Variant report

Variant	nsv1033773
Chromosome Location	chr6:58447068-58774716
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:543)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:543 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:58774342-58780018	K562	blood:	n/a	n/a
2	ATF1	chr6:58773485-58774093	K562	blood:	n/a	n/a
3	BACH1	chr6:58773467-58774102	K562	blood:	n/a	n/a
4	BATF	chr6:58737236-58737386	GM12878	blood:	n/a	n/a
5	BATF	chr6:58773550-58780199	GM12878	blood:	n/a	n/a
6	BATF	chr6:58773483-58774907	GM12878	blood:	n/a	n/a
7	BATF	chr6:58764416-58764615	GM12878	blood:	n/a	n/a
8	BCL11A	chr6:58737244-58737378	GM12878	blood:	n/a	n/a
9	BCL11A	chr6:58773535-58780209	GM12878	blood:	n/a	n/a
10	BCL11A	chr6:58773554-58780191	GM12878	blood:	n/a	n/a
11	BHLHE40	chr6:58773547-58780210	HepG2	liver:	n/a	n/a
12	BHLHE40	chr6:58737228-58737405	HepG2	liver:	n/a	n/a
13	BRCA1	chr6:58773464-58774101	GM12878	blood:	n/a	n/a
14	BRCA1	chr6:58774347-58780025	HepG2	liver:	n/a	n/a
15	BRCA1	chr6:58774350-58780022	GM12878	blood:	n/a	n/a
16	BRCA1	chr6:58773462-58774102	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr6:58774347-58780021	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr6:58524581-58524685	IMR90	lung:	n/a	n/a
19	CEBPB	chr6:58506303-58506382	HepG2	liver:	n/a	n/a
20	CEBPB	chr6:58773594-58774222	GM12878	blood:	n/a	n/a
21	CEBPB	chr6:58524736-58524936	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr6:58576509-58576728	HepG2	liver:	n/a	n/a
23	CEBPB	chr6:58774302-58774846	GM12878	blood:	n/a	n/a
24	CHD1	chr6:58774350-58780020	GM12878	blood:	n/a	n/a
25	CHD1	chr6:58773464-58774101	GM12878	blood:	n/a	n/a
26	CHD2	chr6:58774351-58780021	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr6:58773462-58774101	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr6:58694247-58694254	Fibrobl	skin:	n/a	n/a
29	CTCF	chr6:58686906-58686975	GM20000	blood:	n/a	n/a
30	CTCF	chr6:58507998-58508272	K562	blood:	n/a	chr6:58508122-58508143 chr6:58508127-58508145
31	CTCF	chr6:58698041-58698099	ProgFib	skin:	n/a	n/a
32	CTCF	chr6:58508026-58508280	LNCaP	prostate:	n/a	chr6:58508122-58508143 chr6:58508127-58508145
33	CTCF	chr6:58660153-58660216	GM10266	blood:	n/a	n/a
34	CTCF	chr6:58483898-58483942	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr6:58669851-58669858	LNCaP	prostate:	n/a	n/a
36	CTCF	chr6:58507880-58508030	HMF	breast:	n/a	n/a
37	CTCF	chr6:58666470-58666506	LNCaP	prostate:	n/a	n/a
38	CTCF	chr6:58507900-58508050	HMEC	breast:	n/a	n/a
39	CTCF	chr6:58508050-58508255	GM12878	blood:	n/a	chr6:58508122-58508143 chr6:58508127-58508145
40	CTCF	chr6:58716828-58716881	GM10248	blood:	n/a	n/a
41	CTCF	chr6:58507900-58508050	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr6:58508019-58508260	MCF-7	breast:	n/a	chr6:58508122-58508143 chr6:58508127-58508145
43	CTCF	chr6:58659573-58659667	LNCaP	prostate:	n/a	n/a
44	CTCF	chr6:58507920-58508070	BE2_C	brain:	n/a	n/a
45	CTCF	chr6:58717544-58717644	GM10248	blood:	n/a	n/a
46	CTCF	chr6:58508016-58508262	GM13977	blood:	n/a	chr6:58508122-58508143 chr6:58508127-58508145
47	CTCF	chr6:58484072-58484179	NHEK	skin:	n/a	n/a
48	CTCF	chr6:58508037-58508183	ProgFib	skin:	n/a	chr6:58508122-58508143 chr6:58508127-58508145
49	CTCF	chr6:58507986-58508234	Gliobla	brain:	n/a	chr6:58508122-58508143 chr6:58508127-58508145
50	CTCF	chr6:58462690-58462754	LNCaP	prostate:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:58584053-58584103	HEK293	kidney:	embryo
2	chr6:58584053-58584103	HEEpiC	esophagus:	n/a
3	chr6:58584053-58584103	GM12892	blood:	n/a
4	chr6:58584053-58584103	NHBE	bronchial:	n/a
5	chr6:58584053-58584103	HPAEpiC	pulmonary alveolar:	n/a
6	chr6:58584053-58584103	HIPEpiC	eye:	n/a
7	chr6:58584053-58584103	NH-A	brain:	n/a
8	chr6:58584053-58584103	CMK	blood:	n/a
9	chr6:58584053-58584103	Hepatocyte	liver:	n/a
10	chr6:58584053-58584103	AG04450	lung:	fetal
11	chr6:58584053-58584103	HL-60	blood:	n/a
12	chr6:58584053-58584103	A549	lung:	n/a
13	chr6:58584053-58584103	AoSMC	blood vessel:	n/a
14	chr6:58584053-58584103	SK-N-MC	brain:	n/a
15	chr6:58584053-58584103	MCF10A-Er-Src	breast:	n/a
16	chr6:58584053-58584103	HMEC	breast:	n/a
17	chr6:58584053-58584103	LNCaP	prostate:	n/a
18	chr6:58584053-58584103	BJ	skin:	n/a
19	chr6:58584053-58584103	K562	blood:	n/a
20	chr6:58584053-58584103	BE2_C	brain:	n/a
21	chr6:58584053-58584103	SK-N-SH_RA	brain:	n/a
22	chr6:58584053-58584103	MCF-7	breast:	n/a
23	chr6:58584053-58584103	ECC-1	luminal epithelium:	n/a
24	chr6:58584053-58584103	HepG2	liver:	n/a
25	chr6:58584053-58584103	ovcar-3	ovarian:	n/a
26	chr6:58584053-58584103	SKMC	muscle:	n/a
27	chr6:58584053-58584103	HCM	heart:	n/a
28	chr6:58584053-58584103	NB4	blood:	n/a
29	chr6:58584053-58584103	HRPEpiC	eye:	n/a
30	chr6:58584053-58584103	Jurkat	blood:	n/a
31	chr6:58584053-58584103	Caco-2	colon:	n/a
32	chr6:58584053-58584103	HAEpiC	amniotic membrane:	n/a
33	chr6:58584053-58584103	SAEC	small airway:	n/a
34	chr6:58584053-58584103	GM12878	blood:	n/a
35	chr6:58584053-58584103	PANC-1	pancreas:	n/a
36	chr6:58584053-58584103	NT2-D1	testis:	n/a
37	chr6:58584053-58584103	SK-N-SH	brain:	n/a
38	chr6:58584053-58584103	PrEC	prostate:	n/a
39	chr6:58584053-58584103	AG10803	skin:	n/a
40	chr6:58584053-58584103	NHDF-neo	bronchial:	n/a
41	chr6:58584053-58584103	HNPCEpiC	eye:	n/a
42	chr6:58584053-58584103	ProgFib	skin:	n/a
43	chr6:58584053-58584103	U87	brain:	n/a
44	chr6:58584053-58584103	HCT-116	colon:	n/a
45	chr6:58584053-58584103	IMR90	lung:	fetal
46	chr6:58584053-58584103	Hela-S3	cervix:	n/a
47	chr6:58584053-58584103	GM06990	blood:	n/a
48	chr6:58584053-58584103	PFSK-1	brain:	n/a
49	chr6:58584053-58584103	HRE	kidney:	n/a
50	chr6:58584053-58584103	AG04449	skin:	fetal

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:38032912..38033432-chr6:58774035..58775015,2	MCF-7	breast:
2	chr6:58773141..58775009-chr6:58776566..58778429,2	MCF-7	breast:
3	chr6:58772384..58775379-chr6:58777406..58779060,3	K562	blood:
4	chr19:27738271..27739820-chr6:58772163..58774918,2	MCF-7	breast:
5	chr20:56089136..56089874-chr6:58774030..58774536,2	MCF-7	breast:
6	chr20:36661511..36663112-chr6:58773928..58776889,2	K562	blood:
7	chr6:58772143..58775007-chr6:58776713..58778919,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BAG2-7	chr6:58513504-58513860	ENSG00000223633.2
2	lnc-BAG2-7	chr6:58488888-58489027	ENSG00000223633.2
3	lnc-BAG2-7	chr6:58488888-58489027	ENSG00000223633.1

No data

Variant related genes	Relation type
ENSG00000223633	TF binding region
RBBP4P4	TF binding region
ENSG00000223633	CpG island
RBBP4P4	CpG island
ENSG00000101413	chromatin interactions
ENSG00000101407	chromatin interactions

Extended variants
information (count: 2262 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2262 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2996170	chr6:58449988-58449989	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs547550345	chr6:58450010-58450011	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs566692407	chr6:58450035-58450036	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs567461222	chr6:58450822-58450823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs150184906	chr6:58450831-58450832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs13196183	chr6:58450846-58450847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs550079849	chr6:58450859-58450860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs571258535	chr6:58450947-58450948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538225430	chr6:58450967-58450968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs553831530	chr6:58450994-58450995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs111241310	chr6:58451017-58451018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535930792	chr6:58451023-58451024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs184916279	chr6:58451036-58451037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529648684	chr6:58451054-58451055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs200825410	chr6:58451055-58451056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs202210178	chr6:58451056-58451057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs55909200	chr6:58451057-58451058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs145161722	chr6:58451058-58451059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs576207463	chr6:58451103-58451104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs537381043	chr6:58451115-58451116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs558951128	chr6:58451118-58451119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577190570	chr6:58451129-58451130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541019880	chr6:58451166-58451167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs189676926	chr6:58451237-58451238	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs575028328	chr6:58451252-58451253	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs1461460	chr6:58451356-58451357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs570701409	chr6:58451367-58451368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542341968	chr6:58451390-58451391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561096706	chr6:58451391-58451392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs1461459	chr6:58451416-58451417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs531521122	chr6:58451434-58451435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs550068220	chr6:58451486-58451487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs565008829	chr6:58451576-58451577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs1343380	chr6:58451590-58451591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs1343381	chr6:58451606-58451607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs138743568	chr6:58451616-58451617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs182743789	chr6:58451650-58451651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs1224732	chr6:58451666-58451667	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs188957828	chr6:58451698-58451699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs547864863	chr6:58451713-58451714	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs542931388	chr6:58451723-58451724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs569930451	chr6:58451760-58451761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs1343382	chr6:58451813-58451814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs193133130	chr6:58451830-58451831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs1343383	chr6:58451842-58451843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559207014	chr6:58451858-58451859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs9500288	chr6:58451867-58451868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs535318876	chr6:58451915-58451916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs2996168	chr6:58452026-58452027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs2996167	chr6:58452029-58452030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Neuroblastoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:200 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:58450800-58453400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr6:58451000-58452000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:58452000-58452600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:58452600-58452800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:58452800-58454200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr6:58453400-58454200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr6:58454200-58454800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr6:58454200-58455600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr6:58454400-58454800	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr6:58454800-58455400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr6:58455400-58455600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr6:58518400-58519600	Enhancers	NHEK	skin
13	chr6:58519200-58520000	Enhancers	Muscle Satellite Cultured Cells	--
14	chr6:58519600-58520200	Active TSS	NHEK	skin
15	chr6:58519800-58520200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr6:58520200-58524000	Weak transcription	NHEK	skin
17	chr6:58522000-58522200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr6:58524000-58525800	Enhancers	NHEK	skin
19	chr6:58591000-58591400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr6:58607000-58607400	Active TSS	Stomach Mucosa	stomach
21	chr6:58614800-58617800	Enhancers	NHEK	skin
22	chr6:58668600-58669200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr6:58684400-58685400	Enhancers	NHEK	skin
24	chr6:58748800-58750400	ZNF genes & repeats	Liver	Liver
25	chr6:58762800-58763200	ZNF genes & repeats	Liver	Liver
26	chr6:58764600-58765800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr6:58765200-58769400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr6:58768000-58771000	ZNF genes & repeats	Liver	Liver
29	chr6:58769400-58769800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr6:58769600-58770000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
31	chr6:58769800-58773600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr6:58770000-58773400	Weak transcription	Aorta	Aorta
33	chr6:58770600-58770800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
34	chr6:58770800-58773400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr6:58771000-58773400	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr6:58771000-58773400	Weak transcription	Liver	Liver
37	chr6:58771200-58773400	Weak transcription	Adipose Nuclei	Adipose
38	chr6:58772600-58773200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr6:58773400-58773600	Active TSS	Aorta	Aorta
40	chr6:58773400-58773600	Active TSS	Ovary	ovary
41	chr6:58773400-58773600	Active TSS	Psoas Muscle	Psoas
42	chr6:58773400-58774000	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
43	chr6:58773400-58774000	Flanking Bivalent TSS/Enh	Hela-S3	cervix
44	chr6:58773400-58774800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr6:58773400-58774800	ZNF genes & repeats	Brain Hippocampus Middle	brain
46	chr6:58773400-58774800	ZNF genes & repeats	Colon Smooth Muscle	Colon
47	chr6:58773400-58774800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
48	chr6:58773400-58774800	ZNF genes & repeats	Fetal Lung	lung
49	chr6:58773400-58774800	ZNF genes & repeats	Rectal Smooth Muscle	rectum
50	chr6:58773400-58774800	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon

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