Variant report

Variant	rs114487186
Chromosome Location	chr2:74226916-74226917
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ZNF263	chr2:74226599-74228865	HEK293-T-REx	kidney:	n/a	chr2:74226898-74226907

No.	Distal block	Cell Line	Cell type
1	chr2:74225172..74227834-chr2:74230974..74232570,2	K562	blood:
2	chr2:74225365..74228086-chr2:74337531..74340333,2	K562	blood:
3	chr2:74054453..74058790-chr2:74226313..74230079,4	MCF-7	breast:
4	chr2:74224937..74227638-chr2:74357477..74359947,2	MCF-7	breast:

Variant related genes	Relation type
TET3	TF binding region
ENSG00000124356	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	nsv1011177	chr2:74167343-74239905	Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	esv3584956	chr2:74197109-74317135	Flanking Active TSS Genic enhancers Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
3	nsv818048	chr2:74225434-74313080	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:74215800-74227000	Weak transcription	Right Atrium	heart
2	chr2:74215800-74227400	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr2:74215800-74229200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr2:74216000-74227000	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr2:74216000-74227000	Weak transcription	Small Intestine	intestine
6	chr2:74216400-74229200	Weak transcription	Rectal Smooth Muscle	rectum
7	chr2:74216600-74227400	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr2:74220600-74227400	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr2:74220800-74229200	Weak transcription	Primary hematopoietic stem cells	blood
10	chr2:74221200-74227000	Weak transcription	Adipose Nuclei	Adipose
11	chr2:74221200-74227000	Weak transcription	NHLF	lung
12	chr2:74221200-74227200	Weak transcription	Gastric	stomach
13	chr2:74221200-74228800	Weak transcription	Psoas Muscle	Psoas
14	chr2:74221400-74227200	Weak transcription	HSMMtube	muscle
15	chr2:74221400-74229000	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr2:74222600-74228400	Enhancers	Primary T helper cells PMA-I stimulated	--
17	chr2:74222600-74229200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
18	chr2:74222800-74229000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr2:74222800-74229200	Enhancers	Primary T cells fromperipheralblood	blood
20	chr2:74223600-74227600	Genic enhancers	GM12878-XiMat	blood
21	chr2:74223800-74228800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
22	chr2:74224000-74227000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
23	chr2:74224000-74229200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr2:74224000-74229200	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr2:74224000-74229400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr2:74224000-74230000	Enhancers	Fetal Brain Male	brain
27	chr2:74224200-74227600	Genic enhancers	Primary T cells from cord blood	blood
28	chr2:74224600-74228400	Enhancers	Brain Angular Gyrus	brain
29	chr2:74224800-74227000	Weak transcription	Fetal Thymus	thymus
30	chr2:74224800-74227200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr2:74224800-74229000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr2:74225000-74227200	Weak transcription	Pancreas	Pancrea
33	chr2:74225000-74228000	Enhancers	Brain Anterior Caudate	brain
34	chr2:74225200-74228200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr2:74225400-74228400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr2:74225400-74229200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr2:74225600-74228200	Weak transcription	Primary B cells from cord blood	blood
38	chr2:74225600-74228200	Weak transcription	Thymus	Thymus
39	chr2:74225600-74228600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr2:74225600-74229200	Enhancers	Brain Cingulate Gyrus	brain
41	chr2:74225800-74227000	Weak transcription	Spleen	Spleen
42	chr2:74225800-74228000	Weak transcription	Dnd41	blood
43	chr2:74225800-74229200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
44	chr2:74226000-74227000	Genic enhancers	HepG2	liver
45	chr2:74226000-74227800	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr2:74226000-74229200	Weak transcription	Brain Substantia Nigra	brain
47	chr2:74226000-74229200	Enhancers	Placenta	Placenta
48	chr2:74226000-74229400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr2:74226000-74229400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr2:74226200-74227200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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