Variant report

Variant	rs113790312
Chromosome Location	chr12:4109826-4109827
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530520	chr12:3726841-4601757	Enhancers Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv832316	chr12:3981184-4180381	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	esv2761723	chr12:4096815-4161871	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv13469	chr12:4107971-4109977	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv468982	chr12:4108513-4164815	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv557120	chr12:4108513-4164815	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:4104000-4110200	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr12:4104600-4110000	Enhancers	HepG2	liver
3	chr12:4107000-4112600	Enhancers	Placenta Amnion	Placenta Amnion
4	chr12:4107600-4110000	Enhancers	HMEC	breast
5	chr12:4107600-4121600	Weak transcription	Esophagus	oesophagus
6	chr12:4108200-4110000	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr12:4108800-4111000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr12:4108800-4111000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr12:4109400-4121000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr12:4109600-4112000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr12:4109800-4111000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr12:4109800-4111600	Weak transcription	Fetal Intestine Large	intestine
13	chr12:4109800-4111800	Weak transcription	Pancreas	Pancrea
14	chr12:4109800-4112000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr12:4109800-4112000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr12:4109800-4112000	Weak transcription	Fetal Intestine Small	intestine
17	chr12:4109800-4112000	Weak transcription	Placenta	Placenta
18	chr12:4109800-4112000	Weak transcription	NHEK	skin

Quick Search:

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

what's new

Quick links