Variant report

Variant	rs35379940
Chromosome Location	chr2:110457829-110457830
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:110251030..110252990-chr2:110456796..110459130,2	MCF-7	breast:
2	chr2:110455483..110458569-chr2:110458609..110461502,6	MCF-7	breast:
3	chr2:110456223..110458678-chr2:110473323..110476138,2	MCF-7	breast:
4	chr2:110448146..110451787-chr2:110456949..110458921,3	MCF-7	breast:
5	chr2:110371478..110373330-chr2:110455377..110458240,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000198142	Chromatin interaction
ENSG00000186522	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs57115181	1.00[ASN][1000 genomes]
rs73956135	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874777	chr2:109825516-110693317	Strong transcription Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv1011456	chr2:110290958-110980402	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
3	nsv535861	chr2:110290958-110980402	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
4	nsv1009367	chr2:110349178-110863354	Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
5	esv2762780	chr2:110367969-110462496	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
6	nsv491837	chr2:110381297-110964737	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
7	nsv999552	chr2:110396395-110978224	Enhancers Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
8	nsv428061	chr2:110423940-110714002	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
9	esv2751812	chr2:110457214-110980346	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:110451000-110458000	Weak transcription	Spleen	Spleen
2	chr2:110453200-110458000	Weak transcription	Esophagus	oesophagus
3	chr2:110455400-110461800	Enhancers	Placenta	Placenta
4	chr2:110455800-110461600	Enhancers	Fetal Intestine Small	intestine
5	chr2:110456200-110458600	Enhancers	Duodenum Smooth Muscle	Duodenum
6	chr2:110456200-110459200	Enhancers	Hela-S3	cervix
7	chr2:110456400-110458600	Enhancers	Colon Smooth Muscle	Colon
8	chr2:110456400-110458600	Enhancers	Fetal Muscle Leg	muscle
9	chr2:110456400-110458800	Enhancers	Fetal Heart	heart
10	chr2:110456400-110459200	Enhancers	HMEC	breast
11	chr2:110456400-110460200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr2:110456400-110460200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:110456400-110460200	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr2:110456400-110460400	Enhancers	Stomach Mucosa	stomach
15	chr2:110456400-110461000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr2:110456400-110461800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr2:110456600-110458200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr2:110456600-110458800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr2:110456600-110458800	Enhancers	Right Atrium	heart
20	chr2:110456600-110459000	Enhancers	H1 Cell Line	embryonic stem cell
21	chr2:110456600-110459000	Enhancers	Fetal Stomach	stomach
22	chr2:110456600-110459000	Enhancers	Pancreas	Pancrea
23	chr2:110456600-110459600	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr2:110456600-110459800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr2:110456600-110460000	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr2:110456600-110460200	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr2:110456600-110460200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr2:110456600-110460200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr2:110456600-110461400	Enhancers	Fetal Lung	lung
30	chr2:110456600-110462000	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr2:110456800-110458000	Flanking Active TSS	Duodenum Mucosa	Duodenum
32	chr2:110456800-110458800	Enhancers	Aorta	Aorta
33	chr2:110456800-110459000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr2:110456800-110459400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr2:110456800-110459800	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr2:110456800-110459800	Weak transcription	Liver	Liver
37	chr2:110456800-110460000	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr2:110456800-110460600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr2:110456800-110461000	Enhancers	Small Intestine	intestine
40	chr2:110457000-110458400	Weak transcription	Fetal Kidney	kidney
41	chr2:110457000-110459400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr2:110457200-110459600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr2:110457200-110460200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr2:110457200-110460200	Weak transcription	A549	lung
45	chr2:110457400-110458200	Flanking Active TSS	HUVEC	blood vessel
46	chr2:110457400-110458400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr2:110457400-110458400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr2:110457400-110458600	Enhancers	Colonic Mucosa	Colon
49	chr2:110457400-110459600	Weak transcription	Lung	lung
50	chr2:110457400-110459600	Enhancers	Rectal Mucosa Donor 29	rectum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links