Variant report

Variant	rs73585971
Chromosome Location	chr14:21504467-21504468
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:21498286..21500648-chr14:21502338..21505596,3	K562	blood:
2	chr14:21503364..21505418-chr14:21509371..21512241,2	K562	blood:
3	chr14:21490493..21493487-chr14:21503206..21505661,2	MCF-7	breast:
4	chr14:21502778..21505418-chr14:21509371..21512527,3	K562	blood:

Variant related genes	Relation type
ENSG00000179636	Chromatin interaction
ENSG00000165799	Chromatin interaction
ENSG00000258604	Chromatin interaction
ENSG00000165795	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs73573860	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	nsv427936	chr14:21216108-21531783	Flanking Active TSS Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
2	nsv428293	chr14:21216108-21531783	Enhancers Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
3	nsv832740	chr14:21332060-21545052	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	45 gene(s)	inside rSNPs	diseases
4	nsv530009	chr14:21377022-22044608	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
5	nsv530769	chr14:21407536-22139126	Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
6	nsv1039369	chr14:21499054-21530301	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21495400-21505200	Weak transcription	Spleen	Spleen
2	chr14:21495400-21514200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr14:21500400-21505000	Weak transcription	Brain Angular Gyrus	brain
4	chr14:21500600-21506000	Weak transcription	Liver	Liver
5	chr14:21501200-21504800	Weak transcription	Esophagus	oesophagus
6	chr14:21501200-21505200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr14:21501200-21505400	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr14:21501600-21504600	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr14:21501800-21504800	Weak transcription	Left Ventricle	heart
10	chr14:21501800-21505000	Weak transcription	Psoas Muscle	Psoas
11	chr14:21502000-21504800	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr14:21502000-21505000	Weak transcription	Stomach Smooth Muscle	stomach
13	chr14:21502000-21506000	Weak transcription	Right Atrium	heart
14	chr14:21502000-21536600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr14:21502200-21505000	Weak transcription	Right Ventricle	heart
16	chr14:21502200-21505000	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr14:21502400-21504600	Weak transcription	Brain Substantia Nigra	brain
18	chr14:21502400-21504800	Weak transcription	Brain Anterior Caudate	brain
19	chr14:21502600-21504800	Weak transcription	Fetal Muscle Trunk	muscle
20	chr14:21502800-21504800	Weak transcription	Brain Hippocampus Middle	brain
21	chr14:21503400-21504800	Weak transcription	Brain Cingulate Gyrus	brain
22	chr14:21503400-21504800	Weak transcription	Fetal Muscle Leg	muscle
23	chr14:21503600-21505400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr14:21503600-21506000	Weak transcription	Lung	lung
25	chr14:21503800-21505400	Weak transcription	Fetal Intestine Large	intestine
26	chr14:21503800-21506000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr14:21504000-21505600	Weak transcription	Duodenum Mucosa	Duodenum
28	chr14:21504000-21509600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr14:21504200-21509600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr14:21504400-21507400	Enhancers	Ovary	ovary

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