Variant report

Variant	rs11014336
Chromosome Location	chr10:25277641-25277642
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:25277210..25278984-chr10:25279762..25281866,2	K562	blood:
2	chr10:25246877..25249016-chr10:25275912..25277898,2	K562	blood:
3	chr10:25241921..25243506-chr10:25276442..25278938,2	K562	blood:

Variant related genes	Relation type
ENSG00000273107	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	esv3452797	chr10:25276796-25278244	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	esv3452808	chr10:25276796-25278244	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	esv1965232	chr10:25277423-25277846	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv3395367	chr10:25277580-25277646	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv996389	chr10:25277594-25277641	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv1147591	chr10:25277608-25277656	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv19989	chr10:25277642-25277645	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	n/a	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25264400-25277800	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr10:25264400-25281800	Weak transcription	Fetal Intestine Small	intestine
3	chr10:25264600-25292200	Weak transcription	Ovary	ovary
4	chr10:25269200-25277800	Weak transcription	Brain Angular Gyrus	brain
5	chr10:25271200-25277800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr10:25272400-25277800	Weak transcription	Gastric	stomach
7	chr10:25272400-25281000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr10:25274200-25278200	Weak transcription	A549	lung
9	chr10:25274400-25277800	Weak transcription	Adipose Nuclei	Adipose
10	chr10:25275400-25278400	Enhancers	Brain Hippocampus Middle	brain
11	chr10:25276600-25277800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr10:25276600-25280400	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr10:25276800-25277800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr10:25276800-25277800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr10:25277000-25278200	Weak transcription	Hela-S3	cervix
16	chr10:25277400-25278400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr10:25277400-25278600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr10:25277600-25277800	Enhancers	K562	blood
19	chr10:25277600-25278400	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr10:25277600-25278400	Enhancers	Brain Anterior Caudate	brain
21	chr10:25277600-25278400	Enhancers	Brain Cingulate Gyrus	brain
22	chr10:25277600-25278400	Enhancers	Brain Substantia Nigra	brain
23	chr10:25277600-25278600	Enhancers	Fetal Brain Male	brain

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