Variant report

Variant	rs62026889
Chromosome Location	chr15:76917885-76917886
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:37)
CpG islands
(count:0)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:37 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RAD21	chr15:76917662-76917956	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCF	chr15:76917780-76917930	Caco-2	colon:	n/a	n/a
3	CTCF	chr15:76917800-76917950	GM12873	blood:	n/a	n/a
4	CTCF	chr15:76917740-76917890	HCPEpiC	choroid plexus:	n/a	n/a
5	CTCF	chr15:76917760-76917910	HA-sp	spinal cord:	n/a	n/a
6	CTCF	chr15:76917740-76917890	WI-38	lung:	n/a	n/a
7	RAD21	chr15:76917653-76917952	HepG2	liver:	n/a	n/a
8	CTCF	chr15:76917585-76918014	K562	blood:	n/a	n/a
9	CTCF	chr15:76917621-76917959	K562	blood:	n/a	n/a
10	ZNF143	chr15:76917645-76917946	GM12878	blood:	n/a	n/a
11	CTCF	chr15:76917760-76917910	HepG2	liver:	n/a	n/a
12	CTCF	chr15:76917613-76917929	K562	blood:	n/a	n/a
13	RAD21	chr15:76917646-76917960	HepG2	liver:	n/a	n/a
14	CTCF	chr15:76917684-76917904	MCF-7	breast:	n/a	n/a
15	CTCF	chr15:76917620-76917910	HCM	heart:	n/a	n/a
16	CTCF	chr15:76917740-76917890	A549	lung:	n/a	n/a
17	CTCF	chr15:76917642-76917956	GM12878	blood:	n/a	n/a
18	CTCF	chr15:76917740-76917890	GM12874	blood:	n/a	n/a
19	CTCF	chr15:76917680-76917912	K562	blood:	n/a	n/a
20	CTCF	chr15:76917697-76917885	MCF-7	breast:	n/a	n/a
21	CTCF	chr15:76917740-76917890	HUVEC	blood vessel:	n/a	n/a
22	CTCF	chr15:76917760-76917910	HCFaa	heart:	n/a	n/a
23	CTCF	chr15:76917702-76917896	MCF-7	breast:	n/a	n/a
24	CTCF	chr15:76917644-76917909	MCF-7	breast:	n/a	n/a
25	SMC3	chr15:76917735-76917915	HepG2	liver:	n/a	n/a
26	CTCF	chr15:76917688-76917957	K562	blood:	n/a	n/a
27	CTCF	chr15:76917760-76917910	HPF	lung:	n/a	n/a
28	RAD21	chr15:76917650-76917970	HepG2	liver:	n/a	n/a
29	CTCF	chr15:76917740-76917890	HEEpiC	esophagus:	n/a	n/a
30	ZNF143	chr15:76917718-76917888	K562	blood:	n/a	n/a
31	CTCF	chr15:76917740-76917890	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr15:76917711-76917900	HepG2	liver:	n/a	n/a
33	CTCF	chr15:76917674-76917896	H1-hESC	embryonic stem cell:	n/a	n/a
34	RAD21	chr15:76917506-76917951	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr15:76917688-76917893	MCF-7	breast:	n/a	n/a
36	CTCF	chr15:76917671-76917915	A549	lung:	n/a	n/a
37	RAD21	chr15:76917586-76917916	H1-hESC	embryonic stem cell:	n/a	n/a

No data

Variant related genes	Relation type
SCAPER	TF binding region

Extended variants
information (count: 99 )
Associated
traits (count: 12 )

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs1011083	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1011084	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10152247	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10851888	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10851889	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11072600	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11072602	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11072607	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11072610	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11072612	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11072616	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11072618	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11072619	0.80[EUR][1000 genomes]
rs11072620	0.80[EUR][1000 genomes]
rs11629727	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11630402	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11631082	0.81[EUR][1000 genomes]
rs11631394	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11632670	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11632765	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11635273	0.80[AFR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11637096	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11852777	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11854850	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11855762	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12437981	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12439141	0.80[EUR][1000 genomes]
rs12440511	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12440965	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12591622	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12898416	0.81[EUR][1000 genomes]
rs12898810	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12904149	0.81[EUR][1000 genomes]
rs12904417	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12910081	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12910820	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12914196	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1443115	0.81[EUR][1000 genomes]
rs1603860	0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1809875	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2047504	0.87[EUR][1000 genomes]
rs2120109	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2164102	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2404604	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2404734	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2436996	0.83[EUR][1000 genomes]
rs2454450	0.84[EUR][1000 genomes]
rs2454451	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2459361	0.83[EUR][1000 genomes]
rs28895952	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34103231	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35374222	0.80[EUR][1000 genomes]
rs36114653	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4886816	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4886819	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56339024	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs57682236	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62026898	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7165053	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7181506	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8029283	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs920712	0.81[EUR][1000 genomes]
rs965818	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:36 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv542439	chr15:76762161-77196336	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
2	esv3440794	chr15:76764595-77571114	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv904400	chr15:76772062-77085283	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1053924	chr15:76803849-77089079	Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
5	nsv471254	chr15:76811390-76978139	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
6	nsv570021	chr15:76813920-76978139	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
7	nsv570022	chr15:76816015-76978139	ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
8	nsv904401	chr15:76816015-77085283	Strong transcription Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
9	nsv1042089	chr15:76855098-77016127	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
10	nsv904402	chr15:76863023-76930805	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
11	esv2830013	chr15:76863023-77176158	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
12	nsv1042623	chr15:76863437-76999030	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
13	nsv1039269	chr15:76863437-77057021	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
14	nsv904403	chr15:76869929-76951040	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
15	nsv904404	chr15:76869929-77033934	Strong transcription ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
16	nsv904405	chr15:76869929-77047915	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
17	nsv904406	chr15:76869929-77085283	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
18	nsv904407	chr15:76869929-77121196	Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
19	nsv1052133	chr15:76878362-76962756	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
20	esv1815271	chr15:76883346-76930805	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
21	nsv570023	chr15:76884127-76978139	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
22	nsv904408	chr15:76884127-77085283	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
23	esv1824106	chr15:76891342-76930805	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
24	nsv1049209	chr15:76891615-76920081	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
25	nsv1046858	chr15:76892097-77020971	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
26	nsv542440	chr15:76892097-77020971	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
27	nsv1043066	chr15:76892097-77057021	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
28	nsv542441	chr15:76892097-77057021	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
29	nsv1046137	chr15:76892097-77196336	ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
30	nsv542442	chr15:76892097-77196336	ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
31	nsv904409	chr15:76893186-77033934	Strong transcription ZNF genes & repeats Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
32	nsv904410	chr15:76893186-77047915	ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
33	nsv904411	chr15:76893186-77085283	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
34	nsv1054164	chr15:76895332-76920081	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
35	nsv570109	chr15:76907376-76978139	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
36	nsv904412	chr15:76910031-77085283	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:12)

SNP	Gene	Cis/trans	Tissue	Source
rs62026889	SCAPER	cis	Artery Tibial	GTEx
rs62026889	ISL2	Cis_1M	lymphoblastoid	RTeQTL
rs62026889	SCAPER	cis	Esophagus Mucosa	GTEx
rs62026889	SCAPER	Cis_1M	lymphoblastoid	RTeQTL
rs62026889	SCAPER	cis	Esophagus Muscularis	GTEx
rs62026889	SCAPER	cis	Thyroid	GTEx
rs62026889	SCAPER	cis	Skin Sun Exposed Lower leg	GTEx
rs62026889	ISL2	cis	Whole Blood	GTEx
rs62026889	SCAPER	cis	Stomach	GTEx
rs62026889	SCAPER	cis	Whole Blood	GTEx
rs62026889	SCAPER	cis	lung	GTEx
rs62026889	SCAPER	cis	Adipose Subcutaneous	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76882200-76991400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr15:76898400-76981000	Weak transcription	Pancreas	Pancrea
3	chr15:76902600-76992000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr15:76902800-76926400	Weak transcription	Dnd41	blood
5	chr15:76903400-76940400	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr15:76904000-76927800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr15:76904400-76923600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr15:76904800-76939800	Weak transcription	Aorta	Aorta
9	chr15:76905000-76941000	Weak transcription	Ovary	ovary
10	chr15:76906000-76919000	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr15:76906000-76946800	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr15:76906600-76918600	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr15:76908000-76918200	Weak transcription	Stomach Mucosa	stomach
14	chr15:76908600-76928200	Weak transcription	Duodenum Mucosa	Duodenum
15	chr15:76908800-76928400	Weak transcription	Psoas Muscle	Psoas
16	chr15:76910000-76964200	Weak transcription	Brain Hippocampus Middle	brain
17	chr15:76910200-76918800	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr15:76910200-76919400	Weak transcription	Spleen	Spleen
19	chr15:76910200-76920000	Weak transcription	Primary hematopoietic stem cells	blood
20	chr15:76910200-76926000	Weak transcription	Esophagus	oesophagus
21	chr15:76910200-76941000	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr15:76910200-76959400	Weak transcription	Brain Substantia Nigra	brain
23	chr15:76911400-76990800	Weak transcription	Placenta	Placenta
24	chr15:76911600-76928600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr15:76912400-76918800	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr15:76914000-76918000	Weak transcription	Brain Anterior Caudate	brain
27	chr15:76914000-76928200	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr15:76914000-76928600	Weak transcription	Liver	Liver
29	chr15:76914000-76939800	Weak transcription	Left Ventricle	heart
30	chr15:76914000-76952600	Weak transcription	Brain Angular Gyrus	brain
31	chr15:76914200-76928600	Weak transcription	Adipose Nuclei	Adipose
32	chr15:76914400-76920000	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr15:76915800-76924000	Weak transcription	Fetal Brain Female	brain
34	chr15:76916200-76936200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr15:76917000-76918200	Strong transcription	Primary T cells from cord blood	blood
36	chr15:76917000-76918200	Strong transcription	Fetal Muscle Leg	muscle
37	chr15:76917000-76918400	Strong transcription	Fetal Intestine Large	intestine
38	chr15:76917000-76918400	Strong transcription	Fetal Intestine Small	intestine
39	chr15:76917000-76918400	Strong transcription	Fetal Stomach	stomach
40	chr15:76917200-76918000	Strong transcription	Stomach Smooth Muscle	stomach
41	chr15:76917200-76918600	Strong transcription	Gastric	stomach
42	chr15:76917400-76918200	Strong transcription	Brain Cingulate Gyrus	brain
43	chr15:76917400-76918200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr15:76917400-76918400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr15:76917600-76918000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr15:76917600-76918200	Strong transcription	Thymus	Thymus
47	chr15:76917600-76940800	Weak transcription	Right Ventricle	heart
48	chr15:76917800-76918000	Genic enhancers	Lung	lung
49	chr15:76917800-76918200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
50	chr15:76917800-76918400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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