Variant report

Variant	rs73748687
Chromosome Location	chr5:14218151-14218152
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:14216973..14219606-chr5:14236627..14239606,2	MCF-7	breast:
2	chr5:14218014..14220716-chr5:14221301..14224995,3	MCF-7	breast:
3	chr5:14217173..14219209-chr5:14242160..14244276,2	MCF-7	breast:
4	chr5:14142853..14145531-chr5:14217598..14220636,3	MCF-7	breast:
5	chr5:14212915..14215891-chr5:14216884..14220454,4	MCF-7	breast:
6	chr5:14217255..14219345-chr5:14264896..14267843,2	MCF-7	breast:
7	chr5:14216252..14219175-chr5:14227535..14229395,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000038382	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs16903265	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs16903269	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16903270	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16903321	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16903322	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16903350	0.80[AFR][1000 genomes]
rs56140232	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59499572	0.80[AFR][1000 genomes]
rs59619763	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61011080	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61509800	0.80[AFR][1000 genomes]
rs61665335	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73748679	0.91[AFR][1000 genomes]
rs73748685	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73748688	0.98[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73751311	0.83[AFR][1000 genomes]
rs73751318	0.80[AFR][1000 genomes]
rs73751327	0.80[AFR][1000 genomes]
rs7703674	0.80[AFR][1000 genomes]
rs7705426	0.80[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534466	chr5:13847044-14246208	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
2	esv1830112	chr5:14147376-14222601	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv1825924	chr5:14147376-14270450	Flanking Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv830209	chr5:14154989-14301758	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv948355	chr5:14160447-14395478	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:14205400-14218800	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr5:14206800-14218800	Weak transcription	Esophagus	oesophagus
3	chr5:14212400-14218400	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr5:14212400-14219000	Genic enhancers	HSMM	muscle
5	chr5:14213000-14223600	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr5:14213200-14218200	Enhancers	Thymus	Thymus
7	chr5:14214400-14218800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr5:14214600-14218200	Weak transcription	Fetal Kidney	kidney
9	chr5:14214800-14220800	Enhancers	HepG2	liver
10	chr5:14215000-14222600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr5:14215200-14219600	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr5:14215200-14221000	Enhancers	NHDF-Ad	bronchial
13	chr5:14215200-14222800	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr5:14215400-14220400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr5:14215400-14221600	Enhancers	GM12878-XiMat	blood
16	chr5:14215600-14218200	Enhancers	Fetal Thymus	thymus
17	chr5:14215600-14223400	Enhancers	Sigmoid Colon	Sigmoid Colon
18	chr5:14216000-14218800	Enhancers	A549	lung
19	chr5:14216000-14218800	Enhancers	Osteobl	bone
20	chr5:14216000-14219200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr5:14216000-14219800	Enhancers	HMEC	breast
22	chr5:14216000-14220000	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr5:14216000-14220600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr5:14216000-14221600	Enhancers	Muscle Satellite Cultured Cells	--
25	chr5:14216000-14221600	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr5:14216000-14222000	Enhancers	Primary B cells from peripheral blood	blood
27	chr5:14216000-14223800	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr5:14216000-14225800	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr5:14216200-14218800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr5:14216200-14218800	Enhancers	Rectal Smooth Muscle	rectum
31	chr5:14216200-14219600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr5:14216200-14220600	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr5:14216200-14221000	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr5:14216200-14221400	Enhancers	Small Intestine	intestine
35	chr5:14216200-14221600	Enhancers	Fetal Heart	heart
36	chr5:14216200-14221800	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr5:14216200-14221800	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr5:14216400-14221600	Enhancers	HSMMtube	muscle
39	chr5:14216400-14222600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr5:14216600-14218600	Enhancers	Colonic Mucosa	Colon
41	chr5:14216600-14218800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr5:14216600-14219800	Enhancers	Fetal Stomach	stomach
43	chr5:14216600-14222000	Enhancers	Left Ventricle	heart
44	chr5:14216800-14219000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr5:14216800-14219800	Enhancers	Placenta	Placenta
46	chr5:14216800-14220000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr5:14216800-14221200	Enhancers	Fetal Muscle Leg	muscle
48	chr5:14216800-14221400	Enhancers	Duodenum Mucosa	Duodenum
49	chr5:14216800-14221800	Enhancers	Fetal Intestine Small	intestine
50	chr5:14216800-14222000	Enhancers	Adipose Nuclei	Adipose

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links