Variant report

Variant	nsv546940
Chromosome Location	chr1:104065653-104068782
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:462)
CpG islands
(count:672)
Chromatin interactive
region (count:3)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:462 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:104068398-104069159	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:104068425-104069462	K562	blood:	n/a	n/a
3	ATF2	chr1:104068276-104068823	GM12878	blood:	n/a	n/a
4	ATF2	chr1:104068246-104068748	GM12878	blood:	n/a	n/a
5	BCLAF1	chr1:104068286-104068884	GM12878	blood:	n/a	n/a
6	BHLHE40	chr1:104067893-104069179	K562	blood:	n/a	n/a
7	BHLHE40	chr1:104068347-104069164	GM12878	blood:	n/a	n/a
8	BRCA1	chr1:104068332-104068755	H1-hESC	embryonic stem cell:	n/a	chr1:104068541-104068550
9	BRCA1	chr1:104068338-104068741	HepG2	liver:	n/a	chr1:104068541-104068550
10	BRCA1	chr1:104068257-104069233	Hela-S3	cervix:	n/a	chr1:104068541-104068550
11	BRCA1	chr1:104068347-104068826	GM12878	blood:	n/a	chr1:104068541-104068550
12	CBX3	chr1:104068298-104068668	K562	blood:	n/a	n/a
13	CBX3	chr1:104068335-104068703	K562	blood:	n/a	n/a
14	CCNT2	chr1:104068442-104069153	K562	blood:	n/a	n/a
15	CEBPB	chr1:104067855-104068146	K562	blood:	n/a	n/a
16	CHD1	chr1:104068464-104069301	GM12878	blood:	n/a	chr1:104068541-104068550
17	CHD2	chr1:104067937-104068012	K562	blood:	n/a	n/a
18	CHD2	chr1:104068225-104069285	GM12878	blood:	n/a	chr1:104068541-104068550
19	CHD2	chr1:104068272-104068999	HepG2	liver:	n/a	chr1:104068541-104068550
20	CHD2	chr1:104068290-104068970	H1-hESC	embryonic stem cell:	n/a	chr1:104068541-104068550
21	CHD2	chr1:104067900-104069278	Hela-S3	cervix:	n/a	chr1:104068541-104068550
22	CHD2	chr1:104068248-104069181	K562	blood:	n/a	chr1:104068541-104068550
23	CREB1	chr1:104068282-104068752	A549	lung:	n/a	n/a
24	CREB1	chr1:104068364-104068701	A549	lung:	n/a	n/a
25	CTBP2	chr1:104068522-104069274	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr1:104068700-104068850	GM12864	blood:	n/a	n/a
27	CTCF	chr1:104068680-104068830	SAEC	small airway:	n/a	n/a
28	CTCF	chr1:104068640-104068790	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr1:104068676-104068850	GM12891	blood:	n/a	n/a
30	CTCF	chr1:104068680-104068830	AoAF	blood vessel:	n/a	n/a
31	CTCF	chr1:104068680-104068830	GM12868	blood:	n/a	n/a
32	CTCF	chr1:104068660-104068810	GM12874	blood:	n/a	n/a
33	CTCF	chr1:104068520-104068670	GM12873	blood:	n/a	n/a
34	CTCF	chr1:104068680-104068830	GM12865	blood:	n/a	n/a
35	CTCF	chr1:104068760-104068821	Fibrobl	skin:	n/a	n/a
36	CTCF	chr1:104068700-104068850	GM12871	blood:	n/a	n/a
37	CTCF	chr1:104068688-104068852	GM19239	blood:	n/a	n/a
38	CTCF	chr1:104068460-104068610	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr1:104068700-104068850	GM12873	blood:	n/a	n/a
40	CTCF	chr1:104068682-104068791	GM12878	blood:	n/a	n/a
41	CTCF	chr1:104068720-104068870	GM12871	blood:	n/a	n/a
42	CTCF	chr1:104068678-104068830	GM10266	blood:	n/a	n/a
43	CTCF	chr1:104068640-104068790	GM12872	blood:	n/a	n/a
44	CTCF	chr1:104068640-104068790	GM12875	blood:	n/a	n/a
45	CTCF	chr1:104068661-104068869	GM12892	blood:	n/a	n/a
46	CTCF	chr1:104068652-104068850	GM19240	blood:	n/a	n/a
47	CTCF	chr1:104068620-104068770	GM06990	blood:	n/a	n/a
48	CTCF	chr1:104068700-104068850	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr1:104068660-104068810	HMEC	breast:	n/a	n/a
50	CTCF	chr1:104068720-104068870	NHLF	lung:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:104068121-104068171	HCF	heart:	n/a
2	chr1:104068121-104068171	HCF	heart:	n/a
3	chr1:104068488-104068538	MCF10A-Er-Src	breast:	n/a
4	chr1:104068603-104068653	Caco-2	colon:	n/a
5	chr1:104068567-104068617	Caco-2	colon:	n/a
6	chr1:104068121-104068171	HRPEpiC	eye:	n/a
7	chr1:104068704-104068754	SAEC	small airway:	n/a
8	chr1:104068301-104068351	AG09319	gingival:	n/a
9	chr1:104068121-104068171	HAEpiC	amniotic membrane:	n/a
10	chr1:104068118-104068168	AG04450	lung:	fetal
11	chr1:104068312-104068362	GM19239	blood:	n/a
12	chr1:104068488-104068538	HPAEpiC	pulmonary alveolar:	n/a
13	chr1:104068490-104068540	HCF	heart:	n/a
14	chr1:104068312-104068362	HEEpiC	esophagus:	n/a
15	chr1:104068301-104068351	CMK	blood:	n/a
16	chr1:104068664-104068714	HCPEpiC	choroid plexus:	n/a
17	chr1:104068603-104068653	NHDF-neo	bronchial:	n/a
18	chr1:104068419-104068469	IMR90	lung:	fetal
19	chr1:104068704-104068754	SKMC	muscle:	n/a
20	chr1:104068603-104068653	RPTEC	kidney:	n/a
21	chr1:104068664-104068714	ovcar-3	ovarian:	n/a
22	chr1:104068312-104068362	AG04450	lung:	fetal
23	chr1:104068567-104068617	HRCEpiC	kidney:	n/a
24	chr1:104068567-104068617	RPTEC	kidney:	n/a
25	chr1:104068488-104068538	AG10803	skin:	n/a
26	chr1:104068301-104068351	HRCEpiC	kidney:	n/a
27	chr1:104068490-104068540	AG10803	skin:	n/a
28	chr1:104068301-104068351	HEEpiC	esophagus:	n/a
29	chr1:104068664-104068714	HL-60	blood:	n/a
30	chr1:104068118-104068168	Caco-2	colon:	n/a
31	chr1:104068603-104068653	SK-N-SH	brain:	n/a
32	chr1:104068419-104068469	HCPEpiC	choroid plexus:	n/a
33	chr1:104068118-104068168	HRCEpiC	kidney:	n/a
34	chr1:104068118-104068168	PrEC	prostate:	n/a
35	chr1:104068121-104068171	HIPEpiC	eye:	n/a
36	chr1:104068704-104068754	MCF-7	breast:	n/a
37	chr1:104068312-104068362	AoSMC	blood vessel:	n/a
38	chr1:104068301-104068351	BE2_C	brain:	n/a
39	chr1:104068704-104068754	HepG2	liver:	n/a
40	chr1:104068121-104068171	HEEpiC	esophagus:	n/a
41	chr1:104068488-104068538	AG09319	gingival:	n/a
42	chr1:104068567-104068617	H1-hESC	embryonic stem cell:	embryo
43	chr1:104068490-104068540	PFSK-1	brain:	n/a
44	chr1:104068118-104068168	AG04449	skin:	fetal
45	chr1:104068118-104068168	Jurkat	blood:	n/a
46	chr1:104068301-104068351	HCT-116	colon:	n/a
47	chr1:104068490-104068540	HIPEpiC	eye:	n/a
48	chr1:104068567-104068617	HMEC	breast:	n/a
49	chr1:104068419-104068469	SK-N-SH	brain:	n/a
50	chr1:104068301-104068351	NHDF-neo	bronchial:	n/a

(count:3 , 50 per page) page: 1

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

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

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

No data

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

Extended variants
information (count: 110 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:110 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10881197	chr1:104065653-104065654	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565697654	chr1:104065678-104065679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs146882909	chr1:104065682-104065683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551793418	chr1:104065697-104065698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570375068	chr1:104065729-104065730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs537239660	chr1:104065742-104065743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188329418	chr1:104065792-104065793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs567400725	chr1:104065806-104065807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs529079209	chr1:104065816-104065817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534807735	chr1:104065829-104065830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs376576262	chr1:104065924-104065925	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs140578948	chr1:104065937-104065938	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs150415211	chr1:104066022-104066023	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs138141392	chr1:104066073-104066074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181048518	chr1:104066100-104066101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs186438788	chr1:104066132-104066133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs191155795	chr1:104066138-104066139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561939027	chr1:104066140-104066141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs528964406	chr1:104066168-104066169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs181775969	chr1:104066192-104066193	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs551443467	chr1:104066193-104066194	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs149174428	chr1:104066222-104066223	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs532954282	chr1:104066234-104066235	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs551397262	chr1:104066247-104066248	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs369018462	chr1:104066287-104066288	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs570021339	chr1:104066317-104066318	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs570238730	chr1:104066318-104066319	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs186817507	chr1:104066337-104066338	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs375917152	chr1:104066371-104066372	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs146506955	chr1:104066374-104066375	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs139113880	chr1:104066435-104066436	Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs553047446	chr1:104066439-104066440	Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs113882635	chr1:104066490-104066491	Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs538638392	chr1:104066516-104066517	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs557351588	chr1:104066556-104066557	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs191317906	chr1:104066599-104066600	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs537369520	chr1:104066614-104066615	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs574028055	chr1:104066638-104066639	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs534854396	chr1:104066641-104066642	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs555233465	chr1:104066668-104066669	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs372693762	chr1:104066679-104066680	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs573886708	chr1:104066698-104066699	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs74731736	chr1:104066728-104066729	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs559481121	chr1:104066745-104066746	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs183018459	chr1:104066800-104066801	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs187710519	chr1:104066832-104066833	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs142814924	chr1:104066898-104066899	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs531069506	chr1:104066931-104066932	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs549654312	chr1:104066951-104066952	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs147394836	chr1:104066957-104066958	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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

Chromatin state (count:276 , 50 per page) page: 1 2 3 4 5 6

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	chr1:104059800-104067400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr1:104059800-104067400	Weak transcription	Osteobl	bone
6	chr1:104060400-104067400	Weak transcription	Fetal Heart	heart
7	chr1:104060600-104067200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr1:104060600-104067400	Weak transcription	HUVEC	blood vessel
9	chr1:104061000-104067400	Weak transcription	GM12878-XiMat	blood
10	chr1:104062400-104067400	Weak transcription	Right Ventricle	heart
11	chr1:104064200-104067200	Weak transcription	Hela-S3	cervix
12	chr1:104064800-104067400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr1:104065000-104067400	Weak transcription	Pancreas	Pancrea
14	chr1:104065200-104067800	Enhancers	Fetal Intestine Large	intestine
15	chr1:104065400-104066200	Weak transcription	Fetal Intestine Small	intestine
16	chr1:104065400-104066600	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr1:104065800-104066400	Enhancers	Skeletal Muscle Male	skeletal muscle
18	chr1:104065800-104067800	Weak transcription	Fetal Stomach	stomach
19	chr1:104066200-104066400	Enhancers	Fetal Intestine Small	intestine
20	chr1:104066200-104066400	Enhancers	Fetal Muscle Leg	muscle
21	chr1:104066200-104066400	Enhancers	Psoas Muscle	Psoas
22	chr1:104066200-104067400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
23	chr1:104066400-104066600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr1:104066400-104067200	Weak transcription	Fetal Intestine Small	intestine
25	chr1:104066400-104067400	Active TSS	Psoas Muscle	Psoas
26	chr1:104066400-104067400	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr1:104066600-104067000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr1:104066600-104067600	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr1:104066800-104067400	Enhancers	Dnd41	blood
30	chr1:104066800-104067400	Enhancers	K562	blood
31	chr1:104067000-104067400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr1:104067000-104067400	Enhancers	HepG2	liver
33	chr1:104067000-104067400	Enhancers	NHEK	skin
34	chr1:104067000-104067600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr1:104067200-104067400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr1:104067200-104067400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr1:104067200-104067400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr1:104067200-104067400	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr1:104067200-104067400	Enhancers	Hela-S3	cervix
40	chr1:104067200-104067400	Enhancers	HMEC	breast
41	chr1:104067200-104067600	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr1:104067200-104067800	Enhancers	Fetal Intestine Small	intestine
43	chr1:104067200-104067800	Enhancers	Placenta	Placenta
44	chr1:104067200-104071400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
45	chr1:104067400-104067600	Enhancers	H9 Cell Line	embryonic stem cell
46	chr1:104067400-104067600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr1:104067400-104067600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr1:104067400-104067600	Enhancers	Primary neutrophils fromperipheralblood	blood
49	chr1:104067400-104067600	Enhancers	Primary B cells from peripheral blood	blood
50	chr1:104067400-104067600	Enhancers	Primary T cells from cord blood	blood

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