Variant report

Variant	rs1648307
Chromosome Location	chr15:45471489-45471490
allele	C/T
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	CTCF	chr15:45471480-45471630	HRPEpiC	eye:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471606-45471619 chr15:45471519-45471537 chr15:45471522-45471531
2	CTCF	chr15:45471420-45471570	GM12870	blood:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
3	CTCF	chr15:45471372-45471645	Spleen_OC	spleen:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471606-45471619 chr15:45471519-45471537 chr15:45471522-45471531
4	CTCF	chr15:45471403-45471624	MCF-7	breast:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471606-45471619 chr15:45471519-45471537 chr15:45471522-45471531
5	CTCF	chr15:45471480-45471630	GM12875	blood:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471606-45471619 chr15:45471519-45471537 chr15:45471522-45471531
6	CTCF	chr15:45471433-45471588	A549	lung:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
7	RAD21	chr15:45471269-45471794	ECC-1	luminal epithelium:	n/a	chr15:45471520-45471539
8	CTCF	chr15:45471440-45471590	HMF	breast:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
9	CTCF	chr15:45471241-45471815	K562	blood:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471606-45471619 chr15:45471519-45471537 chr15:45471522-45471531
10	CTCF	chr15:45471340-45471490	HMEC	breast:	n/a	n/a
11	CTCF	chr15:45471413-45471627	HepG2	liver:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471606-45471619 chr15:45471519-45471537 chr15:45471522-45471531
12	RAD21	chr15:45471424-45471597	K562	blood:	n/a	chr15:45471520-45471539
13	CTCF	chr15:45471440-45471590	HUVEC	blood vessel:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
14	CTCF	chr15:45471420-45471570	GM12864	blood:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
15	CTCF	chr15:45471390-45471677	GM19240	blood:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471606-45471619 chr15:45471519-45471537 chr15:45471522-45471531
16	CTCF	chr15:45471440-45471590	HFF-Myc	foreskin:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
17	CTCF	chr15:45471380-45471530	HCPEpiC	choroid plexus:	n/a	n/a
18	SMC3	chr15:45471276-45471703	HepG2	liver:	n/a	chr15:45471521-45471535 chr15:45471521-45471528
19	CTCF	chr15:45471391-45471654	HepG2	liver:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471606-45471619 chr15:45471519-45471537 chr15:45471522-45471531
20	RAD21	chr15:45471347-45471643	H1-hESC	embryonic stem cell:	n/a	chr15:45471520-45471539
21	CTCF	chr15:45471400-45471550	AoAF	blood vessel:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
22	SMC3	chr15:45471345-45471707	Hela-S3	cervix:	n/a	chr15:45471521-45471535 chr15:45471521-45471528
23	RCOR1	chr15:45471449-45471596	HepG2	liver:	n/a	n/a
24	CTCF	chr15:45471480-45471630	NHDF-neo	bronchial:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471606-45471619 chr15:45471519-45471537 chr15:45471522-45471531
25	CTCF	chr15:45471380-45471530	HRE	kidney:	n/a	n/a
26	CTCF	chr15:45471416-45471582	GM10248	blood:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
27	CTCF	chr15:45471460-45471610	HA-sp	spinal cord:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
28	CTCF	chr15:45471400-45471550	GM12866	blood:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
29	CTCF	chr15:45471460-45471610	HRPEpiC	eye:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
30	ZNF143	chr15:45471357-45471722	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr15:45471420-45471570	GM12873	blood:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
32	CTCF	chr15:45471420-45471570	HVMF	connective:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
33	CTCF	chr15:45471403-45471648	GM19239	blood:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471606-45471619 chr15:45471519-45471537 chr15:45471522-45471531
34	CTCF	chr15:45471414-45471576	SK-N-SH_RA	brain:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
35	CTCF	chr15:45471424-45471593	A549	lung:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
36	CTCF	chr15:45471400-45471550	GM06990	blood:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
37	CTCF	chr15:45471460-45471610	BE2_C	brain:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
38	CTCF	chr15:45471400-45471550	AG04450	lung:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
39	CTCF	chr15:45471460-45471610	A549	lung:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
40	ZNF143	chr15:45471394-45471714	GM12878	blood:	n/a	n/a
41	CTCF	chr15:45471385-45471655	Hela-S3	cervix:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471606-45471619 chr15:45471519-45471537 chr15:45471522-45471531
42	CTCF	chr15:45471480-45471630	HCM	heart:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471606-45471619 chr15:45471519-45471537 chr15:45471522-45471531
43	CTCF	chr15:45471440-45471590	GM12872	blood:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
44	CTCF	chr15:45471291-45471743	H1-hESC	embryonic stem cell:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471606-45471619 chr15:45471519-45471537 chr15:45471522-45471531
45	CTCF	chr15:45471440-45471590	BJ	skin:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
46	CTCF	chr15:45471440-45471590	GM12874	blood:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
47	CTCF	chr15:45471420-45471570	MCF-7	breast:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
48	CTCF	chr15:45471331-45471615	HepG2	liver:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531
49	CTCF	chr15:45471384-45471645	MCF-7	breast:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471606-45471619 chr15:45471519-45471537 chr15:45471522-45471531
50	CTCF	chr15:45471400-45471550	BJ	skin:	n/a	chr15:45471524-45471534 chr15:45471519-45471532 chr15:45471520-45471536 chr15:45471521-45471542 chr15:45471519-45471537 chr15:45471522-45471531

No.	Distal block	Cell Line	Cell type
1	chr15:45471040..45471975-chr15:45749448..45750391,3	K562	blood:
2	chr15:45470589..45472995-chr15:45489124..45491462,3	MCF-7	breast:
3	chr15:45458776..45462841-chr15:45467209..45473486,10	K562	blood:
4	chr15:45471459..45472025-chr15:45490883..45491405,2	MCF-7	breast:

Variant related genes	Relation type
SHF	TF binding region
ENSG00000259932	Chromatin interaction
ENSG00000259539	Chromatin interaction
ENSG00000259519	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs1145089	1.00[JPT][hapmap]
rs1620253	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1648304	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1648308	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1648310	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1648312	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1648313	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1648317	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1648318	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1706807	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1706808	1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1706811	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1706812	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1706813	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1706815	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1706817	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1706820	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1706826	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];0.95[MEX][hapmap];0.85[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1706827	0.84[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AMR][1000 genomes]
rs1706829	1.00[JPT][hapmap];0.91[LWK][hapmap];0.85[MKK][hapmap];0.85[YRI][hapmap];0.82[AMR][1000 genomes]
rs2162246	0.84[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2292468	1.00[CEU][hapmap];0.91[TSI][hapmap];0.95[EUR][1000 genomes]
rs2458237	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2467819	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2467820	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4775830	0.82[AMR][1000 genomes]
rs6493143	1.00[JPT][hapmap]
rs7169193	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.98[TSI][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[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	nsv916374	chr15:45058112-45769052	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
2	nsv932147	chr15:45319178-45872076	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv427961	chr15:45338381-45491634	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
4	esv1823029	chr15:45387102-45482245	Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
5	nsv869616	chr15:45401411-45736209	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
6	nsv904187	chr15:45438537-45507738	Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
7	nsv569315	chr15:45446156-45772448	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	75 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs1648307	CCNDBP1	cis	cerebellum	SCAN
rs1648307	ADAL	cis	parietal	SCAN
rs1648307	FSIP1	cis	parietal	SCAN
rs1648307	SHF	cis	cerebellum	SCAN
rs1648307	SHF	cis	parietal	SCAN

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:45459800-45471800	Weak transcription	Small Intestine	intestine
2	chr15:45459800-45478000	Weak transcription	Aorta	Aorta
3	chr15:45460000-45471600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr15:45460000-45471800	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr15:45460000-45472200	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr15:45460000-45474800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr15:45460000-45477200	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr15:45460000-45478600	Weak transcription	Thymus	Thymus
9	chr15:45460200-45478000	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr15:45460400-45475200	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr15:45460600-45471800	Weak transcription	Esophagus	oesophagus
12	chr15:45460600-45475400	Weak transcription	Brain Anterior Caudate	brain
13	chr15:45460600-45475600	Weak transcription	Left Ventricle	heart
14	chr15:45460600-45478000	Weak transcription	Rectal Smooth Muscle	rectum
15	chr15:45460600-45478200	Weak transcription	Adipose Nuclei	Adipose
16	chr15:45461200-45471800	Weak transcription	Pancreas	Pancrea
17	chr15:45461200-45473200	Weak transcription	Fetal Brain Male	brain
18	chr15:45461800-45471800	Strong transcription	Fetal Stomach	stomach
19	chr15:45462200-45477200	Weak transcription	Brain Hippocampus Middle	brain
20	chr15:45462400-45473600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr15:45462800-45471600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr15:45462800-45473800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr15:45463000-45473800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr15:45463200-45471600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr15:45463200-45471600	Strong transcription	HepG2	liver
26	chr15:45463600-45471600	Strong transcription	Fetal Brain Female	brain
27	chr15:45464200-45472400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr15:45464600-45472400	Weak transcription	Colonic Mucosa	Colon
29	chr15:45465600-45471600	Strong transcription	Cortex derived primary cultured neurospheres	brain
30	chr15:45466000-45478800	Weak transcription	Right Ventricle	heart
31	chr15:45466200-45471600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr15:45466400-45471600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr15:45466400-45477600	Weak transcription	Colon Smooth Muscle	Colon
34	chr15:45466800-45472000	Weak transcription	HSMMtube	muscle
35	chr15:45466800-45473800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr15:45467600-45476200	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr15:45467600-45477400	Weak transcription	Brain Angular Gyrus	brain
38	chr15:45467800-45471600	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr15:45467800-45471600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr15:45467800-45473800	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr15:45467800-45477400	Weak transcription	Brain Cingulate Gyrus	brain
42	chr15:45468000-45477800	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr15:45468400-45471800	Weak transcription	Lung	lung
44	chr15:45470000-45473800	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr15:45470200-45471600	Weak transcription	Ovary	ovary
46	chr15:45470200-45472600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr15:45470200-45475600	Weak transcription	Placenta	Placenta
48	chr15:45470400-45471600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr15:45470400-45471600	Weak transcription	Duodenum Mucosa	Duodenum
50	chr15:45470400-45473200	Weak transcription	Stomach Smooth Muscle	stomach

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