Variant report

Variant	esv2761737
Chromosome Location	chr12:47946795-48045722
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:765)
CpG islands
(count:122)
Chromatin interactive
region (count:40)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:48045429-48047004	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:48009566-48009824	K562	blood:	n/a	n/a
3	BACH1	chr12:48030886-48030902	K562	blood:	n/a	n/a
4	BATF	chr12:47968098-47968398	GM12878	blood:	n/a	n/a
5	BCL3	chr12:47990271-47990556	GM12878	blood:	n/a	n/a
6	CBX3	chr12:48001220-48001519	K562	blood:	n/a	n/a
7	CBX3	chr12:48006654-48007105	K562	blood:	n/a	n/a
8	CBX3	chr12:48006668-48007131	HCT-116	colon:	n/a	n/a
9	CBX3	chr12:47947045-47947272	K562	blood:	n/a	n/a
10	CBX3	chr12:48006744-48007063	K562	blood:	n/a	n/a
11	CBX3	chr12:47999499-47999693	K562	blood:	n/a	n/a
12	CCNT2	chr12:48009615-48009815	K562	blood:	n/a	n/a
13	CEBPB	chr12:48010294-48010614	HepG2	liver:	n/a	chr12:48010454-48010465
14	CEBPB	chr12:47990304-47990504	K562	blood:	n/a	chr12:47990388-47990399
15	CEBPB	chr12:48010311-48010625	K562	blood:	n/a	chr12:48010454-48010465
16	CEBPB	chr12:47990257-47990581	HepG2	liver:	n/a	chr12:47990388-47990399
17	CEBPB	chr12:47990321-47990731	Hela-S3	cervix:	n/a	chr12:47990388-47990399
18	CEBPB	chr12:47990252-47990588	IMR90	lung:	n/a	chr12:47990388-47990399
19	CEBPB	chr12:48010270-48010620	IMR90	lung:	n/a	chr12:48010454-48010465
20	CEBPB	chr12:47990261-47990663	A549	lung:	n/a	chr12:47990388-47990399
21	CEBPB	chr12:48010267-48010601	Hela-S3	cervix:	n/a	chr12:48010454-48010465
22	CEBPB	chr12:48010262-48010605	A549	lung:	n/a	chr12:48010454-48010465
23	CEBPB	chr12:47961516-47961727	IMR90	lung:	n/a	chr12:47961609-47961626
24	CEBPD	chr12:48009505-48009968	K562	blood:	n/a	n/a
25	CHD1	chr12:48045392-48045839	IMR90	lung:	n/a	n/a
26	CTCF	chr12:48030966-48031336	K562	blood:	n/a	n/a
27	CTCF	chr12:48045336-48045872	MCF-7	breast:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
28	CTCF	chr12:48045500-48045650	A549	lung:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
29	CTCF	chr12:48045560-48045710	GM06990	blood:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
30	CTCF	chr12:48031080-48031230	NHLF	lung:	n/a	n/a
31	CTCF	chr12:47997087-47997154	MCF-7	breast:	n/a	n/a
32	CTCF	chr12:48031013-48031229	MCF-7	breast:	n/a	n/a
33	CTCF	chr12:48045545-48045663	GM13976	blood:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
34	CTCF	chr12:48045500-48045650	HFF	foreskin:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
35	CTCF	chr12:48045485-48045751	A549	lung:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
36	CTCF	chr12:48045442-48045714	SK-N-SH_RA	brain:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
37	CTCF	chr12:47996840-47996990	HepG2	liver:	n/a	chr12:47996875-47996893 chr12:47996955-47996968
38	CTCF	chr12:48045520-48045670	HPF	lung:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
39	CTCF	chr12:48045520-48045670	SK-N-SH_RA	brain:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
40	CTCF	chr12:48031020-48031170	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr12:48034081-48034183	GM13976	blood:	n/a	n/a
42	CTCF	chr12:48031080-48031230	GM12873	blood:	n/a	n/a
43	CTCF	chr12:48045560-48045710	AG09309	skin:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
44	CTCF	chr12:48045520-48045670	AG09309	skin:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
45	CTCF	chr12:48031006-48031246	Fibrobl	skin:	n/a	n/a
46	CTCF	chr12:48045480-48045630	HAc	cerebellar:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
47	CTCF	chr12:48031061-48031246	GM10248	blood:	n/a	n/a
48	CTCF	chr12:48030808-48031637	A549	lung:	n/a	n/a
49	CTCF	chr12:48031080-48031230	Caco-2	colon:	n/a	n/a
50	CTCF	chr12:48031140-48031290	WI-38	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:48044905-48044955	A549	lung:	n/a
2	chr12:48044905-48044955	K562	blood:	n/a
3	chr12:48044905-48044955	PANC-1	pancreas:	n/a
4	chr12:48044905-48044955	RPTEC	kidney:	n/a
5	chr12:47985234-47985284	AG04449	skin:	fetal
6	chr12:48044905-48044955	HUVEC	blood vessel:	n/a
7	chr12:47985234-47985284	SAEC	small airway:	n/a
8	chr12:47985234-47985284	HRE	kidney:	n/a
9	chr12:48044905-48044955	GM06990	blood:	n/a
10	chr12:47985234-47985284	GM06990	blood:	n/a
11	chr12:48044905-48044955	HIPEpiC	eye:	n/a
12	chr12:47985234-47985284	NHDF-neo	bronchial:	n/a
13	chr12:47985234-47985284	BE2_C	brain:	n/a
14	chr12:48044905-48044955	Hepatocyte	liver:	n/a
15	chr12:47985234-47985284	Caco-2	colon:	n/a
16	chr12:48044905-48044955	AG10803	skin:	n/a
17	chr12:48044905-48044955	PFSK-1	brain:	n/a
18	chr12:47985234-47985284	K562	blood:	n/a
19	chr12:47985234-47985284	T-47D	breast:	n/a
20	chr12:48044905-48044955	SK-N-MC	brain:	n/a
21	chr12:47985234-47985284	HEK293	kidney:	embryo
22	chr12:47985234-47985284	HCT-116	colon:	n/a
23	chr12:47985234-47985284	MCF-7	breast:	n/a
24	chr12:47985234-47985284	HEEpiC	esophagus:	n/a
25	chr12:48044905-48044955	LNCaP	prostate:	n/a
26	chr12:48044905-48044955	ProgFib	skin:	n/a
27	chr12:48044905-48044955	HRPEpiC	eye:	n/a
28	chr12:47985234-47985284	HCPEpiC	choroid plexus:	n/a
29	chr12:47985234-47985284	GM12878	blood:	n/a
30	chr12:48044905-48044955	NH-A	brain:	n/a
31	chr12:48044905-48044955	HMEC	breast:	n/a
32	chr12:48044905-48044955	Caco-2	colon:	n/a
33	chr12:48044905-48044955	Jurkat	blood:	n/a
34	chr12:47985234-47985284	GM12892	blood:	n/a
35	chr12:47985234-47985284	AoSMC	blood vessel:	n/a
36	chr12:47985234-47985284	HRPEpiC	eye:	n/a
37	chr12:47985234-47985284	HPAEpiC	pulmonary alveolar:	n/a
38	chr12:47985234-47985284	GM12891	blood:	n/a
39	chr12:47985234-47985284	AG09319	gingival:	n/a
40	chr12:47985234-47985284	PANC-1	pancreas:	n/a
41	chr12:48044905-48044955	HCT-116	colon:	n/a
42	chr12:47985234-47985284	HNPCEpiC	eye:	n/a
43	chr12:48044905-48044955	H1-hESC	embryonic stem cell:	embryo
44	chr12:48044905-48044955	AG04449	skin:	fetal
45	chr12:48044905-48044955	ovcar-3	ovarian:	n/a
46	chr12:47985234-47985284	Hela-S3	cervix:	n/a
47	chr12:48044905-48044955	NT2-D1	testis:	n/a
48	chr12:48044905-48044955	AG09309	skin:	n/a
49	chr12:48044905-48044955	HAEpiC	amniotic membrane:	n/a
50	chr12:47985234-47985284	MCF10A-Er-Src	breast:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:47954626..47957338-chr12:47968383..47970833,2	K562	blood:
2	chr12:47974012..47976836-chr12:47979914..47981559,2	K562	blood:
3	chr12:48041265..48043377-chr12:48228501..48230073,2	K562	blood:
4	chr12:48014490..48017395-chr12:48029451..48031685,2	MCF-7	breast:
5	chr12:47988486..47990191-chr12:47994085..47995626,2	MCF-7	breast:
6	chr12:47947520..47950380-chr12:47954557..47956247,2	MCF-7	breast:
7	chr12:48045249..48046046-chr12:48080121..48081065,3	MCF-7	breast:
8	chr12:48044022..48046311-chr12:48051570..48054955,3	K562	blood:
9	chr12:47954626..47957338-chr12:47968383..47970833,2	K562	blood:
10	chr12:47969970..47972142-chr12:47972144..47974115,2	K562	blood:
11	chr12:47974012..47976836-chr12:47979914..47981559,2	K562	blood:
12	chr12:47955362..47958310-chr12:48025284..48027406,2	MCF-7	breast:
13	chr12:48042180..48043761-chr12:48096547..48099075,2	K562	blood:
14	chr12:47960869..47963224-chr12:47965190..47966994,3	K562	blood:
15	chr12:48010127..48013715-chr12:48014407..48017154,4	K562	blood:
16	chr12:48044527..48046603-chr12:48048041..48049724,2	K562	blood:
17	chr12:47960869..47963224-chr12:47965190..47966994,3	K562	blood:
18	chr12:48014490..48017395-chr12:48029451..48031685,2	MCF-7	breast:
19	chr12:47947520..47950380-chr12:47954557..47956247,2	MCF-7	breast:
20	chr12:47969081..47971247-chr12:47974364..47977314,2	MCF-7	breast:
21	chr12:47959788..47962194-chr12:47969072..47971219,2	K562	blood:
22	chr12:47951165..47953932-chr12:47955672..47957240,2	MCF-7	breast:
23	chr12:47969970..47972142-chr12:47972144..47974115,2	K562	blood:
24	chr12:47949400..47951691-chr12:47954293..47957038,2	MCF-7	breast:
25	chr12:47949400..47951691-chr12:47954293..47957038,2	MCF-7	breast:
26	chr12:48040105..48042458-chr12:48048872..48051635,2	K562	blood:
27	chr12:48010127..48013715-chr12:48014407..48017154,4	K562	blood:
28	chr12:48038756..48040401-chr12:48092675..48094968,2	K562	blood:
29	chr12:47975336..47978227-chr12:47979914..47982995,4	K562	blood:
30	chr12:47951165..47953932-chr12:47955672..47957240,2	MCF-7	breast:
31	chr12:47969081..47971247-chr12:47974364..47977314,2	MCF-7	breast:
32	chr12:47978595..47981359-chr12:47984602..47986611,2	K562	blood:
33	chr12:47978595..47981359-chr12:47984602..47986611,2	K562	blood:
34	chr12:48045147..48046102-chr12:48080596..48081443,2	K562	blood:
35	chr12:47995378..47998174-chr12:48001804..48005197,3	K562	blood:
36	chr12:47975336..47978227-chr12:47979914..47982995,4	K562	blood:
37	chr12:47959788..47962194-chr12:47969072..47971219,2	K562	blood:
38	chr12:47955362..47958310-chr12:48025284..48027406,2	MCF-7	breast:
39	chr12:47995378..47998174-chr12:48001804..48005197,3	K562	blood:
40	chr12:47988486..47990191-chr12:47994085..47995626,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC48A1-4	chr12:48001617-48001971	NONHSAT027928
2	lnc-SLC48A1-6	chr12:47947058-47947319	expReg_chr12_3796_+

No data

Variant related genes	Relation type
ENSG00000257905	TF binding region
ENSG00000257905	CpG island
ENSG00000005175	chromatin interactions

Extended variants
information (count: 4037 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:4037 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10783205	chr12:47946795-47946796	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536903761	chr12:47946805-47946806	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs149188661	chr12:47946809-47946810	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187173329	chr12:47946810-47946811	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543167362	chr12:47946838-47946839	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs369255265	chr12:47946863-47946864	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs559868404	chr12:47946896-47946897	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs373717801	chr12:47946938-47946939	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs10875662	chr12:47946958-47946959	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs545379246	chr12:47946976-47946977	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs78526254	chr12:47947098-47947099	Weak transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs77371536	chr12:47947118-47947119	Weak transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs192483000	chr12:47947186-47947187	Weak transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs561167672	chr12:47947192-47947193	Weak transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs370071327	chr12:47947204-47947205	Weak transcription Enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
16	rs530208905	chr12:47947213-47947214	Weak transcription Enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
17	rs7296656	chr12:47947223-47947224	Weak transcription Enhancers ZNF genes & repeats	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs146966129	chr12:47947236-47947237	Weak transcription Enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
19	rs545878677	chr12:47947279-47947280	Weak transcription Enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
20	rs137984842	chr12:47947295-47947296	Weak transcription Enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
21	rs571118102	chr12:47947331-47947332	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs564989162	chr12:47947332-47947333	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs564128105	chr12:47947397-47947398	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs11346315	chr12:47947418-47947419	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs141977758	chr12:47947424-47947425	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs556949657	chr12:47947463-47947464	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs145724618	chr12:47947506-47947507	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs183931928	chr12:47947510-47947511	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs553548873	chr12:47947518-47947519	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs377404155	chr12:47947524-47947525	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs757354	chr12:47947551-47947552	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs545131263	chr12:47947572-47947573	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs558924770	chr12:47947594-47947595	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs148273888	chr12:47947627-47947628	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs576833254	chr12:47947722-47947723	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs73109453	chr12:47947779-47947780	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs547957959	chr12:47947814-47947815	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs141387737	chr12:47947870-47947871	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs561231963	chr12:47947884-47947885	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs530271514	chr12:47947892-47947893	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs540425260	chr12:47948040-47948041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs560266611	chr12:47948106-47948107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530170184	chr12:47948130-47948131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528202566	chr12:47948173-47948174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs544162490	chr12:47948223-47948224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs551157623	chr12:47948248-47948249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs186622601	chr12:47948269-47948270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs189901844	chr12:47948312-47948313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550933424	chr12:47948351-47948352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs150796281	chr12:47948356-47948357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	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
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Breast cancer	21785460	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:904 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:47943600-47951600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:47944200-47953000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr12:47945800-47947200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr12:47946000-47947000	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr12:47946400-47946800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr12:47946400-47947000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr12:47946400-47949800	Weak transcription	Colon Smooth Muscle	Colon
8	chr12:47946600-47947200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
9	chr12:47946800-47947400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr12:47947000-47947400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr12:47947000-47948000	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr12:47947200-47948000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr12:47947200-47949400	Enhancers	Dnd41	blood
14	chr12:47947200-47953200	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr12:47947400-47948200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr12:47947400-47951000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr12:47947800-47948400	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr12:47947800-47948800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr12:47948000-47948800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr12:47948000-47949000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr12:47948000-47949000	Weak transcription	HMEC	breast
22	chr12:47948000-47949200	Weak transcription	Primary neutrophils fromperipheralblood	blood
23	chr12:47948200-47948400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr12:47948200-47948600	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr12:47948200-47948600	Enhancers	Primary T killer memory cells from peripheral blood	blood
26	chr12:47949000-47950000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr12:47949000-47953200	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr12:47949200-47950200	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr12:47949600-47951600	Enhancers	HMEC	breast
30	chr12:47949600-47952000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr12:47949800-47950200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr12:47949800-47950800	Enhancers	NHEK	skin
33	chr12:47949800-47953400	Enhancers	Colon Smooth Muscle	Colon
34	chr12:47950000-47950200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr12:47950200-47950400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
36	chr12:47950200-47950400	Enhancers	Esophagus	oesophagus
37	chr12:47950200-47950600	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr12:47950200-47951200	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr12:47950200-47951400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr12:47950200-47951600	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr12:47950200-47952000	Enhancers	Fetal Brain Female	brain
42	chr12:47950200-47952200	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr12:47950200-47952400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr12:47950200-47953200	Enhancers	Rectal Smooth Muscle	rectum
45	chr12:47950400-47950800	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr12:47950400-47951000	Weak transcription	Esophagus	oesophagus
47	chr12:47950400-47952400	Enhancers	Brain Substantia Nigra	brain
48	chr12:47950800-47951400	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr12:47951000-47952000	Enhancers	Esophagus	oesophagus
50	chr12:47951000-47952200	Enhancers	Fetal Brain Male	brain

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