Variant report

Variant	rs4660864
Chromosome Location	chr1:45966582-45966583
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:18)
CpG islands
(count:0)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:18 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr1:45966334-45966644	IMR90	lung:	n/a	n/a
2	CEBPB	chr1:45965469-45966636	HepG2	liver:	n/a	chr1:45966124-45966132
3	ZNF384	chr1:45965683-45966769	GM12878	blood:	n/a	n/a
4	HCFC1	chr1:45964803-45966980	Hela-S3	cervix:	n/a	n/a
5	MAX	chr1:45966359-45966778	K562	blood:	n/a	n/a
6	MXI1	chr1:45964964-45967174	SK-N-SH	brain:	n/a	n/a
7	ZNF384	chr1:45966381-45966794	K562	blood:	n/a	n/a
8	POLR2A	chr1:45964582-45967225	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:45966332-45966723	K562	blood:	n/a	n/a
10	CEBPB	chr1:45965401-45966711	Hela-S3	cervix:	n/a	chr1:45966124-45966132
11	MYBL2	chr1:45966554-45967673	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:45966401-45966622	K562	blood:	n/a	n/a
13	CEBPB	chr1:45965628-45966687	K562	blood:	n/a	chr1:45966124-45966132
14	GTF3C2	chr1:45965481-45966688	Hela-S3	cervix:	n/a	n/a
15	YY1	chr1:45966402-45966645	K562	blood:	n/a	n/a
16	SREBP1	chr1:45964570-45967128	GM12878	blood:	n/a	n/a
17	YY1	chr1:45966357-45966661	GM12878	blood:	n/a	n/a
18	CEBPB	chr1:45965676-45966682	A549	lung:	n/a	chr1:45966124-45966132

No data

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:45239737..45242586-chr1:45965500..45967251,2	K562	blood:
2	chr1:45804114..45807301-chr1:45961577..45967419,8	K562	blood:
3	chr1:45966070..45969060-chr1:46033668..46035384,2	MCF-7	breast:
4	chr1:45185969..45188598-chr1:45964540..45967567,4	K562	blood:
5	chr1:45283510..45287262-chr1:45964108..45968951,6	K562	blood:
6	chr1:45952646..45954421-chr1:45965976..45968197,2	K562	blood:
7	chr1:45768003..45772070-chr1:45964648..45967315,5	K562	blood:
8	chr1:45963397..45969763-chr1:46047572..46053150,23	K562	blood:
9	chr1:45963437..45971807-chr1:46047572..46053150,22	K562	blood:
10	chr1:45965940..45967492-chr1:46038830..46041668,2	K562	blood:
11	chr1:45265558..45267516-chr1:45964222..45967034,2	K562	blood:
12	chr1:45954905..45960579-chr1:45960652..45966878,10	K562	blood:
13	chr1:45964150..45967582-chr1:46014583..46018871,5	K562	blood:
14	chr1:45272934..45277358-chr1:45964626..45967668,4	K562	blood:
15	chr1:45284392..45287262-chr1:45964108..45967526,3	K562	blood:
16	chr1:45804471..45806506-chr1:45965051..45967533,2	K562	blood:
17	chr1:45185644..45188958-chr1:45966067..45969348,3	K562	blood:
18	chr1:45965671..45969478-chr1:45972057..45975317,5	MCF-7	breast:

No data

Variant related genes	Relation type
CCDC163P	TF binding region
ENSG00000188396	Chromatin interaction
ENSG00000202444	Chromatin interaction
ENSG00000132781	Chromatin interaction
ENSG00000200913	Chromatin interaction
ENSG00000117448	Chromatin interaction
ENSG00000199377	Chromatin interaction
ENSG00000264294	Chromatin interaction
ENSG00000173846	Chromatin interaction
ENSG00000142937	Chromatin interaction
ENSG00000132773	Chromatin interaction
ENSG00000132763	Chromatin interaction
ENSG00000162415	Chromatin interaction
ENSG00000132780	Chromatin interaction
ENSG00000225721	Chromatin interaction
ENSG00000070759	Chromatin interaction
ENSG00000222009	Chromatin interaction

Extended variants
information (count: 77 )
Associated
traits (count: 24 )

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10157597	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1044717	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10493120	0.86[GIH][hapmap];1.00[MEX][hapmap]
rs10736426	0.96[CEU][hapmap];0.92[CHD][hapmap];0.96[GIH][hapmap];0.89[MEX][hapmap];0.97[TSI][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10789466	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1088099	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11211110	0.86[GIH][hapmap];1.00[MEX][hapmap]
rs11211113	0.84[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap]
rs11211132	1.00[ASW][hapmap];0.96[CEU][hapmap];0.96[GIH][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11211134	0.91[EUR][1000 genomes]
rs12038608	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12042481	0.85[CHB][hapmap];0.84[CHD][hapmap];0.85[ASN][1000 genomes]
rs12047498	0.85[ASN][1000 genomes]
rs12048936	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12082256	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12145526	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12729974	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12749658	0.91[EUR][1000 genomes]
rs1337902	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1494813	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1691217	0.86[GIH][hapmap];0.89[MEX][hapmap]
rs1765711	1.00[JPT][hapmap]
rs1974271	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2065708	0.85[CHB][hapmap];0.84[CHD][hapmap]
rs2077808	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2152077	0.95[CEU][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2356555	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2356559	1.00[ASW][hapmap];0.96[CEU][hapmap];0.81[CHD][hapmap];0.96[GIH][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs2356560	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2356561	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2991966	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2993257	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2993259	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34315657	0.81[EUR][1000 genomes]
rs3748643	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4233498	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4660306	1.00[ASW][hapmap];0.96[CEU][hapmap];0.96[GIH][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4660309	0.86[EUR][1000 genomes]
rs4660860	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4660862	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4660866	0.86[EUR][1000 genomes]
rs4660867	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4660868	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4660871	0.82[EUR][1000 genomes]
rs4660872	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6429566	0.82[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap]
rs6429567	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6429569	0.96[CEU][hapmap];0.96[GIH][hapmap];0.92[TSI][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6667191	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6673477	0.82[EUR][1000 genomes]
rs6688424	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6688516	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7516006	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7522705	0.96[CEU][hapmap];0.92[CHD][hapmap];0.96[GIH][hapmap];0.89[MEX][hapmap];0.95[TSI][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7534467	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7536557	0.96[CEU][hapmap];0.92[CHD][hapmap];0.96[GIH][hapmap];0.89[MEX][hapmap];0.95[TSI][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7539253	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7543076	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7546268	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7549093	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs781059	0.83[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap]
rs781060	0.83[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap]
rs781061	1.00[JPT][hapmap]
rs781066	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs882803	0.96[CEU][hapmap];0.92[CHD][hapmap];0.96[GIH][hapmap];0.88[MEX][hapmap];0.97[TSI][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs937290	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs945179	1.00[ASW][hapmap];1.00[CEU][hapmap];0.85[CHB][hapmap];0.84[CHD][hapmap];1.00[GIH][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];0.97[TSI][hapmap];0.90[YRI][hapmap];0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9725380	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9803979	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv498036	chr1:45428030-46050934	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
2	esv1795802	chr1:45819489-46009818	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
3	esv1831217	chr1:45819489-46009818	Strong transcription Enhancers Genic enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
4	nsv530016	chr1:45868543-46069020	Flanking Active TSS Genic enhancers Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	149 gene(s)	inside rSNPs	diseases
5	nsv829726	chr1:45897581-46103186	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
6	nsv529631	chr1:45905936-46335246	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	207 gene(s)	inside rSNPs	diseases
7	nsv932680	chr1:45935520-46686477	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	232 gene(s)	inside rSNPs	diseases
8	nsv868828	chr1:45953923-46686477	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	232 gene(s)	inside rSNPs	diseases

mRNA abundance (count:24)

SNP	Gene	Cis/trans	Tissue	Source
rs4660864	CYP4Z2P	cis	parietal	SCAN
rs4660864	MMACHC	cis	multi-tissue	Pritchard
rs4660864	TESK2	cis	lymphoblastoid	seeQTL
rs4660864	LOC126661	cis	multi-tissue	Pritchard
rs4660864	CCDC163P	cis	Stomach	GTEx
rs4660864	TESK2	cis	multi-tissue	Pritchard
rs4660864	CCDC163P	cis	Heart Left Ventricle	GTEx
rs4660864	CCDC163P	cis	Thyroid	GTEx
rs4660864	LOC126661	Cis_1M	lymphoblastoid	RTeQTL
rs4660864	CCDC163P	cis	Esophagus Muscularis	GTEx
rs4660864	CCDC163P	cis	Artery Tibial	GTEx
rs4660864	CCDC163P	cis	Adipose Subcutaneous	GTEx
rs4660864	LOC126661	cis	uninvolved skin	skin_eQTL
rs4660864	CYP4A11	cis	parietal	SCAN
rs4660864	BEND5	cis	cerebellum	SCAN
rs4660864	CCDC163P	cis	lymphoblastoid	seeQTL
rs4660864	CCDC163P	cis	Artery Aorta	GTEx
rs4660864	CCDC163P	cis	lung	GTEx
rs4660864	CCDC163P	cis	Muscle Skeletal	GTEx
rs4660864	CCDC163P	cis	Nerve Tibial	GTEx
rs4660864	ST3GAL3	cis	parietal	SCAN
rs4660864	CCDC163P	cis	Esophagus Mucosa	GTEx
rs4660864	CCDC163P	cis	Skin Sun Exposed Lower leg	GTEx
rs4660864	CCDC163P	cis	Whole Blood	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:45956800-45974000	Weak transcription	Small Intestine	intestine
2	chr1:45964400-45966600	Active TSS	A549	lung
3	chr1:45964400-45966800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr1:45964600-45966600	Active TSS	Rectal Smooth Muscle	rectum
5	chr1:45964800-45966600	Active TSS	H1 Cell Line	embryonic stem cell
6	chr1:45964800-45966600	Active TSS	Ovary	ovary
7	chr1:45964800-45967200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr1:45964800-45967400	Active TSS	HUES64 Cell Line	embryonic stem cell
9	chr1:45965000-45966600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr1:45965000-45966600	Active TSS	iPS-20b Cell Line	embryonic stem cell
11	chr1:45965000-45966600	Flanking Active TSS	Primary B cells from cord blood	blood
12	chr1:45965000-45966600	Active TSS	Pancreas	Pancrea
13	chr1:45965000-45966800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr1:45965000-45966800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
15	chr1:45965000-45966800	Flanking Active TSS	Primary hematopoietic stem cells	blood
16	chr1:45965000-45966800	Active TSS	Fetal Kidney	kidney
17	chr1:45965000-45966800	Active TSS	Pancreatic Islets	Pancreatic Islet
18	chr1:45965000-45966800	Active TSS	NHLF	lung
19	chr1:45965000-45967000	Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr1:45965000-45967000	Flanking Active TSS	Adipose Nuclei	Adipose
21	chr1:45965000-45967200	Active TSS	iPS-15b Cell Line	embryonic stem cell
22	chr1:45965000-45967200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
23	chr1:45965200-45966600	Active TSS	H9 Cell Line	embryonic stem cell
24	chr1:45965200-45966600	Active TSS	HUES48 Cell Line	embryonic stem cell
25	chr1:45965200-45966600	Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr1:45965200-45966600	Active TSS	Breast Myoepithelial Primary Cells	Breast
27	chr1:45965200-45966600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr1:45965200-45966600	Active TSS	Psoas Muscle	Psoas
29	chr1:45965200-45966800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr1:45965200-45966800	Active TSS	Fetal Intestine Large	intestine
31	chr1:45965200-45967000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
32	chr1:45965200-45967000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr1:45965400-45966600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr1:45965400-45966600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr1:45965400-45966600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr1:45965400-45966600	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
37	chr1:45965400-45966600	Active TSS	Primary T helper naive cells from peripheral blood	blood
38	chr1:45965400-45966600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr1:45965400-45966600	Active TSS	Muscle Satellite Cultured Cells	--
40	chr1:45965400-45966600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr1:45965400-45966600	Active TSS	Brain Angular Gyrus	brain
42	chr1:45965400-45966600	Active TSS	Brain Anterior Caudate	brain
43	chr1:45965400-45966600	Active TSS	Brain Cingulate Gyrus	brain
44	chr1:45965400-45966600	Active TSS	Brain Hippocampus Middle	brain
45	chr1:45965400-45966600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
46	chr1:45965400-45966600	Active TSS	Colon Smooth Muscle	Colon
47	chr1:45965400-45966600	Active TSS	Duodenum Mucosa	Duodenum
48	chr1:45965400-45966600	Active TSS	Fetal Intestine Small	intestine
49	chr1:45965400-45966600	Active TSS	Fetal Lung	lung
50	chr1:45965400-45966600	Active TSS	Placenta	Placenta

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