Variant report

Variant	rs1775
Chromosome Location	chr12:48452504-48452505
allele	G/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	KAP1	chr12:48452253-48453303	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:48435313..48437988-chr12:48451982..48454529,2	K562	blood:

Variant related genes	Relation type
ENSG00000240399	TF binding region

Extended variants
information (count: 6 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10128968	1.00[JPT][hapmap]
rs740023	1.00[JPT][hapmap]
rs7975847	1.00[JPT][hapmap]

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	nsv832401	chr12:48347453-48477999	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	esv2758307	chr12:48429702-48825499	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	esv2759898	chr12:48429702-48825499	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:48431800-48456600	Weak transcription	NHLF	lung
2	chr12:48432000-48463400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr12:48432200-48498400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr12:48435200-48476200	Weak transcription	Stomach Mucosa	stomach
5	chr12:48435400-48457200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr12:48437200-48489000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr12:48439200-48453000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr12:48439200-48456800	Weak transcription	HMEC	breast
9	chr12:48439200-48468000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr12:48439600-48455400	Weak transcription	Colonic Mucosa	Colon
11	chr12:48440000-48454000	Weak transcription	HUVEC	blood vessel
12	chr12:48440000-48457200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr12:48440200-48452600	Weak transcription	Brain Germinal Matrix	brain
14	chr12:48440200-48452600	Weak transcription	Right Ventricle	heart
15	chr12:48440200-48453800	Weak transcription	Colon Smooth Muscle	Colon
16	chr12:48440400-48453400	Weak transcription	Esophagus	oesophagus
17	chr12:48441000-48452600	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr12:48441200-48457000	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr12:48441400-48453400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr12:48441400-48453400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr12:48441400-48454400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr12:48441400-48482600	Weak transcription	Small Intestine	intestine
23	chr12:48441600-48452800	Weak transcription	NHEK	skin
24	chr12:48441600-48468000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr12:48442400-48452600	Weak transcription	Fetal Brain Male	brain
26	chr12:48443000-48453200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr12:48443000-48478800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr12:48443400-48453400	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr12:48443400-48453600	Weak transcription	Stomach Smooth Muscle	stomach
30	chr12:48444000-48452800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr12:48444200-48474600	Weak transcription	Gastric	stomach
32	chr12:48444800-48453000	Weak transcription	Fetal Muscle Trunk	muscle
33	chr12:48444800-48468000	Weak transcription	Spleen	Spleen
34	chr12:48445000-48452600	Weak transcription	Fetal Muscle Leg	muscle
35	chr12:48445200-48452600	Weak transcription	Primary T cells fromperipheralblood	blood
36	chr12:48446000-48453800	Weak transcription	Brain Angular Gyrus	brain
37	chr12:48449400-48452600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr12:48449400-48452600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr12:48449400-48452600	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr12:48449400-48452800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr12:48449400-48453400	Weak transcription	Aorta	Aorta
42	chr12:48449400-48453400	Weak transcription	Ovary	ovary
43	chr12:48449400-48453600	Weak transcription	Fetal Stomach	stomach
44	chr12:48449400-48453600	Weak transcription	Lung	lung
45	chr12:48449400-48453600	Weak transcription	Pancreas	Pancrea
46	chr12:48449400-48464400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr12:48452000-48452800	Strong transcription	HSMM	muscle
48	chr12:48452000-48453000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr12:48452000-48453600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr12:48452000-48453800	Weak transcription	Fetal Intestine Small	intestine

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