Variant report

Variant	rs4985407
Chromosome Location	chr16:70285901-70285902
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:684)
CpG islands
(count:0)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:684 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TEAD4	chr16:70285421-70286096	SK-N-SH	brain:	n/a	n/a
2	FOXA2	chr16:70285697-70286062	HepG2	liver:	n/a	n/a
3	TRIM28	chr16:70285545-70286216	K562	blood:	n/a	chr16:70286028-70286036
4	POLR2A	chr16:70285528-70286229	H1-neurons	neurons:	n/a	n/a
5	ELF1	chr16:70285517-70286092	SK-N-SH	brain:	n/a	n/a
6	REST	chr16:70285510-70286056	PFSK-1	brain:	n/a	chr16:70286002-70286015
7	ZBTB33	chr16:70285583-70286096	A549	lung:	n/a	n/a
8	CHD1	chr16:70284609-70286363	IMR90	lung:	n/a	n/a
9	PML	chr16:70285539-70286234	MCF-7	breast:	n/a	chr16:70286028-70286036
10	YY1	chr16:70285577-70286156	SK-N-SH	brain:	n/a	n/a
11	POLR2A	chr16:70284792-70286092	HepG2	liver:	n/a	n/a
12	TAF1	chr16:70285611-70286044	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr16:70284719-70286585	HL-60	blood:	n/a	n/a
14	POLR2A	chr16:70285559-70286091	GM12878	blood:	n/a	n/a
15	GTF2F1	chr16:70285680-70286790	Hela-S3	cervix:	n/a	n/a
16	UBTF	chr16:70284737-70286795	K562	blood:	n/a	n/a
17	POLR2A	chr16:70284547-70286177	H1-hESC	embryonic stem cell:	n/a	n/a
18	KAP1	chr16:70285610-70286878	HEK293	kidney:	n/a	chr16:70286028-70286036
19	POLR2A	chr16:70285129-70286156	ECC-1	luminal epithelium:	n/a	n/a
20	CTCF	chr16:70285820-70285970	BE2_C	brain:	n/a	chr16:70285927-70285936
21	PBX3	chr16:70285503-70286243	A549	lung:	n/a	n/a
22	EP300	chr16:70285395-70286361	ECC-1	luminal epithelium:	n/a	n/a
23	CREB1	chr16:70285484-70286141	H1-hESC	embryonic stem cell:	n/a	n/a
24	TBL1XR1	chr16:70285614-70286010	GM12878	blood:	n/a	n/a
25	POLR2A	chr16:70284594-70286177	GM12878	blood:	n/a	n/a
26	CEBPB	chr16:70285616-70286218	GM12878	blood:	n/a	n/a
27	MAX	chr16:70284710-70286335	HepG2	liver:	n/a	n/a
28	MYC	chr16:70285663-70285971	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr16:70285880-70286030	GM06990	blood:	n/a	chr16:70285927-70285936
30	POLR2A	chr16:70284826-70286040	A549	lung:	n/a	n/a
31	ELF1	chr16:70285565-70286150	SK-N-SH	brain:	n/a	n/a
32	CTCF	chr16:70285860-70286010	GM12865	blood:	n/a	chr16:70285927-70285936
33	POU2F2	chr16:70285667-70285955	GM12878	blood:	n/a	n/a
34	GABPA	chr16:70285454-70286198	MCF-7	breast:	n/a	n/a
35	SIN3AK20	chr16:70285566-70286079	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr16:70285840-70285990	BE2_C	brain:	n/a	chr16:70285927-70285936
37	POLR2A	chr16:70285573-70286039	SK-N-SH	brain:	n/a	n/a
38	REST	chr16:70284832-70286384	H1-neurons	neurons:	n/a	chr16:70286002-70286015
39	ATF2	chr16:70285560-70286287	H1-hESC	embryonic stem cell:	n/a	n/a
40	TAF1	chr16:70285498-70286137	MCF-7	breast:	n/a	n/a
41	MAFK	chr16:70285812-70286483	K562	blood:	n/a	n/a
42	USF1	chr16:70285572-70286107	A549	lung:	n/a	n/a
43	SPI1	chr16:70285688-70285947	GM12878	blood:	n/a	n/a
44	POLR2A	chr16:70285517-70286053	HepG2	liver:	n/a	n/a
45	PAX5	chr16:70285615-70286035	GM12878	blood:	n/a	n/a
46	TAF1	chr16:70285523-70286029	GM12878	blood:	n/a	n/a
47	IRF1	chr16:70285675-70286239	K562	blood:	n/a	n/a
48	TEAD4	chr16:70285550-70286082	A549	lung:	n/a	n/a
49	BCLAF1	chr16:70285551-70286111	GM12878	blood:	n/a	chr16:70285921-70285929
50	MAX	chr16:70284869-70286078	HepG2	liver:	n/a	n/a

No data

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:70283970..70285913-chr16:70380669..70382950,2	K562	blood:
2	chr16:70285343..70285906-chr19:16738980..16739732,2	Hela-S3	cervix:
3	chr1:149982029..149982749-chr16:70285430..70285983,2	Hela-S3	cervix:
4	chr16:70278247..70283453-chr16:70284015..70287841,6	MCF-7	breast:
5	chr16:70285325..70286015-chr8:117886552..117887078,2	HCT-116	colon:
6	chr16:70284207..70286196-chr16:70321648..70323975,3	MCF-7	breast:
7	chr16:70279273..70282169-chr16:70284255..70286204,3	K562	blood:
8	chr16:70285239..70287287-chr16:70556700..70559340,2	K562	blood:
9	chr16:70284511..70286776-chr16:70330314..70334173,3	MCF-7	breast:
10	chr16:70279244..70282169-chr16:70284255..70286230,4	K562	blood:
11	chr16:70284251..70286200-chr16:70298122..70301114,5	MCF-7	breast:
12	chr16:70284271..70287113-chr16:70301564..70303205,2	MCF-7	breast:
13	chr16:70285367..70286970-chr17:73718097..73720794,2	MCF-7	breast:
14	chr16:70284505..70286615-chr16:70556732..70559559,2	MCF-7	breast:
15	chr16:70285081..70287489-chr16:70291525..70295571,5	K562	blood:
16	chr16:70284942..70287057-chr16:70291525..70294943,4	K562	blood:
17	chr11:842040..842913-chr16:70285376..70285907,2	HCT-116	colon:
18	chr16:70285876..70288887-chr16:70302566..70307390,4	K562	blood:

No data

Variant related genes	Relation type
EXOSC6	TF binding region
ENSG00000164754	Chromatin interaction
ENSG00000214063	Chromatin interaction
ENSG00000177700	Chromatin interaction
ENSG00000261556	Chromatin interaction
ENSG00000132470	Chromatin interaction
ENSG00000141979	Chromatin interaction
ENSG00000090861	Chromatin interaction
ENSG00000157349	Chromatin interaction
ENSG00000264875	Chromatin interaction
ENSG00000260537	Chromatin interaction
ENSG00000103051	Chromatin interaction
ENSG00000265230	Chromatin interaction
ENSG00000168872	Chromatin interaction
ENSG00000163113	Chromatin interaction
ENSG00000189091	Chromatin interaction
ENSG00000105085	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 60 )

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1044876	0.83[CEU][hapmap]
rs1134074	0.82[CHD][hapmap]
rs2070203	0.96[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2287983	0.87[JPT][hapmap]
rs28733806	0.83[ASN][1000 genomes]
rs34087264	0.94[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs3859068	0.93[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap]
rs4985525	0.82[CHD][hapmap]
rs7189474	0.93[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.81[YRI][hapmap]
rs7192268	0.93[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.81[YRI][hapmap]
rs73575193	0.84[EUR][1000 genomes]
rs775208	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8058224	0.93[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.81[YRI][hapmap]
rs8062183	0.90[CHD][hapmap];1.00[JPT][hapmap]
rs936994	0.93[CEU][hapmap];0.89[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.93[TSI][hapmap]
rs9934440	0.93[CEU][hapmap];0.89[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.87[MKK][hapmap];0.95[TSI][hapmap]

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	esv2758428	chr16:69855122-70313222	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
2	esv2758652	chr16:69855122-70313222	Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
3	esv1830874	chr16:69968850-70298988	Strong transcription Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
4	nsv428328	chr16:69986563-70313222	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
5	esv1802826	chr16:69988100-70287669	Strong transcription Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
6	esv1820100	chr16:70048808-70311044	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
7	esv33745	chr16:70116599-70319873	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' 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	39 gene(s)	inside rSNPs	diseases
8	esv1801017	chr16:70141558-70303736	Strong transcription Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
9	nsv833271	chr16:70185694-70353334	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS 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	51 gene(s)	inside rSNPs	diseases
10	esv1796562	chr16:70206819-70289517	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
11	esv1825452	chr16:70206819-70289517	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
12	esv1804795	chr16:70206819-70294463	Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
13	nsv978165	chr16:70244012-70286115	Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
14	nsv1061286	chr16:70253809-70331407	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
15	esv1826506	chr16:70253919-70287669	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
16	nsv906868	chr16:70270429-70292810	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
17	esv3338628	chr16:70283151-70287449	Weak transcription Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases
18	esv3505211	chr16:70284351-70286799	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases
19	esv3505212	chr16:70284351-70286799	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases
20	nsv906869	chr16:70285901-70292810	Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	18 gene(s)	inside rSNPs	diseases

mRNA abundance (count:60)

SNP	Gene	Cis/trans	Tissue	Source
rs4985407	PDXDC2P	cis	Artery Tibial	GTEx
rs4985407	EXOSC6	cis	Adipose Subcutaneous	GTEx
rs4985407	EXOSC6	cis	Muscle Skeletal	GTEx
rs4985407	EXOSC6	cis	cerebellum	SCAN
rs4985407	RP11-419C5.2	cis	lung	GTEx
rs4985407	EXOSC6	Cis_1M	lymphoblastoid	RTeQTL
rs4985407	RP11-296I10.6	cis	Muscle Skeletal	GTEx
rs4985407	PDXDC2P	cis	parietal	SCAN
rs4985407	EXOSC6	cis	Artery Tibial	GTEx
rs4985407	EXOSC6	cis	normal skin	skin_eQTL
rs4985407	PDXDC2P	cis	Adipose Subcutaneous	GTEx
rs4985407	CLEC18A	cis	Artery Tibial	GTEx
rs4985407	RP11-296I10.6	cis	Skin Sun Exposed Lower leg	GTEx
rs4985407	CLEC18A	cis	lung	GTEx
rs4985407	PDXDC2P	cis	Thyroid	GTEx
rs4985407	PDXDC2P	cis	Nerve Tibial	GTEx
rs4985407	PDXDC2P	cis	lung	GTEx
rs4985407	RP11-296I10.6	cis	Whole Blood	GTEx
rs4985407	EXOSC6	cis	Esophagus Muscularis	GTEx
rs4985407	RP11-296I10.6	cis	Heart Left Ventricle	GTEx
rs4985407	RP11-296I10.6	cis	Artery Tibial	GTEx
rs4985407	PDXDC2P	cis	Artery Aorta	GTEx
rs4985407	RP11-419C5.2	cis	Skin Sun Exposed Lower leg	GTEx
rs4985407	TMCO7	cis	parietal	SCAN
rs4985407	WWP2	cis	parietal	SCAN
rs4985407	RP11-296I10.6	cis	Stomach	GTEx
rs4985407	RP11-296I10.6	cis	Thyroid	GTEx
rs4985407	CLEC18A	cis	Adipose Subcutaneous	GTEx
rs4985407	RP11-419C5.2	cis	Muscle Skeletal	GTEx
rs4985407	EXOSC6	cis	Heart Left Ventricle	GTEx
rs4985407	RP11-419C5.2	cis	Adipose Subcutaneous	GTEx
rs4985407	EXOSC6	cis	Thyroid	GTEx
rs4985407	AARS	Cis_1M	lymphoblastoid	RTeQTL
rs4985407	CLEC18C	cis	Nerve Tibial	GTEx
rs4985407	RP11-296I10.6	cis	Esophagus Muscularis	GTEx
rs4985407	EXOSC6	cis	lung	GTEx
rs4985407	PDXDC2P	cis	Muscle Skeletal	GTEx
rs4985407	RP11-296I10.6	cis	Artery Aorta	GTEx
rs4985407	RP11-419C5.2	cis	Thyroid	GTEx
rs4985407	EXOSC6	cis	Stomach	GTEx
rs4985407	EXOSC6	cis	Skin Sun Exposed Lower leg	GTEx
rs4985407	EXOSC6	cis	parietal	SCAN
rs4985407	EXOSC6	cis	Esophagus Mucosa	GTEx
rs4985407	RP11-296I10.6	cis	Nerve Tibial	GTEx
rs4985407	CLEC18C	cis	Artery Tibial	GTEx
rs4985407	EXOSC6	cis	Artery Aorta	GTEx
rs4985407	PDXDC2P	cis	Skin Sun Exposed Lower leg	GTEx
rs4985407	CLEC18A	cis	Thyroid	GTEx
rs4985407	RP11-419C5.2	cis	Esophagus Muscularis	GTEx
rs4985407	CLEC18A	cis	Skin Sun Exposed Lower leg	GTEx
rs4985407	EXOSC6	cis	Whole Blood	GTEx
rs4985407	CLEC18A	cis	Whole Blood	GTEx
rs4985407	RP11-296I10.6	cis	lung	GTEx
rs4985407	ENSG00000157344	cis	multi-tissue	Pritchard
rs4985407	RP11-419C5.2	cis	Nerve Tibial	GTEx
rs4985407	EXOSC6	cis	Nerve Tibial	GTEx
rs4985407	CLEC18C	cis	Whole Blood	GTEx
rs4985407	EXOSC6	cis	uninvolved skin	skin_eQTL
rs4985407	PDXDC2P	cis	Esophagus Muscularis	GTEx
rs4985407	RP11-296I10.6	cis	Adipose Subcutaneous	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70283400-70286000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr16:70283400-70286000	Active TSS	A549	lung
3	chr16:70283600-70286000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr16:70283600-70286000	Active TSS	HUES48 Cell Line	embryonic stem cell
5	chr16:70283600-70286000	Active TSS	HUES64 Cell Line	embryonic stem cell
6	chr16:70283600-70286000	Active TSS	iPS-18 Cell Line	embryonic stem cell
7	chr16:70283600-70286000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr16:70283600-70286200	Active TSS	Hela-S3	cervix
9	chr16:70283800-70286000	Active TSS	K562	blood
10	chr16:70284000-70286000	Active TSS	ES-I3 Cell Line	embryonic stem cell
11	chr16:70284000-70286000	Active TSS	NH-A	brain
12	chr16:70284200-70286000	Active TSS	H9 Cell Line	embryonic stem cell
13	chr16:70284200-70286000	Active TSS	iPS-15b Cell Line	embryonic stem cell
14	chr16:70284200-70286000	Active TSS	Fetal Intestine Small	intestine
15	chr16:70284200-70286000	Active TSS	Pancreatic Islets	Pancreatic Islet
16	chr16:70284200-70286000	Active TSS	HSMM	muscle
17	chr16:70284400-70286000	Active TSS	H1 Cell Line	embryonic stem cell
18	chr16:70284400-70286000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr16:70284400-70286000	Active TSS	iPS-20b Cell Line	embryonic stem cell
20	chr16:70284400-70286000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
21	chr16:70284400-70286000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr16:70284400-70286000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr16:70284400-70286000	Active TSS	Primary T helper cells PMA-I stimulated	--
24	chr16:70284400-70286000	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
25	chr16:70284400-70286000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
26	chr16:70284400-70286000	Active TSS	Duodenum Smooth Muscle	Duodenum
27	chr16:70284400-70286000	Active TSS	Fetal Thymus	thymus
28	chr16:70284400-70286000	Active TSS	Rectal Smooth Muscle	rectum
29	chr16:70284400-70286000	Active TSS	HUVEC	blood vessel
30	chr16:70284400-70286000	Active TSS	Osteobl	bone
31	chr16:70284400-70286200	Active TSS	Fetal Brain Female	brain
32	chr16:70284600-70286000	Weak transcription	Fetal Heart	heart
33	chr16:70284600-70286000	Active TSS	Thymus	Thymus
34	chr16:70284600-70286200	Transcr. at gene 5' and 3'	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr16:70284600-70286200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr16:70284800-70286000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr16:70284800-70286000	Active TSS	Muscle Satellite Cultured Cells	--
38	chr16:70284800-70286000	Active TSS	Colon Smooth Muscle	Colon
39	chr16:70284800-70286000	Active TSS	Gastric	stomach
40	chr16:70284800-70286000	Active TSS	Left Ventricle	heart
41	chr16:70284800-70286000	Active TSS	Lung	lung
42	chr16:70284800-70286000	Active TSS	Ovary	ovary
43	chr16:70284800-70286000	Active TSS	Sigmoid Colon	Sigmoid Colon
44	chr16:70284800-70286000	Active TSS	Stomach Smooth Muscle	stomach
45	chr16:70284800-70286000	Active TSS	HMEC	breast
46	chr16:70284800-70286200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
47	chr16:70284800-70286400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr16:70285000-70286000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr16:70285000-70286000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr16:70285000-70286000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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