Variant report

Variant	rs3751742
Chromosome Location	chr16:31719727-31719728
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:21)
CpG islands
(count:0)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:21 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr16:31719245-31721035	HepG2	liver:	n/a	n/a
2	POLR2A	chr16:31719151-31720075	GM12878	blood:	n/a	n/a
3	POLR2A	chr16:31719397-31720901	HepG2	liver:	n/a	n/a
4	POLR2A	chr16:31719685-31719919	HepG2	liver:	n/a	n/a
5	ZNF263	chr16:31719661-31719992	HEK293-T-REx	kidney:	n/a	n/a
6	POLR2A	chr16:31718748-31725396	HepG2	liver:	n/a	n/a
7	POLR2A	chr16:31719083-31719974	HepG2	liver:	n/a	n/a
8	POLR2A	chr16:31719083-31720227	GM12878	blood:	n/a	n/a
9	POLR2A	chr16:31718969-31720098	HepG2	liver:	n/a	n/a
10	POLR2A	chr16:31719678-31719929	K562	blood:	n/a	n/a
11	POLR2A	chr16:31719575-31720542	K562	blood:	n/a	n/a
12	POLR2A	chr16:31719634-31720403	GM12892	blood:	n/a	n/a
13	POLR2A	chr16:31718943-31727784	HepG2	liver:	n/a	n/a
14	POLR2A	chr16:31719438-31720734	GM12878	blood:	n/a	n/a
15	POLR2A	chr16:31719646-31720282	K562	blood:	n/a	n/a
16	POLR2A	chr16:31715130-31726933	HepG2	liver:	n/a	n/a
17	POLR2A	chr16:31719716-31720003	H1-neurons	neurons:	n/a	n/a
18	POLR2A	chr16:31719617-31719945	GM12891	blood:	n/a	n/a
19	POLR2A	chr16:31719335-31720370	GM12891	blood:	n/a	n/a
20	POLR2A	chr16:31718974-31728173	GM12878	blood:	n/a	n/a
21	POLR2A	chr16:31719083-31720878	GM12892	blood:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr16:31469625..31472736-chr16:31718738..31721377,3	K562	blood:
2	chr16:31518291..31520186-chr16:31719579..31721600,2	MCF-7	breast:
3	chr16:31469625..31472005-chr16:31718738..31721377,2	K562	blood:

No data

Variant related genes	Relation type
ZNF720	TF binding region
ENSG00000140688	Chromatin interaction
ENSG00000260267	Chromatin interaction
ENSG00000140691	Chromatin interaction
ENSG00000260625	Chromatin interaction

Extended variants
information (count: 99 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:87)

rs_ID	r²[population]
rs1045483	1.00[CEU][hapmap];0.82[JPT][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1073513	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1104549	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1104550	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11150632	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11150639	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11642525	1.00[CEU][hapmap];0.81[JPT][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11643629	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11862133	0.82[LWK][hapmap]
rs11862739	0.82[LWK][hapmap]
rs12325485	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12386038	0.95[CEU][hapmap];0.81[JPT][hapmap];0.82[EUR][1000 genomes]
rs12921028	1.00[CEU][hapmap];0.82[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12932938	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1304163	1.00[CEU][hapmap];0.82[JPT][hapmap];0.87[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1358485	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1406177	0.82[CEU][hapmap];0.96[MEX][hapmap];0.94[TSI][hapmap]
rs1406178	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]
rs1468158	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];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1468159	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];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1528317	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1534506	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1599855	1.00[CEU][hapmap];0.82[JPT][hapmap];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1609289	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17839526	0.82[LWK][hapmap]
rs1852667	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1881316	0.82[CEU][hapmap];0.96[MEX][hapmap];0.94[TSI][hapmap]
rs1881317	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1881318	1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.97[TSI][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1919039	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2008774	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2078923	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2091521	1.00[CEU][hapmap];0.90[CHB][hapmap];0.91[JPT][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2097683	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2106580	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2141349	0.95[CEU][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2157969	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2188620	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2214139	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2359220	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2359223	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2359228	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2359231	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2359234	0.82[LWK][hapmap]
rs2359455	0.84[MEX][hapmap]
rs2884713	0.84[MEX][hapmap]
rs3088127	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34632985	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3751738	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3937426	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4297693	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4499253	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4572414	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4632148	1.00[CEU][hapmap];0.82[JPT][hapmap];0.87[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4889679	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4889680	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4889687	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6565266	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6565270	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6565271	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6565277	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6565284	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7187074	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7187594	0.82[LWK][hapmap]
rs7188748	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7192274	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7192670	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7192946	0.82[LWK][hapmap]
rs7195700	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7197470	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7197963	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];0.87[YRI][hapmap];0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7198038	1.00[CEU][hapmap];0.82[JPT][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7359491	1.00[CEU][hapmap];0.82[JPT][hapmap];0.87[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7498390	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8043927	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs8048027	0.90[EUR][1000 genomes]
rs8048591	0.84[MEX][hapmap]
rs8048741	1.00[CEU][hapmap];0.82[JPT][hapmap];0.87[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs8052434	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs8054649	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs8062902	0.84[MEX][hapmap]
rs929208	0.84[MEX][hapmap]
rs929209	1.00[CEU][hapmap];0.82[JPT][hapmap];0.87[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9928595	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9929259	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9938037	0.84[MEX][hapmap]
rs9939255	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]

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	nsv905747	chr16:31394179-31888684	Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	123 gene(s)	inside rSNPs	diseases
2	esv3344221	chr16:31526786-31821640	Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
3	esv3323903	chr16:31526802-31821640	Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
4	esv3504445	chr16:31526873-31821580	Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
5	esv3504446	chr16:31526873-31821580	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
6	esv3366795	chr16:31534951-31827424	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
7	nsv833195	chr16:31576112-31763222	ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
8	nsv1057598	chr16:31608831-31726446	Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
9	nsv1067321	chr16:31652036-31959992	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
10	nsv918074	chr16:31669781-31935033	ZNF genes & repeats Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
11	nsv1063037	chr16:31669981-31934894	Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
12	nsv542903	chr16:31669981-31934894	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs3751742	ATP2A1	cis	cerebellum	SCAN
rs3751742	ZNF720	cis	parietal	SCAN

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31712600-31724200	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr16:31712600-31724200	Weak transcription	Psoas Muscle	Psoas
3	chr16:31712600-31724200	Weak transcription	HSMM	muscle
4	chr16:31712800-31724200	Weak transcription	HSMMtube	muscle
5	chr16:31712800-31724200	Weak transcription	NHDF-Ad	bronchial
6	chr16:31712800-31724400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr16:31712800-31724600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr16:31713000-31724400	Weak transcription	Right Atrium	heart
9	chr16:31713200-31724000	Weak transcription	Fetal Heart	heart
10	chr16:31713200-31724200	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr16:31713400-31720000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr16:31713400-31720800	Strong transcription	Cortex derived primary cultured neurospheres	brain
13	chr16:31713400-31722400	Strong transcription	Fetal Intestine Small	intestine
14	chr16:31713400-31724000	Weak transcription	K562	blood
15	chr16:31713400-31724200	Weak transcription	Fetal Brain Male	brain
16	chr16:31713600-31720800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr16:31713600-31722200	Strong transcription	Stomach Smooth Muscle	stomach
18	chr16:31713800-31720000	Strong transcription	Brain Inferior Temporal Lobe	brain
19	chr16:31713800-31720000	Strong transcription	Colonic Mucosa	Colon
20	chr16:31713800-31720400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr16:31713800-31720800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr16:31713800-31721400	Strong transcription	HUES6 Cell Line	embryonic stem cell
23	chr16:31713800-31721400	Strong transcription	Fetal Muscle Trunk	muscle
24	chr16:31713800-31721600	Strong transcription	Primary B cells from peripheral blood	blood
25	chr16:31713800-31721800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr16:31713800-31722200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr16:31713800-31722600	Strong transcription	Fetal Stomach	stomach
28	chr16:31714000-31720400	Strong transcription	H1 Cell Line	embryonic stem cell
29	chr16:31714000-31720400	Strong transcription	Rectal Smooth Muscle	rectum
30	chr16:31714000-31720400	Strong transcription	NHEK	skin
31	chr16:31714000-31720600	Strong transcription	HUES64 Cell Line	embryonic stem cell
32	chr16:31714000-31720600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr16:31714000-31720600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr16:31714000-31720800	Strong transcription	H9 Cell Line	embryonic stem cell
35	chr16:31714000-31720800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr16:31714000-31720800	Strong transcription	Brain Anterior Caudate	brain
37	chr16:31714000-31720800	Strong transcription	Skeletal Muscle Male	skeletal muscle
38	chr16:31714000-31721400	Strong transcription	Fetal Muscle Leg	muscle
39	chr16:31714000-31721800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr16:31714000-31722800	Strong transcription	Fetal Brain Female	brain
41	chr16:31714200-31719800	Strong transcription	A549	lung
42	chr16:31714200-31720000	Strong transcription	Adipose Nuclei	Adipose
43	chr16:31714200-31720000	Strong transcription	Ovary	ovary
44	chr16:31714200-31720200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr16:31714200-31720400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
46	chr16:31714200-31720400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr16:31714200-31720600	Strong transcription	Rectal Mucosa Donor 31	rectum
48	chr16:31714200-31721000	Strong transcription	Rectal Mucosa Donor 29	rectum
49	chr16:31714200-31721400	Strong transcription	Gastric	stomach
50	chr16:31714200-31721600	Strong transcription	Duodenum Mucosa	Duodenum

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