Variant report

Variant	rs2899014
Chromosome Location	chr15:41560878-41560879
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:41554916..41558076-chr15:41560482..41563886,4	K562	blood:
2	chr15:41548726..41552355-chr15:41557074..41560902,3	K562	blood:

Variant related genes	Relation type
ENSG00000187446	Chromatin interaction

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10467974	0.82[EUR][1000 genomes]
rs10518718	0.82[EUR][1000 genomes]
rs11549913	0.82[EUR][1000 genomes]
rs16952331	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16971562	0.86[EUR][1000 genomes]
rs16971576	0.88[EUR][1000 genomes]
rs16971647	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16971651	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16971653	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16971654	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16971733	0.93[ASN][1000 genomes]
rs16971734	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16971735	0.91[ASN][1000 genomes]
rs2083238	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2090826	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2118739	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2412607	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2412610	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28417774	0.91[ASN][1000 genomes]
rs28468975	0.91[ASN][1000 genomes]
rs28478807	0.89[ASN][1000 genomes]
rs28626792	0.93[ASN][1000 genomes]
rs28643296	0.82[EUR][1000 genomes]
rs55787465	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs55952963	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs56262456	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs56815966	0.86[EUR][1000 genomes]
rs57009745	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs57896923	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs58060180	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs58322837	0.82[EUR][1000 genomes]
rs58335029	0.82[EUR][1000 genomes]
rs58436082	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs58851405	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs59441380	0.82[EUR][1000 genomes]
rs60789744	0.82[EUR][1000 genomes]
rs6492996	0.90[ASN][1000 genomes]
rs7165551	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7166182	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7167142	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7167498	0.82[EUR][1000 genomes]
rs7168706	0.82[EUR][1000 genomes]
rs7175690	0.82[EUR][1000 genomes]
rs7175800	0.84[EUR][1000 genomes]
rs7176314	0.82[EUR][1000 genomes]
rs74012251	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs74012252	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs74012253	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs74012255	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8023619	0.82[EUR][1000 genomes]
rs8025660	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs8025916	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8029873	0.90[ASN][1000 genomes]
rs8030033	0.83[ASN][1000 genomes]
rs8030683	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8030706	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8030712	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8030732	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8030954	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8031542	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8034073	0.90[ASN][1000 genomes]
rs8036686	0.90[ASN][1000 genomes]
rs8040375	0.82[EUR][1000 genomes]
rs9672272	0.95[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9672309	0.88[EUR][1000 genomes]
rs9972547	0.82[EUR][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	nsv1045455	chr15:41536624-41620534	Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv1044438	chr15:41560160-41745480	Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Enhancers Genic enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41524200-41563800	Weak transcription	Small Intestine	intestine
2	chr15:41524200-41575800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr15:41524800-41563800	Weak transcription	Esophagus	oesophagus
4	chr15:41525200-41575400	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr15:41525800-41575200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr15:41536600-41573600	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr15:41537400-41570800	Weak transcription	Ovary	ovary
8	chr15:41537600-41562800	Weak transcription	Lung	lung
9	chr15:41542800-41572000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr15:41543000-41575200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr15:41545000-41571400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr15:41549200-41575200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr15:41550400-41571400	Weak transcription	Right Ventricle	heart
14	chr15:41550400-41575600	Weak transcription	Fetal Brain Male	brain
15	chr15:41550600-41564200	Weak transcription	NHDF-Ad	bronchial
16	chr15:41551800-41568600	Weak transcription	Fetal Lung	lung
17	chr15:41551800-41570600	Weak transcription	HMEC	breast
18	chr15:41552400-41574600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr15:41552600-41575200	Weak transcription	GM12878-XiMat	blood
20	chr15:41552800-41575800	Weak transcription	Primary hematopoietic stem cells	blood
21	chr15:41553600-41569200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr15:41554600-41573000	Strong transcription	Primary neutrophils fromperipheralblood	blood
23	chr15:41554800-41563400	Strong transcription	Sigmoid Colon	Sigmoid Colon
24	chr15:41555000-41561400	Strong transcription	Fetal Stomach	stomach
25	chr15:41555400-41569000	Weak transcription	Fetal Kidney	kidney
26	chr15:41555400-41570800	Weak transcription	HSMM	muscle
27	chr15:41555600-41564200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr15:41555600-41566600	Weak transcription	Brain Angular Gyrus	brain
29	chr15:41555600-41569000	Weak transcription	Dnd41	blood
30	chr15:41555600-41570600	Strong transcription	Liver	Liver
31	chr15:41556200-41569000	Weak transcription	K562	blood
32	chr15:41556400-41562800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr15:41556400-41563800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr15:41556400-41571600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr15:41556400-41574400	Strong transcription	Monocytes-CD14+_RO01746	blood
36	chr15:41556600-41561600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr15:41556600-41568400	Weak transcription	Stomach Mucosa	stomach
38	chr15:41556600-41568600	Weak transcription	NH-A	brain
39	chr15:41556600-41570800	Weak transcription	Brain Substantia Nigra	brain
40	chr15:41556800-41561800	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr15:41556800-41562400	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr15:41556800-41562400	Weak transcription	A549	lung
43	chr15:41556800-41562600	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr15:41556800-41563600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr15:41556800-41563800	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr15:41556800-41566200	Weak transcription	Pancreas	Pancrea
47	chr15:41556800-41569200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr15:41556800-41569600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr15:41556800-41571600	Weak transcription	Thymus	Thymus
50	chr15:41556800-41571800	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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