Variant report

Variant	rs552634447
Chromosome Location	chr12:118808810-118808811
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:118789693..118801109-chr12:118805205..118813455,21	K562	blood:
2	chr12:118765311..118767097-chr12:118807777..118809983,2	K562	blood:
3	chr12:118792933..118800473-chr12:118805927..118813309,24	K562	blood:

Variant related genes	Relation type
ENSG00000135090	Chromatin interaction

Extended variants
information (count: 3 )
Associated
traits (count: 0)

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	nsv1053785	chr12:118490955-118874194	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv899547	chr12:118791441-118896304	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	esv3413770	chr12:118808569-118812117	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:118794800-118809000	Weak transcription	Lung	lung
2	chr12:118794800-118809000	Weak transcription	Pancreas	Pancrea
3	chr12:118794800-118809200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr12:118794800-118809200	Weak transcription	Esophagus	oesophagus
5	chr12:118799200-118809000	Weak transcription	HSMM	muscle
6	chr12:118801800-118809000	Weak transcription	Gastric	stomach
7	chr12:118801800-118809000	Weak transcription	Left Ventricle	heart
8	chr12:118804800-118809000	Weak transcription	Spleen	Spleen
9	chr12:118806200-118809000	Weak transcription	Psoas Muscle	Psoas
10	chr12:118806600-118809000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr12:118806800-118809000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr12:118807000-118809200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr12:118807200-118809400	Flanking Active TSS	Primary hematopoietic stem cells	blood
14	chr12:118807200-118811400	Active TSS	NHDF-Ad	bronchial
15	chr12:118808000-118809000	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr12:118808000-118809000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr12:118808000-118809200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr12:118808000-118809400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
19	chr12:118808000-118811400	Active TSS	NHLF	lung
20	chr12:118808200-118809000	Enhancers	Skeletal Muscle Female	skeletal muscle
21	chr12:118808200-118809200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr12:118808200-118809600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr12:118808200-118810000	Flanking Active TSS	Adipose Nuclei	Adipose
24	chr12:118808400-118809000	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
25	chr12:118808400-118809000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr12:118808400-118809000	Enhancers	Primary B cells from peripheral blood	blood
27	chr12:118808400-118809000	Enhancers	Primary T cells fromperipheralblood	blood
28	chr12:118808400-118809000	Enhancers	Primary T killer memory cells from peripheral blood	blood
29	chr12:118808400-118809000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
30	chr12:118808400-118809000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr12:118808400-118809000	Bivalent Enhancer	Fetal Heart	heart
32	chr12:118808400-118809000	Enhancers	Fetal Stomach	stomach
33	chr12:118808400-118809000	Enhancers	Small Intestine	intestine
34	chr12:118808400-118809000	Bivalent Enhancer	Dnd41	blood
35	chr12:118808400-118809000	Flanking Active TSS	NHEK	skin
36	chr12:118808400-118809000	Flanking Active TSS	Osteobl	bone
37	chr12:118808400-118809200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr12:118808400-118809200	Flanking Active TSS	Brain Cingulate Gyrus	brain
39	chr12:118808400-118809400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr12:118808400-118809400	Flanking Active TSS	Brain Germinal Matrix	brain
41	chr12:118808400-118809600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
42	chr12:118808400-118810000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
43	chr12:118808400-118811200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr12:118808400-118811200	Active TSS	Brain Anterior Caudate	brain
45	chr12:118808400-118811200	Active TSS	Duodenum Mucosa	Duodenum
46	chr12:118808400-118811200	Active TSS	Fetal Intestine Large	intestine
47	chr12:118808400-118811600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr12:118808600-118809000	Enhancers	H9 Cell Line	embryonic stem cell
49	chr12:118808600-118809000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr12:118808600-118809000	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell

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