Variant report

Variant	rs763254
Chromosome Location	chr6:118886615-118886616
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:118886471..118886972-chr6:118940114..118940818,2	MCF-7	breast:
2	chr6:118886433..118887071-chr6:119121474..119122076,2	MCF-7	breast:
3	chr6:118886432..118887044-chr6:118901651..118902441,2	MCF-7	breast:
4	chr6:118886488..118887139-chr6:118939697..118940461,3	MCF-7	breast:

Extended variants
information (count: 133 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:112)

rs_ID	r²[population]
rs10456917	0.83[ASN][1000 genomes]
rs10457330	0.82[ASN][1000 genomes]
rs10457331	0.82[ASN][1000 genomes]
rs10457335	0.83[ASN][1000 genomes]
rs10457337	0.84[ASN][1000 genomes]
rs10457338	0.94[CHB][hapmap];0.83[ASN][1000 genomes]
rs10457342	0.83[ASN][1000 genomes]
rs10872167	1.00[ASW][hapmap];0.92[CEU][hapmap];0.94[CHB][hapmap];0.93[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11153734	0.82[ASN][1000 genomes]
rs11153748	0.83[ASN][1000 genomes]
rs11153752	0.94[CHB][hapmap];0.87[ASN][1000 genomes]
rs11153753	0.88[ASN][1000 genomes]
rs11153759	0.92[ASN][1000 genomes]
rs11153763	0.94[CHB][hapmap];0.85[ASN][1000 genomes]
rs11153767	0.83[ASN][1000 genomes]
rs11153768	0.90[ASW][hapmap];0.89[CEU][hapmap];0.94[CHB][hapmap];0.93[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.92[MKK][hapmap];0.95[YRI][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11752626	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11752928	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11753128	0.89[ASN][1000 genomes]
rs11754023	0.83[JPT][hapmap]
rs11755121	0.88[CHB][hapmap];0.89[ASN][1000 genomes]
rs11756438	0.81[JPT][hapmap]
rs11756440	0.83[JPT][hapmap]
rs11758454	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11965985	0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11967375	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11967858	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11968176	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11968351	0.89[CHB][hapmap];0.92[ASN][1000 genomes]
rs11970286	0.81[EUR][1000 genomes]
rs12192682	0.92[ASN][1000 genomes]
rs12192964	0.82[ASN][1000 genomes]
rs12194555	0.94[CHB][hapmap];0.80[CHD][hapmap];0.95[MEX][hapmap];0.86[ASN][1000 genomes]
rs12197337	0.91[ASN][1000 genomes]
rs12198461	0.90[ASN][1000 genomes]
rs12199463	0.94[CHB][hapmap];0.85[MEX][hapmap];0.89[ASN][1000 genomes]
rs12203006	0.92[ASN][1000 genomes]
rs12206329	0.94[CHB][hapmap];0.92[ASN][1000 genomes]
rs12207209	0.89[ASN][1000 genomes]
rs12208253	0.94[CHB][hapmap];0.87[ASN][1000 genomes]
rs12211576	0.92[ASN][1000 genomes]
rs12214483	0.94[CHB][hapmap];0.83[ASN][1000 genomes]
rs12215793	0.83[ASN][1000 genomes]
rs12660455	0.82[ASN][1000 genomes]
rs12661338	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13191610	0.85[ASN][1000 genomes]
rs13192336	0.94[CHB][hapmap];0.92[ASN][1000 genomes]
rs13192574	0.92[ASN][1000 genomes]
rs13217710	0.86[ASN][1000 genomes]
rs13219555	0.87[ASN][1000 genomes]
rs13220480	0.94[CHB][hapmap];0.80[CHD][hapmap];0.95[MEX][hapmap];0.92[ASN][1000 genomes]
rs17226667	0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17227124	0.99[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17349329	0.83[JPT][hapmap]
rs17427116	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17825393	0.97[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17825652	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2078383	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2184402	0.87[ASN][1000 genomes]
rs2213856	0.94[CHB][hapmap];0.86[ASN][1000 genomes]
rs2213857	0.85[ASN][1000 genomes]
rs2356183	0.83[ASN][1000 genomes]
rs2356492	0.94[CHB][hapmap];0.85[ASN][1000 genomes]
rs2356497	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2356498	0.92[ASN][1000 genomes]
rs2798321	0.88[CHB][hapmap];0.81[MEX][hapmap]
rs2798323	0.83[CHB][hapmap]
rs2883956	0.85[ASN][1000 genomes]
rs34479834	0.89[ASN][1000 genomes]
rs35029749	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35730412	0.81[ASN][1000 genomes]
rs35962656	0.92[ASN][1000 genomes]
rs3734381	0.81[CHB][hapmap];0.89[MEX][hapmap];0.80[ASN][1000 genomes]
rs3752581	0.94[CHB][hapmap];0.92[ASN][1000 genomes]
rs3798420	0.94[CHB][hapmap];0.80[CHD][hapmap];0.94[MEX][hapmap];0.83[ASN][1000 genomes]
rs3890198	0.81[ASN][1000 genomes]
rs3951042	0.82[ASN][1000 genomes]
rs3951043	0.82[ASN][1000 genomes]
rs4027880	0.82[ASN][1000 genomes]
rs4307206	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.80[MKK][hapmap];0.98[TSI][hapmap];0.81[YRI][hapmap];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4945623	0.92[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4946347	0.89[ASN][1000 genomes]
rs4946350	0.85[ASN][1000 genomes]
rs55892056	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs57813349	0.82[ASN][1000 genomes]
rs59671368	0.92[ASN][1000 genomes]
rs6569020	0.93[CHB][hapmap];0.85[ASN][1000 genomes]
rs6569024	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs67832971	0.89[ASN][1000 genomes]
rs6902812	0.93[CHB][hapmap];0.87[ASN][1000 genomes]
rs6906287	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6925641	0.94[CHB][hapmap];0.80[CHD][hapmap];0.95[MEX][hapmap];0.89[ASN][1000 genomes]
rs6936178	0.82[ASN][1000 genomes]
rs6938041	0.89[ASN][1000 genomes]
rs6938226	0.89[ASN][1000 genomes]
rs72952771	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72952795	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72958930	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7740645	0.94[CHB][hapmap];0.87[ASN][1000 genomes]
rs7746778	0.80[ASN][1000 genomes]
rs7751467	0.94[CHB][hapmap];0.92[ASN][1000 genomes]
rs7757892	0.88[ASN][1000 genomes]
rs7758614	0.92[ASN][1000 genomes]
rs7763596	0.92[ASN][1000 genomes]
rs7766375	0.90[ASN][1000 genomes]
rs7769001	0.94[CHB][hapmap];0.87[ASN][1000 genomes]
rs7772214	0.84[ASN][1000 genomes]
rs7772921	0.83[ASN][1000 genomes]
rs7773274	0.87[ASN][1000 genomes]
rs9320663	0.89[CHB][hapmap];0.95[MEX][hapmap];0.81[ASN][1000 genomes]
rs9320665	0.89[CHB][hapmap];0.81[ASN][1000 genomes]
rs973944	0.94[CHB][hapmap];0.80[CHD][hapmap];0.94[MEX][hapmap];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532051	chr6:118551027-119044197	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1020463	chr6:118593028-119146363	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv1025403	chr6:118635123-119122551	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv1025456	chr6:118669672-119058789	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers 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	9 gene(s)	inside rSNPs	diseases
5	nsv1027444	chr6:118687556-119121660	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv538428	chr6:118687556-119121660	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
7	nsv949321	chr6:118692304-119137658	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active 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	10 gene(s)	inside rSNPs	diseases
8	nsv432958	chr6:118692307-119010307	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
9	nsv1034448	chr6:118698169-119016383	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
10	nsv1025097	chr6:118699752-119058789	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
11	nsv1020586	chr6:118711098-118900012	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
12	nsv532052	chr6:118711850-119057295	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer 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	9 gene(s)	inside rSNPs	diseases
13	nsv432959	chr6:118716318-119010307	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
14	nsv604556	chr6:118722589-119065365	Active TSS Strong transcription Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
15	nsv949416	chr6:118772508-119033063	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
16	nsv948980	chr6:118772508-119137658	Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
17	nsv604559	chr6:118786486-119113317	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
18	nsv1022865	chr6:118786586-119058789	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
19	nsv1020405	chr6:118786586-119241006	ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
20	nsv1030331	chr6:118874345-118975680	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
21	esv275552	chr6:118878758-118887215	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs763254	SLC35F1	cis	cerebellum	SCAN
rs763254	C6orf204	cis	cerebellum	SCAN

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:118847800-118895400	Weak transcription	Pancreas	Pancrea
2	chr6:118852600-118895200	Weak transcription	Primary B cells from cord blood	blood
3	chr6:118864400-118895200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr6:118868600-118894000	Weak transcription	Fetal Stomach	stomach
5	chr6:118872200-118895200	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr6:118872800-118895200	Weak transcription	HMEC	breast
7	chr6:118873800-118895600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr6:118874600-118895200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr6:118874600-118895200	Weak transcription	K562	blood
10	chr6:118875000-118889200	Weak transcription	Placenta	Placenta
11	chr6:118875400-118895200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr6:118877800-118889200	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr6:118877800-118895200	Weak transcription	Gastric	stomach
14	chr6:118878800-118889200	Weak transcription	Right Atrium	heart
15	chr6:118880200-118890000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr6:118880400-118889200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr6:118880400-118895200	Weak transcription	Left Ventricle	heart
18	chr6:118880400-118895200	Weak transcription	Right Ventricle	heart
19	chr6:118880600-118889400	Weak transcription	Colon Smooth Muscle	Colon
20	chr6:118880800-118894400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr6:118880800-118895000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr6:118881000-118889200	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr6:118881000-118895200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr6:118881200-118886800	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr6:118881800-118895200	Weak transcription	Stomach Smooth Muscle	stomach
26	chr6:118882400-118886800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr6:118882600-118889000	Weak transcription	Fetal Heart	heart
28	chr6:118884200-118886800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr6:118884200-118886800	Weak transcription	Fetal Brain Female	brain
30	chr6:118884200-118889600	Weak transcription	Brain Cingulate Gyrus	brain
31	chr6:118884200-118894600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr6:118884200-118895200	Weak transcription	Aorta	Aorta
33	chr6:118884200-118895400	Weak transcription	NHLF	lung
34	chr6:118884400-118888600	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr6:118884400-118888800	Weak transcription	Brain Hippocampus Middle	brain
36	chr6:118884400-118889000	Weak transcription	Brain Angular Gyrus	brain
37	chr6:118884400-118889000	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr6:118884400-118889800	Weak transcription	NHDF-Ad	bronchial
39	chr6:118884600-118894600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr6:118885000-118886800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr6:118885000-118891800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
42	chr6:118885000-118894000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr6:118885200-118886800	Strong transcription	Primary T cells fromperipheralblood	blood
44	chr6:118885200-118889400	Weak transcription	Stomach Mucosa	stomach
45	chr6:118885400-118889200	Weak transcription	Brain Substantia Nigra	brain
46	chr6:118885400-118895400	Weak transcription	Brain Anterior Caudate	brain
47	chr6:118885600-118887200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr6:118885600-118887400	Strong transcription	HSMM	muscle
49	chr6:118886000-118887600	Strong transcription	Monocytes-CD14+_RO01746	blood
50	chr6:118886000-118888000	Strong transcription	Dnd41	blood

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