Variant report

Variant	rs60357123
Chromosome Location	chr8:108506068-108506069
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:47 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1825819	chr8:108495057-108506185	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv1832361	chr8:108495057-108506185	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv1844679	chr8:108495057-108506185	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv611854	chr8:108503702-108506185	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS	n/a	n/a	inside rSNPs	diseases
5	esv3480583	chr8:108504234-108506607	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
6	nsv824702	chr8:108504672-108506345	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	inside rSNPs	diseases
7	nsv819326	chr8:108504700-108506635	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
8	esv3480581	chr8:108504738-108506441	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
9	esv3480582	chr8:108504805-108506368	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
10	nsv396231	chr8:108504819-108506363	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
11	esv3480584	chr8:108504819-108506365	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
12	esv13179	chr8:108504879-108506388	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
13	esv1824993	chr8:108504907-108506185	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
14	esv1825717	chr8:108504907-108506185	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
15	esv1826614	chr8:108504907-108506185	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
16	esv1829645	chr8:108504907-108506185	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
17	esv1830175	chr8:108504907-108506185	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
18	esv1830213	chr8:108504907-108506185	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	inside rSNPs	diseases
19	esv1832061	chr8:108504907-108506185	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
20	esv1832241	chr8:108504907-108506185	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
21	esv1833404	chr8:108504907-108506185	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
22	esv1842971	chr8:108504907-108506185	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
23	esv1843611	chr8:108504907-108506185	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
24	esv1843851	chr8:108504907-108506185	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
25	esv1844320	chr8:108504907-108506185	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
26	esv1844453	chr8:108504907-108506185	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
27	esv1844592	chr8:108504907-108506185	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
28	esv1844832	chr8:108504907-108506185	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	inside rSNPs	diseases
29	esv1846223	chr8:108504907-108506185	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
30	esv1848547	chr8:108504907-108506185	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
31	esv1848937	chr8:108504907-108506185	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	inside rSNPs	diseases
32	esv1850641	chr8:108504907-108506185	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
33	esv1850649	chr8:108504907-108506185	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	inside rSNPs	diseases
34	esv1851243	chr8:108504907-108506185	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
35	esv1851893	chr8:108504907-108506185	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	inside rSNPs	diseases
36	nsv611860	chr8:108504907-108506185	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
37	nsv611861	chr8:108504907-108509116	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
38	nsv611862	chr8:108504907-108513341	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
39	esv1845767	chr8:108504907-108515373	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
40	esv1849422	chr8:108504907-108515373	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
41	esv1825455	chr8:108504907-108518274	Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
42	nsv611865	chr8:108504961-108506185	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
43	nsv611866	chr8:108504961-108509116	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
44	nsv611868	chr8:108505161-108506185	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	inside rSNPs	diseases
45	nsv611869	chr8:108505161-108509116	Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
46	nsv611870	chr8:108505219-108506185	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
47	nsv611872	chr8:108505425-108506185	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:108497800-108508400	Weak transcription	Left Ventricle	heart
2	chr8:108498200-108506800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr8:108498400-108506800	Weak transcription	Brain Hippocampus Middle	brain
4	chr8:108498400-108507400	Weak transcription	Brain Cingulate Gyrus	brain
5	chr8:108499000-108506600	Weak transcription	Brain Substantia Nigra	brain
6	chr8:108499400-108507000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr8:108499600-108506800	Weak transcription	Fetal Thymus	thymus
8	chr8:108499800-108506800	Weak transcription	Aorta	Aorta
9	chr8:108500400-108507200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr8:108502400-108507600	Weak transcription	Psoas Muscle	Psoas
11	chr8:108502600-108506800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr8:108502800-108506400	Weak transcription	NHDF-Ad	bronchial
13	chr8:108502800-108506400	Weak transcription	NHLF	lung
14	chr8:108502800-108506600	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr8:108502800-108506600	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr8:108502800-108506600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr8:108502800-108506600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr8:108502800-108506600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr8:108502800-108506600	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr8:108502800-108506600	Weak transcription	Brain Germinal Matrix	brain
21	chr8:108502800-108506600	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr8:108502800-108506800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr8:108502800-108506800	Weak transcription	Fetal Brain Female	brain
24	chr8:108502800-108507000	Weak transcription	Ovary	ovary
25	chr8:108502800-108507200	Weak transcription	A549	lung
26	chr8:108502800-108507600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr8:108502800-108509200	Weak transcription	NHEK	skin
28	chr8:108503000-108506600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr8:108503000-108506600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr8:108503000-108506600	Weak transcription	Colon Smooth Muscle	Colon
31	chr8:108503000-108506800	Weak transcription	Adipose Nuclei	Adipose
32	chr8:108503000-108507400	Weak transcription	Rectal Smooth Muscle	rectum
33	chr8:108503000-108508400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr8:108503200-108506200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr8:108503600-108506400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr8:108503800-108506200	Weak transcription	Osteobl	bone
37	chr8:108503800-108506800	Weak transcription	Brain Anterior Caudate	brain
38	chr8:108503800-108506800	Weak transcription	Stomach Smooth Muscle	stomach
39	chr8:108504000-108506400	Weak transcription	Fetal Lung	lung
40	chr8:108504000-108506600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr8:108504000-108506600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr8:108504000-108506600	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr8:108505000-108508800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr8:108505200-108506200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr8:108505200-108506200	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr8:108505200-108506200	Enhancers	Fetal Kidney	kidney
47	chr8:108505200-108506800	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr8:108505200-108507000	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr8:108505200-108507400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr8:108505200-108507800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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