Variant report

Variant	rs367751435
Chromosome Location	chr4:103781870-103781871
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr4:103781708-103781959	K562	blood:	n/a	n/a
2	GATA1	chr4:103781676-103782280	PBDE	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:103741330..103752134-chr4:103778393..103796398,92	K562	blood:
2	chr4:103736995..103756245-chr4:103778393..103800311,117	K562	blood:

Variant related genes	Relation type
ENSG00000238948	TF binding region
ENSG00000246560	Chromatin interaction
ENSG00000109332	Chromatin interaction

Extended variants
information (count: 18 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv594957	chr4:103728010-103870091	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
2	esv1802717	chr4:103765156-103870091	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv10541	chr4:103778446-103785639	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	esv21280	chr4:103779278-103783640	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv594958	chr4:103780496-103782321	ZNF genes & repeats Weak transcription Strong transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv594959	chr4:103780496-103782582	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
7	nsv594960	chr4:103780496-103782764	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
8	nsv594961	chr4:103780496-103783359	ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
9	nsv594962	chr4:103780496-103783412	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
10	esv2757946	chr4:103780705-104057321	Strong transcription Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
11	esv2759270	chr4:103780705-104057321	ZNF genes & repeats Strong transcription Weak transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
12	nsv594963	chr4:103780840-103782764	ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
13	nsv594964	chr4:103780840-103782963	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
14	nsv594965	chr4:103780840-103783359	Genic enhancers ZNF genes & repeats Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
15	nsv594966	chr4:103780840-103783412	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
16	nsv594967	chr4:103780922-103782764	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
17	nsv594968	chr4:103780922-103782963	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
18	nsv594969	chr4:103781574-103783412	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:103750800-103788000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr4:103765000-103783600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr4:103765400-103788800	Weak transcription	Left Ventricle	heart
4	chr4:103779000-103787600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr4:103780000-103782000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
6	chr4:103780000-103788000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr4:103780200-103782200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr4:103780200-103782800	ZNF genes & repeats	Dnd41	blood
9	chr4:103780200-103789200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr4:103780400-103788800	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr4:103780800-103788000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr4:103781000-103783000	Weak transcription	Brain Angular Gyrus	brain
13	chr4:103781000-103785000	Weak transcription	Primary T cells from cord blood	blood
14	chr4:103781000-103788800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr4:103781000-103789400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr4:103781200-103785800	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr4:103781200-103788600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr4:103781400-103782200	Strong transcription	H1 Cell Line	embryonic stem cell
19	chr4:103781400-103782400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
20	chr4:103781400-103782600	ZNF genes & repeats	Fetal Stomach	stomach
21	chr4:103781600-103782200	ZNF genes & repeats	Liver	Liver
22	chr4:103781600-103782200	ZNF genes & repeats	Fetal Thymus	thymus
23	chr4:103781600-103782400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
24	chr4:103781600-103782400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr4:103781600-103782400	ZNF genes & repeats	Fetal Intestine Small	intestine
26	chr4:103781600-103782400	ZNF genes & repeats	GM12878-XiMat	blood
27	chr4:103781600-103783400	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr4:103781800-103782000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr4:103781800-103782200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr4:103781800-103782200	ZNF genes & repeats	Aorta	Aorta
31	chr4:103781800-103782200	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
32	chr4:103781800-103782200	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
33	chr4:103781800-103782400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr4:103781800-103782400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
35	chr4:103781800-103782400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr4:103781800-103782400	ZNF genes & repeats	Fetal Muscle Leg	muscle
37	chr4:103781800-103782600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr4:103781800-103783400	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr4:103781800-103784400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr4:103781800-103788000	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr4:103781800-103789600	Weak transcription	Fetal Brain Male	brain

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