Variant report

Variant	nsv1013911
Chromosome Location	chr1:84619164-84667950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:312)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:312 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:84625274-84625597	K562	blood:	n/a	n/a
2	ATF3	chr1:84639743-84640360	A549	lung:	n/a	n/a
3	ATF3	chr1:84621649-84622441	HCT-116	colon:	n/a	n/a
4	BATF	chr1:84632577-84632840	GM12878	blood:	n/a	chr1:84632738-84632749
5	BATF	chr1:84622058-84622350	GM12878	blood:	n/a	chr1:84622196-84622207
6	BHLHE40	chr1:84622132-84622332	A549	lung:	n/a	n/a
7	CBX3	chr1:84639583-84640587	HCT-116	colon:	n/a	n/a
8	CBX3	chr1:84639712-84640465	HCT-116	colon:	n/a	n/a
9	CBX3	chr1:84621201-84622949	HCT-116	colon:	n/a	chr1:84621269-84621280
10	CBX3	chr1:84621472-84622485	HCT-116	colon:	n/a	n/a
11	CEBPB	chr1:84619166-84619515	IMR90	lung:	n/a	chr1:84619337-84619348
12	CEBPB	chr1:84621648-84622549	HCT-116	colon:	n/a	n/a
13	CEBPB	chr1:84639922-84640406	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr1:84623013-84623236	IMR90	lung:	n/a	n/a
15	CEBPB	chr1:84641972-84642191	A549	lung:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
16	CEBPB	chr1:84641972-84642221	IMR90	lung:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
17	CEBPB	chr1:84639642-84640513	HCT-116	colon:	n/a	n/a
18	CEBPB	chr1:84619289-84619449	HepG2	liver:	n/a	chr1:84619337-84619348
19	CEBPB	chr1:84621953-84622346	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr1:84640217-84640541	A549	lung:	n/a	n/a
21	CEBPB	chr1:84639591-84640709	HCT-116	colon:	n/a	n/a
22	CEBPB	chr1:84646427-84646520	HepG2	liver:	n/a	n/a
23	CEBPB	chr1:84641970-84642235	HepG2	liver:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
24	CTCF	chr1:84629400-84629550	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr1:84651795-84651989	K562	blood:	n/a	n/a
26	CTCF	chr1:84651947-84652024	GM19238	blood:	n/a	n/a
27	CTCF	chr1:84651820-84651970	HCFaa	heart:	n/a	n/a
28	CTCF	chr1:84651920-84652070	GM12872	blood:	n/a	n/a
29	CTCF	chr1:84651820-84651970	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr1:84658864-84658893	Lung_OC	lung:	n/a	n/a
31	CTCF	chr1:84651961-84651988	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr1:84651952-84651975	ProgFib	skin:	n/a	n/a
33	CTCF	chr1:84652020-84652022	A549	lung:	n/a	n/a
34	CTCF	chr1:84651940-84652090	RPTEC	kidney:	n/a	n/a
35	CTCF	chr1:84651820-84651970	HMF	breast:	n/a	n/a
36	CTCF	chr1:84651920-84652070	MCF-7	breast:	n/a	n/a
37	CTCF	chr1:84651900-84652050	AG04449	skin:	n/a	n/a
38	CTCF	chr1:84651880-84652030	HL-60	blood:	n/a	n/a
39	CTCF	chr1:84651900-84652050	AG09319	gingival:	n/a	n/a
40	CTCF	chr1:84651860-84652010	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr1:84651941-84651966	MCF-7	breast:	n/a	n/a
42	CTCF	chr1:84651880-84652030	HEK293	kidney:	n/a	n/a
43	CTCF	chr1:84653585-84653620	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr1:84651840-84651990	HA-sp	spinal cord:	n/a	n/a
45	CTCF	chr1:84651946-84652019	A549	lung:	n/a	n/a
46	CTCF	chr1:84651880-84652030	GM12875	blood:	n/a	n/a
47	CTCF	chr1:84652160-84652310	GM12868	blood:	n/a	n/a
48	CTCF	chr1:84651840-84651990	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr1:84651895-84652005	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr1:84651942-84651996	MCF-7	breast:	n/a	n/a

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:84662036..84663948-chr1:84669561..84672181,4	K562	blood:
2	chr1:84633326..84635826-chr1:84640053..84642677,3	K562	blood:
3	chr1:84639020..84640539-chr1:84647151..84649519,2	MCF-7	breast:
4	chr1:84633326..84636042-chr1:84640053..84642677,3	K562	blood:
5	chr1:84619466..84621949-chr1:84622598..84626604,3	K562	blood:
6	chr1:84639501..84640001-chr11:32381239..32382124,2	MCF-7	breast:
7	chr1:84619466..84621949-chr1:84622598..84626604,3	K562	blood:
8	chr1:84642752..84644786-chr1:84646959..84648659,2	K562	blood:
9	chr1:84628795..84632177-chr1:84635427..84638265,3	K562	blood:
10	chr1:84540791..84543154-chr1:84633401..84635166,2	K562	blood:
11	chr1:84639020..84640539-chr1:84647151..84649519,2	MCF-7	breast:
12	chr1:84633326..84636042-chr1:84640053..84642677,3	K562	blood:
13	chr1:84633326..84635826-chr1:84640053..84642677,3	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SAMD13-1	chr1:84644860-84644903	NONHSAT004190
2	lnc-SAMD13-1	chr1:84640717-84640739	NONHSAT004191
3	lnc-SAMD13-1	chr1:84640716-84640739	NONHSAT004188
4	lnc-SAMD13-1	chr1:84639012-84639035	NONHSAT004188
5	lnc-SAMD13-1	chr1:84644861-84644903	NONHSAT004191
6	lnc-SAMD13-1	chr1:84630387-84630696	NONHSAT004188
7	lnc-SAMD13-1	chr1:84644860-84644921	NONHSAT004188
8	lnc-SAMD13-1	chr1:84630581-84630696	NONHSAT004191
9	lnc-SAMD13-1	chr1:84630580-84630696	NONHSAT004190
10	lnc-SAMD13-1	chr1:84639012-84639035	NONHSAT004190
11	lnc-SAMD13-1	chr1:84639013-84639035	NONHSAT004191
12	lnc-SAMD13-1	chr1:84640716-84640739	NONHSAT004190
13	lnc-SAMD13-1	chr1:84641482-84641490	NONHSAT004190

No data

Variant related genes	Relation type
PRKACB	TF binding region
ENSG00000142875	chromatin interactions
GCFC1	miRNA target sites
GCH1	miRNA target sites
GCNT2	miRNA target sites

Extended variants
information (count: 1556 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1556 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543294865	chr1:84619169-84619170	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs566040987	chr1:84619170-84619171	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563357597	chr1:84619189-84619190	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs146415209	chr1:84619216-84619217	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12746303	chr1:84619247-84619248	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs140820281	chr1:84619305-84619306	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs566952661	chr1:84619349-84619350	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs115709140	chr1:84619381-84619382	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs143862850	chr1:84619448-84619449	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs151327349	chr1:84619454-84619455	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs535891741	chr1:84619481-84619482	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552887594	chr1:84619491-84619492	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557005014	chr1:84619530-84619531	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs183406826	chr1:84619538-84619539	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374622000	chr1:84619539-84619540	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544696348	chr1:84619542-84619543	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs140545379	chr1:84619547-84619548	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2811999	chr1:84619590-84619591	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs575077092	chr1:84619671-84619672	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185782443	chr1:84619682-84619683	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs113599963	chr1:84619741-84619742	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529976276	chr1:84619749-84619750	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs539099201	chr1:84619755-84619756	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs138198042	chr1:84619796-84619797	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs115083203	chr1:84619830-84619831	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs72710861	chr1:84619838-84619839	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs551902948	chr1:84619968-84619969	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564870864	chr1:84620020-84620021	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190690521	chr1:84620072-84620073	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182499679	chr1:84620129-84620130	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs551107617	chr1:84620142-84620143	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186856221	chr1:84620240-84620241	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192916270	chr1:84620348-84620349	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs543514432	chr1:84620362-84620363	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs76672690	chr1:84620383-84620384	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs114681285	chr1:84620435-84620436	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs142402929	chr1:84620442-84620443	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs558217998	chr1:84620444-84620445	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs182456936	chr1:84620519-84620520	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs544101323	chr1:84620564-84620565	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146579694	chr1:84620577-84620578	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs574679768	chr1:84620582-84620583	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs568705369	chr1:84620591-84620592	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs76480077	chr1:84620606-84620607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs550902001	chr1:84620647-84620648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs138990739	chr1:84620716-84620717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559114510	chr1:84620826-84620827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529403822	chr1:84620830-84620831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs528485491	chr1:84620860-84620861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs545380730	chr1:84620896-84620897	Weak transcription Enhancers	n/a	n/a	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:1356 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84610200-84621800	Weak transcription	Aorta	Aorta
2	chr1:84610200-84621800	Weak transcription	Small Intestine	intestine
3	chr1:84610200-84622000	Weak transcription	HSMM	muscle
4	chr1:84610400-84633400	Weak transcription	Fetal Kidney	kidney
5	chr1:84611600-84629800	Weak transcription	Fetal Stomach	stomach
6	chr1:84612600-84621400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr1:84612600-84621400	Weak transcription	NHDF-Ad	bronchial
8	chr1:84612600-84621600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:84612600-84621800	Weak transcription	NH-A	brain
10	chr1:84612800-84621600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr1:84612800-84628800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr1:84613200-84623400	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr1:84614000-84621000	Weak transcription	HUVEC	blood vessel
14	chr1:84614000-84621200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:84614000-84633800	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr1:84614600-84625600	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr1:84614800-84620000	Weak transcription	Dnd41	blood
18	chr1:84614800-84629000	Weak transcription	Brain Hippocampus Middle	brain
19	chr1:84615400-84621600	Weak transcription	Duodenum Mucosa	Duodenum
20	chr1:84615800-84619400	Enhancers	Primary B cells from peripheral blood	blood
21	chr1:84615800-84623800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr1:84615800-84634800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr1:84616000-84623000	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr1:84616200-84622800	Enhancers	Primary T killer memory cells from peripheral blood	blood
25	chr1:84616200-84635200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr1:84616400-84619800	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr1:84616400-84623000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr1:84617000-84619800	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr1:84617600-84620000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
30	chr1:84617800-84619200	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr1:84617800-84621400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr1:84618000-84619200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr1:84618000-84619400	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr1:84618200-84619400	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr1:84618200-84623800	Weak transcription	Thymus	Thymus
36	chr1:84618400-84619200	Enhancers	GM12878-XiMat	blood
37	chr1:84618400-84621000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr1:84618400-84621600	Weak transcription	Psoas Muscle	Psoas
39	chr1:84618600-84623000	Enhancers	Primary T helper naive cells from peripheral blood	blood
40	chr1:84618800-84621600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr1:84618800-84622600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr1:84618800-84623000	Enhancers	Primary T cells from cord blood	blood
43	chr1:84618800-84623600	Weak transcription	Fetal Thymus	thymus
44	chr1:84618800-84630400	Weak transcription	Primary B cells from cord blood	blood
45	chr1:84619000-84619200	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr1:84619000-84621600	Weak transcription	Primary T cells fromperipheralblood	blood
47	chr1:84619000-84621600	Weak transcription	Primary hematopoietic stem cells	blood
48	chr1:84619000-84621600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr1:84619000-84621800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr1:84619000-84628800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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