Variant report

Variant	rs16841653
Chromosome Location	chr3:99436570-99436571
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	chr3:99429413..99432457-chr3:99433966..99437540,3	K562	blood:

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs16841650	1.00[LWK][hapmap];0.87[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs16841712	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs17778804	1.00[ASW][hapmap];1.00[YRI][hapmap]
rs2035400	1.00[YRI][hapmap]
rs6762809	1.00[ASW][hapmap];1.00[YRI][hapmap]
rs6772519	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap]
rs6805703	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap]
rs6808420	1.00[YRI][hapmap]
rs7611313	1.00[ASW][hapmap];1.00[YRI][hapmap]
rs7612083	1.00[YRI][hapmap]
rs7612089	1.00[YRI][hapmap]
rs7619738	1.00[YRI][hapmap]
rs7626214	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap]
rs9756455	1.00[YRI][hapmap]
rs9824017	1.00[YRI][hapmap]
rs9843372	1.00[YRI][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877217	chr3:99418950-99496351	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:99411400-99439600	Weak transcription	NHEK	skin
2	chr3:99423800-99440000	Weak transcription	Adipose Nuclei	Adipose
3	chr3:99426600-99439800	Weak transcription	NHLF	lung
4	chr3:99428000-99439600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr3:99428200-99436800	Weak transcription	Ovary	ovary
6	chr3:99428200-99439800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr3:99428200-99442800	Weak transcription	Aorta	Aorta
8	chr3:99428400-99439600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr3:99433400-99437200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr3:99433600-99449200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr3:99434000-99440000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr3:99435800-99437200	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr3:99435800-99438200	Weak transcription	HUVEC	blood vessel
14	chr3:99435800-99439400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr3:99435800-99440600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr3:99436000-99436800	Weak transcription	NHDF-Ad	bronchial
17	chr3:99436000-99438200	Weak transcription	HSMM	muscle
18	chr3:99436000-99439000	Weak transcription	NH-A	brain
19	chr3:99436000-99439800	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr3:99436000-99440000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr3:99436200-99436800	Weak transcription	Osteobl	bone
22	chr3:99436400-99438200	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr3:99436400-99439800	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr3:99436400-99439800	Weak transcription	HSMMtube	muscle
25	chr3:99436400-99440400	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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