Variant report

Variant	rs16851444
Chromosome Location	chr1:165807812-165807813
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:165737816..165739553-chr1:165807597..165809420,3	MCF-7	breast:
2	chr1:165739953..165741791-chr1:165806314..165808597,2	K562	blood:
3	chr1:165804707..165809840-chr1:165822123..165825220,4	K562	blood:
4	chr1:165806407..165808791-chr1:165825833..165828310,2	MCF-7	breast:
5	chr1:165806807..165812397-chr1:165814507..165819170,6	MCF-7	breast:
6	chr1:165804707..165808619-chr1:165822123..165824856,3	K562	blood:

Variant related genes	Relation type
ENSG00000143183	Chromatin interaction
ENSG00000224358	Chromatin interaction

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

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

rs_ID	r²[population]
rs12091518	1.00[JPT][hapmap]
rs3790662	1.00[JPT][hapmap]
rs4657478	0.89[CEU][hapmap];0.81[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2756102	chr1:165652342-165877342	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv517792	chr1:165785503-165811729	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	31 gene(s)	inside rSNPs	diseases
3	esv2830094	chr1:165785503-165840411	Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	31 gene(s)	inside rSNPs	diseases
4	nsv818544	chr1:165797966-165811729	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases
5	nsv548097	chr1:165797966-165825166	Flanking Active TSS Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:165798600-165811000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr1:165798800-165811000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:165798800-165811000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr1:165798800-165811400	Weak transcription	Esophagus	oesophagus
5	chr1:165798800-165811800	Weak transcription	Primary B cells from cord blood	blood
6	chr1:165798800-165814200	Weak transcription	Fetal Muscle Trunk	muscle
7	chr1:165799000-165810600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr1:165799000-165811000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr1:165799000-165811200	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr1:165799000-165811800	Weak transcription	Colon Smooth Muscle	Colon
11	chr1:165799000-165811800	Weak transcription	Fetal Intestine Large	intestine
12	chr1:165799000-165811800	Weak transcription	Fetal Stomach	stomach
13	chr1:165799000-165818200	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr1:165799200-165811000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr1:165799200-165811400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr1:165799200-165811400	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr1:165799200-165811600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr1:165799200-165815800	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr1:165799400-165810800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr1:165799400-165810800	Weak transcription	NHEK	skin
21	chr1:165799400-165811000	Weak transcription	Fetal Muscle Leg	muscle
22	chr1:165800600-165811600	Weak transcription	Fetal Brain Male	brain
23	chr1:165802600-165809600	Weak transcription	Fetal Intestine Small	intestine
24	chr1:165802800-165809000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr1:165802800-165810600	Weak transcription	HMEC	breast
26	chr1:165802800-165810800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr1:165802800-165810800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr1:165802800-165810800	Weak transcription	NHDF-Ad	bronchial
29	chr1:165802800-165811200	Weak transcription	Ovary	ovary
30	chr1:165804400-165809000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr1:165805400-165808000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr1:165805800-165808000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr1:165805800-165808200	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr1:165805800-165809000	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr1:165806000-165808000	Enhancers	Fetal Thymus	thymus
36	chr1:165806000-165808000	Enhancers	Gastric	stomach
37	chr1:165806000-165808000	Enhancers	Lung	lung
38	chr1:165806000-165808000	Genic enhancers	A549	lung
39	chr1:165806000-165808000	Genic enhancers	K562	blood
40	chr1:165806000-165808200	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr1:165806000-165809000	Enhancers	HUVEC	blood vessel
42	chr1:165806000-165809800	Enhancers	H1 Cell Line	embryonic stem cell
43	chr1:165806000-165810200	Enhancers	Pancreas	Pancrea
44	chr1:165806200-165808000	Enhancers	Stomach Mucosa	stomach
45	chr1:165806200-165810800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr1:165806400-165808000	Strong transcription	HSMM	muscle
47	chr1:165806400-165809200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr1:165806400-165809600	Weak transcription	Fetal Heart	heart
49	chr1:165806400-165810800	Weak transcription	Hela-S3	cervix
50	chr1:165806400-165810800	Weak transcription	Osteobl	bone

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