Variant report

Variant	rs150776626
Chromosome Location	chr11:8057735-8057736
allele	C/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
ENSG00000254921	Chromatin interaction
ENSG00000166402	Chromatin interaction

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 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
3	nsv972907	chr11:8057411-8061563	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:8054200-8057800	Enhancers	Fetal Heart	heart
2	chr11:8054600-8057800	Enhancers	Fetal Intestine Large	intestine
3	chr11:8054600-8058000	Enhancers	Placenta Amnion	Placenta Amnion
4	chr11:8055200-8058000	Enhancers	Adipose Nuclei	Adipose
5	chr11:8055200-8059600	Weak transcription	Brain Angular Gyrus	brain
6	chr11:8055400-8059400	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr11:8055400-8059600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr11:8055400-8059600	Weak transcription	Brain Cingulate Gyrus	brain
9	chr11:8055800-8059600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr11:8055800-8060000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr11:8056200-8057800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr11:8056200-8058000	Enhancers	Left Ventricle	heart
13	chr11:8056200-8059400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr11:8056600-8059200	Weak transcription	Brain Anterior Caudate	brain
15	chr11:8056800-8061400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr11:8057000-8058000	Enhancers	Ovary	ovary
17	chr11:8057000-8058200	Enhancers	Right Ventricle	heart
18	chr11:8057000-8059800	Weak transcription	Fetal Brain Female	brain
19	chr11:8057200-8059200	Weak transcription	Brain Germinal Matrix	brain
20	chr11:8057400-8057800	Enhancers	Fetal Thymus	thymus
21	chr11:8057400-8058600	Weak transcription	Right Atrium	heart
22	chr11:8057600-8059400	Weak transcription	Fetal Brain Male	brain

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