Variant report

Variant	rs6137837
Chromosome Location	chr20:23108362-23108363
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr20:23088338..23089890-chr20:23107180..23109300,2	MCF-7	breast:
2	chr20:23106418..23109174-chr20:23126935..23129451,2	K562	blood:
3	chr20:23103723..23106528-chr20:23107935..23111054,5	K562	blood:
4	chr20:23103623..23110911-chr20:23111294..23114699,12	K562	blood:

Variant related genes	Relation type
ENSG00000233746	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs13045861	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6083009	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6083010	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6083012	0.87[AMR][1000 genomes]
rs6132568	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6137840	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs844828	0.85[EUR][1000 genomes]
rs844829	0.85[EUR][1000 genomes]
rs946369	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[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	esv2758516	chr20:23029404-23173240	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
2	esv2758789	chr20:23029404-23179604	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23085800-23114600	Enhancers	Placenta	Placenta
2	chr20:23097600-23110200	Weak transcription	Pancreas	Pancrea
3	chr20:23100200-23111200	Enhancers	Fetal Thymus	thymus
4	chr20:23101200-23109400	Weak transcription	Liver	Liver
5	chr20:23101800-23109200	Weak transcription	Right Ventricle	heart
6	chr20:23102000-23114000	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr20:23103200-23109800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr20:23104600-23111600	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr20:23105000-23109800	Enhancers	Brain Hippocampus Middle	brain
10	chr20:23105200-23109200	Weak transcription	Fetal Lung	lung
11	chr20:23105200-23111000	Enhancers	Fetal Muscle Leg	muscle
12	chr20:23105600-23108600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr20:23105800-23108400	Enhancers	Lung	lung
14	chr20:23105800-23108600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr20:23105800-23110000	Enhancers	Primary B cells from cord blood	blood
16	chr20:23105800-23110000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr20:23105800-23111000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr20:23106000-23112000	Enhancers	Adipose Nuclei	Adipose
19	chr20:23106200-23110200	Weak transcription	Fetal Intestine Small	intestine
20	chr20:23106400-23108400	Enhancers	Fetal Stomach	stomach
21	chr20:23106400-23108600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr20:23106400-23109600	Enhancers	Primary T cells fromperipheralblood	blood
23	chr20:23106600-23109800	Weak transcription	Right Atrium	heart
24	chr20:23106600-23111000	Enhancers	Spleen	Spleen
25	chr20:23106600-23112600	Weak transcription	Fetal Intestine Large	intestine
26	chr20:23106800-23109800	Weak transcription	Colonic Mucosa	Colon
27	chr20:23106800-23110800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr20:23106800-23114400	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr20:23106800-23116400	Weak transcription	Esophagus	oesophagus
30	chr20:23107000-23108600	Weak transcription	Brain Substantia Nigra	brain
31	chr20:23107200-23109200	Weak transcription	Duodenum Mucosa	Duodenum
32	chr20:23107200-23110800	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr20:23107400-23108800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr20:23107400-23109200	Weak transcription	Fetal Heart	heart
35	chr20:23107600-23108800	Weak transcription	Left Ventricle	heart
36	chr20:23107600-23109200	Weak transcription	K562	blood
37	chr20:23107600-23110000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr20:23107600-23110000	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr20:23107600-23111200	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr20:23107600-23113200	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr20:23107800-23108800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr20:23107800-23111000	Enhancers	Dnd41	blood
43	chr20:23108000-23109400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr20:23108000-23110000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
45	chr20:23108000-23111000	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr20:23108200-23108400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
47	chr20:23108200-23109600	Weak transcription	Primary hematopoietic stem cells	blood
48	chr20:23108200-23110000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
49	chr20:23108200-23110600	Weak transcription	Psoas Muscle	Psoas

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