Variant report

Variant	rs149178937
Chromosome Location	chr20:12731913-12731914
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1058919	chr20:11917331-12733316	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv544183	chr20:11917331-12733316	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv18943	chr20:12627634-12841804	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv585433	chr20:12724326-12756660	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer	lncRNA	n/a	inside rSNPs	diseases
5	nsv1066818	chr20:12729400-12781534	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	lncRNA	n/a	inside rSNPs	diseases
6	nsv1057219	chr20:12729479-13338337	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	nsv1065145	chr20:12729803-12781534	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	lncRNA	n/a	inside rSNPs	diseases
8	nsv522376	chr20:12730872-12771339	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:12728000-12732000	Enhancers	H9 Cell Line	embryonic stem cell
2	chr20:12728600-12733000	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr20:12728600-12733000	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr20:12728800-12733200	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr20:12729600-12733200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr20:12729800-12740800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr20:12730000-12732600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr20:12730200-12732000	Enhancers	Fetal Muscle Leg	muscle
9	chr20:12730400-12732600	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr20:12731000-12732000	Enhancers	H1 Cell Line	embryonic stem cell
11	chr20:12731000-12732000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr20:12731200-12732000	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr20:12731200-12732000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr20:12731600-12732600	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr20:12731800-12732800	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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

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