Variant report

Variant	rs528434096
Chromosome Location	chr8:96250128-96250129
allele	A/C
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:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:96221181..96226002-chr8:96248062..96252220,6	MCF-7	breast:
2	chr8:95907386..95908938-chr8:96249524..96251716,2	MCF-7	breast:
3	chr8:96249492..96251130-chr8:96256592..96259030,2	K562	blood:
4	chr8:96249665..96253673-chr8:96259430..96262765,4	K562	blood:
5	chr8:96145670..96147348-chr8:96249546..96251895,2	MCF-7	breast:
6	chr8:96243081..96246840-chr8:96248821..96252281,5	K562	blood:
7	chr8:96244866..96247715-chr8:96248127..96251735,3	K562	blood:
8	chr8:96218443..96220891-chr8:96249353..96251227,2	MCF-7	breast:
9	chr8:96150317..96152962-chr8:96247980..96250492,2	K562	blood:
10	chr8:96241648..96244611-chr8:96247721..96251221,3	K562	blood:
11	chr8:96231573..96233965-chr8:96249378..96252236,2	K562	blood:

No data

No data

No data

Extended variants
information (count: 2 )
Associated
traits (count: 0)

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	nsv6315	chr8:96216465-96261671	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv971599	chr8:96249324-96255153	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:96219800-96251800	Enhancers	Primary B cells from peripheral blood	blood
2	chr8:96238800-96250200	Weak transcription	Stomach Smooth Muscle	stomach
3	chr8:96242200-96280600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:96243800-96280400	Weak transcription	Primary hematopoietic stem cells	blood
5	chr8:96244200-96250200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr8:96245200-96254600	Weak transcription	Fetal Muscle Leg	muscle
7	chr8:96245200-96269200	Weak transcription	Fetal Muscle Trunk	muscle
8	chr8:96245600-96280400	Weak transcription	Fetal Stomach	stomach
9	chr8:96245600-96280400	Weak transcription	Pancreas	Pancrea
10	chr8:96248400-96262200	Weak transcription	HepG2	liver
11	chr8:96249000-96280800	Weak transcription	Gastric	stomach
12	chr8:96249400-96250600	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr8:96249600-96251400	Enhancers	Primary B cells from cord blood	blood
14	chr8:96249600-96271400	Weak transcription	Aorta	Aorta
15	chr8:96249800-96250200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr8:96249800-96251400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr8:96250000-96250200	Enhancers	GM12878-XiMat	blood
18	chr8:96250000-96250400	Enhancers	Spleen	Spleen

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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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