Variant report

Variant	esv1833126
Chromosome Location	chr1:104092318-104337600
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	chr1:104104781-104104969	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:104332136-104332202	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:104103048-104103509	HepG2	liver:	n/a	n/a
4	ATF2	chr1:104104531-104104991	GM12878	blood:	n/a	n/a
5	BATF	chr1:104163710-104163876	GM12878	blood:	n/a	n/a
6	BATF	chr1:104163708-104163856	GM12878	blood:	n/a	n/a
7	BCL11A	chr1:104163716-104163847	GM12878	blood:	n/a	n/a
8	BCL11A	chr1:104163692-104163866	GM12878	blood:	n/a	n/a
9	BCLAF1	chr1:104104511-104104987	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:104163686-104163884	HepG2	liver:	n/a	n/a
11	BHLHE40	chr1:104104614-104104992	GM12878	blood:	n/a	n/a
12	BRCA1	chr1:104326501-104326782	GM12878	blood:	n/a	n/a
13	CEBPB	chr1:104306952-104307157	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:104128801-104129380	HepG2	liver:	n/a	chr1:104128959-104128968 chr1:104128959-104128968 chr1:104128959-104128968 chr1:104128957-104128970
15	CEBPB	chr1:104117700-104117982	IMR90	lung:	n/a	chr1:104117799-104117810
16	CEBPB	chr1:104109313-104109613	A549	lung:	n/a	chr1:104109438-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109515-104109526 chr1:104109440-104109449 chr1:104109438-104109449 chr1:104109440-104109451 chr1:104109440-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109440-104109449
17	CEBPB	chr1:104109284-104109624	IMR90	lung:	n/a	chr1:104109438-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109515-104109526 chr1:104109440-104109449 chr1:104109438-104109449 chr1:104109440-104109451 chr1:104109440-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109440-104109449
18	CEBPB	chr1:104098729-104098994	HepG2	liver:	n/a	n/a
19	CEBPB	chr1:104104662-104104945	Hela-S3	cervix:	n/a	chr1:104104711-104104723
20	CEBPB	chr1:104120646-104120872	A549	lung:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
21	CEBPB	chr1:104329336-104329610	HepG2	liver:	n/a	chr1:104329485-104329496 chr1:104329484-104329497
22	CEBPB	chr1:104307250-104307433	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr1:104103108-104103415	HepG2	liver:	n/a	n/a
24	CEBPB	chr1:104120629-104120899	HepG2	liver:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
25	CEBPB	chr1:104109287-104109643	HepG2	liver:	n/a	chr1:104109438-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109515-104109526 chr1:104109440-104109449 chr1:104109438-104109449 chr1:104109440-104109451 chr1:104109440-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109440-104109449
26	CEBPB	chr1:104104635-104104975	HepG2	liver:	n/a	chr1:104104711-104104723
27	CEBPB	chr1:104117717-104117917	HepG2	liver:	n/a	chr1:104117799-104117810
28	CEBPB	chr1:104120615-104120913	IMR90	lung:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
29	CEBPD	chr1:104163704-104163928	K562	blood:	n/a	n/a
30	CHD2	chr1:104326467-104326843	GM12878	blood:	n/a	n/a
31	CHD2	chr1:104326567-104326730	HepG2	liver:	n/a	n/a
32	CTCF	chr1:104331131-104331240	HepG2	liver:	n/a	chr1:104331174-104331190 chr1:104331173-104331191 chr1:104331175-104331196
33	CTCF	chr1:104130720-104130870	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr1:104212526-104212596	ProgFib	skin:	n/a	n/a
35	CTCF	chr1:104248353-104248412	GM13976	blood:	n/a	n/a
36	CTCF	chr1:104331049-104331327	A549	lung:	n/a	chr1:104331174-104331190 chr1:104331173-104331191 chr1:104331175-104331196
37	CTCF	chr1:104231384-104231389	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr1:104331096-104331270	H1-hESC	embryonic stem cell:	n/a	chr1:104331174-104331190 chr1:104331173-104331191 chr1:104331175-104331196
39	CTCF	chr1:104104380-104104530	AG10803	skin:	n/a	n/a
40	CTCF	chr1:104136948-104137064	Medullo	brain:	n/a	n/a
41	CTCF	chr1:104250396-104250604	Lung_OC	lung:	n/a	n/a
42	CTCF	chr1:104223571-104223629	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr1:104130740-104130890	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr1:104331099-104331239	GM10248	blood:	n/a	chr1:104331174-104331190 chr1:104331173-104331191 chr1:104331175-104331196
45	CTCF	chr1:104331100-104331250	HL-60	blood:	n/a	chr1:104331174-104331190 chr1:104331173-104331191 chr1:104331175-104331196
46	CTCF	chr1:104238464-104238556	Lung_OC	lung:	n/a	n/a
47	CTCF	chr1:104130620-104130770	GM12873	blood:	n/a	n/a
48	CTCF	chr1:104330980-104331130	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr1:104130760-104130910	A549	lung:	n/a	n/a
50	CTCF	chr1:104331024-104331344	IMR90	lung:	n/a	chr1:104331174-104331190 chr1:104331173-104331191 chr1:104331175-104331196

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:104111877-104111927	ovcar-3	ovarian:	n/a
2	chr1:104111877-104111927	ovcar-3	ovarian:	n/a
3	chr1:104239696-104239746	GM12891	blood:	n/a
4	chr1:104239696-104239746	GM19239	blood:	n/a
5	chr1:104113039-104113089	SK-N-SH_RA	brain:	n/a
6	chr1:104097670-104097720	GM12878	blood:	n/a
7	chr1:104113039-104113089	AG09319	gingival:	n/a
8	chr1:104096517-104096567	SK-N-SH	brain:	n/a
9	chr1:104096621-104096671	SAEC	small airway:	n/a
10	chr1:104113061-104113111	GM12891	blood:	n/a
11	chr1:104096517-104096567	HCT-116	colon:	n/a
12	chr1:104113039-104113089	HRCEpiC	kidney:	n/a
13	chr1:104096621-104096671	NB4	blood:	n/a
14	chr1:104096621-104096671	Jurkat	blood:	n/a
15	chr1:104112143-104112193	HRCEpiC	kidney:	n/a
16	chr1:104096517-104096567	PANC-1	pancreas:	n/a
17	chr1:104113061-104113111	MCF-7	breast:	n/a
18	chr1:104096517-104096567	AoSMC	blood vessel:	n/a
19	chr1:104113039-104113089	AG10803	skin:	n/a
20	chr1:104111877-104111927	SAEC	small airway:	n/a
21	chr1:104160257-104160307	ProgFib	skin:	n/a
22	chr1:104111877-104111927	HUVEC	blood vessel:	n/a
23	chr1:104113039-104113089	HPAEpiC	pulmonary alveolar:	n/a
24	chr1:104160257-104160307	GM12892	blood:	n/a
25	chr1:104160257-104160307	HCPEpiC	choroid plexus:	n/a
26	chr1:104239696-104239746	AG09309	skin:	n/a
27	chr1:104160257-104160307	NHDF-neo	bronchial:	n/a
28	chr1:104096621-104096671	CMK	blood:	n/a
29	chr1:104113039-104113089	NT2-D1	testis:	n/a
30	chr1:104113061-104113111	SK-N-SH	brain:	n/a
31	chr1:104160257-104160307	Caco-2	colon:	n/a
32	chr1:104239696-104239746	GM06990	blood:	n/a
33	chr1:104097670-104097720	GM12892	blood:	n/a
34	chr1:104112143-104112193	HIPEpiC	eye:	n/a
35	chr1:104096517-104096567	AG09309	skin:	n/a
36	chr1:104160257-104160307	A549	lung:	n/a
37	chr1:104239696-104239746	AG04449	skin:	fetal
38	chr1:104113061-104113111	AG10803	skin:	n/a
39	chr1:104096621-104096671	HNPCEpiC	eye:	n/a
40	chr1:104096621-104096671	HMEC	breast:	n/a
41	chr1:104112143-104112193	CMK	blood:	n/a
42	chr1:104160257-104160307	U87	brain:	n/a
43	chr1:104160257-104160307	GM12891	blood:	n/a
44	chr1:104112143-104112193	HCM	heart:	n/a
45	chr1:104111877-104111927	BJ	skin:	n/a
46	chr1:104111877-104111927	AG09319	gingival:	n/a
47	chr1:104097670-104097720	AG09309	skin:	n/a
48	chr1:104160257-104160307	HCM	heart:	n/a
49	chr1:104113039-104113089	GM12878	blood:	n/a
50	chr1:104160257-104160307	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:104120354..104123298-chr1:104128850..104131166,2	K562	blood:
2	chr1:104330211..104331667-chr1:104674701..104675769,4	MCF-7	breast:
3	chr1:104330809..104331725-chr1:104675161..104675727,2	MCF-7	breast:
4	chr1:104068563..104070409-chr1:104091369..104094625,4	MCF-7	breast:
5	chr1:104320249..104323301-chr1:104334806..104337281,3	K562	blood:
6	chr1:104120354..104123298-chr1:104128850..104131166,2	K562	blood:
7	chr1:104087556..104090106-chr1:104096002..104097509,2	K562	blood:
8	chr1:104307678..104310486-chr1:104333154..104335185,2	K562	blood:
9	chr1:104307678..104310486-chr1:104333154..104335185,2	K562	blood:
10	chr1:104320249..104323301-chr1:104334806..104337281,3	K562	blood:

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RNPC3	hsa-miR-192-5p	chr1:104096163-104096184

Variant related genes	Relation type
AMY1C	TF binding region
ACTG1P4	TF binding region
AMY1A	TF binding region
RNPC3	TF binding region
AMY1B	TF binding region
ENSG00000234441	TF binding region
AMY2A	TF binding region
AMYP1	TF binding region
AMY2B	TF binding region
AMY1C	CpG island
ACTG1P4	CpG island
AMY1A	CpG island
RNPC3	CpG island
AMY1B	CpG island
ENSG00000234441	CpG island
AMY2A	CpG island
AMYP1	CpG island
AMY2B	CpG island
ENSG00000185946	chromatin interactions

Extended variants
information (count: 2070 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:2070 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576205527	chr1:104092409-104092410	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs145807684	chr1:104092436-104092437	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs546269780	chr1:104092457-104092458	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs182100833	chr1:104092463-104092464	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs550574850	chr1:104092464-104092465	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs569403889	chr1:104092484-104092485	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs376347618	chr1:104092544-104092545	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs185172882	chr1:104092550-104092551	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs548643057	chr1:104092551-104092552	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs562205469	chr1:104092555-104092556	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs374194919	chr1:104092556-104092557	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs78210641	chr1:104092558-104092559	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs140734482	chr1:104092560-104092561	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs542661724	chr1:104092589-104092590	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs145876159	chr1:104092596-104092597	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs201295055	chr1:104092622-104092623	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs537822348	chr1:104092628-104092629	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs374184978	chr1:104092642-104092643	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs575407320	chr1:104092658-104092659	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs542895764	chr1:104092679-104092680	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs138463967	chr1:104092683-104092684	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs141236586	chr1:104092732-104092733	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs540057247	chr1:104092742-104092743	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs551535618	chr1:104092781-104092782	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs541434330	chr1:104092788-104092789	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs190709578	chr1:104092797-104092798	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs77947722	chr1:104092807-104092808	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs550267592	chr1:104092861-104092862	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs143217868	chr1:104092911-104092912	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs529703641	chr1:104092983-104092984	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs34487026	chr1:104093027-104093028	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs527323435	chr1:104093037-104093038	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs534356148	chr1:104093038-104093039	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs141467136	chr1:104093046-104093047	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs111482163	chr1:104093049-104093050	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs150782673	chr1:104093124-104093125	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs538343853	chr1:104093131-104093132	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs556421603	chr1:104093168-104093169	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs574771541	chr1:104093186-104093187	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs367962701	chr1:104093190-104093191	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs564419905	chr1:104093199-104093200	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs550934146	chr1:104093206-104093207	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs188941348	chr1:104093210-104093211	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs374533518	chr1:104093211-104093212	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs34109337	chr1:104093263-104093264	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs397686893	chr1:104093282-104093283	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs539994554	chr1:104093311-104093312	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs564747507	chr1:104093355-104093356	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs577005613	chr1:104093380-104093381	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs559286976	chr1:104093470-104093471	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	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
Ovarian clear cell carcinoma	21343371	CNVD
Autism	19287141	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:512 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:104069200-104096400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:104069200-104101200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr1:104069400-104097400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr1:104069600-104100000	Weak transcription	Stomach Mucosa	stomach
5	chr1:104070200-104096200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr1:104070800-104092400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr1:104071200-104098800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr1:104071400-104099000	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr1:104071400-104100200	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr1:104071600-104096200	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr1:104071600-104100000	Weak transcription	Fetal Brain Male	brain
12	chr1:104072000-104097800	Strong transcription	Rectal Mucosa Donor 29	rectum
13	chr1:104072800-104092600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr1:104073200-104092800	Strong transcription	Primary B cells from peripheral blood	blood
15	chr1:104073600-104096000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr1:104074600-104098800	Strong transcription	Primary T cells fromperipheralblood	blood
17	chr1:104075000-104100000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr1:104075000-104100000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr1:104075400-104098800	Strong transcription	Rectal Mucosa Donor 31	rectum
20	chr1:104076000-104095600	Strong transcription	Dnd41	blood
21	chr1:104076200-104095800	Strong transcription	HUES48 Cell Line	embryonic stem cell
22	chr1:104076200-104099000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr1:104076200-104100200	Strong transcription	Primary T helper cells fromperipheralblood	blood
24	chr1:104076400-104095400	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr1:104076400-104096000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
26	chr1:104076400-104097000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr1:104076600-104095400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr1:104076600-104096200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr1:104076600-104097000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr1:104076600-104097200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr1:104076600-104097400	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr1:104076600-104098800	Strong transcription	Primary T helper cells PMA-I stimulated	--
33	chr1:104076800-104095200	Strong transcription	Placenta	Placenta
34	chr1:104077400-104092600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr1:104077800-104092600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr1:104077800-104095000	Strong transcription	Duodenum Smooth Muscle	Duodenum
37	chr1:104078800-104096000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr1:104081400-104096800	Weak transcription	Fetal Heart	heart
39	chr1:104082800-104093200	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr1:104082800-104095000	Weak transcription	NHLF	lung
41	chr1:104083400-104103800	Weak transcription	Psoas Muscle	Psoas
42	chr1:104084200-104095400	Strong transcription	Skeletal Muscle Female	skeletal muscle
43	chr1:104085000-104094400	Weak transcription	Brain Cingulate Gyrus	brain
44	chr1:104086400-104092800	Strong transcription	Skeletal Muscle Male	skeletal muscle
45	chr1:104086600-104092600	Strong transcription	Stomach Smooth Muscle	stomach
46	chr1:104086800-104095200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
47	chr1:104087600-104092800	Strong transcription	Cortex derived primary cultured neurospheres	brain
48	chr1:104087600-104095000	Strong transcription	Fetal Intestine Large	intestine
49	chr1:104087800-104092800	Strong transcription	Fetal Thymus	thymus
50	chr1:104088000-104095400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland

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