Variant report

Variant	rs2625183
Chromosome Location	chr5:16926755-16926756
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	chr5:16925356..16927728-chr5:16934819..16936878,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000145555	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs13354237	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2016972	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2016983	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2016997	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2170642	0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2217341	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2434960	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2434962	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2449479	0.88[AFR][1000 genomes];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2454879	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2562351	0.87[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs2562361	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2562362	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2562363	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2562364	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2562365	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2562366	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2562367	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2625177	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs2625178	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2625179	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2625180	0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2625181	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2625182	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2625184	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2625185	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2625186	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2625187	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2625188	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2625191	0.81[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs2650457	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2650458	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2650459	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs29453	0.83[ASN][1000 genomes]
rs31452	0.87[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs31453	0.85[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs31464	0.90[ASN][1000 genomes]
rs40984	0.85[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs922881	0.86[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025225	chr5:16714512-17234866	Enhancers Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv1015247	chr5:16748966-17133274	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	esv2762500	chr5:16815489-16952565	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
4	nsv880277	chr5:16829442-17316288	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
5	esv3485757	chr5:16856475-16966851	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
6	esv3485758	chr5:16856475-16966851	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16902200-16930000	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr5:16904400-16933200	Weak transcription	Fetal Stomach	stomach
3	chr5:16914000-16931600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr5:16914000-16933200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:16914200-16930200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr5:16914600-16934400	Weak transcription	Psoas Muscle	Psoas
7	chr5:16916000-16930800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr5:16918400-16930400	Weak transcription	HSMMtube	muscle
9	chr5:16918600-16930400	Weak transcription	HSMM	muscle
10	chr5:16918600-16930600	Weak transcription	NH-A	brain
11	chr5:16919200-16930000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr5:16919200-16931600	Weak transcription	HMEC	breast
13	chr5:16919600-16929600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr5:16920800-16930800	Weak transcription	Fetal Kidney	kidney
15	chr5:16921000-16927800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr5:16921000-16927800	Weak transcription	NHEK	skin
17	chr5:16921400-16927800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr5:16921600-16929400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr5:16922000-16927600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr5:16922000-16930200	Weak transcription	NHDF-Ad	bronchial
21	chr5:16922000-16930600	Weak transcription	NHLF	lung
22	chr5:16922000-16931400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr5:16922000-16931600	Weak transcription	Osteobl	bone
24	chr5:16923200-16930800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr5:16923200-16932400	Weak transcription	Gastric	stomach
26	chr5:16924400-16927600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr5:16924400-16930800	Weak transcription	Lung	lung
28	chr5:16924600-16929800	Weak transcription	Fetal Lung	lung
29	chr5:16924600-16930200	Weak transcription	Fetal Intestine Large	intestine
30	chr5:16924600-16931600	Weak transcription	Fetal Intestine Small	intestine
31	chr5:16924800-16930000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr5:16924800-16930200	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr5:16924800-16930600	Weak transcription	Duodenum Mucosa	Duodenum
34	chr5:16924800-16930600	Weak transcription	Small Intestine	intestine
35	chr5:16925000-16930200	Weak transcription	Fetal Muscle Leg	muscle
36	chr5:16925400-16926800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr5:16925400-16926800	Enhancers	Pancreas	Pancrea
38	chr5:16925600-16928200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr5:16925800-16927600	Enhancers	A549	lung
40	chr5:16926000-16930200	Weak transcription	Ovary	ovary
41	chr5:16926200-16927600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr5:16926200-16929600	Weak transcription	Stomach Mucosa	stomach
43	chr5:16926200-16933200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr5:16926400-16927200	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr5:16926600-16930000	Weak transcription	HUVEC	blood vessel

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