Variant report

Variant	rs533059664
Chromosome Location	chr1:214794584-214794585
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:214791981..214793760-chr1:214793960..214796575,2	K562	blood:
2	chr1:214775848..214778755-chr1:214793553..214795303,2	K562	blood:
3	chr1:214776329..214778755-chr1:214793412..214795053,3	K562	blood:
4	chr1:214788681..214791513-chr1:214794324..214796385,3	K562	blood:

Variant related genes	Relation type
ENSG00000117724	Chromatin interaction

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1004475	chr1:214763778-215013375	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1005669	chr1:214774522-214994142	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv997864	chr1:214778658-214994142	Enhancers Genic enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1002937	chr1:214793813-214994142	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:214777600-214800400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:214777600-214810800	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr1:214777600-214838600	Weak transcription	Esophagus	oesophagus
4	chr1:214777800-214838400	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr1:214778000-214839200	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr1:214778200-214803600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr1:214781200-214818000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr1:214781800-214795800	Weak transcription	Fetal Intestine Small	intestine
9	chr1:214782000-214803800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr1:214783200-214817800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr1:214783400-214838800	Weak transcription	Fetal Kidney	kidney
12	chr1:214784600-214834000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:214784800-214803600	Weak transcription	Brain Germinal Matrix	brain
14	chr1:214784800-214807400	Weak transcription	Fetal Brain Female	brain
15	chr1:214785600-214819400	Strong transcription	K562	blood
16	chr1:214785600-214843800	Strong transcription	Fetal Thymus	thymus
17	chr1:214785800-214800600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr1:214786000-214794600	Weak transcription	Primary T cells from cord blood	blood
19	chr1:214786200-214843000	Strong transcription	HUES64 Cell Line	embryonic stem cell
20	chr1:214786600-214797200	Strong transcription	H1 Cell Line	embryonic stem cell
21	chr1:214786600-214800200	Strong transcription	HUES48 Cell Line	embryonic stem cell
22	chr1:214786600-214833800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr1:214786600-214843200	Strong transcription	HUES6 Cell Line	embryonic stem cell
24	chr1:214786800-214800400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
25	chr1:214786800-214805200	Strong transcription	Dnd41	blood
26	chr1:214786800-214843800	Strong transcription	Monocytes-CD14+_RO01746	blood
27	chr1:214787200-214798200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr1:214787600-214796600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr1:214787600-214842200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
30	chr1:214787800-214798600	Strong transcription	HepG2	liver
31	chr1:214787800-214800400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr1:214788000-214803800	Weak transcription	Placenta	Placenta
33	chr1:214788000-214810400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
34	chr1:214788200-214820600	Weak transcription	Fetal Heart	heart
35	chr1:214788600-214803800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr1:214789000-214837400	Weak transcription	Small Intestine	intestine
37	chr1:214789200-214796800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr1:214789600-214796200	Strong transcription	A549	lung
39	chr1:214789800-214796800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr1:214790400-214797600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr1:214790600-214795000	Strong transcription	Fetal Muscle Trunk	muscle
42	chr1:214790600-214795000	Strong transcription	Fetal Muscle Leg	muscle
43	chr1:214790600-214795800	Strong transcription	HMEC	breast
44	chr1:214790600-214796000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr1:214790800-214796800	Strong transcription	Osteobl	bone
46	chr1:214790800-214800200	Strong transcription	Hela-S3	cervix
47	chr1:214790800-214800600	Strong transcription	Primary monocytes fromperipheralblood	blood
48	chr1:214790800-214805600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr1:214791000-214795400	Strong transcription	Primary hematopoietic stem cells	blood
50	chr1:214791000-214797200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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