Variant report

Variant	rs11054166
Chromosome Location	chr12:11170042-11170043
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:11169301..11171201-chr12:11322573..11325255,2	MCF-7	breast:
2	chr12:11009323..11011109-chr12:11168207..11170860,2	K562	blood:

Variant related genes	Relation type
ENSG00000111215	Chromatin interaction
ENSG00000256537	Chromatin interaction
ENSG00000256712	Chromatin interaction
ENSG00000212127	Chromatin interaction

Extended variants
information (count: 143 )
Associated
traits (count: 12 )

rSNPs within LD-proxies of this variant (count:119)

rs_ID	r²[population]
rs10161144	0.85[ASN][1000 genomes]
rs1044682	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs1044683	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10743937	0.88[ASN][1000 genomes]
rs10772393	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10772394	0.81[AMR][1000 genomes]
rs10772396	0.85[ASN][1000 genomes]
rs10772418	0.99[ASN][1000 genomes]
rs10772419	0.88[ASN][1000 genomes]
rs10845252	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10845253	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10845254	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10845255	0.81[ASN][1000 genomes]
rs10845256	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10845258	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10845259	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10845260	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10845261	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10845262	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10845263	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10845264	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10845275	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10845283	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11054082	0.81[AMR][1000 genomes]
rs11054084	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054088	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054089	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054090	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054092	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054093	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054094	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054095	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054096	0.81[ASN][1000 genomes]
rs11054097	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054098	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054099	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054101	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054102	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054103	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11054104	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054105	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054106	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054107	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054108	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054109	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054110	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054111	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054112	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054113	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054114	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054115	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054116	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054117	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11054118	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054119	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054120	0.82[ASN][1000 genomes]
rs11054121	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054122	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054123	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054124	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054125	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11054131	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11054148	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11054155	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12367487	0.82[ASN][1000 genomes]
rs12581501	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1376250	0.97[ASN][1000 genomes]
rs1650030	0.95[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]
rs17743605	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs17810798	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs17817150	0.92[JPT][hapmap]
rs2084650	0.85[ASN][1000 genomes]
rs2218820	0.85[ASN][1000 genomes]
rs2418224	0.81[AMR][1000 genomes]
rs2900554	0.85[ASN][1000 genomes]
rs319272	0.95[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]
rs34146423	0.84[AFR][1000 genomes]
rs34373072	0.84[AFR][1000 genomes]
rs34855658	0.82[AFR][1000 genomes]
rs35062230	0.84[AFR][1000 genomes]
rs35093093	0.86[AFR][1000 genomes]
rs35152755	0.84[AFR][1000 genomes]
rs35218320	0.86[AFR][1000 genomes]
rs35304582	0.84[AFR][1000 genomes]
rs35931025	0.86[AFR][1000 genomes]
rs3851589	0.81[AMR][1000 genomes]
rs4132154	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4763231	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4763232	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4763599	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4763602	0.83[ASN][1000 genomes]
rs4763603	0.85[ASN][1000 genomes]
rs4763611	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61912291	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61912292	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61912293	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61912888	0.84[AFR][1000 genomes]
rs6488332	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6488334	0.88[EUR][1000 genomes]
rs7132674	0.86[JPT][hapmap]
rs7134390	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7134527	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7135018	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7136588	0.85[ASN][1000 genomes]
rs7136962	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7137212	0.82[ASN][1000 genomes]
rs7138360	0.82[ASN][1000 genomes]
rs7294858	0.82[ASN][1000 genomes]
rs7295278	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7302227	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7303183	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7305795	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7308469	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7308933	0.82[ASN][1000 genomes]
rs7312169	0.82[ASN][1000 genomes]
rs7314608	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7957791	0.92[ASN][1000 genomes]
rs7974464	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7976950	0.86[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758294	chr12:10969620-11714921	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
2	esv2759879	chr12:10969620-11714921	Genic enhancers Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS 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	52 gene(s)	inside rSNPs	diseases
3	nsv1038277	chr12:11060978-11504091	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
4	nsv428272	chr12:11069845-11714921	Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
5	nsv832330	chr12:11077678-11206957	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
6	nsv898779	chr12:11134701-11174276	Enhancers Genic enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	esv8289	chr12:11144397-11222359	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv898780	chr12:11144994-11251560	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
9	esv3503763	chr12:11161162-11275828	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
10	esv3503774	chr12:11161325-11275786	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
11	nsv1038709	chr12:11165117-11283834	Enhancers Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
12	esv8805	chr12:11166558-11222811	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
13	esv3383115	chr12:11166848-11222150	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
14	esv1804289	chr12:11166879-11294110	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
15	esv7343	chr12:11167352-11223285	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
16	esv3389107	chr12:11167826-11228448	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
17	esv3347626	chr12:11167851-11223280	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
18	nsv8917	chr12:11168232-11293747	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
19	esv1804220	chr12:11168557-11243887	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
20	esv1827548	chr12:11168557-11277324	Weak transcription ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
21	esv3501349	chr12:11169700-11225559	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
22	esv3501348	chr12:11169763-11225525	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
23	esv3501350	chr12:11169763-11225525	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
24	esv3432938	chr12:11169783-11225495	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

mRNA abundance (count:12)

SNP	Gene	Cis/trans	Tissue	Source
rs11054166	PRR4	cis	multi-tissue	Pritchard
rs11054166	PRR4	cis	Thyroid	GTEx
rs11054166	TAS2R14	cis	Nerve Tibial	GTEx
rs11054166	RP11-434C1.1	cis	Nerve Tibial	GTEx
rs11054166	RP11-434C1.1	cis	Heart Left Ventricle	GTEx
rs11054166	PRR4	cis	Heart Left Ventricle	GTEx
rs11054166	RP11-434C1.1	cis	Thyroid	GTEx
rs11054166	PRR4	cis	Muscle Skeletal	GTEx
rs11054166	PRR4	cis	lung	GTEx
rs11054166	TAS2R14	cis	Esophagus Muscularis	GTEx
rs11054166	PRR4	cis	Nerve Tibial	GTEx
rs11054166	RP11-434C1.1	cis	lung	GTEx

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11114400-11180200	Weak transcription	Primary B cells from peripheral blood	blood
2	chr12:11122000-11170200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr12:11136400-11180200	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr12:11136600-11180200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr12:11136600-11196400	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr12:11137400-11203000	Weak transcription	Hela-S3	cervix
7	chr12:11143400-11178800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr12:11145400-11177600	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr12:11147000-11178600	Weak transcription	Fetal Stomach	stomach
10	chr12:11147000-11185400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr12:11147200-11171200	Weak transcription	Primary hematopoietic stem cells	blood
12	chr12:11147200-11176200	Weak transcription	Aorta	Aorta
13	chr12:11147200-11180400	Weak transcription	Pancreas	Pancrea
14	chr12:11148400-11178200	Weak transcription	Dnd41	blood
15	chr12:11154200-11174200	Weak transcription	Primary B cells from cord blood	blood
16	chr12:11154200-11178000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr12:11154200-11178200	Weak transcription	A549	lung
18	chr12:11154200-11178800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr12:11159400-11182000	Weak transcription	NHEK	skin
20	chr12:11159600-11178200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr12:11161400-11178200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr12:11161400-11179200	Weak transcription	Fetal Kidney	kidney
23	chr12:11162400-11172800	Weak transcription	Fetal Brain Female	brain
24	chr12:11163400-11177600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr12:11163400-11178000	Weak transcription	GM12878-XiMat	blood
26	chr12:11163600-11178800	Weak transcription	Ovary	ovary
27	chr12:11163800-11178000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr12:11164400-11178600	Weak transcription	Fetal Thymus	thymus
29	chr12:11164800-11171800	Weak transcription	Lung	lung
30	chr12:11165000-11180800	Weak transcription	HSMM	muscle
31	chr12:11165200-11170800	Enhancers	Brain Substantia Nigra	brain
32	chr12:11165400-11180200	Weak transcription	Esophagus	oesophagus
33	chr12:11165600-11174200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr12:11166000-11192000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr12:11166200-11210000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr12:11166400-11170600	Enhancers	Brain Hippocampus Middle	brain
37	chr12:11166400-11170800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
38	chr12:11166600-11199600	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr12:11167000-11178200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr12:11167400-11170200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr12:11167400-11201800	Weak transcription	Stomach Smooth Muscle	stomach
42	chr12:11167600-11170200	Enhancers	Fetal Intestine Small	intestine
43	chr12:11167600-11178000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr12:11167600-11180000	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr12:11167800-11170800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr12:11167800-11178600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr12:11168000-11177600	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr12:11168400-11170600	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr12:11168800-11201000	Weak transcription	Colon Smooth Muscle	Colon
50	chr12:11168800-11205800	Weak transcription	Osteobl	bone

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