Variant report

Variant	rs1877031
Chromosome Location	chr17:37814080-37814081
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:122)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ZNF263	chr17:37813997-37814431	HEK293-T-REx	kidney:	n/a	chr17:37814194-37814215

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:37814072-37814122	GM06990	blood:	n/a
2	chr17:37814043-37814093	SAEC	small airway:	n/a
3	chr17:37814072-37814122	HepG2	liver:	n/a
4	chr17:37814072-37814122	NT2-D1	testis:	n/a
5	chr17:37814043-37814093	RPTEC	kidney:	n/a
6	chr17:37814072-37814122	MCF-7	breast:	n/a
7	chr17:37814043-37814093	HRE	kidney:	n/a
8	chr17:37814072-37814122	GM12892	blood:	n/a
9	chr17:37814072-37814122	NH-A	brain:	n/a
10	chr17:37814043-37814093	AG09319	gingival:	n/a
11	chr17:37814043-37814093	HCF	heart:	n/a
12	chr17:37814072-37814122	PANC-1	pancreas:	n/a
13	chr17:37814072-37814122	HMEC	breast:	n/a
14	chr17:37814043-37814093	AG04449	skin:	fetal
15	chr17:37814043-37814093	PANC-1	pancreas:	n/a
16	chr17:37814072-37814122	PrEC	prostate:	n/a
17	chr17:37814043-37814093	SK-N-SH_RA	brain:	n/a
18	chr17:37814072-37814122	SK-N-SH	brain:	n/a
19	chr17:37814072-37814122	HCF	heart:	n/a
20	chr17:37814043-37814093	BJ	skin:	n/a
21	chr17:37814043-37814093	HRPEpiC	eye:	n/a
22	chr17:37814043-37814093	GM12892	blood:	n/a
23	chr17:37814072-37814122	HPAEpiC	pulmonary alveolar:	n/a
24	chr17:37814072-37814122	HRE	kidney:	n/a
25	chr17:37814072-37814122	AG04449	skin:	fetal
26	chr17:37814072-37814122	SAEC	small airway:	n/a
27	chr17:37814072-37814122	HRCEpiC	kidney:	n/a
28	chr17:37814043-37814093	A549	lung:	n/a
29	chr17:37814043-37814093	AG10803	skin:	n/a
30	chr17:37814043-37814093	HL-60	blood:	n/a
31	chr17:37814043-37814093	T-47D	breast:	n/a
32	chr17:37814072-37814122	Hepatocyte	liver:	n/a
33	chr17:37814072-37814122	BE2_C	brain:	n/a
34	chr17:37814043-37814093	ECC-1	luminal epithelium:	n/a
35	chr17:37814072-37814122	Jurkat	blood:	n/a
36	chr17:37814072-37814122	HEK293	kidney:	embryo
37	chr17:37814043-37814093	HRCEpiC	kidney:	n/a
38	chr17:37814043-37814093	BE2_C	brain:	n/a
39	chr17:37814072-37814122	AG09309	skin:	n/a
40	chr17:37814072-37814122	GM12891	blood:	n/a
41	chr17:37814043-37814093	Caco-2	colon:	n/a
42	chr17:37814072-37814122	CMK	blood:	n/a
43	chr17:37814072-37814122	HEEpiC	esophagus:	n/a
44	chr17:37814072-37814122	SK-N-MC	brain:	n/a
45	chr17:37814043-37814093	Hela-S3	cervix:	n/a
46	chr17:37814043-37814093	SK-N-MC	brain:	n/a
47	chr17:37814043-37814093	HMEC	breast:	n/a
48	chr17:37814043-37814093	NT2-D1	testis:	n/a
49	chr17:37814072-37814122	NHBE	bronchial:	n/a
50	chr17:37814043-37814093	U87	brain:	n/a

No data

Variant related genes	Relation type
STARD3	TF binding region
STARD3	CpG island

Extended variants
information (count: 86 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs1018246	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1053651	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.92[TSI][hapmap];0.99[ASN][1000 genomes]
rs10852934	0.87[CHB][hapmap];0.83[CHD][hapmap];0.82[JPT][hapmap];0.91[ASN][1000 genomes]
rs11651497	0.91[ASN][1000 genomes]
rs11658786	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11869286	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.91[YRI][hapmap];0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12150298	0.86[CHB][hapmap];0.80[CHD][hapmap];0.88[GIH][hapmap];0.91[JPT][hapmap];0.83[MEX][hapmap];0.87[TSI][hapmap];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12150603	0.94[ASW][hapmap];0.86[CHB][hapmap];0.83[CHD][hapmap];0.88[GIH][hapmap];0.91[JPT][hapmap];0.85[TSI][hapmap];0.91[YRI][hapmap];0.82[AFR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12453682	0.81[ASW][hapmap];0.87[GIH][hapmap];0.85[LWK][hapmap];0.98[MKK][hapmap];0.92[TSI][hapmap];0.91[YRI][hapmap];0.86[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs12940986	0.94[ASW][hapmap];0.86[CHB][hapmap];0.83[CHD][hapmap];0.88[GIH][hapmap];0.91[JPT][hapmap];0.87[MEX][hapmap];0.87[TSI][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs14050	0.91[CHB][hapmap];0.88[CHD][hapmap];0.91[JPT][hapmap];0.83[TSI][hapmap];0.94[ASN][1000 genomes]
rs1476278	0.86[CHB][hapmap];0.83[CHD][hapmap];0.88[GIH][hapmap];0.91[JPT][hapmap];0.87[MEX][hapmap];0.87[TSI][hapmap];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1495099	0.88[AFR][1000 genomes];0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1495100	0.85[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs1495101	0.94[ASN][1000 genomes]
rs1495102	0.94[ASN][1000 genomes]
rs1565920	0.85[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs1565922	0.86[CHB][hapmap];0.83[CHD][hapmap];0.90[JPT][hapmap];0.80[TSI][hapmap];0.94[ASN][1000 genomes]
rs1874228	0.94[ASW][hapmap];0.83[CHB][hapmap];0.83[CHD][hapmap];0.92[GIH][hapmap];0.82[JPT][hapmap];0.92[LWK][hapmap];0.91[MKK][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs2247862	0.91[CHB][hapmap];0.87[CHD][hapmap];0.91[JPT][hapmap];0.83[TSI][hapmap];0.94[ASN][1000 genomes]
rs2271308	0.82[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.95[TSI][hapmap];0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2271309	0.87[CHB][hapmap];0.82[JPT][hapmap];0.91[ASN][1000 genomes]
rs2313171	0.90[JPT][hapmap];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2517952	0.85[ASN][1000 genomes]
rs2517953	0.87[ASN][1000 genomes]
rs2517954	0.86[JPT][hapmap];0.86[ASN][1000 genomes]
rs2517955	0.94[ASW][hapmap];0.85[GIH][hapmap];0.86[JPT][hapmap];0.87[MEX][hapmap];0.85[TSI][hapmap];1.00[YRI][hapmap];0.85[ASN][1000 genomes]
rs2517956	0.86[JPT][hapmap];0.85[ASN][1000 genomes]
rs2517957	0.90[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2517958	0.86[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2517959	0.86[ASN][1000 genomes]
rs2517960	0.85[ASN][1000 genomes]
rs2934951	0.94[ASN][1000 genomes]
rs2934952	0.94[ASN][1000 genomes]
rs2934953	0.81[CHB][hapmap];0.89[JPT][hapmap];0.94[ASN][1000 genomes]
rs2934956	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2941503	0.91[CHB][hapmap];0.88[CHD][hapmap];0.90[JPT][hapmap];0.82[TSI][hapmap];0.94[ASN][1000 genomes]
rs2941504	0.91[CHB][hapmap];0.91[JPT][hapmap];0.82[TSI][hapmap];0.94[ASN][1000 genomes]
rs2941505	0.86[CHB][hapmap];0.91[JPT][hapmap];0.94[ASN][1000 genomes]
rs2941506	0.85[CHB][hapmap];0.84[JPT][hapmap];0.94[ASN][1000 genomes]
rs2952151	0.91[CHB][hapmap];0.88[CHD][hapmap];0.91[JPT][hapmap];0.83[TSI][hapmap];0.94[ASN][1000 genomes]
rs2952152	0.92[ASN][1000 genomes]
rs33953566	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35734596	0.85[ASN][1000 genomes]
rs3751903	0.91[ASN][1000 genomes]
rs3764351	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3764352	0.88[ASW][hapmap];0.87[CHB][hapmap];0.86[CHD][hapmap];0.90[GIH][hapmap];0.82[JPT][hapmap];0.92[LWK][hapmap];0.95[MKK][hapmap];0.91[ASN][1000 genomes]
rs3764353	0.91[ASN][1000 genomes]
rs3794712	0.87[ASN][1000 genomes]
rs3817160	0.91[ASN][1000 genomes]
rs407307	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4794817	0.91[ASN][1000 genomes]
rs4795388	0.83[CHB][hapmap];0.85[ASN][1000 genomes]
rs4795389	0.88[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs4795390	0.91[ASN][1000 genomes]
rs732083	0.87[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs732084	0.94[ASN][1000 genomes]
rs8077172	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8078228	0.85[CHB][hapmap];0.90[JPT][hapmap];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs879606	0.87[CHB][hapmap];0.83[CHD][hapmap];0.82[JPT][hapmap];0.91[ASN][1000 genomes]
rs881844	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs903501	0.86[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap];0.93[ASN][1000 genomes]
rs903502	0.87[ASW][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.82[GIH][hapmap];0.91[JPT][hapmap];0.92[TSI][hapmap];0.84[YRI][hapmap];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs907087	0.91[CHB][hapmap];0.88[CHD][hapmap];0.91[JPT][hapmap];0.83[TSI][hapmap];0.94[ASN][1000 genomes]
rs907088	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs907089	0.86[CHB][hapmap];0.83[CHD][hapmap];0.85[GIH][hapmap];0.91[JPT][hapmap];0.87[TSI][hapmap];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs907090	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs907094	0.88[ASW][hapmap];0.87[CHB][hapmap];0.86[CHD][hapmap];0.90[GIH][hapmap];0.82[JPT][hapmap];0.92[LWK][hapmap];0.95[MKK][hapmap];0.91[ASN][1000 genomes]
rs9303274	0.86[CHB][hapmap];0.83[CHD][hapmap];0.88[GIH][hapmap];0.91[JPT][hapmap];0.87[MEX][hapmap];0.87[TSI][hapmap];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs931992	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[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]
rs9675194	0.86[CHB][hapmap];0.80[CHD][hapmap];0.90[GIH][hapmap];0.91[JPT][hapmap];0.83[MEX][hapmap];0.87[TSI][hapmap];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9915323	0.82[CEU][hapmap];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9972882	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.80[MEX][hapmap];0.85[TSI][hapmap];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932024	chr17:37192290-37850932	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	92 gene(s)	inside rSNPs	diseases
2	esv1825702	chr17:37487168-37876767	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
3	nsv833442	chr17:37692880-37861291	Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
4	nsv908205	chr17:37709422-37830900	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
5	nsv908206	chr17:37709422-37866005	Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
6	nsv908207	chr17:37709422-37922259	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
7	nsv833443	chr17:37725640-37882864	Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
8	nsv457738	chr17:37770005-37831035	Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
9	nsv574991	chr17:37770005-37831035	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
10	nsv516757	chr17:37781849-37834541	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases
11	esv1792029	chr17:37797757-37886460	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh 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	20 gene(s)	inside rSNPs	diseases
12	nsv908213	chr17:37807698-37839493	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
13	nsv528093	chr17:37814080-37866005	Weak transcription Bivalent Enhancer Enhancers Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs1877031	HNF1B	cis	cerebellum	SCAN
rs1877031	PGAP3	cis	lung	GTEx
rs1877031	SLFN14	cis	parietal	SCAN
rs1877031	PGAP3	cis	Thyroid	GTEx
rs1877031	PGAP3	cis	Heart Left Ventricle	GTEx
rs1877031	SPACA3	cis	parietal	SCAN
rs1877031	ORMDL3	Cis_1M	lymphoblastoid	RTeQTL
rs1877031	PGAP3	cis	Nerve Tibial	GTEx

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:37795000-37823800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr17:37795200-37814600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr17:37795400-37818000	Weak transcription	Fetal Kidney	kidney
4	chr17:37799800-37819600	Weak transcription	Osteobl	bone
5	chr17:37800000-37815200	Weak transcription	HUVEC	blood vessel
6	chr17:37800000-37818600	Weak transcription	Hela-S3	cervix
7	chr17:37800000-37820000	Weak transcription	NH-A	brain
8	chr17:37800200-37816800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr17:37800600-37816200	Weak transcription	NHEK	skin
10	chr17:37801000-37814600	Weak transcription	Primary B cells from cord blood	blood
11	chr17:37801800-37817000	Weak transcription	A549	lung
12	chr17:37803400-37814200	Strong transcription	Thymus	Thymus
13	chr17:37803800-37821800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr17:37808400-37819200	Weak transcription	Small Intestine	intestine
15	chr17:37809200-37816200	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr17:37809600-37814200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr17:37809800-37816400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr17:37809800-37819400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr17:37810000-37815000	Strong transcription	Primary monocytes fromperipheralblood	blood
20	chr17:37810000-37815600	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr17:37810000-37817200	Weak transcription	HSMM	muscle
22	chr17:37810000-37819400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr17:37810000-37819600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr17:37810000-37820000	Weak transcription	HSMMtube	muscle
25	chr17:37810000-37820400	Strong transcription	Brain Germinal Matrix	brain
26	chr17:37810200-37815400	Strong transcription	Fetal Stomach	stomach
27	chr17:37810200-37816200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr17:37810200-37816400	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr17:37810200-37816400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr17:37810200-37816600	Strong transcription	Spleen	Spleen
31	chr17:37810200-37819800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr17:37810400-37815000	Weak transcription	Pancreas	Pancrea
33	chr17:37810400-37817600	Weak transcription	Stomach Mucosa	stomach
34	chr17:37810400-37817800	Strong transcription	Rectal Mucosa Donor 29	rectum
35	chr17:37810600-37814200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr17:37810600-37814200	Strong transcription	Primary B cells from peripheral blood	blood
37	chr17:37810600-37814600	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr17:37810600-37814600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr17:37810600-37814600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr17:37810600-37814600	Weak transcription	Liver	Liver
41	chr17:37810600-37815200	Strong transcription	Monocytes-CD14+_RO01746	blood
42	chr17:37810600-37818600	Strong transcription	Fetal Intestine Small	intestine
43	chr17:37810600-37819200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr17:37810600-37819200	Strong transcription	Fetal Intestine Large	intestine
45	chr17:37810600-37820000	Weak transcription	K562	blood
46	chr17:37810600-37821000	Weak transcription	Fetal Brain Male	brain
47	chr17:37810800-37816600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr17:37810800-37819400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
49	chr17:37810800-37819600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr17:37810800-37820600	Strong transcription	Primary neutrophils fromperipheralblood	blood

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