Variant report

Variant	rs12356612
Chromosome Location	chr10:1055055-1055056
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:34)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:34 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	EP300	chr10:1054477-1055669	SK-N-SH	brain:	n/a	chr10:1054792-1054806
2	REST	chr10:1054954-1055394	SK-N-SH	brain:	n/a	n/a
3	POLR2A	chr10:1054972-1055586	K562	blood:	n/a	n/a
4	GATA2	chr10:1054998-1055574	SH-SY5Y	brain:	n/a	n/a
5	GATA1	chr10:1055015-1055771	K562	blood:	n/a	n/a
6	POLR2A	chr10:1055044-1055580	HepG2	liver:	n/a	n/a
7	HMGN3	chr10:1054979-1055455	K562	blood:	n/a	n/a
8	POLR2A	chr10:1054906-1055092	H1-hESC	embryonic stem cell:	n/a	n/a
9	EP300	chr10:1054927-1055379	SK-N-SH_RA	brain:	n/a	n/a
10	POLR2A	chr10:1054934-1055132	A549	lung:	n/a	n/a
11	TCF12	chr10:1054913-1055572	SK-N-SH	brain:	n/a	n/a
12	POLR2A	chr10:1054785-1057747	K562	blood:	n/a	n/a
13	EP300	chr10:1055020-1055545	K562	blood:	n/a	n/a
14	POLR2A	chr10:1054815-1055404	Hela-S3	cervix:	n/a	n/a
15	POLR2A	chr10:1054903-1055513	GM12892	blood:	n/a	n/a
16	CCNT2	chr10:1055021-1055508	K562	blood:	n/a	n/a
17	POLR2A	chr10:1054886-1055392	K562	blood:	n/a	n/a
18	POLR2A	chr10:1054921-1055136	GM12878	blood:	n/a	n/a
19	POLR2A	chr10:1055010-1055484	K562	blood:	n/a	n/a
20	GATA1	chr10:1054954-1055574	PBDE	blood:	n/a	n/a
21	POLR2A	chr10:1054790-1056448	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr10:1054836-1058782	GM12892	blood:	n/a	n/a
23	RCOR1	chr10:1054982-1055603	K562	blood:	n/a	n/a
24	GATA3	chr10:1054963-1055587	SK-N-SH	brain:	n/a	n/a
25	POLR2A	chr10:1054878-1055542	K562	blood:	n/a	n/a
26	POLR2A	chr10:1054852-1055298	GM12878	blood:	n/a	n/a
27	POLR2A	chr10:1054963-1055500	GM12891	blood:	n/a	n/a
28	POLR2A	chr10:1054954-1055108	A549	lung:	n/a	n/a
29	POLR2A	chr10:1054632-1058917	K562	blood:	n/a	n/a
30	POLR2A	chr10:1054952-1055143	GM12878	blood:	n/a	n/a
31	POLR2A	chr10:1054801-1055611	K562	blood:	n/a	n/a
32	POLR2A	chr10:1054218-1059008	A549	lung:	n/a	n/a
33	TEAD4	chr10:1055001-1055570	K562	blood:	n/a	n/a
34	EP300	chr10:1055013-1055467	SK-N-SH_RA	brain:	n/a	n/a

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:1048395..1052203-chr10:1053928..1057241,3	MCF-7	breast:
2	chr10:1054711..1057336-chr10:1093694..1095483,2	MCF-7	breast:
3	chr10:1052939..1055149-chr10:1088165..1090086,2	MCF-7	breast:
4	chr10:1033201..1035981-chr10:1054777..1056323,2	MCF-7	breast:
5	chr10:1052653..1055132-chr10:1094709..1096832,2	K562	blood:
6	chr10:1053366..1056354-chr10:1087658..1089642,2	K562	blood:
7	chr10:1031655..1033355-chr10:1053764..1056440,2	K562	blood:
8	chr10:1053992..1056284-chr10:1061634..1063262,2	K562	blood:
9	chr10:1053366..1056481-chr10:1086210..1089642,3	K562	blood:
10	chr10:1053179..1055951-chr10:1060885..1063576,2	MCF-7	breast:

No data

Variant related genes	Relation type
GTPBP4	TF binding region
ENSG00000205740	Chromatin interaction
ENSG00000047056	Chromatin interaction
ENSG00000067064	Chromatin interaction
ENSG00000107937	Chromatin interaction
ENSG00000238924	Chromatin interaction

Extended variants
information (count: 103 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:83)

rs_ID	r²[population]
rs1013504	1.00[ASN][1000 genomes]
rs10903358	1.00[ASN][1000 genomes]
rs11250228	1.00[CEU][hapmap]
rs11253504	1.00[ASN][1000 genomes]
rs11253518	1.00[ASN][1000 genomes]
rs11253530	1.00[ASN][1000 genomes]
rs11253537	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11253538	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11253539	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11253540	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11253549	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11253550	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11253557	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11253558	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11253559	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11253560	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12354914	1.00[ASN][1000 genomes]
rs12357633	1.00[ASN][1000 genomes]
rs12359796	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1250891	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12761180	1.00[ASN][1000 genomes]
rs12762228	1.00[ASN][1000 genomes]
rs12768348	1.00[ASN][1000 genomes]
rs12769002	1.00[ASN][1000 genomes]
rs12770173	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12770910	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12771179	1.00[ASN][1000 genomes]
rs12771539	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12772979	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12773961	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12774985	1.00[ASN][1000 genomes]
rs12777021	1.00[ASN][1000 genomes]
rs12777788	0.83[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs12777800	1.00[ASN][1000 genomes]
rs12777801	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12778271	1.00[ASN][1000 genomes]
rs12781329	1.00[ASN][1000 genomes]
rs17221456	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17221463	1.00[CEU][hapmap];0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17221491	1.00[CEU][hapmap];1.00[ASN][1000 genomes]
rs17293580	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17293608	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1871621	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1871622	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28512382	1.00[ASN][1000 genomes]
rs34115136	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34159706	1.00[ASN][1000 genomes]
rs34251037	1.00[ASN][1000 genomes]
rs34270668	1.00[ASN][1000 genomes]
rs34318754	1.00[ASN][1000 genomes]
rs34480046	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34487581	1.00[ASN][1000 genomes]
rs34527494	1.00[ASN][1000 genomes]
rs34885925	1.00[ASN][1000 genomes]
rs35028518	1.00[ASN][1000 genomes]
rs35306767	1.00[ASN][1000 genomes]
rs35363972	1.00[ASN][1000 genomes]
rs35443149	1.00[ASN][1000 genomes]
rs35666723	1.00[ASN][1000 genomes]
rs35667562	1.00[ASN][1000 genomes]
rs35670857	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35709890	1.00[ASN][1000 genomes]
rs35957139	1.00[ASN][1000 genomes]
rs41260144	1.00[ASN][1000 genomes]
rs55697724	1.00[ASN][1000 genomes]
rs55708963	1.00[ASN][1000 genomes]
rs55742421	1.00[ASN][1000 genomes]
rs56222464	1.00[ASN][1000 genomes]
rs61830900	1.00[ASN][1000 genomes]
rs61830926	1.00[ASN][1000 genomes]
rs61830931	1.00[ASN][1000 genomes]
rs61830933	1.00[ASN][1000 genomes]
rs61833260	1.00[ASN][1000 genomes]
rs61833265	1.00[ASN][1000 genomes]
rs66462130	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66797613	1.00[ASN][1000 genomes]
rs67205460	1.00[ASN][1000 genomes]
rs67696450	1.00[ASN][1000 genomes]
rs7088956	1.00[ASN][1000 genomes]
rs7093665	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7094031	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72778228	1.00[ASN][1000 genomes]
rs7914758	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916591	chr10:224406-1088734	Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS 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	38 gene(s)	inside rSNPs	diseases
2	nsv540386	chr10:224406-1197416	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
3	nsv1054659	chr10:611444-1133578	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
4	nsv466697	chr10:734229-1129527	ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
5	nsv549765	chr10:734229-1129527	Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
6	nsv530116	chr10:776548-1401075	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
7	nsv1052540	chr10:887562-1300134	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
8	nsv540407	chr10:887562-1300134	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
9	nsv533861	chr10:945438-1382068	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
10	nsv530117	chr10:945438-1729634	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
11	nsv540408	chr10:955835-1260680	Enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
12	nsv817532	chr10:964660-1885945	Bivalent/Poised TSS Enhancers Strong transcription Flanking Active TSS Active TSS Weak 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 miRNA target site	39 gene(s)	inside rSNPs	diseases
13	nsv1050577	chr10:986723-1277854	Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
14	nsv540409	chr10:986723-1277854	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
15	nsv949405	chr10:1010464-1376105	Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
16	nsv1048254	chr10:1016006-1146595	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
17	esv1813158	chr10:1021156-1062915	Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases
18	esv1831483	chr10:1021156-1062915	Active TSS Strong transcription Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases
19	nsv1040178	chr10:1024910-1126104	Strong transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
20	nsv540410	chr10:1024910-1126104	Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 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	chr10:1035000-1094000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr10:1035800-1066200	Strong transcription	NH-A	brain
3	chr10:1036000-1066800	Strong transcription	HUES64 Cell Line	embryonic stem cell
4	chr10:1036200-1061800	Weak transcription	Stomach Mucosa	stomach
5	chr10:1036800-1066000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
6	chr10:1036800-1066800	Strong transcription	HUES48 Cell Line	embryonic stem cell
7	chr10:1036800-1066800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr10:1036800-1066800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr10:1037000-1066000	Strong transcription	Primary T cells fromperipheralblood	blood
10	chr10:1037000-1066200	Strong transcription	H1 Cell Line	embryonic stem cell
11	chr10:1037200-1066800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr10:1037200-1067200	Strong transcription	NHEK	skin
13	chr10:1038000-1066200	Strong transcription	HUVEC	blood vessel
14	chr10:1038000-1066200	Strong transcription	Osteobl	bone
15	chr10:1038000-1067200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr10:1038200-1067000	Strong transcription	HSMM	muscle
17	chr10:1038200-1067200	Strong transcription	Muscle Satellite Cultured Cells	--
18	chr10:1038200-1067400	Strong transcription	HUES6 Cell Line	embryonic stem cell
19	chr10:1038400-1063800	Strong transcription	HepG2	liver
20	chr10:1038400-1064200	Strong transcription	Brain Cingulate Gyrus	brain
21	chr10:1038400-1065600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr10:1038400-1065600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr10:1038400-1066000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
24	chr10:1038400-1066200	Strong transcription	Duodenum Mucosa	Duodenum
25	chr10:1038400-1066200	Strong transcription	Stomach Smooth Muscle	stomach
26	chr10:1038400-1066800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr10:1038400-1066800	Strong transcription	HMEC	breast
28	chr10:1038600-1066200	Strong transcription	Brain Angular Gyrus	brain
29	chr10:1038600-1066800	Strong transcription	Fetal Thymus	thymus
30	chr10:1038600-1066800	Strong transcription	Sigmoid Colon	Sigmoid Colon
31	chr10:1038600-1067000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
32	chr10:1038600-1067200	Strong transcription	Brain Inferior Temporal Lobe	brain
33	chr10:1038600-1068000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr10:1038800-1059600	Strong transcription	Lung	lung
35	chr10:1038800-1064200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr10:1038800-1064400	Strong transcription	Left Ventricle	heart
37	chr10:1038800-1065800	Strong transcription	Brain Anterior Caudate	brain
38	chr10:1038800-1066600	Strong transcription	ES-I3 Cell Line	embryonic stem cell
39	chr10:1038800-1067000	Strong transcription	Rectal Mucosa Donor 29	rectum
40	chr10:1038800-1067400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr10:1038800-1067800	Strong transcription	Skeletal Muscle Female	skeletal muscle
42	chr10:1039000-1060000	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr10:1039000-1064200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
44	chr10:1040600-1058800	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr10:1040600-1065600	Strong transcription	Placenta Amnion	Placenta Amnion
46	chr10:1041000-1063200	Strong transcription	Primary T helper naive cells from peripheral blood	blood
47	chr10:1041200-1067800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr10:1043600-1064200	Strong transcription	Psoas Muscle	Psoas
49	chr10:1046400-1066000	Strong transcription	HSMMtube	muscle
50	chr10:1046800-1068600	Weak transcription	Right Atrium	heart

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