Variant report

Variant	esv1802746
Chromosome Location	chr12:737230-752482
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:958)
CpG islands
(count:611)
Chromatin interactive
region (count:34)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:958 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:741280-741704	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:749111-749150	K562	blood:	n/a	n/a
3	ARID3A	chr12:743086-743324	HepG2	liver:	n/a	n/a
4	ATF2	chr12:739072-739566	GM12878	blood:	n/a	n/a
5	ATF2	chr12:739681-740480	GM12878	blood:	n/a	n/a
6	ATF2	chr12:751604-752174	GM12878	blood:	n/a	n/a
7	ATF2	chr12:745685-746246	GM12878	blood:	n/a	n/a
8	ATF2	chr12:739151-739544	GM12878	blood:	n/a	n/a
9	ATF3	chr12:751842-752074	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr12:751830-752092	K562	blood:	n/a	n/a
11	ATF3	chr12:751751-752142	GM12878	blood:	n/a	chr12:751828-751837
12	ATF3	chr12:741095-742097	A549	lung:	n/a	n/a
13	ATF3	chr12:740929-742235	A549	lung:	n/a	chr12:742131-742139
14	BACH1	chr12:751945-752753	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr12:741558-741930	GM12878	blood:	n/a	chr12:741768-741779
16	BATF	chr12:751594-751825	GM12878	blood:	n/a	n/a
17	BATF	chr12:745878-746123	GM12878	blood:	n/a	n/a
18	BCL11A	chr12:751833-752090	GM12878	blood:	n/a	n/a
19	BCL3	chr12:739181-739461	GM12878	blood:	n/a	n/a
20	BCL3	chr12:740892-742303	A549	lung:	n/a	n/a
21	BCL3	chr12:752331-752877	A549	lung:	n/a	n/a
22	BCL3	chr12:740921-742194	A549	lung:	n/a	n/a
23	BCL3	chr12:751585-752198	GM12878	blood:	n/a	n/a
24	BCLAF1	chr12:739614-740086	GM12878	blood:	n/a	chr12:739944-739957 chr12:739946-739955
25	BCLAF1	chr12:739669-740256	GM12878	blood:	n/a	chr12:739944-739957 chr12:739946-739955
26	BCLAF1	chr12:751703-752097	GM12878	blood:	n/a	n/a
27	BCLAF1	chr12:751697-753147	GM12878	blood:	n/a	n/a
28	BHLHE40	chr12:739686-740235	GM12878	blood:	n/a	n/a
29	BHLHE40	chr12:748786-748900	GM12878	blood:	n/a	n/a
30	BHLHE40	chr12:741019-741584	A549	lung:	n/a	n/a
31	BHLHE40	chr12:751566-752695	GM12878	blood:	n/a	chr12:751804-751820
32	BHLHE40	chr12:737778-737900	K562	blood:	n/a	n/a
33	BHLHE40	chr12:751793-753273	K562	blood:	n/a	chr12:751804-751820
34	BRCA1	chr12:751117-751249	GM12878	blood:	n/a	n/a
35	CBX3	chr12:752477-753062	K562	blood:	n/a	n/a
36	CCNT2	chr12:751817-752596	K562	blood:	n/a	n/a
37	CEBPB	chr12:740921-742309	A549	lung:	n/a	chr12:741185-741197
38	CEBPB	chr12:741347-741704	HepG2	liver:	n/a	n/a
39	CEBPB	chr12:741054-742226	A549	lung:	n/a	chr12:741185-741197
40	CEBPB	chr12:752462-752951	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr12:741132-742098	A549	lung:	n/a	chr12:741185-741197
42	CEBPD	chr12:737055-737369	HepG2	liver:	n/a	n/a
43	CHD1	chr12:740002-740147	H1-hESC	embryonic stem cell:	n/a	chr12:740078-740088 chr12:740034-740044
44	CHD1	chr12:739865-740447	GM12878	blood:	n/a	chr12:740078-740088 chr12:740034-740044
45	CHD1	chr12:739220-739583	GM12878	blood:	n/a	n/a
46	CHD1	chr12:751725-753716	GM12878	blood:	n/a	chr12:751750-751759
47	CHD2	chr12:751766-752686	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr12:741396-741895	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr12:741691-741924	GM12878	blood:	n/a	n/a
50	CHD2	chr12:739729-740247	GM12878	blood:	n/a	chr12:740078-740088 chr12:740034-740044

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:751753-751803	AG10803	skin:	n/a
2	chr12:751753-751803	AG10803	skin:	n/a
3	chr12:740100-740150	GM12878	blood:	n/a
4	chr12:749527-749577	GM12892	blood:	n/a
5	chr12:752290-752340	HCF	heart:	n/a
6	chr12:741507-741557	GM06990	blood:	n/a
7	chr12:739980-740030	LNCaP	prostate:	n/a
8	chr12:739280-739330	PFSK-1	brain:	n/a
9	chr12:739980-740030	Hela-S3	cervix:	n/a
10	chr12:752381-752431	MCF10A-Er-Src	breast:	n/a
11	chr12:740338-740388	ECC-1	luminal epithelium:	n/a
12	chr12:739280-739330	GM12891	blood:	n/a
13	chr12:751692-751742	HCPEpiC	choroid plexus:	n/a
14	chr12:749527-749577	MCF-7	breast:	n/a
15	chr12:749527-749577	NH-A	brain:	n/a
16	chr12:740338-740388	HEEpiC	esophagus:	n/a
17	chr12:740100-740150	HRCEpiC	kidney:	n/a
18	chr12:752381-752431	HMEC	breast:	n/a
19	chr12:739280-739330	NHBE	bronchial:	n/a
20	chr12:739280-739330	AG10803	skin:	n/a
21	chr12:752381-752431	HNPCEpiC	eye:	n/a
22	chr12:740100-740150	SKMC	muscle:	n/a
23	chr12:741507-741557	HL-60	blood:	n/a
24	chr12:741507-741557	GM19239	blood:	n/a
25	chr12:751753-751803	LNCaP	prostate:	n/a
26	chr12:740100-740150	T-47D	breast:	n/a
27	chr12:751753-751803	AG04449	skin:	fetal
28	chr12:749527-749577	LNCaP	prostate:	n/a
29	chr12:741507-741557	SK-N-MC	brain:	n/a
30	chr12:749527-749577	Hela-S3	cervix:	n/a
31	chr12:749527-749577	HRCEpiC	kidney:	n/a
32	chr12:751753-751803	AoSMC	blood vessel:	n/a
33	chr12:740338-740388	AG09309	skin:	n/a
34	chr12:740338-740388	PrEC	prostate:	n/a
35	chr12:751753-751803	SK-N-SH	brain:	n/a
36	chr12:751692-751742	GM19239	blood:	n/a
37	chr12:752381-752431	AG04449	skin:	fetal
38	chr12:739980-740030	ovcar-3	ovarian:	n/a
39	chr12:749527-749577	NHBE	bronchial:	n/a
40	chr12:751753-751803	NHBE	bronchial:	n/a
41	chr12:739980-740030	GM12878	blood:	n/a
42	chr12:752381-752431	SKMC	muscle:	n/a
43	chr12:752381-752431	AG09319	gingival:	n/a
44	chr12:752381-752431	BE2_C	brain:	n/a
45	chr12:751692-751742	GM06990	blood:	n/a
46	chr12:749527-749577	RPTEC	kidney:	n/a
47	chr12:740100-740150	HEK293	kidney:	embryo
48	chr12:752290-752340	NT2-D1	testis:	n/a
49	chr12:752381-752431	SAEC	small airway:	n/a
50	chr12:751692-751742	PANC-1	pancreas:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:747492..749466-chr12:752449..754926,2	MCF-7	breast:
2	chr12:749128..755954-chr12:858463..864495,7	MCF-7	breast:
3	chr12:744135..746381-chr12:747872..750045,2	MCF-7	breast:
4	chr12:740454..743801-chr12:746950..749909,6	MCF-7	breast:
5	chr12:751220..755551-chr12:860416..865761,8	K562	blood:
6	chr12:698993..700663-chr12:750297..752796,2	K562	blood:
7	chr11:62609043..62609718-chr12:740053..741009,2	NB4	blood:
8	chr12:746607..749466-chr12:749610..751934,3	K562	blood:
9	chr12:739608..744885-chr12:750259..753818,8	MCF-7	breast:
10	chr12:736660..739478-chr12:748534..751154,2	K562	blood:
11	chr12:746607..749584-chr12:749610..753132,4	K562	blood:
12	chr12:746884..750259-chr12:756842..758934,3	K562	blood:
13	chr12:742386..744766-chr12:749695..751874,2	K562	blood:
14	chr12:740454..743801-chr12:746950..749909,6	MCF-7	breast:
15	chr12:741380..743074-chr12:743313..746220,2	MCF-7	breast:
16	chr12:508524..511172-chr12:751040..752702,2	MCF-7	breast:
17	chr12:741380..743074-chr12:743313..746220,2	MCF-7	breast:
18	chr12:752081..752621-chr15:68569750..68570655,2	HCT-116	colon:
19	chr12:738549..743434-chr12:750658..753859,6	MCF-7	breast:
20	chr12:696407..698451-chr12:743928..745643,2	MCF-7	breast:
21	chr12:739334..741511-chr12:860709..863370,3	MCF-7	breast:
22	chr12:742386..744973-chr12:747394..751874,4	K562	blood:
23	chr12:738549..743434-chr12:750658..753859,6	MCF-7	breast:
24	chr12:736660..739478-chr12:748534..751154,2	K562	blood:
25	chr12:751801..754339-chr12:772154..775493,3	MCF-7	breast:
26	chr12:739608..744885-chr12:750259..753818,8	MCF-7	breast:
27	chr12:695602..698441-chr12:748222..750831,2	K562	blood:
28	chr12:742026..744558-chr12:860085..862333,2	MCF-7	breast:
29	chr12:748631..750707-chr12:754970..756942,2	MCF-7	breast:
30	chr12:750256..753677-chr12:768929..774136,4	MCF-7	breast:
31	chr12:751953..754697-chr12:859970..862221,2	K562	blood:
32	chr12:749727..757562-chr12:858273..868886,17	MCF-7	breast:
33	chr12:744135..746381-chr12:747872..750045,2	MCF-7	breast:
34	chr12:745810..749958-chr12:750110..752210,4	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-B4GALNT3-2	chr12:752147-752883	ENSG00000177406.4
2	lnc-B4GALNT3-2	chr12:741380-741413	ENSG00000177406.4
3	lnc-B4GALNT3-2	chr12:751859-751904	NONHSAT025358
4	lnc-B4GALNT3-2	chr12:751840-751904	ENSG00000177406.4
5	lnc-B4GALNT3-2	chr12:740057-740151	ENSG00000177406.4
6	lnc-B4GALNT3-2	chr12:741675-741782	ENSG00000177406.4
7	lnc-B4GALNT3-2	chr12:750010-750190	ENSG00000177406.4

No data

Variant related genes	Relation type
ENSG00000177406	TF binding region
ENSG00000177406	CpG island
ENSG00000133316	chromatin interactions
ENSG00000171840	chromatin interactions
ENSG00000060237	chromatin interactions
ENSG00000120647	chromatin interactions
ENSG00000256020	chromatin interactions
ENSG00000177406	chromatin interactions
ENSG00000255825	chromatin interactions
ENSG00000169018	chromatin interactions
ENSG00000260657	chromatin interactions

Extended variants
information (count: 595 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:595 , 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	rs10849359	chr12:737230-737231	Enhancers Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553996142	chr12:737296-737297	Enhancers Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs572719222	chr12:737309-737310	Enhancers Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs547081942	chr12:737392-737393	Enhancers Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs565631910	chr12:737394-737395	Enhancers Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs139634493	chr12:737395-737396	Enhancers Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs536217388	chr12:737463-737464	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs181595479	chr12:737487-737488	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs71045089	chr12:737507-737508	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs542117640	chr12:737534-737535	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs551456101	chr12:737557-737558	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs184140506	chr12:737558-737559	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs188423413	chr12:737698-737699	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs180788220	chr12:737748-737749	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs114974349	chr12:737771-737772	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs368505884	chr12:737824-737825	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs185211441	chr12:737900-737901	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs570986794	chr12:737915-737916	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs192365712	chr12:737917-737918	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs150757809	chr12:738019-738020	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548224392	chr12:738059-738060	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563273088	chr12:738066-738067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371835009	chr12:738085-738086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181957550	chr12:738142-738143	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs139089015	chr12:738191-738192	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570222917	chr12:738234-738235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538818375	chr12:738247-738248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186990897	chr12:738274-738275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566176147	chr12:738295-738296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191531335	chr12:738314-738315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555006455	chr12:738335-738336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570021348	chr12:738345-738346	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149887887	chr12:738346-738347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559044523	chr12:738347-738348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577438556	chr12:738373-738374	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538428483	chr12:738410-738411	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs73598109	chr12:738450-738451	Enhancers Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs144880616	chr12:738468-738469	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs545144018	chr12:738513-738514	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574574108	chr12:738514-738515	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs183395436	chr12:738525-738526	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs563476562	chr12:738548-738549	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs575210685	chr12:738550-738551	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs530385952	chr12:738580-738581	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs186917258	chr12:738582-738583	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs563803101	chr12:738583-738584	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs528157749	chr12:738585-738586	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs6489684	chr12:738597-738598	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs566257373	chr12:738604-738605	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs116039566	chr12:738633-738634	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD

Chromatin state (count:894 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:725800-739800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr12:729600-739200	Weak transcription	Brain Cingulate Gyrus	brain
3	chr12:730400-741400	Weak transcription	Brain Substantia Nigra	brain
4	chr12:731000-741400	Weak transcription	Brain Angular Gyrus	brain
5	chr12:732600-738600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr12:732600-740000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr12:732600-741000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr12:732800-737400	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr12:732800-739200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr12:732800-739400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr12:732800-739800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr12:733000-737400	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr12:733000-737600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr12:733000-738400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr12:733000-750600	Weak transcription	Spleen	Spleen
16	chr12:733200-738400	Weak transcription	Primary T cells from cord blood	blood
17	chr12:733400-739200	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr12:733600-738400	Weak transcription	GM12878-XiMat	blood
19	chr12:733600-739200	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr12:733600-739200	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr12:733600-739200	Weak transcription	Brain Hippocampus Middle	brain
22	chr12:733600-741600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
23	chr12:735400-738800	Enhancers	Left Ventricle	heart
24	chr12:735800-741000	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr12:736400-738600	Enhancers	Right Atrium	heart
26	chr12:736400-738600	Enhancers	HepG2	liver
27	chr12:736600-737800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr12:736600-738000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr12:736600-738000	Enhancers	Adipose Nuclei	Adipose
30	chr12:736600-738000	Enhancers	Liver	Liver
31	chr12:736600-738400	Enhancers	A549	lung
32	chr12:736600-738600	Enhancers	Psoas Muscle	Psoas
33	chr12:736600-738600	Enhancers	Right Ventricle	heart
34	chr12:736600-739200	Enhancers	Primary B cells from peripheral blood	blood
35	chr12:736600-740800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr12:736800-737400	Enhancers	Fetal Muscle Trunk	muscle
37	chr12:736800-737600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr12:736800-737800	Enhancers	Fetal Thymus	thymus
39	chr12:736800-738000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr12:736800-738000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr12:736800-738000	Enhancers	Fetal Muscle Leg	muscle
42	chr12:736800-738000	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr12:736800-738200	Enhancers	Lung	lung
44	chr12:736800-738400	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr12:736800-738600	Enhancers	Esophagus	oesophagus
46	chr12:736800-739200	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr12:736800-739400	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr12:736800-739600	Enhancers	Placenta	Placenta
49	chr12:736800-742200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr12:737000-737600	Enhancers	Primary B cells from cord blood	blood

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