Variant report

Variant	nsv827390
Chromosome Location	chr15:75766087-75795370
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:70)
CpG islands
(count:244)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:70 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr15:75775900-75776050	HUVEC	blood vessel:	n/a	n/a
2	CTCF	chr15:75783628-75783725	Kidney_OC	kidney:	n/a	n/a
3	CTCF	chr15:75774892-75774930	GM10248	blood:	n/a	n/a
4	CTCF	chr15:75793107-75793182	GM20000	blood:	n/a	n/a
5	EP300	chr15:75786095-75786398	T-47D	breast:	n/a	n/a
6	FOS	chr15:75766234-75766433	MCF10A-Er-Src	breast:	n/a	n/a
7	FOS	chr15:75766276-75766451	MCF10A-Er-Src	breast:	n/a	n/a
8	FOXA1	chr15:75786107-75786438	T-47D	breast:	n/a	n/a
9	FOXA1	chr15:75786030-75786435	HepG2	liver:	n/a	n/a
10	FOXA1	chr15:75786113-75786387	T-47D	breast:	n/a	n/a
11	FOXA1	chr15:75786084-75786424	HepG2	liver:	n/a	n/a
12	FOXA2	chr15:75784837-75785038	HepG2	liver:	n/a	n/a
13	HEY1	chr15:75772578-75772925	HepG2	liver:	n/a	n/a
14	HEY1	chr15:75772720-75772923	K562	blood:	n/a	n/a
15	HEY1	chr15:75772751-75772892	HepG2	liver:	n/a	n/a
16	HEY1	chr15:75772732-75772913	K562	blood:	n/a	n/a
17	JUN	chr15:75769554-75769650	HepG2	liver:	n/a	chr15:75769631-75769640 chr15:75769630-75769643
18	JUND	chr15:75769486-75769795	HepG2	liver:	n/a	chr15:75769631-75769640
19	MAFF	chr15:75777496-75777659	HepG2	liver:	n/a	n/a
20	MAFK	chr15:75777477-75777689	HepG2	liver:	n/a	chr15:75777632-75777646
21	MAFK	chr15:75777587-75777776	HepG2	liver:	n/a	chr15:75777632-75777646
22	MYC	chr15:75783360-75783400	MCF-7	breast:	n/a	n/a
23	MYC	chr15:75781800-75781822	GM12878	blood:	n/a	n/a
24	POLR2A	chr15:75766715-75766823	GM12878	blood:	n/a	n/a
25	POLR2A	chr15:75772727-75772891	H1-hESC	embryonic stem cell:	n/a	n/a
26	POLR2A	chr15:75788886-75789216	PFSK-1	brain:	n/a	n/a
27	POLR2A	chr15:75772754-75772950	GM12878	blood:	n/a	n/a
28	POLR2A	chr15:75772759-75772887	A549	lung:	n/a	n/a
29	POLR2A	chr15:75772692-75772992	GM12892	blood:	n/a	n/a
30	POLR2A	chr15:75782935-75783063	HepG2	liver:	n/a	n/a
31	POLR2A	chr15:75776083-75776296	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr15:75778392-75778874	PFSK-1	brain:	n/a	n/a
33	POLR2A	chr15:75788123-75788367	HepG2	liver:	n/a	n/a
34	POLR2A	chr15:75772738-75772902	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr15:75789657-75789944	PFSK-1	brain:	n/a	n/a
36	POLR2A	chr15:75772728-75772975	A549	lung:	n/a	n/a
37	POLR2A	chr15:75789913-75789950	HepG2	liver:	n/a	n/a
38	POLR2A	chr15:75772762-75772883	A549	lung:	n/a	n/a
39	POLR2A	chr15:75793901-75793910	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr15:75776081-75776240	HUVEC	blood vessel:	n/a	n/a
41	POLR2A	chr15:75772747-75772893	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr15:75772690-75772991	GM12878	blood:	n/a	n/a
43	POLR2A	chr15:75791991-75792004	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr15:75772742-75772894	Hela-S3	cervix:	n/a	n/a
45	POLR2A	chr15:75777134-75777187	MCF-7	breast:	n/a	n/a
46	POLR2A	chr15:75791794-75792011	HepG2	liver:	n/a	n/a
47	POLR2A	chr15:75789969-75790019	HepG2	liver:	n/a	n/a
48	POLR2A	chr15:75770474-75770492	HepG2	liver:	n/a	n/a
49	POLR2A	chr15:75788879-75789009	HepG2	liver:	n/a	n/a
50	POLR2A	chr15:75779937-75780211	PFSK-1	brain:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:75771387-75771437	HepG2	liver:	n/a
2	chr15:75768945-75768995	HepG2	liver:	n/a
3	chr15:75775352-75775402	HIPEpiC	eye:	n/a
4	chr15:75768945-75768995	K562	blood:	n/a
5	chr15:75775352-75775402	BJ	skin:	n/a
6	chr15:75772834-75772884	HNPCEpiC	eye:	n/a
7	chr15:75771387-75771437	HNPCEpiC	eye:	n/a
8	chr15:75772834-75772884	Jurkat	blood:	n/a
9	chr15:75768945-75768995	PANC-1	pancreas:	n/a
10	chr15:75771387-75771437	AoSMC	blood vessel:	n/a
11	chr15:75771387-75771437	K562	blood:	n/a
12	chr15:75768945-75768995	SAEC	small airway:	n/a
13	chr15:75771387-75771437	Hepatocyte	liver:	n/a
14	chr15:75775352-75775402	SK-N-SH	brain:	n/a
15	chr15:75772834-75772884	NB4	blood:	n/a
16	chr15:75772834-75772884	A549	lung:	n/a
17	chr15:75768945-75768995	HIPEpiC	eye:	n/a
18	chr15:75775352-75775402	HEEpiC	esophagus:	n/a
19	chr15:75771387-75771437	HRE	kidney:	n/a
20	chr15:75771387-75771437	AG04449	skin:	fetal
21	chr15:75771387-75771437	NHDF-neo	bronchial:	n/a
22	chr15:75775352-75775402	HCM	heart:	n/a
23	chr15:75775352-75775402	HMEC	breast:	n/a
24	chr15:75775352-75775402	HRE	kidney:	n/a
25	chr15:75775352-75775402	Jurkat	blood:	n/a
26	chr15:75768945-75768995	HRPEpiC	eye:	n/a
27	chr15:75772834-75772884	SAEC	small airway:	n/a
28	chr15:75775352-75775402	HepG2	liver:	n/a
29	chr15:75772834-75772884	NHDF-neo	bronchial:	n/a
30	chr15:75768945-75768995	A549	lung:	n/a
31	chr15:75771387-75771437	PANC-1	pancreas:	n/a
32	chr15:75775352-75775402	GM12878	blood:	n/a
33	chr15:75775352-75775402	GM12891	blood:	n/a
34	chr15:75772834-75772884	SK-N-MC	brain:	n/a
35	chr15:75772834-75772884	IMR90	lung:	fetal
36	chr15:75768945-75768995	Hela-S3	cervix:	n/a
37	chr15:75768945-75768995	MCF10A-Er-Src	breast:	n/a
38	chr15:75775352-75775402	CMK	blood:	n/a
39	chr15:75768945-75768995	HCM	heart:	n/a
40	chr15:75771387-75771437	Jurkat	blood:	n/a
41	chr15:75771387-75771437	CMK	blood:	n/a
42	chr15:75775352-75775402	PFSK-1	brain:	n/a
43	chr15:75768945-75768995	HAEpiC	amniotic membrane:	n/a
44	chr15:75775352-75775402	ProgFib	skin:	n/a
45	chr15:75772834-75772884	AG04450	lung:	fetal
46	chr15:75775352-75775402	Hela-S3	cervix:	n/a
47	chr15:75768945-75768995	HCPEpiC	choroid plexus:	n/a
48	chr15:75771387-75771437	ovcar-3	ovarian:	n/a
49	chr15:75772834-75772884	GM06990	blood:	n/a
50	chr15:75772834-75772884	AG09309	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr15:75767969..75769622-chr15:75930822..75933401,2	MCF-7	breast:
2	chr15:75781333..75783165-chr15:75786697..75789671,2	K562	blood:
3	chr15:75743324..75745076-chr15:75777150..75780089,2	MCF-7	breast:
4	chr15:75790680..75793556-chr15:75804189..75806502,2	MCF-7	breast:
5	chr15:75745748..75747907-chr15:75768138..75770692,2	MCF-7	breast:
6	chr15:75743484..75746288-chr15:75777590..75779604,2	K562	blood:
7	chr15:75781333..75783165-chr15:75786697..75789671,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000260165	TF binding region
PTPN9	TF binding region
ENSG00000260165	CpG island
PTPN9	CpG island
ENSG00000169375	chromatin interactions
ENSG00000259931	chromatin interactions
ENSG00000177971	chromatin interactions

Extended variants
information (count: 942 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:942 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186045366	chr15:75766087-75766088	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs200761378	chr15:75766118-75766119	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140659570	chr15:75766171-75766172	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149679493	chr15:75766190-75766191	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537243989	chr15:75766191-75766192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573013429	chr15:75766225-75766226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371756051	chr15:75766235-75766236	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs576496151	chr15:75766260-75766261	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs545462369	chr15:75766261-75766262	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs145506231	chr15:75766283-75766284	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs565281336	chr15:75766289-75766290	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs551247992	chr15:75766304-75766305	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs11855799	chr15:75766322-75766323	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs141261168	chr15:75766341-75766342	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs74609674	chr15:75766358-75766359	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs369097826	chr15:75766401-75766402	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs189574366	chr15:75766422-75766423	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs533876055	chr15:75766463-75766464	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549146196	chr15:75766506-75766507	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146977327	chr15:75766582-75766583	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs11634863	chr15:75766672-75766673	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs556398906	chr15:75766688-75766689	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs138084538	chr15:75766804-75766805	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs142182539	chr15:75766814-75766815	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs560894763	chr15:75766847-75766848	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs529930495	chr15:75766852-75766853	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557737071	chr15:75766858-75766859	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549795028	chr15:75766868-75766869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572957217	chr15:75767014-75767015	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs76479056	chr15:75767038-75767039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369940709	chr15:75767068-75767069	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs74449134	chr15:75767269-75767270	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs369992359	chr15:75767275-75767276	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574163733	chr15:75767284-75767285	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs143162610	chr15:75767357-75767358	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563169671	chr15:75767404-75767405	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182033017	chr15:75767411-75767412	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs148273644	chr15:75767416-75767417	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544980665	chr15:75767417-75767418	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560187169	chr15:75767428-75767429	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs141838249	chr15:75767443-75767444	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569187952	chr15:75767551-75767552	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187647919	chr15:75767603-75767604	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567276846	chr15:75767631-75767632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531504092	chr15:75767638-75767639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549723036	chr15:75767639-75767640	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs13380130	chr15:75767645-75767646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs114171803	chr15:75767646-75767647	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538547317	chr15:75767737-75767738	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs563641142	chr15:75767746-75767747	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	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
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:1009 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:75749000-75797800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr15:75749200-75776800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr15:75749200-75782000	Weak transcription	Right Atrium	heart
4	chr15:75754400-75770800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr15:75755200-75772400	Strong transcription	Cortex derived primary cultured neurospheres	brain
6	chr15:75755200-75772400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr15:75755200-75772600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr15:75755400-75772400	Strong transcription	Fetal Muscle Leg	muscle
9	chr15:75755600-75769800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr15:75755600-75772800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr15:75756200-75772400	Strong transcription	Fetal Stomach	stomach
12	chr15:75756200-75772600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr15:75756200-75772600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr15:75756400-75766600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr15:75756400-75766600	Strong transcription	Fetal Intestine Large	intestine
16	chr15:75756400-75772600	Strong transcription	Fetal Muscle Trunk	muscle
17	chr15:75756600-75772800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr15:75756800-75769800	Strong transcription	Duodenum Mucosa	Duodenum
19	chr15:75757200-75767600	Strong transcription	Dnd41	blood
20	chr15:75757200-75770400	Strong transcription	Rectal Mucosa Donor 31	rectum
21	chr15:75757400-75772400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr15:75757600-75769600	Strong transcription	HUES64 Cell Line	embryonic stem cell
23	chr15:75757800-75766800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
24	chr15:75757800-75767200	Strong transcription	Muscle Satellite Cultured Cells	--
25	chr15:75757800-75768600	Strong transcription	Stomach Smooth Muscle	stomach
26	chr15:75757800-75769800	Strong transcription	HUES6 Cell Line	embryonic stem cell
27	chr15:75757800-75769800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
28	chr15:75757800-75769800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr15:75757800-75772600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr15:75758000-75766600	Strong transcription	Primary B cells from peripheral blood	blood
31	chr15:75758000-75767400	Strong transcription	Primary B cells from cord blood	blood
32	chr15:75758000-75767400	Strong transcription	Rectal Mucosa Donor 29	rectum
33	chr15:75758000-75769400	Strong transcription	H1 Cell Line	embryonic stem cell
34	chr15:75758000-75769400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr15:75758000-75772400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr15:75758000-75772400	Strong transcription	Liver	Liver
37	chr15:75758000-75772400	Strong transcription	Osteobl	bone
38	chr15:75758000-75772600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr15:75758000-75772800	Strong transcription	Primary monocytes fromperipheralblood	blood
40	chr15:75758200-75766400	Strong transcription	Colonic Mucosa	Colon
41	chr15:75758200-75766600	Strong transcription	Brain Hippocampus Middle	brain
42	chr15:75758200-75768200	Strong transcription	Duodenum Smooth Muscle	Duodenum
43	chr15:75758200-75768400	Strong transcription	Primary T helper cells fromperipheralblood	blood
44	chr15:75758200-75769600	Strong transcription	Fetal Thymus	thymus
45	chr15:75758200-75769800	Strong transcription	HUES48 Cell Line	embryonic stem cell
46	chr15:75758200-75770000	Strong transcription	Sigmoid Colon	Sigmoid Colon
47	chr15:75758200-75772200	Strong transcription	Primary T cells fromperipheralblood	blood
48	chr15:75758400-75766800	Strong transcription	Fetal Lung	lung
49	chr15:75758400-75768400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr15:75758400-75769400	Strong transcription	Placenta	Placenta

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