Variant report

Variant	rs2278045
Chromosome Location	chr16:77224863-77224864
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	TBP	chr16:77224374-77225315	HepG2	liver:	n/a	n/a
2	MAZ	chr16:77224265-77226878	IMR90	lung:	n/a	n/a
3	SP2	chr16:77224341-77225069	H1-hESC	embryonic stem cell:	n/a	chr16:77224435-77224458 chr16:77224989-77225012
4	STAT5A	chr16:77224678-77225842	GM12878	blood:	n/a	chr16:77225036-77225059 chr16:77225657-77225669 chr16:77225705-77225712
5	SP1	chr16:77224243-77225255	GM12878	blood:	n/a	chr16:77224735-77224756 chr16:77224347-77224360
6	POLR2A	chr16:77224094-77225735	GM12878	blood:	n/a	n/a
7	E2F6	chr16:77224531-77224889	K562	blood:	n/a	chr16:77224702-77224709 chr16:77224702-77224710 chr16:77224701-77224712 chr16:77224702-77224710 chr16:77224701-77224711
8	JUND	chr16:77224481-77225142	HepG2	liver:	n/a	n/a
9	POLR2A	chr16:77223958-77226689	MCF10A-Er-Src	breast:	n/a	n/a
10	GABPA	chr16:77224542-77225224	HepG2	liver:	n/a	n/a
11	CTCF	chr16:77224800-77224950	NHLF	lung:	n/a	n/a
12	TAF1	chr16:77224213-77225320	MCF-7	breast:	n/a	n/a
13	POLR2A	chr16:77224188-77225482	U87	brain:	n/a	n/a
14	SP1	chr16:77224400-77225047	K562	blood:	n/a	chr16:77224735-77224756
15	MXI1	chr16:77224183-77225745	HepG2	liver:	n/a	n/a
16	POLR2A	chr16:77223956-77225823	GM12892	blood:	n/a	n/a
17	CTCF	chr16:77224780-77224930	AG04449	skin:	n/a	n/a
18	TAF1	chr16:77224777-77225189	Hela-S3	cervix:	n/a	n/a
19	TBP	chr16:77224420-77225354	GM12878	blood:	n/a	n/a
20	CTCF	chr16:77224820-77224970	AG10803	skin:	n/a	n/a
21	RFX5	chr16:77224337-77225263	GM12878	blood:	n/a	n/a
22	POLR2A	chr16:77223928-77228004	GM12878	blood:	n/a	n/a
23	STAT5A	chr16:77224700-77225224	GM12878	blood:	n/a	chr16:77225036-77225059
24	POLR2A	chr16:77224339-77225655	NB4	blood:	n/a	n/a
25	MAZ	chr16:77224273-77225353	HepG2	liver:	n/a	n/a
26	POLR2A	chr16:77224314-77225369	HCT-116	colon:	n/a	n/a
27	RCOR1	chr16:77224139-77225357	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr16:77224840-77224990	HMEC	breast:	n/a	n/a
29	E2F4	chr16:77224164-77225207	K562	blood:	n/a	chr16:77224702-77224709 chr16:77224980-77224992 chr16:77224702-77224710 chr16:77224701-77224712 chr16:77224702-77224710 chr16:77224701-77224711 chr16:77224201-77224213
30	POLR2A	chr16:77224108-77225456	MCF-7	breast:	n/a	n/a
31	ELF1	chr16:77223970-77225648	HCT-116	colon:	n/a	chr16:77225022-77225033 chr16:77225023-77225032 chr16:77225081-77225090 chr16:77225052-77225061 chr16:77225051-77225062 chr16:77225022-77225033 chr16:77225080-77225091 chr16:77225051-77225062 chr16:77225080-77225091
32	TAF1	chr16:77224359-77225252	K562	blood:	n/a	n/a
33	ELF1	chr16:77224004-77225445	K562	blood:	n/a	chr16:77225022-77225033 chr16:77225023-77225032 chr16:77225081-77225090 chr16:77225052-77225061 chr16:77225051-77225062 chr16:77225022-77225033 chr16:77225080-77225091 chr16:77225051-77225062 chr16:77225080-77225091
34	POLR2A	chr16:77224272-77225177	HUVEC	blood vessel:	n/a	n/a
35	RFX5	chr16:77224345-77225172	HepG2	liver:	n/a	n/a
36	POLR2A	chr16:77224737-77225740	HL-60	blood:	n/a	n/a
37	TBP	chr16:77224393-77225288	Hela-S3	cervix:	n/a	n/a
38	GABPA	chr16:77224188-77225748	A549	lung:	n/a	n/a
39	POLR2A	chr16:77224070-77225803	GM12878	blood:	n/a	n/a
40	POLR2A	chr16:77223991-77225829	GM18951	blood:	n/a	n/a
41	POLR2A	chr16:77224315-77225788	HL-60	blood:	n/a	n/a
42	POLR2A	chr16:77224371-77225364	PANC-1	pancreas:	n/a	n/a
43	POLR2A	chr16:77224728-77225139	A549	lung:	n/a	n/a
44	UBTF	chr16:77224362-77225319	K562	blood:	n/a	n/a
45	IRF3	chr16:77224493-77224946	GM12878	blood:	n/a	chr16:77224507-77224521 chr16:77224506-77224518
46	YY1	chr16:77224709-77225273	GM12878	blood:	n/a	n/a
47	NFIC	chr16:77224340-77225344	HepG2	liver:	n/a	n/a
48	USF1	chr16:77224718-77225262	A549	lung:	n/a	n/a
49	CEBPB	chr16:77224206-77225382	A549	lung:	n/a	n/a
50	TAF1	chr16:77224207-77225369	ECC-1	luminal epithelium:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:77223598..77226407-chr16:77245076..77246907,2	MCF-7	breast:
2	chr16:75588082..75590325-chr16:77223299..77225155,3	K562	blood:
3	chr11:66360307..66360987-chr16:77224555..77225280,2	Hela-S3	cervix:
4	chr16:77223287..77227235-chr16:77231893..77237199,5	MCF-7	breast:
5	chr16:77224130..77224935-chr22:41863949..41864740,2	Hela-S3	cervix:
6	chr16:77224632..77225508-chr5:43483543..43484113,2	Hela-S3	cervix:
7	chr16:77224416..77225113-chr9:131940115..131940671,2	Hela-S3	cervix:
8	chr16:77223216..77226884-chr16:77251990..77255920,6	MCF-7	breast:
9	chr16:75680522..75683233-chr16:77224728..77226496,3	MCF-7	breast:
10	chr16:75680135..75682966-chr16:77223241..77226200,3	MCF-7	breast:
11	chr16:77223534..77226455-chr16:77227601..77231752,9	MCF-7	breast:
12	chr1:200638562..200641266-chr16:77224293..77226737,2	MCF-7	breast:
13	chr16:77223627..77226316-chr16:77230976..77234622,5	MCF-7	breast:
14	chr16:77223923..77226639-chr16:77244818..77248823,8	K562	blood:
15	chr16:77224814..77227187-chr16:77245098..77247161,3	K562	blood:

Variant related genes	Relation type
MON1B	TF binding region
ENSG00000205084	Chromatin interaction
ENSG00000173992	Chromatin interaction
ENSG00000103111	Chromatin interaction
ENSG00000249492	Chromatin interaction
ENSG00000226348	Chromatin interaction
ENSG00000205078	Chromatin interaction
ENSG00000151881	Chromatin interaction
ENSG00000188483	Chromatin interaction
ENSG00000260088	Chromatin interaction
ENSG00000182791	Chromatin interaction
ENSG00000118197	Chromatin interaction
ENSG00000100410	Chromatin interaction
ENSG00000065427	Chromatin interaction
ENSG00000166848	Chromatin interaction

Extended variants
information (count: 68 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10781982	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11149970	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11149972	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11149975	0.82[ASN][1000 genomes]
rs11639911	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11649440	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12447059	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12448094	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12716823	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2113282	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2161715	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs2232504	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.92[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2232509	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2241415	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2241416	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34143201	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35660173	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3743759	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];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3743761	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3743762	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3760004	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3760005	0.90[CHB][hapmap];0.80[JPT][hapmap];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3760006	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3760007	1.00[CHB][hapmap];0.88[JPT][hapmap];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4887893	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62049594	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62049596	0.94[ASN][1000 genomes]
rs6420403	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6564404	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6564405	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6564406	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6564407	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6564408	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6564409	1.00[CHB][hapmap];0.84[JPT][hapmap]
rs6564414	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7185297	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7185889	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7194408	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7195255	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7202265	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7204238	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7205119	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8047912	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8048285	0.96[CEU][hapmap];0.92[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.93[MEX][hapmap];0.95[TSI][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8052509	1.00[CEU][hapmap];0.92[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.93[MEX][hapmap];0.93[TSI][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8062063	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9923489	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9924160	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9924694	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9930201	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9930541	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9939130	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9939212	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869201	chr16:76714549-77233646	Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
2	nsv1057677	chr16:76861946-77230013	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
3	nsv1065343	chr16:76927295-77279747	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	nsv542965	chr16:76927295-77279747	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
5	nsv1055234	chr16:77003426-77467286	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
6	nsv1065048	chr16:77003426-77675163	Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
7	esv2830376	chr16:77014551-77658185	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
8	nsv1065149	chr16:77032082-77671890	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
9	nsv1062349	chr16:77039764-77458731	Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
10	nsv542967	chr16:77039764-77458731	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
11	nsv1056676	chr16:77139682-77854848	Strong transcription Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
12	nsv906954	chr16:77197633-77227180	Flanking Active TSS Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	21 gene(s)	inside rSNPs	diseases
13	nsv827756	chr16:77198788-77225812	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	21 gene(s)	inside rSNPs	diseases
14	nsv906955	chr16:77202701-77227180	Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	21 gene(s)	inside rSNPs	diseases
15	esv11803	chr16:77224589-77227011	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2278045	SYCE1L	cis	Artery Tibial	GTEx
rs2278045	MON1B	cis	Whole Blood	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:77223200-77226200	Active TSS	HUES64 Cell Line	embryonic stem cell
2	chr16:77223400-77226600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr16:77223600-77225600	Active TSS	iPS-18 Cell Line	embryonic stem cell
4	chr16:77223600-77226200	Active TSS	H1 Cell Line	embryonic stem cell
5	chr16:77223800-77225600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr16:77223800-77225600	Active TSS	Breast Myoepithelial Primary Cells	Breast
7	chr16:77223800-77225600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr16:77223800-77225600	Active TSS	Pancreatic Islets	Pancreatic Islet
9	chr16:77223800-77225600	Active TSS	Rectal Mucosa Donor 29	rectum
10	chr16:77223800-77225600	Active TSS	HMEC	breast
11	chr16:77223800-77225800	Active TSS	HUES48 Cell Line	embryonic stem cell
12	chr16:77223800-77225800	Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr16:77223800-77225800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr16:77223800-77225800	Active TSS	Placenta Amnion	Placenta Amnion
15	chr16:77223800-77226000	Active TSS	ES-I3 Cell Line	embryonic stem cell
16	chr16:77223800-77226000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr16:77223800-77226000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr16:77223800-77226000	Active TSS	GM12878-XiMat	blood
19	chr16:77223800-77226000	Active TSS	K562	blood
20	chr16:77223800-77226200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
21	chr16:77223800-77226600	Active TSS	HUES6 Cell Line	embryonic stem cell
22	chr16:77224000-77225400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr16:77224000-77225400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr16:77224000-77225400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
25	chr16:77224000-77225400	Active TSS	Primary T helper naive cells from peripheral blood	blood
26	chr16:77224000-77225400	Active TSS	Primary T killer naive cells fromperipheralblood	blood
27	chr16:77224000-77225400	Active TSS	Fetal Lung	lung
28	chr16:77224000-77225400	Active TSS	Fetal Stomach	stomach
29	chr16:77224000-77225400	Active TSS	Left Ventricle	heart
30	chr16:77224000-77225400	Active TSS	Rectal Mucosa Donor 31	rectum
31	chr16:77224000-77225400	Active TSS	Skeletal Muscle Male	skeletal muscle
32	chr16:77224000-77225400	Active TSS	Osteobl	bone
33	chr16:77224000-77225600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr16:77224000-77225600	Active TSS	Primary hematopoietic stem cells short term culture	blood
35	chr16:77224000-77225600	Active TSS	Primary T killer memory cells from peripheral blood	blood
36	chr16:77224000-77225600	Active TSS	Muscle Satellite Cultured Cells	--
37	chr16:77224000-77225600	Active TSS	Liver	Liver
38	chr16:77224000-77225600	Active TSS	Brain Anterior Caudate	brain
39	chr16:77224000-77225600	Active TSS	Brain Cingulate Gyrus	brain
40	chr16:77224000-77225600	Active TSS	Brain Hippocampus Middle	brain
41	chr16:77224000-77225600	Active TSS	Brain Inferior Temporal Lobe	brain
42	chr16:77224000-77225600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
43	chr16:77224000-77225600	Active TSS	Colon Smooth Muscle	Colon
44	chr16:77224000-77225600	Active TSS	Duodenum Smooth Muscle	Duodenum
45	chr16:77224000-77225600	Active TSS	Fetal Brain Male	brain
46	chr16:77224000-77225600	Active TSS	Fetal Brain Female	brain
47	chr16:77224000-77225600	Active TSS	Fetal Heart	heart
48	chr16:77224000-77225600	Active TSS	Pancreas	Pancrea
49	chr16:77224000-77225600	Active TSS	Rectal Smooth Muscle	rectum
50	chr16:77224000-77225600	Active TSS	Right Ventricle	heart

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