Variant report

Variant	rs2492405
Chromosome Location	chr10:43931825-43931826
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	FOS	chr10:43931754-43932026	MCF10A-Er-Src	breast:	n/a	n/a
2	NRF1	chr10:43931813-43932632	GM12878	blood:	n/a	n/a
3	SIN3AK20	chr10:43931690-43932679	K562	blood:	n/a	n/a
4	CREB1	chr10:43931653-43932946	HepG2	liver:	n/a	n/a
5	CHD2	chr10:43931733-43933039	Hela-S3	cervix:	n/a	n/a
6	NFIC	chr10:43931659-43932718	GM12878	blood:	n/a	n/a
7	TCF12	chr10:43931699-43932762	A549	lung:	n/a	chr10:43932408-43932418
8	MYC	chr10:43931607-43932721	K562	blood:	n/a	chr10:43932575-43932584
9	YY1	chr10:43931687-43932824	K562	blood:	n/a	chr10:43932543-43932554 chr10:43932718-43932729
10	POLR2A	chr10:43931750-43932664	ECC-1	luminal epithelium:	n/a	n/a
11	EP300	chr10:43931532-43932622	K562	blood:	n/a	chr10:43932545-43932554
12	HDAC2	chr10:43931696-43933054	MCF-7	breast:	n/a	chr10:43932058-43932077 chr10:43932113-43932127
13	HCFC1	chr10:43931612-43933039	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr10:43931687-43932523	K562	blood:	n/a	n/a
15	POLR2A	chr10:43931818-43932693	K562	blood:	n/a	n/a
16	MYBL2	chr10:43931706-43932584	HepG2	liver:	n/a	n/a
17	TFAP2A	chr10:43931697-43932589	Hela-S3	cervix:	n/a	chr10:43932196-43932208 chr10:43932196-43932208 chr10:43932196-43932208 chr10:43932196-43932208
18	HEY1	chr10:43931621-43932771	K562	blood:	n/a	chr10:43932715-43932730
19	ELF1	chr10:43931719-43932753	MCF-7	breast:	n/a	chr10:43932236-43932248 chr10:43932119-43932130
20	MAX	chr10:43931757-43932670	A549	lung:	n/a	chr10:43932575-43932584
21	POLR2A	chr10:43931673-43932876	PANC-1	pancreas:	n/a	n/a
22	ZBTB7A	chr10:43931765-43932960	K562	blood:	n/a	chr10:43932495-43932504 chr10:43932559-43932568
23	STAT5A	chr10:43931787-43932348	GM12878	blood:	n/a	n/a
24	RAD21	chr10:43931736-43932373	HepG2	liver:	n/a	n/a
25	SMC3	chr10:43931734-43933087	Hela-S3	cervix:	n/a	chr10:43932729-43932739
26	YY1	chr10:43931695-43932730	SK-N-SH	brain:	n/a	chr10:43932543-43932554 chr10:43932718-43932729
27	MXI1	chr10:43931441-43933680	SK-N-SH	brain:	n/a	n/a
28	TEAD4	chr10:43931681-43932357	K562	blood:	n/a	n/a
29	ELF1	chr10:43931700-43932957	GM12878	blood:	n/a	chr10:43932119-43932130 chr10:43932236-43932248
30	TCF7L2	chr10:43931714-43932410	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr10:43931661-43932803	U87	brain:	n/a	n/a
32	TAF1	chr10:43931742-43932876	HepG2	liver:	n/a	n/a
33	RAD21	chr10:43931694-43931900	HepG2	liver:	n/a	n/a
34	POLR2A	chr10:43930733-43932910	HepG2	liver:	n/a	n/a
35	STAT3	chr10:43931772-43932095	GM12878	blood:	n/a	n/a
36	ZNF143	chr10:43931760-43932498	K562	blood:	n/a	chr10:43932233-43932251 chr10:43932236-43932246
37	POLR2A	chr10:43931659-43932753	HepG2	liver:	n/a	n/a
38	MYC	chr10:43931745-43932677	K562	blood:	n/a	chr10:43932575-43932584
39	MXI1	chr10:43931520-43933034	IMR90	lung:	n/a	n/a
40	NR2F2	chr10:43931518-43932846	K562	blood:	n/a	n/a
41	TAF1	chr10:43931802-43932799	K562	blood:	n/a	n/a
42	POLR2A	chr10:43931790-43932638	GM12891	blood:	n/a	n/a
43	POLR2A	chr10:43931712-43932860	HCT-116	colon:	n/a	n/a
44	TAF1	chr10:43931811-43932655	HepG2	liver:	n/a	n/a
45	CTCF	chr10:43931760-43931910	GM12865	blood:	n/a	n/a
46	JUND	chr10:43931712-43932728	K562	blood:	n/a	n/a
47	MAFF	chr10:43931733-43932125	HepG2	liver:	n/a	n/a
48	MAX	chr10:43931740-43932636	GM12878	blood:	n/a	chr10:43932575-43932584
49	GTF2F1	chr10:43931813-43932687	H1-hESC	embryonic stem cell:	n/a	n/a
50	PML	chr10:43931650-43932711	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:43903244..43904543-chr10:43931320..43932838,6	Hela-S3	cervix:
2	chr10:43889891..43893674-chr10:43930869..43934431,5	MCF-7	breast:
3	chr10:43930579..43934633-chr10:43949587..43954210,8	K562	blood:
4	chr10:43912793..43917262-chr10:43929806..43934635,10	MCF-7	breast:
5	chr10:43931567..43932335-chr8:33342087..33342660,2	Hela-S3	cervix:
6	chr10:43931809..43932733-chr9:86594490..86595462,2	Hela-S3	cervix:
7	chr10:43931795..43932553-chr16:68271279..68271889,2	Hela-S3	cervix:
8	chr10:43913553..43915356-chr10:43929097..43931961,3	K562	blood:
9	chr10:43901784..43908257-chr10:43928243..43934263,17	MCF-7	breast:
10	chr10:43930452..43932223-chr17:43227607..43229368,2	K562	blood:
11	chr10:43915403..43918859-chr10:43929644..43933431,7	K562	blood:
12	chr10:43901370..43906375-chr10:43928042..43934083,16	MCF-7	breast:
13	chr10:43914713..43918981-chr10:43928825..43933676,11	MCF-7	breast:

Variant related genes	Relation type
ZNF487	TF binding region
ENSG00000169813	Chromatin interaction
ENSG00000165119	Chromatin interaction
ENSG00000198042	Chromatin interaction
ENSG00000221400	Chromatin interaction
ENSG00000261469	Chromatin interaction
ENSG00000252532	Chromatin interaction
ENSG00000230555	Chromatin interaction

Extended variants
information (count: 97 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:90)

rs_ID	r²[population]
rs10732897	0.85[ASN][1000 genomes]
rs10751319	0.84[AMR][1000 genomes]
rs10793430	0.91[ASN][1000 genomes]
rs10793431	0.89[ASW][hapmap];0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap];0.99[MKK][hapmap];0.94[TSI][hapmap];0.86[YRI][hapmap];0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10899794	0.85[JPT][hapmap]
rs10899795	0.84[CEU][hapmap];0.93[GIH][hapmap];0.86[TSI][hapmap];0.81[EUR][1000 genomes]
rs10899797	0.85[JPT][hapmap]
rs10899798	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10899799	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11238542	0.94[ASN][1000 genomes]
rs1126487	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs12257917	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs12779063	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs1416226	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2066043	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2066044	0.89[ASW][hapmap];0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.86[YRI][hapmap];0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2247860	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2247979	0.89[ASW][hapmap];0.83[CHB][hapmap];0.91[GIH][hapmap];0.85[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.83[YRI][hapmap];0.91[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs2247981	0.89[ASW][hapmap];0.83[CHB][hapmap];0.91[GIH][hapmap];0.85[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.83[YRI][hapmap];0.91[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs2248332	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2248335	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2248469	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2248706	0.91[ASN][1000 genomes]
rs2250444	0.89[ASW][hapmap];0.83[CHB][hapmap];0.91[GIH][hapmap];0.85[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.87[YRI][hapmap];0.90[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs2252783	0.89[ASW][hapmap];0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.90[LWK][hapmap];0.94[MEX][hapmap];0.99[MKK][hapmap];1.00[TSI][hapmap];0.86[YRI][hapmap];0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2252785	0.89[ASW][hapmap];0.94[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];0.94[MEX][hapmap];0.99[MKK][hapmap];1.00[TSI][hapmap];0.86[YRI][hapmap];0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2252800	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs2252804	0.81[AFR][1000 genomes]
rs2255967	0.84[AFR][1000 genomes]
rs2256495	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2256613	0.91[ASN][1000 genomes]
rs2259045	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2260162	0.99[ASN][1000 genomes]
rs2260200	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2261636	0.85[JPT][hapmap];0.87[YRI][hapmap];0.90[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs2261665	0.90[ASN][1000 genomes]
rs2265886	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.94[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];0.82[YRI][hapmap];0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2265887	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs2265888	0.96[AFR][1000 genomes]
rs2265952	0.81[AMR][1000 genomes]
rs2265953	0.83[AMR][1000 genomes]
rs2265954	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2393954	0.91[ASN][1000 genomes]
rs2492403	0.99[ASN][1000 genomes]
rs2492404	0.84[AFR][1000 genomes]
rs2492407	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs2492408	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2492409	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2492410	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2492411	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2492412	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2493648	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2812797	0.89[ASN][1000 genomes]
rs2819021	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2819026	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2819032	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs2819034	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs2999223	0.82[ASN][1000 genomes]
rs2999225	0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2999276	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2999282	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2999286	0.85[AFR][1000 genomes]
rs2999287	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3000700	0.88[AFR][1000 genomes]
rs3006405	0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs3006408	0.89[ASN][1000 genomes]
rs3006409	0.83[ASN][1000 genomes]
rs3750890	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs4551711	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4559639	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4584528	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4597022	0.89[ASW][hapmap];0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];0.94[MEX][hapmap];0.99[MKK][hapmap];1.00[TSI][hapmap];0.86[YRI][hapmap];0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4948726	0.83[CHB][hapmap];0.85[JPT][hapmap];0.87[YRI][hapmap];0.90[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs56059584	0.84[AFR][1000 genomes]
rs61859002	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6421744	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6593513	0.85[JPT][hapmap]
rs7069214	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7070029	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs7070769	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs7081729	0.93[ASN][1000 genomes]
rs7088430	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs7089290	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7092599	0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7894374	0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7905676	0.83[CHB][hapmap];0.85[JPT][hapmap]
rs7914140	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7918726	0.91[ASN][1000 genomes]
rs7920539	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs9422371	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430159	chr10:43291894-43946294	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
2	nsv895087	chr10:43783339-43982390	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
3	nsv831842	chr10:43846541-43987501	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
4	nsv895088	chr10:43871999-44003101	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
5	nsv825354	chr10:43883418-43949936	Flanking Active TSS Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
6	nsv825356	chr10:43893080-43946515	Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	63 gene(s)	inside rSNPs	diseases
7	esv3448813	chr10:43919995-43950867	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 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	chr10:43930400-43933000	Active TSS	Hela-S3	cervix
2	chr10:43930600-43933000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
3	chr10:43930800-43933200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr10:43930800-43933200	Active TSS	Duodenum Smooth Muscle	Duodenum
5	chr10:43931000-43932800	Active TSS	Brain Hippocampus Middle	brain
6	chr10:43931000-43932800	Active TSS	NHEK	skin
7	chr10:43931000-43933000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr10:43931000-43933000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr10:43931000-43933000	Active TSS	HSMM	muscle
10	chr10:43931000-43933200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr10:43931000-43933200	Active TSS	A549	lung
12	chr10:43931200-43932800	Active TSS	Liver	Liver
13	chr10:43931200-43932800	Active TSS	Duodenum Mucosa	Duodenum
14	chr10:43931200-43932800	Active TSS	Stomach Smooth Muscle	stomach
15	chr10:43931200-43932800	Active TSS	Dnd41	blood
16	chr10:43931200-43932800	Active TSS	HMEC	breast
17	chr10:43931200-43932800	Active TSS	K562	blood
18	chr10:43931200-43933200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr10:43931200-43933200	Active TSS	Brain Inferior Temporal Lobe	brain
20	chr10:43931200-43933200	Active TSS	Rectal Mucosa Donor 29	rectum
21	chr10:43931400-43932000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
22	chr10:43931400-43932000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
23	chr10:43931400-43932000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
24	chr10:43931400-43932000	Active TSS	Right Atrium	heart
25	chr10:43931400-43932200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr10:43931400-43932200	Flanking Active TSS	Fetal Muscle Trunk	muscle
27	chr10:43931400-43932200	Flanking Active TSS	Placenta	Placenta
28	chr10:43931400-43932600	Active TSS	Colonic Mucosa	Colon
29	chr10:43931400-43932800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr10:43931400-43932800	Active TSS	Rectal Smooth Muscle	rectum
31	chr10:43931400-43933000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr10:43931400-43933000	Active TSS	Psoas Muscle	Psoas
33	chr10:43931400-43933200	Active TSS	HUES64 Cell Line	embryonic stem cell
34	chr10:43931400-43933200	Active TSS	Fetal Intestine Large	intestine
35	chr10:43931400-43933200	Active TSS	Pancreatic Islets	Pancreatic Islet
36	chr10:43931400-43933200	Active TSS	Skeletal Muscle Male	skeletal muscle
37	chr10:43931400-43933400	Active TSS	Breast Myoepithelial Primary Cells	Breast
38	chr10:43931600-43932000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
39	chr10:43931600-43932000	Flanking Active TSS	Primary B cells from cord blood	blood
40	chr10:43931600-43932000	Flanking Active TSS	Primary B cells from peripheral blood	blood
41	chr10:43931600-43932000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
42	chr10:43931600-43932000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
43	chr10:43931600-43932000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
44	chr10:43931600-43932000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
45	chr10:43931600-43932000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
46	chr10:43931600-43932000	Flanking Active TSS	Fetal Muscle Leg	muscle
47	chr10:43931600-43932000	Flanking Active TSS	Fetal Thymus	thymus
48	chr10:43931600-43932000	Flanking Active TSS	HUVEC	blood vessel
49	chr10:43931600-43932000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
50	chr10:43931600-43932200	Flanking Active TSS	Primary hematopoietic stem cells	blood

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