Variant report

Variant	rs4819383
Chromosome Location	chr21:45573361-45573362
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:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:45573335..45575799-chr21:45659324..45661159,2	MCF-7	breast:
2	chr21:45551834..45580791-chr21:45711953..45732193,97	MCF-7	breast:
3	chr21:45572051..45574951-chr21:45759360..45761487,2	MCF-7	breast:
4	chr21:45571920..45573873-chr21:45586886..45589109,2	MCF-7	breast:
5	chr21:45573023..45575397-chr21:45576610..45579323,3	K562	blood:
6	chr21:45572891..45575841-chr21:45596465..45598354,2	MCF-7	breast:
7	chr21:45553420..45556020-chr21:45571814..45574166,3	MCF-7	breast:
8	chr21:45571851..45574845-chr21:45716576..45719950,3	MCF-7	breast:
9	chr21:45571719..45574629-chr21:45639760..45641612,2	MCF-7	breast:
10	chr21:45571309..45577111-chr21:45620650..45624145,5	MCF-7	breast:
11	chr21:45561894..45565955-chr21:45571282..45575871,6	MCF-7	breast:
12	chr21:45558413..45560351-chr21:45571798..45574177,2	MCF-7	breast:
13	chr21:45573267..45575463-chr21:45578748..45581310,2	MCF-7	breast:
14	chr21:45573193..45575716-chr21:45715248..45717300,2	K562	blood:
15	chr21:45571301..45575033-chr21:45652281..45654701,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000141959	Chromatin interaction
ENSG00000160221	Chromatin interaction
ENSG00000160223	Chromatin interaction
ENSG00000232124	Chromatin interaction
ENSG00000225331	Chromatin interaction

Extended variants
information (count: 133 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:111)

rs_ID	r²[population]
rs1005046	0.86[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs1059813	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11089111	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11089115	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11089117	0.83[AFR][1000 genomes]
rs11700840	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11700919	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12626672	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12627239	0.95[CEU][hapmap];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13046297	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13048551	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1858665	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2006694	0.87[EUR][1000 genomes]
rs2020945	0.94[CEU][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2020946	0.95[CEU][hapmap];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2039272	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2051260	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2071135	0.88[CEU][hapmap]
rs2071142	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2071143	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2071146	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2071147	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2073432	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2073433	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2073434	0.86[ASN][1000 genomes]
rs2073435	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2187313	0.89[CEU][hapmap]
rs2238713	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2242950	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2242953	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2242954	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2243999	0.94[CEU][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2251267	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2255828	0.94[CEU][hapmap]
rs2255922	0.85[EUR][1000 genomes]
rs2255955	0.84[CEU][hapmap]
rs2276530	0.95[CEU][hapmap];0.84[EUR][1000 genomes]
rs2277805	0.84[CEU][hapmap]
rs2277806	0.94[CEU][hapmap];0.84[EUR][1000 genomes]
rs2299815	0.95[CEU][hapmap]
rs2299818	0.84[EUR][1000 genomes]
rs2329707	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2516519	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2516521	0.90[CEU][hapmap];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2776368	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2838469	0.84[CEU][hapmap]
rs2838471	0.84[EUR][1000 genomes]
rs2838473	0.95[CEU][hapmap]
rs2838478	0.80[CEU][hapmap]
rs2838482	0.95[CEU][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2838486	0.94[CEU][hapmap];0.81[EUR][1000 genomes]
rs2838488	0.95[CEU][hapmap];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2838489	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2838490	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2838491	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2838492	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2838493	0.94[CEU][hapmap];0.82[EUR][1000 genomes]
rs2838494	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2838496	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2838498	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2838499	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2838500	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2838501	0.93[AFR][1000 genomes]
rs2838502	0.94[CEU][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2838503	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28480490	0.81[ASN][1000 genomes]
rs2850150	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2850153	0.82[ASN][1000 genomes]
rs2850155	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2850156	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2850157	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28547944	0.91[AFR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2855651	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2855652	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35538274	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4818881	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4818882	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4819370	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4819372	0.84[EUR][1000 genomes]
rs4819373	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4819376	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4819377	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4819378	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4819379	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4819381	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7277269	0.94[CEU][hapmap];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7279319	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7280558	0.90[CEU][hapmap]
rs7280581	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7281270	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7281291	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7281768	0.94[CEU][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7282324	0.90[CEU][hapmap]
rs7283870	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs756553	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs756554	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs756555	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs7676	0.89[CEU][hapmap]
rs8126564	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8130647	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8132918	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs8133610	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs885872	0.89[CEU][hapmap]
rs915772	0.90[CEU][hapmap];0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs915774	0.90[CEU][hapmap];0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9306172	0.94[CEU][hapmap];0.85[EUR][1000 genomes]
rs9680179	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs968713	0.89[CEU][hapmap]
rs968714	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9977564	0.87[EUR][1000 genomes]
rs9981485	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 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	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	nsv913895	chr21:45528919-45595060	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
14	nsv913896	chr21:45528919-45603746	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats 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	31 gene(s)	inside rSNPs	diseases
15	nsv913897	chr21:45528919-45640139	Strong transcription Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
16	esv1825445	chr21:45535566-45754936	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
17	esv1817474	chr21:45540607-45773102	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription 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	65 gene(s)	inside rSNPs	diseases
18	nsv533679	chr21:45551026-45768578	Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	64 gene(s)	inside rSNPs	diseases
19	nsv913898	chr21:45555079-45941566	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS 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	74 gene(s)	inside rSNPs	diseases
20	nsv428042	chr21:45560437-45848190	Enhancers Active TSS Genic enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	61 gene(s)	inside rSNPs	diseases
21	nsv1065479	chr21:45571324-45617878	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
22	esv3362646	chr21:45573322-45573434	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs4819383	PWP2	cis	Muscle Skeletal	GTEx
rs4819383	PWP2	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45561000-45584400	Weak transcription	Aorta	Aorta
2	chr21:45561200-45574200	Weak transcription	Fetal Brain Female	brain
3	chr21:45563800-45574800	Weak transcription	NHLF	lung
4	chr21:45565400-45580600	Weak transcription	Brain Germinal Matrix	brain
5	chr21:45566400-45575000	Weak transcription	Rectal Smooth Muscle	rectum
6	chr21:45567400-45573400	Weak transcription	Brain Angular Gyrus	brain
7	chr21:45568000-45573600	Weak transcription	Brain Anterior Caudate	brain
8	chr21:45570600-45577400	Enhancers	Primary B cells from cord blood	blood
9	chr21:45570800-45573400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr21:45571000-45573400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr21:45571000-45575400	Enhancers	Primary B cells from peripheral blood	blood
12	chr21:45571000-45582600	Weak transcription	Ovary	ovary
13	chr21:45572000-45573400	Enhancers	Primary T cells fromperipheralblood	blood
14	chr21:45572200-45573400	Weak transcription	Left Ventricle	heart
15	chr21:45572200-45573600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr21:45572200-45574200	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr21:45572200-45575000	Enhancers	Primary T killer memory cells from peripheral blood	blood
18	chr21:45572400-45575000	Enhancers	Primary T cells from cord blood	blood
19	chr21:45572400-45577400	Enhancers	Fetal Thymus	thymus
20	chr21:45572800-45573400	Enhancers	Rectal Mucosa Donor 29	rectum
21	chr21:45572800-45573600	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr21:45572800-45573600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr21:45572800-45573800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr21:45572800-45574200	Flanking Active TSS	GM12878-XiMat	blood
25	chr21:45572800-45575600	Enhancers	Duodenum Smooth Muscle	Duodenum
26	chr21:45572800-45577400	Enhancers	Primary hematopoietic stem cells	blood
27	chr21:45573000-45573400	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr21:45573000-45573400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
29	chr21:45573000-45573400	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr21:45573000-45573400	Enhancers	Muscle Satellite Cultured Cells	--
31	chr21:45573000-45573400	Enhancers	Fetal Stomach	stomach
32	chr21:45573000-45573400	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr21:45573000-45573400	Enhancers	HSMMtube	muscle
34	chr21:45573000-45573600	Enhancers	H1 Cell Line	embryonic stem cell
35	chr21:45573000-45573600	Enhancers	H9 Cell Line	embryonic stem cell
36	chr21:45573000-45573600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr21:45573000-45573600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr21:45573000-45573600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
39	chr21:45573000-45573600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr21:45573000-45573600	Enhancers	Fetal Intestine Large	intestine
41	chr21:45573000-45573600	Enhancers	Placenta	Placenta
42	chr21:45573000-45573600	Enhancers	Gastric	stomach
43	chr21:45573000-45573600	Enhancers	Placenta Amnion	Placenta Amnion
44	chr21:45573000-45573800	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr21:45573000-45573800	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr21:45573000-45573800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
47	chr21:45573000-45573800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
48	chr21:45573000-45573800	Enhancers	Fetal Lung	lung
49	chr21:45573000-45573800	Flanking Active TSS	Hela-S3	cervix
50	chr21:45573000-45574000	Enhancers	Fetal Intestine Small	intestine

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