Variant report

Variant	rs10519278
Chromosome Location	chr15:50789163-50789164
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2)
CpG islands
(count:0)
Chromatin interactive
region (count:3)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr15:50789160-50789169	HepG2	liver:	n/a	n/a
2	POLR2A	chr15:50789049-50789231	MCF-7	breast:	n/a	n/a

No data

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:50646468..50650762-chr15:50786083..50789645,4	K562	blood:
2	chr15:50644389..50649393-chr15:50787180..50791359,7	MCF-7	breast:
3	chr15:50781518..50783831-chr15:50786910..50789444,2	MCF-7	breast:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP50-2	chr15:50789094-50789277	ENSG00000259618.1

No data

Variant related genes	Relation type
USP8	TF binding region
ENSG00000244879	Chromatin interaction
ENSG00000138592	Chromatin interaction
ENSG00000104064	Chromatin interaction

Extended variants
information (count: 106 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:84)

rs_ID	r²[population]
rs10519276	0.94[CEU][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11070774	0.93[CEU][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11070775	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11070777	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11070778	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11070779	0.94[CEU][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11070780	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11070781	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11070785	0.94[CEU][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11070786	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11070787	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11070788	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11630309	0.93[CEU][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11631351	0.94[CEU][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11631398	0.93[CEU][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11632697	0.94[CEU][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11632708	0.93[CEU][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11632823	0.94[CEU][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11633608	0.94[CEU][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11633624	0.93[CEU][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11633765	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11634832	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11637031	1.00[CEU][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11637104	0.94[CEU][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11637111	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11638198	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11638390	0.94[CEU][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12439248	0.93[CEU][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12440152	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs16963723	0.88[YRI][hapmap]
rs17519466	0.94[CEU][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17519536	0.94[CEU][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17597852	0.93[CEU][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17597915	0.94[CEU][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17598061	0.94[CEU][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2414044	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2414045	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3887421	0.88[YRI][hapmap]
rs4774569	0.94[CEU][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4774570	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4774571	0.93[CEU][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4774572	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4775883	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4775884	0.94[CEU][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4775885	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4775886	0.93[CEU][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4775888	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4775889	0.93[CEU][hapmap];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62016938	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62016939	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62016940	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62016942	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62016943	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62016944	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62016945	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62016947	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62019074	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62019075	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62019076	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62019077	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62019078	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62019079	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62019080	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62019082	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62019084	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62019085	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62019087	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62019112	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62019113	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62019115	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62019116	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62019117	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7165464	0.88[CEU][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7168783	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7169778	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7170114	0.94[CEU][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7181536	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7182569	0.94[CEU][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7182980	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7494907	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs8030373	0.93[CEU][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs8037446	0.94[CEU][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs8037553	1.00[CEU][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs934636	0.94[CEU][hapmap];0.87[AMR][1000 genomes];0.91[EUR][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	nsv1045456	chr15:50592472-51019873	Strong transcription Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	121 gene(s)	inside rSNPs	diseases
2	nsv948579	chr15:50645530-51045564	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
3	nsv524613	chr15:50656449-50868779	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv1040717	chr15:50715572-50846521	Strong transcription Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer 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
5	nsv1053966	chr15:50715572-51133186	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
6	nsv542383	chr15:50715572-51133186	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer 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	65 gene(s)	inside rSNPs	diseases
7	nsv1043805	chr15:50715572-51208891	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
8	nsv542384	chr15:50715572-51208891	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
9	nsv1049576	chr15:50744781-50843495	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
10	nsv1047443	chr15:50744781-51647023	Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
11	nsv1051990	chr15:50745814-51133186	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
12	nsv1054970	chr15:50761410-51036625	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
13	nsv457134	chr15:50770868-51184583	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers 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	54 gene(s)	inside rSNPs	diseases
14	nsv471242	chr15:50770868-51184583	Genic enhancers ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
15	nsv569396	chr15:50770868-51184583	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
16	nsv457135	chr15:50770868-51189707	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
17	nsv569397	chr15:50770868-51189707	Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
18	nsv1048621	chr15:50775451-51115535	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer 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 miRNA target site	47 gene(s)	inside rSNPs	diseases
19	nsv1047039	chr15:50782070-51187804	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
20	nsv542385	chr15:50782070-51187804	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
21	nsv457136	chr15:50789125-51294995	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
22	nsv569398	chr15:50789125-51294995	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 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	chr15:50738200-50796800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr15:50741800-50797000	Strong transcription	Primary monocytes fromperipheralblood	blood
3	chr15:50746200-50794400	Strong transcription	Primary neutrophils fromperipheralblood	blood
4	chr15:50750000-50794400	Strong transcription	Primary T cells fromperipheralblood	blood
5	chr15:50751000-50792400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr15:50751000-50796600	Strong transcription	Fetal Thymus	thymus
7	chr15:50754400-50797000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr15:50756600-50795800	Strong transcription	Adipose Nuclei	Adipose
9	chr15:50757000-50796600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr15:50757000-50796800	Strong transcription	Liver	Liver
11	chr15:50761800-50794000	Strong transcription	HUES48 Cell Line	embryonic stem cell
12	chr15:50762400-50794000	Strong transcription	Primary T helper cells PMA-I stimulated	--
13	chr15:50763000-50795800	Strong transcription	HUES6 Cell Line	embryonic stem cell
14	chr15:50763600-50796200	Strong transcription	Primary T cells from cord blood	blood
15	chr15:50768000-50796800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr15:50768200-50794000	Strong transcription	Skeletal Muscle Female	skeletal muscle
17	chr15:50768400-50797000	Strong transcription	Duodenum Mucosa	Duodenum
18	chr15:50768400-50797000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr15:50768800-50796000	Strong transcription	Hela-S3	cervix
20	chr15:50770200-50794000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
21	chr15:50771200-50796000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
22	chr15:50772400-50796000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr15:50772800-50796000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr15:50774200-50797600	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr15:50775600-50795400	Weak transcription	Stomach Mucosa	stomach
26	chr15:50776000-50796000	Strong transcription	Fetal Intestine Large	intestine
27	chr15:50776400-50789400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr15:50776400-50792400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr15:50776400-50796000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr15:50777000-50796000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr15:50777200-50791600	Strong transcription	Fetal Muscle Leg	muscle
32	chr15:50777400-50796000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr15:50777800-50789200	Strong transcription	Fetal Stomach	stomach
34	chr15:50777800-50789600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr15:50778400-50796800	Strong transcription	Primary B cells from cord blood	blood
36	chr15:50778800-50796000	Strong transcription	Rectal Mucosa Donor 29	rectum
37	chr15:50779200-50795400	Strong transcription	Primary T helper cells fromperipheralblood	blood
38	chr15:50779400-50794200	Strong transcription	NH-A	brain
39	chr15:50779400-50796000	Strong transcription	Cortex derived primary cultured neurospheres	brain
40	chr15:50779400-50796800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr15:50779600-50793200	Strong transcription	Rectal Mucosa Donor 31	rectum
42	chr15:50779600-50794000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr15:50779600-50794200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr15:50779800-50793800	Strong transcription	Osteobl	bone
45	chr15:50779800-50795800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr15:50779800-50795800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr15:50780000-50792800	Strong transcription	Primary B cells from peripheral blood	blood
48	chr15:50780000-50796200	Strong transcription	Duodenum Smooth Muscle	Duodenum
49	chr15:50780200-50793400	Strong transcription	Fetal Muscle Trunk	muscle
50	chr15:50780200-50796000	Strong transcription	Placenta	Placenta

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