Variant report

Variant	rs2032450
Chromosome Location	chr6:25993114-25993115
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:16)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:25726594..25729863-chr6:25991893..25994558,4	K562	blood:
2	chr6:25992550..25993437-chr6:36561552..36562217,2	NB4	blood:
3	chr6:25962825..25963375-chr6:25992746..25993257,2	K562	blood:
4	chr17:73150234..73151018-chr6:25992234..25993190,2	Hela-S3	cervix:
5	chr6:25990980..25994781-chr6:26019644..26023390,9	MCF-7	breast:
6	chr11:34126629..34127570-chr6:25992649..25993532,2	Hela-S3	cervix:
7	chr6:25991481..25993438-chr6:26015538..26017595,2	MCF-7	breast:
8	chr6:25992274..25993189-chr6:26020579..26021165,3	Hela-S3	cervix:
9	chr6:25867711..25870516-chr6:25992020..25994438,2	K562	blood:
10	chr6:25961783..25964529-chr6:25992813..25995946,4	MCF-7	breast:
11	chr6:25992154..25994849-chr6:27113422..27115157,2	K562	blood:
12	chr6:25991365..25993572-chr6:25997805..26000097,3	MCF-7	breast:
13	chr6:25992957..25995819-chr6:25996424..25999435,3	MCF-7	breast:
14	chr6:25991732..25993497-chr6:26025765..26028422,2	MCF-7	breast:
15	chr6:25992191..25994174-chr6:26011944..26014564,2	MCF-7	breast:
16	chr6:25725442..25728537-chr6:25991436..25993393,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIM38-1	chr6:25992968-25993146	XLOC_005208
2	lnc-TRIM38-1	chr6:25992927-25993146	XLOC_005208
3	lnc-TRIM38-1	chr6:25992890-25993146	ENSG00000272462.2
4	lnc-TRIM38-1	chr6:25992889-25993146	NONHSAT108196

No data

Variant related genes	Relation type
ENSG00000272810	Chromatin interaction
ENSG00000146047	Chromatin interaction
ENSG00000189159	Chromatin interaction
ENSG00000124564	Chromatin interaction
ENSG00000135372	Chromatin interaction
ENSG00000198366	Chromatin interaction
ENSG00000112343	Chromatin interaction
ENSG00000272558	Chromatin interaction
ENSG00000124529	Chromatin interaction
ENSG00000112081	Chromatin interaction
ENSG00000164508	Chromatin interaction
ENSG00000224447	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000196176	Chromatin interaction
ENSG00000184825	Chromatin interaction

Extended variants
information (count: 130 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:117)

rs_ID	r²[population]
rs10807006	0.83[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs10946800	0.83[AMR][1000 genomes]
rs1115920	0.83[AMR][1000 genomes]
rs1130000	1.00[CEU][hapmap];0.94[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12195653	0.81[CEU][hapmap];0.94[CHB][hapmap];0.85[JPT][hapmap];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12209482	0.85[AMR][1000 genomes]
rs1324084	0.85[AMR][1000 genomes]
rs1436306	0.83[AMR][1000 genomes]
rs1436307	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1436309	0.89[CEU][hapmap];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1436310	0.89[CEU][hapmap];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1540273	0.88[CHB][hapmap];0.85[AMR][1000 genomes]
rs1541987	0.82[AMR][1000 genomes]
rs1800702	0.85[CEU][hapmap];1.00[JPT][hapmap]
rs1816546	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1865760	0.87[CHB][hapmap];0.85[AMR][1000 genomes]
rs2006736	0.92[CEU][hapmap];1.00[JPT][hapmap]
rs2008015	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2013063	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2032443	0.83[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs2032445	0.83[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs2032449	0.89[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2051544	0.84[CEU][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap]
rs2071297	0.87[CHB][hapmap];0.87[AMR][1000 genomes]
rs2071298	0.87[CHB][hapmap];0.85[AMR][1000 genomes]
rs2071299	0.87[CHB][hapmap];0.85[AMR][1000 genomes]
rs2071300	0.81[CHB][hapmap]
rs2071301	0.87[CHB][hapmap];0.85[AMR][1000 genomes]
rs2157050	0.92[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2164485	0.83[AMR][1000 genomes]
rs2164487	0.82[AMR][1000 genomes]
rs2328903	0.81[CEU][hapmap];0.94[CHB][hapmap];0.84[JPT][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2794719	0.81[CEU][hapmap];1.00[JPT][hapmap]
rs2794720	0.84[CEU][hapmap];1.00[JPT][hapmap]
rs2876693	0.82[CEU][hapmap];0.94[CHB][hapmap];0.84[JPT][hapmap];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3752419	0.89[CEU][hapmap];0.88[CHB][hapmap];0.95[JPT][hapmap];0.90[YRI][hapmap];0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3752420	0.89[CEU][hapmap];0.83[CHB][hapmap];0.95[JPT][hapmap];0.90[YRI][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3752421	0.87[CHB][hapmap];0.85[AMR][1000 genomes]
rs3799371	0.87[CHB][hapmap];0.84[AMR][1000 genomes]
rs3799372	0.88[CHB][hapmap];0.85[AMR][1000 genomes]
rs3799373	0.88[CHB][hapmap];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs3830057	0.85[AMR][1000 genomes]
rs3846838	0.85[AMR][1000 genomes]
rs4478388	0.83[AMR][1000 genomes]
rs4529296	0.85[CEU][hapmap];1.00[JPT][hapmap]
rs56118523	0.85[AMR][1000 genomes]
rs6456705	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6905887	0.83[AMR][1000 genomes]
rs6910138	0.88[CHB][hapmap];0.85[AMR][1000 genomes]
rs6910174	0.87[CHB][hapmap];0.85[AMR][1000 genomes]
rs6915834	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6928951	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6929805	0.82[AMR][1000 genomes]
rs6932113	0.83[CEU][hapmap];0.87[CHB][hapmap];0.85[AMR][1000 genomes]
rs6938233	0.87[CHB][hapmap];0.85[AMR][1000 genomes]
rs6942196	0.84[CEU][hapmap];1.00[JPT][hapmap]
rs7450342	0.81[CHB][hapmap]
rs7739966	0.85[AMR][1000 genomes]
rs7749342	0.81[CHB][hapmap]
rs7753253	0.86[CHB][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs7753826	0.91[YRI][hapmap]
rs7757666	0.85[AMR][1000 genomes]
rs7766342	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7766478	0.85[AMR][1000 genomes]
rs7770139	0.87[CHB][hapmap];0.87[AMR][1000 genomes]
rs7772312	0.85[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.83[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs9295673	0.83[AMR][1000 genomes]
rs9295677	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9295679	0.81[AMR][1000 genomes]
rs9295680	0.81[AMR][1000 genomes]
rs9295681	0.81[AMR][1000 genomes]
rs9295685	0.90[JPT][hapmap]
rs9295687	0.84[CEU][hapmap];1.00[JPT][hapmap]
rs9295688	0.85[CEU][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap]
rs9348698	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9348704	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9356991	0.80[CEU][hapmap];0.87[CHB][hapmap];0.85[AMR][1000 genomes]
rs9358891	0.81[AMR][1000 genomes]
rs9358892	0.81[AMR][1000 genomes]
rs9358893	0.82[CHB][hapmap];0.85[AMR][1000 genomes]
rs9358895	0.87[AMR][1000 genomes]
rs9358896	0.81[CEU][hapmap];0.94[CHB][hapmap];0.84[JPT][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9358902	0.80[ASN][1000 genomes]
rs9358903	0.81[CEU][hapmap]
rs9366634	0.84[CEU][hapmap];1.00[JPT][hapmap]
rs9379801	0.81[CHB][hapmap]
rs9379806	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9379807	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9379814	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9379815	0.96[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9379818	0.84[CEU][hapmap]
rs9379820	0.85[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.83[AMR][1000 genomes]
rs9379821	1.00[JPT][hapmap];0.83[AMR][1000 genomes]
rs9379825	0.85[CEU][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap]
rs9393675	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9393677	0.81[AMR][1000 genomes]
rs9393678	0.81[AMR][1000 genomes]
rs9393681	0.92[CEU][hapmap];0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9393683	0.81[CEU][hapmap]
rs9461224	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9461227	0.83[AMR][1000 genomes]
rs9461229	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9461230	0.89[CEU][hapmap];0.84[AMR][1000 genomes]
rs9467636	0.82[CHB][hapmap];0.85[AMR][1000 genomes]
rs9467641	0.83[AMR][1000 genomes]
rs9467645	0.83[AMR][1000 genomes]
rs9467646	0.81[CEU][hapmap];0.94[CHB][hapmap];0.84[JPT][hapmap];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9467647	0.83[AMR][1000 genomes]
rs9467648	0.83[AMR][1000 genomes]
rs9467650	0.83[AMR][1000 genomes]
rs9467651	0.83[AMR][1000 genomes]
rs9467652	0.82[AMR][1000 genomes]
rs9467656	0.96[CEU][hapmap];0.96[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9467658	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9467662	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9467663	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9467672	0.85[CEU][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv1030351	chr6:25813178-26352046	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1189 gene(s)	inside rSNPs	diseases
4	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1201 gene(s)	inside rSNPs	diseases
5	nsv1025237	chr6:25874326-26280867	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
6	nsv538163	chr6:25874326-26280867	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
7	nsv432857	chr6:25957109-26072445	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	451 gene(s)	inside rSNPs	diseases
8	nsv1015627	chr6:25973495-26100483	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	447 gene(s)	inside rSNPs	diseases
9	nsv538164	chr6:25973495-26100483	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	447 gene(s)	inside rSNPs	diseases
10	nsv1028456	chr6:25984457-26174993	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	873 gene(s)	inside rSNPs	diseases
11	nsv538165	chr6:25984457-26174993	Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Genic enhancers 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	873 gene(s)	inside rSNPs	diseases
12	nsv428137	chr6:25987413-26351920	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1181 gene(s)	inside rSNPs	diseases
13	nsv916992	chr6:25991630-26280921	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1159 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2032450	U91328.19	cis	Muscle Skeletal	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:25991600-25993600	Active TSS	Liver	Liver
2	chr6:25991600-25994000	Active TSS	Rectal Mucosa Donor 29	rectum
3	chr6:25991800-25993600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr6:25991800-25993800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
5	chr6:25991800-25994000	Active TSS	Hela-S3	cervix
6	chr6:25991800-25994200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr6:25991800-25994200	Active TSS	Stomach Smooth Muscle	stomach
8	chr6:25992000-25993200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr6:25992000-25993200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr6:25992000-25993400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr6:25992000-25993400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr6:25992000-25993400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr6:25992000-25993400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr6:25992000-25993400	Active TSS	Primary T helper naive cells from peripheral blood	blood
15	chr6:25992000-25993400	Active TSS	Primary T killer memory cells from peripheral blood	blood
16	chr6:25992000-25993400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
17	chr6:25992000-25993400	Active TSS	Esophagus	oesophagus
18	chr6:25992000-25993400	Active TSS	Lung	lung
19	chr6:25992000-25993400	Active TSS	Small Intestine	intestine
20	chr6:25992000-25993600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr6:25992000-25993600	Active TSS	iPS-18 Cell Line	embryonic stem cell
22	chr6:25992000-25993600	Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr6:25992000-25993600	Active TSS	Aorta	Aorta
24	chr6:25992000-25993600	Active TSS	Brain Angular Gyrus	brain
25	chr6:25992000-25993600	Active TSS	Brain Anterior Caudate	brain
26	chr6:25992000-25993600	Active TSS	Brain Hippocampus Middle	brain
27	chr6:25992000-25993600	Active TSS	Brain Inferior Temporal Lobe	brain
28	chr6:25992000-25993600	Active TSS	Fetal Brain Female	brain
29	chr6:25992000-25993600	Active TSS	Fetal Kidney	kidney
30	chr6:25992000-25993600	Active TSS	Psoas Muscle	Psoas
31	chr6:25992000-25993600	Active TSS	Osteobl	bone
32	chr6:25992000-25993800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
33	chr6:25992000-25993800	Active TSS	H9 Cell Line	embryonic stem cell
34	chr6:25992000-25993800	Active TSS	Breast Myoepithelial Primary Cells	Breast
35	chr6:25992000-25993800	Active TSS	Colon Smooth Muscle	Colon
36	chr6:25992000-25993800	Active TSS	Duodenum Smooth Muscle	Duodenum
37	chr6:25992000-25993800	Active TSS	Fetal Intestine Small	intestine
38	chr6:25992000-25993800	Active TSS	Pancreatic Islets	Pancreatic Islet
39	chr6:25992000-25993800	Active TSS	Left Ventricle	heart
40	chr6:25992000-25994000	Active TSS	HUES48 Cell Line	embryonic stem cell
41	chr6:25992000-25994000	Active TSS	HUES64 Cell Line	embryonic stem cell
42	chr6:25992000-25994000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr6:25992000-25994000	Active TSS	Fetal Lung	lung
44	chr6:25992000-25994000	Active TSS	Right Atrium	heart
45	chr6:25992000-25994000	Active TSS	Right Ventricle	heart
46	chr6:25992000-25994200	Active TSS	iPS-15b Cell Line	embryonic stem cell
47	chr6:25992000-25994200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr6:25992000-25994200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr6:25992000-25994200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
50	chr6:25992000-25994200	Active TSS	Fetal Intestine Large	intestine

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