Variant report

Variant	rs61795612
Chromosome Location	chr3:120411506-120411507
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:120319897..120322089-chr3:120410422..120413508,3	MCF-7	breast:
2	chr3:120406419..120409773-chr3:120409851..120413198,4	MCF-7	breast:
3	chr3:120411360..120413123-chr3:120418535..120421038,2	K562	blood:
4	chr3:120410148..120412083-chr3:120412165..120413730,2	MCF-7	breast:
5	chr3:120399515..120401916-chr3:120410296..120413269,2	K562	blood:
6	chr3:120403041..120405585-chr3:120409977..120412139,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000113924	Chromatin interaction

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs13082232	1.00[ASN][1000 genomes]
rs388747	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007557	chr3:119892894-120764353	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv536706	chr3:119892894-120764353	Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv1006428	chr3:120015620-120421982	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	esv3369381	chr3:120066425-120425510	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
5	esv3350409	chr3:120066445-120425480	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
6	esv3373301	chr3:120273762-120421260	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
7	nsv877377	chr3:120287683-120426750	Enhancers Strong transcription Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
8	esv3464294	chr3:120303062-120420810	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
9	esv3464295	chr3:120303062-120420810	Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
10	nsv829699	chr3:120308332-120484695	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases
11	nsv869548	chr3:120320731-121076337	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
12	nsv916869	chr3:120360281-120973169	Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
13	nsv877378	chr3:120381530-120606438	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:120397600-120421600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr3:120397800-120412200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr3:120397800-120415800	Weak transcription	Ovary	ovary
4	chr3:120397800-120420600	Weak transcription	Primary B cells from cord blood	blood
5	chr3:120397800-120421800	Weak transcription	Aorta	Aorta
6	chr3:120397800-120424800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr3:120398200-120412200	Weak transcription	Brain Hippocampus Middle	brain
8	chr3:120398200-120412200	Weak transcription	HMEC	breast
9	chr3:120398200-120415200	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr3:120398200-120423200	Weak transcription	Psoas Muscle	Psoas
11	chr3:120398200-120427000	Weak transcription	Stomach Smooth Muscle	stomach
12	chr3:120398200-120427800	Weak transcription	Placenta	Placenta
13	chr3:120398200-120430200	Weak transcription	NHEK	skin
14	chr3:120398200-120438000	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr3:120398400-120412200	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr3:120398400-120412400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr3:120398600-120411800	Weak transcription	HUVEC	blood vessel
18	chr3:120398800-120442200	Weak transcription	Fetal Muscle Leg	muscle
19	chr3:120400000-120412200	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr3:120400200-120421600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr3:120401000-120424800	Weak transcription	Rectal Smooth Muscle	rectum
22	chr3:120402200-120411800	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr3:120402200-120412200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr3:120402400-120423600	Weak transcription	Lung	lung
25	chr3:120402600-120420800	Weak transcription	Primary hematopoietic stem cells	blood
26	chr3:120402800-120412200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr3:120402800-120421800	Weak transcription	Fetal Kidney	kidney
28	chr3:120402800-120456600	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr3:120403200-120412000	Weak transcription	Fetal Intestine Small	intestine
30	chr3:120403600-120423800	Weak transcription	Spleen	Spleen
31	chr3:120404000-120415600	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr3:120404000-120423600	Weak transcription	Pancreas	Pancrea
33	chr3:120404200-120416000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr3:120404800-120421800	Weak transcription	HSMM	muscle
35	chr3:120405000-120412400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr3:120405600-120436800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr3:120406000-120412200	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr3:120406000-120415400	Weak transcription	Left Ventricle	heart
39	chr3:120406000-120421800	Weak transcription	Dnd41	blood
40	chr3:120406400-120415200	Weak transcription	Fetal Muscle Trunk	muscle
41	chr3:120406400-120436600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr3:120406600-120421800	Weak transcription	Colon Smooth Muscle	Colon
43	chr3:120406800-120421200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr3:120407000-120417600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr3:120407000-120421800	Weak transcription	Thymus	Thymus
46	chr3:120407200-120422000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr3:120407400-120412200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr3:120407600-120413800	Weak transcription	Primary B cells from peripheral blood	blood
49	chr3:120407800-120412200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr3:120408400-120412000	Weak transcription	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links