Variant report

Variant	rs2235393
Chromosome Location	chr6:11763403-11763404
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:11763055..11764666-chr6:11765801..11768544,2	MCF-7	breast:
2	chr6:11760325..11763713-chr6:11770760..11773174,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000111863	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs2235394	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2235395	0.80[ASN][1000 genomes]
rs9348976	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758036	chr6:11679753-11822351	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv2759407	chr6:11679753-11822351	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2235393	C6orf105	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:11753200-11763800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr6:11755800-11768400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr6:11759000-11765800	Enhancers	Fetal Intestine Large	intestine
4	chr6:11759200-11764400	Enhancers	Stomach Mucosa	stomach
5	chr6:11759200-11765600	Enhancers	Fetal Intestine Small	intestine
6	chr6:11759400-11763600	Weak transcription	Esophagus	oesophagus
7	chr6:11759400-11769600	Weak transcription	Lung	lung
8	chr6:11759600-11765000	Enhancers	Duodenum Mucosa	Duodenum
9	chr6:11759600-11765800	Weak transcription	Hela-S3	cervix
10	chr6:11759800-11764400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr6:11760400-11765800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr6:11760600-11763600	Weak transcription	Ovary	ovary
13	chr6:11760600-11763600	Weak transcription	Right Atrium	heart
14	chr6:11760600-11766000	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr6:11760600-11770600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr6:11760800-11763600	Weak transcription	Small Intestine	intestine
17	chr6:11761600-11765800	Weak transcription	K562	blood
18	chr6:11762000-11764400	Enhancers	NHEK	skin
19	chr6:11762000-11764600	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr6:11762000-11767200	Enhancers	HSMMtube	muscle
21	chr6:11762200-11763600	Enhancers	Sigmoid Colon	Sigmoid Colon
22	chr6:11762200-11763800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr6:11762200-11764000	Enhancers	Fetal Kidney	kidney
24	chr6:11762200-11764400	Enhancers	Placenta Amnion	Placenta Amnion
25	chr6:11762200-11764600	Enhancers	Fetal Lung	lung
26	chr6:11762200-11764600	Enhancers	NH-A	brain
27	chr6:11762400-11763600	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr6:11762400-11763600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr6:11762400-11763800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr6:11762400-11764000	Enhancers	Osteobl	bone
31	chr6:11762400-11764400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr6:11762400-11764400	Enhancers	HSMM	muscle
33	chr6:11762400-11764600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr6:11762400-11764600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr6:11762400-11765400	Enhancers	Aorta	Aorta
36	chr6:11762400-11768200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr6:11762600-11763600	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr6:11762600-11763600	Weak transcription	Gastric	stomach
39	chr6:11762600-11767200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr6:11762600-11770600	Weak transcription	Spleen	Spleen
41	chr6:11762800-11763600	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr6:11762800-11764400	Weak transcription	A549	lung
43	chr6:11762800-11764600	Enhancers	Muscle Satellite Cultured Cells	--
44	chr6:11762800-11764600	Enhancers	Rectal Smooth Muscle	rectum
45	chr6:11763000-11764400	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr6:11763000-11764400	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr6:11763000-11764600	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr6:11763000-11764800	Enhancers	Colon Smooth Muscle	Colon
49	chr6:11763000-11766000	Genic enhancers	HMEC	breast
50	chr6:11763000-11768000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links