Variant report

Variant	rs576614058
Chromosome Location	chr11:59378767-59378768
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:59332513..59335346-chr11:59377143..59379065,2	K562	blood:
2	chr11:59358338..59361390-chr11:59376004..59379219,3	K562	blood:
3	chr11:59373266..59379105-chr11:59379660..59383510,5	MCF-7	breast:
4	chr11:59367319..59373347-chr11:59375671..59384148,16	K562	blood:
5	chr11:59362508..59365255-chr11:59378234..59380693,3	K562	blood:
6	chr11:59340962..59342782-chr11:59376375..59380389,3	K562	blood:

Variant related genes	Relation type
ENSG00000255008	Chromatin interaction
ENSG00000264559	Chromatin interaction
ENSG00000110048	Chromatin interaction

Extended variants
information (count: 2 )
Associated
traits (count: 0)

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	esv1833978	chr11:59377543-59383631	Strong transcription Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	esv1842135	chr11:59377543-59383631	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:59334200-59382000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr11:59342000-59379000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr11:59343800-59382000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr11:59353400-59378800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr11:59353800-59379400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr11:59354400-59379400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr11:59354600-59379600	Strong transcription	Thymus	Thymus
8	chr11:59355800-59379800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr11:59357400-59379000	Strong transcription	GM12878-XiMat	blood
10	chr11:59357600-59379200	Strong transcription	K562	blood
11	chr11:59357800-59380600	Strong transcription	Primary B cells from cord blood	blood
12	chr11:59358400-59382000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr11:59369800-59379000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr11:59373000-59379400	Strong transcription	Hela-S3	cervix
15	chr11:59374000-59379200	Weak transcription	Small Intestine	intestine
16	chr11:59376200-59378800	Genic enhancers	Fetal Muscle Leg	muscle
17	chr11:59376200-59381200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr11:59376400-59379400	Weak transcription	Right Atrium	heart
19	chr11:59376400-59382200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr11:59376600-59379000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr11:59376600-59380200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr11:59376800-59380800	Genic enhancers	Primary T helper cells fromperipheralblood	blood
23	chr11:59377200-59378800	Weak transcription	Colon Smooth Muscle	Colon
24	chr11:59377200-59378800	Weak transcription	Fetal Brain Male	brain
25	chr11:59377200-59379000	Enhancers	Fetal Heart	heart
26	chr11:59377400-59378800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr11:59377800-59378800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr11:59377800-59378800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr11:59377800-59379000	Weak transcription	Brain Hippocampus Middle	brain
30	chr11:59377800-59379200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr11:59377800-59381200	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr11:59378000-59379000	Weak transcription	Fetal Kidney	kidney
33	chr11:59378000-59379000	Weak transcription	Fetal Lung	lung
34	chr11:59378000-59379200	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr11:59378000-59379200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr11:59378000-59379200	Weak transcription	Brain Substantia Nigra	brain
37	chr11:59378000-59379400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr11:59378000-59379400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr11:59378000-59379400	Weak transcription	Brain Angular Gyrus	brain
40	chr11:59378000-59379400	Weak transcription	Esophagus	oesophagus
41	chr11:59378000-59379400	Weak transcription	Left Ventricle	heart
42	chr11:59378000-59379400	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr11:59378000-59379400	Weak transcription	Spleen	Spleen
44	chr11:59378000-59379400	Weak transcription	A549	lung
45	chr11:59378000-59379600	Weak transcription	Aorta	Aorta
46	chr11:59378000-59380200	Weak transcription	HMEC	breast
47	chr11:59378000-59380600	Weak transcription	Primary hematopoietic stem cells	blood
48	chr11:59378000-59380800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr11:59378000-59381200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr11:59378000-59381400	Genic enhancers	Primary T helper cells PMA-I stimulated	--

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