Variant report

Variant	nsv948700
Chromosome Location	chr12:21008498-21422492
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1421)
CpG islands
(count:366)
Chromatin interactive
region (count:30)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1421 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:21392742-21392928	K562	blood:	n/a	n/a
2	ATF1	chr12:21387015-21387268	K562	blood:	n/a	n/a
3	BACH1	chr12:21380331-21380521	K562	blood:	n/a	n/a
4	BACH1	chr12:21350777-21350898	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr12:21322799-21322999	K562	blood:	n/a	n/a
6	BATF	chr12:21021928-21022137	GM12878	blood:	n/a	chr12:21022019-21022030
7	BATF	chr12:21090344-21090547	GM12878	blood:	n/a	n/a
8	BHLHE40	chr12:21017099-21017177	GM12878	blood:	n/a	n/a
9	BHLHE40	chr12:21138511-21138625	GM12878	blood:	n/a	n/a
10	BRCA1	chr12:21308670-21308879	H1-hESC	embryonic stem cell:	n/a	n/a
11	BRCA1	chr12:21322801-21323167	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr12:21103222-21103500	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr12:21193579-21193868	A549	lung:	n/a	chr12:21193754-21193765
14	CEBPB	chr12:21133477-21133530	HepG2	liver:	n/a	n/a
15	CEBPB	chr12:21358479-21358755	HepG2	liver:	n/a	n/a
16	CEBPB	chr12:21065012-21065124	HepG2	liver:	n/a	chr12:21065034-21065045
17	CEBPB	chr12:21168858-21169067	H1-hESC	embryonic stem cell:	n/a	chr12:21168919-21168930
18	CEBPB	chr12:21409453-21409717	HepG2	liver:	n/a	chr12:21409600-21409611
19	CEBPB	chr12:21394753-21395095	HepG2	liver:	n/a	chr12:21394924-21394935
20	CEBPB	chr12:21358486-21358919	A549	lung:	n/a	n/a
21	CEBPB	chr12:21234037-21234356	A549	lung:	n/a	chr12:21234179-21234190
22	CEBPB	chr12:21114301-21114316	A549	lung:	n/a	n/a
23	CEBPB	chr12:21246783-21246933	HepG2	liver:	n/a	chr12:21246828-21246839
24	CEBPB	chr12:21175930-21176170	HepG2	liver:	n/a	chr12:21176036-21176047 chr12:21176037-21176048 chr12:21176036-21176049 chr12:21176038-21176047
25	CEBPB	chr12:21260029-21260209	A549	lung:	n/a	chr12:21260128-21260137 chr12:21260126-21260137 chr12:21260126-21260139
26	CEBPB	chr12:21038060-21038439	A549	lung:	n/a	n/a
27	CEBPB	chr12:21417548-21417736	H1-hESC	embryonic stem cell:	n/a	chr12:21417620-21417631
28	CEBPB	chr12:21282343-21282678	HepG2	liver:	n/a	chr12:21282598-21282609 chr12:21282528-21282539
29	CEBPB	chr12:21127431-21127656	HepG2	liver:	n/a	chr12:21127518-21127529
30	CEBPB	chr12:21243014-21243312	A549	lung:	n/a	chr12:21243166-21243177
31	CEBPB	chr12:21243036-21243304	IMR90	lung:	n/a	chr12:21243166-21243177
32	CEBPB	chr12:21260027-21260258	HepG2	liver:	n/a	chr12:21260128-21260137 chr12:21260126-21260137 chr12:21260126-21260139
33	CEBPB	chr12:21417474-21417800	A549	lung:	n/a	chr12:21417620-21417631
34	CEBPB	chr12:21215636-21215960	A549	lung:	n/a	n/a
35	CEBPB	chr12:21271000-21271136	HepG2	liver:	n/a	chr12:21271080-21271091
36	CEBPB	chr12:21036268-21036667	A549	lung:	n/a	chr12:21036463-21036474 chr12:21036307-21036318
37	CEBPB	chr12:21015510-21015751	A549	lung:	n/a	n/a
38	CEBPB	chr12:21193602-21193866	HepG2	liver:	n/a	chr12:21193754-21193765
39	CEBPB	chr12:21036155-21036832	A549	lung:	n/a	chr12:21036463-21036474 chr12:21036307-21036318
40	CEBPB	chr12:21417491-21417780	HepG2	liver:	n/a	chr12:21417620-21417631
41	CEBPB	chr12:21418941-21419217	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr12:21168771-21169100	A549	lung:	n/a	chr12:21168919-21168930
43	CEBPB	chr12:21409481-21409705	A549	lung:	n/a	chr12:21409600-21409611
44	CEBPB	chr12:21038089-21038427	A549	lung:	n/a	n/a
45	CEBPB	chr12:21410877-21411098	A549	lung:	n/a	n/a
46	CEBPB	chr12:21234009-21234357	HepG2	liver:	n/a	chr12:21234179-21234190
47	CEBPB	chr12:21356602-21356832	H1-hESC	embryonic stem cell:	n/a	chr12:21356695-21356706
48	CEBPB	chr12:21193722-21193901	H1-hESC	embryonic stem cell:	n/a	chr12:21193754-21193765
49	CEBPB	chr12:21168774-21169104	HepG2	liver:	n/a	chr12:21168919-21168930
50	CEBPB	chr12:21356579-21356809	HepG2	liver:	n/a	chr12:21356695-21356706

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:21015340-21015390	BJ	skin:	n/a
2	chr12:21324585-21324635	HMEC	breast:	n/a
3	chr12:21283725-21283775	NB4	blood:	n/a
4	chr12:21287375-21287425	HRE	kidney:	n/a
5	chr12:21283725-21283775	SAEC	small airway:	n/a
6	chr12:21418929-21418979	GM06990	blood:	n/a
7	chr12:21015340-21015390	AG09309	skin:	n/a
8	chr12:21287375-21287425	AG09319	gingival:	n/a
9	chr12:21015340-21015390	HIPEpiC	eye:	n/a
10	chr12:21014317-21014367	HEK293	kidney:	embryo
11	chr12:21015340-21015390	Jurkat	blood:	n/a
12	chr12:21015340-21015390	Hepatocyte	liver:	n/a
13	chr12:21418929-21418979	Hela-S3	cervix:	n/a
14	chr12:21324585-21324635	NH-A	brain:	n/a
15	chr12:21418929-21418979	GM12892	blood:	n/a
16	chr12:21287375-21287425	LNCaP	prostate:	n/a
17	chr12:21014317-21014367	AG04449	skin:	fetal
18	chr12:21014317-21014367	Jurkat	blood:	n/a
19	chr12:21324585-21324635	PrEC	prostate:	n/a
20	chr12:21014317-21014367	U87	brain:	n/a
21	chr12:21283725-21283775	NH-A	brain:	n/a
22	chr12:21287375-21287425	SK-N-MC	brain:	n/a
23	chr12:21324585-21324635	NHBE	bronchial:	n/a
24	chr12:21014317-21014367	AoSMC	blood vessel:	n/a
25	chr12:21015340-21015390	GM19239	blood:	n/a
26	chr12:21324585-21324635	AG09319	gingival:	n/a
27	chr12:21287375-21287425	HPAEpiC	pulmonary alveolar:	n/a
28	chr12:21418929-21418979	LNCaP	prostate:	n/a
29	chr12:21287375-21287425	HUVEC	blood vessel:	n/a
30	chr12:21418929-21418979	PFSK-1	brain:	n/a
31	chr12:21014317-21014367	PrEC	prostate:	n/a
32	chr12:21283725-21283775	HMEC	breast:	n/a
33	chr12:21287375-21287425	HEEpiC	esophagus:	n/a
34	chr12:21324585-21324635	CMK	blood:	n/a
35	chr12:21287375-21287425	NT2-D1	testis:	n/a
36	chr12:21283725-21283775	Caco-2	colon:	n/a
37	chr12:21418929-21418979	RPTEC	kidney:	n/a
38	chr12:21015340-21015390	GM12892	blood:	n/a
39	chr12:21418929-21418979	AG09319	gingival:	n/a
40	chr12:21283725-21283775	HCM	heart:	n/a
41	chr12:21287375-21287425	GM19239	blood:	n/a
42	chr12:21015340-21015390	PANC-1	pancreas:	n/a
43	chr12:21283725-21283775	HCF	heart:	n/a
44	chr12:21283725-21283775	LNCaP	prostate:	n/a
45	chr12:21283725-21283775	HRPEpiC	eye:	n/a
46	chr12:21287375-21287425	NH-A	brain:	n/a
47	chr12:21014317-21014367	PANC-1	pancreas:	n/a
48	chr12:21014317-21014367	HCF	heart:	n/a
49	chr12:21287375-21287425	MCF-7	breast:	n/a
50	chr12:21283725-21283775	HIPEpiC	eye:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:21099420..21100309-chr12:21218592..21219170,2	MCF-7	breast:
2	chr12:21099420..21100309-chr12:21218592..21219170,2	MCF-7	breast:
3	chr12:21220478..21221206-chr12:21228660..21229307,2	MCF-7	breast:
4	chr12:21103010..21104123-chr12:21218514..21219449,3	MCF-7	breast:
5	chr12:21337800..21339752-chr12:21340612..21342590,2	K562	blood:
6	chr12:21154478..21155199-chr12:21322720..21323314,2	MCF-7	breast:
7	chr12:21220478..21221206-chr12:21228660..21229307,2	MCF-7	breast:
8	chr12:21099378..21100255-chr12:21322524..21323110,2	MCF-7	breast:
9	chr12:21373190..21374871-chr12:21381396..21383038,2	K562	blood:
10	chr12:21354085..21355966-chr12:21358587..21360653,2	K562	blood:
11	chr12:21367379..21369612-chr12:21376922..21378821,2	K562	blood:
12	chr12:21102918..21103853-chr12:21322562..21323307,3	MCF-7	breast:
13	chr12:21193958..21195458-chr17:59872939..59874521,2	MCF-7	breast:
14	chr12:21268556..21269333-chr7:84915114..84915941,2	MCF-7	breast:
15	chr12:21099355..21100332-chr12:21322634..21323175,3	MCF-7	breast:
16	chr12:21368652..21370975-chr12:21374890..21377722,2	K562	blood:
17	chr12:21099355..21100332-chr12:21322634..21323175,3	MCF-7	breast:
18	chr12:21103010..21104123-chr12:21218514..21219449,3	MCF-7	breast:
19	chr12:21099378..21100255-chr12:21322524..21323110,2	MCF-7	breast:
20	chr12:21254641..21256921-chr12:21258871..21260640,2	K562	blood:
21	chr12:21354085..21355966-chr12:21358587..21360653,2	K562	blood:
22	chr12:21102918..21103853-chr12:21322562..21323307,3	MCF-7	breast:
23	chr12:21254641..21256921-chr12:21258871..21260640,2	K562	blood:
24	chr12:21367379..21369612-chr12:21376922..21378821,2	K562	blood:
25	chr12:21154478..21155199-chr12:21322720..21323314,2	MCF-7	breast:
26	chr12:21337800..21339752-chr12:21340612..21342590,2	K562	blood:
27	chr12:21368652..21370975-chr12:21374890..21377722,2	K562	blood:
28	chr12:21373190..21374871-chr12:21381396..21383038,2	K562	blood:
29	chr12:21372629..21374270-chr12:21375812..21377730,2	K562	blood:
30	chr12:21372629..21374270-chr12:21375812..21377730,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLCO1B1-1	chr12:21228194-21228718	NONHSAT027240
2	lnc-SLCO1A2-5	chr12:21083248-21084757	NONHSAT027238
3	lnc-SLCO1B1-1	chr12:21220285-21220317	NONHSAT027240

No data

Variant related genes	Relation type
ENSG00000257062	TF binding region
SLCO1B1	TF binding region
SLCO1B7	TF binding region
SLCO1B3	TF binding region
ENSG00000257062	CpG island
SLCO1B1	CpG island
SLCO1B7	CpG island
SLCO1B3	CpG island

Extended variants
information (count: 13144 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:13144 , 50 per page) page: 1 2 3 4 5 6 7 ... 263

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7303743	chr12:21008498-21008499	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs371185830	chr12:21008512-21008513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373603904	chr12:21008556-21008557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138010878	chr12:21008561-21008562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567202916	chr12:21008592-21008593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs35056493	chr12:21008593-21008594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs35228554	chr12:21008730-21008731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs77638597	chr12:21008846-21008847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143555681	chr12:21008888-21008889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs74067318	chr12:21008908-21008909	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs201000252	chr12:21008970-21008971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543127592	chr12:21008990-21008991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557334065	chr12:21009003-21009004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190885888	chr12:21009012-21009013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183098103	chr12:21009045-21009046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10841672	chr12:21009049-21009050	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs145926334	chr12:21009069-21009070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564922119	chr12:21009080-21009081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531137971	chr12:21009145-21009146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187606474	chr12:21009149-21009150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10841673	chr12:21009213-21009214	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs190566022	chr12:21009218-21009219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10841674	chr12:21009253-21009254	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs529171266	chr12:21009310-21009311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs548945487	chr12:21009329-21009330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10841675	chr12:21009359-21009360	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs138844062	chr12:21009370-21009371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528196926	chr12:21009405-21009406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183199752	chr12:21009408-21009409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141322760	chr12:21009439-21009440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188258324	chr12:21009513-21009514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11045566	chr12:21009514-21009515	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs566524787	chr12:21009534-21009535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536952031	chr12:21009536-21009537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs368485132	chr12:21009539-21009540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs11045567	chr12:21009544-21009545	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs192345698	chr12:21009560-21009561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558599996	chr12:21009574-21009575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575313789	chr12:21009577-21009578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150799544	chr12:21009587-21009588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184291200	chr12:21009618-21009619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567537219	chr12:21009630-21009631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370304669	chr12:21009653-21009654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573898464	chr12:21009654-21009655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542858960	chr12:21009655-21009656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187818617	chr12:21009665-21009666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528259854	chr12:21009683-21009684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7307957	chr12:21009684-21009685	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs192390443	chr12:21009715-21009716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530603866	chr12:21009774-21009775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	16397240	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21364760	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	21346763	CNVD
Breast cancer	22522925	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Lung cancer	21911935	CNVD
Breast cancer	22048815	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Heart disease	21282601	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Gastric cancer	24379144	CNVD
Gastric cancer	19545448	CNVD
Lung cancer	20031968	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung adenocarcinoma	19826477	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19826477	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	17504988	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	19671679	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:254 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:21006200-21011000	Weak transcription	Liver	Liver
2	chr12:21006600-21018000	Weak transcription	A549	lung
3	chr12:21011000-21014600	Strong transcription	Liver	Liver
4	chr12:21014600-21015400	Weak transcription	Liver	Liver
5	chr12:21015400-21018400	Strong transcription	Liver	Liver
6	chr12:21017800-21019200	Enhancers	HUVEC	blood vessel
7	chr12:21018000-21018200	Strong transcription	A549	lung
8	chr12:21018200-21018800	Weak transcription	A549	lung
9	chr12:21018400-21020800	Weak transcription	Liver	Liver
10	chr12:21018800-21020600	Strong transcription	A549	lung
11	chr12:21019800-21020000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr12:21020000-21020400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr12:21020000-21020600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr12:21020600-21021600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr12:21020600-21027400	Weak transcription	A549	lung
16	chr12:21020800-21021200	Strong transcription	Liver	Liver
17	chr12:21020800-21021600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr12:21021200-21024600	Weak transcription	Liver	Liver
19	chr12:21021600-21022200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr12:21024600-21026200	Strong transcription	Liver	Liver
21	chr12:21026200-21027800	Weak transcription	Liver	Liver
22	chr12:21027400-21028400	Strong transcription	A549	lung
23	chr12:21027800-21029600	Strong transcription	Liver	Liver
24	chr12:21028400-21035800	Weak transcription	A549	lung
25	chr12:21029600-21032400	Weak transcription	Liver	Liver
26	chr12:21032400-21035400	Strong transcription	Liver	Liver
27	chr12:21034000-21034200	Enhancers	Rectal Smooth Muscle	rectum
28	chr12:21034400-21035000	Enhancers	Stomach Mucosa	stomach
29	chr12:21034400-21035600	Weak transcription	Rectal Smooth Muscle	rectum
30	chr12:21035000-21035400	Weak transcription	Stomach Mucosa	stomach
31	chr12:21035400-21036000	Enhancers	Stomach Mucosa	stomach
32	chr12:21035400-21039000	Weak transcription	Liver	Liver
33	chr12:21035600-21036200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr12:21035600-21036600	Enhancers	Rectal Smooth Muscle	rectum
35	chr12:21035600-21037800	Enhancers	Colon Smooth Muscle	Colon
36	chr12:21035800-21036600	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr12:21035800-21037000	Enhancers	Adipose Nuclei	Adipose
38	chr12:21035800-21037600	Enhancers	HUVEC	blood vessel
39	chr12:21035800-21038200	Enhancers	A549	lung
40	chr12:21038200-21038400	Flanking Active TSS	A549	lung
41	chr12:21038400-21038800	Enhancers	A549	lung
42	chr12:21038800-21040600	Weak transcription	A549	lung
43	chr12:21039000-21040000	Strong transcription	Liver	Liver
44	chr12:21040000-21046600	Weak transcription	Liver	Liver
45	chr12:21044600-21054200	Weak transcription	A549	lung
46	chr12:21046600-21048400	Strong transcription	Liver	Liver
47	chr12:21048400-21052400	Weak transcription	Liver	Liver
48	chr12:21049800-21050200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr12:21051800-21052200	Weak transcription	Aorta	Aorta
50	chr12:21052400-21052600	Enhancers	Aorta	Aorta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links