Variant report

Variant	rs566475172
Chromosome Location	chr1:62490463-62490464
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:62481608..62483564-chr1:62488703..62491650,2	MCF-7	breast:
2	chr1:62488087..62490869-chr1:62492445..62494953,2	K562	blood:

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv518627	chr1:62279594-62517947	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv522020	chr1:62279594-62517947	Active TSS ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv531876	chr1:62302313-62504349	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv1004446	chr1:62394631-62813533	Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
5	nsv534984	chr1:62394631-62813533	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
6	nsv1001667	chr1:62407786-62649838	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
7	nsv546416	chr1:62437872-62492215	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv945803	chr1:62490443-62495121	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62385000-62494200	Weak transcription	Aorta	Aorta
2	chr1:62409200-62518600	Weak transcription	Pancreas	Pancrea
3	chr1:62424200-62494200	Weak transcription	Esophagus	oesophagus
4	chr1:62458800-62521400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr1:62459000-62516000	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr1:62459000-62530600	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr1:62459200-62511200	Weak transcription	Gastric	stomach
8	chr1:62459200-62550000	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr1:62459400-62493800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr1:62459600-62494200	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr1:62460000-62499600	Weak transcription	Fetal Intestine Large	intestine
12	chr1:62460000-62516400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr1:62460000-62544600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr1:62460200-62516000	Weak transcription	HMEC	breast
15	chr1:62466400-62494200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr1:62469000-62533600	Weak transcription	Rectal Smooth Muscle	rectum
17	chr1:62474200-62518600	Weak transcription	Primary T cells from cord blood	blood
18	chr1:62479400-62493600	Weak transcription	Stomach Smooth Muscle	stomach
19	chr1:62479400-62496000	Weak transcription	Fetal Kidney	kidney
20	chr1:62480600-62513000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr1:62484400-62492800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr1:62484400-62523000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr1:62484400-62562200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr1:62484600-62492400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr1:62484600-62493800	Weak transcription	Duodenum Mucosa	Duodenum
26	chr1:62484600-62494400	Weak transcription	Liver	Liver
27	chr1:62484600-62506000	Weak transcription	NHEK	skin
28	chr1:62484800-62511200	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr1:62485000-62494000	Weak transcription	Fetal Intestine Small	intestine
30	chr1:62486000-62492600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr1:62486200-62517600	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chr1:62488000-62498000	Weak transcription	Fetal Heart	heart
33	chr1:62488400-62491600	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr1:62488400-62494200	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr1:62488400-62494600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr1:62488400-62494600	Weak transcription	Brain Germinal Matrix	brain
37	chr1:62488400-62497600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr1:62488400-62497600	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr1:62488400-62521200	Weak transcription	Ovary	ovary
40	chr1:62488600-62494400	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr1:62488600-62494400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr1:62488600-62499000	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr1:62488800-62491200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr1:62489800-62490600	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr1:62490200-62490600	Enhancers	Fetal Brain Male	brain
46	chr1:62490200-62490600	Enhancers	Fetal Brain Female	brain
47	chr1:62490200-62491800	Enhancers	Left Ventricle	heart
48	chr1:62490200-62491800	Enhancers	Psoas Muscle	Psoas
49	chr1:62490200-62492400	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr1:62490200-62493000	Enhancers	Skeletal Muscle Female	skeletal muscle

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