Variant report

Variant	rs214155
Chromosome Location	chr7:117327842-117327843
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	7:117114628-117119361..7:117326534-117332210	H1-hESC	embryonic stem cell:	embryo
2	7:116307511-116321259..7:117326534-117332210	Hela-S3	cervix:
3	chr7:117314737..117317346-chr7:117324406..117328585,3	MCF-7	breast:
4	7:116957165-116964911..7:117326534-117332210	H1-hESC	embryonic stem cell:	embryo
5	7:116434729-116454408..7:117326534-117332210	H1-hESC	embryonic stem cell:	embryo
6	7:115890993-115892266..7:117326534-117332210	H1-hESC	embryonic stem cell:	embryo
7	7:117100350-117112126..7:117326534-117332210	H1-hESC	embryonic stem cell:	embryo
8	chr7:117321253..117323639-chr7:117325646..117329002,3	K562	blood:
9	7:116500954-116503335..7:117326534-117332210	Hela-S3	cervix:
10	7:116604327-116608063..7:117326534-117332210	Hela-S3	cervix:

No data

No data

No data

Variant related genes	Relation type
ENSG00000105989	Chromatin interaction
ENSG00000228368	Chromatin interaction
ENSG00000135269	Chromatin interaction
ENSG00000198898	Chromatin interaction
ENSG00000001626	Chromatin interaction
ENSG00000105976	Chromatin interaction

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:117322000-117330600	Enhancers	Fetal Intestine Large	intestine
2	chr7:117324000-117328400	Weak transcription	Duodenum Mucosa	Duodenum
3	chr7:117324000-117328400	Weak transcription	Small Intestine	intestine
4	chr7:117327000-117329800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr7:117327000-117335000	Weak transcription	Dnd41	blood
6	chr7:117327000-117376400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr7:117327600-117328600	Weak transcription	Fetal Intestine Small	intestine
8	chr7:117327800-117329000	Enhancers	NHEK	skin

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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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