Variant report

Variant	rs574891867
Chromosome Location	chr11:34349449-34349450
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:34348938..34354072-chr11:34377839..34381430,6	MCF-7	breast:
2	chr11:34295466..34297998-chr11:34348756..34350438,2	MCF-7	breast:
3	chr11:34345030..34348316-chr11:34348388..34351447,3	K562	blood:

Variant related genes	Relation type
ENSG00000166016	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

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	esv2757435	chr11:34220504-34370236	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv2759816	chr11:34220504-34370236	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv818809	chr11:34239730-34354076	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	esv2753052	chr11:34247462-34358300	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv897205	chr11:34248229-34507213	Enhancers Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv897207	chr11:34253683-34621004	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
7	nsv897208	chr11:34257064-34562247	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
8	nsv897209	chr11:34309519-34548906	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
9	nsv818810	chr11:34337564-34354076	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
10	esv2753225	chr11:34338342-34354865	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
11	nsv897210	chr11:34349427-34381075	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34336200-34358200	Weak transcription	Thymus	Thymus
2	chr11:34339000-34357400	Weak transcription	Fetal Thymus	thymus
3	chr11:34340000-34353200	Weak transcription	Small Intestine	intestine
4	chr11:34340800-34352200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr11:34341000-34352400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr11:34341200-34352200	Weak transcription	HSMM	muscle
7	chr11:34343600-34350800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr11:34346600-34351000	Weak transcription	Aorta	Aorta
9	chr11:34346600-34353800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr11:34347000-34349600	Weak transcription	Lung	lung
11	chr11:34347000-34349600	Weak transcription	A549	lung
12	chr11:34347000-34350800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr11:34347000-34355600	Weak transcription	GM12878-XiMat	blood
14	chr11:34347800-34354400	Enhancers	Fetal Stomach	stomach
15	chr11:34348000-34353200	Enhancers	Fetal Muscle Leg	muscle
16	chr11:34348400-34350000	Enhancers	Fetal Muscle Trunk	muscle
17	chr11:34348400-34350200	Enhancers	Left Ventricle	heart
18	chr11:34348400-34350200	Enhancers	Ovary	ovary
19	chr11:34348400-34351200	Enhancers	Fetal Lung	lung
20	chr11:34348400-34351600	Enhancers	Right Ventricle	heart
21	chr11:34348400-34354400	Enhancers	Psoas Muscle	Psoas
22	chr11:34348600-34352800	Enhancers	Fetal Heart	heart
23	chr11:34348600-34353600	Enhancers	Colon Smooth Muscle	Colon
24	chr11:34348600-34353800	Enhancers	Rectal Smooth Muscle	rectum
25	chr11:34348800-34349800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr11:34348800-34350000	Enhancers	Brain Angular Gyrus	brain
27	chr11:34348800-34350200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr11:34348800-34350200	Enhancers	Brain Substantia Nigra	brain
29	chr11:34348800-34350400	Enhancers	Liver	Liver
30	chr11:34348800-34350600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr11:34348800-34351200	Enhancers	Brain Germinal Matrix	brain
32	chr11:34348800-34351800	Enhancers	HepG2	liver
33	chr11:34348800-34352000	Enhancers	Skeletal Muscle Male	skeletal muscle
34	chr11:34349000-34349600	Enhancers	Pancreas	Pancrea
35	chr11:34349000-34349800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
36	chr11:34349000-34349800	Enhancers	Right Atrium	heart
37	chr11:34349000-34349800	Flanking Active TSS	Stomach Smooth Muscle	stomach
38	chr11:34349000-34349800	Enhancers	NHLF	lung
39	chr11:34349000-34350000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr11:34349000-34350200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr11:34349000-34350200	Enhancers	Placenta	Placenta
42	chr11:34349000-34350800	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr11:34349000-34350800	Enhancers	Fetal Brain Male	brain
44	chr11:34349000-34351000	Enhancers	Brain Anterior Caudate	brain
45	chr11:34349000-34351600	Enhancers	Adipose Nuclei	Adipose
46	chr11:34349000-34352000	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr11:34349200-34351000	Enhancers	Duodenum Smooth Muscle	Duodenum
48	chr11:34349400-34349800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr11:34349400-34349800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr11:34349400-34349800	Flanking Active TSS	Brain Cingulate Gyrus	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links