Variant report

Variant	rs55817227
Chromosome Location	chr12:123122570-123122571
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:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:123122086..123123273-chr12:123236757..123237976,12	MCF-7	breast:
2	chr12:123122176..123123128-chr12:123214963..123215579,2	MCF-7	breast:
3	chr12:123120054..123123996-chr12:123234682..123237075,4	MCF-7	breast:
4	chr12:123009865..123013304-chr12:123120249..123122722,3	MCF-7	breast:
5	chr12:123122056..123123058-chr12:123236724..123237693,13	MCF-7	breast:
6	chr12:123120971..123123822-chr12:123241913..123244089,2	MCF-7	breast:
7	chr12:123122176..123123060-chr12:123236746..123237553,10	K562	blood:
8	chr12:123118461..123125368-chr12:123234706..123239529,13	MCF-7	breast:
9	chr12:123122297..123122893-chr12:123215090..123215755,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000111011	Chromatin interaction
ENSG00000196917	Chromatin interaction
ENSG00000184445	Chromatin interaction
ENSG00000139726	Chromatin interaction

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs55935830	0.83[AMR][1000 genomes]
rs56019922	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56990369	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57142071	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57766838	1.00[AMR][1000 genomes]
rs58276954	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60586933	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61062446	1.00[AMR][1000 genomes]
rs61275910	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61585633	1.00[AMR][1000 genomes]
rs6489161	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7134209	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7307052	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7310898	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7960674	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7972727	1.00[AMR][1000 genomes]
rs7973067	1.00[AMR][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	nsv1054458	chr12:123045662-123133545	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123077400-123137600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:123077600-123128200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr12:123101600-123131000	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr12:123105800-123124600	Weak transcription	Fetal Brain Female	brain
5	chr12:123108000-123131400	Weak transcription	NHLF	lung
6	chr12:123108200-123124200	Weak transcription	HMEC	breast
7	chr12:123108400-123128600	Weak transcription	Placenta	Placenta
8	chr12:123109400-123128000	Weak transcription	Primary hematopoietic stem cells	blood
9	chr12:123110600-123128000	Weak transcription	NHDF-Ad	bronchial
10	chr12:123111600-123136200	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr12:123111800-123127600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr12:123112000-123123400	Weak transcription	Hela-S3	cervix
13	chr12:123112000-123126400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr12:123112000-123128400	Weak transcription	Primary T cells from cord blood	blood
15	chr12:123112200-123128200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr12:123112200-123130600	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr12:123112200-123131200	Weak transcription	Osteobl	bone
18	chr12:123112400-123126600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr12:123112400-123128200	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr12:123112400-123129400	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr12:123112400-123131000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr12:123114600-123127600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr12:123115000-123124600	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr12:123115000-123128000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr12:123115000-123131400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr12:123115800-123123600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr12:123116600-123122800	Weak transcription	Fetal Intestine Small	intestine
28	chr12:123117600-123127600	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr12:123119000-123127800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr12:123119000-123128000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr12:123119200-123126800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr12:123119200-123128800	Weak transcription	K562	blood
33	chr12:123119600-123128000	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr12:123119800-123123200	Weak transcription	Thymus	Thymus
35	chr12:123119800-123128000	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr12:123119800-123128400	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr12:123120000-123125400	Weak transcription	Fetal Stomach	stomach
38	chr12:123120000-123128000	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr12:123120200-123127600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr12:123120200-123128000	Weak transcription	HepG2	liver
41	chr12:123120200-123128200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr12:123120200-123131000	Weak transcription	GM12878-XiMat	blood
43	chr12:123120200-123140800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr12:123120400-123127800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr12:123120400-123128200	Weak transcription	Fetal Muscle Leg	muscle
46	chr12:123120400-123131000	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr12:123120600-123127600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr12:123120600-123128000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr12:123120600-123128200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr12:123120600-123129400	Weak transcription	Dnd41	blood

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