Variant report

Variant	nsv1011105
Chromosome Location	chr1:84638386-84674276
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:161)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:161 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr1:84639743-84640360	A549	lung:	n/a	n/a
2	CBX3	chr1:84639712-84640465	HCT-116	colon:	n/a	n/a
3	CBX3	chr1:84639583-84640587	HCT-116	colon:	n/a	n/a
4	CEBPB	chr1:84641970-84642235	HepG2	liver:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
5	CEBPB	chr1:84641972-84642221	IMR90	lung:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
6	CEBPB	chr1:84641972-84642191	A549	lung:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
7	CEBPB	chr1:84639591-84640709	HCT-116	colon:	n/a	n/a
8	CEBPB	chr1:84646427-84646520	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:84639642-84640513	HCT-116	colon:	n/a	n/a
10	CEBPB	chr1:84640217-84640541	A549	lung:	n/a	n/a
11	CEBPB	chr1:84639922-84640406	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr1:84651820-84651970	HCFaa	heart:	n/a	n/a
13	CTCF	chr1:84651941-84651966	MCF-7	breast:	n/a	n/a
14	CTCF	chr1:84651800-84651950	AG09319	gingival:	n/a	n/a
15	CTCF	chr1:84651941-84652037	MCF-7	breast:	n/a	n/a
16	CTCF	chr1:84651920-84652070	MCF-7	breast:	n/a	n/a
17	CTCF	chr1:84651900-84652050	AG04449	skin:	n/a	n/a
18	CTCF	chr1:84651860-84652010	HBMEC	blood vessel:	n/a	n/a
19	CTCF	chr1:84651860-84652010	BJ	skin:	n/a	n/a
20	CTCF	chr1:84651840-84651990	HFF-Myc	foreskin:	n/a	n/a
21	CTCF	chr1:84651920-84652070	GM12872	blood:	n/a	n/a
22	CTCF	chr1:84651795-84651989	K562	blood:	n/a	n/a
23	CTCF	chr1:84651897-84651999	HUVEC	blood vessel:	n/a	n/a
24	CTCF	chr1:84651947-84652024	GM19238	blood:	n/a	n/a
25	CTCF	chr1:84651940-84652090	RPTEC	kidney:	n/a	n/a
26	CTCF	chr1:84651876-84652020	K562	blood:	n/a	n/a
27	CTCF	chr1:84651942-84651996	MCF-7	breast:	n/a	n/a
28	CTCF	chr1:84651923-84651989	MCF-7	breast:	n/a	n/a
29	CTCF	chr1:84651840-84651990	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr1:84651820-84651970	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr1:84651883-84652042	Gliobla	brain:	n/a	n/a
32	CTCF	chr1:84651880-84652030	GM12875	blood:	n/a	n/a
33	CTCF	chr1:84651926-84651993	NHEK	skin:	n/a	n/a
34	CTCF	chr1:84651860-84652010	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr1:84653585-84653620	Spleen_OC	spleen:	n/a	n/a
36	CTCF	chr1:84652020-84652022	A549	lung:	n/a	n/a
37	CTCF	chr1:84651740-84651890	RPTEC	kidney:	n/a	n/a
38	CTCF	chr1:84651840-84651990	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr1:84651933-84652005	GM10266	blood:	n/a	n/a
40	CTCF	chr1:84651820-84651970	HMF	breast:	n/a	n/a
41	CTCF	chr1:84651860-84652010	HVMF	connective:	n/a	n/a
42	CTCF	chr1:84651952-84651975	ProgFib	skin:	n/a	n/a
43	CTCF	chr1:84651946-84652019	A549	lung:	n/a	n/a
44	CTCF	chr1:84651880-84652030	HEK293	kidney:	n/a	n/a
45	CTCF	chr1:84651900-84652050	AG09319	gingival:	n/a	n/a
46	CTCF	chr1:84651895-84652005	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr1:84651820-84651970	GM06990	blood:	n/a	n/a
48	CTCF	chr1:84651880-84652030	HL-60	blood:	n/a	n/a
49	CTCF	chr1:84651840-84651990	AG10803	skin:	n/a	n/a
50	CTCF	chr1:84651961-84651988	H1-hESC	embryonic stem cell:	n/a	n/a

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:84662036..84663948-chr1:84669561..84672181,4	K562	blood:
2	chr1:84639020..84640539-chr1:84647151..84649519,2	MCF-7	breast:
3	chr1:84639020..84640539-chr1:84647151..84649519,2	MCF-7	breast:
4	chr1:84662036..84663948-chr1:84669561..84672181,4	K562	blood:
5	chr1:84633326..84636042-chr1:84640053..84642677,3	K562	blood:
6	chr1:84671668..84674166-chr1:84678982..84681039,2	MCF-7	breast:
7	chr1:84639501..84640001-chr11:32381239..32382124,2	MCF-7	breast:
8	chr1:84633326..84635826-chr1:84640053..84642677,3	K562	blood:
9	chr1:84642752..84644786-chr1:84646959..84648659,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SAMD13-1	chr1:84644860-84644903	NONHSAT004190
2	lnc-SAMD13-1	chr1:84639012-84639035	NONHSAT004190
3	lnc-SAMD13-1	chr1:84639013-84639035	NONHSAT004191
4	lnc-SAMD13-1	chr1:84640717-84640739	NONHSAT004191
5	lnc-SAMD13-1	chr1:84640716-84640739	NONHSAT004190
6	lnc-SAMD13-1	chr1:84641482-84641490	NONHSAT004190
7	lnc-SAMD13-1	chr1:84639012-84639035	NONHSAT004188
8	lnc-SAMD13-1	chr1:84644860-84644921	NONHSAT004188
9	lnc-SAMD13-1	chr1:84644861-84644903	NONHSAT004191
10	lnc-SAMD13-1	chr1:84640716-84640739	NONHSAT004188

No data

Variant related genes	Relation type
PRKACB	TF binding region
ENSG00000142875	chromatin interactions
GCH1	miRNA target sites
GCNT2	miRNA target sites

Extended variants
information (count: 1196 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1196 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547331363	chr1:84638402-84638403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs549166158	chr1:84638434-84638435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559548463	chr1:84638448-84638449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528691245	chr1:84638449-84638450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551658057	chr1:84638463-84638464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs533762908	chr1:84638464-84638465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs565590084	chr1:84638540-84638541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs34765744	chr1:84638583-84638584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531096457	chr1:84638588-84638589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs201881874	chr1:84638665-84638666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187222559	chr1:84638668-84638669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs566917351	chr1:84638678-84638679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs535980958	chr1:84638679-84638680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546681901	chr1:84638785-84638786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568834759	chr1:84638791-84638792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs566398758	chr1:84638828-84638829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs538849257	chr1:84638831-84638832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs114973228	chr1:84638864-84638865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537962541	chr1:84638883-84638884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs191978450	chr1:84638964-84638965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs116630098	chr1:84638976-84638977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs557923832	chr1:84639076-84639077	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183551740	chr1:84639081-84639082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577688798	chr1:84639104-84639105	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574093465	chr1:84639105-84639106	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562770936	chr1:84639120-84639121	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187429101	chr1:84639159-84639160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542996723	chr1:84639174-84639175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553457673	chr1:84639175-84639176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573225282	chr1:84639187-84639188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs375971869	chr1:84639200-84639201	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs565316715	chr1:84639223-84639224	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191613971	chr1:84639240-84639241	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs544491955	chr1:84639360-84639361	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs368830140	chr1:84639450-84639451	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs532551754	chr1:84639468-84639469	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs533816114	chr1:84639508-84639509	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs149453800	chr1:84639589-84639590	Enhancers Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs11163911	chr1:84639626-84639627	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs11163912	chr1:84639630-84639631	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs532091726	chr1:84639642-84639643	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs182631978	chr1:84639654-84639655	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs186632302	chr1:84639668-84639669	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs537998313	chr1:84639674-84639675	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs554906155	chr1:84639682-84639683	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs568337561	chr1:84639713-84639714	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs75865828	chr1:84639728-84639729	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs374239313	chr1:84639779-84639780	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs76974562	chr1:84639805-84639806	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs192790958	chr1:84639820-84639821	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1041 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84623000-84639200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:84624000-84651800	Weak transcription	Thymus	Thymus
3	chr1:84629200-84654000	Weak transcription	Spleen	Spleen
4	chr1:84629400-84644400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr1:84630600-84639800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr1:84630600-84640400	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr1:84630800-84648200	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr1:84632600-84647800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr1:84632800-84647400	Weak transcription	Dnd41	blood
10	chr1:84633000-84648400	Weak transcription	Primary B cells from peripheral blood	blood
11	chr1:84633000-84649600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr1:84634000-84647800	Weak transcription	Primary B cells from cord blood	blood
13	chr1:84634000-84648200	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr1:84634200-84639600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr1:84634600-84639600	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr1:84634800-84649400	Weak transcription	Primary hematopoietic stem cells	blood
17	chr1:84634800-84651400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr1:84634800-84651800	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr1:84635000-84639600	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr1:84635000-84656400	Weak transcription	Fetal Heart	heart
21	chr1:84635200-84639200	Weak transcription	Fetal Brain Male	brain
22	chr1:84635400-84639600	Enhancers	HUVEC	blood vessel
23	chr1:84636000-84639000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr1:84636000-84639800	Weak transcription	Osteobl	bone
25	chr1:84636200-84639600	Weak transcription	Brain Cingulate Gyrus	brain
26	chr1:84636200-84639600	Weak transcription	Brain Hippocampus Middle	brain
27	chr1:84636200-84639600	Weak transcription	Brain Substantia Nigra	brain
28	chr1:84636200-84639800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr1:84636400-84638600	Weak transcription	Primary T helper cells fromperipheralblood	blood
30	chr1:84636400-84639200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr1:84636400-84639200	Weak transcription	Brain Angular Gyrus	brain
32	chr1:84636400-84639600	Weak transcription	Fetal Intestine Small	intestine
33	chr1:84636400-84639800	Weak transcription	Small Intestine	intestine
34	chr1:84636400-84643000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr1:84636400-84652400	Weak transcription	Fetal Brain Female	brain
36	chr1:84636800-84640400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr1:84637000-84639200	Weak transcription	Brain Anterior Caudate	brain
38	chr1:84637400-84640400	Enhancers	Primary T cells from cord blood	blood
39	chr1:84637600-84639600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr1:84637600-84639600	Weak transcription	NHEK	skin
41	chr1:84637800-84638800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr1:84637800-84639400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr1:84638000-84638600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr1:84638000-84639200	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr1:84638000-84639600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr1:84638000-84640000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
47	chr1:84638200-84638800	Weak transcription	A549	lung
48	chr1:84638200-84648200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr1:84638600-84640200	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr1:84638600-84640400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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