Variant report

Variant	rs2735475
Chromosome Location	chr17:34258007-34258008
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	GTF2F1	chr17:34257550-34258011	H1-hESC	embryonic stem cell:	n/a	n/a
2	POLR2A	chr17:34257545-34258139	K562	blood:	n/a	n/a
3	TBP	chr17:34257595-34258132	K562	blood:	n/a	n/a
4	E2F6	chr17:34257561-34258081	A549	lung:	n/a	chr17:34257776-34257785
5	NRF1	chr17:34257569-34258041	GM12878	blood:	n/a	chr17:34257775-34257786 chr17:34257777-34257786 chr17:34257743-34257754 chr17:34257814-34257823 chr17:34257772-34257786 chr17:34257775-34257789 chr17:34257775-34257786
6	E2F4	chr17:34257473-34258524	MCF10A-Er-Src	breast:	n/a	chr17:34257776-34257785
7	YY1	chr17:34257583-34258027	K562	blood:	n/a	n/a
8	IRF1	chr17:34257584-34258162	K562	blood:	n/a	chr17:34257823-34257837
9	CHD2	chr17:34257548-34258043	GM12878	blood:	n/a	n/a
10	E2F6	chr17:34257514-34258039	H1-hESC	embryonic stem cell:	n/a	chr17:34257776-34257785
11	E2F4	chr17:34257595-34258016	GM12878	blood:	n/a	chr17:34257776-34257785
12	E2F6	chr17:34257064-34258140	H1-hESC	embryonic stem cell:	n/a	chr17:34257776-34257785
13	MXI1	chr17:34257745-34258199	K562	blood:	n/a	n/a
14	POLR2A	chr17:34257349-34258087	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr17:34257348-34258295	U87	brain:	n/a	n/a
16	E2F6	chr17:34257251-34258015	K562	blood:	n/a	chr17:34257776-34257785
17	ATF3	chr17:34257587-34258081	A549	lung:	n/a	n/a
18	POLR2A	chr17:34257481-34258179	H1-hESC	embryonic stem cell:	n/a	n/a
19	SETDB1	chr17:34257550-34258191	U2OS	brain:	n/a	chr17:34257776-34257785
20	IRF1	chr17:34257491-34258130	K562	blood:	n/a	chr17:34257823-34257837
21	ZMIZ1	chr17:34257844-34258081	K562	blood:	n/a	n/a
22	POLR2A	chr17:34257394-34258112	GM12892	blood:	n/a	n/a
23	ATF3	chr17:34257493-34258046	A549	lung:	n/a	n/a
24	UBTF	chr17:34257368-34258164	K562	blood:	n/a	n/a
25	BHLHE40	chr17:34257613-34258093	K562	blood:	n/a	n/a
26	POLR2A	chr17:34257432-34258140	PANC-1	pancreas:	n/a	n/a
27	MAX	chr17:34257567-34258048	K562	blood:	n/a	n/a
28	MAX	chr17:34257589-34258100	SK-N-SH	brain:	n/a	n/a
29	POLR2A	chr17:34257323-34258121	GM12891	blood:	n/a	n/a
30	MXI1	chr17:34257425-34258136	GM12878	blood:	n/a	n/a
31	PAX5	chr17:34257541-34258049	GM12878	blood:	n/a	n/a
32	POLR2A	chr17:34257524-34258063	GM18951	blood:	n/a	n/a
33	POLR2A	chr17:34257496-34258058	K562	blood:	n/a	n/a
34	TAF1	chr17:34257559-34258080	PFSK-1	brain:	n/a	n/a
35	POLR2A	chr17:34257212-34259498	K562	blood:	n/a	n/a
36	POLR2A	chr17:34257573-34258040	H1-hESC	embryonic stem cell:	n/a	n/a
37	TBL1XR1	chr17:34257552-34258291	K562	blood:	n/a	n/a
38	POLR2A	chr17:34257540-34258143	K562	blood:	n/a	n/a
39	HEY1	chr17:34257737-34258179	K562	blood:	n/a	n/a
40	ZNF143	chr17:34257793-34258125	K562	blood:	n/a	n/a
41	MAX	chr17:34257441-34258132	ECC-1	luminal epithelium:	n/a	n/a
42	MTA3	chr17:34257282-34258165	GM12878	blood:	n/a	n/a
43	NRF1	chr17:34257582-34258126	K562	blood:	n/a	chr17:34257775-34257786 chr17:34257777-34257786 chr17:34257743-34257754 chr17:34257814-34257823 chr17:34257772-34257786 chr17:34257775-34257789 chr17:34257775-34257786
44	MAX	chr17:34257403-34258174	A549	lung:	n/a	n/a
45	GTF2F1	chr17:34257689-34258065	K562	blood:	n/a	n/a
46	SIN3A	chr17:34257356-34258043	H1-hESC	embryonic stem cell:	n/a	n/a
47	MAX	chr17:34257568-34258016	HepG2	liver:	n/a	n/a
48	POLR2A	chr17:34257468-34258143	SK-N-SH	brain:	n/a	n/a
49	RCOR1	chr17:34257122-34258087	K562	blood:	n/a	n/a
50	CBX3	chr17:34257536-34258177	K562	blood:	n/a	n/a

Variant related genes	Relation type
RDM1	TF binding region

Extended variants
information (count: 125 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:117)

rs_ID	r²[population]
rs11080360	0.88[ASN][1000 genomes]
rs11080361	0.88[ASN][1000 genomes]
rs11080362	0.88[ASN][1000 genomes]
rs11650409	0.87[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs11652536	0.87[CHB][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs11653016	0.88[ASN][1000 genomes]
rs11653051	0.87[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs11653204	0.87[ASN][1000 genomes]
rs11654713	0.89[ASN][1000 genomes]
rs11655533	0.87[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs11656556	0.87[ASN][1000 genomes]
rs11657908	0.87[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs11868801	0.88[ASN][1000 genomes]
rs11869976	0.88[ASN][1000 genomes]
rs16971670	0.88[ASN][1000 genomes]
rs2107538	0.92[GIH][hapmap];0.89[TSI][hapmap];0.86[EUR][1000 genomes]
rs2107540	0.87[ASN][1000 genomes]
rs2251660	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2280787	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2291299	0.96[TSI][hapmap];0.81[EUR][1000 genomes]
rs2376287	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2526327	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];0.86[YRI][hapmap];0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2526328	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2702947	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2702948	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28550999	0.88[ASN][1000 genomes]
rs28722787	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28739295	0.87[ASN][1000 genomes]
rs28912068	0.84[ASN][1000 genomes]
rs34369685	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3760447	0.84[ASN][1000 genomes]
rs3809769	0.87[CHB][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs3817655	0.82[EUR][1000 genomes]
rs3817656	0.81[ASN][1000 genomes]
rs3826404	0.89[TSI][hapmap]
rs4251751	0.81[CHB][hapmap];0.94[JPT][hapmap]
rs4251752	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs4251791	0.80[EUR][1000 genomes]
rs4795089	0.80[CHB][hapmap];0.87[JPT][hapmap]
rs4795090	0.86[GIH][hapmap];0.96[TSI][hapmap]
rs4795095	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs4795099	0.83[ASN][1000 genomes]
rs4795100	0.88[ASN][1000 genomes]
rs4795101	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4796105	0.88[TSI][hapmap]
rs4796107	0.80[CHB][hapmap];0.87[JPT][hapmap]
rs4796108	0.88[JPT][hapmap]
rs4796112	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs4796114	0.85[JPT][hapmap]
rs4796115	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs4796118	0.80[CHB][hapmap];0.94[JPT][hapmap]
rs4796119	0.86[CHB][hapmap];0.93[JPT][hapmap]
rs4796120	0.87[CHB][hapmap];0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs4796123	0.87[CHB][hapmap];0.82[ASN][1000 genomes]
rs4796124	0.87[ASN][1000 genomes]
rs4796125	0.87[ASN][1000 genomes]
rs4796126	0.85[ASN][1000 genomes]
rs4796127	0.87[ASN][1000 genomes]
rs4796128	0.95[GIH][hapmap];0.96[TSI][hapmap];0.88[EUR][1000 genomes]
rs4796130	0.88[ASN][1000 genomes]
rs4796131	0.88[ASN][1000 genomes]
rs4796133	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4796134	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4796136	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4796137	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4796138	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56294660	0.88[ASN][1000 genomes]
rs56344830	0.85[ASN][1000 genomes]
rs59338510	0.87[ASN][1000 genomes]
rs6505496	0.86[GIH][hapmap];0.96[TSI][hapmap]
rs7211393	0.86[EUR][1000 genomes]
rs7213636	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7215845	0.88[EUR][1000 genomes]
rs8066406	0.89[EUR][1000 genomes]
rs9303691	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs9303693	0.88[ASN][1000 genomes]
rs9754	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9789051	0.87[ASN][1000 genomes]
rs9889274	0.80[CHB][hapmap];0.93[JPT][hapmap];0.88[ASN][1000 genomes]
rs9889977	0.88[ASN][1000 genomes]
rs9890583	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9891064	0.88[ASN][1000 genomes]
rs9893004	0.88[ASN][1000 genomes]
rs9894314	0.88[ASN][1000 genomes]
rs9894799	0.88[ASN][1000 genomes]
rs9896265	0.87[ASN][1000 genomes]
rs9896658	0.88[ASN][1000 genomes]
rs9897665	0.88[ASN][1000 genomes]
rs9898132	0.87[CHB][hapmap];0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs9898152	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs9899215	0.88[ASN][1000 genomes]
rs9899866	0.87[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs9899870	0.87[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs9899881	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9900236	0.87[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs9901195	0.88[ASN][1000 genomes]
rs9901418	0.88[ASN][1000 genomes]
rs9903590	0.88[ASN][1000 genomes]
rs9904675	0.86[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs9907145	0.88[ASN][1000 genomes]
rs9907295	0.87[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs9908011	0.87[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs9908525	0.88[ASN][1000 genomes]
rs9908907	0.81[ASN][1000 genomes]
rs9908928	0.81[EUR][1000 genomes]
rs9909050	0.87[CHB][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs9911016	0.88[ASN][1000 genomes]
rs9912049	0.88[ASN][1000 genomes]
rs9912284	0.86[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs9912552	0.81[ASN][1000 genomes]
rs9912571	0.86[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs9912793	0.82[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs9912894	0.88[ASN][1000 genomes]
rs9913488	0.87[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs9913559	1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9914401	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs9914468	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3380735	chr17:34246253-34271932	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1063100	chr17:34246253-34397598	Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv833424	chr17:34246253-34419476	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv1056950	chr17:34246253-34442620	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
5	nsv1059795	chr17:34246253-34442620	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
6	nsv1060457	chr17:34246253-34442620	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
7	nsv543320	chr17:34246253-34442620	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
8	nsv949160	chr17:34246253-34442620	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs2735475	RDM1	cis	Lymphoblastoid	GTEx
rs2735475	AMAC1	cis	cerebellum	SCAN
rs2735475	RDM1	cis	parietal	SCAN
rs2735475	C17orf50	cis	cerebellum	SCAN
rs2735475	RDM1	cis	lymphoblastoid	seeQTL

Chromatin state (count:89 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:34257000-34258200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr17:34257000-34258200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
3	chr17:34257000-34258200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr17:34257000-34258200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr17:34257000-34258200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
6	chr17:34257000-34258200	Flanking Active TSS	Osteobl	bone
7	chr17:34257200-34258200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr17:34257200-34258200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr17:34257200-34258200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
10	chr17:34257200-34258200	Flanking Active TSS	Fetal Lung	lung
11	chr17:34257400-34258200	Active TSS	HUES48 Cell Line	embryonic stem cell
12	chr17:34257400-34258200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr17:34257400-34258200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr17:34257400-34258200	Active TSS	NHDF-Ad	bronchial
15	chr17:34257600-34258200	Active TSS	Fetal Brain Female	brain
16	chr17:34257800-34258200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr17:34257800-34258200	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr17:34257800-34258200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
19	chr17:34257800-34258200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr17:34257800-34258200	Enhancers	Liver	Liver
21	chr17:34257800-34258200	Flanking Active TSS	Fetal Heart	heart
22	chr17:34257800-34258200	Enhancers	Left Ventricle	heart
23	chr17:34257800-34258200	Enhancers	Placenta Amnion	Placenta Amnion
24	chr17:34257800-34258200	Flanking Active TSS	Stomach Smooth Muscle	stomach
25	chr17:34257800-34258200	Flanking Active TSS	GM12878-XiMat	blood
26	chr17:34257800-34258200	Flanking Active TSS	NHLF	lung
27	chr17:34257800-34258400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr17:34257800-34258400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr17:34257800-34258400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
30	chr17:34257800-34258400	Enhancers	Primary hematopoietic stem cells	blood
31	chr17:34257800-34258400	Flanking Active TSS	A549	lung
32	chr17:34257800-34258400	Flanking Active TSS	K562	blood
33	chr17:34257800-34258600	Enhancers	H9 Cell Line	embryonic stem cell
34	chr17:34257800-34259200	Weak transcription	Right Ventricle	heart
35	chr17:34257800-34259400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr17:34257800-34264000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr17:34257800-34266200	Weak transcription	Aorta	Aorta
38	chr17:34258000-34258200	Flanking Active TSS	ES-WA7 Cell Line	embryonic stem cell
39	chr17:34258000-34258200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr17:34258000-34258200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr17:34258000-34258200	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr17:34258000-34258200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr17:34258000-34258200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
44	chr17:34258000-34258200	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr17:34258000-34258200	Enhancers	Primary B cells from cord blood	blood
46	chr17:34258000-34258200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr17:34258000-34258200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr17:34258000-34258200	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr17:34258000-34258200	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr17:34258000-34258200	Enhancers	Primary T regulatory cells fromperipheralblood	blood

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