Variant report

Variant	nsv599934
Chromosome Location	chr5:145068001-145143775
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:578)
CpG islands
(count:122)
Chromatin interactive
region (count:23)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:578 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:145119991-145120065	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:145119613-145119652	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:145076901-145077309	K562	blood:	n/a	n/a
4	ARID3A	chr5:145121930-145122466	HepG2	liver:	n/a	n/a
5	ATF1	chr5:145076819-145077122	K562	blood:	n/a	n/a
6	ATF1	chr5:145115137-145115271	K562	blood:	n/a	n/a
7	BHLHE40	chr5:145076930-145077159	K562	blood:	n/a	n/a
8	CBX3	chr5:145109249-145109584	K562	blood:	n/a	n/a
9	CBX3	chr5:145076871-145077217	K562	blood:	n/a	n/a
10	CBX3	chr5:145106362-145106709	K562	blood:	n/a	n/a
11	CBX3	chr5:145076816-145077250	K562	blood:	n/a	n/a
12	CEBPB	chr5:145070438-145070735	HepG2	liver:	n/a	chr5:145070573-145070584
13	CEBPB	chr5:145129955-145130119	A549	lung:	n/a	chr5:145130011-145130022
14	CEBPB	chr5:145070462-145070752	A549	lung:	n/a	chr5:145070573-145070584
15	CEBPB	chr5:145134159-145134371	IMR90	lung:	n/a	n/a
16	CEBPB	chr5:145129927-145130151	HepG2	liver:	n/a	chr5:145130011-145130022 chr5:145130116-145130127 chr5:145130111-145130128 chr5:145130116-145130127
17	CEBPB	chr5:145129983-145130149	Hela-S3	cervix:	n/a	chr5:145130011-145130022 chr5:145130116-145130127 chr5:145130111-145130128 chr5:145130116-145130127
18	CEBPB	chr5:145076868-145077148	K562	blood:	n/a	n/a
19	CHD2	chr5:145069214-145069246	HepG2	liver:	n/a	n/a
20	CTCF	chr5:145076860-145077010	HFF-Myc	foreskin:	n/a	n/a
21	CTCF	chr5:145098640-145098790	AG04449	skin:	n/a	n/a
22	CTCF	chr5:145098660-145098810	HCM	heart:	n/a	n/a
23	CTCF	chr5:145076811-145077097	K562	blood:	n/a	n/a
24	CTCF	chr5:145076880-145077030	WI-38	lung:	n/a	n/a
25	CTCF	chr5:145098640-145098790	HepG2	liver:	n/a	n/a
26	CTCF	chr5:145098526-145098798	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr5:145098654-145098798	A549	lung:	n/a	n/a
28	CTCF	chr5:145081100-145081250	HCPEpiC	choroid plexus:	n/a	chr5:145081150-145081166 chr5:145081149-145081167 chr5:145081151-145081172
29	CTCF	chr5:145098720-145098870	AG04450	lung:	n/a	n/a
30	CTCF	chr5:145076940-145077090	SAEC	small airway:	n/a	n/a
31	CTCF	chr5:145076869-145077130	Medullo	brain:	n/a	n/a
32	CTCF	chr5:145076815-145077193	IMR90	lung:	n/a	n/a
33	CTCF	chr5:145081020-145081170	HUVEC	blood vessel:	n/a	chr5:145081150-145081166 chr5:145081149-145081167
34	CTCF	chr5:145076859-145077135	HepG2	liver:	n/a	n/a
35	CTCF	chr5:145098720-145098870	A549	lung:	n/a	n/a
36	CTCF	chr5:145098660-145098810	HEK293	kidney:	n/a	n/a
37	CTCF	chr5:145076857-145077158	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr5:145076940-145077090	GM12864	blood:	n/a	n/a
39	CTCF	chr5:145076900-145077050	SAEC	small airway:	n/a	n/a
40	CTCF	chr5:145076920-145077070	GM12875	blood:	n/a	n/a
41	CTCF	chr5:145076900-145077050	HA-sp	spinal cord:	n/a	n/a
42	CTCF	chr5:145076940-145077090	AG04449	skin:	n/a	n/a
43	CTCF	chr5:145076876-145077095	GM19238	blood:	n/a	n/a
44	CTCF	chr5:145098716-145098746	GM10266	blood:	n/a	n/a
45	CTCF	chr5:145076763-145077290	HCT-116	colon:	n/a	n/a
46	CTCF	chr5:145068890-145069002	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr5:145076880-145077099	A549	lung:	n/a	n/a
48	CTCF	chr5:145098640-145098790	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr5:145076880-145077030	HAc	cerebellar:	n/a	n/a
50	CTCF	chr5:145098620-145098770	Caco-2	colon:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:145143495-145143545	AG04450	lung:	fetal
2	chr5:145132641-145132691	Hepatocyte	liver:	n/a
3	chr5:145132641-145132691	HRE	kidney:	n/a
4	chr5:145143495-145143545	HCM	heart:	n/a
5	chr5:145132641-145132691	LNCaP	prostate:	n/a
6	chr5:145132641-145132691	HAEpiC	amniotic membrane:	n/a
7	chr5:145132641-145132691	SK-N-SH_RA	brain:	n/a
8	chr5:145132641-145132691	H1-hESC	embryonic stem cell:	embryo
9	chr5:145132641-145132691	HL-60	blood:	n/a
10	chr5:145143495-145143545	HRE	kidney:	n/a
11	chr5:145132641-145132691	NB4	blood:	n/a
12	chr5:145132641-145132691	SK-N-MC	brain:	n/a
13	chr5:145132641-145132691	PrEC	prostate:	n/a
14	chr5:145143495-145143545	MCF-7	breast:	n/a
15	chr5:145132641-145132691	AG09319	gingival:	n/a
16	chr5:145132641-145132691	PANC-1	pancreas:	n/a
17	chr5:145143495-145143545	HRPEpiC	eye:	n/a
18	chr5:145143495-145143545	GM06990	blood:	n/a
19	chr5:145143495-145143545	NT2-D1	testis:	n/a
20	chr5:145132641-145132691	MCF-7	breast:	n/a
21	chr5:145143495-145143545	HUVEC	blood vessel:	n/a
22	chr5:145132641-145132691	A549	lung:	n/a
23	chr5:145143495-145143545	HCPEpiC	choroid plexus:	n/a
24	chr5:145132641-145132691	HPAEpiC	pulmonary alveolar:	n/a
25	chr5:145132641-145132691	K562	blood:	n/a
26	chr5:145132641-145132691	ovcar-3	ovarian:	n/a
27	chr5:145143495-145143545	NB4	blood:	n/a
28	chr5:145132641-145132691	AG10803	skin:	n/a
29	chr5:145143495-145143545	HPAEpiC	pulmonary alveolar:	n/a
30	chr5:145143495-145143545	Hela-S3	cervix:	n/a
31	chr5:145132641-145132691	GM12892	blood:	n/a
32	chr5:145132641-145132691	HCT-116	colon:	n/a
33	chr5:145132641-145132691	ECC-1	luminal epithelium:	n/a
34	chr5:145143495-145143545	ProgFib	skin:	n/a
35	chr5:145143495-145143545	AG09309	skin:	n/a
36	chr5:145132641-145132691	GM12891	blood:	n/a
37	chr5:145143495-145143545	H1-hESC	embryonic stem cell:	embryo
38	chr5:145143495-145143545	BE2_C	brain:	n/a
39	chr5:145143495-145143545	HAEpiC	amniotic membrane:	n/a
40	chr5:145143495-145143545	HL-60	blood:	n/a
41	chr5:145132641-145132691	HUVEC	blood vessel:	n/a
42	chr5:145143495-145143545	GM12891	blood:	n/a
43	chr5:145143495-145143545	MCF10A-Er-Src	breast:	n/a
44	chr5:145143495-145143545	SK-N-SH	brain:	n/a
45	chr5:145143495-145143545	T-47D	breast:	n/a
46	chr5:145132641-145132691	GM06990	blood:	n/a
47	chr5:145143495-145143545	PFSK-1	brain:	n/a
48	chr5:145143495-145143545	AG04449	skin:	fetal
49	chr5:145143495-145143545	AG09319	gingival:	n/a
50	chr5:145143495-145143545	ECC-1	luminal epithelium:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:145093601..145096391-chr5:145098604..145102525,3	MCF-7	breast:
2	chr5:145060908..145061744-chr5:145098314..145099122,3	MCF-7	breast:
3	chr5:145093601..145096391-chr5:145098604..145102525,3	MCF-7	breast:
4	chr5:145080788..145081576-chr5:145098526..145099103,2	MCF-7	breast:
5	chr5:145081132..145081713-chr5:145205200..145205925,2	MCF-7	breast:
6	chr5:145075981..145078499-chr5:145212662..145215642,2	MCF-7	breast:
7	chr5:145084415..145086296-chr5:145089093..145090802,2	K562	blood:
8	chr5:145087405..145089668-chr5:145092865..145095003,2	K562	blood:
9	chr5:145141507..145143160-chr5:145145225..145147733,2	K562	blood:
10	chr5:145134194..145136208-chr5:145188501..145190902,2	K562	blood:
11	chr5:145076888..145077592-chr5:145191540..145192583,3	MCF-7	breast:
12	chr5:145075276..145075947-chr5:145428743..145429454,2	K562	blood:
13	chr5:145088168..145091039-chr5:145092677..145095003,2	K562	blood:
14	chr5:145076480..145077302-chr5:145266518..145267420,2	K562	blood:
15	chr5:145084415..145086296-chr5:145089093..145090802,2	K562	blood:
16	chr5:145087405..145089668-chr5:145092865..145095003,2	K562	blood:
17	chr5:145130899..145133455-chr5:145134892..145136854,2	K562	blood:
18	chr5:145076760..145077364-chr5:145300197..145301114,2	K562	blood:
19	chr5:145080788..145081576-chr5:145098526..145099103,2	MCF-7	breast:
20	chr5:145088168..145091039-chr5:145092677..145095003,2	K562	blood:
21	chr5:145081237..145084236-chr5:145205534..145207080,2	K562	blood:
22	chr5:145130899..145133455-chr5:145134892..145136854,2	K562	blood:
23	chr5:145050661..145052911-chr5:145067099..145069500,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRELID2-1	chr5:145133728-145133942	NONHSAT104385
2	lnc-GRXCR2-1	chr5:145116948-145117205	expReg_chr5_8822_-
3	lnc-PRELID2-1	chr5:145083655-145083858	NONHSAT104385
4	lnc-SH3RF2-6	chr5:145071374-145071683	NONHSAT104383

No data

Variant related genes	Relation type
ENSG00000249363	TF binding region
PRELID2	TF binding region
ENSG00000249363	CpG island
PRELID2	CpG island
ENSG00000186314	chromatin interactions

Extended variants
information (count: 2940 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2940 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17103619	chr5:145068001-145068002	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs577994151	chr5:145068005-145068006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs17103621	chr5:145068011-145068012	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs370949971	chr5:145068029-145068030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190962267	chr5:145068235-145068236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs375376426	chr5:145068245-145068246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs546073617	chr5:145068258-145068259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs559323831	chr5:145068274-145068275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs183907666	chr5:145068277-145068278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs17103624	chr5:145068303-145068304	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs561384847	chr5:145068304-145068305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187610316	chr5:145068324-145068325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190880549	chr5:145068325-145068326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs1368434	chr5:145068327-145068328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs532736502	chr5:145068332-145068333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375753220	chr5:145068348-145068349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374643549	chr5:145068359-145068360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs183201652	chr5:145068404-145068405	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs542847587	chr5:145068427-145068428	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs187016554	chr5:145068436-145068437	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs76315578	chr5:145068533-145068534	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs368689527	chr5:145068536-145068537	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs562530631	chr5:145068558-145068559	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs567823428	chr5:145068569-145068570	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs149434873	chr5:145068597-145068598	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs556726952	chr5:145068680-145068681	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs62392301	chr5:145068702-145068703	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs369688962	chr5:145068732-145068733	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs539384698	chr5:145068739-145068740	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs373277727	chr5:145068769-145068770	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs553281759	chr5:145068770-145068771	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs6580382	chr5:145068838-145068839	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs542056359	chr5:145068860-145068861	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs73302055	chr5:145068869-145068870	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs147497524	chr5:145068920-145068921	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs62392302	chr5:145068942-145068943	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs563568301	chr5:145068991-145068992	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs532517396	chr5:145069066-145069067	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs552263338	chr5:145069075-145069076	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs566825518	chr5:145069085-145069086	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs13186831	chr5:145069126-145069127	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs76258781	chr5:145069143-145069144	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs528717306	chr5:145069145-145069146	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs140092721	chr5:145069215-145069216	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs568310360	chr5:145069219-145069220	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs536785866	chr5:145069270-145069271	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs550633771	chr5:145069273-145069274	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs571152145	chr5:145069274-145069275	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs76102876	chr5:145069297-145069298	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs549183379	chr5:145069365-145069366	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Intellectual disability	22102821	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	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
Breast cancer	21858162	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
Lung cancer	18438408	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	16864856	CNVD
small cell lung cancer	20016488	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
Acute lymphoblastic leukemia	21339820	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	20864512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:297 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:145060800-145074600	Weak transcription	Aorta	Aorta
2	chr5:145060800-145089600	Weak transcription	Gastric	stomach
3	chr5:145061400-145076800	Weak transcription	Pancreas	Pancrea
4	chr5:145062000-145069200	Weak transcription	HepG2	liver
5	chr5:145062400-145071800	Weak transcription	Rectal Smooth Muscle	rectum
6	chr5:145066600-145084200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr5:145067600-145070600	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr5:145067800-145068400	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr5:145068000-145070400	Enhancers	Brain Substantia Nigra	brain
10	chr5:145068200-145069400	Enhancers	Brain Angular Gyrus	brain
11	chr5:145068400-145069000	Enhancers	Brain Hippocampus Middle	brain
12	chr5:145068400-145069400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr5:145068400-145070000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
14	chr5:145068400-145070200	Enhancers	Brain Cingulate Gyrus	brain
15	chr5:145068600-145068800	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr5:145068600-145069200	Enhancers	GM12878-XiMat	blood
17	chr5:145068600-145069400	Enhancers	Primary B cells from peripheral blood	blood
18	chr5:145068600-145106200	Weak transcription	Duodenum Mucosa	Duodenum
19	chr5:145068800-145069000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
20	chr5:145068800-145069400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr5:145069000-145069200	Active TSS	Brain Inferior Temporal Lobe	brain
22	chr5:145069000-145069400	Flanking Active TSS	Brain Hippocampus Middle	brain
23	chr5:145069000-145069400	Enhancers	Colon Smooth Muscle	Colon
24	chr5:145069200-145069400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
25	chr5:145069200-145069800	Enhancers	HepG2	liver
26	chr5:145069400-145070600	Enhancers	Brain Hippocampus Middle	brain
27	chr5:145069400-145076800	Weak transcription	Brain Angular Gyrus	brain
28	chr5:145070000-145070800	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr5:145074600-145075400	Strong transcription	Aorta	Aorta
30	chr5:145075400-145090200	Weak transcription	Aorta	Aorta
31	chr5:145076600-145088200	Weak transcription	Right Ventricle	heart
32	chr5:145076800-145077000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr5:145076800-145077000	Enhancers	Adipose Nuclei	Adipose
34	chr5:145076800-145077000	Enhancers	Pancreas	Pancrea
35	chr5:145076800-145077400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr5:145076800-145077400	Enhancers	Hela-S3	cervix
37	chr5:145077000-145077400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr5:145077000-145077400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr5:145077000-145077400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr5:145077000-145077400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr5:145077000-145077400	Flanking Active TSS	Adipose Nuclei	Adipose
42	chr5:145077000-145077400	Enhancers	A549	lung
43	chr5:145077000-145077400	Enhancers	HSMM	muscle
44	chr5:145077000-145077400	Active TSS	K562	blood
45	chr5:145077000-145077400	Enhancers	Osteobl	bone
46	chr5:145077000-145091000	Weak transcription	Pancreas	Pancrea
47	chr5:145077200-145077400	Enhancers	Muscle Satellite Cultured Cells	--
48	chr5:145077400-145079400	Weak transcription	Adipose Nuclei	Adipose
49	chr5:145079000-145079800	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr5:145079400-145079800	Enhancers	Adipose Nuclei	Adipose

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