Variant report

Variant	rs78021449
Chromosome Location	chr4:20407896-20407897
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1004503	chr4:20399974-20409944	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv3420991	chr4:20405954-20410452	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3500334	chr4:20406404-20409602	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3500335	chr4:20406404-20409602	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3445244	chr4:20406879-20409727	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3464866	chr4:20407063-20408942	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3464863	chr4:20407416-20408639	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3323769	chr4:20407440-20408631	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3464862	chr4:20407464-20408605	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3464861	chr4:20407468-20408633	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3464865	chr4:20407475-20408557	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3396104	chr4:20407503-20408550	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv2863	chr4:20407510-20408609	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3464867	chr4:20407524-20408533	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv3464868	chr4:20407539-20408531	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
16	esv10699	chr4:20407568-20408857	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
17	nsv821168	chr4:20407568-20408857	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
18	nsv593794	chr4:20407591-20408433	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
19	nsv593795	chr4:20407591-20418308	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:20393200-20408800	Weak transcription	Colon Smooth Muscle	Colon
2	chr4:20405200-20419600	Weak transcription	NHDF-Ad	bronchial
3	chr4:20406000-20409200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr4:20406200-20409200	Weak transcription	Brain Hippocampus Middle	brain
5	chr4:20406200-20420000	Weak transcription	Fetal Lung	lung
6	chr4:20406400-20409000	Weak transcription	Brain Anterior Caudate	brain

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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

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