Variant report

Variant	esv3443258
Chromosome Location	chr15:41644871-41681515
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:233)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:233 , 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	chr15:41676294-41676433	HepG2	liver:	n/a	n/a
2	CEBPB	chr15:41660975-41661010	IMR90	lung:	n/a	n/a
3	CTCF	chr15:41651192-41651276	Lung_OC	lung:	n/a	n/a
4	CTCF	chr15:41672600-41672750	HRPEpiC	eye:	n/a	n/a
5	CTCF	chr15:41665052-41665079	GM10266	blood:	n/a	n/a
6	CTCF	chr15:41672580-41672730	HCPEpiC	choroid plexus:	n/a	n/a
7	CTCF	chr15:41672620-41672770	HPAF	blood vessel:	n/a	n/a
8	E2F4	chr15:41657188-41657260	MCF10A-Er-Src	breast:	n/a	n/a
9	FOS	chr15:41670193-41670503	MCF10A-Er-Src	breast:	n/a	chr15:41670360-41670369 chr15:41670358-41670370 chr15:41670360-41670367 chr15:41670360-41670368
10	FOS	chr15:41644937-41645191	HUVEC	blood vessel:	n/a	chr15:41645033-41645044
11	FOS	chr15:41670243-41670499	MCF10A-Er-Src	breast:	n/a	chr15:41670360-41670369 chr15:41670358-41670370 chr15:41670360-41670367 chr15:41670360-41670368
12	FOS	chr15:41670204-41670473	MCF10A-Er-Src	breast:	n/a	chr15:41670360-41670369 chr15:41670358-41670370 chr15:41670360-41670367 chr15:41670360-41670368
13	FOS	chr15:41648283-41648304	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr15:41644977-41645103	MCF10A-Er-Src	breast:	n/a	chr15:41645033-41645044
15	FOS	chr15:41644903-41645104	MCF10A-Er-Src	breast:	n/a	chr15:41645033-41645044
16	FOS	chr15:41670205-41670502	MCF10A-Er-Src	breast:	n/a	chr15:41670360-41670369 chr15:41670358-41670370 chr15:41670360-41670367 chr15:41670360-41670368
17	JUN	chr15:41648183-41648414	HepG2	liver:	n/a	n/a
18	JUND	chr15:41670190-41670506	HepG2	liver:	n/a	chr15:41670360-41670369 chr15:41670358-41670370 chr15:41670358-41670369 chr15:41670360-41670367 chr15:41670360-41670368
19	JUND	chr15:41648140-41648467	HepG2	liver:	n/a	chr15:41648286-41648297
20	JUND	chr15:41648056-41648636	SK-N-SH	brain:	n/a	chr15:41648286-41648297
21	MAFK	chr15:41656192-41656331	HepG2	liver:	n/a	n/a
22	MAFK	chr15:41644904-41645187	IMR90	lung:	n/a	n/a
23	MAFK	chr15:41656144-41656370	HepG2	liver:	n/a	n/a
24	MYC	chr15:41663007-41663032	MCF-7	breast:	n/a	n/a
25	MYC	chr15:41670320-41670531	MCF10A-Er-Src	breast:	n/a	chr15:41670359-41670368 chr15:41670360-41670369
26	NFIC	chr15:41659687-41660055	ECC-1	luminal epithelium:	n/a	n/a
27	NR2F2	chr15:41675742-41676300	K562	blood:	n/a	n/a
28	NR2F2	chr15:41675857-41676139	K562	blood:	n/a	n/a
29	PML	chr15:41646247-41646856	K562	blood:	n/a	n/a
30	POLR2A	chr15:41669987-41669994	HepG2	liver:	n/a	n/a
31	POLR2A	chr15:41646210-41646780	GM12878	blood:	n/a	n/a
32	POLR2A	chr15:41646200-41646854	GM12892	blood:	n/a	n/a
33	POLR2A	chr15:41645009-41645274	K562	blood:	n/a	n/a
34	POLR2A	chr15:41676368-41676449	MCF-7	breast:	n/a	n/a
35	POLR2A	chr15:41663215-41663217	Hela-S3	cervix:	n/a	n/a
36	POLR2A	chr15:41675153-41675256	GM12878	blood:	n/a	n/a
37	POLR2A	chr15:41671863-41672388	K562	blood:	n/a	n/a
38	POLR2A	chr15:41671315-41671316	K562	blood:	n/a	n/a
39	POLR2A	chr15:41659722-41659784	Hela-S3	cervix:	n/a	n/a
40	POLR2A	chr15:41645554-41645759	K562	blood:	n/a	n/a
41	POLR2A	chr15:41645109-41645242	Hela-S3	cervix:	n/a	n/a
42	POLR2A	chr15:41649236-41649525	K562	blood:	n/a	n/a
43	POLR2A	chr15:41661944-41661951	HepG2	liver:	n/a	n/a
44	POLR2A	chr15:41659222-41659379	Hela-S3	cervix:	n/a	n/a
45	POLR2A	chr15:41676308-41676609	K562	blood:	n/a	n/a
46	POLR2A	chr15:41662837-41663138	K562	blood:	n/a	n/a
47	POLR2A	chr15:41665372-41665535	HepG2	liver:	n/a	n/a
48	POLR2A	chr15:41645565-41645868	K562	blood:	n/a	n/a
49	POLR2A	chr15:41646282-41646481	GM12878	blood:	n/a	n/a
50	POLR2A	chr15:41645483-41645645	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:41673030-41673080	AG09319	gingival:	n/a
2	chr15:41673030-41673080	MCF10A-Er-Src	breast:	n/a
3	chr15:41673030-41673080	HCM	heart:	n/a
4	chr15:41673030-41673080	NHBE	bronchial:	n/a
5	chr15:41673030-41673080	Caco-2	colon:	n/a
6	chr15:41673030-41673080	U87	brain:	n/a
7	chr15:41673030-41673080	HEK293	kidney:	embryo
8	chr15:41673030-41673080	HMEC	breast:	n/a
9	chr15:41673030-41673080	GM12878	blood:	n/a
10	chr15:41673030-41673080	GM19239	blood:	n/a
11	chr15:41673030-41673080	IMR90	lung:	fetal
12	chr15:41673030-41673080	Jurkat	blood:	n/a
13	chr15:41673030-41673080	AG04450	lung:	fetal
14	chr15:41673030-41673080	MCF-7	breast:	n/a
15	chr15:41673030-41673080	ProgFib	skin:	n/a
16	chr15:41673030-41673080	PANC-1	pancreas:	n/a
17	chr15:41673030-41673080	AG04449	skin:	fetal
18	chr15:41673030-41673080	NH-A	brain:	n/a
19	chr15:41673030-41673080	HUVEC	blood vessel:	n/a
20	chr15:41673030-41673080	BJ	skin:	n/a
21	chr15:41673030-41673080	GM06990	blood:	n/a
22	chr15:41673030-41673080	SK-N-SH	brain:	n/a
23	chr15:41673030-41673080	HRE	kidney:	n/a
24	chr15:41673030-41673080	HCT-116	colon:	n/a
25	chr15:41673030-41673080	LNCaP	prostate:	n/a
26	chr15:41673030-41673080	HRPEpiC	eye:	n/a
27	chr15:41673030-41673080	AoSMC	blood vessel:	n/a
28	chr15:41673030-41673080	RPTEC	kidney:	n/a
29	chr15:41673030-41673080	HIPEpiC	eye:	n/a
30	chr15:41673030-41673080	HEEpiC	esophagus:	n/a
31	chr15:41673030-41673080	GM12891	blood:	n/a
32	chr15:41673030-41673080	HNPCEpiC	eye:	n/a
33	chr15:41673030-41673080	ovcar-3	ovarian:	n/a
34	chr15:41673030-41673080	Hepatocyte	liver:	n/a
35	chr15:41673030-41673080	BE2_C	brain:	n/a
36	chr15:41673030-41673080	HRCEpiC	kidney:	n/a
37	chr15:41673030-41673080	SAEC	small airway:	n/a
38	chr15:41673030-41673080	K562	blood:	n/a
39	chr15:41673030-41673080	HAEpiC	amniotic membrane:	n/a
40	chr15:41673030-41673080	A549	lung:	n/a
41	chr15:41673030-41673080	AG09309	skin:	n/a
42	chr15:41673030-41673080	PFSK-1	brain:	n/a
43	chr15:41673030-41673080	ECC-1	luminal epithelium:	n/a
44	chr15:41673030-41673080	SK-N-MC	brain:	n/a
45	chr15:41673030-41673080	GM12892	blood:	n/a
46	chr15:41673030-41673080	NHDF-neo	bronchial:	n/a
47	chr15:41673030-41673080	AG10803	skin:	n/a
48	chr15:41673030-41673080	HCPEpiC	choroid plexus:	n/a
49	chr15:41673030-41673080	HPAEpiC	pulmonary alveolar:	n/a
50	chr15:41673030-41673080	H1-hESC	embryonic stem cell:	embryo

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:41653827..41656033-chr15:41656188..41659095,2	K562	blood:
2	chr15:41672888..41674609-chr15:41676088..41678675,2	K562	blood:
3	chr15:41641575..41643582-chr15:41646821..41649075,2	K562	blood:
4	chr15:41672888..41674609-chr15:41676088..41678675,2	K562	blood:
5	chr15:41646211..41648336-chr15:41650156..41652980,2	K562	blood:
6	chr15:41646211..41648336-chr15:41650156..41652980,2	K562	blood:
7	chr15:41646211..41648331-chr15:41650156..41651809,2	K562	blood:
8	chr15:41646211..41648331-chr15:41650156..41651809,2	K562	blood:
9	chr15:41657846..41659992-chr15:41662423..41664875,3	K562	blood:

No data

Variant related genes	Relation type
NUSAP1	TF binding region
NUSAP1	CpG island
ENSG00000137804	chromatin interactions

Extended variants
information (count: 1391 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1391 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572724537	chr15:41644912-41644913	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs564446149	chr15:41644935-41644936	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191322115	chr15:41644980-41644981	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs546197032	chr15:41645019-41645020	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs566296424	chr15:41645090-41645091	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78463234	chr15:41645093-41645094	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528028071	chr15:41645112-41645113	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs72739633	chr15:41645119-41645120	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs140815826	chr15:41645228-41645229	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs150135435	chr15:41645286-41645287	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563001631	chr15:41645372-41645373	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561761328	chr15:41645376-41645377	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138861179	chr15:41645405-41645406	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181742629	chr15:41645417-41645418	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs540889984	chr15:41645420-41645421	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs143907718	chr15:41645426-41645427	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs370677814	chr15:41645562-41645563	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577127136	chr15:41645601-41645602	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146650599	chr15:41645662-41645663	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs370671982	chr15:41645663-41645664	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528963351	chr15:41645692-41645693	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562867331	chr15:41645745-41645746	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185936960	chr15:41645751-41645752	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs74827458	chr15:41645752-41645753	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560708185	chr15:41645877-41645878	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568930546	chr15:41645906-41645907	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs138982660	chr15:41645927-41645928	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546459994	chr15:41645934-41645935	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191198669	chr15:41645952-41645953	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566479284	chr15:41645953-41645954	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532046642	chr15:41645979-41645980	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552129294	chr15:41646002-41646003	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568906601	chr15:41646018-41646019	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537933206	chr15:41646030-41646031	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555212259	chr15:41646050-41646051	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183362722	chr15:41646194-41646195	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534509163	chr15:41646208-41646209	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs533177274	chr15:41646250-41646251	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577441636	chr15:41646313-41646314	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575298770	chr15:41646314-41646315	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs545921306	chr15:41646330-41646331	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551660980	chr15:41646342-41646343	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs149352614	chr15:41646346-41646347	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541873400	chr15:41646361-41646362	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368420299	chr15:41646365-41646366	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112989375	chr15:41646373-41646374	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529806244	chr15:41646377-41646378	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144821175	chr15:41646381-41646382	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs11854081	chr15:41646398-41646399	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs113710447	chr15:41646421-41646422	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Maculopathy	20981449	CNVD
Gastric adenocarcinoma	19115996	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:800 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41625400-41670200	Weak transcription	Gastric	stomach
2	chr15:41625600-41659200	Weak transcription	Lung	lung
3	chr15:41625800-41665800	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr15:41625800-41694200	Weak transcription	Small Intestine	intestine
5	chr15:41626000-41665200	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr15:41626200-41658200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr15:41626200-41678200	Weak transcription	Liver	Liver
8	chr15:41626200-41680200	Weak transcription	Fetal Brain Male	brain
9	chr15:41626400-41677800	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr15:41626400-41678400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr15:41626800-41686400	Weak transcription	Rectal Smooth Muscle	rectum
12	chr15:41627000-41672800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr15:41627200-41676800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr15:41627400-41668000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr15:41627400-41673000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr15:41628200-41673000	Strong transcription	HUES64 Cell Line	embryonic stem cell
17	chr15:41628600-41672800	Strong transcription	HUES6 Cell Line	embryonic stem cell
18	chr15:41628600-41673800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr15:41628800-41654400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr15:41629000-41672000	Weak transcription	Primary T cells from cord blood	blood
21	chr15:41629000-41673000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr15:41629400-41672400	Strong transcription	Fetal Stomach	stomach
23	chr15:41629400-41672800	Strong transcription	HUES48 Cell Line	embryonic stem cell
24	chr15:41629400-41673600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr15:41629600-41674000	Strong transcription	Fetal Thymus	thymus
26	chr15:41629800-41658800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr15:41630000-41662000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr15:41630400-41649600	Strong transcription	Fetal Muscle Trunk	muscle
29	chr15:41630400-41674000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
30	chr15:41630400-41674200	Strong transcription	H1 Cell Line	embryonic stem cell
31	chr15:41630800-41673800	Strong transcription	Dnd41	blood
32	chr15:41631200-41659200	Weak transcription	Primary B cells from peripheral blood	blood
33	chr15:41631800-41649600	Strong transcription	Cortex derived primary cultured neurospheres	brain
34	chr15:41631800-41679200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr15:41632000-41654600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr15:41632000-41673000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
37	chr15:41632000-41673600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr15:41632200-41646600	Strong transcription	H9 Cell Line	embryonic stem cell
39	chr15:41632200-41646600	Strong transcription	K562	blood
40	chr15:41632200-41649600	Strong transcription	Thymus	Thymus
41	chr15:41632200-41655000	Strong transcription	Primary neutrophils fromperipheralblood	blood
42	chr15:41632200-41659600	Strong transcription	Fetal Muscle Leg	muscle
43	chr15:41632200-41674000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr15:41632400-41651800	Strong transcription	Monocytes-CD14+_RO01746	blood
45	chr15:41632800-41673800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr15:41633400-41649600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr15:41634200-41652200	Strong transcription	GM12878-XiMat	blood
48	chr15:41634600-41646000	Weak transcription	Fetal Intestine Large	intestine
49	chr15:41637000-41646800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr15:41638400-41658800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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