Variant report

Variant	rs8014377
Chromosome Location	chr14:35531057-35531058
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:35519616..35521249-chr14:35528506..35531084,2	MCF-7	breast:
2	chr14:35525027..35526542-chr14:35529643..35531640,2	K562	blood:
3	chr14:35343011..35344577-chr14:35528833..35531225,2	MCF-7	breast:
4	chr14:35520110..35522080-chr14:35529783..35531632,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000198604	Chromatin interaction
ENSG00000258738	Chromatin interaction

Extended variants
information (count: 123 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:101)

rs_ID	r²[population]
rs1028449	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1056879	0.82[CHD][hapmap];0.82[JPT][hapmap]
rs11156875	0.92[CEU][hapmap];0.85[CHB][hapmap];1.00[CHD][hapmap];0.91[JPT][hapmap];0.93[MEX][hapmap];0.96[TSI][hapmap];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11845837	0.80[ASN][1000 genomes]
rs11851907	0.82[JPT][hapmap]
rs12050390	0.85[ASN][1000 genomes]
rs12050402	0.86[ASN][1000 genomes]
rs12050404	0.87[ASN][1000 genomes]
rs12050447	0.87[ASN][1000 genomes]
rs12587376	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12589079	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12589278	0.90[CHB][hapmap]
rs12878219	0.90[CHB][hapmap];0.83[CHD][hapmap];0.95[JPT][hapmap]
rs12880809	0.85[ASN][1000 genomes]
rs12880928	0.88[ASN][1000 genomes]
rs12881698	0.93[ASN][1000 genomes]
rs12887248	0.91[ASN][1000 genomes]
rs12887779	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12887885	0.90[CHB][hapmap];0.83[CHD][hapmap];0.95[JPT][hapmap]
rs12890307	0.80[ASN][1000 genomes]
rs12891343	0.90[CHB][hapmap];0.95[JPT][hapmap]
rs12892552	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12895051	0.95[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap]
rs12896759	0.91[ASN][1000 genomes]
rs17102923	0.80[ASN][1000 genomes]
rs17102967	0.95[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.91[ASN][1000 genomes]
rs17102970	0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs17103005	0.82[JPT][hapmap];0.81[ASN][1000 genomes]
rs17103104	0.85[CEU][hapmap];0.92[TSI][hapmap]
rs17103120	0.85[CEU][hapmap];0.92[TSI][hapmap]
rs17113838	0.83[CEU][hapmap]
rs1712349	0.86[JPT][hapmap]
rs1967723	0.95[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap]
rs2010648	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2038255	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2143950	0.92[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2179890	0.82[CHD][hapmap];0.82[JPT][hapmap];0.84[ASN][1000 genomes]
rs2236167	0.82[CHD][hapmap];0.82[JPT][hapmap]
rs2273158	0.95[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.88[ASN][1000 genomes]
rs2383689	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs2415260	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2415261	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2415262	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28365850	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28397987	0.82[CHD][hapmap]
rs28399702	0.81[EUR][1000 genomes]
rs34286037	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs34678475	0.80[ASN][1000 genomes]
rs34737707	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs35030792	0.93[ASN][1000 genomes]
rs35797365	0.80[ASN][1000 genomes]
rs36112862	0.90[ASN][1000 genomes]
rs3809449	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[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.96[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4456414	0.82[ASN][1000 genomes]
rs4594164	0.82[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.83[MKK][hapmap];0.92[TSI][hapmap];0.83[YRI][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs5014384	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56686328	0.87[ASN][1000 genomes]
rs57075379	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs57725522	0.83[AMR][1000 genomes]
rs58770366	0.84[ASN][1000 genomes]
rs60693825	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61125355	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61136372	0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs62625038	0.99[ASN][1000 genomes]
rs7141292	0.83[ASN][1000 genomes]
rs71421921	0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7142489	0.81[CHB][hapmap];0.82[CHD][hapmap];0.82[JPT][hapmap];0.84[ASN][1000 genomes]
rs7144423	0.91[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7144574	0.83[ASN][1000 genomes]
rs7144617	0.95[CHB][hapmap];0.93[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.94[MKK][hapmap];0.84[TSI][hapmap];0.93[ASN][1000 genomes]
rs7144646	0.80[ASN][1000 genomes]
rs7145474	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7145608	0.87[ASN][1000 genomes]
rs7145883	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7149177	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7153068	0.95[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs7153331	0.92[ASN][1000 genomes]
rs7153550	0.95[CHB][hapmap];0.93[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.82[MKK][hapmap];0.84[TSI][hapmap];0.93[ASN][1000 genomes]
rs7153626	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7154306	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7155696	0.93[ASN][1000 genomes]
rs7156322	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7158416	0.82[JPT][hapmap]
rs7159324	0.85[CEU][hapmap];0.85[CHB][hapmap];1.00[CHD][hapmap];0.91[JPT][hapmap];0.93[MEX][hapmap];0.92[TSI][hapmap];0.80[ASN][1000 genomes]
rs7160160	0.99[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72680650	0.84[ASN][1000 genomes]
rs74046408	0.88[ASN][1000 genomes]
rs799664	0.86[JPT][hapmap]
rs8006583	0.84[ASN][1000 genomes]
rs8007274	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8009093	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8013540	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8015622	0.93[ASN][1000 genomes]
rs8017191	0.88[ASN][1000 genomes]
rs8017225	0.95[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.80[MEX][hapmap];0.94[MKK][hapmap];0.88[ASN][1000 genomes]
rs8018114	0.95[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs8019179	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs932473	0.86[JPT][hapmap]
rs941653	0.92[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9671773	0.82[CHD][hapmap];0.82[JPT][hapmap];0.81[ASN][1000 genomes]
rs9672061	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv901602	chr14:35367889-35571651	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS 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	52 gene(s)	inside rSNPs	diseases
2	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
3	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
4	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
5	nsv901607	chr14:35449467-35540764	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers 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	48 gene(s)	inside rSNPs	diseases
6	nsv901608	chr14:35449467-35571651	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers 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	49 gene(s)	inside rSNPs	diseases
7	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
8	nsv456204	chr14:35466584-35556498	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription 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	26 gene(s)	inside rSNPs	diseases
9	nsv564263	chr14:35466584-35556498	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription 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	26 gene(s)	inside rSNPs	diseases
10	nsv901611	chr14:35470049-35540764	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
11	nsv901612	chr14:35470049-35571651	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers 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	27 gene(s)	inside rSNPs	diseases
12	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
13	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
14	nsv901614	chr14:35485748-35571651	ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers 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
15	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
16	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
17	nsv1043801	chr14:35493065-35539399	Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	26 gene(s)	inside rSNPs	diseases
18	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
19	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
20	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
21	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
22	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

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs8014377	PPP2R3C	cis	lymphoblastoid	seeQTL
rs8014377	PPP2R3C	Cis_1M	lymphoblastoid	RTeQTL
rs8014377	KIAA0391	Cis_1M	lymphoblastoid	RTeQTL
rs8014377	PPP2R3C	cis	Whole Blood	GTEx

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35516400-35537600	Weak transcription	Ovary	ovary
2	chr14:35516400-35552600	Weak transcription	Spleen	Spleen
3	chr14:35516600-35537400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr14:35516800-35536800	Weak transcription	Fetal Kidney	kidney
5	chr14:35516800-35537200	Weak transcription	Fetal Brain Male	brain
6	chr14:35516800-35537600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr14:35516800-35551200	Weak transcription	Right Ventricle	heart
8	chr14:35516800-35552200	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr14:35517200-35547200	Weak transcription	Brain Anterior Caudate	brain
10	chr14:35517400-35537600	Weak transcription	Colon Smooth Muscle	Colon
11	chr14:35517400-35544000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr14:35517400-35578800	Weak transcription	Stomach Mucosa	stomach
13	chr14:35517600-35536400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr14:35517600-35537600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr14:35517600-35537600	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr14:35517600-35545800	Weak transcription	Brain Cingulate Gyrus	brain
17	chr14:35517600-35554400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr14:35517800-35531400	Strong transcription	Fetal Stomach	stomach
19	chr14:35518000-35547400	Weak transcription	GM12878-XiMat	blood
20	chr14:35519400-35532000	Strong transcription	Placenta	Placenta
21	chr14:35519600-35531800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr14:35520200-35550800	Weak transcription	NHLF	lung
23	chr14:35521000-35559400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr14:35521600-35531800	Strong transcription	Liver	Liver
25	chr14:35521600-35540800	Strong transcription	Primary neutrophils fromperipheralblood	blood
26	chr14:35522000-35531800	Strong transcription	Monocytes-CD14+_RO01746	blood
27	chr14:35522000-35532200	Strong transcription	Primary T helper cells fromperipheralblood	blood
28	chr14:35522200-35531600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr14:35522600-35531800	Strong transcription	Primary T helper cells PMA-I stimulated	--
30	chr14:35522800-35531600	Strong transcription	Fetal Muscle Leg	muscle
31	chr14:35523000-35536800	Weak transcription	NHDF-Ad	bronchial
32	chr14:35523400-35537600	Weak transcription	HSMMtube	muscle
33	chr14:35524400-35531400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr14:35524400-35531600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr14:35524400-35532000	Strong transcription	Primary T cells fromperipheralblood	blood
36	chr14:35524800-35531800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr14:35524800-35532000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr14:35525800-35531800	Strong transcription	Primary monocytes fromperipheralblood	blood
39	chr14:35525800-35531800	Strong transcription	Primary B cells from peripheral blood	blood
40	chr14:35525800-35537800	Weak transcription	Psoas Muscle	Psoas
41	chr14:35526200-35531800	Strong transcription	Fetal Intestine Large	intestine
42	chr14:35526200-35532000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr14:35526400-35532000	Strong transcription	Primary B cells from cord blood	blood
44	chr14:35526600-35547200	Weak transcription	Brain Angular Gyrus	brain
45	chr14:35526600-35552400	Weak transcription	Brain Substantia Nigra	brain
46	chr14:35527400-35531400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr14:35527600-35531600	Strong transcription	Stomach Smooth Muscle	stomach
48	chr14:35527600-35532000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr14:35527800-35531400	Strong transcription	Thymus	Thymus
50	chr14:35528200-35547400	Weak transcription	Fetal Thymus	thymus

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