Variant report

Variant	nsv564263
Chromosome Location	chr14:35466584-35556498
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1130)
CpG islands
(count:672)
Chromatin interactive
region (count:94)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:1130 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:35537558-35537700	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:35521017-35521344	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:35547257-35547542	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:35509539-35510010	HepG2	liver:	n/a	chr14:35509792-35509808
5	ARID3A	chr14:35519909-35520120	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:35519876-35520224	K562	blood:	n/a	n/a
7	ARID3A	chr14:35514746-35515759	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:35516133-35516303	HepG2	liver:	n/a	n/a
9	ATF1	chr14:35515122-35515876	K562	blood:	n/a	n/a
10	ATF1	chr14:35519862-35520172	K562	blood:	n/a	n/a
11	ATF1	chr14:35517147-35517386	K562	blood:	n/a	n/a
12	ATF2	chr14:35504149-35504484	GM12878	blood:	n/a	n/a
13	ATF2	chr14:35515054-35515466	GM12878	blood:	n/a	n/a
14	ATF2	chr14:35514853-35515586	GM12878	blood:	n/a	n/a
15	ATF2	chr14:35515000-35515488	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr14:35515153-35515540	H1-hESC	embryonic stem cell:	n/a	n/a
17	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
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	BACH1	chr14:35519638-35520190	K562	blood:	n/a	chr14:35520008-35520022
21	BATF	chr14:35502715-35503130	GM12878	blood:	n/a	chr14:35502942-35502953
22	BATF	chr14:35504265-35504563	GM12878	blood:	n/a	chr14:35504383-35504394
23	BATF	chr14:35504189-35504612	GM12878	blood:	n/a	chr14:35504383-35504394
24	BATF	chr14:35502850-35503057	GM12878	blood:	n/a	chr14:35502942-35502953
25	BATF	chr14:35515132-35515392	GM12878	blood:	n/a	chr14:35515350-35515363
26	BCL11A	chr14:35504236-35504481	GM12878	blood:	n/a	n/a
27	BCL3	chr14:35515416-35515871	A549	lung:	n/a	n/a
28	BCL3	chr14:35515089-35515763	GM12878	blood:	n/a	chr14:35515406-35515415
29	BCLAF1	chr14:35514960-35515869	GM12878	blood:	n/a	chr14:35515406-35515415
30	BHLHE40	chr14:35514866-35515778	K562	blood:	n/a	n/a
31	BHLHE40	chr14:35509723-35509774	K562	blood:	n/a	n/a
32	BHLHE40	chr14:35514837-35515868	HepG2	liver:	n/a	n/a
33	BHLHE40	chr14:35516561-35516712	GM12878	blood:	n/a	n/a
34	BHLHE40	chr14:35514808-35515688	GM12878	blood:	n/a	n/a
35	BHLHE40	chr14:35516483-35516685	K562	blood:	n/a	n/a
36	BRCA1	chr14:35515197-35515787	GM12878	blood:	n/a	n/a
37	BRCA1	chr14:35515067-35515671	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr14:35515159-35515688	H1-hESC	embryonic stem cell:	n/a	n/a
39	BRCA1	chr14:35516063-35516352	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr14:35514954-35516171	HepG2	liver:	n/a	n/a
41	CBX3	chr14:35503722-35504021	K562	blood:	n/a	n/a
42	CBX3	chr14:35503606-35504100	K562	blood:	n/a	n/a
43	CCNT2	chr14:35515159-35516049	K562	blood:	n/a	chr14:35515540-35515549
44	CCNT2	chr14:35519979-35520161	K562	blood:	n/a	n/a
45	CEBPB	chr14:35514743-35514990	K562	blood:	n/a	chr14:35514905-35514918
46	CEBPB	chr14:35530316-35530631	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr14:35514766-35515598	MCF-7	breast:	n/a	chr14:35514905-35514918
48	CEBPB	chr14:35514023-35514086	K562	blood:	n/a	chr14:35514043-35514054
49	CEBPB	chr14:35502339-35502472	HepG2	liver:	n/a	n/a
50	CEBPB	chr14:35537899-35538083	HepG2	liver:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35516283-35516333	HMEC	breast:	n/a
2	chr14:35516283-35516333	HMEC	breast:	n/a
3	chr14:35514333-35514383	HIPEpiC	eye:	n/a
4	chr14:35515291-35515341	GM06990	blood:	n/a
5	chr14:35495536-35495586	HRE	kidney:	n/a
6	chr14:35515414-35515464	HCT-116	colon:	n/a
7	chr14:35495536-35495586	K562	blood:	n/a
8	chr14:35515356-35515406	HEK293	kidney:	embryo
9	chr14:35495536-35495586	SAEC	small airway:	n/a
10	chr14:35540926-35540976	BE2_C	brain:	n/a
11	chr14:35498490-35498540	SKMC	muscle:	n/a
12	chr14:35515116-35515166	CMK	blood:	n/a
13	chr14:35540926-35540976	Hepatocyte	liver:	n/a
14	chr14:35512367-35512417	GM06990	blood:	n/a
15	chr14:35515116-35515166	NB4	blood:	n/a
16	chr14:35515356-35515406	ovcar-3	ovarian:	n/a
17	chr14:35512367-35512417	AG04449	skin:	fetal
18	chr14:35515116-35515166	ProgFib	skin:	n/a
19	chr14:35514333-35514383	IMR90	lung:	fetal
20	chr14:35516283-35516333	GM12891	blood:	n/a
21	chr14:35495536-35495586	GM12892	blood:	n/a
22	chr14:35516283-35516333	HPAEpiC	pulmonary alveolar:	n/a
23	chr14:35515291-35515341	HPAEpiC	pulmonary alveolar:	n/a
24	chr14:35515858-35515908	Caco-2	colon:	n/a
25	chr14:35514333-35514383	SK-N-MC	brain:	n/a
26	chr14:35515356-35515406	HRE	kidney:	n/a
27	chr14:35515858-35515908	ovcar-3	ovarian:	n/a
28	chr14:35498490-35498540	AG09309	skin:	n/a
29	chr14:35514333-35514383	HepG2	liver:	n/a
30	chr14:35515414-35515464	GM12891	blood:	n/a
31	chr14:35516283-35516333	NHDF-neo	bronchial:	n/a
32	chr14:35498490-35498540	GM06990	blood:	n/a
33	chr14:35498490-35498540	T-47D	breast:	n/a
34	chr14:35512367-35512417	ProgFib	skin:	n/a
35	chr14:35515858-35515908	SAEC	small airway:	n/a
36	chr14:35515858-35515908	CMK	blood:	n/a
37	chr14:35540926-35540976	PFSK-1	brain:	n/a
38	chr14:35516283-35516333	IMR90	lung:	fetal
39	chr14:35515291-35515341	AG09309	skin:	n/a
40	chr14:35515116-35515166	AG04450	lung:	fetal
41	chr14:35515858-35515908	MCF-7	breast:	n/a
42	chr14:35514333-35514383	H1-hESC	embryonic stem cell:	embryo
43	chr14:35495536-35495586	AG09309	skin:	n/a
44	chr14:35515291-35515341	GM12878	blood:	n/a
45	chr14:35495536-35495586	ECC-1	luminal epithelium:	n/a
46	chr14:35498490-35498540	HL-60	blood:	n/a
47	chr14:35516283-35516333	SKMC	muscle:	n/a
48	chr14:35515858-35515908	GM12878	blood:	n/a
49	chr14:35495536-35495586	A549	lung:	n/a
50	chr14:35515116-35515166	IMR90	lung:	fetal

(count:94 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:35450099..35453742-chr14:35513316..35517237,10	K562	blood:
2	chr14:35514347..35516079-chr14:35590063..35591815,2	K562	blood:
3	chr14:35542856..35545379-chr14:35545884..35547837,2	K562	blood:
4	chr14:35524936..35527808-chr14:35546522..35548065,2	MCF-7	breast:
5	chr14:35514228..35515878-chr14:35780242..35782321,2	MCF-7	breast:
6	chr14:35519987..35522404-chr14:35523498..35526576,3	K562	blood:
7	chr14:35515362..35516342-chr16:11836358..11837096,2	Hela-S3	cervix:
8	chr14:35465599..35469103-chr14:35471087..35474391,3	MCF-7	breast:
9	chr14:35456800..35459337-chr14:35464974..35467131,2	K562	blood:
10	chr14:35507467..35509940-chr14:35513836..35516152,2	MCF-7	breast:
11	chr14:35517575..35519344-chr14:35683138..35684908,2	MCF-7	breast:
12	chr14:35451620..35453361-chr14:35464939..35467575,2	MCF-7	breast:
13	chr14:35514107..35515830-chr14:35872683..35874428,2	MCF-7	breast:
14	chr14:35546558..35548524-chr14:35548647..35551587,2	K562	blood:
15	chr14:35449839..35454578-chr14:35513316..35515954,7	K562	blood:
16	chr14:35515365..35516134-chr15:65596788..65597492,2	Hela-S3	cervix:
17	chr14:35513511..35517056-chr14:35517636..35522677,6	K562	blood:
18	chr14:35513511..35517056-chr14:35517636..35522677,6	K562	blood:
19	chr11:65266267..65267153-chr14:35515173..35515777,2	Hela-S3	cervix:
20	chr14:35481674..35484183-chr14:35515641..35517435,2	MCF-7	breast:
21	chr14:35556172..35559296-chr14:35562772..35565829,3	MCF-7	breast:
22	chr14:35516520..35518836-chr14:35536161..35537991,2	K562	blood:
23	chr14:35520904..35522612-chr14:35525076..35526619,2	K562	blood:
24	chr14:35473349..35476278-chr14:35514310..35517232,2	MCF-7	breast:
25	chr14:35513731..35517214-chr14:35589119..35593617,5	MCF-7	breast:
26	chr11:62608378..62609108-chr14:35519776..35520391,2	Hela-S3	cervix:
27	chr14:35492619..35494488-chr14:35513893..35516711,2	MCF-7	breast:
28	chr14:35509776..35510382-chr14:35602542..35603513,2	MCF-7	breast:
29	chr14:35520110..35522080-chr14:35529783..35531632,2	MCF-7	breast:
30	chr14:35545880..35548959-chr14:35590371..35593257,4	MCF-7	breast:
31	chr14:35512802..35518057-chr14:35589980..35593805,9	MCF-7	breast:
32	chr14:35515295..35517054-chr14:35528629..35530241,2	MCF-7	breast:
33	chr14:35515172..35516906-chr14:35528396..35530412,2	K562	blood:
34	chr14:35515379..35516132-chr17:56736001..56736995,2	NB4	blood:
35	chr14:35514893..35515885-chr2:74692133..74692798,2	Hela-S3	cervix:
36	chr14:35506932..35507762-chr3:185524185..185525086,2	MCF-7	breast:
37	chr14:35509919..35510459-chr14:35875894..35876731,2	MCF-7	breast:
38	chr14:35450596..35455465-chr14:35514082..35520003,7	MCF-7	breast:
39	chr14:35515655..35516294-chr7:100025920..100026511,2	Hela-S3	cervix:
40	chr14:35515170..35517585-chr14:35518270..35521794,5	K562	blood:
41	chr14:35520110..35522080-chr14:35529783..35531632,2	MCF-7	breast:
42	chr14:35513942..35517116-chr14:35546230..35550128,3	MCF-7	breast:
43	chr14:35525027..35526542-chr14:35529643..35531640,2	K562	blood:
44	chr14:35516667..35519479-chr14:35589018..35592188,3	K562	blood:
45	chr14:35519616..35521249-chr14:35528506..35531084,2	MCF-7	breast:
46	chr14:35518346..35520607-chr14:35589756..35591434,2	MCF-7	breast:
47	chr14:35515994..35521853-chr14:35871391..35874738,9	MCF-7	breast:
48	chr14:35514169..35519549-chr14:35872431..35877872,11	MCF-7	breast:
49	chr14:35519987..35522404-chr14:35523498..35526576,3	K562	blood:
50	chr14:35500902..35503626-chr14:35810015..35811675,2	MCF-7	breast:

(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

(count:6 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	FAM177A1	hsa-miR-186-5p	chr14:35550483-35550504
2	FAM177A1	hsa-miR-124-3p	chr14:35552521-35552538
3	FAM177A1	hsa-miR-155-5p	chr14:35551927-35551947
4	FAM177A1	hsa-miR-142-3p	chr14:35551080-35551101
5	FAM177A1	hsa-miR-186-5p	chr14:35551034-35551055
6	FAM177A1	hsa-miR-124-3p	chr14:35552531-35552538

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

Extended variants
information (count: 3421 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:3421 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs876144	chr14:35466584-35466585	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs559248919	chr14:35466596-35466597	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs148716085	chr14:35466613-35466614	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs142294231	chr14:35466615-35466616	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs34315973	chr14:35466642-35466643	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs181476097	chr14:35466660-35466661	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs530865984	chr14:35466693-35466694	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs551064940	chr14:35466741-35466742	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs570853201	chr14:35466753-35466754	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs185625331	chr14:35466762-35466763	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs190085432	chr14:35466767-35466768	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs528072687	chr14:35466773-35466774	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs536163097	chr14:35466791-35466792	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs180906907	chr14:35466802-35466803	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs185785642	chr14:35466827-35466828	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs192358078	chr14:35466839-35466840	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs556684322	chr14:35466854-35466855	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs576406415	chr14:35466855-35466856	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs560076058	chr14:35466870-35466871	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs147952583	chr14:35466874-35466875	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs567766253	chr14:35466901-35466902	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs535134448	chr14:35466937-35466938	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs552562526	chr14:35466954-35466955	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs12435454	chr14:35466997-35466998	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs542113148	chr14:35467014-35467015	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs183733488	chr14:35467091-35467092	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs575438485	chr14:35467092-35467093	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs551392749	chr14:35467101-35467102	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs544379799	chr14:35467133-35467134	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs74046408	chr14:35467135-35467136	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs533350081	chr14:35467159-35467160	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs546982828	chr14:35467168-35467169	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs560495975	chr14:35467188-35467189	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs529520228	chr14:35467190-35467191	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs117732497	chr14:35467199-35467200	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs558919338	chr14:35467222-35467223	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs564795198	chr14:35467271-35467272	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs368735148	chr14:35467304-35467305	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs369416209	chr14:35467309-35467310	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs140220691	chr14:35467334-35467335	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs145685623	chr14:35467344-35467345	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs552108416	chr14:35467431-35467432	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs550243705	chr14:35467442-35467443	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs187834186	chr14:35467448-35467449	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs539164990	chr14:35467472-35467473	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs114622577	chr14:35467485-35467486	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs112351818	chr14:35467535-35467536	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs117905034	chr14:35467569-35467570	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs532023982	chr14:35467593-35467594	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs147710794	chr14:35467703-35467704	Weak transcription Strong transcription Enhancers	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:2988 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35452800-35478200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr14:35453200-35467200	Weak transcription	Fetal Muscle Trunk	muscle
3	chr14:35453200-35474200	Weak transcription	Aorta	Aorta
4	chr14:35453400-35467400	Weak transcription	Placenta	Placenta
5	chr14:35453600-35467600	Weak transcription	Fetal Intestine Small	intestine
6	chr14:35453600-35468800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr14:35453600-35470600	Weak transcription	Fetal Stomach	stomach
8	chr14:35453600-35474200	Weak transcription	Right Ventricle	heart
9	chr14:35453600-35485600	Weak transcription	HSMMtube	muscle
10	chr14:35453800-35466600	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr14:35453800-35467200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr14:35453800-35467200	Weak transcription	Primary hematopoietic stem cells	blood
13	chr14:35453800-35467200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr14:35453800-35468600	Weak transcription	Colonic Mucosa	Colon
15	chr14:35453800-35472000	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr14:35453800-35473600	Weak transcription	Fetal Lung	lung
17	chr14:35453800-35474000	Weak transcription	NHEK	skin
18	chr14:35453800-35476000	Weak transcription	Rectal Smooth Muscle	rectum
19	chr14:35453800-35499200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr14:35454000-35479200	Weak transcription	Gastric	stomach
21	chr14:35454400-35468800	Weak transcription	Left Ventricle	heart
22	chr14:35454400-35471200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr14:35454400-35481600	Weak transcription	HMEC	breast
24	chr14:35454400-35485200	Weak transcription	Esophagus	oesophagus
25	chr14:35454400-35509800	Weak transcription	Psoas Muscle	Psoas
26	chr14:35454600-35468800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr14:35454600-35474000	Weak transcription	Brain Angular Gyrus	brain
28	chr14:35454800-35466600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr14:35454800-35466600	Weak transcription	Osteobl	bone
30	chr14:35454800-35466800	Weak transcription	Adipose Nuclei	Adipose
31	chr14:35454800-35467000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr14:35454800-35468400	Weak transcription	Fetal Muscle Leg	muscle
33	chr14:35454800-35468600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr14:35454800-35468800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr14:35454800-35469200	Weak transcription	Brain Substantia Nigra	brain
36	chr14:35454800-35471600	Weak transcription	Ovary	ovary
37	chr14:35454800-35471800	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr14:35454800-35472000	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr14:35454800-35474000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr14:35454800-35481600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr14:35454800-35483600	Weak transcription	Small Intestine	intestine
42	chr14:35454800-35484800	Weak transcription	Fetal Brain Male	brain
43	chr14:35455000-35466600	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr14:35455000-35466600	Weak transcription	Brain Cingulate Gyrus	brain
45	chr14:35455000-35468800	Weak transcription	Fetal Heart	heart
46	chr14:35455000-35470600	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr14:35455200-35466600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr14:35455200-35466800	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr14:35455200-35467000	Weak transcription	Primary T cells from cord blood	blood
50	chr14:35455200-35467000	Weak transcription	Duodenum Mucosa	Duodenum

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