Variant report

Variant	rs185462821
Chromosome Location	chr1:69943945-69943946
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:69935852..69938331-chr1:69943499..69946682,3	K562	blood:
2	chr1:69935852..69938420-chr1:69942565..69946682,4	K562	blood:

Extended variants
information (count: 27 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949691	chr1:69749722-70302201	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv870931	chr1:69765592-69959061	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv3384194	chr1:69885024-70275430	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv546451	chr1:69894849-69975660	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv3441556	chr1:69942789-69945337	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3389806	chr1:69943014-69945037	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3355296	chr1:69943464-69944562	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv6225	chr1:69943533-69944303	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv2271565	chr1:69943546-69944218	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3320166	chr1:69943609-69944119	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3486046	chr1:69943622-69944128	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3486044	chr1:69943623-69944117	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv3486045	chr1:69943637-69944072	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3486047	chr1:69943644-69944053	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv4719	chr1:69943644-69944082	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
16	esv3320165	chr1:69943655-69944091	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
17	esv3320163	chr1:69943656-69944092	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
18	esv3486043	chr1:69943659-69944073	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
19	esv3320167	chr1:69943672-69944044	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
20	esv3486042	chr1:69943674-69944066	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
21	esv3406866	chr1:69943679-69944043	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
22	esv3320164	chr1:69943700-69944029	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
23	esv3486048	chr1:69943715-69944022	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
24	esv2518942	chr1:69943716-69944021	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
25	esv3320168	chr1:69943716-69944032	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
26	esv3486049	chr1:69943716-69944032	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
27	esv1350326	chr1:69943725-69944031	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:69943000-69945400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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