Variant report

Variant	rs184155223
Chromosome Location	chr12:106132543-106132544
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1039068	chr12:105935786-106211250	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv899503	chr12:106021477-106175903	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1047810	chr12:106067049-106246582	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1040261	chr12:106068992-106246582	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv899504	chr12:106095906-106135942	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	n/a
6	esv3447181	chr12:106132354-106138639	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:106126600-106133200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr12:106127400-106134600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr12:106129400-106133400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr12:106129400-106134200	Weak transcription	HSMM	muscle
5	chr12:106130000-106137800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr12:106130600-106133000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr12:106130800-106133000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr12:106130800-106133400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr12:106130800-106133600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr12:106130800-106134800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr12:106131000-106132600	Enhancers	Fetal Lung	lung
12	chr12:106131000-106133400	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr12:106131200-106132600	Enhancers	Fetal Heart	heart
14	chr12:106131200-106133200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr12:106131200-106133200	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr12:106131400-106133200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr12:106131400-106134000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr12:106131800-106135000	Enhancers	Fetal Brain Male	brain
19	chr12:106131800-106136600	Enhancers	Right Atrium	heart
20	chr12:106131800-106138000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr12:106132000-106132600	Enhancers	Fetal Muscle Trunk	muscle
22	chr12:106132000-106132600	Enhancers	Ovary	ovary
23	chr12:106132000-106132800	Enhancers	Fetal Stomach	stomach
24	chr12:106132000-106133200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr12:106132000-106133200	Strong transcription	HSMMtube	muscle
26	chr12:106132000-106133800	Enhancers	Left Ventricle	heart
27	chr12:106132200-106132800	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr12:106132200-106133000	Enhancers	Primary T cells fromperipheralblood	blood
29	chr12:106132200-106136200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr12:106132200-106137800	Enhancers	Fetal Muscle Leg	muscle
31	chr12:106132400-106132600	Enhancers	H1 Cell Line	embryonic stem cell
32	chr12:106132400-106132600	Enhancers	H9 Cell Line	embryonic stem cell
33	chr12:106132400-106132600	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr12:106132400-106132600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
35	chr12:106132400-106132600	Enhancers	Aorta	Aorta
36	chr12:106132400-106132600	Enhancers	Brain Anterior Caudate	brain
37	chr12:106132400-106132600	Enhancers	Brain Cingulate Gyrus	brain
38	chr12:106132400-106132600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
39	chr12:106132400-106132600	Enhancers	Right Ventricle	heart
40	chr12:106132400-106132600	Enhancers	Spleen	Spleen
41	chr12:106132400-106132800	Flanking Bivalent TSS/Enh	HUVEC	blood vessel
42	chr12:106132400-106133600	Enhancers	Lung	lung
43	chr12:106132400-106133800	Enhancers	Adipose Nuclei	Adipose

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