Variant report

Variant	rs570614047
Chromosome Location	chr15:40903595-40903596
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:40900479..40903844-chr15:40904116..40906813,4	K562	blood:

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832984	chr15:40794391-40998535	Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
2	esv2758378	chr15:40832545-40995111	Active TSS Flanking Active TSS Strong transcription Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
3	esv2760026	chr15:40832545-40995111	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	esv1843830	chr15:40902453-40915045	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	esv1841263	chr15:40902453-40966765	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:40887600-40941800	Weak transcription	Fetal Intestine Large	intestine
2	chr15:40887800-40933200	Weak transcription	Duodenum Mucosa	Duodenum
3	chr15:40887800-40942200	Weak transcription	Primary B cells from cord blood	blood
4	chr15:40887800-40948200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr15:40887800-40961600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr15:40888000-40956000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr15:40888200-40912800	Weak transcription	HMEC	breast
8	chr15:40888400-40913200	Weak transcription	NHDF-Ad	bronchial
9	chr15:40888400-40913600	Weak transcription	NHLF	lung
10	chr15:40888400-40923200	Weak transcription	Osteobl	bone
11	chr15:40888400-40925800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr15:40888400-40944200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr15:40890800-40904800	Weak transcription	A549	lung
14	chr15:40890800-40925200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr15:40893400-40907200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr15:40893600-40922600	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr15:40895800-40905200	Strong transcription	Fetal Thymus	thymus
18	chr15:40895800-40905600	Strong transcription	Dnd41	blood
19	chr15:40896000-40910200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr15:40896800-40910400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr15:40897800-40957200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr15:40898000-40905400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr15:40898200-40907800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr15:40898800-40903600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr15:40899400-40922600	Weak transcription	Fetal Intestine Small	intestine
26	chr15:40899600-40911600	Weak transcription	Fetal Muscle Trunk	muscle
27	chr15:40899600-40911800	Weak transcription	Fetal Muscle Leg	muscle
28	chr15:40899600-40913200	Weak transcription	Primary hematopoietic stem cells	blood
29	chr15:40900000-40943600	Weak transcription	NH-A	brain
30	chr15:40900200-40912800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr15:40900400-40913200	Weak transcription	NHEK	skin
32	chr15:40900600-40912800	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr15:40901400-40905200	Strong transcription	Thymus	Thymus
34	chr15:40902000-40903600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr15:40902000-40904400	Strong transcription	Fetal Stomach	stomach
36	chr15:40902000-40911200	Weak transcription	HepG2	liver
37	chr15:40902200-40903600	Strong transcription	HUES6 Cell Line	embryonic stem cell
38	chr15:40902200-40903600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr15:40902200-40920400	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr15:40902400-40911000	Weak transcription	HSMM	muscle
41	chr15:40902600-40904400	Weak transcription	Hela-S3	cervix
42	chr15:40902600-40904800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr15:40902600-40904800	Weak transcription	Primary neutrophils fromperipheralblood	blood
44	chr15:40902600-40911000	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr15:40902800-40903600	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr15:40902800-40903600	Strong transcription	GM12878-XiMat	blood
47	chr15:40902800-40911800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr15:40902800-40913000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr15:40903000-40905000	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr15:40903000-40906200	Weak transcription	Primary monocytes fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links