Variant report

Variant	rs13190955
Chromosome Location	chr6:163757025-163757026
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:163751984..163754408-chr6:163756474..163759819,3	K562	blood:
2	chr6:163755571..163762023-chr6:163831891..163837157,6	MCF-7	breast:
3	chr6:163751446..163754906-chr6:163755143..163760328,4	K562	blood:

Variant related genes	Relation type
ENSG00000112531	Chromatin interaction
ENSG00000270419	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs12527711	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12529440	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13196281	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13211088	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13211237	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13214515	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13218916	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17393817	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34418608	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56167893	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs56212042	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6921139	0.84[ASN][1000 genomes]
rs6925566	0.84[ASN][1000 genomes]
rs6928196	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71569403	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9458808	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9458809	0.88[AMR][1000 genomes];0.89[EUR][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	nsv932127	chr6:163000261-163950870	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1022610	chr6:163591786-163814041	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv605188	chr6:163697439-163772096	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv534621	chr6:163731741-163950870	Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	esv1803546	chr6:163749552-163757127	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163745200-163767000	Enhancers	Brain Inferior Temporal Lobe	brain
2	chr6:163745600-163773600	Enhancers	Brain Substantia Nigra	brain
3	chr6:163746600-163759400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:163746600-163759800	Enhancers	Brain Anterior Caudate	brain
5	chr6:163746600-163759800	Enhancers	Brain Hippocampus Middle	brain
6	chr6:163746600-163764400	Enhancers	Brain Cingulate Gyrus	brain
7	chr6:163751600-163759200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:163751600-163759400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr6:163752600-163758200	Enhancers	Adipose Nuclei	Adipose
10	chr6:163753600-163759000	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr6:163754200-163757400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr6:163754200-163760000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr6:163754400-163758200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr6:163754400-163760400	Enhancers	Fetal Muscle Trunk	muscle
15	chr6:163754600-163760200	Enhancers	Left Ventricle	heart
16	chr6:163754600-163760800	Enhancers	Fetal Muscle Leg	muscle
17	chr6:163754800-163757200	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr6:163755000-163757600	Enhancers	Fetal Lung	lung
19	chr6:163755000-163757800	Enhancers	Placenta	Placenta
20	chr6:163755000-163758400	Enhancers	Right Ventricle	heart
21	chr6:163755000-163760200	Enhancers	Lung	lung
22	chr6:163755200-163757200	Enhancers	Fetal Heart	heart
23	chr6:163755200-163758000	Enhancers	Spleen	Spleen
24	chr6:163755200-163758200	Enhancers	Right Atrium	heart
25	chr6:163755200-163758400	Enhancers	Psoas Muscle	Psoas
26	chr6:163755400-163759800	Enhancers	Brain Angular Gyrus	brain
27	chr6:163755800-163758000	Enhancers	HUVEC	blood vessel
28	chr6:163755800-163759400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr6:163756000-163757200	Enhancers	Colon Smooth Muscle	Colon
30	chr6:163756000-163757600	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr6:163756000-163757800	Enhancers	Duodenum Smooth Muscle	Duodenum
32	chr6:163756000-163757800	Enhancers	Stomach Smooth Muscle	stomach
33	chr6:163756000-163758000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr6:163756000-163758200	Bivalent Enhancer	Fetal Stomach	stomach
35	chr6:163756000-163758200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
36	chr6:163756200-163757200	Enhancers	Fetal Thymus	thymus
37	chr6:163756200-163757800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr6:163756200-163758000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr6:163756200-163759800	Weak transcription	Fetal Kidney	kidney
40	chr6:163756400-163757400	Enhancers	Ovary	ovary
41	chr6:163756400-163757600	Enhancers	Primary hematopoietic stem cells	blood
42	chr6:163756400-163759000	Weak transcription	Esophagus	oesophagus
43	chr6:163756600-163757200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr6:163756600-163757200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr6:163756600-163757200	Enhancers	Muscle Satellite Cultured Cells	--
46	chr6:163756600-163757400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr6:163756600-163757400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr6:163756600-163757400	Enhancers	Colonic Mucosa	Colon
49	chr6:163756600-163757400	Enhancers	Fetal Intestine Small	intestine
50	chr6:163756800-163757200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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