Variant report

Variant	rs552128010
Chromosome Location	chr21:39863897-39863898
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1059340	chr21:39817504-39881353	Weak transcription Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1064436	chr21:39846571-39875576	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	esv3491054	chr21:39863789-39864097	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	inside rSNPs	diseases
4	esv3375060	chr21:39863792-39864081	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	inside rSNPs	diseases
5	esv3491050	chr21:39863803-39864029	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	inside rSNPs	diseases
6	esv3455476	chr21:39863814-39864063	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
7	esv2852	chr21:39863818-39864058	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
8	esv3491049	chr21:39863830-39864043	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
9	esv3491053	chr21:39863871-39863994	Weak transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	inside rSNPs	diseases
10	esv3455477	chr21:39863874-39863997	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
11	esv3491051	chr21:39863884-39863997	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	inside rSNPs	diseases
12	esv3455478	chr21:39863888-39863995	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
13	esv3491055	chr21:39863888-39863995	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	inside rSNPs	diseases
14	nsv187113	chr21:39863890-39863994	Weak transcription Genic enhancers Flanking Active TSS Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:39858000-39864000	Enhancers	Fetal Heart	heart
2	chr21:39859600-39865600	Weak transcription	Fetal Muscle Leg	muscle
3	chr21:39859800-39864000	Weak transcription	Fetal Lung	lung
4	chr21:39859800-39864200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr21:39860200-39865400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr21:39860200-39865600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr21:39860200-39865600	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr21:39860400-39879000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr21:39861000-39865800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr21:39861000-39867600	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr21:39861200-39866200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr21:39861400-39865600	Weak transcription	Thymus	Thymus
13	chr21:39861400-39866200	Weak transcription	NH-A	brain
14	chr21:39861600-39864600	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr21:39861800-39867600	Weak transcription	Duodenum Mucosa	Duodenum
16	chr21:39862000-39864800	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr21:39862000-39865600	Weak transcription	HMEC	breast
18	chr21:39862000-39866400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr21:39862000-39866600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr21:39862000-39872200	Weak transcription	Gastric	stomach
21	chr21:39862000-39877400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr21:39862200-39866000	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr21:39862200-39871200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr21:39862400-39864600	Enhancers	Primary B cells from cord blood	blood
25	chr21:39862400-39866800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr21:39862600-39869400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr21:39862800-39865600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr21:39862800-39865600	Weak transcription	Adipose Nuclei	Adipose
29	chr21:39862800-39865600	Weak transcription	Aorta	Aorta
30	chr21:39862800-39865600	Weak transcription	Lung	lung
31	chr21:39862800-39865600	Weak transcription	Pancreas	Pancrea
32	chr21:39862800-39865600	Weak transcription	Spleen	Spleen
33	chr21:39862800-39866200	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr21:39862800-39866600	Weak transcription	Right Ventricle	heart
35	chr21:39863000-39864600	Weak transcription	Fetal Thymus	thymus
36	chr21:39863000-39864800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr21:39863000-39865000	Genic enhancers	Primary hematopoietic stem cells	blood
38	chr21:39863000-39865600	Weak transcription	Left Ventricle	heart
39	chr21:39863000-39865600	Weak transcription	Right Atrium	heart
40	chr21:39863000-39866200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr21:39863400-39864800	Enhancers	HSMMtube	muscle
42	chr21:39863600-39864200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr21:39863600-39865600	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr21:39863600-39865600	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr21:39863800-39865000	Flanking Active TSS	HUVEC	blood vessel
46	chr21:39863800-39865200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr21:39863800-39865600	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr21:39863800-39865600	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr21:39863800-39866600	Weak transcription	H1 Cell Line	embryonic stem cell

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