Variant report

Variant	rs560445583
Chromosome Location	chr12:57400209-57400210
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:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:57398945..57400725-chr12:57479656..57482846,3	MCF-7	breast:
2	chr12:57079674..57082070-chr12:57399337..57401813,2	MCF-7	breast:
3	chr12:57398623..57401161-chr12:57471695..57473634,2	MCF-7	breast:
4	chr12:57398801..57400743-chr12:57521280..57524489,3	K562	blood:
5	chr12:57393282..57404587-chr12:57480276..57487045,17	MCF-7	breast:
6	chr12:57398801..57400719-chr12:57521892..57524489,2	K562	blood:
7	chr12:57156641..57157497-chr12:57399996..57400652,4	MCF-7	breast:
8	chr12:57400180..57401732-chr12:57514933..57516523,2	K562	blood:
9	chr12:57399976..57400833-chr12:57424825..57425490,2	MCF-7	breast:
10	chr12:57145657..57146209-chr12:57399868..57400428,2	MCF-7	breast:
11	chr12:57388586..57390855-chr12:57398700..57400334,2	MCF-7	breast:
12	chr12:56709311..56709830-chr12:57399980..57400910,2	MCF-7	breast:
13	chr12:57399687..57402362-chr12:57503183..57504772,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000144785	Chromatin interaction
ENSG00000123384	Chromatin interaction
ENSG00000166886	Chromatin interaction
ENSG00000166866	Chromatin interaction
ENSG00000257727	Chromatin interaction
ENSG00000166881	Chromatin interaction
ENSG00000166888	Chromatin interaction
ENSG00000268162	Chromatin interaction
ENSG00000258442	Chromatin interaction
ENSG00000263832	Chromatin interaction
ENSG00000110958	Chromatin interaction
ENSG00000025423	Chromatin interaction
ENSG00000198056	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

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	nsv1040850	chr12:57055011-57679209	Strong transcription Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Genic enhancers 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 miRNA target site	181 gene(s)	inside rSNPs	diseases
2	nsv428590	chr12:57329214-57527358	Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
3	nsv832428	chr12:57340609-57535694	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
4	nsv559022	chr12:57394123-57410389	Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	esv3395929	chr12:57399110-57401658	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	18 gene(s)	inside rSNPs	diseases
6	esv3377733	chr12:57399235-57401433	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:57398600-57400800	Active TSS	H1 Cell Line	embryonic stem cell
2	chr12:57399000-57400600	Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr12:57399000-57400600	Active TSS	NHDF-Ad	bronchial
4	chr12:57399000-57400800	Active TSS	HUES64 Cell Line	embryonic stem cell
5	chr12:57399000-57400800	Active TSS	HSMM	muscle
6	chr12:57399200-57400400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr12:57399200-57400400	Active TSS	Lung	lung
8	chr12:57399200-57400600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr12:57399200-57400600	Active TSS	Esophagus	oesophagus
10	chr12:57399200-57400600	Active TSS	Fetal Brain Female	brain
11	chr12:57399200-57400600	Active TSS	Rectal Mucosa Donor 29	rectum
12	chr12:57399200-57400600	Active TSS	Right Ventricle	heart
13	chr12:57399200-57400800	Active TSS	H9 Cell Line	embryonic stem cell
14	chr12:57399200-57400800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr12:57399200-57400800	Active TSS	Left Ventricle	heart
16	chr12:57399200-57400800	Active TSS	Ovary	ovary
17	chr12:57399200-57400800	Active TSS	HSMMtube	muscle
18	chr12:57399200-57401000	Enhancers	Stomach Mucosa	stomach
19	chr12:57399400-57400400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr12:57399400-57400400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr12:57399400-57400400	Active TSS	Fetal Intestine Large	intestine
22	chr12:57399400-57400400	Active TSS	Fetal Muscle Trunk	muscle
23	chr12:57399400-57400400	Active TSS	HepG2	liver
24	chr12:57399400-57400600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr12:57399400-57400600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr12:57399400-57400600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
27	chr12:57399400-57400600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr12:57399400-57400600	Active TSS	Breast Myoepithelial Primary Cells	Breast
29	chr12:57399400-57400600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr12:57399400-57400600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
31	chr12:57399400-57400600	Active TSS	Fetal Kidney	kidney
32	chr12:57399400-57400600	Active TSS	Fetal Stomach	stomach
33	chr12:57399400-57400600	Active TSS	Pancreas	Pancrea
34	chr12:57399400-57400600	Active TSS	Psoas Muscle	Psoas
35	chr12:57399400-57400600	Active TSS	Right Atrium	heart
36	chr12:57399400-57400600	Active TSS	Skeletal Muscle Female	skeletal muscle
37	chr12:57399400-57400600	Active TSS	A549	lung
38	chr12:57399400-57400600	Active TSS	GM12878-XiMat	blood
39	chr12:57399400-57400600	Active TSS	NHLF	lung
40	chr12:57399400-57400800	Active TSS	HUES48 Cell Line	embryonic stem cell
41	chr12:57399400-57400800	Active TSS	Pancreatic Islets	Pancreatic Islet
42	chr12:57399400-57401000	Active TSS	Brain Hippocampus Middle	brain
43	chr12:57399400-57401400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr12:57399600-57400400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr12:57399600-57400400	Active TSS	Primary hematopoietic stem cells short term culture	blood
46	chr12:57399600-57400400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr12:57399600-57400400	Active TSS	Rectal Smooth Muscle	rectum
48	chr12:57399600-57400400	Active TSS	Sigmoid Colon	Sigmoid Colon
49	chr12:57399600-57400400	Active TSS	K562	blood
50	chr12:57399600-57400600	Active TSS	iPS-18 Cell Line	embryonic stem cell

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