Variant report

Variant	rs73412155
Chromosome Location	chr6:33769611-33769612
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:33758412..33760501-chr6:33767524..33770306,2	MCF-7	breast:
2	chr6:33767158..33770119-chr6:33775833..33777551,2	MCF-7	breast:
3	chr6:33762823..33764594-chr6:33767158..33770034,2	K562	blood:
4	chr6:33767719..33770571-chr6:33780655..33782252,3	K562	blood:

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs3828784	0.86[AFR][1000 genomes]
rs60110107	0.87[AFR][1000 genomes]
rs62400072	0.80[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	nsv462897	chr6:33717770-33778964	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv602839	chr6:33717770-33778964	Enhancers Genic enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 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	chr6:33757600-33775800	Weak transcription	Right Atrium	heart
2	chr6:33763600-33771600	Weak transcription	Fetal Intestine Small	intestine
3	chr6:33765800-33770200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr6:33766000-33770200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr6:33766000-33776000	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr6:33766600-33770000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr6:33766800-33769800	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr6:33766800-33776400	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr6:33768200-33770000	Weak transcription	Osteobl	bone
10	chr6:33768400-33770600	Weak transcription	NHDF-Ad	bronchial
11	chr6:33768800-33772400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr6:33769000-33769800	Weak transcription	Fetal Brain Male	brain
13	chr6:33769000-33771400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr6:33769000-33772200	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr6:33769200-33771600	Enhancers	Brain Germinal Matrix	brain
16	chr6:33769200-33773200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr6:33769400-33770200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr6:33769400-33770600	Enhancers	H1 Cell Line	embryonic stem cell
19	chr6:33769400-33770800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr6:33769600-33770400	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr6:33769600-33770800	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr6:33769600-33770800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr6:33769600-33771000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links