Variant report

Variant	nsv901649
Chromosome Location	chr14:38053334-38065813
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1144)
CpG islands
(count:2199)
Chromatin interactive
region (count:106)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1144 , 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	chr14:38062250-38062328	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:38055724-38056888	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:38062570-38065874	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:38057217-38058999	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:38059293-38059710	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:38065271-38065427	K562	blood:	n/a	n/a
7	ATF1	chr14:38065088-38065545	K562	blood:	n/a	n/a
8	BACH1	chr14:38065596-38065808	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr14:38055583-38055770	K562	blood:	n/a	n/a
10	BACH1	chr14:38064935-38065230	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr14:38057273-38058078	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr14:38064346-38064563	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr14:38064974-38065220	K562	blood:	n/a	n/a
14	BCL3	chr14:38065168-38065727	A549	lung:	n/a	chr14:38065574-38065587
15	BHLHE40	chr14:38065019-38065504	K562	blood:	n/a	n/a
16	BHLHE40	chr14:38064021-38065888	HepG2	liver:	n/a	chr14:38064929-38064945 chr14:38064053-38064069 chr14:38065568-38065584
17	BHLHE40	chr14:38064034-38064506	K562	blood:	n/a	chr14:38064053-38064069
18	BHLHE40	chr14:38063317-38063788	K562	blood:	n/a	n/a
19	BHLHE40	chr14:38063300-38063721	HepG2	liver:	n/a	n/a
20	BRCA1	chr14:38057239-38057644	HepG2	liver:	n/a	n/a
21	BRCA1	chr14:38065028-38065362	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr14:38065169-38065626	HepG2	liver:	n/a	n/a
23	BRCA1	chr14:38063097-38063799	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr14:38064049-38064336	HepG2	liver:	n/a	n/a
25	BRCA1	chr14:38064866-38064867	HepG2	liver:	n/a	n/a
26	CCNT2	chr14:38063667-38064544	K562	blood:	n/a	n/a
27	CCNT2	chr14:38064876-38065569	K562	blood:	n/a	chr14:38065466-38065475
28	CEBPB	chr14:38052395-38053418	MCF-7	breast:	n/a	n/a
29	CEBPB	chr14:38057175-38057605	HepG2	liver:	n/a	chr14:38057227-38057240
30	CEBPB	chr14:38064988-38065817	HepG2	liver:	n/a	n/a
31	CEBPB	chr14:38065138-38065610	HepG2	liver:	n/a	n/a
32	CEBPB	chr14:38064367-38065778	MCF-7	breast:	n/a	n/a
33	CEBPB	chr14:38064423-38064489	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr14:38055751-38056011	A549	lung:	n/a	chr14:38055886-38055898 chr14:38055919-38055930 chr14:38055919-38055932 chr14:38055920-38055931
35	CEBPB	chr14:38063406-38063894	Hela-S3	cervix:	n/a	chr14:38063618-38063629
36	CEBPB	chr14:38055737-38056070	HepG2	liver:	n/a	chr14:38055886-38055898 chr14:38055919-38055930 chr14:38055919-38055932 chr14:38055920-38055931
37	CEBPB	chr14:38057036-38057436	H1-hESC	embryonic stem cell:	n/a	chr14:38057227-38057240
38	CEBPB	chr14:38064482-38064614	HepG2	liver:	n/a	n/a
39	CEBPB	chr14:38062196-38062366	HepG2	liver:	n/a	n/a
40	CEBPB	chr14:38055775-38056080	IMR90	lung:	n/a	chr14:38055886-38055898 chr14:38055919-38055930 chr14:38055919-38055932 chr14:38055920-38055931
41	CEBPD	chr14:38063986-38065839	HepG2	liver:	n/a	n/a
42	CEBPD	chr14:38064131-38065690	HepG2	liver:	n/a	n/a
43	CEBPD	chr14:38052481-38053399	HepG2	liver:	n/a	n/a
44	CEBPD	chr14:38056965-38057951	HepG2	liver:	n/a	chr14:38057228-38057239
45	CHD1	chr14:38060477-38060869	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD1	chr14:38064812-38064962	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr14:38063425-38063845	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD1	chr14:38057190-38057567	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr14:38060934-38060995	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr14:38063370-38063743	Hela-S3	cervix:	n/a	n/a

(count:2199 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:38064849-38064899	LNCaP	prostate:	n/a
2	chr14:38057472-38057522	NH-A	brain:	n/a
3	chr14:38065152-38065202	CMK	blood:	n/a
4	chr14:38064849-38064899	LNCaP	prostate:	n/a
5	chr14:38057472-38057522	NH-A	brain:	n/a
6	chr14:38065152-38065202	CMK	blood:	n/a
7	chr14:38065303-38065353	PANC-1	pancreas:	n/a
8	chr14:38057893-38057943	PANC-1	pancreas:	n/a
9	chr14:38053972-38054022	T-47D	breast:	n/a
10	chr14:38058639-38058689	MCF10A-Er-Src	breast:	n/a
11	chr14:38063813-38063863	PANC-1	pancreas:	n/a
12	chr14:38053972-38054022	HCT-116	colon:	n/a
13	chr14:38061458-38061508	U87	brain:	n/a
14	chr14:38064513-38064563	H1-hESC	embryonic stem cell:	embryo
15	chr14:38064490-38064540	A549	lung:	n/a
16	chr14:38055252-38055302	SAEC	small airway:	n/a
17	chr14:38065201-38065251	CMK	blood:	n/a
18	chr14:38065201-38065251	AG09309	skin:	n/a
19	chr14:38061458-38061508	IMR90	lung:	fetal
20	chr14:38064513-38064563	ProgFib	skin:	n/a
21	chr14:38053726-38053776	NHDF-neo	bronchial:	n/a
22	chr14:38065582-38065632	Hepatocyte	liver:	n/a
23	chr14:38053599-38053649	GM12878	blood:	n/a
24	chr14:38060857-38060907	HCM	heart:	n/a
25	chr14:38064513-38064563	BJ	skin:	n/a
26	chr14:38060857-38060907	ProgFib	skin:	n/a
27	chr14:38061326-38061376	MCF10A-Er-Src	breast:	n/a
28	chr14:38064456-38064506	A549	lung:	n/a
29	chr14:38058639-38058689	Jurkat	blood:	n/a
30	chr14:38064456-38064506	IMR90	lung:	fetal
31	chr14:38053972-38054022	GM19239	blood:	n/a
32	chr14:38053378-38053428	LNCaP	prostate:	n/a
33	chr14:38061988-38062038	GM12891	blood:	n/a
34	chr14:38061988-38062038	AG09309	skin:	n/a
35	chr14:38061458-38061508	NB4	blood:	n/a
36	chr14:38053726-38053776	K562	blood:	n/a
37	chr14:38057752-38057802	AG09319	gingival:	n/a
38	chr14:38057752-38057802	A549	lung:	n/a
39	chr14:38065201-38065251	Hepatocyte	liver:	n/a
40	chr14:38061458-38061508	H1-hESC	embryonic stem cell:	embryo
41	chr14:38053726-38053776	AG04449	skin:	fetal
42	chr14:38065303-38065353	SKMC	muscle:	n/a
43	chr14:38053378-38053428	Caco-2	colon:	n/a
44	chr14:38065303-38065353	GM12892	blood:	n/a
45	chr14:38053378-38053428	NB4	blood:	n/a
46	chr14:38064532-38064582	NB4	blood:	n/a
47	chr14:38063564-38063614	HEEpiC	esophagus:	n/a
48	chr14:38063813-38063863	BJ	skin:	n/a
49	chr14:38064493-38064543	HL-60	blood:	n/a
50	chr14:38057752-38057802	GM12892	blood:	n/a

(count:106 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:37996356..38000397-chr14:38056446..38059493,3	MCF-7	breast:
2	chr14:38013523..38020726-chr14:38055776..38060374,10	MCF-7	breast:
3	chr14:38061035..38061673-chr14:38184445..38185002,2	MCF-7	breast:
4	chr12:52638172..52640523-chr14:38063240..38065213,2	MCF-7	breast:
5	chr14:38063715..38066524-chr16:54963024..54965693,2	MCF-7	breast:
6	chr12:7053819..7056575-chr14:38063408..38066179,2	MCF-7	breast:
7	chr14:37924566..37927073-chr14:38060566..38062784,2	MCF-7	breast:
8	chr14:38053183..38055954-chr14:38113662..38116528,3	MCF-7	breast:
9	chr14:38055708..38063394-chr14:38063498..38068319,8	K562	blood:
10	chr14:38065320..38065829-chr14:38119737..38120477,2	MCF-7	breast:
11	chr14:38035462..38036377-chr14:38063741..38064636,2	MCF-7	breast:
12	chr14:38035774..38036456-chr14:38064681..38065639,3	MCF-7	breast:
13	chr14:21736096..21738321-chr14:38062641..38065635,3	MCF-7	breast:
14	chr14:38023383..38025089-chr14:38055151..38056886,2	MCF-7	breast:
15	chr14:38063644..38065305-chr17:59487657..59489465,2	MCF-7	breast:
16	chr14:38056746..38059083-chr14:38363861..38366801,2	MCF-7	breast:
17	chr14:38059772..38062294-chr6:35436080..35437583,2	MCF-7	breast:
18	chr14:38064152..38064718-chr3:172468271..172468926,2	Hela-S3	cervix:
19	chr14:37732063..37736405-chr14:38055420..38059808,4	MCF-7	breast:
20	chr14:38053132..38055336-chr16:8951638..8953945,2	MCF-7	breast:
21	chr14:37977669..37980526-chr14:38060967..38062630,2	MCF-7	breast:
22	chr14:37903287..37907312-chr14:38059908..38064571,5	MCF-7	breast:
23	chr14:38052576..38054584-chr20:45987058..45989218,2	MCF-7	breast:
24	chr14:38010426..38020494-chr14:38050537..38062032,33	MCF-7	breast:
25	chr12:52539263..52541137-chr14:38055892..38058453,2	MCF-7	breast:
26	chr14:38021477..38023434-chr14:38051873..38053665,2	MCF-7	breast:
27	chr14:38064027..38066439-chr20:52209479..52211136,2	MCF-7	breast:
28	chr14:38060569..38062165-chr14:38339643..38341361,2	MCF-7	breast:
29	chr14:38035708..38036563-chr14:38060466..38061108,2	MCF-7	breast:
30	chr14:38052796..38053461-chr20:46130106..46131097,2	MCF-7	breast:
31	chr14:38052164..38054489-chr14:38155614..38158177,2	MCF-7	breast:
32	chr12:120728734..120731323-chr14:38058246..38060152,2	MCF-7	breast:
33	chr14:37703862..37705867-chr14:38056619..38058843,2	MCF-7	breast:
34	chr14:38052799..38056645-chr14:38110576..38115505,4	MCF-7	breast:
35	chr1:249152224..249152732-chr14:38065328..38065950,2	MCF-7	breast:
36	chr14:38061358..38063507-chr3:161089489..161091930,2	MCF-7	breast:
37	chr14:38064575..38066712-chr14:38067823..38069498,2	K562	blood:
38	chr14:38054348..38056983-chr16:85495948..85497819,2	MCF-7	breast:
39	chr14:38035709..38036660-chr14:38064999..38065756,3	MCF-7	breast:
40	chr14:38049811..38051883-chr14:38056230..38058824,2	K562	blood:
41	chr14:38065477..38068089-chr14:38070439..38072783,2	K562	blood:
42	chr14:37641087..37642667-chr14:38063502..38066629,3	MCF-7	breast:
43	chr14:38043804..38045954-chr14:38058287..38060752,2	K562	blood:
44	chr14:38057805..38059842-chr14:38111890..38113627,2	MCF-7	breast:
45	chr14:37709149..37730989-chr14:38048141..38067789,135	MCF-7	breast:
46	chr14:37749616..37751782-chr14:38055400..38058293,2	MCF-7	breast:
47	chr14:37996620..37999759-chr14:38060620..38062986,3	MCF-7	breast:
48	chr14:38055921..38058875-chr14:38061516..38064509,2	K562	blood:
49	chr14:38055655..38059490-chr14:38342768..38346428,4	MCF-7	breast:
50	chr14:38052050..38054072-chr8:119123824..119125742,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC25A21-3	chr14:38063080-38063818	NONHSAT036465
2	lnc-SLC25A21-3	chr14:38064106-38064155	NONHSAT036465

No data

Variant related genes	Relation type
TTC6	TF binding region
FOXA1	TF binding region
TTC6	CpG island
FOXA1	CpG island
ENSG00000259087	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000129514	chromatin interactions
ENSG00000183032	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000198755	chromatin interactions
ENSG00000258708	chromatin interactions
ENSG00000116793	chromatin interactions
ENSG00000152518	chromatin interactions
ENSG00000196542	chromatin interactions
ENSG00000253716	chromatin interactions
ENSG00000171940	chromatin interactions
ENSG00000182054	chromatin interactions
ENSG00000171163	chromatin interactions
ENSG00000104731	chromatin interactions
ENSG00000124151	chromatin interactions
ENSG00000245694	chromatin interactions
ENSG00000124207	chromatin interactions
ENSG00000158805	chromatin interactions
ENSG00000221869	chromatin interactions
ENSG00000176842	chromatin interactions
ENSG00000235505	chromatin interactions
ENSG00000141279	chromatin interactions
ENSG00000151338	chromatin interactions
ENSG00000169398	chromatin interactions
ENSG00000227431	chromatin interactions
ENSG00000270117	chromatin interactions
ENSG00000187013	chromatin interactions
ENSG00000092199	chromatin interactions
ENSG00000135480	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000114346	chromatin interactions
ENSG00000139865	chromatin interactions
ENSG00000182197	chromatin interactions
ENSG00000152475	chromatin interactions
ENSG00000251562	chromatin interactions
ENSG00000259685	chromatin interactions
ENSG00000112787	chromatin interactions
ENSG00000111679	chromatin interactions
ENSG00000050393	chromatin interactions
ENSG00000207046	chromatin interactions
ENSG00000267280	chromatin interactions

Extended variants
information (count: 427 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12432697	chr14:38053334-38053335	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs554491110	chr14:38053400-38053401	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs36080747	chr14:38053401-38053402	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs577309090	chr14:38053402-38053403	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs397751152	chr14:38053417-38053418	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs540226696	chr14:38053444-38053445	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs368745645	chr14:38053511-38053512	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs371495486	chr14:38053523-38053524	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs375810841	chr14:38053588-38053589	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs542328093	chr14:38053608-38053609	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs535911779	chr14:38053611-38053612	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs555901747	chr14:38053631-38053632	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs369411335	chr14:38053635-38053636	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs112373142	chr14:38053640-38053641	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs372066314	chr14:38053746-38053747	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs575837831	chr14:38053751-38053752	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs72674245	chr14:38053817-38053818	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs544974594	chr14:38053837-38053838	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs76472712	chr14:38053842-38053843	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs186870934	chr14:38053849-38053850	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs540652220	chr14:38053854-38053855	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs560495908	chr14:38053885-38053886	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs369627516	chr14:38053960-38053961	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs529372968	chr14:38054004-38054005	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs367677416	chr14:38054037-38054038	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs549500985	chr14:38054048-38054049	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs566077649	chr14:38054067-38054068	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs569469921	chr14:38054068-38054069	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs531972307	chr14:38054078-38054079	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs10149161	chr14:38054085-38054086	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs571935454	chr14:38054086-38054087	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs534243813	chr14:38054089-38054090	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs377748116	chr14:38054114-38054115	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs553315305	chr14:38054118-38054119	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs191769195	chr14:38054147-38054148	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs115952104	chr14:38054152-38054153	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs555889227	chr14:38054160-38054161	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs79015761	chr14:38054164-38054165	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs572838927	chr14:38054168-38054169	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs545223704	chr14:38054185-38054186	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs539847058	chr14:38054200-38054201	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs181843266	chr14:38054245-38054246	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs543940061	chr14:38054286-38054287	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs540983091	chr14:38054293-38054294	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs560478606	chr14:38054310-38054311	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs529352647	chr14:38054315-38054316	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs77888037	chr14:38054375-38054376	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs186294938	chr14:38054389-38054390	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs531787638	chr14:38054397-38054398	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs528992678	chr14:38054483-38054484	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
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
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
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Prostate cancer	21147910	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:923 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:38051800-38053600	Active TSS	HepG2	liver
2	chr14:38051800-38054600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
3	chr14:38052000-38055200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
4	chr14:38052200-38053400	Active TSS	A549	lung
5	chr14:38052200-38053800	Active TSS	Rectal Mucosa Donor 29	rectum
6	chr14:38052200-38054200	Bivalent/Poised TSS	Fetal Intestine Small	intestine
7	chr14:38052400-38053400	Bivalent/Poised TSS	Fetal Intestine Large	intestine
8	chr14:38052400-38053400	Bivalent/Poised TSS	Small Intestine	intestine
9	chr14:38052400-38053400	Active TSS	Hela-S3	cervix
10	chr14:38052400-38053600	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr14:38052400-38053600	Active TSS	Rectal Mucosa Donor 31	rectum
12	chr14:38052400-38054600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr14:38052400-38054800	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
14	chr14:38052400-38054800	Active TSS	Esophagus	oesophagus
15	chr14:38052600-38053400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
16	chr14:38052600-38053400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr14:38052600-38053400	Bivalent/Poised TSS	Colonic Mucosa	Colon
18	chr14:38052600-38053600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr14:38052600-38053600	Enhancers	Pancreas	Pancrea
20	chr14:38052600-38053800	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr14:38052600-38053800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr14:38052600-38053800	Bivalent Enhancer	Fetal Heart	heart
23	chr14:38052600-38053800	Active TSS	Rectal Smooth Muscle	rectum
24	chr14:38052600-38054200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
25	chr14:38052600-38054200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr14:38052600-38054400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr14:38052600-38054400	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr14:38052600-38054400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
29	chr14:38052600-38054600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
30	chr14:38052600-38054600	Bivalent Enhancer	Fetal Brain Female	brain
31	chr14:38052600-38054800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
32	chr14:38052600-38054800	Bivalent Enhancer	Left Ventricle	heart
33	chr14:38052800-38053400	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr14:38052800-38053400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
35	chr14:38052800-38053400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
36	chr14:38052800-38053400	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
37	chr14:38052800-38053400	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr14:38052800-38053400	Flanking Active TSS	Right Atrium	heart
39	chr14:38052800-38053400	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
40	chr14:38052800-38053400	ZNF genes & repeats	Spleen	Spleen
41	chr14:38052800-38053400	Bivalent/Poised TSS	HSMM	muscle
42	chr14:38052800-38053600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr14:38052800-38053600	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr14:38052800-38053600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr14:38052800-38053600	Bivalent/Poised TSS	Right Ventricle	heart
46	chr14:38052800-38053800	Bivalent/Poised TSS	Sigmoid Colon	Sigmoid Colon
47	chr14:38052800-38054200	Bivalent/Poised TSS	NHEK	skin
48	chr14:38052800-38054400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
49	chr14:38052800-38054400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
50	chr14:38052800-38054600	Bivalent Enhancer	Brain Hippocampus Middle	brain

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