Variant report

Variant	rs9634361
Chromosome Location	chr13:30897471-30897472
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:30880917..30883470-chr13:30895639..30898288,2	K562	blood:
2	chr13:30897317..30899409-chr13:30902997..30905720,2	K562	blood:

Variant related genes	Relation type
ENSG00000102781	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs12873373	0.88[EUR][1000 genomes]
rs35962246	0.82[EUR][1000 genomes]
rs4769824	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6490453	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7335432	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs756850	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs763808	0.91[EUR][1000 genomes]
rs7991052	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9506288	0.89[EUR][1000 genomes]
rs9506290	0.93[EUR][1000 genomes]
rs9506291	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9506292	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9508700	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9508701	0.93[EUR][1000 genomes]
rs9508702	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9508703	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9508705	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9508706	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9508711	0.91[EUR][1000 genomes]
rs9551887	0.98[EUR][1000 genomes]

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:30882200-30910800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr13:30882400-30905400	Weak transcription	Right Ventricle	heart
3	chr13:30882400-30905400	Weak transcription	Stomach Smooth Muscle	stomach
4	chr13:30886000-30898400	Weak transcription	Lung	lung
5	chr13:30886800-30900000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr13:30888000-30903400	Weak transcription	Fetal Thymus	thymus
7	chr13:30888000-30909600	Weak transcription	Thymus	Thymus
8	chr13:30889400-30899400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr13:30889400-30906400	Weak transcription	Primary B cells from cord blood	blood
10	chr13:30889600-30898000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr13:30889600-30902400	Weak transcription	Primary hematopoietic stem cells	blood
12	chr13:30892800-30897800	Weak transcription	Right Atrium	heart
13	chr13:30892800-30913400	Weak transcription	Psoas Muscle	Psoas
14	chr13:30894200-30897800	Weak transcription	Fetal Muscle Leg	muscle
15	chr13:30894200-30900200	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr13:30894200-30903000	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr13:30894600-30897600	Weak transcription	Brain Hippocampus Middle	brain
18	chr13:30894800-30905400	Weak transcription	Brain Anterior Caudate	brain
19	chr13:30895800-30898000	Weak transcription	Brain Cingulate Gyrus	brain
20	chr13:30896000-30899600	Weak transcription	Fetal Heart	heart
21	chr13:30896800-30898000	Enhancers	K562	blood
22	chr13:30896800-30898200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr13:30897200-30905600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr13:30897400-30898000	Enhancers	Breast Myoepithelial Primary Cells	Breast

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