Variant report

Variant	rs8038760
Chromosome Location	chr15:75742095-75742096
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:75741578..75748624-chr15:75927989..75935113,20	K562	blood:
2	chr15:75657601..75665504-chr15:75739437..75749700,27	K562	blood:
3	chr15:75741664..75745730-chr15:75869940..75872786,3	MCF-7	breast:
4	chr15:75658070..75664945-chr15:75741625..75749756,25	K562	blood:
5	chr15:75741052..75746522-chr15:75930202..75934500,7	MCF-7	breast:
6	chr15:75741578..75748579-chr15:75928515..75935579,16	K562	blood:
7	chr15:75726359..75728321-chr15:75740878..75743039,2	K562	blood:
8	chr15:75741711..75746813-chr15:75868980..75872679,7	MCF-7	breast:
9	chr15:75656095..75662590-chr15:75739456..75750037,27	MCF-7	breast:
10	chr15:75657484..75665083-chr15:75741604..75749517,41	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000177971	Chromatin interaction
ENSG00000260206	Chromatin interaction
ENSG00000260274	Chromatin interaction
ENSG00000140400	Chromatin interaction
ENSG00000169410	Chromatin interaction

Extended variants
information (count: 99 )
Associated
traits (count: 17 )

rSNPs within LD-proxies of this variant (count:87)

rs_ID	r²[population]
rs10152155	0.92[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs10220738	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10775209	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11072542	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11631052	0.91[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs11632105	0.82[GIH][hapmap]
rs11632813	0.80[GIH][hapmap]
rs11634863	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11636031	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];0.92[MEX][hapmap];0.94[MKK][hapmap];0.95[TSI][hapmap];0.93[YRI][hapmap];0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11636199	0.94[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];0.95[LWK][hapmap];0.84[MEX][hapmap];0.94[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap]
rs11637068	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11637586	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11638974	1.00[CEU][hapmap];0.89[GIH][hapmap];0.93[TSI][hapmap]
rs11639183	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12708518	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12708519	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.92[MEX][hapmap];0.94[MKK][hapmap];0.93[TSI][hapmap];0.89[YRI][hapmap];0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12708520	1.00[CEU][hapmap];0.93[YRI][hapmap]
rs12916964	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13380103	1.00[CEU][hapmap];0.96[YRI][hapmap]
rs13737	0.88[CEU][hapmap]
rs28432989	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs28610581	0.84[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];0.92[MEX][hapmap];0.80[MKK][hapmap];0.95[TSI][hapmap];0.86[YRI][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28693593	0.89[ASW][hapmap];1.00[CEU][hapmap];0.91[GIH][hapmap];0.95[LWK][hapmap];0.84[MEX][hapmap];0.93[MKK][hapmap];0.95[TSI][hapmap];0.89[YRI][hapmap]
rs28737338	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28783769	0.88[CHB][hapmap];0.93[CHD][hapmap];0.89[GIH][hapmap];0.85[JPT][hapmap];0.95[LWK][hapmap];0.92[MKK][hapmap];0.80[YRI][hapmap]
rs3809547	0.94[CEU][hapmap];0.89[CHB][hapmap];0.95[JPT][hapmap];0.89[EUR][1000 genomes]
rs4075522	0.89[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];0.95[LWK][hapmap];0.84[MEX][hapmap];0.93[MKK][hapmap];0.95[TSI][hapmap];0.96[YRI][hapmap]
rs4243033	0.92[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs4297648	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4299117	0.84[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];0.98[TSI][hapmap];0.83[YRI][hapmap];0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4322627	0.89[ASW][hapmap];0.94[CHB][hapmap];0.95[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.95[LWK][hapmap];0.83[MEX][hapmap];0.95[TSI][hapmap];0.88[YRI][hapmap];0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4368141	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4381565	0.84[AMR][1000 genomes]
rs4451914	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];0.92[MEX][hapmap];0.97[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4462560	1.00[CEU][hapmap];0.89[YRI][hapmap];0.86[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4486847	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4526985	0.80[GIH][hapmap]
rs4545784	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4564532	1.00[CEU][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4886443	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.92[MEX][hapmap];0.98[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4886446	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]
rs4886699	1.00[ASW][hapmap];1.00[CEU][hapmap];0.91[GIH][hapmap];0.95[LWK][hapmap];0.92[MEX][hapmap];0.95[MKK][hapmap];0.98[TSI][hapmap];0.89[YRI][hapmap];0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4886700	0.92[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs4886702	0.82[GIH][hapmap]
rs4886703	1.00[ASW][hapmap];1.00[CEU][hapmap];0.91[GIH][hapmap];1.00[LWK][hapmap];0.92[MEX][hapmap];0.97[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4886704	0.80[GIH][hapmap]
rs4886705	0.89[GIH][hapmap]
rs4886706	0.89[GIH][hapmap]
rs4886707	0.84[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4886708	0.94[ASW][hapmap];0.94[CEU][hapmap];0.91[GIH][hapmap];0.90[LWK][hapmap];0.92[MEX][hapmap];0.85[MKK][hapmap];0.98[TSI][hapmap];0.93[YRI][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4886712	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4886716	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs4886722	1.00[CEU][hapmap];0.87[GIH][hapmap];0.86[TSI][hapmap]
rs5745920	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6495171	0.95[JPT][hapmap]
rs6495174	0.80[GIH][hapmap]
rs6495176	0.80[GIH][hapmap]
rs6495181	0.80[GIH][hapmap]
rs6495182	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.95[TSI][hapmap];0.80[YRI][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7163907	0.84[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.89[GIH][hapmap];0.95[JPT][hapmap];0.91[LWK][hapmap];0.92[MEX][hapmap];0.91[TSI][hapmap];0.82[YRI][hapmap]
rs7166281	0.88[CEU][hapmap]
rs7166737	1.00[CEU][hapmap];0.89[YRI][hapmap];0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7171507	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7175852	0.94[ASW][hapmap];0.91[GIH][hapmap];0.95[LWK][hapmap];0.89[MKK][hapmap];0.91[TSI][hapmap];0.89[YRI][hapmap];0.89[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs7176938	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7180574	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7182283	0.80[GIH][hapmap]
rs7184046	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap]
rs7402293	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7402844	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7495610	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs8023268	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs8023815	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];0.92[MEX][hapmap];0.94[MKK][hapmap];0.95[TSI][hapmap];0.93[YRI][hapmap];0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs8024244	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs8027365	0.83[AFR][1000 genomes]
rs8027546	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs8028182	0.94[ASW][hapmap];1.00[LWK][hapmap];0.84[MEX][hapmap];0.85[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs8028277	1.00[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];1.00[LWK][hapmap];0.92[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs8029112	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];0.92[MEX][hapmap];0.95[TSI][hapmap];0.93[YRI][hapmap];0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs8029394	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8030802	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.89[TSI][hapmap];0.86[YRI][hapmap];0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs8034317	0.94[ASW][hapmap];1.00[CEU][hapmap];0.91[GIH][hapmap];0.95[LWK][hapmap];0.92[MEX][hapmap];0.94[MKK][hapmap];0.98[TSI][hapmap];0.93[YRI][hapmap];0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs8035987	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs8036758	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9806241	0.80[GIH][hapmap]
rs9920028	1.00[CEU][hapmap];0.84[TSI][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	nsv827389	chr15:75741918-75749453	Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	61 gene(s)	inside rSNPs	diseases

mRNA abundance (count:17)

SNP	Gene	Cis/trans	Tissue	Source
rs8038760	MAN2C1	cis	Esophagus Muscularis	GTEx
rs8038760	MAN2C1	cis	Artery Tibial	GTEx
rs8038760	SNUPN	cis	Thyroid	GTEx
rs8038760	MAN2C1	cis	Artery Aorta	GTEx
rs8038760	MAN2C1	cis	Heart Left Ventricle	GTEx
rs8038760	MAN2C1	cis	Nerve Tibial	GTEx
rs8038760	MAN2C1	cis	Adipose Subcutaneous	GTEx
rs8038760	SNUPN	Cis_1M	lymphoblastoid	RTeQTL
rs8038760	MAN2C1	cis	parietal	SCAN
rs8038760	MAN2C1	cis	cerebellum	SCAN
rs8038760	MAN2C1	cis	Esophagus Mucosa	GTEx
rs8038760	SNUPN	cis	lymphoblastoid	seeQTL
rs8038760	MAN2C1	cis	Thyroid	GTEx
rs8038760	MAN2C1	cis	Skin Sun Exposed Lower leg	GTEx
rs8038760	MAN2C1	cis	lung	GTEx
rs8038760	MAN2C1	cis	Stomach	GTEx
rs8038760	MAN2C1	cis	Whole Blood	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:75704800-75742200	Weak transcription	Fetal Brain Male	brain
2	chr15:75705400-75742200	Weak transcription	Right Ventricle	heart
3	chr15:75715600-75742200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr15:75717000-75742600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr15:75721200-75742600	Weak transcription	Aorta	Aorta
6	chr15:75722800-75742200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr15:75722800-75742200	Weak transcription	Gastric	stomach
8	chr15:75722800-75742200	Weak transcription	Pancreas	Pancrea
9	chr15:75722800-75742200	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr15:75722800-75742200	Weak transcription	HSMMtube	muscle
11	chr15:75723000-75742600	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr15:75728800-75742600	Weak transcription	Esophagus	oesophagus
13	chr15:75730800-75742200	Weak transcription	Psoas Muscle	Psoas
14	chr15:75735600-75742200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr15:75735600-75742600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr15:75735800-75742400	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr15:75736000-75742200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr15:75736000-75742800	Weak transcription	Lung	lung
19	chr15:75736200-75742200	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr15:75736200-75742200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr15:75736200-75742600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr15:75736400-75742200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
23	chr15:75737000-75742200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
24	chr15:75738400-75742200	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr15:75738800-75742200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr15:75738800-75742200	Weak transcription	Right Atrium	heart
27	chr15:75739400-75742200	Weak transcription	Left Ventricle	heart
28	chr15:75740000-75742200	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr15:75740000-75742200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
30	chr15:75740000-75742400	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr15:75740000-75742600	Weak transcription	Brain Angular Gyrus	brain
32	chr15:75740200-75742200	Weak transcription	Brain Substantia Nigra	brain
33	chr15:75740200-75742200	Weak transcription	Fetal Kidney	kidney
34	chr15:75740200-75742400	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr15:75740200-75742400	Enhancers	Primary T killer memory cells from peripheral blood	blood
36	chr15:75740400-75742200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr15:75740400-75742200	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr15:75740400-75742200	Weak transcription	Spleen	Spleen
39	chr15:75740600-75742200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
40	chr15:75740600-75742400	Enhancers	Primary B cells from cord blood	blood
41	chr15:75740800-75742200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr15:75741000-75742200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr15:75741000-75742200	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr15:75741000-75742200	Enhancers	Thymus	Thymus
45	chr15:75741000-75742400	Enhancers	Brain Germinal Matrix	brain
46	chr15:75741400-75742200	Enhancers	Liver	Liver
47	chr15:75741400-75742200	Enhancers	Colon Smooth Muscle	Colon
48	chr15:75741400-75742200	Enhancers	Fetal Lung	lung
49	chr15:75741400-75742400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr15:75741600-75742200	Enhancers	Cortex derived primary cultured neurospheres	brain

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