Variant report

Variant	rs74901851
Chromosome Location	chr14:68602097-68602098
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:68570562..68573394-chr14:68599517..68602198,2	MCF-7	breast:
2	chr14:68541688..68545482-chr14:68601842..68606347,5	MCF-7	breast:
3	chr14:68600662..68602278-chr14:69257760..69259773,2	MCF-7	breast:
4	chr14:68601379..68608308-chr14:69256404..69263440,24	MCF-7	breast:
5	chr14:68588139..68594823-chr14:68601028..68606199,6	MCF-7	breast:
6	chr14:68600338..68604507-chr14:69260783..69264203,4	MCF-7	breast:
7	chr14:68569098..68575378-chr14:68600721..68608879,10	MCF-7	breast:
8	chr14:68602094..68605658-chr14:68697621..68700210,3	MCF-7	breast:
9	chr14:68601506..68610081-chr14:68654290..68661321,21	MCF-7	breast:
10	chr14:68601301..68602871-chr14:68607372..68610107,2	MCF-7	breast:
11	chr14:68532345..68534667-chr14:68601779..68604351,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000185650	Chromatin interaction

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869154	chr14:68366754-69041768	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	esv3523718	chr14:68601299-68605697	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	esv3421508	chr14:68601799-68604997	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:68592200-68603000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:68592400-68602200	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr14:68592400-68604600	Weak transcription	Psoas Muscle	Psoas
4	chr14:68592400-68606200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr14:68593400-68603400	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr14:68594200-68604400	Weak transcription	Fetal Stomach	stomach
7	chr14:68596200-68604800	Weak transcription	Primary hematopoietic stem cells	blood
8	chr14:68598800-68603800	Weak transcription	Adipose Nuclei	Adipose
9	chr14:68599000-68602200	Weak transcription	NH-A	brain
10	chr14:68599600-68603600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr14:68599600-68603800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr14:68599800-68603000	Weak transcription	Fetal Muscle Leg	muscle
13	chr14:68599800-68604400	Weak transcription	Ovary	ovary
14	chr14:68600000-68604200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr14:68600000-68606200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr14:68601200-68606400	Weak transcription	Brain Hippocampus Middle	brain
17	chr14:68601400-68602400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
18	chr14:68601400-68604400	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr14:68601800-68602200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
20	chr14:68601800-68602200	Enhancers	HSMM	muscle
21	chr14:68601800-68602400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr14:68601800-68602400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr14:68601800-68602400	Enhancers	Fetal Kidney	kidney
24	chr14:68601800-68602400	Enhancers	Rectal Smooth Muscle	rectum
25	chr14:68601800-68602400	Enhancers	GM12878-XiMat	blood
26	chr14:68601800-68602600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr14:68601800-68602600	Enhancers	Colon Smooth Muscle	Colon
28	chr14:68601800-68602600	ZNF genes & repeats	A549	lung
29	chr14:68601800-68602600	Enhancers	NHLF	lung
30	chr14:68601800-68603200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr14:68601800-68604200	Enhancers	Muscle Satellite Cultured Cells	--
32	chr14:68601800-68607200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr14:68601800-68608800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr14:68601800-68613600	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr14:68601800-68614400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr14:68601800-68614800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr14:68601800-68615600	Enhancers	HMEC	breast
38	chr14:68602000-68602200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr14:68602000-68602200	Flanking Active TSS	NHEK	skin
40	chr14:68602000-68602600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr14:68602000-68602600	Enhancers	Osteobl	bone
42	chr14:68602000-68602800	Enhancers	NHDF-Ad	bronchial
43	chr14:68602000-68603200	Enhancers	HSMMtube	muscle
44	chr14:68602000-68607400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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