Variant report

Variant	nsv882735
Chromosome Location	chr5:115254723-115377150
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:976)
CpG islands
(count:1711)
Chromatin interactive
region (count:45)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:115367900-115368175	K562	blood:	n/a	n/a
2	ARID3A	chr5:115305895-115305924	K562	blood:	n/a	n/a
3	ARID3A	chr5:115338438-115338492	HepG2	liver:	n/a	n/a
4	ATF1	chr5:115367730-115368219	K562	blood:	n/a	n/a
5	ATF1	chr5:115342618-115342831	K562	blood:	n/a	n/a
6	ATF2	chr5:115367677-115368276	GM12878	blood:	n/a	n/a
7	ATF2	chr5:115367704-115368194	GM12878	blood:	n/a	n/a
8	ATF3	chr5:115265671-115266431	HCT-116	colon:	n/a	n/a
9	ATF3	chr5:115264135-115264632	HCT-116	colon:	n/a	n/a
10	ATF3	chr5:115367703-115368390	HCT-116	colon:	n/a	n/a
11	ATF3	chr5:115265826-115266223	A549	lung:	n/a	n/a
12	ATF3	chr5:115265657-115266433	HCT-116	colon:	n/a	n/a
13	ATF3	chr5:115367737-115368181	K562	blood:	n/a	n/a
14	BACH1	chr5:115289945-115290173	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr5:115316893-115317171	GM12878	blood:	n/a	n/a
16	BATF	chr5:115367875-115368141	GM12878	blood:	n/a	chr5:115368009-115368020
17	BATF	chr5:115372991-115373241	GM12878	blood:	n/a	chr5:115373126-115373136 chr5:115373125-115373136
18	BATF	chr5:115372974-115373262	GM12878	blood:	n/a	chr5:115373126-115373136 chr5:115373125-115373136
19	BCL11A	chr5:115367806-115368162	GM12878	blood:	n/a	n/a
20	BCL3	chr5:115265804-115266312	GM12878	blood:	n/a	n/a
21	BCLAF1	chr5:115367748-115368206	GM12878	blood:	n/a	n/a
22	BHLHE40	chr5:115367910-115368167	K562	blood:	n/a	n/a
23	BHLHE40	chr5:115341377-115341646	K562	blood:	n/a	n/a
24	BHLHE40	chr5:115341005-115341007	K562	blood:	n/a	n/a
25	BHLHE40	chr5:115298546-115298742	HepG2	liver:	n/a	n/a
26	BHLHE40	chr5:115317842-115317997	K562	blood:	n/a	n/a
27	BHLHE40	chr5:115362354-115362487	K562	blood:	n/a	n/a
28	BRCA1	chr5:115367793-115368308	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr5:115265554-115266476	HCT-116	colon:	n/a	n/a
30	CBX3	chr5:115264727-115267603	HCT-116	colon:	n/a	n/a
31	CBX3	chr5:115276709-115277429	HCT-116	colon:	n/a	n/a
32	CBX3	chr5:115263940-115265316	HCT-116	colon:	n/a	n/a
33	CBX3	chr5:115367615-115368500	HCT-116	colon:	n/a	n/a
34	CBX3	chr5:115263504-115264630	HCT-116	colon:	n/a	n/a
35	CBX3	chr5:115367578-115368433	HCT-116	colon:	n/a	n/a
36	CCNT2	chr5:115295755-115295957	K562	blood:	n/a	n/a
37	CCNT2	chr5:115298759-115298856	K562	blood:	n/a	n/a
38	CEBPB	chr5:115367817-115368143	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr5:115355886-115356153	HepG2	liver:	n/a	chr5:115356018-115356029
40	CEBPB	chr5:115264959-115265284	K562	blood:	n/a	chr5:115265120-115265131
41	CEBPB	chr5:115367773-115368233	A549	lung:	n/a	n/a
42	CEBPB	chr5:115367716-115368247	IMR90	lung:	n/a	n/a
43	CEBPB	chr5:115265555-115266818	HCT-116	colon:	n/a	n/a
44	CEBPB	chr5:115282432-115283344	IMR90	lung:	n/a	n/a
45	CEBPB	chr5:115367720-115368154	A549	lung:	n/a	n/a
46	CEBPB	chr5:115265590-115266415	HCT-116	colon:	n/a	n/a
47	CEBPB	chr5:115377069-115377351	K562	blood:	n/a	chr5:115377191-115377202 chr5:115377189-115377202 chr5:115377191-115377202 chr5:115377189-115377202 chr5:115377189-115377202
48	CEBPB	chr5:115311053-115311271	HepG2	liver:	n/a	chr5:115311119-115311130
49	CEBPB	chr5:115367761-115368163	K562	blood:	n/a	n/a
50	CEBPB	chr5:115377108-115377339	H1-hESC	embryonic stem cell:	n/a	chr5:115377191-115377202 chr5:115377189-115377202 chr5:115377191-115377202 chr5:115377189-115377202 chr5:115377189-115377202

(count:1711 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:115284110-115284160	ECC-1	luminal epithelium:	n/a
2	chr5:115330940-115330990	HCF	heart:	n/a
3	chr5:115322511-115322561	NH-A	brain:	n/a
4	chr5:115284110-115284160	ECC-1	luminal epithelium:	n/a
5	chr5:115330940-115330990	HCF	heart:	n/a
6	chr5:115322511-115322561	NH-A	brain:	n/a
7	chr5:115298511-115298561	PFSK-1	brain:	n/a
8	chr5:115299071-115299121	HUVEC	blood vessel:	n/a
9	chr5:115297853-115297903	ProgFib	skin:	n/a
10	chr5:115298079-115298129	GM12878	blood:	n/a
11	chr5:115298231-115298281	NHDF-neo	bronchial:	n/a
12	chr5:115298079-115298129	Caco-2	colon:	n/a
13	chr5:115294388-115294438	SK-N-MC	brain:	n/a
14	chr5:115299828-115299878	AoSMC	blood vessel:	n/a
15	chr5:115367063-115367113	HEEpiC	esophagus:	n/a
16	chr5:115299646-115299696	NH-A	brain:	n/a
17	chr5:115299071-115299121	PANC-1	pancreas:	n/a
18	chr5:115322511-115322561	HUVEC	blood vessel:	n/a
19	chr5:115330940-115330990	MCF-7	breast:	n/a
20	chr5:115294261-115294311	GM06990	blood:	n/a
21	chr5:115297989-115298039	SAEC	small airway:	n/a
22	chr5:115298079-115298129	CMK	blood:	n/a
23	chr5:115294261-115294311	AG10803	skin:	n/a
24	chr5:115297488-115297538	HIPEpiC	eye:	n/a
25	chr5:115298720-115298770	Hepatocyte	liver:	n/a
26	chr5:115299646-115299696	ProgFib	skin:	n/a
27	chr5:115289176-115289226	HCPEpiC	choroid plexus:	n/a
28	chr5:115297853-115297903	NB4	blood:	n/a
29	chr5:115299071-115299121	BE2_C	brain:	n/a
30	chr5:115297989-115298039	MCF10A-Er-Src	breast:	n/a
31	chr5:115298511-115298561	SK-N-SH_RA	brain:	n/a
32	chr5:115274878-115274928	SK-N-SH_RA	brain:	n/a
33	chr5:115297690-115297740	HEK293	kidney:	embryo
34	chr5:115299088-115299138	HNPCEpiC	eye:	n/a
35	chr5:115297690-115297740	HRE	kidney:	n/a
36	chr5:115298720-115298770	RPTEC	kidney:	n/a
37	chr5:115297989-115298039	AG04449	skin:	fetal
38	chr5:115297690-115297740	AG10803	skin:	n/a
39	chr5:115274878-115274928	HCPEpiC	choroid plexus:	n/a
40	chr5:115298231-115298281	PrEC	prostate:	n/a
41	chr5:115297690-115297740	AG09309	skin:	n/a
42	chr5:115298704-115298754	Hepatocyte	liver:	n/a
43	chr5:115337401-115337451	BE2_C	brain:	n/a
44	chr5:115294388-115294438	HRCEpiC	kidney:	n/a
45	chr5:115363186-115363236	NHBE	bronchial:	n/a
46	chr5:115297723-115297773	SK-N-SH_RA	brain:	n/a
47	chr5:115314451-115314501	HEEpiC	esophagus:	n/a
48	chr5:115367063-115367113	Jurkat	blood:	n/a
49	chr5:115367063-115367113	MCF10A-Er-Src	breast:	n/a
50	chr5:115299071-115299121	HPAEpiC	pulmonary alveolar:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:115350341..115352208-chr5:115356224..115357798,2	K562	blood:
2	chr5:115325159..115327094-chr5:115327462..115329055,2	K562	blood:
3	chr5:115314211..115315757-chr5:115317313..115319872,2	K562	blood:
4	chr5:115311683..115315711-chr5:115317313..115319331,3	K562	blood:
5	chr5:115245411..115247547-chr5:115255771..115257429,2	K562	blood:
6	chr5:115314211..115315757-chr5:115317313..115319872,2	K562	blood:
7	chr5:115318449..115319995-chr5:115320033..115322882,2	MCF-7	breast:
8	chr5:115325159..115327094-chr5:115327462..115329055,2	K562	blood:
9	chr5:115374690..115376752-chr5:115422929..115424884,2	K562	blood:
10	chr5:115325067..115326852-chr5:115339331..115341155,2	K562	blood:
11	chr5:115369299..115371727-chr5:115372016..115373618,2	K562	blood:
12	chr5:115357626..115360379-chr5:115363877..115366832,2	K562	blood:
13	chr5:115355525..115357381-chr5:115358877..115362646,3	MCF-7	breast:
14	chr5:115325463..115327847-chr5:115335444..115338217,2	K562	blood:
15	chr5:115369299..115371727-chr5:115372016..115373618,2	K562	blood:
16	chr5:115345544..115349281-chr5:115349377..115353001,6	K562	blood:
17	chr5:115357626..115360379-chr5:115363877..115366832,2	K562	blood:
18	chr5:115339171..115341772-chr5:115344562..115347685,3	K562	blood:
19	chr5:115325067..115326852-chr5:115339331..115341155,2	K562	blood:
20	chr5:115266649..115268813-chr5:115285639..115288179,2	K562	blood:
21	chr5:115318449..115319995-chr5:115320033..115322882,2	MCF-7	breast:
22	chr5:115358879..115361762-chr5:115363430..115365377,2	K562	blood:
23	chr5:115309826..115311459-chr5:115311683..115313948,2	K562	blood:
24	chr5:115175803..115178911-chr5:115366529..115369436,3	MCF-7	breast:
25	chr5:115316121..115317825-chr5:115326867..115328575,2	K562	blood:
26	chr5:115325463..115327847-chr5:115335444..115338217,2	K562	blood:
27	chr5:115266649..115268813-chr5:115285639..115288179,2	K562	blood:
28	chr5:115374690..115378372-chr5:115418496..115424884,6	K562	blood:
29	chr5:115329359..115331153-chr5:115337694..115340263,2	K562	blood:
30	chr5:115316121..115317825-chr5:115326867..115328575,2	K562	blood:
31	chr5:115338156..115340599-chr5:115341199..115344105,2	K562	blood:
32	chr5:115176344..115179132-chr5:115268451..115271240,2	K562	blood:
33	chr5:115351780..115354393-chr5:115357858..115360108,2	K562	blood:
34	chr5:115164592..115166592-chr5:115332938..115334988,2	K562	blood:
35	chr5:115338156..115340599-chr5:115341199..115344105,2	K562	blood:
36	chr5:115358879..115361762-chr5:115363430..115365377,2	K562	blood:
37	chr16:68772311..68772969-chr5:115376254..115377111,2	MCF-7	breast:
38	chr5:115339914..115341470-chr5:115365898..115367731,2	K562	blood:
39	chr5:115339914..115341470-chr5:115365898..115367731,2	K562	blood:
40	chr4:148160683..148161374-chr5:115362795..115363673,2	MCF-7	breast:
41	chr5:115223617..115224331-chr5:115367917..115368436,2	MCF-7	breast:
42	chr5:115175781..115177499-chr5:115307496..115309644,2	K562	blood:
43	chr5:115345258..115349032-chr5:115349377..115353428,5	K562	blood:
44	chr5:115339171..115341772-chr5:115344562..115347685,3	K562	blood:
45	chr5:115288586..115289484-chr7:18169519..18170041,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COMMD10-8	chr5:115358088-115358163	NONHSAT103346
2	lnc-COMMD10-7	chr5:115365620-115367298	NONHSAT103348
3	lnc-LVRN.1-1	chr5:115292239-115292617	XLOC_004517
4	lnc-LVRN.1-1	chr5:115294126-115295651	XLOC_004517
5	lnc-LVRN.1-1	chr5:115292235-115292617	XLOC_004517
6	lnc-LVRN.1-1	chr5:115296816-115297015	XLOC_004517
7	lnc-COMMD10-8	chr5:115361675-115363300	NONHSAT103346
8	lnc-ATG12-2	chr5:115267146-115267687	NONHSAT103341
9	lnc-LVRN.1-1	chr5:115292235-115292617	XLOC_004517
10	lnc-COMMD10-7	chr5:115367304-115367620	NONHSAT103348
11	lnc-LVRN.1-1	chr5:115294108-115294320	XLOC_004517
12	lnc-COMMD10-8	chr5:115356724-115357449	NONHSAT103346

No data

Variant related genes	Relation type
ENSG00000172901	TF binding region
ENSG00000221778	TF binding region
ENSG00000268714	TF binding region
ENSG00000248295	TF binding region
ENSG00000172901	CpG island
ENSG00000221778	CpG island
ENSG00000268714	CpG island
ENSG00000248295	CpG island
ENSG00000145782	chromatin interactions
ENSG00000248295	chromatin interactions
ENSG00000268714	chromatin interactions
ENSG00000271918	chromatin interactions
ENSG00000145781	chromatin interactions
ENSG00000221778	chromatin interactions
ENSG00000172901	chromatin interactions
ENSG00000177879	chromatin interactions
IGF2BP3	miRNA target sites

Extended variants
information (count: 5958 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:5958 , 50 per page) page: 1 2 3 4 5 6 7 ... 120

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11958116	chr5:115254723-115254724	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs189522255	chr5:115254724-115254725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541708484	chr5:115254763-115254764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143666196	chr5:115254776-115254777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs76794115	chr5:115254786-115254787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551053658	chr5:115254799-115254800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs147196811	chr5:115254804-115254805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs11948179	chr5:115254821-115254822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531398469	chr5:115254826-115254827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34827265	chr5:115254827-115254828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs78504935	chr5:115254857-115254858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181829381	chr5:115254909-115254910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs372111090	chr5:115254943-115254944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs74561168	chr5:115254983-115254984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs540957398	chr5:115254984-115254985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs567252893	chr5:115255007-115255008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554329814	chr5:115255060-115255061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557608651	chr5:115255106-115255107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549532626	chr5:115255112-115255113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs527463816	chr5:115255113-115255114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569524800	chr5:115255126-115255127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539077140	chr5:115255167-115255168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552438968	chr5:115255225-115255226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs149590093	chr5:115255227-115255228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534742001	chr5:115255228-115255229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555279386	chr5:115255253-115255254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575157928	chr5:115255254-115255255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537756360	chr5:115255287-115255288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs185315531	chr5:115255295-115255296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144210873	chr5:115255324-115255325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148728491	chr5:115255346-115255347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375179514	chr5:115255350-115255351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577333440	chr5:115255376-115255377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571986978	chr5:115255386-115255387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375169049	chr5:115255389-115255390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540642743	chr5:115255395-115255396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs369685485	chr5:115255422-115255423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs199862363	chr5:115255439-115255440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560569901	chr5:115255458-115255459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142456808	chr5:115255460-115255461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374784690	chr5:115255466-115255467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189678226	chr5:115255485-115255486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146888023	chr5:115255557-115255558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552624013	chr5:115255564-115255565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs147782117	chr5:115255586-115255587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182251082	chr5:115255590-115255591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535141034	chr5:115255595-115255596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs76284489	chr5:115255613-115255614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186766465	chr5:115255668-115255669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573870145	chr5:115255669-115255670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Sezary syndrome	18413736	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Depressive disorder	21152026	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:892 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:115195400-115263200	Weak transcription	Aorta	Aorta
2	chr5:115219600-115256000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:115234400-115258800	Weak transcription	Primary T cells from cord blood	blood
4	chr5:115234800-115255000	Weak transcription	Stomach Smooth Muscle	stomach
5	chr5:115234800-115255200	Weak transcription	Primary B cells from cord blood	blood
6	chr5:115234800-115255400	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr5:115234800-115257800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr5:115235000-115257800	Weak transcription	NH-A	brain
9	chr5:115240800-115257800	Weak transcription	Fetal Heart	heart
10	chr5:115247800-115261200	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr5:115249600-115258400	Weak transcription	HSMMtube	muscle
12	chr5:115249800-115258400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr5:115251800-115256000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr5:115251800-115259200	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr5:115251800-115259600	Weak transcription	Fetal Muscle Trunk	muscle
16	chr5:115252400-115255200	Weak transcription	Liver	Liver
17	chr5:115252400-115258400	Weak transcription	Fetal Lung	lung
18	chr5:115252400-115259000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr5:115252600-115264200	Weak transcription	Fetal Muscle Leg	muscle
20	chr5:115252800-115256400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr5:115254200-115257800	Weak transcription	NHLF	lung
22	chr5:115256000-115256200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr5:115256000-115256400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr5:115256400-115264800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr5:115257800-115258800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr5:115257800-115259200	Enhancers	Fetal Heart	heart
27	chr5:115258400-115258600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr5:115258400-115258600	Enhancers	HSMMtube	muscle
29	chr5:115258400-115258800	Enhancers	Fetal Lung	lung
30	chr5:115258800-115261200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr5:115263200-115263400	Enhancers	Aorta	Aorta
32	chr5:115263200-115264600	Enhancers	A549	lung
33	chr5:115264200-115266000	Enhancers	Fetal Muscle Leg	muscle
34	chr5:115264600-115265000	Weak transcription	A549	lung
35	chr5:115264800-115265400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr5:115265000-115266000	Enhancers	A549	lung
37	chr5:115265400-115265600	Enhancers	Placenta	Placenta
38	chr5:115266400-115270200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr5:115266600-115266800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr5:115266600-115267000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr5:115266600-115267200	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr5:115266600-115267400	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr5:115266800-115267200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr5:115266800-115269000	Weak transcription	NH-A	brain
45	chr5:115267000-115267400	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr5:115267200-115267400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr5:115267200-115267400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr5:115267200-115269400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr5:115267400-115267800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr5:115267400-115273400	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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