Variant report

Variant	rs9579404
Chromosome Location	chr13:30129816-30129817
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:30128754..30131140-chr13:30168189..30170872,2	MCF-7	breast:
2	chr13:30128662..30130229-chr13:30134308..30136024,2	K562	blood:

Variant related genes	Relation type
ENSG00000139514	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10454589	0.90[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs10454590	0.83[EUR][1000 genomes]
rs12868663	0.97[EUR][1000 genomes]
rs34369885	0.90[AFR][1000 genomes]
rs34496705	0.90[AFR][1000 genomes]
rs34831702	0.99[EUR][1000 genomes]
rs7328329	0.99[EUR][1000 genomes]
rs7333701	0.81[AFR][1000 genomes]
rs819388	1.00[EUR][1000 genomes]
rs9578103	0.90[AFR][1000 genomes]
rs9578105	0.90[AFR][1000 genomes]
rs9578106	0.83[EUR][1000 genomes]
rs9578107	0.83[EUR][1000 genomes]
rs9579383	0.90[AFR][1000 genomes]
rs9579384	0.90[AFR][1000 genomes]
rs9579386	0.90[AFR][1000 genomes]
rs9579390	0.90[AFR][1000 genomes]
rs9579392	0.90[AFR][1000 genomes]
rs9579393	0.90[AFR][1000 genomes]
rs9579394	0.90[AFR][1000 genomes]
rs9579395	0.90[AFR][1000 genomes]
rs9579396	0.90[AFR][1000 genomes]
rs9579398	0.83[EUR][1000 genomes]
rs9579399	0.93[EUR][1000 genomes]
rs9579400	0.93[EUR][1000 genomes]
rs9579401	0.96[EUR][1000 genomes]
rs9579402	0.95[AFR][1000 genomes];0.99[EUR][1000 genomes]
rs9579403	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv979	chr13:30122254-30167821	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:30092200-30133000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr13:30097200-30138400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr13:30103800-30137200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr13:30104200-30135400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr13:30105200-30136800	Weak transcription	Brain Germinal Matrix	brain
6	chr13:30113200-30141600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr13:30113800-30136200	Weak transcription	Rectal Smooth Muscle	rectum
8	chr13:30121400-30130000	Weak transcription	Adipose Nuclei	Adipose
9	chr13:30122600-30131600	Weak transcription	Small Intestine	intestine
10	chr13:30123000-30138600	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr13:30123600-30136200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr13:30125000-30137200	Weak transcription	Brain Anterior Caudate	brain
13	chr13:30125000-30147400	Weak transcription	A549	lung
14	chr13:30125800-30130800	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr13:30125800-30136600	Weak transcription	Brain Hippocampus Middle	brain
16	chr13:30125800-30142200	Weak transcription	K562	blood
17	chr13:30125800-30143200	Weak transcription	Gastric	stomach
18	chr13:30126000-30135800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr13:30126000-30137000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr13:30126000-30138400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr13:30126000-30161400	Weak transcription	Primary B cells from cord blood	blood
22	chr13:30126200-30130600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr13:30126200-30137200	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr13:30126200-30147200	Weak transcription	Spleen	Spleen
25	chr13:30126600-30136000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
26	chr13:30126600-30136000	Weak transcription	HUVEC	blood vessel
27	chr13:30126800-30135200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr13:30127400-30142200	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr13:30127600-30135400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr13:30127600-30135800	Weak transcription	HSMM	muscle
31	chr13:30127600-30137200	Weak transcription	Brain Cingulate Gyrus	brain
32	chr13:30127600-30137800	Weak transcription	Stomach Smooth Muscle	stomach
33	chr13:30127600-30144000	Weak transcription	Fetal Intestine Small	intestine
34	chr13:30127600-30146200	Weak transcription	Right Ventricle	heart
35	chr13:30127600-30151400	Weak transcription	Aorta	Aorta
36	chr13:30127600-30156400	Weak transcription	Lung	lung
37	chr13:30127800-30130600	Weak transcription	NH-A	brain
38	chr13:30127800-30131000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr13:30127800-30131000	Weak transcription	Fetal Brain Female	brain
40	chr13:30127800-30135800	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr13:30127800-30135800	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr13:30127800-30136200	Weak transcription	Ovary	ovary
43	chr13:30127800-30136800	Weak transcription	Brain Angular Gyrus	brain
44	chr13:30127800-30137200	Weak transcription	Pancreas	Pancrea
45	chr13:30127800-30137800	Weak transcription	Brain Substantia Nigra	brain
46	chr13:30127800-30137800	Weak transcription	Colon Smooth Muscle	Colon
47	chr13:30127800-30143200	Weak transcription	Fetal Thymus	thymus
48	chr13:30127800-30147400	Weak transcription	Fetal Intestine Large	intestine
49	chr13:30127800-30147600	Weak transcription	Monocytes-CD14+_RO01746	blood
50	chr13:30128000-30130800	Weak transcription	NHDF-Ad	bronchial

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