Variant report

Variant	rs145404171
Chromosome Location	chr7:39500859-39500860
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	chr7:39493293..39495900-chr7:39499088..39502872,3	K562	blood:
2	chr7:39498982..39501819-chr7:39501974..39504808,2	K562	blood:

Variant related genes	Relation type
ENSG00000106536	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	nsv1021180	chr7:39424988-39642261	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1026951	chr7:39429036-39642261	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv966782	chr7:39454992-39581886	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1018430	chr7:39455497-39643569	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	esv1797871	chr7:39499852-39503496	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39485800-39502000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr7:39492000-39504800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr7:39497200-39503600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:39498200-39504600	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr7:39499200-39504800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr7:39499400-39504400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr7:39499600-39501000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr7:39499600-39501600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr7:39499600-39501800	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr7:39499600-39501800	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr7:39499600-39504400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr7:39499800-39501000	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr7:39499800-39501000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr7:39499800-39501400	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr7:39500600-39501000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr7:39500600-39502400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr7:39500600-39503000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr7:39500600-39504800	Weak transcription	Fetal Brain Male	brain
19	chr7:39500800-39501400	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr7:39500800-39501600	Enhancers	Primary hematopoietic stem cells	blood
21	chr7:39500800-39502600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr7:39500800-39504000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr7:39500800-39504800	Weak transcription	K562	blood

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