Variant report

Variant	nsv462213
Chromosome Location	chr5:76067624-76112869
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1567)
CpG islands
(count:366)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1567 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:76086428-76087095	K562	blood:	n/a	n/a
2	ARID3A	chr5:76070411-76070732	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:76081436-76081712	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:76083060-76083212	K562	blood:	n/a	n/a
5	ARID3A	chr5:76086368-76087004	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:76101782-76102245	K562	blood:	n/a	n/a
7	ATF1	chr5:76086458-76087131	K562	blood:	n/a	n/a
8	ATF1	chr5:76101722-76102174	K562	blood:	n/a	n/a
9	ATF2	chr5:76086364-76086842	GM12878	blood:	n/a	n/a
10	ATF2	chr5:76070318-76070761	GM12878	blood:	n/a	n/a
11	ATF2	chr5:76103843-76104561	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr5:76103823-76104436	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr5:76099975-76100655	A549	lung:	n/a	n/a
14	ATF3	chr5:76081264-76081700	A549	lung:	n/a	n/a
15	ATF3	chr5:76101689-76102467	A549	lung:	n/a	n/a
16	ATF3	chr5:76101627-76102562	A549	lung:	n/a	n/a
17	ATF3	chr5:76086333-76087061	A549	lung:	n/a	n/a
18	ATF3	chr5:76100044-76100672	A549	lung:	n/a	n/a
19	ATF3	chr5:76067852-76068234	A549	lung:	n/a	n/a
20	ATF3	chr5:76081235-76081754	A549	lung:	n/a	n/a
21	ATF3	chr5:76086335-76086970	A549	lung:	n/a	n/a
22	ATF3	chr5:76086822-76087094	K562	blood:	n/a	n/a
23	BACH1	chr5:76103704-76103712	K562	blood:	n/a	n/a
24	BACH1	chr5:76070379-76070679	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr5:76086433-76086741	GM12878	blood:	n/a	chr5:76086559-76086569
26	BATF	chr5:76086446-76086954	GM12878	blood:	n/a	chr5:76086559-76086569
27	BATF	chr5:76102000-76102358	GM12878	blood:	n/a	n/a
28	BCL11A	chr5:76086438-76086837	GM12878	blood:	n/a	n/a
29	BCL11A	chr5:76086459-76086753	GM12878	blood:	n/a	n/a
30	BCL3	chr5:76109782-76110506	A549	lung:	n/a	chr5:76110348-76110357
31	BCL3	chr5:76101545-76102516	A549	lung:	n/a	chr5:76102262-76102271
32	BCL3	chr5:76086213-76087155	A549	lung:	n/a	n/a
33	BCL3	chr5:76101997-76102356	GM12878	blood:	n/a	chr5:76102262-76102271
34	BCL3	chr5:76099974-76100817	A549	lung:	n/a	chr5:76100092-76100100 chr5:76100201-76100210
35	BCL3	chr5:76097061-76097862	A549	lung:	n/a	n/a
36	BCL3	chr5:76086154-76087174	A549	lung:	n/a	n/a
37	BCL3	chr5:76101399-76102582	A549	lung:	n/a	chr5:76102262-76102271
38	BCL3	chr5:76099724-76100840	A549	lung:	n/a	chr5:76100092-76100100 chr5:76100201-76100210
39	BCL3	chr5:76081199-76081823	A549	lung:	n/a	n/a
40	BCL3	chr5:76101972-76102349	GM12878	blood:	n/a	chr5:76102262-76102271
41	BCL3	chr5:76067487-76068377	A549	lung:	n/a	n/a
42	BCL3	chr5:76081377-76081777	A549	lung:	n/a	n/a
43	BCL3	chr5:76109914-76110498	A549	lung:	n/a	chr5:76110348-76110357
44	BCLAF1	chr5:76070255-76070755	GM12878	blood:	n/a	n/a
45	BHLHE40	chr5:76083231-76083423	K562	blood:	n/a	n/a
46	BHLHE40	chr5:76101694-76102239	K562	blood:	n/a	n/a
47	BHLHE40	chr5:76070330-76070841	K562	blood:	n/a	n/a
48	BHLHE40	chr5:76078612-76078808	K562	blood:	n/a	n/a
49	BHLHE40	chr5:76070263-76070754	GM12878	blood:	n/a	n/a
50	BHLHE40	chr5:76090863-76090978	K562	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:76108729-76108779	ProgFib	skin:	n/a
2	chr5:76108191-76108241	IMR90	lung:	fetal
3	chr5:76112776-76112826	MCF10A-Er-Src	breast:	n/a
4	chr5:76108191-76108241	Jurkat	blood:	n/a
5	chr5:76111995-76112045	H1-hESC	embryonic stem cell:	embryo
6	chr5:76111995-76112045	BE2_C	brain:	n/a
7	chr5:76108191-76108241	HMEC	breast:	n/a
8	chr5:76108729-76108779	NHBE	bronchial:	n/a
9	chr5:76112776-76112826	SK-N-SH	brain:	n/a
10	chr5:76112776-76112826	SKMC	muscle:	n/a
11	chr5:76068752-76068802	A549	lung:	n/a
12	chr5:76111995-76112045	HRCEpiC	kidney:	n/a
13	chr5:76087172-76087222	U87	brain:	n/a
14	chr5:76111995-76112045	ProgFib	skin:	n/a
15	chr5:76068752-76068802	ECC-1	luminal epithelium:	n/a
16	chr5:76111995-76112045	NHBE	bronchial:	n/a
17	chr5:76108191-76108241	GM19239	blood:	n/a
18	chr5:76108729-76108779	U87	brain:	n/a
19	chr5:76108191-76108241	HUVEC	blood vessel:	n/a
20	chr5:76087172-76087222	GM06990	blood:	n/a
21	chr5:76111995-76112045	HL-60	blood:	n/a
22	chr5:76112776-76112826	Hela-S3	cervix:	n/a
23	chr5:76108191-76108241	GM12878	blood:	n/a
24	chr5:76108729-76108779	Caco-2	colon:	n/a
25	chr5:76111995-76112045	PFSK-1	brain:	n/a
26	chr5:76087172-76087222	ovcar-3	ovarian:	n/a
27	chr5:76108191-76108241	NHDF-neo	bronchial:	n/a
28	chr5:76087172-76087222	AG09319	gingival:	n/a
29	chr5:76068752-76068802	SK-N-SH_RA	brain:	n/a
30	chr5:76112776-76112826	BE2_C	brain:	n/a
31	chr5:76111995-76112045	Hepatocyte	liver:	n/a
32	chr5:76108729-76108779	GM12891	blood:	n/a
33	chr5:76108729-76108779	GM12892	blood:	n/a
34	chr5:76112776-76112826	HCT-116	colon:	n/a
35	chr5:76108729-76108779	PANC-1	pancreas:	n/a
36	chr5:76112776-76112826	ovcar-3	ovarian:	n/a
37	chr5:76068752-76068802	NH-A	brain:	n/a
38	chr5:76111995-76112045	U87	brain:	n/a
39	chr5:76111995-76112045	PrEC	prostate:	n/a
40	chr5:76068752-76068802	PFSK-1	brain:	n/a
41	chr5:76087172-76087222	IMR90	lung:	fetal
42	chr5:76108729-76108779	HNPCEpiC	eye:	n/a
43	chr5:76111995-76112045	HRE	kidney:	n/a
44	chr5:76068752-76068802	HRPEpiC	eye:	n/a
45	chr5:76108191-76108241	AG04450	lung:	fetal
46	chr5:76068752-76068802	Hepatocyte	liver:	n/a
47	chr5:76112776-76112826	HepG2	liver:	n/a
48	chr5:76112776-76112826	SK-N-MC	brain:	n/a
49	chr5:76108191-76108241	T-47D	breast:	n/a
50	chr5:76108729-76108779	AG04450	lung:	fetal

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:76094721..76097053-chr5:76101788..76104241,2	K562	blood:
2	chr5:76069360..76073048-chr5:76075455..76078776,4	K562	blood:
3	chr5:75896999..75898252-chr5:76070091..76071474,10	K562	blood:
4	chr5:76011366..76011912-chr5:76070358..76071019,2	MCF-7	breast:
5	chr5:76094082..76095930-chr5:76098926..76101541,2	K562	blood:
6	chr5:75898209..75899288-chr5:76070136..76071088,4	MCF-7	breast:
7	chr5:76094082..76095930-chr5:76098926..76101541,2	K562	blood:
8	chr5:76106690..76108652-chr5:76112389..76115245,2	K562	blood:
9	chr5:76110973..76114089-chr5:76116480..76119427,3	K562	blood:
10	chr5:76011519..76012401-chr5:76070136..76070995,3	K562	blood:
11	chr5:76083391..76086055-chr5:76095285..76096948,2	MCF-7	breast:
12	chr5:76101619..76103504-chr5:76111998..76114759,2	K562	blood:
13	chr5:76083391..76086055-chr5:76095285..76096948,2	MCF-7	breast:
14	chr5:75897438..75897959-chr5:76070126..76070803,2	MCF-7	breast:
15	chr5:76103612..76107653-chr5:76108707..76113004,3	MCF-7	breast:
16	chr5:76105222..76108652-chr5:76112389..76115245,3	K562	blood:
17	chr5:76094721..76097053-chr5:76101788..76104241,2	K562	blood:
18	chr5:76069360..76073048-chr5:76075455..76078776,4	K562	blood:
19	chr5:75896963..75898061-chr5:76070096..76071180,9	MCF-7	breast:
20	chr5:76103612..76107653-chr5:76108707..76113004,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000238688	TF binding region
F2RL1	TF binding region
ENSG00000238688	CpG island
F2RL1	CpG island
ENSG00000225407	chromatin interactions
ENSG00000181104	chromatin interactions
ENSG00000164251	chromatin interactions

Extended variants
information (count: 1919 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1919 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs250760	chr5:76067624-76067625	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs567142509	chr5:76067634-76067635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536292093	chr5:76067637-76067638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs151223275	chr5:76067649-76067650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs2067345	chr5:76067685-76067686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs386404161	chr5:76067686-76067687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs397750067	chr5:76067687-76067688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113040604	chr5:76067688-76067689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs376186941	chr5:76067721-76067722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs572929202	chr5:76067724-76067725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs250759	chr5:76067728-76067729	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs559168391	chr5:76067744-76067745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538145095	chr5:76067749-76067750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs530858356	chr5:76067812-76067813	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs374341440	chr5:76067813-76067814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372581850	chr5:76067821-76067822	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544881501	chr5:76067822-76067823	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116399823	chr5:76067824-76067825	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554418631	chr5:76067831-76067832	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs530018045	chr5:76067857-76067858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs187907702	chr5:76067870-76067871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574595649	chr5:76067915-76067916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560299310	chr5:76067916-76067917	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs140052050	chr5:76067971-76067972	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534003446	chr5:76067985-76067986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561280926	chr5:76068026-76068027	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs552255516	chr5:76068038-76068039	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs369231838	chr5:76068061-76068062	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs568766316	chr5:76068063-76068064	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs554274523	chr5:76068098-76068099	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs191544506	chr5:76068128-76068129	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs372780005	chr5:76068154-76068155	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs150294903	chr5:76068155-76068156	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs545840594	chr5:76068159-76068160	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs552900063	chr5:76068176-76068177	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs250758	chr5:76068179-76068180	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs550879332	chr5:76068193-76068194	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs569459484	chr5:76068241-76068242	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs538693395	chr5:76068276-76068277	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs558697629	chr5:76068295-76068296	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs377619949	chr5:76068347-76068348	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs576288804	chr5:76068348-76068349	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs74436288	chr5:76068356-76068357	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs144920051	chr5:76068362-76068363	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs183429794	chr5:76068364-76068365	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs575041441	chr5:76068387-76068388	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs140880974	chr5:76068402-76068403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560449130	chr5:76068411-76068412	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138386585	chr5:76068419-76068420	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545883375	chr5:76068428-76068429	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	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
Hepatocellular carcinoma	16750200	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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:971 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:76060600-76070200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr5:76061600-76074800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr5:76063400-76067800	Weak transcription	NHDF-Ad	bronchial
4	chr5:76067200-76068000	Enhancers	A549	lung
5	chr5:76067400-76067800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr5:76067400-76068200	Enhancers	HepG2	liver
7	chr5:76067400-76068200	Enhancers	NHLF	lung
8	chr5:76067400-76068400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr5:76067400-76068400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr5:76067400-76068800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr5:76067600-76068200	Enhancers	Muscle Satellite Cultured Cells	--
12	chr5:76067600-76068200	Enhancers	Osteobl	bone
13	chr5:76067600-76068400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr5:76067600-76068600	Enhancers	HSMMtube	muscle
15	chr5:76067800-76068200	Enhancers	NHDF-Ad	bronchial
16	chr5:76067800-76068400	Enhancers	K562	blood
17	chr5:76067800-76069000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr5:76068000-76068400	Enhancers	Fetal Kidney	kidney
19	chr5:76068000-76068400	Flanking Active TSS	A549	lung
20	chr5:76068200-76068600	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr5:76068200-76069200	Weak transcription	NHLF	lung
22	chr5:76068200-76070200	Weak transcription	Osteobl	bone
23	chr5:76068200-76070400	Weak transcription	HepG2	liver
24	chr5:76068200-76070800	Weak transcription	NH-A	brain
25	chr5:76068400-76068600	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr5:76068400-76068600	Enhancers	A549	lung
27	chr5:76068400-76068800	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr5:76068400-76070200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr5:76068400-76070200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr5:76068400-76070400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr5:76068600-76069400	Weak transcription	A549	lung
32	chr5:76068600-76069600	Weak transcription	HSMMtube	muscle
33	chr5:76068600-76074600	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr5:76068800-76074400	Weak transcription	Primary neutrophils fromperipheralblood	blood
35	chr5:76069000-76070400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr5:76069400-76070200	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr5:76069400-76072400	Enhancers	A549	lung
38	chr5:76070000-76070200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr5:76070200-76070400	Active TSS	Rectal Mucosa Donor 29	rectum
40	chr5:76070200-76070600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr5:76070200-76070600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr5:76070200-76070600	Enhancers	Primary T cells fromperipheralblood	blood
43	chr5:76070200-76070600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr5:76070200-76070600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr5:76070200-76070600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
46	chr5:76070200-76070600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr5:76070200-76070600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr5:76070200-76070600	Enhancers	Fetal Intestine Small	intestine
49	chr5:76070200-76070600	Enhancers	Stomach Mucosa	stomach
50	chr5:76070200-76070600	Enhancers	HUVEC	blood vessel

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links