Variant report

Variant	rs17603755
Chromosome Location	chr2:11939018-11939019
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:11926063..11932602-chr2:11933029..11939967,9	K562	blood:
2	chr2:11935812..11939126-chr2:11941117..11946129,5	K562	blood:

Variant related genes	Relation type
ENSG00000134324	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10520097	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11679358	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11690125	0.90[CEU][hapmap];1.00[CHB][hapmap];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11694797	0.91[CEU][hapmap];0.86[EUR][1000 genomes]
rs11695081	1.00[CEU][hapmap]
rs11695610	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17603197	0.82[CEU][hapmap];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2289193	0.90[CEU][hapmap]
rs2358125	0.84[AMR][1000 genomes]
rs3762583	0.83[CEU][hapmap];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4129758	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62113359	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62114960	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010506	chr2:11430965-12057286	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
2	nsv535585	chr2:11430965-12057286	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
3	nsv1003899	chr2:11789374-12248081	Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11916800-11961200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr2:11919400-11940400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr2:11919400-11943400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr2:11919400-11961800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr2:11919600-11940800	Strong transcription	Left Ventricle	heart
6	chr2:11919600-11940800	Strong transcription	NHEK	skin
7	chr2:11919600-11968400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr2:11919800-11939600	Strong transcription	Fetal Thymus	thymus
9	chr2:11919800-11940000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr2:11919800-11940000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr2:11919800-11940400	Strong transcription	Dnd41	blood
12	chr2:11919800-11940600	Strong transcription	Primary monocytes fromperipheralblood	blood
13	chr2:11919800-11940600	Strong transcription	Placenta	Placenta
14	chr2:11919800-11948400	Strong transcription	Primary T helper cells PMA-I stimulated	--
15	chr2:11919800-11949000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr2:11919800-11957600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr2:11919800-11957800	Strong transcription	Primary T cells from cord blood	blood
18	chr2:11919800-11959200	Strong transcription	Liver	Liver
19	chr2:11919800-11960400	Weak transcription	Stomach Mucosa	stomach
20	chr2:11919800-11963200	Strong transcription	Primary B cells from peripheral blood	blood
21	chr2:11919800-11967600	Strong transcription	Primary T helper cells fromperipheralblood	blood
22	chr2:11919800-11968400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr2:11919800-11968800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr2:11920000-11940400	Strong transcription	HMEC	breast
25	chr2:11920000-11941000	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr2:11920200-11939600	Strong transcription	Primary T helper naive cells from peripheral blood	blood
27	chr2:11920200-11940800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr2:11920400-11939800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr2:11920400-11940400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr2:11920400-11940400	Strong transcription	Gastric	stomach
31	chr2:11924600-11947800	Weak transcription	Right Atrium	heart
32	chr2:11925200-11940200	Strong transcription	Rectal Mucosa Donor 29	rectum
33	chr2:11925200-11941000	Strong transcription	Ovary	ovary
34	chr2:11925200-11949400	Strong transcription	Duodenum Mucosa	Duodenum
35	chr2:11925200-11964800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr2:11925200-11968600	Strong transcription	NHLF	lung
37	chr2:11925400-11940800	Strong transcription	Stomach Smooth Muscle	stomach
38	chr2:11925600-11939200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr2:11925600-11940400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr2:11925600-11940600	Strong transcription	Brain Hippocampus Middle	brain
41	chr2:11925600-11946400	Strong transcription	Skeletal Muscle Female	skeletal muscle
42	chr2:11925800-11968600	Strong transcription	Primary T cells fromperipheralblood	blood
43	chr2:11926200-11948600	Strong transcription	Primary hematopoietic stem cells	blood
44	chr2:11926400-11940400	Strong transcription	HUES6 Cell Line	embryonic stem cell
45	chr2:11926600-11941200	Strong transcription	Rectal Mucosa Donor 31	rectum
46	chr2:11926800-11940400	Strong transcription	Duodenum Smooth Muscle	Duodenum
47	chr2:11928400-11948800	Strong transcription	HUVEC	blood vessel
48	chr2:11929600-11944600	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr2:11929800-11947000	Weak transcription	Fetal Heart	heart
50	chr2:11929800-11951200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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