Variant report

Variant	rs12554583
Chromosome Location	chr9:100812569-100812570
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:100743537..100749297-chr9:100805473..100813198,12	K562	blood:
2	chr9:100797529..100799265-chr9:100810758..100812808,2	K562	blood:
3	chr9:100812046..100815738-chr9:100818810..100820929,4	K562	blood:

Variant related genes	Relation type
ENSG00000095380	Chromatin interaction
ENSG00000136938	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1059273	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs16912622	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2224773	0.81[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs2281732	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3739670	0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4300105	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4394518	0.81[AFR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4562446	0.80[AFR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4742716	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4743157	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4743158	0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4743159	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55978131	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58427887	0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6478539	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6478556	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7020081	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7034147	0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7038592	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7041811	0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7046514	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7846772	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7846880	0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7848430	0.81[AFR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7862535	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7867404	0.82[AFR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7869762	0.99[EUR][1000 genomes];0.96[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	nsv482635	chr9:100775549-100953239	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	esv3483159	chr9:100806167-100814815	Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
3	esv3483160	chr9:100806167-100814815	Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs12554583	TRIM14	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:100807600-100818400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr9:100808400-100818400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr9:100808400-100818400	Weak transcription	Fetal Thymus	thymus
4	chr9:100808600-100812800	Enhancers	Primary hematopoietic stem cells	blood
5	chr9:100808600-100816200	Weak transcription	Primary B cells from cord blood	blood
6	chr9:100808800-100818200	Weak transcription	Duodenum Mucosa	Duodenum
7	chr9:100808800-100818400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr9:100809000-100818200	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr9:100809600-100815400	Weak transcription	Primary T cells from cord blood	blood
10	chr9:100810200-100818200	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr9:100810200-100818400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr9:100810600-100812800	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr9:100810800-100818200	Weak transcription	HepG2	liver
14	chr9:100811000-100812600	Genic enhancers	K562	blood
15	chr9:100811200-100813000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr9:100812000-100812800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr9:100812000-100818200	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr9:100812200-100812600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr9:100812400-100816800	Weak transcription	GM12878-XiMat	blood
20	chr9:100812400-100817800	Weak transcription	Primary T helper cells PMA-I stimulated	--
21	chr9:100812400-100818200	Weak transcription	Dnd41	blood
22	chr9:100812400-100818400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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