Variant report

Variant	nsv533712
Chromosome Location	chr5:70369930-70657718
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2635)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2635 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:70586985-70587016	HepG2	liver:	n/a	n/a
2	BATF	chr5:70581822-70582238	GM12878	blood:	n/a	n/a
3	BATF	chr5:70585008-70585657	GM12878	blood:	n/a	n/a
4	BATF	chr5:70557168-70557369	GM12878	blood:	n/a	n/a
5	BATF	chr5:70456649-70456978	GM12878	blood:	n/a	n/a
6	BATF	chr5:70585042-70585622	GM12878	blood:	n/a	n/a
7	BATF	chr5:70505333-70505618	GM12878	blood:	n/a	n/a
8	BATF	chr5:70541641-70542422	GM12878	blood:	n/a	n/a
9	BATF	chr5:70583794-70584001	GM12878	blood:	n/a	n/a
10	BATF	chr5:70585975-70586260	GM12878	blood:	n/a	n/a
11	BATF	chr5:70539589-70539933	GM12878	blood:	n/a	n/a
12	BATF	chr5:70545061-70545287	GM12878	blood:	n/a	n/a
13	BATF	chr5:70609718-70609921	GM12878	blood:	n/a	n/a
14	BATF	chr5:70598063-70598280	GM12878	blood:	n/a	n/a
15	BATF	chr5:70558503-70558784	GM12878	blood:	n/a	chr5:70558607-70558616
16	BATF	chr5:70558516-70558791	GM12878	blood:	n/a	chr5:70558607-70558616
17	BATF	chr5:70586371-70586849	GM12878	blood:	n/a	n/a
18	BATF	chr5:70574041-70574264	GM12878	blood:	n/a	n/a
19	BATF	chr5:70456678-70456913	GM12878	blood:	n/a	n/a
20	BATF	chr5:70539526-70539950	GM12878	blood:	n/a	n/a
21	BATF	chr5:70555163-70555361	GM12878	blood:	n/a	n/a
22	BATF	chr5:70580342-70580785	GM12878	blood:	n/a	n/a
23	BATF	chr5:70581590-70581807	GM12878	blood:	n/a	n/a
24	BATF	chr5:70473270-70473572	GM12878	blood:	n/a	n/a
25	BATF	chr5:70538662-70539061	GM12878	blood:	n/a	n/a
26	BATF	chr5:70557586-70557801	GM12878	blood:	n/a	n/a
27	BATF	chr5:70582923-70583350	GM12878	blood:	n/a	n/a
28	BATF	chr5:70590289-70590572	GM12878	blood:	n/a	chr5:70590466-70590476
29	BATF	chr5:70552069-70552305	GM12878	blood:	n/a	n/a
30	BATF	chr5:70523358-70523643	GM12878	blood:	n/a	n/a
31	BATF	chr5:70602705-70602934	GM12878	blood:	n/a	n/a
32	BATF	chr5:70616798-70617022	GM12878	blood:	n/a	n/a
33	BATF	chr5:70584401-70584705	GM12878	blood:	n/a	n/a
34	BATF	chr5:70523279-70523646	GM12878	blood:	n/a	n/a
35	BATF	chr5:70580375-70580726	GM12878	blood:	n/a	n/a
36	BATF	chr5:70549602-70549824	GM12878	blood:	n/a	n/a
37	BATF	chr5:70536594-70536821	GM12878	blood:	n/a	n/a
38	BATF	chr5:70575508-70575709	GM12878	blood:	n/a	chr5:70575634-70575644 chr5:70575633-70575644
39	BATF	chr5:70552028-70552325	GM12878	blood:	n/a	n/a
40	BATF	chr5:70544001-70544158	GM12878	blood:	n/a	n/a
41	BATF	chr5:70586369-70587093	GM12878	blood:	n/a	n/a
42	BATF	chr5:70557634-70557835	GM12878	blood:	n/a	n/a
43	BATF	chr5:70556089-70556296	GM12878	blood:	n/a	n/a
44	BATF	chr5:70572667-70572911	GM12878	blood:	n/a	n/a
45	BATF	chr5:70597986-70598270	GM12878	blood:	n/a	n/a
46	BATF	chr5:70558118-70558400	GM12878	blood:	n/a	n/a
47	BATF	chr5:70572459-70572639	GM12878	blood:	n/a	n/a
48	BATF	chr5:70606094-70606336	GM12878	blood:	n/a	chr5:70606171-70606182
49	BATF	chr5:70575518-70575716	GM12878	blood:	n/a	chr5:70575634-70575644 chr5:70575633-70575644
50	BATF	chr5:70578302-70579195	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:70372505-70372555	NB4	blood:	n/a
2	chr5:70372505-70372555	U87	brain:	n/a
3	chr5:70372505-70372555	AG10803	skin:	n/a
4	chr5:70372505-70372555	IMR90	lung:	fetal
5	chr5:70372505-70372555	K562	blood:	n/a
6	chr5:70372505-70372555	HPAEpiC	pulmonary alveolar:	n/a
7	chr5:70372505-70372555	AG04450	lung:	fetal
8	chr5:70372505-70372555	T-47D	breast:	n/a
9	chr5:70372505-70372555	GM12891	blood:	n/a
10	chr5:70372505-70372555	Jurkat	blood:	n/a
11	chr5:70372505-70372555	ovcar-3	ovarian:	n/a
12	chr5:70372505-70372555	HIPEpiC	eye:	n/a
13	chr5:70372505-70372555	SK-N-SH	brain:	n/a
14	chr5:70372505-70372555	GM12892	blood:	n/a
15	chr5:70372505-70372555	H1-hESC	embryonic stem cell:	embryo
16	chr5:70372505-70372555	GM12878	blood:	n/a
17	chr5:70372505-70372555	PFSK-1	brain:	n/a
18	chr5:70372505-70372555	Hepatocyte	liver:	n/a
19	chr5:70372505-70372555	CMK	blood:	n/a
20	chr5:70372505-70372555	NT2-D1	testis:	n/a
21	chr5:70372505-70372555	LNCaP	prostate:	n/a
22	chr5:70372505-70372555	BE2_C	brain:	n/a
23	chr5:70372505-70372555	MCF10A-Er-Src	breast:	n/a
24	chr5:70372505-70372555	HUVEC	blood vessel:	n/a
25	chr5:70372505-70372555	HNPCEpiC	eye:	n/a
26	chr5:70372505-70372555	HEK293	kidney:	embryo
27	chr5:70372505-70372555	ProgFib	skin:	n/a
28	chr5:70372505-70372555	NH-A	brain:	n/a
29	chr5:70372505-70372555	HAEpiC	amniotic membrane:	n/a
30	chr5:70372505-70372555	RPTEC	kidney:	n/a
31	chr5:70372505-70372555	SK-N-SH_RA	brain:	n/a
32	chr5:70372505-70372555	SAEC	small airway:	n/a
33	chr5:70372505-70372555	NHBE	bronchial:	n/a
34	chr5:70372505-70372555	MCF-7	breast:	n/a
35	chr5:70372505-70372555	AG04449	skin:	fetal
36	chr5:70372505-70372555	AG09309	skin:	n/a
37	chr5:70372505-70372555	AG09319	gingival:	n/a
38	chr5:70372505-70372555	NHDF-neo	bronchial:	n/a
39	chr5:70372505-70372555	PANC-1	pancreas:	n/a
40	chr5:70372505-70372555	HCT-116	colon:	n/a
41	chr5:70372505-70372555	PrEC	prostate:	n/a
42	chr5:70372505-70372555	HMEC	breast:	n/a
43	chr5:70372505-70372555	ECC-1	luminal epithelium:	n/a
44	chr5:70372505-70372555	HepG2	liver:	n/a
45	chr5:70372505-70372555	Hela-S3	cervix:	n/a
46	chr5:70372505-70372555	GM19239	blood:	n/a
47	chr5:70372505-70372555	HCF	heart:	n/a
48	chr5:70372505-70372555	HRPEpiC	eye:	n/a
49	chr5:70372505-70372555	A549	lung:	n/a
50	chr5:70372505-70372555	HCM	heart:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GTF2H2-7	chr5:70493473-70493614	NONHSAT102003
2	lnc-GTF2H2-3	chr5:70647682-70649750	ENSG00000250387
3	lnc-GTF2H2-7	chr5:70493473-70493608	NONHSAT102005
4	lnc-GTF2H2-6	chr5:70528927-70529141	NONHSAT102010
5	lnc-GTF2H2-3	chr5:70649314-70649750	ENSG00000250387
6	lnc-GTF2H2-7	chr5:70492974-70493188	NONHSAT102005
7	lnc-BDP1-5	chr5:70504655-70505021	NONHSAT102007
8	lnc-SMN1-2	chr5:70378669-70379081	NONHSAT101998
9	lnc-GTF2H2-5	chr5:70525720-70525924	NONHSAT102009
10	lnc-GTF2H2-7	chr5:70435716-70435861	NONHSAT102003
11	lnc-GTF2H2-7	chr5:70438472-70438586	NONHSAT102003
12	lnc-GTF2H2-6	chr5:70529887-70530059	NONHSAT102010
13	lnc-SMN1-3	chr5:70485544-70485865	NONHSAT102004
14	lnc-GTF2H2-3	chr5:70647682-70649750	NONHSAT102012

No data

Variant related genes	Relation type
ENSG00000230847	TF binding region
ENSG00000254133	TF binding region
CDH12P4	TF binding region
ENSG00000251634	TF binding region
ENSG00000238451	TF binding region
ENSG00000235558	TF binding region
GUSBP9	TF binding region
ENSG00000254276	TF binding region
ENSG00000230847	CpG island
ENSG00000254133	CpG island
CDH12P4	CpG island
ENSG00000251634	CpG island
ENSG00000238451	CpG island
ENSG00000235558	CpG island
GUSBP9	CpG island
ENSG00000254276	CpG island

Extended variants
information (count: 372 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:372 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370663152	chr5:70369938-70369939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs187675661	chr5:70369956-70369957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570999739	chr5:70369984-70369985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531829869	chr5:70369993-70369994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371115260	chr5:70370043-70370044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2666626	chr5:70370109-70370110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs370774294	chr5:70370154-70370155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568666110	chr5:70370315-70370316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs536194121	chr5:70371081-70371082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553795200	chr5:70371087-70371088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs565714417	chr5:70371096-70371097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539519041	chr5:70371104-70371105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557910121	chr5:70371107-70371108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576151654	chr5:70371128-70371129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543261867	chr5:70371129-70371130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs57441369	chr5:70371135-70371136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555589289	chr5:70371136-70371137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573849762	chr5:70371150-70371151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530136230	chr5:70371373-70371374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540966912	chr5:70372457-70372458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370884961	chr5:70372469-70372470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560097075	chr5:70372506-70372507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs527706110	chr5:70373157-70373158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545862817	chr5:70373174-70373175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs376209441	chr5:70373240-70373241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs193209515	chr5:70373257-70373258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531889709	chr5:70373279-70373280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs256922	chr5:70373280-70373281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550106434	chr5:70373290-70373291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568679772	chr5:70373311-70373312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569997738	chr5:70373513-70373514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529599092	chr5:70373742-70373743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548139342	chr5:70373745-70373746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs256921	chr5:70373763-70373764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539455158	chr5:70373802-70373803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183412136	chr5:70373812-70373813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187498659	chr5:70373826-70373827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537195433	chr5:70373849-70373850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs256920	chr5:70373874-70373875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192327766	chr5:70373913-70373914	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
41	rs184073794	chr5:70374002-70374003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540903483	chr5:70374033-70374034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552867946	chr5:70374080-70374081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572071981	chr5:70374161-70374162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545799083	chr5:70374214-70374215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371463967	chr5:70374351-70374352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375263772	chr5:70374459-70374460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564554228	chr5:70374460-70374461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576452006	chr5:70374513-70374514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369456872	chr5:70374617-70374618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:116)

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
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ovarian cancer	21781307	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	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
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
abnormal development	18461090	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21045282	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelodysplastic syndrome	18663149	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Sezary syndrome	18413736	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21990379	CNVD
Hirschsprung''s Disease	21712996	CNVD
Apoptosis	19488400	CNVD
Breast cancer	22048815	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Acute monocytic leukemia	16498392	CNVD
Colorectal cancer	20459617	CNVD
Gastric adenocarcinoma	19115996	CNVD
Spinal muscular atrophy	17160897	CNVD
Spinal muscular atrophy	17668391	CNVD
Spinal muscular atrophy	17668395	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pseudo-TORCH syndrome	20727516	CNVD
Medullary thyroid carcinoma	18765511	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Autism	22549408	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Disease	19212409	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Recurrent pregnancy loss	19789632	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:70348200-70376200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:70392600-70395000	Weak transcription	Lung	lung
3	chr5:70392600-70395800	Weak transcription	Fetal Muscle Trunk	muscle
4	chr5:70393400-70393800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:70393400-70393800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr5:70393400-70400600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr5:70393600-70393800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr5:70393600-70394200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr5:70393600-70394200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr5:70397400-70408400	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr5:70398800-70408400	Weak transcription	Ovary	ovary
12	chr5:70404800-70408200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr5:70404800-70408200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr5:70404800-70408200	Weak transcription	Fetal Stomach	stomach
15	chr5:70405600-70408000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr5:70405600-70408000	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr5:70405600-70408000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr5:70405600-70408000	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr5:70405600-70408000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr5:70405600-70408000	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr5:70405600-70408000	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr5:70484800-70485000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr5:70492000-70494200	Weak transcription	Fetal Muscle Leg	muscle
24	chr5:70492000-70494200	Weak transcription	Fetal Thymus	thymus
25	chr5:70492200-70494600	Weak transcription	Dnd41	blood
26	chr5:70492400-70494800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr5:70525000-70526600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr5:70525000-70526600	Weak transcription	Fetal Intestine Large	intestine
29	chr5:70525600-70528000	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr5:70525600-70528000	Weak transcription	Primary hematopoietic stem cells	blood
31	chr5:70525800-70528000	Weak transcription	Ovary	ovary
32	chr5:70525800-70528200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr5:70525800-70528200	Weak transcription	Fetal Brain Female	brain
34	chr5:70526600-70527000	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr5:70526600-70527000	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr5:70526600-70527000	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr5:70526600-70527000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
38	chr5:70526600-70527200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr5:70526600-70527200	Strong transcription	Fetal Intestine Large	intestine
40	chr5:70526600-70527400	Enhancers	H1 Cell Line	embryonic stem cell
41	chr5:70527000-70527200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr5:70527000-70527400	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
43	chr5:70527200-70527400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr5:70527200-70527400	Enhancers	Lung	lung
45	chr5:70527200-70528800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr5:70527200-70528800	Weak transcription	Fetal Intestine Large	intestine
47	chr5:70527400-70528200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr5:70575600-70576000	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr5:70575600-70576000	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr5:70575600-70576000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links