Variant report

Variant	rs17033015
Chromosome Location	chr4:103546304-103546305
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:103545322..103548006-chr4:103788328..103790591,2	MCF-7	breast:
2	chr4:103543864..103546409-chr4:103549438..103551075,2	K562	blood:
3	chr4:103534750..103537170-chr4:103544463..103546367,2	K562	blood:
4	chr4:103542281..103545235-chr4:103546204..103549504,3	K562	blood:

Variant related genes	Relation type
ENSG00000109332	Chromatin interaction
ENSG00000145354	Chromatin interaction

Extended variants
information (count: 65 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs1054029	0.90[JPT][hapmap]
rs1054037	0.90[JPT][hapmap]
rs1077358	0.90[JPT][hapmap]
rs11724614	0.91[JPT][hapmap]
rs11727546	0.91[JPT][hapmap]
rs12498722	0.91[JPT][hapmap]
rs12644381	0.91[JPT][hapmap]
rs13106304	0.91[JPT][hapmap]
rs13106325	0.91[JPT][hapmap]
rs1585214	0.91[CEU][hapmap];0.91[JPT][hapmap]
rs1598856	0.91[CEU][hapmap];0.90[JPT][hapmap]
rs179195	0.82[CHB][hapmap];0.95[JPT][hapmap]
rs2125211	0.90[JPT][hapmap]
rs223397	0.80[YRI][hapmap]
rs223498	0.80[YRI][hapmap]
rs2272695	0.91[JPT][hapmap]
rs2272696	0.91[JPT][hapmap]
rs2272697	0.90[JPT][hapmap]
rs227276	0.83[CHB][hapmap];0.91[JPT][hapmap]
rs227277	0.83[CHB][hapmap];0.91[JPT][hapmap]
rs227361	0.82[CHB][hapmap];0.95[JPT][hapmap]
rs227368	0.80[YRI][hapmap]
rs227375	0.80[YRI][hapmap]
rs228611	0.80[JPT][hapmap]
rs228614	0.82[CHB][hapmap];0.95[JPT][hapmap]
rs228617	0.82[CHB][hapmap];0.95[JPT][hapmap]
rs228618	0.86[JPT][hapmap]
rs228619	0.83[CHB][hapmap];0.95[JPT][hapmap]
rs228623	0.81[CHB][hapmap];0.89[JPT][hapmap]
rs230510	0.91[CEU][hapmap];0.91[JPT][hapmap]
rs230530	0.95[CEU][hapmap];0.90[JPT][hapmap]
rs2866407	0.91[JPT][hapmap]
rs2866412	0.91[JPT][hapmap]
rs2866413	0.90[JPT][hapmap]
rs2866414	0.90[JPT][hapmap]
rs2903283	0.90[JPT][hapmap]
rs3733202	0.90[JPT][hapmap]
rs3774932	0.87[CEU][hapmap];0.90[JPT][hapmap]
rs3774968	0.95[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap]
rs4013	0.90[JPT][hapmap]
rs404574	0.85[CHB][hapmap];0.94[JPT][hapmap]
rs434644	0.83[CHB][hapmap];0.95[JPT][hapmap]
rs4496586	0.91[JPT][hapmap]
rs4547797	0.90[JPT][hapmap]
rs4586937	0.90[JPT][hapmap]
rs5026472	0.91[JPT][hapmap]
rs5026473	0.91[JPT][hapmap]
rs5026474	0.91[JPT][hapmap]
rs5026476	0.91[JPT][hapmap]
rs6533020	0.91[JPT][hapmap]
rs6533021	0.95[JPT][hapmap]
rs6810869	0.91[JPT][hapmap]
rs6812747	0.91[JPT][hapmap]
rs6839064	0.91[JPT][hapmap]
rs735403	0.90[JPT][hapmap]
rs735404	0.90[JPT][hapmap]
rs735405	0.90[JPT][hapmap]
rs7674640	0.86[JPT][hapmap]
rs7677509	0.91[JPT][hapmap]
rs7699231	0.91[JPT][hapmap]
rs7699678	0.91[JPT][hapmap]
rs909349	0.90[JPT][hapmap]
rs93059	0.91[CEU][hapmap];0.90[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830020	chr4:103387343-103581284	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv1003618	chr4:103530465-103562161	Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region miRNA target site	10 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs17033015	MANBA	cis	multi-tissue	Pritchard

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:103521400-103554400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:103536200-103552800	Weak transcription	Ovary	ovary
3	chr4:103536200-103595400	Weak transcription	Colonic Mucosa	Colon
4	chr4:103536400-103553400	Weak transcription	Fetal Brain Female	brain
5	chr4:103536600-103550800	Weak transcription	Thymus	Thymus
6	chr4:103536600-103562600	Weak transcription	Brain Germinal Matrix	brain
7	chr4:103536600-103595800	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr4:103538000-103546600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr4:103538000-103552800	Weak transcription	Spleen	Spleen
10	chr4:103538200-103549400	Weak transcription	Fetal Lung	lung
11	chr4:103538200-103550800	Weak transcription	Lung	lung
12	chr4:103538200-103552400	Weak transcription	Primary hematopoietic stem cells	blood
13	chr4:103538200-103555600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr4:103538200-103555600	Weak transcription	Gastric	stomach
15	chr4:103538200-103555800	Weak transcription	Esophagus	oesophagus
16	chr4:103538600-103546600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr4:103538600-103552800	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr4:103538800-103546400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr4:103538800-103546400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr4:103538800-103546400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr4:103538800-103546600	Weak transcription	Primary B cells from peripheral blood	blood
22	chr4:103538800-103552800	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr4:103538800-103552800	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr4:103538800-103552800	Weak transcription	Adipose Nuclei	Adipose
25	chr4:103538800-103555600	Weak transcription	Right Ventricle	heart
26	chr4:103538800-103555800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr4:103539000-103546600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr4:103540000-103546400	Weak transcription	Primary B cells from cord blood	blood
29	chr4:103540200-103546600	Weak transcription	GM12878-XiMat	blood
30	chr4:103541800-103562400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr4:103541800-103571000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr4:103542000-103547400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr4:103542000-103552400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr4:103542200-103552000	Weak transcription	Stomach Smooth Muscle	stomach
35	chr4:103542200-103552800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr4:103542200-103552800	Weak transcription	Colon Smooth Muscle	Colon
37	chr4:103542200-103552800	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr4:103542200-103555400	Weak transcription	Brain Cingulate Gyrus	brain
39	chr4:103542200-103555400	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr4:103542200-103555600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr4:103542200-103555600	Weak transcription	Brain Anterior Caudate	brain
42	chr4:103542400-103549000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr4:103542400-103552800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr4:103542400-103552800	Weak transcription	Fetal Muscle Leg	muscle
45	chr4:103542400-103552800	Weak transcription	Left Ventricle	heart
46	chr4:103542400-103553200	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr4:103542400-103555400	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr4:103542400-103555600	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr4:103542400-103557200	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr4:103542400-103560800	Weak transcription	Brain Substantia Nigra	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links