Variant report

Variant	rs17103044
Chromosome Location	chr14:35575513-35575514
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:35575108..35577004-chr14:35580748..35582498,2	MCF-7	breast:
2	chr14:35016883..35018423-chr14:35574764..35577501,2	MCF-7	breast:

Extended variants
information (count: 128 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:100)

rs_ID	r²[population]
rs10137019	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap]
rs10142846	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap]
rs10144857	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap]
rs10146133	0.91[ASN][1000 genomes]
rs10146691	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs10149823	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap]
rs1064248	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap]
rs11156874	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs11848309	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs11850487	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12100841	0.91[ASW][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];0.84[YRI][hapmap];0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12100944	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17103013	0.91[ASW][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.80[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs17103033	0.81[ASW][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.92[ASN][1000 genomes]
rs17103047	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17103147	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17103166	1.00[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs17386684	0.91[ASN][1000 genomes]
rs17456067	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs1807162	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs2005535	1.00[CHB][hapmap]
rs2008130	0.81[ASW][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];1.00[ASN][1000 genomes]
rs2143948	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2143949	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2277459	0.82[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs2277461	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap]
rs2415258	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2415284	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2899832	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs34509212	0.91[ASN][1000 genomes]
rs4494460	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs55791227	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs55833640	0.82[ASN][1000 genomes]
rs55890055	0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs56142562	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56363117	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs57166048	0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs57338667	0.87[ASN][1000 genomes]
rs57411359	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs60940685	0.81[ASN][1000 genomes]
rs61060564	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61492899	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62625039	0.91[ASN][1000 genomes]
rs6571694	0.91[ASW][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];0.89[YRI][hapmap];0.88[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs6571695	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6571709	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7140462	1.00[ASN][1000 genomes]
rs7154292	0.81[ASW][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];0.84[YRI][hapmap];0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7154637	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap]
rs7155697	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7156704	0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7156770	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7160889	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7218	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap]
rs72664814	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72664816	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72664819	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72664820	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72664829	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72664840	0.84[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs72664843	0.91[ASN][1000 genomes]
rs72664849	0.84[ASN][1000 genomes]
rs72664854	0.91[ASN][1000 genomes]
rs72664855	0.91[ASN][1000 genomes]
rs72680622	0.87[ASN][1000 genomes]
rs72680641	0.87[ASN][1000 genomes]
rs72680648	0.96[ASN][1000 genomes]
rs72680652	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72680655	1.00[ASN][1000 genomes]
rs72680657	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72680662	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72680663	0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7493705	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap]
rs8004236	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs8005079	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs8007337	0.91[ASN][1000 genomes]
rs8007346	0.91[ASN][1000 genomes]
rs8007575	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs8008066	0.82[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];0.84[YRI][hapmap];0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs8009666	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs8011195	0.91[ASN][1000 genomes]
rs8011242	1.00[ASN][1000 genomes]
rs8011549	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];1.00[ASN][1000 genomes]
rs8012905	0.96[ASN][1000 genomes]
rs8014760	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.82[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8016140	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap]
rs8016541	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8017547	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8018116	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8019182	1.00[ASN][1000 genomes]
rs8019482	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8019523	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8019700	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8019709	0.91[ASN][1000 genomes]
rs8019741	0.86[LWK][hapmap];0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs876996	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap]
rs9646144	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9888560	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9888561	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9888597	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949617	chr14:35379923-35825436	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	nsv1043470	chr14:35398522-35754029	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
3	nsv542031	chr14:35398522-35754029	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Active TSS 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	65 gene(s)	inside rSNPs	diseases
4	nsv901609	chr14:35449467-35587767	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
5	nsv901613	chr14:35470049-35587767	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Enhancers Flanking Active TSS 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	30 gene(s)	inside rSNPs	diseases
6	nsv564264	chr14:35482797-35732369	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
7	nsv901615	chr14:35485748-35630175	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
8	nsv870305	chr14:35488290-35852349	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
9	nsv1052800	chr14:35509858-35607117	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Genic enhancers 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	37 gene(s)	inside rSNPs	diseases
10	nsv1044515	chr14:35510785-35756317	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
11	nsv564265	chr14:35512335-35624831	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Genic enhancers 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	38 gene(s)	inside rSNPs	diseases
12	nsv1046992	chr14:35527239-35724227	Flanking Active TSS Strong transcription Weak transcription Enhancers Genic 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	27 gene(s)	inside rSNPs	diseases
13	nsv1051274	chr14:35529529-35724227	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
14	nsv1048823	chr14:35537281-35724892	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking 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	27 gene(s)	inside rSNPs	diseases
15	nsv542032	chr14:35537281-35724892	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
16	nsv1040540	chr14:35537481-35724753	Strong transcription Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
17	nsv542033	chr14:35537481-35724753	Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
18	nsv1042625	chr14:35546094-35680358	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers 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	22 gene(s)	inside rSNPs	diseases
19	nsv1050123	chr14:35546114-35724892	Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers 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	27 gene(s)	inside rSNPs	diseases
20	nsv542034	chr14:35546114-35724892	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
21	nsv1050700	chr14:35548276-35639084	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS 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	21 gene(s)	inside rSNPs	diseases
22	nsv1043692	chr14:35548276-35720016	Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
23	nsv1053604	chr14:35548276-35825805	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
24	nsv542035	chr14:35563220-35607117	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
25	nsv1047992	chr14:35563220-35639084	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
26	nsv1052392	chr14:35563220-35893309	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	83 gene(s)	inside rSNPs	diseases
27	nsv542036	chr14:35563220-35893309	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	83 gene(s)	inside rSNPs	diseases
28	nsv1053978	chr14:35571762-35639084	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35517400-35578800	Weak transcription	Stomach Mucosa	stomach
2	chr14:35529400-35590200	Weak transcription	Esophagus	oesophagus
3	chr14:35530600-35590000	Weak transcription	Fetal Heart	heart
4	chr14:35538200-35581000	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr14:35542000-35589600	Weak transcription	Fetal Brain Male	brain
6	chr14:35543200-35580800	Weak transcription	K562	blood
7	chr14:35545600-35580800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr14:35545600-35582800	Strong transcription	Primary T helper cells fromperipheralblood	blood
9	chr14:35545600-35590000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr14:35546000-35581200	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr14:35546000-35585800	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr14:35546000-35587200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr14:35546200-35585000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr14:35547000-35580800	Strong transcription	HUES48 Cell Line	embryonic stem cell
15	chr14:35547200-35577600	Strong transcription	Placenta	Placenta
16	chr14:35547400-35577800	Strong transcription	Primary B cells from peripheral blood	blood
17	chr14:35547400-35580600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr14:35548000-35581000	Strong transcription	HepG2	liver
19	chr14:35548200-35580800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr14:35548400-35578800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr14:35550200-35586000	Strong transcription	Primary neutrophils fromperipheralblood	blood
22	chr14:35550800-35581000	Strong transcription	Dnd41	blood
23	chr14:35551600-35579400	Weak transcription	NHEK	skin
24	chr14:35552000-35586600	Strong transcription	Fetal Thymus	thymus
25	chr14:35552600-35577600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
26	chr14:35553400-35589800	Weak transcription	Pancreas	Pancrea
27	chr14:35555000-35576000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
28	chr14:35555000-35581200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr14:35555400-35578800	Weak transcription	HMEC	breast
30	chr14:35556200-35578800	Weak transcription	Aorta	Aorta
31	chr14:35557000-35578200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr14:35558600-35576200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr14:35560200-35581200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr14:35560600-35576400	Weak transcription	A549	lung
35	chr14:35560600-35580600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr14:35560600-35580600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr14:35561800-35579000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr14:35564200-35578600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr14:35564200-35589400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr14:35564400-35578800	Weak transcription	Fetal Kidney	kidney
41	chr14:35564400-35579200	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr14:35564400-35580000	Weak transcription	Colonic Mucosa	Colon
43	chr14:35564800-35576000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr14:35564800-35578800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr14:35564800-35579000	Weak transcription	Hela-S3	cervix
46	chr14:35564800-35589800	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr14:35565200-35582000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr14:35565600-35578800	Weak transcription	Small Intestine	intestine
49	chr14:35565800-35578600	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr14:35566000-35578800	Weak transcription	Brain Substantia Nigra	brain

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