Variant report

Variant	rs1506786
Chromosome Location	chr1:92016912-92016913
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:92011701..92014706-chr1:92015449..92018915,4	K562	blood:

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs17879470	1.00[AMR][1000 genomes]
rs2219395	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34011609	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4658227	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs471904	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs516593	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs517460	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs519523	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs529778	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs582636	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs590931	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs594834	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59894382	1.00[AMR][1000 genomes]
rs6661449	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72952916	1.00[AMR][1000 genomes]
rs72970317	1.00[AMR][1000 genomes]
rs72970324	1.00[AMR][1000 genomes]
rs72970332	1.00[AMR][1000 genomes]
rs72970344	1.00[AMR][1000 genomes]
rs72970362	1.00[AMR][1000 genomes]
rs72970365	1.00[AMR][1000 genomes]
rs72970366	1.00[AMR][1000 genomes]
rs72970375	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	nsv949516	chr1:91644418-92109261	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv1009560	chr1:91897078-92270781	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92003600-92018000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr1:92010600-92017000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr1:92011400-92018200	Weak transcription	Right Atrium	heart
4	chr1:92012000-92027400	Enhancers	Primary T helper cells fromperipheralblood	blood
5	chr1:92012800-92018800	Weak transcription	Placenta	Placenta
6	chr1:92013600-92017000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr1:92013800-92018000	Weak transcription	Colon Smooth Muscle	Colon
8	chr1:92013800-92018200	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr1:92014200-92018200	Weak transcription	Small Intestine	intestine
10	chr1:92014600-92020000	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr1:92014600-92020400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr1:92014800-92017000	Enhancers	Primary T cells fromperipheralblood	blood
13	chr1:92014800-92020600	Weak transcription	Fetal Stomach	stomach
14	chr1:92014800-92021400	Weak transcription	Fetal Heart	heart
15	chr1:92014800-92028000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr1:92015000-92018200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr1:92015000-92018800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
18	chr1:92015000-92025600	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr1:92015200-92018400	Weak transcription	Spleen	Spleen
20	chr1:92015200-92020400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr1:92015200-92020600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr1:92015200-92027800	Enhancers	Primary T helper naive cells from peripheral blood	blood
23	chr1:92015400-92017200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr1:92015400-92017200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr1:92015600-92019800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr1:92015600-92020000	Weak transcription	Primary T cells from cord blood	blood
27	chr1:92015600-92020600	Weak transcription	Dnd41	blood
28	chr1:92016400-92017000	Enhancers	GM12878-XiMat	blood
29	chr1:92016400-92022200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr1:92016600-92018200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr1:92016600-92023800	Enhancers	Primary T regulatory cells fromperipheralblood	blood

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