Variant report

Variant	rs12610110
Chromosome Location	chr19:35650969-35650970
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	chr19:35650702..35653470-chr19:35739367..35741084,2	K562	blood:

Variant related genes	Relation type
ENSG00000105699	Chromatin interaction

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10410144	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12608443	0.85[EUR][1000 genomes]
rs16970012	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16970014	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4805109	0.85[EUR][1000 genomes]
rs56115369	0.85[EUR][1000 genomes]
rs56263489	0.80[EUR][1000 genomes]
rs56347218	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56821088	0.85[EUR][1000 genomes]
rs59086958	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61709658	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	nsv432045	chr19:35556260-36520760	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
2	nsv911616	chr19:35577870-35669071	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	40 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:35646400-35655000	Weak transcription	Brain Angular Gyrus	brain
2	chr19:35646600-35652200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr19:35646600-35653600	Weak transcription	HSMMtube	muscle
4	chr19:35646600-35656800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr19:35646800-35651600	Weak transcription	Brain Hippocampus Middle	brain
6	chr19:35646800-35655000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr19:35647000-35652400	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr19:35647000-35652400	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr19:35647000-35653000	Weak transcription	Stomach Mucosa	stomach
10	chr19:35647000-35653400	Weak transcription	Rectal Smooth Muscle	rectum
11	chr19:35647000-35653600	Weak transcription	Colonic Mucosa	Colon
12	chr19:35647000-35654800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr19:35647000-35654800	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr19:35647600-35651000	Strong transcription	ES-I3 Cell Line	embryonic stem cell
15	chr19:35647600-35652000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr19:35647600-35652200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr19:35647600-35652200	Weak transcription	Colon Smooth Muscle	Colon
18	chr19:35647600-35652400	Strong transcription	Primary B cells from cord blood	blood
19	chr19:35647600-35652400	Weak transcription	Right Ventricle	heart
20	chr19:35647600-35653400	Strong transcription	Fetal Intestine Small	intestine
21	chr19:35647600-35653800	Strong transcription	HUES6 Cell Line	embryonic stem cell
22	chr19:35647600-35654200	Strong transcription	NHLF	lung
23	chr19:35647600-35655200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr19:35647800-35652200	Weak transcription	Esophagus	oesophagus
25	chr19:35647800-35652200	Strong transcription	Thymus	Thymus
26	chr19:35647800-35652200	Strong transcription	Monocytes-CD14+_RO01746	blood
27	chr19:35647800-35652400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr19:35647800-35652400	Strong transcription	Primary neutrophils fromperipheralblood	blood
29	chr19:35647800-35652400	Strong transcription	Primary B cells from peripheral blood	blood
30	chr19:35647800-35652400	Strong transcription	Lung	lung
31	chr19:35647800-35652400	Strong transcription	NHEK	skin
32	chr19:35647800-35653200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr19:35647800-35653400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr19:35647800-35657000	Strong transcription	HUES64 Cell Line	embryonic stem cell
35	chr19:35648000-35652000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
36	chr19:35648000-35652200	Strong transcription	GM12878-XiMat	blood
37	chr19:35648000-35652400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr19:35648000-35652400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr19:35648000-35652400	Strong transcription	Primary monocytes fromperipheralblood	blood
40	chr19:35648000-35652400	Strong transcription	Primary T cells from cord blood	blood
41	chr19:35648000-35652400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr19:35648000-35652400	Strong transcription	Placenta	Placenta
43	chr19:35648000-35652600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr19:35648000-35653000	Strong transcription	Spleen	Spleen
45	chr19:35648000-35653200	Strong transcription	HMEC	breast
46	chr19:35648000-35653400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr19:35648000-35653600	Strong transcription	HUVEC	blood vessel
48	chr19:35648000-35653800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr19:35648000-35654200	Strong transcription	Primary hematopoietic stem cells	blood
50	chr19:35648000-35654800	Strong transcription	H9 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links