Variant report

Variant	rs529530319
Chromosome Location	chr12:58352454-58352455
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:58339593..58341366-chr12:58350590..58353556,2	K562	blood:

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	nsv559046	chr12:58162085-58478598	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	261 gene(s)	inside rSNPs	diseases
2	nsv523853	chr12:58350631-58386722	ZNF genes & repeats Enhancers Strong transcription Weak transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv975500	chr12:58351052-58362673	ZNF genes & repeats Weak transcription Strong transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:58336000-58353000	Weak transcription	Small Intestine	intestine
2	chr12:58336200-58353000	Weak transcription	Stomach Mucosa	stomach
3	chr12:58336200-58353400	Weak transcription	Fetal Kidney	kidney
4	chr12:58336200-58353600	Weak transcription	Brain Substantia Nigra	brain
5	chr12:58336200-58353600	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr12:58336200-58353800	Weak transcription	Brain Angular Gyrus	brain
7	chr12:58336200-58353800	Weak transcription	Brain Hippocampus Middle	brain
8	chr12:58336200-58354000	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr12:58336200-58354000	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr12:58336200-58354000	Weak transcription	Psoas Muscle	Psoas
11	chr12:58336200-58356200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr12:58336200-58359600	Weak transcription	A549	lung
13	chr12:58336400-58359600	Weak transcription	HMEC	breast
14	chr12:58336800-58353000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr12:58337200-58358400	Weak transcription	HepG2	liver
16	chr12:58343200-58352600	Weak transcription	Brain Cingulate Gyrus	brain
17	chr12:58345000-58352600	Strong transcription	Dnd41	blood
18	chr12:58346400-58352600	Strong transcription	Primary T helper cells fromperipheralblood	blood
19	chr12:58347800-58352600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr12:58348800-58353800	Weak transcription	Osteobl	bone
21	chr12:58350200-58352600	Strong transcription	Skeletal Muscle Female	skeletal muscle
22	chr12:58350400-58352600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr12:58350400-58352600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr12:58350400-58352600	Strong transcription	Adipose Nuclei	Adipose
25	chr12:58350600-58352800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr12:58350600-58355400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr12:58350800-58352600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr12:58351000-58352600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
29	chr12:58351000-58352600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr12:58351000-58352600	Strong transcription	Colonic Mucosa	Colon
31	chr12:58351000-58352600	Strong transcription	Skeletal Muscle Male	skeletal muscle
32	chr12:58351200-58352600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr12:58351200-58352600	ZNF genes & repeats	Fetal Intestine Small	intestine
34	chr12:58351200-58352600	ZNF genes & repeats	Fetal Stomach	stomach
35	chr12:58351200-58352600	ZNF genes & repeats	Gastric	stomach
36	chr12:58351200-58352600	ZNF genes & repeats	Thymus	Thymus
37	chr12:58351200-58359400	Weak transcription	K562	blood
38	chr12:58351400-58352600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr12:58351400-58352600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
40	chr12:58351400-58352600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
41	chr12:58351400-58352600	Strong transcription	Fetal Lung	lung
42	chr12:58351400-58352600	ZNF genes & repeats	Fetal Muscle Leg	muscle
43	chr12:58351400-58352600	ZNF genes & repeats	Pancreas	Pancrea
44	chr12:58351400-58352600	Strong transcription	Right Ventricle	heart
45	chr12:58351400-58355400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr12:58351600-58352600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
47	chr12:58351600-58352600	Strong transcription	Primary B cells from cord blood	blood
48	chr12:58351600-58352600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
49	chr12:58351800-58352600	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
50	chr12:58351800-58353200	Weak transcription	Brain Inferior Temporal Lobe	brain

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