Variant report

Variant	rs17098454
Chromosome Location	chr12:63263986-63263987
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:63262389..63265887-chr12:63279810..63282418,3	MCF-7	breast:
2	chr12:63263678..63269164-chr12:63325830..63330278,6	MCF-7	breast:
3	chr12:63256130..63258393-chr12:63262684..63264265,2	K562	blood:
4	chr12:63262984..63265194-chr12:63280872..63282464,2	MCF-7	breast:
5	chr12:63260158..63264907-chr12:63265796..63270388,6	MCF-7	breast:

Variant related genes	Relation type
ENSG00000252660	Chromatin interaction
ENSG00000111110	Chromatin interaction

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs17098470	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17822974	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41380144	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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	esv3415227	chr12:63228121-63591615	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 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	chr12:63258200-63277200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr12:63258800-63264400	Enhancers	HepG2	liver
3	chr12:63260200-63275400	Weak transcription	Pancreas	Pancrea
4	chr12:63260600-63270600	Weak transcription	Aorta	Aorta
5	chr12:63260800-63267000	Weak transcription	Placenta	Placenta
6	chr12:63260800-63270000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr12:63260800-63275200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr12:63261000-63264800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr12:63261200-63265800	Weak transcription	Brain Hippocampus Middle	brain
10	chr12:63261200-63275000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr12:63261200-63277800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr12:63261400-63266800	Weak transcription	Fetal Intestine Small	intestine
13	chr12:63261800-63264800	Weak transcription	NH-A	brain
14	chr12:63261800-63267000	Weak transcription	Fetal Intestine Large	intestine
15	chr12:63262000-63269600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr12:63262200-63266800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr12:63262200-63267200	Weak transcription	K562	blood
18	chr12:63262400-63269600	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr12:63262400-63275200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr12:63262400-63277000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr12:63262600-63267200	Weak transcription	A549	lung
22	chr12:63262600-63267800	Weak transcription	Brain Angular Gyrus	brain
23	chr12:63262600-63267800	Weak transcription	Brain Substantia Nigra	brain
24	chr12:63262800-63276000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr12:63263400-63264000	Enhancers	Brain Cingulate Gyrus	brain
26	chr12:63263400-63267000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr12:63263400-63277200	Weak transcription	H9 Cell Line	embryonic stem cell

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