Variant report

Variant	rs28534698
Chromosome Location	chr15:77849724-77849725
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:77847726..77850177-chr15:77859392..77861698,2	K562	blood:
2	chr15:77848566..77850112-chr15:77856631..77859198,2	K562	blood:
3	chr15:77848268..77851249-chr15:77883793..77885346,2	MCF-7	breast:
4	chr15:77840852..77845440-chr15:77846808..77850692,5	K562	blood:
5	chr15:77848438..77851266-chr15:77854844..77857960,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000259420	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11855272	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs16953967	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16968930	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2137111	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs28375490	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28712147	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4243046	0.89[EUR][1000 genomes]
rs4886874	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61097729	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61483316	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs907370	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs907371	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 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
8	nsv904415	chr15:77845959-77943935	Weak transcription Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv904416	chr15:77845959-77967416	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs28534698	TSPAN3	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:77838600-77849800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr15:77842200-77850200	Enhancers	Brain Inferior Temporal Lobe	brain
3	chr15:77842800-77850400	Enhancers	Brain Hippocampus Middle	brain
4	chr15:77844400-77850200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr15:77844600-77850000	Enhancers	Brain Anterior Caudate	brain
6	chr15:77844800-77849800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr15:77844800-77849800	Enhancers	Brain Substantia Nigra	brain
8	chr15:77846200-77850200	Enhancers	Brain Cingulate Gyrus	brain
9	chr15:77846800-77850000	Enhancers	Fetal Lung	lung
10	chr15:77847000-77851200	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr15:77847400-77850800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr15:77847600-77850000	Weak transcription	Spleen	Spleen
13	chr15:77848000-77849800	Enhancers	Brain Germinal Matrix	brain
14	chr15:77848000-77855800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr15:77848600-77849800	Enhancers	Fetal Brain Female	brain
16	chr15:77848600-77850000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr15:77848600-77850000	Enhancers	Brain Angular Gyrus	brain
18	chr15:77848600-77850200	Enhancers	Fetal Intestine Large	intestine
19	chr15:77848600-77850600	Enhancers	Placenta	Placenta
20	chr15:77848800-77850200	Enhancers	Fetal Heart	heart
21	chr15:77848800-77850400	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr15:77849000-77850200	Enhancers	H1 Cell Line	embryonic stem cell
23	chr15:77849000-77850200	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr15:77849000-77850200	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr15:77849000-77850200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr15:77849000-77850200	Enhancers	Gastric	stomach
27	chr15:77849200-77850000	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr15:77849200-77850000	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr15:77849200-77850200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr15:77849200-77850200	Enhancers	K562	blood
31	chr15:77849200-77850600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr15:77849400-77850000	Enhancers	Duodenum Mucosa	Duodenum
33	chr15:77849400-77850400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr15:77849600-77849800	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr15:77849600-77850000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr15:77849600-77850000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr15:77849600-77850000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr15:77849600-77850000	Enhancers	Left Ventricle	heart
39	chr15:77849600-77850200	Enhancers	Right Ventricle	heart

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