Variant report

Variant	nsv901585
Chromosome Location	chr14:31365884-31433473
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:441)
CpG islands
(count:183)
Chromatin interactive
region (count:48)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:441 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:31372571-31372796	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:31376988-31377265	K562	blood:	n/a	n/a
3	ATF1	chr14:31377002-31377168	K562	blood:	n/a	n/a
4	BCLAF1	chr14:31427753-31428225	GM12878	blood:	n/a	chr14:31428044-31428053
5	BHLHE40	chr14:31376174-31376181	GM12878	blood:	n/a	n/a
6	BRCA1	chr14:31367644-31367659	HepG2	liver:	n/a	n/a
7	CEBPB	chr14:31372526-31372822	HepG2	liver:	n/a	chr14:31372663-31372674
8	CEBPB	chr14:31372541-31372770	HepG2	liver:	n/a	chr14:31372663-31372674
9	CEBPB	chr14:31374411-31374761	HepG2	liver:	n/a	chr14:31374573-31374582 chr14:31374572-31374583
10	CEBPB	chr14:31390557-31390875	K562	blood:	n/a	chr14:31390697-31390708
11	CEBPB	chr14:31407840-31408130	MCF-7	breast:	n/a	chr14:31408020-31408031
12	CEBPB	chr14:31390531-31390873	Hela-S3	cervix:	n/a	chr14:31390697-31390708
13	CEBPB	chr14:31374474-31374739	A549	lung:	n/a	chr14:31374573-31374582 chr14:31374572-31374583
14	CEBPB	chr14:31407850-31408210	HepG2	liver:	n/a	chr14:31408020-31408031
15	CEBPB	chr14:31407861-31408215	A549	lung:	n/a	chr14:31408020-31408031
16	CEBPB	chr14:31390541-31390863	IMR90	lung:	n/a	chr14:31390697-31390708
17	CEBPB	chr14:31407827-31408269	A549	lung:	n/a	chr14:31408020-31408031
18	CEBPB	chr14:31407859-31408202	Hela-S3	cervix:	n/a	chr14:31408020-31408031
19	CEBPB	chr14:31374436-31374745	K562	blood:	n/a	chr14:31374573-31374582 chr14:31374572-31374583
20	CEBPB	chr14:31407849-31408190	H1-hESC	embryonic stem cell:	n/a	chr14:31408020-31408031
21	CEBPB	chr14:31374488-31374726	Hela-S3	cervix:	n/a	chr14:31374573-31374582 chr14:31374572-31374583
22	CEBPB	chr14:31407864-31408203	K562	blood:	n/a	chr14:31408020-31408031
23	CEBPB	chr14:31372529-31372820	HepG2	liver:	n/a	chr14:31372663-31372674
24	CEBPB	chr14:31390506-31390821	K562	blood:	n/a	chr14:31390697-31390708
25	CEBPB	chr14:31390567-31390856	HepG2	liver:	n/a	chr14:31390697-31390708
26	CEBPB	chr14:31407822-31408276	MCF-7	breast:	n/a	chr14:31408020-31408031
27	CEBPB	chr14:31374434-31374742	IMR90	lung:	n/a	chr14:31374573-31374582 chr14:31374572-31374583
28	CEBPB	chr14:31397272-31397408	HepG2	liver:	n/a	chr14:31397379-31397390
29	CEBPB	chr14:31407843-31408215	IMR90	lung:	n/a	chr14:31408020-31408031
30	CTCF	chr14:31376120-31376270	HRE	kidney:	n/a	n/a
31	CTCF	chr14:31376060-31376249	K562	blood:	n/a	n/a
32	CTCF	chr14:31376020-31376170	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr14:31375872-31376491	SK-N-SH	brain:	n/a	n/a
34	CTCF	chr14:31376100-31376250	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr14:31376140-31376290	AG04450	lung:	n/a	n/a
36	CTCF	chr14:31376140-31376290	BJ	skin:	n/a	n/a
37	CTCF	chr14:31376080-31376230	HEK293	kidney:	n/a	n/a
38	CTCF	chr14:31376060-31376210	GM12801	blood:	n/a	n/a
39	CTCF	chr14:31376120-31376270	NHLF	lung:	n/a	n/a
40	CTCF	chr14:31373640-31373790	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr14:31376064-31376246	GM10266	blood:	n/a	n/a
42	CTCF	chr14:31376020-31376170	GM12869	blood:	n/a	n/a
43	CTCF	chr14:31376080-31376230	GM12867	blood:	n/a	n/a
44	CTCF	chr14:31391080-31391230	HepG2	liver:	n/a	n/a
45	CTCF	chr14:31376100-31376250	GM12864	blood:	n/a	n/a
46	CTCF	chr14:31412000-31412150	MCF-7	breast:	n/a	n/a
47	CTCF	chr14:31373584-31373699	MCF-7	breast:	n/a	n/a
48	CTCF	chr14:31376080-31376230	GM12874	blood:	n/a	n/a
49	CTCF	chr14:31428680-31428830	HepG2	liver:	n/a	n/a
50	CTCF	chr14:31376060-31376210	HBMEC	blood vessel:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:31398430-31398480	NHBE	bronchial:	n/a
2	chr14:31398430-31398480	HEK293	kidney:	embryo
3	chr14:31408344-31408394	PFSK-1	brain:	n/a
4	chr14:31408344-31408394	HRCEpiC	kidney:	n/a
5	chr14:31408344-31408394	HCT-116	colon:	n/a
6	chr14:31389792-31389842	NH-A	brain:	n/a
7	chr14:31408344-31408394	HepG2	liver:	n/a
8	chr14:31398430-31398480	K562	blood:	n/a
9	chr14:31398430-31398480	RPTEC	kidney:	n/a
10	chr14:31389792-31389842	NT2-D1	testis:	n/a
11	chr14:31398430-31398480	PFSK-1	brain:	n/a
12	chr14:31389792-31389842	AG04449	skin:	fetal
13	chr14:31389792-31389842	NHDF-neo	bronchial:	n/a
14	chr14:31408344-31408394	Hepatocyte	liver:	n/a
15	chr14:31398430-31398480	AG04450	lung:	fetal
16	chr14:31398430-31398480	BJ	skin:	n/a
17	chr14:31408344-31408394	A549	lung:	n/a
18	chr14:31398430-31398480	HIPEpiC	eye:	n/a
19	chr14:31389792-31389842	HAEpiC	amniotic membrane:	n/a
20	chr14:31389792-31389842	H1-hESC	embryonic stem cell:	embryo
21	chr14:31408344-31408394	HCF	heart:	n/a
22	chr14:31408344-31408394	IMR90	lung:	fetal
23	chr14:31398430-31398480	A549	lung:	n/a
24	chr14:31408344-31408394	GM19239	blood:	n/a
25	chr14:31408344-31408394	SK-N-SH_RA	brain:	n/a
26	chr14:31408344-31408394	U87	brain:	n/a
27	chr14:31389792-31389842	HL-60	blood:	n/a
28	chr14:31389792-31389842	IMR90	lung:	fetal
29	chr14:31398430-31398480	SK-N-MC	brain:	n/a
30	chr14:31398430-31398480	HCT-116	colon:	n/a
31	chr14:31408344-31408394	NH-A	brain:	n/a
32	chr14:31389792-31389842	HMEC	breast:	n/a
33	chr14:31398430-31398480	AG10803	skin:	n/a
34	chr14:31408344-31408394	HCPEpiC	choroid plexus:	n/a
35	chr14:31398430-31398480	AG09319	gingival:	n/a
36	chr14:31389792-31389842	ovcar-3	ovarian:	n/a
37	chr14:31408344-31408394	BE2_C	brain:	n/a
38	chr14:31389792-31389842	Hepatocyte	liver:	n/a
39	chr14:31398430-31398480	HRE	kidney:	n/a
40	chr14:31398430-31398480	HCPEpiC	choroid plexus:	n/a
41	chr14:31389792-31389842	BJ	skin:	n/a
42	chr14:31408344-31408394	HEK293	kidney:	embryo
43	chr14:31398430-31398480	HPAEpiC	pulmonary alveolar:	n/a
44	chr14:31408344-31408394	GM12891	blood:	n/a
45	chr14:31389792-31389842	HCT-116	colon:	n/a
46	chr14:31408344-31408394	Caco-2	colon:	n/a
47	chr14:31398430-31398480	HMEC	breast:	n/a
48	chr14:31398430-31398480	GM06990	blood:	n/a
49	chr14:31398430-31398480	AG04449	skin:	fetal
50	chr14:31408344-31408394	AG10803	skin:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:31425052..31427072-chr14:31430189..31431943,2	K562	blood:
2	chr14:31359586..31361884-chr14:31363738..31366139,3	MCF-7	breast:
3	chr14:31402683..31406428-chr14:31407313..31410233,6	K562	blood:
4	chr14:31364498..31367422-chr14:31368554..31370574,2	K562	blood:
5	chr14:31126170..31126990-chr14:31375725..31376423,2	MCF-7	breast:
6	chr14:31417991..31420027-chr14:31423345..31424852,2	K562	blood:
7	chr14:31428661..31430231-chr14:31430956..31433408,2	MCF-7	breast:
8	chr14:31390350..31392275-chr14:31395263..31396767,2	K562	blood:
9	chr14:31363037..31365815-chr14:31368802..31371071,3	MCF-7	breast:
10	chr14:31379170..31380881-chr14:31494382..31497004,2	MCF-7	breast:
11	chr14:31365626..31367876-chr14:31370827..31372505,3	K562	blood:
12	chr14:31428661..31430231-chr14:31430956..31433408,2	MCF-7	breast:
13	chr14:31387011..31389077-chr14:31394255..31396560,2	K562	blood:
14	chr14:31412377..31414525-chr14:31418622..31420542,2	MCF-7	breast:
15	chr14:31357417..31359632-chr14:31378177..31380284,2	K562	blood:
16	chr14:31400245..31402113-chr14:31403843..31406707,2	MCF-7	breast:
17	chr14:31420168..31423130-chr14:31493763..31496178,2	MCF-7	breast:
18	chr14:31397468..31399701-chr14:31410285..31412729,2	MCF-7	breast:
19	chr14:31373196..31374094-chr14:31550924..31551881,2	MCF-7	breast:
20	chr14:31406134..31408433-chr14:31516211..31518078,2	K562	blood:
21	chr14:31397468..31399701-chr14:31410285..31412729,2	MCF-7	breast:
22	chr14:31364498..31367422-chr14:31368554..31370574,2	K562	blood:
23	chr14:31359962..31362507-chr14:31370920..31372508,2	MCF-7	breast:
24	chr14:31368029..31370614-chr14:31372597..31374525,2	MCF-7	breast:
25	chr14:31390350..31392275-chr14:31395263..31396767,2	K562	blood:
26	chr14:31400245..31402113-chr14:31403843..31406707,2	MCF-7	breast:
27	chr14:31398507..31401730-chr14:31402844..31406226,4	K562	blood:
28	chr14:31412013..31413799-chr14:31413815..31415852,2	MCF-7	breast:
29	chr14:31385237..31388114-chr14:31390780..31394488,3	MCF-7	breast:
30	chr14:31376657..31378769-chr14:31384602..31386523,2	MCF-7	breast:
31	chr14:31422050..31424018-chr14:31493292..31496577,3	K562	blood:
32	chr14:31428811..31431049-chr14:31434848..31436931,2	MCF-7	breast:
33	chr14:31387011..31389077-chr14:31394255..31396560,2	K562	blood:
34	chr14:31417991..31420027-chr14:31423345..31424852,2	K562	blood:
35	chr14:31404383..31406657-chr14:31409869..31411808,3	MCF-7	breast:
36	chr14:31362905..31364737-chr14:31367677..31370319,3	K562	blood:
37	chr14:31385492..31389361-chr14:31390065..31392327,4	K562	blood:
38	chr14:31398507..31401730-chr14:31402844..31406226,4	K562	blood:
39	chr14:31365626..31367876-chr14:31370827..31372505,3	K562	blood:
40	chr14:31385492..31389361-chr14:31390065..31392327,4	K562	blood:
41	chr14:31368029..31370614-chr14:31372597..31374525,2	MCF-7	breast:
42	chr14:31425052..31427072-chr14:31430189..31431943,2	K562	blood:
43	chr14:31358985..31361298-chr14:31365493..31368318,2	K562	blood:
44	chr14:31412013..31413799-chr14:31413815..31415852,2	MCF-7	breast:
45	chr14:31385237..31388114-chr14:31390780..31394488,3	MCF-7	breast:
46	chr14:31412377..31414525-chr14:31418622..31420542,2	MCF-7	breast:
47	chr14:31376657..31378769-chr14:31384602..31386523,2	MCF-7	breast:
48	chr14:31345025..31346912-chr14:31378500..31381004,2	K562	blood:

No data

Variant related genes	Relation type
HIGD1AP17	TF binding region
STRN3	TF binding region
HIGD1AP17	CpG island
STRN3	CpG island
ENSG00000100473	chromatin interactions
ENSG00000100478	chromatin interactions
ENSG00000196792	chromatin interactions
ENSG00000258525	chromatin interactions

Extended variants
information (count: 2573 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2573 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10483360	chr14:31365884-31365885	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs557966715	chr14:31365973-31365974	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs143512900	chr14:31365987-31365988	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs148032624	chr14:31365999-31366000	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs114427375	chr14:31366037-31366038	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs573276304	chr14:31366047-31366048	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs59048919	chr14:31366053-31366054	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs562405988	chr14:31366056-31366057	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs369316707	chr14:31366059-31366060	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs191364974	chr14:31366068-31366069	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs560419092	chr14:31366085-31366086	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs377626830	chr14:31366153-31366154	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs113686262	chr14:31366167-31366168	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs116859728	chr14:31366180-31366181	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs139946204	chr14:31366248-31366249	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs569240592	chr14:31366301-31366302	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs539966482	chr14:31366310-31366311	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs10483359	chr14:31366334-31366335	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs566756152	chr14:31366338-31366339	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs534147354	chr14:31366381-31366382	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs557481466	chr14:31366422-31366423	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs8005583	chr14:31366468-31366469	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs116709485	chr14:31366491-31366492	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs377427789	chr14:31366502-31366503	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs184272783	chr14:31366550-31366551	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs8005624	chr14:31366556-31366557	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs543855592	chr14:31366561-31366562	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs187140458	chr14:31366652-31366653	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs12434740	chr14:31366715-31366716	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs146292773	chr14:31366724-31366725	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs192319516	chr14:31366729-31366730	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs527452752	chr14:31366747-31366748	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs185212714	chr14:31366762-31366763	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs377022230	chr14:31366771-31366772	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs540040615	chr14:31366866-31366867	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs17097477	chr14:31366895-31366896	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs374304134	chr14:31366950-31366951	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs8009661	chr14:31366967-31366968	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs374506263	chr14:31366987-31366988	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs76340350	chr14:31367025-31367026	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs139272866	chr14:31367052-31367053	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs569259788	chr14:31367152-31367153	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs368185029	chr14:31367230-31367231	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs368887291	chr14:31367255-31367256	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs190056089	chr14:31367325-31367326	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs182212112	chr14:31367380-31367381	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs78240955	chr14:31367420-31367421	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs146145395	chr14:31367437-31367438	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs150004652	chr14:31367462-31367463	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs573295006	chr14:31367522-31367523	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	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
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1512 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31345000-31435400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr14:31345200-31369200	Weak transcription	Pancreas	Pancrea
3	chr14:31345400-31382600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr14:31346600-31382600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr14:31347000-31384600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr14:31347000-31394800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr14:31348000-31372600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr14:31348200-31376800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr14:31350200-31377800	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr14:31353400-31367400	Weak transcription	NHLF	lung
11	chr14:31353400-31369200	Weak transcription	Fetal Intestine Small	intestine
12	chr14:31355200-31378400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr14:31355800-31414400	Weak transcription	Spleen	Spleen
14	chr14:31356000-31369200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr14:31356200-31367200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr14:31356200-31378800	Weak transcription	Brain Germinal Matrix	brain
17	chr14:31356200-31412800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr14:31357800-31370800	Weak transcription	K562	blood
19	chr14:31358000-31428200	Weak transcription	Small Intestine	intestine
20	chr14:31358400-31378400	Weak transcription	Aorta	Aorta
21	chr14:31359200-31371400	Weak transcription	HUVEC	blood vessel
22	chr14:31359600-31375200	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr14:31360200-31369200	Weak transcription	Fetal Stomach	stomach
24	chr14:31360200-31435600	Weak transcription	Gastric	stomach
25	chr14:31360400-31381800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr14:31361200-31379400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
27	chr14:31361400-31377200	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr14:31361600-31380600	Weak transcription	Stomach Mucosa	stomach
29	chr14:31361600-31384400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr14:31361800-31394200	Weak transcription	Fetal Brain Male	brain
31	chr14:31362000-31381400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr14:31362200-31378800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr14:31362200-31414400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
34	chr14:31362400-31435400	Weak transcription	Colonic Mucosa	Colon
35	chr14:31362600-31366400	Strong transcription	HUES64 Cell Line	embryonic stem cell
36	chr14:31362600-31366600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr14:31362600-31368600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
38	chr14:31362600-31382400	Strong transcription	Liver	Liver
39	chr14:31362800-31366400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
40	chr14:31362800-31369200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr14:31362800-31372200	Strong transcription	HepG2	liver
42	chr14:31363000-31379200	Weak transcription	Fetal Heart	heart
43	chr14:31363000-31394400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr14:31363000-31430600	Weak transcription	Brain Angular Gyrus	brain
45	chr14:31363000-31435200	Weak transcription	Esophagus	oesophagus
46	chr14:31363200-31366200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr14:31363200-31366600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr14:31363400-31371800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr14:31363400-31383000	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr14:31363600-31366000	Strong transcription	Primary monocytes fromperipheralblood	blood

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