Variant report

Variant	nsv1010004
Chromosome Location	chr3:113564233-113620612
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:275)
CpG islands
(count:427)
Chromatin interactive
region (count:7)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:275 , 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	ARID3A	chr3:113592645-113593092	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:113613793-113614046	HepG2	liver:	n/a	n/a
3	CBX3	chr3:113598730-113599055	K562	blood:	n/a	n/a
4	CEBPB	chr3:113566855-113567338	ECC-1	luminal epithelium:	n/a	n/a
5	CEBPB	chr3:113617801-113618158	A549	lung:	n/a	chr3:113617980-113617991 chr3:113617982-113617991
6	CEBPB	chr3:113566882-113567369	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr3:113583765-113584065	HepG2	liver:	n/a	chr3:113583925-113583936
8	CEBPB	chr3:113617789-113618176	IMR90	lung:	n/a	chr3:113617980-113617991 chr3:113617982-113617991
9	CEBPB	chr3:113566941-113567255	A549	lung:	n/a	n/a
10	CEBPB	chr3:113617756-113618171	Hela-S3	cervix:	n/a	chr3:113617980-113617991 chr3:113617982-113617991
11	CEBPB	chr3:113617843-113618107	A549	lung:	n/a	chr3:113617980-113617991 chr3:113617982-113617991
12	CEBPB	chr3:113617816-113618166	HepG2	liver:	n/a	chr3:113617980-113617991 chr3:113617982-113617991
13	CEBPB	chr3:113592722-113593062	HepG2	liver:	n/a	chr3:113592898-113592909 chr3:113592919-113592930
14	CEBPB	chr3:113566853-113567372	HCT-116	colon:	n/a	n/a
15	CEBPB	chr3:113617825-113618142	K562	blood:	n/a	chr3:113617980-113617991 chr3:113617982-113617991
16	CEBPB	chr3:113566783-113567371	HCT-116	colon:	n/a	n/a
17	CEBPB	chr3:113566786-113567374	MCF-7	breast:	n/a	n/a
18	CEBPB	chr3:113566842-113567355	MCF-7	breast:	n/a	n/a
19	CEBPB	chr3:113566962-113567383	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr3:113583800-113584036	A549	lung:	n/a	chr3:113583925-113583936
21	CEBPB	chr3:113567006-113567155	K562	blood:	n/a	n/a
22	CEBPB	chr3:113617811-113618163	H1-hESC	embryonic stem cell:	n/a	chr3:113617980-113617991 chr3:113617982-113617991
23	CEBPB	chr3:113566999-113567271	HepG2	liver:	n/a	n/a
24	CEBPB	chr3:113609114-113609530	MCF-7	breast:	n/a	n/a
25	CEBPB	chr3:113576517-113576704	HepG2	liver:	n/a	n/a
26	CTCF	chr3:113609180-113609330	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr3:113609298-113609342	ProgFib	skin:	n/a	n/a
28	CTCF	chr3:113609240-113609390	Caco-2	colon:	n/a	n/a
29	CTCF	chr3:113609190-113609416	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr3:113609243-113609383	GM19240	blood:	n/a	n/a
31	CTCF	chr3:113609227-113609410	Gliobla	brain:	n/a	n/a
32	CTCF	chr3:113569155-113569200	MCF-7	breast:	n/a	n/a
33	CTCF	chr3:113609160-113609310	GM12873	blood:	n/a	n/a
34	CTCF	chr3:113609220-113609370	HEK293	kidney:	n/a	n/a
35	CTCF	chr3:113609260-113609410	GM12868	blood:	n/a	n/a
36	CTCF	chr3:113609200-113609350	GM12874	blood:	n/a	n/a
37	CTCF	chr3:113609360-113609510	HFF-Myc	foreskin:	n/a	n/a
38	CTCF	chr3:113569146-113569238	MCF-7	breast:	n/a	n/a
39	CTCF	chr3:113609220-113609370	HepG2	liver:	n/a	n/a
40	CTCF	chr3:113609225-113609400	K562	blood:	n/a	n/a
41	CTCF	chr3:113609280-113609430	MCF-7	breast:	n/a	n/a
42	CTCF	chr3:113609220-113609370	BE2_C	brain:	n/a	n/a
43	CTCF	chr3:113609234-113609399	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr3:113609240-113609390	NHEK	skin:	n/a	n/a
45	CTCF	chr3:113582540-113582690	HepG2	liver:	n/a	n/a
46	CTCF	chr3:113609065-113609541	MCF-7	breast:	n/a	n/a
47	CTCF	chr3:113609240-113609390	SAEC	small airway:	n/a	n/a
48	CTCF	chr3:113609280-113609430	GM12872	blood:	n/a	n/a
49	CTCF	chr3:113609149-113609452	MCF-7	breast:	n/a	n/a
50	CTCF	chr3:113582580-113582730	GM12872	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:113602333-113602383	HL-60	blood:	n/a
2	chr3:113604241-113604291	HMEC	breast:	n/a
3	chr3:113604392-113604442	SKMC	muscle:	n/a
4	chr3:113603874-113603924	GM12892	blood:	n/a
5	chr3:113604392-113604442	HCM	heart:	n/a
6	chr3:113606269-113606319	RPTEC	kidney:	n/a
7	chr3:113604241-113604291	BE2_C	brain:	n/a
8	chr3:113604241-113604291	HUVEC	blood vessel:	n/a
9	chr3:113599916-113599966	ProgFib	skin:	n/a
10	chr3:113602333-113602383	ECC-1	luminal epithelium:	n/a
11	chr3:113599916-113599966	IMR90	lung:	fetal
12	chr3:113604183-113604233	ovcar-3	ovarian:	n/a
13	chr3:113599916-113599966	HRCEpiC	kidney:	n/a
14	chr3:113602333-113602383	NT2-D1	testis:	n/a
15	chr3:113603874-113603924	RPTEC	kidney:	n/a
16	chr3:113599916-113599966	NH-A	brain:	n/a
17	chr3:113599916-113599966	HPAEpiC	pulmonary alveolar:	n/a
18	chr3:113599916-113599966	HNPCEpiC	eye:	n/a
19	chr3:113604392-113604442	BE2_C	brain:	n/a
20	chr3:113606269-113606319	SK-N-SH_RA	brain:	n/a
21	chr3:113602333-113602383	HCPEpiC	choroid plexus:	n/a
22	chr3:113604392-113604442	PANC-1	pancreas:	n/a
23	chr3:113604392-113604442	H1-hESC	embryonic stem cell:	embryo
24	chr3:113604241-113604291	GM12892	blood:	n/a
25	chr3:113599916-113599966	Hepatocyte	liver:	n/a
26	chr3:113602333-113602383	HepG2	liver:	n/a
27	chr3:113604183-113604233	ECC-1	luminal epithelium:	n/a
28	chr3:113604183-113604233	K562	blood:	n/a
29	chr3:113602333-113602383	LNCaP	prostate:	n/a
30	chr3:113603874-113603924	HCF	heart:	n/a
31	chr3:113604183-113604233	AG04449	skin:	fetal
32	chr3:113604241-113604291	AG09319	gingival:	n/a
33	chr3:113604241-113604291	AG10803	skin:	n/a
34	chr3:113606269-113606319	BE2_C	brain:	n/a
35	chr3:113603874-113603924	HUVEC	blood vessel:	n/a
36	chr3:113603874-113603924	NB4	blood:	n/a
37	chr3:113604392-113604442	NT2-D1	testis:	n/a
38	chr3:113602333-113602383	HRCEpiC	kidney:	n/a
39	chr3:113604241-113604291	HL-60	blood:	n/a
40	chr3:113604392-113604442	HepG2	liver:	n/a
41	chr3:113606269-113606319	AG04449	skin:	fetal
42	chr3:113599916-113599966	SK-N-MC	brain:	n/a
43	chr3:113606269-113606319	HNPCEpiC	eye:	n/a
44	chr3:113606269-113606319	U87	brain:	n/a
45	chr3:113604241-113604291	IMR90	lung:	fetal
46	chr3:113604392-113604442	ProgFib	skin:	n/a
47	chr3:113606269-113606319	HL-60	blood:	n/a
48	chr3:113606269-113606319	HRCEpiC	kidney:	n/a
49	chr3:113606269-113606319	HPAEpiC	pulmonary alveolar:	n/a
50	chr3:113602333-113602383	PANC-1	pancreas:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:113612373..113614219-chr3:113615941..113617468,2	MCF-7	breast:
2	chr3:113464701..113467422-chr3:113608653..113611479,2	K562	blood:
3	chr3:113615024..113616556-chr3:113664464..113667228,2	MCF-7	breast:
4	chr3:113613642..113617289-chr3:113619230..113622663,4	K562	blood:
5	chr3:113564891..113567125-chr3:113615091..113617846,2	MCF-7	breast:
6	chr3:113608263..113610778-chr3:113614290..113616255,2	MCF-7	breast:
7	chr3:113607843..113610621-chr3:113612739..113615522,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP6V1A-2	chr3:113594331-113594714	NONHSAT091246
2	lnc-NAA50-4	chr3:113569084-113569578	NONHSAT091250
3	lnc-ATP6V1A-2	chr3:113588354-113588438	NONHSAT091246

No data

Variant related genes	Relation type
ENSG00000240776	TF binding region
GRAMD1C	TF binding region
ENSG00000241889	TF binding region
ENSG00000240776	CpG island
GRAMD1C	CpG island
ENSG00000241889	CpG island
ENSG00000178075	chromatin interactions
ENSG00000273394	chromatin interactions
ENSG00000184307	chromatin interactions
ENSG00000121579	chromatin interactions
ENSG00000114573	chromatin interactions
ENSG00000242659	chromatin interactions

Extended variants
information (count: 1726 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1726 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79548880	chr3:113564266-113564267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs7612787	chr3:113564276-113564277	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs562762657	chr3:113564300-113564301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs191791024	chr3:113564333-113564334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539452293	chr3:113564342-113564343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs371652006	chr3:113564349-113564350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182851798	chr3:113564354-113564355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560735637	chr3:113564374-113564375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs368330904	chr3:113564394-113564395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187922969	chr3:113564407-113564408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144960929	chr3:113564441-113564442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555958018	chr3:113564493-113564494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566151662	chr3:113564534-113564535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530203221	chr3:113564552-113564553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192449848	chr3:113564605-113564606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs541790763	chr3:113564653-113564654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560089237	chr3:113564674-113564675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569691573	chr3:113564706-113564707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533622618	chr3:113564735-113564736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545829717	chr3:113564748-113564749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs34307870	chr3:113564760-113564761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs397724335	chr3:113564763-113564764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs563897725	chr3:113564831-113564832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558544283	chr3:113564858-113564859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2712366	chr3:113564918-113564919	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs147950812	chr3:113564945-113564946	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs60131213	chr3:113564958-113564959	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs397990846	chr3:113564970-113564971	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs549594196	chr3:113564978-113564979	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs201758485	chr3:113564988-113564989	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs184358922	chr3:113564995-113564996	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs2052969	chr3:113565029-113565030	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs141564237	chr3:113565049-113565050	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs552751020	chr3:113565074-113565075	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs112330589	chr3:113565086-113565087	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs539317415	chr3:113565089-113565090	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs558157457	chr3:113565099-113565100	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs569931058	chr3:113565127-113565128	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs537587834	chr3:113565128-113565129	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs555574609	chr3:113565181-113565182	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs370233977	chr3:113565195-113565196	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs574133934	chr3:113565196-113565197	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs190562303	chr3:113565199-113565200	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs553567292	chr3:113565207-113565208	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs531597167	chr3:113565249-113565250	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs528016343	chr3:113565262-113565263	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs545693524	chr3:113565287-113565288	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs564142427	chr3:113565349-113565350	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs72952678	chr3:113565386-113565387	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs543553005	chr3:113565462-113565463	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	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
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Attention deficit hyperactivity disorder	22180640	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	22174824	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	19805367	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	19039135	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
early-passage human iPS cells	21368824	CNVD
Glioma	20126413	CNVD

Chromatin state (count:253 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:113558200-113570800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr3:113558400-113566400	Weak transcription	Fetal Intestine Small	intestine
3	chr3:113558600-113566600	Weak transcription	Fetal Kidney	kidney
4	chr3:113558600-113566600	Weak transcription	NHLF	lung
5	chr3:113558600-113574800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr3:113558800-113566600	Weak transcription	HUVEC	blood vessel
7	chr3:113560400-113566600	Weak transcription	Placenta	Placenta
8	chr3:113562600-113566400	Weak transcription	Duodenum Mucosa	Duodenum
9	chr3:113564200-113565400	Weak transcription	Liver	Liver
10	chr3:113565000-113566400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr3:113565400-113565600	Enhancers	Fetal Intestine Large	intestine
12	chr3:113565400-113565600	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr3:113565400-113566400	Enhancers	Liver	Liver
14	chr3:113565600-113566400	Weak transcription	Fetal Intestine Large	intestine
15	chr3:113565600-113566400	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr3:113566200-113566400	Enhancers	Rectal Mucosa Donor 29	rectum
17	chr3:113566200-113567600	Enhancers	Stomach Mucosa	stomach
18	chr3:113566400-113566800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr3:113566400-113566800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
20	chr3:113566400-113566800	Enhancers	Small Intestine	intestine
21	chr3:113566400-113567000	Flanking Active TSS	Liver	Liver
22	chr3:113566400-113567200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr3:113566400-113567600	Enhancers	Duodenum Mucosa	Duodenum
24	chr3:113566400-113567600	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr3:113566400-113568000	Enhancers	Fetal Intestine Large	intestine
26	chr3:113566400-113568000	Enhancers	Fetal Intestine Small	intestine
27	chr3:113566600-113566800	Enhancers	Placenta	Placenta
28	chr3:113566600-113566800	Enhancers	HUVEC	blood vessel
29	chr3:113566600-113566800	Enhancers	NHLF	lung
30	chr3:113566600-113567000	Enhancers	Fetal Kidney	kidney
31	chr3:113566600-113567200	Enhancers	Muscle Satellite Cultured Cells	--
32	chr3:113566600-113567200	Enhancers	Hela-S3	cervix
33	chr3:113566600-113567600	Enhancers	HMEC	breast
34	chr3:113566600-113567600	Enhancers	NHEK	skin
35	chr3:113566600-113568000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr3:113566800-113567000	Active TSS	Rectal Mucosa Donor 29	rectum
37	chr3:113566800-113567400	Weak transcription	Placenta	Placenta
38	chr3:113566800-113571200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr3:113567000-113567600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr3:113567000-113567600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr3:113567000-113568000	Enhancers	Liver	Liver
42	chr3:113567200-113570400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr3:113567400-113567600	Enhancers	Placenta	Placenta
44	chr3:113567600-113569200	Weak transcription	Placenta	Placenta
45	chr3:113568000-113569200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr3:113568000-113571200	Weak transcription	Fetal Intestine Small	intestine
47	chr3:113568000-113571600	Weak transcription	Fetal Intestine Large	intestine
48	chr3:113569200-113569400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr3:113569200-113569400	Enhancers	Placenta	Placenta
50	chr3:113569200-113574400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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