Variant report

Variant	rs2267737
Chromosome Location	chr7:31136610-31136611
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:31136609..31138321-chr7:31142401..31144993,2	K562	blood:

Extended variants
information (count: 10 )
Associated
traits (count: 1 )

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	nsv538811	chr7:30549595-31405593	Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv1016256	chr7:30649212-31163056	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv1023120	chr7:30655070-31185096	Enhancers Strong transcription Bivalent Enhancer Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	esv2761316	chr7:30655082-31166676	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv527038	chr7:30657467-31161945	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
6	nsv916877	chr7:30661135-31154731	Weak transcription Genic enhancers Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
7	nsv1017168	chr7:30663213-31166676	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS 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	18 gene(s)	inside rSNPs	diseases
8	nsv1017808	chr7:30671936-31150473	Enhancers Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
9	nsv519081	chr7:31134317-31136610	Strong transcription Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a
10	nsv915784	chr7:31134685-31870517	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2267737	HOXA13	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:31101000-31137600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr7:31117400-31162000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr7:31125600-31144800	Weak transcription	Brain Substantia Nigra	brain
4	chr7:31129000-31148200	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr7:31132200-31140000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr7:31132400-31137600	Strong transcription	Fetal Brain Female	brain
7	chr7:31132400-31141000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr7:31132600-31137000	Strong transcription	Brain Germinal Matrix	brain
9	chr7:31132600-31137000	Strong transcription	Brain Inferior Temporal Lobe	brain
10	chr7:31133200-31154600	Weak transcription	Brain Angular Gyrus	brain
11	chr7:31133400-31154200	Weak transcription	Fetal Brain Male	brain
12	chr7:31134600-31137200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr7:31135800-31137200	Enhancers	Fetal Muscle Trunk	muscle
14	chr7:31136000-31136800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr7:31136000-31137400	Enhancers	Fetal Muscle Leg	muscle
16	chr7:31136200-31138600	Weak transcription	Fetal Stomach	stomach
17	chr7:31136400-31136800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr7:31136600-31136800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr7:31136600-31137000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr7:31136600-31143000	Weak transcription	Brain Anterior Caudate	brain
21	chr7:31136600-31149600	Weak transcription	Brain Cingulate Gyrus	brain

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