Variant report

Variant	rs183054519
Chromosome Location	chr9:93798905-93798906
allele	A/G
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	chr9:93677265..93679731-chr9:93797817..93800776,2	MCF-7	breast:
2	chr9:93744053..93746493-chr9:93797661..93799337,2	K562	blood:
3	chr9:93797874..93801408-chr9:93805945..93809060,4	MCF-7	breast:
4	chr9:93786992..93789003-chr9:93797212..93799731,2	MCF-7	breast:
5	chr9:93798539..93802041-chr9:94184980..94187268,5	MCF-7	breast:
6	chr9:93798149..93802099-chr9:94185060..94188043,3	K562	blood:
7	chr9:93797668..93803133-chr9:94183972..94188624,9	MCF-7	breast:
8	chr9:93798149..93801072-chr9:94184955..94188043,3	K562	blood:
9	chr9:93747626..93749444-chr9:93797575..93800020,2	MCF-7	breast:
10	chr9:93797970..93799747-chr9:93818400..93820922,2	MCF-7	breast:
11	chr9:93752160..93754281-chr9:93798521..93801349,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000165030	Chromatin interaction
ENSG00000233081	Chromatin interaction

Extended variants
information (count: 3 )
Associated
traits (count: 0)

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	nsv1046989	chr9:93353987-93800416	Transcr. at gene 5' and 3' Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv523562	chr9:93791410-93800017	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	esv3443359	chr9:93798631-93803029	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:93793600-93799400	Weak transcription	Liver	Liver
2	chr9:93794800-93799200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr9:93796000-93800200	Enhancers	Primary B cells from peripheral blood	blood
4	chr9:93796200-93799000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr9:93796400-93799200	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr9:93796800-93799200	Enhancers	HepG2	liver
7	chr9:93797000-93799400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr9:93797400-93801200	Enhancers	Placenta	Placenta
9	chr9:93797600-93800400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr9:93797800-93799000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr9:93797800-93799200	Weak transcription	Spleen	Spleen
12	chr9:93797800-93799800	Enhancers	GM12878-XiMat	blood
13	chr9:93798200-93799200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr9:93798200-93800000	Enhancers	Dnd41	blood
15	chr9:93798200-93801000	Enhancers	Esophagus	oesophagus
16	chr9:93798400-93799200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr9:93798400-93799200	Weak transcription	Fetal Intestine Small	intestine
18	chr9:93798400-93799400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr9:93798400-93800400	Enhancers	Fetal Lung	lung
20	chr9:93798600-93799000	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr9:93798600-93799000	Weak transcription	Stomach Smooth Muscle	stomach
22	chr9:93798600-93799400	Enhancers	Duodenum Mucosa	Duodenum
23	chr9:93798600-93802000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr9:93798600-93802400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr9:93798800-93799200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr9:93798800-93799400	Bivalent Enhancer	Thymus	Thymus
27	chr9:93798800-93799600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
28	chr9:93798800-93800000	Enhancers	Fetal Thymus	thymus
29	chr9:93798800-93800400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr9:93798800-93800600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr9:93798800-93800800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links