Variant report

Variant	nsv976927
Chromosome Location	chr15:42862948-42868443
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:463)
CpG islands
(count:673)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:463 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:42867471-42867507	K562	blood:	n/a	n/a
2	ARID3A	chr15:42867503-42867684	HepG2	liver:	n/a	n/a
3	BACH1	chr15:42867244-42868133	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr15:42867207-42867565	GM12878	blood:	n/a	n/a
5	BHLHE40	chr15:42867126-42868327	K562	blood:	n/a	chr15:42867776-42867792 chr15:42867765-42867781
6	BHLHE40	chr15:42867038-42868340	GM12878	blood:	n/a	chr15:42867776-42867792 chr15:42867765-42867781
7	BHLHE40	chr15:42867207-42868103	HepG2	liver:	n/a	chr15:42867776-42867792 chr15:42867765-42867781
8	BHLHE40	chr15:42866649-42866654	K562	blood:	n/a	n/a
9	BHLHE40	chr15:42867233-42867556	A549	lung:	n/a	n/a
10	BRCA1	chr15:42867171-42867861	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr15:42866894-42868477	K562	blood:	n/a	n/a
12	CBX3	chr15:42867193-42867650	K562	blood:	n/a	n/a
13	CCNT2	chr15:42867230-42868278	K562	blood:	n/a	chr15:42868077-42868086
14	CEBPB	chr15:42867557-42867674	Hela-S3	cervix:	n/a	n/a
15	CEBPD	chr15:42867530-42867895	HepG2	liver:	n/a	n/a
16	CEBPD	chr15:42866559-42866867	K562	blood:	n/a	n/a
17	CEBPD	chr15:42867225-42868075	HepG2	liver:	n/a	n/a
18	CHD1	chr15:42867119-42867328	GM12878	blood:	n/a	n/a
19	CHD1	chr15:42867949-42868231	GM12878	blood:	n/a	n/a
20	CHD2	chr15:42867215-42868277	GM12878	blood:	n/a	n/a
21	CHD2	chr15:42867087-42868355	Hela-S3	cervix:	n/a	n/a
22	CHD2	chr15:42867297-42868030	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr15:42867244-42868221	HepG2	liver:	n/a	n/a
24	CHD2	chr15:42867951-42868219	K562	blood:	n/a	n/a
25	CHD2	chr15:42867366-42867658	K562	blood:	n/a	n/a
26	CREB1	chr15:42867258-42868207	A549	lung:	n/a	n/a
27	CREB1	chr15:42867069-42868412	HepG2	liver:	n/a	n/a
28	CTCF	chr15:42867840-42867990	GM12871	blood:	n/a	n/a
29	CTCF	chr15:42867362-42867493	Spleen_OC	spleen:	n/a	n/a
30	CTCF	chr15:42868040-42868190	HCFaa	heart:	n/a	n/a
31	CTCF	chr15:42868040-42868190	BJ	skin:	n/a	n/a
32	CTCF	chr15:42867940-42868090	HCM	heart:	n/a	n/a
33	CTCF	chr15:42867860-42868010	AG04449	skin:	n/a	n/a
34	CTCF	chr15:42868060-42868210	GM12867	blood:	n/a	n/a
35	CTCF	chr15:42867923-42868144	K562	blood:	n/a	n/a
36	CTCF	chr15:42868080-42868230	GM12870	blood:	n/a	n/a
37	CTCF	chr15:42868040-42868190	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr15:42867980-42868130	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr15:42868020-42868170	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr15:42867300-42867450	GM12869	blood:	n/a	n/a
41	CTCF	chr15:42868100-42868250	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr15:42867980-42868130	AG09319	gingival:	n/a	n/a
43	CTCF	chr15:42868000-42868150	GM06990	blood:	n/a	n/a
44	CTCF	chr15:42867920-42868070	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr15:42867980-42868130	GM12875	blood:	n/a	n/a
46	CTCF	chr15:42867880-42868030	Caco-2	colon:	n/a	n/a
47	CTCF	chr15:42867680-42867830	AG04449	skin:	n/a	n/a
48	CTCF	chr15:42868020-42868170	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr15:42867980-42868130	AG10803	skin:	n/a	n/a
50	CTCF	chr15:42868160-42868310	HVMF	connective:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:42867338-42867388	K562	blood:	n/a
2	chr15:42867875-42867925	ovcar-3	ovarian:	n/a
3	chr15:42867338-42867388	K562	blood:	n/a
4	chr15:42867875-42867925	ovcar-3	ovarian:	n/a
5	chr15:42868114-42868164	ProgFib	skin:	n/a
6	chr15:42867567-42867617	SAEC	small airway:	n/a
7	chr15:42867567-42867617	HRE	kidney:	n/a
8	chr15:42867567-42867617	IMR90	lung:	fetal
9	chr15:42867590-42867640	AG09309	skin:	n/a
10	chr15:42867856-42867906	NH-A	brain:	n/a
11	chr15:42867567-42867617	SKMC	muscle:	n/a
12	chr15:42867875-42867925	Hepatocyte	liver:	n/a
13	chr15:42868443-42868493	GM06990	blood:	n/a
14	chr15:42867856-42867906	HIPEpiC	eye:	n/a
15	chr15:42867888-42867938	BE2_C	brain:	n/a
16	chr15:42867338-42867388	Hepatocyte	liver:	n/a
17	chr15:42867590-42867640	PrEC	prostate:	n/a
18	chr15:42866523-42866573	MCF-7	breast:	n/a
19	chr15:42864583-42864633	NHDF-neo	bronchial:	n/a
20	chr15:42867303-42867353	ProgFib	skin:	n/a
21	chr15:42867856-42867906	HUVEC	blood vessel:	n/a
22	chr15:42867303-42867353	K562	blood:	n/a
23	chr15:42867567-42867617	AG10803	skin:	n/a
24	chr15:42868443-42868493	AG10803	skin:	n/a
25	chr15:42867338-42867388	NHDF-neo	bronchial:	n/a
26	chr15:42867856-42867906	SKMC	muscle:	n/a
27	chr15:42868114-42868164	ECC-1	luminal epithelium:	n/a
28	chr15:42867888-42867938	Caco-2	colon:	n/a
29	chr15:42867567-42867617	A549	lung:	n/a
30	chr15:42868114-42868164	RPTEC	kidney:	n/a
31	chr15:42867875-42867925	AG04449	skin:	fetal
32	chr15:42867590-42867640	HIPEpiC	eye:	n/a
33	chr15:42867888-42867938	MCF10A-Er-Src	breast:	n/a
34	chr15:42867856-42867906	SK-N-SH_RA	brain:	n/a
35	chr15:42864583-42864633	A549	lung:	n/a
36	chr15:42867888-42867938	Hepatocyte	liver:	n/a
37	chr15:42866523-42866573	AG04450	lung:	fetal
38	chr15:42864583-42864633	SKMC	muscle:	n/a
39	chr15:42867338-42867388	A549	lung:	n/a
40	chr15:42866523-42866573	HUVEC	blood vessel:	n/a
41	chr15:42866523-42866573	GM12892	blood:	n/a
42	chr15:42867856-42867906	NB4	blood:	n/a
43	chr15:42868114-42868164	GM12891	blood:	n/a
44	chr15:42867567-42867617	K562	blood:	n/a
45	chr15:42867338-42867388	HPAEpiC	pulmonary alveolar:	n/a
46	chr15:42868114-42868164	GM12892	blood:	n/a
47	chr15:42867590-42867640	U87	brain:	n/a
48	chr15:42867888-42867938	H1-hESC	embryonic stem cell:	embryo
49	chr15:42867590-42867640	PFSK-1	brain:	n/a
50	chr15:42867567-42867617	HEEpiC	esophagus:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:42867986..42870891-chr15:43024060..43026740,2	K562	blood:
2	chr15:42801179..42804150-chr15:42867351..42869271,2	K562	blood:
3	chr15:42854171..42864590-chr15:42864872..42869799,12	K562	blood:
4	chr1:155903608..155904383-chr15:42867723..42868723,3	Hela-S3	cervix:
5	chr15:42785710..42787693-chr15:42866156..42868186,2	K562	blood:
6	chr15:42862243..42864590-chr15:42865875..42867418,2	K562	blood:
7	chr15:42866281..42869584-chr15:42871180..42873707,4	K562	blood:
8	chr15:42840104..42842482-chr15:42865653..42867827,2	K562	blood:
9	chr11:71791137..71792001-chr15:42866964..42867628,2	Hela-S3	cervix:
10	chr15:42842458..42844772-chr15:42862212..42863902,2	K562	blood:
11	chr15:42838345..42842657-chr15:42865696..42868936,4	MCF-7	breast:
12	chr15:42838709..42841070-chr15:42866779..42868984,2	MCF-7	breast:
13	chr15:42867826..42868650-chr21:36260005..36261002,2	Hela-S3	cervix:
14	chr15:42840090..42842755-chr15:42865653..42870684,5	K562	blood:
15	chr15:42866660..42868750-chr15:42872207..42873779,2	K562	blood:
16	chr15:42783274..42784836-chr15:42864927..42867645,2	K562	blood:
17	chr15:42854171..42864590-chr15:42864872..42869799,12	K562	blood:

No data

Variant related genes	Relation type
STARD9	TF binding region
ENSG00000261822	TF binding region
ENSG00000260490	TF binding region
STARD9	CpG island
ENSG00000261822	CpG island
ENSG00000260490	CpG island
ENSG00000137814	chromatin interactions
ENSG00000260282	chromatin interactions
ENSG00000092531	chromatin interactions
ENSG00000260490	chromatin interactions
ENSG00000184154	chromatin interactions
ENSG00000159216	chromatin interactions
ENSG00000159433	chromatin interactions
ENSG00000132680	chromatin interactions
ENSG00000137497	chromatin interactions
ENSG00000261822	chromatin interactions
ENSG00000103994	chromatin interactions
ENSG00000180979	chromatin interactions

Extended variants
information (count: 199 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:199 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528208084	chr15:42862992-42862993	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs551534352	chr15:42863019-42863020	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs536854089	chr15:42863052-42863053	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs73406544	chr15:42863107-42863108	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs202185661	chr15:42863184-42863185	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs201124004	chr15:42863185-42863186	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs368055240	chr15:42863201-42863202	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs144618686	chr15:42863242-42863243	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs372814321	chr15:42863245-42863246	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs573677105	chr15:42863287-42863288	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs181633159	chr15:42863341-42863342	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs550594238	chr15:42863369-42863370	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs567564848	chr15:42863372-42863373	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs553662387	chr15:42863413-42863414	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs372569378	chr15:42863421-42863422	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs145649721	chr15:42863429-42863430	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs73406545	chr15:42863490-42863491	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs62019315	chr15:42863542-42863543	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs560393707	chr15:42863562-42863563	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs185531006	chr15:42863572-42863573	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs34878389	chr15:42863581-42863582	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs8029970	chr15:42863588-42863589	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs537257006	chr15:42863594-42863595	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs188674760	chr15:42863626-42863627	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs367619702	chr15:42863631-42863632	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs574294514	chr15:42863648-42863649	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs542222860	chr15:42863651-42863652	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs559283027	chr15:42863652-42863653	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs572905619	chr15:42863676-42863677	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs556190600	chr15:42863706-42863707	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs545124404	chr15:42863744-42863745	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs148160970	chr15:42863746-42863747	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs181435105	chr15:42863753-42863754	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs111515690	chr15:42863783-42863784	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs138405876	chr15:42863823-42863824	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs560996932	chr15:42863827-42863828	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs186022383	chr15:42863852-42863853	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs190895127	chr15:42863868-42863869	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs150242543	chr15:42863870-42863871	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs183944098	chr15:42863873-42863874	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs542476582	chr15:42863892-42863893	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs138862331	chr15:42863894-42863895	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs200448986	chr15:42863965-42863966	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs201393967	chr15:42863967-42863968	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs67477577	chr15:42863968-42863969	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs112404001	chr15:42863969-42863970	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs3036822	chr15:42863970-42863971	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs186290721	chr15:42863979-42863980	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs143223609	chr15:42864024-42864025	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs573403356	chr15:42864034-42864035	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Melanoma	17363583	CNVD
Cancer	20164919	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:507 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42841600-42866800	Weak transcription	Stomach Mucosa	stomach
2	chr15:42841800-42867000	Weak transcription	Ovary	ovary
3	chr15:42842200-42867000	Weak transcription	Psoas Muscle	Psoas
4	chr15:42842400-42867000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr15:42842600-42867400	Weak transcription	Small Intestine	intestine
6	chr15:42842800-42867000	Weak transcription	Fetal Kidney	kidney
7	chr15:42843000-42863000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr15:42849400-42866800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr15:42851600-42866600	Weak transcription	Fetal Heart	heart
10	chr15:42852000-42867000	Weak transcription	Colonic Mucosa	Colon
11	chr15:42854200-42867000	Weak transcription	HSMMtube	muscle
12	chr15:42854800-42867000	Weak transcription	Pancreas	Pancrea
13	chr15:42855000-42864400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr15:42855200-42867000	Weak transcription	Esophagus	oesophagus
15	chr15:42855200-42867800	Weak transcription	Aorta	Aorta
16	chr15:42856000-42867000	Weak transcription	A549	lung
17	chr15:42857600-42867000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr15:42857800-42867200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr15:42857800-42867200	Weak transcription	Spleen	Spleen
20	chr15:42858000-42867000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr15:42858200-42867000	Weak transcription	Right Ventricle	heart
22	chr15:42858400-42866400	Weak transcription	Rectal Smooth Muscle	rectum
23	chr15:42858800-42867000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr15:42858800-42867000	Weak transcription	Brain Substantia Nigra	brain
25	chr15:42858800-42867000	Weak transcription	Colon Smooth Muscle	Colon
26	chr15:42859000-42867200	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr15:42859000-42868000	Weak transcription	Fetal Brain Male	brain
28	chr15:42859200-42866400	Weak transcription	HepG2	liver
29	chr15:42859200-42867000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr15:42859200-42867000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
31	chr15:42859200-42867000	Weak transcription	Brain Angular Gyrus	brain
32	chr15:42859200-42867000	Weak transcription	Fetal Lung	lung
33	chr15:42859200-42867000	Weak transcription	HSMM	muscle
34	chr15:42859200-42867000	Weak transcription	NH-A	brain
35	chr15:42859200-42867000	Weak transcription	NHEK	skin
36	chr15:42859400-42866800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
37	chr15:42859400-42866800	Weak transcription	Hela-S3	cervix
38	chr15:42859400-42867000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr15:42859400-42867000	Weak transcription	Primary T helper cells PMA-I stimulated	--
40	chr15:42859400-42867000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr15:42859400-42867800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr15:42859600-42863600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr15:42859600-42866400	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr15:42859600-42866400	Weak transcription	K562	blood
45	chr15:42859600-42866600	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr15:42859600-42866800	Weak transcription	Fetal Muscle Leg	muscle
47	chr15:42859600-42866800	Weak transcription	Placenta	Placenta
48	chr15:42859600-42867000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr15:42859600-42867000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
50	chr15:42859600-42867000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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