Variant report

Variant	rs73043413
Chromosome Location	chr3:179041759-179041760
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	RCOR1	chr3:179040162-179041791	Hela-S3	cervix:	n/a	n/a
2	WRNIP1	chr3:179041465-179041785	GM12878	blood:	n/a	n/a
3	MYC	chr3:179039897-179042523	MCF10A-Er-Src	breast:	n/a	chr3:179042200-179042210 chr3:179042171-179042178 chr3:179042168-179042179 chr3:179040898-179040907 chr3:179042164-179042183
4	JUND	chr3:179040194-179041796	K562	blood:	n/a	chr3:179040556-179040565 chr3:179041077-179041085
5	STAT5A	chr3:179040982-179041888	GM12878	blood:	n/a	n/a
6	POLR2A	chr3:179040158-179041832	GM12891	blood:	n/a	n/a
7	POLR2A	chr3:179040298-179041839	GM15510	blood:	n/a	n/a
8	POLR2A	chr3:179040287-179041864	GM12892	blood:	n/a	n/a
9	HCFC1	chr3:179039384-179042423	Hela-S3	cervix:	n/a	n/a
10	E2F6	chr3:179040242-179041760	H1-hESC	embryonic stem cell:	n/a	chr3:179040829-179040838 chr3:179040972-179040981 chr3:179041028-179041038 chr3:179040633-179040648 chr3:179041162-179041174 chr3:179040793-179040805
11	NFIC	chr3:179040176-179041807	ECC-1	luminal epithelium:	n/a	n/a
12	IRF1	chr3:179041586-179042635	K562	blood:	n/a	chr3:179042538-179042551 chr3:179041902-179041916 chr3:179042538-179042552 chr3:179041898-179041918 chr3:179041854-179041868 chr3:179041904-179041917 chr3:179041905-179041922 chr3:179042537-179042551 chr3:179041850-179041870 chr3:179041855-179041869 chr3:179041903-179041917 chr3:179042536-179042550 chr3:179041852-179041866 chr3:179041906-179041920
13	MAX	chr3:179040229-179042627	NB4	blood:	n/a	chr3:179042200-179042210 chr3:179042171-179042178 chr3:179042168-179042179 chr3:179040898-179040907 chr3:179042164-179042183
14	CEBPB	chr3:179040057-179041934	Hela-S3	cervix:	n/a	n/a
15	MAFK	chr3:179041175-179041872	Hela-S3	cervix:	n/a	n/a
16	POLR2A	chr3:179040199-179041827	GM18505	blood:	n/a	n/a
17	RAD21	chr3:179039236-179042655	SK-N-SH	brain:	n/a	chr3:179041123-179041133 chr3:179041353-179041367 chr3:179041292-179041302 chr3:179040968-179040980 chr3:179040969-179040982 chr3:179039549-179039568
18	POLR2A	chr3:179040164-179041818	GM12892	blood:	n/a	n/a
19	MAX	chr3:179039733-179041834	HepG2	liver:	n/a	chr3:179040898-179040907
20	POLR2A	chr3:179040554-179041790	GM12892	blood:	n/a	n/a
21	JUND	chr3:179039219-179041948	SK-N-SH	brain:	n/a	chr3:179040556-179040565 chr3:179041077-179041085
22	SIN3AK20	chr3:179040338-179041775	PANC-1	pancreas:	n/a	n/a
23	BHLHE40	chr3:179039332-179041761	K562	blood:	n/a	chr3:179040974-179040990 chr3:179041029-179041045 chr3:179041288-179041304
24	SIN3A	chr3:179041156-179042085	GM12878	blood:	n/a	chr3:179041489-179041498
25	POLR2A	chr3:179040090-179041847	H1-hESC	embryonic stem cell:	n/a	n/a
26	POLR2A	chr3:179040124-179041866	Hela-S3	cervix:	n/a	n/a
27	REST	chr3:179040112-179042006	H1-neurons	neurons:	n/a	chr3:179040937-179040944 chr3:179041007-179041020
28	POLR2A	chr3:179039299-179043011	MCF10A-Er-Src	breast:	n/a	n/a
29	RCOR1	chr3:179038803-179041761	K562	blood:	n/a	n/a
30	YY1	chr3:179040455-179041851	GM12878	blood:	n/a	chr3:179041008-179041017 chr3:179041030-179041039 chr3:179041015-179041029 chr3:179041024-179041035 chr3:179040972-179040981 chr3:179040861-179040872 chr3:179041027-179041036
31	SIN3AK20	chr3:179039984-179041852	MCF-7	breast:	n/a	n/a
32	UBTF	chr3:179040514-179042581	K562	blood:	n/a	n/a
33	MAX	chr3:179040165-179041773	HepG2	liver:	n/a	chr3:179040898-179040907
34	NR2F2	chr3:179040989-179041797	K562	blood:	n/a	n/a
35	TBL1XR1	chr3:179041075-179041762	K562	blood:	n/a	n/a
36	E2F6	chr3:179040195-179041804	K562	blood:	n/a	chr3:179040829-179040838 chr3:179040972-179040981 chr3:179041028-179041038 chr3:179040633-179040648 chr3:179041162-179041174 chr3:179040793-179040805
37	MYC	chr3:179040394-179042204	A549	lung:	n/a	chr3:179042171-179042178 chr3:179042168-179042179 chr3:179040898-179040907 chr3:179042164-179042183
38	TCF7L2	chr3:179040251-179041795	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr3:179040268-179041802	HepG2	liver:	n/a	n/a
40	POLR2A	chr3:179040181-179041777	Hela-S3	cervix:	n/a	n/a
41	MYC	chr3:179039371-179042652	K562	blood:	n/a	chr3:179042200-179042210 chr3:179042171-179042178 chr3:179042168-179042179 chr3:179040898-179040907 chr3:179042164-179042183
42	POLR2A	chr3:179040110-179041852	K562	blood:	n/a	n/a
43	POLR2A	chr3:179040164-179041826	Hela-S3	cervix:	n/a	n/a
44	MAX	chr3:179041195-179041793	MCF-7	breast:	n/a	n/a
45	MAZ	chr3:179040292-179041846	K562	blood:	n/a	chr3:179040898-179040907
46	MYC	chr3:179039244-179042670	K562	blood:	n/a	chr3:179042200-179042210 chr3:179042171-179042178 chr3:179042168-179042179 chr3:179040898-179040907 chr3:179042164-179042183
47	SMC3	chr3:179039806-179041981	SK-N-SH	brain:	n/a	chr3:179041292-179041306 chr3:179041123-179041133
48	CTCF	chr3:179039275-179041891	SK-N-SH	brain:	n/a	chr3:179039546-179039567 chr3:179039552-179039568 chr3:179041292-179041305
49	POLR2A	chr3:179040258-179041856	GM12878	blood:	n/a	n/a
50	MAX	chr3:179040055-179041896	ECC-1	luminal epithelium:	n/a	chr3:179040898-179040907

No.	Distal block	Cell Line	Cell type
1	chr3:178864344..178867597-chr3:179039214..179042429,8	K562	blood:
2	chr3:178978041..178980864-chr3:179039699..179042008,3	K562	blood:
3	chr3:178977469..178980839-chr3:179038593..179042214,6	K562	blood:
4	chr3:179039679..179043417-chr3:179063023..179066951,5	K562	blood:
5	chr3:179040252..179043387-chr3:179064355..179067344,4	MCF-7	breast:
6	chr3:178787120..178791261-chr3:179039253..179041998,3	K562	blood:
7	chr3:179041141..179044648-chr3:179167085..179169566,4	K562	blood:
8	chr3:179040254..179044115-chr3:179063916..179068626,6	K562	blood:
9	chr3:179037868..179043452-chr3:179279283..179282534,12	K562	blood:
10	chr3:160116021..160118602-chr3:179040566..179042306,2	K562	blood:
11	chr3:179037735..179042391-chr3:179277921..179283824,9	MCF-7	breast:
12	chr3:179039334..179043117-chr3:179061578..179071936,16	MCF-7	breast:
13	chr3:179040074..179043948-chr3:179167085..179170222,5	K562	blood:
14	chr3:179039352..179043378-chr3:179279283..179282999,10	K562	blood:
15	chr3:179039610..179042933-chr3:179054240..179057497,4	MCF-7	breast:
16	chr3:178866029..178868505-chr3:179041655..179043720,2	K562	blood:
17	chr3:178977854..178979821-chr3:179040251..179043018,2	MCF-7	breast:
18	chr3:179040206..179042939-chr3:179043914..179045418,3	MCF-7	breast:
19	chr3:178787618..178789818-chr3:179039518..179042108,2	K562	blood:
20	chr3:179039445..179042481-chr3:179045775..179048078,4	MCF-7	breast:
21	chr3:179040612..179043524-chr3:179043815..179047485,6	K562	blood:
22	chr3:178864492..178868931-chr3:179039553..179043493,6	MCF-7	breast:
23	chr3:179039914..179042763-chr3:179093091..179095772,2	K562	blood:

Variant related genes	Relation type
ZNF639	TF binding region
ENSG00000068885	Chromatin interaction
ENSG00000136518	Chromatin interaction
ENSG00000121864	Chromatin interaction
ENSG00000273190	Chromatin interaction
ENSG00000121879	Chromatin interaction
ENSG00000114450	Chromatin interaction
ENSG00000240429	Chromatin interaction
ENSG00000171109	Chromatin interaction
ENSG00000172667	Chromatin interaction
ENSG00000239255	Chromatin interaction
ENSG00000229102	Chromatin interaction
ENSG00000171121	Chromatin interaction
ENSG00000113810	Chromatin interaction

Extended variants
information (count: 72 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11916825	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11919840	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11925064	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11925248	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11927084	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13317510	0.89[AMR][1000 genomes]
rs16830445	0.89[AMR][1000 genomes]
rs16830460	0.89[AMR][1000 genomes]
rs28512433	0.89[AMR][1000 genomes]
rs28522651	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55805052	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56210820	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs56265474	0.89[AMR][1000 genomes]
rs56280435	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57148977	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57526364	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57795346	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58741861	0.89[AMR][1000 genomes]
rs59062224	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59333548	0.89[AMR][1000 genomes]
rs59511701	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59564372	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59833817	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs60191176	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60746059	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61246771	0.89[AMR][1000 genomes]
rs61325843	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6778235	0.89[AMR][1000 genomes]
rs6800044	0.89[AMR][1000 genomes]
rs6808033	0.89[AMR][1000 genomes]
rs6808866	1.00[AMR][1000 genomes]
rs73043406	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73043407	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73043409	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73043415	0.95[AFR][1000 genomes]
rs73045191	0.89[AMR][1000 genomes]
rs73045195	0.89[AMR][1000 genomes]
rs73045198	0.89[AMR][1000 genomes]
rs73059758	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73059766	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7355835	0.89[AMR][1000 genomes]
rs73883508	0.89[AMR][1000 genomes]
rs73883509	0.89[AMR][1000 genomes]
rs73886620	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7611533	0.89[AMR][1000 genomes]
rs7625719	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9814990	0.89[AMR][1000 genomes]
rs9829054	0.89[AMR][1000 genomes]
rs9834493	0.89[AMR][1000 genomes]
rs9861354	0.89[AMR][1000 genomes]
rs9864857	0.89[AMR][1000 genomes]
rs9872939	0.89[AMR][1000 genomes]
rs9884070	0.89[AMR][1000 genomes]
rs9968068	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9968069	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9968075	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9968076	1.00[AMR][1000 genomes];1.00[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	nsv998253	chr3:178622707-179196274	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	nsv536814	chr3:178622707-179196274	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer 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 miRNA target site	52 gene(s)	inside rSNPs	diseases
3	esv3354111	chr3:178833305-179156908	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
4	nsv1002962	chr3:178943753-179224548	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
5	nsv536815	chr3:178943753-179224548	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
6	nsv1003021	chr3:178944806-179246179	Enhancers Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
7	nsv1006584	chr3:178944822-179241429	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
8	nsv829806	chr3:178952363-179154373	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
9	nsv1010137	chr3:178962897-179050787	Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases
10	nsv471116	chr3:178968634-179252263	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
11	nsv592650	chr3:178968634-179252263	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
12	nsv1010513	chr3:178976107-179196274	Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
13	nsv536816	chr3:178976107-179196274	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
14	nsv1003514	chr3:178990037-179177029	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
15	esv3409455	chr3:179040008-179042256	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	22 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:179038800-179042200	Active TSS	NHLF	lung
2	chr3:179038800-179042800	Active TSS	Ovary	ovary
3	chr3:179039000-179042400	Active TSS	Right Atrium	heart
4	chr3:179039000-179043200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr3:179039200-179042600	Active TSS	Breast Myoepithelial Primary Cells	Breast
6	chr3:179039200-179042600	Active TSS	Colonic Mucosa	Colon
7	chr3:179039200-179042800	Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr3:179039600-179041800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
9	chr3:179039800-179042800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr3:179040000-179041800	Active TSS	Brain Inferior Temporal Lobe	brain
11	chr3:179040000-179042000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr3:179040000-179042200	Active TSS	Brain Angular Gyrus	brain
13	chr3:179040000-179042200	Active TSS	Colon Smooth Muscle	Colon
14	chr3:179040000-179042200	Active TSS	Fetal Intestine Large	intestine
15	chr3:179040000-179042200	Active TSS	Psoas Muscle	Psoas
16	chr3:179040000-179042400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr3:179040000-179042400	Active TSS	HUES6 Cell Line	embryonic stem cell
18	chr3:179040000-179042400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr3:179040000-179042400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr3:179040000-179042400	Active TSS	Right Ventricle	heart
21	chr3:179040000-179042600	Active TSS	H9 Cell Line	embryonic stem cell
22	chr3:179040000-179042600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:179040000-179042800	Active TSS	HSMMtube	muscle
24	chr3:179040000-179043000	Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr3:179040200-179041800	Active TSS	Brain Hippocampus Middle	brain
26	chr3:179040200-179041800	Active TSS	Gastric	stomach
27	chr3:179040200-179041800	Active TSS	Sigmoid Colon	Sigmoid Colon
28	chr3:179040200-179042000	Active TSS	HUES64 Cell Line	embryonic stem cell
29	chr3:179040200-179042000	Active TSS	Placenta Amnion	Placenta Amnion
30	chr3:179040200-179042200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr3:179040200-179042200	Active TSS	iPS-20b Cell Line	embryonic stem cell
32	chr3:179040200-179042200	Active TSS	Fetal Intestine Small	intestine
33	chr3:179040200-179042200	Active TSS	NH-A	brain
34	chr3:179040200-179042400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
35	chr3:179040200-179042400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr3:179040200-179042400	Active TSS	Duodenum Smooth Muscle	Duodenum
37	chr3:179040200-179042400	Active TSS	Left Ventricle	heart
38	chr3:179040200-179042400	Active TSS	Lung	lung
39	chr3:179040200-179042400	Active TSS	A549	lung
40	chr3:179040200-179042600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr3:179040200-179042800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr3:179040200-179042800	Active TSS	Aorta	Aorta
43	chr3:179040200-179042800	Active TSS	NHDF-Ad	bronchial
44	chr3:179040400-179041800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
45	chr3:179040400-179041800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr3:179040400-179041800	Active TSS	Small Intestine	intestine
47	chr3:179040400-179041800	Active TSS	Spleen	Spleen
48	chr3:179040400-179042000	Active TSS	HUES48 Cell Line	embryonic stem cell
49	chr3:179040400-179042000	Active TSS	iPS-18 Cell Line	embryonic stem cell
50	chr3:179040400-179042000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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