Variant report

Variant	rs11884484
Chromosome Location	chr2:182649589-182649590
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:182648713..182650748-chr2:182748851..182753671,4	MCF-7	breast:
2	chr2:182647541..182657734-chr2:182753295..182760748,23	MCF-7	breast:
3	chr2:182642988..182645048-chr2:182649419..182652084,2	MCF-7	breast:
4	chr2:182649357..182651111-chr2:182651745..182654044,2	MCF-7	breast:
5	chr2:182646086..182659083-chr2:182754079..182762654,36	MCF-7	breast:
6	chr2:182607060..182610718-chr2:182648609..182651704,3	MCF-7	breast:
7	chr2:182642047..182644183-chr2:182648360..182651289,2	K562	blood:

Variant related genes	Relation type
ENSG00000138434	Chromatin interaction
ENSG00000260742	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10169250	0.94[YRI][hapmap];0.93[AFR][1000 genomes]
rs10173295	1.00[AMR][1000 genomes]
rs10178791	1.00[AMR][1000 genomes]
rs10183369	1.00[AMR][1000 genomes]
rs11884530	1.00[AMR][1000 genomes]
rs11898883	1.00[AMR][1000 genomes]
rs11903205	0.83[YRI][hapmap];0.83[AFR][1000 genomes]
rs11904481	1.00[AMR][1000 genomes]
rs13385387	1.00[AMR][1000 genomes]
rs13399033	0.85[AFR][1000 genomes]
rs13404097	1.00[AMR][1000 genomes]
rs13412336	1.00[AMR][1000 genomes]
rs13415704	1.00[AMR][1000 genomes]
rs28730957	1.00[AMR][1000 genomes]
rs56043868	1.00[AMR][1000 genomes]
rs59024368	1.00[AMR][1000 genomes]
rs59405729	1.00[AMR][1000 genomes]
rs73030974	1.00[AMR][1000 genomes]
rs73030984	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9288070	1.00[AMR][1000 genomes]
rs9288071	1.00[AMR][1000 genomes]
rs9288072	1.00[AMR][1000 genomes]
rs9630973	1.00[AMR][1000 genomes]
rs9630988	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005870	chr2:181968637-182921439	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv536063	chr2:181968637-182921439	Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv1001558	chr2:182590009-182732738	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:182641800-182649600	Enhancers	Fetal Intestine Large	intestine
2	chr2:182641800-182650000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr2:182642200-182657200	Enhancers	Hela-S3	cervix
4	chr2:182645200-182651800	Weak transcription	Thymus	Thymus
5	chr2:182645400-182650600	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr2:182646000-182651200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr2:182646000-182651800	Weak transcription	Fetal Thymus	thymus
8	chr2:182646200-182651000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr2:182646200-182651200	Weak transcription	Primary hematopoietic stem cells	blood
10	chr2:182646200-182651200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr2:182646400-182650200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr2:182646400-182651600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr2:182646400-182651600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr2:182646600-182651200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr2:182646600-182651200	Weak transcription	Pancreas	Pancrea
16	chr2:182646600-182653400	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr2:182646600-182654800	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr2:182647200-182652600	Enhancers	HepG2	liver
19	chr2:182647200-182652800	Enhancers	Stomach Mucosa	stomach
20	chr2:182647400-182653000	Enhancers	Fetal Intestine Small	intestine
21	chr2:182647600-182650600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr2:182647800-182650000	Enhancers	Fetal Kidney	kidney
23	chr2:182647800-182650200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr2:182648000-182657200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr2:182648200-182650200	Enhancers	Muscle Satellite Cultured Cells	--
26	chr2:182648200-182650800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr2:182648200-182651200	Weak transcription	Placenta	Placenta
28	chr2:182648200-182651800	Weak transcription	Dnd41	blood
29	chr2:182648400-182650000	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr2:182648600-182651000	Enhancers	NH-A	brain
31	chr2:182648600-182651200	Enhancers	Placenta Amnion	Placenta Amnion
32	chr2:182648600-182651400	Enhancers	Osteobl	bone
33	chr2:182648600-182657200	Enhancers	HMEC	breast
34	chr2:182648800-182649600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr2:182648800-182651000	Weak transcription	Small Intestine	intestine
36	chr2:182648800-182654600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr2:182648800-182657000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr2:182649000-182651000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr2:182649000-182651400	Enhancers	HSMM	muscle
40	chr2:182649200-182649600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr2:182649200-182649600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr2:182649200-182649600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr2:182649200-182649600	Enhancers	Fetal Lung	lung
44	chr2:182649200-182650000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr2:182649200-182650000	Flanking Active TSS	NHEK	skin
46	chr2:182649200-182650800	Enhancers	HUVEC	blood vessel
47	chr2:182649200-182651000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr2:182649200-182651000	Enhancers	HSMMtube	muscle
49	chr2:182649200-182651400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr2:182649200-182651400	Enhancers	Rectal Mucosa Donor 31	rectum

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