Variant report

Variant	rs537185204
Chromosome Location	chr22:30099229-30099230
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr22:30086550..30091376-chr22:30091742..30099600,10	MCF-7	breast:
2	chr22:30096975..30100180-chr22:30101896..30105574,4	K562	blood:
3	chr22:30097362..30099278-chr22:30100636..30102663,2	K562	blood:
4	chr22:30091150..30094109-chr22:30098424..30101093,2	K562	blood:
5	chr22:30098350..30101826-chr22:30195223..30196896,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000100325	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	nsv529742	chr22:29677909-30274388	Bivalent Enhancer Enhancers ZNF genes & repeats Strong transcription Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv1064081	chr22:29826745-30623965	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv544677	chr22:29826745-30623965	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
4	nsv529737	chr22:30060946-30109561	Bivalent Enhancer Genic enhancers Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
5	nsv914963	chr22:30075052-30133579	Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
6	nsv914964	chr22:30081715-30150549	Bivalent Enhancer Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv515720	chr22:30081715-30163526	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv914965	chr22:30086144-30112226	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv914966	chr22:30088442-30138548	Weak transcription Bivalent Enhancer Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
10	esv1816879	chr22:30096309-30126906	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
11	esv3407139	chr22:30099177-30101725	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	Chromatin interactive region lncRNA	1 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	chr22:30093000-30099400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr22:30095800-30101400	Enhancers	HSMMtube	muscle
3	chr22:30095800-30101600	Bivalent Enhancer	Fetal Muscle Leg	muscle
4	chr22:30095800-30103000	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr22:30096000-30103600	Enhancers	Fetal Brain Male	brain
6	chr22:30096200-30103200	Enhancers	Fetal Brain Female	brain
7	chr22:30096400-30099400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr22:30096400-30099400	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr22:30096400-30099800	Enhancers	Primary hematopoietic stem cells	blood
10	chr22:30096400-30099800	Bivalent Enhancer	Fetal Intestine Large	intestine
11	chr22:30096400-30100600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
12	chr22:30096400-30100800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr22:30096400-30101400	Bivalent Enhancer	Fetal Intestine Small	intestine
14	chr22:30096400-30103000	Enhancers	Brain Anterior Caudate	brain
15	chr22:30096400-30103200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr22:30096400-30103600	Enhancers	Brain Inferior Temporal Lobe	brain
17	chr22:30096400-30107400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr22:30096600-30099600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr22:30096600-30100400	Enhancers	Rectal Mucosa Donor 29	rectum
20	chr22:30096600-30102000	Enhancers	Skeletal Muscle Female	skeletal muscle
21	chr22:30096600-30103800	Enhancers	Brain Cingulate Gyrus	brain
22	chr22:30096800-30099400	Enhancers	Primary B cells from peripheral blood	blood
23	chr22:30096800-30099600	Enhancers	HSMM	muscle
24	chr22:30096800-30100200	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr22:30096800-30101400	Enhancers	A549	lung
26	chr22:30097000-30099800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
27	chr22:30097000-30100000	Enhancers	Brain Angular Gyrus	brain
28	chr22:30097000-30102200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr22:30097000-30106400	Weak transcription	Psoas Muscle	Psoas
30	chr22:30097400-30099800	Enhancers	Lung	lung
31	chr22:30097600-30101000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr22:30097800-30099600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
33	chr22:30097800-30100400	Enhancers	Brain Substantia Nigra	brain
34	chr22:30098000-30100800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
35	chr22:30098000-30102800	Weak transcription	Esophagus	oesophagus
36	chr22:30098200-30099600	Weak transcription	Gastric	stomach
37	chr22:30098200-30099800	Bivalent Enhancer	Adipose Nuclei	Adipose
38	chr22:30098200-30100000	Bivalent Enhancer	Stomach Mucosa	stomach
39	chr22:30098200-30101600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr22:30098400-30099400	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr22:30098400-30100000	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
42	chr22:30098400-30100000	Enhancers	Primary B cells from cord blood	blood
43	chr22:30098400-30101000	Weak transcription	Pancreas	Pancrea
44	chr22:30098600-30099400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr22:30098600-30099600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
46	chr22:30098600-30099800	Enhancers	Spleen	Spleen
47	chr22:30098600-30100000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
48	chr22:30098600-30100000	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr22:30098600-30100200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr22:30098800-30099400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links