Variant report

Variant	rs4818743
Chromosome Location	chr21:46360297-46360298
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAX	chr21:46359047-46360590	K562	blood:	n/a	chr21:46360118-46360128
2	MAX	chr21:46359325-46360554	HepG2	liver:	n/a	chr21:46360118-46360128
3	POLR2A	chr21:46359340-46360607	H1-hESC	embryonic stem cell:	n/a	n/a
4	POLR2A	chr21:46359562-46360500	Hela-S3	cervix:	n/a	n/a
5	MAZ	chr21:46359456-46360528	K562	blood:	n/a	chr21:46360118-46360128
6	POLR2A	chr21:46358524-46360361	GM18505	blood:	n/a	n/a
7	CHD1	chr21:46359328-46361037	IMR90	lung:	n/a	n/a
8	POLR2A	chr21:46359477-46360455	H1-neurons	neurons:	n/a	n/a
9	GABPA	chr21:46359520-46360408	H1-hESC	embryonic stem cell:	n/a	chr21:46359828-46359842
10	ZBTB7A	chr21:46359583-46360334	ECC-1	luminal epithelium:	n/a	n/a
11	TBP	chr21:46359556-46360341	K562	blood:	n/a	n/a
12	SIN3AK20	chr21:46359520-46360568	K562	blood:	n/a	n/a
13	MXI1	chr21:46358871-46361050	SK-N-SH	brain:	n/a	n/a
14	MYC	chr21:46359525-46360691	K562	blood:	n/a	chr21:46360118-46360128
15	GABPA	chr21:46359434-46360347	GM12878	blood:	n/a	chr21:46359828-46359842
16	GABPA	chr21:46360089-46360387	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr21:46359474-46360363	GM12878	blood:	n/a	n/a
18	POLR2A	chr21:46360157-46360451	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr21:46358166-46360480	SK-N-MC	brain:	n/a	n/a
20	JUN	chr21:46358206-46361110	K562	blood:	n/a	chr21:46358894-46358905
21	HEY1	chr21:46359472-46360599	K562	blood:	n/a	chr21:46359746-46359761 chr21:46359861-46359876
22	MXI1	chr21:46359622-46360382	GM12878	blood:	n/a	n/a
23	POLR2A	chr21:46359456-46360355	H1-hESC	embryonic stem cell:	n/a	n/a
24	GABPA	chr21:46359338-46360563	MCF-7	breast:	n/a	chr21:46359828-46359842
25	TAF1	chr21:46359379-46360399	H1-hESC	embryonic stem cell:	n/a	n/a
26	SMARCB1	chr21:46359494-46360532	Hela-S3	cervix:	n/a	n/a
27	MAX	chr21:46359188-46360520	K562	blood:	n/a	chr21:46360118-46360128
28	MAX	chr21:46359638-46360586	NB4	blood:	n/a	chr21:46360118-46360128
29	POLR2A	chr21:46358504-46360381	GM12878	blood:	n/a	n/a
30	ZNF263	chr21:46359023-46360700	HEK293-T-REx	kidney:	n/a	n/a
31	CREB1	chr21:46359612-46360381	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr21:46359394-46360527	GM12892	blood:	n/a	n/a
33	SMC3	chr21:46360207-46360405	K562	blood:	n/a	n/a
34	GABPA	chr21:46359643-46360374	HepG2	liver:	n/a	chr21:46359828-46359842
35	UBTF	chr21:46359548-46360455	K562	blood:	n/a	n/a
36	MAX	chr21:46359318-46360394	H1-hESC	embryonic stem cell:	n/a	chr21:46360118-46360128
37	MYC	chr21:46359272-46360588	K562	blood:	n/a	chr21:46360118-46360128
38	MAX	chr21:46359537-46360510	Hela-S3	cervix:	n/a	chr21:46360118-46360128
39	ELF1	chr21:46359691-46360440	K562	blood:	n/a	chr21:46359846-46359857 chr21:46359861-46359873 chr21:46359847-46359856 chr21:46360168-46360177 chr21:46359846-46359855 chr21:46359846-46359857 chr21:46359845-46359858 chr21:46360115-46360127 chr21:46359928-46359937
40	POLR2A	chr21:46359261-46360302	PFSK-1	brain:	n/a	n/a
41	E2F6	chr21:46359104-46360366	K562	blood:	n/a	chr21:46360122-46360132 chr21:46359882-46359892
42	CCNT2	chr21:46359520-46360344	K562	blood:	n/a	n/a
43	MXI1	chr21:46359607-46360475	K562	blood:	n/a	n/a
44	MAX	chr21:46359279-46360463	HepG2	liver:	n/a	chr21:46360118-46360128
45	MAZ	chr21:46359485-46360568	IMR90	lung:	n/a	chr21:46360118-46360128
46	IRF1	chr21:46359588-46360715	K562	blood:	n/a	n/a
47	MYC	chr21:46359389-46360610	K562	blood:	n/a	chr21:46360118-46360128
48	POLR2A	chr21:46359519-46360432	K562	blood:	n/a	n/a
49	POLR2A	chr21:46359523-46360508	HL-60	blood:	n/a	n/a
50	MAX	chr21:46359385-46360440	K562	blood:	n/a	chr21:46360118-46360128

No.	Distal block	Cell Line	Cell type
1	chr21:46348854..46378176-chr21:46489799..46500436,75	K562	blood:
2	chr21:46359964..46363434-chr21:46389610..46392494,4	K562	blood:
3	chr21:46293553..46294470-chr21:46359794..46360468,2	Hela-S3	cervix:
4	chr21:46235785..46239443-chr21:46357143..46362674,8	MCF-7	breast:
5	chr21:46291916..46297365-chr21:46358001..46363812,14	MCF-7	breast:
6	chr21:46358715..46360802-chr21:46377914..46380232,3	K562	blood:
7	chr21:46358799..46362946-chr21:46546409..46551680,5	K562	blood:
8	chr21:46153888..46156616-chr21:46360093..46361664,2	MCF-7	breast:
9	chr21:46353923..46356909-chr21:46357554..46361249,6	K562	blood:
10	chr21:46236285..46239693-chr21:46357237..46360614,5	K562	blood:
11	chr21:46355061..46362857-chr21:46490375..46496482,13	K562	blood:
12	chr21:46236918..46239386-chr21:46357793..46361272,3	K562	blood:
13	chr21:46357121..46360685-chr21:46377277..46380905,4	MCF-7	breast:
14	chr21:46218606..46224662-chr21:46357422..46363606,13	MCF-7	breast:
15	chr21:46220260..46222802-chr21:46358731..46365262,8	MCF-7	breast:

Variant related genes	Relation type
C21orf67	TF binding region
ENSG00000183255	Chromatin interaction
ENSG00000236519	Chromatin interaction
ENSG00000160256	Chromatin interaction
ENSG00000272825	Chromatin interaction
ENSG00000184900	Chromatin interaction
ENSG00000268856	Chromatin interaction
ENSG00000184787	Chromatin interaction
ENSG00000197381	Chromatin interaction
ENSG00000235374	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11701378	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11701457	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11702593	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1985483	0.92[CEU][hapmap];1.00[CHB][hapmap];0.90[GIH][hapmap];0.92[JPT][hapmap];1.00[MEX][hapmap];0.82[TSI][hapmap]
rs2005951	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2012438	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.83[JPT][hapmap];0.93[MEX][hapmap];0.91[TSI][hapmap]
rs2294166	0.95[ASN][1000 genomes]
rs2294168	0.82[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs2294170	0.88[ASN][1000 genomes]
rs2838742	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2838743	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2838745	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.95[TSI][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2838751	0.83[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap];0.92[MEX][hapmap]
rs28399723	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28461900	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4143368	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4818748	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];0.92[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4818749	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4818990	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4818993	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55716911	0.87[ASN][1000 genomes]
rs55859454	0.82[ASN][1000 genomes]
rs56213773	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62214491	0.85[ASN][1000 genomes]
rs62214513	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs914205	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916258	chr21:45995986-46624705	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	102 gene(s)	inside rSNPs	diseases
2	nsv1056513	chr21:46254075-46442759	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv913969	chr21:46279505-46472929	Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv913970	chr21:46305175-46487831	Bivalent Enhancer Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	nsv933240	chr21:46305956-46371518	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
6	nsv913974	chr21:46306161-46430792	Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
7	nsv913975	chr21:46306161-46459432	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
8	nsv913976	chr21:46306161-46487831	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
9	nsv834110	chr21:46316183-46505151	Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
10	nsv1064518	chr21:46317690-46413159	Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
11	nsv913977	chr21:46335761-46454391	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
12	nsv913978	chr21:46335761-46466674	Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
13	nsv913979	chr21:46335761-46472929	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
14	nsv913980	chr21:46337565-46454391	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
15	nsv913981	chr21:46344426-46408790	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
16	nsv913982	chr21:46344426-46430792	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
17	nsv913984	chr21:46344426-46435610	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
18	nsv913983	chr21:46344426-46440385	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
19	nsv913985	chr21:46344426-46448142	Weak transcription Genic enhancers Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
20	nsv913986	chr21:46344426-46466674	Strong transcription Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
21	nsv913987	chr21:46344426-46472929	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
22	nsv913988	chr21:46356816-46408790	Genic enhancers Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription 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	16 gene(s)	inside rSNPs	diseases
23	nsv913989	chr21:46356816-46430792	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
24	nsv913990	chr21:46356816-46448142	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
25	nsv913991	chr21:46356816-46472929	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4818743	C21orf70	cis	lymphoblastoid	seeQTL

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:46358800-46360600	Active TSS	iPS-15b Cell Line	embryonic stem cell
2	chr21:46358800-46360800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr21:46358800-46361000	Active TSS	HUES6 Cell Line	embryonic stem cell
4	chr21:46359000-46361000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr21:46359000-46361000	Active TSS	Fetal Kidney	kidney
6	chr21:46359000-46361200	Active TSS	A549	lung
7	chr21:46359000-46361600	Active TSS	H9 Cell Line	embryonic stem cell
8	chr21:46359000-46361600	Active TSS	HUES48 Cell Line	embryonic stem cell
9	chr21:46359200-46360600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr21:46359200-46360600	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr21:46359200-46360800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr21:46359200-46360800	Active TSS	HUES64 Cell Line	embryonic stem cell
13	chr21:46359200-46360800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr21:46359200-46360800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
15	chr21:46359200-46361000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr21:46359200-46361000	Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr21:46359200-46361000	Flanking Active TSS	Primary B cells from cord blood	blood
18	chr21:46359200-46361200	Active TSS	Psoas Muscle	Psoas
19	chr21:46359200-46361200	Active TSS	GM12878-XiMat	blood
20	chr21:46359200-46361400	Active TSS	Left Ventricle	heart
21	chr21:46359200-46361400	Active TSS	HSMMtube	muscle
22	chr21:46359400-46360400	Active TSS	Primary T cells from cord blood	blood
23	chr21:46359400-46360400	Active TSS	Brain Anterior Caudate	brain
24	chr21:46359400-46360400	Active TSS	Brain Hippocampus Middle	brain
25	chr21:46359400-46360400	Active TSS	Duodenum Mucosa	Duodenum
26	chr21:46359400-46360400	Active TSS	Stomach Smooth Muscle	stomach
27	chr21:46359400-46360600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr21:46359400-46360600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr21:46359400-46360600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr21:46359400-46360600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr21:46359400-46360600	Active TSS	Brain Angular Gyrus	brain
32	chr21:46359400-46360600	Active TSS	Brain Inferior Temporal Lobe	brain
33	chr21:46359400-46360600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
34	chr21:46359400-46360600	Active TSS	Brain Substantia Nigra	brain
35	chr21:46359400-46360600	Active TSS	Colon Smooth Muscle	Colon
36	chr21:46359400-46360600	Active TSS	Duodenum Smooth Muscle	Duodenum
37	chr21:46359400-46360600	Active TSS	Fetal Heart	heart
38	chr21:46359400-46360600	Active TSS	Fetal Stomach	stomach
39	chr21:46359400-46360600	Active TSS	Gastric	stomach
40	chr21:46359400-46360600	Active TSS	Lung	lung
41	chr21:46359400-46360600	Active TSS	Placenta Amnion	Placenta Amnion
42	chr21:46359400-46360600	Active TSS	Rectal Mucosa Donor 29	rectum
43	chr21:46359400-46360600	Active TSS	Rectal Mucosa Donor 31	rectum
44	chr21:46359400-46360600	Active TSS	Rectal Smooth Muscle	rectum
45	chr21:46359400-46360600	Active TSS	Small Intestine	intestine
46	chr21:46359400-46360600	Active TSS	Thymus	Thymus
47	chr21:46359400-46360600	Active TSS	Hela-S3	cervix
48	chr21:46359400-46360600	Active TSS	NHLF	lung
49	chr21:46359400-46360800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
50	chr21:46359400-46360800	Active TSS	H1 Cell Line	embryonic stem cell

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