Variant report

Variant	rs9805139
Chromosome Location	chr12:50444506-50444507
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:50440879..50447724-chr12:50448390..50454714,11	K562	blood:
2	chr12:50432660..50433175-chr12:50444120..50444802,2	K562	blood:
3	chr12:50367042..50370413-chr12:50441830..50446012,4	K562	blood:
4	chr12:50441963..50444884-chr12:50445387..50446910,2	MCF-7	breast:
5	chr12:50442392..50444531-chr12:50445010..50447664,2	K562	blood:
6	chr12:50424617..50427330-chr12:50443083..50445011,2	MCF-7	breast:
7	chr12:50443166..50446140-chr12:50448387..50451467,3	K562	blood:
8	chr12:50431093..50436094-chr12:50443171..50446761,5	K562	blood:

No data

Variant related genes	Relation type
ENSG00000161800	Chromatin interaction
ENSG00000110881	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045327	chr12:49975040-50551375	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	170 gene(s)	inside rSNPs	diseases
2	nsv541490	chr12:49975040-50551375	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	170 gene(s)	inside rSNPs	diseases
3	nsv530671	chr12:50233858-50708991	Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
4	nsv469374	chr12:50349765-50467769	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	nsv469375	chr12:50349765-50467769	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
6	nsv558837	chr12:50349765-50467769	Bivalent/Poised TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
7	esv3392138	chr12:50394642-50645326	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
8	esv3324153	chr12:50443735-50446133	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:50443000-50447200	Enhancers	Fetal Brain Male	brain
2	chr12:50443400-50445000	Enhancers	Stomach Mucosa	stomach
3	chr12:50443400-50445400	Enhancers	Duodenum Smooth Muscle	Duodenum
4	chr12:50443400-50445800	Enhancers	Placenta	Placenta
5	chr12:50443600-50445200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
6	chr12:50443800-50444600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr12:50443800-50445400	Enhancers	Placenta Amnion	Placenta Amnion
8	chr12:50444000-50444600	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
9	chr12:50444000-50444600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr12:50444000-50444600	Bivalent/Poised TSS	Muscle Satellite Cultured Cells	--
11	chr12:50444000-50444600	Active TSS	Colon Smooth Muscle	Colon
12	chr12:50444000-50444600	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
13	chr12:50444000-50444600	Flanking Active TSS	K562	blood
14	chr12:50444000-50445200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
15	chr12:50444000-50445200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
16	chr12:50444000-50445400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
17	chr12:50444000-50445400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr12:50444000-50445600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
19	chr12:50444000-50445600	Bivalent Enhancer	Primary B cells from cord blood	blood
20	chr12:50444000-50446200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
21	chr12:50444200-50444600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr12:50444200-50444600	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr12:50444200-50444600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr12:50444200-50444600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
25	chr12:50444200-50444600	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
26	chr12:50444200-50444600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
27	chr12:50444200-50444600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr12:50444200-50444600	Active TSS	Brain Anterior Caudate	brain
29	chr12:50444200-50444600	Active TSS	Brain Inferior Temporal Lobe	brain
30	chr12:50444200-50444600	Bivalent/Poised TSS	Colonic Mucosa	Colon
31	chr12:50444200-50444600	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
32	chr12:50444200-50444600	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
33	chr12:50444200-50444600	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
34	chr12:50444200-50444600	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
35	chr12:50444200-50444600	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
36	chr12:50444200-50444600	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
37	chr12:50444200-50444600	Flanking Active TSS	Pancreas	Pancrea
38	chr12:50444200-50444600	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
39	chr12:50444200-50444600	Active TSS	Rectal Smooth Muscle	rectum
40	chr12:50444200-50444600	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
41	chr12:50444200-50444600	Bivalent/Poised TSS	NH-A	brain
42	chr12:50444200-50444600	Flanking Bivalent TSS/Enh	NHLF	lung
43	chr12:50444200-50444800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr12:50444200-50444800	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr12:50444200-50444800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
46	chr12:50444200-50444800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
47	chr12:50444200-50444800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
48	chr12:50444200-50444800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr12:50444200-50444800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr12:50444200-50444800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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