Variant report

Variant	nsv541329
Chromosome Location	chr12:504573-586674
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1830)
CpG islands
(count:2323)
Chromatin interactive
region (count:49)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1830 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:511331-511652	K562	blood:	n/a	n/a
2	ARID3A	chr12:510180-510242	K562	blood:	n/a	n/a
3	ATF1	chr12:515974-516345	K562	blood:	n/a	n/a
4	ATF1	chr12:510436-510930	K562	blood:	n/a	n/a
5	ATF1	chr12:511278-511685	K562	blood:	n/a	n/a
6	ATF2	chr12:510432-510994	GM12878	blood:	n/a	n/a
7	ATF2	chr12:510426-510971	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr12:515973-516410	K562	blood:	n/a	n/a
9	ATF3	chr12:562477-562737	GM12878	blood:	n/a	n/a
10	ATF3	chr12:562458-562788	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr12:510544-510949	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr12:562530-562764	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr12:515953-516283	K562	blood:	n/a	n/a
14	BACH1	chr12:569939-570255	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr12:529122-529352	GM12878	blood:	n/a	n/a
16	BATF	chr12:562151-562738	GM12878	blood:	n/a	n/a
17	BATF	chr12:529788-530091	GM12878	blood:	n/a	n/a
18	BCL11A	chr12:562080-562805	GM12878	blood:	n/a	n/a
19	BCL11A	chr12:562203-562719	GM12878	blood:	n/a	n/a
20	BCL3	chr12:510404-511202	A549	lung:	n/a	n/a
21	BCL3	chr12:510447-511339	A549	lung:	n/a	n/a
22	BHLHE40	chr12:515401-515749	K562	blood:	n/a	n/a
23	BHLHE40	chr12:551635-551655	K562	blood:	n/a	n/a
24	BHLHE40	chr12:515997-516342	K562	blood:	n/a	n/a
25	BHLHE40	chr12:568683-568808	K562	blood:	n/a	n/a
26	BHLHE40	chr12:562200-562747	GM12878	blood:	n/a	n/a
27	BHLHE40	chr12:510198-511441	K562	blood:	n/a	n/a
28	BHLHE40	chr12:559708-559969	K562	blood:	n/a	n/a
29	BHLHE40	chr12:570572-570903	HepG2	liver:	n/a	n/a
30	BRCA1	chr12:510425-510985	GM12878	blood:	n/a	n/a
31	BRCA1	chr12:510477-510896	HepG2	liver:	n/a	n/a
32	BRCA1	chr12:510458-510903	H1-hESC	embryonic stem cell:	n/a	n/a
33	BRCA1	chr12:510309-510949	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr12:515984-516531	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr12:551492-551762	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr12:561932-562822	K562	blood:	n/a	n/a
37	CBX3	chr12:515966-516383	K562	blood:	n/a	n/a
38	CBX3	chr12:562047-562747	K562	blood:	n/a	n/a
39	CCNT2	chr12:510455-511004	K562	blood:	n/a	chr12:510983-510992
40	CCNT2	chr12:516019-516466	K562	blood:	n/a	n/a
41	CEBPB	chr12:515899-516441	K562	blood:	n/a	chr12:516063-516074
42	CEBPB	chr12:515891-516405	Hela-S3	cervix:	n/a	chr12:516063-516074
43	CEBPB	chr12:515824-516325	A549	lung:	n/a	chr12:516063-516074
44	CEBPB	chr12:551291-551648	HepG2	liver:	n/a	chr12:551414-551425
45	CEBPB	chr12:577001-577239	K562	blood:	n/a	chr12:577070-577081
46	CEBPB	chr12:576948-577229	IMR90	lung:	n/a	chr12:577070-577081
47	CEBPB	chr12:547594-547767	HepG2	liver:	n/a	chr12:547618-547629
48	CEBPB	chr12:568214-568497	A549	lung:	n/a	n/a
49	CEBPB	chr12:559882-559914	K562	blood:	n/a	n/a
50	CEBPB	chr12:568253-568483	HepG2	liver:	n/a	n/a

(count:2323 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:570249-570299	Jurkat	blood:	n/a
2	chr12:568543-568593	K562	blood:	n/a
3	chr12:534917-534967	MCF10A-Er-Src	breast:	n/a
4	chr12:510474-510524	NHBE	bronchial:	n/a
5	chr12:569679-569729	HCT-116	colon:	n/a
6	chr12:570249-570299	Jurkat	blood:	n/a
7	chr12:568543-568593	K562	blood:	n/a
8	chr12:534917-534967	MCF10A-Er-Src	breast:	n/a
9	chr12:510474-510524	NHBE	bronchial:	n/a
10	chr12:569679-569729	HCT-116	colon:	n/a
11	chr12:510474-510524	GM12878	blood:	n/a
12	chr12:562065-562115	GM12878	blood:	n/a
13	chr12:551573-551623	ovcar-3	ovarian:	n/a
14	chr12:569221-569271	SKMC	muscle:	n/a
15	chr12:511111-511161	A549	lung:	n/a
16	chr12:510476-510526	HUVEC	blood vessel:	n/a
17	chr12:510476-510526	HRCEpiC	kidney:	n/a
18	chr12:573270-573320	HCPEpiC	choroid plexus:	n/a
19	chr12:570155-570205	HIPEpiC	eye:	n/a
20	chr12:510594-510644	IMR90	lung:	fetal
21	chr12:568798-568848	Caco-2	colon:	n/a
22	chr12:568826-568876	Hepatocyte	liver:	n/a
23	chr12:564731-564781	MCF-7	breast:	n/a
24	chr12:569733-569783	IMR90	lung:	fetal
25	chr12:564731-564781	ProgFib	skin:	n/a
26	chr12:510550-510600	AoSMC	blood vessel:	n/a
27	chr12:515355-515405	NT2-D1	testis:	n/a
28	chr12:568826-568876	AG04450	lung:	fetal
29	chr12:569679-569729	Hela-S3	cervix:	n/a
30	chr12:568931-568981	U87	brain:	n/a
31	chr12:510594-510644	AG09319	gingival:	n/a
32	chr12:506697-506747	AoSMC	blood vessel:	n/a
33	chr12:534669-534719	SK-N-MC	brain:	n/a
34	chr12:510535-510585	BE2_C	brain:	n/a
35	chr12:535855-535905	HEEpiC	esophagus:	n/a
36	chr12:510665-510715	Hela-S3	cervix:	n/a
37	chr12:573270-573320	AG10803	skin:	n/a
38	chr12:551046-551096	Jurkat	blood:	n/a
39	chr12:535855-535905	HEK293	kidney:	embryo
40	chr12:534917-534967	ProgFib	skin:	n/a
41	chr12:551046-551096	HPAEpiC	pulmonary alveolar:	n/a
42	chr12:510772-510822	PrEC	prostate:	n/a
43	chr12:569679-569729	AG09309	skin:	n/a
44	chr12:510594-510644	GM06990	blood:	n/a
45	chr12:569733-569783	K562	blood:	n/a
46	chr12:510665-510715	ovcar-3	ovarian:	n/a
47	chr12:510594-510644	HRCEpiC	kidney:	n/a
48	chr12:551046-551096	U87	brain:	n/a
49	chr12:568543-568593	HRE	kidney:	n/a
50	chr12:569221-569271	HCPEpiC	choroid plexus:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:562205..562756-chr12:650853..651426,2	MCF-7	breast:
2	chr12:496401..500895-chr12:509695..513736,6	K562	blood:
3	chr12:563544..564514-chr12:655825..656615,2	MCF-7	breast:
4	chr12:562142..562756-chr12:667856..668414,2	MCF-7	breast:
5	chr12:562096..563077-chr12:923022..923690,2	MCF-7	breast:
6	chr12:562235..562796-chr12:678736..679457,3	MCF-7	breast:
7	chr12:541135..544043-chr12:1097640..1100614,2	K562	blood:
8	chr12:552972..554536-chr12:556070..557992,2	MCF-7	breast:
9	chr12:547432..549780-chr12:1702241..1704941,2	MCF-7	breast:
10	chr12:562076..562781-chr12:1058723..1059610,2	K562	blood:
11	chr12:567792..568717-chr12:633148..633750,3	MCF-7	breast:
12	chr12:515684..517646-chr12:519999..522840,2	K562	blood:
13	chr12:553314..555353-chr12:563794..566581,2	MCF-7	breast:
14	chr12:508524..511172-chr12:751040..752702,2	MCF-7	breast:
15	chr12:579325..581351-chr12:586759..589716,2	MCF-7	breast:
16	chr12:567380..570258-chr12:571395..573761,2	MCF-7	breast:
17	chr12:509245..512944-chr12:513140..518002,8	K562	blood:
18	chr12:497611..500419-chr12:508788..511712,2	MCF-7	breast:
19	chr12:563329..565508-chr12:567009..569483,2	MCF-7	breast:
20	chr12:562705..564349-chr12:655693..658061,2	MCF-7	breast:
21	chr12:558395..561077-chr12:566153..568160,2	K562	blood:
22	chr12:563547..564241-chr12:655739..656517,2	MCF-7	breast:
23	chr12:509480..512671-chr12:512718..518002,7	K562	blood:
24	chr12:563329..565508-chr12:567009..569483,2	MCF-7	breast:
25	chr12:510904..511428-chr12:655804..656333,2	MCF-7	breast:
26	chr12:551367..552157-chr12:655845..657279,4	MCF-7	breast:
27	chr12:551637..552181-chr12:1692709..1693253,2	K562	blood:
28	chr12:510462..511217-chr17:8113394..8114106,2	Hela-S3	cervix:
29	chr12:562216..562824-chr12:680454..681003,2	MCF-7	breast:
30	chr12:562294..562804-chr12:608079..608940,2	MCF-7	breast:
31	chr12:561789..563094-chr12:650609..651816,8	MCF-7	breast:
32	chr12:553314..555353-chr12:563794..566581,2	MCF-7	breast:
33	chr12:515684..517646-chr12:519999..522840,2	K562	blood:
34	chr12:558395..561077-chr12:566153..568160,2	K562	blood:
35	chr12:562112..562967-chr12:655719..656711,9	K562	blood:
36	chr12:565368..565882-chr12:633415..633928,2	MCF-7	breast:
37	chr12:549410..550324-chr12:655836..656812,2	K562	blood:
38	chr12:510695..511242-chr7:6098537..6099050,2	Hela-S3	cervix:
39	chr12:563912..565642-chr12:570833..573151,2	K562	blood:
40	chr12:551206..552180-chr12:655785..656728,9	K562	blood:
41	chr12:552972..554536-chr12:556070..557992,2	MCF-7	breast:
42	chr12:562103..563075-chr12:634406..635587,3	MCF-7	breast:
43	chr12:510128..512811-chr12:522624..524245,2	MCF-7	breast:
44	chr12:561777..563247-chr12:653593..656972,77	MCF-7	breast:
45	chr12:561825..562818-chr12:694443..695023,2	MCF-7	breast:
46	chr12:563912..565642-chr12:570833..573151,2	K562	blood:
47	chr12:559544..561291-chr12:645812..647419,2	K562	blood:
48	chr12:562086..563088-chr12:655521..657408,28	MCF-7	breast:
49	chr12:562106..562698-chr12:860790..861501,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-B4GALNT3-5	chr12:518534-518947	NONHSAT025343
2	lnc-B4GALNT3-5	chr12:510817-510850	NONHSAT025343
3	lnc-KDM5A-4	chr12:510484-510565	NONHSAT025342
4	lnc-KDM5A-4	chr12:510059-510216	NONHSAT025342
5	lnc-B4GALNT3-5	chr12:514677-514730	NONHSAT025343

No data

Variant related genes	Relation type
CCDC77	TF binding region
B4GALNT3	TF binding region
CCDC77	CpG island
B4GALNT3	CpG island
ENSG00000139044	chromatin interactions
ENSG00000073614	chromatin interactions
ENSG00000120647	chromatin interactions
ENSG00000171823	chromatin interactions
ENSG00000250132	chromatin interactions
ENSG00000086232	chromatin interactions
ENSG00000177406	chromatin interactions
ENSG00000178999	chromatin interactions
ENSG00000082805	chromatin interactions
ENSG00000002016	chromatin interactions

Extended variants
information (count: 3668 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:3668 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376178660	chr12:504599-504600	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs377487746	chr12:504618-504619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188577811	chr12:504628-504629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs145553990	chr12:504659-504660	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs191464720	chr12:504676-504677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564198705	chr12:504679-504680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183320552	chr12:504717-504718	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371125898	chr12:504767-504768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548239850	chr12:504786-504787	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs2007537	chr12:504797-504798	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs530761603	chr12:504798-504799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138027873	chr12:504826-504827	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187820033	chr12:504860-504861	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs149074897	chr12:504881-504882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554229623	chr12:504929-504930	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548937075	chr12:505003-505004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191437283	chr12:505017-505018	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554997837	chr12:505038-505039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576341665	chr12:505045-505046	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537319300	chr12:505111-505112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558726047	chr12:505120-505121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576980451	chr12:505214-505215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143087182	chr12:505259-505260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559399679	chr12:505284-505285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568710548	chr12:505285-505286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs9805067	chr12:505333-505334	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs146941930	chr12:505374-505375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563241929	chr12:505425-505426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113517665	chr12:505470-505471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183760891	chr12:505473-505474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552453327	chr12:505489-505490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188043679	chr12:505514-505515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374294849	chr12:505522-505523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564282620	chr12:505533-505534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs77565550	chr12:505581-505582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1541462	chr12:505595-505596	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs137905274	chr12:505608-505609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536314648	chr12:505648-505649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192464389	chr12:505718-505719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1541463	chr12:505759-505760	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs185273089	chr12:505799-505800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1541464	chr12:505839-505840	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs143320727	chr12:505847-505848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190307000	chr12:505899-505900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs1541465	chr12:505920-505921	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs574493585	chr12:505932-505933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531421418	chr12:505936-505937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371464925	chr12:505962-505963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147526589	chr12:505966-505967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs181508425	chr12:505973-505974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	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
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Autism	22495309	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Melanoma	20877625	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Pleomorphic liposarcoma	18784837	CNVD
small cell lung cancer	17426248	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2597 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:499200-510000	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr12:499200-510000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr12:499200-510000	Weak transcription	Placenta	Placenta
4	chr12:499200-510000	Weak transcription	Left Ventricle	heart
5	chr12:499200-510000	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr12:499400-509400	Weak transcription	Fetal Intestine Small	intestine
7	chr12:499400-510000	Weak transcription	Primary hematopoietic stem cells	blood
8	chr12:499400-510000	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr12:499400-510000	Weak transcription	Brain Substantia Nigra	brain
10	chr12:499600-510000	Weak transcription	Primary T cells from cord blood	blood
11	chr12:499600-510000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr12:499600-510000	Weak transcription	Brain Anterior Caudate	brain
13	chr12:499600-510000	Weak transcription	Fetal Lung	lung
14	chr12:499600-510000	Weak transcription	Fetal Muscle Leg	muscle
15	chr12:499600-510400	Weak transcription	Fetal Brain Male	brain
16	chr12:499800-510000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr12:499800-510000	Weak transcription	A549	lung
18	chr12:504400-505200	Strong transcription	Fetal Stomach	stomach
19	chr12:505200-510200	Weak transcription	Fetal Stomach	stomach
20	chr12:509400-510000	Enhancers	Fetal Intestine Small	intestine
21	chr12:509400-510000	Enhancers	K562	blood
22	chr12:509400-511800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr12:509600-509800	Enhancers	Dnd41	blood
24	chr12:509600-510000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr12:509600-510000	Enhancers	Fetal Intestine Large	intestine
26	chr12:509600-510000	Enhancers	HepG2	liver
27	chr12:509800-510000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr12:509800-510000	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr12:509800-510000	Enhancers	Primary T killer memory cells from peripheral blood	blood
30	chr12:509800-510000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr12:509800-510000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr12:509800-510000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr12:509800-510000	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr12:509800-510000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr12:509800-510000	Enhancers	Adipose Nuclei	Adipose
36	chr12:509800-510000	Enhancers	Brain Angular Gyrus	brain
37	chr12:509800-510000	Enhancers	Brain Hippocampus Middle	brain
38	chr12:509800-510000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
39	chr12:509800-510000	Enhancers	Colon Smooth Muscle	Colon
40	chr12:509800-510000	Enhancers	Duodenum Mucosa	Duodenum
41	chr12:509800-510000	Enhancers	Fetal Heart	heart
42	chr12:509800-510000	Enhancers	Rectal Smooth Muscle	rectum
43	chr12:509800-510000	Enhancers	Skeletal Muscle Male	skeletal muscle
44	chr12:509800-510000	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr12:509800-510000	Enhancers	GM12878-XiMat	blood
46	chr12:509800-510000	Enhancers	Hela-S3	cervix
47	chr12:509800-510600	Flanking Active TSS	Dnd41	blood
48	chr12:510000-510200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr12:510000-510200	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr12:510000-510200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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