Variant report

Variant	rs6571826
Chromosome Location	chr14:21905703-21905704
allele	A/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	FOXA1	chr14:21905256-21906349	HepG2	liver:	n/a	chr14:21906041-21906053
2	BCL3	chr14:21905060-21905868	A549	lung:	n/a	n/a
3	POLR2A	chr14:21905343-21905855	IMR90	lung:	n/a	n/a
4	POLR2A	chr14:21905211-21905728	HepG2	liver:	n/a	n/a
5	MYC	chr14:21905371-21905770	K562	blood:	n/a	n/a
6	PBX3	chr14:21905045-21905866	SK-N-SH	brain:	n/a	chr14:21905476-21905485
7	ATF1	chr14:21905327-21905918	K562	blood:	n/a	n/a
8	IRF1	chr14:21905209-21905995	K562	blood:	n/a	chr14:21905459-21905468 chr14:21905758-21905772
9	ZNF143	chr14:21905204-21905972	K562	blood:	n/a	chr14:21905219-21905229
10	YY1	chr14:21905256-21905747	GM12878	blood:	n/a	chr14:21905689-21905708 chr14:21905633-21905644
11	NFATC1	chr14:21905141-21905823	GM12878	blood:	n/a	n/a
12	TCF12	chr14:21905127-21905887	ECC-1	luminal epithelium:	n/a	n/a
13	CHD2	chr14:21905233-21905789	Hela-S3	cervix:	n/a	chr14:21905447-21905457 chr14:21905442-21905452
14	POLR2A	chr14:21905069-21905795	GM12892	blood:	n/a	n/a
15	STAT3	chr14:21905419-21905728	MCF10A-Er-Src	breast:	n/a	n/a
16	CHD2	chr14:21905283-21906074	HepG2	liver:	n/a	chr14:21905447-21905457 chr14:21905442-21905452
17	SP1	chr14:21905049-21905904	A549	lung:	n/a	chr14:21905229-21905239 chr14:21905221-21905233 chr14:21905536-21905550 chr14:21905543-21905552 chr14:21905222-21905231 chr14:21905514-21905525 chr14:21905221-21905233 chr14:21905409-21905423 chr14:21905222-21905232 chr14:21905541-21905552 chr14:21905848-21905855 chr14:21905760-21905772 chr14:21905448-21905469 chr14:21905761-21905775 chr14:21905218-21905232
18	MXI1	chr14:21905289-21905780	GM12878	blood:	n/a	n/a
19	ELF1	chr14:21905172-21905716	A549	lung:	n/a	n/a
20	POLR2A	chr14:21905139-21906214	HepG2	liver:	n/a	n/a
21	BCLAF1	chr14:21905069-21905833	GM12878	blood:	n/a	n/a
22	BCLAF1	chr14:21904845-21905739	GM12878	blood:	n/a	n/a
23	REST	chr14:21905275-21905715	SK-N-SH	brain:	n/a	n/a
24	SP1	chr14:21905011-21905935	HCT-116	colon:	n/a	chr14:21905229-21905239 chr14:21905221-21905233 chr14:21905536-21905550 chr14:21905543-21905552 chr14:21905222-21905231 chr14:21905028-21905042 chr14:21905514-21905525 chr14:21905032-21905042 chr14:21905221-21905233 chr14:21905409-21905423 chr14:21905222-21905232 chr14:21905541-21905552 chr14:21905848-21905855 chr14:21905760-21905772 chr14:21905448-21905469 chr14:21905761-21905775 chr14:21905218-21905232 chr14:21905032-21905041
25	NFIC	chr14:21905184-21906213	HepG2	liver:	n/a	n/a
26	MAZ	chr14:21905018-21905812	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr14:21905150-21905866	ECC-1	luminal epithelium:	n/a	n/a
28	BHLHE40	chr14:21905383-21905938	K562	blood:	n/a	n/a
29	EP300	chr14:21905432-21905973	K562	blood:	n/a	n/a
30	TAF1	chr14:21905097-21905854	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTBP2	chr14:21905207-21905865	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr14:21905146-21905730	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPD	chr14:21905053-21905774	HepG2	liver:	n/a	n/a
34	PML	chr14:21905140-21905997	GM12878	blood:	n/a	n/a
35	POLR2A	chr14:21905029-21905963	GM18505	blood:	n/a	n/a
36	TCF12	chr14:21905318-21905704	GM12878	blood:	n/a	n/a
37	POLR2A	chr14:21904933-21905980	GM12878	blood:	n/a	n/a
38	YY1	chr14:21905101-21905932	HepG2	liver:	n/a	chr14:21905689-21905708 chr14:21905633-21905644
39	REST	chr14:21905092-21905784	A549	lung:	n/a	n/a
40	MAX	chr14:21905184-21905905	ECC-1	luminal epithelium:	n/a	n/a
41	NFYA	chr14:21905154-21905821	Hela-S3	cervix:	n/a	chr14:21905459-21905471 chr14:21905458-21905468
42	SP1	chr14:21904979-21905887	HCT-116	colon:	n/a	chr14:21905229-21905239 chr14:21905221-21905233 chr14:21905536-21905550 chr14:21905543-21905552 chr14:21905222-21905231 chr14:21905028-21905042 chr14:21905514-21905525 chr14:21905032-21905042 chr14:21905221-21905233 chr14:21905409-21905423 chr14:21905222-21905232 chr14:21905541-21905552 chr14:21905848-21905855 chr14:21905760-21905772 chr14:21905448-21905469 chr14:21905761-21905775 chr14:21905218-21905232 chr14:21905032-21905041
43	POLR2A	chr14:21905055-21905804	GM12892	blood:	n/a	n/a
44	POLR2A	chr14:21905027-21905817	Raji	blood:	n/a	n/a
45	POLR2A	chr14:21904998-21905882	GM12878	blood:	n/a	n/a
46	ELF1	chr14:21904906-21906001	MCF-7	breast:	n/a	n/a
47	RFX5	chr14:21905360-21905757	Hela-S3	cervix:	n/a	n/a
48	RAD21	chr14:21905340-21905824	HepG2	liver:	n/a	chr14:21905808-21905820
49	TAF1	chr14:21905045-21905951	H1-neurons	neurons:	n/a	n/a
50	NFYA	chr14:21905192-21905810	GM12878	blood:	n/a	chr14:21905459-21905471 chr14:21905458-21905468

No.	Distal block	Cell Line	Cell type
1	chr14:21903199..21908176-chr14:21922150..21927422,17	MCF-7	breast:
2	chr14:21902087..21907117-chr14:21919849..21925728,16	MCF-7	breast:
3	chr14:21874917..21880880-chr14:21901855..21906138,6	MCF-7	breast:
4	chr14:21904269..21906743-chr14:21992458..21995215,2	K562	blood:
5	chr14:21904171..21908174-chr14:21922677..21925847,6	K562	blood:
6	chr14:21903666..21907303-chr14:21944223..21946943,4	K562	blood:
7	chr14:21850845..21853690-chr14:21904139..21906102,2	K562	blood:
8	chr14:21903062..21910356-chr14:21920914..21926084,11	K562	blood:

Variant related genes	Relation type
CHD8	TF binding region
ENSG00000165821	Chromatin interaction
ENSG00000100888	Chromatin interaction
ENSG00000092201	Chromatin interaction
ENSG00000260830	Chromatin interaction
ENSG00000092203	Chromatin interaction
ENSG00000129472	Chromatin interaction

Extended variants
information (count: 77 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs1008268	0.88[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1008269	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10132333	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10134108	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10135022	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10137743	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs10138699	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10139379	0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10143061	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10146717	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10150329	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10151764	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10438064	1.00[CHB][hapmap]
rs1045842	0.80[AMR][1000 genomes]
rs10782384	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs11623599	0.94[ASN][1000 genomes]
rs11623642	0.88[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11623737	0.96[ASN][1000 genomes]
rs11624716	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12885503	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1543494	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1952554	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1983768	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1998330	0.98[ASN][1000 genomes]
rs1998331	0.91[ASN][1000 genomes]
rs1998332	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs1999139	0.80[AMR][1000 genomes]
rs2007434	0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2065096	1.00[CEU][hapmap];0.88[AMR][1000 genomes]
rs2146062	0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2149749	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2181125	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2295865	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2295866	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3762156	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3762157	0.94[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3762158	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3762159	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4144189	1.00[CHB][hapmap];0.82[JPT][hapmap];0.88[ASN][1000 genomes]
rs4246991	0.89[ASN][1000 genomes]
rs4982445	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4982446	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6571770	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6571797	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7145002	0.82[CEU][hapmap]
rs7147024	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7148741	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7152833	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7155123	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7160488	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs8004294	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs8004388	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes]
rs8007893	0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs8008670	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs8009789	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs8011945	1.00[ASN][1000 genomes]
rs8017451	0.80[ASN][1000 genomes]
rs8017630	0.88[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs8018369	0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs8020149	0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs8022395	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs8022755	0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs927412	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs9322978	1.00[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:13 , 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	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	nsv1054013	chr14:21868964-21992109	Enhancers Genic enhancers Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
12	nsv541991	chr14:21868964-21992109	Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
13	nsv530011	chr14:21876973-21985341	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6571826	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	chr14:21903400-21905800	Active TSS	NHLF	lung
2	chr14:21904200-21905800	Active TSS	H1 Cell Line	embryonic stem cell
3	chr14:21904200-21905800	Active TSS	iPS-15b Cell Line	embryonic stem cell
4	chr14:21904200-21906000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr14:21904200-21906000	Active TSS	Right Atrium	heart
6	chr14:21904200-21906200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr14:21904200-21906200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr14:21904200-21906200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr14:21904200-21906200	Active TSS	Psoas Muscle	Psoas
10	chr14:21904400-21905800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr14:21904400-21905800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr14:21904400-21905800	Active TSS	NHDF-Ad	bronchial
13	chr14:21904400-21906000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr14:21904400-21906000	Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr14:21904400-21906200	Active TSS	Pancreatic Islets	Pancreatic Islet
16	chr14:21904400-21906400	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr14:21904600-21905800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr14:21904600-21905800	Active TSS	HUES64 Cell Line	embryonic stem cell
19	chr14:21904600-21905800	Active TSS	Fetal Intestine Large	intestine
20	chr14:21904600-21905800	Active TSS	Left Ventricle	heart
21	chr14:21904600-21906000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr14:21904600-21906000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
23	chr14:21904600-21906000	Active TSS	Colonic Mucosa	Colon
24	chr14:21904600-21906000	Active TSS	Right Ventricle	heart
25	chr14:21904600-21906200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr14:21904600-21906200	Active TSS	Esophagus	oesophagus
27	chr14:21904600-21906200	Active TSS	Fetal Muscle Trunk	muscle
28	chr14:21904600-21906200	Active TSS	Ovary	ovary
29	chr14:21904800-21905800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr14:21904800-21905800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr14:21904800-21905800	Active TSS	Brain Angular Gyrus	brain
32	chr14:21904800-21905800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
33	chr14:21904800-21905800	Active TSS	Fetal Adrenal Gland	Adrenal Gland
34	chr14:21904800-21905800	Active TSS	Fetal Heart	heart
35	chr14:21904800-21905800	Active TSS	Fetal Intestine Small	intestine
36	chr14:21904800-21905800	Active TSS	Fetal Kidney	kidney
37	chr14:21904800-21905800	Active TSS	Fetal Stomach	stomach
38	chr14:21904800-21905800	Active TSS	Fetal Thymus	thymus
39	chr14:21904800-21905800	Active TSS	Gastric	stomach
40	chr14:21904800-21905800	Active TSS	Pancreas	Pancrea
41	chr14:21904800-21905800	Active TSS	Placenta Amnion	Placenta Amnion
42	chr14:21904800-21905800	Active TSS	A549	lung
43	chr14:21904800-21905800	Active TSS	K562	blood
44	chr14:21904800-21906000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
45	chr14:21904800-21906000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr14:21904800-21906000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
47	chr14:21904800-21906000	Active TSS	Aorta	Aorta
48	chr14:21904800-21906000	Active TSS	Brain Substantia Nigra	brain
49	chr14:21904800-21906000	Active TSS	Fetal Brain Female	brain
50	chr14:21904800-21906000	Active TSS	Lung	lung

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