Variant report

Variant	rs373813118
Chromosome Location	chr1:78468673-78468674
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	EP300	chr1:78468615-78470834	K562	blood:	n/a	chr1:78469262-78469276
2	ZNF384	chr1:78468385-78469166	K562	blood:	n/a	n/a
3	MAFK	chr1:78468560-78469502	GM12878	blood:	n/a	chr1:78469158-78469172 chr1:78469157-78469173 chr1:78469162-78469171 chr1:78469155-78469175 chr1:78469154-78469169 chr1:78469159-78469168 chr1:78469155-78469166
4	IRF1	chr1:78468673-78471591	K562	blood:	n/a	chr1:78471360-78471371 chr1:78471360-78471373 chr1:78471361-78471375 chr1:78469905-78469919 chr1:78471360-78471373 chr1:78471359-78471372 chr1:78469257-78469271 chr1:78471360-78471373 chr1:78471360-78471374
5	ARID3A	chr1:78467855-78472242	K562	blood:	n/a	n/a
6	MAFF	chr1:78468581-78471128	K562	blood:	n/a	chr1:78469158-78469172 chr1:78469152-78469170

No.	Distal block	Cell Line	Cell type
1	chr1:78222274..78226935-chr1:78467368..78471641,7	K562	blood:
2	chr1:77813619..77816574-chr1:78468319..78470340,2	K562	blood:
3	chr1:45195514..45197967-chr1:78468300..78470449,2	K562	blood:
4	chr1:78468129..78475881-chr1:78555411..78565499,18	K562	blood:
5	chr1:78434019..78436134-chr1:78467540..78469438,2	MCF-7	breast:
6	chr1:78468665..78470165-chr1:80026349..80029039,2	K562	blood:
7	chr1:78147072..78148946-chr1:78468394..78471551,4	K562	blood:
8	chr1:78223538..78227787-chr1:78468626..78471641,9	K562	blood:
9	chr1:78215243..78217892-chr1:78468395..78470149,2	K562	blood:
10	chr1:78466521..78469448-chr1:78786020..78788848,2	K562	blood:
11	chr1:78391278..78394159-chr1:78467798..78470228,4	K562	blood:
12	chr1:78467305..78472459-chr1:78554681..78560615,12	K562	blood:
13	chr1:78148235..78150616-chr1:78467949..78471468,6	K562	blood:
14	chr1:78466099..78472038-chr1:78511575..78517585,8	K562	blood:
15	chr1:78441900..78447727-chr1:78466477..78473207,15	MCF-7	breast:
16	chr1:78466262..78468828-chr1:85227463..85229470,2	K562	blood:
17	chr1:77684174..77686431-chr1:78467561..78469261,2	K562	blood:
18	chr1:78148970..78151388-chr1:78468544..78472172,4	K562	blood:
19	chr1:78391278..78393665-chr1:78467798..78470228,3	K562	blood:
20	chr1:78468395..78470223-chr1:78565706..78567712,2	K562	blood:
21	chr1:78194511..78196220-chr1:78468665..78470167,2	K562	blood:
22	chr1:78196594..78199188-chr1:78468041..78469700,2	K562	blood:
23	chr1:78441980..78446801-chr1:78467462..78471771,12	MCF-7	breast:
24	chr1:78467898..78469708-chr1:78520081..78522686,2	K562	blood:

Variant related genes	Relation type
DNAJB4	TF binding region
ENSG00000233099	Chromatin interaction
ENSG00000036549	Chromatin interaction
ENSG00000077254	Chromatin interaction
ENSG00000162613	Chromatin interaction
ENSG00000213560	Chromatin interaction
ENSG00000137960	Chromatin interaction
ENSG00000162614	Chromatin interaction
ENSG00000162616	Chromatin interaction
ENSG00000202263	Chromatin interaction
ENSG00000142892	Chromatin interaction
ENSG00000251958	Chromatin interaction
ENSG00000200169	Chromatin interaction

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

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1794082	chr1:78102426-78492221	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
2	esv3434340	chr1:78153780-78607103	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
3	nsv1013008	chr1:78463173-78958701	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
4	nsv535012	chr1:78463173-78958701	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
5	esv1801396	chr1:78468094-78492221	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:78446200-78469600	Weak transcription	Thymus	Thymus
2	chr1:78446400-78469800	Weak transcription	Primary B cells from peripheral blood	blood
3	chr1:78446400-78470200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr1:78446600-78468800	Weak transcription	Primary hematopoietic stem cells	blood
5	chr1:78446600-78468800	Weak transcription	Adipose Nuclei	Adipose
6	chr1:78446600-78468800	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr1:78446600-78469000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr1:78446600-78469000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr1:78446600-78469000	Weak transcription	Fetal Kidney	kidney
10	chr1:78446600-78469600	Weak transcription	Aorta	Aorta
11	chr1:78446600-78469800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr1:78446600-78470200	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr1:78446600-78470400	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr1:78447600-78469800	Weak transcription	Brain Cingulate Gyrus	brain
15	chr1:78447600-78470200	Weak transcription	Fetal Brain Male	brain
16	chr1:78447800-78469600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr1:78448000-78468800	Weak transcription	Brain Hippocampus Middle	brain
18	chr1:78448800-78488200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr1:78450200-78469600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr1:78450200-78469600	Weak transcription	Fetal Intestine Large	intestine
21	chr1:78452400-78468800	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr1:78452400-78468800	Weak transcription	Colon Smooth Muscle	Colon
23	chr1:78452800-78468800	Weak transcription	NH-A	brain
24	chr1:78452800-78470400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr1:78452800-78478800	Weak transcription	Spleen	Spleen
26	chr1:78453000-78469600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr1:78454200-78468800	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr1:78454200-78469200	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr1:78454200-78469800	Weak transcription	Left Ventricle	heart
30	chr1:78454200-78469800	Weak transcription	Psoas Muscle	Psoas
31	chr1:78454200-78485600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr1:78454400-78469800	Weak transcription	Right Ventricle	heart
33	chr1:78455600-78469200	Weak transcription	Primary B cells from cord blood	blood
34	chr1:78455800-78468800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr1:78456000-78469200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr1:78456200-78470400	Weak transcription	Esophagus	oesophagus
37	chr1:78456600-78468800	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr1:78457400-78469000	Weak transcription	GM12878-XiMat	blood
39	chr1:78457400-78469800	Weak transcription	Ovary	ovary
40	chr1:78457400-78470400	Weak transcription	Pancreas	Pancrea
41	chr1:78457800-78469000	Weak transcription	HMEC	breast
42	chr1:78459400-78469800	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr1:78459600-78469600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr1:78460000-78469800	Weak transcription	Fetal Thymus	thymus
45	chr1:78460200-78470200	Weak transcription	Brain Germinal Matrix	brain
46	chr1:78461400-78468800	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr1:78461400-78470000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr1:78461400-78470800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr1:78461600-78468800	Weak transcription	NHEK	skin
50	chr1:78461600-78469400	Weak transcription	Primary T helper cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links