Variant report

Variant	nsv877706
Chromosome Location	chr3:160820175-160826404
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:215)
CpG islands
(count:1040)
Chromatin interactive
region (count:11)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:215 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:160822337-160823250	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr3:160822109-160822390	H1-hESC	embryonic stem cell:	n/a	n/a
3	CCNT2	chr3:160823104-160823304	K562	blood:	n/a	chr3:160823190-160823199
4	CEBPB	chr3:160825637-160825809	A549	lung:	n/a	n/a
5	CEBPB	chr3:160825588-160825803	HepG2	liver:	n/a	n/a
6	CEBPB	chr3:160822350-160822703	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD1	chr3:160822427-160822677	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr3:160822261-160822792	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTBP2	chr3:160822389-160823317	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr3:160823164-160823311	GM10266	blood:	n/a	n/a
11	CTCF	chr3:160822620-160822770	GM12873	blood:	n/a	n/a
12	CTCF	chr3:160822760-160822910	GM12866	blood:	n/a	n/a
13	CTCF	chr3:160823200-160823270	NHEK	skin:	n/a	n/a
14	CTCF	chr3:160823240-160823390	SAEC	small airway:	n/a	n/a
15	CTCF	chr3:160823160-160823310	HRE	kidney:	n/a	n/a
16	CTCF	chr3:160822572-160822698	MCF-7	breast:	n/a	n/a
17	CTCF	chr3:160822520-160822670	GM12864	blood:	n/a	n/a
18	CTCF	chr3:160823340-160823490	GM12869	blood:	n/a	n/a
19	CTCF	chr3:160823160-160823310	SAEC	small airway:	n/a	n/a
20	CTCF	chr3:160823157-160823341	Spleen_OC	spleen:	n/a	n/a
21	CTCF	chr3:160822420-160822570	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr3:160823024-160823314	MCF-7	breast:	n/a	n/a
23	CTCF	chr3:160822720-160822870	AG04449	skin:	n/a	n/a
24	CTCF	chr3:160823165-160823291	GM12892	blood:	n/a	n/a
25	CTCF	chr3:160823080-160823230	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr3:160822660-160822810	GM12870	blood:	n/a	n/a
27	CTCF	chr3:160822620-160822770	GM12867	blood:	n/a	n/a
28	CTCF	chr3:160823098-160823307	MCF-7	breast:	n/a	n/a
29	CTCF	chr3:160822400-160822550	HRE	kidney:	n/a	n/a
30	CTCF	chr3:160822320-160822470	AoAF	blood vessel:	n/a	n/a
31	CTCF	chr3:160822260-160822410	AG04449	skin:	n/a	n/a
32	CTCF	chr3:160823060-160823210	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr3:160823151-160823309	MCF-7	breast:	n/a	n/a
34	CTCF	chr3:160822400-160822550	GM12864	blood:	n/a	n/a
35	CTCF	chr3:160823177-160823258	GM10248	blood:	n/a	n/a
36	CTCF	chr3:160823168-160823294	MCF-7	breast:	n/a	n/a
37	CTCF	chr3:160823163-160823281	GM19240	blood:	n/a	n/a
38	CTCF	chr3:160823240-160823390	GM12865	blood:	n/a	n/a
39	CTCF	chr3:160823101-160823327	GM19238	blood:	n/a	n/a
40	CTCF	chr3:160822663-160822700	GM13977	blood:	n/a	n/a
41	CTCF	chr3:160822280-160822430	AG10803	skin:	n/a	n/a
42	CTCF	chr3:160822760-160822910	Caco-2	colon:	n/a	n/a
43	CTCF	chr3:160823197-160823275	ProgFib	skin:	n/a	n/a
44	CTCF	chr3:160823111-160823320	GM12891	blood:	n/a	n/a
45	CTCF	chr3:160822604-160822726	GM19238	blood:	n/a	n/a
46	CTCF	chr3:160822580-160822730	GM12871	blood:	n/a	n/a
47	CTCF	chr3:160823120-160823270	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr3:160822860-160823010	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr3:160822480-160822630	GM12867	blood:	n/a	n/a
50	CTCF	chr3:160822637-160822677	NHEK	skin:	n/a	n/a

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:160823315-160823365	Caco-2	colon:	n/a
2	chr3:160823255-160823305	AoSMC	blood vessel:	n/a
3	chr3:160823387-160823437	HUVEC	blood vessel:	n/a
4	chr3:160823315-160823365	Caco-2	colon:	n/a
5	chr3:160823255-160823305	AoSMC	blood vessel:	n/a
6	chr3:160823387-160823437	HUVEC	blood vessel:	n/a
7	chr3:160822661-160822711	HL-60	blood:	n/a
8	chr3:160823505-160823555	HPAEpiC	pulmonary alveolar:	n/a
9	chr3:160823231-160823281	HIPEpiC	eye:	n/a
10	chr3:160823231-160823281	MCF-7	breast:	n/a
11	chr3:160822423-160822473	Jurkat	blood:	n/a
12	chr3:160823318-160823368	HMEC	breast:	n/a
13	chr3:160823318-160823368	SKMC	muscle:	n/a
14	chr3:160822720-160822770	HAEpiC	amniotic membrane:	n/a
15	chr3:160822911-160822961	SAEC	small airway:	n/a
16	chr3:160823315-160823365	AG04449	skin:	fetal
17	chr3:160822711-160822761	HCM	heart:	n/a
18	chr3:160822423-160822473	IMR90	lung:	fetal
19	chr3:160822545-160822595	U87	brain:	n/a
20	chr3:160822728-160822778	NHDF-neo	bronchial:	n/a
21	chr3:160823231-160823281	NT2-D1	testis:	n/a
22	chr3:160823231-160823281	HEK293	kidney:	embryo
23	chr3:160823231-160823281	Hela-S3	cervix:	n/a
24	chr3:160823505-160823555	NH-A	brain:	n/a
25	chr3:160822268-160822318	PrEC	prostate:	n/a
26	chr3:160822423-160822473	GM12878	blood:	n/a
27	chr3:160823231-160823281	HRCEpiC	kidney:	n/a
28	chr3:160823505-160823555	AG10803	skin:	n/a
29	chr3:160825607-160825657	AG04449	skin:	fetal
30	chr3:160823315-160823365	MCF-7	breast:	n/a
31	chr3:160825607-160825657	SK-N-SH	brain:	n/a
32	chr3:160822720-160822770	SKMC	muscle:	n/a
33	chr3:160826129-160826179	HCPEpiC	choroid plexus:	n/a
34	chr3:160823255-160823305	Jurkat	blood:	n/a
35	chr3:160823315-160823365	IMR90	lung:	fetal
36	chr3:160822720-160822770	AG09309	skin:	n/a
37	chr3:160822661-160822711	BE2_C	brain:	n/a
38	chr3:160823315-160823365	Hepatocyte	liver:	n/a
39	chr3:160823392-160823442	Caco-2	colon:	n/a
40	chr3:160822545-160822595	ECC-1	luminal epithelium:	n/a
41	chr3:160825607-160825657	HRPEpiC	eye:	n/a
42	chr3:160823255-160823305	PFSK-1	brain:	n/a
43	chr3:160823255-160823305	Hela-S3	cervix:	n/a
44	chr3:160823231-160823281	Caco-2	colon:	n/a
45	chr3:160823315-160823365	SK-N-SH_RA	brain:	n/a
46	chr3:160822423-160822473	RPTEC	kidney:	n/a
47	chr3:160823231-160823281	SKMC	muscle:	n/a
48	chr3:160826129-160826179	GM12878	blood:	n/a
49	chr3:160823231-160823281	AoSMC	blood vessel:	n/a
50	chr3:160823315-160823365	HIPEpiC	eye:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:160823684..160825879-chr3:160830015..160833205,3	MCF-7	breast:
2	chr3:160824011..160825629-chr3:161089025..161091868,3	MCF-7	breast:
3	chr3:160818503..160825890-chr3:160937051..160945986,18	MCF-7	breast:
4	chr3:160819564..160821281-chr3:160942870..160944755,2	MCF-7	breast:
5	chr3:160824125..160825880-chr3:160827918..160829533,2	K562	blood:
6	chr3:160821182..160827138-chr3:160937374..160941314,7	MCF-7	breast:
7	chr3:160824306..160825835-chr3:160990515..160993079,2	MCF-7	breast:
8	chr3:160825465..160827951-chr3:160887384..160889097,2	MCF-7	breast:
9	chr3:160813033..160824577-chr3:161083489..161092050,35	MCF-7	breast:
10	chr3:160819385..160821536-chr3:161081853..161083436,2	MCF-7	breast:
11	chr3:160819969..160822199-chr3:161125222..161127254,2	MCF-7	breast:

(count:22 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 216 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:216 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9869430	chr3:160820175-160820176	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs190996690	chr3:160820216-160820217	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs7627701	chr3:160820249-160820250	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs186837795	chr3:160820252-160820253	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs111711052	chr3:160820255-160820256	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs62278026	chr3:160820319-160820320	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs550217502	chr3:160820345-160820346	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs190202546	chr3:160820366-160820367	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs7650089	chr3:160820401-160820402	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs531352247	chr3:160820406-160820407	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs532764150	chr3:160820410-160820411	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs546421794	chr3:160820427-160820428	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs371503305	chr3:160820434-160820435	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs75252311	chr3:160820450-160820451	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs4557202	chr3:160820524-160820525	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
16	rs34501729	chr3:160820537-160820538	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs138445897	chr3:160820540-160820541	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs538174596	chr3:160820544-160820545	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs574849811	chr3:160820591-160820592	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs571715435	chr3:160820670-160820671	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs561969928	chr3:160820684-160820685	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs34049656	chr3:160820768-160820769	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs574052206	chr3:160820791-160820792	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs542869370	chr3:160820803-160820804	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs182772927	chr3:160820827-160820828	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs576209738	chr3:160820882-160820883	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs371723261	chr3:160820891-160820892	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs545343186	chr3:160820907-160820908	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
29	rs371815176	chr3:160820911-160820912	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
30	rs187320931	chr3:160820962-160820963	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
31	rs34853143	chr3:160820985-160820986	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs537946943	chr3:160821007-160821008	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs149260874	chr3:160821045-160821046	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs540176884	chr3:160821103-160821104	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs36051722	chr3:160821115-160821116	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs528946682	chr3:160821159-160821160	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs548787698	chr3:160821178-160821179	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs369335123	chr3:160821191-160821192	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs185667635	chr3:160821211-160821212	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs531532021	chr3:160821255-160821256	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
41	rs148395014	chr3:160821271-160821272	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
42	rs571526794	chr3:160821322-160821323	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs188930363	chr3:160821338-160821339	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs34791869	chr3:160821436-160821437	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs373892479	chr3:160821443-160821444	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs34112645	chr3:160821483-160821484	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs192545269	chr3:160821510-160821511	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs183776863	chr3:160821538-160821539	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs7650705	chr3:160821551-160821552	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs147321472	chr3:160821584-160821585	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 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:479 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	chr3:160796200-160821800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr3:160797000-160822000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr3:160798600-160821800	Weak transcription	Brain Angular Gyrus	brain
7	chr3:160799800-160821800	Weak transcription	NHLF	lung
8	chr3:160799800-160822000	Weak transcription	HMEC	breast
9	chr3:160800400-160822200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr3:160800400-160822400	Weak transcription	Spleen	Spleen
11	chr3:160801000-160821800	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr3:160801200-160822000	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr3:160801600-160821800	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr3:160802600-160821400	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr3:160802600-160822000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr3:160802600-160822400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr3:160802800-160822000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr3:160803400-160822000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr3:160803800-160822000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr3:160804400-160822000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr3:160804400-160822000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr3:160804600-160820400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr3:160804600-160821800	Weak transcription	Brain Substantia Nigra	brain
24	chr3:160804600-160821800	Weak transcription	HUVEC	blood vessel
25	chr3:160804600-160822200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr3:160807800-160820200	Weak transcription	Pancreas	Pancrea
27	chr3:160809000-160821800	Weak transcription	NHDF-Ad	bronchial
28	chr3:160809000-160822200	Weak transcription	Psoas Muscle	Psoas
29	chr3:160813400-160822000	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr3:160814000-160821600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr3:160814600-160820800	Strong transcription	Fetal Muscle Leg	muscle
32	chr3:160815200-160820800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
33	chr3:160815200-160820800	Strong transcription	Brain Inferior Temporal Lobe	brain
34	chr3:160815600-160821400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr3:160815800-160820800	Strong transcription	Fetal Lung	lung
36	chr3:160816000-160821000	Strong transcription	Fetal Muscle Trunk	muscle
37	chr3:160816000-160822200	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr3:160816200-160820800	Strong transcription	Ovary	ovary
39	chr3:160816400-160820600	Strong transcription	Stomach Smooth Muscle	stomach
40	chr3:160816400-160820800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr3:160816600-160820800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr3:160816800-160821000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr3:160817000-160821200	Strong transcription	Cortex derived primary cultured neurospheres	brain
44	chr3:160817200-160820200	Strong transcription	Brain Hippocampus Middle	brain
45	chr3:160817200-160820600	Strong transcription	Brain Anterior Caudate	brain
46	chr3:160817200-160820800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr3:160817200-160820800	Strong transcription	Osteobl	bone
48	chr3:160817200-160822000	Weak transcription	Rectal Smooth Muscle	rectum
49	chr3:160817400-160821000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr3:160817400-160822000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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