Variant report

Variant	rs533963535
Chromosome Location	chr6:4730877-4730878
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:4730542..4732664-chr6:4733935..4736268,2	K562	blood:
2	chr6:4728025..4731306-chr6:4774544..4778107,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000236336	Chromatin interaction
ENSG00000153046	Chromatin interaction

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	esv3366530	chr6:4471528-4865322	ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv528627	chr6:4614058-4731340	Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv3429586	chr6:4719363-4792438	Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1017938	chr6:4729592-4774914	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1023527	chr6:4729592-5387176	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4724200-4733000	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr6:4724600-4733000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr6:4725000-4732600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr6:4728000-4734400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr6:4728200-4733000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr6:4728400-4733200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr6:4728600-4732400	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr6:4728600-4734400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr6:4728800-4732800	Weak transcription	Placenta	Placenta
10	chr6:4728800-4733000	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr6:4728800-4733000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr6:4728800-4733000	Weak transcription	Colonic Mucosa	Colon
13	chr6:4728800-4733200	Weak transcription	Stomach Mucosa	stomach
14	chr6:4729000-4733000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr6:4729000-4733000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr6:4729400-4732800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr6:4729400-4733000	Weak transcription	Duodenum Mucosa	Duodenum
18	chr6:4729400-4733000	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr6:4729600-4733000	Weak transcription	Fetal Intestine Large	intestine
20	chr6:4729800-4733000	Weak transcription	Fetal Intestine Small	intestine
21	chr6:4730800-4731400	Enhancers	K562	blood

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