Variant report

Variant	rs61267749
Chromosome Location	chr14:69122569-69122570
allele	C/G/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	chr14:68937048..68939834-chr14:69120983..69124190,3	MCF-7	breast:
2	chr14:69120949..69124420-chr14:69255481..69258792,4	MCF-7	breast:
3	chr14:69122320..69125331-chr14:69259876..69262362,3	MCF-7	breast:
4	chr14:69095981..69098144-chr14:69121077..69123082,2	MCF-7	breast:
5	chr14:69112688..69114597-chr14:69122344..69125074,2	K562	blood:
6	chr14:69030473..69032904-chr14:69122357..69124258,2	MCF-7	breast:
7	chr14:68740932..68744536-chr14:69121884..69124192,3	MCF-7	breast:
8	chr14:69111300..69112991-chr14:69119803..69122665,2	MCF-7	breast:
9	chr14:68990793..68991332-chr14:69122376..69122983,2	MCF-7	breast:
10	chr14:69122387..69124084-chr14:69250804..69252456,2	MCF-7	breast:
11	chr14:69115935..69118979-chr14:69121407..69123459,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000182185	Chromatin interaction
ENSG00000185650	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs11846166	1.00[EUR][1000 genomes]
rs73287717	1.00[EUR][1000 genomes]
rs73287719	1.00[EUR][1000 genomes]
rs73287720	1.00[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1798800	chr14:69114353-69131030	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69115200-69123400	Enhancers	Colon Smooth Muscle	Colon
2	chr14:69115400-69130200	Enhancers	Fetal Stomach	stomach
3	chr14:69116000-69123600	Enhancers	Ovary	ovary
4	chr14:69117000-69124000	Enhancers	Rectal Smooth Muscle	rectum
5	chr14:69119000-69122600	Weak transcription	A549	lung
6	chr14:69119000-69125800	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr14:69119600-69125400	Weak transcription	NHDF-Ad	bronchial
8	chr14:69120400-69123400	Enhancers	Spleen	Spleen
9	chr14:69120600-69122600	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr14:69120600-69122600	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr14:69120600-69123000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr14:69120600-69123600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr14:69120800-69122800	Enhancers	Brain Cingulate Gyrus	brain
14	chr14:69120800-69123000	Enhancers	Primary hematopoietic stem cells	blood
15	chr14:69120800-69123000	Enhancers	Fetal Heart	heart
16	chr14:69120800-69123600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr14:69120800-69123800	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr14:69120800-69126800	Enhancers	Fetal Lung	lung
19	chr14:69120800-69127000	Enhancers	Fetal Thymus	thymus
20	chr14:69120800-69139800	Enhancers	Fetal Muscle Leg	muscle
21	chr14:69121000-69122800	Enhancers	Right Ventricle	heart
22	chr14:69121000-69123000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr14:69121000-69123000	Enhancers	Pancreas	Pancrea
24	chr14:69121000-69123200	Enhancers	Primary T cells fromperipheralblood	blood
25	chr14:69121000-69123600	Enhancers	Fetal Intestine Small	intestine
26	chr14:69121000-69123600	Enhancers	Placenta	Placenta
27	chr14:69121000-69123800	Enhancers	Brain Substantia Nigra	brain
28	chr14:69121000-69125800	Enhancers	Fetal Muscle Trunk	muscle
29	chr14:69121200-69122600	Enhancers	Muscle Satellite Cultured Cells	--
30	chr14:69121200-69122800	Enhancers	Left Ventricle	heart
31	chr14:69121200-69122800	Enhancers	Right Atrium	heart
32	chr14:69121200-69122800	Enhancers	Stomach Mucosa	stomach
33	chr14:69121200-69122800	Enhancers	HSMM	muscle
34	chr14:69121200-69122800	Enhancers	HSMMtube	muscle
35	chr14:69121200-69123000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr14:69121200-69123000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr14:69121200-69123000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr14:69121200-69123000	Enhancers	Brain Hippocampus Middle	brain
39	chr14:69121200-69123000	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr14:69121200-69123000	Enhancers	Duodenum Smooth Muscle	Duodenum
41	chr14:69121200-69123000	Enhancers	Fetal Brain Female	brain
42	chr14:69121200-69123000	Enhancers	Lung	lung
43	chr14:69121200-69123000	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr14:69121200-69123400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr14:69121200-69123600	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr14:69121200-69123600	Enhancers	Fetal Intestine Large	intestine
47	chr14:69121200-69123800	Enhancers	Primary B cells from peripheral blood	blood
48	chr14:69121200-69129400	Enhancers	Placenta Amnion	Placenta Amnion
49	chr14:69121400-69122600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr14:69121400-69122800	Enhancers	Fetal Brain Male	brain

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