Variant report

Variant	rs576340306
Chromosome Location	chr1:10860131-10860132
allele	G/T
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	MAX	chr1:10859891-10860132	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:10859540..10861856-chr1:11072997..11074622,2	MCF-7	breast:
2	chr1:10859730..10862103-chr1:10872540..10874271,2	K562	blood:
3	chr1:10859862..10862247-chr1:10862997..10864599,2	MCF-7	breast:

Variant related genes	Relation type
CASZ1	TF binding region
ENSG00000120948	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv29966	chr1:10676800-10874152	Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv870849	chr1:10694125-10894724	Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv529981	chr1:10697093-11353487	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
4	esv2757723	chr1:10742502-11055147	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
5	esv2758921	chr1:10742502-11055147	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	nsv871772	chr1:10832322-10894724	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv870589	chr1:10840905-10901994	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv871617	chr1:10858746-10935232	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv871155	chr1:10858746-10998509	Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10857000-10873600	Weak transcription	Gastric	stomach
2	chr1:10857000-10882600	Weak transcription	Right Atrium	heart
3	chr1:10857200-10860400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr1:10857600-10860600	Weak transcription	Stomach Mucosa	stomach
5	chr1:10859200-10860200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr1:10859600-10860400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
7	chr1:10859800-10860200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
8	chr1:10859800-10860200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
9	chr1:10859800-10860200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
10	chr1:10859800-10860200	Enhancers	Fetal Intestine Large	intestine
11	chr1:10859800-10860200	Bivalent Enhancer	Fetal Muscle Leg	muscle
12	chr1:10859800-10860400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr1:10859800-10860400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr1:10859800-10860400	Bivalent Enhancer	Duodenum Mucosa	Duodenum
15	chr1:10860000-10860200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
16	chr1:10860000-10860200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
17	chr1:10860000-10860200	Enhancers	Fetal Intestine Small	intestine
18	chr1:10860000-10860400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr1:10860000-10860600	Enhancers	Fetal Heart	heart
20	chr1:10860000-10863000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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