Variant report

Variant	nsv5150
Chromosome Location	chr5:177180399-177225918
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	BHLHE40	chr5:177225275-177225490	HepG2	liver:	n/a	n/a
2	CBX3	chr5:177209565-177209833	K562	blood:	n/a	n/a
3	CBX3	chr5:177209512-177209875	K562	blood:	n/a	n/a
4	CEBPB	chr5:177198402-177198415	K562	blood:	n/a	n/a
5	CEBPB	chr5:177198235-177198496	IMR90	lung:	n/a	chr5:177198345-177198358
6	CEBPB	chr5:177198236-177198491	A549	lung:	n/a	chr5:177198345-177198358
7	CTCF	chr5:177224142-177224265	HepG2	liver:	n/a	chr5:177224201-177224219 chr5:177224227-177224235
8	CTCF	chr5:177225406-177225500	GM19239	blood:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
9	CTCF	chr5:177224113-177224272	GM19239	blood:	n/a	chr5:177224201-177224219 chr5:177224227-177224235
10	CTCF	chr5:177225388-177225550	GM19240	blood:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
11	CTCF	chr5:177224140-177224290	SAEC	small airway:	n/a	chr5:177224201-177224219 chr5:177224227-177224235
12	CTCF	chr5:177224286-177224332	Kidney_OC	kidney:	n/a	n/a
13	CTCF	chr5:177225300-177225450	GM12873	blood:	n/a	chr5:177225342-177225350
14	CTCF	chr5:177225378-177225486	HepG2	liver:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
15	CTCF	chr5:177225300-177225450	HepG2	liver:	n/a	chr5:177225342-177225350
16	CTCF	chr5:177224825-177224872	HepG2	liver:	n/a	n/a
17	CTCF	chr5:177225420-177225511	A549	lung:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
18	CTCF	chr5:177225387-177225519	MCF-7	breast:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
19	CTCF	chr5:177224334-177224345	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr5:177211703-177211835	Medullo	brain:	n/a	n/a
21	CTCF	chr5:177225412-177225515	Fibrobl	skin:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
22	CTCF	chr5:177224817-177224870	GM10266	blood:	n/a	n/a
23	CTCF	chr5:177225349-177225697	K562	blood:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
24	CTCF	chr5:177225431-177225623	K562	blood:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
25	CTCF	chr5:177224115-177224299	MCF-7	breast:	n/a	chr5:177224201-177224219 chr5:177224227-177224235
26	CTCF	chr5:177224126-177224271	K562	blood:	n/a	chr5:177224201-177224219 chr5:177224227-177224235
27	CTCF	chr5:177225280-177225430	NB4	blood:	n/a	chr5:177225342-177225350
28	CTCF	chr5:177225393-177225521	Hela-S3	cervix:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
29	CTCF	chr5:177197744-177197783	GM20000	blood:	n/a	n/a
30	CTCF	chr5:177208101-177208143	GM13976	blood:	n/a	n/a
31	CTCF	chr5:177224110-177224277	MCF-7	breast:	n/a	chr5:177224201-177224219 chr5:177224227-177224235
32	CTCF	chr5:177225300-177225450	K562	blood:	n/a	chr5:177225342-177225350
33	CTCF	chr5:177225389-177225540	MCF-7	breast:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
34	CTCF	chr5:177189950-177190021	GM10266	blood:	n/a	n/a
35	CTCF	chr5:177225441-177225502	GM10266	blood:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
36	CTCF	chr5:177225118-177225177	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr5:177225352-177225548	MCF-7	breast:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
38	CTCF	chr5:177224081-177224306	MCF-7	breast:	n/a	chr5:177224088-177224096 chr5:177224201-177224219 chr5:177224227-177224235
39	CTCF	chr5:177224136-177224310	H1-hESC	embryonic stem cell:	n/a	chr5:177224201-177224219 chr5:177224227-177224235
40	CTCF	chr5:177225385-177225556	GM19238	blood:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
41	CTCF	chr5:177211281-177211328	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr5:177225352-177225561	A549	lung:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
43	CTCF	chr5:177224109-177224271	MCF-7	breast:	n/a	chr5:177224201-177224219 chr5:177224227-177224235
44	CTCF	chr5:177223086-177223092	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr5:177225353-177225564	K562	blood:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
46	CTCF	chr5:177224162-177224265	Pancreas_OC	pancreas:	n/a	chr5:177224201-177224219 chr5:177224227-177224235
47	CTCF	chr5:177224174-177224224	GM10248	blood:	n/a	chr5:177224201-177224219
48	CTCF	chr5:177225368-177225554	HepG2	liver:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
49	CTCF	chr5:177224055-177224307	K562	blood:	n/a	chr5:177224088-177224096 chr5:177224201-177224219 chr5:177224227-177224235
50	CTCF	chr5:177225390-177225511	Medullo	brain:	n/a	chr5:177225459-177225472 chr5:177225456-177225474

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:177196865-177196915	ProgFib	skin:	n/a
2	chr5:177209947-177209997	SKMC	muscle:	n/a
3	chr5:177196865-177196915	ProgFib	skin:	n/a
4	chr5:177209947-177209997	SKMC	muscle:	n/a
5	chr5:177209285-177209335	CMK	blood:	n/a
6	chr5:177209285-177209335	Caco-2	colon:	n/a
7	chr5:177209285-177209335	GM19239	blood:	n/a
8	chr5:177212760-177212810	Jurkat	blood:	n/a
9	chr5:177209947-177209997	PrEC	prostate:	n/a
10	chr5:177210257-177210307	AG09309	skin:	n/a
11	chr5:177210257-177210307	U87	brain:	n/a
12	chr5:177196865-177196915	MCF-7	breast:	n/a
13	chr5:177225404-177225454	GM06990	blood:	n/a
14	chr5:177225404-177225454	NHDF-neo	bronchial:	n/a
15	chr5:177210257-177210307	NHDF-neo	bronchial:	n/a
16	chr5:177209285-177209335	Hela-S3	cervix:	n/a
17	chr5:177212760-177212810	ECC-1	luminal epithelium:	n/a
18	chr5:177210257-177210307	HEEpiC	esophagus:	n/a
19	chr5:177210257-177210307	AG04450	lung:	fetal
20	chr5:177196865-177196915	GM12891	blood:	n/a
21	chr5:177212760-177212810	NT2-D1	testis:	n/a
22	chr5:177210257-177210307	SK-N-SH	brain:	n/a
23	chr5:177210257-177210307	HRPEpiC	eye:	n/a
24	chr5:177210257-177210307	HNPCEpiC	eye:	n/a
25	chr5:177210257-177210307	HCM	heart:	n/a
26	chr5:177212760-177212810	HRCEpiC	kidney:	n/a
27	chr5:177210257-177210307	GM12878	blood:	n/a
28	chr5:177212760-177212810	Hela-S3	cervix:	n/a
29	chr5:177209285-177209335	ovcar-3	ovarian:	n/a
30	chr5:177212760-177212810	HEEpiC	esophagus:	n/a
31	chr5:177225404-177225454	HUVEC	blood vessel:	n/a
32	chr5:177209947-177209997	SK-N-MC	brain:	n/a
33	chr5:177210257-177210307	GM12891	blood:	n/a
34	chr5:177209285-177209335	HPAEpiC	pulmonary alveolar:	n/a
35	chr5:177209947-177209997	HMEC	breast:	n/a
36	chr5:177225404-177225454	HNPCEpiC	eye:	n/a
37	chr5:177209285-177209335	HIPEpiC	eye:	n/a
38	chr5:177225404-177225454	HRCEpiC	kidney:	n/a
39	chr5:177196865-177196915	AG09319	gingival:	n/a
40	chr5:177209947-177209997	HCT-116	colon:	n/a
41	chr5:177212760-177212810	NH-A	brain:	n/a
42	chr5:177225404-177225454	MCF-7	breast:	n/a
43	chr5:177212760-177212810	HAEpiC	amniotic membrane:	n/a
44	chr5:177209285-177209335	RPTEC	kidney:	n/a
45	chr5:177210257-177210307	MCF-7	breast:	n/a
46	chr5:177209947-177209997	CMK	blood:	n/a
47	chr5:177209285-177209335	AG04449	skin:	fetal
48	chr5:177209947-177209997	ProgFib	skin:	n/a
49	chr5:177209285-177209335	HCT-116	colon:	n/a
50	chr5:177225404-177225454	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:177034180..177035059-chr5:177223760..177224507,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM193B-7	chr5:177206557-177206718	NONHSAT105468
2	lnc-FAM193B-7	chr5:177189930-177190511	NONHSAT105465
3	lnc-FAM193B-7	chr5:177207450-177207505	NONHSAT105468
4	lnc-FAM193B-7	chr5:177210285-177210365	NONHSAT105465
5	lnc-FAM193B-7	chr5:177207450-177207505	NONHSAT105465
6	lnc-FAM193B-7	chr5:177206498-177206718	NONHSAT105467
7	lnc-FAM193B-7	chr5:177207450-177207505	NONHSAT105467
8	lnc-FAM193B-7	chr5:177208586-177208685	NONHSAT105467
9	lnc-FAM193B-7	chr5:177209744-177209814	NONHSAT105468

Variant related genes	Relation type
FAM153A	TF binding region
ENSG00000249109	TF binding region
FAM153A	CpG island
ENSG00000249109	CpG island
ENSG00000027847	chromatin interactions

Extended variants
information (count: 302 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7735142	chr5:177180958-177180959	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530399397	chr5:177180979-177180980	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs542239509	chr5:177181002-177181003	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs561076286	chr5:177181004-177181005	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs191851096	chr5:177181008-177181009	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs11249686	chr5:177181014-177181015	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
7	rs112597806	chr5:177181045-177181046	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs111370678	chr5:177181072-177181073	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs550864279	chr5:177181147-177181148	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs569149776	chr5:177181148-177181149	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs537486284	chr5:177181187-177181188	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs549098149	chr5:177181200-177181201	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs567795411	chr5:177181205-177181206	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs189483022	chr5:177181206-177181207	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs201568423	chr5:177181215-177181216	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs62398556	chr5:177181217-177181218	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs62398557	chr5:177181228-177181229	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs181921281	chr5:177181231-177181232	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs187659795	chr5:177181232-177181233	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs62398558	chr5:177181235-177181236	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs557261020	chr5:177181279-177181280	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs575518501	chr5:177181317-177181318	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs58736697	chr5:177181364-177181365	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
24	rs560672714	chr5:177181365-177181366	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs531949511	chr5:177188031-177188032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs146300120	chr5:177188040-177188041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs562218699	chr5:177188045-177188046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs528901598	chr5:177188069-177188070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs150050666	chr5:177188090-177188091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs546949942	chr5:177188098-177188099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs62399963	chr5:177188132-177188133	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
32	rs62399964	chr5:177188139-177188140	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
33	rs368337628	chr5:177188217-177188218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs569500107	chr5:177188279-177188280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs536973681	chr5:177188343-177188344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs555654955	chr5:177188349-177188350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs567413251	chr5:177188383-177188384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs535849933	chr5:177188388-177188389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs112266701	chr5:177190273-177190274	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs62399966	chr5:177190808-177190809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530748488	chr5:177190883-177190884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201001417	chr5:177190916-177190917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs548863495	chr5:177190922-177190923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567552972	chr5:177190925-177190926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs373831525	chr5:177190937-177190938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs201720066	chr5:177190950-177190951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs62399967	chr5:177190972-177190973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs554246436	chr5:177191178-177191179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs62399968	chr5:177191190-177191191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs566060814	chr5:177191274-177191275	Enhancers	n/a	n/a	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
Non-syndromic sensorineural hearing loss	19212409	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177188000-177188400	Enhancers	K562	blood
2	chr5:177190800-177191800	Enhancers	Fetal Muscle Leg	muscle
3	chr5:177209000-177209800	Active TSS	Primary T helper cells PMA-I stimulated	--
4	chr5:177209400-177209600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr5:177209400-177209600	Enhancers	Pancreas	Pancrea
6	chr5:177209400-177209800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
7	chr5:177209400-177209800	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
8	chr5:177209400-177210200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr5:177209400-177210400	Active TSS	Primary T helper naive cells fromperipheralblood	blood
10	chr5:177209400-177210400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
11	chr5:177209400-177210600	Active TSS	Ovary	ovary
12	chr5:177209600-177209800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr5:177209600-177209800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr5:177209600-177210400	Active TSS	Primary T cells fromperipheralblood	blood
15	chr5:177209800-177210400	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr5:177210000-177210400	Active TSS	Brain Angular Gyrus	brain
17	chr5:177210000-177210600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr5:177218400-177218600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr5:177218600-177220800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr5:177220800-177222400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
21	chr5:177221400-177221800	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr5:177221400-177221800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr5:177221400-177221800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr5:177221400-177221800	Enhancers	Primary T killer memory cells from peripheral blood	blood
25	chr5:177221400-177222600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
26	chr5:177221400-177222600	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr5:177221400-177222800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
28	chr5:177221600-177222000	Enhancers	Primary T cells fromperipheralblood	blood
29	chr5:177221800-177235600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr5:177222000-177222400	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr5:177222400-177222600	Enhancers	Primary T cells fromperipheralblood	blood
32	chr5:177222400-177230400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr5:177222600-177226400	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr5:177222600-177227400	Weak transcription	Primary T cells fromperipheralblood	blood
35	chr5:177222800-177225400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links