Variant report

Variant	rs180927695
Chromosome Location	chr5:112251913-112251914
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:112249716..112252598-chr5:112302249..112303940,2	MCF-7	breast:
2	chr5:112246563..112249281-chr5:112250414..112253168,3	K562	blood:
3	chr5:112248880..112253416-chr5:112311841..112314795,5	K562	blood:
4	chr5:112243670..112246215-chr5:112250359..112252946,2	K562	blood:

Variant related genes	Relation type
ENSG00000172795	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029271	chr5:112113308-112325943	Strong transcription Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv529536	chr5:112174106-112269758	Genic enhancers Strong transcription Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv599394	chr5:112185491-112446323	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats 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	31 gene(s)	inside rSNPs	diseases
4	nsv1030103	chr5:112197662-112255712	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv537863	chr5:112197662-112255712	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv1019756	chr5:112242315-112325943	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
7	nsv968850	chr5:112250486-112252092	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 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	chr5:112211600-112256400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:112212200-112256400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr5:112215200-112255800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr5:112221800-112256600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:112222000-112256400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr5:112223000-112256400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr5:112223000-112256600	Weak transcription	Thymus	Thymus
8	chr5:112229600-112256600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr5:112237400-112254000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr5:112238400-112252800	Weak transcription	Small Intestine	intestine
11	chr5:112238400-112253800	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr5:112242200-112254200	Weak transcription	Fetal Kidney	kidney
13	chr5:112242400-112252800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr5:112242600-112256800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr5:112243200-112254000	Weak transcription	Fetal Brain Male	brain
16	chr5:112243400-112252800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr5:112245800-112252000	Weak transcription	Fetal Brain Female	brain
18	chr5:112245800-112252400	Weak transcription	Fetal Thymus	thymus
19	chr5:112245800-112252800	Weak transcription	Colonic Mucosa	Colon
20	chr5:112245800-112253200	Weak transcription	Primary hematopoietic stem cells	blood
21	chr5:112245800-112253200	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr5:112246000-112254000	Weak transcription	Esophagus	oesophagus
23	chr5:112246000-112254000	Weak transcription	Rectal Smooth Muscle	rectum
24	chr5:112246200-112254000	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr5:112246600-112252000	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr5:112246800-112253400	Weak transcription	Psoas Muscle	Psoas
27	chr5:112247000-112252600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr5:112247800-112255800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr5:112248000-112255600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr5:112248200-112255600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr5:112248400-112256000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr5:112249000-112252800	Weak transcription	Pancreas	Pancrea
33	chr5:112249200-112254000	Strong transcription	Placenta	Placenta
34	chr5:112249400-112254200	Strong transcription	Liver	Liver
35	chr5:112249400-112254400	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr5:112249400-112255600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
37	chr5:112249600-112252000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
38	chr5:112249600-112254200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr5:112250000-112254600	Strong transcription	H1 Cell Line	embryonic stem cell
40	chr5:112250200-112252800	Weak transcription	Fetal Intestine Small	intestine
41	chr5:112250200-112254000	Strong transcription	Rectal Mucosa Donor 29	rectum
42	chr5:112250200-112254400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr5:112250200-112254800	Genic enhancers	Brain Inferior Temporal Lobe	brain
44	chr5:112250400-112253200	Weak transcription	Gastric	stomach
45	chr5:112250400-112253800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr5:112250400-112253800	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr5:112250400-112254000	Weak transcription	Stomach Mucosa	stomach
48	chr5:112250400-112254200	Genic enhancers	Primary T helper cells fromperipheralblood	blood
49	chr5:112250600-112253200	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr5:112250600-112254000	Weak transcription	Spleen	Spleen

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links