Variant report

Variant	rs11766860
Chromosome Location	chr7:14016664-14016665
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:14006507..14011484-chr7:14016197..14021172,5	K562	blood:
2	chr7:14014823..14017219-chr7:14018906..14020830,2	MCF-7	breast:
3	chr7:14011992..14014933-chr7:14015921..14017592,2	K562	blood:
4	chr7:13991446..13994404-chr7:14016165..14019066,2	K562	blood:

Extended variants
information (count: 14 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs11773782	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17167722	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62454620	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019873	chr7:13707148-14133367	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv887698	chr7:13841798-14056075	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1020543	chr7:13851470-14021121	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv949467	chr7:13938464-14279074	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv887700	chr7:13948517-14042702	Flanking Active TSS Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv887702	chr7:13995209-14027557	Active TSS Flanking Active TSS Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv606279	chr7:13995209-14027991	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv887703	chr7:13997159-14027557	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv887704	chr7:13997159-14029739	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	nsv1030645	chr7:14015533-14078153	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv538739	chr7:14015533-14078153	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11766860	C4orf17	trans	lymphoblastoid	RTeQTL

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:13989000-14019400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:14002400-14019600	Weak transcription	K562	blood
3	chr7:14004000-14017400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr7:14004000-14018600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr7:14004400-14019400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:14005600-14019400	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr7:14005800-14018800	Weak transcription	NH-A	brain
8	chr7:14006000-14018800	Weak transcription	Osteobl	bone
9	chr7:14009800-14019800	Weak transcription	Fetal Kidney	kidney
10	chr7:14010200-14020200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr7:14010400-14017400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
12	chr7:14010400-14027800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr7:14010800-14017400	Strong transcription	HUES64 Cell Line	embryonic stem cell
14	chr7:14011000-14017400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr7:14011200-14017400	Strong transcription	Cortex derived primary cultured neurospheres	brain
16	chr7:14011800-14017200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr7:14011800-14022400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr7:14012200-14017400	Weak transcription	Fetal Brain Female	brain
19	chr7:14012800-14016800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr7:14012800-14027600	Weak transcription	Fetal Stomach	stomach
21	chr7:14013000-14019400	Weak transcription	HSMM	muscle
22	chr7:14013000-14027600	Weak transcription	Liver	Liver
23	chr7:14013000-14027800	Weak transcription	Aorta	Aorta
24	chr7:14013200-14019800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr7:14013200-14020200	Weak transcription	Adipose Nuclei	Adipose
26	chr7:14013400-14017000	Strong transcription	H1 Cell Line	embryonic stem cell
27	chr7:14013400-14017200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
28	chr7:14013600-14019400	Weak transcription	Fetal Brain Male	brain
29	chr7:14013800-14017200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr7:14014000-14016800	Strong transcription	Fetal Muscle Leg	muscle
31	chr7:14014000-14017000	Strong transcription	HUES6 Cell Line	embryonic stem cell
32	chr7:14014000-14017000	Strong transcription	Fetal Lung	lung
33	chr7:14014000-14017200	Strong transcription	HUES48 Cell Line	embryonic stem cell
34	chr7:14014000-14017400	Strong transcription	H9 Cell Line	embryonic stem cell
35	chr7:14014200-14018800	Weak transcription	HUVEC	blood vessel
36	chr7:14014200-14018800	Weak transcription	NHLF	lung
37	chr7:14014600-14017400	Weak transcription	Right Ventricle	heart
38	chr7:14014600-14019200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr7:14014600-14019600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr7:14014800-14017200	Weak transcription	Lung	lung
41	chr7:14014800-14018800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr7:14014800-14019400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr7:14015000-14019800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr7:14015000-14027600	Weak transcription	Fetal Muscle Trunk	muscle
45	chr7:14015800-14023800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr7:14016200-14017000	Genic enhancers	Fetal Heart	heart
47	chr7:14016200-14017000	Strong transcription	NHDF-Ad	bronchial
48	chr7:14016400-14017400	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr7:14016600-14018600	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr7:14016600-14019200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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