Variant report

Variant	rs11848309
Chromosome Location	chr14:35624831-35624832
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:35624804..35627276-chr14:35631634..35634106,2	K562	blood:
2	chr14:35622588..35627460-chr14:35872526..35876521,6	MCF-7	breast:
3	chr14:35622836..35624862-chr14:35627590..35631684,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000100906	Chromatin interaction
ENSG00000259090	Chromatin interaction

Extended variants
information (count: 170 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:143)

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	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs10142846	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs10144857	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs10146133	1.00[ASN][1000 genomes]
rs10146691	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs10147645	1.00[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs10149823	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs1064248	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs11156874	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11844031	0.81[ASN][1000 genomes]
rs11845183	0.81[ASN][1000 genomes]
rs11845364	0.85[ASN][1000 genomes]
rs11849461	0.81[ASN][1000 genomes]
rs11850487	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs11851820	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs11852178	0.81[ASN][1000 genomes]
rs12100582	0.85[ASN][1000 genomes]
rs12100841	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.91[ASN][1000 genomes]
rs12100944	0.91[ASN][1000 genomes]
rs12100980	0.85[ASN][1000 genomes]
rs12436351	0.81[ASN][1000 genomes]
rs17091807	1.00[JPT][hapmap]
rs17103013	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs17103033	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.86[TSI][hapmap];0.84[ASN][1000 genomes]
rs17103044	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs17103047	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs17103111	0.85[ASN][1000 genomes]
rs17103147	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs17103166	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs17386684	1.00[ASN][1000 genomes]
rs17456067	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1807162	1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[ASN][1000 genomes]
rs1884715	0.82[ASN][1000 genomes]
rs2005535	1.00[CHB][hapmap]
rs2008130	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.86[TSI][hapmap];0.91[ASN][1000 genomes]
rs2143948	0.91[ASN][1000 genomes]
rs2143949	0.91[ASN][1000 genomes]
rs2145622	1.00[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs2277459	0.82[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs2277461	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs2415258	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs2415278	0.85[ASN][1000 genomes]
rs2415284	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];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	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs34509212	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4494460	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.88[YRI][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4981267	0.85[EUR][1000 genomes]
rs55785573	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs55791227	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	0.91[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	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.86[TSI][hapmap];1.00[ASN][1000 genomes]
rs6571695	1.00[ASN][1000 genomes]
rs6571709	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs7140462	0.91[ASN][1000 genomes]
rs7144822	0.84[EUR][1000 genomes]
rs7148424	0.85[ASN][1000 genomes]
rs7149602	0.85[ASN][1000 genomes]
rs7153807	0.85[ASN][1000 genomes]
rs7154292	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.86[TSI][hapmap];0.91[ASN][1000 genomes]
rs7154637	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs7155335	0.84[ASN][1000 genomes]
rs7155697	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs7156704	0.91[ASN][1000 genomes]
rs7156770	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs7160889	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs7218	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs72664814	0.91[ASN][1000 genomes]
rs72664816	0.91[ASN][1000 genomes]
rs72664819	0.91[ASN][1000 genomes]
rs72664820	0.84[ASN][1000 genomes]
rs72664829	0.91[ASN][1000 genomes]
rs72664840	1.00[ASN][1000 genomes]
rs72664843	1.00[ASN][1000 genomes]
rs72664849	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[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	0.91[ASN][1000 genomes]
rs72680655	0.91[ASN][1000 genomes]
rs72680657	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	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs8004236	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs8005079	0.91[ASN][1000 genomes]
rs8005261	0.81[ASN][1000 genomes]
rs8007337	0.83[ASN][1000 genomes]
rs8007346	0.83[ASN][1000 genomes]
rs8007575	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs8007822	0.85[ASN][1000 genomes]
rs8008066	0.82[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.86[TSI][hapmap];0.91[ASN][1000 genomes]
rs8009666	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs8010905	0.85[ASN][1000 genomes]
rs8011195	1.00[ASN][1000 genomes]
rs8011242	0.91[ASN][1000 genomes]
rs8011549	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs8012905	0.88[ASN][1000 genomes]
rs8014760	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs8016140	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs8016541	0.91[ASN][1000 genomes]
rs8017547	0.91[ASN][1000 genomes]
rs8018116	0.91[ASN][1000 genomes]
rs8019182	0.91[ASN][1000 genomes]
rs8019482	1.00[ASN][1000 genomes]
rs8019523	1.00[ASN][1000 genomes]
rs8019700	1.00[ASN][1000 genomes]
rs8019709	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8019741	0.91[ASN][1000 genomes]
rs876996	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs9646144	1.00[CHB][hapmap];1.00[JPT][hapmap];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:27 , 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	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	nsv1040300	chr14:35602956-35643888	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
27	nsv1046680	chr14:35608347-35665374	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs11848309	PPP2R3C	cis	lymphoblastoid	seeQTL
rs11848309	FAM177A1	cis	cerebellum	SCAN
rs11848309	PPP2R3C	cis	parietal	SCAN

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35592600-35625200	Weak transcription	Small Intestine	intestine
2	chr14:35593000-35638200	Weak transcription	Fetal Brain Male	brain
3	chr14:35593000-35660400	Weak transcription	Stomach Smooth Muscle	stomach
4	chr14:35593200-35625200	Weak transcription	NH-A	brain
5	chr14:35593200-35625600	Weak transcription	Colon Smooth Muscle	Colon
6	chr14:35593200-35627800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr14:35593200-35635400	Weak transcription	Rectal Smooth Muscle	rectum
8	chr14:35594400-35629000	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr14:35597400-35625000	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr14:35597600-35625000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr14:35603000-35625200	Weak transcription	HSMM	muscle
12	chr14:35603200-35663400	Weak transcription	Fetal Lung	lung
13	chr14:35603400-35625200	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr14:35604200-35625200	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr14:35604200-35625200	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr14:35604200-35628800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr14:35604200-35651400	Weak transcription	Esophagus	oesophagus
18	chr14:35604400-35625200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr14:35604400-35625200	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr14:35604400-35642000	Weak transcription	Lung	lung
21	chr14:35604400-35651800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr14:35604400-35660200	Weak transcription	Aorta	Aorta
23	chr14:35604600-35625200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr14:35604600-35625200	Weak transcription	Adipose Nuclei	Adipose
25	chr14:35604600-35626000	Weak transcription	Placenta	Placenta
26	chr14:35604600-35667400	Weak transcription	Spleen	Spleen
27	chr14:35604800-35625000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr14:35604800-35625200	Weak transcription	Liver	Liver
29	chr14:35604800-35625400	Weak transcription	HSMMtube	muscle
30	chr14:35605000-35625000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr14:35605600-35625200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr14:35605600-35625200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr14:35605600-35625200	Weak transcription	Hela-S3	cervix
34	chr14:35605600-35628000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr14:35606400-35625200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr14:35607400-35628200	Weak transcription	Primary neutrophils fromperipheralblood	blood
37	chr14:35607400-35642800	Weak transcription	Left Ventricle	heart
38	chr14:35607400-35662000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr14:35607600-35625000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr14:35607600-35661200	Weak transcription	Fetal Muscle Leg	muscle
41	chr14:35612000-35659800	Weak transcription	Fetal Muscle Trunk	muscle
42	chr14:35612200-35628200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr14:35612200-35641800	Weak transcription	Fetal Stomach	stomach
44	chr14:35613600-35625200	Weak transcription	Duodenum Mucosa	Duodenum
45	chr14:35613600-35625200	Weak transcription	Thymus	Thymus
46	chr14:35613600-35625400	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr14:35613600-35628000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr14:35613600-35628200	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr14:35613600-35635800	Weak transcription	Brain Substantia Nigra	brain
50	chr14:35613800-35625000	Weak transcription	Primary B cells from cord blood	blood

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