Variant report

Variant	rs162378
Chromosome Location	chr21:44925905-44925906
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:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:44922907..44925146-chr21:44925882..44927883,3	K562	blood:
2	chr21:44925704..44927836-chr21:44928810..44931005,2	K562	blood:
3	chr21:44920414..44926751-chr21:45027970..45034874,9	MCF-7	breast:
4	chr21:44826611..44829527-chr21:44923973..44926200,2	MCF-7	breast:
5	chr21:44839515..44855046-chr21:44918803..44938582,70	MCF-7	breast:
6	chr21:44924498..44927329-chr21:45064955..45067005,2	MCF-7	breast:
7	chr21:44903235..44910338-chr21:44918042..44927375,22	MCF-7	breast:
8	chr21:44924283..44926867-chr21:45004236..45006835,2	MCF-7	breast:
9	chr21:44923746..44926037-chr21:44940122..44942028,2	K562	blood:
10	chr21:44766255..44769691-chr21:44923906..44926026,3	MCF-7	breast:
11	chr21:44846010..44848472-chr21:44925465..44927292,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000142178	Chromatin interaction

Extended variants
information (count: 156 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:137)

rs_ID	r²[population]
rs1003280	1.00[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs1073522	1.00[CHB][hapmap];0.94[JPT][hapmap];0.92[ASN][1000 genomes]
rs1122873	1.00[CHB][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs11701518	0.87[CHB][hapmap];0.83[YRI][hapmap]
rs11909064	0.80[JPT][hapmap]
rs12626757	0.91[ASN][1000 genomes]
rs12627667	1.00[CHB][hapmap];0.93[JPT][hapmap]
rs1378079	1.00[CHB][hapmap];1.00[CHD][hapmap];0.82[JPT][hapmap];0.92[ASN][1000 genomes]
rs1378080	1.00[CHB][hapmap];0.94[JPT][hapmap];0.92[ASN][1000 genomes]
rs141521	1.00[CHB][hapmap];0.96[CHD][hapmap];0.94[JPT][hapmap];0.80[MEX][hapmap];0.94[ASN][1000 genomes]
rs1454648	1.00[CHB][hapmap];0.94[JPT][hapmap];0.80[ASN][1000 genomes]
rs1454650	1.00[CHB][hapmap];0.96[CHD][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs1454651	1.00[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs1584917	1.00[CHB][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs1584918	1.00[CHB][hapmap];0.93[JPT][hapmap];0.90[ASN][1000 genomes]
rs1598206	1.00[CHB][hapmap];0.96[CHD][hapmap];0.94[JPT][hapmap];0.80[MEX][hapmap];0.80[ASN][1000 genomes]
rs162343	0.86[CHB][hapmap];0.93[JPT][hapmap];0.87[ASN][1000 genomes]
rs162344	1.00[CHB][hapmap];0.96[CHD][hapmap];0.93[JPT][hapmap];0.80[MEX][hapmap];0.95[ASN][1000 genomes]
rs162345	1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.84[MKK][hapmap];0.95[ASN][1000 genomes]
rs162366	1.00[CHB][hapmap];0.96[CHD][hapmap];0.93[JPT][hapmap];0.96[ASN][1000 genomes]
rs162367	0.88[ASW][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];0.87[JPT][hapmap];0.85[LWK][hapmap];0.80[MEX][hapmap];0.86[YRI][hapmap];0.92[ASN][1000 genomes]
rs162368	0.96[ASN][1000 genomes]
rs162369	0.97[ASN][1000 genomes]
rs162371	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs162372	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs162373	0.87[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs162374	0.99[ASN][1000 genomes]
rs162375	1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs162376	1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs162377	0.92[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.82[TSI][hapmap];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs162380	0.86[CHB][hapmap];0.93[JPT][hapmap];0.95[ASN][1000 genomes]
rs162381	0.86[CHB][hapmap];0.93[JPT][hapmap];0.93[YRI][hapmap];0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs162388	1.00[CHB][hapmap];0.93[JPT][hapmap];0.83[YRI][hapmap];0.93[ASN][1000 genomes]
rs162389	0.96[ASN][1000 genomes]
rs162390	0.86[CHB][hapmap];0.87[JPT][hapmap];0.90[ASN][1000 genomes]
rs162391	0.94[ASN][1000 genomes]
rs162393	0.92[ASN][1000 genomes]
rs162394	0.95[ASN][1000 genomes]
rs162395	0.92[ASN][1000 genomes]
rs162396	0.92[ASN][1000 genomes]
rs162398	0.83[ASW][hapmap];0.86[CHB][hapmap];0.96[CHD][hapmap];0.93[JPT][hapmap];0.80[MEX][hapmap];0.84[MKK][hapmap];0.92[ASN][1000 genomes]
rs162399	0.86[CHB][hapmap];0.93[JPT][hapmap];0.92[ASN][1000 genomes]
rs162400	0.86[CHB][hapmap];0.96[CHD][hapmap];0.93[JPT][hapmap];0.92[ASN][1000 genomes]
rs162402	0.94[ASN][1000 genomes]
rs162403	0.94[ASN][1000 genomes]
rs162404	0.94[ASN][1000 genomes]
rs167930	0.95[ASN][1000 genomes]
rs1836856	0.87[CHB][hapmap];0.83[YRI][hapmap]
rs189094	0.97[ASN][1000 genomes]
rs2155722	0.80[JPT][hapmap]
rs2236666	0.80[JPT][hapmap]
rs2246602	1.00[CHB][hapmap];0.96[CHD][hapmap];0.94[JPT][hapmap];0.80[ASN][1000 genomes]
rs2250773	0.80[JPT][hapmap]
rs2251253	0.80[JPT][hapmap]
rs229340	0.80[ASN][1000 genomes]
rs229341	0.83[CHD][hapmap]
rs229357	1.00[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs2298561	0.80[JPT][hapmap]
rs230640	0.86[CHB][hapmap];0.93[JPT][hapmap];0.96[ASN][1000 genomes]
rs230642	0.86[CHB][hapmap];0.96[CHD][hapmap];0.93[JPT][hapmap];0.96[ASN][1000 genomes]
rs230643	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs230644	0.91[ASN][1000 genomes]
rs230645	0.86[CHB][hapmap];0.93[JPT][hapmap];0.86[YRI][hapmap];0.85[ASN][1000 genomes]
rs230646	0.86[CHB][hapmap];0.93[JPT][hapmap];0.80[MEX][hapmap];0.96[ASN][1000 genomes]
rs230647	0.96[ASN][1000 genomes]
rs2329442	1.00[CHB][hapmap];0.96[CHD][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs2838316	1.00[CHB][hapmap];0.96[CHD][hapmap];0.93[JPT][hapmap];0.91[ASN][1000 genomes]
rs2838317	1.00[CHB][hapmap];0.94[JPT][hapmap];0.83[YRI][hapmap];0.91[ASN][1000 genomes]
rs2838318	0.81[CHB][hapmap]
rs2838319	1.00[CHB][hapmap];0.94[JPT][hapmap];0.83[YRI][hapmap];0.91[ASN][1000 genomes]
rs2838320	0.86[CHB][hapmap]
rs2838321	1.00[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs2838322	0.91[ASN][1000 genomes]
rs2838323	1.00[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs2838324	1.00[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs2838325	0.81[CHB][hapmap]
rs2838326	0.81[CHB][hapmap]
rs2838328	1.00[CHB][hapmap];0.94[JPT][hapmap];0.92[ASN][1000 genomes]
rs2838329	0.92[ASN][1000 genomes]
rs2838330	1.00[CHB][hapmap];0.94[JPT][hapmap];0.92[ASN][1000 genomes]
rs2838331	1.00[CHB][hapmap];0.96[CHD][hapmap];0.94[JPT][hapmap];0.92[ASN][1000 genomes]
rs2838336	1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[JPT][hapmap];0.80[MEX][hapmap]
rs2838337	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs2838338	1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[JPT][hapmap]
rs2838339	1.00[CHB][hapmap];0.96[CHD][hapmap];0.88[JPT][hapmap]
rs2838340	0.81[CHB][hapmap]
rs2838341	1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[JPT][hapmap];0.80[MEX][hapmap]
rs2838343	1.00[CHB][hapmap];0.87[JPT][hapmap]
rs2838344	0.80[JPT][hapmap]
rs2838348	0.80[JPT][hapmap]
rs2838350	0.80[JPT][hapmap]
rs2838351	0.80[JPT][hapmap]
rs28840140	0.90[ASN][1000 genomes]
rs3788062	1.00[CHB][hapmap];0.94[JPT][hapmap];0.80[YRI][hapmap];0.91[ASN][1000 genomes]
rs3819161	0.80[JPT][hapmap]
rs389278	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs463738	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4818833	0.85[ASN][1000 genomes]
rs4818843	0.91[ASN][1000 genomes]
rs4818850	1.00[CHB][hapmap];0.94[JPT][hapmap];0.92[ASN][1000 genomes]
rs4818856	0.90[ASN][1000 genomes]
rs4818858	0.80[JPT][hapmap]
rs4819212	0.87[CHB][hapmap]
rs4819219	0.87[CHB][hapmap]
rs4819264	0.90[ASN][1000 genomes]
rs4819270	1.00[CHB][hapmap];0.94[JPT][hapmap];0.92[ASN][1000 genomes]
rs4997353	0.85[ASN][1000 genomes]
rs6518301	1.00[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs6518302	1.00[CHB][hapmap];0.96[CHD][hapmap];0.94[JPT][hapmap];0.92[ASN][1000 genomes]
rs6518309	1.00[CHB][hapmap];0.93[JPT][hapmap];0.90[ASN][1000 genomes]
rs6518310	0.80[JPT][hapmap]
rs7275705	0.80[ASN][1000 genomes]
rs7276215	1.00[CHB][hapmap];0.94[JPT][hapmap];0.89[ASN][1000 genomes]
rs7276316	0.85[ASN][1000 genomes]
rs7276633	1.00[CHB][hapmap];0.96[CHD][hapmap];0.88[JPT][hapmap]
rs7277539	0.86[CHB][hapmap];0.96[CHD][hapmap];0.93[JPT][hapmap];0.80[ASN][1000 genomes]
rs7279958	1.00[CHB][hapmap];0.94[JPT][hapmap];0.92[ASN][1000 genomes]
rs7279959	0.86[CHB][hapmap]
rs7279968	1.00[CHB][hapmap];0.88[JPT][hapmap]
rs7282122	0.80[JPT][hapmap]
rs7282933	0.90[ASN][1000 genomes]
rs7283362	0.82[ASW][hapmap];0.87[CHB][hapmap];0.81[CHD][hapmap];0.83[YRI][hapmap]
rs762400	0.80[JPT][hapmap]
rs8131005	0.81[CHB][hapmap]
rs8131020	0.87[CHB][hapmap];0.80[CHD][hapmap];0.83[YRI][hapmap]
rs8133523	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs86138	0.97[ASN][1000 genomes]
rs86139	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs91424	1.00[CEU][hapmap];0.86[CHB][hapmap];0.93[JPT][hapmap];0.93[YRI][hapmap];0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9306159	1.00[CHB][hapmap];0.88[JPT][hapmap];0.80[ASN][1000 genomes]
rs9976441	1.00[CHB][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs9978811	1.00[CHB][hapmap];0.94[JPT][hapmap];0.82[YRI][hapmap];0.91[ASN][1000 genomes]
rs9980185	0.93[CHB][hapmap];0.96[CHD][hapmap];0.94[JPT][hapmap];0.80[ASN][1000 genomes]
rs9981291	1.00[CHB][hapmap];0.96[CHD][hapmap];0.94[JPT][hapmap];0.92[ASN][1000 genomes]
rs9981790	1.00[CHB][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs9983763	1.00[CHB][hapmap];0.96[CHD][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs9984002	0.89[CHD][hapmap];0.94[JPT][hapmap];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv913831	chr21:44563995-44931821	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
2	nsv1057726	chr21:44711850-44957303	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
3	nsv544466	chr21:44711850-44957303	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
4	nsv913838	chr21:44740134-44931821	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
5	nsv913839	chr21:44750200-44931821	Strong transcription Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
6	nsv913847	chr21:44792003-44931821	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
7	nsv913868	chr21:44835508-44954522	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
8	esv1839560	chr21:44864079-44973184	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	56 gene(s)	inside rSNPs	diseases
9	nsv913873	chr21:44879869-45142427	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
10	nsv587689	chr21:44884252-44986050	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
11	nsv1061369	chr21:44886596-44931388	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
12	nsv544468	chr21:44886596-44931388	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
13	nsv1059264	chr21:44895863-44944515	Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
14	nsv1061539	chr21:44915533-45041824	Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
15	nsv1067171	chr21:44921187-45039471	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
16	nsv521700	chr21:44925334-45041790	Enhancers Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
17	nsv470903	chr21:44925334-45061501	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
18	nsv459289	chr21:44925334-45064600	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
19	nsv587690	chr21:44925334-45064600	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs162378	HSF2BP	cis	lymphoblastoid	seeQTL
rs162378	DNMT3L	cis	cerebellum	SCAN
rs162378	HSF2BP	cis	Lymphoblastoid	GTEx
rs162378	PCP4	cis	cerebellum	SCAN
rs162378	NCRNA00175	cis	parietal	SCAN
rs162378	COL18A1	cis	cerebellum	SCAN
rs162378	HSF2BP	cis	multi-tissue	Pritchard

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:44918800-44930200	Weak transcription	Fetal Kidney	kidney
2	chr21:44919800-44936800	Weak transcription	Fetal Brain Female	brain
3	chr21:44921800-44926400	Enhancers	Left Ventricle	heart
4	chr21:44922800-44926800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr21:44922800-44936000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr21:44923200-44926400	Weak transcription	Fetal Lung	lung
7	chr21:44923400-44926000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr21:44923400-44926000	Weak transcription	Fetal Stomach	stomach
9	chr21:44923400-44926200	Weak transcription	Ovary	ovary
10	chr21:44923400-44926400	Weak transcription	Esophagus	oesophagus
11	chr21:44923400-44926400	Weak transcription	NHEK	skin
12	chr21:44923400-44926600	Weak transcription	Psoas Muscle	Psoas
13	chr21:44923400-44929000	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr21:44923400-44934000	Weak transcription	Gastric	stomach
15	chr21:44923400-44936600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr21:44923400-44936600	Weak transcription	Brain Germinal Matrix	brain
17	chr21:44923600-44926400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr21:44924000-44926000	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr21:44924000-44926200	Weak transcription	HepG2	liver
20	chr21:44924000-44926400	Weak transcription	Pancreas	Pancrea
21	chr21:44924000-44926600	Weak transcription	Duodenum Mucosa	Duodenum
22	chr21:44924000-44926600	Weak transcription	Fetal Intestine Large	intestine
23	chr21:44924000-44926600	Weak transcription	Fetal Intestine Small	intestine
24	chr21:44924000-44927200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr21:44924000-44927600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr21:44924000-44930200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr21:44924200-44926200	Weak transcription	Placenta	Placenta
28	chr21:44924200-44929800	Weak transcription	HMEC	breast
29	chr21:44924400-44926400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr21:44924400-44926600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr21:44924400-44927600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr21:44924400-44929200	Weak transcription	A549	lung
33	chr21:44924800-44926200	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr21:44925200-44926200	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr21:44925400-44926200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr21:44925400-44926200	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr21:44925400-44930000	Weak transcription	Right Atrium	heart
38	chr21:44925600-44926000	Weak transcription	Right Ventricle	heart
39	chr21:44925600-44928200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr21:44925800-44926800	Enhancers	HSMM	muscle
41	chr21:44925800-44927600	Enhancers	HSMMtube	muscle

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