Variant report

Variant	rs1111881
Chromosome Location	chr8:102661269-102661270
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:102657037..102659278-chr8:102659929..102662288,2	MCF-7	breast:
2	chr8:102661081..102663898-chr8:102668064..102670538,3	MCF-7	breast:

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10955269	0.93[ASN][1000 genomes]
rs11991426	0.84[EUR][1000 genomes]
rs11994981	0.88[EUR][1000 genomes]
rs12676557	0.89[EUR][1000 genomes]
rs16868138	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16868201	0.88[EUR][1000 genomes]
rs1892753	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1892754	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1892755	0.84[AFR][1000 genomes]
rs1892756	0.81[AFR][1000 genomes]
rs1892757	0.82[AFR][1000 genomes]
rs2387623	0.90[YRI][hapmap];0.85[AFR][1000 genomes]
rs35227396	0.84[EUR][1000 genomes]
rs3824091	0.85[EUR][1000 genomes]
rs4317540	0.92[YRI][hapmap];0.85[AFR][1000 genomes]
rs4734037	0.91[EUR][1000 genomes]
rs4734567	0.93[ASN][1000 genomes]
rs4734570	0.89[EUR][1000 genomes]
rs4734571	0.86[EUR][1000 genomes]
rs59320315	0.85[EUR][1000 genomes]
rs62517420	0.89[EUR][1000 genomes]
rs6468784	0.85[EUR][1000 genomes]
rs6989650	0.88[EUR][1000 genomes]
rs7386202	0.85[EUR][1000 genomes]
rs7829633	0.83[EUR][1000 genomes]
rs7829786	0.82[EUR][1000 genomes]
rs9297307	0.89[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3401576	chr8:102640273-102724495	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:102644600-102663800	Weak transcription	Lung	lung
2	chr8:102644800-102674600	Weak transcription	Ovary	ovary
3	chr8:102648600-102663600	Weak transcription	Rectal Smooth Muscle	rectum
4	chr8:102650600-102664400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
5	chr8:102650800-102662400	Strong transcription	H1 Cell Line	embryonic stem cell
6	chr8:102650800-102664600	Strong transcription	HUES48 Cell Line	embryonic stem cell
7	chr8:102651400-102681200	Weak transcription	Stomach Mucosa	stomach
8	chr8:102655000-102661800	Strong transcription	Fetal Intestine Small	intestine
9	chr8:102655200-102663800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr8:102655200-102669400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr8:102655600-102661800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr8:102655600-102664400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr8:102655600-102664400	Strong transcription	Duodenum Mucosa	Duodenum
14	chr8:102655800-102662000	Strong transcription	H9 Cell Line	embryonic stem cell
15	chr8:102656400-102663800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr8:102657000-102661600	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr8:102657200-102661600	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr8:102657200-102668200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr8:102658400-102661800	Strong transcription	Fetal Intestine Large	intestine
20	chr8:102658400-102661800	Strong transcription	Gastric	stomach
21	chr8:102658400-102663000	Strong transcription	NHEK	skin
22	chr8:102658600-102665800	Strong transcription	Rectal Mucosa Donor 31	rectum
23	chr8:102658800-102662000	Strong transcription	Esophagus	oesophagus
24	chr8:102659000-102661800	Strong transcription	Pancreas	Pancrea
25	chr8:102659000-102664400	Strong transcription	Placenta	Placenta
26	chr8:102659200-102662400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
27	chr8:102659200-102663400	Weak transcription	Right Atrium	heart
28	chr8:102659200-102679400	Weak transcription	HMEC	breast
29	chr8:102660200-102661600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr8:102660200-102661800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr8:102660200-102661800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr8:102660200-102662000	Strong transcription	Sigmoid Colon	Sigmoid Colon
33	chr8:102660200-102662600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
34	chr8:102660200-102663200	Strong transcription	Rectal Mucosa Donor 29	rectum
35	chr8:102660800-102661600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr8:102660800-102661800	Strong transcription	Colonic Mucosa	Colon
37	chr8:102661000-102663400	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr8:102661200-102663800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr8:102661200-102664400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr8:102661200-102678600	Weak transcription	Fetal Stomach	stomach

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