Variant report

Variant	rs2271308
Chromosome Location	chr17:37817482-37817483
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	NFIC	chr17:37817248-37817810	ECC-1	luminal epithelium:	n/a	n/a
2	TCF12	chr17:37817167-37817769	ECC-1	luminal epithelium:	n/a	n/a
3	NR3C1	chr17:37817198-37817626	A549	lung:	n/a	chr17:37817403-37817419 chr17:37817404-37817418 chr17:37817404-37817418 chr17:37817403-37817419 chr17:37817403-37817419 chr17:37817432-37817439 chr17:37817403-37817419
4	TCF12	chr17:37817097-37817765	ECC-1	luminal epithelium:	n/a	n/a
5	NR3C1	chr17:37817070-37817768	A549	lung:	n/a	chr17:37817403-37817419 chr17:37817735-37817748 chr17:37817404-37817418 chr17:37817404-37817418 chr17:37817403-37817419 chr17:37817403-37817419 chr17:37817432-37817439 chr17:37817403-37817419
6	CTCF	chr17:37817360-37817510	WERI-Rb-1	eye:	n/a	n/a
7	NR3C1	chr17:37817076-37817704	A549	lung:	n/a	chr17:37817403-37817419 chr17:37817404-37817418 chr17:37817404-37817418 chr17:37817403-37817419 chr17:37817403-37817419 chr17:37817432-37817439 chr17:37817403-37817419
8	NR3C1	chr17:37817203-37817606	A549	lung:	n/a	chr17:37817403-37817419 chr17:37817404-37817418 chr17:37817404-37817418 chr17:37817403-37817419 chr17:37817403-37817419 chr17:37817432-37817439 chr17:37817403-37817419
9	NR3C1	chr17:37817177-37817641	ECC-1	luminal epithelium:	n/a	chr17:37817403-37817419 chr17:37817404-37817418 chr17:37817404-37817418 chr17:37817403-37817419 chr17:37817403-37817419 chr17:37817432-37817439 chr17:37817403-37817419
10	EP300	chr17:37817062-37817818	ECC-1	luminal epithelium:	n/a	n/a
11	GATA2	chr17:37817319-37817871	SH-SY5Y	brain:	n/a	chr17:37817494-37817507
12	NR3C1	chr17:37817141-37817708	ECC-1	luminal epithelium:	n/a	chr17:37817403-37817419 chr17:37817404-37817418 chr17:37817404-37817418 chr17:37817403-37817419 chr17:37817403-37817419 chr17:37817432-37817439 chr17:37817403-37817419
13	NR3C1	chr17:37817246-37817524	A549	lung:	n/a	chr17:37817403-37817419 chr17:37817404-37817418 chr17:37817404-37817418 chr17:37817403-37817419 chr17:37817403-37817419 chr17:37817432-37817439 chr17:37817403-37817419

No.	Distal block	Cell Line	Cell type
1	chr17:37796408..37798750-chr17:37816714..37819349,2	MCF-7	breast:
2	chr17:37806279..37807957-chr17:37817089..37818610,2	K562	blood:
3	chr17:37815487..37818092-chr17:37864402..37866827,2	MCF-7	breast:
4	chr17:37814865..37817539-chr17:37818088..37820916,2	MCF-7	breast:
5	chr17:37792116..37794246-chr17:37816401..37819185,2	MCF-7	breast:

Variant related genes	Relation type
TCAP	TF binding region
ENSG00000131748	Chromatin interaction
ENSG00000173991	Chromatin interaction
ENSG00000141736	Chromatin interaction

Extended variants
information (count: 103 )
Associated
traits (count: 11 )

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs1018246	0.92[ASN][1000 genomes]
rs1053651	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];0.97[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10852934	0.83[CHB][hapmap];0.81[CHD][hapmap];0.82[JPT][hapmap];0.89[ASN][1000 genomes]
rs11078901	0.85[CEU][hapmap]
rs11078906	0.84[CEU][hapmap]
rs11078907	0.84[CEU][hapmap]
rs11651497	0.89[ASN][1000 genomes]
rs11654018	0.90[CEU][hapmap]
rs11657899	0.85[CEU][hapmap]
rs11658678	0.95[CEU][hapmap]
rs11658786	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11869286	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];0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12150298	0.82[CHB][hapmap];0.81[GIH][hapmap];0.91[JPT][hapmap];0.87[TSI][hapmap];0.92[ASN][1000 genomes]
rs12150603	0.82[CHB][hapmap];0.80[CHD][hapmap];0.81[GIH][hapmap];0.91[JPT][hapmap];0.84[TSI][hapmap];0.92[ASN][1000 genomes]
rs12450559	0.90[CEU][hapmap]
rs12453682	0.86[CEU][hapmap];0.84[GIH][hapmap];0.92[TSI][hapmap];0.86[EUR][1000 genomes]
rs12936996	0.85[CEU][hapmap]
rs12940986	0.82[CHB][hapmap];0.80[CHD][hapmap];0.81[GIH][hapmap];0.91[JPT][hapmap];0.87[TSI][hapmap];0.91[ASN][1000 genomes]
rs14050	0.86[CHB][hapmap];0.85[CHD][hapmap];0.91[JPT][hapmap];0.87[TSI][hapmap];0.92[ASN][1000 genomes]
rs1476278	0.82[CHB][hapmap];0.80[CHD][hapmap];0.81[GIH][hapmap];0.91[JPT][hapmap];0.87[TSI][hapmap];0.91[ASN][1000 genomes]
rs1495099	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1495100	0.92[ASN][1000 genomes]
rs1495101	0.92[ASN][1000 genomes]
rs1495102	0.92[ASN][1000 genomes]
rs1565920	0.91[ASN][1000 genomes]
rs1565922	0.82[CHB][hapmap];0.80[CHD][hapmap];0.90[JPT][hapmap];0.85[TSI][hapmap];0.92[ASN][1000 genomes]
rs1874228	0.95[CEU][hapmap];0.81[CHD][hapmap];0.89[GIH][hapmap];0.82[JPT][hapmap];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1877031	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]
rs2247862	0.86[CHB][hapmap];0.85[CHD][hapmap];0.91[JPT][hapmap];0.87[TSI][hapmap];0.92[ASN][1000 genomes]
rs2271309	0.83[CHB][hapmap];0.82[JPT][hapmap];0.89[ASN][1000 genomes]
rs2303316	0.90[CEU][hapmap]
rs2313171	0.90[JPT][hapmap];0.92[ASN][1000 genomes]
rs2517952	0.83[ASN][1000 genomes]
rs2517953	0.86[ASN][1000 genomes]
rs2517954	0.86[JPT][hapmap];0.85[ASN][1000 genomes]
rs2517955	0.80[CHD][hapmap];0.86[JPT][hapmap];0.85[TSI][hapmap];0.85[ASN][1000 genomes]
rs2517956	0.80[CHD][hapmap];0.86[JPT][hapmap];0.85[ASN][1000 genomes]
rs2517957	0.85[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs2517958	0.81[CHB][hapmap];0.90[JPT][hapmap];0.92[ASN][1000 genomes]
rs2517959	0.85[ASN][1000 genomes]
rs2517960	0.84[ASN][1000 genomes]
rs2934951	0.92[ASN][1000 genomes]
rs2934952	0.92[ASN][1000 genomes]
rs2934953	0.89[JPT][hapmap];0.92[ASN][1000 genomes]
rs2934956	0.92[ASN][1000 genomes]
rs2934971	0.80[CHD][hapmap]
rs2941503	0.86[CHB][hapmap];0.85[CHD][hapmap];0.90[JPT][hapmap];0.87[TSI][hapmap];0.92[ASN][1000 genomes]
rs2941504	0.86[CHB][hapmap];0.91[JPT][hapmap];0.87[TSI][hapmap];0.92[ASN][1000 genomes]
rs2941505	0.82[CHB][hapmap];0.91[JPT][hapmap];0.92[ASN][1000 genomes]
rs2941506	0.84[JPT][hapmap];0.92[ASN][1000 genomes]
rs2952151	0.86[CHB][hapmap];0.85[CHD][hapmap];0.91[JPT][hapmap];0.87[TSI][hapmap];0.92[ASN][1000 genomes]
rs2952152	0.90[ASN][1000 genomes]
rs33953566	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35734596	0.83[ASN][1000 genomes]
rs3751903	0.89[ASN][1000 genomes]
rs3764352	0.83[CHB][hapmap];0.84[CHD][hapmap];0.86[GIH][hapmap];0.82[JPT][hapmap];0.89[ASN][1000 genomes]
rs3764353	0.89[ASN][1000 genomes]
rs3794712	0.85[ASN][1000 genomes]
rs3817160	0.89[ASN][1000 genomes]
rs407307	0.90[ASN][1000 genomes]
rs4239222	0.90[CEU][hapmap]
rs4794814	0.90[CEU][hapmap]
rs4794817	0.89[ASN][1000 genomes]
rs4795388	0.95[CEU][hapmap];0.83[ASN][1000 genomes]
rs4795389	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4795390	0.89[ASN][1000 genomes]
rs7216086	0.90[CEU][hapmap]
rs7225096	0.85[CEU][hapmap]
rs732083	0.92[ASN][1000 genomes]
rs732084	0.92[ASN][1000 genomes]
rs7503069	0.90[CEU][hapmap]
rs7503705	0.90[CEU][hapmap]
rs8065963	0.90[CEU][hapmap]
rs8077172	0.92[ASN][1000 genomes]
rs8078228	0.81[CHB][hapmap];0.90[JPT][hapmap];0.92[ASN][1000 genomes]
rs879606	0.83[CHB][hapmap];0.81[CHD][hapmap];0.82[JPT][hapmap];0.89[ASN][1000 genomes]
rs881844	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs903501	0.82[CHB][hapmap];0.80[CHD][hapmap];0.91[JPT][hapmap];0.91[ASN][1000 genomes]
rs903502	0.86[CHB][hapmap];0.82[CHD][hapmap];0.85[GIH][hapmap];0.91[JPT][hapmap];0.83[MEX][hapmap];0.97[TSI][hapmap];0.91[ASN][1000 genomes]
rs907087	0.86[CHB][hapmap];0.85[CHD][hapmap];0.91[JPT][hapmap];0.87[TSI][hapmap];0.92[ASN][1000 genomes]
rs907088	0.92[ASN][1000 genomes]
rs907089	0.82[CHB][hapmap];0.80[CHD][hapmap];0.91[JPT][hapmap];0.87[TSI][hapmap];0.92[ASN][1000 genomes]
rs907090	0.92[ASN][1000 genomes]
rs907094	0.83[CHB][hapmap];0.84[CHD][hapmap];0.86[GIH][hapmap];0.82[JPT][hapmap];0.89[ASN][1000 genomes]
rs9303274	0.82[CHB][hapmap];0.80[CHD][hapmap];0.81[GIH][hapmap];0.91[JPT][hapmap];0.87[TSI][hapmap];0.91[ASN][1000 genomes]
rs931992	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.95[TSI][hapmap]
rs9675194	0.82[CHB][hapmap];0.83[GIH][hapmap];0.91[JPT][hapmap];0.87[TSI][hapmap];0.92[ASN][1000 genomes]
rs9915323	1.00[CEU][hapmap];0.83[CHB][hapmap];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9972882	0.90[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.90[TSI][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 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
14	nsv908214	chr17:37814224-37861833	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers 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:11)

SNP	Gene	Cis/trans	Tissue	Source
rs2271308	ORMDL3	Cis_1M	lymphoblastoid	RTeQTL
rs2271308	PGAP3	cis	Thyroid	GTEx
rs2271308	PGAP3	cis	cerebellum	SCAN
rs2271308	PGAP3	cis	Heart Left Ventricle	GTEx
rs2271308	PGAP3	cis	Stomach	GTEx
rs2271308	SPACA3	cis	parietal	SCAN
rs2271308	DHRS11	cis	parietal	SCAN
rs2271308	RAD51L3	cis	cerebellum	SCAN
rs2271308	SLFN14	cis	parietal	SCAN
rs2271308	DHRS11	cis	cerebellum	SCAN
rs2271308	CRKRS	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:123 , 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	chr17:37795400-37818000	Weak transcription	Fetal Kidney	kidney
3	chr17:37799800-37819600	Weak transcription	Osteobl	bone
4	chr17:37800000-37818600	Weak transcription	Hela-S3	cervix
5	chr17:37800000-37820000	Weak transcription	NH-A	brain
6	chr17:37803800-37821800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr17:37808400-37819200	Weak transcription	Small Intestine	intestine
8	chr17:37809800-37819400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr17:37810000-37819400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr17:37810000-37819600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
11	chr17:37810000-37820000	Weak transcription	HSMMtube	muscle
12	chr17:37810000-37820400	Strong transcription	Brain Germinal Matrix	brain
13	chr17:37810200-37819800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr17:37810400-37817600	Weak transcription	Stomach Mucosa	stomach
15	chr17:37810400-37817800	Strong transcription	Rectal Mucosa Donor 29	rectum
16	chr17:37810600-37818600	Strong transcription	Fetal Intestine Small	intestine
17	chr17:37810600-37819200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr17:37810600-37819200	Strong transcription	Fetal Intestine Large	intestine
19	chr17:37810600-37820000	Weak transcription	K562	blood
20	chr17:37810600-37821000	Weak transcription	Fetal Brain Male	brain
21	chr17:37810800-37819400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr17:37810800-37819600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr17:37810800-37820600	Strong transcription	Primary neutrophils fromperipheralblood	blood
24	chr17:37811000-37818000	Strong transcription	Esophagus	oesophagus
25	chr17:37811000-37818600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr17:37811000-37818600	Strong transcription	Sigmoid Colon	Sigmoid Colon
27	chr17:37811400-37818600	Strong transcription	Cortex derived primary cultured neurospheres	brain
28	chr17:37811800-37819400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr17:37811800-37820800	Strong transcription	Fetal Brain Female	brain
30	chr17:37812000-37817600	Strong transcription	Gastric	stomach
31	chr17:37812000-37819400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr17:37812000-37819600	Genic enhancers	Lung	lung
33	chr17:37812400-37818200	Genic enhancers	Primary T cells fromperipheralblood	blood
34	chr17:37812400-37819200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr17:37812400-37819600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr17:37812600-37818000	Weak transcription	HMEC	breast
37	chr17:37812600-37818200	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
38	chr17:37812600-37818200	Strong transcription	Duodenum Mucosa	Duodenum
39	chr17:37812600-37819400	Strong transcription	Placenta Amnion	Placenta Amnion
40	chr17:37812600-37819600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr17:37812800-37818000	Strong transcription	Rectal Mucosa Donor 31	rectum
42	chr17:37813000-37818000	Strong transcription	Ovary	ovary
43	chr17:37813000-37820800	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr17:37813400-37819400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr17:37814000-37817800	Strong transcription	Duodenum Smooth Muscle	Duodenum
46	chr17:37814000-37818200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr17:37814000-37818200	Strong transcription	Aorta	Aorta
48	chr17:37814000-37818200	Strong transcription	Brain Angular Gyrus	brain
49	chr17:37814000-37818400	Strong transcription	Colon Smooth Muscle	Colon
50	chr17:37814000-37819200	Strong transcription	Muscle Satellite Cultured Cells	--

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