Variant report

Variant	nsv1039230
Chromosome Location	chr14:69922552-69972002
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1070)
CpG islands
(count:1222)
Chromatin interactive
region (count:53)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1070 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:69926824-69927161	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:69941910-69942131	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:69941879-69942182	K562	blood:	n/a	n/a
4	ARID3A	chr14:69926831-69927180	K562	blood:	n/a	n/a
5	ARID3A	chr14:69970593-69970792	HepG2	liver:	n/a	n/a
6	ATF1	chr14:69926858-69927169	K562	blood:	n/a	n/a
7	BACH1	chr14:69948935-69949141	K562	blood:	n/a	n/a
8	BACH1	chr14:69950648-69951056	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr14:69968018-69968246	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr14:69948920-69949253	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr14:69938610-69938873	GM12878	blood:	n/a	chr14:69938787-69938797 chr14:69938790-69938801
12	BATF	chr14:69938611-69938940	GM12878	blood:	n/a	chr14:69938787-69938797 chr14:69938790-69938801
13	BHLHE40	chr14:69925845-69926040	K562	blood:	n/a	n/a
14	BHLHE40	chr14:69938666-69938985	GM12878	blood:	n/a	n/a
15	BHLHE40	chr14:69926882-69927125	GM12878	blood:	n/a	n/a
16	BHLHE40	chr14:69926849-69927149	K562	blood:	n/a	n/a
17	BRCA1	chr14:69926810-69927151	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr14:69940288-69940504	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr14:69926890-69927205	A549	lung:	n/a	n/a
20	CEBPB	chr14:69923739-69924095	MCF-7	breast:	n/a	n/a
21	CEBPB	chr14:69959052-69959243	A549	lung:	n/a	chr14:69959128-69959139 chr14:69959127-69959140
22	CEBPB	chr14:69935812-69935918	IMR90	lung:	n/a	n/a
23	CEBPB	chr14:69950226-69950924	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPB	chr14:69926851-69927177	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr14:69957851-69957951	K562	blood:	n/a	chr14:69957884-69957895
26	CEBPB	chr14:69959034-69959265	HepG2	liver:	n/a	chr14:69959128-69959139 chr14:69959127-69959140
27	CEBPB	chr14:69926814-69927165	IMR90	lung:	n/a	n/a
28	CEBPB	chr14:69925222-69925301	HepG2	liver:	n/a	n/a
29	CEBPB	chr14:69957726-69958039	HepG2	liver:	n/a	chr14:69957884-69957895
30	CHD2	chr14:69950982-69951100	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr14:69926903-69927066	GM12878	blood:	n/a	n/a
32	CREB1	chr14:69926663-69927279	K562	blood:	n/a	n/a
33	CREB1	chr14:69926855-69927102	A549	lung:	n/a	n/a
34	CREB1	chr14:69926650-69927291	GM12878	blood:	n/a	n/a
35	CREB1	chr14:69926705-69927203	K562	blood:	n/a	n/a
36	CREB1	chr14:69926775-69927172	GM12878	blood:	n/a	n/a
37	CTBP2	chr14:69950474-69951751	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr14:69943620-69943770	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr14:69943640-69943790	RPTEC	kidney:	n/a	n/a
40	CTCF	chr14:69970620-69970770	AG10803	skin:	n/a	n/a
41	CTCF	chr14:69943620-69943770	AoAF	blood vessel:	n/a	n/a
42	CTCF	chr14:69941920-69942070	NHLF	lung:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
43	CTCF	chr14:69970573-69970767	GM13977	blood:	n/a	n/a
44	CTCF	chr14:69926894-69927176	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr14:69926940-69927090	GM12878	blood:	n/a	n/a
46	CTCF	chr14:69943620-69943770	HRE	kidney:	n/a	n/a
47	CTCF	chr14:69926940-69927090	Caco-2	colon:	n/a	n/a
48	CTCF	chr14:69943640-69943790	AG09319	gingival:	n/a	n/a
49	CTCF	chr14:69926900-69927050	MCF-7	breast:	n/a	n/a
50	CTCF	chr14:69970600-69970750	HMEC	breast:	n/a	n/a

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:69950574-69950624	HIPEpiC	eye:	n/a
2	chr14:69950574-69950624	Jurkat	blood:	n/a
3	chr14:69950574-69950624	HIPEpiC	eye:	n/a
4	chr14:69950574-69950624	Jurkat	blood:	n/a
5	chr14:69950574-69950624	LNCaP	prostate:	n/a
6	chr14:69951839-69951889	SAEC	small airway:	n/a
7	chr14:69951211-69951261	GM12892	blood:	n/a
8	chr14:69951322-69951372	HPAEpiC	pulmonary alveolar:	n/a
9	chr14:69951322-69951372	A549	lung:	n/a
10	chr14:69927947-69927997	ECC-1	luminal epithelium:	n/a
11	chr14:69951720-69951770	AG10803	skin:	n/a
12	chr14:69931877-69931927	ProgFib	skin:	n/a
13	chr14:69950043-69950093	IMR90	lung:	fetal
14	chr14:69950574-69950624	GM06990	blood:	n/a
15	chr14:69968273-69968323	HepG2	liver:	n/a
16	chr14:69951422-69951472	SK-N-SH_RA	brain:	n/a
17	chr14:69947271-69947321	HMEC	breast:	n/a
18	chr14:69951305-69951355	LNCaP	prostate:	n/a
19	chr14:69947271-69947321	H1-hESC	embryonic stem cell:	embryo
20	chr14:69952104-69952154	A549	lung:	n/a
21	chr14:69951422-69951472	LNCaP	prostate:	n/a
22	chr14:69954135-69954185	AG10803	skin:	n/a
23	chr14:69951720-69951770	GM12892	blood:	n/a
24	chr14:69952104-69952154	HNPCEpiC	eye:	n/a
25	chr14:69950043-69950093	HCPEpiC	choroid plexus:	n/a
26	chr14:69951311-69951361	HCPEpiC	choroid plexus:	n/a
27	chr14:69951781-69951831	PFSK-1	brain:	n/a
28	chr14:69951322-69951372	GM12878	blood:	n/a
29	chr14:69951839-69951889	HCM	heart:	n/a
30	chr14:69951720-69951770	AG04449	skin:	fetal
31	chr14:69951305-69951355	HCT-116	colon:	n/a
32	chr14:69951322-69951372	HRCEpiC	kidney:	n/a
33	chr14:69951839-69951889	ECC-1	luminal epithelium:	n/a
34	chr14:69951322-69951372	HCM	heart:	n/a
35	chr14:69950043-69950093	HRE	kidney:	n/a
36	chr14:69952003-69952053	ovcar-3	ovarian:	n/a
37	chr14:69952003-69952053	T-47D	breast:	n/a
38	chr14:69951372-69951422	Caco-2	colon:	n/a
39	chr14:69950116-69950166	BE2_C	brain:	n/a
40	chr14:69951781-69951831	Jurkat	blood:	n/a
41	chr14:69951211-69951261	PANC-1	pancreas:	n/a
42	chr14:69952003-69952053	PrEC	prostate:	n/a
43	chr14:69951305-69951355	H1-hESC	embryonic stem cell:	embryo
44	chr14:69951211-69951261	HRPEpiC	eye:	n/a
45	chr14:69951372-69951422	IMR90	lung:	fetal
46	chr14:69951305-69951355	K562	blood:	n/a
47	chr14:69951311-69951361	GM06990	blood:	n/a
48	chr14:69951720-69951770	GM12878	blood:	n/a
49	chr14:69931877-69931927	HEEpiC	esophagus:	n/a
50	chr14:69950043-69950093	ovcar-3	ovarian:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:69920954..69922535-chr14:69924046..69926530,2	MCF-7	breast:
2	chr14:69863461..69868593-chr14:69924955..69929429,6	MCF-7	breast:
3	chr14:69947992..69950774-chr14:69962839..69965276,2	K562	blood:
4	chr14:69941960..69942511-chr14:69967141..69968031,2	MCF-7	breast:
5	chr14:69958713..69961679-chr14:69965168..69967666,2	MCF-7	breast:
6	chr14:69950456..69952040-chr14:70233397..70235258,2	MCF-7	breast:
7	chr14:69877530..69878097-chr14:69941616..69942179,2	MCF-7	breast:
8	chr14:69863597..69866154-chr14:69965430..69966974,2	MCF-7	breast:
9	chr14:69946123..69947705-chr14:69948349..69951147,2	MCF-7	breast:
10	chr14:69951736..69954477-chr14:69954891..69957562,2	MCF-7	breast:
11	chr14:69821722..69824231-chr14:69923203..69925103,2	MCF-7	breast:
12	chr14:69947992..69950774-chr14:69962839..69965276,2	K562	blood:
13	chr14:69829365..69831341-chr14:69925811..69928602,2	MCF-7	breast:
14	chr14:69951443..69953126-chr14:69953457..69956317,2	MCF-7	breast:
15	chr14:69878685..69880394-chr14:69926350..69928996,2	K562	blood:
16	chr14:69708990..69709961-chr14:69926423..69927285,4	MCF-7	breast:
17	chr14:69947992..69950774-chr14:69962839..69965833,3	K562	blood:
18	chr14:69949714..69952374-chr14:70039182..70041131,3	MCF-7	breast:
19	chr14:69952428..69953410-chr5:19316375..19317263,2	MCF-7	breast:
20	chr14:69865072..69867138-chr14:69919938..69922880,2	MCF-7	breast:
21	chr14:69619033..69620696-chr14:69925440..69927325,2	MCF-7	breast:
22	chr14:69708308..69710896-chr14:69926995..69929013,2	MCF-7	breast:
23	chr14:69958713..69961679-chr14:69965168..69967666,2	MCF-7	breast:
24	chr14:69951841..69953361-chr7:104652261..104653928,2	MCF-7	breast:
25	chr14:69709454..69710236-chr14:69926522..69927633,4	K562	blood:
26	chr14:69970369..69971161-chr14:70041166..70042114,4	MCF-7	breast:
27	chr14:69959710..69961607-chr14:69966720..69969108,2	MCF-7	breast:
28	chr14:69932792..69935168-chr14:70232400..70234408,2	K562	blood:
29	chr14:69969961..69971754-chr14:70233921..70235579,2	K562	blood:
30	chr14:69970253..69971296-chr14:70001641..70002581,3	MCF-7	breast:
31	chr14:69813202..69813855-chr14:69926762..69927557,4	MCF-7	breast:
32	chr14:69833381..69834049-chr14:69926658..69927452,2	MCF-7	breast:
33	chr14:69863307..69865409-chr14:69940498..69943105,2	MCF-7	breast:
34	chr14:69815842..69819268-chr14:69923313..69926949,3	MCF-7	breast:
35	chr14:69947861..69950985-chr14:69958572..69961159,3	MCF-7	breast:
36	chr14:69947992..69950774-chr14:69962839..69965833,3	K562	blood:
37	chr14:69865252..69866906-chr14:69922886..69924769,3	MCF-7	breast:
38	chr14:69819465..69821642-chr14:69923369..69926196,2	MCF-7	breast:
39	chr14:69941960..69942511-chr14:69967141..69968031,2	MCF-7	breast:
40	chr14:69951736..69954477-chr14:69954891..69957562,2	MCF-7	breast:
41	chr14:69708985..69710051-chr14:69926386..69927467,4	MCF-7	breast:
42	chr14:69959710..69961607-chr14:69966720..69969108,2	MCF-7	breast:
43	chr14:69940565..69944198-chr14:69948650..69951872,3	MCF-7	breast:
44	chr14:69725416..69728127-chr14:69925008..69927270,2	MCF-7	breast:
45	chr14:69862767..69865090-chr14:69948473..69950881,2	MCF-7	breast:
46	chr14:69714947..69715448-chr14:69926707..69927678,2	MCF-7	breast:
47	chr14:69970211..69971130-chr14:70193442..70194320,2	MCF-7	breast:
48	chr14:69949476..69951469-chr14:70232962..70234565,2	MCF-7	breast:
49	chr14:69951860..69952360-chr7:104652907..104653592,2	Hela-S3	cervix:
50	chr14:69970362..69971107-chr14:70041144..70041646,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ERH-1	chr14:69925417-69926228	ENSG00000249775

No data

Variant related genes	Relation type
PLEKHD1	TF binding region
PLEKHD1	CpG island
ENSG00000175985	chromatin interactions
ENSG00000100626	chromatin interactions
ENSG00000100650	chromatin interactions
ENSG00000267909	chromatin interactions
ENSG00000100632	chromatin interactions
ENSG00000139990	chromatin interactions
ENSG00000029364	chromatin interactions
ENSG00000258520	chromatin interactions
ENSG00000228393	chromatin interactions
DDX17	miRNA target sites

Extended variants
information (count: 1721 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1721 , 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	rs2232059	chr14:69922552-69922553	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs376016493	chr14:69922591-69922592	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs563946460	chr14:69922599-69922600	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs117742817	chr14:69922647-69922648	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs112529420	chr14:69922670-69922671	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs561484429	chr14:69922697-69922698	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs528838053	chr14:69922736-69922737	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs147361756	chr14:69922739-69922740	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs139477373	chr14:69922760-69922761	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs35779467	chr14:69922808-69922809	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs560916626	chr14:69922827-69922828	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs528047368	chr14:69922847-69922848	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs546591900	chr14:69922917-69922918	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs570260219	chr14:69922926-69922927	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs187098200	chr14:69922962-69922963	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs555883735	chr14:69922981-69922982	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs567786577	chr14:69922996-69922997	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs61982402	chr14:69923018-69923019	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs116061271	chr14:69923034-69923035	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs572203476	chr14:69923060-69923061	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs539722832	chr14:69923147-69923148	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs557677538	chr14:69923168-69923169	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs575821534	chr14:69923187-69923188	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs543246543	chr14:69923191-69923192	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs142544417	chr14:69923196-69923197	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs532453147	chr14:69923221-69923222	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs550793215	chr14:69923241-69923242	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs573696699	chr14:69923281-69923282	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs540630175	chr14:69923325-69923326	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs559303484	chr14:69923342-69923343	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs192170997	chr14:69923360-69923361	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs150537910	chr14:69923362-69923363	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs564007139	chr14:69923400-69923401	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs569115111	chr14:69923439-69923440	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs183331290	chr14:69923464-69923465	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs536730839	chr14:69923585-69923586	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs566899436	chr14:69923617-69923618	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs8013221	chr14:69923702-69923703	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs139544592	chr14:69923776-69923777	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs546628319	chr14:69923862-69923863	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs554606508	chr14:69923887-69923888	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs145943038	chr14:69923892-69923893	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs33924796	chr14:69923893-69923894	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs1275675	chr14:69923902-69923903	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs113164473	chr14:69923903-69923904	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs35410490	chr14:69923904-69923905	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs375368251	chr14:69923906-69923907	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs557614265	chr14:69923909-69923910	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs575953911	chr14:69923923-69923924	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs536817620	chr14:69923933-69923934	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
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
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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Hematopoietic stem cell	20738155	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69868000-69923200	Weak transcription	Esophagus	oesophagus
2	chr14:69889200-69923400	Weak transcription	Colon Smooth Muscle	Colon
3	chr14:69889400-69923200	Weak transcription	Pancreas	Pancrea
4	chr14:69891200-69922800	Weak transcription	Colonic Mucosa	Colon
5	chr14:69891200-69923000	Weak transcription	NHLF	lung
6	chr14:69892200-69931400	Weak transcription	K562	blood
7	chr14:69893000-69922800	Weak transcription	Aorta	Aorta
8	chr14:69893200-69926800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr14:69893400-69922600	Weak transcription	Brain Germinal Matrix	brain
10	chr14:69893400-69922800	Weak transcription	Rectal Smooth Muscle	rectum
11	chr14:69893400-69923000	Weak transcription	Lung	lung
12	chr14:69893600-69922800	Weak transcription	Brain Hippocampus Middle	brain
13	chr14:69893600-69923200	Weak transcription	Gastric	stomach
14	chr14:69893600-69925000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr14:69894000-69922800	Weak transcription	Brain Cingulate Gyrus	brain
16	chr14:69894000-69924400	Weak transcription	Brain Angular Gyrus	brain
17	chr14:69894600-69922800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr14:69902400-69927000	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr14:69903600-69937800	Weak transcription	Psoas Muscle	Psoas
20	chr14:69906800-69924400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr14:69906800-69924400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr14:69909000-69933200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr14:69909400-69922800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr14:69910200-69923000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr14:69910400-69927200	Weak transcription	NHEK	skin
26	chr14:69910800-69923000	Weak transcription	Thymus	Thymus
27	chr14:69911600-69922600	Weak transcription	A549	lung
28	chr14:69911600-69925600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr14:69911800-69922800	Weak transcription	NHDF-Ad	bronchial
30	chr14:69915800-69932600	Weak transcription	Fetal Heart	heart
31	chr14:69916200-69927000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr14:69916400-69926400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr14:69918400-69929200	Strong transcription	Primary T cells from cord blood	blood
34	chr14:69919200-69929600	Strong transcription	Primary T helper cells fromperipheralblood	blood
35	chr14:69919600-69926200	Strong transcription	Primary B cells from cord blood	blood
36	chr14:69919600-69929000	Strong transcription	Primary B cells from peripheral blood	blood
37	chr14:69919800-69924000	Strong transcription	GM12878-XiMat	blood
38	chr14:69919800-69925000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr14:69919800-69925800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr14:69919800-69926000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr14:69919800-69926000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
42	chr14:69919800-69926000	Strong transcription	Ovary	ovary
43	chr14:69919800-69926000	Strong transcription	Stomach Smooth Muscle	stomach
44	chr14:69919800-69926400	Strong transcription	Rectal Mucosa Donor 31	rectum
45	chr14:69919800-69926600	Strong transcription	HSMM	muscle
46	chr14:69919800-69928600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr14:69919800-69929000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr14:69919800-69929000	Strong transcription	Dnd41	blood
49	chr14:69919800-69929400	Strong transcription	Fetal Intestine Large	intestine
50	chr14:69919800-69929600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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