Variant report

Variant	nsv539618
Chromosome Location	chr8:53488049-53748168
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3328)
CpG islands
(count:1465)
Chromatin interactive
region (count:134)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:3328 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:53490305-53490673	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:53490268-53490616	K562	blood:	n/a	n/a
3	ARID3A	chr8:53626830-53627890	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:53625837-53626271	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:53655962-53656401	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:53653439-53654157	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:53607839-53608395	K562	blood:	n/a	n/a
8	ARID3A	chr8:53623763-53624376	K562	blood:	n/a	n/a
9	ARID3A	chr8:53649716-53650068	HepG2	liver:	n/a	n/a
10	ARID3A	chr8:53607651-53608431	HepG2	liver:	n/a	n/a
11	ARID3A	chr8:53619391-53620331	K562	blood:	n/a	n/a
12	ARID3A	chr8:53626858-53627017	K562	blood:	n/a	n/a
13	ARID3A	chr8:53625373-53626141	K562	blood:	n/a	n/a
14	ARID3A	chr8:53736377-53736496	HepG2	liver:	n/a	n/a
15	ATF1	chr8:53619393-53619703	K562	blood:	n/a	n/a
16	ATF1	chr8:53600952-53601256	K562	blood:	n/a	n/a
17	ATF1	chr8:53571713-53571874	K562	blood:	n/a	n/a
18	ATF1	chr8:53607852-53608349	K562	blood:	n/a	n/a
19	ATF1	chr8:53625619-53626121	K562	blood:	n/a	n/a
20	ATF2	chr8:53627701-53628173	GM12878	blood:	n/a	n/a
21	ATF2	chr8:53502312-53502692	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr8:53706285-53706764	GM12878	blood:	n/a	n/a
23	ATF2	chr8:53541876-53542312	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr8:53626713-53627724	GM12878	blood:	n/a	n/a
25	ATF2	chr8:53541963-53542396	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF3	chr8:53607833-53608330	A549	lung:	n/a	n/a
27	ATF3	chr8:53625613-53626138	K562	blood:	n/a	n/a
28	ATF3	chr8:53607775-53608234	K562	blood:	n/a	n/a
29	ATF3	chr8:53619369-53619713	K562	blood:	n/a	n/a
30	ATF3	chr8:53625672-53625862	K562	blood:	n/a	n/a
31	ATF3	chr8:53541931-53542300	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr8:53730807-53730831	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr8:53502214-53502830	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr8:53625799-53626136	K562	blood:	n/a	chr8:53626047-53626061
35	BACH1	chr8:53624188-53624203	K562	blood:	n/a	n/a
36	BACH1	chr8:53626943-53627132	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr8:53625880-53626504	H1-hESC	embryonic stem cell:	n/a	chr8:53626047-53626061
38	BACH1	chr8:53737850-53738162	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr8:53512316-53512639	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr8:53669704-53669715	K562	blood:	n/a	n/a
41	BACH1	chr8:53627436-53627545	H1-hESC	embryonic stem cell:	n/a	n/a
42	BATF	chr8:53627832-53628156	GM12878	blood:	n/a	n/a
43	BATF	chr8:53538194-53538450	GM12878	blood:	n/a	n/a
44	BATF	chr8:53627830-53628114	GM12878	blood:	n/a	n/a
45	BCL11A	chr8:53541969-53542167	H1-hESC	embryonic stem cell:	n/a	n/a
46	BCL11A	chr8:53502345-53502607	H1-hESC	embryonic stem cell:	n/a	n/a
47	BCL11A	chr8:53541959-53542415	H1-hESC	embryonic stem cell:	n/a	n/a
48	BCL11A	chr8:53538553-53538791	GM12878	blood:	n/a	n/a
49	BCL3	chr8:53626818-53627345	GM12878	blood:	n/a	chr8:53627003-53627012 chr8:53626964-53626973
50	BCL3	chr8:53607785-53608368	A549	lung:	n/a	n/a

(count:1465 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:53627208-53627258	HCM	heart:	n/a
2	chr8:53627208-53627258	HCM	heart:	n/a
3	chr8:53627369-53627419	GM06990	blood:	n/a
4	chr8:53566460-53566510	HL-60	blood:	n/a
5	chr8:53626947-53626997	Caco-2	colon:	n/a
6	chr8:53626238-53626288	HMEC	breast:	n/a
7	chr8:53566460-53566510	BE2_C	brain:	n/a
8	chr8:53566460-53566510	NH-A	brain:	n/a
9	chr8:53603035-53603085	Hepatocyte	liver:	n/a
10	chr8:53499582-53499632	H1-hESC	embryonic stem cell:	embryo
11	chr8:53627099-53627149	GM12891	blood:	n/a
12	chr8:53626936-53626986	A549	lung:	n/a
13	chr8:53627067-53627117	ECC-1	luminal epithelium:	n/a
14	chr8:53578814-53578864	GM12892	blood:	n/a
15	chr8:53566460-53566510	HRCEpiC	kidney:	n/a
16	chr8:53499558-53499608	AG09309	skin:	n/a
17	chr8:53566460-53566510	SK-N-SH_RA	brain:	n/a
18	chr8:53627628-53627678	IMR90	lung:	fetal
19	chr8:53566460-53566510	NHDF-neo	bronchial:	n/a
20	chr8:53625864-53625914	SK-N-SH_RA	brain:	n/a
21	chr8:53603035-53603085	NHDF-neo	bronchial:	n/a
22	chr8:53627369-53627419	NHDF-neo	bronchial:	n/a
23	chr8:53627771-53627821	ECC-1	luminal epithelium:	n/a
24	chr8:53626939-53626989	U87	brain:	n/a
25	chr8:53536234-53536284	HEK293	kidney:	embryo
26	chr8:53626238-53626288	NHDF-neo	bronchial:	n/a
27	chr8:53566460-53566510	HEK293	kidney:	embryo
28	chr8:53626238-53626288	SK-N-MC	brain:	n/a
29	chr8:53627208-53627258	K562	blood:	n/a
30	chr8:53626238-53626288	SK-N-SH_RA	brain:	n/a
31	chr8:53623995-53624045	ProgFib	skin:	n/a
32	chr8:53626238-53626288	NB4	blood:	n/a
33	chr8:53578814-53578864	HNPCEpiC	eye:	n/a
34	chr8:53499582-53499632	ProgFib	skin:	n/a
35	chr8:53490251-53490301	A549	lung:	n/a
36	chr8:53626947-53626997	BJ	skin:	n/a
37	chr8:53627771-53627821	GM19239	blood:	n/a
38	chr8:53536234-53536284	GM12892	blood:	n/a
39	chr8:53490251-53490301	U87	brain:	n/a
40	chr8:53626936-53626986	IMR90	lung:	fetal
41	chr8:53626939-53626989	HEK293	kidney:	embryo
42	chr8:53627628-53627678	HCPEpiC	choroid plexus:	n/a
43	chr8:53499558-53499608	Hepatocyte	liver:	n/a
44	chr8:53578814-53578864	BJ	skin:	n/a
45	chr8:53623995-53624045	Hepatocyte	liver:	n/a
46	chr8:53608045-53608095	NHBE	bronchial:	n/a
47	chr8:53627067-53627117	Hela-S3	cervix:	n/a
48	chr8:53626436-53626486	K562	blood:	n/a
49	chr8:53490251-53490301	SK-N-MC	brain:	n/a
50	chr8:53528402-53528452	T-47D	breast:	n/a

(count:134 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:53606863..53608934-chr8:53624875..53627041,2	MCF-7	breast:
2	chr8:53558929..53560566-chr8:53563756..53566639,2	K562	blood:
3	chr8:53645160..53646715-chr8:53654221..53656472,2	K562	blood:
4	chr8:53607539..53609203-chr8:53611083..53613444,2	K562	blood:
5	chr8:53742398..53744549-chr8:53749329..53751637,2	K562	blood:
6	chr8:53544573..53546394-chr8:53550090..53551810,2	K562	blood:
7	chr8:53649395..53650276-chr8:53853945..53854772,3	MCF-7	breast:
8	chr8:53619754..53621729-chr8:53622520..53624879,3	K562	blood:
9	chr8:53602830..53605702-chr8:53625745..53627611,2	MCF-7	breast:
10	chr8:53620476..53625575-chr8:53625670..53628222,6	MCF-7	breast:
11	chr8:53558478..53560001-chr8:53562936..53564747,2	K562	blood:
12	chr8:53630266..53632486-chr8:53643679..53645465,2	K562	blood:
13	chr8:53522102..53525092-chr8:53526837..53528370,2	K562	blood:
14	chr1:155293911..155294447-chr8:53626319..53626980,2	Hela-S3	cervix:
15	chr8:53632444..53635231-chr8:53641843..53643770,2	K562	blood:
16	chr8:53527707..53530232-chr8:53540269..53542754,2	K562	blood:
17	chr8:53676710..53678990-chr8:53681046..53682714,2	MCF-7	breast:
18	chr8:53627655..53629298-chr8:53662388..53664857,2	K562	blood:
19	chr8:53689610..53691710-chr8:53692191..53695139,2	K562	blood:
20	chr8:53683660..53686636-chr8:53704958..53706568,2	MCF-7	breast:
21	chr8:53590344..53593070-chr8:53594562..53597118,2	K562	blood:
22	chr8:53490108..53490739-chr8:53649694..53650429,2	MCF-7	breast:
23	chr8:53527707..53530232-chr8:53540269..53542754,2	K562	blood:
24	chr8:53527061..53528646-chr8:53530160..53531706,2	MCF-7	breast:
25	chr8:53599823..53601414-chr8:53625162..53627415,2	MCF-7	breast:
26	chr8:53711623..53712255-chr8:53854248..53854877,2	MCF-7	breast:
27	chr8:53649575..53650317-chrX:24516398..24516929,2	MCF-7	breast:
28	chr8:53606661..53608813-chr8:53627240..53629943,2	MCF-7	breast:
29	chr8:53544573..53546394-chr8:53550090..53551810,2	K562	blood:
30	chr8:53573059..53575717-chr8:53608675..53611203,2	K562	blood:
31	chr8:53563732..53566107-chr8:53606822..53608530,2	K562	blood:
32	chr8:53490029..53490926-chr8:53861444..53862393,2	MCF-7	breast:
33	chr8:53615440..53617336-chr8:53625360..53626968,2	MCF-7	breast:
34	chr8:53532077..53533994-chr8:53547222..53549293,2	K562	blood:
35	chr8:53569082..53571374-chr8:53573595..53575990,2	K562	blood:
36	chr8:53624816..53627483-chr8:54753343..54757526,4	K562	blood:
37	chr8:53636304..53636924-chr8:53649658..53650305,2	K562	blood:
38	chr8:53608190..53609971-chr8:53612097..53614102,2	MCF-7	breast:
39	chr8:53625824..53627381-chr8:53665181..53668029,2	K562	blood:
40	chr8:53600570..53603168-chr8:53623179..53625977,2	K562	blood:
41	chr8:53600327..53602070-chr8:53622453..53624679,2	K562	blood:
42	chr8:53572459..53576424-chr8:53576772..53581609,5	K562	blood:
43	chr8:53610826..53614248-chr8:53624819..53626954,3	MCF-7	breast:
44	chr8:53607539..53609203-chr8:53611083..53613444,2	K562	blood:
45	chr8:53649723..53650709-chr8:53861922..53862952,3	MCF-7	breast:
46	chr8:53627614..53630487-chr8:53664001..53666801,2	K562	blood:
47	chr8:53598610..53601005-chr8:53615440..53617848,2	MCF-7	breast:
48	chr8:53608310..53609817-chr8:53611710..53613536,2	K562	blood:
49	chr8:53601514..53605844-chr8:53607755..53610588,4	K562	blood:
50	chr8:53615440..53617336-chr8:53625360..53626968,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM150A-3	chr8:53599506-53599527	NONHSAT126570
2	lnc-NPBWR1-2	chr8:53635463-53635701	ENSG00000271555.1
3	lnc-NPBWR1-4	chr8:53627118-53631645	NONHSAT126571
4	lnc-FAM150A-3	chr8:53535889-53536031	NONHSAT126570
5	lnc-FAM150A-3	chr8:53626635-53626997	NONHSAT126570

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	RB1CC1	hsa-miR-133b	chr8:53536089-53536082
2	RB1CC1	hsa-miR-375	chr8:53535552-53535573
3	RB1CC1	hsa-miR-133b	chr8:53536083-53536106
4	RB1CC1	hsa-miR-375	chr8:53535026-53535047

Variant related genes	Relation type
RB1CC1	TF binding region
ENSG00000271555	TF binding region
RB1CC1	CpG island
ENSG00000271555	CpG island
ENSG00000187735	chromatin interactions
ENSG00000129521	chromatin interactions
ENSG00000271555	chromatin interactions
ENSG00000197147	chromatin interactions
ENSG00000168010	chromatin interactions
ENSG00000136653	chromatin interactions
ENSG00000181222	chromatin interactions
ENSG00000225855	chromatin interactions
ENSG00000132680	chromatin interactions
ENSG00000047249	chromatin interactions
ENSG00000183729	chromatin interactions
ENSG00000131143	chromatin interactions
ENSG00000160753	chromatin interactions
ENSG00000023287	chromatin interactions
ENSG00000174282	chromatin interactions

Extended variants
information (count: 9191 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:9191 , 50 per page) page: 1 2 3 4 5 6 7 ... 184

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562101676	chr8:53488193-53488194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs529288055	chr8:53488211-53488212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs547399091	chr8:53488212-53488213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs7826532	chr8:53488242-53488243	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs532995188	chr8:53488243-53488244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs552147540	chr8:53488246-53488247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs569512496	chr8:53488330-53488331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147156549	chr8:53488372-53488373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs555029954	chr8:53488388-53488389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs7826811	chr8:53488391-53488392	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs534582550	chr8:53488584-53488585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs554183477	chr8:53488624-53488625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs111742068	chr8:53488653-53488654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs572658368	chr8:53488721-53488722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs546083267	chr8:53488729-53488730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537452301	chr8:53488801-53488802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs139518891	chr8:53488805-53488806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576698533	chr8:53488823-53488824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs543966916	chr8:53488828-53488829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs184651286	chr8:53488866-53488867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs554815584	chr8:53488867-53488868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529323392	chr8:53488989-53488990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541376573	chr8:53489060-53489061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188318474	chr8:53489097-53489098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs533306861	chr8:53489152-53489153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs551378045	chr8:53489201-53489202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs574810502	chr8:53489247-53489248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs569549327	chr8:53489285-53489286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs10559969	chr8:53489344-53489345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs71551910	chr8:53489345-53489346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539672261	chr8:53489347-53489348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs554101742	chr8:53489384-53489385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73593396	chr8:53489429-53489430	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs566987957	chr8:53489449-53489450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs374286020	chr8:53489471-53489472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs79838702	chr8:53489524-53489525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192708076	chr8:53489543-53489544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs546025182	chr8:53489616-53489617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs571152657	chr8:53489666-53489667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs540165072	chr8:53489697-53489698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs563005689	chr8:53489713-53489714	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184785213	chr8:53489722-53489723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576455109	chr8:53489817-53489818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs145470410	chr8:53489915-53489916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs563417631	chr8:53490104-53490105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs4416838	chr8:53490186-53490187	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs148411479	chr8:53490195-53490196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs74473802	chr8:53490215-53490216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561130234	chr8:53490244-53490245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559739967	chr8:53490248-53490249	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
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
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	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
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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Uveal melanoma	20484589	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	21215367	CNVD
Colorectal cancer	21645411	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Gastric cancer	22014070	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21785460	CNVD

Chromatin state (count:4026 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:53487800-53490800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr8:53488600-53489400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr8:53489400-53490800	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr8:53490200-53490800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:53490400-53490800	Enhancers	HMEC	breast
6	chr8:53490400-53491000	Enhancers	Liver	Liver
7	chr8:53490600-53490800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr8:53490600-53490800	Flanking Active TSS	A549	lung
9	chr8:53490600-53490800	Flanking Active TSS	NHLF	lung
10	chr8:53490600-53491000	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr8:53490800-53492000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr8:53492200-53492400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr8:53498600-53499000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr8:53498800-53499600	Active TSS	Stomach Smooth Muscle	stomach
15	chr8:53499000-53502200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr8:53499600-53499800	Weak transcription	Stomach Smooth Muscle	stomach
17	chr8:53499600-53500000	Bivalent Enhancer	Fetal Stomach	stomach
18	chr8:53499600-53500200	Enhancers	Colon Smooth Muscle	Colon
19	chr8:53499600-53500200	Enhancers	Rectal Smooth Muscle	rectum
20	chr8:53499800-53500200	Enhancers	Stomach Smooth Muscle	stomach
21	chr8:53502000-53502200	Enhancers	H1 Cell Line	embryonic stem cell
22	chr8:53502000-53502200	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr8:53502000-53503600	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr8:53502000-53503600	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr8:53502200-53502400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
26	chr8:53502200-53502400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr8:53502200-53502600	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr8:53502200-53502600	Flanking Active TSS	H1 Cell Line	embryonic stem cell
29	chr8:53502200-53502600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr8:53502200-53502600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr8:53502200-53502600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr8:53502200-53502800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr8:53502200-53502800	Enhancers	H9 Cell Line	embryonic stem cell
34	chr8:53502200-53502800	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr8:53502200-53502800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr8:53502200-53503000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr8:53502200-53503800	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr8:53502400-53502600	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr8:53502400-53502600	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr8:53502400-53503000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr8:53502600-53502800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr8:53502600-53503000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
43	chr8:53502600-53514800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr8:53502800-53503600	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr8:53505200-53505400	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr8:53505400-53508400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr8:53508200-53508600	Enhancers	HepG2	liver
48	chr8:53508200-53509800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr8:53508400-53508800	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr8:53508800-53509200	Enhancers	Ovary	ovary

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