Variant report

Variant	rs7122221
Chromosome Location	chr11:76881067-76881068
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:76877108..76882328-chr11:76882354..76886286,6	K562	blood:
2	chr11:76877108..76882092-chr11:76882914..76884987,4	K562	blood:
3	chr11:76868588..76871297-chr11:76879348..76881579,2	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs11601497	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11607721	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3758709	0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4944147	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4945150	0.82[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	esv1816632	chr11:76751285-76927014	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76864800-76882200	Weak transcription	HepG2	liver
2	chr11:76865000-76882800	Strong transcription	Fetal Intestine Large	intestine
3	chr11:76865600-76882000	Strong transcription	Fetal Intestine Small	intestine
4	chr11:76869400-76889200	Weak transcription	Pancreas	Pancrea
5	chr11:76873600-76883000	Weak transcription	Ovary	ovary
6	chr11:76876400-76882800	Weak transcription	Esophagus	oesophagus
7	chr11:76877600-76884000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr11:76878000-76881200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr11:76878800-76881400	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr11:76879000-76881200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr11:76879000-76881400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr11:76879000-76884200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr11:76879200-76882000	Weak transcription	Liver	Liver
14	chr11:76879200-76882800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr11:76879200-76882800	Weak transcription	Spleen	Spleen
16	chr11:76879200-76884000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr11:76879200-76884200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr11:76879400-76883600	Weak transcription	Primary hematopoietic stem cells	blood
19	chr11:76879400-76883600	Weak transcription	HUVEC	blood vessel
20	chr11:76880200-76882800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr11:76880200-76883800	Enhancers	Placenta	Placenta
22	chr11:76880200-76887600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr11:76880400-76916600	Weak transcription	Right Atrium	heart
24	chr11:76881000-76881400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr11:76881000-76881600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr11:76881000-76881600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr11:76881000-76881600	Enhancers	Placenta Amnion	Placenta Amnion
28	chr11:76881000-76883600	Enhancers	H9 Cell Line	embryonic stem cell
29	chr11:76881000-76883600	Enhancers	HUES64 Cell Line	embryonic stem cell

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