Variant report

Variant	rs563033169
Chromosome Location	chr6:165339067-165339068
allele	-/CACT
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:165335824..165337632-chr6:165338882..165340730,2	K562	blood:

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv605232	chr6:164994771-165401154	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv521153	chr6:165279393-165343557	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv886925	chr6:165319631-165705488	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
4	esv3410490	chr6:165337362-165341860	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
5	esv3414452	chr6:165337862-165341160	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a
6	esv3446736	chr6:165338062-165341060	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:165333200-165346200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:165337800-165339400	Enhancers	Fetal Brain Male	brain
3	chr6:165337800-165340400	Enhancers	Brain Cingulate Gyrus	brain
4	chr6:165338000-165340200	Enhancers	Brain Germinal Matrix	brain
5	chr6:165338200-165341200	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr6:165338200-165341400	Enhancers	Fetal Heart	heart
7	chr6:165338600-165339600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:165338600-165339600	Weak transcription	Brain Anterior Caudate	brain
9	chr6:165338600-165339600	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr6:165338600-165341200	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr6:165338600-165341200	Weak transcription	Psoas Muscle	Psoas
12	chr6:165338800-165339200	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr6:165338800-165339200	Weak transcription	Brain Hippocampus Middle	brain
14	chr6:165338800-165339400	Weak transcription	Brain Substantia Nigra	brain
15	chr6:165338800-165339800	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr6:165338800-165340800	Weak transcription	Fetal Muscle Leg	muscle
17	chr6:165338800-165341200	Weak transcription	Fetal Muscle Trunk	muscle
18	chr6:165339000-165339600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr6:165339000-165340800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr6:165339000-165341000	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr6:165339000-165341200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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