Variant report

Variant	nsv984039
Chromosome Location	chr15:30020901-30024443
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:66)
CpG islands
(count:0)
Chromatin interactive
region (count:1)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:66 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr15:30021321-30021542	HepG2	liver:	n/a	n/a
2	CEBPB	chr15:30024232-30024564	ECC-1	luminal epithelium:	n/a	n/a
3	CEBPB	chr15:30024213-30024548	IMR90	lung:	n/a	n/a
4	CEBPB	chr15:30021314-30021647	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr15:30021342-30021552	MCF-7	breast:	n/a	n/a
6	CEBPB	chr15:30021385-30021517	K562	blood:	n/a	n/a
7	CTCF	chr15:30021300-30021450	A549	lung:	n/a	n/a
8	CTCF	chr15:30021340-30021490	HBMEC	blood vessel:	n/a	n/a
9	CTCF	chr15:30021320-30021470	HepG2	liver:	n/a	n/a
10	CTCF	chr15:30021383-30021429	MCF-7	breast:	n/a	n/a
11	CTCF	chr15:30021240-30021390	HCPEpiC	choroid plexus:	n/a	n/a
12	CTCF	chr15:30021394-30021471	Fibrobl	skin:	n/a	n/a
13	CTCF	chr15:30021390-30021401	MCF-7	breast:	n/a	n/a
14	CTCF	chr15:30021375-30021412	MCF-7	breast:	n/a	n/a
15	HEY1	chr15:30022750-30023021	K562	blood:	n/a	n/a
16	HEY1	chr15:30022741-30022884	HepG2	liver:	n/a	n/a
17	HEY1	chr15:30022741-30023037	K562	blood:	n/a	n/a
18	HEY1	chr15:30022654-30022926	HepG2	liver:	n/a	n/a
19	IRF1	chr15:30022255-30022320	K562	blood:	n/a	n/a
20	MAFK	chr15:30021184-30021242	K562	blood:	n/a	n/a
21	POLR2A	chr15:30022663-30023031	GM12878	blood:	n/a	n/a
22	POLR2A	chr15:30022613-30023089	GM12892	blood:	n/a	n/a
23	POLR2A	chr15:30022832-30022858	HUVEC	blood vessel:	n/a	n/a
24	POLR2A	chr15:30020786-30020950	K562	blood:	n/a	n/a
25	POLR2A	chr15:30022774-30022894	HepG2	liver:	n/a	n/a
26	POLR2A	chr15:30023558-30023718	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr15:30023443-30023671	GM12878	blood:	n/a	n/a
28	POLR2A	chr15:30022775-30022919	GM12878	blood:	n/a	n/a
29	POLR2A	chr15:30022791-30022898	A549	lung:	n/a	n/a
30	POLR2A	chr15:30022649-30022653	ProgFib	skin:	n/a	n/a
31	POLR2A	chr15:30022744-30023003	GM12891	blood:	n/a	n/a
32	POLR2A	chr15:30022819-30022993	MCF-7	breast:	n/a	n/a
33	POLR2A	chr15:30022691-30023061	MCF-7	breast:	n/a	n/a
34	POLR2A	chr15:30022783-30022866	HepG2	liver:	n/a	n/a
35	POLR2A	chr15:30020490-30021721	K562	blood:	n/a	n/a
36	POLR2A	chr15:30023581-30023737	K562	blood:	n/a	n/a
37	POLR2A	chr15:30022641-30023018	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr15:30022758-30022920	A549	lung:	n/a	n/a
39	POLR2A	chr15:30022764-30022953	Hela-S3	cervix:	n/a	n/a
40	POLR2A	chr15:30022676-30022694	ProgFib	skin:	n/a	n/a
41	POLR2A	chr15:30022258-30022765	HepG2	liver:	n/a	n/a
42	POLR2A	chr15:30023397-30023672	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr15:30022866-30022923	MCF-7	breast:	n/a	n/a
44	POLR2A	chr15:30022727-30023051	GM12892	blood:	n/a	n/a
45	POLR2A	chr15:30023317-30023617	GM12878	blood:	n/a	n/a
46	POLR2A	chr15:30022733-30022920	GM12892	blood:	n/a	n/a
47	POLR2A	chr15:30022774-30022923	GM12878	blood:	n/a	n/a
48	POLR2A	chr15:30020671-30020926	K562	blood:	n/a	n/a
49	POLR2A	chr15:30023511-30023669	H1-hESC	embryonic stem cell:	n/a	n/a
50	POLR2A	chr15:30022668-30023019	GM12878	blood:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:30023084..30024986-chr15:30029445..30032082,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM189A1-3	chr15:30020390-30021735	ENSG00000259644.1

No data

Variant related genes	Relation type
ENSG00000259644	TF binding region
HMGN2P5	TF binding region

Extended variants
information (count: 152 )
Associated
traits (count: 153 )

Variant overlapped rSNPs/rCNVs (count:152 , 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	rs556769791	chr15:30020911-30020912	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs576916978	chr15:30020971-30020972	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs187425374	chr15:30020998-30020999	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs191796718	chr15:30021020-30021021	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs183032539	chr15:30021024-30021025	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs542099165	chr15:30021036-30021037	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs561971988	chr15:30021045-30021046	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs3809503	chr15:30021157-30021158	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs142830495	chr15:30021168-30021169	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs570027290	chr15:30021210-30021211	Strong transcription Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs532671293	chr15:30021297-30021298	Strong transcription Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs552265857	chr15:30021302-30021303	Strong transcription Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs75200556	chr15:30021358-30021359	Strong transcription Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs534703091	chr15:30021363-30021364	Strong transcription Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs530001582	chr15:30021408-30021409	Strong transcription Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs372112946	chr15:30021409-30021410	Strong transcription Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs554803528	chr15:30021436-30021437	Strong transcription Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs7177230	chr15:30021461-30021462	Strong transcription Weak transcription	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs537245982	chr15:30021476-30021477	Strong transcription Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs557560416	chr15:30021504-30021505	Strong transcription Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs45505998	chr15:30021512-30021513	Strong transcription Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs187566445	chr15:30021540-30021541	Strong transcription Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs553106054	chr15:30021605-30021606	Strong transcription Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs578165873	chr15:30021609-30021610	Strong transcription Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs191828510	chr15:30021646-30021647	Strong transcription Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs72719056	chr15:30021665-30021666	Strong transcription Weak transcription	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs78446367	chr15:30021683-30021684	Strong transcription Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs182456453	chr15:30021762-30021763	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs28697092	chr15:30021780-30021781	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs62016718	chr15:30021794-30021795	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs62016719	chr15:30021798-30021799	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs62016720	chr15:30021799-30021800	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs147892002	chr15:30021805-30021806	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs377688260	chr15:30021840-30021841	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185018969	chr15:30021880-30021881	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559302103	chr15:30021881-30021882	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545379611	chr15:30021884-30021885	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575860826	chr15:30021892-30021893	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs568639646	chr15:30021902-30021903	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373657261	chr15:30021911-30021912	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551006383	chr15:30021916-30021917	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544502400	chr15:30021917-30021918	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540046878	chr15:30021924-30021925	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs142206055	chr15:30021982-30021983	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556984046	chr15:30021985-30021986	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs537342444	chr15:30022005-30022006	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372898413	chr15:30022006-30022007	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190658870	chr15:30022014-30022015	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs17750790	chr15:30022069-30022070	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs567015925	chr15:30022112-30022113	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:153)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
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
idiopathic generalized epilepsy	19843651	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prader-willi syndrome	21504564	CNVD
The inv dup or idic syndrome	19019226	CNVD
Prader-willi syndrome	21233802	CNVD
Angelman syndrome	16617304	CNVD
Angelman syndrome	20970697	CNVD
Autism	22958593	CNVD
Prader-willi syndrome	16617304	CNVD
Prader-willi syndrome	18923514	CNVD
Prader-willi syndrome	20970697	CNVD
Angelman syndrome	16183798	CNVD
Angelman syndrome	18923514	CNVD
Prader-willi syndrome	22241247	CNVD
Epilepsy	20970697	CNVD
Autism	20970697	CNVD
Autism	19935738	CNVD
Autism	22930557	CNVD
Autism	19966786	CNVD
Autism	18923514	CNVD
Autism	18925931	CNVD
Autism	18835857	CNVD
Prader-willi syndrome	18835857	CNVD
Prader-willi syndrome	22152151	CNVD
Autism	22241247	CNVD
15q-syndrome	21725066	CNVD
Prader-willi syndrome	21503198	CNVD
Autism	21956041	CNVD
Prader-willi syndrome	16760730	CNVD
Prader-willi syndrome	22470819	CNVD
prenatal diagnosis	20453657	CNVD
Prader-willi syndrome	17867985	CNVD
Angelman syndrome	21072004	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
Hodgkin''s lymphoma	18641027	CNVD
Prader-willi syndrome	18781185	CNVD
Melanoma	18172304	CNVD
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	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
Gastrointestinal stromal cancer	20818650	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Schizophrenia	19197363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Angelman syndrome	18787571	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Abnormal corpus callosum	21572526	CNVD
Autism	20531469	CNVD
Neuropsychiatric disorder	20506139	CNVD
Austim spectrum disorder	21302340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Mental retardation	17124404	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Autism	19843651	CNVD
Schizophrenia	19843651	CNVD
Schizophrenia	23813976	CNVD
Cognitive impairment	21505072	CNVD
Epilepsy	20502679	CNVD
Autism	22543975	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495309	CNVD
Schizophrenia	20388499	CNVD
Autism	20841430	CNVD
Epilepsy	22499536	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Mental retardation	21956041	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Autism	21269290	CNVD
Intellectual disability	21269290	CNVD
Schizophrenia	21269290	CNVD
Colorectal cancer	21128281	CNVD
Epilepsy	19289393	CNVD
Epilepsy	20643615	CNVD
Mental retardation	19289393	CNVD
Mental retardation	20152051	CNVD
Schizophrenia	19289393	CNVD
dysmorphic features	19289393	CNVD
idiopathic epilepsies	19341504	CNVD
idiopathic generalized epilepsy	19592580	CNVD
idiopathic generalized epilepsy	19136953	CNVD
Autism	22094647	CNVD
Developmental delay	19898479	CNVD
Mental retardation	18278044	CNVD
Mental retardation	19898479	CNVD
Prader-willi syndrome	18854863	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:195 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:29989600-30021200	Strong transcription	Duodenum Smooth Muscle	Duodenum
2	chr15:29989600-30027200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr15:29990200-30028400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr15:29990400-30026400	Strong transcription	Stomach Smooth Muscle	stomach
5	chr15:29991200-30022400	Strong transcription	Skeletal Muscle Female	skeletal muscle
6	chr15:29992000-30026600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr15:29996200-30021400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr15:30005000-30023000	Strong transcription	Muscle Satellite Cultured Cells	--
9	chr15:30005400-30022800	Strong transcription	HSMMtube	muscle
10	chr15:30007200-30021400	Strong transcription	Fetal Kidney	kidney
11	chr15:30007200-30021400	Strong transcription	NHLF	lung
12	chr15:30014800-30021200	Strong transcription	HMEC	breast
13	chr15:30014800-30028400	Strong transcription	NHEK	skin
14	chr15:30015000-30021600	Strong transcription	Brain Angular Gyrus	brain
15	chr15:30015000-30022200	Strong transcription	Osteobl	bone
16	chr15:30015000-30024400	Weak transcription	Psoas Muscle	Psoas
17	chr15:30015000-30028400	Weak transcription	Stomach Mucosa	stomach
18	chr15:30015000-30035000	Strong transcription	Adipose Nuclei	Adipose
19	chr15:30015200-30021200	Strong transcription	Brain Hippocampus Middle	brain
20	chr15:30015200-30021400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr15:30015200-30021400	Strong transcription	Duodenum Mucosa	Duodenum
22	chr15:30015200-30021600	Strong transcription	Ovary	ovary
23	chr15:30015200-30022800	Strong transcription	NH-A	brain
24	chr15:30015200-30023200	Strong transcription	Placenta	Placenta
25	chr15:30015200-30024200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr15:30015400-30026600	Strong transcription	Brain Inferior Temporal Lobe	brain
27	chr15:30015400-30028600	Strong transcription	HUVEC	blood vessel
28	chr15:30015600-30021000	Strong transcription	NHDF-Ad	bronchial
29	chr15:30015600-30021400	Strong transcription	Fetal Lung	lung
30	chr15:30015600-30026600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr15:30015600-30034800	Strong transcription	Fetal Muscle Leg	muscle
32	chr15:30015600-30035200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr15:30015600-30037600	Weak transcription	Small Intestine	intestine
34	chr15:30015800-30023000	Strong transcription	Fetal Stomach	stomach
35	chr15:30015800-30023200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr15:30015800-30026400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr15:30015800-30026800	Strong transcription	Fetal Muscle Trunk	muscle
38	chr15:30015800-30027200	Weak transcription	Rectal Smooth Muscle	rectum
39	chr15:30015800-30027600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr15:30015800-30034400	Strong transcription	Cortex derived primary cultured neurospheres	brain
41	chr15:30016400-30021000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr15:30016600-30021400	Strong transcription	Sigmoid Colon	Sigmoid Colon
43	chr15:30016600-30021400	Strong transcription	HSMM	muscle
44	chr15:30016600-30021800	Strong transcription	HUES6 Cell Line	embryonic stem cell
45	chr15:30016600-30023000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr15:30016600-30025800	Strong transcription	Left Ventricle	heart
47	chr15:30016600-30029800	Strong transcription	H1 Cell Line	embryonic stem cell
48	chr15:30016600-30035200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
49	chr15:30016600-30052000	Weak transcription	Spleen	Spleen
50	chr15:30016600-30068200	Weak transcription	Brain Germinal Matrix	brain

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