Variant report

Variant	rs375855142
Chromosome Location	chrX:138284694-138284695
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	chrX:138273663..138275580-chrX:138283129..138285298,2	K562	blood:
2	chrX:138282011..138285172-chrX:138285245..138287356,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000129682	Chromatin interaction

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525867	chrX:137580983-138439843	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv533984	chrX:137938683-138556308	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv532935	chrX:138281469-138764448	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	esv3346694	chrX:138283686-138289084	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:138277400-138285200	Weak transcription	Pancreas	Pancrea
2	chrX:138277600-138285400	Weak transcription	Liver	Liver
3	chrX:138277600-138286000	Weak transcription	Right Atrium	heart
4	chrX:138279000-138284800	Weak transcription	Gastric	stomach
5	chrX:138282600-138284800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chrX:138282600-138284800	Weak transcription	Psoas Muscle	Psoas
7	chrX:138282800-138285000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chrX:138282800-138285400	Weak transcription	Esophagus	oesophagus
9	chrX:138283000-138285000	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chrX:138283000-138288600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chrX:138284200-138285000	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chrX:138284400-138284800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
13	chrX:138284400-138284800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
14	chrX:138284400-138284800	Flanking Active TSS	K562	blood
15	chrX:138284400-138285000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
16	chrX:138284400-138285000	Enhancers	HSMMtube	muscle
17	chrX:138284400-138285200	Enhancers	Skeletal Muscle Male	skeletal muscle
18	chrX:138284400-138285400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
19	chrX:138284400-138287800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chrX:138284400-138288400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
21	chrX:138284600-138284800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
22	chrX:138284600-138284800	Bivalent/Poised TSS	Adipose Nuclei	Adipose
23	chrX:138284600-138284800	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
24	chrX:138284600-138285000	Bivalent Enhancer	NH-A	brain
25	chrX:138284600-138285200	Active TSS	ES-I3 Cell Line	embryonic stem cell
26	chrX:138284600-138285200	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
27	chrX:138284600-138285200	Flanking Active TSS	Brain Germinal Matrix	brain
28	chrX:138284600-138286400	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
29	chrX:138284600-138287800	Bivalent/Poised TSS	Fetal Brain Female	brain
30	chrX:138284600-138288000	Bivalent/Poised TSS	Fetal Intestine Large	intestine
31	chrX:138284600-138288200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
32	chrX:138284600-138288600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
33	chrX:138284600-138288800	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
34	chrX:138284600-138288800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell

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