Variant report

Variant	esv3462231
Chromosome Location	chr3:100323931-100329687
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:100328325-100328363	K562	blood:	n/a	n/a
2	ATF1	chr3:100328075-100328453	K562	blood:	n/a	n/a
3	BACH1	chr3:100324408-100324438	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr3:100325837-100326298	GM12878	blood:	n/a	n/a
5	CCNT2	chr3:100328275-100328511	K562	blood:	n/a	n/a
6	CEBPB	chr3:100328331-100328552	K562	blood:	n/a	n/a
7	CHD2	chr3:100324442-100324546	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr3:100325860-100326010	GM12869	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
9	CTCF	chr3:100325708-100326147	MCF-7	breast:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
10	CTCF	chr3:100325940-100326090	HAc	cerebellar:	n/a	n/a
11	CTCF	chr3:100325880-100326030	WERI-Rb-1	eye:	n/a	n/a
12	CTCF	chr3:100325900-100326050	HCPEpiC	choroid plexus:	n/a	n/a
13	CTCF	chr3:100325940-100326090	GM12873	blood:	n/a	n/a
14	CTCF	chr3:100327900-100328050	WERI-Rb-1	eye:	n/a	n/a
15	CTCF	chr3:100325700-100325850	RPTEC	kidney:	n/a	n/a
16	CTCF	chr3:100325840-100325990	GM12867	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
17	CTCF	chr3:100325810-100326068	K562	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
18	CTCF	chr3:100325860-100326010	GM12875	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
19	CTCF	chr3:100325080-100325230	GM12864	blood:	n/a	n/a
20	CTCF	chr3:100325860-100325988	Hela-S3	cervix:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
21	CTCF	chr3:100325687-100326092	MCF-7	breast:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
22	CTCF	chr3:100325840-100325990	GM12873	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
23	CTCF	chr3:100325840-100325990	HPAF	blood vessel:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
24	CTCF	chr3:100325820-100325970	GM12867	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
25	CTCF	chr3:100325920-100326070	HCM	heart:	n/a	n/a
26	CTCF	chr3:100325960-100326110	GM12874	blood:	n/a	n/a
27	CTCF	chr3:100325764-100326060	K562	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
28	CTCF	chr3:100325960-100326110	GM12872	blood:	n/a	n/a
29	CTCF	chr3:100325940-100326090	A549	lung:	n/a	n/a
30	CTCF	chr3:100325920-100326070	GM12872	blood:	n/a	n/a
31	CTCF	chr3:100325860-100326010	HPAF	blood vessel:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
32	CTCF	chr3:100325796-100326003	HepG2	liver:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
33	CTCF	chr3:100325960-100326110	GM12866	blood:	n/a	n/a
34	CTCF	chr3:100325860-100326010	GM12865	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
35	CTCF	chr3:100325900-100326050	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr3:100325900-100326050	GM12871	blood:	n/a	n/a
37	CTCF	chr3:100325920-100326070	MCF-7	breast:	n/a	n/a
38	CTCF	chr3:100325820-100325970	GM12872	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
39	CTCF	chr3:100325853-100326019	MCF-7	breast:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
40	CTCF	chr3:100325849-100325851	K562	blood:	n/a	n/a
41	CTCF	chr3:100325820-100325970	GM12870	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
42	CTCF	chr3:100325860-100326010	GM12866	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
43	CTCF	chr3:100325860-100326010	A549	lung:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
44	CTCF	chr3:100325721-100326045	K562	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
45	CTCF	chr3:100325800-100325950	HCPEpiC	choroid plexus:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
46	CTCF	chr3:100325880-100326030	GM12868	blood:	n/a	n/a
47	CTCF	chr3:100325840-100325990	GM12865	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
48	CTCF	chr3:100325840-100325990	GM12871	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
49	CTCF	chr3:100325880-100326030	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr3:100325800-100325950	HepG2	liver:	n/a	chr3:100325868-100325878 chr3:100325865-100325886

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:100328745-100328795	PrEC	prostate:	n/a
2	chr3:100327897-100327947	GM06990	blood:	n/a
3	chr3:100328745-100328795	PrEC	prostate:	n/a
4	chr3:100327897-100327947	GM06990	blood:	n/a
5	chr3:100328745-100328795	NH-A	brain:	n/a
6	chr3:100328265-100328315	H1-hESC	embryonic stem cell:	embryo
7	chr3:100328265-100328315	HNPCEpiC	eye:	n/a
8	chr3:100328265-100328315	MCF-7	breast:	n/a
9	chr3:100328713-100328763	HUVEC	blood vessel:	n/a
10	chr3:100328186-100328236	AoSMC	blood vessel:	n/a
11	chr3:100328745-100328795	SKMC	muscle:	n/a
12	chr3:100328745-100328795	RPTEC	kidney:	n/a
13	chr3:100328265-100328315	GM19239	blood:	n/a
14	chr3:100328745-100328795	NT2-D1	testis:	n/a
15	chr3:100328713-100328763	Hela-S3	cervix:	n/a
16	chr3:100328713-100328763	K562	blood:	n/a
17	chr3:100327897-100327947	NT2-D1	testis:	n/a
18	chr3:100328186-100328236	ovcar-3	ovarian:	n/a
19	chr3:100328713-100328763	LNCaP	prostate:	n/a
20	chr3:100327897-100327947	HCPEpiC	choroid plexus:	n/a
21	chr3:100328265-100328315	PANC-1	pancreas:	n/a
22	chr3:100328745-100328795	A549	lung:	n/a
23	chr3:100328186-100328236	Hepatocyte	liver:	n/a
24	chr3:100328265-100328315	ProgFib	skin:	n/a
25	chr3:100328186-100328236	HepG2	liver:	n/a
26	chr3:100327897-100327947	MCF-7	breast:	n/a
27	chr3:100328186-100328236	SK-N-MC	brain:	n/a
28	chr3:100327897-100327947	HRE	kidney:	n/a
29	chr3:100328713-100328763	SK-N-SH	brain:	n/a
30	chr3:100327897-100327947	Caco-2	colon:	n/a
31	chr3:100328265-100328315	HRCEpiC	kidney:	n/a
32	chr3:100328713-100328763	GM12878	blood:	n/a
33	chr3:100327897-100327947	GM19239	blood:	n/a
34	chr3:100328745-100328795	HUVEC	blood vessel:	n/a
35	chr3:100328745-100328795	HIPEpiC	eye:	n/a
36	chr3:100328186-100328236	NHBE	bronchial:	n/a
37	chr3:100328745-100328795	LNCaP	prostate:	n/a
38	chr3:100328713-100328763	AG10803	skin:	n/a
39	chr3:100327897-100327947	HUVEC	blood vessel:	n/a
40	chr3:100328186-100328236	MCF-7	breast:	n/a
41	chr3:100328186-100328236	HRPEpiC	eye:	n/a
42	chr3:100328745-100328795	Hela-S3	cervix:	n/a
43	chr3:100328265-100328315	HAEpiC	amniotic membrane:	n/a
44	chr3:100328713-100328763	HCPEpiC	choroid plexus:	n/a
45	chr3:100327897-100327947	HCF	heart:	n/a
46	chr3:100328713-100328763	GM12891	blood:	n/a
47	chr3:100328745-100328795	ECC-1	luminal epithelium:	n/a
48	chr3:100327897-100327947	HRPEpiC	eye:	n/a
49	chr3:100327897-100327947	LNCaP	prostate:	n/a
50	chr3:100327897-100327947	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:100325466..100327241-chr3:100349090..100350621,2	K562	blood:
2	chr3:100322209..100326377-chr3:100427335..100430667,5	MCF-7	breast:
3	chr3:100118375..100121332-chr3:100329278..100332064,2	K562	blood:
4	chr3:100325886..100329093-chr3:100426560..100431642,4	MCF-7	breast:
5	chr3:100325407..100326196-chr3:100353394..100354270,2	MCF-7	breast:

Variant related genes	Relation type
GPR128	TF binding region
GPR128	CpG island
ENSG00000154174	chromatin interactions
ENSG00000206535	chromatin interactions
ENSG00000114354	chromatin interactions

Extended variants
information (count: 266 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:266 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576922860	chr3:100323934-100323935	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs138816828	chr3:100323937-100323938	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs77078325	chr3:100323948-100323949	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs141275134	chr3:100323981-100323982	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs193071747	chr3:100324035-100324036	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs146957626	chr3:100324041-100324042	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs185848919	chr3:100324137-100324138	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs563182910	chr3:100324160-100324161	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs575330372	chr3:100324188-100324189	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs545920084	chr3:100324209-100324210	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs112380241	chr3:100324221-100324222	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs528439320	chr3:100324269-100324270	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs9867401	chr3:100324275-100324276	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs562194169	chr3:100324281-100324282	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs1676335	chr3:100324342-100324343	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs137968419	chr3:100324348-100324349	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs368330542	chr3:100324352-100324353	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs149461493	chr3:100324357-100324358	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs188376191	chr3:100324376-100324377	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs535483214	chr3:100324389-100324390	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs537130245	chr3:100324390-100324391	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs193160037	chr3:100324423-100324424	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs570549863	chr3:100324425-100324426	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs17280554	chr3:100324442-100324443	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs1718272	chr3:100324522-100324523	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs539629486	chr3:100324533-100324534	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs143011231	chr3:100324534-100324535	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs535405482	chr3:100324545-100324546	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs374109547	chr3:100324572-100324573	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs9867888	chr3:100324640-100324641	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs575129039	chr3:100324652-100324653	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs573208981	chr3:100324662-100324663	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs142000741	chr3:100324666-100324667	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs71620022	chr3:100324669-100324670	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs2461499	chr3:100324670-100324671	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs12486537	chr3:100324674-100324675	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
37	rs71620024	chr3:100324676-100324677	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs201797094	chr3:100324681-100324682	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs6441359	chr3:100324684-100324685	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
40	rs540259867	chr3:100324685-100324686	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs184012158	chr3:100324696-100324697	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs58942998	chr3:100324703-100324704	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs562161790	chr3:100324712-100324713	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs377681499	chr3:100324723-100324724	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs529591381	chr3:100324727-100324728	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs551332553	chr3:100324737-100324738	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs563191664	chr3:100324741-100324742	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs370428503	chr3:100324746-100324747	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs373594593	chr3:100324750-100324751	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs202025100	chr3:100324754-100324755	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	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
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21785460	CNVD

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:100318200-100324200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr3:100321400-100324200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr3:100322800-100324000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr3:100322800-100324200	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr3:100322800-100325600	Weak transcription	Stomach Mucosa	stomach
6	chr3:100322800-100327800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr3:100322800-100327800	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr3:100322800-100328000	Weak transcription	Colonic Mucosa	Colon
9	chr3:100322800-100328000	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr3:100322800-100328200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr3:100322800-100328200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr3:100322800-100330200	Weak transcription	HepG2	liver
13	chr3:100323000-100324000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:100323000-100325200	Weak transcription	GM12878-XiMat	blood
15	chr3:100323000-100325800	Weak transcription	Primary B cells from peripheral blood	blood
16	chr3:100323000-100325800	Weak transcription	Duodenum Mucosa	Duodenum
17	chr3:100323000-100325800	Weak transcription	Fetal Intestine Large	intestine
18	chr3:100323000-100325800	Weak transcription	Fetal Intestine Small	intestine
19	chr3:100323000-100327800	Weak transcription	Primary T cells from cord blood	blood
20	chr3:100323000-100328000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr3:100323000-100328200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr3:100323000-100328200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr3:100323200-100324400	Weak transcription	Liver	Liver
24	chr3:100323200-100327800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr3:100323200-100328400	Weak transcription	HMEC	breast
26	chr3:100323800-100324200	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr3:100324000-100324200	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr3:100324000-100324400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr3:100324200-100324400	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr3:100324200-100324400	Enhancers	Spleen	Spleen
31	chr3:100324200-100324600	Enhancers	H1 Cell Line	embryonic stem cell
32	chr3:100324200-100324600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr3:100324200-100324600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr3:100324200-100324600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr3:100324400-100325200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr3:100325200-100325800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr3:100325200-100326600	Enhancers	GM12878-XiMat	blood
38	chr3:100325600-100326000	Enhancers	Stomach Mucosa	stomach
39	chr3:100325800-100326200	Enhancers	Primary B cells from peripheral blood	blood
40	chr3:100325800-100326200	Enhancers	Duodenum Mucosa	Duodenum
41	chr3:100325800-100326200	Enhancers	Fetal Intestine Small	intestine
42	chr3:100325800-100326400	Enhancers	Fetal Intestine Large	intestine
43	chr3:100325800-100326800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr3:100326000-100328400	Weak transcription	Stomach Mucosa	stomach
45	chr3:100326200-100327200	Weak transcription	Fetal Intestine Small	intestine
46	chr3:100326200-100327400	Weak transcription	Duodenum Mucosa	Duodenum
47	chr3:100326400-100326800	Weak transcription	Fetal Intestine Large	intestine
48	chr3:100326600-100327000	Flanking Active TSS	GM12878-XiMat	blood
49	chr3:100326800-100328000	Enhancers	Fetal Intestine Large	intestine
50	chr3:100327000-100327200	Enhancers	GM12878-XiMat	blood

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