Variant report

Variant	rs10904416
Chromosome Location	chr10:5137601-5137602
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	SP1	chr10:5136292-5138992	A549	lung:	n/a	chr10:5136552-5136562 chr10:5136548-5136562 chr10:5136551-5136563 chr10:5136551-5136563 chr10:5136552-5136561 chr10:5136507-5136528
2	CTCF	chr10:5137600-5137750	HMF	breast:	n/a	n/a
3	REST	chr10:5135146-5139228	A549	lung:	n/a	n/a
4	SIN3AK20	chr10:5137213-5137765	A549	lung:	n/a	n/a
5	BCL3	chr10:5134993-5138735	A549	lung:	n/a	chr10:5137586-5137595 chr10:5136770-5136779
6	FOSL2	chr10:5135165-5139175	A549	lung:	n/a	chr10:5136821-5136831 chr10:5136823-5136834 chr10:5136821-5136830 chr10:5136821-5136831 chr10:5138903-5138915 chr10:5136822-5136831 chr10:5136820-5136832 chr10:5136822-5136829
7	TAF1	chr10:5136270-5137752	A549	lung:	n/a	n/a
8	BRCA1	chr10:5136453-5137624	Hela-S3	cervix:	n/a	n/a
9	EP300	chr10:5134998-5137746	A549	lung:	n/a	chr10:5135763-5135777 chr10:5136729-5136738 chr10:5137675-5137689 chr10:5136822-5136831
10	TCF12	chr10:5134878-5139332	A549	lung:	n/a	n/a
11	SIX5	chr10:5136756-5139393	A549	lung:	n/a	n/a
12	TBP	chr10:5136188-5137642	Hela-S3	cervix:	n/a	n/a
13	SP1	chr10:5134963-5137699	A549	lung:	n/a	chr10:5136552-5136562 chr10:5136548-5136562 chr10:5136551-5136563 chr10:5136551-5136563 chr10:5136552-5136561 chr10:5136507-5136528
14	RAD21	chr10:5136394-5137664	A549	lung:	n/a	n/a
15	CTCF	chr10:5136062-5138926	A549	lung:	n/a	chr10:5137004-5137025 chr10:5137015-5137024 chr10:5137009-5137027

No.	Distal block	Cell Line	Cell type
1	chr10:4891149..4892494-chr10:5136639..5137645,6	MCF-7	breast:
2	chr10:5135730..5137727-chr10:5144800..5147673,2	K562	blood:
3	chr10:5119351..5122041-chr10:5135538..5138283,2	MCF-7	breast:
4	chr10:5135730..5138906-chr10:5144094..5147673,3	K562	blood:

Variant related genes	Relation type
AKR1C3	TF binding region
ENSG00000239142	TF binding region
ENSG00000196139	Chromatin interaction

Extended variants
information (count: 105 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs10508294	0.96[CEU][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10904415	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10904436	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10904439	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11252928	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11252931	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11252934	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11252935	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11252936	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11252937	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11252941	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11252955	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11252968	0.96[CEU][hapmap];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11252972	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11252978	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11252992	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11253010	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11253012	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11253013	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11253015	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11253016	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11253018	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11253019	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11253020	0.96[CEU][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11253021	0.96[CEU][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11253022	0.96[CEU][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11253036	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11253039	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11492955	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11517338	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11517343	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11517344	0.86[AMR][1000 genomes]
rs12354416	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12354530	1.00[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12357445	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12357449	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12359896	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12360480	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12769156	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1334466	0.83[AMR][1000 genomes]
rs1334467	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1334471	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1334738	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1334739	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17134288	0.96[CEU][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17305952	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1889458	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1937843	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1937909	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2020172	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2210679	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2895061	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2895064	0.86[CEU][hapmap];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs34914591	0.84[AMR][1000 genomes]
rs35219485	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3763676	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4448597	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4880711	0.92[CEU][hapmap];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4880714	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4880715	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4881406	0.96[CEU][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4881407	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6601901	0.86[EUR][1000 genomes]
rs6601907	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6601918	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7069331	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7090349	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7090531	0.96[CEU][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7097295	0.96[CEU][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7097646	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7477623	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7478099	1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7741	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7920141	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7920454	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9730736	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9794203	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv894792	chr10:4832920-5498724	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv948794	chr10:4863093-5227382	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv1045155	chr10:4872239-5211318	Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv1040343	chr10:4872814-5196815	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv540462	chr10:4872814-5196815	Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
6	nsv869470	chr10:4878904-5203685	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
7	nsv466713	chr10:4901798-5319679	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
8	nsv549881	chr10:4901798-5319679	Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
9	nsv534685	chr10:4914018-5853324	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
10	nsv1050246	chr10:4927428-5211318	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
11	nsv549882	chr10:4943518-5203864	Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
12	esv2763913	chr10:4961021-5321407	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
13	nsv1039386	chr10:5008383-5348491	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
14	nsv1036566	chr10:5037926-5261426	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
15	nsv549883	chr10:5037926-5275762	Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
16	nsv1047484	chr10:5076258-5261482	Enhancers Strong transcription Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
17	nsv1036291	chr10:5076258-5456234	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
18	nsv1042487	chr10:5090313-5196900	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
19	nsv540463	chr10:5090313-5196900	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
20	nsv540464	chr10:5108345-5196815	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
21	nsv540465	chr10:5108345-5261482	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
22	nsv540466	chr10:5114577-5196815	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
23	nsv540467	chr10:5114577-5225365	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
24	nsv540468	chr10:5114577-5261482	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
25	nsv540469	chr10:5120774-5225365	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
26	nsv540470	chr10:5120774-5261482	Flanking Active TSS Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
27	nsv540471	chr10:5133561-5261482	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
28	nsv540472	chr10:5133561-5284334	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5135400-5138000	Active TSS	A549	lung
2	chr10:5135800-5138400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr10:5136000-5139400	Active TSS	Duodenum Mucosa	Duodenum
4	chr10:5136200-5138000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr10:5136200-5138400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr10:5136200-5138800	Active TSS	Rectal Mucosa Donor 29	rectum
7	chr10:5136400-5137800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr10:5136400-5137800	Active TSS	Skeletal Muscle Male	skeletal muscle
9	chr10:5136400-5138000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr10:5136400-5138000	Active TSS	Muscle Satellite Cultured Cells	--
11	chr10:5136400-5138000	Active TSS	Thymus	Thymus
12	chr10:5136400-5138400	Active TSS	Primary hematopoietic stem cells	blood
13	chr10:5136400-5138400	Active TSS	Liver	Liver
14	chr10:5136400-5138400	Active TSS	Colon Smooth Muscle	Colon
15	chr10:5136400-5138400	Active TSS	Psoas Muscle	Psoas
16	chr10:5136400-5138400	Active TSS	Hela-S3	cervix
17	chr10:5136400-5138600	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
18	chr10:5136400-5138600	Active TSS	Aorta	Aorta
19	chr10:5136400-5138600	Active TSS	Rectal Smooth Muscle	rectum
20	chr10:5136400-5138600	Active TSS	Stomach Smooth Muscle	stomach
21	chr10:5136400-5138600	Active TSS	HSMMtube	muscle
22	chr10:5136400-5138800	Active TSS	Brain Anterior Caudate	brain
23	chr10:5136400-5139000	Active TSS	Duodenum Smooth Muscle	Duodenum
24	chr10:5136400-5139000	Active TSS	Rectal Mucosa Donor 31	rectum
25	chr10:5136400-5140000	Active TSS	Right Atrium	heart
26	chr10:5136600-5138200	Active TSS	Brain Cingulate Gyrus	brain
27	chr10:5136600-5138600	Active TSS	Brain Hippocampus Middle	brain
28	chr10:5136600-5138600	Active TSS	Left Ventricle	heart
29	chr10:5136600-5138800	Active TSS	Stomach Mucosa	stomach
30	chr10:5136600-5147400	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr10:5136800-5138000	Active TSS	Adipose Nuclei	Adipose
32	chr10:5137000-5138200	Active TSS	Osteobl	bone
33	chr10:5137000-5138400	Active TSS	Fetal Kidney	kidney
34	chr10:5137000-5138400	Active TSS	NHDF-Ad	bronchial
35	chr10:5137000-5138600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr10:5137000-5138800	Active TSS	Skeletal Muscle Female	skeletal muscle
37	chr10:5137000-5141200	Weak transcription	Lung	lung
38	chr10:5137200-5138200	Weak transcription	Gastric	stomach
39	chr10:5137200-5138400	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr10:5137200-5145200	Weak transcription	Esophagus	oesophagus
41	chr10:5137200-5145800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr10:5137200-5149800	Weak transcription	Small Intestine	intestine
43	chr10:5137400-5137800	Weak transcription	Primary T helper cells PMA-I stimulated	--
44	chr10:5137400-5137800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
45	chr10:5137400-5138200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
46	chr10:5137400-5138400	Weak transcription	Colonic Mucosa	Colon
47	chr10:5137400-5138400	Weak transcription	Ovary	ovary
48	chr10:5137400-5138400	Active TSS	HepG2	liver
49	chr10:5137400-5149400	Weak transcription	HSMM	muscle
50	chr10:5137400-5149600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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