Variant report

Variant	rs16848361
Chromosome Location	chr1:228319150-228319151
allele	C/T
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:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:227669108..227669644-chr1:228318559..228319309,2	K562	blood:
2	chr1:228296587..228298134-chr1:228317417..228319245,2	MCF-7	breast:
3	chr1:228318245..228320803-chr1:228645102..228647323,2	MCF-7	breast:
4	chr1:228296837..228298966-chr1:228317403..228319200,2	MCF-7	breast:
5	chr1:228318444..228319355-chr1:228580810..228581597,3	MCF-7	breast:
6	chr1:228317307..228320244-chr1:228593254..228595071,2	MCF-7	breast:
7	chr1:228318795..228319443-chr1:228326879..228327649,2	K562	blood:
8	chr1:228318704..228321290-chr1:228321763..228325598,5	K562	blood:
9	chr1:228317360..228320048-chr1:228643318..228645698,2	K562	blood:
10	chr1:228318929..228320928-chr1:228352510..228356054,3	MCF-7	breast:
11	chr1:228318400..228319358-chr1:228379072..228379959,2	MCF-7	breast:
12	chr1:228318237..228319764-chr1:228400846..228402736,2	K562	blood:
13	chr1:228318799..228319507-chr1:228353439..228354347,2	K562	blood:
14	chr1:228191780..228193444-chr1:228317568..228320348,2	MCF-7	breast:
15	chr1:228318736..228319366-chr1:228328855..228329758,2	K562	blood:
16	chr1:228317576..228320625-chr1:228326165..228329627,4	MCF-7	breast:
17	chr1:228308851..228311913-chr1:228318385..228321498,4	K562	blood:
18	chr1:228317547..228320565-chr1:228350763..228355962,5	MCF-7	breast:
19	chr1:228261534..228262217-chr1:228318541..228319233,2	MCF-7	breast:
20	chr1:228318319..228319575-chr1:228353004..228354801,9	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000162913	Chromatin interaction
ENSG00000143774	Chromatin interaction
ENSG00000227625	Chromatin interaction
ENSG00000196890	Chromatin interaction
ENSG00000162910	Chromatin interaction
ENSG00000181873	Chromatin interaction
ENSG00000154370	Chromatin interaction
ENSG00000203684	Chromatin interaction
ENSG00000181218	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs2231711	1.00[EUR][1000 genomes]
rs34658204	1.00[EUR][1000 genomes]
rs41270181	1.00[EUR][1000 genomes]
rs41314262	1.00[EUR][1000 genomes]
rs45460992	1.00[EUR][1000 genomes]
rs56280452	1.00[EUR][1000 genomes]
rs56394518	1.00[EUR][1000 genomes]
rs57624754	1.00[EUR][1000 genomes]
rs58696607	1.00[EUR][1000 genomes]
rs58787263	1.00[EUR][1000 genomes]
rs60538700	1.00[EUR][1000 genomes]
rs60642596	1.00[EUR][1000 genomes]
rs60777646	1.00[EUR][1000 genomes]
rs61091413	1.00[EUR][1000 genomes]
rs73108778	1.00[EUR][1000 genomes]
rs74140818	1.00[EUR][1000 genomes]
rs74140819	1.00[EUR][1000 genomes]
rs74140821	1.00[EUR][1000 genomes]
rs74140822	1.00[EUR][1000 genomes]
rs74140823	1.00[EUR][1000 genomes]
rs74140994	1.00[EUR][1000 genomes]
rs74143607	1.00[EUR][1000 genomes]
rs74143612	1.00[EUR][1000 genomes]
rs74143614	1.00[EUR][1000 genomes]
rs74143615	1.00[EUR][1000 genomes]
rs74143616	1.00[EUR][1000 genomes]
rs8192631	1.00[EUR][1000 genomes]
rs9662484	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010605	chr1:227770415-228332690	Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	esv32853	chr1:227880116-228806209	Enhancers Genic enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	187 gene(s)	inside rSNPs	diseases
3	nsv826908	chr1:227895386-228691100	Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
4	nsv523935	chr1:228038124-228681749	Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	137 gene(s)	inside rSNPs	diseases
5	nsv873252	chr1:228174528-228371551	Strong transcription Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
6	nsv873253	chr1:228231601-228537942	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
7	nsv873254	chr1:228231601-228543800	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
8	nsv873255	chr1:228254753-228684779	Genic enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	133 gene(s)	inside rSNPs	diseases
9	nsv827019	chr1:228314167-228651020	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	106 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:228318000-228319200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr1:228318200-228319200	Active TSS	H9 Cell Line	embryonic stem cell
3	chr1:228318200-228319200	Enhancers	Primary B cells from peripheral blood	blood
4	chr1:228318200-228319400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr1:228318200-228319800	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr1:228318200-228319800	Enhancers	Fetal Intestine Large	intestine
7	chr1:228318200-228319800	Enhancers	Placenta	Placenta
8	chr1:228318200-228319800	Enhancers	HMEC	breast
9	chr1:228318400-228319200	Active TSS	ES-I3 Cell Line	embryonic stem cell
10	chr1:228318400-228319200	Active TSS	HUES64 Cell Line	embryonic stem cell
11	chr1:228318400-228319200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr1:228318600-228319200	Enhancers	Fetal Lung	lung
13	chr1:228318600-228319200	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr1:228318600-228319600	Enhancers	Hela-S3	cervix
15	chr1:228318800-228319200	Flanking Active TSS	Fetal Kidney	kidney
16	chr1:228318800-228319200	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr1:228318800-228319200	Enhancers	K562	blood
18	chr1:228318800-228319400	Enhancers	HepG2	liver
19	chr1:228318800-228319400	Flanking Active TSS	NHEK	skin
20	chr1:228318800-228319600	Enhancers	Stomach Mucosa	stomach
21	chr1:228318800-228319800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr1:228318800-228319800	Enhancers	Fetal Intestine Small	intestine
23	chr1:228318800-228324000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr1:228318800-228327000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr1:228318800-228327000	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr1:228319000-228319200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
27	chr1:228319000-228319200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
28	chr1:228319000-228319200	Enhancers	Duodenum Smooth Muscle	Duodenum
29	chr1:228319000-228319200	Enhancers	A549	lung
30	chr1:228319000-228323400	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr1:228319000-228323600	Weak transcription	Primary B cells from cord blood	blood
32	chr1:228319000-228323600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr1:228319000-228323600	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr1:228319000-228325000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links