Variant report

Variant	nsv832502
Chromosome Location	chr12:104833729-104908288
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2164)
CpG islands
(count:1588)
Chromatin interactive
region (count:77)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2164 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:104872276-104872568	K562	blood:	n/a	n/a
2	ARID3A	chr12:104850504-104850807	K562	blood:	n/a	n/a
3	ARID3A	chr12:104874813-104874819	K562	blood:	n/a	n/a
4	ARID3A	chr12:104856851-104857119	K562	blood:	n/a	n/a
5	ARID3A	chr12:104860457-104861952	K562	blood:	n/a	n/a
6	ARID3A	chr12:104873665-104874056	K562	blood:	n/a	n/a
7	ARID3A	chr12:104903867-104904401	K562	blood:	n/a	n/a
8	ARID3A	chr12:104888011-104888641	K562	blood:	n/a	n/a
9	ATF1	chr12:104861130-104861643	K562	blood:	n/a	n/a
10	ATF1	chr12:104850414-104850793	K562	blood:	n/a	n/a
11	ATF1	chr12:104873835-104874088	K562	blood:	n/a	n/a
12	ATF1	chr12:104879446-104879870	K562	blood:	n/a	n/a
13	ATF1	chr12:104887942-104888450	K562	blood:	n/a	n/a
14	ATF2	chr12:104853009-104853717	GM12878	blood:	n/a	n/a
15	ATF2	chr12:104856478-104857111	GM12878	blood:	n/a	n/a
16	ATF2	chr12:104871983-104872732	GM12878	blood:	n/a	n/a
17	ATF2	chr12:104850305-104850833	GM12878	blood:	n/a	n/a
18	ATF2	chr12:104856549-104857124	GM12878	blood:	n/a	n/a
19	ATF2	chr12:104887874-104889072	GM12878	blood:	n/a	n/a
20	ATF2	chr12:104850235-104850689	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr12:104891937-104892505	GM12878	blood:	n/a	n/a
22	ATF2	chr12:104888092-104888939	GM12878	blood:	n/a	n/a
23	ATF2	chr12:104871897-104872805	GM12878	blood:	n/a	n/a
24	ATF3	chr12:104851066-104851642	A549	lung:	n/a	n/a
25	ATF3	chr12:104851055-104851650	A549	lung:	n/a	n/a
26	ATF3	chr12:104901542-104901731	K562	blood:	n/a	n/a
27	ATF3	chr12:104861147-104861637	K562	blood:	n/a	n/a
28	ATF3	chr12:104850336-104850972	A549	lung:	n/a	n/a
29	BACH1	chr12:104851180-104851471	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr12:104896474-104896841	K562	blood:	n/a	n/a
31	BACH1	chr12:104890406-104890415	K562	blood:	n/a	n/a
32	BACH1	chr12:104873646-104874045	K562	blood:	n/a	n/a
33	BACH1	chr12:104896276-104896808	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr12:104852062-104852521	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr12:104850287-104850746	H1-hESC	embryonic stem cell:	n/a	n/a
36	BATF	chr12:104888287-104888547	GM12878	blood:	n/a	n/a
37	BATF	chr12:104887835-104888904	GM12878	blood:	n/a	n/a
38	BATF	chr12:104872142-104872520	GM12878	blood:	n/a	n/a
39	BATF	chr12:104856636-104857046	GM12878	blood:	n/a	chr12:104856869-104856878
40	BATF	chr12:104856592-104857100	GM12878	blood:	n/a	chr12:104856869-104856878
41	BCL11A	chr12:104872100-104872745	GM12878	blood:	n/a	chr12:104872310-104872319
42	BCL11A	chr12:104888250-104888561	GM12878	blood:	n/a	n/a
43	BCL11A	chr12:104856657-104857093	GM12878	blood:	n/a	n/a
44	BCL11A	chr12:104888086-104888622	GM12878	blood:	n/a	n/a
45	BCL11A	chr12:104872141-104872686	GM12878	blood:	n/a	chr12:104872310-104872319
46	BCL11A	chr12:104850371-104850664	GM12878	blood:	n/a	chr12:104850647-104850656 chr12:104850400-104850413 chr12:104850628-104850637
47	BCL11A	chr12:104856617-104856979	GM12878	blood:	n/a	n/a
48	BCL3	chr12:104891973-104892394	GM12878	blood:	n/a	chr12:104892103-104892116
49	BCL3	chr12:104882096-104882642	GM12878	blood:	n/a	n/a
50	BCL3	chr12:104871650-104872136	GM12878	blood:	n/a	chr12:104871857-104871866 chr12:104871808-104871816

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:104850576-104850626	HMEC	breast:	n/a
2	chr12:104850695-104850745	HEEpiC	esophagus:	n/a
3	chr12:104850576-104850626	HMEC	breast:	n/a
4	chr12:104850695-104850745	HEEpiC	esophagus:	n/a
5	chr12:104850718-104850768	Hepatocyte	liver:	n/a
6	chr12:104852151-104852201	HEK293	kidney:	embryo
7	chr12:104850219-104850269	GM12878	blood:	n/a
8	chr12:104850716-104850766	PFSK-1	brain:	n/a
9	chr12:104852446-104852496	NT2-D1	testis:	n/a
10	chr12:104850767-104850817	PFSK-1	brain:	n/a
11	chr12:104852151-104852201	HCT-116	colon:	n/a
12	chr12:104852151-104852201	SK-N-SH	brain:	n/a
13	chr12:104849615-104849665	AG09309	skin:	n/a
14	chr12:104852047-104852097	Hela-S3	cervix:	n/a
15	chr12:104850716-104850766	CMK	blood:	n/a
16	chr12:104852439-104852489	PrEC	prostate:	n/a
17	chr12:104850219-104850269	Caco-2	colon:	n/a
18	chr12:104850219-104850269	AoSMC	blood vessel:	n/a
19	chr12:104852047-104852097	AG04450	lung:	fetal
20	chr12:104855500-104855550	AG09319	gingival:	n/a
21	chr12:104850759-104850809	HCF	heart:	n/a
22	chr12:104852047-104852097	PrEC	prostate:	n/a
23	chr12:104850219-104850269	NHDF-neo	bronchial:	n/a
24	chr12:104907103-104907153	GM12891	blood:	n/a
25	chr12:104851909-104851959	AoSMC	blood vessel:	n/a
26	chr12:104852355-104852405	GM06990	blood:	n/a
27	chr12:104850759-104850809	PrEC	prostate:	n/a
28	chr12:104850695-104850745	AG10803	skin:	n/a
29	chr12:104851316-104851366	HCM	heart:	n/a
30	chr12:104850695-104850745	SK-N-SH	brain:	n/a
31	chr12:104852439-104852489	CMK	blood:	n/a
32	chr12:104868173-104868223	HPAEpiC	pulmonary alveolar:	n/a
33	chr12:104907103-104907153	BJ	skin:	n/a
34	chr12:104852446-104852496	HCPEpiC	choroid plexus:	n/a
35	chr12:104852446-104852496	NHBE	bronchial:	n/a
36	chr12:104851172-104851222	HRPEpiC	eye:	n/a
37	chr12:104907103-104907153	T-47D	breast:	n/a
38	chr12:104849615-104849665	NT2-D1	testis:	n/a
39	chr12:104853274-104853324	GM19239	blood:	n/a
40	chr12:104853274-104853324	NHBE	bronchial:	n/a
41	chr12:104852355-104852405	AoSMC	blood vessel:	n/a
42	chr12:104851172-104851222	NHBE	bronchial:	n/a
43	chr12:104850716-104850766	ovcar-3	ovarian:	n/a
44	chr12:104851909-104851959	AG09309	skin:	n/a
45	chr12:104846281-104846331	GM12891	blood:	n/a
46	chr12:104852446-104852496	HepG2	liver:	n/a
47	chr12:104850695-104850745	SK-N-MC	brain:	n/a
48	chr12:104852446-104852496	MCF10A-Er-Src	breast:	n/a
49	chr12:104850219-104850269	GM19239	blood:	n/a
50	chr12:104850326-104850376	ECC-1	luminal epithelium:	n/a

(count:77 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:104898659..104900807-chr12:104906286..104908978,3	K562	blood:
2	chr12:104833181..104835395-chr12:104835605..104837551,2	K562	blood:
3	chr12:104819109..104820894-chr12:104840449..104842365,2	MCF-7	breast:
4	chr12:104902488..104905052-chr12:104962127..104964192,2	K562	blood:
5	chr12:104879669..104882101-chr12:104882975..104884643,2	K562	blood:
6	chr12:104836858..104839359-chr12:104840173..104842812,3	K562	blood:
7	chr12:104858578..104860832-chr12:104863067..104865005,3	K562	blood:
8	chr12:104827188..104830155-chr12:104830427..104833779,3	K562	blood:
9	chr12:104877368..104879686-chr12:104993577..104996445,2	K562	blood:
10	chr12:104878866..104881673-chr12:104885573..104889432,3	K562	blood:
11	chr12:104889682..104892508-chr12:104899984..104902053,3	K562	blood:
12	chr12:104867859..104869379-chr12:104998403..105000393,2	K562	blood:
13	chr12:104876677..104879866-chr12:104887122..104889642,3	K562	blood:
14	chr12:104871756..104873492-chr12:104876935..104879923,2	K562	blood:
15	chr12:104885329..104887209-chr12:104893260..104894913,2	K562	blood:
16	chr12:104897397..104899517-chr12:104972120..104975034,2	K562	blood:
17	chr12:104878866..104881673-chr12:104885573..104889432,3	K562	blood:
18	chr12:104845965..104848831-chr12:104848976..104852004,3	K562	blood:
19	chr12:104869578..104872458-chr12:104877687..104880614,4	K562	blood:
20	chr12:104857257..104859525-chr12:104868712..104871497,3	K562	blood:
21	chr12:104861083..104865275-chr12:104866418..104870159,5	K562	blood:
22	chr12:104897087..104900788-chr12:104905207..104908076,3	MCF-7	breast:
23	chr12:104852839..104855254-chr12:104863893..104866118,2	K562	blood:
24	chr12:104858831..104861040-chr12:104895664..104898086,2	K562	blood:
25	chr12:104876677..104879866-chr12:104887122..104889642,3	K562	blood:
26	chr12:104822038..104824014-chr12:104845954..104848483,2	K562	blood:
27	chr12:104858578..104860832-chr12:104863067..104865005,3	K562	blood:
28	chr12:104882770..104885599-chr12:104898967..104901298,2	K562	blood:
29	chr12:104831707..104833873-chr12:104852450..104855166,2	K562	blood:
30	chr12:104889682..104892508-chr12:104899984..104902053,3	K562	blood:
31	chr12:104893740..104896062-chr12:104897275..104899084,2	K562	blood:
32	chr12:104849161..104852195-chr12:104895253..104897377,3	K562	blood:
33	chr12:104866750..104869514-chr12:104871657..104874435,3	K562	blood:
34	chr12:104892344..104895135-chr12:104897977..104900926,3	MCF-7	breast:
35	chr12:104808930..104811125-chr12:104837946..104840786,2	K562	blood:
36	chr12:104850865..104852398-chr12:104863309..104864984,2	MCF-7	breast:
37	chr12:104850865..104852398-chr12:104863309..104864984,2	MCF-7	breast:
38	chr12:104894805..104896698-chr12:104899476..104901179,2	K562	blood:
39	chr12:104866750..104869514-chr12:104871657..104874435,3	K562	blood:
40	chr12:104857257..104859525-chr12:104868712..104871497,3	K562	blood:
41	chr12:104849098..104852771-chr12:104856010..104858132,3	MCF-7	breast:
42	chr12:104877368..104879475-chr12:104994945..104997533,2	K562	blood:
43	chr12:104861083..104865275-chr12:104866418..104870159,5	K562	blood:
44	chr12:104882770..104885599-chr12:104898967..104901298,2	K562	blood:
45	chr12:104681309..104682923-chr12:104867248..104870196,2	K562	blood:
46	chr12:104869578..104872458-chr12:104877687..104880614,4	K562	blood:
47	chr12:104908202..104911501-chr12:104915065..104918852,3	MCF-7	breast:
48	chr12:104899181..104901734-chr12:104930308..104932411,2	MCF-7	breast:
49	chr12:104841247..104843011-chr12:104850622..104852418,2	K562	blood:
50	chr12:104873432..104875750-chr12:104876830..104879397,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NFYB-2	chr12:104859855-104862733	ENSG00000245335
2	lnc-TXNRD1-5	chr12:104907807-104908217	NONHSAT030428
3	lnc-CHST11-1	chr12:104849073-104849414	NONHSAT030426
4	lnc-CHST11-1	chr12:104850694-104850774	NONHSAT030426
5	lnc-NFYB-2	chr12:104852873-104854222	ENSG00000245335

No data

Variant related genes	Relation type
ENSG00000258111	TF binding region
CHST11	TF binding region
ENSG00000258111	CpG island
CHST11	CpG island
ENSG00000258111	chromatin interactions
ENSG00000198431	chromatin interactions
ENSG00000136051	chromatin interactions
ENSG00000257999	chromatin interactions
ENSG00000171310	chromatin interactions
UBE2Q1	miRNA target sites

Extended variants
information (count: 2690 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:2690 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374429672	chr12:104836839-104836840	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
2	rs79870735	chr12:104836844-104836845	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
3	rs149709841	chr12:104836874-104836875	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
4	rs72035701	chr12:104836881-104836882	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
5	rs71440545	chr12:104836882-104836883	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
6	rs534177153	chr12:104836902-104836903	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
7	rs547423800	chr12:104836903-104836904	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
8	rs549954205	chr12:104836906-104836907	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
9	rs61939008	chr12:104836910-104836911	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
10	rs570532849	chr12:104836928-104836929	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
11	rs113052605	chr12:104836979-104836980	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
12	rs145398792	chr12:104836983-104836984	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
13	rs200565157	chr12:104836984-104836985	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
14	rs539499649	chr12:104836986-104836987	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
15	rs202154741	chr12:104837009-104837010	Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs4619217	chr12:104837029-104837030	Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs181854392	chr12:104837050-104837051	Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs140916061	chr12:104837120-104837121	Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs373998558	chr12:104837126-104837127	Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556001224	chr12:104837189-104837190	Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs7975036	chr12:104837198-104837199	Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs75111979	chr12:104837241-104837242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs146402237	chr12:104837279-104837280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs2254984	chr12:104837294-104837295	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs559160713	chr12:104837321-104837322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs543505199	chr12:104837326-104837327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs186873065	chr12:104837330-104837331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs59262137	chr12:104837333-104837334	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs375339728	chr12:104837367-104837368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs548935057	chr12:104837368-104837369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs115526959	chr12:104837386-104837387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs565265772	chr12:104837409-104837410	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs139115985	chr12:104837438-104837439	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551264718	chr12:104837448-104837449	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs570472095	chr12:104837449-104837450	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369545104	chr12:104837451-104837452	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs539489109	chr12:104837460-104837461	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs549857736	chr12:104837474-104837475	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560913574	chr12:104837493-104837494	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs201839394	chr12:104837508-104837509	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs199902912	chr12:104837509-104837510	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs190581726	chr12:104837554-104837555	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs555644189	chr12:104837618-104837619	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs141679960	chr12:104837619-104837620	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs76219737	chr12:104837641-104837642	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs558500338	chr12:104837722-104837723	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs528332948	chr12:104837736-104837737	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs577705557	chr12:104837750-104837751	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs543490803	chr12:104837755-104837756	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs546240996	chr12:104837824-104837825	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	22032731	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
lymphocytic leukemia	21291569	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Neurocytoma	17123091	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3007 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:104836800-104837200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:104836800-104837200	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
3	chr12:104837000-104837600	Enhancers	Fetal Thymus	thymus
4	chr12:104837400-104838600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr12:104838000-104838200	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:104838000-104838400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr12:104840000-104849800	Weak transcription	Aorta	Aorta
8	chr12:104840200-104840600	Enhancers	Placenta	Placenta
9	chr12:104842200-104843000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr12:104844200-104848200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr12:104844400-104849400	Weak transcription	Spleen	Spleen
12	chr12:104845000-104845200	Enhancers	NHLF	lung
13	chr12:104845600-104846600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr12:104845600-104847400	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr12:104845800-104846000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
16	chr12:104845800-104846200	Enhancers	H9 Cell Line	embryonic stem cell
17	chr12:104845800-104846400	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr12:104845800-104846400	Enhancers	Fetal Brain Male	brain
19	chr12:104845800-104846600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr12:104846000-104846400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr12:104846000-104846600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr12:104846000-104847400	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr12:104846400-104849800	Weak transcription	Fetal Brain Male	brain
24	chr12:104846600-104849200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr12:104847200-104847400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
26	chr12:104847200-104847400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
27	chr12:104847400-104848600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr12:104848200-104848800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr12:104848200-104849800	Enhancers	HMEC	breast
30	chr12:104848200-104849800	Enhancers	NHEK	skin
31	chr12:104848200-104850000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr12:104848400-104848800	Enhancers	A549	lung
33	chr12:104848400-104849800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr12:104848400-104849800	Weak transcription	Fetal Heart	heart
35	chr12:104848600-104848800	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr12:104848600-104848800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
37	chr12:104848600-104849000	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr12:104848600-104849000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr12:104848600-104849000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr12:104848600-104849200	Enhancers	Osteobl	bone
41	chr12:104848600-104849600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr12:104848600-104849600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
43	chr12:104848600-104849600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr12:104848600-104849800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr12:104848600-104849800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr12:104848600-104849800	Enhancers	Muscle Satellite Cultured Cells	--
47	chr12:104848600-104849800	Enhancers	HSMM	muscle
48	chr12:104848600-104849800	Enhancers	HUVEC	blood vessel
49	chr12:104848600-104849800	Enhancers	NH-A	brain
50	chr12:104848600-104849800	Enhancers	NHDF-Ad	bronchial

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