Variant report

Variant	rs1952554
Chromosome Location	chr14:21863716-21863717
allele	C/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	CTCF	chr14:21863710-21863861	HUVEC	blood vessel:	n/a	chr14:21863797-21863815 chr14:21863792-21863813 chr14:21863798-21863814
2	CTCF	chr14:21863700-21863850	HCPEpiC	choroid plexus:	n/a	chr14:21863797-21863815 chr14:21863792-21863813 chr14:21863798-21863814
3	CTCF	chr14:21863620-21863770	AG10803	skin:	n/a	n/a
4	CTCF	chr14:21863660-21863810	HMF	breast:	n/a	n/a
5	CTCF	chr14:21863700-21863850	MCF-7	breast:	n/a	chr14:21863797-21863815 chr14:21863792-21863813 chr14:21863798-21863814
6	CTCF	chr14:21863693-21863838	IMR90	lung:	n/a	chr14:21863797-21863815 chr14:21863792-21863813 chr14:21863798-21863814
7	CTCF	chr14:21863680-21863830	NHDF-neo	bronchial:	n/a	chr14:21863797-21863815 chr14:21863792-21863813 chr14:21863798-21863814
8	RAD21	chr14:21863574-21863997	A549	lung:	n/a	chr14:21863795-21863814
9	CTCF	chr14:21863680-21863830	Caco-2	colon:	n/a	chr14:21863797-21863815 chr14:21863792-21863813 chr14:21863798-21863814
10	CTCF	chr14:21863620-21863770	HCM	heart:	n/a	n/a
11	RAD21	chr14:21863540-21864058	HCT-116	colon:	n/a	chr14:21863795-21863814
12	CTCF	chr14:21863620-21863770	RPTEC	kidney:	n/a	n/a
13	RAD21	chr14:21863704-21863836	SK-N-SH_RA	brain:	n/a	chr14:21863795-21863814
14	RAD21	chr14:21863609-21863997	MCF-7	breast:	n/a	chr14:21863795-21863814
15	CTCF	chr14:21863671-21863937	K562	blood:	n/a	chr14:21863797-21863815 chr14:21863792-21863813 chr14:21863798-21863814
16	RAD21	chr14:21863545-21863978	MCF-7	breast:	n/a	chr14:21863795-21863814
17	CTCF	chr14:21863660-21863910	HMEC	breast:	n/a	chr14:21863797-21863815 chr14:21863792-21863813 chr14:21863798-21863814
18	CTCF	chr14:21863708-21863893	LNCaP	prostate:	n/a	chr14:21863797-21863815 chr14:21863792-21863813 chr14:21863798-21863814
19	CTCF	chr14:21863650-21863957	GM12878	blood:	n/a	chr14:21863797-21863815 chr14:21863792-21863813 chr14:21863798-21863814
20	RAD21	chr14:21863636-21863963	Hela-S3	cervix:	n/a	chr14:21863795-21863814
21	CTCF	chr14:21863716-21863877	Hela-S3	cervix:	n/a	chr14:21863797-21863815 chr14:21863792-21863813 chr14:21863798-21863814
22	CTCF	chr14:21863660-21863810	HepG2	liver:	n/a	n/a
23	CTCF	chr14:21863700-21863850	HRPEpiC	eye:	n/a	chr14:21863797-21863815 chr14:21863792-21863813 chr14:21863798-21863814
24	CTCF	chr14:21863412-21864094	A549	lung:	n/a	chr14:21863797-21863815 chr14:21863792-21863813 chr14:21863798-21863814
25	RAD21	chr14:21863661-21863928	HepG2	liver:	n/a	chr14:21863795-21863814
26	CTCF	chr14:21863680-21863830	HVMF	connective:	n/a	chr14:21863797-21863815 chr14:21863792-21863813 chr14:21863798-21863814
27	CTCF	chr14:21863680-21863950	NHDF-neo	bronchial:	n/a	chr14:21863797-21863815 chr14:21863792-21863813 chr14:21863798-21863814
28	RAD21	chr14:21863601-21864016	HepG2	liver:	n/a	chr14:21863795-21863814

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:21854245..21857483-chr14:21860851..21864599,3	MCF-7	breast:
2	chr14:21850356..21853255-chr14:21861527..21864591,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000241035	TF binding region
SNORD9	TF binding region
CHD8	TF binding region
ENSG00000092201	Chromatin interaction
ENSG00000260830	Chromatin interaction
ENSG00000100888	Chromatin interaction

Extended variants
information (count: 78 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs1008268	0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1008269	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10132333	1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10134108	0.84[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];0.94[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10135022	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10137743	0.91[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.91[TSI][hapmap];0.89[YRI][hapmap];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10138699	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10139379	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10143061	1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.82[TSI][hapmap];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10146717	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10150329	1.00[ASN][1000 genomes]
rs10151764	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap];0.85[YRI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10438064	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs10782384	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11623599	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11623642	0.89[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11623737	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11624716	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12885503	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1543494	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1983768	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1998330	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1998331	0.91[ASN][1000 genomes]
rs1998332	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2007434	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2065096	0.85[AMR][1000 genomes]
rs2146062	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2149749	0.82[ASN][1000 genomes]
rs2181125	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2295865	1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2295866	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3762156	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3762157	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3762158	1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.82[TSI][hapmap];0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3762159	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3762162	0.83[GIH][hapmap];0.82[TSI][hapmap]
rs4144189	1.00[CHB][hapmap];0.82[JPT][hapmap];0.89[YRI][hapmap];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4246991	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4982445	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4982446	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6571770	1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6571797	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6571826	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6571845	0.83[GIH][hapmap];0.83[MEX][hapmap];0.82[TSI][hapmap]
rs7147024	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7148741	0.83[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap];1.00[ASN][1000 genomes]
rs7152833	1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.82[TSI][hapmap];0.87[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7155123	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7160488	1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.82[TSI][hapmap];0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs8004294	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8004388	1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];0.94[MEX][hapmap];0.82[TSI][hapmap];0.87[AMR][1000 genomes]
rs8005163	0.83[GIH][hapmap]
rs8007893	0.89[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs8008670	1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.82[TSI][hapmap];0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs8009789	1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.82[TSI][hapmap];0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs8011945	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8017451	0.80[ASN][1000 genomes]
rs8017630	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs8018369	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs8020149	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs8022395	1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.82[TSI][hapmap];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs8022755	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs927412	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs9322978	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530009	chr14:21377022-22044608	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
2	nsv530769	chr14:21407536-22139126	Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
3	nsv916319	chr14:21507092-21896590	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
4	nsv1036762	chr14:21507093-22101805	Enhancers Strong transcription Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
5	nsv541976	chr14:21507093-22101805	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
6	nsv1043570	chr14:21575068-21899964	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
7	nsv541977	chr14:21575068-21899964	Active TSS Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
8	nsv948957	chr14:21616875-21928338	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
9	nsv1051407	chr14:21692670-21907366	Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
10	nsv541984	chr14:21692670-21907366	Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Enhancers 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	37 gene(s)	inside rSNPs	diseases
11	nsv530010	chr14:21692670-21923767	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
12	nsv428617	chr14:21721165-21871164	Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
13	esv3518898	chr14:21805983-22077584	Flanking Active TSS Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
14	esv3518899	chr14:21805983-22077584	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1952554	TOX4	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21853000-21865000	Weak transcription	Stomach Mucosa	stomach
2	chr14:21853000-21868000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr14:21853200-21863800	Weak transcription	Right Atrium	heart
4	chr14:21853200-21865400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr14:21853200-21884400	Strong transcription	NH-A	brain
6	chr14:21853200-21904000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr14:21853400-21875800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr14:21853400-21876000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr14:21853400-21876200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr14:21853400-21876200	Strong transcription	Osteobl	bone
11	chr14:21853400-21876400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr14:21853400-21877800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr14:21853400-21879800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr14:21853400-21884200	Strong transcription	Colon Smooth Muscle	Colon
15	chr14:21853400-21884400	Strong transcription	Fetal Muscle Leg	muscle
16	chr14:21853400-21884800	Strong transcription	Fetal Brain Female	brain
17	chr14:21853400-21900000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr14:21853400-21900000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr14:21853400-21900000	Strong transcription	Adipose Nuclei	Adipose
20	chr14:21853400-21900000	Strong transcription	Placenta	Placenta
21	chr14:21853400-21900200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr14:21853400-21901800	Strong transcription	HUES64 Cell Line	embryonic stem cell
23	chr14:21853600-21876800	Strong transcription	Fetal Stomach	stomach
24	chr14:21853600-21884000	Strong transcription	Brain Substantia Nigra	brain
25	chr14:21853600-21884400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr14:21853600-21884400	Strong transcription	HSMM	muscle
27	chr14:21853600-21885000	Strong transcription	Stomach Smooth Muscle	stomach
28	chr14:21853600-21885800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr14:21853600-21886800	Strong transcription	Duodenum Smooth Muscle	Duodenum
30	chr14:21853600-21888800	Strong transcription	Fetal Intestine Large	intestine
31	chr14:21853600-21897200	Strong transcription	Fetal Muscle Trunk	muscle
32	chr14:21853600-21900000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr14:21853600-21900200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
34	chr14:21853600-21900200	Strong transcription	Primary neutrophils fromperipheralblood	blood
35	chr14:21853600-21901400	Strong transcription	HUES6 Cell Line	embryonic stem cell
36	chr14:21853600-21902000	Strong transcription	HUES48 Cell Line	embryonic stem cell
37	chr14:21853600-21903400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr14:21853800-21884400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
39	chr14:21853800-21900000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr14:21853800-21900000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr14:21853800-21900200	Strong transcription	Fetal Thymus	thymus
42	chr14:21853800-21901400	Strong transcription	Primary T cells fromperipheralblood	blood
43	chr14:21854000-21873400	Strong transcription	Fetal Intestine Small	intestine
44	chr14:21854000-21885800	Strong transcription	HepG2	liver
45	chr14:21854000-21900200	Strong transcription	Monocytes-CD14+_RO01746	blood
46	chr14:21854000-21904000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr14:21854200-21884400	Strong transcription	H9 Cell Line	embryonic stem cell
48	chr14:21854200-21885400	Strong transcription	H1 Cell Line	embryonic stem cell
49	chr14:21854400-21886400	Strong transcription	Dnd41	blood
50	chr14:21854400-21900000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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