Variant report

Variant	rs992919
Chromosome Location	chr4:94735892-94735893
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

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

rs_ID	r²[population]
rs56905352	1.00[AMR][1000 genomes]
rs59071973	1.00[AMR][1000 genomes]
rs72877822	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]

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	nsv1008055	chr4:94169131-95030074	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv931979	chr4:94289958-95121723	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv821636	chr4:94439636-95116590	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:94732000-94736000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr4:94735000-94736600	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr4:94735200-94736000	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr4:94735200-94736000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr4:94735200-94736200	Enhancers	H9 Cell Line	embryonic stem cell
6	chr4:94735200-94736400	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr4:94735400-94736200	Enhancers	H1 Cell Line	embryonic stem cell
8	chr4:94735400-94736200	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr4:94735400-94736600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr4:94735400-94736600	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr4:94735400-94736600	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr4:94735600-94736000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr4:94735600-94736000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
14	chr4:94735600-94736200	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr4:94735600-94736400	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr4:94735600-94736800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr4:94735800-94736200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr4:94735800-94736200	Enhancers	Dnd41	blood
19	chr4:94735800-94736400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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