Variant report

Variant	rs369460582
Chromosome Location	chr14:69217290-69217291
allele	A/G
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:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:69211410..69213846-chr14:69215945..69218406,2	K562	blood:
2	chr14:69215425..69218916-chr14:69220182..69222789,4	K562	blood:
3	chr14:69217090..69220380-chr14:69222883..69225939,5	K562	blood:
4	chr14:69206060..69208927-chr14:69216486..69218861,2	MCF-7	breast:
5	chr14:69210895..69217826-chr14:69255953..69264501,15	K562	blood:
6	chr14:69212479..69217981-chr14:69255953..69262357,9	K562	blood:
7	chr14:69206574..69210602-chr14:69211879..69218026,8	K562	blood:
8	chr14:69183888..69188009-chr14:69213725..69217312,4	K562	blood:

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	nsv523795	chr14:69216412-69219896	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv456332	chr14:69216412-69230080	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv564963	chr14:69216412-69230080	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69201200-69222600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:69202800-69224600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr14:69204200-69219200	Weak transcription	Adipose Nuclei	Adipose
4	chr14:69212600-69229200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr14:69213800-69217400	Enhancers	HepG2	liver
6	chr14:69213800-69217400	Enhancers	K562	blood
7	chr14:69213800-69217800	Enhancers	Colon Smooth Muscle	Colon
8	chr14:69214400-69221000	Weak transcription	Right Atrium	heart
9	chr14:69214600-69224600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr14:69214800-69219800	Weak transcription	Fetal Lung	lung
11	chr14:69215400-69217400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr14:69215600-69222400	Weak transcription	Pancreas	Pancrea
13	chr14:69215800-69217400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr14:69215800-69221000	Weak transcription	Spleen	Spleen
15	chr14:69215800-69222400	Weak transcription	Right Ventricle	heart
16	chr14:69216400-69219600	Weak transcription	Stomach Mucosa	stomach
17	chr14:69216400-69219800	Weak transcription	Fetal Kidney	kidney
18	chr14:69216600-69224200	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr14:69216800-69218800	Weak transcription	Fetal Stomach	stomach
20	chr14:69217000-69218600	Weak transcription	Fetal Muscle Trunk	muscle
21	chr14:69217000-69218600	Weak transcription	Fetal Muscle Leg	muscle
22	chr14:69217000-69218600	Weak transcription	Left Ventricle	heart
23	chr14:69217000-69218600	Weak transcription	Lung	lung
24	chr14:69217000-69218800	Weak transcription	Fetal Intestine Small	intestine
25	chr14:69217000-69218800	Weak transcription	Rectal Smooth Muscle	rectum
26	chr14:69217000-69222600	Weak transcription	Placenta	Placenta
27	chr14:69217200-69218600	Weak transcription	Fetal Heart	heart

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