Variant report

Variant	rs3838811
Chromosome Location	chr12:105617025-105617026
allele	-/A
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:105616267..105619374-chr12:105619746..105623496,4	MCF-7	breast:
2	chr12:105611067..105613851-chr12:105616365..105618135,2	MCF-7	breast:
3	chr12:105615953..105617646-chr12:105655942..105657913,2	MCF-7	breast:
4	chr12:105604459..105610765-chr12:105612400..105619000,9	MCF-7	breast:
5	chr12:105611185..105613030-chr12:105615764..105617845,2	MCF-7	breast:
6	chr12:105610784..105617210-chr12:105628529..105631630,8	MCF-7	breast:
7	chr12:105615700..105617888-chr12:105626325..105628263,2	K562	blood:
8	chr12:105609229..105612971-chr12:105615964..105620947,4	K562	blood:
9	chr12:105606795..105619301-chr12:105624368..105633184,26	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000136044	Chromatin interaction
ENSG00000235162	Chromatin interaction

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832506	chr12:105461274-105637561	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
2	nsv455704	chr12:105583877-105651356	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
3	nsv560053	chr12:105583877-105651356	Genic enhancers Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
4	nsv899499	chr12:105616297-105722529	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:105546800-105625200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr12:105571400-105617800	Weak transcription	K562	blood
3	chr12:105578000-105623200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr12:105578200-105620000	Strong transcription	Primary T cells fromperipheralblood	blood
5	chr12:105584000-105627000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr12:105590200-105620000	Strong transcription	Primary T helper cells PMA-I stimulated	--
7	chr12:105590400-105618800	Strong transcription	Primary B cells from peripheral blood	blood
8	chr12:105591000-105619400	Strong transcription	Primary T cells from cord blood	blood
9	chr12:105595000-105618800	Strong transcription	Primary T helper cells fromperipheralblood	blood
10	chr12:105596400-105621800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr12:105600800-105626800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr12:105601000-105619200	Weak transcription	GM12878-XiMat	blood
13	chr12:105604400-105618400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr12:105605600-105628400	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr12:105607200-105618600	Genic enhancers	Fetal Intestine Large	intestine
16	chr12:105608600-105618200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr12:105609000-105618600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr12:105609200-105620400	Genic enhancers	Fetal Intestine Small	intestine
19	chr12:105609200-105622400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr12:105609200-105626800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr12:105609200-105628600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr12:105609400-105618600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
23	chr12:105609400-105619400	Strong transcription	Osteobl	bone
24	chr12:105610200-105618800	Strong transcription	Thymus	Thymus
25	chr12:105610800-105620000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr12:105611000-105620000	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr12:105611000-105620200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr12:105611200-105620200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr12:105611200-105621200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr12:105611200-105628200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr12:105611400-105619600	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr12:105611400-105621200	Weak transcription	Hela-S3	cervix
33	chr12:105611600-105621200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr12:105611600-105621600	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr12:105611600-105626200	Weak transcription	Fetal Brain Male	brain
36	chr12:105611800-105621200	Weak transcription	Fetal Kidney	kidney
37	chr12:105612000-105624800	Genic enhancers	NHDF-Ad	bronchial
38	chr12:105612200-105618600	Enhancers	Right Atrium	heart
39	chr12:105612600-105618800	Strong transcription	NHEK	skin
40	chr12:105612800-105618600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr12:105612800-105624200	Strong transcription	Fetal Stomach	stomach
42	chr12:105613000-105623600	Strong transcription	Fetal Muscle Trunk	muscle
43	chr12:105613200-105618400	Strong transcription	Fetal Muscle Leg	muscle
44	chr12:105613200-105620000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr12:105613400-105618000	Strong transcription	Brain Germinal Matrix	brain
46	chr12:105613800-105617200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr12:105613800-105618800	Strong transcription	HSMM	muscle
48	chr12:105613800-105622000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr12:105614000-105617200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr12:105614200-105617800	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain

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