Variant report

Variant	nsv877705
Chromosome Location	chr3:160818188-160836006
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:273)
CpG islands
(count:1100)
Chromatin interactive
region (count:19)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:273 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:160835504-160835704	K562	blood:	n/a	n/a
2	BACH1	chr3:160822337-160823250	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr3:160822109-160822390	H1-hESC	embryonic stem cell:	n/a	n/a
4	CCNT2	chr3:160823104-160823304	K562	blood:	n/a	chr3:160823190-160823199
5	CEBPB	chr3:160822350-160822703	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr3:160825588-160825803	HepG2	liver:	n/a	n/a
7	CEBPB	chr3:160825637-160825809	A549	lung:	n/a	n/a
8	CHD1	chr3:160822427-160822677	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr3:160822261-160822792	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTBP2	chr3:160822389-160823317	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr3:160823168-160823294	MCF-7	breast:	n/a	n/a
12	CTCF	chr3:160822620-160822770	GM12873	blood:	n/a	n/a
13	CTCF	chr3:160822580-160822730	GM12871	blood:	n/a	n/a
14	CTCF	chr3:160823340-160823490	GM12869	blood:	n/a	n/a
15	CTCF	chr3:160822663-160822734	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr3:160822760-160822910	Caco-2	colon:	n/a	n/a
17	CTCF	chr3:160823240-160823390	SAEC	small airway:	n/a	n/a
18	CTCF	chr3:160823060-160823210	BE2_C	brain:	n/a	n/a
19	CTCF	chr3:160823060-160823210	GM12872	blood:	n/a	n/a
20	CTCF	chr3:160823060-160823210	GM12866	blood:	n/a	n/a
21	CTCF	chr3:160822880-160823030	GM12875	blood:	n/a	n/a
22	CTCF	chr3:160823180-160823330	GM12875	blood:	n/a	n/a
23	CTCF	chr3:160823164-160823311	GM10266	blood:	n/a	n/a
24	CTCF	chr3:160823151-160823309	MCF-7	breast:	n/a	n/a
25	CTCF	chr3:160823180-160823330	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr3:160822663-160822700	GM13977	blood:	n/a	n/a
27	CTCF	chr3:160822604-160822726	GM19238	blood:	n/a	n/a
28	CTCF	chr3:160823111-160823320	GM12891	blood:	n/a	n/a
29	CTCF	chr3:160822520-160822670	GM12864	blood:	n/a	n/a
30	CTCF	chr3:160822320-160822470	AoAF	blood vessel:	n/a	n/a
31	CTCF	chr3:160822620-160822770	GM12867	blood:	n/a	n/a
32	CTCF	chr3:160823140-160823290	Caco-2	colon:	n/a	n/a
33	CTCF	chr3:160822560-160822710	GM12871	blood:	n/a	n/a
34	CTCF	chr3:160822986-160823015	GM12891	blood:	n/a	n/a
35	CTCF	chr3:160823200-160823270	NHEK	skin:	n/a	n/a
36	CTCF	chr3:160823160-160823310	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr3:160823080-160823230	AG09319	gingival:	n/a	n/a
38	CTCF	chr3:160823160-160823310	GM12871	blood:	n/a	n/a
39	CTCF	chr3:160823207-160823241	MCF-7	breast:	n/a	n/a
40	CTCF	chr3:160826540-160826690	HMF	breast:	n/a	n/a
41	CTCF	chr3:160822660-160822810	GM12870	blood:	n/a	n/a
42	CTCF	chr3:160822400-160822550	AG04449	skin:	n/a	n/a
43	CTCF	chr3:160823118-160823239	Fibrobl	skin:	n/a	n/a
44	CTCF	chr3:160822596-160822732	GM12891	blood:	n/a	n/a
45	CTCF	chr3:160822992-160823330	GM19239	blood:	n/a	n/a
46	CTCF	chr3:160822720-160822870	AG04449	skin:	n/a	n/a
47	CTCF	chr3:160822420-160822570	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr3:160822560-160822710	GM12875	blood:	n/a	n/a
49	CTCF	chr3:160822560-160822710	GM12873	blood:	n/a	n/a
50	CTCF	chr3:160822760-160822910	GM12866	blood:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:160823387-160823437	NT2-D1	testis:	n/a
2	chr3:160826129-160826179	SAEC	small airway:	n/a
3	chr3:160823387-160823437	NT2-D1	testis:	n/a
4	chr3:160826129-160826179	SAEC	small airway:	n/a
5	chr3:160825607-160825657	PrEC	prostate:	n/a
6	chr3:160823315-160823365	AG09309	skin:	n/a
7	chr3:160820084-160820134	LNCaP	prostate:	n/a
8	chr3:160826129-160826179	SK-N-MC	brain:	n/a
9	chr3:160822545-160822595	AG09319	gingival:	n/a
10	chr3:160823505-160823555	HCT-116	colon:	n/a
11	chr3:160823318-160823368	Jurkat	blood:	n/a
12	chr3:160822711-160822761	AG10803	skin:	n/a
13	chr3:160822728-160822778	BE2_C	brain:	n/a
14	chr3:160820084-160820134	HUVEC	blood vessel:	n/a
15	chr3:160822545-160822595	IMR90	lung:	fetal
16	chr3:160822545-160822595	AoSMC	blood vessel:	n/a
17	chr3:160823255-160823305	MCF-7	breast:	n/a
18	chr3:160822911-160822961	Hepatocyte	liver:	n/a
19	chr3:160823505-160823555	SAEC	small airway:	n/a
20	chr3:160822423-160822473	HRE	kidney:	n/a
21	chr3:160822268-160822318	MCF-7	breast:	n/a
22	chr3:160823387-160823437	GM19239	blood:	n/a
23	chr3:160823392-160823442	PANC-1	pancreas:	n/a
24	chr3:160822720-160822770	HIPEpiC	eye:	n/a
25	chr3:160826129-160826179	HNPCEpiC	eye:	n/a
26	chr3:160823505-160823555	RPTEC	kidney:	n/a
27	chr3:160822423-160822473	BE2_C	brain:	n/a
28	chr3:160822911-160822961	PrEC	prostate:	n/a
29	chr3:160822720-160822770	GM12892	blood:	n/a
30	chr3:160822545-160822595	GM06990	blood:	n/a
31	chr3:160826129-160826179	HRCEpiC	kidney:	n/a
32	chr3:160822720-160822770	SK-N-SH	brain:	n/a
33	chr3:160823318-160823368	HMEC	breast:	n/a
34	chr3:160822661-160822711	CMK	blood:	n/a
35	chr3:160822728-160822778	HAEpiC	amniotic membrane:	n/a
36	chr3:160822661-160822711	NT2-D1	testis:	n/a
37	chr3:160823318-160823368	HCF	heart:	n/a
38	chr3:160822661-160822711	NB4	blood:	n/a
39	chr3:160825607-160825657	NT2-D1	testis:	n/a
40	chr3:160822423-160822473	HRCEpiC	kidney:	n/a
41	chr3:160823387-160823437	PFSK-1	brain:	n/a
42	chr3:160822545-160822595	BE2_C	brain:	n/a
43	chr3:160822268-160822318	PFSK-1	brain:	n/a
44	chr3:160823231-160823281	Jurkat	blood:	n/a
45	chr3:160823392-160823442	PFSK-1	brain:	n/a
46	chr3:160823392-160823442	HL-60	blood:	n/a
47	chr3:160822720-160822770	U87	brain:	n/a
48	chr3:160822728-160822778	HEK293	kidney:	embryo
49	chr3:160822661-160822711	HRE	kidney:	n/a
50	chr3:160823387-160823437	HepG2	liver:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:160821182..160827138-chr3:160937374..160941314,7	MCF-7	breast:
2	chr3:160819564..160821281-chr3:160942870..160944755,2	MCF-7	breast:
3	chr3:160824306..160825835-chr3:160990515..160993079,2	MCF-7	breast:
4	chr3:160835167..160838027-chr3:160903594..160905386,2	MCF-7	breast:
5	chr3:160826732..160829358-chr3:160938079..160940393,2	K562	blood:
6	chr3:160824125..160825880-chr3:160827918..160829533,2	K562	blood:
7	chr3:160786642..160788388-chr3:160816154..160818351,2	MCF-7	breast:
8	chr3:160823684..160825879-chr3:160830015..160833205,3	MCF-7	breast:
9	chr3:160815084..160818315-chr3:161137399..161140050,3	MCF-7	breast:
10	chr3:160819969..160822199-chr3:161125222..161127254,2	MCF-7	breast:
11	chr3:160813033..160824577-chr3:161083489..161092050,35	MCF-7	breast:
12	chr3:160823684..160825879-chr3:160830015..160833205,3	MCF-7	breast:
13	chr3:160825465..160827951-chr3:160887384..160889097,2	MCF-7	breast:
14	chr3:160827858..160830677-chr3:160937623..160940393,2	K562	blood:
15	chr3:160819385..160821536-chr3:161081853..161083436,2	MCF-7	breast:
16	chr3:160824125..160825880-chr3:160827918..160829533,2	K562	blood:
17	chr3:160818503..160825890-chr3:160937051..160945986,18	MCF-7	breast:
18	chr3:160816932..160819441-chr3:160937058..160940131,3	MCF-7	breast:
19	chr3:160824011..160825629-chr3:161089025..161091868,3	MCF-7	breast:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-B3GALNT1-1	chr3:160822107-160822194	NONHSAT093006
2	lnc-B3GALNT1-1	chr3:160823023-160823093	NONHSAT093008
3	lnc-B3GALNT1-1	chr3:160822107-160822194	NONHSAT093007
4	lnc-B3GALNT1-1	chr3:160823023-160823172	NONHSAT093006
5	lnc-B3GALNT1-1	chr3:160821215-160821305	NONHSAT093005
6	lnc-B3GALNT1-1	chr3:160822791-160823033	NONHSAT093009
7	lnc-B3GALNT1-1	chr3:160822107-160822194	NONHSAT093005
8	lnc-B3GALNT1-1	chr3:160820901-160820993	NONHSAT093006
9	lnc-B3GALNT1-1	chr3:160821215-160821305	NONHSAT093008
10	lnc-B3GALNT1-1	chr3:160821215-160821305	NONHSAT093007
11	lnc-B3GALNT1-1	chr3:160821215-160821305	NONHSAT093006
12	lnc-B3GALNT1-1	chr3:160823023-160823172	NONHSAT093005
13	lnc-B3GALNT1-1	chr3:160820901-160820993	NONHSAT093007
14	lnc-B3GALNT1-1	chr3:160822573-160822683	NONHSAT093005
15	lnc-B3GALNT1-1	chr3:160821746-160821893	NONHSAT093008
16	lnc-B3GALNT1-1	chr3:160821215-160821305	NONHSAT093009
17	lnc-B3GALNT1-1	chr3:160818927-160819021	NONHSAT093005
18	lnc-B3GALNT1-1	chr3:160822573-160822683	NONHSAT093008
19	lnc-B3GALNT1-1	chr3:160823023-160823055	NONHSAT093007
20	lnc-B3GALNT1-1	chr3:160818927-160819021	NONHSAT093006
21	lnc-B3GALNT1-1	chr3:160820930-160820993	NONHSAT093009
22	lnc-B3GALNT1-1	chr3:160822107-160822194	NONHSAT093008
23	lnc-B3GALNT1-1	chr3:160821746-160821893	NONHSAT093007
24	lnc-B3GALNT1-1	chr3:160822107-160822194	NONHSAT093009
25	lnc-B3GALNT1-1	chr3:160818927-160819021	NONHSAT093007
26	lnc-B3GALNT1-1	chr3:160818952-160819021	NONHSAT093008

No data

Variant related genes	Relation type
B3GALNT1	TF binding region
NMD3	TF binding region
B3GALNT1	CpG island
NMD3	CpG island
ENSG00000196542	chromatin interactions
ENSG00000271052	chromatin interactions
ENSG00000169251	chromatin interactions

Extended variants
information (count: 645 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:645 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34793753	chr3:160818188-160818189	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs552852857	chr3:160818194-160818195	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs374682062	chr3:160818340-160818341	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs368086118	chr3:160818359-160818360	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs200432895	chr3:160818369-160818370	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs368098790	chr3:160818509-160818510	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs76399864	chr3:160818520-160818521	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs542224861	chr3:160818549-160818550	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs144756152	chr3:160818612-160818613	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs76740998	chr3:160818621-160818622	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs575575134	chr3:160818743-160818744	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs145748620	chr3:160818758-160818759	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs564559820	chr3:160818833-160818834	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs148940463	chr3:160818856-160818857	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs547166906	chr3:160818912-160818913	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs558556676	chr3:160818940-160818941	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
17	rs189375137	chr3:160818950-160818951	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
18	rs537812741	chr3:160818978-160818979	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
19	rs34798602	chr3:160819001-160819002	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs375715896	chr3:160819025-160819026	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs556179596	chr3:160819081-160819082	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs181051568	chr3:160819094-160819095	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs151025209	chr3:160819118-160819119	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs536646572	chr3:160819130-160819131	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs550270417	chr3:160819137-160819138	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs34865754	chr3:160819166-160819167	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs61166195	chr3:160819212-160819213	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs35474158	chr3:160819224-160819225	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs184132746	chr3:160819227-160819228	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs188702873	chr3:160819303-160819304	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs574752490	chr3:160819340-160819341	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs138065889	chr3:160819342-160819343	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs368426136	chr3:160819346-160819347	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs560735028	chr3:160819419-160819420	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs531421233	chr3:160819430-160819431	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs34007980	chr3:160819435-160819436	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs9826857	chr3:160819460-160819461	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs575586518	chr3:160819504-160819505	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs116135633	chr3:160819525-160819526	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs555411029	chr3:160819538-160819539	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs374750559	chr3:160819549-160819550	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs578122882	chr3:160819564-160819565	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs540844687	chr3:160819586-160819587	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs181436491	chr3:160819597-160819598	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs142537910	chr3:160819622-160819623	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs35985783	chr3:160819623-160819624	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs563157069	chr3:160819634-160819635	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs530427856	chr3:160819639-160819640	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs186177804	chr3:160819701-160819702	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs570229027	chr3:160819762-160819763	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21364760	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Sudden cardiac death	19188705	CNVD
Mantle cell lymphoma	19029149	CNVD
Malformation	19546859	CNVD
Schizophrenia	19546859	CNVD
Breast cancer	17133270	CNVD

Chromatin state (count:536 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:160780800-160821400	Weak transcription	Fetal Brain Male	brain
2	chr3:160781800-160822000	Weak transcription	Thymus	Thymus
3	chr3:160787000-160822000	Weak transcription	Primary T cells from cord blood	blood
4	chr3:160787200-160818800	Weak transcription	Brain Germinal Matrix	brain
5	chr3:160789600-160818800	Weak transcription	Esophagus	oesophagus
6	chr3:160796200-160821800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr3:160797000-160822000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr3:160798600-160821800	Weak transcription	Brain Angular Gyrus	brain
9	chr3:160799800-160821800	Weak transcription	NHLF	lung
10	chr3:160799800-160822000	Weak transcription	HMEC	breast
11	chr3:160800200-160818200	Weak transcription	Fetal Intestine Small	intestine
12	chr3:160800200-160820000	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr3:160800400-160818800	Weak transcription	Gastric	stomach
14	chr3:160800400-160822200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr3:160800400-160822400	Weak transcription	Spleen	Spleen
16	chr3:160801000-160821800	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr3:160801200-160822000	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr3:160801600-160818800	Weak transcription	Placenta	Placenta
19	chr3:160801600-160821800	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr3:160802600-160821400	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr3:160802600-160822000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr3:160802600-160822400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr3:160802800-160822000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr3:160803400-160819200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr3:160803400-160822000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr3:160803800-160822000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr3:160804400-160818200	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr3:160804400-160822000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr3:160804400-160822000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr3:160804600-160820400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr3:160804600-160821800	Weak transcription	Brain Substantia Nigra	brain
32	chr3:160804600-160821800	Weak transcription	HUVEC	blood vessel
33	chr3:160804600-160822200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr3:160805800-160818800	Weak transcription	Lung	lung
35	chr3:160807000-160818800	Weak transcription	Fetal Kidney	kidney
36	chr3:160807800-160818800	Weak transcription	Adipose Nuclei	Adipose
37	chr3:160807800-160820200	Weak transcription	Pancreas	Pancrea
38	chr3:160809000-160821800	Weak transcription	NHDF-Ad	bronchial
39	chr3:160809000-160822200	Weak transcription	Psoas Muscle	Psoas
40	chr3:160813400-160818800	Weak transcription	Right Atrium	heart
41	chr3:160813400-160822000	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr3:160813800-160818800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr3:160814000-160821600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr3:160814600-160820800	Strong transcription	Fetal Muscle Leg	muscle
45	chr3:160815200-160820800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr3:160815200-160820800	Strong transcription	Brain Inferior Temporal Lobe	brain
47	chr3:160815600-160821400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr3:160815800-160820800	Strong transcription	Fetal Lung	lung
49	chr3:160816000-160819800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr3:160816000-160820000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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