Variant report

Variant	rs1472118
Chromosome Location	chr12:40498326-40498327
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:39835235..39837376-chr12:40497652..40499874,2	K562	blood:
2	chr12:40494859..40496427-chr12:40496570..40499467,2	MCF-7	breast:
3	chr11:62607295..62609623-chr12:40497021..40499693,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000133316	Chromatin interaction
ENSG00000252974	Chromatin interaction
ENSG00000139116	Chromatin interaction

Extended variants
information (count: 129 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:106)

rs_ID	r²[population]
rs1031996	0.95[CHB][hapmap];0.94[JPT][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10748014	0.82[CHB][hapmap];0.84[JPT][hapmap]
rs10784370	0.82[CHB][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10784381	0.95[CHB][hapmap];0.95[JPT][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10784386	0.95[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10878089	0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs10878113	0.81[EUR][1000 genomes]
rs10878222	0.82[CHB][hapmap]
rs10878224	0.84[CHB][hapmap]
rs1117378	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11175024	0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs11175275	0.88[EUR][1000 genomes]
rs11175326	0.95[CHB][hapmap];0.95[JPT][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11175327	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11175656	0.82[CHB][hapmap];0.84[JPT][hapmap]
rs12230710	0.80[EUR][1000 genomes]
rs12813098	0.96[YRI][hapmap];0.83[AFR][1000 genomes]
rs12823555	0.93[YRI][hapmap];0.86[AFR][1000 genomes]
rs1352876	0.95[CHB][hapmap];0.95[JPT][hapmap]
rs1388589	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1388590	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1388591	0.89[JPT][hapmap];0.82[ASN][1000 genomes]
rs1463719	0.90[CHB][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs1463720	0.87[ASN][1000 genomes]
rs1482284	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1482285	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1482287	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1482288	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1491927	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1491929	0.84[ASN][1000 genomes]
rs1491930	0.82[ASN][1000 genomes]
rs1491931	0.95[CHB][hapmap];0.95[JPT][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1844921	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1844922	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1873612	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1905121	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1948380	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2131082	0.84[ASN][1000 genomes]
rs2131083	0.84[ASN][1000 genomes]
rs2170503	0.86[CHB][hapmap];0.95[JPT][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2201143	0.84[ASN][1000 genomes]
rs2220677	0.84[ASN][1000 genomes]
rs2248928	0.89[JPT][hapmap]
rs2249010	0.89[JPT][hapmap]
rs2249017	0.89[JPT][hapmap]
rs2404573	0.82[CHB][hapmap];0.89[JPT][hapmap];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2638231	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2638232	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2638245	0.95[CHB][hapmap];0.83[JPT][hapmap];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2638249	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2638251	0.82[ASN][1000 genomes]
rs2638254	0.95[CHB][hapmap];0.95[JPT][hapmap];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2638257	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2638258	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2638259	0.86[ASN][1000 genomes]
rs2638260	0.95[CHB][hapmap];0.95[JPT][hapmap];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2638262	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2638263	0.84[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2638264	0.90[CHB][hapmap];0.95[JPT][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2638266	0.95[CHB][hapmap];0.95[JPT][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2638267	0.89[JPT][hapmap];0.82[ASN][1000 genomes]
rs2708449	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2708464	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2708466	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2708467	0.84[ASN][1000 genomes]
rs2708470	0.84[ASN][1000 genomes]
rs2708472	0.84[ASN][1000 genomes]
rs2708473	0.95[CHB][hapmap];0.95[JPT][hapmap];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2708474	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2708476	0.82[ASN][1000 genomes]
rs2708477	0.89[JPT][hapmap]
rs2708479	0.89[JPT][hapmap]
rs2708480	0.95[CHB][hapmap];0.95[JPT][hapmap];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2708481	0.89[JPT][hapmap]
rs2708485	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2708488	0.82[ASN][1000 genomes]
rs2708491	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2708492	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2708493	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2708494	0.91[CHB][hapmap];0.84[JPT][hapmap];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2896825	0.86[YRI][hapmap]
rs2896905	0.96[YRI][hapmap];0.83[AFR][1000 genomes]
rs3812791	0.80[CHB][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3925535	0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs4360759	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4363681	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4767960	0.84[AFR][1000 genomes]
rs6581504	0.96[YRI][hapmap];0.86[AFR][1000 genomes]
rs6581514	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6581519	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7132203	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs716231	0.95[CHB][hapmap];0.95[JPT][hapmap];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs716268	0.86[AFR][1000 genomes]
rs722817	0.82[ASN][1000 genomes]
rs728622	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs728623	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs729216	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7306140	1.00[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7310430	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7313231	0.81[YRI][hapmap]
rs878010	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs900253	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs937109	0.95[CHB][hapmap];0.95[JPT][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs937110	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs937111	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9669240	0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.80[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv558596	chr12:40413698-40591117	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv899028	chr12:40478652-40524180	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
3	nsv899029	chr12:40478652-40536061	Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	esv1816874	chr12:40492814-40499934	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	n/a
5	esv1822895	chr12:40492814-40499934	Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	n/a
6	esv1838004	chr12:40492814-40499934	Flanking Active TSS Bivalent/Poised TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	n/a
7	esv1841992	chr12:40492814-40499934	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	n/a
8	esv1850635	chr12:40492814-40499934	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	n/a
9	esv1836585	chr12:40492814-40540939	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
10	esv1839483	chr12:40492814-40540939	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
11	esv1839896	chr12:40493591-40499908	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	n/a
12	esv1834762	chr12:40496733-40499934	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a
13	esv1799112	chr12:40497095-40499908	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a
14	esv1840625	chr12:40497095-40499908	Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a
15	esv3359383	chr12:40498110-40500658	Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a
16	esv1841522	chr12:40498190-40499803	Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a
17	esv1822852	chr12:40498190-40499934	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a
18	esv1844742	chr12:40498190-40499934	Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a
19	esv1847923	chr12:40498190-40499934	Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a
20	esv1835713	chr12:40498326-40499803	Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a
21	esv1836654	chr12:40498326-40499908	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a
22	esv1839194	chr12:40498326-40499908	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a
23	esv1845368	chr12:40498326-40499908	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs1472118	AC079630.2	cis	Esophagus Mucosa	GTEx
rs1472118	SLC2A13	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40476600-40498400	Weak transcription	Fetal Stomach	stomach
2	chr12:40488200-40498600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:40492400-40498600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr12:40492800-40498600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr12:40492800-40498600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr12:40492800-40498600	Weak transcription	Lung	lung
7	chr12:40496800-40498400	Enhancers	Primary T helper cells fromperipheralblood	blood
8	chr12:40496800-40498600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr12:40496800-40498600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr12:40496800-40499000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
11	chr12:40496800-40500400	Active TSS	Stomach Smooth Muscle	stomach
12	chr12:40496800-40501600	Active TSS	Brain Cingulate Gyrus	brain
13	chr12:40496800-40501600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
14	chr12:40496800-40501600	Active TSS	Pancreatic Islets	Pancreatic Islet
15	chr12:40497000-40498400	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr12:40497000-40498400	Enhancers	Stomach Mucosa	stomach
17	chr12:40497000-40498600	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr12:40497000-40498600	Enhancers	Liver	Liver
19	chr12:40497000-40498600	Weak transcription	Psoas Muscle	Psoas
20	chr12:40497000-40498600	Active TSS	Right Ventricle	heart
21	chr12:40497000-40498800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr12:40497000-40498800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr12:40497000-40498800	Flanking Active TSS	Hela-S3	cervix
24	chr12:40497000-40499000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr12:40497000-40500200	Active TSS	Brain Angular Gyrus	brain
26	chr12:40497000-40501600	Active TSS	Brain Inferior Temporal Lobe	brain
27	chr12:40497000-40501600	Active TSS	Fetal Kidney	kidney
28	chr12:40497200-40498400	Active TSS	HUES6 Cell Line	embryonic stem cell
29	chr12:40497200-40498400	Enhancers	Fetal Muscle Leg	muscle
30	chr12:40497200-40498400	Active TSS	K562	blood
31	chr12:40497200-40498600	Weak transcription	Pancreas	Pancrea
32	chr12:40497200-40498800	Enhancers	Primary T helper naive cells from peripheral blood	blood
33	chr12:40497200-40499000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
34	chr12:40497200-40502200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr12:40497400-40498600	Active TSS	Brain Anterior Caudate	brain
36	chr12:40497400-40498800	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
37	chr12:40497400-40498800	Enhancers	Fetal Heart	heart
38	chr12:40497400-40499000	Flanking Active TSS	Fetal Intestine Small	intestine
39	chr12:40497400-40500000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr12:40497400-40501600	Active TSS	Right Atrium	heart
41	chr12:40497600-40498400	Active TSS	HUES64 Cell Line	embryonic stem cell
42	chr12:40497600-40498400	Enhancers	Adipose Nuclei	Adipose
43	chr12:40497600-40498400	Enhancers	NHDF-Ad	bronchial
44	chr12:40497600-40498600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr12:40497600-40499000	Flanking Active TSS	Duodenum Mucosa	Duodenum
46	chr12:40497600-40500400	Active TSS	Fetal Brain Female	brain
47	chr12:40497800-40498400	Active TSS	ES-I3 Cell Line	embryonic stem cell
48	chr12:40497800-40498400	Enhancers	Primary B cells from peripheral blood	blood
49	chr12:40497800-40498400	Active TSS	Muscle Satellite Cultured Cells	--
50	chr12:40497800-40498400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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