Variant report

Variant	rs367727871
Chromosome Location	chr7:100319149-100319150
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:100314177..100318194-chr7:100318771..100321626,3	K562	blood:
2	chr7:100183516..100185859-chr7:100318860..100320461,2	MCF-7	breast:
3	chr7:100317495..100321039-chr7:100423744..100425687,3	MCF-7	breast:
4	chr7:100302553..100308135-chr7:100314195..100322207,16	MCF-7	breast:
5	chr7:100302051..100306591-chr7:100312993..100321692,11	MCF-7	breast:

Variant related genes	Relation type
ENSG00000172336	Chromatin interaction
ENSG00000146828	Chromatin interaction
ENSG00000077454	Chromatin interaction
ENSG00000196411	Chromatin interaction
ENSG00000106336	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	esv1829095	chr7:99814675-100494084	Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	393 gene(s)	inside rSNPs	diseases
2	nsv831072	chr7:100162503-100362835	Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
3	nsv888791	chr7:100221867-100371114	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
4	nsv607933	chr7:100240191-100365613	Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
5	nsv470381	chr7:100240191-100431980	Strong transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
6	nsv8184	chr7:100240737-100345945	Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
7	nsv888792	chr7:100252918-100329189	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
8	esv1804951	chr7:100275135-100374093	Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
9	nsv1020837	chr7:100313122-100508635	Genic enhancers Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
10	nsv888796	chr7:100313420-100423365	Genic enhancers Strong transcription Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
11	esv3410635	chr7:100317416-100319614	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
12	esv1829284	chr7:100318927-100337055	Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100317200-100319400	Bivalent Enhancer	Fetal Intestine Small	intestine
2	chr7:100317600-100319400	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
3	chr7:100317800-100319200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
4	chr7:100317800-100319200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
5	chr7:100317800-100319200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr7:100317800-100319400	Bivalent Enhancer	Fetal Muscle Leg	muscle
7	chr7:100317800-100321000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
8	chr7:100318000-100319200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
9	chr7:100318000-100319400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr7:100318000-100319600	Enhancers	Pancreas	Pancrea
11	chr7:100318000-100319800	Bivalent Enhancer	Colonic Mucosa	Colon
12	chr7:100318400-100319200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
13	chr7:100318400-100319400	Flanking Active TSS	Liver	Liver
14	chr7:100318600-100319200	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr7:100318600-100319200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
16	chr7:100318600-100320400	Flanking Active TSS	HepG2	liver
17	chr7:100318800-100319200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
18	chr7:100318800-100319200	Enhancers	Right Atrium	heart
19	chr7:100318800-100319400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:100318800-100319400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
21	chr7:100318800-100319400	Enhancers	K562	blood
22	chr7:100318800-100319600	Bivalent Enhancer	Placenta	Placenta
23	chr7:100319000-100319200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
24	chr7:100319000-100319200	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr7:100319000-100319200	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
26	chr7:100319000-100319200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr7:100319000-100319200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr7:100319000-100319200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr7:100319000-100319200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr7:100319000-100319200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr7:100319000-100319200	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr7:100319000-100319200	Bivalent Enhancer	Duodenum Mucosa	Duodenum
33	chr7:100319000-100319200	Bivalent Enhancer	Fetal Thymus	thymus
34	chr7:100319000-100319200	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
35	chr7:100319000-100319200	Bivalent Enhancer	NHEK	skin
36	chr7:100319000-100319400	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr7:100319000-100319400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr7:100319000-100319400	Bivalent Enhancer	Fetal Intestine Large	intestine

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