Variant report

Variant	rs546881028
Chromosome Location	chr22:27707273-27707274
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CRYBA4-8	chr22:27706612-27711010	XLOC_014197
2	lnc-CRYBA4-8	chr22:27706612-27711010	ENSG00000226741

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	esv3413125	chr22:27404463-28121577	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
2	nsv459860	chr22:27527005-28181436	Strong transcription Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv588872	chr22:27527005-28181436	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	nsv834166	chr22:27628570-27814359	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	esv3406339	chr22:27705377-27707925	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	esv3359531	chr22:27706552-27710850	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:27704200-27708600	Weak transcription	Right Atrium	heart
2	chr22:27704600-27707600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr22:27705600-27708400	Enhancers	Fetal Brain Male	brain
4	chr22:27705800-27707800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
5	chr22:27705800-27708400	Enhancers	H9 Cell Line	embryonic stem cell
6	chr22:27705800-27709400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr22:27705800-27710800	Enhancers	Ovary	ovary
8	chr22:27706000-27708400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr22:27706000-27709200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr22:27706000-27709400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
11	chr22:27706000-27709600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr22:27706200-27707600	Enhancers	Brain Germinal Matrix	brain
13	chr22:27706200-27708000	Weak transcription	Aorta	Aorta
14	chr22:27706200-27708200	Bivalent Enhancer	Fetal Muscle Leg	muscle
15	chr22:27706600-27708400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr22:27706800-27707600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
17	chr22:27706800-27707800	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr22:27706800-27707800	Bivalent Enhancer	Fetal Stomach	stomach
19	chr22:27706800-27707800	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr22:27706800-27708800	Enhancers	Spleen	Spleen
21	chr22:27706800-27709000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr22:27706800-27709000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr22:27706800-27709400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr22:27706800-27715400	Enhancers	Fetal Intestine Large	intestine
25	chr22:27707000-27707400	Weak transcription	Brain Anterior Caudate	brain
26	chr22:27707000-27707600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
27	chr22:27707000-27708000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr22:27707000-27708200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
29	chr22:27707000-27708400	Flanking Active TSS	Fetal Brain Female	brain
30	chr22:27707000-27708800	Enhancers	Placenta Amnion	Placenta Amnion
31	chr22:27707000-27709400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr22:27707000-27710200	Enhancers	Duodenum Mucosa	Duodenum
33	chr22:27707000-27710800	Enhancers	Rectal Mucosa Donor 29	rectum
34	chr22:27707200-27707400	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
35	chr22:27707200-27707400	Enhancers	NH-A	brain
36	chr22:27707200-27707600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr22:27707200-27707600	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr22:27707200-27707800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
39	chr22:27707200-27708200	Enhancers	H1 Cell Line	embryonic stem cell
40	chr22:27707200-27710400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr22:27707200-27715400	Enhancers	Fetal Intestine Small	intestine

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