Variant report

Variant	rs8027324
Chromosome Location	chr15:45887684-45887685
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	chr15:45887440..45889797-chr15:45894911..45896652,2	K562	blood:

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10152775	0.86[AMR][1000 genomes]
rs10152792	0.86[AMR][1000 genomes]
rs13376	1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs1442797	1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1529353	0.86[AMR][1000 genomes]
rs1529354	0.93[AMR][1000 genomes]
rs1559892	0.86[AMR][1000 genomes]
rs16944305	0.93[AMR][1000 genomes]
rs16945588	0.96[YRI][hapmap]
rs16945605	0.96[YRI][hapmap]
rs1970374	0.86[AMR][1000 genomes]
rs3858908	0.86[AMR][1000 genomes]
rs4598849	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58055978	0.86[AMR][1000 genomes]
rs58078831	0.86[AMR][1000 genomes]
rs60561729	0.97[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs61169737	0.86[AMR][1000 genomes]
rs61186343	0.86[AMR][1000 genomes]
rs61500896	0.86[AMR][1000 genomes]
rs61756712	0.86[AMR][1000 genomes]
rs6493153	0.86[AMR][1000 genomes]
rs679569	0.96[YRI][hapmap]
rs7163098	0.93[AMR][1000 genomes]
rs7165838	0.80[YRI][hapmap]
rs7165846	0.86[AMR][1000 genomes]
rs7166434	0.93[AMR][1000 genomes]
rs7168313	0.81[AMR][1000 genomes]
rs7168672	0.86[AMR][1000 genomes]
rs7169748	0.84[YRI][hapmap]
rs7170941	0.86[AMR][1000 genomes]
rs7173046	0.86[AMR][1000 genomes]
rs7173983	0.84[YRI][hapmap]
rs7183382	1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs719018	0.86[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs719019	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73414486	0.86[AMR][1000 genomes]
rs73416403	0.86[AMR][1000 genomes]
rs73416407	0.86[AMR][1000 genomes]
rs73416479	0.86[AMR][1000 genomes]
rs73416487	0.86[AMR][1000 genomes]
rs73418308	0.86[AMR][1000 genomes]
rs73418387	0.86[AMR][1000 genomes]
rs73418395	0.86[AMR][1000 genomes]
rs73420403	0.86[AMR][1000 genomes]
rs73420405	0.86[AMR][1000 genomes]
rs73420406	0.86[AMR][1000 genomes]
rs73420408	0.86[AMR][1000 genomes]
rs73420409	0.86[AMR][1000 genomes]
rs73420412	0.86[AMR][1000 genomes]
rs73420415	0.86[AMR][1000 genomes]
rs73420427	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73420437	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73420438	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73420456	0.97[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs7342662	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7495403	0.86[AMR][1000 genomes]
rs751819	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8025600	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8029983	0.86[AMR][1000 genomes]
rs8034420	0.86[AMR][1000 genomes]
rs8042179	0.86[AMR][1000 genomes]
rs8042253	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs8042662	1.00[YRI][hapmap];1.00[AFR][1000 genomes];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	nsv904188	chr15:45801035-45941689	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	nsv904189	chr15:45821158-46298458	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:45880400-45900400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr15:45881000-45888600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr15:45881000-45900200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr15:45881000-45908600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr15:45881000-45908800	Weak transcription	Esophagus	oesophagus
6	chr15:45881200-45888200	Weak transcription	Aorta	Aorta
7	chr15:45881200-45888200	Weak transcription	Fetal Muscle Leg	muscle
8	chr15:45881200-45888200	Weak transcription	Right Ventricle	heart
9	chr15:45881200-45889600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr15:45881200-45890200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr15:45881200-45895800	Weak transcription	Spleen	Spleen
12	chr15:45881200-45898000	Weak transcription	Pancreas	Pancrea
13	chr15:45881200-45899800	Weak transcription	Small Intestine	intestine
14	chr15:45881200-45900200	Weak transcription	Colonic Mucosa	Colon
15	chr15:45881200-45900200	Weak transcription	Gastric	stomach
16	chr15:45881200-45909000	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr15:45881400-45888200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr15:45881400-45898200	Weak transcription	HSMMtube	muscle
19	chr15:45881600-45901800	Weak transcription	Psoas Muscle	Psoas
20	chr15:45881800-45888000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr15:45881800-45888200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr15:45881800-45889000	Weak transcription	A549	lung
23	chr15:45881800-45891800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr15:45881800-45896400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr15:45881800-45896800	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr15:45881800-45898000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr15:45881800-45898200	Weak transcription	Stomach Smooth Muscle	stomach
28	chr15:45881800-45903400	Weak transcription	Brain Substantia Nigra	brain
29	chr15:45881800-45904800	Weak transcription	NHEK	skin
30	chr15:45882000-45888400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr15:45882000-45889400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr15:45882000-45908600	Weak transcription	NHLF	lung
33	chr15:45882200-45898200	Weak transcription	HSMM	muscle
34	chr15:45882400-45888400	Weak transcription	Fetal Kidney	kidney
35	chr15:45883000-45888400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr15:45883000-45888400	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr15:45883000-45898600	Weak transcription	NHDF-Ad	bronchial
38	chr15:45883000-45899000	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr15:45883400-45888200	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr15:45883400-45898000	Weak transcription	Brain Cingulate Gyrus	brain
41	chr15:45883800-45888000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr15:45884000-45888600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr15:45884000-45890200	Strong transcription	Monocytes-CD14+_RO01746	blood
44	chr15:45884000-45896400	Weak transcription	Brain Angular Gyrus	brain
45	chr15:45884000-45898600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
46	chr15:45884200-45887800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr15:45884200-45888200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr15:45884400-45888400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
49	chr15:45884400-45888600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr15:45884400-45889400	Strong transcription	Brain Hippocampus Middle	brain

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