Variant report

Variant	rs907371
Chromosome Location	chr15:77844375-77844376
allele	C/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	chr15:77842609..77845174-chr8:144895503..144897609,2	MCF-7	breast:
3	chr15:77840852..77845440-chr15:77846808..77850692,5	K562	blood:

Variant related genes	Relation type
ENSG00000180900	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11855272	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11856084	0.82[JPT][hapmap]
rs12324211	0.82[JPT][hapmap]
rs1317320	0.89[JPT][hapmap];0.82[MEX][hapmap]
rs16953967	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs16968895	0.89[JPT][hapmap]
rs16968897	0.86[CEU][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes]
rs16968900	0.81[EUR][1000 genomes]
rs16968930	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]
rs17394448	0.89[JPT][hapmap];0.82[MEX][hapmap]
rs17471697	0.80[JPT][hapmap]
rs2137111	0.93[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.95[ASN][1000 genomes]
rs2307141	0.82[JPT][hapmap]
rs28375490	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28534698	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28712147	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3784788	0.82[JPT][hapmap]
rs4243046	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4886874	1.00[CEU][hapmap];0.93[CHB][hapmap];0.88[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61097729	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61483316	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs907370	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs907398	0.82[JPT][hapmap]

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:6)

SNP	Gene	Cis/trans	Tissue	Source
rs907371	TSPAN3	Cis_1M	lymphoblastoid	RTeQTL
rs907371	CYP1A2	cis	cerebellum	SCAN
rs907371	STRA6	cis	cerebellum	SCAN
rs907371	PSTPIP1	cis	multi-tissue	Pritchard
rs907371	TSPAN3	cis	cerebellum	SCAN
rs907371	HMG20A	cis	parietal	SCAN

Chromatin state (count:37 , 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	chr15:77840800-77845200	Enhancers	Placenta	Placenta
10	chr15:77841400-77846600	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr15:77841600-77844600	Weak transcription	Brain Anterior Caudate	brain
12	chr15:77841600-77844800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr15:77841600-77845400	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr15:77841600-77845600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr15:77841600-77846000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr15:77841600-77846800	Weak transcription	Spleen	Spleen
17	chr15:77841600-77847000	Weak transcription	Fetal Brain Female	brain
18	chr15:77841600-77849600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr15:77842200-77844600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr15:77842200-77844600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr15:77842200-77850200	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr15:77842800-77850400	Enhancers	Brain Hippocampus Middle	brain
23	chr15:77843000-77845000	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr15:77843400-77846400	Weak transcription	Fetal Stomach	stomach
25	chr15:77843600-77844800	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr15:77843600-77846200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr15:77843800-77844800	Weak transcription	Brain Angular Gyrus	brain
28	chr15:77843800-77844800	Weak transcription	Brain Substantia Nigra	brain
29	chr15:77843800-77845800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr15:77843800-77846000	Bivalent Enhancer	HepG2	liver
31	chr15:77843800-77847400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr15:77844000-77844400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr15:77844000-77844400	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr15:77844000-77846000	Weak transcription	Fetal Muscle Leg	muscle
35	chr15:77844000-77846600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr15:77844200-77844400	Enhancers	Fetal Intestine Small	intestine
37	chr15:77844200-77844600	Weak transcription	Brain Cingulate Gyrus	brain

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