Variant report

Variant	rs359666
Chromosome Location	chr7:127991090-127991091
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:127988874..127991097-chr7:127995362..127997136,2	K562	blood:
2	chr7:127990359..127992194-chr7:128021875..128024379,2	MCF-7	breast:
3	chr7:127989978..127992194-chr7:128000923..128002456,2	K562	blood:
4	chr7:127991021..127992566-chr7:128027560..128029110,2	MCF-7	breast:
5	chr7:127989814..127992283-chr7:128027367..128029799,2	MCF-7	breast:
6	chr7:127989735..127992397-chr7:128023905..128026447,2	K562	blood:
7	chr7:127990878..127995208-chr7:127998293..128004686,6	K562	blood:
8	chr7:127982717..127985560-chr7:127989854..127991998,3	K562	blood:
9	chr7:127986655..127989567-chr7:127989980..127992814,3	K562	blood:

No data

No data

No data

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs359638	1.00[EUR][1000 genomes]
rs359641	1.00[EUR][1000 genomes]
rs359665	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831124	chr7:127970345-128147910	Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
2	nsv889191	chr7:127973133-128073326	Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
3	nsv608400	chr7:127978820-128048194	Weak transcription Strong transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases
4	esv2493565	chr7:127985695-128053377	Weak transcription Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
5	esv3478325	chr7:127986726-128053483	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	esv3478326	chr7:127986726-128053483	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
7	esv3355435	chr7:127989716-127994314	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
8	esv3406494	chr7:127990366-127992864	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:127988200-127992200	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr7:127989200-127991200	Bivalent Enhancer	Fetal Muscle Leg	muscle
3	chr7:127990000-127991600	Weak transcription	Esophagus	oesophagus
4	chr7:127990400-127991200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
5	chr7:127990400-127994400	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr7:127990800-127991200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr7:127991000-127991200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr7:127991000-127991200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr7:127991000-127991400	Bivalent Enhancer	Fetal Brain Female	brain
10	chr7:127991000-127991400	Bivalent Enhancer	Fetal Thymus	thymus
11	chr7:127991000-127991400	Enhancers	Right Ventricle	heart
12	chr7:127991000-127991600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
13	chr7:127991000-127991600	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
14	chr7:127991000-127992800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr7:127991000-127993000	Bivalent/Poised TSS	iPS-15b 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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