Variant report

Variant	rs7806567
Chromosome Location	chr7:64465502-64465503
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:64463794..64465655-chr7:64465725..64468714,2	MCF-7	breast:
2	chr7:64433625..64435948-chr7:64463259..64466229,2	K562	blood:
3	chr7:64464158..64466866-chr7:64514284..64516776,2	MCF-7	breast:
4	chr7:64365308..64368250-chr7:64464896..64466671,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ERV3-1-2	chr7:64464047-64465572	NONHSAT121063

Variant related genes	Relation type
ENSG00000152926	Chromatin interaction
ENSG00000213462	Chromatin interaction

Extended variants
information (count: 116 )
Associated
traits (count: 35 )

rSNPs within LD-proxies of this variant (count:96)

rs_ID	r²[population]
rs10229485	0.84[AMR][1000 genomes]
rs10237971	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10243523	0.85[AMR][1000 genomes]
rs10252925	0.80[AMR][1000 genomes]
rs1060383	0.83[EUR][1000 genomes]
rs10949955	0.88[CEU][hapmap];0.83[EUR][1000 genomes]
rs11760504	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11764811	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11769801	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11771269	0.85[EUR][1000 genomes]
rs11771529	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11978852	0.85[EUR][1000 genomes]
rs12056025	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12056103	0.95[YRI][hapmap];0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12530729	0.83[EUR][1000 genomes]
rs12538992	0.82[EUR][1000 genomes]
rs12670240	0.84[EUR][1000 genomes]
rs13222578	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13226855	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13229762	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13233376	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13238842	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13243536	0.82[EUR][1000 genomes]
rs13244300	0.85[EUR][1000 genomes]
rs13245077	0.85[EUR][1000 genomes]
rs1540833	0.92[CEU][hapmap];0.83[EUR][1000 genomes]
rs1709515	0.80[AMR][1000 genomes]
rs1818916	0.89[CEU][hapmap];0.83[CHB][hapmap];0.94[YRI][hapmap]
rs1852026	0.85[EUR][1000 genomes]
rs2091224	0.92[CEU][hapmap];0.85[EUR][1000 genomes]
rs2103146	0.84[EUR][1000 genomes]
rs2103148	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2419256	1.00[CEU][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28510371	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28835689	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28872832	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3088174	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34171289	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34362307	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34636014	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34639489	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34897549	0.80[AMR][1000 genomes]
rs35079894	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35189858	0.84[EUR][1000 genomes]
rs35281840	0.83[EUR][1000 genomes]
rs35586133	0.81[EUR][1000 genomes]
rs35679667	0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35953728	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3807068	0.92[CEU][hapmap];0.83[EUR][1000 genomes]
rs3807069	0.85[CEU][hapmap];0.82[EUR][1000 genomes]
rs3823471	0.93[CEU][hapmap];0.83[EUR][1000 genomes]
rs3982216	0.95[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4266535	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4379351	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4481471	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4499978	0.80[EUR][1000 genomes]
rs4718177	0.83[EUR][1000 genomes]
rs4718178	0.84[EUR][1000 genomes]
rs4718180	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.95[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4718187	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4718188	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.95[YRI][hapmap];0.83[AMR][1000 genomes]
rs4718190	0.96[CHB][hapmap];0.86[JPT][hapmap];0.95[YRI][hapmap]
rs55762719	0.83[AMR][1000 genomes]
rs55959098	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs56294715	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56303509	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs56340521	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs57449421	0.83[AMR][1000 genomes]
rs58134413	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs62455989	0.95[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62455992	0.81[ASN][1000 genomes]
rs62457195	0.83[AMR][1000 genomes]
rs6460216	0.89[CEU][hapmap];0.84[EUR][1000 genomes]
rs66688157	0.82[AMR][1000 genomes]
rs67499519	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs67896886	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6947903	0.86[AMR][1000 genomes]
rs6950807	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6955268	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6961678	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6962429	0.86[AMR][1000 genomes]
rs6965099	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6965753	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6968439	0.84[EUR][1000 genomes]
rs6971128	0.81[AMR][1000 genomes]
rs6974079	0.81[AMR][1000 genomes]
rs6978332	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7780100	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7789394	0.85[EUR][1000 genomes]
rs7803542	0.85[EUR][1000 genomes]
rs7807855	0.85[EUR][1000 genomes]
rs9638216	0.83[EUR][1000 genomes]
rs9638417	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9647852	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9770557	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9770631	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422405	chr7:63709739-64632341	Enhancers Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
2	nsv464518	chr7:63881238-64506904	Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv607312	chr7:63881238-64506904	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats 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 miRNA target site	43 gene(s)	inside rSNPs	diseases
4	nsv888275	chr7:63990100-64468590	Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
5	nsv888276	chr7:63990100-64511564	Strong transcription ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS 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 miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
6	nsv1022042	chr7:64226499-64566945	Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
7	nsv888282	chr7:64299645-64511564	Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
8	esv3506582	chr7:64323055-64563984	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
9	esv3506583	chr7:64323055-64563984	Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
10	nsv1019180	chr7:64329889-64512842	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
11	nsv888283	chr7:64343985-64511564	Weak transcription Active TSS ZNF genes & repeats Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
12	esv2752165	chr7:64345822-65208605	Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
13	nsv888284	chr7:64406439-64562139	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
14	nsv970505	chr7:64441807-64494987	ZNF genes & repeats Weak transcription Active TSS Genic enhancers Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
15	nsv1033517	chr7:64443052-64942418	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
16	nsv538893	chr7:64443052-64942418	Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
17	nsv1034625	chr7:64456197-64850413	Genic enhancers Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
18	nsv1019089	chr7:64456197-64874187	Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
19	nsv1023699	chr7:64456197-64942418	Active TSS Flanking Bivalent TSS/Enh Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
20	nsv517778	chr7:64462326-65326821	ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases

mRNA abundance (count:35)

SNP	Gene	Cis/trans	Tissue	Source
rs7806567	AC104057.1	cis	Adipose Subcutaneous	GTEx
rs7806567	INTS4L1	cis	Nerve Tibial	GTEx
rs7806567	ERV3-1	cis	Artery Aorta	GTEx
rs7806567	ERV3	cis	multi-tissue	Pritchard
rs7806567	RP11-460N20.4	cis	Esophagus Mucosa	GTEx
rs7806567	RP11-667F9.1	cis	Nerve Tibial	GTEx
rs7806567	RP11-797H7.3	cis	Adipose Subcutaneous	GTEx
rs7806567	RP11-460N20.5	cis	Artery Tibial	GTEx
rs7806567	RP11-460N20.4	cis	Esophagus Muscularis	GTEx
rs7806567	CCT6P3	cis	Nerve Tibial	GTEx
rs7806567	RP11-797H7.3	cis	lung	GTEx
rs7806567	RP11-797H7.3	cis	Thyroid	GTEx
rs7806567	RP11-460N20.5	cis	Nerve Tibial	GTEx
rs7806567	ZNF273	cis	Thyroid	GTEx
rs7806567	RP11-797H7.5	cis	lung	GTEx
rs7806567	INTS4L1	cis	Esophagus Muscularis	GTEx
rs7806567	ZNF273	cis	lung	GTEx
rs7806567	RP11-797H7.3	cis	Artery Tibial	GTEx
rs7806567	CCT6P3	cis	Esophagus Mucosa	GTEx
rs7806567	RP11-667F9.1	cis	Adipose Subcutaneous	GTEx
rs7806567	RP11-460N20.5	cis	Thyroid	GTEx
rs7806567	RP11-797H7.5	cis	Adipose Subcutaneous	GTEx
rs7806567	RP11-797H7.3	cis	Nerve Tibial	GTEx
rs7806567	INTS4L1	cis	Adipose Subcutaneous	GTEx
rs7806567	RP11-460N20.4	cis	Adipose Subcutaneous	GTEx
rs7806567	RP11-460N20.4	cis	lung	GTEx
rs7806567	CCT6P3	cis	Skin Sun Exposed Lower leg	GTEx
rs7806567	RP11-797H7.5	cis	Thyroid	GTEx
rs7806567	RP11-460N20.5	cis	Whole Blood	GTEx
rs7806567	INTS4L1	cis	Skin Sun Exposed Lower leg	GTEx
rs7806567	RP11-460N20.5	cis	lung	GTEx
rs7806567	RP11-460N20.5	cis	Artery Aorta	GTEx
rs7806567	RP11-460N20.5	cis	Esophagus Mucosa	GTEx
rs7806567	CCT6P3	cis	Adipose Subcutaneous	GTEx
rs7806567	RP11-460N20.5	cis	Adipose Subcutaneous	GTEx

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:64433400-64465600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:64458600-64466200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr7:64459600-64466000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr7:64459600-64466000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr7:64459600-64466000	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr7:64459600-64466000	Weak transcription	HSMMtube	muscle
7	chr7:64459800-64465800	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr7:64459800-64466000	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr7:64459800-64466400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr7:64460800-64465600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
11	chr7:64460800-64465600	ZNF genes & repeats	Fetal Intestine Small	intestine
12	chr7:64461200-64465600	ZNF genes & repeats	Primary B cells from cord blood	blood
13	chr7:64461600-64466000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr7:64462000-64466000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr7:64462000-64466200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr7:64462200-64465600	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr7:64462200-64466000	Weak transcription	Fetal Kidney	kidney
18	chr7:64462200-64466000	Weak transcription	HSMM	muscle
19	chr7:64462200-64466400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr7:64462200-64466400	Weak transcription	Aorta	Aorta
21	chr7:64462400-64466000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr7:64463400-64465600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr7:64463400-64465600	Enhancers	Gastric	stomach
24	chr7:64463600-64465600	Enhancers	Spleen	Spleen
25	chr7:64463800-64465800	ZNF genes & repeats	A549	lung
26	chr7:64463800-64466200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr7:64464000-64466000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
28	chr7:64464200-64466200	Enhancers	Colon Smooth Muscle	Colon
29	chr7:64464400-64465600	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr7:64464400-64465600	Enhancers	Pancreas	Pancrea
31	chr7:64464400-64465800	Enhancers	Ovary	ovary
32	chr7:64464400-64465800	ZNF genes & repeats	GM12878-XiMat	blood
33	chr7:64464400-64466000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr7:64464400-64466200	Enhancers	Primary B cells from peripheral blood	blood
35	chr7:64464400-64466200	Enhancers	Primary T cells fromperipheralblood	blood
36	chr7:64464400-64466200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr7:64464400-64466400	Transcr. at gene 5' and 3'	K562	blood
38	chr7:64464600-64465800	Enhancers	Duodenum Smooth Muscle	Duodenum
39	chr7:64464600-64466000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr7:64464600-64466000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr7:64464600-64466400	Flanking Active TSS	Adipose Nuclei	Adipose
42	chr7:64464800-64465600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr7:64464800-64465600	Strong transcription	Primary hematopoietic stem cells	blood
44	chr7:64464800-64465800	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
45	chr7:64464800-64466000	Weak transcription	Fetal Intestine Large	intestine
46	chr7:64464800-64466400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
47	chr7:64464800-64467800	Enhancers	Fetal Heart	heart
48	chr7:64465000-64465600	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr7:64465000-64465600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
50	chr7:64465000-64465600	Enhancers	Lung	lung

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