Variant report

Variant	rs603015
Chromosome Location	chr5:89825035-89825036
allele	A/G
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	UBTF	chr5:89824326-89826236	K562	blood:	n/a	n/a
2	ZEB1	chr5:89824743-89825678	GM12878	blood:	n/a	chr5:89825161-89825170 chr5:89825258-89825270 chr5:89825162-89825173
3	TCF12	chr5:89824687-89826218	A549	lung:	n/a	chr5:89825149-89825159
4	ZNF143	chr5:89824771-89826429	K562	blood:	n/a	n/a
5	SP1	chr5:89825004-89826212	A549	lung:	n/a	chr5:89825476-89825488 chr5:89825473-89825487 chr5:89825477-89825486 chr5:89825215-89825224 chr5:89825214-89825226 chr5:89825215-89825229 chr5:89825478-89825487 chr5:89825215-89825225 chr5:89825214-89825226 chr5:89825476-89825488 chr5:89825216-89825225
6	POLR2A	chr5:89824308-89826235	K562	blood:	n/a	n/a
7	EGR1	chr5:89824768-89825761	K562	blood:	n/a	chr5:89825152-89825162 chr5:89825463-89825477 chr5:89825373-89825384 chr5:89825543-89825552 chr5:89825216-89825226 chr5:89825372-89825385 chr5:89825479-89825493 chr5:89825478-89825491 chr5:89825152-89825165
8	EGR1	chr5:89824874-89825748	K562	blood:	n/a	chr5:89825152-89825162 chr5:89825463-89825477 chr5:89825373-89825384 chr5:89825543-89825552 chr5:89825216-89825226 chr5:89825372-89825385 chr5:89825479-89825493 chr5:89825478-89825491 chr5:89825152-89825165
9	POLR2A	chr5:89824932-89825458	GM12878	blood:	n/a	n/a
10	TAF1	chr5:89825024-89825821	HepG2	liver:	n/a	n/a
11	YY1	chr5:89824998-89825593	ECC-1	luminal epithelium:	n/a	chr5:89825374-89825383 chr5:89825251-89825273 chr5:89825294-89825306 chr5:89825478-89825489 chr5:89825417-89825426
12	CEBPB	chr5:89824300-89826211	Hela-S3	cervix:	n/a	n/a
13	TCF7L2	chr5:89824647-89826132	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr5:89825028-89825857	HepG2	liver:	n/a	n/a
15	POLR2A	chr5:89824923-89826359	K562	blood:	n/a	n/a
16	ETS1	chr5:89824998-89825505	K562	blood:	n/a	chr5:89825417-89825428 chr5:89825374-89825385 chr5:89825147-89825160
17	RFX5	chr5:89824952-89826099	HepG2	liver:	n/a	n/a
18	CTCF	chr5:89824880-89826659	SK-N-SH	brain:	n/a	chr5:89825024-89825032
19	YY1	chr5:89824907-89825635	HepG2	liver:	n/a	chr5:89825374-89825383 chr5:89825251-89825273 chr5:89825294-89825306 chr5:89825478-89825489 chr5:89825417-89825426
20	MAX	chr5:89824802-89826148	K562	blood:	n/a	n/a
21	POLR2A	chr5:89824811-89826159	H1-neurons	neurons:	n/a	n/a
22	IRF1	chr5:89824705-89826239	K562	blood:	n/a	chr5:89824857-89824871 chr5:89826042-89826051
23	POLR2A	chr5:89824317-89826185	GM12878	blood:	n/a	n/a
24	POLR2A	chr5:89824567-89826134	K562	blood:	n/a	n/a
25	MAFK	chr5:89824825-89825078	HepG2	liver:	n/a	chr5:89824870-89824887
26	TAF1	chr5:89824965-89826079	ECC-1	luminal epithelium:	n/a	n/a
27	PAX5	chr5:89825025-89825745	GM12878	blood:	n/a	n/a
28	POLR2A	chr5:89821851-89826472	K562	blood:	n/a	n/a
29	RFX5	chr5:89824759-89826402	Hela-S3	cervix:	n/a	n/a
30	YY1	chr5:89825004-89825556	SK-N-SH_RA	brain:	n/a	chr5:89825374-89825383 chr5:89825251-89825273 chr5:89825294-89825306 chr5:89825478-89825489 chr5:89825417-89825426
31	SIN3AK20	chr5:89824821-89825578	K562	blood:	n/a	n/a
32	POLR2A	chr5:89824732-89826153	Raji	blood:	n/a	n/a
33	ELF1	chr5:89825013-89826167	GM12878	blood:	n/a	chr5:89825374-89825383 chr5:89825137-89825149 chr5:89826021-89826034 chr5:89825417-89825426
34	EP300	chr5:89824639-89826652	K562	blood:	n/a	chr5:89826147-89826156 chr5:89825539-89825555
35	TRIM28	chr5:89825033-89826579	K562	blood:	n/a	chr5:89826149-89826158
36	MAX	chr5:89824954-89826266	A549	lung:	n/a	chr5:89826147-89826156
37	POLR2A	chr5:89824937-89826062	ProgFib	skin:	n/a	n/a
38	BCLAF1	chr5:89824942-89825599	GM12878	blood:	n/a	chr5:89825478-89825487
39	ELK4	chr5:89824917-89825588	Hela-S3	cervix:	n/a	n/a
40	YY1	chr5:89825034-89825553	K562	blood:	n/a	chr5:89825374-89825383 chr5:89825251-89825273 chr5:89825294-89825306 chr5:89825478-89825489 chr5:89825417-89825426
41	MAX	chr5:89824963-89825634	MCF-7	breast:	n/a	n/a
42	MAZ	chr5:89824971-89826286	GM12878	blood:	n/a	chr5:89826147-89826156
43	POLR2A	chr5:89824978-89826038	A549	lung:	n/a	n/a
44	SIN3A	chr5:89824870-89826086	GM12878	blood:	n/a	n/a
45	POLR2A	chr5:89824228-89826067	HepG2	liver:	n/a	n/a
46	YY1	chr5:89824968-89826117	GM12892	blood:	n/a	chr5:89825374-89825383 chr5:89825251-89825273 chr5:89825294-89825306 chr5:89825478-89825489 chr5:89825417-89825426 chr5:89825908-89825917
47	SIN3AK20	chr5:89824882-89825674	PANC-1	pancreas:	n/a	n/a
48	HMGN3	chr5:89824817-89826053	K562	blood:	n/a	n/a
49	HEY1	chr5:89825027-89825833	HepG2	liver:	n/a	n/a
50	ELF1	chr5:89825008-89826161	MCF-7	breast:	n/a	chr5:89825374-89825383 chr5:89825137-89825149 chr5:89826021-89826034 chr5:89825417-89825426

No.	Distal block	Cell Line	Cell type
1	chr5:89703358..89707086-chr5:89823955..89827154,6	MCF-7	breast:
2	chr5:89766469..89774126-chr5:89823341..89829105,11	K562	blood:
3	chr5:89822684..89827061-chr5:89851623..89857043,7	MCF-7	breast:
4	chr5:89705290..89707109-chr5:89824364..89826854,3	MCF-7	breast:
5	chr5:89704960..89708059-chr5:89823269..89827144,6	K562	blood:
6	chr5:89768855..89773751-chr5:89822671..89829297,12	K562	blood:
7	chr5:89768691..89773005-chr5:89822332..89827140,9	MCF-7	breast:
8	chr5:89703407..89707223-chr5:89822965..89826833,10	K562	blood:
9	chr5:89767818..89772796-chr5:89823286..89827702,11	MCF-7	breast:

Variant related genes	Relation type
GPR98	TF binding region
ENSG00000113356	Chromatin interaction
ENSG00000176055	Chromatin interaction
ENSG00000255647	Chromatin interaction
ENSG00000164199	Chromatin interaction
ENSG00000153140	Chromatin interaction

Extended variants
information (count: 100 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:93)

rs_ID	r²[population]
rs10036980	0.85[JPT][hapmap]
rs10043836	0.85[JPT][hapmap]
rs10058765	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs10060427	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs10062714	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs10062924	0.86[CHB][hapmap];0.85[JPT][hapmap]
rs10067181	0.85[JPT][hapmap]
rs10068473	0.85[JPT][hapmap]
rs10072105	0.81[CHB][hapmap];0.92[JPT][hapmap]
rs1028191	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs1028192	0.85[JPT][hapmap]
rs1033290	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs10462342	0.82[CEU][hapmap];0.93[CHB][hapmap];0.92[JPT][hapmap]
rs10473936	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1047787	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10514327	0.85[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10514333	0.81[CHB][hapmap];0.83[JPT][hapmap]
rs10942596	0.82[CHB][hapmap];0.84[JPT][hapmap]
rs10942597	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];0.93[YRI][hapmap];0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10942605	0.85[JPT][hapmap]
rs10942606	0.85[JPT][hapmap]
rs1160121	0.85[JPT][hapmap]
rs11743030	0.81[CHB][hapmap]
rs12188928	0.85[JPT][hapmap]
rs12516985	0.83[JPT][hapmap]
rs12655180	0.80[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13182165	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13185955	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1533603	0.85[JPT][hapmap]
rs1673378	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1673379	0.92[JPT][hapmap]
rs16868957	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs1700510	0.96[CEU][hapmap];0.81[CHB][hapmap];0.83[JPT][hapmap];0.86[EUR][1000 genomes]
rs1700511	0.92[JPT][hapmap]
rs1812737	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1878878	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs1993474	0.84[JPT][hapmap]
rs2176624	0.85[JPT][hapmap]
rs2222242	0.85[JPT][hapmap]
rs2366771	0.81[CHB][hapmap];0.92[JPT][hapmap]
rs2366773	0.92[JPT][hapmap]
rs2366774	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs2366777	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs3087840	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35407205	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs3805483	1.00[CHB][hapmap];0.82[CHD][hapmap];0.92[JPT][hapmap];0.85[MEX][hapmap];0.88[ASN][1000 genomes]
rs474800	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs490812	0.92[JPT][hapmap]
rs4916681	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs4916684	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs4916686	0.85[JPT][hapmap]
rs4916813	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs4916815	0.83[JPT][hapmap]
rs498491	0.86[CHB][hapmap];0.92[JPT][hapmap]
rs499148	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.98[TSI][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs501640	0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs502596	0.92[JPT][hapmap]
rs552314	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs558809	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs587818	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs603870	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs616379	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs617379	0.81[CHB][hapmap];0.92[JPT][hapmap]
rs618355	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.97[TSI][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs623761	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs637442	0.92[JPT][hapmap]
rs6452906	0.85[JPT][hapmap]
rs645652	0.81[CHB][hapmap];0.85[CHD][hapmap];0.92[JPT][hapmap]
rs648430	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.95[TSI][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs666659	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs67376567	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6863710	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs6878917	0.81[CHB][hapmap];0.92[JPT][hapmap]
rs6881412	0.85[JPT][hapmap]
rs6883872	0.92[JPT][hapmap]
rs6888355	0.85[CHB][hapmap];0.91[JPT][hapmap]
rs688956	1.00[CEU][hapmap];0.81[CHB][hapmap];0.92[CHD][hapmap];0.93[GIH][hapmap];0.92[JPT][hapmap];0.91[TSI][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs688960	0.81[CHB][hapmap];0.92[JPT][hapmap]
rs6897910	1.00[CEU][hapmap];0.93[CHB][hapmap];0.89[CHD][hapmap];0.97[GIH][hapmap];0.92[JPT][hapmap];1.00[MEX][hapmap];0.81[MKK][hapmap];0.98[TSI][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6898209	0.85[JPT][hapmap]
rs7703588	0.85[JPT][hapmap]
rs7716979	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7717423	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7721198	0.82[JPT][hapmap]
rs7723259	0.84[JPT][hapmap]
rs7724806	0.85[JPT][hapmap]
rs7726624	0.81[CHB][hapmap];0.92[JPT][hapmap]
rs7729703	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs7732169	0.85[JPT][hapmap]
rs9293550	0.85[JPT][hapmap]
rs963866	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs977906	0.85[JPT][hapmap]
rs9790907	0.81[CHB][hapmap];0.92[JPT][hapmap]

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	nsv1021142	chr5:89102893-89897826	Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	nsv537804	chr5:89102893-89897826	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv917025	chr5:89208994-89855436	Enhancers Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
4	nsv432750	chr5:89410113-90137144	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
5	nsv432751	chr5:89457044-90090444	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
6	nsv529544	chr5:89523963-90412409	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
7	nsv882365	chr5:89770768-89882618	Flanking Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	13 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs603015	LYSMD3	Cis_1M	lymphoblastoid	RTeQTL
rs603015	LYSMD3	cis	normal skin	skin_eQTL
rs603015	GPR98	cis	cerebellum	SCAN

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89822600-89826600	Active TSS	Breast Myoepithelial Primary Cells	Breast
2	chr5:89823200-89826200	Active TSS	Right Atrium	heart
3	chr5:89823200-89826200	Active TSS	NHLF	lung
4	chr5:89823400-89826400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr5:89823600-89825200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr5:89823600-89826000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr5:89823600-89826200	Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr5:89823600-89826200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr5:89823600-89826200	Active TSS	Fetal Intestine Large	intestine
10	chr5:89823600-89826200	Active TSS	K562	blood
11	chr5:89823600-89826200	Active TSS	NH-A	brain
12	chr5:89823600-89826200	Active TSS	NHDF-Ad	bronchial
13	chr5:89823600-89826400	Active TSS	Duodenum Smooth Muscle	Duodenum
14	chr5:89823600-89826400	Active TSS	GM12878-XiMat	blood
15	chr5:89823800-89825200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr5:89823800-89826200	Active TSS	Brain Inferior Temporal Lobe	brain
17	chr5:89823800-89826200	Active TSS	HMEC	breast
18	chr5:89823800-89826400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr5:89824000-89825200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
20	chr5:89824000-89826000	Active TSS	NHEK	skin
21	chr5:89824000-89826200	Active TSS	ES-I3 Cell Line	embryonic stem cell
22	chr5:89824000-89826200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr5:89824000-89826200	Active TSS	Colonic Mucosa	Colon
24	chr5:89824000-89826200	Active TSS	Colon Smooth Muscle	Colon
25	chr5:89824000-89826200	Active TSS	Right Ventricle	heart
26	chr5:89824000-89826400	Active TSS	H1 Cell Line	embryonic stem cell
27	chr5:89824000-89826400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr5:89824000-89826600	Active TSS	HUES6 Cell Line	embryonic stem cell
29	chr5:89824000-89826600	Active TSS	Aorta	Aorta
30	chr5:89824000-89826600	Active TSS	Pancreatic Islets	Pancreatic Islet
31	chr5:89824000-89826600	Active TSS	HSMMtube	muscle
32	chr5:89824200-89825200	Flanking Active TSS	Primary B cells from cord blood	blood
33	chr5:89824200-89825200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
34	chr5:89824200-89825200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
35	chr5:89824200-89825200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
36	chr5:89824200-89826000	Active TSS	iPS-18 Cell Line	embryonic stem cell
37	chr5:89824200-89826000	Active TSS	Placenta	Placenta
38	chr5:89824200-89826000	Active TSS	Placenta Amnion	Placenta Amnion
39	chr5:89824200-89826200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr5:89824200-89826200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr5:89824200-89826200	Active TSS	Brain Angular Gyrus	brain
42	chr5:89824200-89826200	Active TSS	Brain Anterior Caudate	brain
43	chr5:89824200-89826200	Active TSS	Fetal Intestine Small	intestine
44	chr5:89824200-89826200	Active TSS	Fetal Muscle Trunk	muscle
45	chr5:89824200-89826200	Active TSS	Rectal Mucosa Donor 29	rectum
46	chr5:89824200-89826200	Active TSS	HSMM	muscle
47	chr5:89824200-89826400	Active TSS	Brain Hippocampus Middle	brain
48	chr5:89824200-89826400	Active TSS	Fetal Stomach	stomach
49	chr5:89824200-89826600	Active TSS	Ovary	ovary
50	chr5:89824400-89825200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood

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