Variant report

Variant	rs9810881
Chromosome Location	chr3:46968122-46968123
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	POLR2A	chr3:46967180-46969276	GM19099	blood:	n/a	n/a
2	POLR2A	chr3:46966327-46969602	GM12878	blood:	n/a	n/a
3	FOXM1	chr3:46967934-46969255	GM12878	blood:	n/a	n/a
4	MXI1	chr3:46967257-46968645	IMR90	lung:	n/a	n/a
5	POLR2A	chr3:46967958-46969376	K562	blood:	n/a	n/a
6	EBF1	chr3:46968063-46969292	GM12878	blood:	n/a	chr3:46968194-46968203 chr3:46968900-46968911
7	RUNX3	chr3:46968037-46969500	GM12878	blood:	n/a	n/a
8	POLR2A	chr3:46966735-46970133	GM12878	blood:	n/a	n/a
9	RUNX3	chr3:46967320-46969539	GM12878	blood:	n/a	n/a
10	CTCF	chr3:46968100-46968250	HUVEC	blood vessel:	n/a	n/a
11	POLR2A	chr3:46967468-46969287	GM12892	blood:	n/a	n/a
12	ATF2	chr3:46968000-46969217	GM12878	blood:	n/a	n/a
13	POLR2A	chr3:46968103-46968753	Hela-S3	cervix:	n/a	n/a
14	CHD1	chr3:46968119-46969339	GM12878	blood:	n/a	chr3:46969055-46969065
15	SPI1	chr3:46968085-46969541	GM12878	blood:	n/a	chr3:46969350-46969363 chr3:46968823-46968836 chr3:46968166-46968179
16	TCF12	chr3:46968078-46969129	GM12878	blood:	n/a	chr3:46968141-46968151 chr3:46968275-46968282 chr3:46968117-46968127
17	MTA3	chr3:46966876-46970269	GM12878	blood:	n/a	n/a
18	POLR2A	chr3:46966700-46969363	GM18951	blood:	n/a	n/a
19	MTA3	chr3:46968092-46969485	GM12878	blood:	n/a	n/a
20	POLR2A	chr3:46967011-46969467	GM12891	blood:	n/a	n/a
21	ELF1	chr3:46967998-46969492	GM12878	blood:	n/a	n/a
22	NFIC	chr3:46968093-46970282	GM12878	blood:	n/a	n/a
23	POLR2A	chr3:46967978-46968850	GM12878	blood:	n/a	n/a
24	EBF1	chr3:46968039-46969240	GM12878	blood:	n/a	chr3:46968194-46968203 chr3:46968900-46968911
25	POLR2A	chr3:46967431-46969383	GM12878	blood:	n/a	n/a
26	ZEB1	chr3:46968005-46969198	GM12878	blood:	n/a	chr3:46968231-46968238
27	POLR2A	chr3:46966650-46969522	GM12891	blood:	n/a	n/a
28	POLR2A	chr3:46967362-46969388	GM12878	blood:	n/a	n/a
29	BCL3	chr3:46968088-46969113	GM12878	blood:	n/a	chr3:46968830-46968839 chr3:46968099-46968108
30	POLR2A	chr3:46968119-46968345	HepG2	liver:	n/a	n/a
31	POLR2A	chr3:46956505-46971093	K562	blood:	n/a	n/a
32	STAT5A	chr3:46967744-46970468	GM12878	blood:	n/a	chr3:46967978-46967986 chr3:46968254-46968266 chr3:46968830-46968841 chr3:46968696-46968708 chr3:46968403-46968410 chr3:46968086-46968109 chr3:46968321-46968329
33	POLR2A	chr3:46966882-46970456	GM12891	blood:	n/a	n/a
34	FOXM1	chr3:46968085-46969234	GM12878	blood:	n/a	n/a
35	POLR2A	chr3:46966435-46970329	GM18505	blood:	n/a	n/a
36	RCOR1	chr3:46967450-46968435	IMR90	lung:	n/a	n/a
37	POLR2A	chr3:46966857-46969609	GM12892	blood:	n/a	n/a
38	WRNIP1	chr3:46967596-46969273	GM12878	blood:	n/a	n/a
39	USF2	chr3:46968102-46969152	GM12878	blood:	n/a	n/a
40	POLR2A	chr3:46967351-46969467	GM19193	blood:	n/a	n/a
41	POLR2A	chr3:46966326-46969534	GM12892	blood:	n/a	n/a
42	POLR2A	chr3:46966461-46969470	GM12892	blood:	n/a	n/a
43	POLR2A	chr3:46966406-46968245	A549	lung:	n/a	n/a
44	POLR2A	chr3:46966707-46970065	GM12878	blood:	n/a	n/a
45	POLR2A	chr3:46967606-46969273	GM12878	blood:	n/a	n/a
46	CHD2	chr3:46968024-46969309	GM12878	blood:	n/a	chr3:46969055-46969065
47	IKZF1	chr3:46968091-46969290	GM12878	blood:	n/a	n/a
48	POLR2A	chr3:46966311-46969582	GM12892	blood:	n/a	n/a
49	EBF1	chr3:46967776-46969497	GM12878	blood:	n/a	chr3:46968194-46968203 chr3:46968900-46968911
50	SPI1	chr3:46968084-46969173	GM12891	blood:	n/a	chr3:46968823-46968836 chr3:46968166-46968179

No.	Distal block	Cell Line	Cell type
1	chr3:46967009..46980239-chr3:47015804..47024437,23	MCF-7	breast:
2	chr3:46966733..46968938-chr3:47035742..47038273,2	K562	blood:
3	chr3:46967306..46968929-chr3:46979271..46981150,2	K562	blood:
4	chr3:46966739..46968792-chr3:46972024..46974475,2	K562	blood:
5	chr3:46967003..46969518-chr3:47029296..47031281,2	K562	blood:
6	chr3:46967003..46969094-chr3:47027907..47030796,2	K562	blood:
7	chr3:46966170..46968321-chr3:47021061..47023040,2	K562	blood:
8	chr3:46965883..46969429-chr3:47022291..47025425,4	MCF-7	breast:
9	chr3:46966646..46969252-chr3:47031389..47034280,2	MCF-7	breast:

Variant related genes	Relation type
CCDC12	TF binding region
ENSG00000160799	Chromatin interaction
ENSG00000160796	Chromatin interaction

Extended variants
information (count: 151 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:142)

rs_ID	r²[population]
rs10461017	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10461019	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10865945	1.00[EUR][1000 genomes]
rs11130108	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11130109	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11706212	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11708257	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11709693	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11709876	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11713537	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11928558	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12330516	1.00[EUR][1000 genomes]
rs12487763	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13062185	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13079416	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13082531	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13323092	1.00[EUR][1000 genomes]
rs1378818	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1463394	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1466272	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1466273	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1466274	0.89[AMR][1000 genomes]
rs1473382	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1473384	1.00[EUR][1000 genomes]
rs1473385	1.00[EUR][1000 genomes]
rs1563431	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1563432	1.00[EUR][1000 genomes]
rs1814564	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1869870	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1979736	1.00[EUR][1000 genomes]
rs2124509	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2124510	1.00[AMR][1000 genomes]
rs2385863	1.00[EUR][1000 genomes]
rs2385868	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2385869	1.00[AMR][1000 genomes]
rs28735306	1.00[EUR][1000 genomes]
rs2891887	1.00[AMR][1000 genomes]
rs2891893	0.89[AMR][1000 genomes]
rs34147581	1.00[EUR][1000 genomes]
rs35366910	1.00[EUR][1000 genomes]
rs3930202	1.00[EUR][1000 genomes]
rs4018904	1.00[EUR][1000 genomes]
rs4282092	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4289375	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4324490	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4373094	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4378998	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4389512	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4450857	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4478107	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4522803	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4525902	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4543047	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4682828	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4682832	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4682833	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4682834	1.00[EUR][1000 genomes]
rs4682835	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4682836	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4682838	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4682840	0.89[AMR][1000 genomes]
rs4682841	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4682843	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4682846	1.00[EUR][1000 genomes]
rs4682847	1.00[EUR][1000 genomes]
rs4683277	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4683279	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4683283	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4683284	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4683285	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4683286	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4683288	1.00[EUR][1000 genomes]
rs4683289	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4683290	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4683291	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4683292	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4683293	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4683303	1.00[EUR][1000 genomes]
rs6442041	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6442042	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6442043	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6442044	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6442047	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6442048	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6766676	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6768169	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6775797	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6780994	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6785462	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6804732	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6806521	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6808052	1.00[EUR][1000 genomes]
rs6808629	1.00[EUR][1000 genomes]
rs6809904	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73831482	1.00[EUR][1000 genomes]
rs7615774	1.00[EUR][1000 genomes]
rs7621530	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7624549	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7625011	0.89[AMR][1000 genomes]
rs7630154	1.00[EUR][1000 genomes]
rs7630904	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7638549	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7641494	1.00[EUR][1000 genomes]
rs7643868	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7644382	1.00[EUR][1000 genomes]
rs7646076	1.00[EUR][1000 genomes]
rs7649941	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7650142	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7652492	1.00[EUR][1000 genomes]
rs936173	1.00[EUR][1000 genomes]
rs936177	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs936178	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs936179	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs936180	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs936181	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs936182	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs936185	1.00[EUR][1000 genomes]
rs936186	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs939409	1.00[EUR][1000 genomes]
rs939410	1.00[EUR][1000 genomes]
rs939411	1.00[EUR][1000 genomes]
rs939412	1.00[EUR][1000 genomes]
rs939413	1.00[EUR][1000 genomes]
rs939415	1.00[EUR][1000 genomes]
rs9812407	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9819344	1.00[EUR][1000 genomes]
rs9819475	1.00[EUR][1000 genomes]
rs9823480	1.00[EUR][1000 genomes]
rs9826488	1.00[EUR][1000 genomes]
rs9827293	1.00[EUR][1000 genomes]
rs9828473	1.00[EUR][1000 genomes]
rs9833500	1.00[EUR][1000 genomes]
rs9836801	1.00[EUR][1000 genomes]
rs9850151	1.00[EUR][1000 genomes]
rs9852167	1.00[EUR][1000 genomes]
rs9861265	1.00[EUR][1000 genomes]
rs9862711	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9869489	1.00[EUR][1000 genomes]
rs9878813	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9883152	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9883909	1.00[EUR][1000 genomes]
rs9990284	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007449	chr3:46652343-46986578	Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
2	nsv536554	chr3:46652343-46986578	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
3	esv2757869	chr3:46680452-46972489	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
4	esv2759147	chr3:46680452-46972489	Genic enhancers Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
5	nsv536558	chr3:46706571-47024756	Enhancers Bivalent Enhancer Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
6	nsv915922	chr3:46768104-47009805	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
7	nsv876755	chr3:46895109-47061183	Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
8	nsv460526	chr3:46935527-47001350	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
9	nsv3800	chr3:46961648-47007241	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46958200-46968200	Strong transcription	Rectal Mucosa Donor 31	rectum
2	chr3:46958200-46968800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr3:46958400-46968200	Strong transcription	Dnd41	blood
4	chr3:46958600-46970200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
5	chr3:46959000-46971400	Strong transcription	K562	blood
6	chr3:46959400-46968200	Strong transcription	Sigmoid Colon	Sigmoid Colon
7	chr3:46959600-46970600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr3:46959800-46969200	Strong transcription	NHEK	skin
9	chr3:46959800-46971200	Strong transcription	Hela-S3	cervix
10	chr3:46960200-46968600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr3:46960200-46971200	Strong transcription	HUES64 Cell Line	embryonic stem cell
12	chr3:46960400-46968400	Strong transcription	H1 Cell Line	embryonic stem cell
13	chr3:46960400-46969400	Strong transcription	HUES6 Cell Line	embryonic stem cell
14	chr3:46960400-46970400	Strong transcription	HUES48 Cell Line	embryonic stem cell
15	chr3:46960400-46970400	Strong transcription	Fetal Lung	lung
16	chr3:46960600-46969800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr3:46961000-46970000	Strong transcription	Brain Germinal Matrix	brain
18	chr3:46961200-46968400	Strong transcription	H9 Cell Line	embryonic stem cell
19	chr3:46961400-46970400	Strong transcription	Fetal Brain Female	brain
20	chr3:46961800-46971200	Strong transcription	HepG2	liver
21	chr3:46962000-46969200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
22	chr3:46962600-46969200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr3:46962600-46972400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr3:46962800-46972400	Weak transcription	Fetal Kidney	kidney
25	chr3:46964000-46970200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr3:46964200-46970000	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr3:46964400-46969600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr3:46964600-46969400	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr3:46964600-46969400	Genic enhancers	Stomach Smooth Muscle	stomach
30	chr3:46964600-46975600	Weak transcription	Fetal Brain Male	brain
31	chr3:46964800-46968800	Genic enhancers	Primary T cells fromperipheralblood	blood
32	chr3:46964800-46969400	Genic enhancers	Gastric	stomach
33	chr3:46964800-46972800	Enhancers	Fetal Heart	heart
34	chr3:46965000-46969600	Genic enhancers	Right Ventricle	heart
35	chr3:46965000-46971200	Genic enhancers	Primary T helper cells fromperipheralblood	blood
36	chr3:46965200-46968200	Genic enhancers	Primary hematopoietic stem cells	blood
37	chr3:46965200-46968200	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
38	chr3:46965200-46968200	Genic enhancers	Spleen	Spleen
39	chr3:46965400-46969600	Genic enhancers	Fetal Muscle Trunk	muscle
40	chr3:46965400-46970000	Genic enhancers	Esophagus	oesophagus
41	chr3:46965600-46968200	Genic enhancers	Duodenum Mucosa	Duodenum
42	chr3:46965800-46969800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr3:46965800-46970000	Strong transcription	Cortex derived primary cultured neurospheres	brain
44	chr3:46966000-46969800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr3:46966400-46968400	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr3:46966400-46968600	Genic enhancers	Placenta	Placenta
47	chr3:46966400-46969600	Enhancers	Right Atrium	heart
48	chr3:46966400-46969800	Genic enhancers	Fetal Muscle Leg	muscle
49	chr3:46966400-46971400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr3:46966600-46968200	Genic enhancers	Primary monocytes fromperipheralblood	blood

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