Variant report

Variant	rs4923884
Chromosome Location	chr15:41036448-41036449
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr15:41036325-41036467	ProgFib	skin:	n/a	n/a
2	NR2F2	chr15:41036233-41036890	MCF-7	breast:	n/a	chr15:41036604-41036619
3	POLR2A	chr15:41036351-41036718	U87	brain:	n/a	n/a
4	JUND	chr15:41036368-41036756	Hela-S3	cervix:	n/a	chr15:41036699-41036708 chr15:41036700-41036709
5	MYC	chr15:41036343-41036690	NB4	blood:	n/a	chr15:41036512-41036519
6	USF2	chr15:41036142-41036902	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr15:41036375-41036833	A549	lung:	n/a	chr15:41036554-41036565 chr15:41036556-41036567 chr15:41036554-41036567
8	POLR2A	chr15:41036085-41037433	Hela-S3	cervix:	n/a	n/a
9	JUND	chr15:41036210-41036736	K562	blood:	n/a	chr15:41036699-41036708 chr15:41036700-41036709
10	EP300	chr15:41036383-41036753	Hela-S3	cervix:	n/a	chr15:41036529-41036536
11	POLR2A	chr15:41036087-41036686	K562	blood:	n/a	n/a
12	STAT3	chr15:41036320-41036650	MCF10A-Er-Src	breast:	n/a	chr15:41036501-41036513
13	MAX	chr15:41036126-41036763	K562	blood:	n/a	chr15:41036697-41036707 chr15:41036512-41036519
14	POLR2A	chr15:41036315-41036734	U87	brain:	n/a	n/a
15	CUX1	chr15:41036401-41036618	K562	blood:	n/a	n/a
16	FOS	chr15:41036320-41036729	MCF10A-Er-Src	breast:	n/a	chr15:41036699-41036708 chr15:41036700-41036709
17	MYC	chr15:41036254-41036737	MCF10A-Er-Src	breast:	n/a	chr15:41036697-41036707 chr15:41036512-41036519
18	JUN	chr15:41035587-41036904	K562	blood:	n/a	chr15:41036699-41036708 chr15:41036700-41036709 chr15:41035682-41035692 chr15:41035684-41035695
19	CEBPB	chr15:41036364-41036723	MCF-7	breast:	n/a	chr15:41036554-41036565 chr15:41036556-41036567 chr15:41036554-41036567
20	CHD2	chr15:41036109-41036726	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr15:41036001-41036661	K562	blood:	n/a	n/a
22	CEBPB	chr15:41036324-41036777	IMR90	lung:	n/a	chr15:41036554-41036565 chr15:41036556-41036567 chr15:41036554-41036567
23	ELK1	chr15:41036185-41036720	Hela-S3	cervix:	n/a	n/a
24	FOS	chr15:41036330-41036723	MCF10A-Er-Src	breast:	n/a	chr15:41036699-41036708 chr15:41036700-41036709
25	MAX	chr15:41036247-41036762	A549	lung:	n/a	chr15:41036697-41036707 chr15:41036512-41036519
26	MAX	chr15:41036332-41036723	Hela-S3	cervix:	n/a	chr15:41036697-41036707 chr15:41036512-41036519
27	CEBPB	chr15:41036374-41036750	A549	lung:	n/a	chr15:41036554-41036565 chr15:41036556-41036567 chr15:41036554-41036567
28	FOSL1	chr15:41036419-41036751	K562	blood:	n/a	chr15:41036699-41036708 chr15:41036700-41036709
29	CEBPB	chr15:41036334-41036747	K562	blood:	n/a	chr15:41036554-41036565 chr15:41036556-41036567 chr15:41036554-41036567
30	MAX	chr15:41036257-41036750	Hela-S3	cervix:	n/a	chr15:41036697-41036707 chr15:41036512-41036519
31	NR2F2	chr15:41036136-41036943	K562	blood:	n/a	chr15:41036604-41036619
32	MYC	chr15:41036369-41036714	Hela-S3	cervix:	n/a	chr15:41036697-41036707 chr15:41036512-41036519
33	RAD21	chr15:41036400-41036769	Hela-S3	cervix:	n/a	n/a
34	GATA1	chr15:41035628-41036571	PBDE	blood:	n/a	chr15:41035751-41035760 chr15:41036045-41036066 chr15:41036050-41036059 chr15:41035753-41035763 chr15:41035750-41035762 chr15:41035751-41035761 chr15:41036047-41036063 chr15:41036050-41036059 chr15:41035753-41035760 chr15:41036047-41036063 chr15:41036050-41036060 chr15:41035748-41035764
35	ESR1	chr15:41036438-41036665	ECC-1	luminal epithelium:	n/a	chr15:41036573-41036590 chr15:41036574-41036589 chr15:41036574-41036591
36	NR2F2	chr15:41036344-41036766	K562	blood:	n/a	chr15:41036604-41036619
37	POLR2A	chr15:41036045-41036682	HL-60	blood:	n/a	n/a
38	GTF2F1	chr15:41036343-41036747	Hela-S3	cervix:	n/a	n/a
39	FOS	chr15:41036231-41036714	MCF10A-Er-Src	breast:	n/a	chr15:41036699-41036708 chr15:41036700-41036709
40	POLR2A	chr15:41036446-41036544	GM12878	blood:	n/a	n/a
41	CEBPB	chr15:41036344-41036925	Hela-S3	cervix:	n/a	chr15:41036554-41036565 chr15:41036556-41036567 chr15:41036554-41036567
42	MAFK	chr15:41036297-41037067	Hela-S3	cervix:	n/a	chr15:41036456-41036470 chr15:41036857-41036872
43	JUN	chr15:41036324-41036723	Hela-S3	cervix:	n/a	chr15:41036699-41036708 chr15:41036700-41036709
44	STAT3	chr15:41036391-41036666	MCF10A-Er-Src	breast:	n/a	chr15:41036501-41036513
45	EGR1	chr15:41036361-41036663	K562	blood:	n/a	n/a
46	MAX	chr15:41036351-41036687	NB4	blood:	n/a	chr15:41036512-41036519
47	MAX	chr15:41036341-41036704	MCF-7	breast:	n/a	chr15:41036512-41036519
48	CEBPB	chr15:41036342-41036676	A549	lung:	n/a	chr15:41036554-41036565 chr15:41036556-41036567 chr15:41036554-41036567
49	STAT3	chr15:41036369-41036754	Hela-S3	cervix:	n/a	chr15:41036677-41036688 chr15:41036501-41036513
50	FOS	chr15:41036247-41036729	MCF10A-Er-Src	breast:	n/a	chr15:41036699-41036708 chr15:41036700-41036709

No.	Distal block	Cell Line	Cell type
1	chr15:41035825..41037680-chr15:41060818..41063658,2	K562	blood:
2	chr15:41029851..41031693-chr15:41035155..41036764,2	K562	blood:
3	chr15:41035271..41040468-chr15:41046040..41049485,6	MCF-7	breast:

Variant related genes	Relation type
RMDN3	TF binding region
ENSG00000104129	Chromatin interaction
ENSG00000137824	Chromatin interaction
ENSG00000188277	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 15 )

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10775121	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11070291	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11070293	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.81[MKK][hapmap];0.98[TSI][hapmap];0.89[YRI][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11631563	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11633269	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];0.98[TSI][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11852786	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11855560	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.85[JPT][hapmap];0.83[LWK][hapmap];0.94[MKK][hapmap];0.98[TSI][hapmap];0.96[YRI][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11858337	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11858338	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12372947	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12439683	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12441514	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12442845	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12593359	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.85[JPT][hapmap];0.83[LWK][hapmap];0.84[MEX][hapmap];0.94[MKK][hapmap];0.98[TSI][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12908284	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12912742	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2263551	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2304582	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.96[YRI][hapmap];0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2412546	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];0.95[TSI][hapmap];0.96[YRI][hapmap];0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2412547	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];0.98[TSI][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2412548	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2412549	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2577564	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2619679	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];0.89[TSI][hapmap];0.96[YRI][hapmap];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2619680	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2619683	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2917955	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2928140	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.93[JPT][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];0.95[TSI][hapmap];0.96[YRI][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3092982	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[YRI][hapmap];0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3092983	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.85[YRI][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3101861	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34400306	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs36106105	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs45495293	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4924493	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4924495	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4924501	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];0.98[TSI][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4924503	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];0.97[MKK][hapmap];0.98[TSI][hapmap];0.92[YRI][hapmap];0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56042757	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6492961	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7164339	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7167854	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7169010	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7172195	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7173646	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7174551	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7175401	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs752012	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8025883	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8033829	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8036817	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1053173	chr15:40933163-41094127	Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	nsv542363	chr15:40933163-41094127	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv904099	chr15:40949526-41041875	Genic enhancers Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	nsv904101	chr15:40979651-41275014	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
5	esv1819092	chr15:41017682-41255750	Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases

mRNA abundance (count:15)

SNP	Gene	Cis/trans	Tissue	Source
rs4923884	MRPL42P5	cis	multi-tissue	Pritchard
rs4923884	SPINT1	cis	multi-tissue	Pritchard
rs4923884	PLA2G4D	cis	cerebellum	SCAN
rs4923884	GPR176	cis	cerebellum	SCAN
rs4923884	RAD51	cis	multi-tissue	Pritchard
rs4923884	C15orf57	cis	parietal	SCAN
rs4923884	C15orf57	cis	cerebellum	SCAN
rs4923884	MAPKBP1	cis	cerebellum	SCAN
rs4923884	RP11-111A22.1	cis	Artery Tibial	GTEx
rs4923884	C15orf57	cis	Adipose Subcutaneous	GTEx
rs4923884	C15orf57	cis	lung	GTEx
rs4923884	C15orf57	cis	Nerve Tibial	GTEx
rs4923884	RP11-111A22.1	cis	lung	GTEx
rs4923884	CCDC32	cis	multi-tissue	Pritchard
rs4923884	C15orf57	cis	Artery Tibial	GTEx

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:40998800-41038000	Weak transcription	Stomach Mucosa	stomach
2	chr15:41008200-41046600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr15:41019400-41046200	Strong transcription	Fetal Stomach	stomach
4	chr15:41020000-41043600	Strong transcription	Dnd41	blood
5	chr15:41020400-41037600	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr15:41020600-41036800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr15:41020600-41037800	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr15:41020600-41038200	Strong transcription	Primary neutrophils fromperipheralblood	blood
9	chr15:41020800-41045400	Strong transcription	Fetal Muscle Trunk	muscle
10	chr15:41021800-41044600	Strong transcription	Brain Germinal Matrix	brain
11	chr15:41023200-41045200	Strong transcription	Thymus	Thymus
12	chr15:41023600-41036800	Strong transcription	Fetal Muscle Leg	muscle
13	chr15:41023800-41038400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr15:41023800-41045200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr15:41025600-41045000	Strong transcription	Primary T cells from cord blood	blood
16	chr15:41025600-41045400	Strong transcription	Stomach Smooth Muscle	stomach
17	chr15:41026000-41044600	Strong transcription	Sigmoid Colon	Sigmoid Colon
18	chr15:41026200-41044600	Strong transcription	Lung	lung
19	chr15:41026600-41037600	Strong transcription	HUVEC	blood vessel
20	chr15:41026600-41038200	Strong transcription	Brain Anterior Caudate	brain
21	chr15:41026800-41045200	Strong transcription	Brain Inferior Temporal Lobe	brain
22	chr15:41027200-41038400	Strong transcription	Brain Hippocampus Middle	brain
23	chr15:41027800-41038200	Strong transcription	Rectal Mucosa Donor 31	rectum
24	chr15:41028000-41037800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr15:41029000-41041800	Weak transcription	Fetal Kidney	kidney
26	chr15:41030800-41044000	Weak transcription	Psoas Muscle	Psoas
27	chr15:41031000-41046600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr15:41032000-41037200	Strong transcription	HUES64 Cell Line	embryonic stem cell
29	chr15:41032000-41043000	Weak transcription	Fetal Brain Male	brain
30	chr15:41032400-41036800	Weak transcription	Small Intestine	intestine
31	chr15:41032400-41038000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr15:41032600-41046200	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr15:41032600-41046600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr15:41032600-41046600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr15:41033200-41037600	Strong transcription	HUES48 Cell Line	embryonic stem cell
36	chr15:41033200-41039200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr15:41033200-41042000	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr15:41034000-41037400	Strong transcription	HUES6 Cell Line	embryonic stem cell
39	chr15:41034000-41037400	Strong transcription	Colonic Mucosa	Colon
40	chr15:41034000-41037600	Strong transcription	Brain Cingulate Gyrus	brain
41	chr15:41034000-41038400	Strong transcription	Aorta	Aorta
42	chr15:41034200-41037600	Strong transcription	Primary hematopoietic stem cells	blood
43	chr15:41034200-41038400	Strong transcription	Brain Angular Gyrus	brain
44	chr15:41034200-41045800	Strong transcription	Rectal Mucosa Donor 29	rectum
45	chr15:41034400-41044400	Strong transcription	Duodenum Smooth Muscle	Duodenum
46	chr15:41034400-41044600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr15:41034400-41045200	Strong transcription	Cortex derived primary cultured neurospheres	brain
48	chr15:41034600-41036600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
49	chr15:41034600-41036800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr15:41034600-41037200	Strong transcription	Primary B cells from cord blood	blood

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