Variant report

Variant	nsv546939
Chromosome Location	chr1:104056846-104068680
allele	n/a
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	ARID3A	chr1:104068425-104069462	K562	blood:	n/a	n/a
2	ARID3A	chr1:104068398-104069159	HepG2	liver:	n/a	n/a
3	ATF2	chr1:104068246-104068748	GM12878	blood:	n/a	n/a
4	ATF2	chr1:104060069-104060653	GM12878	blood:	n/a	n/a
5	ATF2	chr1:104068276-104068823	GM12878	blood:	n/a	n/a
6	ATF2	chr1:104060167-104060706	GM12878	blood:	n/a	n/a
7	BATF	chr1:104059876-104060357	GM12878	blood:	n/a	chr1:104060014-104060024 chr1:104060094-104060103
8	BCLAF1	chr1:104057548-104057847	GM12878	blood:	n/a	n/a
9	BCLAF1	chr1:104068286-104068884	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:104067893-104069179	K562	blood:	n/a	n/a
11	BHLHE40	chr1:104068347-104069164	GM12878	blood:	n/a	n/a
12	BRCA1	chr1:104068257-104069233	Hela-S3	cervix:	n/a	chr1:104068541-104068550
13	BRCA1	chr1:104068338-104068741	HepG2	liver:	n/a	chr1:104068541-104068550
14	BRCA1	chr1:104068347-104068826	GM12878	blood:	n/a	chr1:104068541-104068550
15	BRCA1	chr1:104068332-104068755	H1-hESC	embryonic stem cell:	n/a	chr1:104068541-104068550
16	CBX3	chr1:104068298-104068668	K562	blood:	n/a	n/a
17	CBX3	chr1:104068335-104068703	K562	blood:	n/a	n/a
18	CCNT2	chr1:104068442-104069153	K562	blood:	n/a	n/a
19	CEBPB	chr1:104059336-104059587	IMR90	lung:	n/a	n/a
20	CEBPB	chr1:104067855-104068146	K562	blood:	n/a	n/a
21	CEBPB	chr1:104063491-104063778	IMR90	lung:	n/a	n/a
22	CHD1	chr1:104068464-104069301	GM12878	blood:	n/a	chr1:104068541-104068550
23	CHD2	chr1:104068225-104069285	GM12878	blood:	n/a	chr1:104068541-104068550
24	CHD2	chr1:104068248-104069181	K562	blood:	n/a	chr1:104068541-104068550
25	CHD2	chr1:104068290-104068970	H1-hESC	embryonic stem cell:	n/a	chr1:104068541-104068550
26	CHD2	chr1:104068272-104068999	HepG2	liver:	n/a	chr1:104068541-104068550
27	CHD2	chr1:104067937-104068012	K562	blood:	n/a	n/a
28	CHD2	chr1:104067900-104069278	Hela-S3	cervix:	n/a	chr1:104068541-104068550
29	CREB1	chr1:104068364-104068701	A549	lung:	n/a	n/a
30	CREB1	chr1:104068282-104068752	A549	lung:	n/a	n/a
31	CTBP2	chr1:104068522-104069274	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr1:104068660-104068810	GM12874	blood:	n/a	n/a
33	CTCF	chr1:104068680-104068830	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr1:104057720-104057870	MCF-7	breast:	n/a	chr1:104057729-104057750 chr1:104057739-104057747
35	CTCF	chr1:104057680-104057830	HEEpiC	esophagus:	n/a	chr1:104057729-104057750 chr1:104057739-104057747
36	CTCF	chr1:104057640-104057790	HCT-116	colon:	n/a	chr1:104057729-104057750 chr1:104057739-104057747
37	CTCF	chr1:104057624-104057853	Kidney_OC	kidney:	n/a	chr1:104057729-104057750 chr1:104057739-104057747
38	CTCF	chr1:104057660-104057810	HCFaa	heart:	n/a	chr1:104057729-104057750 chr1:104057739-104057747
39	CTCF	chr1:104057680-104057830	HBMEC	blood vessel:	n/a	chr1:104057729-104057750 chr1:104057739-104057747
40	CTCF	chr1:104057557-104057826	A549	lung:	n/a	chr1:104057729-104057750 chr1:104057739-104057747
41	CTCF	chr1:104057641-104057840	GM10248	blood:	n/a	chr1:104057729-104057750 chr1:104057739-104057747
42	CTCF	chr1:104068660-104068810	HMEC	breast:	n/a	n/a
43	CTCF	chr1:104057619-104057836	HepG2	liver:	n/a	chr1:104057729-104057750 chr1:104057739-104057747
44	CTCF	chr1:104057604-104057878	Lung_OC	lung:	n/a	chr1:104057729-104057750 chr1:104057739-104057747
45	CTCF	chr1:104057620-104057770	HFF	foreskin:	n/a	chr1:104057729-104057750 chr1:104057739-104057747
46	CTCF	chr1:104057720-104057870	AoAF	blood vessel:	n/a	chr1:104057729-104057750 chr1:104057739-104057747
47	CTCF	chr1:104057660-104057810	AG10803	skin:	n/a	chr1:104057729-104057750 chr1:104057739-104057747
48	CTCF	chr1:104057501-104057985	GM12878	blood:	n/a	chr1:104057729-104057750 chr1:104057739-104057747
49	CTCF	chr1:104057680-104057824	GM20000	blood:	n/a	chr1:104057729-104057750 chr1:104057739-104057747
50	CTCF	chr1:104068620-104068770	GM06990	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:104068118-104068168	CMK	blood:	n/a
2	chr1:104065263-104065313	HRPEpiC	eye:	n/a
3	chr1:104068121-104068171	PANC-1	pancreas:	n/a
4	chr1:104068490-104068540	HRPEpiC	eye:	n/a
5	chr1:104068490-104068540	NB4	blood:	n/a
6	chr1:104068567-104068617	HPAEpiC	pulmonary alveolar:	n/a
7	chr1:104065263-104065313	HMEC	breast:	n/a
8	chr1:104068121-104068171	HRPEpiC	eye:	n/a
9	chr1:104068312-104068362	ProgFib	skin:	n/a
10	chr1:104068603-104068653	HCPEpiC	choroid plexus:	n/a
11	chr1:104068121-104068171	T-47D	breast:	n/a
12	chr1:104068567-104068617	AG10803	skin:	n/a
13	chr1:104068664-104068714	HAEpiC	amniotic membrane:	n/a
14	chr1:104068301-104068351	ProgFib	skin:	n/a
15	chr1:104068603-104068653	HRE	kidney:	n/a
16	chr1:104068312-104068362	HEK293	kidney:	embryo
17	chr1:104068118-104068168	SK-N-SH_RA	brain:	n/a
18	chr1:104068567-104068617	Hepatocyte	liver:	n/a
19	chr1:104068567-104068617	Caco-2	colon:	n/a
20	chr1:104068312-104068362	T-47D	breast:	n/a
21	chr1:104068419-104068469	ovcar-3	ovarian:	n/a
22	chr1:104068664-104068714	AG04449	skin:	fetal
23	chr1:104068419-104068469	HUVEC	blood vessel:	n/a
24	chr1:104068567-104068617	HCF	heart:	n/a
25	chr1:104068121-104068171	GM12892	blood:	n/a
26	chr1:104068664-104068714	HRE	kidney:	n/a
27	chr1:104068121-104068171	AG04450	lung:	fetal
28	chr1:104068488-104068538	HepG2	liver:	n/a
29	chr1:104068312-104068362	HIPEpiC	eye:	n/a
30	chr1:104068301-104068351	LNCaP	prostate:	n/a
31	chr1:104068312-104068362	H1-hESC	embryonic stem cell:	embryo
32	chr1:104065263-104065313	SAEC	small airway:	n/a
33	chr1:104068118-104068168	LNCaP	prostate:	n/a
34	chr1:104068567-104068617	CMK	blood:	n/a
35	chr1:104068488-104068538	HMEC	breast:	n/a
36	chr1:104068121-104068171	NHDF-neo	bronchial:	n/a
37	chr1:104068121-104068171	A549	lung:	n/a
38	chr1:104068603-104068653	IMR90	lung:	fetal
39	chr1:104068664-104068714	IMR90	lung:	fetal
40	chr1:104068121-104068171	HCM	heart:	n/a
41	chr1:104068490-104068540	HIPEpiC	eye:	n/a
42	chr1:104068301-104068351	GM12892	blood:	n/a
43	chr1:104068488-104068538	HUVEC	blood vessel:	n/a
44	chr1:104068312-104068362	NHBE	bronchial:	n/a
45	chr1:104068118-104068168	HEEpiC	esophagus:	n/a
46	chr1:104068121-104068171	HAEpiC	amniotic membrane:	n/a
47	chr1:104068118-104068168	ProgFib	skin:	n/a
48	chr1:104068603-104068653	HRPEpiC	eye:	n/a
49	chr1:104068664-104068714	K562	blood:	n/a
50	chr1:104068603-104068653	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:104068563..104070409-chr1:104091369..104094625,4	MCF-7	breast:
2	chr1:104068373..104071907-chr1:104081557..104086760,7	K562	blood:
3	chr1:104067956..104068800-chr18:9474823..9475445,2	Hela-S3	cervix:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMY1B-1	chr1:104068018-104068105	XLOC_000945
2	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
3	lnc-AMY1B-1	chr1:104068018-104068083	ENSG00000224613.2
4	lnc-AMY1B-1	chr1:104068018-104068115	XLOC_000945
5	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
6	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
7	lnc-RNPC3-4	chr1:104066184-104066501	NONHSAT004893

Variant related genes	Relation type
RNPC3	TF binding region
RN7SKP285	TF binding region
ENSG00000224613	TF binding region
RNPC3	CpG island
RN7SKP285	CpG island
ENSG00000224613	CpG island
ENSG00000017797	chromatin interactions
ENSG00000185946	chromatin interactions
TOMM34	miRNA target sites

Extended variants
information (count: 371 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:371 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10785714	chr1:104056846-104056847	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs546189635	chr1:104056905-104056906	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182726744	chr1:104056922-104056923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545046741	chr1:104056928-104056929	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs564028942	chr1:104056948-104056949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531532989	chr1:104057018-104057019	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368146428	chr1:104057067-104057068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs149512677	chr1:104057078-104057079	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs564842336	chr1:104057079-104057080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147180593	chr1:104057090-104057091	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187367173	chr1:104057158-104057159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140660370	chr1:104057175-104057176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144508432	chr1:104057210-104057211	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565634744	chr1:104057213-104057214	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539439348	chr1:104057235-104057236	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs114488891	chr1:104057310-104057311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570349929	chr1:104057376-104057377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537374005	chr1:104057526-104057527	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555901111	chr1:104057569-104057570	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544025374	chr1:104057579-104057580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192044420	chr1:104057589-104057590	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs535070141	chr1:104057756-104057757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs182973825	chr1:104057758-104057759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs11184298	chr1:104057790-104057791	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs544984086	chr1:104057829-104057830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563368530	chr1:104057919-104057920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs547734133	chr1:104057936-104057937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs187555883	chr1:104057937-104057938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569623001	chr1:104057967-104057968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538164785	chr1:104057968-104057969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs12084058	chr1:104058017-104058018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs564840004	chr1:104058129-104058130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs529083876	chr1:104058134-104058135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547617960	chr1:104058152-104058153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs182716379	chr1:104058156-104058157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566138893	chr1:104058189-104058190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527322168	chr1:104058202-104058203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs551375633	chr1:104058207-104058208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs569690914	chr1:104058209-104058210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs527879385	chr1:104058227-104058228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs188150182	chr1:104058230-104058231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs369502203	chr1:104058239-104058240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs192713521	chr1:104058258-104058259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs115213012	chr1:104058314-104058315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs184466366	chr1:104058335-104058336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs190574107	chr1:104058337-104058338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs374831074	chr1:104058352-104058353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147781039	chr1:104058362-104058363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs570751530	chr1:104058412-104058413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs368961996	chr1:104058457-104058458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	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
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Cancer	22429812	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Lung cancer	17086460	CNVD
Gastric cancer	16891809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Multiple myeloma	17550852	CNVD
Schizophrenia	20967226	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	19287141	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:310 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:104043200-104067400	Weak transcription	Aorta	Aorta
2	chr1:104050000-104067400	Weak transcription	Left Ventricle	heart
3	chr1:104054400-104066200	Weak transcription	Psoas Muscle	Psoas
4	chr1:104054800-104062600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr1:104056200-104060600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:104056400-104057600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr1:104056400-104059800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr1:104056800-104058400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:104056800-104058400	Weak transcription	Osteobl	bone
10	chr1:104057200-104058200	Weak transcription	HMEC	breast
11	chr1:104057600-104059000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr1:104057800-104058600	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr1:104058200-104060400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr1:104058200-104060400	Enhancers	NH-A	brain
15	chr1:104058200-104060600	Enhancers	HMEC	breast
16	chr1:104058400-104059800	Enhancers	Osteobl	bone
17	chr1:104058400-104060400	Enhancers	NHEK	skin
18	chr1:104058400-104060600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr1:104058400-104060600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr1:104058600-104059600	Weak transcription	Primary T helper cells PMA-I stimulated	--
21	chr1:104058800-104060000	Enhancers	Muscle Satellite Cultured Cells	--
22	chr1:104058800-104060600	Enhancers	HUVEC	blood vessel
23	chr1:104059000-104059200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr1:104059200-104060400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:104059400-104060200	Enhancers	GM12878-XiMat	blood
26	chr1:104059600-104060000	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr1:104059800-104067400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr1:104059800-104067400	Weak transcription	Osteobl	bone
29	chr1:104060200-104060400	Enhancers	Fetal Heart	heart
30	chr1:104060200-104060400	Enhancers	Sigmoid Colon	Sigmoid Colon
31	chr1:104060200-104060400	Flanking Active TSS	GM12878-XiMat	blood
32	chr1:104060400-104060800	Active TSS	GM12878-XiMat	blood
33	chr1:104060400-104067400	Weak transcription	Fetal Heart	heart
34	chr1:104060600-104067200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:104060600-104067400	Weak transcription	HUVEC	blood vessel
36	chr1:104060800-104061000	Flanking Active TSS	GM12878-XiMat	blood
37	chr1:104061000-104067400	Weak transcription	GM12878-XiMat	blood
38	chr1:104062400-104067400	Weak transcription	Right Ventricle	heart
39	chr1:104062600-104062800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr1:104062800-104063600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr1:104063600-104064800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr1:104064000-104064200	Enhancers	Hela-S3	cervix
43	chr1:104064200-104067200	Weak transcription	Hela-S3	cervix
44	chr1:104064800-104065000	Enhancers	Pancreas	Pancrea
45	chr1:104064800-104067400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr1:104065000-104067400	Weak transcription	Pancreas	Pancrea
47	chr1:104065200-104065400	Enhancers	Fetal Intestine Small	intestine
48	chr1:104065200-104067800	Enhancers	Fetal Intestine Large	intestine
49	chr1:104065400-104066200	Weak transcription	Fetal Intestine Small	intestine
50	chr1:104065400-104066600	Weak transcription	Skeletal Muscle Female	skeletal muscle

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