Variant report

Variant	rs180890883
Chromosome Location	chr2:55514005-55514006
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:55513717..55517670-chr2:55518024..55521740,6	K562	blood:
2	chr2:55495418..55497283-chr2:55513358..55515845,2	MCF-7	breast:
3	chr2:55509373..55510992-chr2:55512785..55514521,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000085760	Chromatin interaction
ENSG00000162997	Chromatin interaction

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

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv522016	chr2:55404794-55560298	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv874156	chr2:55474026-55636351	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv874157	chr2:55483020-55571085	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	esv1799450	chr2:55494904-55520842	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
5	nsv874158	chr2:55513738-55619923	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv874159	chr2:55513738-55636351	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:55501000-55517000	Weak transcription	Hela-S3	cervix
2	chr2:55509000-55541200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:55509400-55515600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:55509400-55545200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr2:55509600-55522600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr2:55509800-55514600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr2:55509800-55518600	Weak transcription	HMEC	breast
8	chr2:55509800-55521800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr2:55510000-55514400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr2:55510000-55515400	Weak transcription	Brain Substantia Nigra	brain
11	chr2:55510000-55516200	Weak transcription	Fetal Lung	lung
12	chr2:55510000-55518800	Weak transcription	Brain Angular Gyrus	brain
13	chr2:55510000-55521600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr2:55510000-55521600	Weak transcription	Brain Cingulate Gyrus	brain
15	chr2:55510000-55521800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr2:55510000-55521800	Weak transcription	Fetal Brain Male	brain
17	chr2:55510000-55521800	Weak transcription	NHEK	skin
18	chr2:55510000-55522000	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr2:55510000-55522200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr2:55510000-55522200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr2:55510000-55522400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr2:55510000-55522400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr2:55510000-55522600	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr2:55510000-55541600	Weak transcription	Esophagus	oesophagus
25	chr2:55510000-55553600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr2:55510000-55578800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr2:55510200-55514600	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr2:55510200-55516000	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr2:55510200-55516200	Weak transcription	NHDF-Ad	bronchial
30	chr2:55510200-55516600	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr2:55510200-55517400	Weak transcription	Fetal Brain Female	brain
32	chr2:55510200-55519200	Weak transcription	Ovary	ovary
33	chr2:55510200-55520600	Weak transcription	HSMMtube	muscle
34	chr2:55510200-55521800	Weak transcription	Fetal Kidney	kidney
35	chr2:55510200-55522200	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr2:55510200-55522400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr2:55510200-55522400	Weak transcription	NHLF	lung
38	chr2:55510200-55522600	Weak transcription	Aorta	Aorta
39	chr2:55510200-55542200	Weak transcription	Fetal Intestine Large	intestine
40	chr2:55510200-55559000	Weak transcription	Psoas Muscle	Psoas
41	chr2:55510200-55616800	Weak transcription	Fetal Intestine Small	intestine
42	chr2:55510400-55515200	Weak transcription	HUVEC	blood vessel
43	chr2:55510400-55515600	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr2:55510400-55522400	Weak transcription	Left Ventricle	heart
45	chr2:55510400-55529000	Weak transcription	Placenta	Placenta
46	chr2:55510600-55514400	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr2:55510600-55514800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr2:55510600-55519400	Weak transcription	Primary B cells from cord blood	blood
49	chr2:55510600-55521800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr2:55510600-55522400	Weak transcription	A549	lung

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