Variant report

Variant	rs12600694
Chromosome Location	chr17:18091019-18091020
allele	A/G
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	MYC	chr17:18090763-18091798	MCF10A-Er-Src	breast:	n/a	n/a
2	CHD1	chr17:18085856-18091134	IMR90	lung:	n/a	n/a
3	MXI1	chr17:18085581-18092228	SK-N-SH	brain:	n/a	chr17:18086672-18086687 chr17:18088362-18088377
4	GATA1	chr17:18090662-18091857	PBDE	blood:	n/a	n/a
5	EP300	chr17:18087589-18092262	SK-N-SH	brain:	n/a	chr17:18089998-18090012
6	WRNIP1	chr17:18087774-18091201	GM12878	blood:	n/a	n/a
7	KAP1	chr17:18087725-18091513	HEK293	kidney:	n/a	chr17:18091056-18091064
8	TCF12	chr17:18090282-18091198	SK-N-SH	brain:	n/a	n/a
9	GATA2	chr17:18090537-18091829	SH-SY5Y	brain:	n/a	n/a
10	PBX3	chr17:18090445-18091121	SK-N-SH	brain:	n/a	n/a
11	POLR2A	chr17:18090884-18091110	K562	blood:	n/a	n/a
12	GATA3	chr17:18090355-18092100	SK-N-SH	brain:	n/a	n/a
13	NFIC	chr17:18090468-18092116	SK-N-SH	brain:	n/a	n/a
14	PBX3	chr17:18090416-18091082	SK-N-SH	brain:	n/a	n/a
15	POLR2A	chr17:18090614-18091050	HepG2	liver:	n/a	n/a
16	MXI1	chr17:18086003-18091020	IMR90	lung:	n/a	chr17:18086672-18086687 chr17:18088362-18088377
17	YY1	chr17:18090422-18091105	SK-N-SH_RA	brain:	n/a	n/a
18	EP300	chr17:18090411-18091040	SK-N-SH_RA	brain:	n/a	n/a
19	USF2	chr17:18090863-18091218	Hela-S3	cervix:	n/a	n/a
20	TCF12	chr17:18089654-18092249	SK-N-SH	brain:	n/a	n/a
21	EP300	chr17:18090320-18091075	SK-N-SH_RA	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:18088851..18092330-chr17:18106978..18109728,3	K562	blood:
2	chr17:18081720..18083275-chr17:18090040..18091651,2	MCF-7	breast:
3	chr17:18089295..18091873-chr17:18217649..18220179,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000266677	TF binding region
ENSG00000176994	Chromatin interaction
ENSG00000177302	Chromatin interaction

Extended variants
information (count: 89 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs10048161	0.94[CEU][hapmap];1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10451244	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11078411	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[GIH][hapmap];0.87[LWK][hapmap];0.93[MEX][hapmap];0.88[TSI][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11078412	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[GIH][hapmap];0.87[LWK][hapmap];0.93[MEX][hapmap];0.88[TSI][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11652964	1.00[CHB][hapmap];0.84[EUR][1000 genomes]
rs11653988	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11654146	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11654177	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11654741	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11655588	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[GIH][hapmap];0.87[LWK][hapmap];0.93[MEX][hapmap];0.88[TSI][hapmap];0.96[YRI][hapmap];0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11655731	1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11655797	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11656035	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11657194	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11658477	0.94[CEU][hapmap];1.00[CHB][hapmap];0.84[GIH][hapmap];0.85[MEX][hapmap];0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11868832	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11868886	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11869582	0.80[CEU][hapmap]
rs11871039	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11871491	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[YRI][hapmap];0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12449313	0.91[GIH][hapmap]
rs13284	1.00[ASW][hapmap];0.94[CEU][hapmap];0.97[GIH][hapmap];0.82[LWK][hapmap];0.85[TSI][hapmap];0.95[YRI][hapmap];0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1563371	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[GIH][hapmap];0.87[LWK][hapmap];0.93[MEX][hapmap];0.88[TSI][hapmap];0.96[YRI][hapmap];0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1563373	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[YRI][hapmap];0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs16960980	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[GIH][hapmap];0.87[LWK][hapmap];0.93[MEX][hapmap];0.88[TSI][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16960983	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[GIH][hapmap];0.87[LWK][hapmap];0.93[MEX][hapmap];0.88[TSI][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16960986	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[GIH][hapmap];0.87[LWK][hapmap];0.88[TSI][hapmap];0.96[YRI][hapmap];0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16960990	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[GIH][hapmap];0.87[LWK][hapmap];0.93[MEX][hapmap];0.88[TSI][hapmap];0.96[YRI][hapmap];0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16960996	0.94[CEU][hapmap];1.00[CHB][hapmap];0.96[YRI][hapmap];0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16961153	0.91[GIH][hapmap]
rs2015336	0.88[CEU][hapmap];1.00[CHB][hapmap];0.97[GIH][hapmap];0.85[MEX][hapmap];0.85[TSI][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2071242	0.87[GIH][hapmap]
rs2290502	0.87[GIH][hapmap]
rs2290503	0.87[GIH][hapmap]
rs2294913	0.91[GIH][hapmap]
rs28364628	0.87[GIH][hapmap]
rs28811342	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3088233	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[GIH][hapmap];0.87[LWK][hapmap];0.93[MEX][hapmap];0.88[TSI][hapmap];0.96[YRI][hapmap];0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34474249	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs36058389	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3817992	0.91[GIH][hapmap]
rs3829956	0.91[GIH][hapmap]
rs55918833	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs58441148	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59354912	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs60285171	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62072464	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62072465	0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62072466	0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62072467	0.83[EUR][1000 genomes]
rs62072468	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62072496	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62072497	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62072498	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62072500	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62073602	0.83[EUR][1000 genomes]
rs62073603	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62073604	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62073605	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62073606	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62073607	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62073608	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62073609	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62073611	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62073615	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62073649	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62073650	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6502640	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[GIH][hapmap];0.87[LWK][hapmap];0.93[MEX][hapmap];0.88[TSI][hapmap];0.96[YRI][hapmap];0.80[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7207276	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7215678	0.87[GIH][hapmap]
rs735960	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7498	0.87[GIH][hapmap]
rs8065026	0.88[CEU][hapmap];1.00[CHB][hapmap];0.84[GIH][hapmap];0.85[MEX][hapmap];0.82[EUR][1000 genomes]
rs8069094	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8077577	0.88[CEU][hapmap];0.97[GIH][hapmap];0.85[MEX][hapmap];0.88[TSI][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9909104	0.97[GIH][hapmap]
rs9913139	0.87[GIH][hapmap]
rs9916193	0.82[EUR][1000 genomes]
rs997315	0.94[CEU][hapmap];1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531183	chr17:17571035-18205309	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	123 gene(s)	inside rSNPs	diseases
2	nsv916653	chr17:17651916-18454952	Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
3	nsv533142	chr17:17691726-18236686	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
4	nsv482491	chr17:17959577-18153920	Enhancers Genic enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
5	nsv1061162	chr17:17978838-18259234	Flanking Active TSS Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
6	nsv492305	chr17:17980441-18424702	Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
7	nsv907770	chr17:18003845-18098018	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
8	nsv907771	chr17:18013560-18098018	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
9	nsv907772	chr17:18030524-18098018	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
10	nsv510702	chr17:18037676-18116801	Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs12600694	LOC162632	cis	parietal	SCAN
rs12600694	SHMT1	cis	lymphoblastoid	seeQTL
rs12600694	SHMT1	cis	cerebellum	SCAN
rs12600694	LOC162632	cis	cerebellum	SCAN
rs12600694	FLII	cis	cerebellum	SCAN
rs12600694	SLC47A1	cis	cerebellum	SCAN
rs12600694	PLD6	cis	cerebellum	SCAN

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:18087800-18091200	Flanking Active TSS	Adipose Nuclei	Adipose
2	chr17:18087800-18092000	Transcr. at gene 5' and 3'	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr17:18087800-18092200	Transcr. at gene 5' and 3'	Dnd41	blood
4	chr17:18088000-18091200	Transcr. at gene 5' and 3'	Fetal Stomach	stomach
5	chr17:18088000-18091800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
6	chr17:18088000-18092000	Flanking Active TSS	HUVEC	blood vessel
7	chr17:18088000-18093000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr17:18088200-18091200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr17:18088200-18091200	Flanking Active TSS	Fetal Brain Male	brain
10	chr17:18088200-18091400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
11	chr17:18088200-18091400	Transcr. at gene 5' and 3'	Thymus	Thymus
12	chr17:18088200-18092000	Flanking Active TSS	Brain Germinal Matrix	brain
13	chr17:18088200-18092000	Flanking Active TSS	NH-A	brain
14	chr17:18088400-18091200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
15	chr17:18088800-18091200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
16	chr17:18088800-18091200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr17:18088800-18091200	Transcr. at gene 5' and 3'	A549	lung
18	chr17:18088800-18091400	Flanking Active TSS	Brain Anterior Caudate	brain
19	chr17:18088800-18091400	Flanking Active TSS	Psoas Muscle	Psoas
20	chr17:18088800-18092000	Flanking Active TSS	Brain Hippocampus Middle	brain
21	chr17:18088800-18092000	Transcr. at gene 5' and 3'	NHEK	skin
22	chr17:18088800-18092200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
23	chr17:18088800-18092200	Flanking Active TSS	Osteobl	bone
24	chr17:18089000-18091200	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell
25	chr17:18089000-18091200	Transcr. at gene 5' and 3'	Primary T cells fromperipheralblood	blood
26	chr17:18089000-18091200	Flanking Active TSS	Fetal Heart	heart
27	chr17:18089000-18091400	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr17:18089000-18091600	Transcr. at gene 5' and 3'	K562	blood
29	chr17:18089000-18091800	Flanking Active TSS	Colon Smooth Muscle	Colon
30	chr17:18089000-18091800	Transcr. at gene 5' and 3'	Skeletal Muscle Female	skeletal muscle
31	chr17:18089000-18092000	Flanking Active TSS	Brain Angular Gyrus	brain
32	chr17:18089000-18092000	Flanking Active TSS	Rectal Smooth Muscle	rectum
33	chr17:18089000-18095400	Enhancers	Small Intestine	intestine
34	chr17:18089200-18091200	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr17:18089200-18091200	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr17:18089200-18091600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
37	chr17:18089200-18092000	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr17:18089200-18092000	Flanking Active TSS	Brain Cingulate Gyrus	brain
39	chr17:18089200-18092000	Flanking Active TSS	NHDF-Ad	bronchial
40	chr17:18089200-18092200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr17:18089200-18092200	Genic enhancers	Primary monocytes fromperipheralblood	blood
42	chr17:18089400-18091200	Transcr. at gene 5' and 3'	Left Ventricle	heart
43	chr17:18089400-18091400	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
44	chr17:18089400-18091400	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr17:18089400-18092000	Flanking Active TSS	Colonic Mucosa	Colon
46	chr17:18089400-18092000	Flanking Active TSS	HMEC	breast
47	chr17:18089400-18092200	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
48	chr17:18089600-18091200	Transcr. at gene 5' and 3'	Fetal Muscle Trunk	muscle
49	chr17:18089600-18091400	Flanking Active TSS	HSMMtube	muscle
50	chr17:18089600-18092000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain

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