Variant report

Variant	nsv822201
Chromosome Location	chr3:100325319-100329560
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	BCLAF1	chr3:100325837-100326298	GM12878	blood:	n/a	n/a
4	CCNT2	chr3:100328275-100328511	K562	blood:	n/a	n/a
5	CEBPB	chr3:100328331-100328552	K562	blood:	n/a	n/a
6	CTCF	chr3:100325920-100326070	GM12872	blood:	n/a	n/a
7	CTCF	chr3:100325853-100326019	MCF-7	breast:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
8	CTCF	chr3:100325860-100326010	GM12878	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
9	CTCF	chr3:100325860-100325988	Hela-S3	cervix:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
10	CTCF	chr3:100325860-100326010	GM12875	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
11	CTCF	chr3:100325820-100325970	AG10803	skin:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
12	CTCF	chr3:100325940-100326090	HAc	cerebellar:	n/a	n/a
13	CTCF	chr3:100325920-100326070	HCM	heart:	n/a	n/a
14	CTCF	chr3:100325880-100326030	NHDF-neo	bronchial:	n/a	n/a
15	CTCF	chr3:100325900-100326050	GM12871	blood:	n/a	n/a
16	CTCF	chr3:100325820-100325970	GM12870	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
17	CTCF	chr3:100325860-100326010	A549	lung:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
18	CTCF	chr3:100325940-100326090	A549	lung:	n/a	n/a
19	CTCF	chr3:100325900-100326050	HCPEpiC	choroid plexus:	n/a	n/a
20	CTCF	chr3:100325840-100325990	GM12871	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
21	CTCF	chr3:100325960-100326110	AG04449	skin:	n/a	n/a
22	CTCF	chr3:100325818-100326026	MCF-7	breast:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
23	CTCF	chr3:100325810-100326068	K562	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
24	CTCF	chr3:100325840-100325990	AG04449	skin:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
25	CTCF	chr3:100325840-100325990	GM12865	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
26	CTCF	chr3:100325820-100325970	GM12867	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
27	CTCF	chr3:100325840-100325990	GM12873	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
28	CTCF	chr3:100325860-100326010	HBMEC	blood vessel:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
29	CTCF	chr3:100325860-100326010	HMF	breast:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
30	CTCF	chr3:100325800-100325950	HepG2	liver:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
31	CTCF	chr3:100325687-100326092	MCF-7	breast:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
32	CTCF	chr3:100325869-100325965	HepG2	liver:	n/a	n/a
33	CTCF	chr3:100325960-100326110	GM12874	blood:	n/a	n/a
34	CTCF	chr3:100325860-100326010	HPAF	blood vessel:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
35	CTCF	chr3:100325840-100325990	HPAF	blood vessel:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
36	CTCF	chr3:100325860-100326010	GM12869	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
37	CTCF	chr3:100325880-100326030	GM12873	blood:	n/a	n/a
38	CTCF	chr3:100325810-100326010	K562	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
39	CTCF	chr3:100325820-100325970	GM12874	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
40	CTCF	chr3:100325820-100325970	BE2_C	brain:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
41	CTCF	chr3:100325764-100326060	K562	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
42	CTCF	chr3:100325880-100326030	GM12868	blood:	n/a	n/a
43	CTCF	chr3:100325860-100326010	GM06990	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
44	CTCF	chr3:100325840-100325990	HCT-116	colon:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
45	CTCF	chr3:100325853-100326018	K562	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
46	CTCF	chr3:100325860-100326010	GM12866	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
47	CTCF	chr3:100325721-100326045	K562	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
48	CTCF	chr3:100325780-100325930	MCF-7	breast:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
49	CTCF	chr3:100325760-100325910	NHLF	lung:	n/a	chr3:100325868-100325878 chr3:100325865-100325886
50	CTCF	chr3:100325820-100325970	GM12872	blood:	n/a	chr3:100325868-100325878 chr3:100325865-100325886

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:100327897-100327947	AG04449	skin:	fetal
2	chr3:100327897-100327947	AG04449	skin:	fetal
3	chr3:100328745-100328795	ECC-1	luminal epithelium:	n/a
4	chr3:100328265-100328315	IMR90	lung:	fetal
5	chr3:100328186-100328236	SK-N-SH	brain:	n/a
6	chr3:100328713-100328763	HCPEpiC	choroid plexus:	n/a
7	chr3:100328265-100328315	SAEC	small airway:	n/a
8	chr3:100328265-100328315	PFSK-1	brain:	n/a
9	chr3:100328745-100328795	NHBE	bronchial:	n/a
10	chr3:100328713-100328763	HUVEC	blood vessel:	n/a
11	chr3:100328713-100328763	K562	blood:	n/a
12	chr3:100327897-100327947	AG10803	skin:	n/a
13	chr3:100328745-100328795	SK-N-SH	brain:	n/a
14	chr3:100328186-100328236	HIPEpiC	eye:	n/a
15	chr3:100327897-100327947	HCT-116	colon:	n/a
16	chr3:100328186-100328236	HUVEC	blood vessel:	n/a
17	chr3:100328186-100328236	ovcar-3	ovarian:	n/a
18	chr3:100328186-100328236	BJ	skin:	n/a
19	chr3:100328265-100328315	K562	blood:	n/a
20	chr3:100328745-100328795	HUVEC	blood vessel:	n/a
21	chr3:100328265-100328315	SK-N-MC	brain:	n/a
22	chr3:100328745-100328795	NH-A	brain:	n/a
23	chr3:100328186-100328236	GM12891	blood:	n/a
24	chr3:100327897-100327947	NH-A	brain:	n/a
25	chr3:100328713-100328763	T-47D	breast:	n/a
26	chr3:100328186-100328236	ProgFib	skin:	n/a
27	chr3:100328745-100328795	PFSK-1	brain:	n/a
28	chr3:100328745-100328795	GM12891	blood:	n/a
29	chr3:100328186-100328236	HRCEpiC	kidney:	n/a
30	chr3:100328745-100328795	AG09319	gingival:	n/a
31	chr3:100327897-100327947	CMK	blood:	n/a
32	chr3:100328265-100328315	HCM	heart:	n/a
33	chr3:100328265-100328315	GM06990	blood:	n/a
34	chr3:100327897-100327947	A549	lung:	n/a
35	chr3:100327897-100327947	IMR90	lung:	fetal
36	chr3:100328265-100328315	HCF	heart:	n/a
37	chr3:100328713-100328763	HCF	heart:	n/a
38	chr3:100328745-100328795	T-47D	breast:	n/a
39	chr3:100328186-100328236	IMR90	lung:	fetal
40	chr3:100328713-100328763	SKMC	muscle:	n/a
41	chr3:100328186-100328236	Hepatocyte	liver:	n/a
42	chr3:100328745-100328795	ovcar-3	ovarian:	n/a
43	chr3:100328186-100328236	SK-N-MC	brain:	n/a
44	chr3:100327897-100327947	MCF10A-Er-Src	breast:	n/a
45	chr3:100328713-100328763	AG09319	gingival:	n/a
46	chr3:100328713-100328763	SK-N-MC	brain:	n/a
47	chr3:100328713-100328763	AG09309	skin:	n/a
48	chr3:100327897-100327947	HUVEC	blood vessel:	n/a
49	chr3:100328745-100328795	AG04449	skin:	fetal
50	chr3:100328745-100328795	HEEpiC	esophagus:	n/a

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

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: 166 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:166 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556636316	chr3:100325324-100325325	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs578249213	chr3:100325359-100325360	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs550631893	chr3:100325381-100325382	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs182006022	chr3:100325383-100325384	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs185360334	chr3:100325417-100325418	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs527850409	chr3:100325475-100325476	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs374276964	chr3:100325508-100325509	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs561398237	chr3:100325573-100325574	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs142217482	chr3:100325634-100325635	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs190026163	chr3:100325689-100325690	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs547317288	chr3:100325698-100325699	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs550149565	chr3:100325740-100325741	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs568543235	chr3:100325761-100325762	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs533064433	chr3:100325771-100325772	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs551620006	chr3:100325778-100325779	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs34868268	chr3:100325791-100325792	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs566677441	chr3:100325808-100325809	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs182655322	chr3:100325826-100325827	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs147837501	chr3:100325846-100325847	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs567031331	chr3:100325927-100325928	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs185044882	chr3:100325991-100325992	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs538389518	chr3:100326029-100326030	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs529322536	chr3:100326075-100326076	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs112210598	chr3:100326107-100326108	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs578095569	chr3:100326153-100326154	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs538671383	chr3:100326194-100326195	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs554417478	chr3:100326239-100326240	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs141342086	chr3:100326259-100326260	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs9811156	chr3:100326263-100326264	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs543164747	chr3:100326279-100326280	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs561184153	chr3:100326281-100326282	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs573396519	chr3:100326322-100326323	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs543939968	chr3:100326335-100326336	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs540128280	chr3:100326347-100326348	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs532915739	chr3:100326389-100326390	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs551094094	chr3:100326396-100326397	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs560356761	chr3:100326428-100326429	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs191226131	chr3:100326430-100326431	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs183657735	chr3:100326444-100326445	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs1718273	chr3:100326455-100326456	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs79063208	chr3:100326458-100326459	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs189100401	chr3:100326505-100326506	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs534171742	chr3:100326548-100326549	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs538326265	chr3:100326712-100326713	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs570671714	chr3:100326772-100326773	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs114824188	chr3:100326778-100326779	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs571670587	chr3:100326789-100326790	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs34085401	chr3:100326790-100326791	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs371949695	chr3:100326796-100326797	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs538974998	chr3:100326819-100326820	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 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:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:100322800-100325600	Weak transcription	Stomach Mucosa	stomach
2	chr3:100322800-100327800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr3:100322800-100327800	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr3:100322800-100328000	Weak transcription	Colonic Mucosa	Colon
5	chr3:100322800-100328000	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr3:100322800-100328200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr3:100322800-100328200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr3:100322800-100330200	Weak transcription	HepG2	liver
9	chr3:100323000-100325800	Weak transcription	Primary B cells from peripheral blood	blood
10	chr3:100323000-100325800	Weak transcription	Duodenum Mucosa	Duodenum
11	chr3:100323000-100325800	Weak transcription	Fetal Intestine Large	intestine
12	chr3:100323000-100325800	Weak transcription	Fetal Intestine Small	intestine
13	chr3:100323000-100327800	Weak transcription	Primary T cells from cord blood	blood
14	chr3:100323000-100328000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr3:100323000-100328200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr3:100323000-100328200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr3:100323200-100327800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr3:100323200-100328400	Weak transcription	HMEC	breast
19	chr3:100325200-100325800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr3:100325200-100326600	Enhancers	GM12878-XiMat	blood
21	chr3:100325600-100326000	Enhancers	Stomach Mucosa	stomach
22	chr3:100325800-100326200	Enhancers	Primary B cells from peripheral blood	blood
23	chr3:100325800-100326200	Enhancers	Duodenum Mucosa	Duodenum
24	chr3:100325800-100326200	Enhancers	Fetal Intestine Small	intestine
25	chr3:100325800-100326400	Enhancers	Fetal Intestine Large	intestine
26	chr3:100325800-100326800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr3:100326000-100328400	Weak transcription	Stomach Mucosa	stomach
28	chr3:100326200-100327200	Weak transcription	Fetal Intestine Small	intestine
29	chr3:100326200-100327400	Weak transcription	Duodenum Mucosa	Duodenum
30	chr3:100326400-100326800	Weak transcription	Fetal Intestine Large	intestine
31	chr3:100326600-100327000	Flanking Active TSS	GM12878-XiMat	blood
32	chr3:100326800-100328000	Enhancers	Fetal Intestine Large	intestine
33	chr3:100327000-100327200	Enhancers	GM12878-XiMat	blood
34	chr3:100327200-100328400	Enhancers	Fetal Intestine Small	intestine
35	chr3:100327400-100327600	Enhancers	Duodenum Mucosa	Duodenum
36	chr3:100327600-100334200	Active TSS	Duodenum Mucosa	Duodenum
37	chr3:100327800-100328000	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr3:100327800-100328200	Enhancers	Fetal Thymus	thymus
39	chr3:100327800-100328600	Enhancers	Dnd41	blood
40	chr3:100327800-100328800	Enhancers	Primary T cells from cord blood	blood
41	chr3:100327800-100329000	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr3:100327800-100329000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr3:100327800-100330200	Weak transcription	Liver	Liver
44	chr3:100328000-100328200	Enhancers	Colonic Mucosa	Colon
45	chr3:100328000-100328400	Flanking Active TSS	Fetal Intestine Large	intestine
46	chr3:100328000-100328400	Active TSS	Rectal Mucosa Donor 29	rectum
47	chr3:100328000-100328600	Enhancers	Rectal Mucosa Donor 31	rectum
48	chr3:100328000-100328600	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr3:100328000-100328800	Enhancers	Primary hematopoietic stem cells	blood
50	chr3:100328000-100328800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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