Variant report

Variant	rs4760622
Chromosome Location	chr12:48591960-48591961
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	NRF1	chr12:48591917-48592199	H1-hESC	embryonic stem cell:	n/a	n/a
2	POLR2A	chr12:48591419-48593567	GM12891	blood:	n/a	n/a
3	ATF1	chr12:48591606-48592377	K562	blood:	n/a	n/a
4	RUNX3	chr12:48591330-48592637	GM12878	blood:	n/a	n/a
5	NFYA	chr12:48591433-48592320	K562	blood:	n/a	chr12:48592013-48592028 chr12:48592014-48592028 chr12:48592009-48592027 chr12:48592016-48592026 chr12:48592013-48592028
6	HDAC2	chr12:48591756-48591986	H1-hESC	embryonic stem cell:	n/a	n/a
7	POLR2A	chr12:48591707-48592002	A549	lung:	n/a	n/a
8	FOS	chr12:48591848-48592240	K562	blood:	n/a	chr12:48592015-48592024
9	MAX	chr12:48591515-48592328	H1-hESC	embryonic stem cell:	n/a	n/a
10	E2F6	chr12:48591437-48592538	A549	lung:	n/a	chr12:48592017-48592026
11	CUX1	chr12:48591336-48592190	K562	blood:	n/a	n/a
12	POLR2A	chr12:48591664-48592792	K562	blood:	n/a	n/a
13	MYC	chr12:48591438-48592759	K562	blood:	n/a	n/a
14	POLR2A	chr12:48591608-48592625	H1-hESC	embryonic stem cell:	n/a	n/a
15	WRNIP1	chr12:48591567-48592781	GM12878	blood:	n/a	n/a
16	CTCF	chr12:48591820-48591970	GM12864	blood:	n/a	n/a
17	YY1	chr12:48591767-48592325	HCT-116	colon:	n/a	chr12:48592212-48592226 chr12:48592177-48592187 chr12:48592072-48592086
18	TEAD4	chr12:48591248-48592854	K562	blood:	n/a	n/a
19	MAX	chr12:48591206-48592554	ECC-1	luminal epithelium:	n/a	n/a
20	RAD21	chr12:48591266-48592332	H1-hESC	embryonic stem cell:	n/a	n/a
21	TAF1	chr12:48591666-48592471	A549	lung:	n/a	n/a
22	NFIC	chr12:48591466-48592502	GM12878	blood:	n/a	n/a
23	FOXM1	chr12:48591634-48592548	GM12878	blood:	n/a	n/a
24	YY1	chr12:48591615-48592558	ECC-1	luminal epithelium:	n/a	chr12:48592212-48592226 chr12:48592177-48592187 chr12:48592072-48592086
25	TBL1XR1	chr12:48591706-48592656	K562	blood:	n/a	n/a
26	POLR2A	chr12:48591589-48593345	GM12878	blood:	n/a	n/a
27	STAT1	chr12:48591481-48592458	GM12878	blood:	n/a	n/a
28	MAX	chr12:48591620-48592364	H1-hESC	embryonic stem cell:	n/a	n/a
29	RELA	chr12:48591517-48592446	GM19099	blood:	n/a	n/a
30	E2F4	chr12:48591715-48592451	K562	blood:	n/a	chr12:48592017-48592026
31	CTCF	chr12:48591820-48591970	K562	blood:	n/a	n/a
32	CTCF	chr12:48591688-48591967	GM19239	blood:	n/a	n/a
33	RFX5	chr12:48591877-48592374	H1-hESC	embryonic stem cell:	n/a	chr12:48592016-48592025
34	CTCF	chr12:48591620-48591962	GM19238	blood:	n/a	n/a
35	POU2F2	chr12:48591622-48592399	GM12878	blood:	n/a	n/a
36	CTCF	chr12:48591565-48592163	K562	blood:	n/a	n/a
37	E2F6	chr12:48591666-48592410	H1-hESC	embryonic stem cell:	n/a	chr12:48592017-48592026
38	ZEB1	chr12:48591670-48592103	GM12878	blood:	n/a	n/a
39	TAF1	chr12:48591717-48592753	K562	blood:	n/a	n/a
40	RCOR1	chr12:48591318-48592282	K562	blood:	n/a	n/a
41	TBP	chr12:48591392-48592699	GM12878	blood:	n/a	n/a
42	POLR2A	chr12:48591576-48592494	Hela-S3	cervix:	n/a	n/a
43	USF1	chr12:48591643-48592285	A549	lung:	n/a	n/a
44	YY1	chr12:48591767-48592851	NT2-D1	testis:	n/a	chr12:48592212-48592226 chr12:48592177-48592187 chr12:48592072-48592086
45	TAF1	chr12:48591742-48592856	K562	blood:	n/a	n/a
46	POLR2A	chr12:48591661-48592446	ECC-1	luminal epithelium:	n/a	n/a
47	POLR2A	chr12:48591712-48592758	K562	blood:	n/a	n/a
48	POU2F2	chr12:48591574-48592433	GM12891	blood:	n/a	n/a
49	ELF1	chr12:48591719-48592824	GM12878	blood:	n/a	n/a
50	SIN3A	chr12:48591484-48592469	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:48583311..48584177-chr12:48591097..48592094,2	K562	blood:
2	chr12:48549910..48551454-chr12:48590661..48592818,2	K562	blood:
3	chr12:48549661..48552655-chr12:48590661..48593368,4	K562	blood:
4	chr12:48589603..48591970-chr12:48853785..48856420,2	MCF-7	breast:
5	chr12:48590039..48593666-chr12:48742360..48744824,3	K562	blood:

Variant related genes	Relation type
ENSG00000269514	TF binding region
ENSG00000167528	Chromatin interaction
ENSG00000177981	Chromatin interaction
ENSG00000257735	Chromatin interaction

Extended variants
information (count: 128 )
Associated
traits (count: 13 )

rSNPs within LD-proxies of this variant (count:122)

rs_ID	r²[population]
rs10082861	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs1021313	0.88[ASN][1000 genomes]
rs10219623	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs10431526	0.82[ASN][1000 genomes]
rs10437919	0.88[ASN][1000 genomes]
rs10437920	0.88[ASN][1000 genomes]
rs10467101	0.88[CHB][hapmap];0.84[JPT][hapmap];0.90[ASN][1000 genomes]
rs10783234	0.93[ASN][1000 genomes]
rs10875724	0.93[JPT][hapmap]
rs10875725	0.81[GIH][hapmap];1.00[JPT][hapmap]
rs10875732	0.85[CEU][hapmap];1.00[JPT][hapmap]
rs10875735	0.85[CEU][hapmap]
rs10875745	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap]
rs10875746	0.94[CHB][hapmap];0.88[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap]
rs10875747	0.84[EUR][1000 genomes]
rs10875748	0.84[EUR][1000 genomes]
rs10875750	0.93[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.83[MKK][hapmap];0.94[TSI][hapmap];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10875756	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10875762	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10875764	0.94[ASN][1000 genomes]
rs10875767	0.81[CEU][hapmap];0.88[CHB][hapmap];0.93[JPT][hapmap];0.92[ASN][1000 genomes]
rs10875768	0.90[ASN][1000 genomes]
rs10875769	0.84[ASN][1000 genomes]
rs10875770	0.81[CEU][hapmap];0.89[CHB][hapmap];0.94[CHD][hapmap];0.93[JPT][hapmap];0.83[MEX][hapmap];0.81[TSI][hapmap];0.92[ASN][1000 genomes]
rs10875772	0.81[CEU][hapmap];0.89[CHB][hapmap];0.94[CHD][hapmap];0.93[JPT][hapmap];0.91[MEX][hapmap];0.90[MKK][hapmap];0.81[TSI][hapmap];0.90[ASN][1000 genomes]
rs10875777	0.88[ASN][1000 genomes]
rs10875778	0.88[ASN][1000 genomes]
rs10875779	0.88[ASN][1000 genomes]
rs10875782	0.85[ASN][1000 genomes]
rs10875792	0.86[CHB][hapmap];0.85[JPT][hapmap];0.82[ASN][1000 genomes]
rs10875793	0.80[CEU][hapmap];0.82[CHB][hapmap];0.92[JPT][hapmap];0.82[ASN][1000 genomes]
rs11168355	0.88[GIH][hapmap]
rs11168357	0.85[GIH][hapmap];0.93[JPT][hapmap]
rs11168369	0.81[CEU][hapmap];1.00[JPT][hapmap]
rs11168371	0.87[CEU][hapmap];0.85[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.84[TSI][hapmap]
rs11168403	1.00[JPT][hapmap]
rs11168413	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11168414	0.93[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.83[MKK][hapmap];0.94[TSI][hapmap];0.83[EUR][1000 genomes]
rs11168418	0.93[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.82[MKK][hapmap];0.94[TSI][hapmap];0.85[YRI][hapmap];0.82[EUR][1000 genomes]
rs11168420	0.89[ASW][hapmap];0.93[CEU][hapmap];0.94[CHB][hapmap];0.91[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.83[MKK][hapmap];0.94[TSI][hapmap];0.83[EUR][1000 genomes]
rs11168421	0.94[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap]
rs11168422	0.82[EUR][1000 genomes]
rs11168425	0.94[CHB][hapmap];0.94[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap]
rs11168427	0.93[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.83[MKK][hapmap];0.94[TSI][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11168433	0.93[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.97[MKK][hapmap];0.91[TSI][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11168450	0.94[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs11168459	0.81[CEU][hapmap];0.89[CHB][hapmap];0.94[CHD][hapmap];0.93[JPT][hapmap];0.83[MEX][hapmap];0.81[TSI][hapmap];0.92[ASN][1000 genomes]
rs11168483	0.85[ASN][1000 genomes]
rs11168487	0.88[ASN][1000 genomes]
rs11168493	0.81[ASN][1000 genomes]
rs11168508	0.83[ASN][1000 genomes]
rs11168510	0.83[ASN][1000 genomes]
rs11168514	0.82[ASN][1000 genomes]
rs11168516	0.81[CEU][hapmap];0.83[CHB][hapmap];0.87[JPT][hapmap];0.82[ASN][1000 genomes]
rs11558768	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12227601	0.83[ASN][1000 genomes]
rs12297470	1.00[CHB][hapmap];0.94[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs12300647	0.85[ASN][1000 genomes]
rs12304476	0.87[CEU][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.94[TSI][hapmap]
rs12305182	0.93[JPT][hapmap]
rs12305511	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12305647	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12306451	0.87[CEU][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.91[TSI][hapmap]
rs12310813	1.00[CHB][hapmap];0.94[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs12312134	1.00[CHB][hapmap];0.93[JPT][hapmap];0.85[YRI][hapmap];0.89[ASN][1000 genomes]
rs12317751	0.88[ASN][1000 genomes]
rs12318705	0.85[ASN][1000 genomes]
rs1471997	0.86[JPT][hapmap]
rs17122666	0.93[CEU][hapmap];0.94[CHB][hapmap];0.88[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.94[TSI][hapmap];0.85[EUR][1000 genomes]
rs17122812	0.89[CHB][hapmap];0.93[JPT][hapmap];0.92[ASN][1000 genomes]
rs1859445	1.00[CHB][hapmap];0.91[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap]
rs2012773	0.94[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2079295	0.93[JPT][hapmap]
rs2107638	0.94[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs2171642	0.85[ASN][1000 genomes]
rs2228500	0.93[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.83[MKK][hapmap];0.94[TSI][hapmap];0.84[EUR][1000 genomes]
rs2269933	0.94[CHB][hapmap];0.88[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap]
rs2269935	0.93[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.94[TSI][hapmap];0.83[EUR][1000 genomes]
rs2269936	1.00[JPT][hapmap]
rs2279464	0.82[CHB][hapmap];0.87[JPT][hapmap];0.82[ASN][1000 genomes]
rs2286021	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2409005	0.83[ASN][1000 genomes]
rs2634675	0.87[JPT][hapmap]
rs2732439	0.87[JPT][hapmap]
rs2732465	0.87[JPT][hapmap]
rs2898065	0.87[ASN][1000 genomes]
rs2898066	0.83[ASN][1000 genomes]
rs3185921	0.87[JPT][hapmap]
rs3751273	0.87[JPT][hapmap]
rs3782910	0.87[CEU][hapmap];1.00[JPT][hapmap]
rs4760609	0.88[GIH][hapmap];0.93[JPT][hapmap]
rs4760619	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs4760625	0.83[ASN][1000 genomes]
rs4760681	0.93[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.83[MKK][hapmap];0.94[TSI][hapmap];0.84[YRI][hapmap];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4760687	0.94[CHB][hapmap];0.94[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs4760689	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4760690	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4760695	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4760696	0.94[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs4760697	0.94[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs4760699	0.81[ASN][1000 genomes]
rs61940962	0.92[ASN][1000 genomes]
rs61941003	0.88[ASN][1000 genomes]
rs61941006	0.88[ASN][1000 genomes]
rs6580659	0.92[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7135779	0.94[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs716553	0.88[ASN][1000 genomes]
rs719008	0.93[JPT][hapmap]
rs725454	0.93[CEU][hapmap];0.94[CHB][hapmap];0.88[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.83[MKK][hapmap];0.94[TSI][hapmap];0.85[YRI][hapmap];0.83[EUR][1000 genomes]
rs7297298	0.83[ASN][1000 genomes]
rs7299135	0.93[JPT][hapmap]
rs7299271	0.93[JPT][hapmap]
rs7302466	0.85[ASN][1000 genomes]
rs7303055	0.88[ASN][1000 genomes]
rs7485355	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7486008	0.88[ASN][1000 genomes]
rs7486424	0.94[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs7975956	0.85[ASN][1000 genomes]
rs8804	0.93[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.83[MKK][hapmap];0.94[TSI][hapmap];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs886588	0.87[CEU][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.94[TSI][hapmap]
rs9634261	0.81[CEU][hapmap];0.83[CHB][hapmap];0.87[JPT][hapmap];0.83[ASN][1000 genomes]
rs989144	0.87[CEU][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758307	chr12:48429702-48825499	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	esv2759898	chr12:48429702-48825499	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv8971	chr12:48536526-48758501	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	esv34439	chr12:48541757-48779562	Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
5	esv2757502	chr12:48547128-48779562	Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
6	esv33956	chr12:48565643-48645561	Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:13)

SNP	Gene	Cis/trans	Tissue	Source
rs4760622	RP1-228P16.1	cis	Skin Sun Exposed Lower leg	GTEx
rs4760622	PRKAG1	cis	parietal	SCAN
rs4760622	RP1-228P16.1	cis	lung	GTEx
rs4760622	SENP1	cis	cerebellum	SCAN
rs4760622	ASB8	cis	cerebellum	SCAN
rs4760622	RP1-228P16.1	cis	Thyroid	GTEx
rs4760622	SENP1	cis	parietal	SCAN
rs4760622	FAM186B	cis	parietal	SCAN
rs4760622	H1FNT	cis	cerebellum	SCAN
rs4760622	RP1-228P16.1	cis	Adipose Subcutaneous	GTEx
rs4760622	LOC255411	cis	cerebellum	SCAN
rs4760622	RP1-228P16.1	cis	Artery Tibial	GTEx
rs4760622	RP1-228P16.1	cis	Esophagus Mucosa	GTEx

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:48590800-48592400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr12:48590800-48592600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr12:48590800-48593000	Active TSS	Breast Myoepithelial Primary Cells	Breast
4	chr12:48591000-48592000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
5	chr12:48591000-48592000	Flanking Active TSS	GM12878-XiMat	blood
6	chr12:48591000-48592000	Flanking Active TSS	HMEC	breast
7	chr12:48591000-48592000	Flanking Active TSS	K562	blood
8	chr12:48591000-48592200	Active TSS	NHLF	lung
9	chr12:48591000-48592600	Active TSS	Stomach Smooth Muscle	stomach
10	chr12:48591000-48592800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
11	chr12:48591000-48593000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr12:48591000-48593000	Active TSS	Duodenum Mucosa	Duodenum
13	chr12:48591000-48593200	Active TSS	Right Ventricle	heart
14	chr12:48591200-48592000	Active TSS	HUES64 Cell Line	embryonic stem cell
15	chr12:48591200-48592000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
16	chr12:48591200-48592000	Flanking Active TSS	Primary T cells from cord blood	blood
17	chr12:48591200-48592000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
18	chr12:48591200-48592000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr12:48591200-48592000	Flanking Active TSS	HUVEC	blood vessel
20	chr12:48591200-48592400	Active TSS	H1 Cell Line	embryonic stem cell
21	chr12:48591200-48592600	Active TSS	ES-I3 Cell Line	embryonic stem cell
22	chr12:48591200-48592600	Active TSS	Aorta	Aorta
23	chr12:48591200-48592600	Active TSS	Fetal Lung	lung
24	chr12:48591200-48592800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
25	chr12:48591200-48592800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr12:48591200-48592800	Active TSS	iPS-15b Cell Line	embryonic stem cell
27	chr12:48591200-48592800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
28	chr12:48591200-48592800	Active TSS	Psoas Muscle	Psoas
29	chr12:48591200-48592800	Active TSS	Hela-S3	cervix
30	chr12:48591200-48593000	Active TSS	Colon Smooth Muscle	Colon
31	chr12:48591200-48593000	Flanking Active TSS	Osteobl	bone
32	chr12:48591200-48593200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
33	chr12:48591200-48593200	Active TSS	Duodenum Smooth Muscle	Duodenum
34	chr12:48591200-48593200	Active TSS	Left Ventricle	heart
35	chr12:48591200-48593200	Active TSS	NHDF-Ad	bronchial
36	chr12:48591200-48593400	Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr12:48591200-48594200	Flanking Active TSS	Primary hematopoietic stem cells	blood
38	chr12:48591400-48592000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr12:48591400-48592000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
40	chr12:48591400-48592400	Active TSS	HUES48 Cell Line	embryonic stem cell
41	chr12:48591400-48592400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr12:48591400-48592400	Active TSS	Primary B cells from peripheral blood	blood
43	chr12:48591400-48592400	Active TSS	Fetal Brain Male	brain
44	chr12:48591400-48592600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr12:48591400-48592600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
46	chr12:48591400-48592600	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
47	chr12:48591400-48592600	Active TSS	Primary T killer memory cells from peripheral blood	blood
48	chr12:48591400-48592600	Active TSS	Liver	Liver
49	chr12:48591400-48592600	Active TSS	Fetal Heart	heart
50	chr12:48591400-48592600	Active TSS	Fetal Intestine Small	intestine

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