Variant report

Variant	rs72851735
Chromosome Location	chr17:67024935-67024936
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:67017236..67020123-chr17:67021606..67025957,3	K562	blood:

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs61697543	1.00[AMR][1000 genomes]
rs7217005	1.00[AMR][1000 genomes]
rs72844578	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72844581	1.00[AMR][1000 genomes]
rs72851720	0.87[AMR][1000 genomes]
rs72851722	0.87[AMR][1000 genomes]
rs72851723	1.00[AMR][1000 genomes]
rs72851731	1.00[AMR][1000 genomes]
rs72851733	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72851734	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8068047	0.87[AMR][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	nsv1067334	chr17:66695039-67221585	Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
2	nsv543411	chr17:66695039-67221585	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
3	nsv833526	chr17:66980758-67137034	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:66977800-67027400	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr17:67000200-67044200	Weak transcription	Right Ventricle	heart
3	chr17:67003800-67030600	Weak transcription	Brain Angular Gyrus	brain
4	chr17:67007600-67042200	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr17:67008400-67044000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr17:67009200-67043200	Weak transcription	Pancreas	Pancrea
7	chr17:67009400-67044000	Weak transcription	Colon Smooth Muscle	Colon
8	chr17:67010400-67041200	Weak transcription	NHDF-Ad	bronchial
9	chr17:67011400-67027200	Weak transcription	Fetal Muscle Trunk	muscle
10	chr17:67011400-67032600	Weak transcription	Fetal Muscle Leg	muscle
11	chr17:67011600-67039200	Weak transcription	Left Ventricle	heart
12	chr17:67014000-67044200	Weak transcription	Psoas Muscle	Psoas
13	chr17:67016200-67025800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr17:67022400-67032000	Strong transcription	Skeletal Muscle Female	skeletal muscle
15	chr17:67023200-67027000	Weak transcription	Ovary	ovary
16	chr17:67023200-67033000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr17:67024000-67025600	Weak transcription	Adipose Nuclei	Adipose
18	chr17:67024000-67039200	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr17:67024200-67043200	Weak transcription	Fetal Lung	lung
20	chr17:67024400-67027000	Weak transcription	Liver	Liver
21	chr17:67024800-67026800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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