Variant report

Variant	rs17027826
Chromosome Location	chr4:99526005-99526006
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10005706	1.00[CEU][hapmap]
rs10007752	1.00[CEU][hapmap]
rs10029528	1.00[CEU][hapmap]
rs10030396	1.00[CEU][hapmap]
rs10031904	1.00[CEU][hapmap]
rs10032578	1.00[CEU][hapmap]
rs17027682	1.00[CEU][hapmap]
rs17027707	1.00[CEU][hapmap]
rs17027758	1.00[CEU][hapmap]
rs17027760	1.00[CEU][hapmap]
rs17027831	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17027835	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17027841	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.80[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17027843	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17027845	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17027853	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][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	esv2754250	chr4:99094922-99527122	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv1004181	chr4:99208152-99529576	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:99522200-99532200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
2	chr4:99522400-99526600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
3	chr4:99522400-99528800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
4	chr4:99523000-99527200	Enhancers	Osteobl	bone
5	chr4:99523000-99545000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:99523400-99528400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr4:99523600-99532200	Weak transcription	HMEC	breast
8	chr4:99523800-99527000	Weak transcription	Thymus	Thymus
9	chr4:99524000-99530400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr4:99524000-99535400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr4:99524200-99526800	Enhancers	Muscle Satellite Cultured Cells	--
12	chr4:99524400-99529400	Weak transcription	Primary T cells from cord blood	blood
13	chr4:99524600-99527200	Enhancers	NHLF	lung
14	chr4:99524600-99529800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr4:99524800-99527000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr4:99525000-99527000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr4:99525000-99527800	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr4:99525000-99528000	Weak transcription	Fetal Thymus	thymus
19	chr4:99525200-99526400	Weak transcription	Ovary	ovary
20	chr4:99525200-99530200	Enhancers	Fetal Heart	heart
21	chr4:99525400-99526400	Weak transcription	HSMM	muscle
22	chr4:99525400-99527000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr4:99525400-99527000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr4:99525400-99527000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr4:99525400-99529400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr4:99525400-99529600	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr4:99525400-99530400	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr4:99525400-99531000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr4:99525400-99533200	Weak transcription	Fetal Lung	lung
30	chr4:99525600-99526200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
31	chr4:99525600-99526400	Weak transcription	Fetal Brain Male	brain
32	chr4:99525600-99527000	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr4:99525600-99527000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr4:99525600-99527200	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr4:99525600-99527400	Enhancers	NHDF-Ad	bronchial
36	chr4:99525600-99527600	Enhancers	Brain Germinal Matrix	brain
37	chr4:99525600-99528200	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr4:99525600-99528400	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr4:99525600-99529400	Weak transcription	Brain Angular Gyrus	brain
40	chr4:99525600-99529400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr4:99525800-99526800	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr4:99525800-99527000	Weak transcription	Fetal Brain Female	brain
43	chr4:99525800-99527200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr4:99525800-99527200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr4:99525800-99527400	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr4:99525800-99527600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr4:99525800-99527600	Enhancers	Brain Hippocampus Middle	brain
48	chr4:99525800-99528000	Enhancers	Brain Cingulate Gyrus	brain
49	chr4:99525800-99529400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
50	chr4:99525800-99529400	Weak transcription	Brain Substantia Nigra	brain

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