Variant report

Variant	rs571701256
Chromosome Location	chr1:178977980-178977981
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3320853	chr1:178977290-178979832	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv3320854	chr1:178977334-178979772	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3320855	chr1:178977334-178979772	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv12219	chr1:178977936-178979438	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv548266	chr1:178977963-178978956	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv548267	chr1:178977963-178979112	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv548268	chr1:178977963-178979300	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:178972400-178986000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:178972600-178978000	Weak transcription	Adipose Nuclei	Adipose
3	chr1:178972600-178981200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr1:178972800-178978000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr1:178973200-178979600	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr1:178973400-178980200	Weak transcription	Fetal Intestine Small	intestine
7	chr1:178973400-178980200	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr1:178973600-178983200	Weak transcription	K562	blood
9	chr1:178976600-178978600	Enhancers	Osteobl	bone
10	chr1:178977000-178985400	Weak transcription	A549	lung
11	chr1:178977000-178985600	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr1:178977200-178978000	Weak transcription	HepG2	liver
13	chr1:178977200-178979600	Weak transcription	Stomach Mucosa	stomach
14	chr1:178977200-178981600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:178977400-178978000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr1:178977800-178978000	Enhancers	Stomach Smooth Muscle	stomach
17	chr1:178977800-178978200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr1:178977800-178978600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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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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