Variant report

Variant	rs12672665
Chromosome Location	chr7:100483731-100483732
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:46)
CpG islands
(count:0)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:46 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr7:100482512-100488569	K562	blood:	n/a	n/a
2	POLR2A	chr7:100483677-100484223	GM12878	blood:	n/a	n/a
3	POLR2A	chr7:100480317-100488960	GM12878	blood:	n/a	n/a
4	PBX3	chr7:100483398-100484160	A549	lung:	n/a	n/a
5	POLR2A	chr7:100483366-100487362	GM12891	blood:	n/a	n/a
6	BCL3	chr7:100483054-100483762	A549	lung:	n/a	n/a
7	POLR2A	chr7:100483608-100483735	A549	lung:	n/a	n/a
8	POLR2A	chr7:100483321-100487299	GM12878	blood:	n/a	n/a
9	POLR2A	chr7:100483474-100484274	A549	lung:	n/a	n/a
10	POLR2A	chr7:100483100-100488395	MCF-7	breast:	n/a	n/a
11	POLR2A	chr7:100483710-100484066	GM12892	blood:	n/a	n/a
12	POLR2A	chr7:100483376-100488553	K562	blood:	n/a	n/a
13	POLR2A	chr7:100483603-100484125	HCT-116	colon:	n/a	n/a
14	POLR2A	chr7:100480382-100488921	K562	blood:	n/a	n/a
15	POLR2A	chr7:100483712-100484074	GM12891	blood:	n/a	n/a
16	POLR2A	chr7:100483382-100487701	GM12892	blood:	n/a	n/a
17	POLR2A	chr7:100481058-100488237	Hela-S3	cervix:	n/a	n/a
18	POLR2A	chr7:100483115-100484333	GM12891	blood:	n/a	n/a
19	POLR2A	chr7:100483381-100489176	H1-hESC	embryonic stem cell:	n/a	n/a
20	POLR2A	chr7:100483511-100488697	PANC-1	pancreas:	n/a	n/a
21	POLR2A	chr7:100482821-100484160	GM12891	blood:	n/a	n/a
22	POLR2A	chr7:100482969-100488603	PFSK-1	brain:	n/a	n/a
23	POLR2A	chr7:100480707-100488395	K562	blood:	n/a	n/a
24	POLR2A	chr7:100483684-100484244	GM12878	blood:	n/a	n/a
25	POLR2A	chr7:100483553-100484722	K562	blood:	n/a	n/a
26	POLR2A	chr7:100482275-100488325	SK-N-MC	brain:	n/a	n/a
27	POLR2A	chr7:100483635-100487800	GM12892	blood:	n/a	n/a
28	POLR2A	chr7:100483702-100483739	ProgFib	skin:	n/a	n/a
29	POLR2A	chr7:100483068-100483812	HepG2	liver:	n/a	n/a
30	POLR2A	chr7:100482776-100487720	GM12892	blood:	n/a	n/a
31	POLR2A	chr7:100483200-100483865	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr7:100483567-100483876	Hela-S3	cervix:	n/a	n/a
33	POLR2A	chr7:100482414-100488528	HepG2	liver:	n/a	n/a
34	POLR2A	chr7:100482812-100488482	SK-N-SH	brain:	n/a	n/a
35	POLR2A	chr7:100483214-100488865	GM12878	blood:	n/a	n/a
36	POLR2A	chr7:100483655-100484644	U87	brain:	n/a	n/a
37	POLR2A	chr7:100483708-100484235	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr7:100483622-100483822	HepG2	liver:	n/a	n/a
39	POLR2A	chr7:100482998-100488699	K562	blood:	n/a	n/a
40	POLR2A	chr7:100482415-100488355	Hela-S3	cervix:	n/a	n/a
41	POLR2A	chr7:100483457-100483741	MCF10A-Er-Src	breast:	n/a	n/a
42	ZNF263	chr7:100483685-100486719	HEK293-T-REx	kidney:	n/a	chr7:100484483-100484504
43	POLR2A	chr7:100481005-100489061	K562	blood:	n/a	n/a
44	POLR2A	chr7:100483480-100484224	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr7:100483514-100483763	A549	lung:	n/a	n/a
46	POLR2A	chr7:100481367-100484271	HL-60	blood:	n/a	n/a

No data

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:100274295..100276245-chr7:100482186..100484644,2	K562	blood:
2	chr7:100421802..100424702-chr7:100482689..100484467,2	MCF-7	breast:
3	chr7:100302365..100304789-chr7:100482401..100486103,3	K562	blood:

No data

Variant related genes	Relation type
SRRT	TF binding region
ENSG00000172336	Chromatin interaction
ENSG00000146828	Chromatin interaction
ENSG00000196411	Chromatin interaction
ENSG00000172354	Chromatin interaction

Extended variants
information (count: 70 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs1054391	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11973000	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12666785	0.96[CEU][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.95[TSI][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12669120	0.96[CEU][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs12705094	0.96[CEU][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs12705097	0.86[EUR][1000 genomes]
rs13225631	0.85[EUR][1000 genomes]
rs13226043	0.98[ASN][1000 genomes]
rs13232524	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13240020	0.86[EUR][1000 genomes]
rs13241786	0.89[CEU][hapmap];0.84[CHB][hapmap];0.97[CHD][hapmap];0.90[JPT][hapmap];0.90[MEX][hapmap];0.89[TSI][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs15624	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1799806	0.87[EUR][1000 genomes]
rs2405973	0.90[EUR][1000 genomes]
rs2405974	0.89[EUR][1000 genomes]
rs2405975	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2571598	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs28852509	0.85[EUR][1000 genomes]
rs2894713	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3087504	0.96[CEU][hapmap];0.86[CHB][hapmap];0.97[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs314329	0.81[EUR][1000 genomes]
rs314332	0.84[ASN][1000 genomes]
rs314369	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs314371	0.96[ASN][1000 genomes]
rs314372	0.93[ASN][1000 genomes]
rs314374	0.96[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs314375	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];0.95[MEX][hapmap];0.94[MKK][hapmap];0.93[TSI][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs314376	0.96[CEU][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs314377	1.00[CEU][hapmap];0.86[CHB][hapmap];0.91[JPT][hapmap];0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs314378	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];0.95[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];0.93[YRI][hapmap];0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34005963	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3757869	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3757870	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3757871	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3843541	0.85[EUR][1000 genomes]
rs3843542	0.88[EUR][1000 genomes]
rs3847063	0.96[CEU][hapmap]
rs3847064	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3847068	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3931823	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4727469	0.96[CEU][hapmap]
rs4729615	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4729616	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];0.95[MEX][hapmap];0.94[MKK][hapmap];0.95[TSI][hapmap]
rs4729617	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];0.98[TSI][hapmap];0.83[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4729618	1.00[CEU][hapmap];0.84[CHB][hapmap];0.91[GIH][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.85[YRI][hapmap]
rs4729619	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4729620	0.96[CEU][hapmap]
rs6465776	0.83[ASW][hapmap];1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.95[TSI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6942607	0.96[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs6954151	0.96[CEU][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs6976053	0.92[CEU][hapmap]
rs7783457	0.96[CEU][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7783543	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7798613	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7801015	0.98[ASN][1000 genomes]
rs7803865	0.96[CEU][hapmap]
rs9718841	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1829095	chr7:99814675-100494084	Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	393 gene(s)	inside rSNPs	diseases
2	nsv1020837	chr7:100313122-100508635	Genic enhancers Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
3	esv1832517	chr7:100355490-100749246	Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
4	esv2758125	chr7:100355490-100749246	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
5	esv2759547	chr7:100355490-100749246	Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
6	nsv464647	chr7:100374087-100497131	Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
7	nsv607965	chr7:100374087-100497131	Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
8	nsv1032673	chr7:100382250-100606794	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
9	nsv888799	chr7:100406144-100497131	Enhancers Bivalent Enhancer Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
10	nsv888801	chr7:100416250-100497131	Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
11	nsv464648	chr7:100422156-100518458	Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
12	nsv607966	chr7:100422156-100518458	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS 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 miRNA target site	90 gene(s)	inside rSNPs	diseases
13	nsv831073	chr7:100425659-100544888	Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs12672665	SHFM1	cis	cerebellum	SCAN
rs12672665	C7orf59	cis	parietal	SCAN
rs12672665	PLOD3	cis	cerebellum	SCAN
rs12672665	ZNF3	cis	parietal	SCAN

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100473600-100486600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:100473800-100485600	Weak transcription	Right Atrium	heart
3	chr7:100474600-100484400	Strong transcription	Placenta	Placenta
4	chr7:100474600-100484400	Strong transcription	Fetal Thymus	thymus
5	chr7:100474600-100484600	Strong transcription	HUES6 Cell Line	embryonic stem cell
6	chr7:100474600-100484800	Strong transcription	H1 Cell Line	embryonic stem cell
7	chr7:100474600-100485000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
8	chr7:100474600-100485800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
9	chr7:100474600-100486000	Strong transcription	HUES48 Cell Line	embryonic stem cell
10	chr7:100474800-100484000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr7:100474800-100484400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr7:100474800-100484600	Strong transcription	Rectal Mucosa Donor 31	rectum
13	chr7:100474800-100484800	Strong transcription	A549	lung
14	chr7:100474800-100485000	Strong transcription	Fetal Stomach	stomach
15	chr7:100474800-100485000	Strong transcription	Sigmoid Colon	Sigmoid Colon
16	chr7:100474800-100485600	Strong transcription	HSMM	muscle
17	chr7:100474800-100485800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr7:100474800-100485800	Strong transcription	HUES64 Cell Line	embryonic stem cell
19	chr7:100474800-100486000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr7:100475000-100484800	Strong transcription	Adipose Nuclei	Adipose
21	chr7:100475000-100485800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr7:100475200-100485400	Strong transcription	Fetal Intestine Large	intestine
23	chr7:100475200-100486000	Strong transcription	Ovary	ovary
24	chr7:100475400-100484800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr7:100475400-100484800	Strong transcription	Liver	Liver
26	chr7:100475600-100484600	Strong transcription	Rectal Mucosa Donor 29	rectum
27	chr7:100475600-100484800	Strong transcription	Fetal Lung	lung
28	chr7:100475800-100486000	Strong transcription	NHLF	lung
29	chr7:100475800-100486200	Weak transcription	Fetal Brain Male	brain
30	chr7:100476000-100484200	Strong transcription	Fetal Muscle Leg	muscle
31	chr7:100476000-100484400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr7:100476000-100484800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr7:100476000-100484800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr7:100476000-100485200	Strong transcription	Muscle Satellite Cultured Cells	--
35	chr7:100476200-100485000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr7:100476200-100485000	Strong transcription	Thymus	Thymus
37	chr7:100476200-100485200	Strong transcription	NHEK	skin
38	chr7:100476400-100484600	Strong transcription	Hela-S3	cervix
39	chr7:100476400-100485400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr7:100476400-100485800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr7:100476400-100486000	Strong transcription	Osteobl	bone
42	chr7:100476600-100484000	Strong transcription	HUVEC	blood vessel
43	chr7:100476600-100484600	Strong transcription	Duodenum Mucosa	Duodenum
44	chr7:100476600-100485800	Strong transcription	NH-A	brain
45	chr7:100477200-100485800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr7:100477400-100483800	Strong transcription	Primary hematopoietic stem cells	blood
47	chr7:100477400-100484200	Strong transcription	Primary T cells from cord blood	blood
48	chr7:100477400-100486000	Strong transcription	Aorta	Aorta
49	chr7:100477600-100485800	Strong transcription	H9 Cell Line	embryonic stem cell
50	chr7:100477800-100484000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland

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