Variant report

Variant	rs554668365
Chromosome Location	chr4:745798-745799
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:745562..749408-chr4:752726..755779,3	MCF-7	breast:
2	chr4:745534..748731-chr4:756775..761109,4	MCF-7	breast:
3	chr4:744377..748508-chr4:749329..752035,5	K562	blood:
4	chr4:741073..743262-chr4:744150..746174,2	K562	blood:
5	chr4:744377..747557-chr4:749370..752035,4	K562	blood:
6	chr4:743968..746769-chr4:761390..763211,2	MCF-7	breast:
7	chr4:732543..739360-chr4:740100..745945,6	K562	blood:
8	chr4:745543..747300-chr4:747376..749196,2	K562	blood:
9	chr4:579661..581575-chr4:744162..745804,2	MCF-7	breast:
10	chr4:711689..713819-chr4:744477..746857,2	MCF-7	breast:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CPLX1-11	chr4:744922-746968	ncRnaDb_ncrna_FR374492_1

No data

Variant related genes	Relation type
ENSG00000233799	Chromatin interaction
ENSG00000272588	Chromatin interaction
ENSG00000185619	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011715	chr4:43860-823487	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	nsv532702	chr4:72447-755236	Active TSS ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
3	nsv1005224	chr4:507005-900281	Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Strong transcription Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	nsv536976	chr4:507005-900281	Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
5	nsv822425	chr4:540105-1413799	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
6	esv2757916	chr4:603208-931354	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
7	esv2759217	chr4:603208-931354	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
8	nsv878247	chr4:607202-925149	Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
9	nsv530490	chr4:614355-1399150	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
10	esv1829397	chr4:655939-1041957	Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
11	nsv829834	chr4:665477-775524	Active TSS Genic enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
12	nsv593209	chr4:686563-747810	Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
13	esv1833383	chr4:708887-753697	Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
14	nsv878253	chr4:708932-771587	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
15	nsv878254	chr4:708932-899143	Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
16	nsv878255	chr4:708932-1052488	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
17	nsv878257	chr4:712222-852313	Strong transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
18	nsv878258	chr4:712222-1058358	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
19	nsv878259	chr4:713920-852313	Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
20	nsv878260	chr4:713920-1052488	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
21	nsv4195	chr4:727187-768059	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
22	esv1833385	chr4:738603-753697	Genic enhancers Strong transcription Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
23	esv1002699	chr4:742779-747297	Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
24	nsv966467	chr4:744990-760620	Strong transcription Genic enhancers Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:702200-754800	Weak transcription	Hela-S3	cervix
2	chr4:715600-750200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:727000-767600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr4:728600-755800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr4:728600-763400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr4:729000-754600	Weak transcription	Fetal Kidney	kidney
7	chr4:729000-762600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr4:729600-753800	Weak transcription	Psoas Muscle	Psoas
9	chr4:729600-760800	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr4:733600-753800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr4:733800-747400	Weak transcription	Primary B cells from cord blood	blood
12	chr4:736600-752000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr4:741400-749200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr4:741400-749400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr4:741400-749400	Strong transcription	Thymus	Thymus
16	chr4:741400-749600	Strong transcription	Primary monocytes fromperipheralblood	blood
17	chr4:741400-749600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
18	chr4:741400-751000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr4:741400-751400	Strong transcription	Fetal Brain Female	brain
20	chr4:741400-751800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr4:741400-752000	Strong transcription	Fetal Intestine Small	intestine
22	chr4:741400-752400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr4:741400-752400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr4:741400-752800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr4:741400-752800	Strong transcription	Fetal Thymus	thymus
26	chr4:741600-747200	Strong transcription	HUES48 Cell Line	embryonic stem cell
27	chr4:741600-747200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
28	chr4:741600-748000	Strong transcription	Fetal Intestine Large	intestine
29	chr4:741600-749200	Strong transcription	Primary T cells from cord blood	blood
30	chr4:741600-749400	Strong transcription	Gastric	stomach
31	chr4:741600-749400	Strong transcription	Sigmoid Colon	Sigmoid Colon
32	chr4:741600-750400	Strong transcription	Fetal Lung	lung
33	chr4:741600-750600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr4:741600-750800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr4:741600-751200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr4:741600-751600	Strong transcription	Dnd41	blood
37	chr4:741600-752400	Strong transcription	H1 Cell Line	embryonic stem cell
38	chr4:741600-752400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr4:741600-752400	Strong transcription	Monocytes-CD14+_RO01746	blood
40	chr4:741600-752800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr4:741800-747200	Strong transcription	Primary B cells from peripheral blood	blood
42	chr4:741800-748600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr4:741800-749200	Strong transcription	Duodenum Mucosa	Duodenum
44	chr4:741800-751800	Strong transcription	HUES6 Cell Line	embryonic stem cell
45	chr4:742000-746000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr4:742200-749200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr4:742200-749200	ZNF genes & repeats	Fetal Stomach	stomach
48	chr4:742200-749600	Strong transcription	Stomach Smooth Muscle	stomach
49	chr4:742600-751800	Strong transcription	Placenta	Placenta
50	chr4:742600-754400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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