Variant report

Variant	rs7222225
Chromosome Location	chr17:45693497-45693498
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	CTCF	chr17:45693163-45693551	A549	lung:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
2	CTCF	chr17:45693314-45693538	Gliobla	brain:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
3	CTCF	chr17:45693176-45693507	A549	lung:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
4	POLR2A	chr17:45693075-45693688	HCT-116	colon:	n/a	n/a
5	RAD21	chr17:45693156-45693642	H1-hESC	embryonic stem cell:	n/a	chr17:45693370-45693389 chr17:45693378-45693390 chr17:45693380-45693387
6	ARID3A	chr17:45693174-45693540	K562	blood:	n/a	n/a
7	CTCF	chr17:45693329-45693506	MCF-7	breast:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
8	ZNF143	chr17:45693228-45693516	K562	blood:	n/a	n/a
9	RAD21	chr17:45693126-45693582	Hela-S3	cervix:	n/a	chr17:45693370-45693389 chr17:45693378-45693390 chr17:45693380-45693387
10	CTCF	chr17:45693420-45693570	HFF-Myc	foreskin:	n/a	n/a
11	CTCF	chr17:45693071-45693680	MCF-7	breast:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
12	RAD21	chr17:45693184-45693622	ECC-1	luminal epithelium:	n/a	chr17:45693370-45693389 chr17:45693378-45693390 chr17:45693380-45693387
13	CTCF	chr17:45693360-45693510	K562	blood:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
14	RAD21	chr17:45693135-45693528	GM12878	blood:	n/a	chr17:45693370-45693389 chr17:45693378-45693390 chr17:45693380-45693387
15	CTCF	chr17:45692637-45693913	SK-N-SH	brain:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
16	SMC3	chr17:45693174-45693590	K562	blood:	n/a	chr17:45693374-45693388
17	RAD21	chr17:45692839-45693921	SK-N-SH	brain:	n/a	chr17:45693370-45693389 chr17:45693378-45693390 chr17:45693380-45693387
18	RAD21	chr17:45693081-45693617	A549	lung:	n/a	chr17:45693370-45693389 chr17:45693378-45693390 chr17:45693380-45693387
19	CTCF	chr17:45693298-45693549	MCF-7	breast:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
20	POLR2A	chr17:45693085-45693587	SK-N-SH	brain:	n/a	n/a
21	RAD21	chr17:45693006-45693650	HepG2	liver:	n/a	chr17:45693370-45693389 chr17:45693378-45693390 chr17:45693380-45693387
22	RAD21	chr17:45693062-45693694	SK-N-SH_RA	brain:	n/a	chr17:45693370-45693389 chr17:45693378-45693390 chr17:45693380-45693387
23	RAD21	chr17:45693128-45693606	H1-hESC	embryonic stem cell:	n/a	chr17:45693370-45693389 chr17:45693378-45693390 chr17:45693380-45693387
24	CTCF	chr17:45693203-45693530	SK-N-SH_RA	brain:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
25	RAD21	chr17:45693126-45693569	HepG2	liver:	n/a	chr17:45693370-45693389 chr17:45693378-45693390 chr17:45693380-45693387
26	CTCF	chr17:45693380-45693530	GM12875	blood:	n/a	n/a
27	CTCF	chr17:45693360-45693510	AG09309	skin:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
28	SMC3	chr17:45693155-45693590	GM12878	blood:	n/a	chr17:45693374-45693388
29	CTCF	chr17:45693360-45693510	HCPEpiC	choroid plexus:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
30	RAD21	chr17:45693134-45693562	GM12878	blood:	n/a	chr17:45693370-45693389 chr17:45693378-45693390 chr17:45693380-45693387
31	CTCF	chr17:45693166-45693598	K562	blood:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
32	POLR2A	chr17:45693208-45693548	K562	blood:	n/a	n/a
33	CTCF	chr17:45693360-45693510	GM12873	blood:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
34	RAD21	chr17:45693172-45693550	GM12878	blood:	n/a	chr17:45693370-45693389 chr17:45693378-45693390 chr17:45693380-45693387
35	CTCF	chr17:45693176-45693613	GM12878	blood:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
36	RAD21	chr17:45693136-45693567	SK-N-SH_RA	brain:	n/a	chr17:45693370-45693389 chr17:45693378-45693390 chr17:45693380-45693387
37	RAD21	chr17:45693275-45693506	K562	blood:	n/a	chr17:45693370-45693389 chr17:45693378-45693390 chr17:45693380-45693387
38	YY1	chr17:45693189-45693554	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr17:45693108-45693621	A549	lung:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
40	CTCF	chr17:45693151-45693626	MCF-7	breast:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
41	CTCF	chr17:45693213-45693507	HepG2	liver:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
42	CTCF	chr17:45693380-45693530	GM12873	blood:	n/a	n/a
43	CTCF	chr17:45693380-45693530	GM12872	blood:	n/a	n/a
44	RAD21	chr17:45693036-45693622	ECC-1	luminal epithelium:	n/a	chr17:45693370-45693389 chr17:45693378-45693390 chr17:45693380-45693387
45	CTCF	chr17:45693268-45693518	K562	blood:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
46	CTCF	chr17:45692712-45693783	A549	lung:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
47	CHD1	chr17:45693022-45693789	IMR90	lung:	n/a	n/a
48	CTCF	chr17:45693360-45693510	MCF-7	breast:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
49	CTCF	chr17:45693247-45693525	GM12878	blood:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
50	CTCF	chr17:45693360-45693510	HRE	kidney:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:45399473..45401724-chr17:45692079..45694320,2	K562	blood:

Variant related genes	Relation type
NPEPPS	TF binding region
ENSG00000178852	Chromatin interaction
ENSG00000263293	Chromatin interaction

Extended variants
information (count: 62 )
Associated
traits (count: 13 )

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10163469	0.92[AFR][1000 genomes]
rs11079783	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11079784	0.81[CEU][hapmap];0.88[LWK][hapmap];0.81[TSI][hapmap]
rs11656056	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11656855	0.87[AFR][1000 genomes]
rs11656856	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11871606	0.80[LWK][hapmap];0.81[TSI][hapmap]
rs12936468	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1912486	0.89[CEU][hapmap];0.90[JPT][hapmap]
rs1912487	0.85[CEU][hapmap]
rs1962307	0.93[ASW][hapmap];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];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2013383	0.89[CEU][hapmap];0.82[CHD][hapmap];0.81[JPT][hapmap]
rs34200664	0.80[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3760370	0.86[ASW][hapmap];0.95[LWK][hapmap];0.81[TSI][hapmap];0.88[AFR][1000 genomes]
rs3760371	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3826536	0.88[CEU][hapmap];0.91[JPT][hapmap]
rs4239162	0.81[TSI][hapmap]
rs4267364	0.82[CHD][hapmap];0.81[JPT][hapmap]
rs4289035	0.80[ASW][hapmap];0.81[TSI][hapmap]
rs4497739	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4793836	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs4793842	0.86[ASW][hapmap];0.95[LWK][hapmap];0.81[TSI][hapmap]
rs4793908	0.88[AFR][1000 genomes]
rs4793913	0.84[AFR][1000 genomes]
rs4793978	0.86[LWK][hapmap];0.81[TSI][hapmap]
rs4794001	0.81[TSI][hapmap]
rs4794047	0.85[CEU][hapmap];0.89[TSI][hapmap]
rs4794052	0.89[CEU][hapmap];0.84[CHD][hapmap];0.81[JPT][hapmap]
rs4794053	0.89[CEU][hapmap];0.84[CHD][hapmap];0.81[JPT][hapmap]
rs4794058	0.86[ASW][hapmap];0.82[LWK][hapmap];0.81[TSI][hapmap]
rs62074016	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6503796	0.84[CEU][hapmap];0.81[GIH][hapmap];0.93[TSI][hapmap]
rs6503804	0.89[CEU][hapmap];0.84[CHD][hapmap];0.81[JPT][hapmap]
rs6503807	0.89[CEU][hapmap];0.84[CHD][hapmap];0.81[JPT][hapmap]
rs6505048	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6505049	0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6505062	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7207542	0.89[AFR][1000 genomes]
rs7213086	0.84[EUR][1000 genomes]
rs7214799	0.93[ASW][hapmap];0.92[CEU][hapmap];1.00[LWK][hapmap];0.88[MEX][hapmap];0.80[MKK][hapmap];0.93[TSI][hapmap];0.94[YRI][hapmap];0.99[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs8072644	0.86[ASW][hapmap];0.95[LWK][hapmap];0.81[TSI][hapmap]
rs8075411	0.86[ASW][hapmap];0.95[LWK][hapmap];0.81[TSI][hapmap];0.83[AFR][1000 genomes]
rs8075566	0.89[CEU][hapmap];0.84[CHD][hapmap];0.81[JPT][hapmap]
rs8078309	0.89[CEU][hapmap];0.84[CHD][hapmap];0.81[JPT][hapmap]
rs9891111	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9893901	0.85[TSI][hapmap]
rs9905581	0.92[CEU][hapmap]
rs9912311	0.85[CEU][hapmap]
rs9913503	0.85[CEU][hapmap];0.80[TSI][hapmap]
rs9915919	0.85[CEU][hapmap];0.84[TSI][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	nsv1062983	chr17:45030095-45789543	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
2	nsv516872	chr17:45419139-45702280	Strong transcription Genic enhancers Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv525267	chr17:45451894-45735706	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
4	nsv469573	chr17:45511582-45698942	Strong transcription Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv471701	chr17:45511583-45698942	Genic enhancers Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	esv1811231	chr17:45520374-45764956	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
7	esv1813964	chr17:45520374-45764956	Active TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
8	esv2758458	chr17:45520374-45764956	Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
9	esv2758693	chr17:45520374-45764956	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
10	nsv428344	chr17:45520374-45764956	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
11	nsv471403	chr17:45608444-45700642	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
12	nsv482203	chr17:45608444-45700642	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

mRNA abundance (count:13)

SNP	Gene	Cis/trans	Tissue	Source
rs7222225	KRTAP9-3	cis	cerebellum	SCAN
rs7222225	TBKBP1	cis	Artery Aorta	GTEx
rs7222225	TBKBP1	cis	Artery Tibial	GTEx
rs7222225	TBKBP1	cis	lymphoblastoid	seeQTL
rs7222225	MRPL45P2	cis	lymphoblastoid	seeQTL
rs7222225	TBKBP1	cis	lung	GTEx
rs7222225	HOXB6	cis	cerebellum	SCAN
rs7222225	TBKBP1	cis	Skin Sun Exposed Lower leg	GTEx
rs7222225	C17orf57	cis	cerebellum	SCAN
rs7222225	TBKBP1	cis	Nerve Tibial	GTEx
rs7222225	CDK5RAP3	cis	cerebellum	SCAN
rs7222225	KLHL11	cis	cerebellum	SCAN
rs7222225	VPS25	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45659200-45698800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr17:45663800-45702800	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr17:45664800-45695000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr17:45665600-45698200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr17:45666000-45694200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr17:45666800-45693600	Strong transcription	HUES6 Cell Line	embryonic stem cell
7	chr17:45667200-45698600	Strong transcription	HUES64 Cell Line	embryonic stem cell
8	chr17:45667400-45718200	Strong transcription	Primary neutrophils fromperipheralblood	blood
9	chr17:45668200-45699000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr17:45670000-45703000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr17:45670200-45698600	Weak transcription	Fetal Heart	heart
12	chr17:45670400-45698200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr17:45672400-45704200	Strong transcription	Fetal Muscle Trunk	muscle
14	chr17:45672600-45703000	Strong transcription	Primary monocytes fromperipheralblood	blood
15	chr17:45679000-45696000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr17:45679200-45695800	Weak transcription	Small Intestine	intestine
17	chr17:45679600-45695600	Weak transcription	Fetal Brain Male	brain
18	chr17:45679800-45695800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr17:45682200-45699000	Strong transcription	Fetal Muscle Leg	muscle
20	chr17:45682200-45699200	Weak transcription	Right Atrium	heart
21	chr17:45682800-45698800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr17:45682800-45702000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr17:45683000-45695600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr17:45683400-45695600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr17:45683800-45695800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr17:45685600-45695600	Weak transcription	Primary hematopoietic stem cells	blood
27	chr17:45685600-45695800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr17:45685600-45695800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr17:45686800-45699400	Strong transcription	Fetal Intestine Small	intestine
30	chr17:45686800-45703400	Strong transcription	Fetal Stomach	stomach
31	chr17:45687600-45693600	Strong transcription	HUVEC	blood vessel
32	chr17:45687600-45701400	Strong transcription	Sigmoid Colon	Sigmoid Colon
33	chr17:45687800-45693800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr17:45688000-45693800	Strong transcription	Cortex derived primary cultured neurospheres	brain
35	chr17:45688000-45701600	Strong transcription	Primary T cells from cord blood	blood
36	chr17:45688400-45697200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
37	chr17:45688600-45693600	Strong transcription	Left Ventricle	heart
38	chr17:45688600-45697400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr17:45688600-45701400	Strong transcription	Dnd41	blood
40	chr17:45688800-45693800	Strong transcription	Skeletal Muscle Female	skeletal muscle
41	chr17:45688800-45701600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr17:45688800-45702400	Strong transcription	Duodenum Mucosa	Duodenum
43	chr17:45688800-45702400	Strong transcription	Rectal Mucosa Donor 29	rectum
44	chr17:45688800-45703000	Strong transcription	Placenta	Placenta
45	chr17:45689000-45693800	Strong transcription	Duodenum Smooth Muscle	Duodenum
46	chr17:45689000-45698400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr17:45689000-45703000	Strong transcription	Fetal Thymus	thymus
48	chr17:45689200-45693600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr17:45689200-45693600	Strong transcription	Fetal Lung	lung
50	chr17:45689200-45693800	Strong transcription	Skeletal Muscle Male	skeletal muscle

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