Variant report

Variant	rs13075568
Chromosome Location	chr3:119213913-119213914
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr3:119213780-119213930	HVMF	connective:	n/a	n/a
2	CTCF	chr3:119213780-119213930	NHEK	skin:	n/a	n/a

No data

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:119201366..119207142-chr3:119210949..119217240,7	K562	blood:
2	chr3:119181522..119184148-chr3:119211730..119214140,2	K562	blood:
3	chr3:119213354..119215944-chr3:119217357..119219322,2	K562	blood:
4	chr3:119186615..119189309-chr3:119211919..119214620,2	MCF-7	breast:

No data

Variant related genes	Relation type
TIMMDC1	TF binding region
ENSG00000163389	Chromatin interaction
ENSG00000176142	Chromatin interaction
ENSG00000113845	Chromatin interaction

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1131265	0.94[YRI][hapmap]
rs12695388	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1523311	0.90[ASN][1000 genomes]
rs2293370	0.94[YRI][hapmap]
rs2629396	0.90[ASN][1000 genomes]
rs4688014	0.89[AFR][1000 genomes]
rs6805225	0.88[ASN][1000 genomes]
rs7611041	0.95[ASN][1000 genomes]
rs7615155	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9855093	0.98[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9869760	0.85[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]

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	esv3487859	chr3:118570588-119419623	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	esv3487860	chr3:118570588-119419623	Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
3	nsv829695	chr3:119178890-119367996	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:119188400-119216200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr3:119188400-119216800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr3:119188600-119216200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr3:119188800-119216200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr3:119189000-119216200	Weak transcription	Stomach Mucosa	stomach
6	chr3:119189000-119216200	Weak transcription	HUVEC	blood vessel
7	chr3:119189000-119216600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr3:119189800-119216000	Weak transcription	Fetal Heart	heart
9	chr3:119190800-119216400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr3:119191000-119216400	Weak transcription	Fetal Brain Male	brain
11	chr3:119192400-119216400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr3:119196400-119216200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr3:119196400-119216600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr3:119196800-119216800	Weak transcription	Small Intestine	intestine
15	chr3:119197000-119216400	Weak transcription	Colon Smooth Muscle	Colon
16	chr3:119197400-119216600	Weak transcription	Aorta	Aorta
17	chr3:119204800-119216400	Weak transcription	Rectal Smooth Muscle	rectum
18	chr3:119205000-119216000	Weak transcription	Fetal Kidney	kidney
19	chr3:119205400-119216400	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr3:119205600-119216600	Weak transcription	Colonic Mucosa	Colon
21	chr3:119205600-119216600	Weak transcription	Esophagus	oesophagus
22	chr3:119205600-119216600	Weak transcription	Gastric	stomach
23	chr3:119205800-119216000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr3:119205800-119216200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr3:119205800-119216200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr3:119205800-119216200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr3:119205800-119216600	Weak transcription	Pancreas	Pancrea
28	chr3:119205800-119217000	Weak transcription	Spleen	Spleen
29	chr3:119206000-119216200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr3:119206000-119216200	Weak transcription	Fetal Lung	lung
31	chr3:119206000-119216200	Weak transcription	Psoas Muscle	Psoas
32	chr3:119206000-119216600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr3:119206200-119216000	Weak transcription	NHLF	lung
34	chr3:119206200-119216200	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr3:119206200-119216200	Weak transcription	NH-A	brain
36	chr3:119206400-119216200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr3:119206800-119216200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr3:119206800-119216200	Weak transcription	Brain Anterior Caudate	brain
39	chr3:119207000-119216800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
40	chr3:119207200-119215800	Weak transcription	HepG2	liver
41	chr3:119207200-119216200	Weak transcription	Hela-S3	cervix
42	chr3:119207200-119216600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr3:119207400-119216600	Weak transcription	Ovary	ovary
44	chr3:119207600-119216200	Weak transcription	HSMMtube	muscle
45	chr3:119207600-119216400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr3:119207800-119216600	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr3:119208200-119216200	Weak transcription	Brain Cingulate Gyrus	brain
48	chr3:119208600-119216600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr3:119208800-119216200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr3:119208800-119216200	Weak transcription	Fetal Intestine Small	intestine

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