Variant report

Variant	nsv1025480
Chromosome Location	chr8:43504529-43824036
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3910)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3910 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:43786577-43787136	K562	blood:	n/a	n/a
2	ATF1	chr8:43792645-43793396	K562	blood:	n/a	n/a
3	ATF1	chr8:43785555-43785668	K562	blood:	n/a	n/a
4	ATF1	chr8:43819080-43819187	K562	blood:	n/a	n/a
5	BACH1	chr8:43779446-43779599	K562	blood:	n/a	n/a
6	BACH1	chr8:43818947-43819136	K562	blood:	n/a	n/a
7	BACH1	chr8:43790059-43790248	K562	blood:	n/a	n/a
8	BACH1	chr8:43572418-43572443	K562	blood:	n/a	n/a
9	BACH1	chr8:43820379-43820751	K562	blood:	n/a	n/a
10	BACH1	chr8:43717526-43717725	K562	blood:	n/a	n/a
11	BACH1	chr8:43654724-43654750	K562	blood:	n/a	n/a
12	BATF	chr8:43795705-43796262	GM12878	blood:	n/a	n/a
13	BATF	chr8:43790975-43791219	GM12878	blood:	n/a	n/a
14	BATF	chr8:43817222-43817499	GM12878	blood:	n/a	n/a
15	BATF	chr8:43771245-43771622	GM12878	blood:	n/a	n/a
16	BATF	chr8:43795406-43795581	GM12878	blood:	n/a	n/a
17	BATF	chr8:43806260-43806536	GM12878	blood:	n/a	n/a
18	BATF	chr8:43816105-43816326	GM12878	blood:	n/a	n/a
19	BATF	chr8:43776273-43776586	GM12878	blood:	n/a	n/a
20	BATF	chr8:43823238-43824120	GM12878	blood:	n/a	n/a
21	BATF	chr8:43810454-43810881	GM12878	blood:	n/a	n/a
22	BATF	chr8:43800254-43800627	GM12878	blood:	n/a	n/a
23	BATF	chr8:43771212-43771629	GM12878	blood:	n/a	n/a
24	BATF	chr8:43802641-43802856	GM12878	blood:	n/a	n/a
25	BATF	chr8:43785488-43786069	GM12878	blood:	n/a	n/a
26	BATF	chr8:43782910-43783364	GM12878	blood:	n/a	n/a
27	BATF	chr8:43801979-43802190	GM12878	blood:	n/a	n/a
28	BATF	chr8:43805556-43805832	GM12878	blood:	n/a	n/a
29	BATF	chr8:43772038-43772467	GM12878	blood:	n/a	n/a
30	BATF	chr8:43821252-43822263	GM12878	blood:	n/a	n/a
31	BATF	chr8:43778905-43779151	GM12878	blood:	n/a	n/a
32	BATF	chr8:43801571-43801907	GM12878	blood:	n/a	n/a
33	BATF	chr8:43820362-43821200	GM12878	blood:	n/a	n/a
34	BATF	chr8:43800956-43801154	GM12878	blood:	n/a	n/a
35	BATF	chr8:43803567-43803962	GM12878	blood:	n/a	n/a
36	BATF	chr8:43761208-43761764	GM12878	blood:	n/a	n/a
37	BATF	chr8:43802702-43802924	GM12878	blood:	n/a	n/a
38	BATF	chr8:43818959-43819224	GM12878	blood:	n/a	n/a
39	BATF	chr8:43821328-43821864	GM12878	blood:	n/a	n/a
40	BATF	chr8:43760193-43760718	GM12878	blood:	n/a	n/a
41	BATF	chr8:43809305-43809681	GM12878	blood:	n/a	n/a
42	BATF	chr8:43793089-43793493	GM12878	blood:	n/a	n/a
43	BATF	chr8:43811590-43811948	GM12878	blood:	n/a	n/a
44	BATF	chr8:43785460-43785804	GM12878	blood:	n/a	n/a
45	BATF	chr8:43783535-43783800	GM12878	blood:	n/a	n/a
46	BATF	chr8:43797348-43797784	GM12878	blood:	n/a	n/a
47	BATF	chr8:43822263-43823134	GM12878	blood:	n/a	n/a
48	BATF	chr8:43823254-43823632	GM12878	blood:	n/a	n/a
49	BATF	chr8:43809217-43809758	GM12878	blood:	n/a	n/a
50	BATF	chr8:43759902-43760143	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:43794595-43794645	BE2_C	brain:	n/a
2	chr8:43794595-43794645	HEEpiC	esophagus:	n/a
3	chr8:43794595-43794645	HEK293	kidney:	embryo
4	chr8:43794595-43794645	HRPEpiC	eye:	n/a
5	chr8:43794595-43794645	AG04450	lung:	fetal
6	chr8:43794595-43794645	AG10803	skin:	n/a
7	chr8:43794595-43794645	HUVEC	blood vessel:	n/a
8	chr8:43794595-43794645	SK-N-MC	brain:	n/a
9	chr8:43794595-43794645	NHDF-neo	bronchial:	n/a
10	chr8:43794595-43794645	PrEC	prostate:	n/a
11	chr8:43794595-43794645	NH-A	brain:	n/a
12	chr8:43794595-43794645	HCF	heart:	n/a
13	chr8:43794595-43794645	IMR90	lung:	fetal
14	chr8:43794595-43794645	Caco-2	colon:	n/a
15	chr8:43794595-43794645	U87	brain:	n/a
16	chr8:43794595-43794645	SKMC	muscle:	n/a
17	chr8:43794595-43794645	GM19239	blood:	n/a
18	chr8:43794595-43794645	T-47D	breast:	n/a
19	chr8:43794595-43794645	HNPCEpiC	eye:	n/a
20	chr8:43794595-43794645	MCF10A-Er-Src	breast:	n/a
21	chr8:43794595-43794645	SAEC	small airway:	n/a
22	chr8:43794595-43794645	HL-60	blood:	n/a
23	chr8:43794595-43794645	GM12891	blood:	n/a
24	chr8:43794595-43794645	LNCaP	prostate:	n/a
25	chr8:43794595-43794645	H1-hESC	embryonic stem cell:	embryo
26	chr8:43794595-43794645	ovcar-3	ovarian:	n/a
27	chr8:43794595-43794645	BJ	skin:	n/a
28	chr8:43794595-43794645	MCF-7	breast:	n/a
29	chr8:43794595-43794645	HMEC	breast:	n/a
30	chr8:43794595-43794645	A549	lung:	n/a
31	chr8:43794595-43794645	Jurkat	blood:	n/a
32	chr8:43794595-43794645	AG09319	gingival:	n/a
33	chr8:43794595-43794645	HepG2	liver:	n/a
34	chr8:43794595-43794645	ECC-1	luminal epithelium:	n/a
35	chr8:43794595-43794645	HPAEpiC	pulmonary alveolar:	n/a
36	chr8:43794595-43794645	CMK	blood:	n/a
37	chr8:43794595-43794645	SK-N-SH_RA	brain:	n/a
38	chr8:43794595-43794645	HIPEpiC	eye:	n/a
39	chr8:43794595-43794645	SK-N-SH	brain:	n/a
40	chr8:43794595-43794645	GM12878	blood:	n/a
41	chr8:43794595-43794645	HAEpiC	amniotic membrane:	n/a
42	chr8:43794595-43794645	NT2-D1	testis:	n/a
43	chr8:43794595-43794645	HCPEpiC	choroid plexus:	n/a
44	chr8:43794595-43794645	PFSK-1	brain:	n/a
45	chr8:43794595-43794645	HRCEpiC	kidney:	n/a
46	chr8:43794595-43794645	HCT-116	colon:	n/a
47	chr8:43794595-43794645	ProgFib	skin:	n/a
48	chr8:43794595-43794645	HCM	heart:	n/a
49	chr8:43794595-43794645	GM12892	blood:	n/a
50	chr8:43794595-43794645	RPTEC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:43092429..43093269-chr8:43823893..43824414,2	MCF-7	breast:
2	chr15:63385860..63386443-chr8:43553599..43554374,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNF170-9	chr8:43529413-43529734	NONHSAT126368
2	lnc-HGSNAT-12	chr8:43527966-43528218	NONHSAT126367

No data

Variant related genes	Relation type
ENSG00000253845	TF binding region
ENSG00000253198	TF binding region
ENSG00000253845	CpG island
ENSG00000253198	CpG island

Extended variants
information (count: 20866 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:20866 , 50 per page) page: 1 2 3 4 5 6 7 ... 418

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554903564	chr8:43504531-43504532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs552791049	chr8:43504533-43504534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs543675034	chr8:43504548-43504549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149662588	chr8:43504558-43504559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs532549109	chr8:43504575-43504576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs62516434	chr8:43504595-43504596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559177486	chr8:43504721-43504722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528132384	chr8:43504735-43504736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547877702	chr8:43504746-43504747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs568016551	chr8:43504749-43504750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530840125	chr8:43504750-43504751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs10101287	chr8:43504751-43504752	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs191770286	chr8:43504756-43504757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10104294	chr8:43504759-43504760	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs145419110	chr8:43504764-43504765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369149677	chr8:43504782-43504783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373221313	chr8:43504783-43504784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554560227	chr8:43504794-43504795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184315328	chr8:43504811-43504812	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs149818818	chr8:43504836-43504837	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs557218077	chr8:43504862-43504863	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs577066551	chr8:43504866-43504867	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs546081059	chr8:43504890-43504891	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs566412789	chr8:43504893-43504894	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs528180470	chr8:43504923-43504924	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs376187982	chr8:43504952-43504953	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs77277249	chr8:43504969-43504970	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs541872229	chr8:43504970-43504971	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs115194063	chr8:43504973-43504974	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs530496396	chr8:43504987-43504988	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs7461444	chr8:43504996-43504997	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs114109111	chr8:43505000-43505001	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs375518634	chr8:43505014-43505015	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs188103394	chr8:43505015-43505016	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs11984737	chr8:43505031-43505032	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs546487492	chr8:43505074-43505075	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs566626061	chr8:43505085-43505086	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs191513685	chr8:43505148-43505149	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs79888261	chr8:43505169-43505170	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs71239828	chr8:43505171-43505172	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs397745998	chr8:43505173-43505174	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs375266784	chr8:43505176-43505177	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs367824431	chr8:43505178-43505179	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs548257347	chr8:43505251-43505252	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs568152728	chr8:43505257-43505258	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs112707526	chr8:43505266-43505267	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs370522839	chr8:43505268-43505269	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs185425455	chr8:43505291-43505292	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs149205731	chr8:43505295-43505296	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs577467496	chr8:43505301-43505302	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Seminomas	18059402	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21785460	CNVD
Rhabdomyosarcoma	16790082	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	23813976	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20967226	CNVD
Bipolar disorder	19214233	CNVD

Chromatin state (count:1202 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:43502200-43504800	Weak transcription	Liver	Liver
2	chr8:43504800-43511800	ZNF genes & repeats	Liver	Liver
3	chr8:43505800-43507600	ZNF genes & repeats	Adipose Nuclei	Adipose
4	chr8:43506600-43508400	ZNF genes & repeats	Psoas Muscle	Psoas
5	chr8:43508600-43515000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr8:43509200-43515200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
7	chr8:43509600-43512000	ZNF genes & repeats	Adipose Nuclei	Adipose
8	chr8:43514200-43519600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
9	chr8:43515800-43521200	ZNF genes & repeats	Liver	Liver
10	chr8:43518200-43528000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr8:43522600-43532400	ZNF genes & repeats	Liver	Liver
12	chr8:43523200-43528400	ZNF genes & repeats	Adipose Nuclei	Adipose
13	chr8:43523400-43523800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr8:43525400-43527800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
15	chr8:43526600-43529400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
16	chr8:43529600-43530800	ZNF genes & repeats	Adipose Nuclei	Adipose
17	chr8:43531600-43532000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
18	chr8:43535200-43539600	ZNF genes & repeats	Liver	Liver
19	chr8:43538400-43541800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr8:43539800-43541600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
21	chr8:43540000-43540400	Active TSS	Fetal Heart	heart
22	chr8:43541800-43543800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr8:43543800-43545600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr8:43545200-43546200	ZNF genes & repeats	Liver	Liver
25	chr8:43552400-43552800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
26	chr8:43553600-43554200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
27	chr8:43554200-43555000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
28	chr8:43555600-43557000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
29	chr8:43565800-43568800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
30	chr8:43567000-43569000	ZNF genes & repeats	Psoas Muscle	Psoas
31	chr8:43567200-43568800	ZNF genes & repeats	Liver	Liver
32	chr8:43567400-43569800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr8:43571800-43573600	ZNF genes & repeats	Liver	Liver
34	chr8:43572200-43574600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr8:43572200-43576600	ZNF genes & repeats	Adipose Nuclei	Adipose
36	chr8:43575000-43579400	ZNF genes & repeats	Liver	Liver
37	chr8:43575400-43578400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
38	chr8:43575800-43576400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
39	chr8:43582200-43594800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr8:43582800-43584000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
41	chr8:43584800-43591400	ZNF genes & repeats	Liver	Liver
42	chr8:43585600-43588000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
43	chr8:43586600-43589600	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
44	chr8:43589200-43592000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
45	chr8:43591000-43592600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
46	chr8:43591400-43593400	ZNF genes & repeats	Adipose Nuclei	Adipose
47	chr8:43591800-43593800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
48	chr8:43592000-43594600	ZNF genes & repeats	Liver	Liver
49	chr8:43595800-43602200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr8:43603600-43605600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links