Variant report

Variant	rs16849934
Chromosome Location	chr4:74600673-74600674
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:74596146..74598686-chr4:74599662..74602190,5	K562	blood:
2	chr4:74591810..74594488-chr4:74595060..74600715,5	MCF-7	breast:
3	chr4:74596146..74597922-chr4:74599662..74601519,2	K562	blood:
4	chr4:74572825..74575404-chr4:74599407..74602314,2	K562	blood:
5	chr4:74588963..74591805-chr4:74598001..74600687,2	MCF-7	breast:
6	chr4:74599752..74603059-chr4:74603100..74608923,6	K562	blood:

Variant related genes	Relation type
ENSG00000169429	Chromatin interaction

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs16849925	0.86[AFR][1000 genomes]
rs1957074	1.00[MEX][hapmap]
rs2227525	0.93[AFR][1000 genomes]
rs2227532	0.82[ASW][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes]
rs2227545	0.93[AFR][1000 genomes]
rs2463883	1.00[MEX][hapmap]
rs57818652	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59914288	0.92[AFR][1000 genomes];1.00[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:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:74595000-74602400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr4:74595200-74601800	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr4:74596400-74605400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:74596400-74606000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr4:74597400-74601400	Weak transcription	Lung	lung
6	chr4:74597800-74601800	Enhancers	HUVEC	blood vessel
7	chr4:74598000-74605200	Weak transcription	Left Ventricle	heart
8	chr4:74598400-74602000	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr4:74598400-74602200	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr4:74598800-74601600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr4:74599000-74601600	Enhancers	GM12878-XiMat	blood
12	chr4:74599800-74600800	Enhancers	Colon Smooth Muscle	Colon
13	chr4:74599800-74602000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr4:74600000-74601000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr4:74600000-74601000	Enhancers	K562	blood
16	chr4:74600000-74601200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr4:74600000-74601200	Enhancers	NHLF	lung
18	chr4:74600000-74601400	Enhancers	Osteobl	bone
19	chr4:74600000-74601600	Enhancers	Primary hematopoietic stem cells	blood
20	chr4:74600000-74601600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr4:74600200-74600800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr4:74600200-74600800	Enhancers	NH-A	brain
23	chr4:74600200-74601200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr4:74600400-74600800	Enhancers	HMEC	breast
25	chr4:74600400-74601200	Enhancers	Adipose Nuclei	Adipose
26	chr4:74600400-74601600	Enhancers	A549	lung
27	chr4:74600400-74602200	Enhancers	NHDF-Ad	bronchial
28	chr4:74600400-74605400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr4:74600400-74606200	Weak transcription	Primary B cells from cord blood	blood
30	chr4:74600600-74600800	Enhancers	Muscle Satellite Cultured Cells	--
31	chr4:74600600-74601200	Enhancers	Hela-S3	cervix
32	chr4:74600600-74601400	Enhancers	NHEK	skin
33	chr4:74600600-74601600	Weak transcription	HSMM	muscle
34	chr4:74600600-74605200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr4:74600600-74606200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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