Variant report

Variant	rs1565922
Chromosome Location	chr17:37831035-37831036
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:37827266..37833048-chr17:37842420..37846685,6	MCF-7	breast:
2	chr17:37829376..37831831-chr17:37883917..37885766,2	K562	blood:
3	chr17:37793727..37796192-chr17:37829753..37832726,2	MCF-7	breast:
4	chr17:37827137..37831259-chr17:37846824..37848519,3	K562	blood:
5	chr17:37829760..37835390-chr17:37853762..37858979,8	MCF-7	breast:
6	chr17:37806036..37809512-chr17:37829090..37833058,4	K562	blood:
7	chr17:37829190..37831806-chr17:37886312..37888416,2	MCF-7	breast:
8	chr17:37829895..37831934-chr17:37839264..37841541,2	MCF-7	breast:
9	chr17:37824143..37826951-chr17:37830490..37832127,2	MCF-7	breast:
10	chr17:37830304..37832769-chr17:37860083..37864558,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000141741	Chromatin interaction
ENSG00000141736	Chromatin interaction
ENSG00000141744	Chromatin interaction
ENSG00000161395	Chromatin interaction
ENSG00000131748	Chromatin interaction

Extended variants
information (count: 90 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs1018246	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1053651	0.86[CHB][hapmap];0.83[CHD][hapmap];0.90[JPT][hapmap];0.87[TSI][hapmap];0.94[ASN][1000 genomes]
rs10852934	0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs11651497	0.87[ASN][1000 genomes]
rs11658786	0.92[ASN][1000 genomes]
rs11869286	0.86[CHB][hapmap];0.83[CHD][hapmap];0.90[JPT][hapmap];0.80[TSI][hapmap];0.95[ASN][1000 genomes]
rs12150298	0.89[ASW][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12150603	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12940986	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs14050	0.94[ASW][hapmap];0.86[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];0.91[MEX][hapmap];0.94[MKK][hapmap];0.97[TSI][hapmap];0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1476278	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1495099	0.88[ASN][1000 genomes]
rs1495100	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1495101	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1495102	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1565920	0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1810132	0.87[CHB][hapmap];0.92[CHD][hapmap];0.97[GIH][hapmap];0.87[MEX][hapmap]
rs1874228	0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs1877031	0.86[CHB][hapmap];0.83[CHD][hapmap];0.90[JPT][hapmap];0.80[TSI][hapmap];0.94[ASN][1000 genomes]
rs2247862	0.84[ASW][hapmap];0.86[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.94[MKK][hapmap];0.97[TSI][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2271308	0.82[CHB][hapmap];0.80[CHD][hapmap];0.90[JPT][hapmap];0.85[TSI][hapmap];0.92[ASN][1000 genomes]
rs2271309	0.82[JPT][hapmap];0.88[ASN][1000 genomes]
rs2313171	0.90[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2517952	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2517953	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2517954	0.81[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2517955	0.91[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.92[MEX][hapmap];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2517956	0.84[ASW][hapmap];0.81[CEU][hapmap];0.91[CHB][hapmap];0.95[CHD][hapmap];0.92[GIH][hapmap];0.95[JPT][hapmap];0.83[MEX][hapmap];0.84[TSI][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2517957	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2517958	0.95[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2517959	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2517960	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2934951	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2934952	0.85[CEU][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2934953	0.86[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2934956	0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2934971	0.87[CHB][hapmap];0.95[CHD][hapmap];0.97[GIH][hapmap];0.83[MEX][hapmap];0.82[TSI][hapmap]
rs2941503	0.90[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];0.97[TSI][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2941504	0.84[ASW][hapmap];0.86[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.95[MKK][hapmap];0.97[TSI][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2941505	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2941506	1.00[CHB][hapmap];0.94[JPT][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2952151	0.86[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.81[MKK][hapmap];0.97[TSI][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2952152	0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2952155	0.87[CHB][hapmap]
rs2952156	0.82[CHB][hapmap]
rs33953566	0.87[ASN][1000 genomes]
rs35734596	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3751903	0.88[ASN][1000 genomes]
rs3764352	0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs3764353	0.87[ASN][1000 genomes]
rs3794712	0.84[ASN][1000 genomes]
rs3817160	0.88[ASN][1000 genomes]
rs407307	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4794817	0.88[ASN][1000 genomes]
rs4795388	0.82[ASN][1000 genomes]
rs4795389	0.86[ASN][1000 genomes]
rs4795390	0.87[ASN][1000 genomes]
rs732083	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs732084	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8077172	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8078228	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs879606	0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs881844	0.82[CHB][hapmap];0.90[JPT][hapmap];0.91[ASN][1000 genomes]
rs903501	0.84[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.87[TSI][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs903502	0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.87[TSI][hapmap];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs907087	0.86[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.97[TSI][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs907088	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs907089	0.89[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs907090	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs907094	0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs9303274	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs931992	0.82[CHB][hapmap];0.80[CHD][hapmap];0.90[JPT][hapmap];0.80[TSI][hapmap]
rs9675194	0.89[ASW][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9915323	0.80[ASN][1000 genomes]
rs9972882	0.86[CHB][hapmap];0.83[CHD][hapmap];0.86[GIH][hapmap];0.90[JPT][hapmap];0.95[TSI][hapmap];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 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	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	nsv908215	chr17:37818561-37834541	Strong transcription Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
15	esv1848656	chr17:37830900-37834998	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs1565922	DHRS11	cis	parietal	SCAN
rs1565922	PGAP3	cis	Thyroid	GTEx
rs1565922	SLFN14	cis	parietal	SCAN
rs1565922	DHRS11	cis	cerebellum	SCAN
rs1565922	PGAP3	cis	cerebellum	SCAN
rs1565922	PNMT	cis	parietal	SCAN
rs1565922	PGAP3	cis	Heart Left Ventricle	GTEx
rs1565922	SPACA3	cis	parietal	SCAN
rs1565922	GSDMB	cis	cerebellum	SCAN
rs1565922	ORMDL3	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:37824800-37833200	Enhancers	Fetal Heart	heart
2	chr17:37825200-37831200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr17:37825200-37832600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr17:37825200-37833000	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr17:37825800-37833000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr17:37826400-37833000	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr17:37827600-37832800	Enhancers	Fetal Intestine Large	intestine
8	chr17:37827800-37837800	Genic enhancers	Fetal Intestine Small	intestine
9	chr17:37828400-37832000	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr17:37828400-37832200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr17:37828400-37832400	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr17:37828400-37832600	Weak transcription	Fetal Brain Female	brain
13	chr17:37828400-37834000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr17:37828400-37834200	Weak transcription	Fetal Kidney	kidney
15	chr17:37828600-37831400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr17:37828600-37831400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr17:37828600-37831400	Weak transcription	Brain Cingulate Gyrus	brain
18	chr17:37828600-37831600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr17:37828600-37831600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr17:37828600-37831800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr17:37828600-37831800	Weak transcription	Adipose Nuclei	Adipose
22	chr17:37828600-37832000	Weak transcription	Liver	Liver
23	chr17:37828600-37832200	Weak transcription	Brain Angular Gyrus	brain
24	chr17:37828600-37832200	Weak transcription	Brain Substantia Nigra	brain
25	chr17:37828600-37833000	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr17:37828600-37833200	Weak transcription	Brain Anterior Caudate	brain
27	chr17:37828600-37834200	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr17:37828600-37836000	Weak transcription	Ovary	ovary
29	chr17:37828600-37843200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr17:37828800-37831200	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr17:37828800-37831200	Weak transcription	Brain Hippocampus Middle	brain
32	chr17:37828800-37831200	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr17:37828800-37831600	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr17:37828800-37831800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr17:37828800-37831800	Weak transcription	Lung	lung
36	chr17:37828800-37832000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr17:37828800-37832600	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr17:37828800-37835400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr17:37828800-37839800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr17:37829000-37839600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr17:37829000-37839800	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr17:37829200-37831200	Weak transcription	Stomach Smooth Muscle	stomach
43	chr17:37829200-37833000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr17:37829400-37832200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr17:37829400-37834000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr17:37829400-37837400	Enhancers	Primary B cells from cord blood	blood
47	chr17:37829600-37832200	Weak transcription	Fetal Brain Male	brain
48	chr17:37829600-37835600	Weak transcription	Brain Germinal Matrix	brain
49	chr17:37829600-37837600	Enhancers	Primary B cells from peripheral blood	blood
50	chr17:37829800-37833000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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