Variant report

Variant	rs77710972
Chromosome Location	chr7:25902995-25902996
allele	G/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:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:25900891..25903409-chr7:25932154..25934177,2	K562	blood:
2	chr7:25902422..25904176-chr7:25907218..25908860,2	K562	blood:
3	chr7:25900989..25903469-chr7:26394737..26397654,2	K562	blood:
4	chr7:25901881..25903574-chr7:26239063..26240949,2	MCF-7	breast:
5	chr7:25901871..25903514-chr7:25989852..25991943,2	K562	blood:
6	chr7:25901385..25904121-chr7:25989908..25991928,2	MCF-7	breast:
7	chr7:25901348..25903877-chr7:25904726..25907059,2	K562	blood:
8	chr7:25902131..25903827-chr7:25913868..25916119,2	K562	blood:
9	chr7:25901765..25903846-chr7:25928862..25931823,2	K562	blood:
10	chr7:25900544..25903827-chr7:25911333..25915801,5	K562	blood:
11	chr7:25900551..25904078-chr7:26238740..26241514,6	K562	blood:

No data

Variant related genes	Relation type
ENSG00000122566	Chromatin interaction
ENSG00000122565	Chromatin interaction

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016813	chr7:25405859-26150509	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	108 gene(s)	inside rSNPs	diseases
2	nsv538803	chr7:25405859-26150509	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	108 gene(s)	inside rSNPs	diseases
3	nsv830928	chr7:25820147-25965014	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	esv1792444	chr7:25902015-25964180	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:25900000-25903800	Active TSS	K562	blood
2	chr7:25901400-25903000	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
3	chr7:25901400-25903000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
4	chr7:25901600-25903000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:25901600-25903000	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
6	chr7:25901800-25903000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
7	chr7:25901800-25903000	Bivalent Enhancer	Fetal Stomach	stomach
8	chr7:25901800-25903000	Bivalent Enhancer	Stomach Mucosa	stomach
9	chr7:25902000-25903000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
10	chr7:25902400-25903000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
11	chr7:25902400-25903000	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
12	chr7:25902400-25903000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr7:25902400-25903000	Bivalent Enhancer	Fetal Intestine Large	intestine
14	chr7:25902400-25903000	Enhancers	HMEC	breast
15	chr7:25902600-25903000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
16	chr7:25902600-25903000	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
17	chr7:25902600-25903000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
18	chr7:25902600-25903000	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
19	chr7:25902600-25903000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr7:25902600-25903000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr7:25902600-25903000	Bivalent Enhancer	Colon Smooth Muscle	Colon
22	chr7:25902600-25903000	Bivalent Enhancer	Fetal Muscle Leg	muscle
23	chr7:25902600-25903000	Flanking Active TSS	NHEK	skin
24	chr7:25902600-25903800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
25	chr7:25902600-25904000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
26	chr7:25902600-25904000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
27	chr7:25902600-25904200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
28	chr7:25902600-25904200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr7:25902800-25903000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr7:25902800-25903000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr7:25902800-25903000	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr7:25902800-25903000	Bivalent Enhancer	Primary T cells from cord blood	blood
33	chr7:25902800-25903000	Flanking Bivalent TSS/Enh	Primary T helper naive cells from peripheral blood	blood
34	chr7:25902800-25903000	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
35	chr7:25902800-25903000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
36	chr7:25902800-25903000	Bivalent Enhancer	Adipose Nuclei	Adipose
37	chr7:25902800-25903000	Enhancers	Duodenum Mucosa	Duodenum
38	chr7:25902800-25903000	Bivalent Enhancer	Fetal Lung	lung
39	chr7:25902800-25903000	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
40	chr7:25902800-25903000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
41	chr7:25902800-25903000	Bivalent/Poised TSS	Thymus	Thymus
42	chr7:25902800-25903000	Bivalent Enhancer	Hela-S3	cervix
43	chr7:25902800-25903200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr7:25902800-25903400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
45	chr7:25902800-25903400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
46	chr7:25902800-25903600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell

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