Variant report

Variant	rs14050
Chromosome Location	chr17:37828072-37828073
allele	A/G
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:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:37827266..37833048-chr17:37842420..37846685,6	MCF-7	breast:
2	chr17:37797245..37799083-chr17:37827034..37828829,2	K562	blood:
3	chr17:37827137..37831259-chr17:37846824..37848519,3	K562	blood:
4	chr17:37827978..37830738-chr17:37885762..37888440,2	MCF-7	breast:
5	chr17:37776904..37777847-chr17:37827993..37828988,2	MCF-7	breast:
6	chr17:37775807..37781695-chr17:37822673..37828377,10	K562	blood:
7	chr17:37827616..37829893-chr17:37861352..37863685,3	MCF-7	breast:
8	chr17:37777847..37779169-chr17:37827001..37829318,18	K562	blood:
9	chr17:37825246..37828511-chr17:37865302..37868982,3	K562	blood:
10	chr17:37775807..37779827-chr17:37826059..37828358,3	K562	blood:
11	chr17:37822828..37824535-chr17:37827629..37829192,2	MCF-7	breast:
12	chr17:37826293..37828141-chr17:37893095..37895694,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000141738	Chromatin interaction
ENSG00000141736	Chromatin interaction
ENSG00000141744	Chromatin interaction
ENSG00000141741	Chromatin interaction
ENSG00000161395	Chromatin interaction
ENSG00000214546	Chromatin interaction

Extended variants
information (count: 92 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs1018246	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1053651	0.91[CHB][hapmap];0.88[CHD][hapmap];0.91[JPT][hapmap];0.90[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	0.91[CHB][hapmap];0.88[CHD][hapmap];0.90[JPT][hapmap];0.83[TSI][hapmap];0.95[ASN][1000 genomes]
rs12150298	0.83[ASW][hapmap];0.90[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12150603	0.91[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12453682	0.82[TSI][hapmap]
rs12940986	0.91[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1476278	0.91[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1495099	0.88[ASN][1000 genomes]
rs1495100	0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1495101	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1495102	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1565920	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1565922	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]
rs1565923	0.90[CEU][hapmap]
rs1810132	0.90[CEU][hapmap];0.83[CHB][hapmap];0.88[CHD][hapmap];0.97[GIH][hapmap];0.87[MEX][hapmap]
rs1874228	0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs1877031	0.91[CHB][hapmap];0.88[CHD][hapmap];0.91[JPT][hapmap];0.83[TSI][hapmap];0.94[ASN][1000 genomes]
rs2247862	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2271308	0.86[CHB][hapmap];0.85[CHD][hapmap];0.91[JPT][hapmap];0.87[TSI][hapmap];0.92[ASN][1000 genomes]
rs2271309	0.82[JPT][hapmap];0.88[ASN][1000 genomes]
rs2313171	0.90[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2517952	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2517953	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2517954	0.95[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2517955	0.86[CEU][hapmap];0.87[CHB][hapmap];0.90[CHD][hapmap];0.95[JPT][hapmap];0.84[MEX][hapmap];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2517956	0.95[CEU][hapmap];0.87[CHB][hapmap];0.90[CHD][hapmap];0.92[GIH][hapmap];0.95[JPT][hapmap];0.91[MEX][hapmap];0.87[TSI][hapmap];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2517957	0.91[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2517958	0.91[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2517959	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2517960	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2934951	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2934952	1.00[CEU][hapmap];0.83[YRI][hapmap];0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2934953	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2934956	0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2934971	0.90[CEU][hapmap];0.83[CHB][hapmap];0.90[CHD][hapmap];0.97[GIH][hapmap];0.83[MEX][hapmap];0.84[TSI][hapmap]
rs2941503	0.84[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2941504	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2941505	0.91[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2941506	0.90[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2952151	0.84[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2952152	0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2952155	0.83[CHB][hapmap]
rs2952156	0.90[CEU][hapmap]
rs33953566	0.87[ASN][1000 genomes]
rs35734596	0.80[EUR][1000 genomes];0.89[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	0.89[EUR][1000 genomes];0.95[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	0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs732084	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8077172	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8078228	0.90[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs879606	0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs881844	0.86[CHB][hapmap];0.91[JPT][hapmap];0.91[ASN][1000 genomes]
rs903501	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.89[TSI][hapmap];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs903502	0.91[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.90[TSI][hapmap];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs907087	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs907088	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs907089	0.83[ASW][hapmap];0.91[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs907090	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs907094	0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs9303274	0.91[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs931992	0.86[CHB][hapmap];0.85[CHD][hapmap];0.91[JPT][hapmap];0.83[TSI][hapmap]
rs9675194	0.83[ASW][hapmap];0.91[CEU][hapmap];0.95[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9915323	0.80[ASN][1000 genomes]
rs9972882	0.91[CHB][hapmap];0.88[CHD][hapmap];0.86[GIH][hapmap];0.91[JPT][hapmap];0.83[MEX][hapmap];0.97[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	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
15	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

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs14050	DHRS11	cis	cerebellum	SCAN
rs14050	PNMT	cis	parietal	SCAN
rs14050	PGAP3	cis	Thyroid	GTEx
rs14050	ORMDL3	Cis_1M	lymphoblastoid	RTeQTL
rs14050	SLFN14	cis	parietal	SCAN
rs14050	PGAP3	cis	Heart Left Ventricle	GTEx
rs14050	GSDMB	cis	cerebellum	SCAN
rs14050	SPACA3	cis	parietal	SCAN

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:37824600-37831000	Weak transcription	Gastric	stomach
2	chr17:37824800-37833200	Enhancers	Fetal Heart	heart
3	chr17:37825200-37828200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr17:37825200-37828200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr17:37825200-37828200	Weak transcription	Lung	lung
6	chr17:37825200-37828800	Weak transcription	Primary B cells from cord blood	blood
7	chr17:37825200-37831200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr17:37825200-37832600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr17:37825200-37833000	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr17:37825800-37833000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr17:37826000-37828200	Weak transcription	K562	blood
12	chr17:37826400-37828200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr17:37826400-37829000	Enhancers	Left Ventricle	heart
14	chr17:37826400-37833000	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr17:37826600-37828200	Weak transcription	Right Atrium	heart
16	chr17:37826800-37830800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr17:37827000-37828200	Bivalent Enhancer	Duodenum Mucosa	Duodenum
18	chr17:37827000-37828400	Bivalent Enhancer	Fetal Muscle Leg	muscle
19	chr17:37827000-37829400	Enhancers	Right Ventricle	heart
20	chr17:37827200-37828600	Enhancers	Brain Anterior Caudate	brain
21	chr17:37827200-37828600	Enhancers	Brain Substantia Nigra	brain
22	chr17:37827200-37829000	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr17:37827400-37828200	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr17:37827400-37828800	Enhancers	Brain Hippocampus Middle	brain
25	chr17:37827600-37828400	Enhancers	Fetal Brain Female	brain
26	chr17:37827600-37829000	Enhancers	Fetal Brain Male	brain
27	chr17:37827600-37829000	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr17:37827600-37829200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
29	chr17:37827600-37829200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
30	chr17:37827600-37832800	Enhancers	Fetal Intestine Large	intestine
31	chr17:37827800-37828200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr17:37827800-37828400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
33	chr17:37827800-37828400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr17:37827800-37828400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr17:37827800-37828400	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr17:37827800-37828400	Enhancers	Rectal Mucosa Donor 29	rectum
37	chr17:37827800-37828600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr17:37827800-37828600	Enhancers	Brain Cingulate Gyrus	brain
39	chr17:37827800-37828600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
40	chr17:37827800-37828600	Flanking Bivalent TSS/Enh	HepG2	liver
41	chr17:37827800-37828800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr17:37827800-37828800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr17:37827800-37829200	Enhancers	Primary B cells from peripheral blood	blood
44	chr17:37827800-37829200	Enhancers	Stomach Mucosa	stomach
45	chr17:37827800-37829400	Enhancers	Esophagus	oesophagus
46	chr17:37827800-37829600	Enhancers	Placenta	Placenta
47	chr17:37827800-37837800	Genic enhancers	Fetal Intestine Small	intestine
48	chr17:37828000-37828200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr17:37828000-37828200	Bivalent Enhancer	Colonic Mucosa	Colon
50	chr17:37828000-37828200	Enhancers	Fetal Lung	lung

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