Variant report

Variant	nsv1066091
Chromosome Location	chr20:29991219-30057182
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	chr20:30033920-30034156	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:30048349-30048657	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:30037622-30037661	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:30001402-30001664	HepG2	liver:	n/a	n/a
5	ATF1	chr20:30049793-30049839	K562	blood:	n/a	n/a
6	ATF3	chr20:30048382-30048621	K562	blood:	n/a	n/a
7	BATF	chr20:30048389-30048584	GM12878	blood:	n/a	n/a
8	BHLHE40	chr20:30048429-30048635	GM12878	blood:	n/a	n/a
9	BRCA1	chr20:30048382-30048663	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr20:30047414-30047475	IMR90	lung:	n/a	chr20:30047426-30047437 chr20:30047447-30047458
11	CEBPB	chr20:30034509-30034535	HepG2	liver:	n/a	n/a
12	CEBPB	chr20:30021121-30021265	HepG2	liver:	n/a	n/a
13	CEBPB	chr20:30023127-30023161	HepG2	liver:	n/a	chr20:30023145-30023156
14	CEBPB	chr20:30043112-30043298	A549	lung:	n/a	chr20:30043163-30043174
15	CEBPB	chr20:30043140-30043294	HepG2	liver:	n/a	chr20:30043163-30043174
16	CEBPB	chr20:30013786-30013875	HepG2	liver:	n/a	chr20:30013846-30013859 chr20:30013846-30013857
17	CEBPB	chr20:30016863-30016945	HepG2	liver:	n/a	chr20:30016923-30016934
18	CEBPB	chr20:30043004-30043199	IMR90	lung:	n/a	chr20:30043163-30043174
19	CEBPB	chr20:30042832-30043031	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr20:30047340-30047550	K562	blood:	n/a	chr20:30047426-30047437 chr20:30047447-30047458
21	CEBPB	chr20:30047429-30047586	Hela-S3	cervix:	n/a	chr20:30047447-30047458
22	CEBPB	chr20:30043057-30043355	MCF-7	breast:	n/a	chr20:30043163-30043174
23	CEBPB	chr20:30047333-30047596	HepG2	liver:	n/a	chr20:30047426-30047437 chr20:30047447-30047458
24	CEBPZ	chr20:30047540-30047706	HepG2	liver:	n/a	n/a
25	CHD2	chr20:30041847-30041872	K562	blood:	n/a	n/a
26	CTCF	chr20:30001440-30001590	GM12865	blood:	n/a	n/a
27	CTCF	chr20:30048420-30048570	MCF-7	breast:	n/a	chr20:30048462-30048483
28	CTCF	chr20:30001540-30001690	HRE	kidney:	n/a	n/a
29	CTCF	chr20:30048282-30048669	K562	blood:	n/a	chr20:30048462-30048483
30	CTCF	chr20:30028140-30028290	HEK293	kidney:	n/a	chr20:30028233-30028254 chr20:30028239-30028255 chr20:30028238-30028256 chr20:30028240-30028253 chr20:30028240-30028253
31	CTCF	chr20:30048440-30048590	MCF-7	breast:	n/a	chr20:30048462-30048483
32	CTCF	chr20:30028120-30028270	GM12872	blood:	n/a	chr20:30028233-30028254 chr20:30028239-30028255 chr20:30028238-30028256 chr20:30028240-30028253 chr20:30028240-30028253
33	CTCF	chr20:30028161-30028369	MCF-7	breast:	n/a	chr20:30028233-30028254 chr20:30028239-30028255 chr20:30028238-30028256 chr20:30028240-30028253 chr20:30028240-30028253
34	CTCF	chr20:30048347-30048622	HUVEC	blood vessel:	n/a	chr20:30048462-30048483
35	CTCF	chr20:30048440-30048590	GM12864	blood:	n/a	chr20:30048462-30048483
36	CTCF	chr20:30028160-30028310	GM12871	blood:	n/a	chr20:30028233-30028254 chr20:30028239-30028255 chr20:30028238-30028256 chr20:30028240-30028253 chr20:30028240-30028253
37	CTCF	chr20:30028180-30028330	GM12867	blood:	n/a	chr20:30028233-30028254 chr20:30028239-30028255 chr20:30028238-30028256 chr20:30028240-30028253 chr20:30028240-30028253
38	CTCF	chr20:30028161-30028389	MCF-7	breast:	n/a	chr20:30028233-30028254 chr20:30028239-30028255 chr20:30028238-30028256 chr20:30028240-30028253 chr20:30028240-30028253
39	CTCF	chr20:30001460-30001610	AG09309	skin:	n/a	n/a
40	CTCF	chr20:30028160-30028310	AG04449	skin:	n/a	chr20:30028233-30028254 chr20:30028239-30028255 chr20:30028238-30028256 chr20:30028240-30028253 chr20:30028240-30028253
41	CTCF	chr20:30048284-30048664	H1-hESC	embryonic stem cell:	n/a	chr20:30048462-30048483
42	CTCF	chr20:30001480-30001630	GM12873	blood:	n/a	n/a
43	CTCF	chr20:30001460-30001610	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr20:30028120-30028270	BE2_C	brain:	n/a	chr20:30028233-30028254 chr20:30028239-30028255 chr20:30028238-30028256 chr20:30028240-30028253 chr20:30028240-30028253
45	CTCF	chr20:30042299-30042390	LNCaP	prostate:	n/a	chr20:30042359-30042372 chr20:30042352-30042373 chr20:30042357-30042375
46	CTCF	chr20:30028100-30028250	A549	lung:	n/a	n/a
47	CTCF	chr20:30027940-30028230	Hela-S3	cervix:	n/a	chr20:30028005-30028023 chr20:30028008-30028021 chr20:30028008-30028017
48	CTCF	chr20:30027953-30028475	K562	blood:	n/a	chr20:30028005-30028023 chr20:30028233-30028254 chr20:30028239-30028255 chr20:30028238-30028256 chr20:30028240-30028253 chr20:30028008-30028021 chr20:30028008-30028017 chr20:30028240-30028253
49	CTCF	chr20:30028180-30028330	GM12865	blood:	n/a	chr20:30028233-30028254 chr20:30028239-30028255 chr20:30028238-30028256 chr20:30028240-30028253 chr20:30028240-30028253
50	CTCF	chr20:30042320-30042470	HCT-116	colon:	n/a	chr20:30042359-30042372 chr20:30042352-30042373 chr20:30042357-30042375

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:30028292-30028342	Jurkat	blood:	n/a
2	chr20:29994846-29994896	LNCaP	prostate:	n/a
3	chr20:30028292-30028342	Jurkat	blood:	n/a
4	chr20:29994846-29994896	LNCaP	prostate:	n/a
5	chr20:30028292-30028342	NB4	blood:	n/a
6	chr20:30028223-30028273	Caco-2	colon:	n/a
7	chr20:30028229-30028279	SK-N-SH_RA	brain:	n/a
8	chr20:30028229-30028279	SK-N-MC	brain:	n/a
9	chr20:29994192-29994242	HIPEpiC	eye:	n/a
10	chr20:30008986-30009036	GM12878	blood:	n/a
11	chr20:30028418-30028468	K562	blood:	n/a
12	chr20:29994173-29994223	T-47D	breast:	n/a
13	chr20:30028292-30028342	HCPEpiC	choroid plexus:	n/a
14	chr20:30028229-30028279	BJ	skin:	n/a
15	chr20:29994173-29994223	GM12891	blood:	n/a
16	chr20:29994192-29994242	HPAEpiC	pulmonary alveolar:	n/a
17	chr20:30008142-30008192	SK-N-SH_RA	brain:	n/a
18	chr20:30008986-30009036	AG09309	skin:	n/a
19	chr20:30028062-30028112	GM12878	blood:	n/a
20	chr20:30028241-30028291	H1-hESC	embryonic stem cell:	embryo
21	chr20:30053333-30053383	GM12891	blood:	n/a
22	chr20:29994192-29994242	BJ	skin:	n/a
23	chr20:30028062-30028112	HL-60	blood:	n/a
24	chr20:29994173-29994223	MCF10A-Er-Src	breast:	n/a
25	chr20:29994173-29994223	HEEpiC	esophagus:	n/a
26	chr20:30028241-30028291	HCF	heart:	n/a
27	chr20:29994192-29994242	ovcar-3	ovarian:	n/a
28	chr20:30028223-30028273	AG09319	gingival:	n/a
29	chr20:29993663-29993713	U87	brain:	n/a
30	chr20:30012193-30012243	NHDF-neo	bronchial:	n/a
31	chr20:30008986-30009036	HMEC	breast:	n/a
32	chr20:30028418-30028468	AG09309	skin:	n/a
33	chr20:30028292-30028342	T-47D	breast:	n/a
34	chr20:29993663-29993713	HNPCEpiC	eye:	n/a
35	chr20:29994846-29994896	HMEC	breast:	n/a
36	chr20:29994192-29994242	HEK293	kidney:	embryo
37	chr20:30028241-30028291	HRCEpiC	kidney:	n/a
38	chr20:30007925-30007975	HEK293	kidney:	embryo
39	chr20:30028418-30028468	Jurkat	blood:	n/a
40	chr20:30028418-30028468	HNPCEpiC	eye:	n/a
41	chr20:29995343-29995393	SK-N-MC	brain:	n/a
42	chr20:30028292-30028342	HEEpiC	esophagus:	n/a
43	chr20:30028229-30028279	IMR90	lung:	fetal
44	chr20:30028292-30028342	PFSK-1	brain:	n/a
45	chr20:30028418-30028468	HCPEpiC	choroid plexus:	n/a
46	chr20:30028418-30028468	NH-A	brain:	n/a
47	chr20:30028223-30028273	NH-A	brain:	n/a
48	chr20:29994192-29994242	SKMC	muscle:	n/a
49	chr20:30028223-30028273	AG10803	skin:	n/a
50	chr20:30028229-30028279	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:30001111..30001772-chr20:30200396..30200937,2	MCF-7	breast:
2	chr20:30042574..30044997-chr20:30046543..30048384,2	MCF-7	breast:
3	chr20:30006873..30009795-chr20:30012384..30014922,2	MCF-7	breast:
4	chr20:29900644..29901274-chr20:30041865..30042847,4	MCF-7	breast:
5	chr20:30023186..30025887-chr20:30031461..30033796,2	K562	blood:
6	chr20:30001098..30001991-chr20:30090702..30091623,2	MCF-7	breast:
7	chr20:30045212..30046827-chr20:30114550..30117367,2	K562	blood:
8	chr20:30027160..30029164-chr20:30031582..30034603,3	K562	blood:
9	chr20:29900754..29901422-chr20:30042008..30042651,2	MCF-7	breast:
10	chr20:30050729..30053291-chr20:30054906..30056770,2	K562	blood:
11	chr20:29992014..29994023-chr20:30071484..30073415,2	K562	blood:
12	chr20:29984307..29986959-chr20:29988552..29991737,3	K562	blood:
13	chr20:30031405..30034135-chr20:30036580..30038805,2	K562	blood:
14	chr20:30043021..30045109-chr20:30047141..30048737,2	K562	blood:
15	chr20:30001115..30001627-chr20:30090661..30091593,2	MCF-7	breast:
16	chr20:30043021..30045109-chr20:30047141..30048737,2	K562	blood:
17	chr20:30001102..30001956-chr20:30200407..30201209,2	MCF-7	breast:
18	chr20:30042574..30044997-chr20:30046543..30048384,2	MCF-7	breast:
19	chr20:29976860..29979727-chr20:29989751..29991908,2	MCF-7	breast:
20	chr20:30048029..30048980-chr20:30090666..30091556,3	MCF-7	breast:
21	chr20:30031405..30034135-chr20:30036580..30038805,2	K562	blood:
22	chr20:30047555..30048272-chr4:189297803..189298552,2	MCF-7	breast:
23	chr20:30034296..30036142-chr20:30059251..30061850,2	K562	blood:
24	chr20:30023186..30025887-chr20:30031461..30033796,2	K562	blood:
25	chr20:30048218..30048964-chr20:30090625..30091177,2	K562	blood:
26	chr20:30027160..30029656-chr20:30030161..30033253,3	K562	blood:
27	chr20:30006873..30009795-chr20:30012384..30014922,2	MCF-7	breast:
28	chr20:30050729..30053291-chr20:30054906..30056770,2	K562	blood:
29	chr20:30048067..30048963-chr20:30311751..30312260,2	K562	blood:
30	chr20:30048219..30048754-chr20:30090655..30091410,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB121-1	chr20:30009242-30009481	NONHSAT079292
2	lnc-DEFB121-1	chr20:30011613-30011670	NONHSAT079292

Variant related genes	Relation type
DEFB122	TF binding region
DEFB123	TF binding region
DEFB121	TF binding region
DEFB122	CpG island
DEFB123	CpG island
DEFB121	CpG island
ENSG00000171552	chromatin interactions
ENSG00000180383	chromatin interactions
ENSG00000180424	chromatin interactions
ENSG00000180483	chromatin interactions

Extended variants
information (count: 967 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:967 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6088109	chr20:29991219-29991220	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs376211207	chr20:29991230-29991231	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs377161717	chr20:29991235-29991236	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs73906251	chr20:29991274-29991275	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs553288503	chr20:29991318-29991319	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs566787132	chr20:29991319-29991320	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs538903813	chr20:29991343-29991344	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs370825724	chr20:29991409-29991410	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs192388445	chr20:29991456-29991457	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs575544776	chr20:29991466-29991467	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs36029631	chr20:29991479-29991480	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs6088112	chr20:29991509-29991510	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs554414346	chr20:29991510-29991511	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs77652142	chr20:29991548-29991549	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs539858946	chr20:29991568-29991569	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs560060193	chr20:29991590-29991591	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs377133067	chr20:29991594-29991595	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs146128698	chr20:29991609-29991610	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs535373912	chr20:29991638-29991639	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs545324828	chr20:29991639-29991640	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs565225706	chr20:29991654-29991655	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs73108042	chr20:29991657-29991658	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs551152970	chr20:29991685-29991686	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs184716407	chr20:29991712-29991713	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs189008847	chr20:29991728-29991729	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs180853912	chr20:29991739-29991740	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs186140232	chr20:29991757-29991758	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs189748585	chr20:29991767-29991768	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs558934602	chr20:29991788-29991789	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs139843372	chr20:29991797-29991798	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs115332635	chr20:29991821-29991822	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs554709780	chr20:29991835-29991836	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs181378699	chr20:29991869-29991870	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs144190719	chr20:29994090-29994091	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs554485515	chr20:29994103-29994104	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs74647926	chr20:29994130-29994131	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs113870794	chr20:29994173-29994174	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
38	rs371119986	chr20:29994192-29994193	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs576415213	chr20:29994230-29994231	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs571160147	chr20:29994847-29994848	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs534388290	chr20:29994874-29994875	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs184394086	chr20:29995343-29995344	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs538005481	chr20:29995364-29995365	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs534705339	chr20:29995366-29995367	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
45	rs374684913	chr20:30000665-30000666	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs541758952	chr20:30000666-30000667	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs112836532	chr20:30000680-30000681	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs79134092	chr20:30000681-30000682	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs182210974	chr20:30000691-30000692	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs138938805	chr20:30000704-30000705	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
Autism	22495311	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21806811	CNVD
Melanoma	21693616	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
colon cancer	17210682	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	22028636	CNVD
Breast cancer	21264507	CNVD
Thyroid cancer	19087340	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Soft tissue tumor	16732325	CNVD
Colorectal cancer	19359472	CNVD
Gastric cancer	17167181	CNVD
Myeloproliferative neoplasm	19047681	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	22860045	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Lung cancer	18438408	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Oral cancer	21386901	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Gastric cancer	22014070	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:30001400-30001600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr20:30002200-30002800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr20:30006200-30006600	Active TSS	K562	blood
4	chr20:30012800-30013600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr20:30013000-30013600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr20:30018200-30019000	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr20:30024800-30025000	Enhancers	Spleen	Spleen
8	chr20:30025000-30028400	Weak transcription	Spleen	Spleen
9	chr20:30027800-30028800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
10	chr20:30028000-30028600	Enhancers	K562	blood
11	chr20:30028000-30028800	Active TSS	ES-I3 Cell Line	embryonic stem cell
12	chr20:30028000-30029800	Bivalent Enhancer	HepG2	liver
13	chr20:30028200-30028800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr20:30028200-30029400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
15	chr20:30028400-30028800	Enhancers	Spleen	Spleen
16	chr20:30028600-30029400	Weak transcription	K562	blood
17	chr20:30028800-30029200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr20:30029200-30030000	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr20:30029400-30029600	Enhancers	K562	blood
20	chr20:30029600-30033800	Weak transcription	K562	blood
21	chr20:30029800-30030400	Enhancers	HepG2	liver
22	chr20:30030000-30034000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr20:30030400-30030800	Weak transcription	HepG2	liver
24	chr20:30030800-30031000	Enhancers	HepG2	liver
25	chr20:30031000-30033600	Weak transcription	HepG2	liver
26	chr20:30033600-30034200	Enhancers	HepG2	liver
27	chr20:30033600-30034600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr20:30033600-30034600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr20:30033800-30034400	Enhancers	K562	blood
30	chr20:30034000-30034600	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr20:30034200-30034600	Flanking Active TSS	HepG2	liver
32	chr20:30034400-30034600	Flanking Active TSS	K562	blood
33	chr20:30034600-30034800	Active TSS	K562	blood
34	chr20:30034600-30037200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr20:30034600-30037800	Enhancers	HepG2	liver
36	chr20:30037000-30037400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr20:30037200-30037600	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr20:30037800-30038000	Flanking Active TSS	HepG2	liver
39	chr20:30038000-30038200	Enhancers	HepG2	liver
40	chr20:30040200-30040800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr20:30040200-30040800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr20:30040200-30041000	Enhancers	HSMMtube	muscle
43	chr20:30048000-30048200	Bivalent Enhancer	HepG2	liver
44	chr20:30048000-30048400	Enhancers	Primary B cells from peripheral blood	blood
45	chr20:30048000-30048400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
46	chr20:30048000-30048400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
47	chr20:30048200-30048400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
48	chr20:30048200-30048400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
49	chr20:30048200-30048400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr20:30048200-30048400	Bivalent Enhancer	Fetal Muscle Leg	muscle

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