Variant report

Variant	rs8139244
Chromosome Location	chr22:27842207-27842208
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs10222263	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8137037	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3413125	chr22:27404463-28121577	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
2	nsv459860	chr22:27527005-28181436	Strong transcription Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv588872	chr22:27527005-28181436	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	nsv834167	chr22:27758395-27910985	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv459864	chr22:27760086-27865344	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv588875	chr22:27760086-27865344	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv471192	chr22:27821656-27865344	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs8139244	FABP4	trans	brain	seeQTL

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:27829600-27844000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr22:27832800-27843400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr22:27832800-27844000	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr22:27839000-27843800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr22:27839400-27843600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr22:27839600-27843200	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr22:27839800-27844000	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr22:27840000-27843400	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr22:27840000-27844000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr22:27840200-27843200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr22:27840200-27843400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr22:27840200-27843600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr22:27840200-27843800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr22:27841600-27842400	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr22:27841600-27842600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
16	chr22:27841600-27843800	Enhancers	Fetal Stomach	stomach
17	chr22:27841800-27842400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr22:27841800-27842400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr22:27841800-27842400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr22:27841800-27842400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
21	chr22:27841800-27842400	Bivalent Enhancer	Fetal Muscle Leg	muscle
22	chr22:27841800-27842600	Enhancers	Fetal Intestine Small	intestine
23	chr22:27841800-27842600	Enhancers	Ovary	ovary
24	chr22:27841800-27842600	Enhancers	Spleen	Spleen
25	chr22:27842000-27843000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr22:27842200-27842600	Enhancers	Placenta	Placenta

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