Variant report

Variant	rs11681157
Chromosome Location	chr2:47196484-47196485
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:47194084..47197081-chr2:47210689..47213163,3	MCF-7	breast:
2	chr2:47196068..47199021-chr2:47522197..47525047,2	K562	blood:
3	chr2:47194544..47196937-chr2:47423756..47426631,2	MCF-7	breast:
4	chr2:11678126..11680963-chr2:47194547..47197041,2	MCF-7	breast:
5	chr2:47196076..47198728-chr2:47417712..47420454,3	MCF-7	breast:
6	chr2:47194294..47196907-chr2:47548954..47551761,2	MCF-7	breast:
7	chr2:47191916..47197742-chr2:47401234..47405560,7	MCF-7	breast:
8	chr2:47195860..47200774-chr2:47207735..47210386,4	K562	blood:
9	chr2:47195345..47199186-chr2:47202255..47204268,3	MCF-7	breast:
10	chr2:47166867..47170590-chr2:47194468..47200247,20	MCF-7	breast:
11	chr2:47164675..47170526-chr2:47188235..47196918,12	MCF-7	breast:
12	chr2:47196446..47198984-chr2:47567520..47569154,2	MCF-7	breast:
13	chr2:47182604..47186847-chr2:47193837..47196503,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000272814	Chromatin interaction
ENSG00000143933	Chromatin interaction
ENSG00000196208	Chromatin interaction
ENSG00000068724	Chromatin interaction
ENSG00000264010	Chromatin interaction
ENSG00000180398	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10183233	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11125106	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11125107	0.84[ASN][1000 genomes]
rs11125108	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11680029	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12052808	0.81[ASN][1000 genomes]
rs13002842	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13395498	0.81[ASN][1000 genomes]
rs13406452	0.80[ASN][1000 genomes]
rs17480779	0.84[ASN][1000 genomes]
rs1865262	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2347260	0.88[ASN][1000 genomes]
rs2881587	0.81[ASN][1000 genomes]
rs35779609	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6716882	0.87[ASN][1000 genomes]
rs6731862	0.87[ASN][1000 genomes]
rs6731875	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6734201	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs736683	0.81[ASN][1000 genomes]
rs7560371	0.88[ASN][1000 genomes]
rs993847	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817517	chr2:46819371-47715140	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
2	nsv457352	chr2:47004788-47325973	Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv581749	chr2:47004788-47325973	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	nsv1004828	chr2:47056849-47814482	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
5	nsv524970	chr2:47162739-47302095	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
6	nsv1000377	chr2:47189386-47344029	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
7	esv1009804	chr2:47193130-47196785	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:47169800-47214600	Weak transcription	Fetal Kidney	kidney
2	chr2:47174400-47212400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr2:47177200-47210400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr2:47181600-47210800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:47184600-47197600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr2:47184600-47205000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr2:47185000-47206000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr2:47185200-47210200	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr2:47185400-47205800	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr2:47185400-47210400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr2:47186200-47200800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr2:47186400-47205600	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr2:47186800-47205200	Weak transcription	Gastric	stomach
14	chr2:47186800-47205800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr2:47187200-47197000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr2:47187400-47206000	Weak transcription	Fetal Brain Female	brain
17	chr2:47187800-47203200	Weak transcription	Brain Germinal Matrix	brain
18	chr2:47187800-47210200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr2:47188000-47205200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr2:47188000-47207000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr2:47188200-47196800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr2:47190000-47197000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr2:47190400-47196800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr2:47191200-47198800	Enhancers	Placenta	Placenta
25	chr2:47191400-47197000	Enhancers	HepG2	liver
26	chr2:47192200-47197000	Weak transcription	GM12878-XiMat	blood
27	chr2:47193800-47204000	Strong transcription	Primary T cells from cord blood	blood
28	chr2:47194800-47197600	Weak transcription	Primary neutrophils fromperipheralblood	blood
29	chr2:47194800-47198800	Enhancers	Placenta Amnion	Placenta Amnion
30	chr2:47194800-47200200	Strong transcription	Thymus	Thymus
31	chr2:47195000-47198800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr2:47195000-47198800	Genic enhancers	Fetal Intestine Small	intestine
33	chr2:47195200-47197600	Weak transcription	Primary hematopoietic stem cells	blood
34	chr2:47195200-47202200	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr2:47195400-47197000	Weak transcription	Brain Angular Gyrus	brain
36	chr2:47195400-47202000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr2:47195600-47196600	Strong transcription	Fetal Thymus	thymus
38	chr2:47195600-47196800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr2:47195600-47196800	Weak transcription	Primary B cells from cord blood	blood
40	chr2:47195600-47196800	Weak transcription	Colonic Mucosa	Colon
41	chr2:47195600-47196800	Weak transcription	Spleen	Spleen
42	chr2:47195600-47197000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr2:47195600-47197000	Weak transcription	Primary T helper cells fromperipheralblood	blood
44	chr2:47195600-47197000	Weak transcription	Right Ventricle	heart
45	chr2:47195600-47197200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr2:47195600-47197200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr2:47195600-47197200	Weak transcription	Lung	lung
48	chr2:47195600-47197400	Weak transcription	Right Atrium	heart
49	chr2:47195600-47197600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr2:47195600-47199000	Enhancers	Breast Myoepithelial Primary Cells	Breast

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