Variant report

Variant	rs17007714
Chromosome Location	chr4:124898374-124898375
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

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

rs_ID	r²[population]
rs1433209	1.00[AMR][1000 genomes]
rs2043345	1.00[AMR][1000 genomes]
rs7668990	1.00[AMR][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	esv34581	chr4:124271321-125247395	Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv830049	chr4:124793932-124955708	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv879875	chr4:124821888-124904592	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv868977	chr4:124841128-125550637	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv879876	chr4:124847477-124908231	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv879877	chr4:124847477-124935698	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv879878	chr4:124850901-124935698	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv879879	chr4:124893772-124971109	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:124893600-124903800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:124895600-124899200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr4:124895600-124899200	Enhancers	Fetal Lung	lung
4	chr4:124895600-124899400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr4:124895600-124899400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr4:124895800-124899200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr4:124896000-124899000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr4:124896000-124899200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr4:124896400-124899000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr4:124896600-124899200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr4:124896800-124899200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr4:124897000-124899000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr4:124897000-124899000	Enhancers	HUVEC	blood vessel
14	chr4:124897000-124899200	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr4:124897200-124898800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr4:124897200-124899000	Enhancers	Fetal Kidney	kidney
17	chr4:124897400-124898400	Enhancers	NHLF	lung
18	chr4:124897400-124899200	Enhancers	H1 Cell Line	embryonic stem cell
19	chr4:124897400-124899400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr4:124897600-124898400	Enhancers	H9 Cell Line	embryonic stem cell
21	chr4:124897600-124898400	Enhancers	Primary B cells from cord blood	blood
22	chr4:124897600-124898400	Enhancers	Fetal Brain Male	brain
23	chr4:124897600-124898400	Enhancers	Fetal Muscle Leg	muscle
24	chr4:124897600-124898800	Enhancers	Fetal Intestine Large	intestine
25	chr4:124897600-124899000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr4:124897600-124899000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr4:124897600-124899200	Enhancers	Stomach Mucosa	stomach
28	chr4:124897600-124899400	Enhancers	HepG2	liver
29	chr4:124898000-124899000	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr4:124898200-124898800	Weak transcription	NHDF-Ad	bronchial

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