Variant report

Variant	rs74038894
Chromosome Location	chr14:24298742-24298743
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:24137621..24139131-chr14:24297384..24299665,2	MCF-7	breast:
2	chr14:24285592..24288155-chr14:24298380..24300344,2	K562	blood:

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

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

rs_ID	r²[population]
rs11627053	0.94[AFR][1000 genomes]
rs17097763	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17097766	1.00[AFR][1000 genomes]
rs2332142	1.00[AMR][1000 genomes]
rs74038887	1.00[AMR][1000 genomes]
rs8006078	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043299	chr14:23766696-24351724	Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
2	esv3405661	chr14:24189883-24670942	Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	131 gene(s)	inside rSNPs	diseases
3	nsv564045	chr14:24224245-24348343	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv901494	chr14:24243637-24386159	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr14:24295800-24302000	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr14:24296400-24299800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr14:24296400-24302000	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr14:24296400-24302000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr14:24296600-24301200	Enhancers	HSMMtube	muscle
6	chr14:24296600-24301800	Enhancers	HSMM	muscle
7	chr14:24297000-24298800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr14:24297000-24299000	Enhancers	Primary hematopoietic stem cells	blood
9	chr14:24297200-24301000	Enhancers	Hela-S3	cervix
10	chr14:24297400-24298800	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr14:24297400-24298800	Enhancers	Small Intestine	intestine
12	chr14:24297400-24299200	Enhancers	Colon Smooth Muscle	Colon
13	chr14:24297400-24299200	Enhancers	Rectal Mucosa Donor 29	rectum
14	chr14:24297400-24301600	Enhancers	Muscle Satellite Cultured Cells	--
15	chr14:24297600-24299800	Enhancers	Rectal Smooth Muscle	rectum
16	chr14:24297600-24300400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr14:24297600-24300400	Weak transcription	Ovary	ovary
18	chr14:24298200-24298800	Enhancers	Stomach Mucosa	stomach
19	chr14:24298200-24300200	Enhancers	NHDF-Ad	bronchial
20	chr14:24298400-24298800	Enhancers	Duodenum Smooth Muscle	Duodenum
21	chr14:24298400-24299200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr14:24298400-24299200	Bivalent Enhancer	HepG2	liver
23	chr14:24298400-24300000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr14:24298400-24300000	Enhancers	HMEC	breast
25	chr14:24298400-24300600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr14:24298600-24298800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr14:24298600-24299000	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr14:24298600-24299200	Flanking Active TSS	A549	lung
29	chr14:24298600-24300000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr14:24298600-24300000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr14:24298600-24300000	Enhancers	HUVEC	blood vessel
32	chr14:24298600-24300000	Enhancers	NH-A	brain
33	chr14:24298600-24300000	Enhancers	NHEK	skin
34	chr14:24298600-24300200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr14:24298600-24300600	Enhancers	Osteobl	bone

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