Variant report

Variant	rs561450957
Chromosome Location	chr11:8056627-8056628
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:8055622..8058095-chr11:8058750..8061229,2	K562	blood:
2	chr11:8047756..8050115-chr11:8056077..8058244,2	MCF-7	breast:
3	chr11:8050565..8052197-chr11:8055086..8058020,2	MCF-7	breast:
4	chr11:8055622..8058575-chr11:8058750..8061293,2	K562	blood:
5	chr11:8011622..8013297-chr11:8056375..8059181,2	K562	blood:

Variant related genes	Relation type
ENSG00000166402	Chromatin interaction
ENSG00000254921	Chromatin interaction

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1052808	chr11:8011647-8129191	Bivalent Enhancer Strong transcription Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers 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	11 gene(s)	inside rSNPs	diseases
2	nsv983216	chr11:8056182-8060154	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:8054200-8057800	Enhancers	Fetal Heart	heart
2	chr11:8054400-8057200	Enhancers	Fetal Intestine Small	intestine
3	chr11:8054600-8057000	Enhancers	Fetal Brain Female	brain
4	chr11:8054600-8057600	Enhancers	Fetal Brain Male	brain
5	chr11:8054600-8057600	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr11:8054600-8057800	Enhancers	Fetal Intestine Large	intestine
7	chr11:8054600-8058000	Enhancers	Placenta Amnion	Placenta Amnion
8	chr11:8054800-8057200	Enhancers	Brain Germinal Matrix	brain
9	chr11:8055000-8057400	Enhancers	Fetal Stomach	stomach
10	chr11:8055200-8056800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr11:8055200-8057600	Enhancers	Duodenum Mucosa	Duodenum
12	chr11:8055200-8058000	Enhancers	Adipose Nuclei	Adipose
13	chr11:8055200-8059600	Weak transcription	Brain Angular Gyrus	brain
14	chr11:8055400-8056800	Weak transcription	Fetal Lung	lung
15	chr11:8055400-8057000	Weak transcription	Ovary	ovary
16	chr11:8055400-8059400	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr11:8055400-8059600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr11:8055400-8059600	Weak transcription	Brain Cingulate Gyrus	brain
19	chr11:8055600-8056800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr11:8055800-8057000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr11:8055800-8057400	Weak transcription	Fetal Thymus	thymus
22	chr11:8055800-8059600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr11:8055800-8060000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr11:8056000-8057000	Weak transcription	Right Ventricle	heart
25	chr11:8056200-8057400	Enhancers	Right Atrium	heart
26	chr11:8056200-8057800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr11:8056200-8058000	Enhancers	Left Ventricle	heart
28	chr11:8056200-8059400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr11:8056400-8057600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr11:8056600-8057000	Weak transcription	Esophagus	oesophagus
31	chr11:8056600-8059200	Weak transcription	Brain Anterior Caudate	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links