Variant report

Variant	rs8111491
Chromosome Location	chr19:18449498-18449499
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	HNF4A	chr19:18449403-18449665	HepG2	liver:	n/a	chr19:18449575-18449590 chr19:18449576-18449589 chr19:18449575-18449588 chr19:18449576-18449584 chr19:18449575-18449588 chr19:18449576-18449588 chr19:18449575-18449590 chr19:18449574-18449589 chr19:18449575-18449590
2	HEY1	chr19:18449421-18449734	HepG2	liver:	n/a	n/a
3	HNF4G	chr19:18449429-18449710	HepG2	liver:	n/a	chr19:18449575-18449590 chr19:18449576-18449589 chr19:18449575-18449588 chr19:18449576-18449584 chr19:18449575-18449588 chr19:18449576-18449588 chr19:18449575-18449590 chr19:18449573-18449588 chr19:18449575-18449590
4	HNF4A	chr19:18449431-18449715	HepG2	liver:	n/a	chr19:18449575-18449590 chr19:18449576-18449589 chr19:18449575-18449588 chr19:18449576-18449584 chr19:18449575-18449588 chr19:18449576-18449588 chr19:18449575-18449590 chr19:18449574-18449589 chr19:18449575-18449590

No.	Distal block	Cell Line	Cell type
1	chr19:18448228..18453626-chr19:18495351..18501647,22	K562	blood:
2	chr19:18448952..18453435-chr19:18523841..18530143,7	K562	blood:
3	chr19:18449115..18453939-chr19:18483257..18487784,7	K562	blood:
4	chr19:18388723..18391469-chr19:18447700..18450655,3	MCF-7	breast:
5	chr19:18388917..18393354-chr19:18447866..18453758,9	MCF-7	breast:
6	chr19:18441208..18448128-chr19:18448861..18453326,10	K562	blood:

Variant related genes	Relation type
PGPEP1	TF binding region
ENSG00000130513	Chromatin interaction
ENSG00000264175	Chromatin interaction
ENSG00000130522	Chromatin interaction
ENSG00000130511	Chromatin interaction
ENSG00000239821	Chromatin interaction
ENSG00000267959	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs6512257	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7251109	0.92[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532614	chr19:18033043-18573963	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	204 gene(s)	inside rSNPs	diseases
2	nsv916325	chr19:18244780-18534927	Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	167 gene(s)	inside rSNPs	diseases
3	esv3323899	chr19:18343484-18620429	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	162 gene(s)	inside rSNPs	diseases
4	nsv911271	chr19:18362940-18453124	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	135 gene(s)	inside rSNPs	diseases
5	nsv911273	chr19:18386798-18454825	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	134 gene(s)	inside rSNPs	diseases
6	nsv911274	chr19:18440942-18691942	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18434800-18450600	Weak transcription	Spleen	Spleen
2	chr19:18440000-18450600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr19:18440400-18450600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr19:18440400-18450600	Weak transcription	Stomach Mucosa	stomach
5	chr19:18440400-18450600	Weak transcription	Stomach Smooth Muscle	stomach
6	chr19:18440400-18450800	Weak transcription	Right Ventricle	heart
7	chr19:18440600-18450800	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr19:18444000-18450800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr19:18444200-18451000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr19:18445000-18450600	Weak transcription	K562	blood
11	chr19:18445000-18450800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr19:18445000-18451000	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr19:18446600-18450600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr19:18446600-18450600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr19:18446600-18450600	Weak transcription	Placenta	Placenta
16	chr19:18446600-18451000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr19:18446800-18450600	Weak transcription	Lung	lung
18	chr19:18446800-18450800	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr19:18447400-18450600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr19:18447400-18450800	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr19:18447600-18449600	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr19:18448000-18450800	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr19:18448400-18450000	Flanking Active TSS	HepG2	liver
24	chr19:18448400-18450600	Weak transcription	Primary hematopoietic stem cells	blood
25	chr19:18448400-18450600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr19:18448400-18450600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr19:18448400-18450600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr19:18448600-18450800	Enhancers	Fetal Intestine Large	intestine
29	chr19:18448600-18450800	Enhancers	Fetal Intestine Small	intestine
30	chr19:18448600-18451000	Enhancers	Liver	Liver
31	chr19:18448800-18450600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr19:18448800-18450600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr19:18448800-18450600	Weak transcription	Adipose Nuclei	Adipose
34	chr19:18449000-18449800	Weak transcription	Monocytes-CD14+_RO01746	blood
35	chr19:18449000-18450600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr19:18449000-18450600	Enhancers	Duodenum Mucosa	Duodenum
37	chr19:18449000-18450600	Weak transcription	Fetal Muscle Leg	muscle
38	chr19:18449200-18450600	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr19:18449200-18450800	Weak transcription	Left Ventricle	heart
40	chr19:18449200-18450800	Enhancers	Pancreas	Pancrea
41	chr19:18449400-18450600	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr19:18449400-18450800	Weak transcription	Fetal Heart	heart

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