Variant report

Variant	nsv1239
Chromosome Location	chr14:35477657-35522987
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:988)
CpG islands
(count:611)
Chromatin interactive
region (count:63)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:988 , 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	chr14:35519909-35520120	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:35509539-35510010	HepG2	liver:	n/a	chr14:35509792-35509808
3	ARID3A	chr14:35521017-35521344	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:35516133-35516303	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:35519876-35520224	K562	blood:	n/a	n/a
6	ARID3A	chr14:35514746-35515759	HepG2	liver:	n/a	n/a
7	ATF1	chr14:35519862-35520172	K562	blood:	n/a	n/a
8	ATF1	chr14:35517147-35517386	K562	blood:	n/a	n/a
9	ATF1	chr14:35515122-35515876	K562	blood:	n/a	n/a
10	ATF2	chr14:35515054-35515466	GM12878	blood:	n/a	n/a
11	ATF2	chr14:35515153-35515540	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr14:35515000-35515488	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr14:35514853-35515586	GM12878	blood:	n/a	n/a
14	ATF2	chr14:35504149-35504484	GM12878	blood:	n/a	n/a
15	ATF3	chr14:35515137-35515513	K562	blood:	n/a	chr14:35515349-35515364 chr14:35515353-35515360 chr14:35515353-35515361 chr14:35515353-35515363 chr14:35515352-35515360 chr14:35515350-35515363 chr14:35515353-35515363
16	BACH1	chr14:35519638-35520190	K562	blood:	n/a	chr14:35520008-35520022
17	BACH1	chr14:35515145-35516116	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr14:35519875-35520207	H1-hESC	embryonic stem cell:	n/a	chr14:35520008-35520022
19	BATF	chr14:35515132-35515392	GM12878	blood:	n/a	chr14:35515350-35515363
20	BATF	chr14:35504265-35504563	GM12878	blood:	n/a	chr14:35504383-35504394
21	BATF	chr14:35504189-35504612	GM12878	blood:	n/a	chr14:35504383-35504394
22	BATF	chr14:35502715-35503130	GM12878	blood:	n/a	chr14:35502942-35502953
23	BATF	chr14:35502850-35503057	GM12878	blood:	n/a	chr14:35502942-35502953
24	BCL11A	chr14:35504236-35504481	GM12878	blood:	n/a	n/a
25	BCL3	chr14:35515089-35515763	GM12878	blood:	n/a	chr14:35515406-35515415
26	BCL3	chr14:35515416-35515871	A549	lung:	n/a	n/a
27	BCLAF1	chr14:35514960-35515869	GM12878	blood:	n/a	chr14:35515406-35515415
28	BHLHE40	chr14:35514866-35515778	K562	blood:	n/a	n/a
29	BHLHE40	chr14:35516561-35516712	GM12878	blood:	n/a	n/a
30	BHLHE40	chr14:35514808-35515688	GM12878	blood:	n/a	n/a
31	BHLHE40	chr14:35514837-35515868	HepG2	liver:	n/a	n/a
32	BHLHE40	chr14:35516483-35516685	K562	blood:	n/a	n/a
33	BHLHE40	chr14:35509723-35509774	K562	blood:	n/a	n/a
34	BRCA1	chr14:35515197-35515787	GM12878	blood:	n/a	n/a
35	BRCA1	chr14:35514954-35516171	HepG2	liver:	n/a	n/a
36	BRCA1	chr14:35515159-35515688	H1-hESC	embryonic stem cell:	n/a	n/a
37	BRCA1	chr14:35515067-35515671	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr14:35516063-35516352	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr14:35503722-35504021	K562	blood:	n/a	n/a
40	CBX3	chr14:35503606-35504100	K562	blood:	n/a	n/a
41	CCNT2	chr14:35515159-35516049	K562	blood:	n/a	chr14:35515540-35515549
42	CCNT2	chr14:35519979-35520161	K562	blood:	n/a	n/a
43	CEBPB	chr14:35514752-35515485	H1-hESC	embryonic stem cell:	n/a	chr14:35514905-35514918
44	CEBPB	chr14:35514743-35514990	K562	blood:	n/a	chr14:35514905-35514918
45	CEBPB	chr14:35513979-35514078	HepG2	liver:	n/a	chr14:35514043-35514054
46	CEBPB	chr14:35514730-35515680	Hela-S3	cervix:	n/a	chr14:35514905-35514918
47	CEBPB	chr14:35520889-35521243	MCF-7	breast:	n/a	chr14:35521070-35521081
48	CEBPB	chr14:35514771-35515021	HepG2	liver:	n/a	chr14:35514905-35514918
49	CEBPB	chr14:35514747-35515160	A549	lung:	n/a	chr14:35514905-35514918
50	CEBPB	chr14:35514023-35514086	K562	blood:	n/a	chr14:35514043-35514054

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35515116-35515166	HRCEpiC	kidney:	n/a
2	chr14:35515116-35515166	HRCEpiC	kidney:	n/a
3	chr14:35515356-35515406	HCF	heart:	n/a
4	chr14:35512367-35512417	Caco-2	colon:	n/a
5	chr14:35512367-35512417	NB4	blood:	n/a
6	chr14:35514333-35514383	HIPEpiC	eye:	n/a
7	chr14:35515356-35515406	HEEpiC	esophagus:	n/a
8	chr14:35495536-35495586	SK-N-MC	brain:	n/a
9	chr14:35515414-35515464	NH-A	brain:	n/a
10	chr14:35515356-35515406	BE2_C	brain:	n/a
11	chr14:35515291-35515341	HNPCEpiC	eye:	n/a
12	chr14:35514333-35514383	NB4	blood:	n/a
13	chr14:35516283-35516333	HAEpiC	amniotic membrane:	n/a
14	chr14:35515291-35515341	A549	lung:	n/a
15	chr14:35515858-35515908	HCM	heart:	n/a
16	chr14:35515414-35515464	LNCaP	prostate:	n/a
17	chr14:35512367-35512417	SK-N-SH	brain:	n/a
18	chr14:35495536-35495586	IMR90	lung:	fetal
19	chr14:35498490-35498540	LNCaP	prostate:	n/a
20	chr14:35514333-35514383	HRCEpiC	kidney:	n/a
21	chr14:35515414-35515464	NHBE	bronchial:	n/a
22	chr14:35515116-35515166	HPAEpiC	pulmonary alveolar:	n/a
23	chr14:35515356-35515406	GM12891	blood:	n/a
24	chr14:35515116-35515166	SAEC	small airway:	n/a
25	chr14:35498490-35498540	GM12878	blood:	n/a
26	chr14:35516283-35516333	HRE	kidney:	n/a
27	chr14:35515116-35515166	HEK293	kidney:	embryo
28	chr14:35515116-35515166	SK-N-SH_RA	brain:	n/a
29	chr14:35495536-35495586	HAEpiC	amniotic membrane:	n/a
30	chr14:35515414-35515464	BE2_C	brain:	n/a
31	chr14:35495536-35495586	HRE	kidney:	n/a
32	chr14:35514333-35514383	RPTEC	kidney:	n/a
33	chr14:35498490-35498540	MCF10A-Er-Src	breast:	n/a
34	chr14:35515414-35515464	HEEpiC	esophagus:	n/a
35	chr14:35515291-35515341	GM19239	blood:	n/a
36	chr14:35495536-35495586	ECC-1	luminal epithelium:	n/a
37	chr14:35515356-35515406	CMK	blood:	n/a
38	chr14:35515356-35515406	H1-hESC	embryonic stem cell:	embryo
39	chr14:35515414-35515464	GM06990	blood:	n/a
40	chr14:35515414-35515464	NB4	blood:	n/a
41	chr14:35495536-35495586	HCT-116	colon:	n/a
42	chr14:35515356-35515406	SKMC	muscle:	n/a
43	chr14:35515356-35515406	HCT-116	colon:	n/a
44	chr14:35516283-35516333	GM12891	blood:	n/a
45	chr14:35498490-35498540	NT2-D1	testis:	n/a
46	chr14:35514333-35514383	HMEC	breast:	n/a
47	chr14:35495536-35495586	GM12878	blood:	n/a
48	chr14:35515414-35515464	RPTEC	kidney:	n/a
49	chr14:35498490-35498540	K562	blood:	n/a
50	chr14:35515414-35515464	HCM	heart:	n/a

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:35499235..35502810-chr14:35514800..35516736,3	MCF-7	breast:
2	chr14:35519616..35521249-chr14:35528506..35531084,2	MCF-7	breast:
3	chr14:35481674..35484183-chr14:35515641..35517435,2	MCF-7	breast:
4	chr14:35514107..35515830-chr14:35872683..35874428,2	MCF-7	breast:
5	chr14:35455186..35457809-chr14:35509575..35512529,2	K562	blood:
6	chr1:44115905..44116421-chr14:35515198..35515970,2	NB4	blood:
7	chr14:35450596..35455465-chr14:35514082..35520003,7	MCF-7	breast:
8	chr14:35509386..35510378-chr14:35891186..35892042,3	MCF-7	breast:
9	chr14:35515362..35516342-chr16:11836358..11837096,2	Hela-S3	cervix:
10	chr14:35492619..35494488-chr14:35513893..35516711,2	MCF-7	breast:
11	chr14:35516667..35519479-chr14:35589018..35592188,3	K562	blood:
12	chr14:35513511..35517056-chr14:35517636..35522677,6	K562	blood:
13	chr14:35481674..35484183-chr14:35515641..35517435,2	MCF-7	breast:
14	chr14:35514228..35515878-chr14:35780242..35782321,2	MCF-7	breast:
15	chr14:35515609..35516589-chr15:49169955..49170611,2	Hela-S3	cervix:
16	chr14:35500902..35503626-chr14:35810015..35811675,2	MCF-7	breast:
17	chr11:62608378..62609108-chr14:35519776..35520391,2	Hela-S3	cervix:
18	chr14:35509919..35510459-chr14:35875894..35876731,2	MCF-7	breast:
19	chr14:35505958..35507461-chr14:35513757..35515783,2	K562	blood:
20	chr14:35520110..35522080-chr14:35529783..35531632,2	MCF-7	breast:
21	chr14:35514893..35515885-chr2:74692133..74692798,2	Hela-S3	cervix:
22	chr14:35515177..35515679-chr14:105957265..105957988,2	Hela-S3	cervix:
23	chr14:35519987..35522404-chr14:35523498..35526576,3	K562	blood:
24	chr14:35518346..35520607-chr14:35589756..35591434,2	MCF-7	breast:
25	chr14:35509776..35510382-chr14:35602542..35603513,2	MCF-7	breast:
26	chr14:35484859..35486804-chr14:35511078..35512949,2	K562	blood:
27	chr14:35517575..35519344-chr14:35683138..35684908,2	MCF-7	breast:
28	chr14:35343382..35345457-chr14:35494554..35496991,2	MCF-7	breast:
29	chr14:35489417..35492128-chr14:35497418..35499039,2	K562	blood:
30	chr14:35460081..35462987-chr14:35513991..35516983,2	MCF-7	breast:
31	chr14:35513731..35517214-chr14:35589119..35593617,5	MCF-7	breast:
32	chr14:35507467..35509940-chr14:35513836..35516152,2	MCF-7	breast:
33	chr14:35343911..35346253-chr14:35481173..35482947,2	MCF-7	breast:
34	chr14:35515379..35516132-chr17:56736001..56736995,2	NB4	blood:
35	chr14:35514347..35518167-chr14:35589018..35591815,3	K562	blood:
36	chr14:35511724..35513872-chr14:35864570..35867392,2	MCF-7	breast:
37	chr11:65266267..65267153-chr14:35515173..35515777,2	Hela-S3	cervix:
38	chr14:35508976..35512360-chr14:35513729..35517203,6	K562	blood:
39	chr14:35515655..35516294-chr7:100025920..100026511,2	Hela-S3	cervix:
40	chr14:35514347..35516079-chr14:35590063..35591815,2	K562	blood:
41	chr14:35519480..35523190-chr14:35588742..35592990,5	MCF-7	breast:
42	chr14:35489417..35492128-chr14:35497418..35499039,2	K562	blood:
43	chr14:35512802..35518057-chr14:35589980..35593805,9	MCF-7	breast:
44	chr14:35515355..35516338-chr5:171710986..171711486,2	Hela-S3	cervix:
45	chr14:35506932..35507762-chr3:185524185..185525086,2	MCF-7	breast:
46	chr14:35500095..35502926-chr14:35557815..35560264,2	MCF-7	breast:
47	chr14:35519075..35520594-chr14:35524910..35527892,2	MCF-7	breast:
48	chr14:35515559..35516081-chr3:127771292..127771801,2	Hela-S3	cervix:
49	chr14:35484859..35486804-chr14:35511078..35512949,2	K562	blood:
50	chr14:35515170..35517585-chr14:35518270..35521794,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM177A1-2	chr14:35488172-35488564	NONHSAT036358
2	lnc-FAM177A1-2	chr14:35487835-35487971	NONHSAT036358

No data

Variant related genes	Relation type
SRP54	TF binding region
FAM177A1	TF binding region
SRP54	CpG island
FAM177A1	CpG island
ENSG00000078487	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000198604	chromatin interactions
ENSG00000235883	chromatin interactions
ENSG00000185634	chromatin interactions
ENSG00000092020	chromatin interactions
ENSG00000153066	chromatin interactions
ENSG00000100890	chromatin interactions
ENSG00000255302	chromatin interactions
ENSG00000100906	chromatin interactions
ENSG00000258790	chromatin interactions
ENSG00000151327	chromatin interactions
ENSG00000258704	chromatin interactions
ENSG00000118454	chromatin interactions
ENSG00000115275	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000251562	chromatin interactions
ENSG00000129518	chromatin interactions
ENSG00000066135	chromatin interactions
ENSG00000058262	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000185347	chromatin interactions
ENSG00000168246	chromatin interactions
ENSG00000258738	chromatin interactions
ENSG00000100902	chromatin interactions
ENSG00000100883	chromatin interactions

Extended variants
information (count: 1698 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1698 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554853406	chr14:35477674-35477675	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs575131305	chr14:35477677-35477678	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542720699	chr14:35477749-35477750	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556326431	chr14:35477753-35477754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372371127	chr14:35477759-35477760	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs1712351	chr14:35477785-35477786	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs201049561	chr14:35477795-35477796	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs199909535	chr14:35477804-35477805	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs368641782	chr14:35477836-35477837	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191230389	chr14:35477846-35477847	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527550341	chr14:35477847-35477848	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541358017	chr14:35477911-35477912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560746894	chr14:35477924-35477925	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs550060792	chr14:35477928-35477929	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs151006158	chr14:35477933-35477934	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549847744	chr14:35477954-35477955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569783383	chr14:35477956-35477957	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115840076	chr14:35477965-35477966	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138737163	chr14:35478032-35478033	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs373569690	chr14:35478068-35478069	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375369187	chr14:35478069-35478070	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs71435843	chr14:35478090-35478091	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs35812379	chr14:35478091-35478092	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs397748151	chr14:35478110-35478111	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566076567	chr14:35478132-35478133	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs535001247	chr14:35478143-35478144	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182230318	chr14:35478173-35478174	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566830667	chr14:35478190-35478191	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs111329857	chr14:35478291-35478292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568650719	chr14:35478295-35478296	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535524559	chr14:35478396-35478397	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs36112862	chr14:35478433-35478434	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs544465974	chr14:35478449-35478450	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563140700	chr14:35478463-35478464	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs115416044	chr14:35478467-35478468	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148561640	chr14:35478549-35478550	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374855729	chr14:35478550-35478551	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552059209	chr14:35478552-35478553	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2747010	chr14:35478560-35478561	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs558259451	chr14:35478562-35478563	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs367992023	chr14:35478578-35478579	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186531518	chr14:35478606-35478607	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540946222	chr14:35478711-35478712	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs377247493	chr14:35478721-35478722	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572850199	chr14:35478735-35478736	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560882471	chr14:35478749-35478750	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs17102962	chr14:35478782-35478783	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs543187395	chr14:35478787-35478788	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567406454	chr14:35478793-35478794	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563147959	chr14:35478794-35478795	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Glioma	24330732	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21858162	CNVD
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:1627 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35452800-35478200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr14:35453600-35485600	Weak transcription	HSMMtube	muscle
3	chr14:35453800-35499200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr14:35454000-35479200	Weak transcription	Gastric	stomach
5	chr14:35454400-35481600	Weak transcription	HMEC	breast
6	chr14:35454400-35485200	Weak transcription	Esophagus	oesophagus
7	chr14:35454400-35509800	Weak transcription	Psoas Muscle	Psoas
8	chr14:35454800-35481600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr14:35454800-35483600	Weak transcription	Small Intestine	intestine
10	chr14:35454800-35484800	Weak transcription	Fetal Brain Male	brain
11	chr14:35455200-35482800	Weak transcription	A549	lung
12	chr14:35455200-35487200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr14:35455600-35481600	Weak transcription	NHLF	lung
14	chr14:35456400-35483400	Weak transcription	Pancreas	Pancrea
15	chr14:35459400-35480200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr14:35464000-35478000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr14:35464000-35480200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr14:35465200-35500600	Strong transcription	HepG2	liver
19	chr14:35465600-35482400	Weak transcription	Brain Hippocampus Middle	brain
20	chr14:35465600-35500200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr14:35465800-35489000	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr14:35466000-35501400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr14:35466000-35503800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr14:35466200-35500600	Strong transcription	Rectal Mucosa Donor 29	rectum
25	chr14:35466400-35498200	Weak transcription	Spleen	Spleen
26	chr14:35466600-35502000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr14:35466800-35483600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr14:35466800-35502800	Strong transcription	Primary T helper cells PMA-I stimulated	--
29	chr14:35467000-35482600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr14:35467000-35496600	Weak transcription	K562	blood
31	chr14:35467400-35482400	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr14:35467400-35484800	Weak transcription	Brain Cingulate Gyrus	brain
33	chr14:35467600-35478400	Weak transcription	Brain Germinal Matrix	brain
34	chr14:35467600-35503600	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr14:35467800-35480000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr14:35468400-35480400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr14:35468600-35493600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr14:35468600-35501600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr14:35469000-35488000	Weak transcription	Colonic Mucosa	Colon
40	chr14:35469400-35480600	Weak transcription	NHDF-Ad	bronchial
41	chr14:35469400-35484800	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr14:35469600-35482600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr14:35469600-35482800	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr14:35469600-35484600	Weak transcription	Fetal Heart	heart
45	chr14:35470200-35483000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
46	chr14:35470600-35502600	Strong transcription	Liver	Liver
47	chr14:35471200-35483200	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr14:35471200-35486600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr14:35471800-35479000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr14:35471800-35501600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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