Variant report

Variant	rs1727331
Chromosome Location	chr12:123718879-123718880
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:9)
CpG islands
(count:0)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:9 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MXI1	chr12:123716346-123718916	IMR90	lung:	n/a	n/a
2	NR2F2	chr12:123716903-123719098	K562	blood:	n/a	n/a
3	MTA3	chr12:123716877-123718956	GM12878	blood:	n/a	n/a
4	ZNF384	chr12:123718302-123718969	K562	blood:	n/a	n/a
5	ELF1	chr12:123718610-123718934	K562	blood:	n/a	n/a
6	POLR2A	chr12:123717040-123718886	K562	blood:	n/a	n/a
7	MXI1	chr12:123716350-123718974	SK-N-SH	brain:	n/a	n/a
8	HCFC1	chr12:123716685-123718970	Hela-S3	cervix:	n/a	n/a
9	GATA1	chr12:123716297-123719103	K562	blood:	n/a	chr12:123717946-123717967 chr12:123717953-123717960 chr12:123717953-123717960 chr12:123716547-123716557 chr12:123717953-123717960

No data

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:123494754..123497414-chr12:123717630..123719730,2	K562	blood:
2	chr12:123344301..123346489-chr12:123716077..123720315,3	K562	blood:
3	chr12:123465881..123468570-chr12:123716034..123719414,3	K562	blood:
4	chr12:123717253..123719001-chr12:123746538..123748497,2	K562	blood:
5	chr12:123377844..123381497-chr12:123716230..123718980,3	K562	blood:
6	chr12:123470053..123472975-chr12:123718822..123721771,2	K562	blood:
7	chr12:123715622..123719446-chr12:123735072..123738647,4	K562	blood:
8	chr12:123714199..123721299-chr12:123733822..123739052,7	MCF-7	breast:
9	chr12:123716817..123718990-chr12:124117809..124119418,3	K562	blood:
10	chr12:123457894..123461734-chr12:123715409..123718960,7	K562	blood:
11	chr12:123715746..123718967-chr12:123870796..123875270,4	K562	blood:
12	chr12:123452751..123454277-chr12:123718785..123720840,2	MCF-7	breast:
13	chr12:123463210..123468211-chr12:123716151..123721062,7	MCF-7	breast:
14	chr12:123718175..123719849-chr12:123755538..123757797,2	MCF-7	breast:
15	chr12:123715079..123721002-chr12:123721919..123730378,16	K562	blood:
16	chr12:123459054..123462367-chr12:123715409..123720380,5	K562	blood:
17	chr12:123465824..123467766-chr12:123717384..123719608,2	MCF-7	breast:
18	chr12:123632948..123634613-chr12:123717747..123719847,2	K562	blood:
19	chr12:123716636..123719469-chr12:124192807..124195608,2	K562	blood:
20	chr12:123717082..123719698-chr12:123751267..123753093,2	K562	blood:
21	chr12:123716734..123718943-chr12:124067701..124069242,2	MCF-7	breast:
22	chr12:123558968..123563276-chr12:123716606..123719909,6	MCF-7	breast:
23	chr12:123449332..123452871-chr12:123717386..123719515,4	K562	blood:
24	chr12:123449701..123452611-chr12:123716445..123719411,3	K562	blood:
25	chr12:123442313..123444976-chr12:123717456..123719233,2	K562	blood:
26	chr12:123458147..123462549-chr12:123715608..123720287,8	MCF-7	breast:
27	chr12:123717014..123719935-chr12:123753310..123757333,7	K562	blood:
28	chr12:123716353..123719935-chr12:123753594..123757800,6	K562	blood:

No data

Variant related genes	Relation type
MPHOSPH9	TF binding region
ENSG00000265526	Chromatin interaction
ENSG00000090975	Chromatin interaction
ENSG00000255839	Chromatin interaction
ENSG00000256028	Chromatin interaction
ENSG00000086598	Chromatin interaction
ENSG00000269980	Chromatin interaction
ENSG00000111328	Chromatin interaction
ENSG00000130787	Chromatin interaction
ENSG00000111358	Chromatin interaction
ENSG00000111361	Chromatin interaction
ENSG00000130921	Chromatin interaction
ENSG00000150967	Chromatin interaction
ENSG00000111325	Chromatin interaction
ENSG00000183955	Chromatin interaction
ENSG00000182196	Chromatin interaction
ENSG00000051825	Chromatin interaction
ENSG00000139722	Chromatin interaction

Extended variants
information (count: 152 )
Associated
traits (count: 11 )

rSNPs within LD-proxies of this variant (count:145)

rs_ID	r²[population]
rs10444439	0.81[JPT][hapmap]
rs1051431	0.80[CEU][hapmap]
rs1060105	0.85[GIH][hapmap]
rs10732573	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10734901	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10744150	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10744151	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10744152	0.94[JPT][hapmap]
rs10772997	0.95[CHB][hapmap];0.94[JPT][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10772998	0.90[CEU][hapmap];0.82[EUR][1000 genomes]
rs10772999	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10773000	0.83[CHD][hapmap];0.84[JPT][hapmap]
rs10773002	0.95[CEU][hapmap];1.00[CHB][hapmap];0.85[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.89[TSI][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10846486	0.80[CEU][hapmap]
rs10846489	0.84[JPT][hapmap]
rs10846517	0.94[JPT][hapmap]
rs10846519	0.94[JPT][hapmap]
rs10846520	0.88[JPT][hapmap]
rs10846523	0.94[JPT][hapmap]
rs11057189	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11057202	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11057204	0.82[EUR][1000 genomes]
rs11057205	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11057206	0.81[EUR][1000 genomes]
rs11057207	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11057209	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11057223	0.83[CHB][hapmap];0.84[JPT][hapmap]
rs11057287	0.94[JPT][hapmap]
rs1106240	0.80[CEU][hapmap]
rs1106241	0.80[CEU][hapmap]
rs1109559	0.84[JPT][hapmap]
rs1109560	0.83[JPT][hapmap]
rs11554169	0.85[ASN][1000 genomes]
rs12298826	0.85[GIH][hapmap]
rs12316131	0.85[GIH][hapmap]
rs12322888	0.85[GIH][hapmap]
rs1402274	0.80[CEU][hapmap]
rs1402275	0.84[GIH][hapmap]
rs1533703	0.83[CEU][hapmap]
rs1568427	0.90[CEU][hapmap];0.95[CHB][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.95[TSI][hapmap];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1568428	0.84[JPT][hapmap]
rs1569068	0.80[CEU][hapmap]
rs1609520	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[TSI][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1615350	0.90[CEU][hapmap];0.91[MEX][hapmap];0.86[TSI][hapmap];0.87[AMR][1000 genomes]
rs1660	0.88[JPT][hapmap]
rs1716157	0.80[CEU][hapmap]
rs1716160	0.80[CEU][hapmap]
rs1716164	0.80[CEU][hapmap]
rs1716165	0.80[CEU][hapmap]
rs1716167	0.80[CEU][hapmap]
rs1716168	0.80[CEU][hapmap]
rs1716170	0.80[CEU][hapmap];0.88[GIH][hapmap];0.81[EUR][1000 genomes]
rs1716171	0.80[CEU][hapmap];0.88[GIH][hapmap];0.81[EUR][1000 genomes]
rs1716175	0.80[CEU][hapmap]
rs1716176	0.80[CEU][hapmap]
rs1716177	0.80[CEU][hapmap]
rs1727296	0.80[CEU][hapmap]
rs1727302	0.90[CEU][hapmap];0.86[MEX][hapmap];0.86[TSI][hapmap]
rs1727306	0.80[CEU][hapmap]
rs1727309	0.80[CEU][hapmap]
rs1727313	0.80[CEU][hapmap]
rs1727315	0.80[CEU][hapmap]
rs1727319	0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1727320	0.80[CEU][hapmap]
rs1727323	0.80[CEU][hapmap]
rs1727324	0.80[CEU][hapmap]
rs1727325	0.80[CEU][hapmap]
rs1727332	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1727334	0.81[EUR][1000 genomes]
rs1790095	0.80[CEU][hapmap]
rs1790098	0.80[CEU][hapmap]
rs1790100	0.80[CEU][hapmap]
rs1790108	0.80[CEU][hapmap]
rs1790123	0.80[CEU][hapmap]
rs1790131	0.80[CEU][hapmap]
rs1879379	0.85[CHD][hapmap];0.84[JPT][hapmap]
rs1879380	0.80[CEU][hapmap];0.88[GIH][hapmap]
rs1969354	0.85[CEU][hapmap];0.88[GIH][hapmap]
rs1969355	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1980251	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1980252	0.85[CEU][hapmap]
rs2049114	0.80[CEU][hapmap]
rs2090764	0.89[ASN][1000 genomes]
rs2102949	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2271976	0.84[JPT][hapmap]
rs2280424	1.00[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs2337934	0.85[CEU][hapmap];0.85[GIH][hapmap]
rs2682434	0.80[CEU][hapmap]
rs2695478	0.80[CEU][hapmap]
rs2695482	0.80[CEU][hapmap]
rs28362667	0.92[ASN][1000 genomes]
rs28362669	0.90[ASN][1000 genomes]
rs28406193	0.85[GIH][hapmap]
rs28414347	0.94[JPT][hapmap]
rs28458312	0.85[GIH][hapmap]
rs28472704	0.85[GIH][hapmap]
rs28501453	0.94[JPT][hapmap]
rs2851443	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2851447	0.89[CEU][hapmap];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs28587386	0.94[JPT][hapmap]
rs28595660	0.94[JPT][hapmap]
rs28613486	0.94[JPT][hapmap]
rs28636834	0.85[GIH][hapmap]
rs36121382	0.87[ASN][1000 genomes]
rs3759111	0.91[CHB][hapmap];0.89[JPT][hapmap];0.85[ASN][1000 genomes]
rs3759113	0.91[CHB][hapmap];0.89[JPT][hapmap];0.80[ASN][1000 genomes]
rs3759114	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs3803001	0.94[JPT][hapmap]
rs3825141	0.94[JPT][hapmap]
rs4372492	0.80[CEU][hapmap]
rs4460848	0.90[CEU][hapmap];0.91[CHB][hapmap];0.84[GIH][hapmap];0.89[JPT][hapmap];0.95[MEX][hapmap];0.89[TSI][hapmap];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4474478	0.93[ASN][1000 genomes]
rs4474479	0.93[ASN][1000 genomes]
rs4594040	0.93[ASN][1000 genomes]
rs4759367	0.90[CHB][hapmap];0.88[JPT][hapmap]
rs4759371	0.85[CEU][hapmap];0.88[GIH][hapmap]
rs4759372	0.86[ASN][1000 genomes]
rs4759406	0.84[ASN][1000 genomes]
rs4759407	0.91[CHB][hapmap];0.89[JPT][hapmap];0.85[ASN][1000 genomes]
rs4759408	0.92[ASN][1000 genomes]
rs4759409	0.85[CEU][hapmap];0.83[EUR][1000 genomes]
rs4759411	0.95[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs4759413	0.91[CHB][hapmap];0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs4759414	0.95[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs4759415	0.85[CEU][hapmap];0.88[GIH][hapmap]
rs4759418	0.87[ASN][1000 genomes]
rs57676984	0.92[ASN][1000 genomes]
rs60077920	0.92[ASN][1000 genomes]
rs60254089	0.83[ASN][1000 genomes]
rs60296110	0.84[ASN][1000 genomes]
rs61231969	0.87[ASN][1000 genomes]
rs61519741	0.95[ASN][1000 genomes]
rs7137286	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7139321	0.84[JPT][hapmap];0.83[ASN][1000 genomes]
rs7297649	0.94[JPT][hapmap]
rs7304782	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7313483	0.90[CEU][hapmap]
rs73231928	0.83[ASN][1000 genomes]
rs7953929	0.80[CEU][hapmap];0.85[GIH][hapmap]
rs7959415	0.94[JPT][hapmap]
rs884548	0.80[CEU][hapmap]
rs941305	0.80[CEU][hapmap];0.81[EUR][1000 genomes]
rs941306	0.80[CEU][hapmap];0.81[EUR][1000 genomes]
rs9795522	0.81[EUR][1000 genomes]
rs9795593	0.94[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv427924	chr12:123412172-123722059	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
2	esv1825473	chr12:123582855-123822503	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
3	nsv870326	chr12:123585990-123719323	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS 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	56 gene(s)	inside rSNPs	diseases
4	esv2761773	chr12:123616003-123723460	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
5	esv1803368	chr12:123640853-123822503	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS 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	70 gene(s)	inside rSNPs	diseases
6	esv1830566	chr12:123640853-123822503	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
7	esv1836043	chr12:123709409-123822503	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases

mRNA abundance (count:11)

SNP	Gene	Cis/trans	Tissue	Source
rs1727331	ANAPC5	cis	parietal	SCAN
rs1727331	SBNO1	Cis_1M	lymphoblastoid	RTeQTL
rs1727331	ARL6IP4	Cis_1M	lymphoblastoid	RTeQTL
rs1727331	CDK2AP1	cis	Esophagus Mucosa	GTEx
rs1727331	PITPNM2	cis	cerebellum	SCAN
rs1727331	TMEM120B	cis	parietal	SCAN
rs1727331	MPHOSPH9	Cis_1M	lymphoblastoid	RTeQTL
rs1727331	CCDC92	cis	cerebellum	SCAN
rs1727331	CDK2AP1	Cis_1M	lymphoblastoid	RTeQTL
rs1727331	MPHOSPH9	cis	multi-tissue	Pritchard
rs1727331	RP11-282O18.3	cis	Esophagus Mucosa	GTEx

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123716200-123719000	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr12:123716200-123719400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr12:123716200-123719400	Active TSS	GM12878-XiMat	blood
4	chr12:123716200-123719800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr12:123716400-123719000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr12:123716400-123719000	Active TSS	HUES6 Cell Line	embryonic stem cell
7	chr12:123716400-123719000	Active TSS	iPS-20b Cell Line	embryonic stem cell
8	chr12:123716400-123719400	Active TSS	NHLF	lung
9	chr12:123716600-123719000	Active TSS	H1 Cell Line	embryonic stem cell
10	chr12:123716600-123719200	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr12:123716600-123719400	Active TSS	NHDF-Ad	bronchial
12	chr12:123716800-123719000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr12:123716800-123719000	Active TSS	HUES48 Cell Line	embryonic stem cell
14	chr12:123716800-123719000	Active TSS	HUES64 Cell Line	embryonic stem cell
15	chr12:123716800-123719000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr12:123716800-123719000	Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr12:123716800-123719000	Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr12:123716800-123719000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr12:123716800-123719000	Active TSS	Brain Anterior Caudate	brain
20	chr12:123716800-123719000	Active TSS	Fetal Thymus	thymus
21	chr12:123716800-123719000	Active TSS	HSMM	muscle
22	chr12:123716800-123719000	Active TSS	HSMMtube	muscle
23	chr12:123716800-123719000	Active TSS	K562	blood
24	chr12:123716800-123719200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr12:123716800-123719200	Active TSS	Ovary	ovary
26	chr12:123716800-123719200	Active TSS	Right Atrium	heart
27	chr12:123716800-123719200	Active TSS	Hela-S3	cervix
28	chr12:123716800-123719400	Active TSS	Breast Myoepithelial Primary Cells	Breast
29	chr12:123716800-123719400	Active TSS	A549	lung
30	chr12:123717000-123719000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr12:123717000-123719000	Active TSS	Gastric	stomach
32	chr12:123717000-123719000	Active TSS	Right Ventricle	heart
33	chr12:123717000-123719200	Active TSS	NHEK	skin
34	chr12:123717000-123719400	Active TSS	Thymus	Thymus
35	chr12:123717200-123719200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr12:123717200-123719200	Active TSS	Primary T helper cells PMA-I stimulated	--
37	chr12:123718000-123719600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
38	chr12:123718200-123719000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr12:123718200-123719000	Flanking Active TSS	Primary B cells from cord blood	blood
40	chr12:123718200-123719000	Flanking Active TSS	Primary hematopoietic stem cells	blood
41	chr12:123718200-123719000	Flanking Active TSS	Adipose Nuclei	Adipose
42	chr12:123718200-123719000	Flanking Active TSS	Duodenum Mucosa	Duodenum
43	chr12:123718200-123719000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
44	chr12:123718200-123719200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
45	chr12:123718400-123719000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr12:123718400-123719000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
47	chr12:123718400-123719000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr12:123718400-123719000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr12:123718400-123719000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
50	chr12:123718400-123719000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin

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