Variant report

Variant	rs17106775
Chromosome Location	chr5:146854214-146854215
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:146852615..146855525-chr5:146856529..146860037,3	K562	blood:

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11952079	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11956835	0.85[AFR][1000 genomes]
rs11958380	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13340366	1.00[AMR][1000 genomes]
rs17106746	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59676350	1.00[AMR][1000 genomes]
rs6580475	1.00[AMR][1000 genomes]
rs6885214	1.00[AMR][1000 genomes]
rs6896608	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv5055	chr5:146812672-146857424	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv992285	chr5:146843809-146854803	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:146835800-146858800	Weak transcription	NH-A	brain
2	chr5:146840000-146859200	Weak transcription	NHLF	lung
3	chr5:146842600-146857600	Weak transcription	Osteobl	bone
4	chr5:146844400-146857800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr5:146846600-146858000	Weak transcription	Stomach Smooth Muscle	stomach
6	chr5:146846600-146863600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr5:146849000-146859200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr5:146850600-146858800	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr5:146851400-146856000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr5:146851800-146856000	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr5:146851800-146859400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr5:146851800-146883000	Weak transcription	Psoas Muscle	Psoas
13	chr5:146852600-146855600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr5:146852800-146858000	Weak transcription	Aorta	Aorta
15	chr5:146852800-146858800	Weak transcription	Fetal Stomach	stomach
16	chr5:146853400-146857400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr5:146853400-146858000	Weak transcription	Colon Smooth Muscle	Colon
18	chr5:146853400-146858800	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr5:146853600-146858800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr5:146853800-146854400	Enhancers	Rectal Smooth Muscle	rectum
21	chr5:146853800-146856000	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr5:146853800-146858000	Weak transcription	Ovary	ovary
23	chr5:146854000-146854400	Weak transcription	Brain Germinal Matrix	brain
24	chr5:146854000-146856800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr5:146854200-146854600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr5:146854200-146855200	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr5:146854200-146856000	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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