Variant report

Variant	rs533644592
Chromosome Location	chr1:67201557-67201558
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869413	chr1:67082512-67414286	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv830093	chr1:67173594-67348264	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv3429399	chr1:67200514-67202512	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv2571464	chr1:67200525-67202090	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv6908	chr1:67200969-67201745	Weak transcription Strong transcription Enhancers	n/a	n/a	inside rSNPs	diseases
6	esv2094631	chr1:67201030-67201749	Strong transcription Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv3320149	chr1:67201087-67201613	Weak transcription Strong transcription Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv3519350	chr1:67201111-67201621	Weak transcription Enhancers Strong transcription	n/a	n/a	inside rSNPs	diseases
9	esv3519353	chr1:67201116-67201650	Enhancers Weak transcription Strong transcription	n/a	n/a	inside rSNPs	diseases
10	esv3519355	chr1:67201136-67201586	Weak transcription Enhancers Strong transcription	n/a	n/a	inside rSNPs	diseases
11	esv3320150	chr1:67201141-67201629	Weak transcription Enhancers Strong transcription	n/a	n/a	inside rSNPs	diseases
12	esv3320148	chr1:67201143-67201607	Weak transcription Enhancers Strong transcription	n/a	n/a	inside rSNPs	diseases
13	esv3519351	chr1:67201155-67201595	Weak transcription Enhancers Strong transcription	n/a	n/a	inside rSNPs	diseases
14	esv3320152	chr1:67201156-67201576	Weak transcription Enhancers Strong transcription	n/a	n/a	inside rSNPs	diseases
15	esv4277	chr1:67201160-67201623	Weak transcription Strong transcription Enhancers	n/a	n/a	inside rSNPs	diseases
16	esv3519354	chr1:67201166-67201583	Weak transcription Enhancers Strong transcription	n/a	n/a	inside rSNPs	diseases
17	esv3442582	chr1:67201175-67201565	Weak transcription Enhancers Strong transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:67157000-67208800	Weak transcription	Brain Germinal Matrix	brain
2	chr1:67165400-67206800	Weak transcription	Fetal Brain Male	brain
3	chr1:67186400-67205000	Weak transcription	Fetal Heart	heart
4	chr1:67188600-67217400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr1:67191800-67204600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr1:67191800-67204800	Weak transcription	Lung	lung
7	chr1:67192000-67204600	Weak transcription	Aorta	Aorta
8	chr1:67192000-67204800	Weak transcription	Left Ventricle	heart
9	chr1:67192000-67217200	Weak transcription	Brain Angular Gyrus	brain
10	chr1:67192000-67217400	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr1:67192200-67204600	Weak transcription	Brain Hippocampus Middle	brain
12	chr1:67192200-67208200	Weak transcription	Brain Substantia Nigra	brain
13	chr1:67192400-67204200	Weak transcription	Brain Anterior Caudate	brain
14	chr1:67196600-67212800	Weak transcription	Fetal Brain Female	brain
15	chr1:67197000-67217600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr1:67197600-67204600	Weak transcription	Brain Cingulate Gyrus	brain
17	chr1:67198200-67203800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr1:67199200-67204600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr1:67199600-67203000	Weak transcription	Primary hematopoietic stem cells	blood
20	chr1:67199600-67203600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr1:67199600-67204000	Weak transcription	NHDF-Ad	bronchial
22	chr1:67199600-67204800	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr1:67199600-67205000	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr1:67199600-67205200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr1:67199600-67205600	Weak transcription	NHLF	lung
26	chr1:67199600-67206400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr1:67199800-67205000	Weak transcription	Dnd41	blood
28	chr1:67199800-67205000	Weak transcription	Osteobl	bone
29	chr1:67201200-67203000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr1:67201200-67203400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr1:67201200-67203600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links