Variant report

Variant	nsv830093
Chromosome Location	chr1:67173594-67348264
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1421)
CpG islands
(count:1467)
Chromatin interactive
region (count:38)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1421 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:67223627-67224294	K562	blood:	n/a	n/a
2	ARID3A	chr1:67230720-67231090	K562	blood:	n/a	n/a
3	ARID3A	chr1:67215591-67215797	K562	blood:	n/a	n/a
4	ARID3A	chr1:67297766-67297945	K562	blood:	n/a	n/a
5	ARID3A	chr1:67243630-67243644	K562	blood:	n/a	n/a
6	ATF1	chr1:67230379-67230445	K562	blood:	n/a	n/a
7	ATF1	chr1:67223801-67224364	K562	blood:	n/a	n/a
8	ATF2	chr1:67223717-67224224	GM12878	blood:	n/a	n/a
9	ATF2	chr1:67223708-67224310	GM12878	blood:	n/a	n/a
10	ATF3	chr1:67223808-67224357	K562	blood:	n/a	chr1:67224063-67224072
11	BATF	chr1:67254300-67254480	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:67230554-67230787	K562	blood:	n/a	n/a
13	BHLHE40	chr1:67223909-67224191	GM12878	blood:	n/a	n/a
14	BHLHE40	chr1:67223871-67224578	K562	blood:	n/a	n/a
15	BHLHE40	chr1:67191673-67192051	K562	blood:	n/a	n/a
16	CBX3	chr1:67223830-67224417	K562	blood:	n/a	n/a
17	CBX3	chr1:67191642-67192106	HCT-116	colon:	n/a	n/a
18	CCNT2	chr1:67233388-67233588	K562	blood:	n/a	chr1:67233422-67233442
19	CCNT2	chr1:67225410-67225646	K562	blood:	n/a	n/a
20	CCNT2	chr1:67223864-67224289	K562	blood:	n/a	n/a
21	CCNT2	chr1:67230587-67230898	K562	blood:	n/a	n/a
22	CEBPB	chr1:67298863-67299164	HepG2	liver:	n/a	chr1:67298988-67298999
23	CEBPB	chr1:67257043-67257273	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr1:67297667-67297728	K562	blood:	n/a	n/a
25	CEBPB	chr1:67298846-67299169	K562	blood:	n/a	chr1:67298988-67298999
26	CEBPB	chr1:67333258-67333506	HepG2	liver:	n/a	chr1:67333356-67333367
27	CEBPB	chr1:67321438-67321705	IMR90	lung:	n/a	chr1:67321573-67321584
28	CEBPB	chr1:67321486-67321698	A549	lung:	n/a	chr1:67321573-67321584
29	CEBPB	chr1:67226762-67227204	A549	lung:	n/a	n/a
30	CEBPB	chr1:67302852-67303045	K562	blood:	n/a	n/a
31	CEBPB	chr1:67280053-67280114	HepG2	liver:	n/a	n/a
32	CEBPB	chr1:67223628-67223691	K562	blood:	n/a	n/a
33	CEBPB	chr1:67223862-67224358	K562	blood:	n/a	n/a
34	CEBPB	chr1:67191696-67192046	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr1:67270119-67270281	HepG2	liver:	n/a	n/a
36	CEBPB	chr1:67280010-67280235	K562	blood:	n/a	chr1:67280107-67280118
37	CEBPB	chr1:67226731-67227307	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr1:67336043-67336059	A549	lung:	n/a	n/a
39	CEBPB	chr1:67256996-67257312	K562	blood:	n/a	n/a
40	CEBPB	chr1:67333192-67333532	K562	blood:	n/a	chr1:67333356-67333367
41	CEBPB	chr1:67321548-67321610	H1-hESC	embryonic stem cell:	n/a	chr1:67321573-67321584
42	CEBPB	chr1:67298840-67299137	IMR90	lung:	n/a	chr1:67298988-67298999
43	CEBPB	chr1:67191679-67191905	HepG2	liver:	n/a	n/a
44	CEBPB	chr1:67182840-67183114	HepG2	liver:	n/a	chr1:67182996-67183007
45	CEBPB	chr1:67257003-67257307	HepG2	liver:	n/a	n/a
46	CEBPB	chr1:67321407-67321704	K562	blood:	n/a	chr1:67321573-67321584
47	CEBPB	chr1:67282436-67282636	K562	blood:	n/a	chr1:67282528-67282541 chr1:67282528-67282541 chr1:67282528-67282541 chr1:67282530-67282541
48	CEBPB	chr1:67190927-67191211	HepG2	liver:	n/a	n/a
49	CEBPB	chr1:67282485-67282556	IMR90	lung:	n/a	chr1:67282528-67282541 chr1:67282528-67282541 chr1:67282528-67282541 chr1:67282530-67282541
50	CEBPB	chr1:67333288-67333495	H1-hESC	embryonic stem cell:	n/a	chr1:67333356-67333367

(count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:67218275-67218325	AG04449	skin:	fetal
2	chr1:67268315-67268365	BJ	skin:	n/a
3	chr1:67244062-67244112	SK-N-MC	brain:	n/a
4	chr1:67218275-67218325	AG04449	skin:	fetal
5	chr1:67268315-67268365	BJ	skin:	n/a
6	chr1:67244062-67244112	SK-N-MC	brain:	n/a
7	chr1:67218090-67218140	CMK	blood:	n/a
8	chr1:67218135-67218185	HepG2	liver:	n/a
9	chr1:67204147-67204197	AG09319	gingival:	n/a
10	chr1:67217769-67217819	AG04449	skin:	fetal
11	chr1:67266410-67266460	A549	lung:	n/a
12	chr1:67218275-67218325	AG04450	lung:	fetal
13	chr1:67218505-67218555	MCF-7	breast:	n/a
14	chr1:67178638-67178688	AoSMC	blood vessel:	n/a
15	chr1:67217950-67218000	ECC-1	luminal epithelium:	n/a
16	chr1:67218090-67218140	Hela-S3	cervix:	n/a
17	chr1:67218275-67218325	GM12878	blood:	n/a
18	chr1:67266801-67266851	IMR90	lung:	fetal
19	chr1:67267129-67267179	Hepatocyte	liver:	n/a
20	chr1:67218165-67218215	MCF-7	breast:	n/a
21	chr1:67244062-67244112	HEK293	kidney:	embryo
22	chr1:67218505-67218555	HCPEpiC	choroid plexus:	n/a
23	chr1:67266801-67266851	Caco-2	colon:	n/a
24	chr1:67244062-67244112	Hela-S3	cervix:	n/a
25	chr1:67268315-67268365	HNPCEpiC	eye:	n/a
26	chr1:67191531-67191581	NHDF-neo	bronchial:	n/a
27	chr1:67217950-67218000	GM12891	blood:	n/a
28	chr1:67191531-67191581	MCF-7	breast:	n/a
29	chr1:67218165-67218215	IMR90	lung:	fetal
30	chr1:67218135-67218185	K562	blood:	n/a
31	chr1:67220432-67220482	HNPCEpiC	eye:	n/a
32	chr1:67267129-67267179	AG04449	skin:	fetal
33	chr1:67268315-67268365	HIPEpiC	eye:	n/a
34	chr1:67267855-67267905	LNCaP	prostate:	n/a
35	chr1:67218505-67218555	HMEC	breast:	n/a
36	chr1:67267855-67267905	GM06990	blood:	n/a
37	chr1:67218505-67218555	GM12878	blood:	n/a
38	chr1:67244062-67244112	MCF10A-Er-Src	breast:	n/a
39	chr1:67244062-67244112	T-47D	breast:	n/a
40	chr1:67220432-67220482	HCPEpiC	choroid plexus:	n/a
41	chr1:67218135-67218185	NH-A	brain:	n/a
42	chr1:67217950-67218000	LNCaP	prostate:	n/a
43	chr1:67218080-67218130	GM19239	blood:	n/a
44	chr1:67217950-67218000	CMK	blood:	n/a
45	chr1:67218165-67218215	BJ	skin:	n/a
46	chr1:67217886-67217936	HEEpiC	esophagus:	n/a
47	chr1:67217853-67217903	SKMC	muscle:	n/a
48	chr1:67218135-67218185	HCPEpiC	choroid plexus:	n/a
49	chr1:67267129-67267179	LNCaP	prostate:	n/a
50	chr1:67218275-67218325	HMEC	breast:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:67166132..67168879-chr1:67189803..67192452,2	K562	blood:
2	chr1:67216842..67220056-chr1:67223090..67226284,3	K562	blood:
3	chr1:67230464..67231736-chr1:67614522..67615465,5	K562	blood:
4	chr1:67230218..67231048-chr1:67461528..67462349,2	K562	blood:
5	chr1:67305339..67308328-chr1:67451037..67452745,2	K562	blood:
6	chr1:67279522..67281219-chr1:67285864..67287900,2	K562	blood:
7	chr1:67195090..67196807-chr1:67198511..67200575,2	K562	blood:
8	chr1:67293404..67295635-chr1:67298470..67301604,3	K562	blood:
9	chr1:67325715..67327422-chr1:67337207..67338944,2	K562	blood:
10	chr1:67203426..67206890-chr1:67208390..67210914,3	K562	blood:
11	chr1:67279434..67281250-chr1:67282705..67284237,2	K562	blood:
12	chr1:67195090..67197829-chr1:67199075..67200938,2	K562	blood:
13	chr1:67325715..67327422-chr1:67337207..67338944,2	K562	blood:
14	chr1:67293404..67295635-chr1:67298470..67301604,3	K562	blood:
15	chr1:67197999..67199929-chr1:67205946..67207947,2	K562	blood:
16	chr1:67230851..67231401-chr1:67614599..67615362,2	MCF-7	breast:
17	chr1:67221443..67223945-chr1:67224724..67227311,3	K562	blood:
18	chr1:67221443..67223945-chr1:67224724..67227311,3	K562	blood:
19	chr1:67264702..67266931-chr1:67273930..67275533,2	K562	blood:
20	chr1:67333615..67337326-chr1:67338154..67341461,3	K562	blood:
21	chr1:67264702..67266931-chr1:67273930..67275533,2	K562	blood:
22	chr1:67295036..67296845-chr1:67297127..67301169,3	K562	blood:
23	chr1:67203426..67206890-chr1:67208390..67210914,3	K562	blood:
24	chr1:67172247..67174334-chr1:67176397..67179152,3	K562	blood:
25	chr1:67229958..67230621-chr1:67677554..67678086,2	MCF-7	breast:
26	chr1:67279522..67281219-chr1:67285864..67287900,2	K562	blood:
27	chr1:67220223..67221912-chr1:67222295..67224131,2	K562	blood:
28	chr1:67232486..67234665-chr1:67239762..67241784,2	K562	blood:
29	chr1:67333615..67337326-chr1:67338154..67341461,3	K562	blood:
30	chr1:67197999..67199929-chr1:67205946..67207947,2	K562	blood:
31	chr1:67104788..67107666-chr1:67181908..67183681,2	K562	blood:
32	chr1:67222037..67222621-chr14:53256990..53257660,2	MCF-7	breast:
33	chr1:67220223..67221912-chr1:67222295..67224131,2	K562	blood:
34	chr1:67172247..67174334-chr1:67176397..67179152,3	K562	blood:
35	chr1:67279434..67281250-chr1:67282705..67284237,2	K562	blood:
36	chr1:67072874..67073739-chr1:67191676..67192371,2	K562	blood:
37	chr1:67265658..67268510-chr1:67270646..67272649,2	K562	blood:
38	chr1:67295036..67296845-chr1:67297127..67301169,3	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-INSL5-1	chr1:67326396-67326522	NONHSAT003768
2	lnc-SGIP1-2	chr1:67218215-67218267	NONHSAT003765
3	lnc-SGIP1-2	chr1:67220339-67220460	NONHSAT003765
4	lnc-SGIP1-1	chr1:67240729-67241023	ENSG00000227787.1
5	lnc-SGIP1-2	chr1:67234342-67234443	NONHSAT003765
6	lnc-SGIP1-2	chr1:67221363-67221456	NONHSAT003765
7	lnc-SGIP1-2	chr1:67236070-67236190	NONHSAT003765
8	lnc-INSL5-1	chr1:67327830-67327987	NONHSAT003768
9	lnc-SGIP1-1	chr1:67241197-67241261	ENSG00000227787.1

No data

Variant related genes	Relation type
WDR78	TF binding region
ENSG00000221655	TF binding region
INSL5	TF binding region
ENSG00000231080	TF binding region
TCTEX1D1	TF binding region
WDR78	CpG island
ENSG00000221655	CpG island
INSL5	CpG island
ENSG00000231080	CpG island
TCTEX1D1	CpG island
ENSG00000172410	chromatin interactions
ENSG00000152760	chromatin interactions
ENSG00000221655	chromatin interactions
ENSG00000152763	chromatin interactions

Extended variants
information (count: 5716 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:5716 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567246646	chr1:67173646-67173647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs536212375	chr1:67173655-67173656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs75019572	chr1:67173686-67173687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186352750	chr1:67173751-67173752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1853772	chr1:67173760-67173761	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs1280280	chr1:67173903-67173904	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs560105565	chr1:67173953-67173954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs60980438	chr1:67173954-67173955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566228380	chr1:67173956-67173957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138541790	chr1:67174036-67174037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs555265469	chr1:67174074-67174075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs141620297	chr1:67174097-67174098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs542235555	chr1:67174098-67174099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs150749850	chr1:67174101-67174102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576047209	chr1:67174184-67174185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189191037	chr1:67174236-67174237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs564642980	chr1:67174262-67174263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537563153	chr1:67174321-67174322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540844369	chr1:67174421-67174422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs523188	chr1:67174422-67174423	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs523132	chr1:67174440-67174441	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs113153556	chr1:67174446-67174447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs367713825	chr1:67174460-67174461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs371467676	chr1:67174461-67174462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374930663	chr1:67174462-67174463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549907398	chr1:67174468-67174469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs75904555	chr1:67174507-67174508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs111916321	chr1:67174529-67174530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35690185	chr1:67174537-67174538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181548984	chr1:67174552-67174553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs17129365	chr1:67174554-67174555	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs186731725	chr1:67174580-67174581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566191729	chr1:67174589-67174590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191172189	chr1:67174605-67174606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554621853	chr1:67174613-67174614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568766489	chr1:67174633-67174634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368987208	chr1:67174654-67174655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537788733	chr1:67174661-67174662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371875691	chr1:67174662-67174663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369347828	chr1:67174689-67174690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557380620	chr1:67174695-67174696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575815473	chr1:67174718-67174719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114834780	chr1:67174725-67174726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369864679	chr1:67174735-67174736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544701020	chr1:67174755-67174756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183103358	chr1:67174762-67174763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138020547	chr1:67174764-67174765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186015550	chr1:67174770-67174771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564491143	chr1:67174847-67174848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149511682	chr1:67174980-67174981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Myelofibrosis	22110671	CNVD
CNS Malformation Syndrome	17530927	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	20459617	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal cancer	21851588	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Ewing''s sarcoma	17952124	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:67155800-67177200	Weak transcription	Brain Anterior Caudate	brain
2	chr1:67156000-67177200	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr1:67156800-67191400	Weak transcription	Fetal Brain Female	brain
4	chr1:67157000-67208800	Weak transcription	Brain Germinal Matrix	brain
5	chr1:67157200-67189600	Weak transcription	Brain Hippocampus Middle	brain
6	chr1:67157400-67191600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr1:67158200-67189400	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr1:67158400-67191400	Weak transcription	Left Ventricle	heart
9	chr1:67158600-67189400	Weak transcription	Brain Cingulate Gyrus	brain
10	chr1:67160400-67189400	Weak transcription	Brain Angular Gyrus	brain
11	chr1:67165200-67191400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr1:67165400-67187600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr1:67165400-67191600	Weak transcription	Aorta	Aorta
14	chr1:67165400-67206800	Weak transcription	Fetal Brain Male	brain
15	chr1:67168000-67185000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr1:67170200-67186800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr1:67171400-67189400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr1:67171400-67198000	Weak transcription	NHLF	lung
19	chr1:67177200-67177600	Enhancers	Brain Anterior Caudate	brain
20	chr1:67177200-67177600	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr1:67177400-67177600	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr1:67177600-67178400	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr1:67177600-67189400	Weak transcription	Brain Anterior Caudate	brain
24	chr1:67177600-67189400	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr1:67178000-67178800	Enhancers	H9 Cell Line	embryonic stem cell
26	chr1:67178400-67178800	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr1:67178400-67179200	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr1:67179600-67185000	Weak transcription	Primary hematopoietic stem cells	blood
29	chr1:67179600-67191400	Weak transcription	NHDF-Ad	bronchial
30	chr1:67181000-67181200	Enhancers	Brain Substantia Nigra	brain
31	chr1:67181200-67191200	Weak transcription	Brain Substantia Nigra	brain
32	chr1:67182400-67182800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr1:67182600-67182800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr1:67182800-67183800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr1:67182800-67184400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr1:67183800-67184000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr1:67184000-67184800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr1:67184400-67186400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr1:67184800-67185000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr1:67184800-67199400	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr1:67185000-67185400	Enhancers	Primary hematopoietic stem cells	blood
42	chr1:67185000-67185800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr1:67185000-67188600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr1:67185400-67191200	Weak transcription	Primary hematopoietic stem cells	blood
45	chr1:67185800-67186000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr1:67186000-67189800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr1:67186000-67190600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr1:67186200-67188200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr1:67186400-67190200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr1:67186400-67205000	Weak transcription	Fetal Heart	heart

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