Variant report

Variant	nsv569584
Chromosome Location	chr15:57644267-57775806
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1187)
CpG islands
(count:1772)
Chromatin interactive
region (count:36)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1187 , 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	chr15:57675122-57675478	K562	blood:	n/a	n/a
2	ARID3A	chr15:57698812-57699080	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:57767593-57767849	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:57673166-57673314	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:57709023-57709306	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:57683674-57684095	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:57769934-57770658	HepG2	liver:	n/a	n/a
8	ATF1	chr15:57739082-57739221	K562	blood:	n/a	n/a
9	ATF1	chr15:57675232-57675432	K562	blood:	n/a	n/a
10	ATF2	chr15:57648804-57649568	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr15:57677879-57679030	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr15:57677951-57678684	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr15:57668896-57669038	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr15:57649168-57649224	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr15:57678068-57678736	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr15:57738064-57738618	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr15:57738124-57738415	K562	blood:	n/a	n/a
18	BCL11A	chr15:57648928-57649135	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL11A	chr15:57648891-57649186	H1-hESC	embryonic stem cell:	n/a	n/a
20	BHLHE40	chr15:57675229-57675611	K562	blood:	n/a	n/a
21	BHLHE40	chr15:57683205-57684026	HepG2	liver:	n/a	n/a
22	BHLHE40	chr15:57768791-57768792	GM12878	blood:	n/a	n/a
23	BHLHE40	chr15:57769828-57770706	HepG2	liver:	n/a	n/a
24	BRCA1	chr15:57649151-57649161	H1-hESC	embryonic stem cell:	n/a	n/a
25	CCNT2	chr15:57675201-57675501	K562	blood:	n/a	n/a
26	CEBPB	chr15:57719462-57720034	A549	lung:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
27	CEBPB	chr15:57644762-57645091	HepG2	liver:	n/a	chr15:57644878-57644889
28	CEBPB	chr15:57664442-57664743	A549	lung:	n/a	n/a
29	CEBPB	chr15:57645104-57645259	HepG2	liver:	n/a	n/a
30	CEBPB	chr15:57753678-57754168	MCF-7	breast:	n/a	n/a
31	CEBPB	chr15:57664441-57664787	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr15:57644830-57645208	K562	blood:	n/a	chr15:57644878-57644889
33	CEBPB	chr15:57645133-57645231	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr15:57755183-57755257	K562	blood:	n/a	chr15:57755215-57755226
35	CEBPB	chr15:57719550-57719876	HepG2	liver:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
36	CEBPB	chr15:57719546-57719910	IMR90	lung:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
37	CEBPB	chr15:57698709-57699074	HepG2	liver:	n/a	chr15:57698876-57698887
38	CEBPB	chr15:57679152-57679246	K562	blood:	n/a	n/a
39	CEBPB	chr15:57675162-57675437	K562	blood:	n/a	n/a
40	CEBPB	chr15:57644775-57645006	HepG2	liver:	n/a	chr15:57644878-57644889
41	CEBPB	chr15:57669326-57669420	K562	blood:	n/a	chr15:57669334-57669345
42	CEBPB	chr15:57755052-57755277	HepG2	liver:	n/a	chr15:57755215-57755226
43	CEBPB	chr15:57767622-57767921	HepG2	liver:	n/a	n/a
44	CEBPB	chr15:57768816-57769016	IMR90	lung:	n/a	n/a
45	CEBPB	chr15:57719370-57720131	A549	lung:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
46	CEBPB	chr15:57753700-57754104	MCF-7	breast:	n/a	n/a
47	CEBPB	chr15:57737280-57737551	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr15:57669119-57669538	HepG2	liver:	n/a	chr15:57669334-57669345
49	CEBPB	chr15:57669187-57669508	H1-hESC	embryonic stem cell:	n/a	chr15:57669334-57669345
50	CEBPB	chr15:57719529-57719914	A549	lung:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726

(count:1772 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:57682357-57682407	H1-hESC	embryonic stem cell:	embryo
2	chr15:57655799-57655849	NHBE	bronchial:	n/a
3	chr15:57731055-57731105	Caco-2	colon:	n/a
4	chr15:57682357-57682407	H1-hESC	embryonic stem cell:	embryo
5	chr15:57655799-57655849	NHBE	bronchial:	n/a
6	chr15:57731055-57731105	Caco-2	colon:	n/a
7	chr15:57769667-57769717	HepG2	liver:	n/a
8	chr15:57668261-57668311	LNCaP	prostate:	n/a
9	chr15:57668895-57668945	MCF10A-Er-Src	breast:	n/a
10	chr15:57668812-57668862	SK-N-SH	brain:	n/a
11	chr15:57680479-57680529	GM06990	blood:	n/a
12	chr15:57655799-57655849	SK-N-SH_RA	brain:	n/a
13	chr15:57647657-57647707	AG09309	skin:	n/a
14	chr15:57668247-57668297	BJ	skin:	n/a
15	chr15:57680479-57680529	RPTEC	kidney:	n/a
16	chr15:57668087-57668137	Hela-S3	cervix:	n/a
17	chr15:57669179-57669229	HPAEpiC	pulmonary alveolar:	n/a
18	chr15:57724857-57724907	SK-N-MC	brain:	n/a
19	chr15:57668039-57668089	PANC-1	pancreas:	n/a
20	chr15:57695943-57695993	ProgFib	skin:	n/a
21	chr15:57724857-57724907	T-47D	breast:	n/a
22	chr15:57668539-57668589	GM19239	blood:	n/a
23	chr15:57677507-57677557	HCT-116	colon:	n/a
24	chr15:57668039-57668089	CMK	blood:	n/a
25	chr15:57671034-57671084	SK-N-MC	brain:	n/a
26	chr15:57647657-57647707	HL-60	blood:	n/a
27	chr15:57668812-57668862	NH-A	brain:	n/a
28	chr15:57668539-57668589	SK-N-MC	brain:	n/a
29	chr15:57668812-57668862	AG09309	skin:	n/a
30	chr15:57664490-57664540	HAEpiC	amniotic membrane:	n/a
31	chr15:57668261-57668311	HUVEC	blood vessel:	n/a
32	chr15:57671034-57671084	CMK	blood:	n/a
33	chr15:57668087-57668137	HUVEC	blood vessel:	n/a
34	chr15:57668812-57668862	SK-N-SH_RA	brain:	n/a
35	chr15:57719252-57719302	RPTEC	kidney:	n/a
36	chr15:57682357-57682407	Jurkat	blood:	n/a
37	chr15:57731166-57731216	HIPEpiC	eye:	n/a
38	chr15:57724857-57724907	NB4	blood:	n/a
39	chr15:57668552-57668602	HCPEpiC	choroid plexus:	n/a
40	chr15:57668812-57668862	SAEC	small airway:	n/a
41	chr15:57664490-57664540	GM06990	blood:	n/a
42	chr15:57769667-57769717	PrEC	prostate:	n/a
43	chr15:57695943-57695993	HMEC	breast:	n/a
44	chr15:57680479-57680529	T-47D	breast:	n/a
45	chr15:57731648-57731698	HRE	kidney:	n/a
46	chr15:57695943-57695993	HRCEpiC	kidney:	n/a
47	chr15:57682357-57682407	HNPCEpiC	eye:	n/a
48	chr15:57671034-57671084	AG09319	gingival:	n/a
49	chr15:57668087-57668137	NHBE	bronchial:	n/a
50	chr15:57769667-57769717	HCF	heart:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:57703606..57706122-chr15:57710560..57712105,2	MCF-7	breast:
2	chr15:57637767..57638513-chr15:57664087..57664757,2	MCF-7	breast:
3	chr15:57668435..57670141-chr15:57674647..57676838,2	MCF-7	breast:
4	chr1:121483186..121485028-chr15:57701904..57703998,2	MCF-7	breast:
5	chr15:57708825..57710984-chr15:57719096..57721370,2	K562	blood:
6	chr15:57676218..57678168-chr15:57687344..57689139,2	K562	blood:
7	chr15:57731299..57732946-chr15:57744601..57746731,2	MCF-7	breast:
8	chr15:57750506..57752282-chr15:57753554..57755712,2	K562	blood:
9	chr15:57753396..57757139-chr15:57762848..57768344,4	K562	blood:
10	chr15:57667349..57669479-chr15:57681702..57683974,2	K562	blood:
11	chr15:57760042..57761755-chr15:57765442..57768496,3	K562	blood:
12	chr15:57705802..57707350-chr15:57713092..57715307,2	K562	blood:
13	chr15:57720229..57721976-chr15:57725417..57727742,2	K562	blood:
14	chr15:57708825..57710984-chr15:57719096..57721370,2	K562	blood:
15	chr15:57760042..57761755-chr15:57765442..57768496,3	K562	blood:
16	chr15:57761779..57763343-chr15:57766139..57768515,2	K562	blood:
17	chr15:57761779..57763343-chr15:57766139..57768515,2	K562	blood:
18	chr15:57667871..57669464-chr15:57819823..57821848,2	MCF-7	breast:
19	chr15:57745679..57747449-chr15:57751511..57754366,2	MCF-7	breast:
20	chr15:57705802..57707350-chr15:57713092..57715307,2	K562	blood:
21	chr15:57698192..57700092-chr15:57702299..57704451,2	K562	blood:
22	chr15:57669468..57670026-chr15:57819642..57820286,2	MCF-7	breast:
23	chr15:57753396..57757139-chr15:57762848..57768344,4	K562	blood:
24	chr15:57750506..57752282-chr15:57753554..57755712,2	K562	blood:
25	chr15:57653032..57655514-chr15:57656834..57658857,2	K562	blood:
26	chr15:57731299..57732946-chr15:57744601..57746731,2	MCF-7	breast:
27	chr15:57676218..57678168-chr15:57687344..57689139,2	K562	blood:
28	chr15:57720476..57722936-chr15:57724611..57727742,3	K562	blood:
29	chr15:57668102..57670225-chr15:57677163..57679480,2	MCF-7	breast:
30	chr15:57703606..57706122-chr15:57710560..57712105,2	MCF-7	breast:
31	chr15:57720476..57722936-chr15:57724611..57727742,3	K562	blood:
32	chr15:57720229..57721976-chr15:57725417..57727742,2	K562	blood:
33	chr15:57653032..57655514-chr15:57656834..57658857,2	K562	blood:
34	chr15:57745679..57747449-chr15:57751511..57754366,2	MCF-7	breast:
35	chr15:57662175..57664160-chr15:57665608..57668558,2	K562	blood:
36	chr15:57698192..57700092-chr15:57702299..57704451,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CGNL1-2	chr15:57730183-57730215	NONHSAT044072
2	lnc-CGNL1-2	chr15:57686151-57686289	NONHSAT044073
3	lnc-ALDH1A2-4	chr15:57769682-57769812	ENSG00000261489.1
4	lnc-CGNL1-2	chr15:57694859-57694912	NONHSAT044073
5	lnc-ALDH1A2-6	chr15:57741444-57741697	expReg_chr15_4576_-
6	lnc-CGNL1-2	chr15:57689122-57689304	NONHSAT044073
7	lnc-CGNL1-2	chr15:57668165-57668468	NONHSAT044072
8	lnc-CGNL1-2	chr15:57669124-57669363	NONHSAT044072
9	lnc-CGNL1-2	chr15:57669344-57669363	NONHSAT044073
10	lnc-CGNL1-2	chr15:57699171-57699474	NONHSAT044073
11	lnc-CGNL1-2	chr15:57694217-57694236	NONHSAT044073
12	lnc-CGNL1-2	chr15:57690539-57690628	NONHSAT044073
13	lnc-ALDH1A2-4	chr15:57770404-57770527	ENSG00000261489.1
14	lnc-CGNL1-2	chr15:57698164-57698262	NONHSAT044073

No data

Variant related genes	Relation type
RNU6-844P	TF binding region
CGNL1	TF binding region
ENSG00000261489	TF binding region
RNU6-844P	CpG island
CGNL1	CpG island
ENSG00000261489	CpG island
ENSG00000128849	chromatin interactions
ENSG00000261265	chromatin interactions

Extended variants
information (count: 6049 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:6049 , 50 per page) page: 1 2 3 4 5 6 7 ... 121

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs935322	chr15:57644267-57644268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs376791176	chr15:57644272-57644273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs78595815	chr15:57644309-57644310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs539689938	chr15:57644375-57644376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534137125	chr15:57644400-57644401	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs554335892	chr15:57644409-57644410	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs935321	chr15:57644412-57644413	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs542724950	chr15:57644421-57644422	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs199515226	chr15:57644422-57644423	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs935320	chr15:57644442-57644443	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs735609	chr15:57644456-57644457	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs565037700	chr15:57644459-57644460	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs527542065	chr15:57644466-57644467	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs540913535	chr15:57644482-57644483	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs4622453	chr15:57644505-57644506	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs140808522	chr15:57644508-57644509	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs935319	chr15:57644533-57644534	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs144561518	chr15:57644534-57644535	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs531599855	chr15:57644543-57644544	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs551320060	chr15:57644558-57644559	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs571885335	chr15:57644562-57644563	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs534505297	chr15:57644566-57644567	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs935318	chr15:57644573-57644574	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs554099889	chr15:57644591-57644592	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs539552400	chr15:57644609-57644610	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs182142830	chr15:57644610-57644611	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs556318565	chr15:57644627-57644628	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs575835116	chr15:57644628-57644629	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs148193574	chr15:57644650-57644651	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs2431042	chr15:57644656-57644657	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
31	rs558516901	chr15:57644658-57644659	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs141227201	chr15:57644659-57644660	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs541300335	chr15:57644671-57644672	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs35204236	chr15:57644720-57644721	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs34623171	chr15:57644758-57644759	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs560988408	chr15:57644771-57644772	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs74663971	chr15:57644793-57644794	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs547299387	chr15:57644812-57644813	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs369605760	chr15:57644857-57644858	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs531682523	chr15:57644868-57644869	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs551533343	chr15:57644890-57644891	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs571596331	chr15:57644894-57644895	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs528011049	chr15:57644902-57644903	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs187216981	chr15:57644925-57644926	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs567838917	chr15:57644949-57644950	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs4411458	chr15:57644977-57644978	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs374462138	chr15:57645021-57645022	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs569810706	chr15:57645029-57645030	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs538713566	chr15:57645051-57645052	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs112690708	chr15:57645066-57645067	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:2575 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:57627600-57668200	Weak transcription	Right Atrium	heart
2	chr15:57636200-57647200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr15:57638400-57645000	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr15:57638400-57645600	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr15:57638600-57645200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr15:57638600-57647200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr15:57642200-57644600	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr15:57643600-57645400	Enhancers	Fetal Muscle Trunk	muscle
9	chr15:57643600-57646000	Enhancers	Fetal Muscle Leg	muscle
10	chr15:57643600-57646400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr15:57644000-57644400	Enhancers	HepG2	liver
12	chr15:57644000-57645000	Weak transcription	Fetal Kidney	kidney
13	chr15:57644200-57644400	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr15:57644200-57647800	Enhancers	Fetal Heart	heart
15	chr15:57644400-57644600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr15:57644400-57645200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr15:57644400-57645400	Flanking Active TSS	HepG2	liver
18	chr15:57644400-57646000	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr15:57644400-57649800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr15:57644600-57644800	Enhancers	H1 Cell Line	embryonic stem cell
21	chr15:57644600-57646200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr15:57644600-57646200	Enhancers	Placenta	Placenta
23	chr15:57644800-57645600	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr15:57645000-57645200	Enhancers	Fetal Kidney	kidney
25	chr15:57645000-57645400	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr15:57645000-57645400	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr15:57645200-57645400	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr15:57645200-57645600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr15:57645200-57646000	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr15:57645200-57646200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr15:57645200-57646200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr15:57645200-57646200	Enhancers	Fetal Stomach	stomach
33	chr15:57645200-57646400	Weak transcription	Fetal Kidney	kidney
34	chr15:57645200-57646600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr15:57645400-57646000	Flanking Bivalent TSS/Enh	HepG2	liver
36	chr15:57645400-57646200	Enhancers	Fetal Intestine Small	intestine
37	chr15:57645400-57646400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
38	chr15:57645400-57648000	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr15:57645400-57648200	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr15:57645600-57645800	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr15:57645600-57646000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr15:57645600-57646200	Enhancers	H9 Cell Line	embryonic stem cell
43	chr15:57645600-57646600	Enhancers	H1 Cell Line	embryonic stem cell
44	chr15:57645800-57646000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr15:57645800-57646400	Enhancers	Fetal Intestine Large	intestine
46	chr15:57645800-57646800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr15:57646000-57646200	Bivalent Enhancer	Fetal Muscle Leg	muscle
48	chr15:57646000-57646400	Bivalent Enhancer	HepG2	liver
49	chr15:57646000-57647000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr15:57646000-57647800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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