Variant report

Variant	rs73257437
Chromosome Location	chr5:114595440-114595441
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ZC3H11A	chr5:114595406-114595446	K562	blood:	n/a	n/a

No data

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:114585052..114588251-chr5:114594409..114598098,3	MCF-7	breast:
2	chr5:114592752..114595570-chr5:114596936..114601339,4	K562	blood:
3	chr5:114594074..114596339-chr5:114629566..114632305,2	MCF-7	breast:
4	chr5:114593995..114595570-chr5:114596536..114598747,2	K562	blood:
5	chr5:114594025..114596331-chr5:114597028..114599085,3	MCF-7	breast:
6	chr5:114593990..114598856-chr5:114605325..114609897,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000271797	TF binding region
ENSG00000164221	Chromatin interaction
ENSG00000271797	Chromatin interaction
ENSG00000243304	Chromatin interaction
ENSG00000164219	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs17132480	1.00[AFR][1000 genomes]
rs17137549	1.00[AFR][1000 genomes]
rs17137556	1.00[AFR][1000 genomes]
rs17137563	1.00[AFR][1000 genomes]
rs35940728	0.92[AFR][1000 genomes]
rs57979677	0.82[AFR][1000 genomes]
rs58955791	1.00[AFR][1000 genomes]
rs59891755	0.92[AFR][1000 genomes]
rs59955726	1.00[AFR][1000 genomes]
rs60460575	1.00[AFR][1000 genomes]
rs73253428	0.84[AFR][1000 genomes]
rs73253432	1.00[AFR][1000 genomes]
rs73253434	1.00[AFR][1000 genomes]
rs73253440	1.00[AFR][1000 genomes]
rs73253463	1.00[AFR][1000 genomes]
rs73253466	1.00[AFR][1000 genomes]
rs73255427	1.00[AFR][1000 genomes]
rs73255447	1.00[AFR][1000 genomes]
rs73255479	1.00[AFR][1000 genomes]
rs73255484	1.00[AFR][1000 genomes]
rs73255489	1.00[AFR][1000 genomes]
rs73255491	1.00[AFR][1000 genomes]
rs73255494	1.00[AFR][1000 genomes]
rs73255498	1.00[AFR][1000 genomes]
rs73257403	0.96[AFR][1000 genomes]
rs73257406	1.00[AFR][1000 genomes]
rs73257411	0.93[AFR][1000 genomes]
rs73257413	1.00[AFR][1000 genomes]
rs73257417	0.93[AFR][1000 genomes]
rs73257425	1.00[AFR][1000 genomes]
rs73257446	0.92[AFR][1000 genomes]
rs73257462	0.92[AFR][1000 genomes]
rs73257485	0.92[AFR][1000 genomes]
rs73257491	0.85[AFR][1000 genomes]
rs73257494	0.85[AFR][1000 genomes]
rs73259410	0.85[AFR][1000 genomes]
rs73259416	0.85[AFR][1000 genomes]
rs73259426	0.85[AFR][1000 genomes]
rs7703973	1.00[AFR][1000 genomes]
rs7711888	1.00[AFR][1000 genomes]
rs7724266	1.00[AFR][1000 genomes]
rs7725609	1.00[AFR][1000 genomes]
rs7726219	1.00[AFR][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	nsv830454	chr5:114453864-114607159	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:114547800-114596600	Weak transcription	Brain Germinal Matrix	brain
2	chr5:114548400-114596800	Weak transcription	K562	blood
3	chr5:114549400-114597200	Weak transcription	Aorta	Aorta
4	chr5:114563400-114597600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr5:114565200-114597400	Weak transcription	Colonic Mucosa	Colon
6	chr5:114575000-114597000	Weak transcription	Fetal Stomach	stomach
7	chr5:114575800-114597000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr5:114576000-114596800	Weak transcription	Fetal Kidney	kidney
9	chr5:114576000-114596800	Weak transcription	Rectal Smooth Muscle	rectum
10	chr5:114576200-114596000	Weak transcription	Hela-S3	cervix
11	chr5:114576200-114596800	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr5:114576600-114596200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:114576600-114596400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr5:114576600-114597000	Weak transcription	Brain Substantia Nigra	brain
15	chr5:114576800-114596000	Weak transcription	NHDF-Ad	bronchial
16	chr5:114576800-114596400	Weak transcription	Fetal Lung	lung
17	chr5:114576800-114597000	Weak transcription	Thymus	Thymus
18	chr5:114576800-114597400	Weak transcription	Fetal Muscle Trunk	muscle
19	chr5:114577000-114596800	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr5:114577000-114596800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr5:114577000-114597200	Weak transcription	Placenta	Placenta
22	chr5:114577200-114596800	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr5:114577400-114596800	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr5:114579600-114596000	Weak transcription	HSMM	muscle
25	chr5:114579600-114596600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr5:114579600-114597000	Weak transcription	Small Intestine	intestine
27	chr5:114579800-114597000	Weak transcription	Fetal Intestine Small	intestine
28	chr5:114579800-114597400	Weak transcription	Left Ventricle	heart
29	chr5:114584600-114596800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr5:114584600-114597000	Weak transcription	Primary hematopoietic stem cells	blood
31	chr5:114584600-114597000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr5:114584600-114597000	Weak transcription	Fetal Intestine Large	intestine
33	chr5:114584600-114597000	Weak transcription	Fetal Muscle Leg	muscle
34	chr5:114584600-114597200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr5:114585400-114596000	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr5:114585400-114597000	Weak transcription	Primary T cells fromperipheralblood	blood
37	chr5:114585400-114597200	Weak transcription	Fetal Thymus	thymus
38	chr5:114587400-114596000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr5:114587800-114596000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr5:114587800-114597000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr5:114588600-114595800	Weak transcription	NHEK	skin
42	chr5:114589800-114596000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr5:114591000-114597000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr5:114591600-114597000	Weak transcription	Adipose Nuclei	Adipose
45	chr5:114592000-114596000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr5:114592000-114596000	Weak transcription	Brain Anterior Caudate	brain
47	chr5:114592000-114596400	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr5:114592400-114595600	Weak transcription	HepG2	liver
49	chr5:114592400-114597000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr5:114592600-114595800	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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