Variant report

Variant	rs564100388
Chromosome Location	chr4:3390079-3390080
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:3294234..3297919-chr4:3387466..3390148,3	MCF-7	breast:
2	chr4:3385272..3387718-chr4:3389014..3391654,3	MCF-7	breast:
3	chr4:3388642..3391528-chr4:3405332..3407484,2	MCF-7	breast:
4	chr4:3388406..3390149-chr4:3442407..3445401,2	MCF-7	breast:
5	chr4:3388256..3390546-chr4:3393263..3395293,2	MCF-7	breast:
6	chr4:3356602..3361196-chr4:3388835..3391854,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000109758	Chromatin interaction
ENSG00000159788	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3418626	chr4:2741174-3461492	Genic enhancers Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
2	esv3397632	chr4:2741239-3460583	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats 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	63 gene(s)	inside rSNPs	diseases
3	nsv878456	chr4:3215835-3467519	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
4	nsv428106	chr4:3226182-3752322	Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS 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	33 gene(s)	inside rSNPs	diseases
5	nsv878462	chr4:3311548-3505448	Strong transcription Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
6	nsv1007847	chr4:3317904-3527357	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
7	nsv537001	chr4:3317904-3527357	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats 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	13 gene(s)	inside rSNPs	diseases
8	nsv878463	chr4:3363994-3498896	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv428435	chr4:3386773-3623321	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
10	esv2328657	chr4:3389734-3390188	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3378400-3390400	Weak transcription	Ovary	ovary
2	chr4:3386200-3391400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr4:3386400-3390800	Enhancers	Fetal Lung	lung
4	chr4:3386400-3391200	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr4:3386600-3390800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:3386600-3392400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr4:3386600-3393800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr4:3386800-3393600	Enhancers	H1 Cell Line	embryonic stem cell
9	chr4:3386800-3393600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr4:3386800-3395800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr4:3387600-3390600	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr4:3387600-3390600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr4:3387600-3392600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr4:3387800-3391000	Active TSS	Esophagus	oesophagus
15	chr4:3388000-3390200	Active TSS	HMEC	breast
16	chr4:3388000-3394400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr4:3388400-3391200	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr4:3388400-3392000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
19	chr4:3388400-3393600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr4:3388600-3392000	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr4:3388600-3392400	Enhancers	Fetal Muscle Trunk	muscle
22	chr4:3388600-3394400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:3388800-3390200	Enhancers	H9 Cell Line	embryonic stem cell
24	chr4:3388800-3390200	Enhancers	Brain Angular Gyrus	brain
25	chr4:3388800-3390800	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr4:3388800-3391200	Enhancers	Fetal Intestine Small	intestine
27	chr4:3388800-3391400	Enhancers	Fetal Heart	heart
28	chr4:3388800-3391600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr4:3388800-3391800	Enhancers	Fetal Muscle Leg	muscle
30	chr4:3388800-3392000	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr4:3388800-3392600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr4:3388800-3392600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr4:3388800-3392800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr4:3388800-3394400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr4:3389000-3390600	Enhancers	Fetal Brain Male	brain
36	chr4:3389000-3390600	Flanking Active TSS	GM12878-XiMat	blood
37	chr4:3389000-3391600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
38	chr4:3389000-3391800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr4:3389000-3393400	Enhancers	Brain Germinal Matrix	brain
40	chr4:3389200-3390200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr4:3389200-3390400	Enhancers	Fetal Stomach	stomach
42	chr4:3389200-3390400	Enhancers	HSMMtube	muscle
43	chr4:3389200-3390600	Weak transcription	Liver	Liver
44	chr4:3389200-3391000	Active TSS	Duodenum Mucosa	Duodenum
45	chr4:3389200-3391200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr4:3389200-3391200	Active TSS	Rectal Mucosa Donor 31	rectum
47	chr4:3389200-3391400	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr4:3389200-3391400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr4:3389200-3391400	Flanking Active TSS	Adipose Nuclei	Adipose
50	chr4:3389200-3395000	Weak transcription	HepG2	liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links