Variant report

Variant	rs61474216
Chromosome Location	chr2:48048162-48048163
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs11885260	1.00[AMR][1000 genomes]
rs17036985	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17037025	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56064148	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72876821	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998096	chr2:47939614-48131697	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv1009769	chr2:47972642-48509765	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	nsv535680	chr2:47972642-48509765	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
4	nsv930955	chr2:48040218-48121218	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:48012600-48065000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:48016200-48050400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
3	chr2:48017000-48049400	Strong transcription	Fetal Intestine Large	intestine
4	chr2:48017200-48053200	Strong transcription	HUES48 Cell Line	embryonic stem cell
5	chr2:48017400-48049600	Strong transcription	Primary T cells fromperipheralblood	blood
6	chr2:48021200-48051600	Strong transcription	Placenta	Placenta
7	chr2:48021400-48067600	Strong transcription	Dnd41	blood
8	chr2:48021600-48067000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr2:48022200-48050200	Strong transcription	Rectal Mucosa Donor 29	rectum
10	chr2:48022800-48049200	Strong transcription	Rectal Mucosa Donor 31	rectum
11	chr2:48022800-48050000	Strong transcription	HUVEC	blood vessel
12	chr2:48023200-48065000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr2:48030200-48067600	Strong transcription	HUES64 Cell Line	embryonic stem cell
14	chr2:48030400-48067000	Strong transcription	HUES6 Cell Line	embryonic stem cell
15	chr2:48030800-48049400	Strong transcription	Fetal Muscle Trunk	muscle
16	chr2:48030800-48049600	Strong transcription	Duodenum Mucosa	Duodenum
17	chr2:48030800-48067000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr2:48030800-48067000	Strong transcription	Fetal Thymus	thymus
19	chr2:48031000-48049400	Strong transcription	Fetal Brain Female	brain
20	chr2:48031000-48053000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr2:48031000-48067000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr2:48031000-48067000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr2:48031000-48067200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr2:48031200-48048600	Strong transcription	K562	blood
25	chr2:48031200-48049600	Strong transcription	Primary B cells from cord blood	blood
26	chr2:48031200-48053800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr2:48031200-48065800	Strong transcription	Liver	Liver
28	chr2:48031200-48066800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
29	chr2:48031400-48050000	Strong transcription	Cortex derived primary cultured neurospheres	brain
30	chr2:48031400-48051400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr2:48031400-48060600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr2:48031400-48066800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr2:48031400-48067000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr2:48031400-48067800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr2:48031400-48067800	Strong transcription	Primary T helper cells PMA-I stimulated	--
36	chr2:48031400-48072600	Weak transcription	Stomach Mucosa	stomach
37	chr2:48032000-48058000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
38	chr2:48032200-48067000	Strong transcription	Primary T helper cells fromperipheralblood	blood
39	chr2:48032400-48066800	Strong transcription	Primary neutrophils fromperipheralblood	blood
40	chr2:48032400-48068400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr2:48033600-48067000	Strong transcription	Primary monocytes fromperipheralblood	blood
42	chr2:48033800-48067400	Strong transcription	Monocytes-CD14+_RO01746	blood
43	chr2:48036000-48067800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr2:48037600-48049400	Strong transcription	Fetal Muscle Leg	muscle
45	chr2:48038000-48061200	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr2:48038200-48051800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr2:48038200-48071400	Weak transcription	Fetal Heart	heart
48	chr2:48038400-48066600	Strong transcription	Adipose Nuclei	Adipose
49	chr2:48038600-48054400	Strong transcription	HepG2	liver
50	chr2:48039200-48049600	Strong transcription	Skeletal Muscle Female	skeletal muscle

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