Variant report

Variant	nsv882211
Chromosome Location	chr5:76100536-76125577
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1161)
CpG islands
(count:1464)
Chromatin interactive
region (count:14)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:76116209-76116734	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:76113989-76114292	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:76114553-76114860	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:76101782-76102245	K562	blood:	n/a	n/a
5	ATF1	chr5:76101722-76102174	K562	blood:	n/a	n/a
6	ATF2	chr5:76103823-76104436	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr5:76103843-76104561	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr5:76113947-76114568	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr5:76114079-76115052	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr5:76101689-76102467	A549	lung:	n/a	n/a
11	ATF3	chr5:76099975-76100655	A549	lung:	n/a	n/a
12	ATF3	chr5:76100044-76100672	A549	lung:	n/a	n/a
13	ATF3	chr5:76101627-76102562	A549	lung:	n/a	n/a
14	ATF3	chr5:76114447-76115003	A549	lung:	n/a	chr5:76114977-76114986 chr5:76114862-76114870
15	ATF3	chr5:76114432-76115010	A549	lung:	n/a	chr5:76114977-76114986 chr5:76114862-76114870
16	BACH1	chr5:76103704-76103712	K562	blood:	n/a	n/a
17	BACH1	chr5:76114200-76116153	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr5:76102000-76102358	GM12878	blood:	n/a	n/a
19	BCL3	chr5:76109914-76110498	A549	lung:	n/a	chr5:76110348-76110357
20	BCL3	chr5:76115978-76116822	A549	lung:	n/a	n/a
21	BCL3	chr5:76101972-76102349	GM12878	blood:	n/a	chr5:76102262-76102271
22	BCL3	chr5:76109782-76110506	A549	lung:	n/a	chr5:76110348-76110357
23	BCL3	chr5:76101545-76102516	A549	lung:	n/a	chr5:76102262-76102271
24	BCL3	chr5:76114082-76115135	A549	lung:	n/a	chr5:76114962-76114971 chr5:76114691-76114704
25	BCL3	chr5:76099974-76100817	A549	lung:	n/a	chr5:76100092-76100100 chr5:76100201-76100210
26	BCL3	chr5:76099724-76100840	A549	lung:	n/a	chr5:76100092-76100100 chr5:76100201-76100210
27	BCL3	chr5:76101399-76102582	A549	lung:	n/a	chr5:76102262-76102271
28	BCL3	chr5:76101997-76102356	GM12878	blood:	n/a	chr5:76102262-76102271
29	BHLHE40	chr5:76101694-76102239	K562	blood:	n/a	n/a
30	BHLHE40	chr5:76121429-76121600	A549	lung:	n/a	n/a
31	BRCA1	chr5:76110002-76110390	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr5:76114112-76114340	H1-hESC	embryonic stem cell:	n/a	n/a
33	BRCA1	chr5:76115005-76115163	H1-hESC	embryonic stem cell:	n/a	n/a
34	BRCA1	chr5:76101731-76102250	Hela-S3	cervix:	n/a	n/a
35	CBX3	chr5:76101564-76102624	HCT-116	colon:	n/a	n/a
36	CCNT2	chr5:76114655-76114931	K562	blood:	n/a	chr5:76114770-76114779
37	CCNT2	chr5:76101842-76102246	K562	blood:	n/a	n/a
38	CEBPB	chr5:76100129-76100798	A549	lung:	n/a	chr5:76100726-76100737
39	CEBPB	chr5:76104856-76105149	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr5:76101670-76102398	IMR90	lung:	n/a	n/a
41	CEBPB	chr5:76122283-76122416	HepG2	liver:	n/a	n/a
42	CEBPB	chr5:76101772-76102360	MCF-7	breast:	n/a	n/a
43	CEBPB	chr5:76100651-76100772	K562	blood:	n/a	chr5:76100726-76100737
44	CEBPB	chr5:76107132-76107390	IMR90	lung:	n/a	chr5:76107135-76107143
45	CEBPB	chr5:76101664-76102489	A549	lung:	n/a	n/a
46	CEBPB	chr5:76109982-76110434	A549	lung:	n/a	n/a
47	CEBPB	chr5:76100079-76100911	A549	lung:	n/a	chr5:76100726-76100737
48	CEBPB	chr5:76109834-76110522	A549	lung:	n/a	n/a
49	CEBPB	chr5:76100039-76100821	A549	lung:	n/a	chr5:76100726-76100737
50	CEBPB	chr5:76100560-76100761	HepG2	liver:	n/a	chr5:76100726-76100737

(count:1464 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:76115309-76115359	HEEpiC	esophagus:	n/a
2	chr5:76114373-76114423	ECC-1	luminal epithelium:	n/a
3	chr5:76114822-76114872	HRE	kidney:	n/a
4	chr5:76108729-76108779	H1-hESC	embryonic stem cell:	embryo
5	chr5:76114933-76114983	MCF10A-Er-Src	breast:	n/a
6	chr5:76115974-76116024	PFSK-1	brain:	n/a
7	chr5:76114812-76114862	HUVEC	blood vessel:	n/a
8	chr5:76115974-76116024	HAEpiC	amniotic membrane:	n/a
9	chr5:76117747-76117797	BJ	skin:	n/a
10	chr5:76114522-76114572	CMK	blood:	n/a
11	chr5:76119931-76119981	AG10803	skin:	n/a
12	chr5:76114822-76114872	HCF	heart:	n/a
13	chr5:76112996-76113046	RPTEC	kidney:	n/a
14	chr5:76108729-76108779	SAEC	small airway:	n/a
15	chr5:76116169-76116219	MCF-7	breast:	n/a
16	chr5:76114571-76114621	HCPEpiC	choroid plexus:	n/a
17	chr5:76115868-76115918	HEK293	kidney:	embryo
18	chr5:76112996-76113046	HRCEpiC	kidney:	n/a
19	chr5:76116088-76116138	SK-N-MC	brain:	n/a
20	chr5:76112776-76112826	HIPEpiC	eye:	n/a
21	chr5:76114684-76114734	PANC-1	pancreas:	n/a
22	chr5:76114684-76114734	NT2-D1	testis:	n/a
23	chr5:76114684-76114734	Jurkat	blood:	n/a
24	chr5:76117747-76117797	HUVEC	blood vessel:	n/a
25	chr5:76115672-76115722	NB4	blood:	n/a
26	chr5:76114822-76114872	GM12891	blood:	n/a
27	chr5:76116169-76116219	SK-N-MC	brain:	n/a
28	chr5:76119931-76119981	AG09309	skin:	n/a
29	chr5:76115309-76115359	HAEpiC	amniotic membrane:	n/a
30	chr5:76111995-76112045	HCM	heart:	n/a
31	chr5:76114822-76114872	GM19239	blood:	n/a
32	chr5:76108191-76108241	AG09309	skin:	n/a
33	chr5:76108729-76108779	HL-60	blood:	n/a
34	chr5:76116169-76116219	Hela-S3	cervix:	n/a
35	chr5:76114822-76114872	U87	brain:	n/a
36	chr5:76115868-76115918	NT2-D1	testis:	n/a
37	chr5:76116088-76116138	SK-N-SH	brain:	n/a
38	chr5:76115810-76115860	HPAEpiC	pulmonary alveolar:	n/a
39	chr5:76117747-76117797	U87	brain:	n/a
40	chr5:76115810-76115860	Jurkat	blood:	n/a
41	chr5:76114571-76114621	HCF	heart:	n/a
42	chr5:76117747-76117797	HPAEpiC	pulmonary alveolar:	n/a
43	chr5:76112996-76113046	PANC-1	pancreas:	n/a
44	chr5:76114571-76114621	NHDF-neo	bronchial:	n/a
45	chr5:76114822-76114872	AoSMC	blood vessel:	n/a
46	chr5:76115810-76115860	ovcar-3	ovarian:	n/a
47	chr5:76108729-76108779	BJ	skin:	n/a
48	chr5:76114812-76114862	HepG2	liver:	n/a
49	chr5:76115672-76115722	GM12892	blood:	n/a
50	chr5:76116088-76116138	ovcar-3	ovarian:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:796813..797729-chr5:76114268..76115162,3	HCT-116	colon:
2	chr5:76115218..76117725-chr5:76325993..76327834,2	MCF-7	breast:
3	chr5:76113078..76116046-chr5:76145704..76148210,2	K562	blood:
4	chr5:76103612..76107653-chr5:76108707..76113004,3	MCF-7	breast:
5	chr5:76103612..76107653-chr5:76108707..76113004,3	MCF-7	breast:
6	chr5:76115175..76117196-chr5:76160540..76162682,2	MCF-7	breast:
7	chr5:76110973..76114089-chr5:76116480..76119427,3	K562	blood:
8	chr5:76105222..76108652-chr5:76112389..76115245,3	K562	blood:
9	chr5:76094082..76095930-chr5:76098926..76101541,2	K562	blood:
10	chr5:76123012..76125302-chr5:76125595..76128318,2	MCF-7	breast:
11	chr5:76101619..76103504-chr5:76111998..76114759,2	K562	blood:
12	chr5:76094721..76097053-chr5:76101788..76104241,2	K562	blood:
13	chr5:76110973..76114089-chr5:76116480..76119427,3	K562	blood:
14	chr5:76106690..76108652-chr5:76112389..76115245,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-S100Z-1	chr5:76114806-76115096	NONHSAT102251

No data

Variant related genes	Relation type
F2RL1	TF binding region
F2RL1	CpG island
ENSG00000011304	chromatin interactions
ENSG00000171643	chromatin interactions
ENSG00000164251	chromatin interactions
ENSG00000164252	chromatin interactions

Extended variants
information (count: 1078 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1078 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13177258	chr5:76100536-76100537	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs558506969	chr5:76100702-76100703	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs575199504	chr5:76100713-76100714	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs62365101	chr5:76100717-76100718	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs554330462	chr5:76100736-76100737	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs183377538	chr5:76100754-76100755	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs540400886	chr5:76100755-76100756	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs144255344	chr5:76100777-76100778	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs577098946	chr5:76100794-76100795	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs62365102	chr5:76100798-76100799	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs562889667	chr5:76100849-76100850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs531565187	chr5:76100857-76100858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs556019299	chr5:76100934-76100935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548563758	chr5:76100939-76100940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs188489110	chr5:76100942-76100943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs2435056	chr5:76100952-76100953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs2435057	chr5:76100955-76100956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192905166	chr5:76100966-76100967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs56238109	chr5:76100971-76100972	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs546799062	chr5:76100973-76100974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs114153225	chr5:76101058-76101059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs62365104	chr5:76101074-76101075	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs386689247	chr5:76101106-76101107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs62365105	chr5:76101107-76101108	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs537398517	chr5:76101111-76101112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs554572931	chr5:76101118-76101119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs374001035	chr5:76101153-76101154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs183136734	chr5:76101206-76101207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs13157422	chr5:76101240-76101241	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs369615751	chr5:76101241-76101242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs563909674	chr5:76101265-76101266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs577062755	chr5:76101309-76101310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs374778758	chr5:76101383-76101384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371814727	chr5:76101387-76101388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs140570129	chr5:76101388-76101389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs6886202	chr5:76101399-76101400	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs66493305	chr5:76101402-76101403	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556532868	chr5:76101468-76101469	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576693250	chr5:76101488-76101489	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541822028	chr5:76101503-76101504	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373804818	chr5:76101513-76101514	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs527761913	chr5:76101584-76101585	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550230002	chr5:76101594-76101595	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541587822	chr5:76101619-76101620	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs142487903	chr5:76101645-76101646	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs560380666	chr5:76101654-76101655	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs187824229	chr5:76101726-76101727	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs12186639	chr5:76101781-76101782	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs569029971	chr5:76101793-76101794	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs529394838	chr5:76101794-76101795	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	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
Breast cancer	22522925	CNVD

Chromatin state (count:972 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:76088200-76101400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr5:76091000-76101800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr5:76095000-76101400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr5:76097400-76101400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr5:76097400-76101600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr5:76097600-76101400	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr5:76097800-76101400	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr5:76097800-76101400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr5:76097800-76101400	Weak transcription	NHDF-Ad	bronchial
10	chr5:76097800-76101600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr5:76098000-76101400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr5:76098000-76101400	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr5:76098000-76101400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr5:76098000-76101400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr5:76098000-76101400	Weak transcription	Hela-S3	cervix
16	chr5:76098000-76101400	Weak transcription	HSMMtube	muscle
17	chr5:76098000-76101400	Weak transcription	NHEK	skin
18	chr5:76098000-76101400	Weak transcription	NHLF	lung
19	chr5:76098000-76101600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr5:76098000-76104000	Weak transcription	Spleen	Spleen
21	chr5:76098000-76105000	Weak transcription	Right Atrium	heart
22	chr5:76098200-76101600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr5:76098200-76101600	Weak transcription	HMEC	breast
24	chr5:76099600-76101800	Weak transcription	Gastric	stomach
25	chr5:76099800-76100600	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr5:76099800-76100800	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr5:76099800-76100800	Enhancers	NH-A	brain
28	chr5:76099800-76102200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr5:76099800-76102600	Enhancers	Fetal Intestine Small	intestine
30	chr5:76099800-76103400	Enhancers	Fetal Intestine Large	intestine
31	chr5:76100000-76100600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr5:76100000-76100600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr5:76100000-76100800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr5:76100000-76100800	Flanking Active TSS	A549	lung
35	chr5:76100000-76102400	Enhancers	HepG2	liver
36	chr5:76100000-76104200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr5:76100200-76101600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr5:76100200-76104400	Enhancers	HUVEC	blood vessel
39	chr5:76100400-76100600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr5:76100400-76100600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr5:76100400-76100600	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr5:76100400-76100600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr5:76100400-76100600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr5:76100400-76101400	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr5:76100400-76101400	Weak transcription	Osteobl	bone
46	chr5:76100400-76101800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr5:76100400-76102200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr5:76100400-76102200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr5:76100400-76103000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr5:76100600-76101200	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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