Variant report

Variant	rs13048551
Chromosome Location	chr21:45567977-45567978
allele	C/T
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:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:45567022..45569875-chr21:45667189..45669320,3	MCF-7	breast:
2	chr21:45551834..45580791-chr21:45711953..45732193,97	MCF-7	breast:
3	chr21:45566754..45568641-chr21:45735540..45737926,2	K562	blood:
4	chr21:45567927..45569479-chr21:45614833..45617390,2	K562	blood:
5	chr21:45567275..45569280-chr21:45626977..45629250,2	MCF-7	breast:
6	chr21:45564856..45569821-chr21:45659868..45664299,6	MCF-7	breast:
7	chr21:45556726..45571792-chr21:45714286..45731454,46	K562	blood:
8	chr21:45566333..45568357-chr21:45695334..45697584,2	K562	blood:
9	chr21:45567167..45569134-chr21:45587063..45589096,2	MCF-7	breast:
10	chr21:45564255..45569334-chr21:45585754..45591354,8	K562	blood:
11	chr21:45566699..45568772-chr21:45598220..45601195,2	K562	blood:
12	chr21:45567094..45569672-chr21:45625935..45627743,3	MCF-7	breast:
13	chr21:45564263..45568124-chr21:45686122..45689149,5	K562	blood:
14	chr21:45567116..45569541-chr21:45751438..45754407,2	K562	blood:
15	chr21:45565598..45568910-chr21:45683665..45687558,4	MCF-7	breast:
16	chr21:45553509..45556020-chr21:45565323..45568081,3	MCF-7	breast:
17	chr21:45557962..45571522-chr21:45714618..45733273,43	K562	blood:
18	chr21:45566230..45568537-chr21:45744712..45747553,2	K562	blood:
19	chr21:45566742..45569322-chr21:45613127..45615094,2	MCF-7	breast:
20	chr21:45565762..45568425-chr21:45616246..45618901,2	MCF-7	breast:
21	chr21:45566882..45568614-chr21:45741030..45743410,2	K562	blood:
22	chr21:45557511..45570034-chr21:45715093..45723808,43	MCF-7	breast:
23	chr21:45565601..45570300-chr21:45658772..45665940,10	MCF-7	breast:
24	chr21:45566739..45568032-chr21:45687189..45688228,8	K562	blood:

No data

Variant related genes	Relation type
ENSG00000141959	Chromatin interaction
ENSG00000160226	Chromatin interaction
ENSG00000160221	Chromatin interaction
ENSG00000232698	Chromatin interaction
ENSG00000160223	Chromatin interaction

Extended variants
information (count: 121 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:101)

rs_ID	r²[population]
rs1005046	0.83[ASN][1000 genomes]
rs1059813	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11089111	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11089115	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11700840	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11700919	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12626672	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12627239	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13046297	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1858665	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2006694	0.87[EUR][1000 genomes]
rs2020945	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2020946	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2039272	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2051260	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2071142	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2071143	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2071146	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2071147	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2073432	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2073433	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2073434	0.86[ASN][1000 genomes]
rs2073435	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2187313	0.81[EUR][1000 genomes]
rs2238713	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2242950	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2242953	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2242954	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2243999	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2251267	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2255716	0.80[AMR][1000 genomes]
rs2255922	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2276530	0.84[EUR][1000 genomes]
rs2277806	0.84[EUR][1000 genomes]
rs2299818	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2329707	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2516519	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2516521	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2776368	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2838471	0.84[EUR][1000 genomes]
rs2838482	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2838486	0.81[EUR][1000 genomes]
rs2838488	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2838489	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2838490	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2838491	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2838492	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2838493	0.82[EUR][1000 genomes]
rs2838494	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2838496	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2838498	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2838499	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2838500	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2838501	0.89[AFR][1000 genomes]
rs2838502	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2838503	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28480490	0.80[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2850150	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2850153	0.82[ASN][1000 genomes]
rs2850155	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2850156	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2850157	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28547944	0.81[AFR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2855651	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2855652	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35538274	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3788108	0.81[EUR][1000 genomes]
rs4818881	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4818882	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4819370	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4819372	0.84[EUR][1000 genomes]
rs4819373	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4819376	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4819377	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4819378	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4819379	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4819381	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4819383	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7277269	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7279319	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7280581	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7281270	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7281291	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7281768	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7283870	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs756553	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs756554	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs756555	0.89[EUR][1000 genomes]
rs7676	0.81[EUR][1000 genomes]
rs8126564	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8130647	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8132918	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs8133610	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs915772	0.80[AFR][1000 genomes];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs915774	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9306172	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9680179	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs968714	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9975978	0.80[AMR][1000 genomes]
rs9977564	0.87[EUR][1000 genomes]
rs9981485	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 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

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs13048551	PWP2	Cis_1M	lymphoblastoid	RTeQTL
rs13048551	PWP2	cis	Muscle Skeletal	GTEx

Chromatin state (count:83 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45558200-45573000	Weak transcription	NH-A	brain
2	chr21:45559600-45572800	Weak transcription	Hela-S3	cervix
3	chr21:45559600-45573000	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr21:45559600-45573000	Weak transcription	HMEC	breast
5	chr21:45560000-45568600	Enhancers	Primary hematopoietic stem cells	blood
6	chr21:45560400-45573200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr21:45560800-45568400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr21:45561000-45573000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr21:45561000-45584400	Weak transcription	Aorta	Aorta
10	chr21:45561200-45574200	Weak transcription	Fetal Brain Female	brain
11	chr21:45561400-45573000	Weak transcription	Small Intestine	intestine
12	chr21:45561600-45568200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr21:45563800-45574800	Weak transcription	NHLF	lung
14	chr21:45564400-45568400	Enhancers	Fetal Thymus	thymus
15	chr21:45564600-45568000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
16	chr21:45564600-45568600	Enhancers	Placenta	Placenta
17	chr21:45564800-45570400	Weak transcription	Psoas Muscle	Psoas
18	chr21:45565000-45568000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
19	chr21:45565000-45568400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr21:45565000-45568400	Enhancers	Colonic Mucosa	Colon
21	chr21:45565000-45573200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr21:45565200-45568000	Enhancers	Stomach Mucosa	stomach
23	chr21:45565400-45573000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr21:45565400-45580600	Weak transcription	Brain Germinal Matrix	brain
25	chr21:45565600-45568600	Enhancers	Primary B cells from cord blood	blood
26	chr21:45565600-45569600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr21:45565600-45573000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr21:45565600-45573200	Weak transcription	Colon Smooth Muscle	Colon
29	chr21:45565800-45568200	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr21:45565800-45568200	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr21:45565800-45568200	Enhancers	Primary T killer memory cells from peripheral blood	blood
32	chr21:45566000-45568200	Enhancers	Primary T cells from cord blood	blood
33	chr21:45566000-45568600	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr21:45566000-45569000	Enhancers	Primary T cells fromperipheralblood	blood
35	chr21:45566200-45568000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr21:45566200-45568000	Enhancers	Fetal Muscle Trunk	muscle
37	chr21:45566200-45568600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
38	chr21:45566400-45568400	Enhancers	Brain Hippocampus Middle	brain
39	chr21:45566400-45568600	Enhancers	Primary T helper cells fromperipheralblood	blood
40	chr21:45566400-45575000	Weak transcription	Rectal Smooth Muscle	rectum
41	chr21:45566600-45568400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr21:45566600-45568600	Enhancers	Fetal Muscle Leg	muscle
43	chr21:45566600-45568800	Enhancers	Primary B cells from peripheral blood	blood
44	chr21:45566600-45569400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr21:45566800-45568000	Enhancers	Brain Anterior Caudate	brain
46	chr21:45566800-45568200	Enhancers	Fetal Stomach	stomach
47	chr21:45566800-45568400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
48	chr21:45566800-45569400	Enhancers	GM12878-XiMat	blood
49	chr21:45567000-45568000	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr21:45567000-45568800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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