Variant report

Variant	rs559961233
Chromosome Location	chr1:210405154-210405155
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:210398376..210400495-chr1:210402941..210405832,2	K562	blood:
2	chr1:210404317..210408653-chr1:210545033..210548956,7	MCF-7	breast:
3	chr1:210404553..210406882-chr6:30538400..30541136,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000204574	Chromatin interaction
ENSG00000200972	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	nsv1014034	chr1:209759648-210501731	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv8769	chr1:210403509-210564588	Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
3	esv3422029	chr1:210404854-210407702	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr1:210403800-210405200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr1:210403800-210405600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr1:210403800-210405600	Enhancers	NHEK	skin
4	chr1:210404200-210405200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr1:210404400-210405200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
6	chr1:210404400-210405200	Enhancers	Colon Smooth Muscle	Colon
7	chr1:210404400-210405200	Enhancers	Rectal Smooth Muscle	rectum
8	chr1:210404400-210405600	Bivalent Enhancer	Fetal Heart	heart
9	chr1:210405000-210405200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
10	chr1:210405000-210405200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
11	chr1:210405000-210405200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
12	chr1:210405000-210405200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:210405000-210405200	Enhancers	Muscle Satellite Cultured Cells	--
14	chr1:210405000-210405200	Enhancers	Placenta Amnion	Placenta Amnion
15	chr1:210405000-210405400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr1:210405000-210405400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
17	chr1:210405000-210405400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr1:210405000-210405400	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr1:210405000-210405400	Bivalent Enhancer	Fetal Muscle Leg	muscle
20	chr1:210405000-210405400	Enhancers	Left Ventricle	heart
21	chr1:210405000-210405400	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr1:210405000-210405400	Bivalent Enhancer	NHDF-Ad	bronchial
23	chr1:210405000-210405600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr1:210405000-210405600	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr1:210405000-210405600	Bivalent Enhancer	Thymus	Thymus
26	chr1:210405000-210407400	Active TSS	Stomach Smooth Muscle	stomach
27	chr1:210405000-210407600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell

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