Variant report

Variant	rs34667294
Chromosome Location	chr6:150471296-150471297
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:150469308..150480268-chr6:150484066..150492629,15	K562	blood:
2	chr6:150469487..150471945-chr6:150477081..150478644,2	K562	blood:
3	chr6:150471157..150474765-chr6:150475895..150479622,5	K562	blood:

Variant related genes	Relation type
ENSG00000238594	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs17079360	0.89[ASN][1000 genomes]
rs4869836	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886770	chr6:150395424-150499889	Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv1026690	chr6:150419115-150485583	Bivalent Enhancer Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150465600-150471600	Weak transcription	Psoas Muscle	Psoas
2	chr6:150465600-150471800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:150467800-150472600	Enhancers	NHEK	skin
4	chr6:150467800-150473400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr6:150467800-150473400	Weak transcription	Right Atrium	heart
6	chr6:150468200-150472800	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr6:150469400-150472200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:150469600-150471600	Enhancers	Fetal Heart	heart
9	chr6:150469800-150471600	Weak transcription	Right Ventricle	heart
10	chr6:150470000-150476800	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr6:150470200-150471400	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr6:150470200-150471400	Bivalent Enhancer	Fetal Kidney	kidney
13	chr6:150470200-150472800	Enhancers	HMEC	breast
14	chr6:150470600-150471800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr6:150470800-150471400	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr6:150470800-150471800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr6:150470800-150471800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
18	chr6:150470800-150472000	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr6:150470800-150472600	Weak transcription	Fetal Brain Male	brain
20	chr6:150471000-150472200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
21	chr6:150471000-150472400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
22	chr6:150471000-150472600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr6:150471200-150471400	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr6:150471200-150471400	Transcr. at gene 5' and 3'	K562	blood
25	chr6:150471200-150472400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
26	chr6:150471200-150472400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
27	chr6:150471200-150472800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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