Variant report

Variant	rs7931316
Chromosome Location	chr11:119585681-119585682
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:119579836..119582330-chr11:119583549..119585842,2	MCF-7	breast:
2	chr11:119576493..119579043-chr11:119584398..119586423,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000255247	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10892438	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10892441	0.87[EUR][1000 genomes]
rs11217421	1.00[EUR][1000 genomes]
rs11217423	0.84[EUR][1000 genomes]
rs35301288	0.85[EUR][1000 genomes]
rs7944015	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898421	chr11:119499014-119631325	Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv898422	chr11:119518006-119601779	Bivalent Enhancer Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv898423	chr11:119541332-119659753	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv468880	chr11:119564496-119588062	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv556471	chr11:119564496-119588062	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1051769	chr11:119572865-119630769	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:119568400-119587000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr11:119568600-119590400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr11:119572600-119592000	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr11:119573000-119591800	Weak transcription	Left Ventricle	heart
5	chr11:119574000-119597200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr11:119575200-119591600	Weak transcription	Stomach Smooth Muscle	stomach
7	chr11:119576800-119587200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr11:119579600-119589200	Genic enhancers	Fetal Intestine Small	intestine
9	chr11:119580800-119597000	Weak transcription	Lung	lung
10	chr11:119581000-119586400	Weak transcription	Ovary	ovary
11	chr11:119581000-119591600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr11:119581000-119591600	Weak transcription	Colonic Mucosa	Colon
13	chr11:119581200-119588400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr11:119581200-119590600	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr11:119581400-119585800	Weak transcription	Brain Cingulate Gyrus	brain
16	chr11:119581400-119586400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr11:119581400-119587000	Weak transcription	Brain Substantia Nigra	brain
18	chr11:119581600-119586800	Weak transcription	Brain Germinal Matrix	brain
19	chr11:119581800-119586400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr11:119582200-119585800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr11:119582200-119586200	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr11:119582200-119589000	Enhancers	Duodenum Mucosa	Duodenum
23	chr11:119582200-119593600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr11:119582400-119585800	Enhancers	Fetal Thymus	thymus
25	chr11:119582400-119586600	Enhancers	Liver	Liver
26	chr11:119582400-119587000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr11:119582400-119587800	Enhancers	Fetal Intestine Large	intestine
28	chr11:119582800-119586400	Weak transcription	Brain Angular Gyrus	brain
29	chr11:119582800-119587600	Weak transcription	Fetal Brain Female	brain
30	chr11:119582800-119589200	Enhancers	H1 Cell Line	embryonic stem cell
31	chr11:119583000-119586200	Enhancers	Fetal Muscle Leg	muscle
32	chr11:119583400-119586000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr11:119583400-119586800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr11:119583400-119589400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr11:119583600-119586000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr11:119583600-119586400	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr11:119583600-119588000	Weak transcription	Fetal Kidney	kidney
38	chr11:119583800-119586000	Enhancers	NHEK	skin
39	chr11:119583800-119587400	Weak transcription	Fetal Brain Male	brain
40	chr11:119583800-119588000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr11:119583800-119588400	Weak transcription	Brain Anterior Caudate	brain
42	chr11:119583800-119589200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr11:119584000-119586000	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr11:119584000-119586600	Weak transcription	GM12878-XiMat	blood
45	chr11:119584000-119587600	Weak transcription	Brain Hippocampus Middle	brain
46	chr11:119584200-119586000	Enhancers	HMEC	breast
47	chr11:119584200-119587200	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr11:119584600-119587200	Weak transcription	Fetal Lung	lung
49	chr11:119584600-119587600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr11:119584600-119591600	Weak transcription	Fetal Heart	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links