Variant report

Variant	rs3795315
Chromosome Location	chr1:46906793-46906794
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:46905639..46908191-chr1:46929446..46931823,2	K562	blood:
2	chr1:46901693..46905847-chr1:46906304..46911340,7	K562	blood:
3	chr1:46899022..46900983-chr1:46906400..46908672,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAAH-1	chr1:46906766-46906874	NR_045483
2	lnc-FAAH-1	chr1:46906769-46906874	NONHSAT003013

Variant related genes	Relation type
ENSG00000232022	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10890396	0.96[EUR][1000 genomes]
rs11211276	1.00[CEU][hapmap];0.82[JPT][hapmap];0.90[YRI][hapmap];1.00[AFR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11211278	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11211279	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12126376	1.00[AFR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12407178	0.91[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12409747	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2031249	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2281774	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2281775	0.97[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs2404584	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3737742	0.81[YRI][hapmap]
rs4660347	0.97[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs4660929	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4660935	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4660936	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72637962	1.00[AFR][1000 genomes];0.99[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7538292	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7542172	0.84[CHB][hapmap]
rs7549865	0.89[YRI][hapmap]
rs868650	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005189	chr1:46335186-46949309	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv534946	chr1:46335186-46949309	ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
3	esv2761743	chr1:46339858-47026743	Active TSS Weak transcription Bivalent Enhancer Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
4	nsv1001455	chr1:46828004-47326539	Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
5	nsv534950	chr1:46828004-47326539	Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
6	nsv1000562	chr1:46832451-47027044	Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:46872800-46908000	Weak transcription	Right Atrium	heart
2	chr1:46882000-46908200	Weak transcription	Brain Anterior Caudate	brain
3	chr1:46890800-46908200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr1:46899800-46908200	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr1:46901800-46907800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:46902200-46908000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr1:46902600-46908200	Weak transcription	Esophagus	oesophagus
8	chr1:46903800-46908000	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr1:46904000-46908000	Weak transcription	Gastric	stomach
10	chr1:46904000-46908400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr1:46904600-46907600	Weak transcription	K562	blood
12	chr1:46904600-46908200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr1:46905400-46908000	Weak transcription	Spleen	Spleen

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