Variant report

Variant	rs533508234
Chromosome Location	chr16:30968610-30968611
allele	A/G
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	FOS	chr16:30968270-30968621	MCF10A-Er-Src	breast:	n/a	chr16:30968443-30968453 chr16:30968443-30968453 chr16:30968440-30968451 chr16:30968444-30968452
2	BRCA1	chr16:30968272-30969162	Hela-S3	cervix:	n/a	n/a
3	PML	chr16:30967973-30969524	GM12878	blood:	n/a	chr16:30968445-30968454
4	SP1	chr16:30968002-30969953	HCT-116	colon:	n/a	chr16:30969028-30969035 chr16:30968557-30968569 chr16:30969720-30969730 chr16:30968576-30968590 chr16:30969742-30969752 chr16:30969023-30969037 chr16:30969412-30969426 chr16:30968558-30968568 chr16:30969024-30969033 chr16:30969023-30969032 chr16:30968576-30968586 chr16:30968557-30968569 chr16:30969737-30969746 chr16:30968559-30968568 chr16:30968427-30968436 chr16:30968558-30968572 chr16:30969706-30969720 chr16:30969539-30969553 chr16:30968575-30968587 chr16:30969540-30969549 chr16:30969022-30969034 chr16:30969741-30969753 chr16:30969732-30969746 chr16:30968558-30968568 chr16:30969735-30969747 chr16:30969023-30969033 chr16:30969720-30969730 chr16:30969719-30969731 chr16:30968943-30968955 chr16:30969416-30969425 chr16:30969716-30969730 chr16:30968575-30968587 chr16:30968558-30968567 chr16:30969538-30969550 chr16:30968577-30968586 chr16:30969741-30969753 chr16:30969720-30969729 chr16:30969721-30969730 chr16:30969538-30969550 chr16:30969735-30969747 chr16:30969736-30969745 chr16:30968576-30968585 chr16:30969023-30969033 chr16:30969719-30969731 chr16:30968558-30968567 chr16:30969721-30969730 chr16:30969539-30969549 chr16:30969742-30969751 chr16:30968943-30968955 chr16:30969736-30969746 chr16:30968576-30968586 chr16:30968944-30968953 chr16:30969022-30969034 chr16:30969023-30969032
5	CHD1	chr16:30968346-30969342	GM12878	blood:	n/a	chr16:30969022-30969032
6	CTCF	chr16:30968412-30968613	Fibrobl	skin:	n/a	chr16:30968516-30968529 chr16:30968527-30968537
7	EP300	chr16:30968358-30969341	SK-N-SH_RA	brain:	n/a	n/a
8	MYC	chr16:30968365-30968659	K562	blood:	n/a	chr16:30968576-30968586
9	CTCF	chr16:30968356-30968648	GM12892	blood:	n/a	chr16:30968516-30968529 chr16:30968527-30968537
10	MAX	chr16:30968261-30969490	SK-N-SH	brain:	n/a	chr16:30968576-30968586
11	JUND	chr16:30968239-30969255	K562	blood:	n/a	chr16:30968443-30968453 chr16:30968946-30968955 chr16:30968442-30968453 chr16:30968443-30968453 chr16:30968440-30968451 chr16:30968444-30968452
12	POLR2A	chr16:30968217-30969537	H1-hESC	embryonic stem cell:	n/a	n/a
13	POLR2A	chr16:30968238-30968615	GM12878	blood:	n/a	n/a
14	MAX	chr16:30968167-30969931	K562	blood:	n/a	chr16:30968576-30968586 chr16:30969718-30969728 chr16:30969711-30969721
15	RCOR1	chr16:30968153-30969386	HepG2	liver:	n/a	n/a
16	CTCF	chr16:30968253-30968810	K562	blood:	n/a	chr16:30968516-30968529 chr16:30968527-30968537
17	POLR2A	chr16:30968206-30969403	Hela-S3	cervix:	n/a	n/a
18	EP300	chr16:30968081-30969588	ECC-1	luminal epithelium:	n/a	chr16:30969460-30969476
19	CTCF	chr16:30968381-30968627	MCF-7	breast:	n/a	chr16:30968516-30968529 chr16:30968527-30968537
20	POLR2A	chr16:30967872-30969892	U87	brain:	n/a	n/a
21	POLR2A	chr16:30968094-30969449	SK-N-SH	brain:	n/a	n/a
22	MYC	chr16:30968345-30968644	HepG2	liver:	n/a	chr16:30968576-30968586
23	TAF1	chr16:30968204-30969526	H1-hESC	embryonic stem cell:	n/a	n/a
24	REST	chr16:30968521-30969023	A549	lung:	n/a	chr16:30968576-30968589
25	MAX	chr16:30968199-30969835	MCF-7	breast:	n/a	chr16:30968576-30968586 chr16:30969718-30969728 chr16:30969711-30969721
26	ELF1	chr16:30968200-30969391	K562	blood:	n/a	chr16:30968519-30968528 chr16:30969225-30969234 chr16:30968577-30968589
27	HEY1	chr16:30968090-30969842	HepG2	liver:	n/a	chr16:30969684-30969699 chr16:30969460-30969475
28	POLR2A	chr16:30968014-30969865	H1-hESC	embryonic stem cell:	n/a	n/a
29	MXI1	chr16:30968373-30969293	K562	blood:	n/a	n/a
30	CTCFL	chr16:30968401-30968615	K562	blood:	n/a	chr16:30968526-30968535
31	ARID3A	chr16:30968256-30969315	HepG2	liver:	n/a	n/a
32	MAX	chr16:30968181-30968703	K562	blood:	n/a	chr16:30968576-30968586
33	REST	chr16:30968299-30969342	HepG2	liver:	n/a	chr16:30968576-30968589
34	TEAD4	chr16:30968226-30969235	HepG2	liver:	n/a	n/a
35	GABPA	chr16:30968344-30969435	SK-N-SH	brain:	n/a	chr16:30968945-30968954 chr16:30968577-30968586
36	GABPA	chr16:30968259-30969379	MCF-7	breast:	n/a	chr16:30968945-30968954 chr16:30968577-30968586
37	EP300	chr16:30968239-30969033	K562	blood:	n/a	n/a
38	CTCF	chr16:30968387-30968646	GM19240	blood:	n/a	chr16:30968516-30968529 chr16:30968527-30968537
39	TBP	chr16:30968298-30969363	K562	blood:	n/a	chr16:30968668-30968679
40	POLR2A	chr16:30967869-30970016	HL-60	blood:	n/a	n/a
41	CTCF	chr16:30968379-30968650	GM19238	blood:	n/a	chr16:30968516-30968529 chr16:30968527-30968537
42	RUNX3	chr16:30968008-30969394	GM12878	blood:	n/a	n/a
43	POLR2A	chr16:30968170-30969667	HepG2	liver:	n/a	n/a
44	MYC	chr16:30968369-30968689	MCF10A-Er-Src	breast:	n/a	chr16:30968576-30968586
45	STAT5A	chr16:30968082-30969666	GM12878	blood:	n/a	chr16:30969507-30969519 chr16:30969416-30969428 chr16:30969543-30969555 chr16:30969019-30969031
46	E2F4	chr16:30968386-30969512	K562	blood:	n/a	chr16:30968554-30968564 chr16:30968945-30968954 chr16:30969465-30969474
47	CTCF	chr16:30968460-30968610	Hela-S3	cervix:	n/a	chr16:30968516-30968529 chr16:30968527-30968537
48	TAF1	chr16:30968286-30969760	HepG2	liver:	n/a	n/a
49	POLR2A	chr16:30968197-30969691	Raji	blood:	n/a	n/a
50	TAF1	chr16:30968609-30969031	H1-neurons	neurons:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:56367774..56368423-chr16:30968400..30968917,2	Hela-S3	cervix:
2	chr16:30967331..30971455-chr16:31189672..31193521,14	K562	blood:
3	chr16:30932533..30935734-chr16:30966751..30970803,5	K562	blood:
4	chr16:30968063..30971621-chr16:31128915..31132343,4	K562	blood:
5	chr16:30966729..30970735-chr16:31118988..31121519,3	MCF-7	breast:
6	chr16:30967313..30970142-chr16:31190595..31192726,3	MCF-7	breast:
7	chr16:30885130..30887903-chr16:30968069..30970202,3	MCF-7	breast:
8	chr16:30967183..30971961-chr16:31469060..31471569,4	MCF-7	breast:
9	chr16:30906472..30908810-chr16:30967387..30969859,2	K562	blood:
10	chr16:30967372..30970193-chr16:31225350..31227883,2	MCF-7	breast:
11	chr16:30967872..30970200-chr16:31160526..31163254,2	K562	blood:
12	chr16:30936648..30939511-chr16:30968022..30970933,3	MCF-7	breast:
13	chr16:30967386..30971624-chr16:31189375..31193961,9	K562	blood:
14	chr16:30967392..30969268-chr16:31053446..31056130,2	MCF-7	breast:
15	chr16:30787481..30790093-chr16:30968266..30970450,2	K562	blood:
16	chr16:30967600..30970776-chr16:31084507..31087266,4	MCF-7	breast:
17	chr16:30905169..30907164-chr16:30967632..30970611,2	K562	blood:
18	chr16:30968251..30971465-chr16:31104162..31108928,5	MCF-7	breast:
19	chr16:30968345..30970795-chr16:30996661..31000962,4	MCF-7	breast:
20	chr16:30932533..30936330-chr16:30966882..30969248,5	K562	blood:
21	chr16:30968101..30970312-chr16:30994646..30997121,3	MCF-7	breast:
22	chr16:30968509..30970515-chr16:31884126..31886399,2	K562	blood:
23	chr16:30967393..30971949-chr16:31083830..31088417,7	K562	blood:
24	chr16:30661294..30664208-chr16:30968481..30971665,3	MCF-7	breast:
25	chr16:30967074..30970924-chr16:31469051..31472537,7	K562	blood:
26	chr16:30968166..30970668-chr16:31152878..31154603,2	MCF-7	breast:
27	chr16:30968323..30969136-chr5:1344950..1345807,2	Hela-S3	cervix:
28	chr16:30952078..30954988-chr16:30967257..30969018,2	MCF-7	breast:
29	chr16:30968024..30972662-chr16:31101043..31106214,4	MCF-7	breast:
30	chr16:30967179..30972282-chr16:31082507..31088894,13	MCF-7	breast:
31	chr16:30771826..30774840-chr16:30967351..30969175,3	K562	blood:
32	chr16:30931053..30936697-chr16:30966530..30971104,6	MCF-7	breast:
33	chr16:30967074..30970924-chr16:31469051..31472279,6	K562	blood:
34	chr16:30933863..30936209-chr16:30967329..30971439,5	MCF-7	breast:
35	chr16:30967808..30970715-chr16:30993015..30997033,4	K562	blood:
36	chr16:30708565..30710498-chr16:30967693..30970480,3	K562	blood:
37	chr16:30967863..30970561-chr16:31152190..31155312,3	K562	blood:
38	chr16:30796561..30800264-chr16:30966265..30969481,3	MCF-7	breast:
39	chr16:30968533..30970596-chr16:31206944..31209887,2	K562	blood:
40	chr16:30787481..30790193-chr16:30968511..30970450,2	K562	blood:
41	chr16:30967393..30971385-chr16:31083259..31086232,6	K562	blood:
42	chr16:30708936..30712121-chr16:30967511..30970972,5	K562	blood:
43	chr16:30537776..30539709-chr16:30967467..30970104,2	MCF-7	breast:
44	chr16:30762720..30764607-chr16:30967390..30969922,2	MCF-7	breast:
45	chr16:30967350..30969220-chr16:31127239..31129159,2	MCF-7	breast:

Variant related genes	Relation type
SETD1A	TF binding region
ENSG00000167394	Chromatin interaction
ENSG00000089280	Chromatin interaction
ENSG00000167397	Chromatin interaction
ENSG00000150281	Chromatin interaction
ENSG00000103510	Chromatin interaction
ENSG00000262026	Chromatin interaction
ENSG00000099377	Chromatin interaction
ENSG00000260267	Chromatin interaction
ENSG00000196118	Chromatin interaction
ENSG00000140691	Chromatin interaction
ENSG00000169957	Chromatin interaction
ENSG00000049656	Chromatin interaction
ENSG00000167395	Chromatin interaction
ENSG00000260083	Chromatin interaction
ENSG00000260911	Chromatin interaction
ENSG00000103507	Chromatin interaction
ENSG00000260060	Chromatin interaction
ENSG00000099364	Chromatin interaction
ENSG00000261840	Chromatin interaction
ENSG00000211591	Chromatin interaction
ENSG00000252809	Chromatin interaction
ENSG00000099385	Chromatin interaction
ENSG00000268863	Chromatin interaction
ENSG00000169900	Chromatin interaction
ENSG00000260852	Chromatin interaction
ENSG00000156858	Chromatin interaction
ENSG00000265991	Chromatin interaction
ENSG00000262766	Chromatin interaction
ENSG00000102870	Chromatin interaction
ENSG00000255439	Chromatin interaction
ENSG00000262721	Chromatin interaction
ENSG00000178226	Chromatin interaction
ENSG00000111540	Chromatin interaction
ENSG00000185947	Chromatin interaction
ENSG00000103549	Chromatin interaction
ENSG00000080603	Chromatin interaction
ENSG00000156873	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062456	chr16:30442166-31253997	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
2	nsv542898	chr16:30442166-31253997	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
3	nsv1064134	chr16:30640293-31087327	Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	238 gene(s)	inside rSNPs	diseases
4	nsv905729	chr16:30642867-31247924	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	387 gene(s)	inside rSNPs	diseases
5	esv1825223	chr16:30669091-30971810	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
6	nsv431451	chr16:30682399-31340999	Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	350 gene(s)	inside rSNPs	diseases
7	nsv905733	chr16:30796919-31004812	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	112 gene(s)	inside rSNPs	diseases
8	nsv833190	chr16:30845051-31007863	Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	105 gene(s)	inside rSNPs	diseases
9	nsv833191	chr16:30864242-31048051	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Bivalent/Poised 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 miRNA target site	115 gene(s)	inside rSNPs	diseases
10	nsv905734	chr16:30877544-31191482	Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
11	nsv905735	chr16:30890538-31247924	Strong transcription Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	264 gene(s)	inside rSNPs	diseases
12	nsv905736	chr16:30900235-30995528	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
13	nsv905737	chr16:30900235-31014179	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	95 gene(s)	inside rSNPs	diseases
14	nsv457483	chr16:30903679-31191482	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	253 gene(s)	inside rSNPs	diseases
15	nsv571820	chr16:30903679-31191482	Enhancers Genic enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	253 gene(s)	inside rSNPs	diseases
16	nsv905738	chr16:30906274-30973926	Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
17	esv1797877	chr16:30948643-31188432	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
18	nsv833193	chr16:30960796-31133604	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
19	esv3508669	chr16:30968201-30971099	Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	46 gene(s)	inside rSNPs	n/a
20	esv3508670	chr16:30968201-30971099	Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	46 gene(s)	inside rSNPs	n/a
21	esv3359616	chr16:30968476-30971024	Genic enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	46 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:30967600-30968800	Flanking Active TSS	Dnd41	blood
2	chr16:30967800-30970000	Active TSS	HUES64 Cell Line	embryonic stem cell
3	chr16:30967800-30970000	Active TSS	Brain Substantia Nigra	brain
4	chr16:30968000-30968800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
5	chr16:30968000-30968800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
6	chr16:30968000-30969000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
7	chr16:30968000-30969000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr16:30968000-30969000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr16:30968000-30969400	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr16:30968000-30969800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr16:30968000-30969800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr16:30968000-30969800	Active TSS	Rectal Smooth Muscle	rectum
13	chr16:30968000-30970000	Active TSS	H9 Cell Line	embryonic stem cell
14	chr16:30968000-30970000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr16:30968000-30970000	Active TSS	HUES48 Cell Line	embryonic stem cell
16	chr16:30968000-30970000	Active TSS	HUES6 Cell Line	embryonic stem cell
17	chr16:30968000-30970000	Active TSS	iPS-20b Cell Line	embryonic stem cell
18	chr16:30968000-30970000	Active TSS	Muscle Satellite Cultured Cells	--
19	chr16:30968000-30970000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr16:30968000-30970000	Active TSS	Brain Anterior Caudate	brain
21	chr16:30968000-30970000	Active TSS	HSMM	muscle
22	chr16:30968000-30970200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr16:30968000-30970200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr16:30968000-30970200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr16:30968000-30970400	Active TSS	iPS-15b Cell Line	embryonic stem cell
26	chr16:30968000-30970400	Active TSS	iPS-18 Cell Line	embryonic stem cell
27	chr16:30968200-30968800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
28	chr16:30968200-30968800	Flanking Active TSS	Liver	Liver
29	chr16:30968200-30969000	Flanking Active TSS	Primary B cells from cord blood	blood
30	chr16:30968200-30969000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
31	chr16:30968200-30969000	Active TSS	Fetal Brain Male	brain
32	chr16:30968200-30969200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
33	chr16:30968200-30969800	Active TSS	Primary T cells from cord blood	blood
34	chr16:30968200-30969800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr16:30968200-30969800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
36	chr16:30968200-30969800	Active TSS	Fetal Brain Female	brain
37	chr16:30968200-30969800	Active TSS	Placenta Amnion	Placenta Amnion
38	chr16:30968200-30969800	Active TSS	Osteobl	bone
39	chr16:30968200-30970000	Active TSS	H1 Cell Line	embryonic stem cell
40	chr16:30968200-30970000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr16:30968200-30970000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
42	chr16:30968200-30970000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr16:30968200-30970000	Active TSS	Duodenum Smooth Muscle	Duodenum
44	chr16:30968200-30970000	Active TSS	Psoas Muscle	Psoas
45	chr16:30968200-30970000	Active TSS	HSMMtube	muscle
46	chr16:30968200-30970200	Active TSS	ES-I3 Cell Line	embryonic stem cell
47	chr16:30968200-30970200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr16:30968200-30970200	Active TSS	A549	lung
49	chr16:30968200-30970400	Active TSS	Fetal Kidney	kidney
50	chr16:30968200-30970400	Active TSS	Pancreatic Islets	Pancreatic Islet

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