Variant report

Variant	rs2192741
Chromosome Location	chr7:12132417-12132418
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10226395	0.96[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs12667855	0.82[ASN][1000 genomes]
rs1990602	0.82[ASN][1000 genomes]
rs1990603	0.81[ASN][1000 genomes]
rs2215992	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4721029	0.94[ASN][1000 genomes]
rs7788863	0.87[ASN][1000 genomes]
rs7807762	0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv606199	chr7:11506143-12486659	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv887614	chr7:11778424-12211198	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv830906	chr7:12001764-12177869	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1023608	chr7:12064114-12247520	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv887626	chr7:12119520-12151476	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1031893	chr7:12127098-12155796	Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12127200-12142600	Weak transcription	Fetal Lung	lung
2	chr7:12131400-12132600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:12131400-12133600	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr7:12131400-12133600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr7:12131600-12133000	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr7:12131600-12133800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr7:12131600-12134400	Weak transcription	Placenta	Placenta
8	chr7:12131800-12133800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr7:12132000-12132600	Enhancers	A549	lung
10	chr7:12132000-12133800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr7:12132000-12133800	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr7:12132200-12133600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr7:12132400-12132600	Enhancers	H1 Cell Line	embryonic stem cell
14	chr7:12132400-12132600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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