Variant report

Variant	rs8007618
Chromosome Location	chr14:67877192-67877193
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:67869261..67871633-chr14:67875881..67878692,2	MCF-7	breast:
2	chr14:67826231..67828926-chr14:67875874..67878480,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000134001	Chromatin interaction
ENSG00000100554	Chromatin interaction

Extended variants
information (count: 201 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:190)

rs_ID	r²[population]
rs10129779	0.80[CHB][hapmap];0.81[JPT][hapmap];0.86[ASN][1000 genomes]
rs10131175	0.90[CHB][hapmap];0.82[JPT][hapmap];0.90[ASN][1000 genomes]
rs10131212	0.86[CHB][hapmap];0.93[CHD][hapmap];0.88[GIH][hapmap];0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs10132093	0.82[JPT][hapmap]
rs10135163	0.88[ASN][1000 genomes]
rs10135498	0.88[ASN][1000 genomes]
rs10135727	0.81[ASN][1000 genomes]
rs10135903	0.90[CHB][hapmap];0.82[JPT][hapmap];0.84[ASN][1000 genomes]
rs10136710	0.88[ASN][1000 genomes]
rs10137026	0.83[ASN][1000 genomes]
rs10137557	0.90[CHB][hapmap];0.85[JPT][hapmap];0.88[ASN][1000 genomes]
rs10138755	0.89[CHB][hapmap];0.84[JPT][hapmap];0.86[ASN][1000 genomes]
rs10138824	0.86[CHB][hapmap];0.93[CHD][hapmap];0.90[GIH][hapmap];0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs10138932	0.86[ASN][1000 genomes]
rs10139015	0.95[ASN][1000 genomes]
rs10139585	0.92[ASN][1000 genomes]
rs10139684	0.92[ASN][1000 genomes]
rs10140817	0.86[CHB][hapmap];0.82[JPT][hapmap];0.84[ASN][1000 genomes]
rs10141180	0.87[GIH][hapmap]
rs10141879	0.93[CHD][hapmap];0.90[GIH][hapmap];0.90[JPT][hapmap];0.81[ASN][1000 genomes]
rs10143251	0.92[ASN][1000 genomes]
rs10143916	0.86[ASN][1000 genomes]
rs10144090	0.81[CHB][hapmap];0.93[CHD][hapmap];0.90[GIH][hapmap];0.86[JPT][hapmap]
rs10144401	0.86[CHB][hapmap];0.90[CHD][hapmap];0.90[GIH][hapmap];0.82[JPT][hapmap];0.84[ASN][1000 genomes]
rs10144417	0.90[CHB][hapmap];0.90[CHD][hapmap];0.92[GIH][hapmap];0.82[JPT][hapmap];0.89[ASN][1000 genomes]
rs10145586	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs10146663	0.86[CHB][hapmap];0.90[CHD][hapmap];0.90[GIH][hapmap];0.82[JPT][hapmap];0.84[ASN][1000 genomes]
rs10146722	0.84[JPT][hapmap];0.83[ASN][1000 genomes]
rs10147640	0.84[ASN][1000 genomes]
rs10147852	0.81[CHB][hapmap];0.93[CHD][hapmap];0.88[GIH][hapmap];0.82[JPT][hapmap]
rs10150902	0.86[CHB][hapmap];0.90[CHD][hapmap];0.90[GIH][hapmap];0.82[JPT][hapmap];0.84[ASN][1000 genomes]
rs10151464	0.86[CHB][hapmap];0.82[JPT][hapmap];0.84[ASN][1000 genomes]
rs10431718	0.93[CHD][hapmap];0.90[GIH][hapmap];0.82[JPT][hapmap]
rs1044750	0.86[ASN][1000 genomes]
rs1045060	0.90[CHB][hapmap];0.90[CHD][hapmap];0.90[GIH][hapmap];0.86[JPT][hapmap];0.86[ASN][1000 genomes]
rs10459453	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs1073604	0.80[ASN][1000 genomes]
rs1073607	0.80[CHB][hapmap];0.82[JPT][hapmap]
rs1078194	0.81[CHB][hapmap];0.91[JPT][hapmap]
rs11158658	0.81[CHB][hapmap];0.87[JPT][hapmap];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12323494	0.85[CHB][hapmap];0.81[JPT][hapmap]
rs12323911	0.81[CHB][hapmap];0.90[CHD][hapmap];0.88[GIH][hapmap];0.82[JPT][hapmap]
rs12586552	0.89[CHB][hapmap];0.84[JPT][hapmap];0.84[ASN][1000 genomes]
rs12586609	0.86[ASN][1000 genomes]
rs12586640	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12587134	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12588292	0.85[GIH][hapmap]
rs12588355	0.86[ASN][1000 genomes]
rs12588388	0.86[ASN][1000 genomes]
rs12588478	0.85[CHB][hapmap];0.81[JPT][hapmap];0.89[ASN][1000 genomes]
rs12589091	0.84[CHB][hapmap];0.85[JPT][hapmap];0.81[ASN][1000 genomes]
rs12589218	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs12589325	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12589606	0.86[ASN][1000 genomes]
rs12589671	0.90[CHB][hapmap];0.82[JPT][hapmap];0.88[ASN][1000 genomes]
rs12589983	0.85[ASN][1000 genomes]
rs12590952	0.85[ASN][1000 genomes]
rs12590956	0.91[JPT][hapmap]
rs1318914	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs13379142	0.90[CHB][hapmap];0.80[JPT][hapmap];0.88[ASN][1000 genomes]
rs13379368	0.90[CHB][hapmap];0.82[JPT][hapmap];0.88[ASN][1000 genomes]
rs1473733	0.84[ASN][1000 genomes]
rs1475128	0.86[ASN][1000 genomes]
rs1475129	0.86[ASN][1000 genomes]
rs1535489	0.86[ASN][1000 genomes]
rs1535490	0.86[ASN][1000 genomes]
rs1535491	0.81[CHB][hapmap];0.93[CHD][hapmap];0.90[GIH][hapmap];0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs1536271	0.90[CHB][hapmap];0.82[JPT][hapmap];0.88[ASN][1000 genomes]
rs1536272	0.86[CHB][hapmap];0.82[JPT][hapmap];0.88[ASN][1000 genomes]
rs1536273	0.88[ASN][1000 genomes]
rs1555853	1.00[ASW][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17093616	0.84[ASN][1000 genomes]
rs17104223	0.84[ASN][1000 genomes]
rs17104224	0.84[ASN][1000 genomes]
rs17248526	0.81[CHB][hapmap];0.93[CHD][hapmap];0.90[GIH][hapmap];0.82[JPT][hapmap]
rs17248567	0.86[ASN][1000 genomes]
rs17248616	0.85[CHB][hapmap];0.80[JPT][hapmap];0.85[ASN][1000 genomes]
rs17248714	0.88[ASN][1000 genomes]
rs17248895	0.86[CHD][hapmap];0.87[JPT][hapmap]
rs17248909	0.93[MEX][hapmap];0.93[AMR][1000 genomes]
rs17564263	0.82[ASN][1000 genomes]
rs17836702	0.86[ASN][1000 genomes]
rs17836750	0.82[GIH][hapmap]
rs1885589	0.86[CHB][hapmap];0.81[JPT][hapmap];0.86[ASN][1000 genomes]
rs1885590	0.87[GIH][hapmap]
rs1980817	0.91[ASN][1000 genomes]
rs2031563	0.86[CHB][hapmap];0.90[CHD][hapmap];0.92[GIH][hapmap];0.86[ASN][1000 genomes]
rs2057396	0.86[CHB][hapmap];0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs2094162	0.85[GIH][hapmap]
rs2146229	0.86[CHB][hapmap];0.93[CHD][hapmap];0.90[GIH][hapmap];0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs2146230	0.81[CHB][hapmap];0.93[CHD][hapmap];0.90[GIH][hapmap];0.82[JPT][hapmap]
rs2236333	0.86[CHB][hapmap];0.82[JPT][hapmap];0.85[ASN][1000 genomes]
rs2274335	0.90[CHB][hapmap];0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs2274336	0.86[ASN][1000 genomes]
rs2274338	0.90[CHB][hapmap];0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs2296560	0.90[CHB][hapmap];0.93[CHD][hapmap];0.92[GIH][hapmap];0.82[JPT][hapmap];0.90[ASN][1000 genomes]
rs28405138	0.83[ASN][1000 genomes]
rs28422832	0.86[ASN][1000 genomes]
rs28441403	0.94[ASN][1000 genomes]
rs28456209	0.88[ASN][1000 genomes]
rs28458235	0.85[ASN][1000 genomes]
rs28472807	0.82[ASN][1000 genomes]
rs28558916	0.89[ASN][1000 genomes]
rs28562402	0.81[ASN][1000 genomes]
rs28584286	0.84[ASN][1000 genomes]
rs28607485	0.86[ASN][1000 genomes]
rs28617290	0.84[ASN][1000 genomes]
rs28668536	0.86[ASN][1000 genomes]
rs28706091	0.86[ASN][1000 genomes]
rs35104910	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3759755	0.90[CHB][hapmap];0.90[CHD][hapmap];0.92[GIH][hapmap];0.82[JPT][hapmap];0.89[ASN][1000 genomes]
rs3784081	0.86[ASN][1000 genomes]
rs3784085	0.88[GIH][hapmap]
rs3809387	0.86[ASN][1000 genomes]
rs3818467	0.90[CHB][hapmap];0.90[CHD][hapmap];0.90[GIH][hapmap];0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs3818468	0.95[CHB][hapmap];0.98[CHD][hapmap];0.95[GIH][hapmap];0.86[JPT][hapmap];0.90[ASN][1000 genomes]
rs3825722	0.86[ASN][1000 genomes]
rs4058254	0.85[CHB][hapmap];0.83[ASN][1000 genomes]
rs4143908	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57025434	0.86[ASN][1000 genomes]
rs57234033	0.92[ASN][1000 genomes]
rs61510566	0.80[ASN][1000 genomes]
rs6573760	0.90[CHD][hapmap];0.91[JPT][hapmap]
rs6573763	0.94[JPT][hapmap];0.80[ASN][1000 genomes]
rs6573769	0.88[GIH][hapmap]
rs7144928	0.84[ASN][1000 genomes]
rs7149535	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs7152903	0.93[CHD][hapmap];0.90[GIH][hapmap]
rs7153350	0.94[ASN][1000 genomes]
rs7153725	0.83[CHB][hapmap];0.90[GIH][hapmap]
rs7153965	0.86[ASN][1000 genomes]
rs7154607	0.83[CHB][hapmap];0.83[GIH][hapmap];0.83[JPT][hapmap]
rs7156441	0.90[CHB][hapmap];0.90[CHD][hapmap];0.92[GIH][hapmap];0.86[JPT][hapmap];0.89[ASN][1000 genomes]
rs7157211	0.82[ASN][1000 genomes]
rs7158743	0.84[ASN][1000 genomes]
rs7158751	0.83[ASN][1000 genomes]
rs7160238	0.83[ASN][1000 genomes]
rs72476727	0.86[ASN][1000 genomes]
rs73280932	0.80[ASN][1000 genomes]
rs73282706	0.85[ASN][1000 genomes]
rs73282711	0.84[ASN][1000 genomes]
rs73282717	0.84[ASN][1000 genomes]
rs73282734	0.83[ASN][1000 genomes]
rs73282746	0.84[ASN][1000 genomes]
rs73282766	0.84[ASN][1000 genomes]
rs73282772	0.86[ASN][1000 genomes]
rs73282775	0.86[ASN][1000 genomes]
rs73282776	0.86[ASN][1000 genomes]
rs73282798	0.86[ASN][1000 genomes]
rs73284805	0.81[ASN][1000 genomes]
rs73284810	0.85[ASN][1000 genomes]
rs73284812	0.84[ASN][1000 genomes]
rs8004148	0.90[CHD][hapmap];0.90[JPT][hapmap]
rs8004267	0.83[CHB][hapmap];0.88[CHD][hapmap];0.91[JPT][hapmap];0.81[ASN][1000 genomes]
rs8004332	0.95[CHB][hapmap];0.95[CHD][hapmap];0.95[GIH][hapmap];0.86[JPT][hapmap];0.93[ASN][1000 genomes]
rs8004864	1.00[CHB][hapmap];0.86[JPT][hapmap];0.95[ASN][1000 genomes]
rs8005876	0.83[CHB][hapmap];0.90[GIH][hapmap]
rs8005900	0.93[ASN][1000 genomes]
rs8006042	0.85[GIH][hapmap]
rs8006391	0.90[CHB][hapmap];0.81[JPT][hapmap];0.89[ASN][1000 genomes]
rs8006519	0.90[CHB][hapmap];0.88[CHD][hapmap];0.88[GIH][hapmap];0.88[ASN][1000 genomes]
rs8007033	0.90[CHB][hapmap];0.93[CHD][hapmap];0.92[GIH][hapmap];0.82[JPT][hapmap];0.90[ASN][1000 genomes]
rs8007866	0.86[CHB][hapmap]
rs8008155	0.80[ASN][1000 genomes]
rs8008236	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs8008619	0.90[CHB][hapmap];0.90[CHD][hapmap];0.92[GIH][hapmap];0.82[JPT][hapmap];0.88[ASN][1000 genomes]
rs8008724	0.90[CHB][hapmap];0.90[CHD][hapmap];0.92[GIH][hapmap];0.82[JPT][hapmap];0.90[ASN][1000 genomes]
rs8009318	0.82[JPT][hapmap]
rs8014104	0.86[ASN][1000 genomes]
rs8014259	0.86[ASN][1000 genomes]
rs8014871	0.82[ASN][1000 genomes]
rs8014966	0.85[CHB][hapmap];0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs8015302	0.84[ASN][1000 genomes]
rs8015641	0.81[CHB][hapmap]
rs8015862	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs8015950	0.86[CHD][hapmap];0.87[JPT][hapmap]
rs8016024	0.88[GIH][hapmap]
rs8016037	0.81[CHB][hapmap];0.93[CHD][hapmap];0.90[GIH][hapmap];0.82[JPT][hapmap]
rs8016623	0.88[ASN][1000 genomes]
rs8018623	0.81[ASN][1000 genomes]
rs8019398	0.81[ASN][1000 genomes]
rs8020262	0.88[CHD][hapmap];0.87[JPT][hapmap]
rs8020720	0.85[ASN][1000 genomes]
rs8020850	0.85[GIH][hapmap]
rs8021227	0.84[ASN][1000 genomes]
rs8021621	0.94[ASN][1000 genomes]
rs8021730	0.88[CHD][hapmap];0.87[JPT][hapmap]
rs8021896	0.86[CHB][hapmap];0.93[CHD][hapmap];0.90[GIH][hapmap];0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs9743911	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs9743912	0.81[GIH][hapmap]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2751285	chr14:67364747-67886781	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv1045518	chr14:67529049-67959582	Strong transcription Bivalent Enhancer Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	nsv456331	chr14:67732861-68103780	Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	nsv564961	chr14:67732861-68103780	Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
5	nsv470651	chr14:67732861-68113293	Active TSS Strong transcription Flanking Active TSS Weak transcription Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
6	nsv1054389	chr14:67804987-67922598	Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
7	nsv542121	chr14:67804987-67922598	Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
8	nsv1319	chr14:67863561-67908725	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA	12 gene(s)	inside rSNPs	diseases
9	esv3487440	chr14:67863754-67892047	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
10	esv3487442	chr14:67863758-67892045	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
11	nsv902066	chr14:67873128-68103780	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs8007618	EIF2S1	cis	lymphoblastoid	seeQTL
rs8007618	EIF2S1	cis	multi-tissue	Pritchard

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:67850200-67878400	Weak transcription	Lung	lung
2	chr14:67860800-67878000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr14:67862800-67878400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr14:67875200-67877600	Transcr. at gene 5' and 3'	NHEK	skin
5	chr14:67875400-67877600	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr14:67875400-67877800	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr14:67875400-67878400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr14:67875800-67878000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr14:67875800-67878400	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr14:67876000-67877600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr14:67876200-67877200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr14:67876200-67877200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr14:67876200-67877800	Enhancers	K562	blood
14	chr14:67876200-67878400	Flanking Active TSS	Hela-S3	cervix
15	chr14:67876200-67878600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr14:67876200-67879000	Enhancers	Fetal Heart	heart
17	chr14:67876400-67877400	Enhancers	Placenta	Placenta
18	chr14:67876400-67877600	Enhancers	HepG2	liver
19	chr14:67876400-67878000	Enhancers	Fetal Intestine Large	intestine
20	chr14:67876600-67877200	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr14:67876600-67877200	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr14:67876600-67877600	Enhancers	Esophagus	oesophagus
23	chr14:67876600-67878000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr14:67876600-67878000	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr14:67876800-67878000	Enhancers	Colonic Mucosa	Colon
26	chr14:67876800-67878400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
27	chr14:67876800-67878400	Weak transcription	Right Atrium	heart
28	chr14:67876800-67878600	Flanking Active TSS	Duodenum Mucosa	Duodenum
29	chr14:67877000-67877200	Flanking Active TSS	Fetal Intestine Small	intestine
30	chr14:67877000-67877400	Active TSS	Rectal Mucosa Donor 29	rectum
31	chr14:67877000-67877400	Flanking Active TSS	Stomach Mucosa	stomach
32	chr14:67877000-67877400	Transcr. at gene 5' and 3'	HMEC	breast
33	chr14:67877000-67877800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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