Variant report

Variant	rs72816873
Chromosome Location	chr16:46723370-46723371
allele	A/C
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	chr16:46722396-46723889	K562	blood:	n/a	chr16:46723128-46723138 chr16:46723102-46723111 chr16:46722716-46722732
2	SIN3AK20	chr16:46723349-46723778	HepG2	liver:	n/a	n/a
3	MAX	chr16:46722355-46724350	MCF-7	breast:	n/a	chr16:46723128-46723138 chr16:46723102-46723111 chr16:46722716-46722732
4	MAX	chr16:46722637-46723686	A549	lung:	n/a	chr16:46723128-46723138 chr16:46723102-46723111 chr16:46722716-46722732
5	CREB1	chr16:46722149-46724005	K562	blood:	n/a	n/a
6	MAX	chr16:46722104-46724407	A549	lung:	n/a	chr16:46723128-46723138 chr16:46723102-46723111 chr16:46722716-46722732
7	GABPA	chr16:46722939-46723440	K562	blood:	n/a	chr16:46723144-46723153
8	HEY1	chr16:46723174-46723807	K562	blood:	n/a	n/a
9	PBX3	chr16:46722925-46723600	A549	lung:	n/a	chr16:46723464-46723473 chr16:46723237-46723257 chr16:46723173-46723182
10	MXI1	chr16:46722350-46723720	H1-hESC	embryonic stem cell:	n/a	n/a
11	MYBL2	chr16:46722274-46724273	HepG2	liver:	n/a	n/a
12	MXI1	chr16:46721916-46725345	IMR90	lung:	n/a	n/a
13	USF1	chr16:46722385-46723541	HCT-116	colon:	n/a	chr16:46723072-46723088
14	POLR2A	chr16:46722350-46724205	K562	blood:	n/a	n/a
15	RUNX3	chr16:46722103-46723734	GM12878	blood:	n/a	n/a
16	POLR2A	chr16:46722412-46724164	GM12878	blood:	n/a	n/a
17	POLR2A	chr16:46722415-46724206	Gliobla	brain:	n/a	n/a
18	IRF3	chr16:46723182-46723603	Hela-S3	cervix:	n/a	chr16:46723518-46723532 chr16:46723281-46723295
19	POLR2A	chr16:46722321-46724227	GM19099	blood:	n/a	n/a
20	POLR2A	chr16:46722839-46724244	GM12878	blood:	n/a	n/a
21	MAZ	chr16:46722610-46723475	HepG2	liver:	n/a	chr16:46723128-46723138 chr16:46723102-46723111 chr16:46722716-46722732
22	POLR2A	chr16:46722448-46724285	PFSK-1	brain:	n/a	n/a
23	SIN3AK20	chr16:46722346-46724251	HepG2	liver:	n/a	n/a
24	SIN3AK20	chr16:46722340-46723399	H1-hESC	embryonic stem cell:	n/a	n/a
25	ZNF143	chr16:46722941-46723708	GM12878	blood:	n/a	n/a
26	POLR2A	chr16:46722177-46724269	Hela-S3	cervix:	n/a	n/a
27	SP1	chr16:46723069-46723583	K562	blood:	n/a	chr16:46723143-46723153 chr16:46723520-46723529 chr16:46723518-46723530 chr16:46723128-46723138 chr16:46723519-46723528 chr16:46723142-46723154 chr16:46723127-46723139 chr16:46723144-46723153 chr16:46723518-46723530 chr16:46723200-46723221 chr16:46723143-46723153 chr16:46723519-46723529 chr16:46723127-46723139 chr16:46723129-46723138 chr16:46723142-46723154 chr16:46723143-46723152 chr16:46723519-46723529 chr16:46723143-46723152 chr16:46723281-46723293 chr16:46723128-46723137
28	MAZ	chr16:46722806-46723757	GM12878	blood:	n/a	chr16:46723128-46723138 chr16:46723102-46723111
29	MAFK	chr16:46723210-46723466	Hela-S3	cervix:	n/a	n/a
30	TAF1	chr16:46722344-46724316	ECC-1	luminal epithelium:	n/a	n/a
31	YY1	chr16:46722472-46724275	HepG2	liver:	n/a	chr16:46723144-46723153 chr16:46723039-46723051 chr16:46723771-46723782 chr16:46723770-46723779
32	USF1	chr16:46722767-46723387	H1-hESC	embryonic stem cell:	n/a	chr16:46723072-46723088
33	POLR2A	chr16:46722198-46724309	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr16:46722324-46723806	HepG2	liver:	n/a	n/a
35	POLR2A	chr16:46722438-46724222	GM18526	blood:	n/a	n/a
36	SP1	chr16:46722833-46723783	HepG2	liver:	n/a	chr16:46723143-46723153 chr16:46723520-46723529 chr16:46723518-46723530 chr16:46723128-46723138 chr16:46723519-46723528 chr16:46723142-46723154 chr16:46723127-46723139 chr16:46723144-46723153 chr16:46722982-46722996 chr16:46723518-46723530 chr16:46723200-46723221 chr16:46723143-46723153 chr16:46723519-46723529 chr16:46723127-46723139 chr16:46723129-46723138 chr16:46723142-46723154 chr16:46723143-46723152 chr16:46723519-46723529 chr16:46723143-46723152 chr16:46723281-46723293 chr16:46723128-46723137
37	POLR2A	chr16:46722347-46724542	H1-hESC	embryonic stem cell:	n/a	n/a
38	SP4	chr16:46722804-46723434	H1-hESC	embryonic stem cell:	n/a	chr16:46723125-46723141 chr16:46723140-46723156 chr16:46723277-46723293
39	POLR2A	chr16:46722390-46724330	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr16:46722358-46724192	K562	blood:	n/a	n/a
41	MTA3	chr16:46721999-46723587	GM12878	blood:	n/a	n/a
42	POLR2A	chr16:46722349-46724257	K562	blood:	n/a	n/a
43	RFX5	chr16:46722386-46723667	Hela-S3	cervix:	n/a	chr16:46722815-46722829 chr16:46723464-46723473
44	MYC	chr16:46722207-46723632	MCF10A-Er-Src	breast:	n/a	chr16:46723128-46723138 chr16:46723102-46723111 chr16:46722716-46722732
45	POLR2A	chr16:46723198-46723786	HepG2	liver:	n/a	n/a
46	PAX5	chr16:46723180-46723809	GM12878	blood:	n/a	n/a
47	FOXA2	chr16:46723103-46723502	A549	lung:	n/a	n/a
48	MYC	chr16:46722141-46724290	NB4	blood:	n/a	chr16:46723128-46723138 chr16:46723102-46723111 chr16:46722716-46722732
49	TAF1	chr16:46722107-46723657	H1-neurons	neurons:	n/a	n/a
50	BHLHE40	chr16:46722889-46723497	HepG2	liver:	n/a	chr16:46723072-46723088

No.	Distal block	Cell Line	Cell type
1	chr16:46723293..46723894-chr6:26020511..26021178,2	Hela-S3	cervix:
2	chr15:50646591..50647385-chr16:46723275..46723855,2	Hela-S3	cervix:
3	chr16:46720929..46723857-chr16:46796007..46798416,2	MCF-7	breast:
4	chr16:46723337..46723856-chr16:67312562..67313464,2	Hela-S3	cervix:
5	chr16:46722783..46723664-chr19:49990885..49991440,2	Hela-S3	cervix:
6	chr16:46721087..46725989-chr16:46862740..46865236,7	K562	blood:
7	chr1:210547382..210548026-chr16:46722608..46723579,2	Hela-S3	cervix:
8	chr1:180123484..180124292-chr16:46722902..46723601,2	HCT-116	colon:
9	chr16:46721417..46725620-chr16:46861860..46865482,8	K562	blood:
10	chr16:46722548..46723423-chr16:87425505..87426277,2	Hela-S3	cervix:
11	chr1:75198609..75199364-chr16:46723157..46724066,2	Hela-S3	cervix:
12	chr16:46723133..46724018-chr9:139440419..139440966,2	NB4	blood:
13	chr16:46722901..46723856-chr5:108083974..108084613,2	Hela-S3	cervix:
14	chr16:46653721..46656886-chr16:46721851..46724551,4	K562	blood:
15	chr16:46711146..46713693-chr16:46721499..46723929,2	K562	blood:
16	chr1:153935466..153936188-chr16:46723180..46724080,2	Hela-S3	cervix:
17	chr16:46715468..46717180-chr16:46722050..46724165,2	MCF-7	breast:
18	chr16:46721631..46724836-chr16:46779909..46784170,7	K562	blood:
19	chr16:46723042..46725138-chr16:46863743..46865908,3	MCF-7	breast:
20	chr16:46681844..46684169-chr16:46721518..46723822,2	K562	blood:
21	chr16:46721630..46725552-chr16:46779076..46784170,6	K562	blood:

Variant related genes	Relation type
VPS35	TF binding region
ORC6	TF binding region
ENSG00000140795	Chromatin interaction
ENSG00000069329	Chromatin interaction
ENSG00000198366	Chromatin interaction
ENSG00000200972	Chromatin interaction
ENSG00000140941	Chromatin interaction
ENSG00000265181	Chromatin interaction
ENSG00000237886	Chromatin interaction
ENSG00000151422	Chromatin interaction
ENSG00000171241	Chromatin interaction
ENSG00000103264	Chromatin interaction
ENSG00000196155	Chromatin interaction
ENSG00000104064	Chromatin interaction
ENSG00000142541	Chromatin interaction
ENSG00000162623	Chromatin interaction
ENSG00000116260	Chromatin interaction
ENSG00000155330	Chromatin interaction
ENSG00000116791	Chromatin interaction
ENSG00000143570	Chromatin interaction
ENSG00000260909	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs35444809	1.00[AFR][1000 genomes]
rs55658937	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72810496	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72816832	0.92[AMR][1000 genomes]
rs72818807	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]

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	esv1799780	chr16:46386457-46875496	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv1060734	chr16:46463770-46768102	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv1064289	chr16:46463770-46801977	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
4	nsv1059456	chr16:46463770-47307580	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
5	nsv1066115	chr16:46463770-47318415	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
6	esv1797185	chr16:46489836-46731413	Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
7	nsv1066048	chr16:46500740-46998694	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
8	nsv542908	chr16:46500740-46998694	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
9	nsv1059147	chr16:46500740-47010960	Flanking Active TSS Active TSS Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers 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	54 gene(s)	inside rSNPs	diseases
10	nsv542909	chr16:46500740-47010960	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
11	nsv916976	chr16:46505597-46801868	Active TSS Bivalent Enhancer Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
12	nsv526656	chr16:46539392-46846663	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
13	nsv572536	chr16:46694649-46727385	Enhancers Strong transcription Genic enhancers Active TSS Weak transcription Flanking Active TSS 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 miRNA target site	30 gene(s)	inside rSNPs	diseases
14	esv1799771	chr16:46705343-46731413	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers 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	29 gene(s)	inside rSNPs	diseases
15	esv1792701	chr16:46709686-46751452	Bivalent/Poised TSS Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
16	nsv1059598	chr16:46721805-46762219	Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
17	nsv542913	chr16:46721805-46762219	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
18	nsv1064272	chr16:46721805-46768134	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription 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	29 gene(s)	inside rSNPs	diseases
19	nsv542914	chr16:46721805-46768134	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
20	nsv1067038	chr16:46721805-46797514	Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
21	nsv1066472	chr16:46721805-46801769	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
22	nsv1065253	chr16:46721805-46824369	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers 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	31 gene(s)	inside rSNPs	diseases
23	nsv1059049	chr16:46721805-46859239	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
24	nsv1061651	chr16:46721805-46915511	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
25	nsv1060982	chr16:46721805-46938858	Enhancers Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:46720000-46724200	Active TSS	Fetal Intestine Large	intestine
2	chr16:46720600-46724200	Active TSS	Fetal Intestine Small	intestine
3	chr16:46721000-46724800	Active TSS	NHDF-Ad	bronchial
4	chr16:46721000-46725000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr16:46721200-46724600	Active TSS	HUES6 Cell Line	embryonic stem cell
6	chr16:46721200-46725000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr16:46721200-46725600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr16:46721400-46724000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr16:46721400-46724800	Active TSS	H9 Cell Line	embryonic stem cell
10	chr16:46721400-46724800	Active TSS	HUES48 Cell Line	embryonic stem cell
11	chr16:46721400-46725800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr16:46721600-46724800	Active TSS	iPS-15b Cell Line	embryonic stem cell
13	chr16:46721600-46724800	Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr16:46721600-46724800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr16:46721600-46725200	Active TSS	ES-I3 Cell Line	embryonic stem cell
16	chr16:46721800-46723800	Active TSS	Fetal Muscle Trunk	muscle
17	chr16:46721800-46723800	Active TSS	Pancreas	Pancrea
18	chr16:46721800-46724000	Active TSS	Breast Myoepithelial Primary Cells	Breast
19	chr16:46721800-46724000	Active TSS	Brain Angular Gyrus	brain
20	chr16:46721800-46724000	Active TSS	Duodenum Mucosa	Duodenum
21	chr16:46721800-46724000	Active TSS	Left Ventricle	heart
22	chr16:46721800-46724000	Active TSS	Sigmoid Colon	Sigmoid Colon
23	chr16:46721800-46724200	Active TSS	Ovary	ovary
24	chr16:46721800-46724200	Active TSS	Psoas Muscle	Psoas
25	chr16:46721800-46724200	Active TSS	Right Ventricle	heart
26	chr16:46721800-46724200	Active TSS	Stomach Mucosa	stomach
27	chr16:46721800-46724400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr16:46721800-46724400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr16:46721800-46724400	Active TSS	Pancreatic Islets	Pancreatic Islet
30	chr16:46721800-46724400	Active TSS	Right Atrium	heart
31	chr16:46721800-46724600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr16:46721800-46724800	Active TSS	H1 Cell Line	embryonic stem cell
33	chr16:46721800-46724800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr16:46721800-46724800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr16:46721800-46724800	Active TSS	Esophagus	oesophagus
36	chr16:46721800-46724800	Active TSS	A549	lung
37	chr16:46721800-46725000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr16:46721800-46725000	Active TSS	Colonic Mucosa	Colon
39	chr16:46721800-46725200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr16:46721800-46725200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr16:46721800-46725200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr16:46721800-46725200	Active TSS	GM12878-XiMat	blood
43	chr16:46721800-46725800	Active TSS	NHLF	lung
44	chr16:46722000-46723800	Active TSS	Primary monocytes fromperipheralblood	blood
45	chr16:46722000-46723800	Active TSS	Placenta	Placenta
46	chr16:46722000-46724000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
47	chr16:46722000-46724000	Active TSS	Fetal Muscle Leg	muscle
48	chr16:46722000-46724000	Active TSS	Fetal Stomach	stomach
49	chr16:46722000-46724000	Active TSS	Rectal Smooth Muscle	rectum
50	chr16:46722000-46724200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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