Variant report

Variant	rs150601314
Chromosome Location	chr9:100806648-100806649
allele	-/CTC
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	chr9:100679327..100688755-chr9:100804829..100810921,12	K562	blood:
2	chr9:100743537..100749297-chr9:100805473..100813198,12	K562	blood:
3	chr9:100799367..100802266-chr9:100805470..100807708,2	MCF-7	breast:
4	chr9:100806291..100808002-chr9:100817271..100819268,2	MCF-7	breast:
5	chr9:100458298..100461061-chr9:100806544..100809239,2	K562	blood:
6	chr9:100743649..100747393-chr9:100806371..100809307,4	K562	blood:
7	chr9:100744535..100746584-chr9:100805455..100807504,2	MCF-7	breast:
8	chr9:100686261..100688755-chr9:100806613..100809213,2	K562	blood:
9	chr9:100806589..100809484-chr9:100810464..100812482,2	MCF-7	breast:

No data

No data

No data

Variant related genes	Relation type
ENSG00000136938	Chromatin interaction
ENSG00000136936	Chromatin interaction
ENSG00000136932	Chromatin interaction
ENSG00000095380	Chromatin interaction

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv482635	chr9:100775549-100953239	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	esv3483159	chr9:100806167-100814815	Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
3	esv3483160	chr9:100806167-100814815	Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:100798000-100807000	Weak transcription	Spleen	Spleen
2	chr9:100798000-100807600	Weak transcription	HSMMtube	muscle
3	chr9:100798200-100807400	Weak transcription	Primary B cells from cord blood	blood
4	chr9:100800200-100807000	Weak transcription	K562	blood
5	chr9:100801800-100807400	Weak transcription	HSMM	muscle
6	chr9:100802400-100809600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr9:100802800-100807600	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr9:100804800-100807800	Enhancers	Primary B cells from peripheral blood	blood
9	chr9:100805200-100807000	Enhancers	GM12878-XiMat	blood
10	chr9:100805800-100807400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr9:100806000-100807000	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr9:100806000-100807200	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr9:100806000-100808000	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr9:100806400-100807200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr9:100806600-100807400	Weak transcription	Primary hematopoietic stem cells	blood
16	chr9:100806600-100807400	Enhancers	Monocytes-CD14+_RO01746	blood

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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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