Variant report

Variant	rs978141
Chromosome Location	chr15:62266783-62266784
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:62259986..62262200-chr15:62266004..62268197,2	K562	blood:
2	chr15:62266682..62269656-chr15:62302600..62304271,2	K562	blood:

Extended variants
information (count: 132 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:104)

rs_ID	r²[population]
rs1052306	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs11071640	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11071644	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11555593	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs11555596	0.96[EUR][1000 genomes]
rs11629559	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs11629598	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11629645	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11629741	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes]
rs11629851	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs11629900	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11631273	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11632560	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11634077	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11634306	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11634312	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs11635880	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs11636652	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs11637599	0.89[ASN][1000 genomes]
rs11637606	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs11637693	0.96[ASN][1000 genomes]
rs11637967	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11638455	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs11639286	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12148573	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs12185103	1.00[EUR][1000 genomes]
rs12898715	1.00[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs12898859	1.00[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs12901036	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12901055	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12901735	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12902859	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs12905103	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12905264	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12905403	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12907534	1.00[CEU][hapmap];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12907567	1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12909386	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs12909673	0.96[ASN][1000 genomes]
rs12911422	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12912477	1.00[CEU][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12913358	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12915283	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12915585	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12916410	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12917339	0.96[ASN][1000 genomes]
rs17238096	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs17271291	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17271312	0.96[ASN][1000 genomes]
rs17303887	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs17303894	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes]
rs17303915	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2303405	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34017665	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34042779	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34088392	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34173668	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34234705	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34257602	1.00[AFR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34282385	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34311301	0.96[ASN][1000 genomes]
rs34424197	1.00[AFR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34435758	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34486946	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34556569	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34589937	0.98[EUR][1000 genomes]
rs34646089	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34796280	0.98[EUR][1000 genomes]
rs34853395	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34933463	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34958705	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34997975	0.98[EUR][1000 genomes]
rs35119291	0.96[ASN][1000 genomes]
rs35259011	1.00[AFR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35324423	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35523559	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35559361	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs35607089	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35633657	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35764401	0.96[EUR][1000 genomes]
rs35785804	0.96[ASN][1000 genomes]
rs35984535	1.00[EUR][1000 genomes]
rs36004142	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs36056548	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs36126734	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs36175042	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs36185332	0.98[EUR][1000 genomes]
rs4143844	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4143845	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62006964	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62006969	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62007448	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62007764	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62007768	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62007791	1.00[AFR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62009074	0.98[EUR][1000 genomes]
rs62009078	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs62009082	1.00[EUR][1000 genomes]
rs62009106	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62009109	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs71411468	1.00[EUR][1000 genomes]
rs71411469	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs71411471	1.00[EUR][1000 genomes]
rs957348	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv521334	chr15:62129809-62340126	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv527451	chr15:62129809-62340126	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv904286	chr15:62146598-62313373	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv904287	chr15:62146598-62338797	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
5	nsv904288	chr15:62146598-62356386	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
6	nsv569641	chr15:62155282-62287456	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
7	nsv904289	chr15:62156690-62287456	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
8	nsv516639	chr15:62175134-62340126	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv904290	chr15:62175134-62356386	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	nsv904291	chr15:62178695-62287456	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv904292	chr15:62178695-62313373	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv904293	chr15:62178695-62338797	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv904294	chr15:62178695-62356386	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
14	nsv457176	chr15:62178695-62519658	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
15	nsv569643	chr15:62178695-62519658	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
16	nsv904296	chr15:62198564-62313373	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
17	nsv471247	chr15:62202481-62519658	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
18	nsv904297	chr15:62202482-62313373	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
19	nsv569645	chr15:62202482-62319307	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
20	nsv569646	chr15:62202482-62519658	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
21	esv1816724	chr15:62205104-62285146	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
22	nsv569647	chr15:62214607-62284101	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
23	nsv904298	chr15:62218689-62338797	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
24	nsv569648	chr15:62239697-62340126	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
25	nsv457177	chr15:62243197-62301094	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
26	nsv569649	chr15:62243197-62301094	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
27	nsv569650	chr15:62243197-62313373	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
28	nsv569651	chr15:62243197-62313417	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs978141	VPS13C	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:62150000-62276200	Weak transcription	Psoas Muscle	Psoas
2	chr15:62185600-62333600	Weak transcription	Right Ventricle	heart
3	chr15:62185800-62300000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr15:62188600-62309400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr15:62194600-62266800	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr15:62195600-62285400	Strong transcription	Primary monocytes fromperipheralblood	blood
7	chr15:62208200-62290200	Weak transcription	Aorta	Aorta
8	chr15:62221400-62327600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr15:62229400-62280200	Weak transcription	K562	blood
10	chr15:62230800-62317200	Weak transcription	Pancreas	Pancrea
11	chr15:62235600-62277400	Strong transcription	Primary B cells from peripheral blood	blood
12	chr15:62235800-62285000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr15:62236000-62267000	Strong transcription	Primary T helper cells PMA-I stimulated	--
14	chr15:62236200-62267000	Strong transcription	Primary T helper cells fromperipheralblood	blood
15	chr15:62244600-62350400	Weak transcription	Small Intestine	intestine
16	chr15:62244800-62266800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr15:62244800-62278600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr15:62245000-62266800	Weak transcription	Fetal Heart	heart
19	chr15:62245800-62278400	Strong transcription	Dnd41	blood
20	chr15:62248000-62281400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr15:62254000-62303600	Weak transcription	Spleen	Spleen
22	chr15:62254200-62287800	Weak transcription	Lung	lung
23	chr15:62254200-62297800	Weak transcription	Fetal Intestine Small	intestine
24	chr15:62255200-62268600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr15:62255200-62275800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr15:62255400-62266800	Strong transcription	NHDF-Ad	bronchial
27	chr15:62255800-62276600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr15:62257200-62276000	Weak transcription	HSMMtube	muscle
29	chr15:62257600-62267400	Strong transcription	Fetal Intestine Large	intestine
30	chr15:62258000-62272400	Weak transcription	Brain Cingulate Gyrus	brain
31	chr15:62259200-62276000	Weak transcription	HMEC	breast
32	chr15:62259400-62276000	Weak transcription	Brain Substantia Nigra	brain
33	chr15:62259400-62327200	Weak transcription	HepG2	liver
34	chr15:62259600-62276000	Weak transcription	Brain Angular Gyrus	brain
35	chr15:62259600-62278200	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr15:62261000-62279600	Weak transcription	Esophagus	oesophagus
37	chr15:62261400-62268000	Strong transcription	Primary B cells from cord blood	blood
38	chr15:62261400-62276600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr15:62262200-62267600	Strong transcription	Primary hematopoietic stem cells	blood
40	chr15:62262200-62269400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
41	chr15:62262200-62276400	Strong transcription	Duodenum Mucosa	Duodenum
42	chr15:62262600-62312600	Weak transcription	NHEK	skin
43	chr15:62262800-62271400	Strong transcription	HSMM	muscle
44	chr15:62263800-62276000	Weak transcription	Thymus	Thymus
45	chr15:62263800-62287800	Weak transcription	Fetal Stomach	stomach
46	chr15:62263800-62290200	Weak transcription	Gastric	stomach
47	chr15:62264000-62267200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr15:62264000-62272000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr15:62264000-62276000	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr15:62264000-62281600	Weak transcription	Fetal Brain Female	brain

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