Variant report

Variant	rs12901735
Chromosome Location	chr15:62243559-62243560
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	chr15:62242750..62243662-chr5:173738637..173739199,2	MCF-7	breast:
2	chr15:62236123..62237658-chr15:62241444..62244261,2	K562	blood:

Extended variants
information (count: 135 )
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];0.96[EUR][1000 genomes]
rs11071640	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11071644	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11555593	0.98[EUR][1000 genomes]
rs11555596	0.96[EUR][1000 genomes]
rs11629559	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[EUR][1000 genomes]
rs11629598	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11629645	0.82[CEU][hapmap];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[EUR][1000 genomes]
rs11629900	1.00[CEU][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11631273	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.82[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	0.98[EUR][1000 genomes]
rs11637599	0.89[ASN][1000 genomes]
rs11637606	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11637693	0.96[ASN][1000 genomes]
rs11637967	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11638455	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes]
rs11639286	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12148573	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs12185103	1.00[EUR][1000 genomes]
rs12898715	0.87[EUR][1000 genomes]
rs12898859	0.87[EUR][1000 genomes]
rs12901036	1.00[AFR][1000 genomes];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[EUR][1000 genomes]
rs12902859	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[EUR][1000 genomes]
rs12905103	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12905264	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12905403	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12907534	1.00[CEU][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12907567	1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12909386	0.82[CEU][hapmap];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];1.00[AFR][1000 genomes];1.00[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[EUR][1000 genomes]
rs12915585	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12916410	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];0.96[EUR][1000 genomes]
rs17271291	0.82[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];0.98[EUR][1000 genomes]
rs17303894	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes]
rs17303915	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs2303405	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34017665	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34042779	0.94[EUR][1000 genomes];1.00[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	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34257602	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34282385	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34311301	0.96[ASN][1000 genomes]
rs34424197	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34435758	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34486946	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34556569	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34589937	0.98[EUR][1000 genomes]
rs34646089	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34796280	0.98[EUR][1000 genomes]
rs34853395	0.82[AMR][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	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35119291	0.96[ASN][1000 genomes]
rs35259011	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35324423	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35523559	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35559361	0.98[EUR][1000 genomes]
rs35607089	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[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	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs36004142	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs36056548	0.88[AMR][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	0.83[AMR][1000 genomes];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	0.89[EUR][1000 genomes]
rs62006964	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62006969	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62007448	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62007764	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62007768	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62007791	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62009074	0.98[EUR][1000 genomes]
rs62009078	0.98[EUR][1000 genomes]
rs62009082	1.00[EUR][1000 genomes]
rs62009106	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62009109	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs71411468	1.00[EUR][1000 genomes]
rs71411469	1.00[EUR][1000 genomes]
rs71411471	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs957348	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs978141	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]

Variant overlapped rSNPs/rCNVs (count:31 , 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	nsv904285	chr15:62146598-62246864	Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	nsv904295	chr15:62198564-62259637	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
18	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
19	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
20	nsv569644	chr15:62202482-62247067	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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
31	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
rs12901735	VPS13C	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:62142400-62253000	Weak transcription	Spleen	Spleen
2	chr15:62150000-62276200	Weak transcription	Psoas Muscle	Psoas
3	chr15:62185600-62262200	Weak transcription	Gastric	stomach
4	chr15:62185600-62333600	Weak transcription	Right Ventricle	heart
5	chr15:62185800-62300000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr15:62187200-62246000	Weak transcription	A549	lung
7	chr15:62188600-62309400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr15:62194600-62266800	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr15:62195600-62285400	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr15:62207800-62263200	Weak transcription	Fetal Brain Female	brain
11	chr15:62208200-62263200	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr15:62208200-62290200	Weak transcription	Aorta	Aorta
13	chr15:62208400-62253200	Weak transcription	Thymus	Thymus
14	chr15:62209800-62250600	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr15:62209800-62252400	Weak transcription	Brain Cingulate Gyrus	brain
16	chr15:62214800-62250800	Weak transcription	NH-A	brain
17	chr15:62214800-62253600	Weak transcription	HepG2	liver
18	chr15:62214800-62265600	Weak transcription	Fetal Kidney	kidney
19	chr15:62219600-62253000	Weak transcription	Fetal Intestine Small	intestine
20	chr15:62221400-62327600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr15:62221600-62244400	Weak transcription	Small Intestine	intestine
22	chr15:62221600-62245800	Weak transcription	Fetal Thymus	thymus
23	chr15:62221600-62253000	Weak transcription	Fetal Stomach	stomach
24	chr15:62222600-62253600	Weak transcription	Colon Smooth Muscle	Colon
25	chr15:62223400-62266600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr15:62228200-62255800	Weak transcription	HSMMtube	muscle
27	chr15:62229200-62246600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr15:62229400-62280200	Weak transcription	K562	blood
29	chr15:62229800-62260800	Strong transcription	Duodenum Mucosa	Duodenum
30	chr15:62230800-62317200	Weak transcription	Pancreas	Pancrea
31	chr15:62234200-62258600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr15:62234800-62257000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr15:62235400-62244000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr15:62235600-62247600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr15:62235600-62277400	Strong transcription	Primary B cells from peripheral blood	blood
36	chr15:62235800-62285000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr15:62236000-62255800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr15:62236000-62267000	Strong transcription	Primary T helper cells PMA-I stimulated	--
39	chr15:62236200-62245000	Strong transcription	Liver	Liver
40	chr15:62236200-62267000	Strong transcription	Primary T helper cells fromperipheralblood	blood
41	chr15:62236600-62251600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr15:62236800-62251600	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr15:62237000-62244600	Strong transcription	Primary hematopoietic stem cells	blood
44	chr15:62237200-62249200	Weak transcription	Hela-S3	cervix
45	chr15:62237200-62264400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr15:62237400-62244000	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr15:62237400-62244200	Weak transcription	Brain Angular Gyrus	brain
48	chr15:62237400-62244200	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr15:62237400-62244200	Weak transcription	HUVEC	blood vessel
50	chr15:62237400-62252000	Weak transcription	Fetal Muscle Leg	muscle

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