Variant report

Variant	rs528634200
Chromosome Location	chr4:2850290-2850291
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	ZNF384	chr4:2850162-2850542	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:2843889..2847586-chr4:2849028..2855037,6	K562	blood:
2	chr4:2848510..2850735-chr4:2868206..2870939,2	K562	blood:
3	chr4:2843310..2847623-chr4:2847879..2851865,7	K562	blood:
4	chr4:2842030..2853279-chr4:2934021..2940851,24	MCF-7	breast:
5	chr4:2850138..2853377-chr4:2934213..2937642,3	MCF-7	breast:

Variant related genes	Relation type
ADD1	TF binding region
ENSG00000109736	Chromatin interaction
ENSG00000087274	Chromatin interaction
ENSG00000249673	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv878444	chr4:2689449-2861090	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	esv3418626	chr4:2741174-3461492	Genic enhancers Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
3	esv3397632	chr4:2741239-3460583	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
4	nsv878450	chr4:2760222-2861090	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv593435	chr4:2770772-2881256	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	nsv878451	chr4:2785556-2856687	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv1010533	chr4:2792848-2873441	Enhancers Bivalent/Poised TSS Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	nsv521858	chr4:2846799-2881256	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv526059	chr4:2850142-2861090	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv524060	chr4:2850142-2881256	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:2846400-2851000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:2846600-2854400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:2846600-2862400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr4:2846800-2851000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr4:2846800-2854200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:2846800-2855400	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr4:2846800-2855400	Weak transcription	Placenta	Placenta
8	chr4:2846800-2855600	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr4:2846800-2857400	Weak transcription	Aorta	Aorta
10	chr4:2846800-2861800	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr4:2846800-2861800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr4:2846800-2862000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr4:2846800-2862600	Weak transcription	Esophagus	oesophagus
14	chr4:2847000-2850600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr4:2847000-2851000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr4:2847200-2850400	Weak transcription	Brain Cingulate Gyrus	brain
17	chr4:2847200-2850800	Weak transcription	Fetal Brain Female	brain
18	chr4:2847200-2851200	Weak transcription	HSMM	muscle
19	chr4:2847200-2852000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr4:2847200-2853600	Weak transcription	Fetal Muscle Trunk	muscle
21	chr4:2847200-2862200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr4:2847400-2850400	Weak transcription	Fetal Intestine Large	intestine
23	chr4:2847400-2850400	Weak transcription	NHDF-Ad	bronchial
24	chr4:2847400-2851000	Weak transcription	Right Atrium	heart
25	chr4:2847400-2851000	Weak transcription	HSMMtube	muscle
26	chr4:2847400-2852800	Weak transcription	Fetal Thymus	thymus
27	chr4:2847400-2854400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr4:2847400-2854400	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr4:2847400-2859800	Weak transcription	A549	lung
30	chr4:2847400-2863600	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr4:2847800-2850400	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr4:2847800-2850600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr4:2847800-2851000	Weak transcription	Brain Substantia Nigra	brain
34	chr4:2847800-2851200	Weak transcription	Fetal Kidney	kidney
35	chr4:2847800-2852000	Enhancers	K562	blood
36	chr4:2847800-2852600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr4:2847800-2854200	Enhancers	Primary B cells from peripheral blood	blood
38	chr4:2847800-2854200	Weak transcription	NH-A	brain
39	chr4:2847800-2854200	Weak transcription	Osteobl	bone
40	chr4:2847800-2854600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr4:2847800-2854800	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr4:2847800-2855400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr4:2847800-2856200	Weak transcription	HMEC	breast
44	chr4:2848000-2850400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr4:2848000-2850400	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr4:2848000-2851400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr4:2848000-2853000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr4:2848000-2854200	Weak transcription	HUVEC	blood vessel
49	chr4:2848000-2854400	Weak transcription	NHEK	skin
50	chr4:2848000-2855400	Weak transcription	Fetal Stomach	stomach

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