Variant report

Variant	rs183813787
Chromosome Location	chr1:94282701-94282702
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	chr1:94145260..94147356-chr1:94280674..94282798,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000137936	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

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	nsv546822	chr1:94246577-94289863	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	esv1815663	chr1:94246577-94291252	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1877	chr1:94247756-94292908	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv508415	chr1:94256122-94305339	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	esv1802380	chr1:94272119-94291252	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	esv1822452	chr1:94278128-94320233	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	121 gene(s)	inside rSNPs	diseases
7	esv1005153	chr1:94281705-94283362	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:94273600-94282800	Weak transcription	Lung	lung
2	chr1:94275800-94284200	Enhancers	Hela-S3	cervix
3	chr1:94275800-94285000	Enhancers	HMEC	breast
4	chr1:94276000-94283600	Enhancers	HSMM	muscle
5	chr1:94276000-94285200	Enhancers	Placenta	Placenta
6	chr1:94276800-94283800	Enhancers	NHEK	skin
7	chr1:94277000-94284400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr1:94277000-94285000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr1:94277600-94284600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:94278200-94282800	Weak transcription	Right Ventricle	heart
11	chr1:94278600-94283200	Enhancers	Osteobl	bone
12	chr1:94278600-94284000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr1:94279400-94282800	Weak transcription	Duodenum Mucosa	Duodenum
14	chr1:94279400-94284400	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr1:94279600-94302800	Weak transcription	Stomach Smooth Muscle	stomach
16	chr1:94279800-94284400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr1:94279800-94284600	Enhancers	Primary hematopoietic stem cells	blood
18	chr1:94280000-94282800	Weak transcription	Fetal Intestine Large	intestine
19	chr1:94280000-94285600	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr1:94280000-94290000	Weak transcription	Brain Angular Gyrus	brain
21	chr1:94280200-94284000	Weak transcription	Brain Hippocampus Middle	brain
22	chr1:94280400-94282800	Weak transcription	Fetal Muscle Trunk	muscle
23	chr1:94280400-94285000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr1:94280800-94282800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr1:94280800-94283200	Enhancers	HSMMtube	muscle
26	chr1:94280800-94283400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr1:94280800-94285800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr1:94281000-94284400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr1:94281200-94283400	Enhancers	NH-A	brain
30	chr1:94281200-94284800	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr1:94281200-94289600	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr1:94281400-94285000	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr1:94281400-94285600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr1:94281400-94285800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr1:94281600-94283000	Enhancers	Primary B cells from cord blood	blood
36	chr1:94281600-94285000	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr1:94281600-94285400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr1:94281800-94284200	Enhancers	Primary B cells from peripheral blood	blood
39	chr1:94281800-94285600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr1:94282200-94283200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr1:94282200-94284200	Enhancers	Adipose Nuclei	Adipose
42	chr1:94282200-94284200	Enhancers	Dnd41	blood
43	chr1:94282200-94284400	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr1:94282200-94284400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr1:94282400-94282800	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr1:94282400-94282800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
47	chr1:94282400-94283000	Enhancers	Duodenum Smooth Muscle	Duodenum
48	chr1:94282400-94283000	Enhancers	NHDF-Ad	bronchial
49	chr1:94282400-94283200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
50	chr1:94282400-94283200	Enhancers	Fetal Lung	lung

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