Variant report

Variant	rs2972809
Chromosome Location	chr16:30670074-30670075
allele	C/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	TBL1XR1	chr16:30668824-30670667	K562	blood:	n/a	n/a
2	JUND	chr16:30669001-30670787	H1-hESC	embryonic stem cell:	n/a	chr16:30670017-30670026
3	MAX	chr16:30668608-30671540	K562	blood:	n/a	chr16:30670803-30670813 chr16:30670487-30670497 chr16:30669313-30669322
4	EGR1	chr16:30669256-30670391	K562	blood:	n/a	chr16:30669318-30669327 chr16:30669764-30669778 chr16:30669319-30669328
5	YY1	chr16:30669626-30670233	K562	blood:	n/a	n/a
6	POLR2A	chr16:30668793-30670833	HepG2	liver:	n/a	n/a
7	E2F4	chr16:30668708-30670356	MCF10A-Er-Src	breast:	n/a	chr16:30669318-30669327 chr16:30669323-30669331 chr16:30669228-30669237 chr16:30670030-30670037
8	POLR2A	chr16:30668902-30670927	ECC-1	luminal epithelium:	n/a	n/a
9	TCF7L2	chr16:30668939-30670682	PANC-1	pancreas:	n/a	n/a
10	POLR2A	chr16:30668948-30671717	GM18951	blood:	n/a	n/a
11	RFX5	chr16:30669160-30670715	HepG2	liver:	n/a	n/a
12	POLR2A	chr16:30668093-30671519	PANC-1	pancreas:	n/a	n/a
13	SPI1	chr16:30670037-30670393	K562	blood:	n/a	chr16:30670266-30670279 chr16:30670269-30670278 chr16:30670267-30670280
14	TBP	chr16:30669053-30670746	HepG2	liver:	n/a	n/a
15	RFX5	chr16:30669164-30670549	GM12878	blood:	n/a	n/a
16	FOSL2	chr16:30669254-30670582	A549	lung:	n/a	chr16:30670017-30670026
17	UBTF	chr16:30669793-30670142	K562	blood:	n/a	n/a
18	POLR2A	chr16:30668870-30671538	MCF-7	breast:	n/a	n/a
19	SPI1	chr16:30669504-30670450	HL-60	blood:	n/a	chr16:30670266-30670279 chr16:30670269-30670278 chr16:30670267-30670280
20	POLR2A	chr16:30669650-30670265	SK-N-SH	brain:	n/a	n/a
21	MYBL2	chr16:30668685-30670680	HepG2	liver:	n/a	n/a
22	MBD4	chr16:30669609-30670471	HepG2	liver:	n/a	n/a
23	POLR2A	chr16:30668961-30671625	ProgFib	skin:	n/a	n/a
24	USF2	chr16:30669555-30670116	HepG2	liver:	n/a	n/a
25	MAX	chr16:30668902-30670907	MCF-7	breast:	n/a	chr16:30670803-30670813 chr16:30670487-30670497 chr16:30669313-30669322
26	IRF1	chr16:30668955-30670637	K562	blood:	n/a	chr16:30670012-30670026 chr16:30669147-30669164 chr16:30669656-30669670 chr16:30669457-30669471 chr16:30670017-30670031 chr16:30669584-30669598 chr16:30669515-30669529
27	SPI1	chr16:30669179-30670618	HL-60	blood:	n/a	chr16:30670266-30670279 chr16:30670454-30670461 chr16:30670452-30670465 chr16:30670269-30670278 chr16:30670267-30670280
28	POLR2A	chr16:30668652-30670941	K562	blood:	n/a	n/a
29	POLR2A	chr16:30669506-30670565	GM12891	blood:	n/a	n/a
30	RFX5	chr16:30668990-30670584	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr16:30668555-30671681	HUVEC	blood vessel:	n/a	n/a
32	YY1	chr16:30669787-30670278	ECC-1	luminal epithelium:	n/a	n/a
33	SRF	chr16:30669788-30670174	GM12878	blood:	n/a	chr16:30670026-30670043 chr16:30670032-30670046
34	SIN3A	chr16:30668967-30670905	GM12878	blood:	n/a	chr16:30670064-30670077 chr16:30670546-30670555
35	KAT2A	chr16:30669933-30670232	GM12878	blood:	n/a	n/a
36	NRF1	chr16:30669029-30670651	GM12878	blood:	n/a	chr16:30669224-30669238 chr16:30669319-30669328 chr16:30669227-30669241 chr16:30669317-30669328 chr16:30669227-30669238 chr16:30669317-30669331 chr16:30669226-30669237
37	POLR2A	chr16:30668573-30670993	GM12891	blood:	n/a	n/a
38	STAT3	chr16:30669748-30670431	GM12878	blood:	n/a	n/a
39	EGR1	chr16:30669222-30670397	K562	blood:	n/a	chr16:30669318-30669327 chr16:30669764-30669778 chr16:30669319-30669328 chr16:30669228-30669237
40	TBP	chr16:30669103-30670763	K562	blood:	n/a	n/a
41	FOS	chr16:30669217-30670555	MCF10A-Er-Src	breast:	n/a	chr16:30670017-30670026
42	CREB1	chr16:30668912-30670826	GM12878	blood:	n/a	n/a
43	TAF1	chr16:30669611-30670296	K562	blood:	n/a	n/a
44	ELK4	chr16:30669306-30670377	Hela-S3	cervix:	n/a	n/a
45	SPI1	chr16:30669394-30670723	GM12878	blood:	n/a	chr16:30670266-30670279 chr16:30670454-30670461 chr16:30670452-30670465 chr16:30670269-30670278 chr16:30670267-30670280
46	RAD21	chr16:30668735-30671034	SK-N-SH	brain:	n/a	chr16:30670623-30670633 chr16:30670732-30670741 chr16:30669221-30669235
47	MAZ	chr16:30669138-30670909	GM12878	blood:	n/a	chr16:30670803-30670813 chr16:30670487-30670497 chr16:30669313-30669322
48	SP1	chr16:30669102-30670622	HepG2	liver:	n/a	chr16:30669581-30669595 chr16:30670015-30670024 chr16:30669659-30669673 chr16:30670020-30670034 chr16:30669515-30669527 chr16:30670083-30670090 chr16:30669659-30669668 chr16:30669515-30669527 chr16:30670433-30670440 chr16:30670016-30670025 chr16:30669658-30669670 chr16:30670539-30670546 chr16:30670014-30670026 chr16:30669584-30669596 chr16:30670228-30670242 chr16:30670014-30670026 chr16:30669786-30669797 chr16:30669517-30669526 chr16:30669492-30669513 chr16:30670019-30670031 chr16:30669658-30669670 chr16:30669512-30669526 chr16:30670015-30670024 chr16:30670020-30670029
49	YY1	chr16:30668751-30671388	HepG2	liver:	n/a	chr16:30669304-30669318 chr16:30670751-30670765 chr16:30669221-30669235 chr16:30669304-30669313 chr16:30670800-30670814 chr16:30670969-30670989 chr16:30669348-30669362 chr16:30670802-30670811 chr16:30669306-30669315 chr16:30669227-30669241 chr16:30669298-30669312
50	CHD2	chr16:30669270-30670301	H1-hESC	embryonic stem cell:	n/a	chr16:30670030-30670037 chr16:30670024-30670034

No.	Distal block	Cell Line	Cell type
1	chr10:118764190..118764920-chr16:30669483..30670147,2	Hela-S3	cervix:
2	chr1:154946241..154946985-chr16:30669609..30670152,2	Hela-S3	cervix:
3	chr16:30581443..30584852-chr16:30667885..30670811,3	MCF-7	breast:
4	chr16:30669436..30672389-chr17:73774530..73776217,2	MCF-7	breast:
5	chr16:30534881..30538738-chr16:30669014..30672874,5	MCF-7	breast:
6	chr16:30545060..30546594-chr16:30668041..30670734,2	K562	blood:
7	chr16:30382922..30384905-chr16:30669904..30671484,2	MCF-7	breast:
8	chr16:30665738..30673826-chr16:30707321..30713630,33	K562	blood:
9	chr16:30668135..30670286-chr16:30783767..30786640,2	K562	blood:
10	chr16:30544819..30547359-chr16:30669370..30671346,2	MCF-7	breast:
11	chr16:30665347..30684079-chr16:30697204..30714344,66	MCF-7	breast:
12	chr11:118972613..118973169-chr16:30669774..30670547,2	Hela-S3	cervix:
13	chr16:30669411..30670219-chr6:26156502..26157804,4	Hela-S3	cervix:
14	chr16:30669272..30672997-chr16:30933501..30936286,4	MCF-7	breast:
15	chr16:30668245..30671978-chr16:30750248..30754870,9	MCF-7	breast:
16	chr16:29815810..29818051-chr16:30669124..30671964,2	MCF-7	breast:
17	chr16:30666829..30670641-chr16:30932372..30935048,3	K562	blood:
18	chr16:30583091..30585681-chr16:30668404..30671562,3	K562	blood:
19	chr16:30454464..30457358-chr16:30669384..30671896,3	K562	blood:
20	chr16:30669439..30671139-chr16:30758137..30761003,2	K562	blood:
21	chr16:30595796..30598242-chr16:30667877..30670406,3	MCF-7	breast:
22	chr16:30669616..30672714-chr16:30750078..30754286,5	MCF-7	breast:
23	chr16:30669453..30671146-chr16:30759344..30760999,2	MCF-7	breast:
24	chr16:30669682..30670192-chr6:32939798..32940431,2	Hela-S3	cervix:
25	chr16:30581724..30584025-chr16:30669136..30672320,3	MCF-7	breast:
26	chr16:30667507..30674392-chr16:30704170..30712522,40	MCF-7	breast:
27	chr16:30669667..30670243-chr19:41221082..41221648,2	Hela-S3	cervix:
28	chr16:30365632..30367992-chr16:30667854..30670358,2	MCF-7	breast:
29	chr16:30625309..30627910-chr16:30669048..30671707,2	K562	blood:
30	chr16:30667897..30670733-chr16:30759554..30761748,2	K562	blood:
31	chr16:30537270..30540938-chr16:30667776..30670897,3	K562	blood:
32	chr16:30626674..30628950-chr16:30669542..30671226,2	MCF-7	breast:
33	chr16:30626410..30628513-chr16:30668495..30670548,2	K562	blood:
34	chr16:30667783..30674540-chr16:30707310..30714065,38	K562	blood:
35	chr16:30389121..30392604-chr16:30668490..30671197,4	K562	blood:
36	chr16:30134421..30136289-chr16:30669224..30670756,2	K562	blood:
37	chr16:30669722..30670291-chr9:130565565..130566502,2	Hela-S3	cervix:
38	chr16:30568254..30570090-chr16:30667629..30670948,3	K562	blood:
39	chr16:30439350..30443248-chr16:30667549..30670129,3	MCF-7	breast:
40	chr16:30438691..30441643-chr16:30669537..30671666,4	MCF-7	breast:
41	chr16:30455343..30457757-chr16:30668968..30672214,3	MCF-7	breast:
42	chr16:30535862..30538141-chr16:30667987..30671632,3	K562	blood:
43	chr16:30669265..30670159-chr5:43017610..43018584,2	Hela-S3	cervix:
44	chr16:30345814..30348548-chr16:30669791..30672071,2	MCF-7	breast:

Variant related genes	Relation type
FBRS	TF binding region
ENSG00000179918	Chromatin interaction
ENSG00000080603	Chromatin interaction
ENSG00000172269	Chromatin interaction
ENSG00000260899	Chromatin interaction
ENSG00000229809	Chromatin interaction
ENSG00000235560	Chromatin interaction
ENSG00000103549	Chromatin interaction
ENSG00000260219	Chromatin interaction
ENSG00000136877	Chromatin interaction
ENSG00000103495	Chromatin interaction
ENSG00000168298	Chromatin interaction
ENSG00000183604	Chromatin interaction
ENSG00000156873	Chromatin interaction
ENSG00000180035	Chromatin interaction
ENSG00000204256	Chromatin interaction
ENSG00000251131	Chromatin interaction
ENSG00000123815	Chromatin interaction
ENSG00000169217	Chromatin interaction
ENSG00000260167	Chromatin interaction
ENSG00000187164	Chromatin interaction
ENSG00000179958	Chromatin interaction
ENSG00000239791	Chromatin interaction
ENSG00000169951	Chromatin interaction
ENSG00000261459	Chromatin interaction
ENSG00000099364	Chromatin interaction
ENSG00000172375	Chromatin interaction
ENSG00000180209	Chromatin interaction
ENSG00000169957	Chromatin interaction
ENSG00000197162	Chromatin interaction
ENSG00000132475	Chromatin interaction
ENSG00000260678	Chromatin interaction
ENSG00000261840	Chromatin interaction
ENSG00000260869	Chromatin interaction
ENSG00000222287	Chromatin interaction
ENSG00000169955	Chromatin interaction
ENSG00000160691	Chromatin interaction
ENSG00000102882	Chromatin interaction
ENSG00000260852	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs11150594	0.85[AFR][1000 genomes]
rs11150595	0.81[YRI][hapmap]
rs1348039	1.00[MKK][hapmap]
rs1530201	1.00[MKK][hapmap]
rs1550477	0.81[YRI][hapmap]
rs2099754	0.81[YRI][hapmap]
rs2099755	0.81[YRI][hapmap]
rs2919430	0.80[AFR][1000 genomes]
rs2919431	0.81[YRI][hapmap];0.84[AFR][1000 genomes]
rs2919432	0.82[ASW][hapmap];0.81[LWK][hapmap];1.00[MKK][hapmap];0.87[YRI][hapmap];0.93[AFR][1000 genomes]
rs2972804	0.80[AFR][1000 genomes]
rs2972807	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2972808	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2972815	0.93[AFR][1000 genomes]
rs4889500	0.81[LWK][hapmap];0.81[YRI][hapmap];0.84[AFR][1000 genomes]
rs4889502	1.00[MKK][hapmap]
rs4889503	0.82[ASW][hapmap];0.81[LWK][hapmap];1.00[MKK][hapmap];0.87[YRI][hapmap];0.81[AFR][1000 genomes]
rs4889504	0.81[YRI][hapmap]
rs4889505	0.82[ASW][hapmap];0.81[LWK][hapmap];1.00[MKK][hapmap];0.87[YRI][hapmap]
rs4889506	1.00[MKK][hapmap]
rs4889508	0.81[YRI][hapmap]
rs4889509	0.81[YRI][hapmap]
rs55635617	0.84[AFR][1000 genomes]
rs56209507	0.84[AFR][1000 genomes]
rs57225118	0.84[AFR][1000 genomes]
rs57643871	0.80[AFR][1000 genomes]
rs7185136	0.81[LWK][hapmap];0.81[YRI][hapmap]
rs7188927	1.00[MKK][hapmap]
rs7195583	0.81[LWK][hapmap];0.81[YRI][hapmap]
rs73536457	0.93[AFR][1000 genomes]
rs73536466	0.84[AFR][1000 genomes]
rs73536474	0.84[AFR][1000 genomes]
rs73536488	0.93[AFR][1000 genomes]
rs73536498	0.84[AFR][1000 genomes]
rs73536499	0.84[AFR][1000 genomes]
rs8045484	0.81[YRI][hapmap]
rs8045624	0.81[YRI][hapmap]
rs8048656	0.82[ASW][hapmap];0.81[LWK][hapmap];1.00[MKK][hapmap];0.87[YRI][hapmap]
rs8050578	0.86[YRI][hapmap]
rs893924	1.00[MKK][hapmap]
rs893925	1.00[MKK][hapmap]
rs893927	0.81[YRI][hapmap]
rs9921630	0.81[YRI][hapmap]
rs9941201	0.80[YRI][hapmap]
rs9941300	0.81[LWK][hapmap];0.81[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:14 , 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	nsv905727	chr16:30564526-30689696	Active TSS Flanking Active TSS Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
4	nsv469724	chr16:30632445-30840263	Strong transcription Transcr. at gene 5' and 3' Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	143 gene(s)	inside rSNPs	diseases
5	nsv482704	chr16:30632445-30840263	Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	143 gene(s)	inside rSNPs	diseases
6	nsv833188	chr16:30632446-30840263	Active TSS Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	143 gene(s)	inside rSNPs	diseases
7	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
8	nsv905728	chr16:30642867-30928970	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	171 gene(s)	inside rSNPs	diseases
9	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
10	nsv905730	chr16:30667031-30681816	Genic enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
11	nsv905731	chr16:30667031-30685089	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
12	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
13	esv3506214	chr16:30670001-30672099	Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	46 gene(s)	inside rSNPs	diseases
14	esv3506215	chr16:30670001-30672099	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	46 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	chr16:30668600-30672800	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr16:30668800-30671000	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr16:30668800-30671000	Active TSS	HUES64 Cell Line	embryonic stem cell
4	chr16:30668800-30671200	Active TSS	iPS-18 Cell Line	embryonic stem cell
5	chr16:30668800-30671400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr16:30668800-30671400	Active TSS	H9 Cell Line	embryonic stem cell
7	chr16:30668800-30671400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr16:30668800-30671400	Active TSS	Fetal Brain Female	brain
9	chr16:30668800-30671400	Active TSS	Psoas Muscle	Psoas
10	chr16:30668800-30671800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr16:30668800-30672000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr16:30668800-30672000	Active TSS	Gastric	stomach
13	chr16:30669000-30670400	Active TSS	Fetal Heart	heart
14	chr16:30669000-30670800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
15	chr16:30669000-30671000	Active TSS	iPS-20b Cell Line	embryonic stem cell
16	chr16:30669000-30671000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr16:30669000-30671000	Active TSS	Cortex derived primary cultured neurospheres	brain
18	chr16:30669000-30671200	Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr16:30669000-30671200	Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr16:30669000-30671200	Active TSS	iPS-15b Cell Line	embryonic stem cell
21	chr16:30669000-30671200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
22	chr16:30669000-30671200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr16:30669000-30671200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr16:30669000-30671200	Active TSS	Brain Germinal Matrix	brain
25	chr16:30669000-30671400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr16:30669000-30671400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr16:30669000-30671400	Active TSS	Brain Cingulate Gyrus	brain
28	chr16:30669000-30671400	Active TSS	Brain Hippocampus Middle	brain
29	chr16:30669000-30671600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr16:30669000-30671600	Active TSS	Fetal Kidney	kidney
31	chr16:30669000-30671600	Active TSS	Placenta Amnion	Placenta Amnion
32	chr16:30669000-30671600	Active TSS	Spleen	Spleen
33	chr16:30669000-30671600	Active TSS	Osteobl	bone
34	chr16:30669000-30671800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr16:30669000-30671800	Active TSS	Breast Myoepithelial Primary Cells	Breast
36	chr16:30669000-30671800	Active TSS	Left Ventricle	heart
37	chr16:30669000-30671800	Active TSS	Rectal Smooth Muscle	rectum
38	chr16:30669000-30671800	Active TSS	Sigmoid Colon	Sigmoid Colon
39	chr16:30669000-30671800	Active TSS	A549	lung
40	chr16:30669000-30671800	Active TSS	HSMMtube	muscle
41	chr16:30669000-30672000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr16:30669000-30672200	Active TSS	Esophagus	oesophagus
43	chr16:30669000-30672200	Active TSS	Small Intestine	intestine
44	chr16:30669200-30670200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
45	chr16:30669200-30670400	Active TSS	Fetal Brain Male	brain
46	chr16:30669200-30670800	Active TSS	Primary hematopoietic stem cells	blood
47	chr16:30669200-30671000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr16:30669200-30671000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr16:30669200-30671200	Active TSS	H1 Cell Line	embryonic stem cell
50	chr16:30669200-30671200	Active TSS	Primary monocytes fromperipheralblood	blood

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