Variant report

Variant	rs570077314
Chromosome Location	chr6:150869313-150869314
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	nsv1020067	chr6:150730783-150870708	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv886772	chr6:150743364-151024280	Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh 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	nsv464079	chr6:150836676-150873766	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv604850	chr6:150836676-150873766	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv522578	chr6:150868443-150873766	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150866200-150871000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:150867400-150869400	Enhancers	Fetal Muscle Leg	muscle
3	chr6:150867400-150869400	Enhancers	Right Ventricle	heart
4	chr6:150867400-150869800	Enhancers	Fetal Kidney	kidney
5	chr6:150867600-150869400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
6	chr6:150867600-150869600	Enhancers	Liver	Liver
7	chr6:150867600-150869600	Enhancers	Ovary	ovary
8	chr6:150867800-150869400	Enhancers	Spleen	Spleen
9	chr6:150868000-150870200	Weak transcription	Lung	lung
10	chr6:150868000-150870800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr6:150868000-150871200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr6:150868200-150869600	Enhancers	Fetal Intestine Small	intestine
13	chr6:150869000-150869400	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr6:150869000-150870200	Weak transcription	Fetal Muscle Trunk	muscle
15	chr6:150869000-150870600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr6:150869200-150869400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr6:150869200-150869400	Enhancers	Duodenum Mucosa	Duodenum
18	chr6:150869200-150869400	Flanking Active TSS	HepG2	liver
19	chr6:150869200-150870200	Weak transcription	Cortex derived primary cultured neurospheres	brain

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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