Variant report

Variant	nsv1016948
Chromosome Location	chr8:86850606-86861743
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:243)
CpG islands
(count:0)
Chromatin interactive
region (count:31)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:243 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:86851632-86852291	K562	blood:	n/a	n/a
2	ARID3A	chr8:86860947-86861211	K562	blood:	n/a	n/a
3	ARID3A	chr8:86860057-86860260	K562	blood:	n/a	n/a
4	ARID3A	chr8:86860674-86860711	K562	blood:	n/a	n/a
5	ARID3A	chr8:86855400-86856788	K562	blood:	n/a	chr8:86856408-86856424
6	ARID3A	chr8:86854067-86854193	K562	blood:	n/a	n/a
7	ATF1	chr8:86858572-86858850	K562	blood:	n/a	n/a
8	ATF1	chr8:86851680-86851940	K562	blood:	n/a	n/a
9	ATF3	chr8:86853960-86854338	K562	blood:	n/a	n/a
10	BACH1	chr8:86854704-86854857	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr8:86855556-86855909	K562	blood:	n/a	n/a
12	BHLHE40	chr8:86860851-86861210	K562	blood:	n/a	n/a
13	BHLHE40	chr8:86851452-86852081	K562	blood:	n/a	n/a
14	CBX3	chr8:86855246-86855994	K562	blood:	n/a	n/a
15	CCNT2	chr8:86851412-86851908	K562	blood:	n/a	n/a
16	CCNT2	chr8:86855767-86856007	K562	blood:	n/a	n/a
17	CEBPB	chr8:86855387-86855903	K562	blood:	n/a	n/a
18	CEBPB	chr8:86858744-86859178	K562	blood:	n/a	chr8:86858989-86859000
19	CEBPB	chr8:86853219-86853518	K562	blood:	n/a	n/a
20	CEBPB	chr8:86858898-86859037	HepG2	liver:	n/a	chr8:86858989-86859000
21	CEBPB	chr8:86854020-86854265	K562	blood:	n/a	n/a
22	CEBPB	chr8:86855485-86855973	MCF-7	breast:	n/a	n/a
23	CEBPB	chr8:86855406-86856007	MCF-7	breast:	n/a	n/a
24	CEBPB	chr8:86852999-86853917	MCF-7	breast:	n/a	chr8:86853134-86853151
25	CEBPB	chr8:86852955-86853850	MCF-7	breast:	n/a	chr8:86853134-86853151
26	CEBPD	chr8:86851586-86852041	K562	blood:	n/a	n/a
27	CHD2	chr8:86851732-86852074	K562	blood:	n/a	n/a
28	CHD2	chr8:86853434-86853507	K562	blood:	n/a	n/a
29	CTCF	chr8:86854180-86854330	MCF-7	breast:	n/a	n/a
30	CTCF	chr8:86855360-86855510	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr8:86855758-86855854	K562	blood:	n/a	n/a
32	CTCF	chr8:86851500-86851650	Caco-2	colon:	n/a	chr8:86851525-86851532
33	CTCF	chr8:86860120-86860270	HA-sp	spinal cord:	n/a	n/a
34	CTCF	chr8:86859106-86859175	GM20000	blood:	n/a	n/a
35	CTCF	chr8:86857379-86857443	Lung_OC	lung:	n/a	n/a
36	E2F4	chr8:86855498-86856242	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr8:86857600-86857775	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F6	chr8:86851911-86852046	K562	blood:	n/a	n/a
39	EGR1	chr8:86856731-86857029	K562	blood:	n/a	chr8:86856841-86856854 chr8:86856842-86856853 chr8:86856841-86856854 chr8:86856840-86856855
40	ELF1	chr8:86854642-86855194	MCF-7	breast:	n/a	n/a
41	EP300	chr8:86851550-86851956	K562	blood:	n/a	n/a
42	EP300	chr8:86860139-86860248	K562	blood:	n/a	n/a
43	EP300	chr8:86855763-86855933	GM12878	blood:	n/a	n/a
44	EP300	chr8:86855701-86855947	SK-N-SH_RA	brain:	n/a	n/a
45	EP300	chr8:86860870-86861152	K562	blood:	n/a	n/a
46	EP300	chr8:86852523-86853988	MCF-7	breast:	n/a	chr8:86853573-86853587 chr8:86853574-86853588 chr8:86852819-86852828
47	EP300	chr8:86855403-86856324	K562	blood:	n/a	chr8:86856156-86856165 chr8:86856113-86856127
48	EP300	chr8:86852876-86854010	MCF-7	breast:	n/a	chr8:86853573-86853587 chr8:86853574-86853588
49	ESR1	chr8:86853005-86853412	ECC-1	luminal epithelium:	n/a	chr8:86853223-86853240
50	ESR1	chr8:86852957-86853432	ECC-1	luminal epithelium:	n/a	chr8:86853223-86853240

No data

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:86852831..86853539-chr8:86919503..86920015,2	MCF-7	breast:
2	chr8:86364996..86367147-chr8:86853567..86855147,2	MCF-7	breast:
3	chr8:86855854..86858107-chr8:86860014..86862808,3	K562	blood:
4	chr8:86852142..86856180-chr8:86917083..86921619,8	MCF-7	breast:
5	chr8:86852235..86854715-chr8:86982807..86985769,2	MCF-7	breast:
6	chr8:86372229..86378702-chr8:86846475..86858080,32	MCF-7	breast:
7	chr8:86853963..86856746-chr8:86949985..86952408,2	K562	blood:
8	chr8:86855854..86858107-chr8:86860014..86862808,3	K562	blood:
9	chr8:86854583..86856864-chr8:86887493..86890271,2	MCF-7	breast:
10	chr8:86853239..86855562-chr8:86941096..86942635,2	MCF-7	breast:
11	chr8:86375109..86376361-chr8:86852746..86853757,4	MCF-7	breast:
12	chr8:86853239..86855144-chr8:86935082..86937255,2	MCF-7	breast:
13	chr8:86855854..86858675-chr8:86858692..86862985,4	K562	blood:
14	chr8:86849937..86852745-chr8:86855936..86857800,2	K562	blood:
15	chr8:86373353..86377706-chr8:86848632..86856784,15	MCF-7	breast:
16	chr8:86853963..86856698-chr8:86950908..86953530,2	K562	blood:
17	chr8:86853468..86855962-chr8:86866121..86867816,2	MCF-7	breast:
18	chr8:86464673..86465447-chr8:86852772..86853973,3	MCF-7	breast:
19	chr8:86849418..86851109-chr8:86874092..86876828,2	MCF-7	breast:
20	chr8:86854256..86855844-chr8:86962935..86965322,2	K562	blood:
21	chr8:86852107..86854370-chr8:86972859..86974722,2	MCF-7	breast:
22	chr8:86855854..86858675-chr8:86858692..86862985,4	K562	blood:
23	chr8:86855992..86858469-chr8:86859660..86861283,2	MCF-7	breast:
24	chr3:61613244..61613971-chr8:86852933..86853873,2	MCF-7	breast:
25	chr8:86854974..86856986-chr8:86861959..86864314,2	MCF-7	breast:
26	chr8:86849039..86851736-chr8:87015052..87016845,2	MCF-7	breast:
27	chr16:75285561..75287264-chr8:86851129..86852972,2	MCF-7	breast:
28	chr8:86855992..86858469-chr8:86859660..86861283,2	MCF-7	breast:
29	chr8:86850726..86853148-chr8:86853230..86857704,4	K562	blood:
30	chr8:86852733..86854770-chr8:86972857..86974930,2	K562	blood:
31	chr8:86852831..86853452-chr8:86919492..86920015,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP6V0D2-2	chr8:86851934-86852014	NONHSAT127540
2	lnc-ATP6V0D2-2	chr8:86851934-86852014	ENSG00000253154

No data

Variant related genes	Relation type
ENSG00000253154	TF binding region
ENSG00000253549	chromatin interactions
ENSG00000104267	chromatin interactions
ENSG00000253154	chromatin interactions
ENSG00000050820	chromatin interactions

Extended variants
information (count: 360 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:360 , 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	rs185769744	chr8:86850675-86850676	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs533002678	chr8:86850739-86850740	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs549803537	chr8:86850761-86850762	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs74682239	chr8:86850798-86850799	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs529041395	chr8:86850809-86850810	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs573521703	chr8:86850840-86850841	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs190279100	chr8:86850878-86850879	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs111453400	chr8:86850897-86850898	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs534493264	chr8:86850933-86850934	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs554187721	chr8:86851045-86851046	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs570975007	chr8:86851059-86851060	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs540840845	chr8:86851109-86851110	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs183252075	chr8:86851145-86851146	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs187634750	chr8:86851183-86851184	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs576124675	chr8:86851192-86851193	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs541947034	chr8:86851201-86851202	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs555325721	chr8:86851202-86851203	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs572122390	chr8:86851233-86851234	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs142330557	chr8:86851240-86851241	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs536403154	chr8:86851275-86851276	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs562809861	chr8:86851278-86851279	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs5892957	chr8:86851279-86851280	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs369298435	chr8:86851280-86851281	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs151282465	chr8:86851282-86851283	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs373881834	chr8:86851283-86851284	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs543243695	chr8:86851286-86851287	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs556450138	chr8:86851287-86851288	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs11358933	chr8:86851288-86851289	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs528977013	chr8:86851317-86851318	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs73688536	chr8:86851319-86851320	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs565648854	chr8:86851338-86851339	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs528074962	chr8:86851368-86851369	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs548027491	chr8:86851416-86851417	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs571045435	chr8:86851431-86851432	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs540172717	chr8:86851439-86851440	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs556315918	chr8:86851495-86851496	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs529020497	chr8:86851536-86851537	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs529146436	chr8:86851543-86851544	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs569949142	chr8:86851558-86851559	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs535521039	chr8:86851565-86851566	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs555463236	chr8:86851693-86851694	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs572061899	chr8:86851699-86851700	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs534718271	chr8:86851710-86851711	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs558173891	chr8:86851713-86851714	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs577858342	chr8:86851775-86851776	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs190855284	chr8:86851785-86851786	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs550617368	chr8:86851858-86851859	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs140624209	chr8:86851874-86851875	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs562379263	chr8:86851935-86851936	Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
50	rs80232238	chr8:86851962-86851963	Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	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
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Acute monocytic leukemia	16498392	CNVD
Autism	20841430	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:191 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86846800-86851600	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr8:86847400-86851200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:86848200-86854800	Weak transcription	Osteobl	bone
4	chr8:86848400-86851400	Weak transcription	Stomach Mucosa	stomach
5	chr8:86848400-86855000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr8:86848600-86851200	Weak transcription	Placenta	Placenta
7	chr8:86849200-86851200	Weak transcription	K562	blood
8	chr8:86849400-86850800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr8:86849400-86852800	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr8:86849400-86852800	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr8:86849600-86852800	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr8:86849600-86854000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr8:86849600-86854400	Weak transcription	Fetal Lung	lung
14	chr8:86849600-86855400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:86849800-86852200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr8:86849800-86854200	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr8:86849800-86855200	Weak transcription	NH-A	brain
18	chr8:86850000-86851400	Weak transcription	Brain Angular Gyrus	brain
19	chr8:86850000-86852600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr8:86850000-86853000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr8:86850000-86853200	Weak transcription	Brain Cingulate Gyrus	brain
22	chr8:86850000-86855200	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr8:86850000-86859000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr8:86850000-86861000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr8:86850200-86859000	Weak transcription	Brain Anterior Caudate	brain
26	chr8:86850400-86851400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr8:86850400-86851400	Weak transcription	HMEC	breast
28	chr8:86850400-86852200	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr8:86850400-86852400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr8:86850400-86852600	Weak transcription	NHEK	skin
31	chr8:86850400-86852800	Weak transcription	Hela-S3	cervix
32	chr8:86850400-86853600	Weak transcription	Brain Substantia Nigra	brain
33	chr8:86850400-86853800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr8:86850400-86854400	Weak transcription	Fetal Muscle Leg	muscle
35	chr8:86850400-86855000	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr8:86850400-86855000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr8:86850400-86855000	Weak transcription	Brain Hippocampus Middle	brain
38	chr8:86850600-86853200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr8:86850800-86853600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr8:86851200-86851400	Enhancers	K562	blood
41	chr8:86851200-86851600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr8:86851400-86851600	Enhancers	Brain Angular Gyrus	brain
43	chr8:86851400-86851600	Enhancers	Stomach Mucosa	stomach
44	chr8:86851400-86851600	Enhancers	HMEC	breast
45	chr8:86851400-86851800	Flanking Active TSS	K562	blood
46	chr8:86851400-86852400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr8:86851600-86852000	Weak transcription	HMEC	breast
48	chr8:86851600-86852200	Weak transcription	Stomach Mucosa	stomach
49	chr8:86851600-86853000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr8:86851600-86853800	Weak transcription	Cortex derived primary cultured neurospheres	brain

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