Variant report

Variant	rs1051981
Chromosome Location	chr21:45525685-45525686
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:8)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:8 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TEAD4	chr21:45525410-45525855	K562	blood:	n/a	n/a
2	EP300	chr21:45525502-45525776	K562	blood:	n/a	n/a
3	ARID3A	chr21:45525257-45526502	K562	blood:	n/a	n/a
4	TEAD4	chr21:45525405-45525886	K562	blood:	n/a	n/a
5	EP300	chr21:45525462-45525808	K562	blood:	n/a	n/a
6	POLR2A	chr21:45524792-45525688	K562	blood:	n/a	n/a
7	TAL1	chr21:45525346-45525834	K562	blood:	n/a	n/a
8	TBL1XR1	chr21:45525507-45525732	K562	blood:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr21:45430507..45434109-chr21:45525660..45529122,6	K562	blood:
2	chr21:45429712..45433999-chr21:45522896..45529122,10	K562	blood:
3	chr21:45525373..45527219-chr21:45757637..45759650,2	K562	blood:
4	chr21:45443004..45445894-chr21:45525431..45527091,3	K562	blood:
5	chr21:45430262..45433765-chr21:45524105..45528370,12	MCF-7	breast:
6	chr21:45514673..45516174-chr21:45524050..45526937,2	MCF-7	breast:
7	chr21:45443004..45445894-chr21:45525520..45527091,2	K562	blood:
8	chr21:45525043..45527455-chr21:45658553..45661169,2	K562	blood:
9	chr21:45515403..45518351-chr21:45523507..45526490,2	K562	blood:
10	chr21:45430220..45433985-chr21:45525454..45528690,3	MCF-7	breast:

No data

Variant related genes	Relation type
PWP2	TF binding region
ENSG00000160218	Chromatin interaction
ENSG00000160226	Chromatin interaction
ENSG00000232969	Chromatin interaction
ENSG00000160223	Chromatin interaction

Extended variants
information (count: 144 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:129)

rs_ID	r²[population]
rs1059813	0.84[EUR][1000 genomes]
rs11089111	0.86[EUR][1000 genomes]
rs11700919	0.86[EUR][1000 genomes]
rs12627239	0.83[CEU][hapmap];0.90[EUR][1000 genomes]
rs13047030	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13047214	0.82[ASN][1000 genomes]
rs13048791	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs17004630	0.90[CHB][hapmap];0.89[CHD][hapmap];0.85[GIH][hapmap];0.92[JPT][hapmap];0.81[ASN][1000 genomes]
rs1858665	0.87[EUR][1000 genomes]
rs2006694	0.90[CHB][hapmap];0.85[JPT][hapmap];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2020945	0.84[CEU][hapmap];0.91[TSI][hapmap];0.86[EUR][1000 genomes]
rs2020946	0.83[CEU][hapmap];0.86[EUR][1000 genomes]
rs2039272	0.90[EUR][1000 genomes]
rs2051260	0.83[EUR][1000 genomes]
rs2071135	0.93[CEU][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2071142	0.91[TSI][hapmap];0.85[EUR][1000 genomes]
rs2071143	0.94[TSI][hapmap];0.84[EUR][1000 genomes]
rs2071146	0.84[EUR][1000 genomes]
rs2071147	0.84[EUR][1000 genomes]
rs2071152	0.80[TSI][hapmap]
rs2071154	0.80[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.94[MKK][hapmap];0.84[TSI][hapmap];0.96[YRI][hapmap];0.81[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs2073432	0.83[EUR][1000 genomes]
rs2073433	0.84[EUR][1000 genomes]
rs2073435	0.85[EUR][1000 genomes]
rs2187313	0.93[ASW][hapmap];0.89[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[TSI][hapmap];0.88[YRI][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2238711	0.83[TSI][hapmap]
rs2238713	0.84[EUR][1000 genomes]
rs2242950	0.84[CEU][hapmap];0.89[EUR][1000 genomes]
rs2242951	0.92[ASN][1000 genomes]
rs2242953	0.85[EUR][1000 genomes]
rs2242954	0.81[EUR][1000 genomes]
rs2243999	0.84[CEU][hapmap];0.91[TSI][hapmap];0.86[EUR][1000 genomes]
rs2245462	0.83[TSI][hapmap]
rs2251267	0.94[TSI][hapmap];0.84[EUR][1000 genomes]
rs2255016	0.86[ASN][1000 genomes]
rs2255828	0.83[CEU][hapmap];0.88[TSI][hapmap]
rs2255922	0.84[EUR][1000 genomes]
rs2255955	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2276530	0.83[CEU][hapmap];0.83[EUR][1000 genomes]
rs2276532	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs2277805	0.93[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.91[YRI][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2277806	0.84[CEU][hapmap];0.97[TSI][hapmap];0.88[EUR][1000 genomes]
rs2299815	0.83[CEU][hapmap]
rs2299816	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.87[ASN][1000 genomes]
rs2299817	1.00[CHB][hapmap];0.96[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs2299818	0.83[EUR][1000 genomes]
rs2329707	0.87[EUR][1000 genomes]
rs2516519	0.86[EUR][1000 genomes]
rs2516521	0.87[EUR][1000 genomes]
rs2776368	0.86[EUR][1000 genomes]
rs2838464	0.90[CHB][hapmap];1.00[JPT][hapmap];0.80[TSI][hapmap]
rs2838469	0.94[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.90[TSI][hapmap];0.85[EUR][1000 genomes]
rs2838471	0.85[EUR][1000 genomes]
rs2838473	0.83[CEU][hapmap]
rs2838478	0.85[CEU][hapmap]
rs2838482	0.83[CEU][hapmap];0.84[EUR][1000 genomes]
rs2838486	0.84[CEU][hapmap];0.88[TSI][hapmap];0.81[EUR][1000 genomes]
rs2838488	0.90[EUR][1000 genomes]
rs2838489	0.84[EUR][1000 genomes]
rs2838490	0.91[TSI][hapmap];0.85[EUR][1000 genomes]
rs2838491	0.94[TSI][hapmap];0.84[EUR][1000 genomes]
rs2838492	0.84[EUR][1000 genomes]
rs2838493	0.88[CEU][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2838494	0.82[EUR][1000 genomes]
rs2838496	0.83[EUR][1000 genomes]
rs2838498	0.82[EUR][1000 genomes]
rs2838499	0.83[EUR][1000 genomes]
rs2838502	0.91[TSI][hapmap]
rs2838503	0.88[TSI][hapmap]
rs2838507	0.89[CHB][hapmap];0.83[JPT][hapmap]
rs2838508	0.93[CHD][hapmap];0.92[GIH][hapmap];0.83[JPT][hapmap];0.88[TSI][hapmap]
rs2838509	0.90[CHB][hapmap];0.93[CHD][hapmap];0.92[GIH][hapmap];0.83[JPT][hapmap];0.87[TSI][hapmap]
rs28385580	0.82[ASN][1000 genomes]
rs2850150	0.89[EUR][1000 genomes]
rs2850154	0.92[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2850155	0.86[EUR][1000 genomes]
rs2850156	0.85[EUR][1000 genomes]
rs2850157	0.85[EUR][1000 genomes]
rs2855651	0.87[EUR][1000 genomes]
rs2855652	0.85[EUR][1000 genomes]
rs2855653	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35524612	0.99[ASN][1000 genomes]
rs35538274	0.81[EUR][1000 genomes]
rs3788102	0.87[ASN][1000 genomes]
rs3788104	0.90[CHB][hapmap];0.92[JPT][hapmap];0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3788108	0.90[CHB][hapmap];0.92[JPT][hapmap];0.84[YRI][hapmap];0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4818881	0.83[EUR][1000 genomes]
rs4818886	0.90[CHB][hapmap];0.89[CHD][hapmap]
rs4819361	0.90[CHB][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap]
rs4819362	0.90[CHB][hapmap];0.91[JPT][hapmap]
rs4819370	0.87[EUR][1000 genomes]
rs4819372	0.86[EUR][1000 genomes]
rs4819373	0.86[EUR][1000 genomes]
rs4819375	0.90[CHB][hapmap];0.92[JPT][hapmap];0.81[ASN][1000 genomes]
rs4819376	0.91[TSI][hapmap];0.85[EUR][1000 genomes]
rs4819377	0.84[EUR][1000 genomes]
rs4819378	0.82[EUR][1000 genomes]
rs4819379	0.83[EUR][1000 genomes]
rs4819380	0.90[ASN][1000 genomes]
rs4819381	0.82[EUR][1000 genomes]
rs59675192	0.89[ASN][1000 genomes]
rs62226688	1.00[ASN][1000 genomes]
rs7276709	0.82[ASN][1000 genomes]
rs7277269	0.94[TSI][hapmap];0.87[EUR][1000 genomes]
rs7280558	0.88[TSI][hapmap]
rs7280581	0.84[EUR][1000 genomes]
rs7281270	0.90[EUR][1000 genomes]
rs7281768	0.82[CEU][hapmap];0.84[EUR][1000 genomes]
rs7282324	0.88[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs756553	0.85[EUR][1000 genomes]
rs756554	0.94[TSI][hapmap];0.83[EUR][1000 genomes]
rs756555	0.82[CEU][hapmap];0.85[EUR][1000 genomes]
rs7676	1.00[ASW][hapmap];0.89[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.93[TSI][hapmap];0.88[YRI][hapmap];0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8126564	0.82[EUR][1000 genomes]
rs8130647	0.87[EUR][1000 genomes]
rs8132918	0.88[EUR][1000 genomes]
rs8133610	0.87[EUR][1000 genomes]
rs885872	0.93[ASW][hapmap];0.82[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[TSI][hapmap];0.87[YRI][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs915774	0.83[TSI][hapmap]
rs9306169	0.82[ASN][1000 genomes]
rs9306171	0.83[TSI][hapmap]
rs9306172	0.84[CEU][hapmap];0.94[TSI][hapmap];0.84[EUR][1000 genomes]
rs965733	1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap]
rs9680179	0.81[EUR][1000 genomes]
rs968713	0.88[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs968714	0.94[TSI][hapmap];0.84[EUR][1000 genomes]
rs9977564	0.86[EUR][1000 genomes]
rs9981485	0.85[EUR][1000 genomes]
rs9985064	0.90[CHB][hapmap];0.83[JPT][hapmap]

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	esv33817	chr21:45169412-46031810	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	121 gene(s)	inside rSNPs	diseases
2	nsv913887	chr21:45344799-45670770	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv459293	chr21:45415913-45555079	Active TSS Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	nsv587721	chr21:45415913-45555079	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
5	nsv1064420	chr21:45460089-45814986	Enhancers Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
6	nsv544472	chr21:45460089-45814986	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
7	nsv432155	chr21:45479055-45772388	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
8	nsv913890	chr21:45482950-45603746	Genic enhancers Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
9	nsv459294	chr21:45499171-45595060	Active TSS Flanking Active TSS Strong transcription Genic enhancers Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
10	nsv587722	chr21:45499171-45595060	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
11	nsv913891	chr21:45508561-45588518	Strong transcription Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
12	nsv913892	chr21:45508561-45595060	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
13	nsv913893	chr21:45508561-45603746	Flanking Active TSS Strong transcription Genic enhancers Active TSS Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
14	nsv913894	chr21:45508561-45627976	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
15	nsv984522	chr21:45514579-45542066	Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs1051981	PWP2	cis	lymphoblastoid	seeQTL
rs1051981	PWP2	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45473000-45526600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr21:45495600-45526800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr21:45514000-45525800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr21:45514600-45526600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr21:45517400-45527600	Weak transcription	Fetal Brain Male	brain
6	chr21:45518600-45526600	Weak transcription	Fetal Kidney	kidney
7	chr21:45518800-45526400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr21:45519400-45526200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr21:45519400-45526200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr21:45520200-45527600	Weak transcription	Fetal Heart	heart
11	chr21:45520400-45526600	Weak transcription	HUVEC	blood vessel
12	chr21:45522400-45526800	Weak transcription	NH-A	brain
13	chr21:45522600-45526800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr21:45523000-45526800	Weak transcription	Stomach Mucosa	stomach
15	chr21:45523400-45526600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr21:45523400-45526600	Weak transcription	HMEC	breast
17	chr21:45523600-45526400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr21:45523600-45526400	Weak transcription	A549	lung
19	chr21:45523600-45526600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr21:45523600-45526600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr21:45523600-45526800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr21:45523800-45526400	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr21:45523800-45526400	Weak transcription	Brain Anterior Caudate	brain
24	chr21:45523800-45526400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr21:45523800-45526600	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr21:45523800-45526600	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr21:45523800-45526600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr21:45523800-45526600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr21:45523800-45526600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr21:45523800-45526600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr21:45523800-45526600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr21:45523800-45526600	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr21:45523800-45526600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr21:45523800-45526600	Weak transcription	Fetal Lung	lung
35	chr21:45523800-45526600	Weak transcription	Ovary	ovary
36	chr21:45523800-45526600	Weak transcription	HepG2	liver
37	chr21:45523800-45526600	Weak transcription	NHEK	skin
38	chr21:45523800-45526600	Weak transcription	NHLF	lung
39	chr21:45523800-45526800	Weak transcription	Aorta	Aorta
40	chr21:45523800-45526800	Weak transcription	Esophagus	oesophagus
41	chr21:45524000-45526000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
42	chr21:45524000-45526400	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr21:45524000-45526400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr21:45524000-45526600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr21:45524000-45526600	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr21:45524000-45526600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr21:45524000-45526600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr21:45524000-45526600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr21:45524000-45526600	Weak transcription	Brain Angular Gyrus	brain
50	chr21:45524000-45526600	Weak transcription	Brain Cingulate Gyrus	brain

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