Variant report

Variant	nsv826534
Chromosome Location	chr12:123859610-123876354
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1473)
CpG islands
(count:1344)
Chromatin interactive
region (count:58)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1473 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:123869109-123869429	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:123868068-123868703	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:123868155-123868705	K562	blood:	n/a	n/a
4	ARID3A	chr12:123872141-123873037	K562	blood:	n/a	n/a
5	ATF1	chr12:123868169-123868701	K562	blood:	n/a	n/a
6	ATF1	chr12:123872000-123873150	K562	blood:	n/a	n/a
7	ATF1	chr12:123870215-123870528	K562	blood:	n/a	n/a
8	ATF2	chr12:123872859-123873307	GM12878	blood:	n/a	n/a
9	ATF2	chr12:123868036-123868738	GM12878	blood:	n/a	n/a
10	ATF3	chr12:123869504-123869922	K562	blood:	n/a	chr12:123869745-123869755
11	ATF3	chr12:123870254-123870529	K562	blood:	n/a	n/a
12	BACH1	chr12:123869332-123869397	K562	blood:	n/a	n/a
13	BACH1	chr12:123868886-123869420	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr12:123872212-123873052	K562	blood:	n/a	n/a
15	BACH1	chr12:123867130-123867332	K562	blood:	n/a	n/a
16	BCL3	chr12:123868005-123868486	A549	lung:	n/a	n/a
17	BCL3	chr12:123868933-123869471	A549	lung:	n/a	chr12:123869288-123869301 chr12:123869100-123869109
18	BCL3	chr12:123867985-123868609	A549	lung:	n/a	n/a
19	BCLAF1	chr12:123872847-123873364	GM12878	blood:	n/a	n/a
20	BHLHE40	chr12:123869219-123869565	K562	blood:	n/a	n/a
21	BHLHE40	chr12:123868075-123868594	HepG2	liver:	n/a	n/a
22	BHLHE40	chr12:123868103-123868843	GM12878	blood:	n/a	n/a
23	BHLHE40	chr12:123868214-123868477	A549	lung:	n/a	n/a
24	BHLHE40	chr12:123872863-123873228	GM12878	blood:	n/a	n/a
25	BHLHE40	chr12:123868075-123868887	K562	blood:	n/a	n/a
26	BHLHE40	chr12:123871961-123873162	K562	blood:	n/a	n/a
27	BHLHE40	chr12:123873472-123873547	GM12878	blood:	n/a	n/a
28	BRCA1	chr12:123873103-123873374	GM12878	blood:	n/a	n/a
29	BRCA1	chr12:123868207-123868398	H1-hESC	embryonic stem cell:	n/a	n/a
30	BRCA1	chr12:123868151-123868708	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr12:123869568-123869828	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr12:123867174-123867543	K562	blood:	n/a	n/a
33	CBX3	chr12:123867843-123868917	K562	blood:	n/a	n/a
34	CBX3	chr12:123872436-123873022	K562	blood:	n/a	n/a
35	CBX3	chr12:123871927-123873272	K562	blood:	n/a	n/a
36	CBX3	chr12:123867074-123867622	K562	blood:	n/a	n/a
37	CCNT2	chr12:123868077-123869491	K562	blood:	n/a	n/a
38	CCNT2	chr12:123872168-123874833	K562	blood:	n/a	n/a
39	CEBPB	chr12:123870330-123870385	IMR90	lung:	n/a	n/a
40	CEBPB	chr12:123868004-123868917	ECC-1	luminal epithelium:	n/a	n/a
41	CEBPB	chr12:123868462-123868832	A549	lung:	n/a	n/a
42	CEBPB	chr12:123869586-123869931	H1-hESC	embryonic stem cell:	n/a	chr12:123869754-123869765
43	CEBPB	chr12:123869459-123869934	A549	lung:	n/a	chr12:123869754-123869765
44	CEBPB	chr12:123870242-123870443	A549	lung:	n/a	n/a
45	CEBPB	chr12:123867317-123867451	K562	blood:	n/a	chr12:123867404-123867415
46	CEBPB	chr12:123868040-123868923	K562	blood:	n/a	n/a
47	CEBPB	chr12:123868043-123868867	HepG2	liver:	n/a	n/a
48	CEBPB	chr12:123869508-123869960	A549	lung:	n/a	chr12:123869754-123869765
49	CEBPB	chr12:123868551-123868760	K562	blood:	n/a	n/a
50	CEBPB	chr12:123869614-123869891	K562	blood:	n/a	chr12:123869754-123869765

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:123868662-123868712	AG09319	gingival:	n/a
2	chr12:123874243-123874293	SAEC	small airway:	n/a
3	chr12:123868662-123868712	AG09319	gingival:	n/a
4	chr12:123874243-123874293	SAEC	small airway:	n/a
5	chr12:123874456-123874506	MCF10A-Er-Src	breast:	n/a
6	chr12:123868268-123868318	A549	lung:	n/a
7	chr12:123868662-123868712	SK-N-SH	brain:	n/a
8	chr12:123868625-123868675	Hepatocyte	liver:	n/a
9	chr12:123868268-123868318	ProgFib	skin:	n/a
10	chr12:123868662-123868712	CMK	blood:	n/a
11	chr12:123869060-123869110	GM06990	blood:	n/a
12	chr12:123869060-123869110	HRCEpiC	kidney:	n/a
13	chr12:123869502-123869552	AG04450	lung:	fetal
14	chr12:123868728-123868778	HCT-116	colon:	n/a
15	chr12:123869502-123869552	IMR90	lung:	fetal
16	chr12:123868665-123868715	PFSK-1	brain:	n/a
17	chr12:123867383-123867433	Hepatocyte	liver:	n/a
18	chr12:123868310-123868360	NHDF-neo	bronchial:	n/a
19	chr12:123869060-123869110	MCF10A-Er-Src	breast:	n/a
20	chr12:123869502-123869552	HAEpiC	amniotic membrane:	n/a
21	chr12:123874298-123874348	HUVEC	blood vessel:	n/a
22	chr12:123873524-123873574	SKMC	muscle:	n/a
23	chr12:123869060-123869110	PrEC	prostate:	n/a
24	chr12:123868647-123868697	HPAEpiC	pulmonary alveolar:	n/a
25	chr12:123868728-123868778	HCF	heart:	n/a
26	chr12:123868728-123868778	NT2-D1	testis:	n/a
27	chr12:123874466-123874516	HCPEpiC	choroid plexus:	n/a
28	chr12:123868625-123868675	HUVEC	blood vessel:	n/a
29	chr12:123868698-123868748	NH-A	brain:	n/a
30	chr12:123868545-123868595	Hepatocyte	liver:	n/a
31	chr12:123868665-123868715	K562	blood:	n/a
32	chr12:123869334-123869384	NHBE	bronchial:	n/a
33	chr12:123874707-123874757	BJ	skin:	n/a
34	chr12:123868427-123868477	AG04449	skin:	fetal
35	chr12:123868647-123868697	HMEC	breast:	n/a
36	chr12:123868665-123868715	SAEC	small airway:	n/a
37	chr12:123865592-123865642	T-47D	breast:	n/a
38	chr12:123868728-123868778	GM12891	blood:	n/a
39	chr12:123868310-123868360	PFSK-1	brain:	n/a
40	chr12:123868268-123868318	HCF	heart:	n/a
41	chr12:123868545-123868595	NHDF-neo	bronchial:	n/a
42	chr12:123871695-123871745	U87	brain:	n/a
43	chr12:123868625-123868675	HPAEpiC	pulmonary alveolar:	n/a
44	chr12:123868698-123868748	HMEC	breast:	n/a
45	chr12:123868698-123868748	NHBE	bronchial:	n/a
46	chr12:123865592-123865642	ovcar-3	ovarian:	n/a
47	chr12:123874243-123874293	BE2_C	brain:	n/a
48	chr12:123869502-123869552	PrEC	prostate:	n/a
49	chr12:123868310-123868360	ovcar-3	ovarian:	n/a
50	chr12:123874298-123874348	HPAEpiC	pulmonary alveolar:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:123857490..123859672-chr12:123865984..123869016,3	K562	blood:
2	chr12:123753349..123756927-chr12:123873006..123875020,4	MCF-7	breast:
3	chr12:123873719..123876506-chr12:124067448..124069174,2	K562	blood:
4	chr12:123873866..123876385-chr12:123942538..123944226,2	MCF-7	breast:
5	chr12:123848194..123850354-chr12:123858475..123860838,2	K562	blood:
6	chr12:123872223..123875553-chr12:124085591..124088201,3	MCF-7	breast:
7	chr12:123855413..123857472-chr12:123866745..123868291,2	K562	blood:
8	chr12:123872784..123874602-chr17:59484787..59486930,2	MCF-7	breast:
9	chr12:123755389..123758333-chr12:123866833..123870129,4	K562	blood:
10	chr12:123846590..123852305-chr12:123861449..123873718,39	K562	blood:
11	chr12:123847204..123849398-chr12:123874460..123876425,2	K562	blood:
12	chr12:123871220..123873431-chr12:123897619..123900288,2	K562	blood:
13	chr12:123871392..123873266-chr12:123879118..123880787,2	K562	blood:
14	chr12:123845591..123852236-chr12:123866929..123875043,19	MCF-7	breast:
15	chr12:123862454..123865045-chr12:123865570..123867094,2	K562	blood:
16	chr12:123873193..123874940-chr12:123942406..123944140,2	K562	blood:
17	chr12:123874611..123876401-chr12:123967217..123969868,2	K562	blood:
18	chr12:123754511..123756318-chr12:123868404..123870683,2	MCF-7	breast:
19	chr12:123715746..123718967-chr12:123870796..123875270,4	K562	blood:
20	chr12:123866977..123869044-chr12:124085781..124087608,2	MCF-7	breast:
21	chr12:123857727..123860926-chr12:123866777..123869016,5	K562	blood:
22	chr12:123868262..123871053-chr17:58155484..58156988,2	MCF-7	breast:
23	chr12:123847748..123850760-chr12:123875045..123877875,5	MCF-7	breast:
24	chr12:123755164..123758333-chr12:123868507..123873426,5	K562	blood:
25	chr12:123867386..123869300-chr12:124085669..124087822,2	K562	blood:
26	chr12:123866599..123869577-chr12:123942434..123944403,3	MCF-7	breast:
27	chr11:45825943..45826929-chr12:123873071..123873715,2	Hela-S3	cervix:
28	chr12:123849812..123851534-chr12:123858422..123861381,2	MCF-7	breast:
29	chr12:123847741..123850160-chr12:123863172..123865699,2	MCF-7	breast:
30	chr12:123869164..123871955-chr12:123947898..123950371,2	K562	blood:
31	chr12:123872056..123874942-chr12:124085224..124088307,3	MCF-7	breast:
32	chr12:123752887..123754431-chr12:123868251..123870818,2	K562	blood:
33	chr12:123868443..123871332-chr12:123941328..123944744,4	K562	blood:
34	chr12:123866701..123869300-chr12:124085669..124087764,2	K562	blood:
35	chr12:123753572..123756952-chr12:123872035..123874712,3	MCF-7	breast:
36	chr12:123876121..123878212-chr12:124088472..124090706,2	MCF-7	breast:
37	chr12:123872778..123876196-chr12:124065295..124071344,6	MCF-7	breast:
38	chr12:123846880..123851536-chr12:123865445..123870876,12	MCF-7	breast:
39	chr12:123754082..123756520-chr12:123873506..123875645,3	K562	blood:
40	chr12:123717467..123721119-chr12:123869942..123873013,3	K562	blood:
41	chr12:123872765..123874584-chr2:91935567..91938569,3	MCF-7	breast:
42	chr12:123866820..123869752-chr12:123919792..123923261,3	K562	blood:
43	chr12:123872416..123876102-chr12:124017252..124019601,4	MCF-7	breast:
44	chr12:123753478..123757222-chr12:123871925..123875006,5	K562	blood:
45	chr12:123458609..123460830-chr12:123870435..123872750,2	K562	blood:
46	chr12:123870366..123875219-chr12:124064500..124069174,6	K562	blood:
47	chr12:123862454..123865045-chr12:123865570..123867094,2	K562	blood:
48	chr12:123859632..123861218-chr12:123970833..123973407,2	K562	blood:
49	chr12:123574636..123576162-chr12:123864283..123866660,2	K562	blood:
50	chr12:123754759..123757395-chr12:123866766..123872450,7	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNRNP35-4	chr12:123868720-123868755	NONHSAT031588
2	lnc-SNRNP35-4	chr12:123872989-123873304	NONHSAT031588

No data

Variant related genes	Relation type
SETD8	TF binding region
SETD8	CpG island
ENSG00000150967	chromatin interactions
ENSG00000068097	chromatin interactions
ENSG00000150977	chromatin interactions
ENSG00000232531	chromatin interactions
ENSG00000188026	chromatin interactions
ENSG00000267416	chromatin interactions
ENSG00000139697	chromatin interactions
ENSG00000111328	chromatin interactions
ENSG00000183955	chromatin interactions
ENSG00000111364	chromatin interactions
ENSG00000247373	chromatin interactions
ENSG00000111325	chromatin interactions
ENSG00000256092	chromatin interactions
ENSG00000184209	chromatin interactions
ENSG00000130921	chromatin interactions
ENSG00000256028	chromatin interactions
ENSG00000181830	chromatin interactions
ENSG00000051825	chromatin interactions
ENSG00000121068	chromatin interactions
ENSG00000086598	chromatin interactions

Extended variants
information (count: 581 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:581 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567719257	chr12:123859656-123859657	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs181204370	chr12:123859659-123859660	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs184317373	chr12:123859671-123859672	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs116954591	chr12:123859684-123859685	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs559001058	chr12:123859704-123859705	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs28688145	chr12:123859708-123859709	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs577797240	chr12:123859729-123859730	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs533646718	chr12:123859731-123859732	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs146486070	chr12:123859737-123859738	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs563314036	chr12:123859763-123859764	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs375718308	chr12:123859857-123859858	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs139949145	chr12:123859862-123859863	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs112231508	chr12:123859885-123859886	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs79359209	chr12:123859942-123859943	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs560868831	chr12:123859998-123859999	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs528088663	chr12:123860002-123860003	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs546415820	chr12:123860009-123860010	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs564975290	chr12:123860013-123860014	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs532623127	chr12:123860022-123860023	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs28414347	chr12:123860025-123860026	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs60930365	chr12:123860041-123860042	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs145916877	chr12:123860118-123860119	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs372002272	chr12:123860134-123860135	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs372282014	chr12:123860172-123860173	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs558276265	chr12:123860244-123860245	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs151240199	chr12:123860247-123860248	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs189091360	chr12:123860248-123860249	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs140434560	chr12:123860260-123860261	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs376938211	chr12:123860384-123860385	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs28875264	chr12:123860401-123860402	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs77793639	chr12:123860405-123860406	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs369722626	chr12:123860424-123860425	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs28786830	chr12:123860472-123860473	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs575465704	chr12:123860480-123860481	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs145242492	chr12:123860481-123860482	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs142436864	chr12:123860483-123860484	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs113298289	chr12:123860536-123860537	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs572907547	chr12:123860541-123860542	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs553868297	chr12:123860549-123860550	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs187582215	chr12:123860569-123860570	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs574404028	chr12:123860627-123860628	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs532249765	chr12:123860641-123860642	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs543929558	chr12:123860645-123860646	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs112539727	chr12:123860652-123860653	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs146684068	chr12:123860709-123860710	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs371799018	chr12:123860722-123860723	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs528732221	chr12:123860740-123860741	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs376826213	chr12:123860787-123860788	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs569602582	chr12:123860804-123860805	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs371864486	chr12:123860809-123860810	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1333 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123850600-123867200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr12:123850600-123867800	Weak transcription	Right Atrium	heart
3	chr12:123857400-123860000	Enhancers	K562	blood
4	chr12:123858400-123860000	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr12:123859200-123867200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr12:123859600-123863400	Weak transcription	A549	lung
7	chr12:123859600-123863400	Weak transcription	HepG2	liver
8	chr12:123860000-123861000	Weak transcription	K562	blood
9	chr12:123860000-123863200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr12:123861000-123861400	Enhancers	K562	blood
11	chr12:123861400-123866800	Weak transcription	K562	blood
12	chr12:123863200-123864600	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr12:123863400-123864000	Enhancers	HepG2	liver
14	chr12:123863400-123864200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr12:123863400-123864200	Enhancers	A549	lung
16	chr12:123863400-123864400	Enhancers	NHEK	skin
17	chr12:123863600-123864000	Enhancers	Placenta	Placenta
18	chr12:123863800-123864400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr12:123863800-123864400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr12:123863800-123864400	Enhancers	HMEC	breast
21	chr12:123864000-123866800	Weak transcription	HepG2	liver
22	chr12:123864000-123867200	Weak transcription	Placenta	Placenta
23	chr12:123864200-123867200	Weak transcription	A549	lung
24	chr12:123864200-123867400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr12:123864400-123867000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr12:123864400-123867200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr12:123864400-123867800	Weak transcription	HMEC	breast
28	chr12:123864400-123867800	Weak transcription	NHEK	skin
29	chr12:123864600-123868000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr12:123865600-123866600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr12:123865600-123867200	Weak transcription	Psoas Muscle	Psoas
32	chr12:123866600-123866800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr12:123866800-123867000	Enhancers	K562	blood
34	chr12:123866800-123867200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr12:123866800-123867200	Enhancers	HepG2	liver
36	chr12:123867000-123867200	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr12:123867000-123867200	Enhancers	Hela-S3	cervix
38	chr12:123867000-123867600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr12:123867000-123867600	Flanking Active TSS	K562	blood
40	chr12:123867000-123868000	Enhancers	GM12878-XiMat	blood
41	chr12:123867000-123869600	Active TSS	HSMM	muscle
42	chr12:123867200-123867400	Enhancers	H1 Cell Line	embryonic stem cell
43	chr12:123867200-123867400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr12:123867200-123867400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr12:123867200-123867400	Enhancers	Lung	lung
46	chr12:123867200-123867400	Enhancers	Psoas Muscle	Psoas
47	chr12:123867200-123867600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr12:123867200-123867600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr12:123867200-123867600	Enhancers	Fetal Muscle Trunk	muscle
50	chr12:123867200-123867600	Enhancers	Placenta	Placenta

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