Variant report

Variant	esv3385471
Chromosome Location	chr5:177098196-177106694
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	BACH1	chr5:177099131-177099156	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr5:177103493-177103545	K562	blood:	n/a	n/a
3	CTCF	chr5:177102250-177102455	MCF-7	breast:	n/a	n/a
4	CTCF	chr5:177102283-177102439	GM19240	blood:	n/a	n/a
5	CTCF	chr5:177102393-177102434	Medullo	brain:	n/a	n/a
6	CTCF	chr5:177102363-177102390	MCF-7	breast:	n/a	n/a
7	CTCF	chr5:177102271-177102442	GM19239	blood:	n/a	n/a
8	CTCF	chr5:177102261-177102462	K562	blood:	n/a	n/a
9	CTCF	chr5:177098971-177098999	NHEK	skin:	n/a	n/a
10	CTCF	chr5:177102279-177102438	NHEK	skin:	n/a	n/a
11	CTCF	chr5:177102287-177102424	ProgFib	skin:	n/a	n/a
12	CTCF	chr5:177102263-177102459	GM12878	blood:	n/a	n/a
13	CTCF	chr5:177102280-177102447	A549	lung:	n/a	n/a
14	CTCF	chr5:177098901-177098990	GM12892	blood:	n/a	n/a
15	CTCF	chr5:177102350-177102370	Pancreas_OC	pancreas:	n/a	n/a
16	CTCF	chr5:177102266-177102422	HepG2	liver:	n/a	n/a
17	CTCF	chr5:177102109-177102470	A549	lung:	n/a	n/a
18	CTCF	chr5:177098921-177099028	MCF-7	breast:	n/a	n/a
19	CTCF	chr5:177102291-177102422	Fibrobl	skin:	n/a	n/a
20	CTCF	chr5:177102278-177102430	MCF-7	breast:	n/a	n/a
21	CTCF	chr5:177102286-177102442	HUVEC	blood vessel:	n/a	n/a
22	CTCF	chr5:177098901-177099025	Fibrobl	skin:	n/a	n/a
23	CTCF	chr5:177102259-177102440	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr5:177102294-177102414	Lung_OC	lung:	n/a	n/a
25	CTCF	chr5:177102247-177102527	A549	lung:	n/a	n/a
26	CTCF	chr5:177102198-177102433	A549	lung:	n/a	n/a
27	CTCF	chr5:177098926-177099013	GM19239	blood:	n/a	n/a
28	CTCF	chr5:177102258-177102450	GM19238	blood:	n/a	n/a
29	CTCF	chr5:177102255-177102452	Gliobla	brain:	n/a	n/a
30	CTCF	chr5:177102316-177102433	Spleen_OC	spleen:	n/a	n/a
31	CTCF	chr5:177102324-177102426	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr5:177102288-177102433	GM12892	blood:	n/a	n/a
33	E2F6	chr5:177099063-177099257	K562	blood:	n/a	n/a
34	EBF1	chr5:177100258-177100467	GM12878	blood:	n/a	n/a
35	EGR1	chr5:177099150-177099310	ECC-1	luminal epithelium:	n/a	chr5:177099242-177099256 chr5:177099182-177099196 chr5:177099227-177099241
36	EGR1	chr5:177099114-177099355	HCT-116	colon:	n/a	chr5:177099242-177099256 chr5:177099182-177099196 chr5:177099227-177099241
37	EGR1	chr5:177099108-177099265	K562	blood:	n/a	chr5:177099242-177099256 chr5:177099182-177099196 chr5:177099227-177099241
38	EGR1	chr5:177099109-177099332	GM12878	blood:	n/a	chr5:177099242-177099256 chr5:177099182-177099196 chr5:177099227-177099241
39	EGR1	chr5:177099052-177099277	K562	blood:	n/a	chr5:177099242-177099256 chr5:177099182-177099196 chr5:177099227-177099241
40	EGR1	chr5:177099117-177099250	GM12878	blood:	n/a	chr5:177099182-177099196 chr5:177099227-177099241
41	EGR1	chr5:177099146-177099304	MCF-7	breast:	n/a	chr5:177099242-177099256 chr5:177099182-177099196 chr5:177099227-177099241
42	ELF1	chr5:177098935-177099373	GM12878	blood:	n/a	chr5:177098961-177098973 chr5:177099325-177099337
43	EP300	chr5:177099369-177099557	GM12878	blood:	n/a	chr5:177099400-177099414
44	EP300	chr5:177099102-177099351	SK-N-SH	brain:	n/a	chr5:177099325-177099341
45	GATA2	chr5:177102141-177102525	K562	blood:	n/a	n/a
46	HEY1	chr5:177098155-177098416	K562	blood:	n/a	n/a
47	HEY1	chr5:177098972-177099283	HepG2	liver:	n/a	n/a
48	HEY1	chr5:177098841-177099256	K562	blood:	n/a	n/a
49	HEY1	chr5:177098426-177098824	K562	blood:	n/a	chr5:177098534-177098549
50	HEY1	chr5:177098964-177099235	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:177100448-177100498	NH-A	brain:	n/a
2	chr5:177099102-177099152	CMK	blood:	n/a
3	chr5:177100428-177100478	GM06990	blood:	n/a
4	chr5:177099378-177099428	GM12891	blood:	n/a
5	chr5:177099378-177099428	HMEC	breast:	n/a
6	chr5:177099102-177099152	GM06990	blood:	n/a
7	chr5:177103100-177103150	K562	blood:	n/a
8	chr5:177099378-177099428	H1-hESC	embryonic stem cell:	embryo
9	chr5:177099378-177099428	AG09309	skin:	n/a
10	chr5:177099644-177099694	HepG2	liver:	n/a
11	chr5:177100428-177100478	CMK	blood:	n/a
12	chr5:177100428-177100478	PFSK-1	brain:	n/a
13	chr5:177100428-177100478	GM12892	blood:	n/a
14	chr5:177100448-177100498	Caco-2	colon:	n/a
15	chr5:177099251-177099301	AG04449	skin:	fetal
16	chr5:177099251-177099301	GM12891	blood:	n/a
17	chr5:177099102-177099152	Jurkat	blood:	n/a
18	chr5:177099378-177099428	NHBE	bronchial:	n/a
19	chr5:177100428-177100478	U87	brain:	n/a
20	chr5:177099378-177099428	HEK293	kidney:	embryo
21	chr5:177100428-177100478	HL-60	blood:	n/a
22	chr5:177103100-177103150	Hepatocyte	liver:	n/a
23	chr5:177099644-177099694	NHBE	bronchial:	n/a
24	chr5:177103100-177103150	Caco-2	colon:	n/a
25	chr5:177103100-177103150	SK-N-SH_RA	brain:	n/a
26	chr5:177099373-177099423	NT2-D1	testis:	n/a
27	chr5:177099102-177099152	GM12891	blood:	n/a
28	chr5:177100448-177100498	HCF	heart:	n/a
29	chr5:177099378-177099428	Hepatocyte	liver:	n/a
30	chr5:177099644-177099694	MCF10A-Er-Src	breast:	n/a
31	chr5:177103100-177103150	MCF-7	breast:	n/a
32	chr5:177099102-177099152	Hela-S3	cervix:	n/a
33	chr5:177099373-177099423	LNCaP	prostate:	n/a
34	chr5:177099373-177099423	GM12892	blood:	n/a
35	chr5:177099378-177099428	Caco-2	colon:	n/a
36	chr5:177099373-177099423	BE2_C	brain:	n/a
37	chr5:177099251-177099301	IMR90	lung:	fetal
38	chr5:177099102-177099152	Hepatocyte	liver:	n/a
39	chr5:177103100-177103150	SKMC	muscle:	n/a
40	chr5:177099373-177099423	MCF10A-Er-Src	breast:	n/a
41	chr5:177100448-177100498	HEK293	kidney:	embryo
42	chr5:177100448-177100498	SK-N-SH_RA	brain:	n/a
43	chr5:177100428-177100478	HRPEpiC	eye:	n/a
44	chr5:177099373-177099423	HCT-116	colon:	n/a
45	chr5:177099378-177099428	HCF	heart:	n/a
46	chr5:177100428-177100478	MCF-7	breast:	n/a
47	chr5:177099373-177099423	HepG2	liver:	n/a
48	chr5:177099378-177099428	NB4	blood:	n/a
49	chr5:177099378-177099428	GM06990	blood:	n/a
50	chr5:177099251-177099301	A549	lung:	n/a

Variant related genes	Relation type
ENSG00000249849	TF binding region
ENSG00000246596	TF binding region
ENSG00000249849	CpG island
ENSG00000246596	CpG island

Extended variants
information (count: 95 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:95 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371541858	chr5:177098271-177098272	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs529623473	chr5:177098288-177098289	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541552301	chr5:177098342-177098343	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559812532	chr5:177098353-177098354	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs527521363	chr5:177098361-177098362	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs552044460	chr5:177099047-177099048	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs575822496	chr5:177099069-177099070	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs531478993	chr5:177099208-177099209	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs551011239	chr5:177099239-177099240	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs369791757	chr5:177099365-177099366	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs536628978	chr5:177099378-177099379	Active TSS Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs200105127	chr5:177099403-177099404	Active TSS Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs368969585	chr5:177099610-177099611	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs62398500	chr5:177099623-177099624	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs566845362	chr5:177099689-177099690	Weak transcription Enhancers Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs534415689	chr5:177099728-177099729	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs558854406	chr5:177099779-177099780	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs192391920	chr5:177099792-177099793	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs74955780	chr5:177099964-177099965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs577480397	chr5:177100091-177100092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs374026251	chr5:177100174-177100175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538179362	chr5:177100206-177100207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556414794	chr5:177100340-177100341	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs574141574	chr5:177100341-177100342	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs541414805	chr5:177100342-177100343	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs559823083	chr5:177100348-177100349	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs10075483	chr5:177100425-177100426	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs546002061	chr5:177100433-177100434	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs564092002	chr5:177100478-177100479	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs112900015	chr5:177100527-177100528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs2650327	chr5:177100562-177100563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182236250	chr5:177100572-177100573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs111309508	chr5:177100574-177100575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs370855165	chr5:177100591-177100592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs550130308	chr5:177100644-177100645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561963817	chr5:177100649-177100650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530159434	chr5:177100656-177100657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs548564573	chr5:177100691-177100692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs186913074	chr5:177100696-177100697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs190669449	chr5:177100803-177100804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs182524470	chr5:177100902-177100903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs570982664	chr5:177100912-177100913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs373183575	chr5:177100933-177100934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538045721	chr5:177100986-177100987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs556479201	chr5:177100987-177100988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554431766	chr5:177102128-177102129	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs187683450	chr5:177102187-177102188	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs193236768	chr5:177102203-177102204	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs10045871	chr5:177102261-177102262	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs567118725	chr5:177102282-177102283	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Autism	20841430	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177076800-177098200	Weak transcription	Fetal Stomach	stomach
2	chr5:177077000-177098200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr5:177094200-177098200	Weak transcription	Ovary	ovary
4	chr5:177095600-177098200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr5:177096000-177098200	Enhancers	Primary B cells from peripheral blood	blood
6	chr5:177096600-177098200	Enhancers	Dnd41	blood
7	chr5:177096800-177098400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
8	chr5:177097000-177098200	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr5:177097000-177098200	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr5:177097000-177098200	Weak transcription	Adipose Nuclei	Adipose
11	chr5:177097000-177099000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr5:177097000-177099000	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr5:177097200-177098200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr5:177097200-177098200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr5:177097200-177098200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr5:177097200-177099000	Weak transcription	Thymus	Thymus
17	chr5:177097400-177098200	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr5:177097400-177098200	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr5:177097400-177098200	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr5:177097400-177098200	Weak transcription	Stomach Mucosa	stomach
21	chr5:177097400-177098200	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr5:177097400-177099600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
23	chr5:177097400-177100600	Weak transcription	Primary B cells from cord blood	blood
24	chr5:177097600-177099200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr5:177098000-177098200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr5:177098000-177098600	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr5:177098200-177098400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
28	chr5:177098200-177098400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr5:177098200-177098400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
30	chr5:177098200-177098400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr5:177098200-177098400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
32	chr5:177098200-177098400	Flanking Active TSS	Primary B cells from peripheral blood	blood
33	chr5:177098200-177098400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr5:177098200-177098400	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr5:177098200-177098400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr5:177098200-177098400	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr5:177098200-177098400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr5:177098200-177098400	Flanking Active TSS	Adipose Nuclei	Adipose
39	chr5:177098200-177098400	Enhancers	Colonic Mucosa	Colon
40	chr5:177098200-177098400	Enhancers	Fetal Brain Male	brain
41	chr5:177098200-177098400	Enhancers	Right Atrium	heart
42	chr5:177098200-177098400	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr5:177098200-177098400	Enhancers	Stomach Mucosa	stomach
44	chr5:177098200-177098400	Enhancers	A549	lung
45	chr5:177098200-177098400	Flanking Active TSS	Dnd41	blood
46	chr5:177098200-177098400	Enhancers	HUVEC	blood vessel
47	chr5:177098200-177098600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
48	chr5:177098200-177098600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
49	chr5:177098200-177098600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr5:177098200-177098600	Active TSS	Duodenum Smooth Muscle	Duodenum

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