Variant report

Variant	rs16849896
Chromosome Location	chr4:74591152-74591153
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:74571713..74573594-chr4:74589343..74591305,2	K562	blood:
2	chr4:74588963..74591805-chr4:74598001..74600687,2	MCF-7	breast:
3	chr4:74590489..74596671-chr4:74604726..74609497,7	MCF-7	breast:

Variant related genes	Relation type
ENSG00000169429	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs1745250	0.85[YRI][hapmap];0.83[AMR][1000 genomes]
rs6446952	0.83[AMR][1000 genomes]
rs73827890	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73827892	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7654490	0.81[LWK][hapmap];0.81[YRI][hapmap];0.83[AMR][1000 genomes]
rs7654906	0.83[AMR][1000 genomes]

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	nsv1001725	chr4:74354050-74860924	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv530126	chr4:74376622-74843892	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv1008104	chr4:74468434-74621952	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv1012198	chr4:74487793-74621952	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
5	nsv537139	chr4:74487793-74621952	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
6	nsv1005231	chr4:74555497-74680079	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 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	chr4:74585000-74591600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr4:74587400-74592600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr4:74587600-74591200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr4:74587600-74592000	Weak transcription	Placenta	Placenta
5	chr4:74587800-74591600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr4:74588000-74591200	Weak transcription	NHEK	skin
7	chr4:74588000-74595000	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr4:74588000-74595200	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr4:74588200-74591200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr4:74588200-74591600	Weak transcription	NHLF	lung
11	chr4:74588600-74591200	Weak transcription	A549	lung
12	chr4:74588600-74591200	Weak transcription	HSMM	muscle
13	chr4:74588600-74591400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr4:74588600-74592000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr4:74588800-74591200	Weak transcription	Osteobl	bone
16	chr4:74589000-74591200	Weak transcription	NH-A	brain
17	chr4:74589000-74591400	Weak transcription	K562	blood
18	chr4:74589000-74592000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr4:74589200-74591200	Weak transcription	NHDF-Ad	bronchial
20	chr4:74589200-74591400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr4:74589200-74591800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr4:74589400-74591200	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr4:74589400-74592200	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr4:74589600-74591200	Weak transcription	Hela-S3	cervix
25	chr4:74590800-74592400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr4:74590800-74593000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr4:74590800-74596400	Enhancers	HUVEC	blood vessel
28	chr4:74591000-74592600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr4:74591000-74592800	Enhancers	HMEC	breast
30	chr4:74591000-74594000	Enhancers	Placenta Amnion	Placenta Amnion

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