Variant report

Variant	rs55661489
Chromosome Location	chr1:211824254-211824255
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:211750437..211753125-chr1:211823737..211827672,4	MCF-7	breast:
2	chr1:211750060..211753695-chr1:211824093..211827463,4	MCF-7	breast:
3	chr1:211772625..211775526-chr1:211823895..211826461,2	K562	blood:
4	chr1:211749200..211754595-chr1:211816014..211824648,8	K562	blood:
5	chr1:211781693..211784457-chr1:211822859..211825401,2	K562	blood:
6	chr1:211824090..211825687-chr1:211827375..211829045,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000170385	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs56094815	1.00[ASN][1000 genomes]
rs6659316	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7511687	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7516189	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7526473	0.82[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs7539988	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7551341	0.82[EUR][1000 genomes]
rs7553718	0.82[EUR][1000 genomes]
rs7554588	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211811400-211829600	Enhancers	Fetal Intestine Small	intestine
2	chr1:211811600-211828200	Enhancers	Fetal Intestine Large	intestine
3	chr1:211817400-211827000	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr1:211817400-211827400	Weak transcription	Fetal Heart	heart
5	chr1:211817600-211826800	Weak transcription	Gastric	stomach
6	chr1:211817600-211827000	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr1:211817600-211830600	Weak transcription	Right Atrium	heart
8	chr1:211818400-211828400	Weak transcription	Adipose Nuclei	Adipose
9	chr1:211819600-211824400	Enhancers	Duodenum Mucosa	Duodenum
10	chr1:211820400-211826800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr1:211820800-211824400	Enhancers	HepG2	liver
12	chr1:211821800-211828400	Weak transcription	Colonic Mucosa	Colon
13	chr1:211822000-211826800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr1:211822000-211826800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr1:211822200-211827000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr1:211822200-211827000	Weak transcription	NHEK	skin
17	chr1:211822200-211828400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr1:211822400-211827000	Weak transcription	K562	blood
19	chr1:211822600-211826800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr1:211822800-211827600	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr1:211822800-211828200	Weak transcription	Liver	Liver
22	chr1:211822800-211828200	Weak transcription	Pancreas	Pancrea
23	chr1:211823000-211825600	Genic enhancers	Hela-S3	cervix
24	chr1:211823200-211827000	Weak transcription	A549	lung
25	chr1:211823400-211826400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr1:211823400-211826800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr1:211824000-211826600	Weak transcription	HUVEC	blood vessel
28	chr1:211824000-211826800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr1:211824000-211828200	Weak transcription	Stomach Mucosa	stomach
30	chr1:211824200-211825800	Weak transcription	Placenta	Placenta
31	chr1:211824200-211826400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links