Variant report

Variant	nsv871339
Chromosome Location	chr1:70605735-70634463
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:345)
CpG islands
(count:61)
Chromatin interactive
region (count:23)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:345 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:70606204-70606214	K562	blood:	n/a	n/a
2	ARID3A	chr1:70622219-70622512	K562	blood:	n/a	n/a
3	ATF1	chr1:70607942-70608040	K562	blood:	n/a	n/a
4	ATF1	chr1:70622256-70622578	K562	blood:	n/a	n/a
5	BACH1	chr1:70629532-70629602	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:70611113-70611144	K562	blood:	n/a	n/a
7	BHLHE40	chr1:70622275-70622600	K562	blood:	n/a	n/a
8	CCNT2	chr1:70622326-70622531	K562	blood:	n/a	n/a
9	CEBPB	chr1:70615554-70615701	H1-hESC	embryonic stem cell:	n/a	chr1:70615659-70615670
10	CEBPB	chr1:70615484-70615771	K562	blood:	n/a	chr1:70615659-70615670
11	CEBPB	chr1:70615643-70615741	IMR90	lung:	n/a	chr1:70615659-70615670
12	CEBPB	chr1:70615554-70615756	HepG2	liver:	n/a	chr1:70615659-70615670
13	CEBPB	chr1:70617738-70618012	HepG2	liver:	n/a	n/a
14	CTCF	chr1:70608880-70609030	AG04450	lung:	n/a	chr1:70608930-70608951
15	CTCF	chr1:70608586-70609303	SK-N-SH	brain:	n/a	chr1:70608930-70608951
16	CTCF	chr1:70608880-70609030	HFF-Myc	foreskin:	n/a	chr1:70608930-70608951
17	CTCF	chr1:70607940-70608090	NHDF-neo	bronchial:	n/a	chr1:70607992-70608008
18	CTCF	chr1:70608851-70609027	SK-N-SH_RA	brain:	n/a	chr1:70608930-70608951
19	CTCF	chr1:70607860-70608010	K562	blood:	n/a	chr1:70607992-70608008
20	CTCF	chr1:70607940-70608090	HBMEC	blood vessel:	n/a	chr1:70607992-70608008
21	CTCF	chr1:70607880-70608030	MCF-7	breast:	n/a	chr1:70607992-70608008
22	CTCF	chr1:70606480-70606630	HEK293	kidney:	n/a	chr1:70606578-70606591
23	CTCF	chr1:70619540-70619690	HepG2	liver:	n/a	n/a
24	CTCF	chr1:70607920-70608070	HPF	lung:	n/a	chr1:70607992-70608008
25	CTCF	chr1:70607929-70608060	Medullo	brain:	n/a	chr1:70607992-70608008
26	CTCF	chr1:70608860-70609010	HVMF	connective:	n/a	chr1:70608930-70608951
27	CTCF	chr1:70608860-70609010	Hela-S3	cervix:	n/a	chr1:70608930-70608951
28	CTCF	chr1:70608901-70609014	K562	blood:	n/a	chr1:70608930-70608951
29	CTCF	chr1:70607798-70608179	K562	blood:	n/a	chr1:70607992-70608008
30	CTCF	chr1:70607960-70608110	HRPEpiC	eye:	n/a	chr1:70607992-70608008
31	CTCF	chr1:70615306-70615429	K562	blood:	n/a	n/a
32	CTCF	chr1:70607932-70608096	Pancreas_OC	pancreas:	n/a	chr1:70607992-70608008
33	CTCF	chr1:70606720-70606870	AG10803	skin:	n/a	n/a
34	CTCF	chr1:70607960-70608110	NHDF-neo	bronchial:	n/a	chr1:70607992-70608008
35	CTCF	chr1:70608720-70608870	HMEC	breast:	n/a	n/a
36	CTCF	chr1:70607931-70608052	MCF-7	breast:	n/a	chr1:70607992-70608008
37	CTCF	chr1:70607900-70608050	HRPEpiC	eye:	n/a	chr1:70607992-70608008
38	CTCF	chr1:70607920-70608070	AG09309	skin:	n/a	chr1:70607992-70608008
39	CTCF	chr1:70608860-70609010	HRE	kidney:	n/a	chr1:70608930-70608951
40	CTCF	chr1:70608860-70609010	HMF	breast:	n/a	chr1:70608930-70608951
41	CTCF	chr1:70607969-70608061	HepG2	liver:	n/a	chr1:70607992-70608008
42	CTCF	chr1:70608806-70609032	H1-hESC	embryonic stem cell:	n/a	chr1:70608930-70608951
43	CTCF	chr1:70608880-70609030	AG04449	skin:	n/a	chr1:70608930-70608951
44	CTCF	chr1:70609200-70609350	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr1:70607906-70608079	HUVEC	blood vessel:	n/a	chr1:70607992-70608008
46	CTCF	chr1:70607912-70608081	MCF-7	breast:	n/a	chr1:70607992-70608008
47	CTCF	chr1:70608061-70608063	Medullo	brain:	n/a	n/a
48	CTCF	chr1:70608760-70608910	HAc	cerebellar:	n/a	n/a
49	CTCF	chr1:70608820-70608970	NHEK	skin:	n/a	chr1:70608930-70608951
50	CTCF	chr1:70608800-70608950	NHDF-neo	bronchial:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:70606906-70606956	HPAEpiC	pulmonary alveolar:	n/a
2	chr1:70606906-70606956	AG09309	skin:	n/a
3	chr1:70606906-70606956	HUVEC	blood vessel:	n/a
4	chr1:70606906-70606956	NHDF-neo	bronchial:	n/a
5	chr1:70606906-70606956	GM06990	blood:	n/a
6	chr1:70606906-70606956	GM12878	blood:	n/a
7	chr1:70606906-70606956	T-47D	breast:	n/a
8	chr1:70606906-70606956	SK-N-SH	brain:	n/a
9	chr1:70606906-70606956	NH-A	brain:	n/a
10	chr1:70606906-70606956	PrEC	prostate:	n/a
11	chr1:70606906-70606956	AG04450	lung:	fetal
12	chr1:70606906-70606956	MCF10A-Er-Src	breast:	n/a
13	chr1:70606906-70606956	Jurkat	blood:	n/a
14	chr1:70606906-70606956	ECC-1	luminal epithelium:	n/a
15	chr1:70606906-70606956	HL-60	blood:	n/a
16	chr1:70606906-70606956	HNPCEpiC	eye:	n/a
17	chr1:70606906-70606956	AG10803	skin:	n/a
18	chr1:70606906-70606956	NB4	blood:	n/a
19	chr1:70606906-70606956	ovcar-3	ovarian:	n/a
20	chr1:70606906-70606956	AoSMC	blood vessel:	n/a
21	chr1:70606906-70606956	K562	blood:	n/a
22	chr1:70606906-70606956	SK-N-SH_RA	brain:	n/a
23	chr1:70606906-70606956	RPTEC	kidney:	n/a
24	chr1:70606906-70606956	H1-hESC	embryonic stem cell:	embryo
25	chr1:70606906-70606956	BJ	skin:	n/a
26	chr1:70606906-70606956	HEK293	kidney:	embryo
27	chr1:70606906-70606956	GM19239	blood:	n/a
28	chr1:70606906-70606956	MCF-7	breast:	n/a
29	chr1:70606906-70606956	BE2_C	brain:	n/a
30	chr1:70606906-70606956	HEEpiC	esophagus:	n/a
31	chr1:70606906-70606956	PANC-1	pancreas:	n/a
32	chr1:70606906-70606956	CMK	blood:	n/a
33	chr1:70606906-70606956	NHBE	bronchial:	n/a
34	chr1:70606906-70606956	HRCEpiC	kidney:	n/a
35	chr1:70606906-70606956	HAEpiC	amniotic membrane:	n/a
36	chr1:70606906-70606956	HRPEpiC	eye:	n/a
37	chr1:70606906-70606956	ProgFib	skin:	n/a
38	chr1:70606906-70606956	SAEC	small airway:	n/a
39	chr1:70606906-70606956	HMEC	breast:	n/a
40	chr1:70606906-70606956	U87	brain:	n/a
41	chr1:70606906-70606956	HRE	kidney:	n/a
42	chr1:70606906-70606956	GM12891	blood:	n/a
43	chr1:70606906-70606956	Hela-S3	cervix:	n/a
44	chr1:70606906-70606956	HepG2	liver:	n/a
45	chr1:70606906-70606956	HCPEpiC	choroid plexus:	n/a
46	chr1:70606906-70606956	NT2-D1	testis:	n/a
47	chr1:70606906-70606956	LNCaP	prostate:	n/a
48	chr1:70606906-70606956	HIPEpiC	eye:	n/a
49	chr1:70606906-70606956	AG04449	skin:	fetal
50	chr1:70606906-70606956	A549	lung:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:70613655..70615821-chr1:70616886..70621035,3	K562	blood:
2	chr1:70610824..70612517-chr1:70634874..70637196,2	K562	blood:
3	chr1:70622913..70625686-chr1:70626879..70630763,3	K562	blood:
4	chr1:70629583..70631880-chr1:70637700..70639670,3	K562	blood:
5	chr1:70613655..70615821-chr1:70616886..70621035,3	K562	blood:
6	chr1:70608921..70611354-chr1:70613745..70615584,2	K562	blood:
7	chr1:70623869..70625686-chr1:70628190..70630763,2	K562	blood:
8	chr1:70499914..70500706-chr1:70608453..70608981,2	MCF-7	breast:
9	chr1:70625805..70628227-chr1:70630477..70632879,2	K562	blood:
10	chr1:70608921..70611354-chr1:70613745..70615584,2	K562	blood:
11	chr1:70607998..70610574-chr1:70685135..70686722,2	K562	blood:
12	chr1:70613770..70615406-chr1:70693382..70695005,2	K562	blood:
13	chr1:70606579..70609498-chr1:70685222..70687844,2	K562	blood:
14	chr1:70613655..70616182-chr1:70616886..70621035,4	K562	blood:
15	chr1:70623869..70625686-chr1:70628190..70630763,2	K562	blood:
16	chr1:70611242..70612910-chr1:70616232..70618034,2	K562	blood:
17	chr1:70632648..70635188-chr1:70637548..70640122,2	K562	blood:
18	chr1:70591297..70593707-chr1:70608586..70610156,2	K562	blood:
19	chr1:70622913..70625686-chr1:70626879..70630763,3	K562	blood:
20	chr1:70634010..70636931-chr1:70644146..70645771,2	K562	blood:
21	chr1:70630351..70632302-chr1:70652266..70654580,2	K562	blood:
22	chr1:70625805..70628227-chr1:70630477..70632879,2	K562	blood:
23	chr1:70613655..70616182-chr1:70616886..70621035,4	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC7-1	chr1:70607065-70610047	ENSG00000261223.1
2	lnc-LRRC7-2	chr1:70612804-70612878	ENSG00000231835.1
3	lnc-LRRC7-2	chr1:70617431-70617628	ENSG00000231835.1
4	lnc-LRRC7-2	chr1:70613572-70613688	ENSG00000231835.1

No data

(count:6 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	LRRC40	hsa-miR-26b-5p	chr1:70610727-70610747
2	LRRC40	hsa-miR-155-5p	chr1:70610660-70610683
3	LRRC40	hsa-miR-26b-5p	chr1:70611043-70611063
4	LRRC40	hsa-miR-34a-5p	chr1:70611312-70611336
5	LRRC40	hsa-miR-26b-5p	chr1:70610788-70610810
6	LRRC40	hsa-miR-34a-5p	chr1:70611318-70611311

Variant related genes	Relation type
LRRC7	TF binding region
LRRC7	CpG island
ENSG00000228988	chromatin interactions
ENSG00000033122	chromatin interactions
ENSG00000116754	chromatin interactions

Extended variants
information (count: 941 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:941 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11805173	chr1:70605735-70605736	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs74586623	chr1:70605737-70605738	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs546504528	chr1:70605744-70605745	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs113758060	chr1:70605760-70605761	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs531061450	chr1:70605800-70605801	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs535045459	chr1:70605801-70605802	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs554763496	chr1:70605818-70605819	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs373555617	chr1:70605877-70605878	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs371124886	chr1:70605888-70605889	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs74346722	chr1:70605922-70605923	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs537159991	chr1:70605950-70605951	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs557544208	chr1:70605967-70605968	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs151111941	chr1:70605995-70605996	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs564288158	chr1:70606097-70606098	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs540105847	chr1:70606098-70606099	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs553740018	chr1:70606150-70606151	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs572730894	chr1:70606152-70606153	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs541847569	chr1:70606162-70606163	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs76875131	chr1:70606320-70606321	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs184987588	chr1:70606393-70606394	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs575251501	chr1:70606407-70606408	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs543993291	chr1:70606416-70606417	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs574766894	chr1:70606418-70606419	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs563903161	chr1:70606419-70606420	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs532993974	chr1:70606420-70606421	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs546467775	chr1:70606458-70606459	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs560062717	chr1:70606487-70606488	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs200469465	chr1:70606535-70606536	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs531448218	chr1:70606573-70606574	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs528467326	chr1:70606592-70606593	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs548525078	chr1:70606595-70606596	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs568366397	chr1:70606628-70606629	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs35221172	chr1:70606648-70606649	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs36029606	chr1:70606668-70606669	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs537526926	chr1:70606725-70606726	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs551111611	chr1:70606795-70606796	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs571044865	chr1:70606828-70606829	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs540069671	chr1:70606831-70606832	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs553690965	chr1:70606835-70606836	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs112245695	chr1:70606952-70606953	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs373328377	chr1:70606958-70606959	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs573357515	chr1:70606964-70606965	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs565082207	chr1:70606981-70606982	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs535774482	chr1:70607096-70607097	Enhancers Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs555313633	chr1:70607132-70607133	Enhancers Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
46	rs113233816	chr1:70607135-70607136	Enhancers Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
47	rs190022506	chr1:70607183-70607184	Enhancers Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
48	rs181134376	chr1:70607211-70607212	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
49	rs563866532	chr1:70607227-70607228	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
50	rs547142511	chr1:70607229-70607230	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
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
Melanoma	17363583	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
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal cancer	21851588	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:513 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:70596800-70609200	Weak transcription	Liver	Liver
2	chr1:70599000-70606000	Weak transcription	Osteobl	bone
3	chr1:70599000-70606600	Weak transcription	K562	blood
4	chr1:70599000-70609600	Weak transcription	GM12878-XiMat	blood
5	chr1:70600200-70606000	Weak transcription	Aorta	Aorta
6	chr1:70600400-70605800	Weak transcription	NHDF-Ad	bronchial
7	chr1:70601000-70615400	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr1:70601000-70643200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr1:70601200-70606000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr1:70601200-70606200	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr1:70601200-70652000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr1:70603000-70614800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr1:70603400-70648800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr1:70604600-70608600	Enhancers	Fetal Lung	lung
15	chr1:70604800-70605800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr1:70604800-70606400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr1:70605200-70606200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr1:70605200-70606200	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr1:70605200-70607000	Enhancers	Brain Germinal Matrix	brain
20	chr1:70605200-70607000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr1:70605200-70607000	Enhancers	Ovary	ovary
22	chr1:70605200-70607200	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr1:70605200-70612200	Weak transcription	Primary B cells from cord blood	blood
24	chr1:70605400-70605800	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr1:70605400-70606200	Weak transcription	Psoas Muscle	Psoas
26	chr1:70605400-70606600	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr1:70605400-70608000	Enhancers	Fetal Stomach	stomach
28	chr1:70605400-70608200	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr1:70605400-70639400	Weak transcription	Brain Anterior Caudate	brain
30	chr1:70605600-70605800	Weak transcription	Fetal Heart	heart
31	chr1:70605600-70606000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr1:70605600-70606000	Enhancers	Fetal Brain Male	brain
33	chr1:70605600-70606000	Flanking Active TSS	Fetal Brain Female	brain
34	chr1:70605600-70606400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:70605800-70606000	Enhancers	H9 Cell Line	embryonic stem cell
36	chr1:70605800-70606200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
37	chr1:70605800-70606400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr1:70605800-70606600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr1:70605800-70606800	Enhancers	Fetal Heart	heart
40	chr1:70605800-70606800	Enhancers	Fetal Kidney	kidney
41	chr1:70605800-70607000	Enhancers	Fetal Muscle Leg	muscle
42	chr1:70605800-70607400	Enhancers	Colon Smooth Muscle	Colon
43	chr1:70605800-70608000	Enhancers	Adipose Nuclei	Adipose
44	chr1:70605800-70608800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr1:70605800-70609200	Enhancers	NHDF-Ad	bronchial
46	chr1:70605800-70609200	Enhancers	NHLF	lung
47	chr1:70605800-70609600	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr1:70606000-70606200	Flanking Active TSS	Fetal Brain Male	brain
49	chr1:70606000-70606600	Enhancers	Fetal Intestine Small	intestine
50	chr1:70606000-70606800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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