Variant report

Variant	rs1704913
Chromosome Location	chr12:104921343-104921344
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:104919275..104922640-chr12:104923988..104926677,3	K562	blood:
2	chr12:104919574..104922787-chr12:104926132..104929881,3	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs17811302	1.00[CHB][hapmap]
rs1795860	1.00[ASN][1000 genomes]
rs1795869	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs35634504	1.00[ASN][1000 genomes]
rs7133778	0.82[EUR][1000 genomes]
rs7962759	1.00[CHB][hapmap];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832504	chr12:104853331-105028245	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:104911000-104921800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
2	chr12:104915600-104936600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr12:104916600-104923000	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr12:104917200-104925800	Weak transcription	Lung	lung
5	chr12:104917600-104924600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr12:104917800-104922600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr12:104917800-104922600	Weak transcription	NHEK	skin
8	chr12:104917800-104922800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr12:104917800-104928200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr12:104918000-104934200	Weak transcription	A549	lung
11	chr12:104918200-104921400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr12:104918200-104928200	Weak transcription	Osteobl	bone
13	chr12:104918200-104928400	Weak transcription	Ovary	ovary
14	chr12:104918400-104927400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr12:104918400-104928200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr12:104918600-104925400	Weak transcription	Spleen	Spleen
17	chr12:104918600-104926600	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr12:104918600-104926800	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr12:104918600-104927600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr12:104919000-104921400	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr12:104919200-104923800	Weak transcription	Rectal Smooth Muscle	rectum
22	chr12:104919200-104925600	Weak transcription	Primary T helper cells fromperipheralblood	blood
23	chr12:104919200-104935000	Weak transcription	Primary T cells from cord blood	blood
24	chr12:104919400-104926000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr12:104919400-104928000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr12:104920000-104921400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr12:104920000-104926400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr12:104920200-104922000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr12:104920200-104922400	Enhancers	Primary T cells fromperipheralblood	blood
30	chr12:104920200-104922600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr12:104920400-104921400	Enhancers	H1 Cell Line	embryonic stem cell
32	chr12:104920400-104921400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr12:104920400-104922200	Enhancers	H9 Cell Line	embryonic stem cell
34	chr12:104920400-104927400	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr12:104920600-104921400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr12:104920600-104921400	Enhancers	Left Ventricle	heart
37	chr12:104920600-104921400	Enhancers	Pancreas	Pancrea
38	chr12:104920600-104922600	Weak transcription	Placenta	Placenta
39	chr12:104920600-104926200	Weak transcription	Fetal Thymus	thymus
40	chr12:104920600-104929400	Weak transcription	Colon Smooth Muscle	Colon
41	chr12:104920800-104921400	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr12:104920800-104921400	Enhancers	Fetal Heart	heart
43	chr12:104920800-104922400	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
44	chr12:104920800-104923000	ZNF genes & repeats	Primary B cells from peripheral blood	blood
45	chr12:104920800-104924200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
46	chr12:104920800-104926200	Strong transcription	Dnd41	blood
47	chr12:104921000-104921400	Enhancers	Gastric	stomach
48	chr12:104921000-104921400	Enhancers	Right Atrium	heart
49	chr12:104921000-104922600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr12:104921000-104922800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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