Variant report

Variant	rs28533064
Chromosome Location	chr1:184431294-184431295
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:184412654..184414882-chr1:184428797..184431309,2	MCF-7	breast:
2	chr1:184429671..184432533-chr1:184459614..184461411,2	K562	blood:
3	chr1:184424018..184426734-chr1:184430772..184432362,2	K562	blood:
4	chr1:184353853..184357203-chr1:184430668..184434777,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000116667	Chromatin interaction
ENSG00000271387	Chromatin interaction

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

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

rs_ID	r²[population]
rs13374072	0.89[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530079	chr1:183797938-184639971	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	esv2756618	chr1:184393343-184674343	Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:184419200-184438400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr1:184419600-184432600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:184421400-184433000	Enhancers	Skeletal Muscle Male	skeletal muscle
4	chr1:184424000-184436400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr1:184425400-184442200	Weak transcription	Primary hematopoietic stem cells	blood
6	chr1:184427000-184431400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr1:184427400-184443800	Weak transcription	Esophagus	oesophagus
8	chr1:184427400-184444000	Weak transcription	Lung	lung
9	chr1:184427400-184448400	Weak transcription	Fetal Muscle Leg	muscle
10	chr1:184428600-184431600	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr1:184429000-184454800	Weak transcription	Aorta	Aorta
12	chr1:184429200-184431400	Weak transcription	Colon Smooth Muscle	Colon
13	chr1:184429400-184431400	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr1:184429400-184432800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr1:184429400-184432800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr1:184429400-184434800	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr1:184429400-184449600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr1:184429600-184434600	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr1:184429600-184442200	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr1:184429800-184436600	Weak transcription	Brain Angular Gyrus	brain
21	chr1:184430000-184431400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr1:184430000-184431400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr1:184430000-184431400	Enhancers	Stomach Smooth Muscle	stomach
24	chr1:184430000-184431800	Enhancers	Adipose Nuclei	Adipose
25	chr1:184430200-184431600	Enhancers	NHLF	lung
26	chr1:184430200-184431800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr1:184430200-184431800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr1:184430400-184431400	Weak transcription	Spleen	Spleen
29	chr1:184430400-184431800	Enhancers	Fetal Heart	heart
30	chr1:184430400-184439000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr1:184430600-184431400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr1:184430600-184431600	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr1:184430600-184431600	Enhancers	NHEK	skin
34	chr1:184430600-184433800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr1:184430600-184434600	Weak transcription	Right Atrium	heart
36	chr1:184430600-184436400	Weak transcription	Pancreas	Pancrea
37	chr1:184430600-184444000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr1:184430600-184449800	Weak transcription	Right Ventricle	heart
39	chr1:184430600-184450000	Weak transcription	Fetal Stomach	stomach
40	chr1:184430800-184431600	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr1:184430800-184432800	Weak transcription	Psoas Muscle	Psoas
42	chr1:184430800-184434800	Weak transcription	Left Ventricle	heart
43	chr1:184431000-184431600	Enhancers	Brain Germinal Matrix	brain
44	chr1:184431000-184431600	Enhancers	Duodenum Smooth Muscle	Duodenum
45	chr1:184431000-184436400	Weak transcription	Ovary	ovary
46	chr1:184431200-184431400	Enhancers	Brain Anterior Caudate	brain
47	chr1:184431200-184431800	Enhancers	Fetal Intestine Large	intestine
48	chr1:184431200-184431800	Enhancers	Fetal Intestine Small	intestine
49	chr1:184431200-184431800	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr1:184431200-184432000	Enhancers	Duodenum Mucosa	Duodenum

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