Variant report

Variant	rs79204974
Chromosome Location	chr11:8849076-8849077
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:8847441..8849119-chr11:9018204..9019722,2	K562	blood:
2	chr11:8847275..8850671-chr11:8853327..8856938,3	K562	blood:

Variant related genes	Relation type
ENSG00000166444	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758256	chr11:8784813-9009573	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	esv2759803	chr11:8784813-9009573	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv527920	chr11:8816695-8856822	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv435923	chr11:8839325-9000602	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
5	esv3372624	chr11:8848476-8852774	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:8833200-8859800	Weak transcription	Aorta	Aorta
2	chr11:8836400-8849800	Weak transcription	Fetal Intestine Small	intestine
3	chr11:8836600-8850400	Weak transcription	Fetal Lung	lung
4	chr11:8837000-8850000	Weak transcription	Lung	lung
5	chr11:8839000-8849400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr11:8839200-8849600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr11:8845200-8854200	Weak transcription	Psoas Muscle	Psoas
8	chr11:8845800-8860000	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr11:8846600-8854400	Weak transcription	Fetal Intestine Large	intestine
10	chr11:8847000-8849200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr11:8847000-8849400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr11:8847000-8852800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr11:8847200-8849200	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr11:8847200-8849200	Enhancers	NHDF-Ad	bronchial
15	chr11:8847200-8849400	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr11:8847200-8849400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr11:8847200-8849400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr11:8847200-8849800	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr11:8847200-8849800	Enhancers	NHLF	lung
20	chr11:8847400-8849200	Enhancers	Fetal Heart	heart
21	chr11:8847400-8849200	Enhancers	HepG2	liver
22	chr11:8847400-8850400	Enhancers	K562	blood
23	chr11:8847600-8849200	Enhancers	Placenta Amnion	Placenta Amnion
24	chr11:8847600-8849400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr11:8847600-8849600	Enhancers	Placenta	Placenta
26	chr11:8847600-8850400	Enhancers	Ovary	ovary
27	chr11:8847600-8852600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr11:8847800-8849200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:8848000-8849200	Enhancers	H9 Cell Line	embryonic stem cell
30	chr11:8848000-8849200	Enhancers	NH-A	brain
31	chr11:8848000-8849200	Enhancers	NHEK	skin
32	chr11:8848000-8849400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr11:8848000-8849600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr11:8848000-8850200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr11:8848000-8850400	Enhancers	H1 Cell Line	embryonic stem cell
36	chr11:8848000-8852800	Enhancers	Fetal Thymus	thymus
37	chr11:8848200-8849600	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr11:8848200-8853400	Weak transcription	Rectal Smooth Muscle	rectum
39	chr11:8848400-8849200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr11:8848400-8849200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr11:8848400-8849200	Enhancers	Colon Smooth Muscle	Colon
42	chr11:8848400-8849400	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr11:8848400-8849600	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr11:8848400-8850400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr11:8848400-8850400	Weak transcription	Fetal Kidney	kidney
46	chr11:8848400-8850400	Enhancers	HSMMtube	muscle
47	chr11:8848400-8850800	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr11:8848600-8849200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr11:8848600-8849200	Weak transcription	Brain Hippocampus Middle	brain
50	chr11:8848600-8849200	Enhancers	Right Atrium	heart

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