Variant report

Variant	nsv1043801
Chromosome Location	chr14:35493065-35539399
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1012)
CpG islands
(count:610)
Chromatin interactive
region (count:70)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1012 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:35519876-35520224	K562	blood:	n/a	n/a
2	ARID3A	chr14:35514746-35515759	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:35537558-35537700	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:35521017-35521344	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:35519909-35520120	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:35516133-35516303	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:35509539-35510010	HepG2	liver:	n/a	chr14:35509792-35509808
8	ATF1	chr14:35519862-35520172	K562	blood:	n/a	n/a
9	ATF1	chr14:35517147-35517386	K562	blood:	n/a	n/a
10	ATF1	chr14:35515122-35515876	K562	blood:	n/a	n/a
11	ATF2	chr14:35515054-35515466	GM12878	blood:	n/a	n/a
12	ATF2	chr14:35514853-35515586	GM12878	blood:	n/a	n/a
13	ATF2	chr14:35515000-35515488	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr14:35504149-35504484	GM12878	blood:	n/a	n/a
15	ATF2	chr14:35515153-35515540	H1-hESC	embryonic stem cell:	n/a	n/a
16	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
17	BACH1	chr14:35519638-35520190	K562	blood:	n/a	chr14:35520008-35520022
18	BACH1	chr14:35519875-35520207	H1-hESC	embryonic stem cell:	n/a	chr14:35520008-35520022
19	BACH1	chr14:35515145-35516116	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr14:35504189-35504612	GM12878	blood:	n/a	chr14:35504383-35504394
21	BATF	chr14:35515132-35515392	GM12878	blood:	n/a	chr14:35515350-35515363
22	BATF	chr14:35504265-35504563	GM12878	blood:	n/a	chr14:35504383-35504394
23	BATF	chr14:35502715-35503130	GM12878	blood:	n/a	chr14:35502942-35502953
24	BATF	chr14:35502850-35503057	GM12878	blood:	n/a	chr14:35502942-35502953
25	BCL11A	chr14:35504236-35504481	GM12878	blood:	n/a	n/a
26	BCL3	chr14:35515089-35515763	GM12878	blood:	n/a	chr14:35515406-35515415
27	BCL3	chr14:35515416-35515871	A549	lung:	n/a	n/a
28	BCLAF1	chr14:35514960-35515869	GM12878	blood:	n/a	chr14:35515406-35515415
29	BHLHE40	chr14:35516561-35516712	GM12878	blood:	n/a	n/a
30	BHLHE40	chr14:35514866-35515778	K562	blood:	n/a	n/a
31	BHLHE40	chr14:35514808-35515688	GM12878	blood:	n/a	n/a
32	BHLHE40	chr14:35509723-35509774	K562	blood:	n/a	n/a
33	BHLHE40	chr14:35514837-35515868	HepG2	liver:	n/a	n/a
34	BHLHE40	chr14:35516483-35516685	K562	blood:	n/a	n/a
35	BRCA1	chr14:35515067-35515671	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr14:35515197-35515787	GM12878	blood:	n/a	n/a
37	BRCA1	chr14:35516063-35516352	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr14:35514954-35516171	HepG2	liver:	n/a	n/a
39	BRCA1	chr14:35515159-35515688	H1-hESC	embryonic stem cell:	n/a	n/a
40	CBX3	chr14:35503606-35504100	K562	blood:	n/a	n/a
41	CBX3	chr14:35503722-35504021	K562	blood:	n/a	n/a
42	CCNT2	chr14:35519979-35520161	K562	blood:	n/a	n/a
43	CCNT2	chr14:35515159-35516049	K562	blood:	n/a	chr14:35515540-35515549
44	CEBPB	chr14:35514766-35516188	HepG2	liver:	n/a	chr14:35514905-35514918
45	CEBPB	chr14:35514752-35515485	H1-hESC	embryonic stem cell:	n/a	chr14:35514905-35514918
46	CEBPB	chr14:35516129-35516272	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr14:35506053-35506254	HepG2	liver:	n/a	n/a
48	CEBPB	chr14:35514586-35515500	A549	lung:	n/a	chr14:35514905-35514918
49	CEBPB	chr14:35514722-35515427	K562	blood:	n/a	chr14:35514905-35514918
50	CEBPB	chr14:35514719-35515467	A549	lung:	n/a	chr14:35514905-35514918

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35515414-35515464	ovcar-3	ovarian:	n/a
2	chr14:35515116-35515166	AG10803	skin:	n/a
3	chr14:35515356-35515406	HepG2	liver:	n/a
4	chr14:35515356-35515406	HMEC	breast:	n/a
5	chr14:35516283-35516333	HCPEpiC	choroid plexus:	n/a
6	chr14:35516283-35516333	CMK	blood:	n/a
7	chr14:35512367-35512417	GM06990	blood:	n/a
8	chr14:35498490-35498540	IMR90	lung:	fetal
9	chr14:35515414-35515464	T-47D	breast:	n/a
10	chr14:35495536-35495586	HCF	heart:	n/a
11	chr14:35515414-35515464	GM12892	blood:	n/a
12	chr14:35498490-35498540	NH-A	brain:	n/a
13	chr14:35516283-35516333	HRCEpiC	kidney:	n/a
14	chr14:35514333-35514383	HNPCEpiC	eye:	n/a
15	chr14:35515858-35515908	HL-60	blood:	n/a
16	chr14:35515356-35515406	GM12892	blood:	n/a
17	chr14:35512367-35512417	Hepatocyte	liver:	n/a
18	chr14:35515291-35515341	MCF-7	breast:	n/a
19	chr14:35515414-35515464	A549	lung:	n/a
20	chr14:35515858-35515908	HPAEpiC	pulmonary alveolar:	n/a
21	chr14:35512367-35512417	NT2-D1	testis:	n/a
22	chr14:35498490-35498540	HNPCEpiC	eye:	n/a
23	chr14:35516283-35516333	GM12891	blood:	n/a
24	chr14:35514333-35514383	SK-N-SH	brain:	n/a
25	chr14:35514333-35514383	HMEC	breast:	n/a
26	chr14:35515414-35515464	K562	blood:	n/a
27	chr14:35512367-35512417	ovcar-3	ovarian:	n/a
28	chr14:35514333-35514383	HEEpiC	esophagus:	n/a
29	chr14:35498490-35498540	H1-hESC	embryonic stem cell:	embryo
30	chr14:35516283-35516333	Hela-S3	cervix:	n/a
31	chr14:35514333-35514383	BE2_C	brain:	n/a
32	chr14:35515291-35515341	BJ	skin:	n/a
33	chr14:35498490-35498540	K562	blood:	n/a
34	chr14:35515356-35515406	SK-N-SH	brain:	n/a
35	chr14:35515116-35515166	HAEpiC	amniotic membrane:	n/a
36	chr14:35514333-35514383	LNCaP	prostate:	n/a
37	chr14:35515291-35515341	AG09319	gingival:	n/a
38	chr14:35512367-35512417	HCM	heart:	n/a
39	chr14:35515858-35515908	MCF10A-Er-Src	breast:	n/a
40	chr14:35512367-35512417	HUVEC	blood vessel:	n/a
41	chr14:35498490-35498540	BE2_C	brain:	n/a
42	chr14:35515414-35515464	AG10803	skin:	n/a
43	chr14:35514333-35514383	ProgFib	skin:	n/a
44	chr14:35498490-35498540	PANC-1	pancreas:	n/a
45	chr14:35516283-35516333	HAEpiC	amniotic membrane:	n/a
46	chr14:35515858-35515908	HRE	kidney:	n/a
47	chr14:35515356-35515406	ProgFib	skin:	n/a
48	chr14:35515116-35515166	NB4	blood:	n/a
49	chr14:35495536-35495586	SK-N-MC	brain:	n/a
50	chr14:35498490-35498540	HRPEpiC	eye:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:35516520..35518836-chr14:35536161..35537991,2	K562	blood:
2	chr1:70819918..70820461-chr14:35515383..35516234,2	Hela-S3	cervix:
3	chr14:35460081..35462987-chr14:35513991..35516983,2	MCF-7	breast:
4	chr14:35515559..35516081-chr3:127771292..127771801,2	Hela-S3	cervix:
5	chr14:35516520..35518836-chr14:35536161..35537991,2	K562	blood:
6	chr14:35449839..35454578-chr14:35513316..35515954,7	K562	blood:
7	chr14:35484859..35486804-chr14:35511078..35512949,2	K562	blood:
8	chr14:35508976..35512360-chr14:35513729..35517203,6	K562	blood:
9	chr14:35514107..35515830-chr14:35872683..35874428,2	MCF-7	breast:
10	chr14:35507467..35509940-chr14:35513836..35516152,2	MCF-7	breast:
11	chr14:35514169..35519549-chr14:35872431..35877872,11	MCF-7	breast:
12	chr14:35519480..35523190-chr14:35588742..35592990,5	MCF-7	breast:
13	chr14:35450596..35455465-chr14:35514082..35520003,7	MCF-7	breast:
14	chr14:35516667..35519479-chr14:35589018..35592188,3	K562	blood:
15	chr14:35513511..35517056-chr14:35517636..35522677,6	K562	blood:
16	chr14:35525027..35526542-chr14:35529643..35531640,2	K562	blood:
17	chr14:35515365..35516134-chr15:65596788..65597492,2	Hela-S3	cervix:
18	chr11:62608378..62609108-chr14:35519776..35520391,2	Hela-S3	cervix:
19	chr14:35515355..35516338-chr5:171710986..171711486,2	Hela-S3	cervix:
20	chr14:35515655..35516294-chr7:100025920..100026511,2	Hela-S3	cervix:
21	chr14:35455186..35457809-chr14:35509575..35512529,2	K562	blood:
22	chr1:44115905..44116421-chr14:35515198..35515970,2	NB4	blood:
23	chr14:35520110..35522080-chr14:35529783..35531632,2	MCF-7	breast:
24	chr14:35450099..35453742-chr14:35513316..35517237,10	K562	blood:
25	chr14:35515362..35516342-chr16:11836358..11837096,2	Hela-S3	cervix:
26	chr14:35520110..35522080-chr14:35529783..35531632,2	MCF-7	breast:
27	chr14:35520311..35523520-chr14:35872932..35875311,3	MCF-7	breast:
28	chr14:35517575..35519344-chr14:35683138..35684908,2	MCF-7	breast:
29	chr14:35515170..35517585-chr14:35518270..35521794,5	K562	blood:
30	chr14:35519075..35520594-chr14:35524910..35527892,2	MCF-7	breast:
31	chr14:35519987..35522404-chr14:35523498..35526576,3	K562	blood:
32	chr14:35514347..35516079-chr14:35590063..35591815,2	K562	blood:
33	chr14:35524936..35527808-chr14:35546522..35548065,2	MCF-7	breast:
34	chr14:35515172..35516906-chr14:35528396..35530412,2	K562	blood:
35	chr14:35512802..35518057-chr14:35589980..35593805,9	MCF-7	breast:
36	chr14:35514893..35515885-chr2:74692133..74692798,2	Hela-S3	cervix:
37	chr14:35492619..35494488-chr14:35513893..35516711,2	MCF-7	breast:
38	chr14:35518346..35520607-chr14:35589756..35591434,2	MCF-7	breast:
39	chr11:65266267..65267153-chr14:35515173..35515777,2	Hela-S3	cervix:
40	chr14:35505958..35507461-chr14:35513757..35515783,2	K562	blood:
41	chr14:35500902..35503626-chr14:35810015..35811675,2	MCF-7	breast:
42	chr14:35515177..35515679-chr14:105957265..105957988,2	Hela-S3	cervix:
43	chr14:35515379..35516132-chr17:56736001..56736995,2	NB4	blood:
44	chr14:35520904..35522612-chr14:35525076..35526619,2	K562	blood:
45	chr14:35514228..35515878-chr14:35780242..35782321,2	MCF-7	breast:
46	chr14:35513511..35517056-chr14:35517636..35522677,6	K562	blood:
47	chr14:35449656..35453109-chr14:35514529..35517063,4	MCF-7	breast:
48	chr14:35500095..35502926-chr14:35557815..35560264,2	MCF-7	breast:
49	chr14:35509386..35510378-chr14:35891186..35892042,3	MCF-7	breast:
50	chr14:35489417..35492128-chr14:35497418..35499039,2	K562	blood:

No data

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

Extended variants
information (count: 1715 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1715 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529794457	chr14:35493148-35493149	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs549651517	chr14:35493160-35493161	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs558145579	chr14:35493161-35493162	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs181563048	chr14:35493203-35493204	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs538200036	chr14:35493207-35493208	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs368803902	chr14:35493258-35493259	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs575762919	chr14:35493261-35493262	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs373514664	chr14:35493268-35493269	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs578135561	chr14:35493333-35493334	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs117153277	chr14:35493381-35493382	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs565602986	chr14:35493392-35493393	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs377579722	chr14:35493407-35493408	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs554726013	chr14:35493442-35493443	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs571517286	chr14:35493479-35493480	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs574590440	chr14:35493484-35493485	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs141367035	chr14:35493486-35493487	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs557448605	chr14:35493504-35493505	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs114237788	chr14:35493530-35493531	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs574895727	chr14:35493560-35493561	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs184201723	chr14:35493564-35493565	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs573558456	chr14:35493592-35493593	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs150764522	chr14:35493621-35493622	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs562299419	chr14:35493653-35493654	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs139149375	chr14:35493660-35493661	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs116314320	chr14:35493678-35493679	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs532092492	chr14:35493691-35493692	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs188609957	chr14:35493727-35493728	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs565364172	chr14:35493774-35493775	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs534911900	chr14:35493856-35493857	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs201139535	chr14:35493867-35493868	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs202181267	chr14:35493869-35493870	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs75047337	chr14:35493880-35493881	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs78510688	chr14:35493881-35493882	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs548226098	chr14:35493889-35493890	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs568351384	chr14:35493904-35493905	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs536820189	chr14:35493958-35493959	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs149999027	chr14:35494018-35494019	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs577403284	chr14:35494019-35494020	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs539969606	chr14:35494154-35494155	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs553401596	chr14:35494183-35494184	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs573198820	chr14:35494209-35494210	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs542217357	chr14:35494227-35494228	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs562198153	chr14:35494231-35494232	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs370888747	chr14:35494270-35494271	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs557196209	chr14:35494285-35494286	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs575916139	chr14:35494328-35494329	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs181181476	chr14:35494335-35494336	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs375680645	chr14:35494353-35494354	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs564372474	chr14:35494388-35494389	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs532054828	chr14:35494389-35494390	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	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:1838 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35453800-35499200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr14:35454400-35509800	Weak transcription	Psoas Muscle	Psoas
3	chr14:35465200-35500600	Strong transcription	HepG2	liver
4	chr14:35465600-35500200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr14:35466000-35501400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr14:35466000-35503800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr14:35466200-35500600	Strong transcription	Rectal Mucosa Donor 29	rectum
8	chr14:35466400-35498200	Weak transcription	Spleen	Spleen
9	chr14:35466600-35502000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
10	chr14:35466800-35502800	Strong transcription	Primary T helper cells PMA-I stimulated	--
11	chr14:35467000-35496600	Weak transcription	K562	blood
12	chr14:35467600-35503600	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr14:35468600-35493600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr14:35468600-35501600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr14:35470600-35502600	Strong transcription	Liver	Liver
16	chr14:35471800-35501600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr14:35473400-35501800	Strong transcription	HUES64 Cell Line	embryonic stem cell
18	chr14:35474200-35501400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr14:35474400-35503400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr14:35475000-35495400	Weak transcription	Aorta	Aorta
21	chr14:35475800-35500200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr14:35475800-35503200	Strong transcription	Adipose Nuclei	Adipose
23	chr14:35477000-35499000	Strong transcription	Placenta	Placenta
24	chr14:35477000-35502800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr14:35477200-35493800	Strong transcription	Skeletal Muscle Female	skeletal muscle
26	chr14:35477200-35499000	Strong transcription	Osteobl	bone
27	chr14:35477200-35502200	Strong transcription	Primary T cells fromperipheralblood	blood
28	chr14:35477200-35502800	Strong transcription	Primary T helper cells fromperipheralblood	blood
29	chr14:35477200-35502800	Strong transcription	Duodenum Mucosa	Duodenum
30	chr14:35477400-35502400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr14:35480000-35493400	Strong transcription	HUES48 Cell Line	embryonic stem cell
32	chr14:35480000-35495400	Weak transcription	Gastric	stomach
33	chr14:35480000-35503200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr14:35480400-35504000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr14:35481400-35493600	Strong transcription	Fetal Muscle Trunk	muscle
36	chr14:35481400-35498800	Strong transcription	GM12878-XiMat	blood
37	chr14:35481600-35495200	Strong transcription	HUES6 Cell Line	embryonic stem cell
38	chr14:35481600-35501200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr14:35481600-35502400	Strong transcription	Dnd41	blood
40	chr14:35482200-35501000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr14:35482600-35493200	Strong transcription	Sigmoid Colon	Sigmoid Colon
42	chr14:35482600-35494800	Strong transcription	Rectal Mucosa Donor 31	rectum
43	chr14:35482800-35503200	Weak transcription	Stomach Mucosa	stomach
44	chr14:35483800-35498200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr14:35483800-35501200	Strong transcription	Fetal Intestine Large	intestine
46	chr14:35484600-35495400	Weak transcription	Pancreas	Pancrea
47	chr14:35484600-35498800	Strong transcription	NH-A	brain
48	chr14:35485000-35493200	Strong transcription	Fetal Lung	lung
49	chr14:35485600-35497600	Weak transcription	Fetal Heart	heart
50	chr14:35485800-35501800	Weak transcription	Esophagus	oesophagus

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