Variant report

Variant	rs147153441
Chromosome Location	chr10:98970711-98970712
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:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:98877113..98877837-chr10:98970293..98970909,2	MCF-7	breast:
2	chr10:98970157..98971031-chr10:99114717..99115659,2	MCF-7	breast:
3	chr10:98797178..98797761-chr10:98970351..98971056,2	MCF-7	breast:
4	chr10:98841084..98842088-chr10:98969940..98970900,4	MCF-7	breast:
5	chr10:98897666..98898578-chr10:98969950..98970807,6	MCF-7	breast:
6	chr10:98897585..98899016-chr10:98969998..98971139,5	MCF-7	breast:
7	chr10:98832347..98833305-chr10:98969570..98970861,6	MCF-7	breast:
8	chr10:98970315..98970824-chr10:98993860..98994647,2	MCF-7	breast:
9	chr10:98970361..98971335-chr10:98994318..98994830,2	K562	blood:
10	chr10:98832501..98833370-chr10:98969951..98970951,5	K562	blood:
11	chr10:98859426..98860138-chr10:98970400..98970959,2	K562	blood:
12	chr10:98832312..98833311-chr10:98969943..98970883,4	MCF-7	breast:
13	chr10:98833592..98834496-chr10:98970236..98971005,2	K562	blood:
14	chr10:98796818..98797761-chr10:98969942..98970829,2	K562	blood:

No data

No data

No data

Extended variants
information (count: 6 )
Associated
traits (count: 0)

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	nsv532232	chr10:98360775-99141797	Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv1041614	chr10:98928281-99083056	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	esv3361060	chr10:98939103-99025202	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
4	nsv1045553	chr10:98944397-99122203	Strong transcription Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv540750	chr10:98944397-99122203	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
6	nsv433513	chr10:98970664-98976923	Weak transcription Enhancers Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:98956600-98976000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr10:98968000-98977600	Weak transcription	GM12878-XiMat	blood
3	chr10:98968000-98979000	Weak transcription	Fetal Thymus	thymus
4	chr10:98968000-98982200	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr10:98968000-98982600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr10:98968200-98980600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr10:98970400-98974400	Weak transcription	Fetal Brain Male	brain
8	chr10:98970400-98982000	Weak transcription	Fetal Kidney	kidney

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

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