Variant report

Variant	rs2198015
Chromosome Location	chr3:67704102-67704103
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	POLR2A	chr3:67703925-67705390	U87	brain:	n/a	n/a
2	CHD1	chr3:67703735-67705408	GM12878	blood:	n/a	n/a
3	POLR2A	chr3:67703041-67705477	IMR90	lung:	n/a	n/a
4	POLR2A	chr3:67703977-67705477	GM18526	blood:	n/a	n/a
5	MAX	chr3:67704045-67705368	NB4	blood:	n/a	chr3:67704510-67704520 chr3:67704511-67704520 chr3:67704508-67704521 chr3:67704510-67704519 chr3:67704508-67704521 chr3:67704512-67704528 chr3:67704509-67704520 chr3:67704508-67704521 chr3:67704509-67704519 chr3:67704510-67704519 chr3:67704508-67704521 chr3:67704509-67704520
6	MEF2A	chr3:67703346-67704299	GM12878	blood:	n/a	chr3:67703875-67703889 chr3:67703870-67703891 chr3:67703877-67703888 chr3:67703874-67703889 chr3:67703858-67703866 chr3:67703874-67703890
7	POLR2A	chr3:67703060-67706271	HepG2	liver:	n/a	n/a
8	NFIC	chr3:67703316-67704366	GM12878	blood:	n/a	n/a
9	POLR2A	chr3:67703950-67705613	GM12878	blood:	n/a	n/a
10	MYC	chr3:67703998-67705240	K562	blood:	n/a	chr3:67704510-67704520 chr3:67704511-67704520 chr3:67704508-67704521 chr3:67704510-67704519 chr3:67704508-67704521 chr3:67704512-67704528 chr3:67704509-67704520 chr3:67704508-67704521 chr3:67704509-67704519 chr3:67704510-67704519 chr3:67704508-67704521 chr3:67704509-67704520
11	POLR2A	chr3:67703304-67705555	GM12892	blood:	n/a	n/a
12	POLR2A	chr3:67704033-67704609	GM12891	blood:	n/a	n/a
13	MEF2A	chr3:67703592-67704214	GM12878	blood:	n/a	chr3:67703875-67703889 chr3:67703870-67703891 chr3:67703877-67703888 chr3:67703874-67703889 chr3:67703858-67703866 chr3:67703874-67703890
14	POLR2A	chr3:67704093-67705422	GM15510	blood:	n/a	n/a
15	HCFC1	chr3:67703883-67705592	Hela-S3	cervix:	n/a	n/a
16	POLR2A	chr3:67704061-67704492	GM12891	blood:	n/a	n/a
17	MYC	chr3:67703978-67705239	MCF10A-Er-Src	breast:	n/a	chr3:67704510-67704520 chr3:67704511-67704520 chr3:67704508-67704521 chr3:67704510-67704519 chr3:67704508-67704521 chr3:67704512-67704528 chr3:67704509-67704520 chr3:67704508-67704521 chr3:67704509-67704519 chr3:67704510-67704519 chr3:67704508-67704521 chr3:67704509-67704520
18	CHD2	chr3:67703967-67705580	GM12878	blood:	n/a	n/a
19	WRNIP1	chr3:67704079-67704710	GM12878	blood:	n/a	n/a
20	RUNX3	chr3:67703701-67704295	GM12878	blood:	n/a	n/a
21	POLR2A	chr3:67703530-67705582	MCF10A-Er-Src	breast:	n/a	n/a
22	POLR2A	chr3:67703877-67705560	MCF10A-Er-Src	breast:	n/a	n/a
23	MXI1	chr3:67704005-67705693	SK-N-SH	brain:	n/a	n/a
24	MTA3	chr3:67703325-67704527	GM12878	blood:	n/a	n/a
25	MXI1	chr3:67703457-67705425	GM12878	blood:	n/a	n/a
26	BRCA1	chr3:67703993-67704482	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr3:67704000-67705199	GM12891	blood:	n/a	n/a
28	POLR2A	chr3:67703934-67706381	GM12878	blood:	n/a	n/a
29	POLR2A	chr3:67704062-67705486	GM18951	blood:	n/a	n/a
30	POLR2A	chr3:67703807-67705390	U87	brain:	n/a	n/a
31	POLR2A	chr3:67704073-67704390	GM12891	blood:	n/a	n/a
32	POLR2A	chr3:67703941-67705602	GM12892	blood:	n/a	n/a
33	POLR2A	chr3:67703966-67705284	K562	blood:	n/a	n/a
34	POLR2A	chr3:67704067-67705588	Raji	blood:	n/a	n/a
35	POLR2A	chr3:67703990-67705485	GM12892	blood:	n/a	n/a
36	ATF2	chr3:67703532-67704260	GM12878	blood:	n/a	n/a
37	POLR2A	chr3:67704063-67705563	GM19099	blood:	n/a	n/a
38	SPI1	chr3:67703863-67704260	GM12891	blood:	n/a	n/a
39	POLR2A	chr3:67704036-67705317	U87	brain:	n/a	n/a
40	POLR2A	chr3:67703969-67705589	GM18505	blood:	n/a	n/a
41	MXI1	chr3:67703997-67705224	Hela-S3	cervix:	n/a	n/a
42	NFIC	chr3:67703409-67704816	GM12878	blood:	n/a	n/a
43	POLR2A	chr3:67703993-67705538	GM12878	blood:	n/a	n/a
44	POLR2A	chr3:67703969-67704515	GM12892	blood:	n/a	n/a
45	TBL1XR1	chr3:67703473-67705246	GM12878	blood:	n/a	n/a
46	POLR2A	chr3:67704084-67705494	Hela-S3	cervix:	n/a	n/a
47	RELA	chr3:67704032-67705343	GM15510	blood:	n/a	n/a
48	EBF1	chr3:67703874-67704469	GM12878	blood:	n/a	n/a
49	POLR2A	chr3:67703041-67705669	GM12891	blood:	n/a	n/a
50	BCL11A	chr3:67703945-67704174	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:67644182..67646267-chr3:67702951..67705002,2	MCF-7	breast:
2	chr3:67701996..67704573-chr3:67817178..67820032,3	MCF-7	breast:
3	chr3:67703523..67705706-chr3:68980414..68982098,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000241316	TF binding region
ENSG00000163377	Chromatin interaction

Extended variants
information (count: 70 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs11707967	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11712921	0.85[EUR][1000 genomes]
rs11717561	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11719952	0.87[EUR][1000 genomes]
rs12714500	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13065696	1.00[CEU][hapmap];0.93[CHB][hapmap];0.94[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13068759	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13068996	0.84[EUR][1000 genomes]
rs13069212	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13069251	1.00[CEU][hapmap];0.86[JPT][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13070332	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13076100	1.00[CEU][hapmap];0.86[CHB][hapmap];0.87[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13077262	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13081838	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13083820	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13086260	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13090197	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13091275	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13091330	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13092662	0.96[CEU][hapmap];0.82[CHB][hapmap];0.90[CHD][hapmap];0.87[JPT][hapmap];0.94[MEX][hapmap];0.95[TSI][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13099253	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1376028	1.00[CEU][hapmap];0.93[CHB][hapmap];0.95[CHD][hapmap];0.93[GIH][hapmap];0.94[JPT][hapmap];0.91[LWK][hapmap];0.87[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1376029	1.00[CEU][hapmap];0.82[CHB][hapmap];0.90[CHD][hapmap];0.87[JPT][hapmap];0.87[MEX][hapmap];0.95[TSI][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1376030	1.00[CEU][hapmap];0.86[MEX][hapmap];0.90[TSI][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1450345	0.92[EUR][1000 genomes]
rs1473351	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1814519	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1823476	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2167181	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2198016	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2218796	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2362453	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2362455	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62256429	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6766403	1.00[CEU][hapmap];0.93[CHB][hapmap];0.95[CHD][hapmap];0.93[GIH][hapmap];0.94[JPT][hapmap];0.84[LWK][hapmap];0.86[MEX][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6774971	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6778266	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6779395	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6786211	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6787200	1.00[CEU][hapmap];0.93[CHB][hapmap];0.84[JPT][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6787642	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6787853	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6788874	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6790771	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6791337	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6793868	1.00[CEU][hapmap];0.87[CHB][hapmap];0.92[CHD][hapmap];0.82[GIH][hapmap];0.87[JPT][hapmap];0.87[MEX][hapmap];0.95[TSI][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6797010	0.86[EUR][1000 genomes]
rs6797460	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6798228	1.00[CEU][hapmap];0.87[CHB][hapmap];0.92[CHD][hapmap];0.86[GIH][hapmap];0.87[JPT][hapmap];0.86[MEX][hapmap];0.92[TSI][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6806285	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.93[GIH][hapmap];0.87[JPT][hapmap];0.83[LWK][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6806536	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6808106	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs71621318	0.84[EUR][1000 genomes]
rs7434004	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7610446	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7615766	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7632886	0.82[EUR][1000 genomes]
rs7639427	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.93[GIH][hapmap];0.93[JPT][hapmap];0.93[MEX][hapmap];0.97[TSI][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7647518	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7653350	0.82[EUR][1000 genomes]
rs881948	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs881949	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs935734	1.00[CEU][hapmap];0.93[CHB][hapmap];0.95[CHD][hapmap];0.93[GIH][hapmap];0.94[JPT][hapmap];0.86[LWK][hapmap];0.86[MEX][hapmap];0.82[MKK][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9811187	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv470638	chr3:67367341-67814738	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv460700	chr3:67393629-67712970	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv590560	chr3:67393629-67712970	Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	esv3359258	chr3:67589615-67828274	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv876922	chr3:67635506-67755257	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv428739	chr3:67656829-67730379	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs2198015	RP11-81N13.1	cis	Thyroid	GTEx
rs2198015	LRIG1	cis	parietal	SCAN
rs2198015	SUCLG2	cis	lymphoblastoid	seeQTL
rs2198015	RP11-81N13.1	cis	lung	GTEx
rs2198015	SUCLG2	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:67681800-67704200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr3:67697400-67704200	Enhancers	Small Intestine	intestine
3	chr3:67697600-67704200	Weak transcription	Lung	lung
4	chr3:67698400-67704200	Weak transcription	Placenta	Placenta
5	chr3:67698800-67704200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr3:67699000-67704400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr3:67700200-67704200	Enhancers	Primary B cells from peripheral blood	blood
8	chr3:67701400-67704200	Weak transcription	Ovary	ovary
9	chr3:67701600-67704200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr3:67702000-67704200	Weak transcription	Left Ventricle	heart
11	chr3:67702000-67704200	Weak transcription	Pancreas	Pancrea
12	chr3:67702200-67704400	Weak transcription	Spleen	Spleen
13	chr3:67702400-67704200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr3:67702400-67704200	Weak transcription	Gastric	stomach
15	chr3:67702400-67704600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
16	chr3:67703000-67704600	Flanking Active TSS	Primary T cells from cord blood	blood
17	chr3:67703200-67704200	Weak transcription	Fetal Brain Male	brain
18	chr3:67703200-67704800	Flanking Active TSS	Primary B cells from cord blood	blood
19	chr3:67703400-67704200	Enhancers	Brain Substantia Nigra	brain
20	chr3:67703400-67704400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr3:67703400-67704400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr3:67703400-67704400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
23	chr3:67703400-67704400	Flanking Active TSS	Duodenum Mucosa	Duodenum
24	chr3:67703400-67704400	Flanking Active TSS	Osteobl	bone
25	chr3:67703400-67704600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
26	chr3:67703400-67704600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
27	chr3:67703400-67704600	Flanking Active TSS	Dnd41	blood
28	chr3:67703400-67704600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr3:67703400-67705800	Active TSS	NHLF	lung
30	chr3:67703600-67704200	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr3:67703600-67704200	Enhancers	Fetal Heart	heart
32	chr3:67703600-67704200	Enhancers	Placenta Amnion	Placenta Amnion
33	chr3:67703600-67704200	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr3:67703600-67704400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
35	chr3:67703600-67704400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
36	chr3:67703600-67704600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr3:67703600-67704600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
38	chr3:67703600-67704800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
39	chr3:67703600-67705200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr3:67703600-67705200	Active TSS	GM12878-XiMat	blood
41	chr3:67703600-67705800	Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr3:67703600-67706000	Active TSS	Pancreatic Islets	Pancreatic Islet
43	chr3:67703600-67706000	Active TSS	A549	lung
44	chr3:67703600-67706400	Active TSS	Colonic Mucosa	Colon
45	chr3:67703600-67706400	Active TSS	Duodenum Smooth Muscle	Duodenum
46	chr3:67703800-67704200	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr3:67703800-67704200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr3:67703800-67704200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr3:67703800-67704200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
50	chr3:67703800-67704400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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