Variant report

Variant	rs73613022
Chromosome Location	chr6:149652063-149652064
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:149643934..149646869-chr6:149651768..149654461,2	K562	blood:
2	chr6:149636994..149642058-chr6:149649092..149655125,9	MCF-7	breast:
3	chr6:149649733..149652455-chr6:149658613..149661110,2	K562	blood:
4	chr6:149648554..149650974-chr6:149651371..149654134,3	K562	blood:
5	chr6:149646598..149650161-chr6:149650268..149655691,6	MCF-7	breast:
6	chr6:149637223..149641886-chr6:149650956..149658366,12	K562	blood:

Variant related genes	Relation type
ENSG00000055208	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs34029621	1.00[AFR][1000 genomes]
rs35852678	1.00[AFR][1000 genomes]
rs59632689	1.00[AFR][1000 genomes]
rs61090105	1.00[AFR][1000 genomes]
rs73611041	1.00[AFR][1000 genomes]
rs73611045	1.00[AFR][1000 genomes]
rs73613025	1.00[AFR][1000 genomes]
rs73613039	1.00[AFR][1000 genomes]
rs73613054	1.00[AFR][1000 genomes]
rs73613059	1.00[AFR][1000 genomes]
rs73613069	1.00[AFR][1000 genomes]
rs73613071	1.00[AFR][1000 genomes]
rs73613086	1.00[AFR][1000 genomes]
rs73614909	1.00[AFR][1000 genomes]
rs73615957	1.00[AFR][1000 genomes]
rs73617919	0.87[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024776	chr6:149398652-149654593	Weak transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1024106	chr6:149622349-149745053	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv522875	chr6:149643709-149762537	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149640200-149655400	Weak transcription	Esophagus	oesophagus
2	chr6:149640200-149655600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:149640800-149652800	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr6:149640800-149653200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr6:149641200-149657400	Weak transcription	Aorta	Aorta
6	chr6:149641200-149681400	Weak transcription	Fetal Stomach	stomach
7	chr6:149641400-149655600	Weak transcription	Placenta	Placenta
8	chr6:149641600-149652600	Weak transcription	Brain Germinal Matrix	brain
9	chr6:149641600-149656000	Weak transcription	Lung	lung
10	chr6:149641600-149660200	Enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr6:149641800-149660200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr6:149642400-149652600	Weak transcription	NH-A	brain
13	chr6:149642400-149652600	Weak transcription	NHLF	lung
14	chr6:149642600-149652600	Weak transcription	NHDF-Ad	bronchial
15	chr6:149642600-149657200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr6:149643000-149653400	Weak transcription	HSMM	muscle
17	chr6:149643400-149652200	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr6:149645000-149666400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chr6:149645600-149652600	Weak transcription	Osteobl	bone
20	chr6:149645800-149652800	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr6:149646000-149652600	Weak transcription	HMEC	breast
22	chr6:149646200-149653400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr6:149646200-149654400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
24	chr6:149646200-149657400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
25	chr6:149646400-149652600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr6:149646400-149652600	Weak transcription	Adipose Nuclei	Adipose
27	chr6:149646400-149652600	Weak transcription	Fetal Lung	lung
28	chr6:149646600-149652800	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr6:149646800-149652400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr6:149647000-149653000	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr6:149647200-149653000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr6:149647200-149654400	Weak transcription	Ovary	ovary
33	chr6:149647200-149655400	Weak transcription	Pancreas	Pancrea
34	chr6:149648400-149660600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr6:149648600-149652400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr6:149648600-149654600	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr6:149648600-149655000	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr6:149648600-149655200	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr6:149648600-149656600	Enhancers	Fetal Heart	heart
40	chr6:149648600-149659200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr6:149648600-149659600	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr6:149648800-149656000	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr6:149649000-149652600	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr6:149649000-149657200	Weak transcription	Fetal Intestine Large	intestine
45	chr6:149649000-149660200	Weak transcription	Fetal Intestine Small	intestine
46	chr6:149649200-149652600	Weak transcription	Brain Cingulate Gyrus	brain
47	chr6:149649200-149653000	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr6:149649200-149654200	Weak transcription	Fetal Kidney	kidney
49	chr6:149649200-149654600	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr6:149649200-149657200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood

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