Variant report

Variant	rs3806694
Chromosome Location	chr3:48672334-48672335
allele	C/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	MAZ	chr3:48672120-48673490	K562	blood:	n/a	chr3:48672634-48672644
2	TBP	chr3:48672222-48672422	GM12878	blood:	n/a	n/a
3	POLR2A	chr3:48672030-48673534	Hela-S3	cervix:	n/a	n/a
4	POLR2A	chr3:48672179-48673263	Gliobla	brain:	n/a	n/a
5	HCFC1	chr3:48671808-48673623	Hela-S3	cervix:	n/a	n/a
6	WRNIP1	chr3:48672211-48672357	GM12878	blood:	n/a	n/a
7	POLR2A	chr3:48672136-48673338	K562	blood:	n/a	n/a
8	POLR2A	chr3:48672287-48673323	HepG2	liver:	n/a	n/a
9	SP1	chr3:48672215-48673514	A549	lung:	n/a	chr3:48672979-48672991 chr3:48672637-48672649 chr3:48672980-48672989 chr3:48672980-48672990 chr3:48672981-48672990 chr3:48672632-48672646 chr3:48672346-48672358 chr3:48672346-48672358 chr3:48672979-48672991 chr3:48672631-48672643 chr3:48672981-48672990 chr3:48672368-48672380 chr3:48672633-48672642 chr3:48672963-48672984
10	SIN3AK20	chr3:48672177-48672441	SK-N-SH	brain:	n/a	n/a
11	MAZ	chr3:48672228-48673456	Hela-S3	cervix:	n/a	chr3:48672634-48672644
12	CTCF	chr3:48672220-48672370	AG10803	skin:	n/a	n/a
13	POLR2A	chr3:48672210-48673264	MCF-7	breast:	n/a	n/a
14	POLR2A	chr3:48672285-48672555	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr3:48672204-48673674	GM12878	blood:	n/a	n/a
16	FOSL1	chr3:48672069-48672476	K562	blood:	n/a	chr3:48672401-48672415
17	POLR2A	chr3:48672262-48672563	K562	blood:	n/a	n/a
18	CTCF	chr3:48672048-48673737	SK-N-SH	brain:	n/a	chr3:48672369-48672382 chr3:48673315-48673328 chr3:48672884-48672900
19	POLR2A	chr3:48672041-48673703	H1-hESC	embryonic stem cell:	n/a	n/a
20	FOSL2	chr3:48672020-48672504	A549	lung:	n/a	chr3:48672401-48672415
21	POLR2A	chr3:48672220-48673411	U87	brain:	n/a	n/a
22	YY1	chr3:48672331-48672468	K562	blood:	n/a	n/a
23	POLR2A	chr3:48672173-48673390	PBDE	blood:	n/a	n/a
24	POLR2A	chr3:48672082-48673433	Hela-S3	cervix:	n/a	n/a
25	POLR2A	chr3:48672242-48673570	GM18951	blood:	n/a	n/a
26	SMARCB1	chr3:48672251-48673521	Hela-S3	cervix:	n/a	n/a
27	ZBTB7A	chr3:48672083-48672394	K562	blood:	n/a	n/a
28	JUND	chr3:48672313-48672502	H1-hESC	embryonic stem cell:	n/a	chr3:48672401-48672415
29	TCF7L2	chr3:48672240-48673320	HCT-116	colon:	n/a	chr3:48672287-48672296
30	POLR2A	chr3:48672238-48673568	Hela-S3	cervix:	n/a	n/a
31	FOS	chr3:48672079-48672513	HUVEC	blood vessel:	n/a	chr3:48672285-48672296 chr3:48672401-48672415
32	FOS	chr3:48672178-48672365	MCF10A-Er-Src	breast:	n/a	chr3:48672285-48672296
33	MYC	chr3:48672107-48672347	MCF10A-Er-Src	breast:	n/a	n/a
34	POLR2A	chr3:48672147-48673223	MCF-7	breast:	n/a	n/a
35	CTCF	chr3:48672303-48672365	K562	blood:	n/a	n/a
36	ELK1	chr3:48672289-48672381	Hela-S3	cervix:	n/a	n/a
37	NR2F2	chr3:48672004-48672393	K562	blood:	n/a	n/a
38	MAZ	chr3:48671966-48674071	IMR90	lung:	n/a	chr3:48672634-48672644
39	POLR2A	chr3:48672322-48672626	A549	lung:	n/a	n/a
40	TAF1	chr3:48672199-48673611	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr3:48672129-48673476	Hela-S3	cervix:	n/a	n/a
42	POLR2A	chr3:48672249-48673381	K562	blood:	n/a	n/a
43	CTCF	chr3:48672200-48672350	AG09319	gingival:	n/a	n/a
44	MYC	chr3:48672309-48672379	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr3:48672323-48673221	H1-neurons	neurons:	n/a	n/a
46	POLR2A	chr3:48671859-48673656	K562	blood:	n/a	n/a
47	TAF1	chr3:48672287-48673252	HepG2	liver:	n/a	n/a
48	CHD2	chr3:48672268-48672360	K562	blood:	n/a	n/a
49	POLR2A	chr3:48672245-48672602	GM12878	blood:	n/a	n/a
50	REST	chr3:48672330-48673294	H1-neurons	neurons:	n/a	chr3:48672525-48672538 chr3:48672498-48672511 chr3:48672920-48672940 chr3:48673077-48673090 chr3:48672920-48672940 chr3:48672471-48672484 chr3:48673089-48673107 chr3:48673211-48673219 chr3:48672923-48672936

No.	Distal block	Cell Line	Cell type
1	chr17:8076447..8077190-chr3:48672013..48672607,2	HCT-116	colon:
2	chr3:48644319..48649140-chr3:48667292..48673836,7	K562	blood:
3	chr3:48592797..48594664-chr3:48671142..48674033,2	MCF-7	breast:
4	chr3:48620158..48621979-chr3:48670195..48672558,2	K562	blood:
5	chr3:48671184..48673366-chr3:48722826..48724747,2	K562	blood:
6	chr3:48608865..48611269-chr3:48670330..48672389,2	K562	blood:
7	chr3:48593498..48596370-chr3:48671883..48674161,2	K562	blood:
8	chr3:48670869..48673258-chr3:48680752..48682540,2	K562	blood:
9	chr3:48670764..48674544-chr3:48698929..48702803,9	K562	blood:
10	chr3:48645687..48647354-chr3:48671015..48673103,2	MCF-7	breast:
11	chr3:48670764..48674544-chr3:48699167..48702803,6	K562	blood:
12	chr3:48671382..48674659-chr3:48676453..48680538,5	MCF-7	breast:
13	chr3:48631986..48633856-chr3:48672080..48674450,2	K562	blood:
14	chr3:48665788..48669314-chr3:48669500..48672901,6	K562	blood:
15	chr3:48641673..48644998-chr3:48670911..48673807,4	K562	blood:
16	chr3:48669740..48673837-chr3:48676132..48680334,3	MCF-7	breast:
17	chr3:48631939..48633856-chr3:48671693..48673580,2	K562	blood:
18	chr3:48670890..48672785-chr3:48672866..48675614,2	MCF-7	breast:
19	chr3:48670997..48674874-chr3:48698947..48702118,7	MCF-7	breast:
20	chr3:48541156..48543765-chr3:48670075..48672910,2	K562	blood:
21	chr3:48667529..48675453-chr3:48697968..48703139,10	MCF-7	breast:
22	chr17:2206809..2207404-chr3:48672320..48672914,2	Hela-S3	cervix:
23	chr3:48594423..48596370-chr3:48671883..48674168,2	K562	blood:
24	chr3:48594247..48597141-chr3:48671392..48674077,2	MCF-7	breast:

Variant related genes	Relation type
SLC26A6	TF binding region
ENSG00000010256	Chromatin interaction
ENSG00000213672	Chromatin interaction
ENSG00000164054	Chromatin interaction
ENSG00000167720	Chromatin interaction
ENSG00000008300	Chromatin interaction
ENSG00000114270	Chromatin interaction
ENSG00000070366	Chromatin interaction
ENSG00000225697	Chromatin interaction
ENSG00000114268	Chromatin interaction
ENSG00000263898	Chromatin interaction
ENSG00000228350	Chromatin interaction
ENSG00000200463	Chromatin interaction

Extended variants
information (count: 90 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs10470687	1.00[JPT][hapmap]
rs11706983	1.00[JPT][hapmap]
rs11708786	1.00[JPT][hapmap]
rs11719291	1.00[JPT][hapmap]
rs11928552	1.00[JPT][hapmap]
rs12107252	1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12107418	1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12493578	1.00[JPT][hapmap]
rs12497850	1.00[JPT][hapmap]
rs12715429	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13060933	1.00[JPT][hapmap]
rs13062576	1.00[CHB][hapmap]
rs13063312	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13070798	1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13076269	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13091944	1.00[JPT][hapmap]
rs13096357	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13319651	1.00[JPT][hapmap]
rs13324119	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13324142	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13434258	1.00[JPT][hapmap]
rs1352420	1.00[JPT][hapmap]
rs17080289	0.81[ASN][1000 genomes]
rs17080319	1.00[JPT][hapmap]
rs2006871	1.00[JPT][hapmap]
rs2276850	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2276852	1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2286651	0.81[AFR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2286652	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.81[AFR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2302295	1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2310996	1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2310997	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28452701	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2854394	1.00[JPT][hapmap]
rs34096717	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34368826	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34638686	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35064573	1.00[JPT][hapmap]
rs35343040	0.83[ASN][1000 genomes]
rs35796820	0.81[ASN][1000 genomes]
rs3733086	0.81[AFR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3821875	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3821876	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4858798	1.00[JPT][hapmap]
rs4858828	1.00[JPT][hapmap]
rs4858831	1.00[JPT][hapmap]
rs57334642	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6768448	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6773261	1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6781283	1.00[JPT][hapmap]
rs6788650	1.00[JPT][hapmap]
rs6792156	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs6792525	1.00[JPT][hapmap]
rs68042649	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6806059	1.00[JPT][hapmap]
rs73078349	0.82[EUR][1000 genomes]
rs740787	1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7428949	1.00[JPT][hapmap]
rs7620853	1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7631574	1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9809222	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9810549	1.00[JPT][hapmap]
rs9811027	1.00[JPT][hapmap]
rs9811318	1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9812200	1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9812977	0.81[ASN][1000 genomes]
rs9821797	1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9830581	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs9834996	1.00[JPT][hapmap]
rs9836462	1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9837687	1.00[JPT][hapmap]
rs9841602	1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9843316	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs9850102	1.00[JPT][hapmap]
rs9868809	0.94[YRI][hapmap];0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9869698	1.00[JPT][hapmap]
rs9871180	1.00[JPT][hapmap]
rs9873726	1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9878063	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9878950	1.00[JPT][hapmap]
rs9882549	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008232	chr3:48517121-48702416	Transcr. at gene 5' and 3' Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv523981	chr3:48520289-48721040	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh 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
3	nsv834685	chr3:48565009-48745774	Strong transcription Active TSS Genic enhancers Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
4	nsv876762	chr3:48591481-48731487	Strong transcription Enhancers Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Flanking Active TSS Active TSS 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	53 gene(s)	inside rSNPs	diseases
5	nsv818138	chr3:48610925-48731487	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS 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	49 gene(s)	inside rSNPs	diseases
6	nsv590246	chr3:48628014-48721040	Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Enhancers Strong transcription Active TSS 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	47 gene(s)	inside rSNPs	diseases
7	nsv590247	chr3:48661985-48801929	Transcr. at gene 5' and 3' Strong transcription Active TSS Genic enhancers Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
8	esv3430072	chr3:48668048-48673146	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	14 gene(s)	inside rSNPs	diseases
9	nsv876763	chr3:48669648-48710310	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs3806694	WDR6	cis	Adipose Subcutaneous	GTEx
rs3806694	WDR6	cis	Esophagus Mucosa	GTEx
rs3806694	WDR6	cis	Skin Sun Exposed Lower leg	GTEx
rs3806694	SLC26A6	cis	lung	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:48670000-48673200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr3:48671200-48672400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr3:48671200-48672400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr3:48671200-48672400	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr3:48671200-48672400	Flanking Active TSS	Dnd41	blood
6	chr3:48671200-48672400	Flanking Active TSS	Hela-S3	cervix
7	chr3:48671400-48672400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
8	chr3:48671400-48672400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr3:48671400-48672400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
10	chr3:48671400-48673600	Active TSS	Gastric	stomach
11	chr3:48671400-48674400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
12	chr3:48671600-48672400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr3:48671600-48672400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr3:48671600-48672400	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr3:48671600-48672400	Flanking Active TSS	Colon Smooth Muscle	Colon
16	chr3:48671600-48672400	Flanking Active TSS	Duodenum Mucosa	Duodenum
17	chr3:48671600-48672400	Flanking Active TSS	HSMM	muscle
18	chr3:48671600-48672800	Flanking Active TSS	Colonic Mucosa	Colon
19	chr3:48671600-48672800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
20	chr3:48671600-48674200	Active TSS	HUES64 Cell Line	embryonic stem cell
21	chr3:48671800-48672400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr3:48671800-48672400	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr3:48671800-48672400	Flanking Active TSS	Primary T cells from cord blood	blood
24	chr3:48671800-48672400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr3:48671800-48672400	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
26	chr3:48671800-48672400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
27	chr3:48671800-48672400	Flanking Active TSS	NH-A	brain
28	chr3:48671800-48672600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
29	chr3:48671800-48672600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
30	chr3:48671800-48672600	Flanking Active TSS	Brain Hippocampus Middle	brain
31	chr3:48671800-48672800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
32	chr3:48671800-48672800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
33	chr3:48671800-48673600	Active TSS	HUES48 Cell Line	embryonic stem cell
34	chr3:48671800-48673800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
35	chr3:48671800-48673800	Active TSS	Pancreatic Islets	Pancreatic Islet
36	chr3:48671800-48674000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
37	chr3:48671800-48674000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr3:48671800-48674000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr3:48671800-48674000	Flanking Active TSS	Stomach Smooth Muscle	stomach
40	chr3:48672000-48672400	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr3:48672000-48672400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr3:48672000-48672400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
43	chr3:48672000-48672400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
44	chr3:48672000-48672400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
45	chr3:48672000-48672400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
46	chr3:48672000-48672400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
47	chr3:48672000-48672400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
48	chr3:48672000-48672400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
49	chr3:48672000-48672400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
50	chr3:48672000-48672400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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