Variant report

Variant	rs201335673
Chromosome Location	chr1:150691769-150691770
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006838	chr1:150440214-150722783	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Genic enhancers 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	175 gene(s)	inside rSNPs	diseases
2	esv2829859	chr1:150608894-150937329	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv872417	chr1:150618632-150759979	Strong transcription Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv872418	chr1:150683512-150860471	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
5	esv3334316	chr1:150690728-150692726	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv2609983	chr1:150690733-150692316	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3514553	chr1:150691046-150692585	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3397972	chr1:150691228-150692226	Weak transcription	n/a	n/a	inside rSNPs	diseases
9	esv2238986	chr1:150691243-150691965	Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv9188	chr1:150691252-150692021	Weak transcription	n/a	n/a	inside rSNPs	diseases
11	esv3354612	chr1:150691317-150691839	Weak transcription	n/a	n/a	inside rSNPs	diseases
12	esv3514549	chr1:150691346-150691852	Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv3514551	chr1:150691346-150691886	Weak transcription	n/a	n/a	inside rSNPs	diseases
14	esv3514550	chr1:150691363-150691826	Weak transcription	n/a	n/a	inside rSNPs	diseases
15	esv3514548	chr1:150691367-150691803	Weak transcription	n/a	n/a	inside rSNPs	diseases
16	esv3514547	chr1:150691378-150691820	Weak transcription	n/a	n/a	inside rSNPs	diseases
17	esv3320694	chr1:150691379-150691812	Weak transcription	n/a	n/a	inside rSNPs	diseases
18	esv3320695	chr1:150691387-150691789	Weak transcription	n/a	n/a	inside rSNPs	diseases
19	esv3514545	chr1:150691397-150691803	Weak transcription	n/a	n/a	inside rSNPs	diseases
20	esv3378164	chr1:150691398-150691790	Weak transcription	n/a	n/a	inside rSNPs	diseases
21	esv3600	chr1:150691402-150691865	Weak transcription	n/a	n/a	inside rSNPs	diseases
22	esv3320697	chr1:150691422-150691774	Weak transcription	n/a	n/a	inside rSNPs	diseases
23	esv3514546	chr1:150691434-150691769	Weak transcription	n/a	n/a	inside rSNPs	diseases
24	esv992009	chr1:150691436-150691769	Weak transcription	n/a	n/a	inside rSNPs	diseases
25	esv3320698	chr1:150691436-150691786	Weak transcription	n/a	n/a	inside rSNPs	diseases
26	esv3514554	chr1:150691436-150691786	Weak transcription	n/a	n/a	inside rSNPs	diseases
27	esv2482983	chr1:150691440-150691773	Weak transcription	n/a	n/a	inside rSNPs	diseases
28	esv1594619	chr1:150691451-150691785	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:150670600-150702600	Weak transcription	Hela-S3	cervix
2	chr1:150679200-150698600	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr1:150681600-150702600	Weak transcription	A549	lung
4	chr1:150690800-150702400	Weak transcription	Primary neutrophils fromperipheralblood	blood

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