Variant report

Variant	rs74017935
Chromosome Location	chr16:48399445-48399446
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	KAP1	chr16:48398837-48399846	U2OS	brain:	n/a	n/a
2	MTA3	chr16:48399254-48400963	GM12878	blood:	n/a	n/a
3	NR2F2	chr16:48399419-48400743	K562	blood:	n/a	n/a
4	POLR2A	chr16:48398316-48401000	A549	lung:	n/a	n/a
5	RELA	chr16:48399405-48400889	GM15510	blood:	n/a	n/a
6	POLR2A	chr16:48398255-48402133	HepG2	liver:	n/a	n/a
7	GTF2F1	chr16:48399351-48400816	Hela-S3	cervix:	n/a	n/a
8	POLR2A	chr16:48399196-48400647	GM19193	blood:	n/a	n/a
9	POLR2A	chr16:48399215-48400737	PBDE	blood:	n/a	n/a
10	POLR2A	chr16:48399298-48400768	Hela-S3	cervix:	n/a	n/a
11	POLR2A	chr16:48399384-48400808	K562	blood:	n/a	n/a
12	FOXA1	chr16:48399019-48400039	HepG2	liver:	n/a	n/a
13	TEAD4	chr16:48399350-48400304	K562	blood:	n/a	n/a
14	POLR2A	chr16:48399445-48400763	GM12892	blood:	n/a	n/a
15	MAZ	chr16:48398908-48400774	K562	blood:	n/a	chr16:48399984-48399993 chr16:48399995-48400005 chr16:48400548-48400557
16	SMC3	chr16:48399239-48399809	HepG2	liver:	n/a	chr16:48399437-48399447
17	MAX	chr16:48399199-48400751	K562	blood:	n/a	chr16:48399984-48399993 chr16:48399995-48400005 chr16:48400548-48400557
18	SIN3A	chr16:48399360-48400779	H1-hESC	embryonic stem cell:	n/a	n/a
19	MYC	chr16:48398993-48400894	K562	blood:	n/a	chr16:48399984-48399993 chr16:48399995-48400005 chr16:48400548-48400557
20	CHD1	chr16:48399444-48400758	GM12878	blood:	n/a	n/a
21	MXI1	chr16:48399334-48400958	SK-N-SH	brain:	n/a	n/a
22	CTCF	chr16:48399400-48399550	HCM	heart:	n/a	chr16:48399434-48399447
23	MYC	chr16:48399426-48400771	K562	blood:	n/a	chr16:48399984-48399993 chr16:48399995-48400005 chr16:48400548-48400557
24	MYBL2	chr16:48399417-48400808	HepG2	liver:	n/a	n/a
25	SIN3AK20	chr16:48399409-48400163	MCF-7	breast:	n/a	n/a
26	POLR2A	chr16:48399163-48400940	U87	brain:	n/a	n/a
27	MAZ	chr16:48399414-48400254	HepG2	liver:	n/a	chr16:48399984-48399993 chr16:48399995-48400005
28	POLR2A	chr16:48399350-48400235	ECC-1	luminal epithelium:	n/a	n/a
29	CTCF	chr16:48399440-48399590	HBMEC	blood vessel:	n/a	n/a
30	POLR2A	chr16:48398880-48400775	U87	brain:	n/a	n/a
31	POLR2A	chr16:48399259-48400743	MCF10A-Er-Src	breast:	n/a	n/a
32	FOXA1	chr16:48399131-48399487	HepG2	liver:	n/a	n/a
33	POLR2A	chr16:48398185-48400983	GM12891	blood:	n/a	n/a
34	TAF1	chr16:48399425-48400045	A549	lung:	n/a	n/a
35	POLR2A	chr16:48399166-48400260	K562	blood:	n/a	n/a
36	POLR2A	chr16:48399412-48400104	HL-60	blood:	n/a	n/a
37	POLR2A	chr16:48399440-48400250	PFSK-1	brain:	n/a	n/a
38	POLR2A	chr16:48399316-48401060	HCT-116	colon:	n/a	n/a
39	POLR2A	chr16:48398274-48400807	K562	blood:	n/a	n/a
40	JUND	chr16:48398887-48400764	K562	blood:	n/a	chr16:48399960-48399969 chr16:48399118-48399127
41	POLR2A	chr16:48398921-48400728	K562	blood:	n/a	n/a
42	EP300	chr16:48399430-48399958	HepG2	liver:	n/a	chr16:48399758-48399767
43	CTCF	chr16:48399400-48399550	HAc	cerebellar:	n/a	chr16:48399434-48399447
44	PML	chr16:48399251-48400871	GM12878	blood:	n/a	n/a
45	FOSL2	chr16:48399157-48400236	HepG2	liver:	n/a	chr16:48399960-48399969
46	POLR2A	chr16:48398492-48400809	GM12878	blood:	n/a	n/a
47	ZMIZ1	chr16:48399078-48400794	K562	blood:	n/a	n/a
48	BHLHE40	chr16:48399088-48400804	K562	blood:	n/a	n/a
49	UBTF	chr16:48398863-48400763	K562	blood:	n/a	n/a
50	TBP	chr16:48399350-48400773	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:48398121..48402229-chr16:48414201..48420573,11	MCF-7	breast:
2	chr16:48390430..48396082-chr16:48398412..48402671,6	MCF-7	breast:
3	chr16:48396253..48404408-chr16:48411826..48421166,27	K562	blood:
4	chr16:48397931..48401931-chr16:48416758..48423536,12	MCF-7	breast:
5	chr16:48398982..48401730-chr16:48643542..48645764,2	K562	blood:
6	chr16:48387428..48394420-chr16:48394893..48400608,15	K562	blood:

Variant related genes	Relation type
SIAH1	TF binding region
ENSG00000102910	Chromatin interaction
ENSG00000102921	Chromatin interaction
ENSG00000196470	Chromatin interaction

Extended variants
information (count: 211 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:200)

rs_ID	r²[population]
rs13330237	1.00[AMR][1000 genomes]
rs13339188	1.00[AMR][1000 genomes]
rs16946016	1.00[AMR][1000 genomes]
rs16946018	1.00[AMR][1000 genomes]
rs16946020	1.00[AMR][1000 genomes]
rs16946022	1.00[AMR][1000 genomes]
rs16946024	1.00[AMR][1000 genomes]
rs16946028	1.00[AMR][1000 genomes]
rs16946031	1.00[AMR][1000 genomes]
rs16946033	1.00[AMR][1000 genomes]
rs16946035	1.00[AMR][1000 genomes]
rs16946042	1.00[AMR][1000 genomes]
rs16946044	1.00[AMR][1000 genomes]
rs16946046	1.00[AMR][1000 genomes]
rs16946047	1.00[AMR][1000 genomes]
rs16946049	1.00[AMR][1000 genomes]
rs16946050	1.00[AMR][1000 genomes]
rs16946055	1.00[AMR][1000 genomes]
rs16946056	1.00[AMR][1000 genomes]
rs16946077	1.00[AMR][1000 genomes]
rs16946084	1.00[AMR][1000 genomes]
rs16946088	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16946097	1.00[AMR][1000 genomes]
rs16946106	1.00[AMR][1000 genomes]
rs16946113	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16946115	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16946118	1.00[AMR][1000 genomes]
rs16946120	1.00[AMR][1000 genomes]
rs16946145	1.00[AMR][1000 genomes]
rs16946162	1.00[AMR][1000 genomes]
rs16946199	1.00[AMR][1000 genomes]
rs2046528	1.00[AMR][1000 genomes]
rs2046529	1.00[AMR][1000 genomes]
rs2046530	1.00[AMR][1000 genomes]
rs2160564	1.00[AMR][1000 genomes]
rs2353650	1.00[AMR][1000 genomes]
rs28387003	1.00[AMR][1000 genomes]
rs28407298	1.00[AMR][1000 genomes]
rs28699264	1.00[AMR][1000 genomes]
rs28722105	1.00[AMR][1000 genomes]
rs34437640	1.00[AMR][1000 genomes]
rs35730749	1.00[AMR][1000 genomes]
rs4583238	1.00[AMR][1000 genomes]
rs4619404	1.00[AMR][1000 genomes]
rs55650659	1.00[AMR][1000 genomes]
rs55650780	1.00[AMR][1000 genomes]
rs55727534	1.00[AMR][1000 genomes]
rs55759468	1.00[AMR][1000 genomes]
rs55767683	1.00[AMR][1000 genomes]
rs55791428	1.00[AMR][1000 genomes]
rs55894153	1.00[AMR][1000 genomes]
rs55939380	1.00[AMR][1000 genomes]
rs55945004	1.00[AMR][1000 genomes]
rs56006148	1.00[AMR][1000 genomes]
rs56039807	1.00[AMR][1000 genomes]
rs56056936	1.00[AMR][1000 genomes]
rs56068904	1.00[AMR][1000 genomes]
rs56153325	1.00[AMR][1000 genomes]
rs56183549	1.00[AMR][1000 genomes]
rs56210528	1.00[AMR][1000 genomes]
rs56252717	1.00[AMR][1000 genomes]
rs56270052	1.00[AMR][1000 genomes]
rs56379814	1.00[AMR][1000 genomes]
rs56403551	1.00[AMR][1000 genomes]
rs56739366	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57031394	1.00[AMR][1000 genomes]
rs57045758	1.00[AMR][1000 genomes]
rs57276104	1.00[AMR][1000 genomes]
rs57435271	1.00[AMR][1000 genomes]
rs57646139	1.00[AMR][1000 genomes]
rs57760532	1.00[AMR][1000 genomes]
rs57815195	1.00[AMR][1000 genomes]
rs57850865	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57858756	1.00[AMR][1000 genomes]
rs58068024	1.00[AMR][1000 genomes]
rs58095119	1.00[AMR][1000 genomes]
rs58315149	1.00[AMR][1000 genomes]
rs58405777	1.00[AMR][1000 genomes]
rs58531648	1.00[AMR][1000 genomes]
rs58909828	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58952249	1.00[AMR][1000 genomes]
rs59077393	1.00[AMR][1000 genomes]
rs59103644	1.00[AMR][1000 genomes]
rs59174783	1.00[AMR][1000 genomes]
rs59247940	1.00[AMR][1000 genomes]
rs59295735	1.00[AMR][1000 genomes]
rs59382226	1.00[AMR][1000 genomes]
rs59893238	1.00[AMR][1000 genomes]
rs59966044	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60162759	1.00[AMR][1000 genomes]
rs60230358	1.00[AMR][1000 genomes]
rs60461572	1.00[AMR][1000 genomes]
rs60494112	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60659794	1.00[AMR][1000 genomes]
rs60731420	1.00[AMR][1000 genomes]
rs60791230	1.00[AMR][1000 genomes]
rs60944057	1.00[AMR][1000 genomes]
rs60962209	1.00[AMR][1000 genomes]
rs60983423	1.00[AMR][1000 genomes]
rs61055548	1.00[AMR][1000 genomes]
rs61173366	1.00[AMR][1000 genomes]
rs61238817	1.00[AMR][1000 genomes]
rs61528456	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74016321	1.00[AMR][1000 genomes]
rs74016322	1.00[AMR][1000 genomes]
rs74016323	1.00[AMR][1000 genomes]
rs74016324	1.00[AMR][1000 genomes]
rs74016326	1.00[AMR][1000 genomes]
rs74016331	1.00[AMR][1000 genomes]
rs74016333	1.00[AMR][1000 genomes]
rs74016334	1.00[AMR][1000 genomes]
rs74016335	1.00[AMR][1000 genomes]
rs74016337	1.00[AMR][1000 genomes]
rs74016338	1.00[AMR][1000 genomes]
rs74016339	1.00[AMR][1000 genomes]
rs74016340	1.00[AMR][1000 genomes]
rs74016341	1.00[AMR][1000 genomes]
rs74016342	1.00[AMR][1000 genomes]
rs74016343	1.00[AMR][1000 genomes]
rs74016344	1.00[AMR][1000 genomes]
rs74016345	1.00[AMR][1000 genomes]
rs74016346	1.00[AMR][1000 genomes]
rs74016347	1.00[AMR][1000 genomes]
rs74016348	1.00[AMR][1000 genomes]
rs74016349	1.00[AMR][1000 genomes]
rs74016350	1.00[AMR][1000 genomes]
rs74016351	1.00[AMR][1000 genomes]
rs74016352	1.00[AMR][1000 genomes]
rs74016353	1.00[AMR][1000 genomes]
rs74016355	1.00[AMR][1000 genomes]
rs74016357	1.00[AMR][1000 genomes]
rs74016358	1.00[AMR][1000 genomes]
rs74016362	1.00[AMR][1000 genomes]
rs74016363	1.00[AMR][1000 genomes]
rs74016367	1.00[AMR][1000 genomes]
rs74016372	1.00[AMR][1000 genomes]
rs74016375	1.00[AMR][1000 genomes]
rs74016376	1.00[AMR][1000 genomes]
rs74016377	1.00[AMR][1000 genomes]
rs74016378	1.00[AMR][1000 genomes]
rs74016379	1.00[AMR][1000 genomes]
rs74016381	1.00[AMR][1000 genomes]
rs74016382	1.00[AMR][1000 genomes]
rs74016383	1.00[AMR][1000 genomes]
rs74016384	1.00[AMR][1000 genomes]
rs74016385	1.00[AMR][1000 genomes]
rs74016386	1.00[AMR][1000 genomes]
rs74016387	1.00[AMR][1000 genomes]
rs74016388	1.00[AMR][1000 genomes]
rs74016389	1.00[AMR][1000 genomes]
rs74016390	1.00[AMR][1000 genomes]
rs74016391	1.00[AMR][1000 genomes]
rs74016392	1.00[AMR][1000 genomes]
rs74016393	1.00[AMR][1000 genomes]
rs74016394	1.00[AMR][1000 genomes]
rs74016396	1.00[AMR][1000 genomes]
rs74016397	1.00[AMR][1000 genomes]
rs74016398	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74016399	1.00[AMR][1000 genomes]
rs74016400	1.00[AMR][1000 genomes]
rs74016401	1.00[AMR][1000 genomes]
rs74016402	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74017903	1.00[AMR][1000 genomes]
rs74017904	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74017905	1.00[AMR][1000 genomes]
rs74017907	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74017908	1.00[AMR][1000 genomes]
rs74017909	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74017910	1.00[AMR][1000 genomes]
rs74017913	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74017914	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74017917	1.00[AMR][1000 genomes]
rs74017920	1.00[AMR][1000 genomes]
rs74017922	1.00[AMR][1000 genomes]
rs74017923	1.00[AMR][1000 genomes]
rs74017924	1.00[AMR][1000 genomes]
rs74017927	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74017928	1.00[AMR][1000 genomes]
rs74017929	1.00[AMR][1000 genomes]
rs74017930	1.00[AMR][1000 genomes]
rs74017931	1.00[AMR][1000 genomes]
rs74017932	1.00[AMR][1000 genomes]
rs74017933	1.00[AMR][1000 genomes]
rs74017934	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74017938	1.00[AMR][1000 genomes]
rs74017943	1.00[AMR][1000 genomes]
rs74017945	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74017946	1.00[AMR][1000 genomes]
rs74017947	1.00[AMR][1000 genomes]
rs74017948	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74017950	1.00[AMR][1000 genomes]
rs74017951	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74017952	1.00[AMR][1000 genomes]
rs74017955	1.00[AMR][1000 genomes]
rs74017956	1.00[AMR][1000 genomes]
rs9925219	1.00[AMR][1000 genomes]
rs9926097	1.00[AMR][1000 genomes]
rs9928523	1.00[AMR][1000 genomes]
rs9937947	1.00[AMR][1000 genomes]
rs9940809	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1061316	chr16:48264175-48594219	Weak transcription Strong transcription Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' 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
2	esv1821072	chr16:48268318-48504364	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv833219	chr16:48290595-48459301	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv1061708	chr16:48304343-48482594	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
5	nsv542917	chr16:48304343-48482594	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
6	esv2758424	chr16:48329437-48479754	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
7	esv2758645	chr16:48329437-48479754	ZNF genes & repeats Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
8	esv1837150	chr16:48375777-48470715	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
9	esv1802902	chr16:48394626-48419662	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	22 gene(s)	inside rSNPs	diseases
10	esv1836876	chr16:48395527-48459558	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent Enhancer 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	26 gene(s)	inside rSNPs	diseases
11	esv1842331	chr16:48395527-48459558	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 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	chr16:48397400-48399600	Enhancers	Sigmoid Colon	Sigmoid Colon
2	chr16:48398200-48399600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr16:48398200-48399800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr16:48398200-48399800	Flanking Active TSS	Adipose Nuclei	Adipose
5	chr16:48398400-48399600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr16:48398400-48399600	Enhancers	Small Intestine	intestine
7	chr16:48398400-48399600	Flanking Active TSS	HMEC	breast
8	chr16:48398400-48399800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
9	chr16:48398400-48399800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr16:48398400-48399800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
11	chr16:48398400-48399800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
12	chr16:48398400-48400400	Weak transcription	Dnd41	blood
13	chr16:48398600-48399600	Flanking Active TSS	Stomach Smooth Muscle	stomach
14	chr16:48398600-48399600	Flanking Active TSS	K562	blood
15	chr16:48398600-48399600	Flanking Active TSS	NHEK	skin
16	chr16:48398600-48399800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
17	chr16:48398600-48399800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
18	chr16:48398600-48400600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
19	chr16:48398800-48399600	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr16:48398800-48399600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
21	chr16:48398800-48399600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr16:48398800-48399600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
23	chr16:48398800-48399600	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
24	chr16:48398800-48399600	Enhancers	Placenta Amnion	Placenta Amnion
25	chr16:48398800-48399800	Flanking Active TSS	H1 Cell Line	embryonic stem cell
26	chr16:48398800-48399800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr16:48398800-48399800	Flanking Active TSS	Fetal Heart	heart
28	chr16:48398800-48399800	Flanking Active TSS	Stomach Mucosa	stomach
29	chr16:48398800-48399800	Flanking Active TSS	GM12878-XiMat	blood
30	chr16:48399000-48399600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr16:48399000-48399600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
32	chr16:48399000-48399600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
33	chr16:48399000-48399600	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr16:48399000-48399600	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr16:48399000-48399600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
36	chr16:48399000-48399600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr16:48399000-48399600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr16:48399000-48399600	Flanking Active TSS	Brain Cingulate Gyrus	brain
39	chr16:48399000-48399600	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
40	chr16:48399000-48399600	Flanking Active TSS	Colonic Mucosa	Colon
41	chr16:48399000-48399600	Flanking Active TSS	Rectal Smooth Muscle	rectum
42	chr16:48399000-48399800	Flanking Active TSS	Brain Angular Gyrus	brain
43	chr16:48399000-48399800	Flanking Active TSS	Duodenum Mucosa	Duodenum
44	chr16:48399000-48399800	Flanking Active TSS	Fetal Stomach	stomach
45	chr16:48399000-48399800	Flanking Active TSS	Hela-S3	cervix
46	chr16:48399000-48399800	Flanking Active TSS	HSMM	muscle
47	chr16:48399000-48399800	Flanking Active TSS	HSMMtube	muscle
48	chr16:48399000-48399800	Flanking Active TSS	NHLF	lung
49	chr16:48399000-48399800	Flanking Active TSS	Osteobl	bone
50	chr16:48399000-48400000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin

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