Variant report

Variant	rs73265166
Chromosome Location	chr6:166798902-166798903
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:166753320..166757958-chr6:166794622..166799153,8	K562	blood:
2	chr6:166746293..166747904-chr6:166796894..166799021,2	K562	blood:
3	chr6:166751804..166757558-chr6:166793969..166799153,5	K562	blood:
4	chr6:166798810..166800534-chr6:166801868..166804204,3	K562	blood:
5	chr6:166796680..166799689-chr6:166808021..166810118,3	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FGFR1OP-2	chr6:166796964-166802453	NONHSAT116046

No data

Variant related genes	Relation type
ENSG00000198818	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs2017204	1.00[AMR][1000 genomes]
rs2017647	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73267203	1.00[AMR][1000 genomes]
rs7750474	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3490076	chr6:166727901-167306743	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
2	esv3490077	chr6:166727901-167306743	Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
3	nsv523548	chr6:166796433-166819774	Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr6:166797400-166801600	Weak transcription	Lung	lung
2	chr6:166797600-166801000	Weak transcription	Adipose Nuclei	Adipose
3	chr6:166797600-166801600	Weak transcription	Brain Germinal Matrix	brain
4	chr6:166797600-166801600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr6:166797600-166803000	Weak transcription	Brain Substantia Nigra	brain
6	chr6:166797600-166804200	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr6:166797600-166808200	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr6:166797600-166835800	Weak transcription	Right Atrium	heart
9	chr6:166797800-166801000	Weak transcription	Fetal Intestine Small	intestine
10	chr6:166797800-166801000	Weak transcription	Fetal Lung	lung
11	chr6:166797800-166801200	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr6:166797800-166801200	Weak transcription	Fetal Brain Female	brain
13	chr6:166797800-166802200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr6:166797800-166803800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr6:166797800-166804000	Weak transcription	Brain Angular Gyrus	brain
16	chr6:166798000-166799000	Weak transcription	Primary B cells from cord blood	blood
17	chr6:166798000-166801000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr6:166798000-166801200	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr6:166798000-166801200	Weak transcription	Fetal Intestine Large	intestine
20	chr6:166798000-166802400	Weak transcription	Colon Smooth Muscle	Colon
21	chr6:166798000-166803000	Weak transcription	Pancreas	Pancrea
22	chr6:166798000-166803200	Weak transcription	Fetal Muscle Leg	muscle
23	chr6:166798000-166812200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr6:166798200-166799000	Weak transcription	Liver	Liver
25	chr6:166798200-166800800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr6:166798200-166801000	Enhancers	HepG2	liver
27	chr6:166798200-166801200	Weak transcription	Monocytes-CD14+_RO01746	blood

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