Variant report

Variant	esv3517833
Chromosome Location	chr1:145124709-145183497
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1043)
CpG islands
(count:306)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1043 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:145129724-145130023	GM12878	blood:	n/a	n/a
2	ATF2	chr1:145129655-145130099	GM12878	blood:	n/a	n/a
3	ATF2	chr1:145159486-145159715	GM12878	blood:	n/a	n/a
4	BATF	chr1:145138847-145139218	GM12878	blood:	n/a	n/a
5	BATF	chr1:145129688-145130263	GM12878	blood:	n/a	n/a
6	BATF	chr1:145128460-145128759	GM12878	blood:	n/a	n/a
7	BATF	chr1:145154309-145155270	GM12878	blood:	n/a	n/a
8	BATF	chr1:145153039-145153342	GM12878	blood:	n/a	n/a
9	BATF	chr1:145171479-145171789	GM12878	blood:	n/a	n/a
10	BATF	chr1:145154286-145155318	GM12878	blood:	n/a	n/a
11	BATF	chr1:145159043-145159865	GM12878	blood:	n/a	n/a
12	BATF	chr1:145129645-145130292	GM12878	blood:	n/a	n/a
13	BATF	chr1:145152894-145153398	GM12878	blood:	n/a	n/a
14	BATF	chr1:145138847-145139124	GM12878	blood:	n/a	n/a
15	BATF	chr1:145139292-145139563	GM12878	blood:	n/a	n/a
16	BATF	chr1:145159059-145159858	GM12878	blood:	n/a	n/a
17	BCL11A	chr1:145129685-145130188	GM12878	blood:	n/a	chr1:145129761-145129770
18	BCL11A	chr1:145159061-145159897	GM12878	blood:	n/a	chr1:145159481-145159490
19	BCL11A	chr1:145153041-145153282	GM12878	blood:	n/a	n/a
20	BCL11A	chr1:145154599-145155238	GM12878	blood:	n/a	n/a
21	BCL11A	chr1:145159326-145159774	GM12878	blood:	n/a	chr1:145159481-145159490
22	BCL11A	chr1:145159097-145159259	GM12878	blood:	n/a	n/a
23	BCL11A	chr1:145154296-145155300	GM12878	blood:	n/a	n/a
24	BCL11A	chr1:145152888-145153390	GM12878	blood:	n/a	n/a
25	BCL11A	chr1:145138795-145139137	GM12878	blood:	n/a	n/a
26	BCL11A	chr1:145144553-145144865	GM12878	blood:	n/a	n/a
27	BCL11A	chr1:145139734-145139968	GM12878	blood:	n/a	chr1:145139838-145139847
28	BCL11A	chr1:145139604-145139939	GM12878	blood:	n/a	chr1:145139838-145139847
29	BCL11A	chr1:145129672-145130317	GM12878	blood:	n/a	chr1:145129761-145129770
30	BCL11A	chr1:145138954-145139127	GM12878	blood:	n/a	n/a
31	BCL11A	chr1:145154296-145154577	GM12878	blood:	n/a	n/a
32	BCLAF1	chr1:145129649-145130203	GM12878	blood:	n/a	chr1:145129761-145129770
33	BHLHE40	chr1:145159350-145159641	GM12878	blood:	n/a	n/a
34	BHLHE40	chr1:145129772-145130100	GM12878	blood:	n/a	n/a
35	CBX3	chr1:145144450-145144949	K562	blood:	n/a	n/a
36	CBX3	chr1:145138713-145140124	K562	blood:	n/a	n/a
37	CEBPB	chr1:145129721-145130225	GM12878	blood:	n/a	n/a
38	CEBPB	chr1:145127933-145128246	K562	blood:	n/a	n/a
39	CEBPB	chr1:145144618-145144655	IMR90	lung:	n/a	n/a
40	CEBPB	chr1:145173818-145173894	HepG2	liver:	n/a	n/a
41	CEBPB	chr1:145127930-145128247	K562	blood:	n/a	n/a
42	CEBPB	chr1:145159283-145159768	GM12878	blood:	n/a	n/a
43	CEBPB	chr1:145160809-145160847	IMR90	lung:	n/a	n/a
44	CEBPB	chr1:145181255-145181435	A549	lung:	n/a	n/a
45	CEBPB	chr1:145159615-145159623	IMR90	lung:	n/a	n/a
46	CEBPD	chr1:145139668-145140151	K562	blood:	n/a	n/a
47	CHD1	chr1:145129599-145130344	IMR90	lung:	n/a	n/a
48	CHD1	chr1:145160716-145160940	IMR90	lung:	n/a	n/a
49	CHD2	chr1:145129850-145130048	GM12878	blood:	n/a	n/a
50	CTCF	chr1:145126820-145126970	HCM	heart:	n/a	chr1:145126948-145126969 chr1:145126949-145126962 chr1:145126946-145126964

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:145139896-145139946	HNPCEpiC	eye:	n/a
2	chr1:145139896-145139946	HNPCEpiC	eye:	n/a
3	chr1:145139063-145139113	NHBE	bronchial:	n/a
4	chr1:145139473-145139523	NH-A	brain:	n/a
5	chr1:145139896-145139946	HRCEpiC	kidney:	n/a
6	chr1:145139679-145139729	GM06990	blood:	n/a
7	chr1:145139063-145139113	HRE	kidney:	n/a
8	chr1:145139908-145139958	AG09309	skin:	n/a
9	chr1:145139679-145139729	NT2-D1	testis:	n/a
10	chr1:145139896-145139946	AG10803	skin:	n/a
11	chr1:145139473-145139523	HCPEpiC	choroid plexus:	n/a
12	chr1:145139063-145139113	ProgFib	skin:	n/a
13	chr1:145139063-145139113	HCM	heart:	n/a
14	chr1:145139908-145139958	Caco-2	colon:	n/a
15	chr1:145139896-145139946	ovcar-3	ovarian:	n/a
16	chr1:145139896-145139946	PrEC	prostate:	n/a
17	chr1:145139679-145139729	HRPEpiC	eye:	n/a
18	chr1:145139908-145139958	H1-hESC	embryonic stem cell:	embryo
19	chr1:145139908-145139958	ECC-1	luminal epithelium:	n/a
20	chr1:145139908-145139958	ovcar-3	ovarian:	n/a
21	chr1:145139896-145139946	HUVEC	blood vessel:	n/a
22	chr1:145139679-145139729	SAEC	small airway:	n/a
23	chr1:145139896-145139946	NHBE	bronchial:	n/a
24	chr1:145139679-145139729	HNPCEpiC	eye:	n/a
25	chr1:145139908-145139958	AoSMC	blood vessel:	n/a
26	chr1:145139908-145139958	PFSK-1	brain:	n/a
27	chr1:145139063-145139113	HPAEpiC	pulmonary alveolar:	n/a
28	chr1:145139679-145139729	AoSMC	blood vessel:	n/a
29	chr1:145139063-145139113	HEK293	kidney:	embryo
30	chr1:145139908-145139958	GM12891	blood:	n/a
31	chr1:145139473-145139523	RPTEC	kidney:	n/a
32	chr1:145139063-145139113	HAEpiC	amniotic membrane:	n/a
33	chr1:145139908-145139958	HEK293	kidney:	embryo
34	chr1:145139473-145139523	IMR90	lung:	fetal
35	chr1:145139896-145139946	NB4	blood:	n/a
36	chr1:145139063-145139113	CMK	blood:	n/a
37	chr1:145139473-145139523	NT2-D1	testis:	n/a
38	chr1:145139908-145139958	BE2_C	brain:	n/a
39	chr1:145139473-145139523	GM12878	blood:	n/a
40	chr1:145139063-145139113	MCF-7	breast:	n/a
41	chr1:145139679-145139729	HepG2	liver:	n/a
42	chr1:145139679-145139729	HEK293	kidney:	embryo
43	chr1:145139473-145139523	PANC-1	pancreas:	n/a
44	chr1:145139896-145139946	HEEpiC	esophagus:	n/a
45	chr1:145139896-145139946	K562	blood:	n/a
46	chr1:145139473-145139523	SKMC	muscle:	n/a
47	chr1:145139896-145139946	BE2_C	brain:	n/a
48	chr1:145139063-145139113	GM12892	blood:	n/a
49	chr1:145139473-145139523	AG04449	skin:	fetal
50	chr1:145139908-145139958	HCM	heart:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:145138455..145140955-chr1:145381729..145384293,2	MCF-7	breast:
2	chr1:145124431..145127072-chr1:145381606..145383214,2	K562	blood:
3	chr1:120688084..120688694-chr1:145126764..145127269,2	MCF-7	breast:
4	chr1:145130093..145132779-chr1:145291052..145292604,2	K562	blood:
5	chr1:145134469..145136133-chr1:145381459..145383025,2	MCF-7	breast:
6	chr1:145128744..145130626-chr1:145382573..145384459,2	MCF-7	breast:
7	chr1:145137959..145140660-chr1:145381811..145384748,2	K562	blood:

No data

Variant related genes	Relation type
NUDT4P1	TF binding region
RNU6-1071P	TF binding region
NUDT4P1	CpG island
RNU6-1071P	CpG island
ENSG00000233396	chromatin interactions
ENSG00000201558	chromatin interactions

Extended variants
information (count: 1775 )
Associated
traits (count: 171 )

Variant overlapped rSNPs/rCNVs (count:1775 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587682471	chr1:145124712-145124713	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs587718836	chr1:145124717-145124718	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs587593955	chr1:145124744-145124745	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs3927721	chr1:145124804-145124805	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs57861480	chr1:145124808-145124809	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs587722050	chr1:145124846-145124847	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs4265385	chr1:145124860-145124861	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs587634705	chr1:145124870-145124871	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs587669459	chr1:145124905-145124906	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs587747149	chr1:145124921-145124922	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs587622503	chr1:145124922-145124923	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs374858960	chr1:145124940-145124941	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs3927722	chr1:145124975-145124976	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs587693617	chr1:145124994-145124995	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs587757062	chr1:145125054-145125055	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs587622988	chr1:145125055-145125056	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs199561588	chr1:145125103-145125104	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs587686380	chr1:145125204-145125205	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs3927723	chr1:145125230-145125231	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs112094261	chr1:145125235-145125236	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs587771716	chr1:145125279-145125280	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs587672906	chr1:145125289-145125290	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs587727625	chr1:145125303-145125304	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs587774410	chr1:145125320-145125321	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs111708331	chr1:145125327-145125328	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs142987667	chr1:145125340-145125341	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs587637994	chr1:145125353-145125354	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs587711872	chr1:145125409-145125410	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs74467869	chr1:145125421-145125422	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs587663854	chr1:145125426-145125427	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs587713044	chr1:145125457-145125458	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs587612875	chr1:145125469-145125470	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs587667461	chr1:145125474-145125475	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs370979410	chr1:145125475-145125476	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs200679982	chr1:145125495-145125496	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs587620455	chr1:145125611-145125612	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs201324456	chr1:145125740-145125741	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs587727969	chr1:145125742-145125743	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs147685693	chr1:145125761-145125762	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs71664039	chr1:145125812-145125813	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs71664040	chr1:145125862-145125863	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs71664041	chr1:145125884-145125885	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs201065629	chr1:145125919-145125920	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs587631901	chr1:145125964-145125965	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs587691438	chr1:145125986-145125987	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs587752339	chr1:145126027-145126028	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs587647867	chr1:145126031-145126032	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs144733052	chr1:145126037-145126038	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs3927724	chr1:145126055-145126056	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs587705338	chr1:145126064-145126065	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:171)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17142309	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Tetralogy of Fallot	22912587	CNVD
Bladder cancer	21909424	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	23813976	CNVD
Lung adenocarcinoma	21935476	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	19843651	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	20531469	CNVD
Autism	20858243	CNVD
Autism	22543975	CNVD
Epilepsy	20502679	CNVD
Autism	20841430	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	20808228	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21720365	CNVD

Chromatin state (count:1108 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:145097800-145130000	Weak transcription	Right Ventricle	heart
2	chr1:145113200-145129600	Weak transcription	Fetal Heart	heart
3	chr1:145115200-145130000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr1:145115600-145128200	Weak transcription	HMEC	breast
5	chr1:145116200-145130000	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr1:145116400-145130000	Weak transcription	Thymus	Thymus
7	chr1:145116800-145128200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr1:145116800-145128200	Weak transcription	Colon Smooth Muscle	Colon
9	chr1:145116800-145129600	Weak transcription	Fetal Thymus	thymus
10	chr1:145117000-145128200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr1:145117200-145128200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr1:145118400-145124800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:145118400-145125000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr1:145118400-145125000	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr1:145118400-145127200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr1:145118400-145127200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr1:145118400-145127400	Weak transcription	HSMM	muscle
18	chr1:145118400-145128200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr1:145118400-145128200	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr1:145118400-145128200	Weak transcription	Adipose Nuclei	Adipose
21	chr1:145118400-145128200	Weak transcription	Aorta	Aorta
22	chr1:145118400-145128200	Weak transcription	Liver	Liver
23	chr1:145118400-145128200	Weak transcription	HUVEC	blood vessel
24	chr1:145118400-145128200	Weak transcription	NH-A	brain
25	chr1:145118400-145128200	Weak transcription	NHLF	lung
26	chr1:145118400-145128400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr1:145118400-145128400	Weak transcription	Primary hematopoietic stem cells	blood
28	chr1:145118400-145128800	Weak transcription	Primary B cells from cord blood	blood
29	chr1:145118400-145130000	Weak transcription	Gastric	stomach
30	chr1:145118400-145130000	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr1:145120600-145126200	Weak transcription	Osteobl	bone
32	chr1:145122600-145127200	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr1:145122600-145139200	Weak transcription	Right Atrium	heart
34	chr1:145122800-145128200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr1:145122800-145128400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr1:145123000-145128200	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr1:145123000-145128200	Weak transcription	NHDF-Ad	bronchial
38	chr1:145124600-145125000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr1:145124800-145126800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr1:145125000-145125200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr1:145125000-145125400	Enhancers	Muscle Satellite Cultured Cells	--
42	chr1:145125200-145126600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr1:145125400-145128200	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr1:145126200-145128200	Enhancers	Osteobl	bone
45	chr1:145126600-145127400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr1:145126800-145127000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr1:145126800-145127200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr1:145127000-145128200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
49	chr1:145127200-145127400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr1:145127200-145127400	Enhancers	Primary T helper naive cells from peripheral blood	blood

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