Variant report

Variant	rs1626422
Chromosome Location	chr12:104940373-104940374
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:104933677..104936423-chr12:104938909..104940435,2	K562	blood:
2	chr12:104939073..104940663-chr12:104943081..104945935,2	K562	blood:
3	chr12:104938513..104940949-chr12:104944779..104947009,2	MCF-7	breast:
4	chr12:104938854..104940380-chr12:104941878..104944270,2	K562	blood:

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs1005922	0.91[AFR][1000 genomes]
rs1553836	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1553839	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1625417	0.83[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs1628116	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1704903	0.82[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs1704905	0.83[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs1704915	0.91[EUR][1000 genomes]
rs1704916	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1704917	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1704918	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1704921	0.90[EUR][1000 genomes]
rs1704922	0.91[EUR][1000 genomes]
rs1704924	0.92[EUR][1000 genomes]
rs1704925	0.92[EUR][1000 genomes]
rs1704926	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1704927	0.92[EUR][1000 genomes]
rs1704929	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1795851	0.90[EUR][1000 genomes]
rs1795852	0.92[EUR][1000 genomes]
rs1795853	0.92[EUR][1000 genomes]
rs1795854	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1795855	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1795856	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1795857	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1795859	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1795861	0.92[EUR][1000 genomes]
rs1795862	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1795864	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1795865	0.89[ASN][1000 genomes]
rs1795867	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1795868	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1795870	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1795872	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1973589	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2055861	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2141861	0.93[AFR][1000 genomes]
rs2665748	0.82[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2706273	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6539157	0.91[AFR][1000 genomes]
rs6539158	0.91[AFR][1000 genomes]
rs6539159	0.91[AFR][1000 genomes]
rs6539160	0.91[AFR][1000 genomes]
rs7968613	0.95[AFR][1000 genomes]
rs907097	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832504	chr12:104853331-105028245	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:104927200-104943000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr12:104929200-104940400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr12:104929200-104942800	Weak transcription	Pancreas	Pancrea
4	chr12:104930200-104957600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr12:104930800-104940800	Weak transcription	Colon Smooth Muscle	Colon
6	chr12:104930800-104943800	Weak transcription	Small Intestine	intestine
7	chr12:104933600-104941600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr12:104935200-104947400	Weak transcription	Aorta	Aorta
9	chr12:104935400-104943000	Weak transcription	A549	lung
10	chr12:104935400-104946400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr12:104935400-104947000	Weak transcription	Primary T cells from cord blood	blood
12	chr12:104935800-104940600	Weak transcription	Brain Anterior Caudate	brain
13	chr12:104935800-104943800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr12:104937000-104941000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr12:104938400-104943200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr12:104938600-104940400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr12:104938600-104940600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr12:104938600-104941200	Enhancers	Primary T cells fromperipheralblood	blood
19	chr12:104938600-104941200	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr12:104938600-104941600	Enhancers	Primary hematopoietic stem cells	blood
21	chr12:104938600-104944000	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr12:104938800-104940400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr12:104938800-104940400	Enhancers	GM12878-XiMat	blood
24	chr12:104938800-104940800	Genic enhancers	Dnd41	blood
25	chr12:104938800-104941200	Enhancers	Placenta	Placenta
26	chr12:104939000-104940400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr12:104939000-104940400	Enhancers	HMEC	breast
28	chr12:104939000-104940800	Enhancers	Primary T helper cells PMA-I stimulated	--
29	chr12:104939000-104941000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
30	chr12:104939000-104941200	Enhancers	Thymus	Thymus
31	chr12:104939000-104941400	Enhancers	Fetal Thymus	thymus
32	chr12:104939000-104941400	Enhancers	Lung	lung
33	chr12:104939000-104941800	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr12:104939000-104942000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr12:104939000-104946600	Enhancers	Primary B cells from peripheral blood	blood
36	chr12:104939200-104941400	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr12:104939200-104943800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr12:104939200-104943800	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr12:104939200-104944800	Weak transcription	Brain Germinal Matrix	brain
40	chr12:104939200-104945400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr12:104939200-104951200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr12:104939400-104940400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr12:104939400-104940400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr12:104939400-104941000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr12:104939400-104945000	Weak transcription	HSMMtube	muscle
46	chr12:104939600-104940600	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr12:104939600-104941600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr12:104939800-104940800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr12:104939800-104941200	Enhancers	Brain Hippocampus Middle	brain
50	chr12:104939800-104943600	Weak transcription	Cortex derived primary cultured neurospheres	brain

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