Variant report

Variant	nsv871313
Chromosome Location	chr1:71391646-71489438
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:490)
CpG islands
(count:122)
Chromatin interactive
region (count:27)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:71468699-71468724	K562	blood:	n/a	n/a
2	ARID3A	chr1:71472265-71472284	K562	blood:	n/a	n/a
3	ARID3A	chr1:71436198-71436440	K562	blood:	n/a	n/a
4	ARID3A	chr1:71460522-71460848	K562	blood:	n/a	n/a
5	ARID3A	chr1:71481128-71481217	K562	blood:	n/a	n/a
6	ATF1	chr1:71451500-71451902	K562	blood:	n/a	n/a
7	ATF1	chr1:71445230-71445327	K562	blood:	n/a	n/a
8	ATF1	chr1:71427045-71427515	K562	blood:	n/a	n/a
9	BACH1	chr1:71468156-71468161	K562	blood:	n/a	n/a
10	BHLHE40	chr1:71485053-71485253	K562	blood:	n/a	n/a
11	BHLHE40	chr1:71465554-71465707	K562	blood:	n/a	n/a
12	BHLHE40	chr1:71480894-71480941	K562	blood:	n/a	n/a
13	BHLHE40	chr1:71427278-71427427	K562	blood:	n/a	n/a
14	BHLHE40	chr1:71436134-71436325	K562	blood:	n/a	n/a
15	CCNT2	chr1:71474825-71475012	K562	blood:	n/a	n/a
16	CEBPB	chr1:71422052-71422132	K562	blood:	n/a	chr1:71422081-71422092
17	CEBPB	chr1:71483442-71483555	IMR90	lung:	n/a	n/a
18	CEBPB	chr1:71470760-71470839	HepG2	liver:	n/a	chr1:71470810-71470821
19	CEBPB	chr1:71485706-71485857	A549	lung:	n/a	chr1:71485756-71485767
20	CEBPB	chr1:71474287-71474494	K562	blood:	n/a	n/a
21	CEBPB	chr1:71413585-71413825	A549	lung:	n/a	chr1:71413682-71413693 chr1:71413711-71413724
22	CEBPB	chr1:71421987-71422201	HepG2	liver:	n/a	chr1:71422081-71422092
23	CEBPB	chr1:71467353-71467636	A549	lung:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
24	CEBPB	chr1:71485618-71485862	IMR90	lung:	n/a	chr1:71485756-71485767
25	CEBPB	chr1:71467360-71467695	K562	blood:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
26	CEBPB	chr1:71467330-71467690	HepG2	liver:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
27	CEBPB	chr1:71469996-71470196	K562	blood:	n/a	chr1:71470127-71470140 chr1:71470129-71470140
28	CEBPB	chr1:71458228-71458549	K562	blood:	n/a	chr1:71458394-71458405 chr1:71458394-71458407
29	CEBPB	chr1:71467358-71467677	IMR90	lung:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
30	CEBPB	chr1:71444470-71444536	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr1:71413576-71413806	HepG2	liver:	n/a	chr1:71413682-71413693 chr1:71413711-71413724
32	CEBPB	chr1:71477312-71477504	HepG2	liver:	n/a	chr1:71477360-71477371
33	CEBPB	chr1:71467389-71467679	H1-hESC	embryonic stem cell:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
34	CEBPB	chr1:71423305-71423526	K562	blood:	n/a	n/a
35	CEBPB	chr1:71423310-71423611	IMR90	lung:	n/a	n/a
36	CEBPB	chr1:71458240-71458524	HepG2	liver:	n/a	chr1:71458394-71458405 chr1:71458394-71458407
37	CEBPB	chr1:71410721-71410977	HepG2	liver:	n/a	chr1:71410833-71410844
38	CEBPB	chr1:71477204-71477504	K562	blood:	n/a	chr1:71477360-71477371
39	CEBPD	chr1:71438637-71439063	K562	blood:	n/a	n/a
40	CTCF	chr1:71431860-71431899	GM20000	blood:	n/a	n/a
41	CTCF	chr1:71429182-71429437	K562	blood:	n/a	n/a
42	CTCF	chr1:71398382-71398422	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr1:71429229-71429378	ProgFib	skin:	n/a	n/a
44	CTCF	chr1:71436260-71436410	BE2_C	brain:	n/a	n/a
45	CTCF	chr1:71431820-71431970	HMF	breast:	n/a	n/a
46	CTCF	chr1:71431840-71431990	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr1:71431734-71432074	IMR90	lung:	n/a	n/a
48	CTCF	chr1:71429219-71429343	GM12878	blood:	n/a	n/a
49	CTCF	chr1:71431820-71431970	K562	blood:	n/a	n/a
50	CTCF	chr1:71429160-71429310	AG09309	skin:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:71418388-71418438	GM12892	blood:	n/a
2	chr1:71418388-71418438	HRPEpiC	eye:	n/a
3	chr1:71418388-71418438	HCPEpiC	choroid plexus:	n/a
4	chr1:71418388-71418438	GM06990	blood:	n/a
5	chr1:71472738-71472788	HCF	heart:	n/a
6	chr1:71418388-71418438	MCF-7	breast:	n/a
7	chr1:71418388-71418438	HCF	heart:	n/a
8	chr1:71472738-71472788	HUVEC	blood vessel:	n/a
9	chr1:71472738-71472788	SAEC	small airway:	n/a
10	chr1:71472738-71472788	MCF10A-Er-Src	breast:	n/a
11	chr1:71418388-71418438	GM12878	blood:	n/a
12	chr1:71472738-71472788	HRPEpiC	eye:	n/a
13	chr1:71418388-71418438	AG04450	lung:	fetal
14	chr1:71472738-71472788	LNCaP	prostate:	n/a
15	chr1:71472738-71472788	NHBE	bronchial:	n/a
16	chr1:71418388-71418438	GM19239	blood:	n/a
17	chr1:71472738-71472788	ECC-1	luminal epithelium:	n/a
18	chr1:71472738-71472788	SK-N-SH	brain:	n/a
19	chr1:71418388-71418438	HCM	heart:	n/a
20	chr1:71418388-71418438	NHBE	bronchial:	n/a
21	chr1:71472738-71472788	U87	brain:	n/a
22	chr1:71418388-71418438	SK-N-SH_RA	brain:	n/a
23	chr1:71472738-71472788	SKMC	muscle:	n/a
24	chr1:71418388-71418438	NH-A	brain:	n/a
25	chr1:71472738-71472788	SK-N-SH_RA	brain:	n/a
26	chr1:71418388-71418438	Hela-S3	cervix:	n/a
27	chr1:71472738-71472788	HepG2	liver:	n/a
28	chr1:71472738-71472788	HRCEpiC	kidney:	n/a
29	chr1:71472738-71472788	ovcar-3	ovarian:	n/a
30	chr1:71418388-71418438	HPAEpiC	pulmonary alveolar:	n/a
31	chr1:71472738-71472788	PrEC	prostate:	n/a
32	chr1:71418388-71418438	HMEC	breast:	n/a
33	chr1:71472738-71472788	GM12892	blood:	n/a
34	chr1:71418388-71418438	HRE	kidney:	n/a
35	chr1:71472738-71472788	CMK	blood:	n/a
36	chr1:71418388-71418438	CMK	blood:	n/a
37	chr1:71472738-71472788	GM06990	blood:	n/a
38	chr1:71472738-71472788	HNPCEpiC	eye:	n/a
39	chr1:71418388-71418438	A549	lung:	n/a
40	chr1:71472738-71472788	A549	lung:	n/a
41	chr1:71472738-71472788	BE2_C	brain:	n/a
42	chr1:71472738-71472788	Caco-2	colon:	n/a
43	chr1:71418388-71418438	AoSMC	blood vessel:	n/a
44	chr1:71418388-71418438	HEK293	kidney:	embryo
45	chr1:71418388-71418438	ovcar-3	ovarian:	n/a
46	chr1:71418388-71418438	HL-60	blood:	n/a
47	chr1:71418388-71418438	Jurkat	blood:	n/a
48	chr1:71418388-71418438	H1-hESC	embryonic stem cell:	embryo
49	chr1:71418388-71418438	HEEpiC	esophagus:	n/a
50	chr1:71472738-71472788	HL-60	blood:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:71443738..71447073-chr1:71448870..71451609,5	K562	blood:
2	chr1:71423003..71424991-chr1:71446277..71448535,2	K562	blood:
3	chr1:71402954..71404643-chr1:71411844..71413632,2	K562	blood:
4	chr1:71398892..71400673-chr1:71400772..71403313,2	K562	blood:
5	chr1:71486485..71490048-chr1:71491402..71493576,3	K562	blood:
6	chr1:71443738..71447073-chr1:71448870..71451609,5	K562	blood:
7	chr1:71484257..71486555-chr1:71489083..71490597,2	MCF-7	breast:
8	chr1:71440403..71443013-chr1:71443324..71446288,2	K562	blood:
9	chr1:71423003..71424991-chr1:71446277..71448535,2	K562	blood:
10	chr1:71381219..71383532-chr1:71401301..71402871,2	K562	blood:
11	chr1:71427617..71429337-chr1:71437684..71440303,2	K562	blood:
12	chr1:71440403..71443013-chr1:71443324..71446288,2	K562	blood:
13	chr1:71475910..71477737-chr1:71480653..71482581,2	MCF-7	breast:
14	chr1:71484257..71486555-chr1:71489083..71490597,2	MCF-7	breast:
15	chr1:71467023..71468927-chr1:71512007..71514052,2	K562	blood:
16	chr1:70975940..70976451-chr1:71428828..71429462,2	MCF-7	breast:
17	chr1:71150765..71151639-chr1:71429287..71429792,2	MCF-7	breast:
18	chr1:71488156..71490050-chr1:71494544..71497230,2	K562	blood:
19	chr1:71475910..71477737-chr1:71480653..71482581,2	MCF-7	breast:
20	chr1:71488605..71491550-chr1:71545533..71547496,2	K562	blood:
21	chr1:71427617..71429337-chr1:71437684..71440303,2	K562	blood:
22	chr1:71398892..71400673-chr1:71400772..71403313,2	K562	blood:
23	chr1:71442791..71448002-chr1:71448870..71452211,5	K562	blood:
24	chr1:71473756..71476164-chr1:71480981..71482752,2	K562	blood:
25	chr1:71411854..71414751-chr1:71416719..71419463,2	K562	blood:
26	chr1:71442791..71448002-chr1:71448870..71452211,5	K562	blood:
27	chr1:71473756..71476164-chr1:71480981..71482752,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTH-3	chr1:71416418-71416476	ENSG00000235782.1
2	lnc-CTH-3	chr1:71413062-71413158	ENSG00000235782.1
3	lnc-CTH-14	chr1:71461328-71461385	l_71_chr1:71319635-71475982_testes
4	lnc-ZRANB2-3	chr1:71471537-71472185	ENSG00000269933.1
5	lnc-CTH-14	chr1:71475401-71475924	l_71_chr1:71319635-71475982_testes
6	lnc-CTH-14	chr1:71475926-71475982	l_71_chr1:71319635-71475982_testes
7	lnc-CTH-12	chr1:71426588-71426941	NONHSAT003873
8	lnc-CTH-12	chr1:71430529-71431707	NONHSAT003873
9	lnc-CTH-3	chr1:71416584-71417176	ENSG00000235782.1
10	lnc-ZRANB2-2	chr1:71472542-71473814	NONHSAT003875
11	lnc-CTH-13	chr1:71489270-71489329	NONHSAT003876

No data

Variant related genes	Relation type
ENSG00000269933	TF binding region
ENSG00000235782	TF binding region
ENSG00000269933	CpG island
ENSG00000235782	CpG island
ENSG00000050628	chromatin interactions
ENSG00000229956	chromatin interactions
ENSG00000132485	chromatin interactions
ENSG00000235782	chromatin interactions

Extended variants
information (count: 3555 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:3555 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368015517	chr1:71394217-71394218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs573782869	chr1:71394274-71394275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs542830238	chr1:71394298-71394299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs199531935	chr1:71394330-71394331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189214429	chr1:71394331-71394332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs139010361	chr1:71394337-71394338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs143113425	chr1:71394348-71394349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs79406116	chr1:71394349-71394350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182958794	chr1:71394357-71394358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567174123	chr1:71394367-71394368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs535261399	chr1:71394380-71394381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535637039	chr1:71394381-71394382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs72669163	chr1:71394388-71394389	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs187668637	chr1:71394395-71394396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565367888	chr1:71394432-71394433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191125507	chr1:71394446-71394447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs645618	chr1:71394458-71394459	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs577748039	chr1:71394459-71394460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534059166	chr1:71394463-71394464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs11576593	chr1:71394480-71394481	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs557205567	chr1:71394502-71394503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575265127	chr1:71394512-71394513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs75551853	chr1:71394539-71394540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs375891821	chr1:71394551-71394552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201292072	chr1:71394552-71394553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs149343501	chr1:71394569-71394570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568041983	chr1:71394571-71394572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs34765576	chr1:71394579-71394580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113239977	chr1:71394581-71394582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77739902	chr1:71394599-71394600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs562747645	chr1:71394677-71394678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544711083	chr1:71394682-71394683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs578096	chr1:71394683-71394684	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs147472891	chr1:71394687-71394688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs533125677	chr1:71394766-71394767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546602949	chr1:71394775-71394776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs138506184	chr1:71394827-71394828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs141944154	chr1:71394855-71394856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549310811	chr1:71394865-71394866	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs6670616	chr1:71394883-71394884	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs183997151	chr1:71394891-71394892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs376060542	chr1:71394948-71394949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571389184	chr1:71394984-71394985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573256151	chr1:71394991-71394992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs17090681	chr1:71395022-71395023	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs561740131	chr1:71395036-71395037	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567444071	chr1:71395103-71395104	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536590080	chr1:71395114-71395115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs493489	chr1:71395182-71395183	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs17090682	chr1:71395231-71395232	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:104)

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
Schizophrenia	23813976	CNVD

Chromatin state (count:212 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:71394200-71394400	Enhancers	Pancreas	Pancrea
2	chr1:71394400-71397200	Weak transcription	Pancreas	Pancrea
3	chr1:71394600-71395200	Enhancers	Dnd41	blood
4	chr1:71394800-71396000	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr1:71394800-71396000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr1:71394800-71396000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr1:71395200-71395400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr1:71395200-71395600	Weak transcription	Dnd41	blood
9	chr1:71395600-71396200	Enhancers	Adipose Nuclei	Adipose
10	chr1:71395600-71396200	Enhancers	Dnd41	blood
11	chr1:71395800-71396000	Enhancers	Fetal Kidney	kidney
12	chr1:71395800-71396200	Enhancers	Primary T cells from cord blood	blood
13	chr1:71396000-71399000	Weak transcription	Fetal Kidney	kidney
14	chr1:71397000-71397400	Active TSS	Spleen	Spleen
15	chr1:71397200-71397400	Enhancers	Pancreas	Pancrea
16	chr1:71399000-71400200	Enhancers	Fetal Kidney	kidney
17	chr1:71399200-71400800	Enhancers	Rectal Smooth Muscle	rectum
18	chr1:71399600-71401000	Enhancers	Colon Smooth Muscle	Colon
19	chr1:71399800-71400800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr1:71399800-71401000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr1:71400000-71400800	Enhancers	Fetal Heart	heart
22	chr1:71400400-71400600	Enhancers	Aorta	Aorta
23	chr1:71400600-71404800	Weak transcription	Aorta	Aorta
24	chr1:71400800-71412400	Weak transcription	Rectal Smooth Muscle	rectum
25	chr1:71401000-71406400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr1:71401600-71401800	Active TSS	Sigmoid Colon	Sigmoid Colon
27	chr1:71401800-71402200	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr1:71404800-71405600	Strong transcription	Aorta	Aorta
29	chr1:71405600-71407600	Weak transcription	Aorta	Aorta
30	chr1:71406400-71408000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr1:71406400-71408200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr1:71407000-71407800	Active TSS	HSMMtube	muscle
33	chr1:71407000-71408000	Enhancers	NHDF-Ad	bronchial
34	chr1:71407600-71408000	Enhancers	Adipose Nuclei	Adipose
35	chr1:71407800-71408000	Enhancers	HSMMtube	muscle
36	chr1:71408000-71413800	Weak transcription	Adipose Nuclei	Adipose
37	chr1:71408200-71412400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr1:71410800-71412600	Enhancers	Colon Smooth Muscle	Colon
39	chr1:71411800-71412800	Enhancers	Fetal Heart	heart
40	chr1:71412400-71412800	Enhancers	Rectal Smooth Muscle	rectum
41	chr1:71412400-71413800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr1:71413000-71413600	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr1:71413000-71413800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr1:71413200-71415200	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr1:71413600-71415000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
46	chr1:71413800-71414400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr1:71413800-71414400	Enhancers	Adipose Nuclei	Adipose
48	chr1:71413800-71415600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr1:71414200-71415000	Active TSS	NHDF-Ad	bronchial
50	chr1:71414400-71414600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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