Variant report

Variant	rs17386684
Chromosome Location	chr14:35602087-35602088
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	chr14:35590482..35592799-chr14:35601392..35603277,2	MCF-7	breast:
2	chr14:35591208..35595473-chr14:35600554..35604133,4	K562	blood:

Variant related genes	Relation type
ENSG00000258790	Chromatin interaction
ENSG00000100890	Chromatin interaction
ENSG00000092020	Chromatin interaction

Extended variants
information (count: 170 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:137)

rs_ID	r²[population]
rs10047949	0.85[ASN][1000 genomes]
rs10131625	0.85[ASN][1000 genomes]
rs10132920	0.85[ASN][1000 genomes]
rs10134308	0.85[ASN][1000 genomes]
rs10136978	0.85[ASN][1000 genomes]
rs10137019	0.85[ASN][1000 genomes]
rs10142846	0.85[ASN][1000 genomes]
rs10144857	0.85[ASN][1000 genomes]
rs10146133	1.00[ASN][1000 genomes]
rs10146691	0.88[ASN][1000 genomes]
rs10147645	0.81[ASN][1000 genomes]
rs1064248	0.85[ASN][1000 genomes]
rs11156874	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11844031	0.81[ASN][1000 genomes]
rs11845183	0.81[ASN][1000 genomes]
rs11845364	0.85[ASN][1000 genomes]
rs11848309	1.00[ASN][1000 genomes]
rs11849461	0.81[ASN][1000 genomes]
rs11850487	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11851820	0.81[ASN][1000 genomes]
rs11852178	0.81[ASN][1000 genomes]
rs12100582	0.85[ASN][1000 genomes]
rs12100841	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12100944	0.91[ASN][1000 genomes]
rs12100980	0.85[ASN][1000 genomes]
rs12436351	0.81[ASN][1000 genomes]
rs17103013	0.84[ASN][1000 genomes]
rs17103033	0.84[ASN][1000 genomes]
rs17103044	0.91[ASN][1000 genomes]
rs17103047	0.91[ASN][1000 genomes]
rs17103111	0.85[ASN][1000 genomes]
rs17103147	0.85[ASN][1000 genomes]
rs17103166	0.88[ASN][1000 genomes]
rs17456067	1.00[ASN][1000 genomes]
rs1807162	1.00[ASN][1000 genomes]
rs1884715	0.82[ASN][1000 genomes]
rs2008130	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2143948	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2143949	0.91[ASN][1000 genomes]
rs2145622	0.81[ASN][1000 genomes]
rs2277459	0.85[ASN][1000 genomes]
rs2277461	0.85[ASN][1000 genomes]
rs2415258	0.91[ASN][1000 genomes]
rs2415278	0.85[ASN][1000 genomes]
rs2415284	0.85[ASN][1000 genomes]
rs28470932	0.85[ASN][1000 genomes]
rs28504476	0.82[ASN][1000 genomes]
rs28595436	0.85[ASN][1000 genomes]
rs28665705	0.85[ASN][1000 genomes]
rs28708376	0.85[ASN][1000 genomes]
rs28736779	0.85[ASN][1000 genomes]
rs2899832	0.85[ASN][1000 genomes]
rs34509212	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4494460	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55791227	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs55890055	0.91[ASN][1000 genomes]
rs55907319	0.85[ASN][1000 genomes]
rs56142562	0.83[ASN][1000 genomes]
rs56363117	0.87[ASN][1000 genomes]
rs57166048	0.91[ASN][1000 genomes]
rs57411359	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs58064181	0.81[ASN][1000 genomes]
rs60940685	0.88[ASN][1000 genomes]
rs61060564	0.91[ASN][1000 genomes]
rs61492899	0.91[ASN][1000 genomes]
rs62625039	1.00[ASN][1000 genomes]
rs6571694	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6571695	1.00[ASN][1000 genomes]
rs6571709	0.85[ASN][1000 genomes]
rs7140462	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7148424	0.85[ASN][1000 genomes]
rs7149602	0.85[ASN][1000 genomes]
rs7153807	0.85[ASN][1000 genomes]
rs7154292	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7154637	0.85[ASN][1000 genomes]
rs7155335	0.84[ASN][1000 genomes]
rs7155697	0.91[ASN][1000 genomes]
rs7156704	0.91[ASN][1000 genomes]
rs7156770	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7160889	0.91[ASN][1000 genomes]
rs7218	0.85[ASN][1000 genomes]
rs72664814	0.91[ASN][1000 genomes]
rs72664816	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72664819	0.91[ASN][1000 genomes]
rs72664820	0.84[ASN][1000 genomes]
rs72664829	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72664840	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72664843	1.00[ASN][1000 genomes]
rs72664849	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72664854	1.00[ASN][1000 genomes]
rs72664855	1.00[ASN][1000 genomes]
rs72680648	0.87[ASN][1000 genomes]
rs72680652	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs72680655	0.91[ASN][1000 genomes]
rs72680657	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs72680662	0.91[ASN][1000 genomes]
rs72680663	0.91[ASN][1000 genomes]
rs73239026	0.82[ASN][1000 genomes]
rs73239030	0.82[ASN][1000 genomes]
rs73239072	0.85[ASN][1000 genomes]
rs73239074	0.85[ASN][1000 genomes]
rs73240720	0.81[ASN][1000 genomes]
rs73240721	0.81[ASN][1000 genomes]
rs74043875	0.81[ASN][1000 genomes]
rs743226	0.85[ASN][1000 genomes]
rs743227	0.85[ASN][1000 genomes]
rs7493705	0.85[ASN][1000 genomes]
rs8004236	0.85[ASN][1000 genomes]
rs8005079	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8005261	0.81[ASN][1000 genomes]
rs8007337	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs8007346	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs8007575	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs8007822	0.85[ASN][1000 genomes]
rs8008066	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs8009666	0.85[ASN][1000 genomes]
rs8010905	0.85[ASN][1000 genomes]
rs8011195	1.00[ASN][1000 genomes]
rs8011242	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs8011549	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs8012905	0.88[ASN][1000 genomes]
rs8014760	0.91[ASN][1000 genomes]
rs8016140	0.85[ASN][1000 genomes]
rs8016541	0.91[ASN][1000 genomes]
rs8017547	0.91[ASN][1000 genomes]
rs8018116	0.91[ASN][1000 genomes]
rs8019182	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs8019482	1.00[ASN][1000 genomes]
rs8019523	1.00[ASN][1000 genomes]
rs8019700	1.00[ASN][1000 genomes]
rs8019709	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8019741	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs876996	0.85[ASN][1000 genomes]
rs9646144	0.85[ASN][1000 genomes]
rs9888560	0.91[ASN][1000 genomes]
rs9888561	0.91[ASN][1000 genomes]
rs9888597	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:33 , 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	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	nsv534182	chr14:35579022-35620232	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats 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	19 gene(s)	inside rSNPs	diseases
28	nsv564266	chr14:35594442-35611552	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
29	nsv564267	chr14:35594442-35614319	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
30	nsv564268	chr14:35596092-35610276	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
31	nsv564269	chr14:35596092-35613619	Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
32	nsv564270	chr14:35596092-35614319	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
33	nsv1240	chr14:35599027-35625361	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs17386684	PPP2R3C	cis	Adipose Subcutaneous	GTEx

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35592400-35603000	Weak transcription	Ovary	ovary
2	chr14:35592600-35602800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr14:35592600-35602800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr14:35592600-35602800	Weak transcription	Spleen	Spleen
5	chr14:35592600-35603000	Weak transcription	Esophagus	oesophagus
6	chr14:35592600-35603000	Weak transcription	Gastric	stomach
7	chr14:35592600-35603200	Weak transcription	Left Ventricle	heart
8	chr14:35592600-35603200	Weak transcription	Pancreas	Pancrea
9	chr14:35592600-35603400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr14:35592600-35625200	Weak transcription	Small Intestine	intestine
11	chr14:35592800-35603200	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr14:35592800-35611000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr14:35593000-35602800	Weak transcription	Adipose Nuclei	Adipose
14	chr14:35593000-35602800	Weak transcription	Placenta	Placenta
15	chr14:35593000-35602800	Weak transcription	Lung	lung
16	chr14:35593000-35602800	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr14:35593000-35603400	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr14:35593000-35603400	Weak transcription	Right Atrium	heart
19	chr14:35593000-35603800	Weak transcription	Brain Anterior Caudate	brain
20	chr14:35593000-35603800	Weak transcription	Right Ventricle	heart
21	chr14:35593000-35605200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr14:35593000-35610200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr14:35593000-35613400	Weak transcription	Stomach Mucosa	stomach
24	chr14:35593000-35638200	Weak transcription	Fetal Brain Male	brain
25	chr14:35593000-35660400	Weak transcription	Stomach Smooth Muscle	stomach
26	chr14:35593200-35602400	Weak transcription	Fetal Brain Female	brain
27	chr14:35593200-35602600	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr14:35593200-35602800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr14:35593200-35602800	Weak transcription	Aorta	Aorta
30	chr14:35593200-35602800	Weak transcription	Brain Cingulate Gyrus	brain
31	chr14:35593200-35602800	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr14:35593200-35603000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr14:35593200-35603000	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr14:35593200-35603000	Weak transcription	NHLF	lung
35	chr14:35593200-35603400	Weak transcription	Brain Angular Gyrus	brain
36	chr14:35593200-35603400	Weak transcription	Brain Hippocampus Middle	brain
37	chr14:35593200-35603800	Weak transcription	Fetal Heart	heart
38	chr14:35593200-35604000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr14:35593200-35625200	Weak transcription	NH-A	brain
40	chr14:35593200-35625600	Weak transcription	Colon Smooth Muscle	Colon
41	chr14:35593200-35627800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr14:35593200-35635400	Weak transcription	Rectal Smooth Muscle	rectum
43	chr14:35593400-35602400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr14:35593400-35603600	Weak transcription	HMEC	breast
45	chr14:35593400-35613200	Weak transcription	Osteobl	bone
46	chr14:35593400-35617200	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr14:35594000-35615800	Weak transcription	HUVEC	blood vessel
48	chr14:35594200-35602800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr14:35594400-35602600	Weak transcription	Liver	Liver
50	chr14:35594400-35629000	Weak transcription	Rectal Mucosa Donor 31	rectum

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