Variant report

Variant	nsv611819
Chromosome Location	chr8:102847202-102929460
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:812)
CpG islands
(count:183)
Chromatin interactive
region (count:47)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:812 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:102914752-102914954	K562	blood:	n/a	n/a
2	ATF1	chr8:102854400-102854466	K562	blood:	n/a	n/a
3	ATF1	chr8:102901312-102901533	K562	blood:	n/a	n/a
4	ATF1	chr8:102914633-102915254	K562	blood:	n/a	n/a
5	ATF2	chr8:102914316-102915387	GM12878	blood:	n/a	n/a
6	ATF2	chr8:102920194-102920982	GM12878	blood:	n/a	n/a
7	ATF2	chr8:102923246-102924445	GM12878	blood:	n/a	n/a
8	ATF2	chr8:102855019-102855788	GM12878	blood:	n/a	n/a
9	ATF2	chr8:102914417-102915486	GM12878	blood:	n/a	n/a
10	ATF2	chr8:102854982-102855874	GM12878	blood:	n/a	n/a
11	ATF2	chr8:102858789-102859307	GM12878	blood:	n/a	n/a
12	ATF2	chr8:102923714-102924368	GM12878	blood:	n/a	n/a
13	BACH1	chr8:102876039-102876124	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr8:102914480-102915357	GM12878	blood:	n/a	chr8:102914680-102914690
15	BATF	chr8:102855126-102855769	GM12878	blood:	n/a	chr8:102855445-102855456
16	BATF	chr8:102858820-102859151	GM12878	blood:	n/a	chr8:102858993-102859004
17	BATF	chr8:102914459-102915163	GM12878	blood:	n/a	chr8:102914680-102914690
18	BATF	chr8:102858786-102859207	GM12878	blood:	n/a	chr8:102858993-102859004
19	BATF	chr8:102855111-102855830	GM12878	blood:	n/a	chr8:102855445-102855456
20	BATF	chr8:102923825-102924171	GM12878	blood:	n/a	chr8:102924082-102924095
21	BCL11A	chr8:102914516-102915210	GM12878	blood:	n/a	chr8:102915129-102915138 chr8:102914848-102914855
22	BCL11A	chr8:102920486-102920859	GM12878	blood:	n/a	n/a
23	BCL11A	chr8:102914895-102915184	GM12878	blood:	n/a	chr8:102915129-102915138
24	BCL11A	chr8:102855336-102855836	GM12878	blood:	n/a	n/a
25	BCL11A	chr8:102923806-102924160	GM12878	blood:	n/a	n/a
26	BCL11A	chr8:102923812-102924195	GM12878	blood:	n/a	n/a
27	BCL11A	chr8:102855465-102855759	GM12878	blood:	n/a	n/a
28	BCL3	chr8:102923819-102924322	GM12878	blood:	n/a	n/a
29	BCL3	chr8:102855177-102855774	GM12878	blood:	n/a	n/a
30	BCLAF1	chr8:102855021-102855772	GM12878	blood:	n/a	n/a
31	BCLAF1	chr8:102914409-102915469	GM12878	blood:	n/a	chr8:102915129-102915138 chr8:102914848-102914855
32	BCLAF1	chr8:102855069-102855789	GM12878	blood:	n/a	n/a
33	BCLAF1	chr8:102923791-102924282	GM12878	blood:	n/a	n/a
34	BCLAF1	chr8:102923733-102924340	GM12878	blood:	n/a	n/a
35	BCLAF1	chr8:102914465-102915383	GM12878	blood:	n/a	chr8:102915129-102915138 chr8:102914848-102914855
36	BCLAF1	chr8:102920259-102920919	GM12878	blood:	n/a	n/a
37	BCLAF1	chr8:102920416-102920828	GM12878	blood:	n/a	n/a
38	BHLHE40	chr8:102914713-102914997	K562	blood:	n/a	n/a
39	BHLHE40	chr8:102853520-102853731	GM12878	blood:	n/a	n/a
40	BHLHE40	chr8:102854974-102855834	GM12878	blood:	n/a	n/a
41	BHLHE40	chr8:102915048-102915251	HepG2	liver:	n/a	chr8:102915081-102915097
42	BHLHE40	chr8:102923819-102924246	GM12878	blood:	n/a	n/a
43	BHLHE40	chr8:102858848-102859248	GM12878	blood:	n/a	n/a
44	BHLHE40	chr8:102920330-102920892	GM12878	blood:	n/a	n/a
45	BHLHE40	chr8:102914572-102915402	GM12878	blood:	n/a	chr8:102915081-102915097
46	CBX3	chr8:102904021-102904298	K562	blood:	n/a	n/a
47	CBX3	chr8:102914609-102915052	K562	blood:	n/a	n/a
48	CBX3	chr8:102903427-102903809	HCT-116	colon:	n/a	n/a
49	CBX3	chr8:102903513-102903838	K562	blood:	n/a	n/a
50	CEBPB	chr8:102879656-102879695	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:102898712-102898762	AG09319	gingival:	n/a
2	chr8:102876411-102876461	SK-N-SH	brain:	n/a
3	chr8:102876411-102876461	GM12892	blood:	n/a
4	chr8:102898712-102898762	HepG2	liver:	n/a
5	chr8:102876411-102876461	HepG2	liver:	n/a
6	chr8:102876411-102876461	GM12878	blood:	n/a
7	chr8:102876411-102876461	NHDF-neo	bronchial:	n/a
8	chr8:102903909-102903959	HPAEpiC	pulmonary alveolar:	n/a
9	chr8:102903909-102903959	NH-A	brain:	n/a
10	chr8:102898712-102898762	RPTEC	kidney:	n/a
11	chr8:102898712-102898762	HCM	heart:	n/a
12	chr8:102898712-102898762	HPAEpiC	pulmonary alveolar:	n/a
13	chr8:102876411-102876461	PANC-1	pancreas:	n/a
14	chr8:102876411-102876461	HUVEC	blood vessel:	n/a
15	chr8:102876411-102876461	Hela-S3	cervix:	n/a
16	chr8:102876411-102876461	T-47D	breast:	n/a
17	chr8:102876411-102876461	HCPEpiC	choroid plexus:	n/a
18	chr8:102903909-102903959	A549	lung:	n/a
19	chr8:102876411-102876461	AG04450	lung:	fetal
20	chr8:102898712-102898762	HL-60	blood:	n/a
21	chr8:102898712-102898762	HRCEpiC	kidney:	n/a
22	chr8:102876411-102876461	LNCaP	prostate:	n/a
23	chr8:102876411-102876461	A549	lung:	n/a
24	chr8:102903909-102903959	BE2_C	brain:	n/a
25	chr8:102898712-102898762	HEEpiC	esophagus:	n/a
26	chr8:102903909-102903959	NHBE	bronchial:	n/a
27	chr8:102903909-102903959	HepG2	liver:	n/a
28	chr8:102898712-102898762	PrEC	prostate:	n/a
29	chr8:102876411-102876461	H1-hESC	embryonic stem cell:	embryo
30	chr8:102876411-102876461	GM19239	blood:	n/a
31	chr8:102876411-102876461	PrEC	prostate:	n/a
32	chr8:102876411-102876461	BJ	skin:	n/a
33	chr8:102876411-102876461	NT2-D1	testis:	n/a
34	chr8:102876411-102876461	HPAEpiC	pulmonary alveolar:	n/a
35	chr8:102903909-102903959	SK-N-SH	brain:	n/a
36	chr8:102903909-102903959	ECC-1	luminal epithelium:	n/a
37	chr8:102876411-102876461	MCF10A-Er-Src	breast:	n/a
38	chr8:102898712-102898762	AG09309	skin:	n/a
39	chr8:102898712-102898762	PFSK-1	brain:	n/a
40	chr8:102903909-102903959	T-47D	breast:	n/a
41	chr8:102903909-102903959	MCF-7	breast:	n/a
42	chr8:102903909-102903959	ovcar-3	ovarian:	n/a
43	chr8:102876411-102876461	MCF-7	breast:	n/a
44	chr8:102903909-102903959	PANC-1	pancreas:	n/a
45	chr8:102876411-102876461	BE2_C	brain:	n/a
46	chr8:102898712-102898762	HEK293	kidney:	embryo
47	chr8:102903909-102903959	Hepatocyte	liver:	n/a
48	chr8:102898712-102898762	GM06990	blood:	n/a
49	chr8:102898712-102898762	ovcar-3	ovarian:	n/a
50	chr8:102903909-102903959	HCM	heart:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:102878654..102880299-chr8:102886876..102888668,2	MCF-7	breast:
2	chr8:102852494..102855006-chr8:102859200..102861225,2	MCF-7	breast:
3	chr8:102864772..102866695-chr8:102870312..102872200,2	MCF-7	breast:
4	chr8:102841778..102844657-chr8:102844886..102847440,3	K562	blood:
5	chr8:102886318..102888246-chr8:102888335..102890712,2	MCF-7	breast:
6	chr8:102857484..102859004-chr8:102860794..102863721,2	K562	blood:
7	chr8:102889173..102891724-chr8:102892647..102895312,2	MCF-7	breast:
8	chr8:102847583..102849623-chr8:102851249..102854014,2	MCF-7	breast:
9	chr8:102912593..102916375-chr8:102916443..102918583,3	K562	blood:
10	chr8:102848832..102850431-chr8:102850962..102852555,2	MCF-7	breast:
11	chr8:102921170..102923851-chr8:102931011..102933896,3	MCF-7	breast:
12	chr8:102504416..102506326-chr8:102917856..102920529,2	MCF-7	breast:
13	chr8:102916266..102919129-chr8:102925767..102928340,2	MCF-7	breast:
14	chr8:102503238..102506028-chr8:102887232..102889960,2	MCF-7	breast:
15	chr8:102918268..102920256-chr8:102922072..102924621,2	K562	blood:
16	chr8:102859142..102861704-chr8:102870345..102872066,2	K562	blood:
17	chr8:102864772..102866695-chr8:102870312..102872200,2	MCF-7	breast:
18	chr19:27731229..27733214-chr8:102884050..102885632,2	MCF-7	breast:
19	chr8:102847609..102850390-chr8:102853581..102855226,2	MCF-7	breast:
20	chr8:102886318..102888246-chr8:102888335..102890712,2	MCF-7	breast:
21	chr8:102912593..102916375-chr8:102916443..102918583,3	K562	blood:
22	chr8:102878636..102880767-chr8:102882100..102885005,2	MCF-7	breast:
23	chr8:102895916..102899783-chr8:102900314..102903177,4	MCF-7	breast:
24	chr4:172177030..172177816-chr8:102919199..102919846,2	MCF-7	breast:
25	chr8:102916207..102919330-chr8:102919877..102923677,3	MCF-7	breast:
26	chr8:102876704..102878618-chr8:102883254..102885597,2	K562	blood:
27	chr8:102916207..102919330-chr8:102919877..102923677,3	MCF-7	breast:
28	chr8:102878636..102880767-chr8:102882100..102885005,2	MCF-7	breast:
29	chr8:102876704..102878618-chr8:102883254..102885597,2	K562	blood:
30	chr1:153598533..153600803-chr8:102895391..102897521,2	MCF-7	breast:
31	chr8:102918268..102920256-chr8:102922072..102924621,2	K562	blood:
32	chr8:102878654..102880299-chr8:102886876..102888668,2	MCF-7	breast:
33	chr8:102857484..102859004-chr8:102860794..102863721,2	K562	blood:
34	chr8:102915036..102919130-chr8:102919959..102923677,4	MCF-7	breast:
35	chr8:102879891..102881804-chr8:102883261..102884982,2	K562	blood:
36	chr8:102847583..102849623-chr8:102851249..102854014,2	MCF-7	breast:
37	chr8:102849681..102851432-chr8:102857073..102859191,2	MCF-7	breast:
38	chr8:102895916..102899783-chr8:102900314..102903177,4	MCF-7	breast:
39	chr8:102843199..102845818-chr8:102888680..102891293,2	MCF-7	breast:
40	chr8:102879891..102881804-chr8:102883261..102884982,2	K562	blood:
41	chr8:102848832..102850431-chr8:102850962..102852555,2	MCF-7	breast:
42	chr8:102849681..102851432-chr8:102857073..102859191,2	MCF-7	breast:
43	chr8:102915036..102919130-chr8:102919959..102923677,4	MCF-7	breast:
44	chr8:102842176..102845083-chr8:102849432..102850991,2	K562	blood:
45	chr8:102847609..102850390-chr8:102853581..102855226,2	MCF-7	breast:
46	chr8:102889173..102891724-chr8:102892647..102895312,2	MCF-7	breast:
47	chr8:102916266..102919129-chr8:102925767..102928340,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RRM2B-8	chr8:102927740-102928086	NONHSAT128075
2	lnc-RRM2B-8	chr8:102928037-102928086	NONHSAT128070

No data

Variant related genes	Relation type
ENSG00000238372	TF binding region
ENSG00000238372	CpG island
ENSG00000238372	chromatin interactions
ENSG00000254024	chromatin interactions
ENSG00000189171	chromatin interactions
ENSG00000160678	chromatin interactions
ENSG00000083307	chromatin interactions

Extended variants
information (count: 3025 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:3025 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2155939	chr8:102847202-102847203	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs560824196	chr8:102847230-102847231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531187606	chr8:102847231-102847232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs573187859	chr8:102847260-102847261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs2155938	chr8:102847262-102847263	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs565163933	chr8:102847279-102847280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs73277008	chr8:102847283-102847284	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs369392344	chr8:102847316-102847317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577640938	chr8:102847336-102847337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs550751534	chr8:102847346-102847347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs142535488	chr8:102847377-102847378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs369294956	chr8:102847380-102847381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs10113096	chr8:102847390-102847391	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs534054173	chr8:102847391-102847392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs73277009	chr8:102847438-102847439	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs139065688	chr8:102847439-102847440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533912304	chr8:102847443-102847444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs188435030	chr8:102847464-102847465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73277012	chr8:102847465-102847466	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs73277014	chr8:102847526-102847527	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs556670706	chr8:102847565-102847566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568865744	chr8:102847604-102847605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs73696644	chr8:102847617-102847618	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs34864723	chr8:102847636-102847637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149372459	chr8:102847670-102847671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572903267	chr8:102847704-102847705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs374236109	chr8:102847728-102847729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs144740373	chr8:102847767-102847768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs117718818	chr8:102847775-102847776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs35390274	chr8:102847835-102847836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs148656255	chr8:102847859-102847860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544085775	chr8:102847902-102847903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs562669654	chr8:102847910-102847911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs574050203	chr8:102847925-102847926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530158535	chr8:102847927-102847928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541949224	chr8:102847932-102847933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368670195	chr8:102847934-102847935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs73277017	chr8:102847974-102847975	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs371473122	chr8:102847982-102847983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs372736541	chr8:102847985-102847986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs527720161	chr8:102848148-102848149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs142166608	chr8:102848149-102848150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561824887	chr8:102848307-102848308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs190239244	chr8:102848328-102848329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs531988713	chr8:102848329-102848330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs183143055	chr8:102848348-102848349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs536033540	chr8:102848367-102848368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs558719025	chr8:102848378-102848379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs554747613	chr8:102848397-102848398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs150787948	chr8:102848401-102848402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Sezary syndrome	18413736	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Cancer	20164920	CNVD
Urothelial cell carcinoma	18451213	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	20409316	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21611746	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Autism	22495309	CNVD

Chromatin state (count:910 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:102803600-102870600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr8:102835000-102852000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:102838600-102848400	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr8:102842200-102851000	Weak transcription	Fetal Kidney	kidney
5	chr8:102843800-102848000	Enhancers	HMEC	breast
6	chr8:102844200-102847400	Weak transcription	Esophagus	oesophagus
7	chr8:102844600-102849400	Weak transcription	Right Ventricle	heart
8	chr8:102845400-102847400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr8:102845400-102847400	Weak transcription	NHEK	skin
10	chr8:102845400-102847800	Weak transcription	Right Atrium	heart
11	chr8:102845400-102849400	Weak transcription	Fetal Heart	heart
12	chr8:102845400-102862000	Weak transcription	Left Ventricle	heart
13	chr8:102845600-102855000	Weak transcription	Aorta	Aorta
14	chr8:102846800-102849400	Weak transcription	Ovary	ovary
15	chr8:102846800-102851200	Weak transcription	Fetal Muscle Leg	muscle
16	chr8:102846800-102866400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr8:102847000-102847800	Weak transcription	Psoas Muscle	Psoas
18	chr8:102847400-102847600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr8:102847400-102848200	Enhancers	Esophagus	oesophagus
20	chr8:102847400-102848200	Enhancers	NHEK	skin
21	chr8:102847600-102849600	Enhancers	Fetal Stomach	stomach
22	chr8:102847800-102848000	Enhancers	Psoas Muscle	Psoas
23	chr8:102847800-102848000	Enhancers	Right Atrium	heart
24	chr8:102847800-102849000	Enhancers	Fetal Lung	lung
25	chr8:102848000-102848200	Enhancers	Fetal Brain Male	brain
26	chr8:102848000-102848800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr8:102848000-102853400	Weak transcription	Psoas Muscle	Psoas
28	chr8:102848000-102854200	Weak transcription	HMEC	breast
29	chr8:102848600-102848800	Enhancers	Colon Smooth Muscle	Colon
30	chr8:102848600-102848800	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr8:102849400-102849600	Enhancers	Fetal Heart	heart
32	chr8:102849400-102849600	Enhancers	Ovary	ovary
33	chr8:102849400-102850000	Enhancers	Right Ventricle	heart
34	chr8:102850000-102852000	Weak transcription	Right Ventricle	heart
35	chr8:102851000-102851400	Enhancers	Fetal Kidney	kidney
36	chr8:102851200-102852200	Enhancers	Fetal Muscle Leg	muscle
37	chr8:102852000-102852200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr8:102852000-102852200	Enhancers	Right Ventricle	heart
39	chr8:102852000-102854600	Enhancers	GM12878-XiMat	blood
40	chr8:102852200-102854800	Weak transcription	Fetal Muscle Leg	muscle
41	chr8:102853400-102853800	Enhancers	Psoas Muscle	Psoas
42	chr8:102853800-102854800	Weak transcription	Psoas Muscle	Psoas
43	chr8:102854200-102854600	Enhancers	HMEC	breast
44	chr8:102854200-102855000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr8:102854400-102854800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr8:102854600-102855600	Flanking Active TSS	GM12878-XiMat	blood
47	chr8:102854800-102855000	Enhancers	Fetal Muscle Leg	muscle
48	chr8:102854800-102855000	Enhancers	Psoas Muscle	Psoas
49	chr8:102854800-102866200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr8:102855000-102855200	Enhancers	Aorta	Aorta

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