hESC	embryonic stem cell:	n/a	chr1:71353861-71353872
49	CEBPB	chr1:71467353-71467636	A549	lung:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
50	CEBPB	chr1:71329098-71329416	A549	lung:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:71354374-71354424	AG09309	skin:	n/a
2	chr1:71354374-71354424	AG09309	skin:	n/a
3	chr1:71418388-71418438	ECC-1	luminal epithelium:	n/a
4	chr1:71472738-71472788	AoSMC	blood vessel:	n/a
5	chr1:71418388-71418438	Caco-2	colon:	n/a
6	chr1:71354374-71354424	ECC-1	luminal epithelium:	n/a
7	chr1:71418388-71418438	U87	brain:	n/a
8	chr1:71418388-71418438	AG04450	lung:	fetal
9	chr1:71354374-71354424	HCPEpiC	choroid plexus:	n/a
10	chr1:71472738-71472788	HRE	kidney:	n/a
11	chr1:71354374-71354424	BJ	skin:	n/a
12	chr1:71418388-71418438	GM12891	blood:	n/a
13	chr1:71472738-71472788	HRCEpiC	kidney:	n/a
14	chr1:71354374-71354424	HRCEpiC	kidney:	n/a
15	chr1:71472738-71472788	IMR90	lung:	fetal
16	chr1:71354374-71354424	HMEC	breast:	n/a
17	chr1:71354374-71354424	PANC-1	pancreas:	n/a
18	chr1:71472738-71472788	GM19239	blood:	n/a
19	chr1:71472738-71472788	AG10803	skin:	n/a
20	chr1:71354374-71354424	HUVEC	blood vessel:	n/a
21	chr1:71354374-71354424	SKMC	muscle:	n/a
22	chr1:71472738-71472788	A549	lung:	n/a
23	chr1:71472738-71472788	SK-N-MC	brain:	n/a
24	chr1:71472738-71472788	T-47D	breast:	n/a
25	chr1:71354374-71354424	HPAEpiC	pulmonary alveolar:	n/a
26	chr1:71472738-71472788	HEK293	kidney:	embryo
27	chr1:71472738-71472788	BE2_C	brain:	n/a
28	chr1:71354374-71354424	SAEC	small airway:	n/a
29	chr1:71418388-71418438	MCF10A-Er-Src	breast:	n/a
30	chr1:71472738-71472788	HUVEC	blood vessel:	n/a
31	chr1:71418388-71418438	AG09309	skin:	n/a
32	chr1:71418388-71418438	NHDF-neo	bronchial:	n/a
33	chr1:71472738-71472788	NHBE	bronchial:	n/a
34	chr1:71354374-71354424	T-47D	breast:	n/a
35	chr1:71472738-71472788	SK-N-SH_RA	brain:	n/a
36	chr1:71418388-71418438	A549	lung:	n/a
37	chr1:71418388-71418438	HAEpiC	amniotic membrane:	n/a
38	chr1:71418388-71418438	SKMC	muscle:	n/a
39	chr1:71354374-71354424	NH-A	brain:	n/a
40	chr1:71354374-71354424	SK-N-SH_RA	brain:	n/a
41	chr1:71418388-71418438	AG09319	gingival:	n/a
42	chr1:71354374-71354424	ovcar-3	ovarian:	n/a
43	chr1:71472738-71472788	GM12878	blood:	n/a
44	chr1:71472738-71472788	BJ	skin:	n/a
45	chr1:71418388-71418438	HNPCEpiC	eye:	n/a
46	chr1:71472738-71472788	HCF	heart:	n/a
47	chr1:71354374-71354424	HEK293	kidney:	embryo
48	chr1:71418388-71418438	SK-N-SH_RA	brain:	n/a
49	chr1:71472738-71472788	AG09319	gingival:	n/a
50	chr1:71354374-71354424	U87	brain:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:71372779..71374433-chr1:71377421..71380381,2	K562	blood:
2	chr1:71389776..71391612-chr1:71519550..71521085,2	K562	blood:
3	chr1:71348952..71350575-chr1:71372335..71374257,2	K562	blood:
4	chr1:71312320..71315164-chr1:71322380..71324396,3	K562	blood:
5	chr1:71475910..71477737-chr1:71480653..71482581,2	MCF-7	breast:
6	chr1:71440403..71443013-chr1:71443324..71446288,2	K562	blood:
7	chr1:71374929..71377417-chr1:71518030..71520956,2	K562	blood:
8	chr1:71361958..71362473-chr1:71515591..71516340,2	MCF-7	breast:
9	chr1:71378991..71380997-chr1:71383679..71385899,2	K562	blood:
10	chr1:71381219..71383532-chr1:71401301..71402871,2	K562	blood:
11	chr1:71372779..71374433-chr1:71377421..71380381,2	K562	blood:
12	chr1:71340555..71343191-chr1:71344242..71347755,3	MCF-7	breast:
13	chr1:71427617..71429337-chr1:71437684..71440303,2	K562	blood:
14	chr1:71443738..71447073-chr1:71448870..71451609,5	K562	blood:
15	chr1:71357369..71360235-chr1:71360695..71362626,2	K562	blood:
16	chr1:71210586..71211482-chr1:71361701..71362695,3	MCF-7	breast:
17	chr1:71442791..71448002-chr1:71448870..71452211,5	K562	blood:
18	chr1:71378991..71380997-chr1:71383679..71385899,2	K562	blood:
19	chr1:71326560..71329237-chr1:71329964..71332164,2	K562	blood:
20	chr1:71402954..71404643-chr1:71411844..71413632,2	K562	blood:
21	chr1:71475910..71477737-chr1:71480653..71482581,2	MCF-7	breast:
22	chr1:71427617..71429337-chr1:71437684..71440303,2	K562	blood:
23	chr1:71381219..71383532-chr1:71401301..71402871,2	K562	blood:
24	chr1:71150765..71151639-chr1:71429287..71429792,2	MCF-7	breast:
25	chr1:71340555..71343191-chr1:71344242..71347755,3	MCF-7	breast:
26	chr1:71313216..71315164-chr1:71322380..71324396,2	K562	blood:
27	chr1:71323872..71326494-chr1:71327391..71329274,2	K562	blood:
28	chr1:71332208..71332839-chr1:71513027..71513694,2	MCF-7	breast:
29	chr1:71442791..71448002-chr1:71448870..71452211,5	K562	blood:
30	chr1:71443738..71447073-chr1:71448870..71451609,5	K562	blood:
31	chr1:71347287..71350966-chr1:71352408..71354626,3	K562	blood:
32	chr1:71473756..71476164-chr1:71480981..71482752,2	K562	blood:
33	chr1:71323872..71326494-chr1:71327391..71329274,2	K562	blood:
34	chr1:71467023..71468927-chr1:71512007..71514052,2	K562	blood:
35	chr1:71350292..71353402-chr1:71355074..71357779,3	MCF-7	breast:
36	chr1:71340625..71342302-chr1:71347493..71349338,2	MCF-7	breast:
37	chr1:71347287..71350966-chr1:71352408..71354626,3	K562	blood:
38	chr1:71348952..71350575-chr1:71372335..71374257,2	K562	blood:
39	chr1:71326560..71329237-chr1:71329964..71332164,2	K562	blood:
40	chr1:71357369..71360235-chr1:71360695..71362626,2	K562	blood:
41	chr1:71423003..71424991-chr1:71446277..71448535,2	K562	blood:
42	chr1:71313216..71315164-chr1:71322380..71324396,2	K562	blood:
43	chr1:71473756..71476164-chr1:71480981..71482752,2	K562	blood:
44	chr1:71398892..71400673-chr1:71400772..71403313,2	K562	blood:
45	chr1:71340625..71342302-chr1:71347493..71349338,2	MCF-7	breast:
46	chr1:71373472..71375942-chr1:71510520..71512137,2	K562	blood:
47	chr1:71411854..71414751-chr1:71416719..71419463,2	K562	blood:
48	chr1:71350292..71353402-chr1:71355074..71357779,3	MCF-7	breast:
49	chr1:71398892..71400673-chr1:71400772..71403313,2	K562	blood:
50	chr1:71371588..71372088-chr13:111314049..111314743,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTH-14	chr1:71319636-71319684	l_71_chr1:71319635-71475982_testes
2	lnc-ZRANB2-2	chr1:71472542-71473814	NONHSAT003875
3	lnc-ZRANB2-3	chr1:71471537-71472185	ENSG00000269933.1
4	lnc-CTH-3	chr1:71416584-71417176	ENSG00000235782.1
5	lnc-CTH-14	chr1:71461328-71461385	l_71_chr1:71319635-71475982_testes
6	lnc-CTH-14	chr1:71475401-71475924	l_71_chr1:71319635-71475982_testes
7	lnc-CTH-14	chr1:71329935-71329975	l_71_chr1:71319635-71475982_testes
8	lnc-CTH-12	chr1:71430529-71431707	NONHSAT003873
9	lnc-CTH-3	chr1:71416418-71416476	ENSG00000235782.1
10	lnc-CTH-3	chr1:71413062-71413158	ENSG00000235782.1
11	lnc-CTH-12	chr1:71426588-71426941	NONHSAT003873
12	lnc-CTH-14	chr1:71475926-71475982	l_71_chr1:71319635-71475982_testes

No data

Variant related genes	Relation type
ENSG00000269933	TF binding region
ENSG00000235782	TF binding region
ENSG00000269933	CpG island
ENSG00000235782	CpG island
ENSG00000050628	chromatin interactions
ENSG00000235782	chromatin interactions

Extended variants
information (count: 5371 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:5371 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143136827	chr1:71312645-71312646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs572327674	chr1:71312659-71312660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534916525	chr1:71312673-71312674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554634323	chr1:71312732-71312733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574487990	chr1:71312787-71312788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570562051	chr1:71312855-71312856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs144709186	chr1:71312862-71312863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs192720376	chr1:71312871-71312872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373058430	chr1:71312879-71312880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs114247431	chr1:71312918-71312919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs528153380	chr1:71312946-71312947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs559558197	chr1:71312999-71313000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs118103129	chr1:71313004-71313005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148141850	chr1:71313046-71313047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs141939456	chr1:71313051-71313052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs150704365	chr1:71313090-71313091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs566133510	chr1:71313096-71313097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550111318	chr1:71313135-71313136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs569732403	chr1:71313170-71313171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs536803141	chr1:71313201-71313202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538918955	chr1:71313202-71313203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs183614426	chr1:71313232-71313233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs145284543	chr1:71313243-71313244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs369086627	chr1:71313253-71313254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140169672	chr1:71313256-71313257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs148249425	chr1:71313304-71313305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs55958766	chr1:71313321-71313322	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs554910690	chr1:71313344-71313345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs574425866	chr1:71313364-71313365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs374002527	chr1:71313419-71313420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs556881178	chr1:71313432-71313433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566246601	chr1:71313591-71313592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191164708	chr1:71319661-71319662	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs549144840	chr1:71319674-71319675	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs78785290	chr1:71319679-71319680	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs6424406	chr1:71326810-71326811	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs189294748	chr1:71326833-71326834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs551337060	chr1:71326834-71326835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs35162116	chr1:71326845-71326846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs199876847	chr1:71326897-71326898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs75719142	chr1:71326910-71326911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs140678681	chr1:71326932-71326933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs79943212	chr1:71327034-71327035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529908315	chr1:71327085-71327086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114678445	chr1:71327088-71327089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7530345	chr1:71327092-71327093	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs531854061	chr1:71327183-71327184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144762006	chr1:71327303-71327304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs181065581	chr1:71327339-71327340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs7540868	chr1:71327362-71327363	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:106)

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
Cancer	20164920	CNVD
Glioblastoma multiforme	21510904	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:436 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:71312600-71313000	Enhancers	H1 Cell Line	embryonic stem cell
2	chr1:71312600-71313000	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr1:71312600-71313000	Enhancers	Adipose Nuclei	Adipose
4	chr1:71312600-71313200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr1:71312600-71313200	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr1:71312600-71313400	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr1:71312600-71313600	Enhancers	Fetal Heart	heart
8	chr1:71326800-71327000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr1:71327000-71328000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:71327200-71327400	Enhancers	Adipose Nuclei	Adipose
11	chr1:71327400-71328400	Weak transcription	Adipose Nuclei	Adipose
12	chr1:71327600-71328600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:71328000-71330800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr1:71328400-71330400	Enhancers	Adipose Nuclei	Adipose
15	chr1:71328400-71331000	Enhancers	NHDF-Ad	bronchial
16	chr1:71328600-71329000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr1:71329000-71329400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr1:71329400-71329800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr1:71329800-71332800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr1:71330000-71330800	Enhancers	K562	blood
21	chr1:71330200-71331200	Enhancers	A549	lung
22	chr1:71330400-71331000	Enhancers	Primary T cells from cord blood	blood
23	chr1:71330400-71331200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr1:71330800-71331600	Enhancers	Fetal Heart	heart
25	chr1:71330800-71343200	Weak transcription	K562	blood
26	chr1:71331000-71331600	Flanking Active TSS	Primary T cells from cord blood	blood
27	chr1:71331000-71332400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr1:71331400-71331600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr1:71331400-71332800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr1:71331400-71334800	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr1:71331600-71332000	Enhancers	Primary T cells from cord blood	blood
32	chr1:71331600-71332000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr1:71331600-71333200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr1:71331600-71333200	Enhancers	Dnd41	blood
35	chr1:71331600-71333600	Enhancers	Primary hematopoietic stem cells	blood
36	chr1:71331600-71337200	Weak transcription	Fetal Heart	heart
37	chr1:71331800-71333200	Enhancers	Fetal Thymus	thymus
38	chr1:71332000-71333000	Flanking Active TSS	Primary T cells from cord blood	blood
39	chr1:71332000-71333400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr1:71332200-71332800	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr1:71332400-71332800	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr1:71332800-71336600	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr1:71332800-71337000	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr1:71332800-71338800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr1:71333000-71334400	Enhancers	Primary T cells from cord blood	blood
46	chr1:71335800-71336200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr1:71336600-71337000	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr1:71337000-71337400	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr1:71337000-71339600	Weak transcription	Monocytes-CD14+_RO01746	blood
50	chr1:71337200-71338800	Enhancers	Fetal Heart	heart

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