Variant report

Variant	rs2075614
Chromosome Location	chr5:52345035-52345036
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:52340133..52343071-chr5:52343982..52345648,2	K562	blood:

Extended variants
information (count: 34 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10041086	0.92[ASN][1000 genomes]
rs11741738	0.83[ASN][1000 genomes]
rs1445941	0.92[AMR][1000 genomes]
rs1445942	0.87[AMR][1000 genomes]
rs17298242	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs1900182	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs2287950	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2303124	0.89[AMR][1000 genomes]
rs3212430	0.91[ASN][1000 genomes]
rs3212433	0.91[ASN][1000 genomes]
rs3212435	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3212436	0.92[ASN][1000 genomes]
rs3212446	1.00[ASN][1000 genomes]
rs3212483	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3212537	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3212556	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3212603	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3776788	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3776789	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3797494	0.86[ASN][1000 genomes]
rs3797497	0.91[ASN][1000 genomes]
rs3797500	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62357234	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949005	chr5:52188028-52808229	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv830296	chr5:52209528-52410253	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv880425	chr5:52291279-52345868	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv881652	chr5:52323568-52385312	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv880389	chr5:52333420-52375199	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv881071	chr5:52334774-52362765	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv881359	chr5:52339114-52345868	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv881388	chr5:52339234-52375536	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv881477	chr5:52339843-52345868	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv881148	chr5:52341064-52346527	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv880600	chr5:52342760-52362765	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:52314200-52348000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr5:52324400-52356400	Weak transcription	Brain Anterior Caudate	brain
3	chr5:52328000-52369200	Weak transcription	Fetal Intestine Small	intestine
4	chr5:52328800-52348000	Weak transcription	Fetal Intestine Large	intestine
5	chr5:52333800-52348800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr5:52333800-52369800	Weak transcription	Colonic Mucosa	Colon
7	chr5:52333800-52392600	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr5:52334000-52360800	Weak transcription	Small Intestine	intestine
9	chr5:52334400-52348000	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr5:52334600-52348400	Weak transcription	Lung	lung
11	chr5:52334800-52348000	Weak transcription	Brain Substantia Nigra	brain
12	chr5:52334800-52380800	Weak transcription	Stomach Mucosa	stomach
13	chr5:52334800-52391200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr5:52336400-52399800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr5:52337200-52353400	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr5:52337400-52346400	Weak transcription	Duodenum Mucosa	Duodenum
17	chr5:52337400-52348800	Weak transcription	A549	lung
18	chr5:52337400-52355200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr5:52337400-52369000	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr5:52337400-52370200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr5:52338000-52348200	Weak transcription	Brain Cingulate Gyrus	brain
22	chr5:52341200-52346400	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr5:52341200-52396400	Strong transcription	HMEC	breast
24	chr5:52341400-52345800	Weak transcription	NH-A	brain
25	chr5:52341400-52346400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
26	chr5:52341400-52348600	Weak transcription	Dnd41	blood
27	chr5:52341400-52359000	Weak transcription	NHDF-Ad	bronchial
28	chr5:52341400-52396400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr5:52341800-52347800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr5:52341800-52358800	Weak transcription	Osteobl	bone
31	chr5:52342000-52367200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr5:52342400-52363600	Weak transcription	Rectal Smooth Muscle	rectum
33	chr5:52342600-52383800	Strong transcription	NHEK	skin
34	chr5:52343000-52348600	Weak transcription	Fetal Muscle Leg	muscle
35	chr5:52343000-52359000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr5:52343200-52346800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr5:52343200-52350800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr5:52343200-52351800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr5:52343200-52361800	Strong transcription	HepG2	liver
40	chr5:52343400-52350000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr5:52343400-52357200	Strong transcription	HUVEC	blood vessel
42	chr5:52343400-52392800	Weak transcription	Left Ventricle	heart
43	chr5:52343600-52348000	Weak transcription	Spleen	Spleen
44	chr5:52344000-52348600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr5:52344000-52369200	Weak transcription	Pancreas	Pancrea
46	chr5:52344200-52356000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr5:52344400-52348000	Weak transcription	Brain Hippocampus Middle	brain
48	chr5:52344400-52348200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr5:52344400-52356400	Weak transcription	Esophagus	oesophagus
50	chr5:52344400-52356400	Weak transcription	Gastric	stomach

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