Variant report

Variant	rs16968930
Chromosome Location	chr15:77843434-77843435
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:77837146..77840341-chr15:77840841..77844639,4	K562	blood:
2	chr15:77841651..77843844-chr15:77860587..77863167,2	K562	blood:
3	chr15:77842609..77845174-chr8:144895503..144897609,2	MCF-7	breast:
4	chr15:77840852..77845440-chr15:77846808..77850692,5	K562	blood:

Variant related genes	Relation type
ENSG00000180900	Chromatin interaction
ENSG00000259420	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11855272	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11856084	0.82[JPT][hapmap]
rs1317320	0.89[JPT][hapmap]
rs16953967	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs16968895	0.83[CEU][hapmap];0.90[JPT][hapmap]
rs16968897	0.86[CEU][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes]
rs16968900	0.81[EUR][1000 genomes]
rs17394448	0.89[JPT][hapmap]
rs17471697	0.80[JPT][hapmap]
rs2137111	0.92[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs28375490	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28534698	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28712147	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4243046	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4886874	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61097729	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61483316	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs907370	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs907371	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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	nsv1040852	chr15:77160237-78137541	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv916323	chr15:77485765-78121259	Enhancers Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv1043284	chr15:77740632-77884026	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
4	nsv570139	chr15:77762493-77865459	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	nsv570140	chr15:77787469-77851535	Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv833060	chr15:77816654-78035204	Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	esv1806097	chr15:77817889-78301377	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs16968930	TSPAN3	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:77827000-77845400	Weak transcription	Fetal Kidney	kidney
2	chr15:77829400-77844800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr15:77836200-77846600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr15:77838600-77849800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr15:77838800-77849000	Weak transcription	Gastric	stomach
6	chr15:77839000-77844400	Weak transcription	Stomach Mucosa	stomach
7	chr15:77839800-77846400	Weak transcription	Fetal Heart	heart
8	chr15:77840600-77848600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr15:77840800-77844000	Enhancers	Fetal Muscle Leg	muscle
10	chr15:77840800-77845200	Enhancers	Placenta	Placenta
11	chr15:77841200-77843600	Enhancers	Fetal Muscle Trunk	muscle
12	chr15:77841400-77846600	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr15:77841600-77844600	Weak transcription	Brain Anterior Caudate	brain
14	chr15:77841600-77844800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr15:77841600-77845400	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr15:77841600-77845600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr15:77841600-77846000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr15:77841600-77846800	Weak transcription	Spleen	Spleen
19	chr15:77841600-77847000	Weak transcription	Fetal Brain Female	brain
20	chr15:77841600-77849600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr15:77842200-77844600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr15:77842200-77844600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr15:77842200-77850200	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr15:77842600-77843800	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr15:77842800-77843600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr15:77842800-77843600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
27	chr15:77842800-77843800	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chr15:77842800-77843800	Enhancers	HSMMtube	muscle
29	chr15:77842800-77844000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr15:77842800-77850400	Enhancers	Brain Hippocampus Middle	brain
31	chr15:77843000-77843800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr15:77843000-77843800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr15:77843000-77843800	Enhancers	Brain Angular Gyrus	brain
34	chr15:77843000-77843800	Enhancers	Brain Substantia Nigra	brain
35	chr15:77843000-77844000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr15:77843000-77845000	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr15:77843200-77843600	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr15:77843200-77844000	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr15:77843200-77844200	Enhancers	Brain Cingulate Gyrus	brain
40	chr15:77843400-77843800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr15:77843400-77843800	Enhancers	Placenta Amnion	Placenta Amnion
42	chr15:77843400-77844000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
43	chr15:77843400-77846400	Weak transcription	Fetal Stomach	stomach

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