Variant report

Variant	rs572249606
Chromosome Location	chr12:62393912-62393913
allele	C/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	nsv1039741	chr12:62046850-62491052	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv559151	chr12:62390768-62394361	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3323443	chr12:62392085-62396383	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv559152	chr12:62392548-62395774	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv1820144	chr12:62393257-62394361	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv1823662	chr12:62393257-62394361	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv1843366	chr12:62393257-62394361	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv1844580	chr12:62393257-62394361	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv1848150	chr12:62393257-62394361	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv1850527	chr12:62393257-62394361	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv2633161	chr12:62393516-62395086	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv6636	chr12:62393709-62394748	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv2028037	chr12:62393773-62394689	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3487986	chr12:62393826-62394601	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv3487953	chr12:62393884-62394570	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
16	esv3487964	chr12:62393891-62394565	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
17	esv3487997	chr12:62393903-62394524	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:62392600-62394200	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr12:62393400-62396600	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr12:62393600-62396600	Weak transcription	Primary monocytes fromperipheralblood	blood

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links