Variant report

Variant	nsv1048882
Chromosome Location	chr14:69920881-69976694
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1103)
CpG islands
(count:1223)
Chromatin interactive
region (count:53)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1103 , 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	chr14:69926824-69927161	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:69926831-69927180	K562	blood:	n/a	n/a
3	ARID3A	chr14:69970593-69970792	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:69941879-69942182	K562	blood:	n/a	n/a
5	ARID3A	chr14:69941910-69942131	HepG2	liver:	n/a	n/a
6	ATF1	chr14:69926858-69927169	K562	blood:	n/a	n/a
7	BACH1	chr14:69948920-69949253	H1-hESC	embryonic stem cell:	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	chr14:69948935-69949141	K562	blood:	n/a	n/a
11	BATF	chr14:69938611-69938940	GM12878	blood:	n/a	chr14:69938787-69938797 chr14:69938790-69938801
12	BATF	chr14:69938610-69938873	GM12878	blood:	n/a	chr14:69938787-69938797 chr14:69938790-69938801
13	BCL3	chr14:69973295-69973474	GM12878	blood:	n/a	n/a
14	BHLHE40	chr14:69925845-69926040	K562	blood:	n/a	n/a
15	BHLHE40	chr14:69938666-69938985	GM12878	blood:	n/a	n/a
16	BHLHE40	chr14:69926882-69927125	GM12878	blood:	n/a	n/a
17	BHLHE40	chr14:69926849-69927149	K562	blood:	n/a	n/a
18	BRCA1	chr14:69926810-69927151	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr14:69925222-69925301	HepG2	liver:	n/a	n/a
20	CEBPB	chr14:69959034-69959265	HepG2	liver:	n/a	chr14:69959128-69959139 chr14:69959127-69959140
21	CEBPB	chr14:69926851-69927177	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr14:69957726-69958039	HepG2	liver:	n/a	chr14:69957884-69957895
23	CEBPB	chr14:69926890-69927205	A549	lung:	n/a	n/a
24	CEBPB	chr14:69957851-69957951	K562	blood:	n/a	chr14:69957884-69957895
25	CEBPB	chr14:69959052-69959243	A549	lung:	n/a	chr14:69959128-69959139 chr14:69959127-69959140
26	CEBPB	chr14:69950226-69950924	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr14:69940288-69940504	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr14:69926814-69927165	IMR90	lung:	n/a	n/a
29	CEBPB	chr14:69935812-69935918	IMR90	lung:	n/a	n/a
30	CEBPB	chr14:69923739-69924095	MCF-7	breast:	n/a	n/a
31	CHD2	chr14:69950982-69951100	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr14:69926903-69927066	GM12878	blood:	n/a	n/a
33	CREB1	chr14:69926705-69927203	K562	blood:	n/a	n/a
34	CREB1	chr14:69926855-69927102	A549	lung:	n/a	n/a
35	CREB1	chr14:69926775-69927172	GM12878	blood:	n/a	n/a
36	CREB1	chr14:69926650-69927291	GM12878	blood:	n/a	n/a
37	CREB1	chr14:69926663-69927279	K562	blood:	n/a	n/a
38	CTBP2	chr14:69950474-69951751	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr14:69941943-69942209	A549	lung:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
40	CTCF	chr14:69970554-69970771	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr14:69941980-69942130	GM12874	blood:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
42	CTCF	chr14:69941940-69942090	GM12872	blood:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066
43	CTCF	chr14:69970600-69970750	AoAF	blood vessel:	n/a	n/a
44	CTCF	chr14:69926820-69927220	K562	blood:	n/a	n/a
45	CTCF	chr14:69941880-69942030	HCT-116	colon:	n/a	n/a
46	CTCF	chr14:69970445-69971256	SK-N-SH	brain:	n/a	chr14:69970988-69971006
47	CTCF	chr14:69943620-69943770	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr14:69926900-69927050	WI-38	lung:	n/a	n/a
49	CTCF	chr14:69970620-69970770	HepG2	liver:	n/a	n/a
50	CTCF	chr14:69941976-69942204	GM19239	blood:	n/a	chr14:69942046-69942059 chr14:69942043-69942061 chr14:69942045-69942066

(count:1223 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:69968273-69968323	PANC-1	pancreas:	n/a
2	chr14:69951311-69951361	AoSMC	blood vessel:	n/a
3	chr14:69951311-69951361	MCF-7	breast:	n/a
4	chr14:69968273-69968323	PANC-1	pancreas:	n/a
5	chr14:69951311-69951361	AoSMC	blood vessel:	n/a
6	chr14:69951311-69951361	MCF-7	breast:	n/a
7	chr14:69951495-69951545	Jurkat	blood:	n/a
8	chr14:69950116-69950166	GM12878	blood:	n/a
9	chr14:69968273-69968323	IMR90	lung:	fetal
10	chr14:69950116-69950166	GM19239	blood:	n/a
11	chr14:69951495-69951545	NHDF-neo	bronchial:	n/a
12	chr14:69950043-69950093	HPAEpiC	pulmonary alveolar:	n/a
13	chr14:69947271-69947321	BE2_C	brain:	n/a
14	chr14:69951372-69951422	K562	blood:	n/a
15	chr14:69951372-69951422	HRE	kidney:	n/a
16	chr14:69951311-69951361	SK-N-SH_RA	brain:	n/a
17	chr14:69968273-69968323	SK-N-SH_RA	brain:	n/a
18	chr14:69951211-69951261	HRE	kidney:	n/a
19	chr14:69951720-69951770	AG10803	skin:	n/a
20	chr14:69951422-69951472	RPTEC	kidney:	n/a
21	chr14:69951211-69951261	ECC-1	luminal epithelium:	n/a
22	chr14:69950043-69950093	MCF-7	breast:	n/a
23	chr14:69927947-69927997	HUVEC	blood vessel:	n/a
24	chr14:69951839-69951889	HUVEC	blood vessel:	n/a
25	chr14:69931877-69931927	Jurkat	blood:	n/a
26	chr14:69952104-69952154	HCT-116	colon:	n/a
27	chr14:69952104-69952154	PANC-1	pancreas:	n/a
28	chr14:69952104-69952154	HIPEpiC	eye:	n/a
29	chr14:69951720-69951770	AoSMC	blood vessel:	n/a
30	chr14:69968273-69968323	BE2_C	brain:	n/a
31	chr14:69931877-69931927	MCF10A-Er-Src	breast:	n/a
32	chr14:69951305-69951355	IMR90	lung:	fetal
33	chr14:69951781-69951831	BJ	skin:	n/a
34	chr14:69951781-69951831	U87	brain:	n/a
35	chr14:69950116-69950166	IMR90	lung:	fetal
36	chr14:69968273-69968323	Caco-2	colon:	n/a
37	chr14:69951311-69951361	AG09319	gingival:	n/a
38	chr14:69968273-69968323	AG10803	skin:	n/a
39	chr14:69951422-69951472	AG09319	gingival:	n/a
40	chr14:69952104-69952154	ProgFib	skin:	n/a
41	chr14:69968273-69968323	HRCEpiC	kidney:	n/a
42	chr14:69951211-69951261	BE2_C	brain:	n/a
43	chr14:69951372-69951422	Caco-2	colon:	n/a
44	chr14:69950574-69950624	RPTEC	kidney:	n/a
45	chr14:69954135-69954185	BJ	skin:	n/a
46	chr14:69951372-69951422	SK-N-SH	brain:	n/a
47	chr14:69951781-69951831	SAEC	small airway:	n/a
48	chr14:69951322-69951372	HRCEpiC	kidney:	n/a
49	chr14:69927947-69927997	ECC-1	luminal epithelium:	n/a
50	chr14:69950574-69950624	GM19239	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:69958713..69961679-chr14:69965168..69967666,2	MCF-7	breast:
2	chr14:69947992..69950774-chr14:69962839..69965276,2	K562	blood:
3	chr14:69865072..69867138-chr14:69919938..69922880,2	MCF-7	breast:
4	chr14:69829365..69831341-chr14:69925811..69928602,2	MCF-7	breast:
5	chr14:69714947..69715448-chr14:69926707..69927678,2	MCF-7	breast:
6	chr14:69946123..69947705-chr14:69948349..69951147,2	MCF-7	breast:
7	chr14:69878685..69880394-chr14:69926350..69928996,2	K562	blood:
8	chr14:69959710..69961607-chr14:69966720..69969108,2	MCF-7	breast:
9	chr14:69708985..69710051-chr14:69926386..69927467,4	MCF-7	breast:
10	chr14:69950456..69952040-chr14:70233397..70235258,2	MCF-7	breast:
11	chr14:69949476..69951469-chr14:70232962..70234565,2	MCF-7	breast:
12	chr14:69932792..69935168-chr14:70232400..70234408,2	K562	blood:
13	chr14:69952428..69953410-chr5:19316375..19317263,2	MCF-7	breast:
14	chr14:69862767..69865090-chr14:69948473..69950881,2	MCF-7	breast:
15	chr14:69940565..69944198-chr14:69948650..69951872,3	MCF-7	breast:
16	chr14:69813202..69813855-chr14:69926762..69927557,4	MCF-7	breast:
17	chr14:69946123..69947705-chr14:69948349..69951147,2	MCF-7	breast:
18	chr14:69725416..69728127-chr14:69925008..69927270,2	MCF-7	breast:
19	chr14:69949714..69952374-chr14:70039182..70041131,3	MCF-7	breast:
20	chr14:69969961..69971754-chr14:70233921..70235579,2	K562	blood:
21	chr14:69947992..69950774-chr14:69962839..69965833,3	K562	blood:
22	chr14:69865252..69866906-chr14:69922886..69924769,3	MCF-7	breast:
23	chr14:69941960..69942511-chr14:69967141..69968031,2	MCF-7	breast:
24	chr14:69941960..69942511-chr14:69967141..69968031,2	MCF-7	breast:
25	chr14:69619033..69620696-chr14:69925440..69927325,2	MCF-7	breast:
26	chr14:69970362..69971107-chr14:70041144..70041646,2	K562	blood:
27	chr14:69821722..69824231-chr14:69923203..69925103,2	MCF-7	breast:
28	chr14:69833381..69834049-chr14:69926658..69927452,2	MCF-7	breast:
29	chr14:69877530..69878097-chr14:69941616..69942179,2	MCF-7	breast:
30	chr14:69863307..69865409-chr14:69940498..69943105,2	MCF-7	breast:
31	chr14:69815842..69819268-chr14:69923313..69926949,3	MCF-7	breast:
32	chr14:69920954..69922535-chr14:69924046..69926530,2	MCF-7	breast:
33	chr14:69947861..69950985-chr14:69958572..69961159,3	MCF-7	breast:
34	chr14:69947992..69950774-chr14:69962839..69965276,2	K562	blood:
35	chr14:69951736..69954477-chr14:69954891..69957562,2	MCF-7	breast:
36	chr14:69951736..69954477-chr14:69954891..69957562,2	MCF-7	breast:
37	chr14:69958713..69961679-chr14:69965168..69967666,2	MCF-7	breast:
38	chr14:69947861..69950985-chr14:69958572..69961159,3	MCF-7	breast:
39	chr14:69708990..69709961-chr14:69926423..69927285,4	MCF-7	breast:
40	chr14:69864699..69866812-chr14:69943113..69945643,2	MCF-7	breast:
41	chr14:69951443..69953126-chr14:69953457..69956317,2	MCF-7	breast:
42	chr14:69863461..69868593-chr14:69924955..69929429,6	MCF-7	breast:
43	chr14:69959710..69961607-chr14:69966720..69969108,2	MCF-7	breast:
44	chr14:69819465..69821642-chr14:69923369..69926196,2	MCF-7	breast:
45	chr14:69708308..69710896-chr14:69926995..69929013,2	MCF-7	breast:
46	chr14:69951860..69952360-chr7:104652907..104653592,2	Hela-S3	cervix:
47	chr14:69951841..69953361-chr7:104652261..104653928,2	MCF-7	breast:
48	chr14:69970211..69971130-chr14:70193442..70194320,2	MCF-7	breast:
49	chr14:69947992..69950774-chr14:69962839..69965833,3	K562	blood:
50	chr14:69970253..69971296-chr14:70001641..70002581,3	MCF-7	breast:

(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
SLC39A9	TF binding region
PLEKHD1	TF binding region
SLC39A9	CpG island
PLEKHD1	CpG island
ENSG00000100632	chromatin interactions
ENSG00000029364	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000100650	chromatin interactions
ENSG00000267909	chromatin interactions
ENSG00000258520	chromatin interactions
ENSG00000175985	chromatin interactions
ENSG00000100626	chromatin interactions
ENSG00000139990	chromatin interactions
DDX17	miRNA target sites

Extended variants
information (count: 1838 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1838 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543867574	chr14:69920906-69920907	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs562746774	chr14:69920921-69920922	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs530035632	chr14:69920925-69920926	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs138300844	chr14:69920932-69920933	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs560092487	chr14:69920942-69920943	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs527529631	chr14:69920959-69920960	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs142884834	chr14:69920979-69920980	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs373141789	chr14:69921010-69921011	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs570560104	chr14:69921041-69921042	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs537426193	chr14:69921056-69921057	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs549387257	chr14:69921114-69921115	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs34910925	chr14:69921126-69921127	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs532260443	chr14:69921164-69921165	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs377344466	chr14:69921166-69921167	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs568377161	chr14:69921200-69921201	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs76677476	chr14:69921244-69921245	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs150225542	chr14:69921313-69921314	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs536791147	chr14:69921334-69921335	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs554941812	chr14:69921405-69921406	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs540060246	chr14:69921445-69921446	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs557951523	chr14:69921449-69921450	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs2232057	chr14:69921479-69921480	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs538001390	chr14:69921504-69921505	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs543807274	chr14:69921508-69921509	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs368194737	chr14:69921523-69921524	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs555807922	chr14:69921561-69921562	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs534487237	chr14:69921574-69921575	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs368250989	chr14:69921673-69921674	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs2232058	chr14:69921674-69921675	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs542142508	chr14:69921720-69921721	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs560438845	chr14:69921747-69921748	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs527477689	chr14:69921749-69921750	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs138875248	chr14:69921762-69921763	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs376719621	chr14:69921832-69921833	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs149407275	chr14:69922028-69922029	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs531320541	chr14:69922030-69922031	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs11844453	chr14:69922036-69922037	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs567719305	chr14:69922041-69922042	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs528901188	chr14:69922093-69922094	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs547761853	chr14:69922102-69922103	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs577127725	chr14:69922110-69922111	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs144814941	chr14:69922113-69922114	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs539619977	chr14:69922132-69922133	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs71423362	chr14:69922134-69922135	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs558348330	chr14:69922153-69922154	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs182107002	chr14:69922183-69922184	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs562788153	chr14:69922194-69922195	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs537545828	chr14:69922225-69922226	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs574983716	chr14:69922256-69922257	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs555944940	chr14:69922276-69922277	Weak transcription Strong transcription	Chromatin interactive region	2 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:970 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69868000-69923200	Weak transcription	Esophagus	oesophagus
2	chr14:69889200-69922400	Weak transcription	Brain Substantia Nigra	brain
3	chr14:69889200-69923400	Weak transcription	Colon Smooth Muscle	Colon
4	chr14:69889400-69923200	Weak transcription	Pancreas	Pancrea
5	chr14:69890000-69922400	Weak transcription	Fetal Brain Male	brain
6	chr14:69890800-69922400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr14:69891200-69922800	Weak transcription	Colonic Mucosa	Colon
8	chr14:69891200-69923000	Weak transcription	NHLF	lung
9	chr14:69892200-69931400	Weak transcription	K562	blood
10	chr14:69893000-69922800	Weak transcription	Aorta	Aorta
11	chr14:69893200-69926800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr14:69893400-69922200	Weak transcription	Left Ventricle	heart
13	chr14:69893400-69922400	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr14:69893400-69922600	Weak transcription	Brain Germinal Matrix	brain
15	chr14:69893400-69922800	Weak transcription	Rectal Smooth Muscle	rectum
16	chr14:69893400-69923000	Weak transcription	Lung	lung
17	chr14:69893600-69922000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr14:69893600-69922400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr14:69893600-69922400	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr14:69893600-69922800	Weak transcription	Brain Hippocampus Middle	brain
21	chr14:69893600-69923200	Weak transcription	Gastric	stomach
22	chr14:69893600-69925000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr14:69894000-69922200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr14:69894000-69922800	Weak transcription	Brain Cingulate Gyrus	brain
25	chr14:69894000-69924400	Weak transcription	Brain Angular Gyrus	brain
26	chr14:69894600-69921800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr14:69894600-69922200	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr14:69894600-69922800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr14:69895600-69921400	Weak transcription	NH-A	brain
30	chr14:69896800-69922400	Weak transcription	Brain Anterior Caudate	brain
31	chr14:69897000-69922000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr14:69902400-69927000	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr14:69903600-69922200	Weak transcription	Small Intestine	intestine
34	chr14:69903600-69937800	Weak transcription	Psoas Muscle	Psoas
35	chr14:69906600-69921400	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr14:69906800-69921200	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr14:69906800-69921400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr14:69906800-69922400	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr14:69906800-69924400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr14:69906800-69924400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr14:69908400-69922400	Weak transcription	Fetal Brain Female	brain
42	chr14:69909000-69933200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr14:69909200-69921400	Weak transcription	Fetal Kidney	kidney
44	chr14:69909200-69922400	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr14:69909400-69922800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr14:69909800-69921400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr14:69910200-69923000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
48	chr14:69910400-69922200	Weak transcription	HUVEC	blood vessel
49	chr14:69910400-69927200	Weak transcription	NHEK	skin
50	chr14:69910800-69923000	Weak transcription	Thymus	Thymus

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