Variant report

Variant	nsv830424
Chromosome Location	chr5:99298081-99476578
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:786)
CpG islands
(count:366)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:786 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:99379244-99379565	GM12878	blood:	n/a	n/a
2	ATF2	chr5:99379165-99379540	GM12878	blood:	n/a	n/a
3	BACH1	chr5:99384887-99385260	K562	blood:	n/a	n/a
4	BATF	chr5:99432041-99432354	GM12878	blood:	n/a	n/a
5	BATF	chr5:99382105-99382281	GM12878	blood:	n/a	n/a
6	BATF	chr5:99389500-99389704	GM12878	blood:	n/a	n/a
7	BATF	chr5:99388507-99388698	GM12878	blood:	n/a	n/a
8	BATF	chr5:99382104-99382381	GM12878	blood:	n/a	n/a
9	BATF	chr5:99389889-99390099	GM12878	blood:	n/a	n/a
10	BATF	chr5:99389499-99389705	GM12878	blood:	n/a	n/a
11	BATF	chr5:99432046-99432361	GM12878	blood:	n/a	n/a
12	BATF	chr5:99385890-99386051	GM12878	blood:	n/a	n/a
13	BATF	chr5:99385000-99385307	GM12878	blood:	n/a	n/a
14	BATF	chr5:99384368-99384728	GM12878	blood:	n/a	n/a
15	BATF	chr5:99388504-99388666	GM12878	blood:	n/a	n/a
16	BATF	chr5:99379238-99379445	GM12878	blood:	n/a	n/a
17	BATF	chr5:99388145-99388297	GM12878	blood:	n/a	n/a
18	BATF	chr5:99383113-99383549	GM12878	blood:	n/a	n/a
19	BATF	chr5:99383118-99383547	GM12878	blood:	n/a	n/a
20	BATF	chr5:99389007-99389272	GM12878	blood:	n/a	n/a
21	BATF	chr5:99384412-99384822	GM12878	blood:	n/a	n/a
22	BATF	chr5:99384985-99385295	GM12878	blood:	n/a	n/a
23	BATF	chr5:99379275-99379445	GM12878	blood:	n/a	n/a
24	BATF	chr5:99387907-99388092	GM12878	blood:	n/a	n/a
25	BCL11A	chr5:99387915-99388066	GM12878	blood:	n/a	n/a
26	BCL11A	chr5:99389507-99389698	GM12878	blood:	n/a	n/a
27	BCL11A	chr5:99385767-99386189	GM12878	blood:	n/a	n/a
28	BCL11A	chr5:99383178-99383545	H1-hESC	embryonic stem cell:	n/a	n/a
29	BCL11A	chr5:99432032-99432400	GM12878	blood:	n/a	n/a
30	BCL11A	chr5:99388377-99388810	GM12878	blood:	n/a	n/a
31	BCL11A	chr5:99384943-99385335	GM12878	blood:	n/a	n/a
32	BCL11A	chr5:99385899-99386040	GM12878	blood:	n/a	n/a
33	BCL11A	chr5:99382065-99382284	GM12878	blood:	n/a	n/a
34	BCL11A	chr5:99388998-99389358	GM12878	blood:	n/a	n/a
35	BCL11A	chr5:99384271-99384770	GM12878	blood:	n/a	n/a
36	BCL11A	chr5:99383106-99383811	GM12878	blood:	n/a	n/a
37	BCL11A	chr5:99384966-99385376	GM12878	blood:	n/a	n/a
38	BCL11A	chr5:99383124-99383473	GM12878	blood:	n/a	n/a
39	BCL11A	chr5:99388493-99388759	GM12878	blood:	n/a	n/a
40	BCL11A	chr5:99381820-99382422	GM12878	blood:	n/a	n/a
41	BCL11A	chr5:99384419-99384722	GM12878	blood:	n/a	n/a
42	BCL11A	chr5:99387897-99388305	GM12878	blood:	n/a	n/a
43	BCL11A	chr5:99389955-99390140	GM12878	blood:	n/a	n/a
44	BCL11A	chr5:99389488-99389768	GM12878	blood:	n/a	n/a
45	BCL11A	chr5:99388153-99388292	GM12878	blood:	n/a	n/a
46	BHLHE40	chr5:99388899-99389375	HepG2	liver:	n/a	n/a
47	BHLHE40	chr5:99389491-99389718	HepG2	liver:	n/a	n/a
48	BHLHE40	chr5:99384917-99385380	HepG2	liver:	n/a	n/a
49	BHLHE40	chr5:99387743-99388449	HepG2	liver:	n/a	n/a
50	BHLHE40	chr5:99390309-99390484	HepG2	liver:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:99381840-99381890	ECC-1	luminal epithelium:	n/a
2	chr5:99389821-99389871	NB4	blood:	n/a
3	chr5:99382144-99382194	CMK	blood:	n/a
4	chr5:99381964-99382014	HNPCEpiC	eye:	n/a
5	chr5:99382140-99382190	PrEC	prostate:	n/a
6	chr5:99388688-99388738	GM12892	blood:	n/a
7	chr5:99381840-99381890	Hela-S3	cervix:	n/a
8	chr5:99381964-99382014	K562	blood:	n/a
9	chr5:99381964-99382014	RPTEC	kidney:	n/a
10	chr5:99388688-99388738	HEEpiC	esophagus:	n/a
11	chr5:99382140-99382190	IMR90	lung:	fetal
12	chr5:99381840-99381890	NHDF-neo	bronchial:	n/a
13	chr5:99382144-99382194	BE2_C	brain:	n/a
14	chr5:99381964-99382014	NHBE	bronchial:	n/a
15	chr5:99389821-99389871	HCF	heart:	n/a
16	chr5:99381964-99382014	HUVEC	blood vessel:	n/a
17	chr5:99382144-99382194	PrEC	prostate:	n/a
18	chr5:99389821-99389871	AG04449	skin:	fetal
19	chr5:99389821-99389871	U87	brain:	n/a
20	chr5:99388688-99388738	GM19239	blood:	n/a
21	chr5:99382144-99382194	PFSK-1	brain:	n/a
22	chr5:99382144-99382194	LNCaP	prostate:	n/a
23	chr5:99381964-99382014	IMR90	lung:	fetal
24	chr5:99381964-99382014	NT2-D1	testis:	n/a
25	chr5:99382140-99382190	NHBE	bronchial:	n/a
26	chr5:99381840-99381890	BJ	skin:	n/a
27	chr5:99381964-99382014	NB4	blood:	n/a
28	chr5:99381840-99381890	SK-N-MC	brain:	n/a
29	chr5:99389821-99389871	AG09309	skin:	n/a
30	chr5:99381840-99381890	HCT-116	colon:	n/a
31	chr5:99388688-99388738	NHBE	bronchial:	n/a
32	chr5:99382144-99382194	BJ	skin:	n/a
33	chr5:99382140-99382190	BJ	skin:	n/a
34	chr5:99389821-99389871	LNCaP	prostate:	n/a
35	chr5:99382140-99382190	NHDF-neo	bronchial:	n/a
36	chr5:99382144-99382194	NHDF-neo	bronchial:	n/a
37	chr5:99389821-99389871	GM12892	blood:	n/a
38	chr5:99381964-99382014	HCM	heart:	n/a
39	chr5:99388688-99388738	PFSK-1	brain:	n/a
40	chr5:99381840-99381890	HRPEpiC	eye:	n/a
41	chr5:99381840-99381890	SK-N-SH_RA	brain:	n/a
42	chr5:99381964-99382014	SK-N-SH	brain:	n/a
43	chr5:99389821-99389871	NT2-D1	testis:	n/a
44	chr5:99389821-99389871	H1-hESC	embryonic stem cell:	embryo
45	chr5:99389821-99389871	BE2_C	brain:	n/a
46	chr5:99382144-99382194	A549	lung:	n/a
47	chr5:99381964-99382014	AG04450	lung:	fetal
48	chr5:99382144-99382194	GM12891	blood:	n/a
49	chr5:99382140-99382190	CMK	blood:	n/a
50	chr5:99382140-99382190	LNCaP	prostate:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:99354562..99356518-chr5:99358881..99360827,2	K562	blood:
2	chr5:99444286..99447276-chr5:99447518..99449591,2	MCF-7	breast:
3	chr5:99336948..99339437-chr5:99341088..99343626,2	K562	blood:
4	chr5:99354562..99356518-chr5:99358881..99360827,2	K562	blood:
5	chr5:99336948..99339437-chr5:99341088..99343626,2	K562	blood:
6	chr5:99444286..99447276-chr5:99447518..99449591,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ST8SIA4-10	chr5:99386063-99386354	NONHSAT102989
2	lnc-FAM174A-4	chr5:99382154-99382674	NONHSAT102986

No data

Variant related genes	Relation type
ENSG00000270230	TF binding region
ENSG00000271480	TF binding region
ENSG00000270225	TF binding region
EEF1A1P20	TF binding region
ENSG00000270350	TF binding region
ENSG00000270388	TF binding region
ENSG00000264839	TF binding region
MTATP6P2	TF binding region
MTND5P10	TF binding region
ENSG00000199378	TF binding region
ENSG00000270232	TF binding region
ENSG00000270906	TF binding region
ENSG00000271207	TF binding region
ENSG00000270230	CpG island
ENSG00000271480	CpG island
ENSG00000270225	CpG island
EEF1A1P20	CpG island
ENSG00000270350	CpG island
ENSG00000270388	CpG island
ENSG00000264839	CpG island
MTATP6P2	CpG island
MTND5P10	CpG island
ENSG00000199378	CpG island
ENSG00000270232	CpG island
ENSG00000270906	CpG island
ENSG00000271207	CpG island

Extended variants
information (count: 1596 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1596 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186304778	chr5:99303439-99303440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs537625664	chr5:99303454-99303455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs556058328	chr5:99303486-99303487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs190808704	chr5:99303529-99303530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543016367	chr5:99303536-99303537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs10038624	chr5:99303557-99303558	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs573186897	chr5:99303596-99303597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs148745873	chr5:99303661-99303662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs141715915	chr5:99303686-99303687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs183034689	chr5:99303723-99303724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs113413748	chr5:99303732-99303733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs150567594	chr5:99303812-99303813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs563185225	chr5:99303829-99303830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139589257	chr5:99303845-99303846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs187371824	chr5:99303848-99303849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs566386967	chr5:99303865-99303866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs149743758	chr5:99303879-99303880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs201198712	chr5:99303884-99303885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs147443996	chr5:99303895-99303896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs115206007	chr5:99303903-99303904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs369780501	chr5:99303931-99303932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs547530800	chr5:99305806-99305807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191486433	chr5:99305834-99305835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559601243	chr5:99305835-99305836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs117165887	chr5:99305841-99305842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs13163913	chr5:99305937-99305938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs116267557	chr5:99305971-99305972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538222130	chr5:99306004-99306005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184372605	chr5:99306027-99306028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574840055	chr5:99306070-99306071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535679184	chr5:99306073-99306074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188810463	chr5:99306076-99306077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572543799	chr5:99306143-99306144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370751255	chr5:99306161-99306162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs546128966	chr5:99306162-99306163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs558013239	chr5:99306189-99306190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569799879	chr5:99306207-99306208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10061652	chr5:99306209-99306210	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs542980861	chr5:99306283-99306284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149065156	chr5:99306289-99306290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs33977980	chr5:99306329-99306330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201271869	chr5:99306332-99306333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570679269	chr5:99306369-99306370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540766308	chr5:99306400-99306401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559542772	chr5:99306451-99306452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564229798	chr5:99306454-99306455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142128910	chr5:99306456-99306457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551728934	chr5:99306461-99306462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs10054880	chr5:99306483-99306484	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs553346543	chr5:99306497-99306498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	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
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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	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
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	22522925	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:99303400-99304000	Enhancers	HUVEC	blood vessel
2	chr5:99305800-99309200	Weak transcription	Fetal Lung	lung
3	chr5:99309200-99309400	Enhancers	Fetal Lung	lung
4	chr5:99311000-99311400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:99311400-99312600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr5:99312600-99313000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr5:99340200-99341200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr5:99340200-99341200	Enhancers	NHEK	skin
9	chr5:99345200-99345400	ZNF genes & repeats	Gastric	stomach
10	chr5:99351000-99353200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr5:99351200-99351400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr5:99351400-99353200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr5:99351600-99352600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr5:99352600-99353200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr5:99352600-99355000	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr5:99353200-99353600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr5:99353200-99353600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr5:99353200-99354000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr5:99353600-99354000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr5:99353600-99355400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr5:99354000-99355200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr5:99359000-99360200	Enhancers	Fetal Lung	lung
23	chr5:99360200-99363600	Weak transcription	Fetal Lung	lung
24	chr5:99360800-99361000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr5:99361200-99361600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr5:99361200-99361600	Bivalent/Poised TSS	GM12878-XiMat	blood
27	chr5:99361200-99361600	Active TSS	HSMM	muscle
28	chr5:99361200-99361600	Active TSS	HUVEC	blood vessel
29	chr5:99361400-99361600	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
30	chr5:99363600-99364000	Enhancers	Fetal Lung	lung
31	chr5:99374800-99375800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr5:99375000-99376200	Enhancers	Brain Germinal Matrix	brain
33	chr5:99375400-99375800	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr5:99375400-99375800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr5:99378400-99379000	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr5:99378400-99379200	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr5:99416400-99417200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr5:99458200-99458600	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr5:99458400-99458800	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr5:99458400-99458800	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr5:99458400-99459000	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr5:99458600-99459000	Enhancers	Fetal Brain Male	brain
43	chr5:99458800-99459000	Enhancers	Fetal Lung	lung
44	chr5:99459000-99459800	Weak transcription	Fetal Lung	lung
45	chr5:99459000-99460800	Weak transcription	Fetal Brain Male	brain
46	chr5:99459800-99461400	Enhancers	Fetal Lung	lung
47	chr5:99460800-99461400	Enhancers	Fetal Brain Male	brain
48	chr5:99461200-99461400	Enhancers	Fetal Kidney	kidney
49	chr5:99461400-99464000	Weak transcription	Fetal Kidney	kidney
50	chr5:99464000-99464200	Enhancers	Fetal Kidney	kidney

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