Variant report

Variant	rs4886446
Chromosome Location	chr15:75770521-75770522
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:75745748..75747907-chr15:75768138..75770692,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000169375	Chromatin interaction

Extended variants
information (count: 119 )
Associated
traits (count: 14 )

rSNPs within LD-proxies of this variant (count:107)

rs_ID	r²[population]
rs10152155	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10220738	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs10775209	0.82[EUR][1000 genomes]
rs10851882	0.82[CHB][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs11072542	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11072544	0.82[CHB][hapmap];0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs11072552	0.84[GIH][hapmap]
rs1128933	0.82[CHB][hapmap];0.81[CHD][hapmap];0.86[GIH][hapmap]
rs11631052	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11632105	0.82[CHB][hapmap];0.86[CHD][hapmap];0.89[GIH][hapmap]
rs11632813	0.82[CHB][hapmap];0.86[CHD][hapmap];0.89[GIH][hapmap]
rs11634402	0.82[GIH][hapmap]
rs11634863	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11636031	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.90[LWK][hapmap];0.98[MKK][hapmap];0.89[YRI][hapmap];0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11636199	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.97[MKK][hapmap];0.96[YRI][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11637068	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11637263	0.92[ASN][1000 genomes]
rs11637586	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11638974	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];0.98[GIH][hapmap];0.90[JPT][hapmap];0.81[MKK][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11639183	0.88[EUR][1000 genomes]
rs11855087	0.81[CHB][hapmap]
rs12324230	0.81[CHB][hapmap];0.83[CHD][hapmap];0.89[GIH][hapmap]
rs12708518	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12708519	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.98[MKK][hapmap];0.85[YRI][hapmap];0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12708520	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12909863	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12916964	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13380103	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13737	0.89[CEU][hapmap]
rs28432989	0.99[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28610581	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.83[MKK][hapmap];0.82[YRI][hapmap];0.80[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs28623700	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28693593	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];0.90[LWK][hapmap];0.98[MKK][hapmap];0.84[YRI][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28737338	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28783769	0.95[GIH][hapmap];0.90[LWK][hapmap];0.97[MKK][hapmap];0.84[YRI][hapmap];0.83[EUR][1000 genomes]
rs3809547	0.94[CEU][hapmap];0.80[EUR][1000 genomes]
rs3809549	0.82[CHB][hapmap];0.81[CHD][hapmap];0.86[GIH][hapmap]
rs4075522	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];0.98[MKK][hapmap];0.92[YRI][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4243033	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4297648	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4299117	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.90[LWK][hapmap];1.00[MKK][hapmap];0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4322627	0.94[ASW][hapmap];1.00[GIH][hapmap];0.90[LWK][hapmap];0.88[YRI][hapmap];0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4368141	0.84[EUR][1000 genomes]
rs4381565	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4430707	0.82[CHB][hapmap];0.86[CHD][hapmap];0.86[GIH][hapmap]
rs4451914	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.95[LWK][hapmap];0.97[MKK][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4462560	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.84[YRI][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4486847	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4526985	0.81[CHD][hapmap];0.89[GIH][hapmap]
rs4545784	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4564532	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4886443	0.94[ASW][hapmap];1.00[CEU][hapmap];0.98[GIH][hapmap];0.92[LWK][hapmap];0.97[MKK][hapmap];0.96[YRI][hapmap];0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4886699	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.95[MKK][hapmap];0.85[YRI][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4886700	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4886702	0.82[CHB][hapmap];0.81[CHD][hapmap];0.89[GIH][hapmap]
rs4886703	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];0.97[MKK][hapmap];0.96[YRI][hapmap];0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4886704	0.82[CHB][hapmap];0.88[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs4886705	0.82[CHB][hapmap];0.88[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs4886706	0.82[CHB][hapmap];0.81[CHD][hapmap];0.81[GIH][hapmap]
rs4886707	1.00[CEU][hapmap];0.89[GIH][hapmap];0.83[MKK][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4886708	1.00[ASW][hapmap];0.94[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[LWK][hapmap];0.92[MKK][hapmap];0.89[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4886712	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4886715	0.85[EUR][1000 genomes]
rs4886716	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs4886718	0.82[GIH][hapmap]
rs4886722	1.00[CEU][hapmap];0.95[GIH][hapmap]
rs5745920	0.82[EUR][1000 genomes]
rs60972074	0.83[EUR][1000 genomes]
rs62027181	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6495174	0.82[CHB][hapmap];0.88[CHD][hapmap];0.89[GIH][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs6495176	0.82[CHB][hapmap];0.81[CHD][hapmap];0.89[GIH][hapmap]
rs6495181	0.82[CHB][hapmap];0.86[CHD][hapmap];0.89[GIH][hapmap]
rs6495182	0.84[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.82[MKK][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7163451	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7163907	0.89[ASW][hapmap];1.00[CEU][hapmap];0.98[GIH][hapmap];0.86[LWK][hapmap];0.83[MKK][hapmap];0.85[EUR][1000 genomes]
rs7164541	0.82[CHB][hapmap];0.88[CHD][hapmap];0.89[GIH][hapmap]
rs7165469	0.83[ASN][1000 genomes]
rs7166281	0.88[CEU][hapmap];0.86[GIH][hapmap]
rs7166737	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7170660	0.85[ASN][1000 genomes]
rs7171507	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7175852	0.89[ASW][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.89[MKK][hapmap];0.85[YRI][hapmap];0.85[EUR][1000 genomes]
rs7176938	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7180574	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7182283	0.82[CHB][hapmap];0.85[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap]
rs7184046	1.00[CEU][hapmap];0.84[YRI][hapmap];0.82[EUR][1000 genomes]
rs7402293	0.82[EUR][1000 genomes]
rs7402844	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7495610	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs8023268	1.00[CEU][hapmap];0.89[YRI][hapmap];0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs8023815	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.90[LWK][hapmap];0.98[MKK][hapmap];0.89[YRI][hapmap];0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs8024244	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs8027365	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs8027546	0.89[EUR][1000 genomes]
rs8028182	0.89[ASW][hapmap];0.84[GIH][hapmap];0.97[LWK][hapmap];0.96[YRI][hapmap]
rs8028277	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];0.95[MKK][hapmap];0.89[YRI][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8029112	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.90[LWK][hapmap];0.89[YRI][hapmap];0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs8029394	0.84[EUR][1000 genomes]
rs8030802	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.82[YRI][hapmap];0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs8034317	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];1.00[MKK][hapmap];0.89[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8035987	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs8036758	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs8036884	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs8038760	0.94[ASW][hapmap];1.00[CEU][hapmap];0.91[GIH][hapmap];0.95[LWK][hapmap];0.95[MKK][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9806241	0.82[CHB][hapmap];0.86[CHD][hapmap];0.89[GIH][hapmap]
rs9920028	1.00[CEU][hapmap];0.86[GIH][hapmap]
rs9944207	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531901	chr15:75600108-76019966	Genic enhancers Flanking Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
2	esv3445070	chr15:75623136-76045948	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
3	nsv530345	chr15:75628556-75951011	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	158 gene(s)	inside rSNPs	diseases
4	nsv1048028	chr15:75637515-76019967	Strong transcription Genic enhancers Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	161 gene(s)	inside rSNPs	diseases
5	nsv542436	chr15:75637515-76019967	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	161 gene(s)	inside rSNPs	diseases
6	nsv482802	chr15:75686519-75899896	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
7	esv1800424	chr15:75692303-75991451	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	124 gene(s)	inside rSNPs	diseases
8	nsv904387	chr15:75706296-75806911	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
9	nsv531902	chr15:75724505-75919237	Flanking Active TSS Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
10	nsv904388	chr15:75730182-75804543	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
11	nsv904389	chr15:75739824-75806911	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
12	nsv827390	chr15:75766087-75795370	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:14)

SNP	Gene	Cis/trans	Tissue	Source
rs4886446	MAN2C1	cis	Whole Blood	GTEx
rs4886446	MAN2C1	cis	Artery Aorta	GTEx
rs4886446	SNUPN	Cis_1M	lymphoblastoid	RTeQTL
rs4886446	MAN2C1	cis	Heart Left Ventricle	GTEx
rs4886446	MAN2C1	cis	Stomach	GTEx
rs4886446	MAN2C1	cis	Adipose Subcutaneous	GTEx
rs4886446	MAN2C1	cis	Skin Sun Exposed Lower leg	GTEx
rs4886446	MAN2C1	cis	Esophagus Muscularis	GTEx
rs4886446	MAN2C1	cis	lung	GTEx
rs4886446	MAN2C1	cis	Nerve Tibial	GTEx
rs4886446	MAN2C1	cis	Esophagus Mucosa	GTEx
rs4886446	MAN2C1	cis	Artery Tibial	GTEx
rs4886446	SNUPN	cis	Thyroid	GTEx
rs4886446	MAN2C1	cis	Thyroid	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:75749000-75797800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr15:75749200-75776800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr15:75749200-75782000	Weak transcription	Right Atrium	heart
4	chr15:75754400-75770800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr15:75755200-75772400	Strong transcription	Cortex derived primary cultured neurospheres	brain
6	chr15:75755200-75772400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr15:75755200-75772600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr15:75755400-75772400	Strong transcription	Fetal Muscle Leg	muscle
9	chr15:75755600-75772800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr15:75756200-75772400	Strong transcription	Fetal Stomach	stomach
11	chr15:75756200-75772600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr15:75756200-75772600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr15:75756400-75772600	Strong transcription	Fetal Muscle Trunk	muscle
14	chr15:75756600-75772800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr15:75757400-75772400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
16	chr15:75757800-75772600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr15:75758000-75772400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr15:75758000-75772400	Strong transcription	Liver	Liver
19	chr15:75758000-75772400	Strong transcription	Osteobl	bone
20	chr15:75758000-75772600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr15:75758000-75772800	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr15:75758200-75772200	Strong transcription	Primary T cells fromperipheralblood	blood
23	chr15:75758400-75772200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr15:75758600-75772000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr15:75758600-75772200	Strong transcription	Fetal Intestine Small	intestine
26	chr15:75761600-75785200	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr15:75761800-75772600	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr15:75762000-75771600	Weak transcription	Stomach Mucosa	stomach
29	chr15:75762200-75775400	Weak transcription	Fetal Heart	heart
30	chr15:75762200-75798000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr15:75762400-75771800	Weak transcription	Right Ventricle	heart
32	chr15:75762400-75771800	Weak transcription	K562	blood
33	chr15:75762400-75773000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr15:75762400-75792000	Weak transcription	Esophagus	oesophagus
35	chr15:75762400-75797800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr15:75762400-75798000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
37	chr15:75762800-75770800	Weak transcription	Gastric	stomach
38	chr15:75762800-75770800	Weak transcription	GM12878-XiMat	blood
39	chr15:75762800-75771000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr15:75763000-75770800	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr15:75763200-75775200	Weak transcription	Brain Germinal Matrix	brain
42	chr15:75763400-75771600	Weak transcription	Primary hematopoietic stem cells	blood
43	chr15:75763400-75776600	Weak transcription	Hela-S3	cervix
44	chr15:75763400-75777000	Weak transcription	Small Intestine	intestine
45	chr15:75763400-75778600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
46	chr15:75763400-75780000	Weak transcription	Pancreas	Pancrea
47	chr15:75763600-75770600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr15:75763600-75771000	Weak transcription	Rectal Smooth Muscle	rectum
49	chr15:75763600-75771600	Weak transcription	NHLF	lung
50	chr15:75763600-75785800	Weak transcription	Psoas Muscle	Psoas

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