Variant report

Variant	rs227422
Chromosome Location	chr14:70457653-70457654
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr14:70456335-70461656	Hela-S3	cervix:	n/a	n/a
2	POLR2A	chr14:70456315-70459260	Hela-S3	cervix:	n/a	n/a

Variant related genes	Relation type
SMOC1	TF binding region

Extended variants
information (count: 28 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs12050076	0.83[CHB][hapmap];0.91[JPT][hapmap];0.90[ASN][1000 genomes]
rs12433177	0.91[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs1471243	0.83[CHB][hapmap];0.83[JPT][hapmap];0.84[ASN][1000 genomes]
rs17107547	0.83[ASN][1000 genomes]
rs17107592	0.82[JPT][hapmap];0.90[ASN][1000 genomes]
rs182745	0.81[CHB][hapmap]
rs192024	0.86[CHB][hapmap];0.82[ASN][1000 genomes]
rs227412	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.89[AFR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs227416	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs227417	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap]
rs227419	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.98[ASN][1000 genomes]
rs227420	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs227423	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs227424	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs227425	0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs227426	0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs227427	0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs227437	0.83[ASN][1000 genomes]
rs227438	0.99[ASN][1000 genomes]
rs227439	0.99[ASN][1000 genomes]
rs227444	0.91[JPT][hapmap]
rs56031625	0.90[ASN][1000 genomes]
rs61305	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs67294558	0.83[ASN][1000 genomes]
rs7151788	0.83[CHB][hapmap];0.83[JPT][hapmap];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv456336	chr14:70081956-70574149	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
2	nsv565007	chr14:70081956-70574149	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
3	nsv832824	chr14:70320639-70511401	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs227422	SMOC1	cis	Artery Tibial	GTEx

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70439000-70458800	Weak transcription	Gastric	stomach
2	chr14:70439800-70477200	Weak transcription	Spleen	Spleen
3	chr14:70450000-70458600	Weak transcription	Aorta	Aorta
4	chr14:70450600-70464800	Weak transcription	Fetal Stomach	stomach
5	chr14:70450600-70477200	Weak transcription	Fetal Brain Female	brain
6	chr14:70451800-70459200	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr14:70452400-70458400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr14:70452800-70460600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr14:70453000-70464800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr14:70453200-70457800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr14:70453200-70458600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr14:70453200-70462600	Weak transcription	NHEK	skin
13	chr14:70453600-70462600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr14:70454600-70458600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr14:70454800-70460800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr14:70455800-70458600	Enhancers	Liver	Liver
17	chr14:70456400-70457800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr14:70456400-70457800	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr14:70456400-70458600	Enhancers	Brain Germinal Matrix	brain
20	chr14:70456400-70459200	Enhancers	Brain Hippocampus Middle	brain
21	chr14:70456600-70457800	Enhancers	Brain Substantia Nigra	brain
22	chr14:70456800-70459000	Enhancers	Fetal Intestine Large	intestine
23	chr14:70456800-70463800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr14:70456800-70463800	Weak transcription	Pancreas	Pancrea
25	chr14:70457000-70458000	Enhancers	Fetal Brain Male	brain
26	chr14:70457000-70459400	Weak transcription	Hela-S3	cervix
27	chr14:70457200-70457800	Enhancers	Brain Angular Gyrus	brain
28	chr14:70457400-70458200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr14:70457400-70464200	Weak transcription	HepG2	liver

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