Variant report

Variant	rs7159438
Chromosome Location	chr14:72922485-72922486
allele	C/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:8)

rs_ID	r²[population]
rs2238182	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2238190	0.82[JPT][hapmap]
rs4903020	0.95[YRI][hapmap]
rs4903023	0.96[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4903027	0.81[CEU][hapmap]
rs7143134	0.82[JPT][hapmap]
rs7160223	1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs719064	0.87[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530794	chr14:72113818-73034008	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv948800	chr14:72462557-73150701	Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:72913800-72922600	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr14:72918000-72924400	Weak transcription	Spleen	Spleen
3	chr14:72918000-72930000	Weak transcription	Right Atrium	heart
4	chr14:72918200-72929000	Weak transcription	Brain Cingulate Gyrus	brain
5	chr14:72918200-72930000	Weak transcription	Left Ventricle	heart
6	chr14:72918400-72924200	Weak transcription	HSMM	muscle
7	chr14:72918800-72924200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr14:72919000-72924200	Weak transcription	NH-A	brain
9	chr14:72919000-72931400	Weak transcription	Adipose Nuclei	Adipose
10	chr14:72919400-72926800	Weak transcription	Fetal Intestine Small	intestine
11	chr14:72919400-72945200	Weak transcription	Brain Germinal Matrix	brain
12	chr14:72919800-72923200	Weak transcription	Esophagus	oesophagus
13	chr14:72919800-72924000	Weak transcription	HSMMtube	muscle
14	chr14:72919800-72924400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr14:72919800-72927400	Weak transcription	Fetal Muscle Leg	muscle
16	chr14:72921400-72924400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr14:72922400-72924400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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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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