Variant report

Variant	rs11934177
Chromosome Location	chr4:128629876-128629877
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:128620470..128623327-chr4:128629151..128632115,2	K562	blood:

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11929869	1.00[AMR][1000 genomes]
rs11931600	1.00[AMR][1000 genomes]
rs11933107	1.00[AMR][1000 genomes]
rs11933179	1.00[AMR][1000 genomes]
rs11934725	1.00[AMR][1000 genomes]
rs11939438	1.00[AMR][1000 genomes]
rs11941076	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11946033	1.00[AMR][1000 genomes]
rs11946082	1.00[AMR][1000 genomes]
rs1514305	1.00[AMR][1000 genomes]
rs16997972	1.00[AMR][1000 genomes]
rs17012450	1.00[AMR][1000 genomes]
rs17012474	1.00[AMR][1000 genomes]
rs17012487	1.00[AMR][1000 genomes]
rs17012665	1.00[AMR][1000 genomes]
rs17012675	1.00[AMR][1000 genomes]
rs17012679	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879915	chr4:128167093-129150590	Strong transcription Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv1029214	chr4:128292215-128683123	Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv537247	chr4:128292215-128683123	Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv817326	chr4:128292216-128915201	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	nsv879916	chr4:128422400-128694288	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv879917	chr4:128478408-128841252	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv830056	chr4:128517139-128676557	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv879918	chr4:128543742-128694288	Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv879919	chr4:128543742-128697519	Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
10	nsv879920	chr4:128554404-128694288	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv879921	chr4:128554404-128766074	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
12	nsv879922	chr4:128554404-128901402	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
13	nsv879923	chr4:128554404-129068179	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
14	esv1801492	chr4:128566686-128934513	Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
15	esv1792644	chr4:128566686-129133826	Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
16	esv1795770	chr4:128566686-129145581	Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
17	esv1793579	chr4:128577439-128871309	Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
18	esv1792152	chr4:128585215-128752829	Strong transcription Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
19	nsv879925	chr4:128586241-128665981	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
20	nsv830057	chr4:128591288-128788777	Strong transcription Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:83 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:128554600-128644800	Weak transcription	Lung	lung
2	chr4:128566600-128644600	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr4:128597000-128630200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:128597000-128651600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr4:128597600-128632000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr4:128597600-128632000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr4:128598200-128638200	Weak transcription	Esophagus	oesophagus
8	chr4:128604400-128634400	Weak transcription	Fetal Heart	heart
9	chr4:128606200-128638200	Weak transcription	Brain Cingulate Gyrus	brain
10	chr4:128608400-128630200	Weak transcription	Gastric	stomach
11	chr4:128608400-128643800	Weak transcription	Right Ventricle	heart
12	chr4:128609800-128636600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr4:128612200-128632200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr4:128615200-128642000	Weak transcription	Brain Hippocampus Middle	brain
15	chr4:128615200-128648800	Weak transcription	Fetal Kidney	kidney
16	chr4:128615400-128630200	Weak transcription	Brain Germinal Matrix	brain
17	chr4:128616200-128646200	Weak transcription	Colon Smooth Muscle	Colon
18	chr4:128617000-128643400	Weak transcription	Fetal Intestine Small	intestine
19	chr4:128617200-128635600	Weak transcription	Fetal Brain Male	brain
20	chr4:128619000-128631600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr4:128620000-128630400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr4:128620200-128638400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr4:128620600-128630000	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr4:128620600-128630200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr4:128620600-128630200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr4:128620600-128630200	Weak transcription	HSMM	muscle
27	chr4:128620600-128630400	Weak transcription	HMEC	breast
28	chr4:128620800-128630400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr4:128622400-128630400	Weak transcription	Small Intestine	intestine
30	chr4:128622400-128630800	Weak transcription	Rectal Smooth Muscle	rectum
31	chr4:128622400-128632000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr4:128622600-128636600	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr4:128624200-128630200	Weak transcription	Psoas Muscle	Psoas
34	chr4:128624200-128632200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr4:128625400-128632800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr4:128626000-128632600	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr4:128626200-128632800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr4:128626400-128630600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr4:128626600-128630000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
40	chr4:128626600-128631000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr4:128626600-128631800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr4:128626600-128634200	Strong transcription	HUES64 Cell Line	embryonic stem cell
43	chr4:128627000-128633800	Strong transcription	HUES48 Cell Line	embryonic stem cell
44	chr4:128627200-128630200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr4:128627400-128630400	Weak transcription	Duodenum Mucosa	Duodenum
46	chr4:128627400-128630600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr4:128627400-128630600	Strong transcription	Brain Inferior Temporal Lobe	brain
48	chr4:128627400-128630600	Strong transcription	Fetal Brain Female	brain
49	chr4:128627400-128630600	Strong transcription	Stomach Smooth Muscle	stomach
50	chr4:128627800-128630800	Strong transcription	Fetal Intestine Large	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links