Variant report

Variant	rs17844794
Chromosome Location	chr12:56234664-56234665
allele	C/T
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:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:56222506..56227501-chr12:56233677..56237355,4	K562	blood:
2	chr12:56224688..56227501-chr12:56233908..56236745,4	K562	blood:
3	chr12:56228843..56232382-chr12:56234016..56237333,4	K562	blood:
4	chr12:56233687..56236115-chr12:56320248..56323583,3	MCF-7	breast:
5	chr12:56220285..56224153-chr12:56233677..56238372,4	K562	blood:
6	chr12:56136251..56138283-chr12:56233199..56235588,2	MCF-7	breast:
7	chr12:56232558..56234911-chr9:128508305..128510267,2	MCF-7	breast:
8	chr12:56232360..56237326-chr12:56316163..56320896,5	K562	blood:

No data

Variant related genes	Relation type
ENSG00000170473	Chromatin interaction
ENSG00000135414	Chromatin interaction
ENSG00000065357	Chromatin interaction
ENSG00000257390	Chromatin interaction
ENSG00000167081	Chromatin interaction
ENSG00000229582	Chromatin interaction
ENSG00000182796	Chromatin interaction
ENSG00000123342	Chromatin interaction
ENSG00000135392	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11171678	1.00[CEU][hapmap]
rs1681072	1.00[MEX][hapmap]
rs17117976	1.00[LWK][hapmap];0.81[MKK][hapmap]
rs2071024	1.00[CEU][hapmap];1.00[MEX][hapmap]
rs4359251	1.00[CEU][hapmap]
rs6581081	1.00[LWK][hapmap];0.81[MKK][hapmap]
rs7296036	1.00[LWK][hapmap];0.81[MKK][hapmap]

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	nsv832423	chr12:56080822-56253698	Flanking Active TSS Strong transcription Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	119 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:56225400-56236000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr12:56225400-56236000	Weak transcription	NHEK	skin
3	chr12:56225400-56236600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:56225400-56237000	Weak transcription	GM12878-XiMat	blood
5	chr12:56225600-56235200	Weak transcription	NHDF-Ad	bronchial
6	chr12:56225600-56235400	Weak transcription	HSMMtube	muscle
7	chr12:56225600-56235800	Weak transcription	Duodenum Mucosa	Duodenum
8	chr12:56225600-56236000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr12:56225600-56236000	Weak transcription	NH-A	brain
10	chr12:56225800-56236200	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr12:56225800-56244000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr12:56226000-56235600	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr12:56226000-56236200	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr12:56226200-56235400	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr12:56226200-56236000	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr12:56226200-56236600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr12:56226400-56234800	Weak transcription	Colonic Mucosa	Colon
18	chr12:56226800-56234800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr12:56226800-56235800	Weak transcription	Fetal Lung	lung
20	chr12:56226800-56241400	Weak transcription	Brain Cingulate Gyrus	brain
21	chr12:56227000-56236000	Weak transcription	Right Ventricle	heart
22	chr12:56227000-56236200	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr12:56227400-56235400	Weak transcription	Right Atrium	heart
24	chr12:56227400-56236000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr12:56227400-56236000	Weak transcription	Colon Smooth Muscle	Colon
26	chr12:56227400-56236000	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr12:56227400-56236200	Weak transcription	Esophagus	oesophagus
28	chr12:56227600-56241200	Weak transcription	Brain Hippocampus Middle	brain
29	chr12:56228000-56235000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr12:56228600-56234800	Strong transcription	Muscle Satellite Cultured Cells	--
31	chr12:56228600-56235000	Strong transcription	Fetal Stomach	stomach
32	chr12:56229000-56240800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr12:56229400-56236400	Weak transcription	Thymus	Thymus
34	chr12:56229600-56234800	Strong transcription	NHLF	lung
35	chr12:56230000-56236600	Weak transcription	Fetal Intestine Large	intestine
36	chr12:56230400-56241000	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr12:56231000-56234800	Weak transcription	Fetal Muscle Trunk	muscle
38	chr12:56231200-56236400	Weak transcription	Fetal Intestine Small	intestine
39	chr12:56232200-56236200	Enhancers	Placenta	Placenta
40	chr12:56232400-56235400	Weak transcription	Gastric	stomach
41	chr12:56232400-56236400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr12:56232400-56241000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr12:56232600-56235000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr12:56232800-56235200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr12:56233200-56235000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr12:56233200-56235200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr12:56233400-56234800	Genic enhancers	Adipose Nuclei	Adipose
48	chr12:56233600-56235400	Weak transcription	Ovary	ovary
49	chr12:56233600-56236000	Weak transcription	Aorta	Aorta
50	chr12:56233600-56241000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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