Variant report

Variant	rs9461977
Chromosome Location	chr6:34253108-34253109
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:5)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:34251031..34253241-chr6:34259138..34261085,2	MCF-7	breast:
2	chr6:34243359..34245671-chr6:34250933..34253670,2	MCF-7	breast:
3	chr6:34203148..34206017-chr6:34251263..34253790,3	K562	blood:
4	chr6:34251466..34254255-chr6:34254972..34256784,2	MCF-7	breast:
5	chr6:34251313..34254635-chr6:34272399..34275413,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HMGA1-3	chr6:34252267-34254545	ENSG00000232157.1
2	lnc-HMGA1-2	chr6:34251650-34254539	NONHSAT112120
3	lnc-HMGA1-2	chr6:34246917-34254539	NONHSAT112121
4	lnc-HMGA1-2	chr6:34247456-34254545	ENSG00000225339.2

No data

Variant related genes	Relation type
ENSG00000137309	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs9469771	1.00[ASW][hapmap];1.00[YRI][hapmap];1.00[EUR][1000 genomes]
rs9469788	1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv462903	chr6:34110257-34263743	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv602863	chr6:34110257-34263743	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
3	esv1798756	chr6:34203406-34319041	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
4	esv1798835	chr6:34204183-34319041	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
5	esv1792088	chr6:34204285-34318837	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
6	esv1793127	chr6:34204285-34319041	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34218200-34255000	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr6:34238400-34259400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr6:34240200-34255200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr6:34240400-34255000	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr6:34240400-34259800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr6:34240400-34259800	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr6:34240600-34269200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr6:34240800-34261000	Weak transcription	Fetal Kidney	kidney
9	chr6:34241400-34260000	Weak transcription	Esophagus	oesophagus
10	chr6:34243600-34257200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:34244200-34260000	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr6:34244400-34256600	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr6:34244400-34273400	Weak transcription	Rectal Smooth Muscle	rectum
14	chr6:34245000-34259800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr6:34245000-34260000	Weak transcription	NH-A	brain
16	chr6:34245000-34262600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr6:34245000-34263400	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr6:34245200-34255000	Weak transcription	Ovary	ovary
19	chr6:34245200-34259600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr6:34245200-34260800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr6:34245400-34260800	Weak transcription	Aorta	Aorta
22	chr6:34245600-34255200	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr6:34245600-34257400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr6:34245600-34261600	Weak transcription	Gastric	stomach
25	chr6:34245800-34254800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr6:34245800-34255000	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr6:34245800-34260000	Weak transcription	HSMMtube	muscle
28	chr6:34246000-34253800	Strong transcription	Fetal Muscle Trunk	muscle
29	chr6:34246000-34264400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr6:34246600-34256800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
31	chr6:34246600-34264000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr6:34246600-34264000	Strong transcription	Dnd41	blood
33	chr6:34247200-34259600	Weak transcription	Fetal Heart	heart
34	chr6:34247400-34256400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr6:34247400-34259800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr6:34247800-34260600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr6:34248200-34256400	Weak transcription	Hela-S3	cervix
38	chr6:34248400-34255000	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr6:34248600-34255000	Weak transcription	Stomach Smooth Muscle	stomach
40	chr6:34249000-34253200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr6:34249200-34255000	Weak transcription	Fetal Intestine Large	intestine
42	chr6:34249200-34259400	Weak transcription	Lung	lung
43	chr6:34249400-34259800	Weak transcription	Fetal Lung	lung
44	chr6:34249600-34255000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr6:34249600-34257200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr6:34249800-34254400	Enhancers	Adipose Nuclei	Adipose
47	chr6:34250000-34257800	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr6:34250200-34253600	Weak transcription	HSMM	muscle
49	chr6:34250400-34253400	Genic enhancers	Fetal Thymus	thymus
50	chr6:34250400-34255000	Genic enhancers	K562	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links