Variant report

Variant	rs1899
Chromosome Location	chr15:41689232-41689233
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:41685725..41690620-chr15:41692934..41695677,5	K562	blood:
2	chr15:41687654..41690620-chr15:41692610..41695958,4	K562	blood:
3	chr15:41681566..41684125-chr15:41686638..41690389,3	K562	blood:

Variant related genes	Relation type
ENSG00000137806	Chromatin interaction

Extended variants
information (count: 116 )
Associated
traits (count: 27 )

rSNPs within LD-proxies of this variant (count:110)

rs_ID	r²[population]
rs10518717	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11070328	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11629979	1.00[ASN][1000 genomes]
rs11630656	0.87[CEU][hapmap];1.00[CHB][hapmap];0.83[GIH][hapmap];0.80[MEX][hapmap];0.97[TSI][hapmap];1.00[ASN][1000 genomes]
rs11630799	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11635269	1.00[ASN][1000 genomes]
rs11635565	1.00[ASN][1000 genomes]
rs11635906	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];0.82[LWK][hapmap];0.82[MEX][hapmap];0.89[TSI][hapmap];0.88[YRI][hapmap];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11854081	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11854632	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11854820	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11858068	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11858812	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[LWK][hapmap];0.88[MEX][hapmap];0.92[MKK][hapmap];0.94[TSI][hapmap];0.88[YRI][hapmap];0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13313520	0.91[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13329235	1.00[ASN][1000 genomes]
rs13380007	1.00[YRI][hapmap];0.80[AFR][1000 genomes]
rs1617832	0.90[LWK][hapmap];0.81[YRI][hapmap]
rs16971726	1.00[CHB][hapmap]
rs1757468	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[YRI][hapmap];0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17730589	0.91[ASW][hapmap];0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17730888	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];0.86[LWK][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1866399	1.00[ASN][1000 genomes]
rs2118740	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs2448402	1.00[ASN][1000 genomes]
rs2730056	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];0.81[MEX][hapmap];0.94[TSI][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2730058	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28374715	1.00[CHB][hapmap]
rs28377562	1.00[ASN][1000 genomes]
rs28382348	1.00[ASN][1000 genomes]
rs28416360	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28421136	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28437576	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28456082	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28458941	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28459164	0.95[EUR][1000 genomes]
rs28463309	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28477406	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28492932	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28493087	1.00[ASN][1000 genomes]
rs28493702	0.93[CEU][hapmap];1.00[CHB][hapmap];0.89[GIH][hapmap];0.87[MEX][hapmap];0.97[TSI][hapmap];0.94[YRI][hapmap];1.00[ASN][1000 genomes]
rs28535540	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28554139	1.00[CHB][hapmap];0.81[YRI][hapmap]
rs28555198	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28557159	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.82[MEX][hapmap];0.85[TSI][hapmap];1.00[ASN][1000 genomes]
rs28576457	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28584379	0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28617619	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28623183	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28631111	1.00[CHB][hapmap]
rs28661013	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28663426	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28673484	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28687846	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28700583	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28703570	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28712264	1.00[ASN][1000 genomes]
rs28716689	1.00[ASN][1000 genomes]
rs28827035	1.00[ASN][1000 genomes]
rs28897479	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs316604	1.00[ASW][hapmap];0.93[CEU][hapmap];0.96[GIH][hapmap];0.95[LWK][hapmap];0.82[MEX][hapmap];0.88[MKK][hapmap];0.86[TSI][hapmap];0.88[YRI][hapmap];0.82[AFR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs316606	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs316607	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];0.81[MEX][hapmap];0.92[TSI][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs316611	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];0.81[MEX][hapmap];0.94[TSI][hapmap];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs316616	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs316618	0.81[YRI][hapmap]
rs3204853	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34040639	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[GIH][hapmap];0.81[MEX][hapmap];0.89[TSI][hapmap];0.86[EUR][1000 genomes]
rs34285452	0.91[EUR][1000 genomes]
rs34665396	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4924549	1.00[CHB][hapmap]
rs513280	1.00[ASN][1000 genomes]
rs521890	1.00[ASN][1000 genomes]
rs522063	1.00[ASN][1000 genomes]
rs55725658	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56341337	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs56400990	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59000092	1.00[ASN][1000 genomes]
rs6493000	1.00[ASN][1000 genomes]
rs6493003	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs691011	1.00[ASN][1000 genomes]
rs691906	1.00[ASN][1000 genomes]
rs691907	1.00[ASN][1000 genomes]
rs7162231	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7163989	1.00[ASN][1000 genomes]
rs7164211	0.91[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];0.95[LWK][hapmap];0.88[MEX][hapmap];0.92[MKK][hapmap];0.97[TSI][hapmap];0.94[YRI][hapmap];0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7164684	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];0.81[MEX][hapmap];0.97[TSI][hapmap];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7165396	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7165914	0.91[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];0.86[LWK][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7167706	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7168002	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7168307	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.82[MEX][hapmap];0.81[TSI][hapmap];1.00[ASN][1000 genomes]
rs7168431	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];0.93[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7169543	0.91[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7181982	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7182324	1.00[ASN][1000 genomes]
rs72737786	1.00[ASN][1000 genomes]
rs72737792	1.00[ASN][1000 genomes]
rs72737793	1.00[ASN][1000 genomes]
rs72739630	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72739644	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8023530	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.82[MEX][hapmap];0.85[TSI][hapmap];1.00[ASN][1000 genomes]
rs8034840	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8036026	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8036734	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8037574	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.82[MEX][hapmap];0.81[TSI][hapmap];1.00[ASN][1000 genomes]
rs8038132	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs8038983	1.00[ASN][1000 genomes]
rs8041809	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8043237	1.00[ASN][1000 genomes]
rs9568	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044438	chr15:41560160-41745480	Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Enhancers Genic enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
2	nsv1038923	chr15:41585028-41754890	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
3	nsv1045142	chr15:41585044-41738314	Weak transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
4	nsv1039283	chr15:41620499-41745480	Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	63 gene(s)	inside rSNPs	diseases
5	nsv933757	chr15:41641236-41773058	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	27 gene(s)	inside rSNPs	diseases
6	nsv524476	chr15:41689232-41820200	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases

mRNA abundance (count:27)

SNP	Gene	Cis/trans	Tissue	Source
rs1899	GPR176	cis	parietal	SCAN
rs1899	OIP5-AS1	cis	Adipose Subcutaneous	GTEx
rs1899	KRTAP4-7	cis	lesional skin	skin_eQTL
rs1899	RASGRP1	cis	cerebellum	SCAN
rs1899	ZFP106	cis	parietal	SCAN
rs1899	KRTAP4-7	cis	normal skin	skin_eQTL
rs1899	NDUFAF1	cis	lymphoblastoid	seeQTL
rs1899	KRTAP4-7	Cis_1M	lymphoblastoid	RTeQTL
rs1899	NDUFAF1	cis	multi-tissue	Pritchard
rs1899	OIP5-AS1	cis	Nerve Tibial	GTEx
rs1899	OIP5-AS1	cis	Artery Tibial	GTEx
rs1899	NDUFAF1	cis	cerebellum	SCAN
rs1899	RPAP1	cis	parietal	SCAN
rs1899	SPINT1	cis	cerebellum	SCAN
rs1899	GPR176	cis	cerebellum	SCAN
rs1899	NDUFAF1	cis	Whole Blood	GTEx
rs1899	NUSAP1	cis	parietal	SCAN
rs1899	OIP5-AS1	cis	Esophagus Mucosa	GTEx
rs1899	NDUFAF1	cis	Heart Left Ventricle	GTEx
rs1899	NDUFAF1	cis	Esophagus Muscularis	GTEx
rs1899	NDUFAF1	cis	Muscle Skeletal	GTEx
rs1899	NDUFAF1	Cis_1M	lymphoblastoid	RTeQTL
rs1899	NUSAP1	cis	cerebellum	SCAN
rs1899	LOC729082	Cis_1M	lymphoblastoid	RTeQTL
rs1899	NDUFAF1	cis	lung	GTEx
rs1899	NDUFAF1	cis	Thyroid	GTEx
rs1899	NDUFAF1	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41625800-41694200	Weak transcription	Small Intestine	intestine
2	chr15:41660200-41693800	Weak transcription	Right Ventricle	heart
3	chr15:41661800-41693200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr15:41672000-41693600	Weak transcription	Colonic Mucosa	Colon
5	chr15:41673400-41693800	Weak transcription	HMEC	breast
6	chr15:41673600-41693800	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr15:41673600-41693800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr15:41673800-41693600	Weak transcription	Primary hematopoietic stem cells	blood
9	chr15:41674000-41693800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr15:41674000-41693800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr15:41676400-41689400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr15:41676400-41689400	Strong transcription	Fetal Muscle Trunk	muscle
13	chr15:41676400-41689400	Strong transcription	Fetal Thymus	thymus
14	chr15:41676400-41692200	Strong transcription	Fetal Stomach	stomach
15	chr15:41677000-41693400	Weak transcription	HepG2	liver
16	chr15:41677200-41693400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr15:41678400-41693800	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr15:41679200-41693800	Weak transcription	Stomach Mucosa	stomach
19	chr15:41680000-41691400	Strong transcription	Fetal Muscle Leg	muscle
20	chr15:41680000-41694000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr15:41681200-41693800	Weak transcription	NHDF-Ad	bronchial
22	chr15:41682000-41693200	Weak transcription	Psoas Muscle	Psoas
23	chr15:41683400-41689400	Strong transcription	Brain Angular Gyrus	brain
24	chr15:41683600-41689400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
25	chr15:41683600-41689400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr15:41683600-41689400	Strong transcription	Fetal Intestine Large	intestine
27	chr15:41684600-41689400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr15:41684600-41689400	Strong transcription	Stomach Smooth Muscle	stomach
29	chr15:41684800-41689400	Strong transcription	Brain Cingulate Gyrus	brain
30	chr15:41684800-41689400	Strong transcription	Placenta	Placenta
31	chr15:41685000-41689600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr15:41685200-41689400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr15:41685400-41691600	Strong transcription	Fetal Intestine Small	intestine
34	chr15:41685400-41693800	Weak transcription	Fetal Heart	heart
35	chr15:41686200-41689400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr15:41686400-41689400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr15:41686400-41689400	Strong transcription	Primary T cells from cord blood	blood
38	chr15:41686400-41689400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr15:41686400-41689400	Strong transcription	Cortex derived primary cultured neurospheres	brain
40	chr15:41686400-41689400	Strong transcription	Brain Hippocampus Middle	brain
41	chr15:41686400-41689400	Strong transcription	Fetal Brain Female	brain
42	chr15:41686400-41689400	Strong transcription	Placenta Amnion	Placenta Amnion
43	chr15:41686600-41689400	Strong transcription	HUES64 Cell Line	embryonic stem cell
44	chr15:41686600-41689400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr15:41686600-41689400	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr15:41687000-41689400	Strong transcription	Dnd41	blood
47	chr15:41687400-41693600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr15:41687400-41693800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr15:41687400-41693800	Weak transcription	A549	lung
50	chr15:41687400-41694000	Weak transcription	Fetal Kidney	kidney

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