Variant report

Variant	nsv879505
Chromosome Location	chr4:79887043-80293046
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2545)
CpG islands
(count:1284)
Chromatin interactive
region (count:97)
LncRNA
region (count:56)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2545 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:80137484-80137627	K562	blood:	n/a	n/a
2	ARID3A	chr4:80252423-80252604	K562	blood:	n/a	n/a
3	ARID3A	chr4:79946392-79946697	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:79963283-79963590	K562	blood:	n/a	n/a
5	ARID3A	chr4:80273490-80274890	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:80134780-80135117	K562	blood:	n/a	n/a
7	ARID3A	chr4:79963365-79963515	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:80132360-80133178	K562	blood:	n/a	n/a
9	ARID3A	chr4:80215223-80215720	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:80131117-80132132	K562	blood:	n/a	n/a
11	ARID3A	chr4:80146546-80146807	K562	blood:	n/a	n/a
12	ARID3A	chr4:80133611-80134555	K562	blood:	n/a	n/a
13	ARID3A	chr4:80119960-80120407	K562	blood:	n/a	n/a
14	ARID3A	chr4:80014814-80014884	K562	blood:	n/a	n/a
15	ATF1	chr4:80132469-80132933	K562	blood:	n/a	n/a
16	ATF1	chr4:80252450-80252692	K562	blood:	n/a	n/a
17	ATF1	chr4:80273388-80274894	K562	blood:	n/a	n/a
18	ATF1	chr4:80120027-80120648	K562	blood:	n/a	n/a
19	ATF1	chr4:80247086-80247400	K562	blood:	n/a	n/a
20	ATF1	chr4:80131154-80131695	K562	blood:	n/a	n/a
21	ATF1	chr4:80096662-80096856	K562	blood:	n/a	n/a
22	ATF2	chr4:80098428-80099006	GM12878	blood:	n/a	n/a
23	ATF2	chr4:80103408-80103743	GM12878	blood:	n/a	n/a
24	ATF2	chr4:80085071-80085548	GM12878	blood:	n/a	n/a
25	ATF2	chr4:80091185-80091615	GM12878	blood:	n/a	n/a
26	ATF2	chr4:80098415-80098967	GM12878	blood:	n/a	n/a
27	ATF2	chr4:80091193-80091628	GM12878	blood:	n/a	n/a
28	ATF3	chr4:80119950-80120391	K562	blood:	n/a	n/a
29	ATF3	chr4:80274370-80274695	HepG2	liver:	n/a	n/a
30	ATF3	chr4:80131338-80131528	K562	blood:	n/a	n/a
31	ATF3	chr4:80273388-80274887	K562	blood:	n/a	n/a
32	BACH1	chr4:80138195-80138482	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr4:79948958-79949016	K562	blood:	n/a	n/a
34	BACH1	chr4:80004620-80004896	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr4:80228375-80228565	K562	blood:	n/a	n/a
36	BACH1	chr4:80274154-80274894	K562	blood:	n/a	n/a
37	BATF	chr4:80085130-80085526	GM12878	blood:	n/a	chr4:80085140-80085149 chr4:80085294-80085305
38	BATF	chr4:80273420-80274218	GM12878	blood:	n/a	n/a
39	BATF	chr4:80157752-80158023	GM12878	blood:	n/a	n/a
40	BATF	chr4:80103384-80103619	GM12878	blood:	n/a	chr4:80103484-80103495
41	BATF	chr4:80085167-80085489	GM12878	blood:	n/a	chr4:80085294-80085305
42	BATF	chr4:80213221-80213393	GM12878	blood:	n/a	n/a
43	BATF	chr4:80098563-80098841	GM12878	blood:	n/a	chr4:80098707-80098718
44	BATF	chr4:80273590-80273972	GM12878	blood:	n/a	n/a
45	BATF	chr4:80213169-80213498	GM12878	blood:	n/a	n/a
46	BATF	chr4:80098516-80098835	GM12878	blood:	n/a	chr4:80098707-80098718
47	BATF	chr4:79999738-79999918	GM12878	blood:	n/a	n/a
48	BCL11A	chr4:80098574-80098811	GM12878	blood:	n/a	n/a
49	BCL11A	chr4:80259355-80259631	GM12878	blood:	n/a	chr4:80259451-80259460
50	BCL11A	chr4:80273428-80273908	GM12878	blood:	n/a	n/a

(count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:80004287-80004337	GM12878	blood:	n/a
2	chr4:80247217-80247267	GM19239	blood:	n/a
3	chr4:80203299-80203349	BE2_C	brain:	n/a
4	chr4:80004287-80004337	GM12878	blood:	n/a
5	chr4:80247217-80247267	GM19239	blood:	n/a
6	chr4:80203299-80203349	BE2_C	brain:	n/a
7	chr4:80243325-80243375	SK-N-SH	brain:	n/a
8	chr4:79971432-79971482	GM12892	blood:	n/a
9	chr4:80247281-80247331	H1-hESC	embryonic stem cell:	embryo
10	chr4:80246899-80246949	BJ	skin:	n/a
11	chr4:80246899-80246949	HCF	heart:	n/a
12	chr4:80247171-80247221	HCT-116	colon:	n/a
13	chr4:80247271-80247321	ProgFib	skin:	n/a
14	chr4:80246899-80246949	SK-N-MC	brain:	n/a
15	chr4:79971408-79971458	NT2-D1	testis:	n/a
16	chr4:80247171-80247221	AG09319	gingival:	n/a
17	chr4:80138126-80138176	CMK	blood:	n/a
18	chr4:80247179-80247229	Caco-2	colon:	n/a
19	chr4:80247524-80247574	PFSK-1	brain:	n/a
20	chr4:79971177-79971227	PFSK-1	brain:	n/a
21	chr4:79971462-79971512	PANC-1	pancreas:	n/a
22	chr4:80166298-80166348	HEEpiC	esophagus:	n/a
23	chr4:80243325-80243375	HEEpiC	esophagus:	n/a
24	chr4:80243325-80243375	NH-A	brain:	n/a
25	chr4:80138126-80138176	GM12892	blood:	n/a
26	chr4:80243325-80243375	SK-N-MC	brain:	n/a
27	chr4:79971408-79971458	PFSK-1	brain:	n/a
28	chr4:80243325-80243375	HRCEpiC	kidney:	n/a
29	chr4:80138126-80138176	PrEC	prostate:	n/a
30	chr4:79971177-79971227	AG09309	skin:	n/a
31	chr4:80246713-80246763	NHBE	bronchial:	n/a
32	chr4:79971235-79971285	AG10803	skin:	n/a
33	chr4:80138126-80138176	BE2_C	brain:	n/a
34	chr4:80246899-80246949	BE2_C	brain:	n/a
35	chr4:80246713-80246763	IMR90	lung:	fetal
36	chr4:80247524-80247574	HMEC	breast:	n/a
37	chr4:79891402-79891452	SK-N-MC	brain:	n/a
38	chr4:80203299-80203349	HCM	heart:	n/a
39	chr4:80138126-80138176	Caco-2	colon:	n/a
40	chr4:80243325-80243375	ProgFib	skin:	n/a
41	chr4:79971462-79971512	HCPEpiC	choroid plexus:	n/a
42	chr4:79971408-79971458	AG04449	skin:	fetal
43	chr4:80247217-80247267	IMR90	lung:	fetal
44	chr4:80166298-80166348	H1-hESC	embryonic stem cell:	embryo
45	chr4:79971408-79971458	HCM	heart:	n/a
46	chr4:80138126-80138176	IMR90	lung:	fetal
47	chr4:79971177-79971227	GM12891	blood:	n/a
48	chr4:79971235-79971285	Jurkat	blood:	n/a
49	chr4:79971462-79971512	T-47D	breast:	n/a
50	chr4:80246713-80246763	HRE	kidney:	n/a

(count:97 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:80227909..80229912-chr4:80235316..80237436,2	K562	blood:
2	chr4:80162418..80164734-chr4:80169603..80171885,2	K562	blood:
3	chr4:80169525..80172231-chr4:80176265..80177995,2	K562	blood:
4	chr4:80152607..80154450-chr4:80154654..80156454,2	K562	blood:
5	chr4:79959121..79962093-chr4:79967361..79969057,2	K562	blood:
6	chr4:79963329..79963907-chr4:80497328..80498247,2	K562	blood:
7	chr4:80208255..80210046-chr4:80212366..80215215,2	K562	blood:
8	chr4:80162418..80164734-chr4:80169603..80171885,2	K562	blood:
9	chr4:80122838..80125677-chr4:80129112..80131710,3	K562	blood:
10	chr4:79944609..79947579-chr4:79951684..79954668,2	K562	blood:
11	chr4:79963311..79963867-chr4:80497354..80497886,2	MCF-7	breast:
12	chr4:80103781..80106633-chr4:80109334..80111501,3	K562	blood:
13	chr4:80277590..80280070-chr4:80281677..80284459,2	K562	blood:
14	chr4:79963103..79964922-chr4:79966258..79968873,2	K562	blood:
15	chr4:80223511..80225551-chr4:80241282..80243094,2	K562	blood:
16	chr4:80134202..80136141-chr4:80140133..80142135,2	K562	blood:
17	chr4:80148564..80150117-chr4:80152749..80155436,2	K562	blood:
18	chr4:80163067..80163617-chr4:80497361..80497863,2	MCF-7	breast:
19	chr4:80152607..80154450-chr4:80154654..80156454,2	K562	blood:
20	chr4:79906212..79908512-chr4:79912830..79915570,2	K562	blood:
21	chr4:80126178..80129035-chr4:80131457..80134013,3	K562	blood:
22	chr4:79959717..79962130-chr4:79962284..79964886,2	K562	blood:
23	chr4:80232851..80234372-chr4:80234440..80236664,2	K562	blood:
24	chr4:79963314..79963869-chr4:80218868..80219372,2	K562	blood:
25	chr4:79959121..79962093-chr4:79967361..79969057,2	K562	blood:
26	chr4:80119166..80122635-chr4:80123196..80126603,4	K562	blood:
27	chr4:80256204..80257804-chr4:80261590..80263826,2	K562	blood:
28	chr4:80119134..80120875-chr4:80131892..80134221,2	K562	blood:
29	chr4:80129511..80131347-chr4:80133541..80135090,2	K562	blood:
30	chr4:80148564..80151434-chr4:80151473..80154249,2	K562	blood:
31	chr4:79998907..80000572-chr4:80006530..80008071,2	K562	blood:
32	chr4:80137428..80140426-chr4:80156226..80159142,2	K562	blood:
33	chr4:80241626..80244306-chr4:80246795..80249112,2	K562	blood:
34	chr4:80130065..80132388-chr4:80165360..80168173,2	K562	blood:
35	chr4:80002356..80003863-chr4:80013961..80016777,2	K562	blood:
36	chr4:79998907..80000572-chr4:80006530..80008071,2	K562	blood:
37	chr4:79959717..79962130-chr4:79962284..79964886,2	K562	blood:
38	chr4:79962952..79963679-chr4:81105091..81105941,3	MCF-7	breast:
39	chr1:28974942..28975673-chr4:80186406..80186906,3	Hela-S3	cervix:
40	chr4:79944609..79947579-chr4:79951684..79954668,2	K562	blood:
41	chr4:80053807..80054491-chr8:125501594..125502544,2	MCF-7	breast:
42	chr16:33957128..33958102-chr4:80274126..80274833,2	MCF-7	breast:
43	chr4:80133076..80134964-chr4:100869138..100871543,2	K562	blood:
44	chr4:80169525..80172231-chr4:80176265..80177995,2	K562	blood:
45	chr4:80148564..80151434-chr4:80151473..80154249,2	K562	blood:
46	chr4:80126283..80129035-chr4:80131457..80134013,2	K562	blood:
47	chr4:79963382..79963898-chr4:80312179..80313004,2	K562	blood:
48	chr4:80281030..80283740-chr4:80487916..80490045,2	K562	blood:
49	chr4:79875322..79875845-chr4:79962992..79963610,2	MCF-7	breast:
50	chr4:79943664..79946142-chr9:83452129..83453630,2	MCF-7	breast:

(count:56 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BMP2K-1	chr4:80006393-80006501	ENSG00000249307.1
2	lnc-BMP2K-1	chr4:79894154-79894206	ENSG00000249307.1
3	lnc-BMP2K-1	chr4:80227845-80227882	ENSG00000249307.1
4	lnc-BMP2K-1	chr4:80132839-80132958	ENSG00000249307.1
5	lnc-BMP2K-1	chr4:80116990-80117086	ENSG00000249307.1
6	lnc-BMP2K-1	chr4:80116990-80117086	NONHSAT097098
7	lnc-BMP2K-1	chr4:80227845-80227882	ENSG00000249307.1
8	lnc-BMP2K-1	chr4:80031166-80031247	NONHSAT097101
9	lnc-BMP2K-1	chr4:80225375-80225525	l_2674_chr4:80088967-80336103_prostate
10	lnc-BMP2K-1	chr4:80229427-80229809	ENSG00000249307.1
11	lnc-BMP2K-7	chr4:80292624-80292696	NONHSAT097111
12	lnc-BMP2K-1	chr4:79894154-79894206	NONHSAT097098
13	lnc-BMP2K-1	chr4:79892902-79893030	NONHSAT097098
14	lnc-BMP2K-1	chr4:80226277-80226336	ENSG00000249307.1
15	lnc-BMP2K-1	chr4:80250190-80250247	l_2674_chr4:80088967-80336103_prostate
16	lnc-BMP2K-1	chr4:80148366-80149110	ENSG00000249307.1
17	lnc-BMP2K-1	chr4:80126100-80126506	l_2674_chr4:80088967-80336103_prostate
18	lnc-BMP2K-1	chr4:80111678-80112054	l_2674_chr4:80088967-80336103_prostate
19	lnc-BMP2K-1	chr4:80227845-80227882	ENSG00000249307.1
20	lnc-BMP2K-1	chr4:80227845-80227882	ENSG00000249307.1
21	lnc-BMP2K-1	chr4:80116991-80117086	ENSG00000249307.1
22	lnc-BMP2K-1	chr4:80227845-80227882	ENSG00000249307.1
23	lnc-BMP2K-1	chr4:80088968-80089050	l_2674_chr4:80088967-80336103_prostate
24	lnc-BMP2K-1	chr4:80227845-80227882	ENSG00000249307.1
25	lnc-BMP2K-1	chr4:80179935-80180193	ENSG00000249307.1
26	lnc-BMP2K-1	chr4:80116988-80117086	ENSG00000249307.1
27	lnc-BMP2K-1	chr4:80118695-80118798	ENSG00000249307.1
28	lnc-BMP2K-1	chr4:80116990-80117086	ENSG00000249307.1
29	lnc-BMP2K-1	chr4:80227845-80227882	ENSG00000249307.1
30	lnc-BMP2K-1	chr4:80228218-80228385	ENSG00000249307.1
31	lnc-BMP2K-1	chr4:80007244-80007416	NONHSAT097101
32	lnc-BMP2K-1	chr4:80226269-80226440	l_2674_chr4:80088967-80336103_prostate
33	lnc-BMP2K-1	chr4:80007244-80007416	NONHSAT097102
34	lnc-BMP2K-6	chr4:80053270-80053529	expReg_chr4_4185_+
35	lnc-BMP2K-1	chr4:80229427-80229953	NONHSAT097098
36	lnc-BMP2K-1	chr4:80229427-80229626	ENSG00000249307.1
37	lnc-BMP2K-1	chr4:80148366-80149040	ENSG00000249307.1
38	lnc-BMP2K-1	chr4:79892902-79893030	ENSG00000249307.1
39	lnc-BMP2K-1	chr4:79892902-79893030	ENSG00000249307.1
40	lnc-BMP2K-1	chr4:80007250-80007416	NONHSAT097098
41	lnc-BMP2K-1	chr4:80007250-80007416	ENSG00000249307.1
42	lnc-BMP2K-1	chr4:80220155-80220719	ENSG00000249307.1
43	lnc-BMP2K-1	chr4:80007250-80007416	ENSG00000249307.1
44	lnc-BMP2K-1	chr4:80229427-80229807	ENSG00000249307.1
45	lnc-BMP2K-1	chr4:80229427-80229808	ENSG00000249307.1
46	lnc-BMP2K-1	chr4:80229427-80229698	ENSG00000249307.1
47	lnc-BMP2K-1	chr4:80007250-80007416	ENSG00000249307.1
48	lnc-BMP2K-1	chr4:80113178-80113230	l_2674_chr4:80088967-80336103_prostate
49	lnc-BMP2K-7	chr4:80289843-80289955	NONHSAT097111
50	lnc-BMP2K-5	chr4:80010301-80010583	expReg_chr4_4149_+

No data

Variant related genes	Relation type
LINC01088	TF binding region
NAA11	TF binding region
LINC01088	CpG island
NAA11	CpG island
ENSG00000245322	chromatin interactions
ENSG00000156269	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000164032	chromatin interactions
ENSG00000152784	chromatin interactions
ENSG00000249307	chromatin interactions

Extended variants
information (count: 10705 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:10705 , 50 per page) page: 1 2 3 4 5 6 7 ... 215

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13150370	chr4:79887043-79887044	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs546515168	chr4:79887059-79887060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566315042	chr4:79887126-79887127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185865377	chr4:79887136-79887137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372752170	chr4:79887163-79887164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs34192580	chr4:79887185-79887186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565379905	chr4:79887235-79887236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs115672059	chr4:79887247-79887248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs557449159	chr4:79887275-79887276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188819786	chr4:79887297-79887298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532748311	chr4:79887300-79887301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192597763	chr4:79887358-79887359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551823618	chr4:79887380-79887381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184446872	chr4:79887386-79887387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs116088537	chr4:79887405-79887406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs115944401	chr4:79887423-79887424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188462332	chr4:79887428-79887429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs72862598	chr4:79887435-79887436	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs567691771	chr4:79887451-79887452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528440289	chr4:79887469-79887470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181310190	chr4:79887484-79887485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546699956	chr4:79887486-79887487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2867523	chr4:79887506-79887507	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs553721405	chr4:79887510-79887511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs578145192	chr4:79887569-79887570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374001728	chr4:79887570-79887571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs111826611	chr4:79887584-79887585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530902565	chr4:79887586-79887587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs72862599	chr4:79887658-79887659	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs563587742	chr4:79887669-79887670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs373965818	chr4:79887696-79887697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs76101924	chr4:79887707-79887708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558583362	chr4:79887743-79887744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs147567607	chr4:79887748-79887749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528306122	chr4:79887821-79887822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115074876	chr4:79887874-79887875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs72862600	chr4:79887875-79887876	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs536642311	chr4:79887899-79887900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570361494	chr4:79887916-79887917	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs377343712	chr4:79887928-79887929	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs556643124	chr4:79887988-79887989	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs567257902	chr4:79888016-79888017	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs536515922	chr4:79888022-79888023	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs141923870	chr4:79888073-79888074	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs573458371	chr4:79888091-79888092	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs184303611	chr4:79888121-79888122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs4975152	chr4:79888137-79888138	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs575846454	chr4:79888160-79888161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544699322	chr4:79888166-79888167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561078408	chr4:79888275-79888276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Bipolar disorder	19114987	CNVD
Myelodysplastic syndrome	18508791	CNVD
Chronic lymphocytic leukemia	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1182 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:79883400-79892800	Weak transcription	Primary hematopoietic stem cells	blood
2	chr4:79892000-79892800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr4:79892000-79894400	Enhancers	Duodenum Smooth Muscle	Duodenum
4	chr4:79892200-79893200	Enhancers	Adipose Nuclei	Adipose
5	chr4:79892400-79893200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr4:79892400-79894400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr4:79892400-79894600	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr4:79892400-79894800	Active TSS	Aorta	Aorta
9	chr4:79892600-79893200	Enhancers	Colon Smooth Muscle	Colon
10	chr4:79892600-79894600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr4:79892800-79893200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr4:79892800-79893200	Enhancers	Fetal Muscle Leg	muscle
13	chr4:79892800-79893200	Enhancers	Rectal Smooth Muscle	rectum
14	chr4:79892800-79893200	Enhancers	Right Atrium	heart
15	chr4:79892800-79893200	Active TSS	Stomach Smooth Muscle	stomach
16	chr4:79892800-79894000	Enhancers	Primary hematopoietic stem cells	blood
17	chr4:79892800-79894400	Active TSS	Brain Anterior Caudate	brain
18	chr4:79892800-79894400	Active TSS	Brain Hippocampus Middle	brain
19	chr4:79892800-79895800	Active TSS	Brain Substantia Nigra	brain
20	chr4:79892800-79896200	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr4:79893000-79894000	Active TSS	Psoas Muscle	Psoas
22	chr4:79893200-79894200	Weak transcription	Right Atrium	heart
23	chr4:79894000-79895600	Weak transcription	Psoas Muscle	Psoas
24	chr4:79894400-79894600	Enhancers	Right Atrium	heart
25	chr4:79894400-79896800	Weak transcription	Brain Hippocampus Middle	brain
26	chr4:79894800-79895000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr4:79894800-79895800	Flanking Active TSS	Aorta	Aorta
28	chr4:79895400-79896000	Enhancers	HSMMtube	muscle
29	chr4:79895600-79895800	Active TSS	Psoas Muscle	Psoas
30	chr4:79895800-79896000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr4:79895800-79896000	Active TSS	Aorta	Aorta
32	chr4:79896000-79896800	Weak transcription	Aorta	Aorta
33	chr4:79896800-79897200	Enhancers	Aorta	Aorta
34	chr4:79896800-79897400	Enhancers	Brain Hippocampus Middle	brain
35	chr4:79897200-79897400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr4:79897200-79903600	Weak transcription	Aorta	Aorta
37	chr4:79903600-79903800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
38	chr4:79903600-79904000	ZNF genes & repeats	Aorta	Aorta
39	chr4:79903800-79904200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr4:79904000-79904800	Weak transcription	Aorta	Aorta
41	chr4:79904200-79906200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr4:79904800-79905000	ZNF genes & repeats	Aorta	Aorta
43	chr4:79905000-79917600	Weak transcription	Aorta	Aorta
44	chr4:79905800-79906800	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr4:79906200-79906800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr4:79906400-79906800	Bivalent Enhancer	Stomach Mucosa	stomach
47	chr4:79906800-79907400	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr4:79906800-79908600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr4:79908600-79909400	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr4:79908600-79910400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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