Variant report

Variant	rs7783457
Chromosome Location	chr7:100471595-100471596
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:53)
CpG islands
(count:0)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:53 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	JUN	chr7:100471425-100473881	K562	blood:	n/a	n/a
2	POLR2A	chr7:100471347-100473431	ECC-1	luminal epithelium:	n/a	n/a
3	POLR2A	chr7:100471510-100473062	HCT-116	colon:	n/a	n/a
4	POLR2A	chr7:100471458-100473578	GM12892	blood:	n/a	n/a
5	POLR2A	chr7:100471301-100473584	PANC-1	pancreas:	n/a	n/a
6	NRF1	chr7:100471386-100473412	SK-N-SH	brain:	n/a	chr7:100472752-100472763 chr7:100473013-100473022
7	POLR2A	chr7:100471193-100473615	GM12878	blood:	n/a	n/a
8	POLR2A	chr7:100471531-100473407	K562	blood:	n/a	n/a
9	POLR2A	chr7:100471443-100473296	K562	blood:	n/a	n/a
10	POLR2A	chr7:100471145-100473554	GM12892	blood:	n/a	n/a
11	POLR2A	chr7:100471266-100473670	SK-N-MC	brain:	n/a	n/a
12	POLR2A	chr7:100470747-100473785	U87	brain:	n/a	n/a
13	POLR2A	chr7:100471570-100473348	K562	blood:	n/a	n/a
14	CBX3	chr7:100471542-100473355	K562	blood:	n/a	n/a
15	POLR2A	chr7:100471571-100473389	Raji	blood:	n/a	n/a
16	POLR2A	chr7:100471246-100473602	H1-hESC	embryonic stem cell:	n/a	n/a
17	POLR2A	chr7:100471451-100473476	GM12892	blood:	n/a	n/a
18	POLR2A	chr7:100471353-100473352	K562	blood:	n/a	n/a
19	PML	chr7:100471322-100473602	K562	blood:	n/a	chr7:100472991-100472999
20	ZNF263	chr7:100471590-100472872	HEK293-T-REx	kidney:	n/a	chr7:100471618-100471627 chr7:100471870-100471891
21	POLR2A	chr7:100471548-100472133	GM12878	blood:	n/a	n/a
22	POLR2A	chr7:100471470-100472113	GM12891	blood:	n/a	n/a
23	POLR2A	chr7:100471367-100473533	HL-60	blood:	n/a	n/a
24	POLR2A	chr7:100471547-100473357	U87	brain:	n/a	n/a
25	POLR2A	chr7:100471328-100473625	K562	blood:	n/a	n/a
26	POLR2A	chr7:100471564-100473385	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr7:100471387-100473519	GM12892	blood:	n/a	n/a
28	POLR2A	chr7:100471326-100473567	K562	blood:	n/a	n/a
29	MTA3	chr7:100471350-100473478	GM12878	blood:	n/a	n/a
30	POLR2A	chr7:100471193-100473514	HepG2	liver:	n/a	n/a
31	POLR2A	chr7:100471569-100473318	PFSK-1	brain:	n/a	n/a
32	POLR2A	chr7:100471563-100472134	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr7:100471387-100473462	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr7:100471566-100473311	HepG2	liver:	n/a	n/a
35	POLR2A	chr7:100471310-100472952	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr7:100471248-100473785	U87	brain:	n/a	n/a
37	POLR2A	chr7:100471337-100473610	GM12878	blood:	n/a	n/a
38	POLR2A	chr7:100471260-100473508	K562	blood:	n/a	n/a
39	POLR2A	chr7:100471434-100472951	K562	blood:	n/a	n/a
40	POLR2A	chr7:100471477-100473484	HL-60	blood:	n/a	n/a
41	HEY1	chr7:100471514-100473499	K562	blood:	n/a	chr7:100472975-100472990
42	POLR2A	chr7:100471529-100473431	GM12878	blood:	n/a	n/a
43	HEY1	chr7:100471528-100473359	K562	blood:	n/a	chr7:100472975-100472990
44	PML	chr7:100471519-100473712	GM12878	blood:	n/a	chr7:100472991-100472999
45	POLR2A	chr7:100471529-100473456	GM12878	blood:	n/a	n/a
46	POLR2A	chr7:100471431-100473434	GM12878	blood:	n/a	n/a
47	NR2F2	chr7:100471468-100473371	K562	blood:	n/a	n/a
48	POLR2A	chr7:100471377-100473643	PFSK-1	brain:	n/a	n/a
49	POLR2A	chr7:100471582-100473472	GM12891	blood:	n/a	n/a
50	POLR2A	chr7:100471390-100471668	HCT-116	colon:	n/a	n/a

No data

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:99699125..99701845-chr7:100470033..100472730,2	MCF-7	breast:
2	chr7:100027156..100028676-chr7:100470715..100472560,2	K562	blood:
3	chr7:100448186..100450905-chr7:100471509..100474207,3	K562	blood:
4	chr7:100423829..100426174-chr7:100471078..100472627,2	K562	blood:
5	chr7:100433319..100435177-chr7:100470244..100472636,2	MCF-7	breast:
6	chr7:100409902..100411461-chr7:100471183..100472697,2	MCF-7	breast:
7	chr7:100470889..100475047-chr7:100805272..100809585,4	MCF-7	breast:
8	chr7:100083221..100085283-chr7:100471464..100473239,2	K562	blood:
9	chr7:100471127..100473629-chr7:100728368..100730220,3	K562	blood:
10	chr2:232573730..232575283-chr7:100471498..100474384,2	MCF-7	breast:
11	chr7:100285374..100287070-chr7:100470986..100472980,2	K562	blood:
12	chr7:100452256..100454865-chr7:100471094..100473854,2	K562	blood:
13	chr7:100470857..100473840-chr8:103875332..103878147,2	K562	blood:
14	chr7:100422126..100425537-chr7:100471170..100475559,4	MCF-7	breast:
15	chr7:100274266..100277220-chr7:100470078..100472629,2	K562	blood:
16	chr7:100025223..100027930-chr7:100471250..100474138,3	MCF-7	breast:
17	chr7:100182521..100184068-chr7:100470982..100473122,2	K562	blood:
18	chr7:100470877..100472471-chr7:100728438..100731050,2	MCF-7	breast:
19	chr7:100471473..100474219-chr7:100797756..100799384,2	MCF-7	breast:
20	chr7:100448750..100454655-chr7:100469427..100474218,6	MCF-7	breast:

No data

Variant related genes	Relation type
SRRT	TF binding region
ENSG00000077454	Chromatin interaction
ENSG00000172354	Chromatin interaction
ENSG00000166924	Chromatin interaction
ENSG00000187514	Chromatin interaction
ENSG00000236305	Chromatin interaction
ENSG00000128564	Chromatin interaction
ENSG00000169871	Chromatin interaction
ENSG00000155096	Chromatin interaction
ENSG00000253320	Chromatin interaction
ENSG00000146830	Chromatin interaction
ENSG00000221838	Chromatin interaction
ENSG00000146834	Chromatin interaction
ENSG00000166508	Chromatin interaction
ENSG00000196411	Chromatin interaction
ENSG00000078487	Chromatin interaction
ENSG00000106367	Chromatin interaction
ENSG00000146828	Chromatin interaction
ENSG00000106336	Chromatin interaction

Extended variants
information (count: 50 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1054391	0.96[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs10953305	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12666785	0.92[CEU][hapmap];0.93[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs12669120	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];0.95[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.91[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12672665	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	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];0.91[YRI][hapmap];0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13226043	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13241786	0.85[CEU][hapmap];0.97[CHD][hapmap];0.90[JPT][hapmap];0.90[ASN][1000 genomes]
rs15624	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]
rs3087504	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.91[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs314332	0.84[ASN][1000 genomes]
rs314368	0.89[EUR][1000 genomes]
rs314369	0.89[ASN][1000 genomes]
rs314371	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs314372	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs314374	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs314375	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]
rs314376	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];0.95[MEX][hapmap];1.00[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs314377	0.96[CEU][hapmap];0.91[JPT][hapmap];0.96[ASN][1000 genomes]
rs314378	0.96[CEU][hapmap];0.85[CHB][hapmap];0.97[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs3847063	1.00[CEU][hapmap];0.86[CHB][hapmap];0.93[GIH][hapmap];0.87[MEX][hapmap];0.93[TSI][hapmap];0.91[YRI][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4727469	1.00[CEU][hapmap];0.91[YRI][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4727470	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4729615	0.96[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs4729616	0.92[CEU][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap]
rs4729617	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]
rs4729618	0.96[CEU][hapmap];0.85[GIH][hapmap]
rs4729620	1.00[CEU][hapmap];0.91[YRI][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6465776	0.96[CEU][hapmap];0.93[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs6942607	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6954151	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.91[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6976053	0.96[CEU][hapmap];0.93[GIH][hapmap];0.87[MEX][hapmap];0.93[TSI][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7783543	0.96[ASN][1000 genomes]
rs7801015	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7803865	1.00[CEU][hapmap];0.93[GIH][hapmap];0.82[MEX][hapmap];0.93[TSI][hapmap];0.91[YRI][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 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	nsv888797	chr7:100386900-100482026	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
10	nsv888798	chr7:100406144-100472826	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
11	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
12	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
13	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
14	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
15	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:3)

SNP	Gene	Cis/trans	Tissue	Source
rs7783457	MYH16	cis	parietal	SCAN
rs7783457	SHFM1	cis	cerebellum	SCAN
rs7783457	MCM7	cis	cerebellum	SCAN

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100465600-100471800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr7:100465600-100471800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr7:100465600-100471800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr7:100465600-100472000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr7:100465800-100472000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr7:100466000-100471600	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr7:100466000-100471800	Weak transcription	Fetal Brain Male	brain
8	chr7:100466200-100471600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr7:100466200-100471600	Weak transcription	Brain Angular Gyrus	brain
10	chr7:100466200-100471600	Weak transcription	Brain Germinal Matrix	brain
11	chr7:100466200-100472000	Weak transcription	Fetal Kidney	kidney
12	chr7:100466400-100471600	Weak transcription	Primary B cells from peripheral blood	blood
13	chr7:100466400-100471600	Weak transcription	Right Atrium	heart
14	chr7:100466400-100471800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr7:100466400-100471800	Weak transcription	Fetal Heart	heart
16	chr7:100466600-100471600	Weak transcription	Fetal Brain Female	brain
17	chr7:100466600-100471800	Strong transcription	H1 Cell Line	embryonic stem cell
18	chr7:100466600-100471800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
19	chr7:100466600-100471800	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr7:100466600-100471800	Weak transcription	Primary B cells from cord blood	blood
21	chr7:100466600-100472000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr7:100466800-100471600	Strong transcription	Cortex derived primary cultured neurospheres	brain
23	chr7:100466800-100471600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr7:100466800-100471800	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr7:100467000-100471600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr7:100467000-100471600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr7:100467000-100471600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr7:100467000-100471600	Strong transcription	Stomach Smooth Muscle	stomach
29	chr7:100467200-100471600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr7:100467200-100471800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr7:100467200-100471800	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr7:100467400-100471600	Strong transcription	Fetal Thymus	thymus
33	chr7:100467600-100471600	Strong transcription	HMEC	breast
34	chr7:100467600-100471800	Strong transcription	HUES48 Cell Line	embryonic stem cell
35	chr7:100467600-100471800	Strong transcription	HUES6 Cell Line	embryonic stem cell
36	chr7:100467600-100471800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
37	chr7:100467600-100471800	Strong transcription	Fetal Intestine Large	intestine
38	chr7:100467800-100471600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr7:100467800-100471600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr7:100467800-100471600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr7:100467800-100471600	Strong transcription	Adipose Nuclei	Adipose
42	chr7:100467800-100471800	Strong transcription	H9 Cell Line	embryonic stem cell
43	chr7:100467800-100471800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:100467800-100471800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
45	chr7:100467800-100471800	Strong transcription	Fetal Lung	lung
46	chr7:100467800-100471800	Strong transcription	HUVEC	blood vessel
47	chr7:100467800-100471800	Strong transcription	Osteobl	bone
48	chr7:100468000-100471600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr7:100468000-100471600	Strong transcription	Fetal Muscle Trunk	muscle
50	chr7:100468000-100471800	Strong transcription	HSMM	muscle

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