Variant report

Variant	rs111318836
Chromosome Location	chr5:98356806-98356807
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:98356545..98359049-chr5:98366364..98368367,2	K562	blood:
2	chr5:98263973..98268060-chr5:98355511..98358159,6	K562	blood:
3	chr5:98264797..98266835-chr5:98354593..98357011,2	K562	blood:
4	chr5:98355578..98358107-chr5:98362158..98365732,4	K562	blood:
5	chr5:98262156..98264317-chr5:98355438..98358771,4	K562	blood:
6	chr5:98250951..98253126-chr5:98356611..98358893,2	K562	blood:

Variant related genes	Relation type
ENSG00000153922	Chromatin interaction
ENSG00000248489	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1826071	chr5:98312447-98358852	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv1827754	chr5:98312447-98358852	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv1837772	chr5:98312447-98358852	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv1838335	chr5:98312447-98358852	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	esv1845131	chr5:98312447-98358852	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv599100	chr5:98345182-98357415	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	esv1794778	chr5:98345182-98358852	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	esv1825119	chr5:98345182-98358852	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv599113	chr5:98345632-98357415	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	nsv1024391	chr5:98355665-98653657	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:98353600-98358000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr5:98353600-98361600	Weak transcription	Small Intestine	intestine
3	chr5:98354600-98357000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr5:98354600-98357000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr5:98354800-98357000	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr5:98355000-98358200	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr5:98355000-98358400	Enhancers	Fetal Intestine Small	intestine
8	chr5:98355000-98358600	Enhancers	Fetal Intestine Large	intestine
9	chr5:98355400-98357000	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr5:98355400-98357000	Enhancers	Liver	Liver
11	chr5:98355400-98357400	Enhancers	Duodenum Mucosa	Duodenum
12	chr5:98355600-98358400	Enhancers	HepG2	liver
13	chr5:98356000-98360600	Weak transcription	Colonic Mucosa	Colon
14	chr5:98356400-98357200	Weak transcription	K562	blood
15	chr5:98356400-98357600	Weak transcription	Stomach Mucosa	stomach
16	chr5:98356400-98360400	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr5:98356400-98360400	Weak transcription	GM12878-XiMat	blood
18	chr5:98356400-98361000	Weak transcription	Primary hematopoietic stem cells	blood
19	chr5:98356400-98361000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr5:98356400-98361000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr5:98356400-98361200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr5:98356400-98361200	Weak transcription	Fetal Stomach	stomach
23	chr5:98356400-98361600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr5:98356400-98361800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr5:98356400-98362400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr5:98356600-98357000	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr5:98356800-98357000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
28	chr5:98356800-98358200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr5:98356800-98361000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr5:98356800-98361000	Weak transcription	A549	lung
31	chr5:98356800-98361000	Weak transcription	HUVEC	blood vessel
32	chr5:98356800-98361200	Weak transcription	Adipose Nuclei	Adipose

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