Variant report

Variant	rs692214
Chromosome Location	chr7:129173710-129173711
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs608336	1.00[EUR][1000 genomes]
rs610588	1.00[EUR][1000 genomes]
rs664746	1.00[EUR][1000 genomes]
rs686470	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs692710	1.00[EUR][1000 genomes]
rs712734	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831128	chr7:129063040-129240800	Weak transcription Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	esv3478069	chr7:129157163-129204221	Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	esv3478070	chr7:129157177-129204220	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	esv3407180	chr7:129170016-129174514	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:129150800-129175400	Weak transcription	Right Atrium	heart
2	chr7:129169400-129174800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:129171200-129175200	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr7:129171600-129174000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr7:129171600-129174400	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr7:129171800-129174200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr7:129172200-129173800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr7:129172200-129175400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr7:129172400-129175800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr7:129172600-129176000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr7:129172800-129174400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr7:129173200-129173800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr7:129173200-129173800	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr7:129173200-129174400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr7:129173200-129174600	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr7:129173400-129173800	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr7:129173400-129174200	Enhancers	H1 Cell Line	embryonic stem cell
18	chr7:129173600-129173800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr7:129173600-129174000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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