Variant report

Variant	rs572859924
Chromosome Location	chr8:48966151-48966152
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:48957775..48961134-chr8:48963246..48966717,4	K562	blood:
2	chr8:48957775..48961134-chr8:48963246..48966621,3	K562	blood:
3	chr8:48965207..48966957-chr8:48986549..48988912,2	K562	blood:

Extended variants
information (count: 14 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931032	chr8:48744329-49091359	Strong transcription Flanking Active TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	esv2758156	chr8:48788293-49008014	Strong transcription Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	esv2759611	chr8:48788293-49008014	Strong transcription Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv427820	chr8:48788293-49008014	Strong transcription Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv831309	chr8:48815290-48977856	Strong transcription Genic enhancers Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
6	nsv890850	chr8:48954143-49018790	Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv890851	chr8:48954143-49031082	Strong transcription Weak transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	esv1793797	chr8:48955683-48992093	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
9	esv1798949	chr8:48960737-48976333	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv890852	chr8:48964607-49022082	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
11	nsv890853	chr8:48964607-49031082	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
12	nsv1025169	chr8:48965133-49024711	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
13	nsv1020050	chr8:48965133-49028634	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
14	nsv1033298	chr8:48965133-49048832	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:48921800-48966800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:48922400-48975400	Weak transcription	Fetal Brain Male	brain
3	chr8:48953200-48983400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr8:48953800-48974800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
5	chr8:48954400-48967000	Strong transcription	Placenta	Placenta
6	chr8:48954600-48975200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr8:48954600-48975600	Weak transcription	Pancreas	Pancrea
8	chr8:48954800-48971800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr8:48954800-48975800	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr8:48955000-48975000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr8:48955400-48969600	Strong transcription	Dnd41	blood
12	chr8:48955600-48966200	Strong transcription	Primary neutrophils fromperipheralblood	blood
13	chr8:48955600-48967000	Strong transcription	Adipose Nuclei	Adipose
14	chr8:48955800-48975000	Strong transcription	Primary monocytes fromperipheralblood	blood
15	chr8:48956000-48967000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr8:48956000-48974800	Strong transcription	Primary T helper cells fromperipheralblood	blood
17	chr8:48956800-48973200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr8:48957200-48975400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr8:48957600-48974400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr8:48958000-48980600	Weak transcription	Small Intestine	intestine
21	chr8:48958200-48975600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr8:48958600-48966800	Weak transcription	Colon Smooth Muscle	Colon
23	chr8:48959400-48969600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr8:48959400-48969600	Strong transcription	Liver	Liver
25	chr8:48959600-48973600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr8:48960400-48975800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr8:48960600-48967800	Strong transcription	HUES48 Cell Line	embryonic stem cell
28	chr8:48960800-48969400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr8:48960800-48973400	Weak transcription	Fetal Heart	heart
30	chr8:48961000-48967000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr8:48961000-48975800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr8:48961000-48976800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr8:48961800-48967000	Strong transcription	Cortex derived primary cultured neurospheres	brain
34	chr8:48962200-48967200	Strong transcription	Rectal Mucosa Donor 29	rectum
35	chr8:48962400-48967000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr8:48962400-48967400	Strong transcription	Fetal Intestine Large	intestine
37	chr8:48962400-48975000	Strong transcription	Primary T cells fromperipheralblood	blood
38	chr8:48962600-48966200	Strong transcription	GM12878-XiMat	blood
39	chr8:48962600-48970800	Strong transcription	Primary T helper cells PMA-I stimulated	--
40	chr8:48962800-48967000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr8:48962800-48967000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr8:48962800-48967000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr8:48962800-48967000	Strong transcription	Fetal Muscle Leg	muscle
44	chr8:48962800-48967400	Strong transcription	Sigmoid Colon	Sigmoid Colon
45	chr8:48962800-48967400	Strong transcription	Skeletal Muscle Male	skeletal muscle
46	chr8:48963000-48967000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr8:48963000-48967000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr8:48963000-48967000	Strong transcription	Fetal Muscle Trunk	muscle
49	chr8:48963000-48967600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr8:48963200-48966800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell

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