Variant report

Variant	rs181852135
Chromosome Location	chr7:101383612-101383613
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:101376217..101377768-chr7:101381798..101384550,2	MCF-7	breast:
2	chr7:101371362..101372936-chr7:101382706..101384319,2	MCF-7	breast:
3	chr7:101383126..101385865-chr7:101398297..101401164,2	MCF-7	breast:
4	chr7:101376174..101379277-chr7:101381131..101384556,3	MCF-7	breast:
5	chr7:101358883..101362441-chr7:101383235..101387377,4	MCF-7	breast:
6	chr7:101383224..101388686-chr7:101455921..101460973,10	K562	blood:
7	chr7:101381459..101384895-chr7:101386139..101388176,3	K562	blood:

Variant related genes	Relation type
ENSG00000257923	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933653	chr7:100701931-101515782	Active TSS ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv1018544	chr7:101225639-101424889	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv539045	chr7:101225639-101424889	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv482758	chr7:101231458-101395219	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic 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
5	nsv831079	chr7:101273495-101466776	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
6	nsv1021797	chr7:101342353-101466957	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
7	nsv539046	chr7:101342353-101466957	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
8	nsv1024319	chr7:101368299-101668159	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
9	nsv539047	chr7:101368299-101668159	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
10	esv2534796	chr7:101381535-101384376	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	esv3477438	chr7:101382413-101383963	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	esv3477437	chr7:101382450-101384103	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101377200-101386600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:101377400-101384200	Weak transcription	Colonic Mucosa	Colon
3	chr7:101381000-101384200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr7:101381200-101384200	Enhancers	Fetal Thymus	thymus
5	chr7:101382200-101384000	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr7:101382400-101384200	Enhancers	Thymus	Thymus
7	chr7:101382400-101384200	Enhancers	GM12878-XiMat	blood
8	chr7:101382600-101383800	Enhancers	Hela-S3	cervix
9	chr7:101382600-101384000	Enhancers	Dnd41	blood
10	chr7:101382600-101384200	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr7:101382600-101384200	Enhancers	Primary B cells from cord blood	blood
12	chr7:101382600-101384400	Enhancers	Primary hematopoietic stem cells	blood
13	chr7:101382800-101384200	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr7:101382800-101385000	Enhancers	Stomach Mucosa	stomach
15	chr7:101382800-101386600	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr7:101383000-101386400	Enhancers	Primary B cells from peripheral blood	blood
17	chr7:101383000-101386400	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chr7:101383000-101386600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr7:101383000-101386600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr7:101383200-101384400	Weak transcription	Placenta	Placenta
21	chr7:101383200-101384400	Weak transcription	Gastric	stomach
22	chr7:101383200-101384400	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr7:101383200-101384400	Weak transcription	HUVEC	blood vessel
24	chr7:101383200-101384800	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr7:101383200-101386200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr7:101383200-101386200	Enhancers	Primary T cells from cord blood	blood
27	chr7:101383200-101386400	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr7:101383200-101386600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr7:101383400-101384000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr7:101383400-101384200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr7:101383400-101384200	Enhancers	Primary T cells fromperipheralblood	blood
32	chr7:101383400-101384400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr7:101383400-101385800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr7:101383400-101386200	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr7:101383400-101386200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
36	chr7:101383400-101386400	Weak transcription	A549	lung
37	chr7:101383400-101386400	Weak transcription	HMEC	breast
38	chr7:101383400-101386600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr7:101383400-101386600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr7:101383400-101386600	Weak transcription	Pancreas	Pancrea
41	chr7:101383400-101386600	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr7:101383600-101384000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr7:101383600-101384000	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr7:101383600-101384000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr7:101383600-101384000	Weak transcription	HepG2	liver
46	chr7:101383600-101384000	Weak transcription	K562	blood

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