Variant report

Variant	nsv1053978
Chromosome Location	chr14:35571762-35639084
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1175)
CpG islands
(count:976)
Chromatin interactive
region (count:99)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1175 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:35628515-35629631	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:35628114-35628276	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:35590633-35592472	HepG2	liver:	n/a	chr14:35591480-35591488
4	ARID3A	chr14:35613218-35613555	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:35615869-35616033	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:35609838-35610282	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:35591026-35591699	K562	blood:	n/a	chr14:35591480-35591488
8	ATF1	chr14:35590856-35592000	K562	blood:	n/a	n/a
9	ATF1	chr14:35629215-35629517	K562	blood:	n/a	n/a
10	ATF2	chr14:35590769-35591863	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr14:35590456-35592108	GM12878	blood:	n/a	n/a
12	ATF2	chr14:35591095-35591822	GM12878	blood:	n/a	n/a
13	ATF2	chr14:35590839-35591575	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr14:35591326-35591632	K562	blood:	n/a	chr14:35591484-35591504
15	ATF3	chr14:35591062-35591829	GM12878	blood:	n/a	chr14:35591484-35591504
16	ATF3	chr14:35591368-35591602	GM12878	blood:	n/a	chr14:35591484-35591504
17	ATF3	chr14:35591254-35591787	A549	lung:	n/a	chr14:35591484-35591504
18	ATF3	chr14:35629129-35629373	K562	blood:	n/a	n/a
19	ATF3	chr14:35590988-35592153	HepG2	liver:	n/a	chr14:35591484-35591504
20	ATF3	chr14:35591305-35591773	H1-hESC	embryonic stem cell:	n/a	chr14:35591484-35591504
21	ATF3	chr14:35591069-35591891	HepG2	liver:	n/a	chr14:35591484-35591504
22	BATF	chr14:35629052-35629485	GM12878	blood:	n/a	chr14:35629286-35629297 chr14:35629287-35629297
23	BATF	chr14:35629074-35629473	GM12878	blood:	n/a	chr14:35629286-35629297 chr14:35629287-35629297
24	BATF	chr14:35591663-35591964	GM12878	blood:	n/a	n/a
25	BCL11A	chr14:35629109-35629431	GM12878	blood:	n/a	chr14:35629290-35629299 chr14:35629289-35629298
26	BCL3	chr14:35590607-35591936	A549	lung:	n/a	n/a
27	BCL3	chr14:35590950-35592103	A549	lung:	n/a	n/a
28	BCL3	chr14:35628914-35629626	A549	lung:	n/a	chr14:35629290-35629299 chr14:35629289-35629298
29	BCLAF1	chr14:35590870-35592203	GM12878	blood:	n/a	n/a
30	BCLAF1	chr14:35590896-35592186	GM12878	blood:	n/a	n/a
31	BHLHE40	chr14:35590665-35592190	K562	blood:	n/a	n/a
32	BHLHE40	chr14:35590781-35592288	GM12878	blood:	n/a	n/a
33	BHLHE40	chr14:35591280-35591665	A549	lung:	n/a	n/a
34	BHLHE40	chr14:35628362-35628811	HepG2	liver:	n/a	n/a
35	BHLHE40	chr14:35590749-35592231	HepG2	liver:	n/a	n/a
36	BRCA1	chr14:35591074-35592013	HepG2	liver:	n/a	n/a
37	BRCA1	chr14:35613335-35613393	GM12878	blood:	n/a	n/a
38	BRCA1	chr14:35590611-35592191	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr14:35590603-35591644	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr14:35629077-35629584	Hela-S3	cervix:	n/a	n/a
41	CBX3	chr14:35602360-35602546	K562	blood:	n/a	n/a
42	CBX3	chr14:35602269-35602685	K562	blood:	n/a	n/a
43	CBX3	chr14:35580846-35581125	K562	blood:	n/a	n/a
44	CBX3	chr14:35580902-35581120	K562	blood:	n/a	n/a
45	CBX3	chr14:35590828-35591964	K562	blood:	n/a	n/a
46	CCNT2	chr14:35629331-35629550	K562	blood:	n/a	n/a
47	CCNT2	chr14:35590784-35592019	K562	blood:	n/a	n/a
48	CEBPB	chr14:35629005-35629607	A549	lung:	n/a	n/a
49	CEBPB	chr14:35629119-35629473	IMR90	lung:	n/a	n/a
50	CEBPB	chr14:35628942-35629670	HCT-116	colon:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35591779-35591829	AG09309	skin:	n/a
2	chr14:35589334-35589384	NHBE	bronchial:	n/a
3	chr14:35591473-35591523	BE2_C	brain:	n/a
4	chr14:35594356-35594406	K562	blood:	n/a
5	chr14:35591252-35591302	PrEC	prostate:	n/a
6	chr14:35591572-35591622	BJ	skin:	n/a
7	chr14:35591625-35591675	PFSK-1	brain:	n/a
8	chr14:35591572-35591622	Caco-2	colon:	n/a
9	chr14:35589334-35589384	NHDF-neo	bronchial:	n/a
10	chr14:35589334-35589384	HepG2	liver:	n/a
11	chr14:35591951-35592001	HCF	heart:	n/a
12	chr14:35589334-35589384	A549	lung:	n/a
13	chr14:35591781-35591831	HPAEpiC	pulmonary alveolar:	n/a
14	chr14:35591840-35591890	LNCaP	prostate:	n/a
15	chr14:35591781-35591831	HCF	heart:	n/a
16	chr14:35591625-35591675	HCM	heart:	n/a
17	chr14:35583718-35583768	SKMC	muscle:	n/a
18	chr14:35591473-35591523	AoSMC	blood vessel:	n/a
19	chr14:35591695-35591745	GM12878	blood:	n/a
20	chr14:35591840-35591890	RPTEC	kidney:	n/a
21	chr14:35592116-35592166	SK-N-SH_RA	brain:	n/a
22	chr14:35591252-35591302	NH-A	brain:	n/a
23	chr14:35589334-35589384	HIPEpiC	eye:	n/a
24	chr14:35591840-35591890	HEEpiC	esophagus:	n/a
25	chr14:35591572-35591622	SAEC	small airway:	n/a
26	chr14:35591781-35591831	HepG2	liver:	n/a
27	chr14:35591695-35591745	BE2_C	brain:	n/a
28	chr14:35591252-35591302	Jurkat	blood:	n/a
29	chr14:35591252-35591302	HRPEpiC	eye:	n/a
30	chr14:35591252-35591302	SAEC	small airway:	n/a
31	chr14:35583718-35583768	Jurkat	blood:	n/a
32	chr14:35589334-35589384	HCF	heart:	n/a
33	chr14:35594356-35594406	PANC-1	pancreas:	n/a
34	chr14:35591781-35591831	HNPCEpiC	eye:	n/a
35	chr14:35591252-35591302	PFSK-1	brain:	n/a
36	chr14:35629311-35629361	HEEpiC	esophagus:	n/a
37	chr14:35587750-35587800	ProgFib	skin:	n/a
38	chr14:35591695-35591745	GM19239	blood:	n/a
39	chr14:35592116-35592166	HPAEpiC	pulmonary alveolar:	n/a
40	chr14:35594356-35594406	Hepatocyte	liver:	n/a
41	chr14:35591840-35591890	Jurkat	blood:	n/a
42	chr14:35591951-35592001	NH-A	brain:	n/a
43	chr14:35591695-35591745	HEEpiC	esophagus:	n/a
44	chr14:35587750-35587800	T-47D	breast:	n/a
45	chr14:35591572-35591622	RPTEC	kidney:	n/a
46	chr14:35587750-35587800	SKMC	muscle:	n/a
47	chr14:35591840-35591890	ovcar-3	ovarian:	n/a
48	chr14:35583718-35583768	RPTEC	kidney:	n/a
49	chr14:35592116-35592166	T-47D	breast:	n/a
50	chr14:35591695-35591745	AG04449	skin:	fetal

(count:99 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:35589827..35591407-chr14:35592886..35594751,2	K562	blood:
2	chr14:35571820..35573660-chr14:35580909..35583356,2	MCF-7	breast:
3	chr14:35016883..35018423-chr14:35574764..35577501,2	MCF-7	breast:
4	chr1:45196086..45196947-chr14:35590878..35591536,2	Hela-S3	cervix:
5	chr14:35593860..35596443-chr14:35605517..35607732,2	MCF-7	breast:
6	chr14:35622836..35624862-chr14:35627590..35631684,4	MCF-7	breast:
7	chr14:35579453..35581651-chr14:35585942..35587733,2	K562	blood:
8	chr14:35591775..35593424-chr14:35873275..35875126,2	K562	blood:
9	chr14:35582794..35584767-chr14:35585993..35588866,2	MCF-7	breast:
10	chr14:35628255..35632944-chr14:35633604..35637748,5	MCF-7	breast:
11	chr14:35609923..35610592-chr14:35882131..35883118,2	K562	blood:
12	chr14:35577086..35580056-chr14:35580213..35583818,4	MCF-7	breast:
13	chr14:35625181..35627591-chr14:35627623..35631343,4	MCF-7	breast:
14	chr14:35624804..35627276-chr14:35631634..35634106,2	K562	blood:
15	chr14:35614979..35617041-chr14:35619996..35622805,3	K562	blood:
16	chr14:35628567..35630693-chr14:35872213..35874122,2	MCF-7	breast:
17	chr14:35605217..35606991-chr14:35607370..35609971,2	MCF-7	breast:
18	chr14:35590512..35592667-chr14:35626960..35629855,2	MCF-7	breast:
19	chr14:35590512..35592667-chr14:35626960..35629855,2	MCF-7	breast:
20	chr14:35614979..35617041-chr14:35619996..35622805,3	K562	blood:
21	chr14:35509776..35510382-chr14:35602542..35603513,2	MCF-7	breast:
22	chr14:35590482..35592799-chr14:35601392..35603277,2	MCF-7	breast:
23	chr14:35579884..35582908-chr14:35589580..35593400,4	MCF-7	breast:
24	chr14:35593618..35595181-chr14:35595674..35598084,2	K562	blood:
25	chr14:35593883..35596766-chr14:35627445..35630133,2	MCF-7	breast:
26	chr14:35565651..35568101-chr14:35571541..35574493,2	K562	blood:
27	chr14:35514347..35518167-chr14:35589018..35591815,3	K562	blood:
28	chr14:35592944..35595456-chr14:35809160..35811582,2	K562	blood:
29	chr14:35636279..35638693-chr14:35643286..35645234,2	K562	blood:
30	chr14:35628320..35630476-chr14:35639523..35641227,2	MCF-7	breast:
31	chr14:35583719..35588379-chr14:35588655..35591956,6	MCF-7	breast:
32	chr14:35604150..35607008-chr14:35873146..35874686,2	MCF-7	breast:
33	chr14:35617849..35620759-chr14:35622945..35624771,2	K562	blood:
34	chr14:35575108..35577004-chr14:35580748..35582498,2	MCF-7	breast:
35	chr14:35342813..35344956-chr14:35595359..35597712,2	K562	blood:
36	chr14:35515793..35518719-chr14:35585868..35588915,3	K562	blood:
37	chr14:35624804..35627276-chr14:35631634..35634106,2	K562	blood:
38	chr14:35582794..35584767-chr14:35585993..35588866,2	MCF-7	breast:
39	chr14:35342738..35344659-chr14:35589687..35591484,2	K562	blood:
40	chr14:35604060..35606513-chr14:35608346..35611320,2	K562	blood:
41	chr14:35341168..35344675-chr14:35590606..35593872,6	MCF-7	breast:
42	chr14:35589196..35594400-chr14:35871301..35877730,13	MCF-7	breast:
43	chr14:35450042..35454830-chr14:35589505..35593708,8	K562	blood:
44	chr14:35627605..35629327-chr14:35631788..35633814,2	MCF-7	breast:
45	chr1:1709416..1709919-chr14:35590889..35591481,2	Hela-S3	cervix:
46	chr14:35341498..35344850-chr14:35591184..35593267,3	K562	blood:
47	chr14:35583308..35588876-chr14:35589178..35593731,8	MCF-7	breast:
48	chr14:35583281..35585103-chr14:35589464..35591782,2	K562	blood:
49	chr14:35450906..35453739-chr14:35588377..35591005,2	K562	blood:
50	chr14:35450146..35454994-chr14:35588530..35593322,8	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPP2R3C-1	chr14:35613227-35613686	NONHSAT036366
2	lnc-BAZ1A-3	chr14:35579129-35579835	NONHSAT036363
3	lnc-BAZ1A-3	chr14:35591108-35591185	NONHSAT036363
4	lnc-BAZ1A-3	chr14:35585816-35585943	NONHSAT036363
5	lnc-PPP2R3C-2	chr14:35627110-35628305	NONHSAT036367
6	lnc-RP11-173D9.3.1-1	chr14:35568882-35571935	ENSG00000247658
7	lnc-RP11-173D9.3.1-1	chr14:35579101-35579166	ENSG00000247658
8	lnc-RP11-173D9.3.1-1	chr14:35579776-35579932	ENSG00000247658
9	lnc-RP11-173D9.3.1-1	chr14:35575573-35575690	ENSG00000247658

No data

Variant related genes	Relation type
ENSG00000241052	TF binding region
ENSG00000259090	TF binding region
KIAA0391	TF binding region
ENSG00000258790	TF binding region
PPP2R3C	TF binding region
ENSG00000241052	CpG island
ENSG00000259090	CpG island
KIAA0391	CpG island
ENSG00000258790	CpG island
PPP2R3C	CpG island
ENSG00000092020	chromatin interactions
ENSG00000094916	chromatin interactions
ENSG00000100890	chromatin interactions
ENSG00000259090	chromatin interactions
ENSG00000174851	chromatin interactions
ENSG00000258704	chromatin interactions
ENSG00000198604	chromatin interactions
ENSG00000258738	chromatin interactions
ENSG00000008130	chromatin interactions
ENSG00000196547	chromatin interactions
ENSG00000165752	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000151327	chromatin interactions
ENSG00000100883	chromatin interactions
ENSG00000100906	chromatin interactions
ENSG00000258790	chromatin interactions
C2CD4A	miRNA target sites
SAMD4B	miRNA target sites
FNDC3A	miRNA target sites
NEFM	miRNA target sites

Extended variants
information (count: 2624 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2624 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541995605	chr14:35571780-35571781	Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
2	rs562107247	chr14:35571808-35571809	Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
3	rs540041767	chr14:35571815-35571816	Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
4	rs567673804	chr14:35571816-35571817	Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
5	rs530854336	chr14:35571838-35571839	Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs145877447	chr14:35571863-35571864	Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs181297407	chr14:35571948-35571949	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs12100944	chr14:35572005-35572006	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs11625810	chr14:35572042-35572043	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs567097094	chr14:35572091-35572092	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs375981276	chr14:35572109-35572110	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs111778408	chr14:35572163-35572164	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs568151210	chr14:35572175-35572176	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs536603204	chr14:35572186-35572187	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs556556478	chr14:35572193-35572194	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs12323698	chr14:35572197-35572198	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs539378747	chr14:35572227-35572228	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs552736863	chr14:35572235-35572236	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs572997832	chr14:35572249-35572250	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs542308576	chr14:35572257-35572258	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs561997531	chr14:35572262-35572263	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs575705143	chr14:35572266-35572267	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs544585322	chr14:35572267-35572268	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs564495185	chr14:35572281-35572282	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs2143950	chr14:35572357-35572358	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs61492899	chr14:35572360-35572361	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs560727142	chr14:35572389-35572390	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs185415997	chr14:35572411-35572412	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563021123	chr14:35572506-35572507	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143991082	chr14:35572536-35572537	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs7144423	chr14:35572547-35572548	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs530650879	chr14:35572564-35572565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189620188	chr14:35572572-35572573	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570146514	chr14:35572598-35572599	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371920964	chr14:35572643-35572644	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs375584047	chr14:35572704-35572705	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs552892453	chr14:35572759-35572760	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs566764102	chr14:35572777-35572778	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs535257547	chr14:35572789-35572790	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs555554724	chr14:35572839-35572840	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs180845212	chr14:35572889-35572890	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544746960	chr14:35572897-35572898	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs558168464	chr14:35572960-35572961	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs530157520	chr14:35572965-35572966	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs578101415	chr14:35573014-35573015	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs540635234	chr14:35573072-35573073	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs569304894	chr14:35573083-35573084	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560582732	chr14:35573109-35573110	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs529605075	chr14:35573130-35573131	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs368549968	chr14:35573153-35573154	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Lung adenocarcinoma	17982442	CNVD

Chromatin state (count:2447 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35517400-35578800	Weak transcription	Stomach Mucosa	stomach
2	chr14:35529400-35590200	Weak transcription	Esophagus	oesophagus
3	chr14:35530600-35590000	Weak transcription	Fetal Heart	heart
4	chr14:35538200-35581000	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr14:35542000-35589600	Weak transcription	Fetal Brain Male	brain
6	chr14:35543200-35580800	Weak transcription	K562	blood
7	chr14:35545600-35580800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr14:35545600-35582800	Strong transcription	Primary T helper cells fromperipheralblood	blood
9	chr14:35545600-35590000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr14:35546000-35581200	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr14:35546000-35585800	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr14:35546000-35587200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr14:35546200-35585000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr14:35546800-35571800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr14:35547000-35580800	Strong transcription	HUES48 Cell Line	embryonic stem cell
16	chr14:35547200-35574400	Strong transcription	Primary T cells fromperipheralblood	blood
17	chr14:35547200-35577600	Strong transcription	Placenta	Placenta
18	chr14:35547400-35574000	Strong transcription	Adipose Nuclei	Adipose
19	chr14:35547400-35577800	Strong transcription	Primary B cells from peripheral blood	blood
20	chr14:35547400-35580600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr14:35548000-35581000	Strong transcription	HepG2	liver
22	chr14:35548200-35580800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr14:35548400-35578800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr14:35550200-35586000	Strong transcription	Primary neutrophils fromperipheralblood	blood
25	chr14:35550800-35581000	Strong transcription	Dnd41	blood
26	chr14:35551000-35572800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr14:35551600-35579400	Weak transcription	NHEK	skin
28	chr14:35552000-35586600	Strong transcription	Fetal Thymus	thymus
29	chr14:35552600-35577600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
30	chr14:35553400-35589800	Weak transcription	Pancreas	Pancrea
31	chr14:35555000-35576000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr14:35555000-35581200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr14:35555400-35578800	Weak transcription	HMEC	breast
34	chr14:35556200-35578800	Weak transcription	Aorta	Aorta
35	chr14:35557000-35578200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr14:35558600-35576200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr14:35560200-35581200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr14:35560600-35576400	Weak transcription	A549	lung
39	chr14:35560600-35580600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr14:35560600-35580600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr14:35560800-35572600	Strong transcription	Fetal Muscle Leg	muscle
42	chr14:35561800-35579000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr14:35563200-35573000	Strong transcription	Skeletal Muscle Female	skeletal muscle
44	chr14:35564200-35578600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr14:35564200-35589400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr14:35564400-35572000	Weak transcription	Psoas Muscle	Psoas
47	chr14:35564400-35578800	Weak transcription	Fetal Kidney	kidney
48	chr14:35564400-35579200	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr14:35564400-35580000	Weak transcription	Colonic Mucosa	Colon
50	chr14:35564800-35572400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood

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