Variant report

Variant	rs61880367
Chromosome Location	chr11:34048803-34048804
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3399258	chr11:34046901-34049749	Enhancers Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv3438684	chr11:34047026-34049824	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3420049	chr11:34047526-34049324	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3502318	chr11:34048450-34048911	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3477953	chr11:34048485-34048872	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3427216	chr11:34048486-34048896	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv5117	chr11:34048504-34048850	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3432667	chr11:34048537-34048849	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3384101	chr11:34048557-34048819	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3477964	chr11:34048598-34048804	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3502320	chr11:34048598-34048804	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34046600-34049400	Weak transcription	Aorta	Aorta
2	chr11:34048800-34049200	Enhancers	Liver	Liver
3	chr11:34048800-34049400	Enhancers	Sigmoid Colon	Sigmoid Colon
4	chr11:34048800-34049600	Enhancers	H9 Cell Line	embryonic stem cell
5	chr11:34048800-34050200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:34048800-34050400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr11:34048800-34050400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr11:34048800-34050400	Enhancers	Pancreas	Pancrea
9	chr11:34048800-34050600	Enhancers	Fetal Intestine Small	intestine
10	chr11:34048800-34052400	Enhancers	Cortex derived primary cultured neurospheres	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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