Variant report

Variant	rs1133642
Chromosome Location	chr15:31267147-31267148
allele	A/C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:31258278..31261400-chr15:31264720..31267542,4	K562	blood:

Variant related genes	Relation type
ENSG00000166912	Chromatin interaction

Extended variants
information (count: 120 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:102)

rs_ID	r²[population]
rs10153041	0.84[CHB][hapmap]
rs10163148	0.91[CHB][hapmap];0.83[CHD][hapmap]
rs10519726	0.82[CHB][hapmap]
rs11070678	0.91[CHB][hapmap]
rs11070718	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11631543	0.80[EUR][1000 genomes]
rs11638295	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[JPT][hapmap];0.87[TSI][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12437580	0.85[ASN][1000 genomes]
rs12439664	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12441318	0.92[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs12442333	0.81[CHB][hapmap]
rs12443369	0.81[ASN][1000 genomes]
rs12901022	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs12905872	0.89[ASN][1000 genomes]
rs12906480	0.85[ASN][1000 genomes]
rs12913397	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12914207	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12914438	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1404468	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1404469	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1404470	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1425291	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1474381	0.91[CHB][hapmap]
rs1474382	0.91[CHB][hapmap];0.83[CHD][hapmap]
rs1524876	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16956341	0.82[CHB][hapmap]
rs16956362	0.82[CHB][hapmap]
rs16956366	0.82[CHB][hapmap]
rs16956414	0.82[CHB][hapmap]
rs16956422	0.82[CHB][hapmap]
rs1880499	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2042613	1.00[CHB][hapmap]
rs2113945	0.91[CHB][hapmap];0.83[CHD][hapmap]
rs2113946	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs2272218	0.91[CHB][hapmap];0.89[CHD][hapmap];0.85[ASN][1000 genomes]
rs2272219	0.91[CHB][hapmap];0.85[ASN][1000 genomes]
rs2293314	0.92[ASW][hapmap];0.96[CEU][hapmap];0.84[CHB][hapmap];0.90[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];0.88[MKK][hapmap];0.98[TSI][hapmap];0.81[YRI][hapmap];0.81[EUR][1000 genomes]
rs2293319	0.91[CHB][hapmap];0.83[CHD][hapmap]
rs2293320	0.91[CHB][hapmap];0.89[CHD][hapmap]
rs28564430	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28693590	0.91[CHB][hapmap];0.83[CHD][hapmap]
rs2873	0.84[ASW][hapmap];0.93[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.86[YRI][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2949566	0.80[EUR][1000 genomes]
rs2949567	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2949569	0.93[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2949570	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2949571	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2949573	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2949574	0.87[GIH][hapmap];0.84[MKK][hapmap];0.91[TSI][hapmap]
rs2949575	0.91[CHB][hapmap];0.85[ASN][1000 genomes]
rs2949576	0.91[CHB][hapmap];0.89[CHD][hapmap];0.85[ASN][1000 genomes]
rs2949577	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2949578	0.91[CHB][hapmap];0.89[CHD][hapmap];0.82[ASN][1000 genomes]
rs2955783	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2955787	0.91[CHB][hapmap];0.85[ASN][1000 genomes]
rs2955790	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.98[TSI][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2955791	0.91[CHB][hapmap]
rs2955794	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2955795	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2955796	0.92[CEU][hapmap];0.92[CHB][hapmap];0.90[JPT][hapmap];0.80[EUR][1000 genomes]
rs2955798	0.80[EUR][1000 genomes]
rs2959039	0.96[CEU][hapmap];0.92[CHB][hapmap];0.90[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.81[EUR][1000 genomes]
rs2959047	0.85[ASN][1000 genomes]
rs2959049	0.91[CHB][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2959050	0.85[ASN][1000 genomes]
rs2959054	0.87[GIH][hapmap];0.91[TSI][hapmap]
rs3743231	0.91[CHB][hapmap];0.89[CHD][hapmap];0.82[ASN][1000 genomes]
rs3743233	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3784588	0.82[CHB][hapmap]
rs3794594	0.85[CEU][hapmap];0.91[GIH][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap]
rs4344701	0.82[ASN][1000 genomes]
rs4779794	0.80[CEU][hapmap];0.91[GIH][hapmap];1.00[TSI][hapmap]
rs4779796	0.91[CHB][hapmap]
rs4779797	0.91[CHB][hapmap];0.83[CHD][hapmap]
rs58083498	0.89[ASN][1000 genomes]
rs6493358	0.82[CHB][hapmap]
rs6493387	0.89[ASN][1000 genomes]
rs6493388	0.89[ASN][1000 genomes]
rs7161812	0.90[CHB][hapmap]
rs7164530	0.85[ASN][1000 genomes]
rs7164939	0.82[CHB][hapmap];0.82[ASN][1000 genomes]
rs7165798	1.00[CHB][hapmap]
rs7169064	0.91[CHB][hapmap];0.83[CHD][hapmap]
rs7170710	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7170772	0.81[ASN][1000 genomes]
rs7175256	0.85[ASN][1000 genomes]
rs7175951	0.91[CHB][hapmap];0.89[CHD][hapmap];0.85[ASN][1000 genomes]
rs7175967	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7176351	0.91[CHB][hapmap];0.83[CHD][hapmap]
rs7178375	0.91[CHB][hapmap]
rs7178533	0.91[CHB][hapmap]
rs7182143	1.00[CHB][hapmap]
rs7183880	0.85[ASN][1000 genomes]
rs798088	0.84[CHB][hapmap]
rs798101	0.92[CHB][hapmap];0.81[JPT][hapmap]
rs8040989	0.92[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.87[TSI][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8041717	0.91[CHB][hapmap];0.89[CHD][hapmap];0.85[ASN][1000 genomes]
rs811768	0.84[CHB][hapmap]
rs871312	0.82[CHB][hapmap]
rs872843	0.82[CHB][hapmap]
rs964925	0.91[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs9806159	0.91[CHB][hapmap];0.83[CHD][hapmap]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv427955	chr15:30467980-31273174	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	nsv531138	chr15:30653877-31609679	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
3	nsv916936	chr15:30921917-31337510	Active TSS Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	nsv525795	chr15:30936285-31324531	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	nsv903831	chr15:30986051-31723279	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
6	nsv1046874	chr15:31008133-31294654	Enhancers Strong transcription Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
7	nsv1054147	chr15:31014507-31972706	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
8	nsv542306	chr15:31014507-31972706	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
9	nsv832951	chr15:31131239-31304469	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
10	nsv1039037	chr15:31140415-31277268	Strong transcription ZNF genes & repeats Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
11	nsv542309	chr15:31140415-31277268	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
12	nsv1036018	chr15:31140415-31544888	Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
13	nsv521842	chr15:31140700-31272670	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
14	nsv903834	chr15:31179534-31293774	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
15	esv33507	chr15:31183324-31471023	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers 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	35 gene(s)	inside rSNPs	diseases
16	nsv832952	chr15:31204426-31333998	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
17	nsv1052722	chr15:31261834-31609680	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
18	nsv542315	chr15:31261834-31609680	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31226200-31269200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr15:31227000-31269600	Strong transcription	Primary monocytes fromperipheralblood	blood
3	chr15:31233400-31269200	Strong transcription	Liver	Liver
4	chr15:31237200-31269600	Strong transcription	Primary B cells from cord blood	blood
5	chr15:31242000-31282800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr15:31243200-31267600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr15:31245000-31276400	Weak transcription	Brain Germinal Matrix	brain
8	chr15:31247000-31270200	Weak transcription	K562	blood
9	chr15:31248800-31283000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr15:31249000-31269600	Strong transcription	HUVEC	blood vessel
11	chr15:31249000-31270200	Weak transcription	Stomach Mucosa	stomach
12	chr15:31249000-31276000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr15:31250200-31282200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr15:31250800-31270600	Weak transcription	Small Intestine	intestine
15	chr15:31250800-31282400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr15:31251200-31272400	Weak transcription	Aorta	Aorta
17	chr15:31251200-31277200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr15:31251200-31282400	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr15:31251600-31282200	Weak transcription	Hela-S3	cervix
20	chr15:31252000-31272200	Weak transcription	Spleen	Spleen
21	chr15:31252800-31282400	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr15:31253400-31270200	Weak transcription	Ovary	ovary
23	chr15:31254600-31276400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr15:31254600-31277200	Weak transcription	HSMMtube	muscle
25	chr15:31254800-31270400	Weak transcription	Fetal Heart	heart
26	chr15:31254800-31272000	Weak transcription	Esophagus	oesophagus
27	chr15:31255200-31269200	Strong transcription	Placenta	Placenta
28	chr15:31255200-31276800	Weak transcription	Fetal Brain Female	brain
29	chr15:31255400-31270000	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr15:31255400-31271600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr15:31255600-31270000	Strong transcription	Primary T helper cells fromperipheralblood	blood
32	chr15:31255600-31277000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr15:31255800-31269000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr15:31255800-31269600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr15:31255800-31277000	Weak transcription	Fetal Intestine Small	intestine
36	chr15:31255800-31277000	Weak transcription	Fetal Stomach	stomach
37	chr15:31256000-31282400	Weak transcription	Fetal Brain Male	brain
38	chr15:31256800-31268800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr15:31257800-31271400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr15:31258200-31270200	Weak transcription	Right Ventricle	heart
41	chr15:31258200-31277000	Weak transcription	Placenta Amnion	Placenta Amnion
42	chr15:31258200-31277800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr15:31258400-31272400	Weak transcription	Pancreas	Pancrea
44	chr15:31258400-31277000	Weak transcription	Gastric	stomach
45	chr15:31258800-31270000	Weak transcription	Left Ventricle	heart
46	chr15:31258800-31271200	Weak transcription	Stomach Smooth Muscle	stomach
47	chr15:31258800-31271800	Weak transcription	Thymus	Thymus
48	chr15:31258800-31273400	Weak transcription	Lung	lung
49	chr15:31259600-31274800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr15:31260600-31267800	Strong transcription	Primary hematopoietic stem cells	blood

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