Variant report

Variant	esv3457027
Chromosome Location	chr2:100103045-100105893
allele	n/a
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:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:100091970..100094649-chr2:100104238..100106048,2	MCF-7	breast:
2	chr2:100104879..100106389-chr2:100120710..100122893,2	MCF-7	breast:
3	chr2:99950324..99955285-chr2:100104603..100108030,8	MCF-7	breast:
4	chr2:100099713..100102517-chr2:100102817..100104971,3	MCF-7	breast:
5	chr2:100064922..100067755-chr2:100103657..100105818,3	MCF-7	breast:
6	chr2:99950963..99955972-chr2:100104881..100108306,7	MCF-7	breast:
7	chr2:99952415..99954577-chr2:100101593..100103318,2	MCF-7	breast:
8	chr2:99951055..99957153-chr2:100104418..100108530,14	K562	blood:
9	chr2:100075556..100080404-chr2:100103648..100108163,7	K562	blood:
10	chr11:63580406..63581266-chr2:100105797..100106443,2	MCF-7	breast:
11	chr2:99952384..99954745-chr2:100101155..100103970,2	K562	blood:
12	chr2:100019850..100022413-chr2:100104870..100107869,3	MCF-7	breast:
13	chr2:100045644..100048567-chr2:100103283..100105124,2	K562	blood:
14	chr2:99951256..99955616-chr2:100104663..100107649,9	K562	blood:
15	chr2:99485026..99487433-chr2:100105196..100107704,3	MCF-7	breast:
16	chr2:100103127..100105220-chr2:100105235..100107072,2	MCF-7	breast:
17	chr2:99796371..99799059-chr2:100100777..100103682,2	MCF-7	breast:
18	chr2:100104533..100107300-chr2:100936927..100940750,3	MCF-7	breast:
19	chr2:99796217..99799127-chr2:100105224..100108883,4	K562	blood:
20	chr2:100019781..100021613-chr2:100105810..100107711,2	MCF-7	breast:
21	chr2:100011720..100013891-chr2:100102274..100104165,2	K562	blood:
22	chr2:99796217..99798600-chr2:100104908..100107681,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000170500	chromatin interactions
ENSG00000273306	chromatin interactions
ENSG00000158417	chromatin interactions
ENSG00000241962	chromatin interactions
ENSG00000185414	chromatin interactions
ENSG00000115514	chromatin interactions
ENSG00000158411	chromatin interactions
ENSG00000135945	chromatin interactions
ENSG00000168005	chromatin interactions
ENSG00000196872	chromatin interactions

Extended variants
information (count: 93 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:93 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185000737	chr2:100103070-100103071	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs564193112	chr2:100103171-100103172	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs532914543	chr2:100103257-100103258	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs535827045	chr2:100103324-100103325	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs527752389	chr2:100103347-100103348	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs569793003	chr2:100103359-100103360	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs78254852	chr2:100103380-100103381	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs532683218	chr2:100103387-100103388	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs189463633	chr2:100103415-100103416	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs147466475	chr2:100103428-100103429	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs566004538	chr2:100103465-100103466	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs375675652	chr2:100103512-100103513	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs114222077	chr2:100103513-100103514	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs553903197	chr2:100103637-100103638	Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs553909018	chr2:100103643-100103644	Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs572489853	chr2:100103660-100103661	Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs377674533	chr2:100103713-100103714	Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs577262791	chr2:100103776-100103777	Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs545899891	chr2:100103781-100103782	Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs139361076	chr2:100103804-100103805	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs556625814	chr2:100103981-100103982	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs576180712	chr2:100103989-100103990	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs181849723	chr2:100104097-100104098	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs566094023	chr2:100104100-100104101	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs562010461	chr2:100104152-100104153	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs143165153	chr2:100104158-100104159	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs541000628	chr2:100104184-100104185	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs563972955	chr2:100104237-100104238	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs186968586	chr2:100104266-100104267	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs115525963	chr2:100104370-100104371	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs370328392	chr2:100104459-100104460	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs563378234	chr2:100104558-100104559	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs147516707	chr2:100104613-100104614	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs80215199	chr2:100104694-100104695	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs565955824	chr2:100104701-100104702	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs528419164	chr2:100104702-100104703	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs547759028	chr2:100104723-100104724	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs570714798	chr2:100104737-100104738	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs374710192	chr2:100104754-100104755	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs202217893	chr2:100104779-100104780	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs539822720	chr2:100104799-100104800	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs556354090	chr2:100104825-100104826	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs569830335	chr2:100105026-100105027	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs543278811	chr2:100105041-100105042	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs561999382	chr2:100105083-100105084	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs535638136	chr2:100105099-100105100	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs191641933	chr2:100105113-100105114	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs555569767	chr2:100105125-100105126	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs572404077	chr2:100105166-100105167	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs541403203	chr2:100105185-100105186	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioblastoma multiforme	21138945	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:562 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:100076200-100105000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:100076600-100104200	Weak transcription	NHLF	lung
3	chr2:100078800-100105000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr2:100079200-100104000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr2:100080400-100103200	Weak transcription	Fetal Stomach	stomach
6	chr2:100080800-100103200	Weak transcription	HSMM	muscle
7	chr2:100088000-100104800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr2:100091400-100103200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr2:100091800-100103400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr2:100092600-100103600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr2:100092600-100104200	Weak transcription	Osteobl	bone
12	chr2:100092800-100103600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr2:100092800-100104600	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr2:100092800-100105000	Weak transcription	Placenta	Placenta
15	chr2:100094000-100103400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr2:100094800-100104800	Weak transcription	Colonic Mucosa	Colon
17	chr2:100095200-100103400	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr2:100095400-100103400	Weak transcription	HUVEC	blood vessel
19	chr2:100095600-100103400	Weak transcription	Primary B cells from peripheral blood	blood
20	chr2:100095600-100103600	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr2:100095600-100103600	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr2:100097200-100104000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr2:100097200-100104200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr2:100097200-100105000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr2:100097800-100103200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr2:100098000-100103200	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr2:100098600-100105200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr2:100098600-100105200	Weak transcription	Gastric	stomach
29	chr2:100098800-100103200	Weak transcription	Adipose Nuclei	Adipose
30	chr2:100098800-100103400	Weak transcription	Brain Substantia Nigra	brain
31	chr2:100098800-100103400	Weak transcription	Stomach Mucosa	stomach
32	chr2:100098800-100104800	Weak transcription	Spleen	Spleen
33	chr2:100098800-100105000	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr2:100098800-100105200	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr2:100099000-100103200	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr2:100099000-100103200	Weak transcription	Fetal Intestine Small	intestine
37	chr2:100099000-100103200	Weak transcription	Rectal Smooth Muscle	rectum
38	chr2:100099000-100103200	Weak transcription	NHDF-Ad	bronchial
39	chr2:100099000-100103600	Weak transcription	Primary T cells from cord blood	blood
40	chr2:100099000-100103800	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr2:100099000-100105000	Weak transcription	Pancreas	Pancrea
42	chr2:100099200-100103600	Weak transcription	Primary hematopoietic stem cells	blood
43	chr2:100099800-100103600	Enhancers	HMEC	breast
44	chr2:100099800-100103800	Enhancers	Fetal Heart	heart
45	chr2:100100000-100103200	Enhancers	Psoas Muscle	Psoas
46	chr2:100100200-100103200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr2:100100200-100103200	Enhancers	HepG2	liver
48	chr2:100100200-100103800	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chr2:100100600-100103200	Enhancers	Primary T helper cells PMA-I stimulated	--
50	chr2:100100800-100105000	Weak transcription	Esophagus	oesophagus

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