Variant report

Variant	nsv590233
Chromosome Location	chr3:47798700-47829277
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1060)
CpG islands
(count:1039)
Chromatin interactive
region (count:61)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1060 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:47802732-47802844	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:47823180-47823697	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:47821421-47821618	K562	blood:	n/a	n/a
4	ARID3A	chr3:47803679-47804149	K562	blood:	n/a	n/a
5	ARID3A	chr3:47824522-47824674	K562	blood:	n/a	n/a
6	ATF1	chr3:47803757-47804142	K562	blood:	n/a	n/a
7	ATF2	chr3:47823379-47824042	GM12878	blood:	n/a	n/a
8	ATF2	chr3:47823224-47824309	GM12878	blood:	n/a	n/a
9	ATF2	chr3:47823353-47823818	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr3:47803657-47804193	K562	blood:	n/a	n/a
11	BACH1	chr3:47822846-47823713	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr3:47823495-47823776	GM12878	blood:	n/a	n/a
13	BATF	chr3:47823375-47824031	GM12878	blood:	n/a	n/a
14	BCL11A	chr3:47823503-47823789	GM12878	blood:	n/a	n/a
15	BCL11A	chr3:47823445-47823916	GM12878	blood:	n/a	n/a
16	BCL3	chr3:47823164-47824010	GM12878	blood:	n/a	n/a
17	BCL3	chr3:47823281-47823798	A549	lung:	n/a	n/a
18	BCLAF1	chr3:47822671-47824083	GM12878	blood:	n/a	n/a
19	BCLAF1	chr3:47821285-47821812	GM12878	blood:	n/a	chr3:47821556-47821565
20	BHLHE40	chr3:47819410-47819570	GM12878	blood:	n/a	n/a
21	BHLHE40	chr3:47822804-47823739	HepG2	liver:	n/a	chr3:47823032-47823048
22	BHLHE40	chr3:47824471-47824790	GM12878	blood:	n/a	n/a
23	BHLHE40	chr3:47822472-47823929	K562	blood:	n/a	chr3:47823032-47823048
24	BHLHE40	chr3:47819897-47820060	GM12878	blood:	n/a	n/a
25	BHLHE40	chr3:47803848-47804062	K562	blood:	n/a	n/a
26	BHLHE40	chr3:47822141-47824170	GM12878	blood:	n/a	chr3:47823032-47823048
27	BHLHE40	chr3:47821488-47821702	GM12878	blood:	n/a	n/a
28	BRCA1	chr3:47821939-47822883	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr3:47823134-47823621	HepG2	liver:	n/a	n/a
30	BRCA1	chr3:47823134-47823695	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr3:47823123-47823740	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr3:47823030-47823762	GM12878	blood:	n/a	n/a
33	CBX3	chr3:47821788-47822211	K562	blood:	n/a	n/a
34	CBX3	chr3:47803625-47804188	K562	blood:	n/a	n/a
35	CBX3	chr3:47823147-47824694	K562	blood:	n/a	n/a
36	CCNT2	chr3:47803778-47804129	K562	blood:	n/a	n/a
37	CCNT2	chr3:47822656-47823958	K562	blood:	n/a	chr3:47823002-47823011
38	CEBPB	chr3:47815817-47816018	K562	blood:	n/a	chr3:47815963-47815974
39	CEBPB	chr3:47824247-47824583	K562	blood:	n/a	n/a
40	CEBPB	chr3:47799864-47800093	MCF-7	breast:	n/a	n/a
41	CEBPB	chr3:47823315-47824715	GM12878	blood:	n/a	n/a
42	CEBPB	chr3:47815841-47816076	HepG2	liver:	n/a	chr3:47815963-47815974
43	CEBPB	chr3:47821639-47822233	K562	blood:	n/a	n/a
44	CEBPB	chr3:47799897-47800058	K562	blood:	n/a	n/a
45	CEBPB	chr3:47799859-47800049	HepG2	liver:	n/a	n/a
46	CEBPB	chr3:47824227-47824577	K562	blood:	n/a	n/a
47	CEBPB	chr3:47803733-47804207	K562	blood:	n/a	n/a
48	CEBPB	chr3:47803804-47804050	K562	blood:	n/a	n/a
49	CEBPB	chr3:47815958-47815996	A549	lung:	n/a	chr3:47815963-47815974
50	CEBPB	chr3:47815891-47816079	IMR90	lung:	n/a	chr3:47815963-47815974

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:47823067-47823117	AG09309	skin:	n/a
2	chr3:47823067-47823117	HRCEpiC	kidney:	n/a
3	chr3:47823067-47823117	AG09309	skin:	n/a
4	chr3:47823067-47823117	HRCEpiC	kidney:	n/a
5	chr3:47823067-47823117	HIPEpiC	eye:	n/a
6	chr3:47823638-47823688	GM06990	blood:	n/a
7	chr3:47825578-47825628	SKMC	muscle:	n/a
8	chr3:47823638-47823688	SK-N-MC	brain:	n/a
9	chr3:47827617-47827667	GM12878	blood:	n/a
10	chr3:47823121-47823171	HPAEpiC	pulmonary alveolar:	n/a
11	chr3:47823560-47823610	HRE	kidney:	n/a
12	chr3:47823674-47823724	T-47D	breast:	n/a
13	chr3:47823423-47823473	BJ	skin:	n/a
14	chr3:47823291-47823341	U87	brain:	n/a
15	chr3:47823524-47823574	ovcar-3	ovarian:	n/a
16	chr3:47823614-47823664	HCF	heart:	n/a
17	chr3:47821924-47821974	AG09309	skin:	n/a
18	chr3:47820852-47820902	U87	brain:	n/a
19	chr3:47823291-47823341	RPTEC	kidney:	n/a
20	chr3:47823531-47823581	PFSK-1	brain:	n/a
21	chr3:47823531-47823581	U87	brain:	n/a
22	chr3:47823560-47823610	PrEC	prostate:	n/a
23	chr3:47823524-47823574	ProgFib	skin:	n/a
24	chr3:47823995-47824045	ProgFib	skin:	n/a
25	chr3:47823674-47823724	HCPEpiC	choroid plexus:	n/a
26	chr3:47823614-47823664	BJ	skin:	n/a
27	chr3:47823291-47823341	HRCEpiC	kidney:	n/a
28	chr3:47823423-47823473	GM06990	blood:	n/a
29	chr3:47823531-47823581	SKMC	muscle:	n/a
30	chr3:47821924-47821974	SK-N-SH	brain:	n/a
31	chr3:47827617-47827667	HUVEC	blood vessel:	n/a
32	chr3:47820852-47820902	CMK	blood:	n/a
33	chr3:47821924-47821974	HEEpiC	esophagus:	n/a
34	chr3:47823291-47823341	HIPEpiC	eye:	n/a
35	chr3:47823291-47823341	HEEpiC	esophagus:	n/a
36	chr3:47821224-47821274	K562	blood:	n/a
37	chr3:47821924-47821974	K562	blood:	n/a
38	chr3:47823524-47823574	ECC-1	luminal epithelium:	n/a
39	chr3:47820852-47820902	HCPEpiC	choroid plexus:	n/a
40	chr3:47823423-47823473	AG04449	skin:	fetal
41	chr3:47823560-47823610	SAEC	small airway:	n/a
42	chr3:47823614-47823664	GM12892	blood:	n/a
43	chr3:47823638-47823688	HIPEpiC	eye:	n/a
44	chr3:47823560-47823610	SKMC	muscle:	n/a
45	chr3:47823291-47823341	NHBE	bronchial:	n/a
46	chr3:47823067-47823117	SKMC	muscle:	n/a
47	chr3:47823638-47823688	SKMC	muscle:	n/a
48	chr3:47823638-47823688	NB4	blood:	n/a
49	chr3:47823614-47823664	AG04449	skin:	fetal
50	chr3:47823674-47823724	Hela-S3	cervix:	n/a

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:47807190..47809534-chr3:47813516..47815766,2	K562	blood:
2	chr3:47819996..47824833-chr3:47866390..47869916,6	K562	blood:
3	chr3:47579787..47581854-chr3:47822138..47824570,2	K562	blood:
4	chr3:47809506..47818715-chr3:47820075..47824996,15	MCF-7	breast:
5	chr3:47582862..47584388-chr3:47823797..47825986,2	K562	blood:
6	chr3:47821651..47823502-chr3:172427414..172429681,2	MCF-7	breast:
7	chr3:47765075..47767679-chr3:47818543..47820695,2	K562	blood:
8	chr3:47821442..47824826-chr3:47842672..47846080,5	MCF-7	breast:
9	chr3:47139097..47140627-chr3:47822792..47824576,2	K562	blood:
10	chr3:47821496..47825290-chr3:47843622..47845759,4	MCF-7	breast:
11	chr3:47827524..47829723-chr3:47850586..47853080,2	K562	blood:
12	chr3:47783474..47786163-chr3:47820894..47822857,2	MCF-7	breast:
13	chr3:47823164..47824038-chr3:187871696..187872523,2	Hela-S3	cervix:
14	chr3:47553771..47557534-chr3:47822005..47824702,4	K562	blood:
15	chr3:47822503..47823283-chr9:96928496..96929478,2	Hela-S3	cervix:
16	chr3:47808223..47811235-chr3:47813033..47816575,4	MCF-7	breast:
17	chr3:47821014..47824119-chr3:47842599..47847365,10	K562	blood:
18	chr20:49346523..49348276-chr3:47822543..47824569,2	MCF-7	breast:
19	chr3:47801338..47803180-chr3:47822974..47824547,2	K562	blood:
20	chr3:47799964..47802084-chr3:47803507..47806480,3	K562	blood:
21	chr3:47822834..47823428-chr9:115479877..115480684,2	Hela-S3	cervix:
22	chr3:47787198..47789332-chr3:47822441..47824997,2	K562	blood:
23	chr3:47819746..47821257-chr3:47823167..47825022,2	MCF-7	breast:
24	chr3:47807190..47809534-chr3:47813516..47815766,2	K562	blood:
25	chr3:47819738..47825460-chr3:47843094..47847845,6	K562	blood:
26	chr3:47775553..47777861-chr3:47823812..47825481,2	K562	blood:
27	chr3:47822067..47822622-chr5:131825519..131826350,2	Hela-S3	cervix:
28	chr3:47799964..47802084-chr3:47803507..47806480,3	K562	blood:
29	chr3:47823020..47823962-chr6:43597169..43598056,2	Hela-S3	cervix:
30	chr3:47803418..47807540-chr3:47810492..47813252,3	MCF-7	breast:
31	chr3:47555986..47558236-chr3:47820565..47823335,2	MCF-7	breast:
32	chr3:47820608..47822821-chr3:47870608..47873437,2	K562	blood:
33	chr3:47809807..47812260-chr3:47814251..47817184,2	K562	blood:
34	chr2:10262084..10262617-chr3:47822855..47823557,2	Hela-S3	cervix:
35	chr3:47821493..47825300-chr3:47828979..47831183,6	K562	blood:
36	chr3:47807226..47809643-chr3:47821048..47823302,2	MCF-7	breast:
37	chr3:47821721..47824833-chr3:47865723..47867890,4	K562	blood:
38	chr3:47555068..47558623-chr3:47821026..47823771,5	K562	blood:
39	chr3:47017679..47019433-chr3:47821354..47822860,2	K562	blood:
40	chr3:47807226..47809643-chr3:47821048..47823302,2	MCF-7	breast:
41	chr3:47812305..47815018-chr3:47821120..47824532,4	MCF-7	breast:
42	chr15:45878972..45879914-chr3:47822992..47823712,2	Hela-S3	cervix:
43	chr3:47562617..47565330-chr3:47829264..47832654,4	MCF-7	breast:
44	chr3:47803866..47805515-chr3:47821094..47823324,2	K562	blood:
45	chr3:47617723..47621182-chr3:47821900..47825077,3	MCF-7	breast:
46	chr3:47555041..47556961-chr3:47821638..47825112,3	MCF-7	breast:
47	chr1:110527265..110527945-chr3:47823077..47824066,2	Hela-S3	cervix:
48	chr3:47587613..47590274-chr3:47819316..47821047,2	K562	blood:
49	chr3:47803866..47805515-chr3:47821094..47823324,2	K562	blood:
50	chr3:47798148..47800331-chr3:47801413..47803600,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000266457	TF binding region
SMARCC1	TF binding region
ENSG00000266457	CpG island
SMARCC1	CpG island
ENSG00000173473	chromatin interactions
ENSG00000145012	chromatin interactions
ENSG00000266443	chromatin interactions
ENSG00000029363	chromatin interactions
ENSG00000270959	chromatin interactions
ENSG00000163832	chromatin interactions
ENSG00000114646	chromatin interactions
ENSG00000124171	chromatin interactions
ENSG00000181555	chromatin interactions
ENSG00000132153	chromatin interactions
ENSG00000124688	chromatin interactions
ENSG00000160799	chromatin interactions
ENSG00000148153	chromatin interactions
ENSG00000227036	chromatin interactions
ENSG00000144959	chromatin interactions
ENSG00000104164	chromatin interactions
ENSG00000125347	chromatin interactions
ENSG00000168710	chromatin interactions
ENSG00000266457	chromatin interactions
ENSG00000260170	chromatin interactions
ENSG00000269946	chromatin interactions
ENSG00000171848	chromatin interactions
ENSG00000081791	chromatin interactions

Extended variants
information (count: 1091 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1091 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9811453	chr3:47798700-47798701	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs190758800	chr3:47798741-47798742	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs572763484	chr3:47798762-47798763	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs111679482	chr3:47798778-47798779	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs182925897	chr3:47798934-47798935	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187222775	chr3:47798955-47798956	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs574272358	chr3:47799000-47799001	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192088255	chr3:47799101-47799102	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs149006296	chr3:47799107-47799108	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs578109508	chr3:47799118-47799119	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545182251	chr3:47799126-47799127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552399934	chr3:47799166-47799167	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs527711846	chr3:47799188-47799189	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540504060	chr3:47799223-47799224	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561874119	chr3:47799228-47799229	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529050502	chr3:47799231-47799232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs143779799	chr3:47799252-47799253	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568718686	chr3:47799261-47799262	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374548060	chr3:47799273-47799274	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs60788109	chr3:47799289-47799290	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532828177	chr3:47799347-47799348	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs551208293	chr3:47799386-47799387	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532048407	chr3:47799401-47799402	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533588604	chr3:47799425-47799426	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs570948787	chr3:47799489-47799490	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs556019482	chr3:47799497-47799498	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs568009966	chr3:47799532-47799533	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538879738	chr3:47799596-47799597	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs111562325	chr3:47799621-47799622	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557169162	chr3:47799662-47799663	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs538542725	chr3:47799673-47799674	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs138465986	chr3:47799685-47799686	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs7637950	chr3:47799694-47799695	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs545461315	chr3:47799702-47799703	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs531926405	chr3:47799734-47799735	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs554007200	chr3:47799841-47799842	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572395429	chr3:47799868-47799869	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs542701802	chr3:47799875-47799876	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs71070227	chr3:47799877-47799878	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs112295334	chr3:47799900-47799901	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs78841252	chr3:47799918-47799919	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529110141	chr3:47799921-47799922	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs544113359	chr3:47799945-47799946	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs55823596	chr3:47800031-47800032	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs533010173	chr3:47800048-47800049	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs551443851	chr3:47800075-47800076	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs566489021	chr3:47800081-47800082	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs182684943	chr3:47800085-47800086	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs78866407	chr3:47800108-47800109	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs143547469	chr3:47800212-47800213	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1351 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:47701600-47800400	Strong transcription	Dnd41	blood
2	chr3:47701600-47819800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr3:47727600-47819400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr3:47769600-47812400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr3:47769800-47817800	Weak transcription	Pancreas	Pancrea
6	chr3:47772800-47821000	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr3:47774200-47799000	Weak transcription	NHEK	skin
8	chr3:47774200-47820600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr3:47777000-47817600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr3:47777200-47801400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr3:47777200-47805200	Weak transcription	Esophagus	oesophagus
12	chr3:47777200-47812400	Weak transcription	Brain Hippocampus Middle	brain
13	chr3:47777200-47813600	Weak transcription	A549	lung
14	chr3:47777200-47819000	Weak transcription	Fetal Brain Male	brain
15	chr3:47777200-47819800	Weak transcription	Small Intestine	intestine
16	chr3:47777400-47799600	Weak transcription	Spleen	Spleen
17	chr3:47777400-47802000	Weak transcription	Aorta	Aorta
18	chr3:47777400-47805400	Weak transcription	Gastric	stomach
19	chr3:47777400-47805600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr3:47777400-47812600	Weak transcription	Colon Smooth Muscle	Colon
21	chr3:47777400-47819800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr3:47777400-47821000	Weak transcription	Brain Cingulate Gyrus	brain
23	chr3:47777400-47821000	Weak transcription	Brain Substantia Nigra	brain
24	chr3:47777400-47821800	Weak transcription	Right Ventricle	heart
25	chr3:47777600-47812800	Weak transcription	NHDF-Ad	bronchial
26	chr3:47777600-47820600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr3:47777600-47820800	Weak transcription	NHLF	lung
28	chr3:47777800-47802000	Weak transcription	Fetal Kidney	kidney
29	chr3:47778800-47805400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr3:47778800-47814200	Weak transcription	Rectal Smooth Muscle	rectum
31	chr3:47781200-47802600	Weak transcription	Ovary	ovary
32	chr3:47784000-47816000	Strong transcription	Fetal Stomach	stomach
33	chr3:47784400-47811800	Weak transcription	Left Ventricle	heart
34	chr3:47784800-47799400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr3:47784800-47820800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr3:47785200-47805400	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr3:47785600-47803600	Weak transcription	Fetal Heart	heart
38	chr3:47786400-47805400	Weak transcription	Stomach Smooth Muscle	stomach
39	chr3:47786600-47805000	Weak transcription	HMEC	breast
40	chr3:47786600-47814200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr3:47787200-47801800	Weak transcription	Fetal Lung	lung
42	chr3:47787200-47808200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr3:47787200-47811000	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr3:47787400-47801400	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr3:47787400-47805400	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr3:47787400-47808000	Weak transcription	Adipose Nuclei	Adipose
47	chr3:47787400-47811800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr3:47787400-47812600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr3:47787400-47820800	Weak transcription	Brain Angular Gyrus	brain
50	chr3:47787600-47805600	Weak transcription	Primary hematopoietic stem cells	blood

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