Variant report

Variant	rs73708865
Chromosome Location	chr7:96761374-96761375
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:96745462..96747973-chr7:96759232..96761431,3	K562	blood:
2	chr7:96759320..96762416-chr7:96764442..96769272,6	K562	blood:
3	chr7:96748869..96751979-chr7:96758718..96762589,5	K562	blood:

Variant related genes	Relation type
ENSG00000196636	Chromatin interaction
ENSG00000224551	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10265264	0.83[AMR][1000 genomes]
rs56962196	0.83[AMR][1000 genomes]
rs58839243	0.83[AMR][1000 genomes]
rs73708847	1.00[AMR][1000 genomes]
rs73708849	1.00[AMR][1000 genomes]
rs73708852	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73708854	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73708858	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73708859	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73708861	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73708863	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73708864	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73708872	0.90[AFR][1000 genomes]
rs73708874	0.90[AFR][1000 genomes]
rs73708875	0.90[AFR][1000 genomes]
rs73708876	0.82[AFR][1000 genomes]
rs73708890	0.83[AMR][1000 genomes]

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	nsv1019725	chr7:96749866-96850819	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv539029	chr7:96749866-96850819	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:96747600-96768200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr7:96747800-96768200	Weak transcription	Aorta	Aorta
3	chr7:96748400-96767200	Weak transcription	Fetal Stomach	stomach
4	chr7:96748400-96768200	Weak transcription	Right Ventricle	heart
5	chr7:96748400-96768400	Weak transcription	Psoas Muscle	Psoas
6	chr7:96749000-96768200	Weak transcription	Right Atrium	heart
7	chr7:96749200-96768000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr7:96749400-96768000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr7:96749400-96768200	Weak transcription	Primary T cells from cord blood	blood
10	chr7:96752400-96766000	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr7:96755000-96766800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr7:96755000-96768000	Weak transcription	Adipose Nuclei	Adipose
13	chr7:96756000-96762600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:96756200-96767800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr7:96756400-96765600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr7:96756600-96766400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr7:96756600-96768000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr7:96756600-96768000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr7:96759200-96768400	Weak transcription	Brain Hippocampus Middle	brain
20	chr7:96760000-96763400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr7:96760000-96767200	Weak transcription	Fetal Intestine Small	intestine
22	chr7:96760000-96768000	Weak transcription	Duodenum Mucosa	Duodenum
23	chr7:96760000-96768000	Weak transcription	Spleen	Spleen
24	chr7:96760000-96768200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr7:96760000-96768200	Weak transcription	Esophagus	oesophagus
26	chr7:96760200-96762600	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr7:96760200-96767800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr7:96760200-96768000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr7:96760200-96768200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr7:96760400-96766400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr7:96760400-96766600	Weak transcription	K562	blood
32	chr7:96760400-96767400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr7:96760400-96768000	Weak transcription	Liver	Liver
34	chr7:96760400-96768000	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr7:96760400-96768200	Weak transcription	Gastric	stomach
36	chr7:96760400-96768200	Weak transcription	Left Ventricle	heart
37	chr7:96760400-96796800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr7:96760600-96762200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr7:96760600-96762400	Weak transcription	HepG2	liver
40	chr7:96760600-96762600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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