Variant report

Variant	rs694461
Chromosome Location	chr15:44096063-44096064
allele	C/T
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	chr15:44096020-44096187	H1-hESC	embryonic stem cell:	n/a	n/a
2	POLR2A	chr15:44094963-44096478	PFSK-1	brain:	n/a	n/a
3	POLR2A	chr15:44094846-44096127	GM12892	blood:	n/a	n/a
4	POLR2A	chr15:44096023-44096648	Hela-S3	cervix:	n/a	n/a
5	POLR2A	chr15:44096014-44096183	MCF-7	breast:	n/a	n/a
6	POLR2A	chr15:44095970-44096602	PANC-1	pancreas:	n/a	n/a
7	POLR2A	chr15:44094183-44096675	HepG2	liver:	n/a	n/a
8	POLR2A	chr15:44096012-44096644	SK-N-MC	brain:	n/a	n/a
9	POLR2A	chr15:44094982-44096304	K562	blood:	n/a	n/a
10	POLR2A	chr15:44095048-44096278	GM12892	blood:	n/a	n/a
11	POLR2A	chr15:44096007-44097841	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:44067637..44070234-chr15:44095073..44096785,2	MCF-7	breast:
2	chr15:44062113..44074982-chr15:44088756..44097846,29	MCF-7	breast:

Variant related genes	Relation type
SERINC4	TF binding region
ENSG00000262560	TF binding region
ENSG00000140264	Chromatin interaction
ENSG00000167004	Chromatin interaction
ENSG00000128886	Chromatin interaction

Extended variants
information (count: 138 )
Associated
traits (count: 18 )

rSNPs within LD-proxies of this variant (count:127)

rs_ID	r²[population]
rs10163054	0.95[CHB][hapmap];0.92[CHD][hapmap];0.90[JPT][hapmap];0.83[ASN][1000 genomes]
rs10438303	1.00[CHB][hapmap];0.94[CHD][hapmap];0.95[JPT][hapmap]
rs1053492	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11070408	1.00[CHB][hapmap];0.94[CHD][hapmap];0.90[JPT][hapmap]
rs11070410	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.93[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11070412	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11638972	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11852840	0.92[ASN][1000 genomes]
rs11856495	0.91[ASN][1000 genomes]
rs11856795	1.00[CHB][hapmap];0.97[CHD][hapmap];0.84[JPT][hapmap];0.83[ASN][1000 genomes]
rs12101756	0.84[ASN][1000 genomes]
rs12440573	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12441127	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs12441861	1.00[CHB][hapmap];0.94[CHD][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs12441984	1.00[CHB][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs12442129	0.87[ASN][1000 genomes]
rs12443102	0.89[CHB][hapmap];0.88[JPT][hapmap]
rs12702	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12899922	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12908467	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13380397	0.88[ASN][1000 genomes]
rs16950562	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs16963953	0.95[ASN][1000 genomes]
rs16965120	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs16977724	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs16977798	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs1965794	0.87[ASN][1000 genomes]
rs1965795	0.94[ASN][1000 genomes]
rs1975364	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2228368	1.00[ASN][1000 genomes]
rs2277531	1.00[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs2411284	0.85[EUR][1000 genomes]
rs2412823	0.82[CEU][hapmap]
rs2447193	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs2447208	1.00[CHB][hapmap];0.91[CHD][hapmap];0.90[JPT][hapmap]
rs2467402	0.95[CHB][hapmap];0.94[CHD][hapmap];0.95[JPT][hapmap]
rs2470121	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs2614811	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs2614819	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs2788	1.00[CHB][hapmap];0.94[CHD][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs28377539	0.87[ASN][1000 genomes]
rs28413704	0.94[ASN][1000 genomes]
rs28476182	0.94[ASN][1000 genomes]
rs28509275	1.00[CHB][hapmap];0.97[CHD][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs28513374	1.00[CHB][hapmap];0.95[ASN][1000 genomes]
rs28519630	0.94[ASN][1000 genomes]
rs28524541	0.95[ASN][1000 genomes]
rs28531819	0.95[ASN][1000 genomes]
rs28546844	0.90[ASN][1000 genomes]
rs28564774	0.95[ASN][1000 genomes]
rs28578398	0.93[ASN][1000 genomes]
rs28583806	1.00[ASN][1000 genomes]
rs28590651	0.98[ASN][1000 genomes]
rs28595038	0.85[ASN][1000 genomes]
rs28636829	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs28674750	0.98[ASN][1000 genomes]
rs28678901	0.94[ASN][1000 genomes]
rs28679673	0.95[ASN][1000 genomes]
rs28684672	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs28687459	0.95[ASN][1000 genomes]
rs28696802	0.95[ASN][1000 genomes]
rs28707214	0.95[ASN][1000 genomes]
rs28718261	0.85[ASN][1000 genomes]
rs28780699	0.95[ASN][1000 genomes]
rs28781888	0.95[ASN][1000 genomes]
rs28823973	0.86[ASN][1000 genomes]
rs28858500	0.85[ASN][1000 genomes]
rs28866846	0.93[ASN][1000 genomes]
rs28891769	0.93[ASN][1000 genomes]
rs2920781	0.90[CHB][hapmap];0.91[CHD][hapmap];0.90[JPT][hapmap]
rs2927071	0.95[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap]
rs2927072	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs2927085	0.86[CEU][hapmap]
rs2955969	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3087657	1.00[CEU][hapmap];0.86[GIH][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3101443	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs35654783	0.82[EUR][1000 genomes]
rs35866764	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3736180	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs3742982	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs3759790	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs3759791	0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs3816792	0.95[CHB][hapmap];0.97[CHD][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs3825783	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs3862142	1.00[CHB][hapmap];0.91[CHD][hapmap];0.94[JPT][hapmap]
rs4332723	0.88[EUR][1000 genomes]
rs4617832	0.85[EUR][1000 genomes]
rs4924720	0.82[EUR][1000 genomes]
rs4924722	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4997480	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs524908	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap];0.93[TSI][hapmap];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs533143	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap]
rs56008017	0.94[ASN][1000 genomes]
rs56909447	0.95[ASN][1000 genomes]
rs575082	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60883262	0.94[ASN][1000 genomes]
rs61390361	0.83[ASN][1000 genomes]
rs62018947	0.85[EUR][1000 genomes]
rs62018952	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs663214	1.00[CEU][hapmap];0.93[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.81[YRI][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs667476	0.91[CEU][hapmap];0.95[CHB][hapmap]
rs68079546	0.95[ASN][1000 genomes]
rs686666	0.95[CEU][hapmap];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs688009	0.95[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs693919	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];0.95[TSI][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7168158	0.85[ASN][1000 genomes]
rs7169322	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs7169382	1.00[ASN][1000 genomes]
rs7169988	0.90[CHB][hapmap];0.90[JPT][hapmap]
rs7170167	0.86[ASN][1000 genomes]
rs7170751	0.88[ASN][1000 genomes]
rs7171750	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs7174208	1.00[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs7175032	1.00[CHB][hapmap];0.94[CHD][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs7175129	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.88[EUR][1000 genomes]
rs7178343	0.85[EUR][1000 genomes]
rs7179388	0.95[ASN][1000 genomes]
rs7180818	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7183809	0.95[ASN][1000 genomes]
rs8023458	1.00[CHB][hapmap];0.94[CHD][hapmap];0.95[JPT][hapmap]
rs8023508	1.00[CHB][hapmap];1.00[CHD][hapmap];0.85[JPT][hapmap];0.82[ASN][1000 genomes]
rs8032649	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs8034451	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs8040839	0.97[ASN][1000 genomes]
rs8042868	1.00[CHB][hapmap];0.91[CHD][hapmap];0.90[JPT][hapmap]
rs9944216	1.00[CHB][hapmap];0.91[CHD][hapmap];0.84[JPT][hapmap];0.83[ASN][1000 genomes]
rs9989313	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1846172	chr15:43632138-44116986	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
2	esv1846701	chr15:43759774-44116986	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
3	esv2758379	chr15:43823158-44148641	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
4	esv2760028	chr15:43823158-44148641	Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
5	nsv427960	chr15:43823158-44148641	Flanking Active TSS Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
6	nsv1037786	chr15:43888926-44318587	Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
7	nsv542370	chr15:43888926-44318587	Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
8	nsv431387	chr15:43929378-44862930	Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	158 gene(s)	inside rSNPs	diseases
9	nsv931051	chr15:43988761-44833518	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	154 gene(s)	inside rSNPs	diseases
10	nsv1036318	chr15:44053617-44160773	Flanking Active TSS Strong transcription Genic enhancers Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
11	nsv1050263	chr15:44093927-44204047	Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	n/a

mRNA abundance (count:18)

SNP	Gene	Cis/trans	Tissue	Source
rs694461	TGM5	cis	lymphoblastoid	seeQTL
rs694461	ELL3	cis	multi-tissue	Pritchard
rs694461	STRCP1	cis	Thyroid	GTEx
rs694461	CKMT1A	cis	Esophagus Mucosa	GTEx
rs694461	AC011330.5	cis	Thyroid	GTEx
rs694461	STRCP1	cis	Whole Blood	GTEx
rs694461	ZNF690	cis	multi-tissue	Pritchard
rs694461	NAP1L2	trans	lymphoblastoid	seeQTL
rs694461	C15orf43	cis	cerebellum	SCAN
rs694461	ADAL	cis	parietal	SCAN
rs694461	AC011330.5	cis	Artery Tibial	GTEx
rs694461	TGM5	cis	Lymphoblastoid	GTEx
rs694461	DUOX2	cis	parietal	SCAN
rs694461	SERF2	cis	lymphoblastoid	seeQTL
rs694461	ZSCAN29	cis	Thyroid	GTEx
rs694461	STRC	cis	multi-tissue	Pritchard
rs694461	WDR76	cis	parietal	SCAN
rs694461	PATL2	cis	cerebellum	SCAN

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:44093600-44097000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:44093600-44097000	Weak transcription	Aorta	Aorta
3	chr15:44093600-44097000	Weak transcription	Gastric	stomach
4	chr15:44093600-44098200	Weak transcription	Small Intestine	intestine
5	chr15:44093600-44103400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr15:44093600-44116000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr15:44093600-44116400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr15:44093800-44096600	Weak transcription	Brain Angular Gyrus	brain
9	chr15:44093800-44105400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr15:44093800-44107000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr15:44093800-44109000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr15:44093800-44112800	Strong transcription	Thymus	Thymus
13	chr15:44093800-44113800	Weak transcription	Stomach Mucosa	stomach
14	chr15:44093800-44115800	Weak transcription	Right Atrium	heart
15	chr15:44094000-44096200	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr15:44094000-44096400	Weak transcription	Primary B cells from cord blood	blood
17	chr15:44094000-44096400	Weak transcription	Primary hematopoietic stem cells	blood
18	chr15:44094000-44096400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr15:44094000-44096400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr15:44094000-44096400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr15:44094000-44096400	Weak transcription	Colon Smooth Muscle	Colon
22	chr15:44094000-44096400	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr15:44094000-44096400	Weak transcription	Fetal Brain Male	brain
24	chr15:44094000-44096400	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr15:44094000-44096400	Weak transcription	Rectal Smooth Muscle	rectum
26	chr15:44094000-44096400	Weak transcription	NHLF	lung
27	chr15:44094000-44096600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr15:44094000-44096800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr15:44094000-44097000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr15:44094000-44097000	Weak transcription	Colonic Mucosa	Colon
31	chr15:44094000-44097000	Weak transcription	Left Ventricle	heart
32	chr15:44094000-44097000	Weak transcription	Right Ventricle	heart
33	chr15:44094000-44097200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr15:44094000-44097200	Weak transcription	Esophagus	oesophagus
35	chr15:44094000-44097200	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr15:44094000-44097200	Weak transcription	Psoas Muscle	Psoas
37	chr15:44094000-44100400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr15:44094000-44100600	Strong transcription	Primary monocytes fromperipheralblood	blood
39	chr15:44094000-44100600	Strong transcription	Fetal Intestine Small	intestine
40	chr15:44094000-44100600	Strong transcription	Monocytes-CD14+_RO01746	blood
41	chr15:44094000-44107800	Strong transcription	Lung	lung
42	chr15:44094000-44109800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr15:44094000-44110000	Strong transcription	Brain Anterior Caudate	brain
44	chr15:44094000-44110000	Strong transcription	Placenta	Placenta
45	chr15:44094000-44110000	Strong transcription	Fetal Thymus	thymus
46	chr15:44094000-44110000	Strong transcription	Skeletal Muscle Female	skeletal muscle
47	chr15:44094000-44110000	Strong transcription	Stomach Smooth Muscle	stomach
48	chr15:44094000-44110200	Strong transcription	HUES64 Cell Line	embryonic stem cell
49	chr15:44094000-44110200	Strong transcription	Primary T cells fromperipheralblood	blood
50	chr15:44094000-44110200	Strong transcription	Fetal Intestine Large	intestine

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