Variant report

Variant	rs1329248
Chromosome Location	chr10:25793215-25793216
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10508698	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11014579	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs11014588	1.00[ASN][1000 genomes]
rs11014592	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[YRI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11014593	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11014627	0.82[CEU][hapmap]
rs11591807	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs12248413	1.00[JPT][hapmap]
rs16926123	0.82[CEU][hapmap]
rs16926129	0.85[CEU][hapmap]
rs16926165	0.82[CEU][hapmap]
rs1855674	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34229386	0.91[ASN][1000 genomes]
rs35075874	0.97[ASN][1000 genomes]
rs4316420	0.85[CEU][hapmap];1.00[CHB][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs67192203	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7090929	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7093822	0.91[ASN][1000 genomes]
rs72788296	0.83[EUR][1000 genomes]
rs7902586	1.00[CEU][hapmap];0.96[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	esv3349863	chr10:25614571-25946379	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25783200-25797200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr10:25791600-25794600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr10:25791600-25800400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr10:25791800-25794600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr10:25791800-25794800	Weak transcription	Fetal Heart	heart
6	chr10:25791800-25796800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr10:25791800-25796800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr10:25791800-25797200	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr10:25791800-25797200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr10:25791800-25797200	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr10:25791800-25797200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr10:25791800-25797200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr10:25792000-25796000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr10:25792000-25796600	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr10:25792000-25797400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr10:25792400-25797000	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr10:25792600-25797000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr10:25792600-25797000	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr10:25792800-25811600	Weak transcription	Cortex derived primary cultured neurospheres	brain

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