Variant report

Variant	rs1045204
Chromosome Location	chr15:34634138-34634139
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 99 )
Associated
traits (count: 16 )

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs104017	0.94[CHB][hapmap];0.92[CHD][hapmap];0.90[JPT][hapmap]
rs1045194	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1045238	0.83[AMR][1000 genomes]
rs1133154	0.91[GIH][hapmap]
rs11631094	0.82[CHB][hapmap];0.92[CHD][hapmap];0.81[JPT][hapmap]
rs12591967	0.82[ASW][hapmap];0.88[CHB][hapmap];0.91[CHD][hapmap];0.97[GIH][hapmap];0.90[JPT][hapmap];0.82[MKK][hapmap];0.85[TSI][hapmap];0.94[YRI][hapmap]
rs12593384	0.83[AMR][1000 genomes]
rs12594569	0.92[CHD][hapmap]
rs12595504	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];0.89[YRI][hapmap]
rs16958878	0.91[GIH][hapmap]
rs16958954	0.88[CHB][hapmap];0.92[CHD][hapmap];0.97[GIH][hapmap];0.90[JPT][hapmap];0.85[TSI][hapmap]
rs16958995	0.82[CHB][hapmap];0.90[JPT][hapmap]
rs16959012	0.94[CHB][hapmap];0.95[JPT][hapmap]
rs16959021	0.94[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];0.93[MEX][hapmap]
rs180886	0.94[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];0.93[MEX][hapmap]
rs1845773	0.83[AMR][1000 genomes]
rs2219668	0.83[AMR][1000 genomes]
rs2644243	0.82[CHB][hapmap]
rs2644247	0.92[CHD][hapmap]
rs2705343	0.81[CHD][hapmap]
rs2705348	0.88[CHB][hapmap];0.85[JPT][hapmap]
rs3063	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.83[AMR][1000 genomes]
rs34639726	0.83[AMR][1000 genomes]
rs347818	0.92[CHD][hapmap]
rs347827	0.94[CHB][hapmap];0.90[JPT][hapmap]
rs347830	0.94[CHB][hapmap];0.92[CHD][hapmap];0.90[JPT][hapmap]
rs347834	0.94[CHB][hapmap];0.95[JPT][hapmap]
rs347836	0.94[CHB][hapmap];0.90[JPT][hapmap]
rs347842	0.88[CHB][hapmap];0.94[CHD][hapmap];0.90[JPT][hapmap]
rs347845	0.92[CHD][hapmap]
rs347848	0.88[CHB][hapmap]
rs347849	0.88[CHB][hapmap];0.94[CHD][hapmap]
rs347851	0.88[CHB][hapmap]
rs347861	0.92[CHD][hapmap]
rs422388	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs4238572	0.88[GIH][hapmap]
rs426634	0.88[CHB][hapmap];0.92[CHD][hapmap]
rs436552	0.89[CHD][hapmap]
rs4569235	0.83[AMR][1000 genomes]
rs56057955	0.85[AMR][1000 genomes]
rs56762274	0.83[AMR][1000 genomes]
rs59452641	0.82[AMR][1000 genomes]
rs59861881	0.85[AMR][1000 genomes]
rs6495660	0.88[CHB][hapmap];0.90[JPT][hapmap]
rs6495661	0.83[AMR][1000 genomes]
rs6495662	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];0.88[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];0.86[TSI][hapmap];1.00[YRI][hapmap];0.83[AMR][1000 genomes]
rs7163195	0.93[CHB][hapmap];0.95[JPT][hapmap]
rs7164902	0.92[CHD][hapmap]
rs7175028	0.88[CHB][hapmap];0.92[CHD][hapmap];0.97[GIH][hapmap];0.90[JPT][hapmap];0.85[TSI][hapmap]
rs7176426	0.88[CHB][hapmap];0.90[JPT][hapmap]
rs7181260	0.87[CHB][hapmap];0.89[JPT][hapmap];0.92[YRI][hapmap]
rs7182584	0.83[AMR][1000 genomes]
rs72486679	0.83[AMR][1000 genomes]
rs73374500	0.85[AMR][1000 genomes]
rs73374502	0.83[AMR][1000 genomes]
rs756086	0.94[CHB][hapmap];0.90[JPT][hapmap]
rs8023583	0.94[CHB][hapmap];0.95[JPT][hapmap];0.94[YRI][hapmap];0.82[AMR][1000 genomes]
rs8025057	1.00[ASW][hapmap];0.82[CHB][hapmap];0.92[CHD][hapmap];0.94[GIH][hapmap];0.90[JPT][hapmap];0.82[LWK][hapmap];0.92[MKK][hapmap];0.85[TSI][hapmap];0.94[YRI][hapmap]
rs8028600	0.80[JPT][hapmap]
rs8031145	0.94[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];0.86[MEX][hapmap]
rs8031147	0.94[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];0.93[MEX][hapmap]
rs8031404	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];0.89[YRI][hapmap]
rs8032347	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs8033032	0.80[AMR][1000 genomes]
rs8038177	0.94[CHB][hapmap];0.90[JPT][hapmap]
rs924065	0.94[CHB][hapmap];0.95[JPT][hapmap];0.87[YRI][hapmap];0.82[AMR][1000 genomes]
rs9630418	0.94[CHB][hapmap];0.95[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:32 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1052804	chr15:34498529-34841447	Active TSS Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv542341	chr15:34498529-34841447	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	esv1798578	chr15:34543021-34988247	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
4	esv1804312	chr15:34543021-34988247	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
5	esv1821622	chr15:34543021-34988247	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers 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	45 gene(s)	inside rSNPs	diseases
6	esv1850950	chr15:34543021-34988247	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
7	esv2758376	chr15:34543021-34988247	Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
8	esv2760024	chr15:34543021-34988247	Flanking Active TSS Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
9	nsv428303	chr15:34543021-34988247	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
10	nsv1036475	chr15:34552879-34841587	Bivalent/Poised TSS Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
11	nsv542342	chr15:34552879-34841587	Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
12	nsv1048550	chr15:34553078-34841447	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
13	nsv542343	chr15:34553078-34841447	Active TSS Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
14	nsv471682	chr15:34560451-34882630	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
15	nsv469547	chr15:34594557-34757807	Genic enhancers Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS 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	33 gene(s)	inside rSNPs	diseases
16	nsv482528	chr15:34594557-34757807	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Strong transcription 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	33 gene(s)	inside rSNPs	diseases
17	esv1817014	chr15:34598601-34911177	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer 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	39 gene(s)	inside rSNPs	diseases
18	esv1817924	chr15:34598601-34911177	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
19	esv1847172	chr15:34598601-34911177	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
20	esv1802396	chr15:34598601-34988247	Flanking Active TSS Active TSS Enhancers Strong transcription Weak transcription 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	45 gene(s)	inside rSNPs	diseases
21	esv1809360	chr15:34598601-34988247	Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
22	esv1844776	chr15:34598601-34988247	Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
23	nsv427957	chr15:34598601-34988247	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
24	nsv1039577	chr15:34624178-34962093	Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
25	nsv542344	chr15:34624178-34962093	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
26	nsv542345	chr15:34626815-34841586	Strong transcription Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
27	nsv542346	chr15:34627015-34841447	Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
28	nsv915918	chr15:34627109-34841422	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
29	nsv916680	chr15:34627109-34964198	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
30	esv1822549	chr15:34628041-34909164	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
31	nsv1038524	chr15:34628041-34962093	Flanking Bivalent TSS/Enh Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
32	nsv542347	chr15:34628041-34962093	Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases

mRNA abundance (count:16)

SNP	Gene	Cis/trans	Tissue	Source
rs1045204	NOP10	cis	Skin Sun Exposed Lower leg	GTEx
rs1045204	PGBD4	cis	cerebellum	SCAN
rs1045204	NOP10	cis	Artery Tibial	GTEx
rs1045204	NOP10	cis	lung	GTEx
rs1045204	NOP10	cis	Artery Aorta	GTEx
rs1045204	NOP10	cis	cerebellum	SCAN
rs1045204	NOP10	cis	Esophagus Mucosa	GTEx
rs1045204	TMEM85	cis	cerebellum	SCAN
rs1045204	NOP10	cis	Heart Left Ventricle	GTEx
rs1045204	NOP10	cis	Nerve Tibial	GTEx
rs1045204	NOP10	cis	Muscle Skeletal	GTEx
rs1045204	NOP10	cis	Esophagus Muscularis	GTEx
rs1045204	SLC12A6	cis	Thyroid	GTEx
rs1045204	NOP10	cis	Thyroid	GTEx
rs1045204	NOP10	cis	Stomach	GTEx
rs1045204	NOP10	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34630600-34634200	Weak transcription	Aorta	Aorta
2	chr15:34630600-34635000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr15:34630800-34634200	Weak transcription	Brain Angular Gyrus	brain
4	chr15:34630800-34634200	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr15:34630800-34634400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr15:34630800-34634400	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr15:34631800-34634600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr15:34632000-34634400	Genic enhancers	Primary T helper cells fromperipheralblood	blood
9	chr15:34632400-34634200	Strong transcription	Fetal Stomach	stomach
10	chr15:34632400-34634200	Genic enhancers	Lung	lung
11	chr15:34632400-34634400	Genic enhancers	Primary T cells fromperipheralblood	blood
12	chr15:34633200-34634400	Genic enhancers	Primary B cells from peripheral blood	blood
13	chr15:34633200-34634400	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
14	chr15:34633200-34634800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr15:34633400-34634400	Transcr. at gene 5' and 3'	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr15:34633400-34634600	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr15:34633400-34634600	Enhancers	Primary T killer memory cells from peripheral blood	blood
18	chr15:34633600-34634200	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell
19	chr15:34633600-34634200	Transcr. at gene 5' and 3'	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr15:34633600-34634200	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr15:34633600-34634200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr15:34633600-34634200	Transcr. at gene 5' and 3'	Muscle Satellite Cultured Cells	--
23	chr15:34633600-34634200	Enhancers	Brain Hippocampus Middle	brain
24	chr15:34633600-34634200	Enhancers	Placenta Amnion	Placenta Amnion
25	chr15:34633600-34634200	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
26	chr15:34633600-34634200	Transcr. at gene 5' and 3'	K562	blood
27	chr15:34633600-34634400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr15:34633600-34634400	Transcr. at gene 5' and 3'	HUES64 Cell Line	embryonic stem cell
29	chr15:34633600-34634400	Transcr. at gene 5' and 3'	Primary neutrophils fromperipheralblood	blood
30	chr15:34633600-34634400	Enhancers	Fetal Lung	lung
31	chr15:34633600-34634400	Transcr. at gene 5' and 3'	Dnd41	blood
32	chr15:34633600-34634800	Enhancers	Small Intestine	intestine
33	chr15:34633800-34634200	Transcr. at gene 5' and 3'	Primary B cells from cord blood	blood
34	chr15:34633800-34634200	Genic enhancers	Esophagus	oesophagus
35	chr15:34633800-34634200	Genic enhancers	Rectal Mucosa Donor 29	rectum
36	chr15:34633800-34634200	Transcr. at gene 5' and 3'	HUVEC	blood vessel
37	chr15:34633800-34634400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr15:34633800-34634400	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
39	chr15:34633800-34634400	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr15:34633800-34634400	Transcr. at gene 5' and 3'	Hela-S3	cervix
41	chr15:34633800-34634400	Transcr. at gene 5' and 3'	NHEK	skin
42	chr15:34633800-34634600	Flanking Active TSS	Primary T cells from cord blood	blood
43	chr15:34633800-34634800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
44	chr15:34633800-34634800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
45	chr15:34633800-34635400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr15:34633800-34635400	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
47	chr15:34634000-34634200	Transcr. at gene 5' and 3'	ES-I3 Cell Line	embryonic stem cell
48	chr15:34634000-34634200	Transcr. at gene 5' and 3'	H1 Cell Line	embryonic stem cell
49	chr15:34634000-34634200	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr15:34634000-34634200	Flanking Active TSS	H9 Cell Line	embryonic stem cell

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