Variant report

Variant	rs6006207
Chromosome Location	chr22:30013967-30013968
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr22:30013839..30015515-chr22:30021150..30023734,2	MCF-7	breast:
2	chr22:30006178..30007796-chr22:30012477..30014335,2	MCF-7	breast:
3	chr22:29997853..30001127-chr22:30012116..30016282,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000186575	Chromatin interaction

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs12157558	1.00[AFR][1000 genomes]
rs5763347	1.00[YRI][hapmap]
rs5997498	1.00[AFR][1000 genomes]
rs6006214	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 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	nsv1058156	chr22:29772043-30024013	Strong transcription Enhancers Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv544675	chr22:29772043-30024013	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv1062373	chr22:29826745-30092448	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
5	nsv544676	chr22:29826745-30092448	Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
6	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
7	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
8	nsv834172	chr22:29899036-30057948	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
9	nsv817417	chr22:29998464-30035142	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30000400-30026600	Weak transcription	Gastric	stomach
2	chr22:30001000-30019400	Weak transcription	Thymus	Thymus
3	chr22:30001400-30014000	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr22:30002000-30014200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr22:30002000-30017600	Weak transcription	Primary T cells from cord blood	blood
6	chr22:30002600-30014000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr22:30002800-30017600	Weak transcription	Lung	lung
8	chr22:30003000-30016600	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr22:30003200-30014000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr22:30003400-30014000	Weak transcription	Right Atrium	heart
11	chr22:30003400-30017200	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr22:30003600-30014000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr22:30003600-30016400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr22:30003800-30032800	Weak transcription	Fetal Muscle Trunk	muscle
15	chr22:30005200-30019400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr22:30005400-30017800	Weak transcription	Primary B cells from cord blood	blood
17	chr22:30006800-30019000	Weak transcription	Fetal Thymus	thymus
18	chr22:30007400-30016800	Weak transcription	Fetal Muscle Leg	muscle
19	chr22:30007600-30017400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr22:30009600-30017600	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr22:30011000-30015600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr22:30011000-30017800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr22:30011600-30016800	Weak transcription	Esophagus	oesophagus
24	chr22:30011800-30017000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr22:30011800-30017200	Weak transcription	Primary B cells from peripheral blood	blood
26	chr22:30011800-30026200	Weak transcription	Fetal Stomach	stomach
27	chr22:30013000-30017600	Enhancers	HMEC	breast
28	chr22:30013000-30018400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr22:30013200-30014400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
30	chr22:30013200-30014800	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr22:30013200-30014800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr22:30013200-30015000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr22:30013200-30015000	Enhancers	Hela-S3	cervix
34	chr22:30013200-30015000	Enhancers	HUVEC	blood vessel
35	chr22:30013200-30015200	Enhancers	Muscle Satellite Cultured Cells	--
36	chr22:30013200-30015200	Enhancers	NHDF-Ad	bronchial
37	chr22:30013200-30017200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr22:30013200-30017800	Enhancers	NHLF	lung
39	chr22:30013400-30014000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr22:30013400-30014200	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr22:30013400-30014200	Weak transcription	Brain Cingulate Gyrus	brain
42	chr22:30013400-30014200	Enhancers	Ovary	ovary
43	chr22:30013400-30014200	Enhancers	Stomach Smooth Muscle	stomach
44	chr22:30013400-30014200	Enhancers	A549	lung
45	chr22:30013400-30014200	Flanking Active TSS	GM12878-XiMat	blood
46	chr22:30013400-30014400	Enhancers	Primary T helper cells fromperipheralblood	blood
47	chr22:30013400-30014400	Enhancers	Small Intestine	intestine
48	chr22:30013400-30014800	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr22:30013400-30014800	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr22:30013400-30014800	Enhancers	Colon Smooth Muscle	Colon

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