Variant report

Variant	nsv832528
Chromosome Location	chr12:119638211-119793401
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:984)
CpG islands
(count:1039)
Chromatin interactive
region (count:24)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:984 , 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	ATF1	chr12:119778457-119778752	K562	blood:	n/a	n/a
2	ATF3	chr12:119778421-119778778	K562	blood:	n/a	chr12:119778607-119778618 chr12:119778607-119778620 chr12:119778608-119778619 chr12:119778606-119778616 chr12:119778606-119778619 chr12:119778609-119778619 chr12:119778606-119778619 chr12:119778609-119778619 chr12:119778609-119778616 chr12:119778608-119778616 chr12:119778605-119778620 chr12:119778607-119778618 chr12:119778605-119778618
3	ATF3	chr12:119741129-119741350	K562	blood:	n/a	n/a
4	ATF3	chr12:119741184-119741308	GM12878	blood:	n/a	n/a
5	ATF3	chr12:119741124-119741413	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr12:119656099-119656299	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr12:119674225-119674313	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr12:119765991-119766222	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr12:119712493-119712720	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr12:119776785-119777103	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr12:119757656-119757836	K562	blood:	n/a	n/a
12	BHLHE40	chr12:119741114-119741379	K562	blood:	n/a	n/a
13	BHLHE40	chr12:119676273-119676298	K562	blood:	n/a	n/a
14	BRCA1	chr12:119713921-119714003	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr12:119772882-119772889	GM12878	blood:	n/a	n/a
16	CEBPB	chr12:119691039-119691397	IMR90	lung:	n/a	n/a
17	CEBPB	chr12:119691086-119691405	MCF-7	breast:	n/a	n/a
18	CEBPB	chr12:119663345-119663698	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr12:119696097-119696384	H1-hESC	embryonic stem cell:	n/a	chr12:119696249-119696266 chr12:119696251-119696262 chr12:119696250-119696263
20	CEBPB	chr12:119683724-119684097	HepG2	liver:	n/a	chr12:119683917-119683928
21	CEBPB	chr12:119739252-119739625	MCF-7	breast:	n/a	n/a
22	CEBPB	chr12:119646421-119646850	Hela-S3	cervix:	n/a	chr12:119646651-119646662
23	CEBPB	chr12:119736371-119736694	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr12:119739407-119739537	HepG2	liver:	n/a	n/a
25	CEBPB	chr12:119651060-119651116	A549	lung:	n/a	n/a
26	CEBPB	chr12:119646522-119646774	K562	blood:	n/a	chr12:119646651-119646662
27	CEBPB	chr12:119739316-119739526	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr12:119683814-119684027	A549	lung:	n/a	chr12:119683917-119683928
29	CEBPB	chr12:119691060-119691392	HepG2	liver:	n/a	n/a
30	CEBPB	chr12:119691126-119691317	A549	lung:	n/a	n/a
31	CEBPB	chr12:119736449-119736550	A549	lung:	n/a	n/a
32	CEBPB	chr12:119691033-119691394	A549	lung:	n/a	n/a
33	CEBPB	chr12:119683776-119684001	HepG2	liver:	n/a	chr12:119683917-119683928
34	CEBPB	chr12:119646388-119646901	MCF-7	breast:	n/a	chr12:119646651-119646662
35	CEBPB	chr12:119646496-119646788	H1-hESC	embryonic stem cell:	n/a	chr12:119646651-119646662
36	CEBPB	chr12:119730940-119731019	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr12:119672789-119673204	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr12:119672874-119673151	HepG2	liver:	n/a	n/a
39	CEBPB	chr12:119739293-119739581	K562	blood:	n/a	n/a
40	CEBPB	chr12:119739274-119739559	A549	lung:	n/a	n/a
41	CEBPB	chr12:119646442-119646812	A549	lung:	n/a	chr12:119646651-119646662
42	CEBPB	chr12:119646466-119646825	HepG2	liver:	n/a	chr12:119646651-119646662
43	CEBPB	chr12:119727720-119727767	HepG2	liver:	n/a	chr12:119727741-119727752
44	CEBPB	chr12:119683844-119683984	H1-hESC	embryonic stem cell:	n/a	chr12:119683917-119683928
45	CEBPB	chr12:119696114-119696396	Hela-S3	cervix:	n/a	chr12:119696249-119696266 chr12:119696251-119696262 chr12:119696250-119696263
46	CEBPB	chr12:119691034-119691385	K562	blood:	n/a	n/a
47	CEBPB	chr12:119646418-119646818	IMR90	lung:	n/a	chr12:119646651-119646662
48	CEBPB	chr12:119696097-119696390	HepG2	liver:	n/a	chr12:119696249-119696266 chr12:119696251-119696262 chr12:119696250-119696263
49	CEBPB	chr12:119691041-119691378	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr12:119663452-119663563	HepG2	liver:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:119776178-119776228	Hepatocyte	liver:	n/a
2	chr12:119715090-119715140	ECC-1	luminal epithelium:	n/a
3	chr12:119776178-119776228	Hepatocyte	liver:	n/a
4	chr12:119715090-119715140	ECC-1	luminal epithelium:	n/a
5	chr12:119742417-119742467	HRPEpiC	eye:	n/a
6	chr12:119772421-119772471	T-47D	breast:	n/a
7	chr12:119772354-119772404	K562	blood:	n/a
8	chr12:119740840-119740890	AoSMC	blood vessel:	n/a
9	chr12:119771257-119771307	ovcar-3	ovarian:	n/a
10	chr12:119771596-119771646	Hela-S3	cervix:	n/a
11	chr12:119772381-119772431	SK-N-SH_RA	brain:	n/a
12	chr12:119771257-119771307	ECC-1	luminal epithelium:	n/a
13	chr12:119772577-119772627	GM12891	blood:	n/a
14	chr12:119772577-119772627	GM12878	blood:	n/a
15	chr12:119772577-119772627	SK-N-SH	brain:	n/a
16	chr12:119772421-119772471	SK-N-SH	brain:	n/a
17	chr12:119715090-119715140	NB4	blood:	n/a
18	chr12:119772381-119772431	AG10803	skin:	n/a
19	chr12:119776178-119776228	LNCaP	prostate:	n/a
20	chr12:119740840-119740890	IMR90	lung:	fetal
21	chr12:119772381-119772431	K562	blood:	n/a
22	chr12:119771257-119771307	H1-hESC	embryonic stem cell:	embryo
23	chr12:119771596-119771646	AoSMC	blood vessel:	n/a
24	chr12:119772421-119772471	HAEpiC	amniotic membrane:	n/a
25	chr12:119741254-119741304	SAEC	small airway:	n/a
26	chr12:119772381-119772431	AoSMC	blood vessel:	n/a
27	chr12:119769357-119769407	GM19239	blood:	n/a
28	chr12:119776178-119776228	H1-hESC	embryonic stem cell:	embryo
29	chr12:119772354-119772404	SK-N-SH	brain:	n/a
30	chr12:119715090-119715140	U87	brain:	n/a
31	chr12:119772381-119772431	NH-A	brain:	n/a
32	chr12:119772381-119772431	HepG2	liver:	n/a
33	chr12:119776178-119776228	Caco-2	colon:	n/a
34	chr12:119715090-119715140	SK-N-MC	brain:	n/a
35	chr12:119771135-119771185	SK-N-SH_RA	brain:	n/a
36	chr12:119772421-119772471	SK-N-MC	brain:	n/a
37	chr12:119742417-119742467	ovcar-3	ovarian:	n/a
38	chr12:119772364-119772414	H1-hESC	embryonic stem cell:	embryo
39	chr12:119771135-119771185	AG09319	gingival:	n/a
40	chr12:119663566-119663616	GM19239	blood:	n/a
41	chr12:119772354-119772404	ovcar-3	ovarian:	n/a
42	chr12:119741507-119741557	BJ	skin:	n/a
43	chr12:119741254-119741304	HIPEpiC	eye:	n/a
44	chr12:119741507-119741557	HCF	heart:	n/a
45	chr12:119772421-119772471	AoSMC	blood vessel:	n/a
46	chr12:119715090-119715140	AG04450	lung:	fetal
47	chr12:119772354-119772404	HRE	kidney:	n/a
48	chr12:119715090-119715140	GM06990	blood:	n/a
49	chr12:119772577-119772627	T-47D	breast:	n/a
50	chr12:119663566-119663616	GM12878	blood:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:119717074..119719997-chr12:119720891..119724603,3	K562	blood:
2	chr12:119685139..119687783-chr12:119693154..119694704,2	K562	blood:
3	chr12:119739534..119741521-chr12:119743131..119745914,2	MCF-7	breast:
4	chr12:119774496..119776327-chr12:119777022..119779114,2	K562	blood:
5	chr12:119774496..119776327-chr12:119777022..119779114,2	K562	blood:
6	chr12:119765671..119766355-chr12:119850911..119851698,3	K562	blood:
7	chr12:119616176..119619939-chr12:119645007..119648032,3	MCF-7	breast:
8	chr12:119717074..119719997-chr12:119720891..119724603,3	K562	blood:
9	chr12:119765655..119766458-chr12:119850699..119851560,2	MCF-7	breast:
10	chr12:119685139..119687783-chr12:119693154..119694704,2	K562	blood:
11	chr12:119777510..119778281-chr3:182539096..182539983,2	MCF-7	breast:
12	chr12:119639986..119643300-chr12:119644923..119647932,3	MCF-7	breast:
13	chr12:119662826..119664972-chr12:119720982..119723971,2	MCF-7	breast:
14	chr12:119764864..119767176-chr12:119782140..119784942,2	MCF-7	breast:
15	chr12:119615775..119617389-chr12:119662533..119665044,2	MCF-7	breast:
16	chr12:119634370..119636287-chr12:119638890..119640452,2	MCF-7	breast:
17	chr12:119552783..119553783-chr12:119712402..119713111,2	MCF-7	breast:
18	chr12:119717872..119719890-chr12:119720891..119722921,2	K562	blood:
19	chr12:119662826..119664972-chr12:119720982..119723971,2	MCF-7	breast:
20	chr12:119764864..119767176-chr12:119782140..119784942,2	MCF-7	breast:
21	chr12:119639986..119643300-chr12:119644923..119647932,3	MCF-7	breast:
22	chr12:119739534..119741521-chr12:119743131..119745914,2	MCF-7	breast:
23	chr12:119717872..119719890-chr12:119720891..119722921,2	K562	blood:
24	chr12:119641619..119642425-chr21:40721169..40721890,2	MCF-7	breast:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CIT-2	chr12:119739414-119739836	XLOC_010217
2	lnc-CIT-2	chr12:119723322-119723541	NONHSAT031078
3	lnc-CIT-3	chr12:119663639-119663668	ENSG00000256311.1
4	lnc-SRRM4-1	chr12:119658519-119658735	XLOC_009909
5	lnc-SRRM4-1	chr12:119658518-119658735	NONHSAT031073
6	lnc-CIT-2	chr12:119741140-119741185	XLOC_010217
7	lnc-CIT-2	chr12:119722577-119722592	XLOC_010217
8	lnc-CIT-3	chr12:119674429-119674565	ENSG00000256311.1
9	lnc-CIT-9	chr12:119710068-119710249	NONHSAT031076
10	lnc-CIT-2	chr12:119721823-119722486	XLOC_010217
11	lnc-SRRM4-1	chr12:119651506-119651546	XLOC_009909
12	lnc-CIT-2	chr12:119721630-119722486	XLOC_010217
13	lnc-CIT-9	chr12:119698581-119698874	NONHSAT031076
14	lnc-HSPB8-7	chr12:119773016-119773071	NONHSAT031079
15	lnc-CIT-2	chr12:119722573-119722665	NONHSAT031078
16	lnc-CIT-2	chr12:119731250-119731344	NONHSAT031078
17	lnc-CIT-3	chr12:119664192-119664352	ENSG00000256311.1
18	lnc-CIT-3	chr12:119696754-119696822	ENSG00000256311.1
19	lnc-CIT-2	chr12:119722577-119723541	XLOC_010217
20	lnc-SRRM4-1	chr12:119651505-119651546	NONHSAT031073
21	lnc-CIT-3	chr12:119674718-119674821	ENSG00000256311.1

No data

Variant related genes	Relation type
ENSG00000256311	TF binding region
CCDC60	TF binding region
ENSG00000256311	CpG island
CCDC60	CpG island
ENSG00000152137	chromatin interactions
ENSG00000205581	chromatin interactions
MEST	miRNA target sites
METAP1	miRNA target sites

Extended variants
information (count: 5511 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:5511 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73213461	chr12:119638280-119638281	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564585409	chr12:119638281-119638282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs375638485	chr12:119638282-119638283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs527271592	chr12:119638290-119638291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs182195778	chr12:119638305-119638306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs150670880	chr12:119638328-119638329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs35835842	chr12:119638356-119638357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs561216710	chr12:119638368-119638369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs529921331	chr12:119638376-119638377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs548347282	chr12:119638377-119638378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569817318	chr12:119638384-119638385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs1426629	chr12:119638495-119638496	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs551894609	chr12:119638582-119638583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571583741	chr12:119638595-119638596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs572973546	chr12:119638599-119638600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375958073	chr12:119638600-119638601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs372828782	chr12:119638620-119638621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs553850987	chr12:119638701-119638702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554988091	chr12:119638711-119638712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs536506603	chr12:119638726-119638727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs139759187	chr12:119638740-119638741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs576225701	chr12:119638741-119638742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs149811352	chr12:119638780-119638781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs564622911	chr12:119638783-119638784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs73412047	chr12:119638791-119638792	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs199578661	chr12:119638829-119638830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs12424136	chr12:119638903-119638904	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs144674168	chr12:119638904-119638905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560690998	chr12:119638922-119638923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530013419	chr12:119639043-119639044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539112226	chr12:119639047-119639048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs550093671	chr12:119639057-119639058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs185841231	chr12:119639129-119639130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs527394331	chr12:119639134-119639135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs374744145	chr12:119639135-119639136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs547046309	chr12:119639161-119639162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs139829077	chr12:119639212-119639213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs718021	chr12:119639264-119639265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs571734020	chr12:119639277-119639278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs534001647	chr12:119639316-119639317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs570115249	chr12:119639412-119639413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs539041995	chr12:119639488-119639489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs79768463	chr12:119639544-119639545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs77948989	chr12:119639621-119639622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536596026	chr12:119639650-119639651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs190250047	chr12:119639654-119639655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576264502	chr12:119639664-119639665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs11064706	chr12:119639668-119639669	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs558858490	chr12:119639681-119639682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs377042918	chr12:119639682-119639683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	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
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:836 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:119618800-119639600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:119619200-119639000	Weak transcription	Colonic Mucosa	Colon
3	chr12:119620000-119639200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr12:119620000-119639600	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr12:119627000-119641600	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr12:119627200-119639000	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr12:119627600-119641600	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr12:119627800-119646600	Weak transcription	Gastric	stomach
9	chr12:119628400-119641200	Weak transcription	Fetal Heart	heart
10	chr12:119631200-119639200	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr12:119632000-119642200	Weak transcription	Brain Substantia Nigra	brain
12	chr12:119632200-119642200	Weak transcription	Psoas Muscle	Psoas
13	chr12:119632400-119638600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr12:119632400-119638600	Weak transcription	Fetal Lung	lung
15	chr12:119632400-119641400	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr12:119632400-119641400	Weak transcription	HSMMtube	muscle
17	chr12:119632400-119642200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr12:119633400-119638800	Weak transcription	Fetal Muscle Leg	muscle
19	chr12:119633400-119638800	Weak transcription	Left Ventricle	heart
20	chr12:119633400-119640200	Weak transcription	Right Ventricle	heart
21	chr12:119633800-119639600	Weak transcription	Fetal Muscle Trunk	muscle
22	chr12:119633800-119640600	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr12:119633800-119641600	Weak transcription	Adipose Nuclei	Adipose
24	chr12:119634400-119640400	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr12:119634400-119642000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr12:119634800-119639000	Weak transcription	Lung	lung
27	chr12:119635400-119638400	Enhancers	Placenta	Placenta
28	chr12:119636600-119640200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr12:119636600-119644200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr12:119636600-119645000	Weak transcription	Brain Anterior Caudate	brain
31	chr12:119636800-119638400	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr12:119636800-119640000	Weak transcription	Right Atrium	heart
33	chr12:119637400-119638400	Weak transcription	Colon Smooth Muscle	Colon
34	chr12:119637400-119640200	Weak transcription	Rectal Smooth Muscle	rectum
35	chr12:119637400-119640400	Weak transcription	Stomach Smooth Muscle	stomach
36	chr12:119637400-119645800	Weak transcription	Esophagus	oesophagus
37	chr12:119638200-119638600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr12:119638400-119639000	Enhancers	Colon Smooth Muscle	Colon
39	chr12:119638400-119639200	Enhancers	Placenta Amnion	Placenta Amnion
40	chr12:119638400-119640600	Weak transcription	Placenta	Placenta
41	chr12:119638600-119638800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr12:119638600-119642000	Enhancers	Fetal Lung	lung
43	chr12:119638600-119643400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr12:119638800-119639000	Enhancers	Left Ventricle	heart
45	chr12:119638800-119642000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr12:119638800-119643600	Enhancers	Fetal Muscle Leg	muscle
47	chr12:119639000-119639200	Enhancers	Lung	lung
48	chr12:119639000-119639400	Weak transcription	Left Ventricle	heart
49	chr12:119639000-119640000	Weak transcription	Colon Smooth Muscle	Colon
50	chr12:119639000-119642800	Enhancers	H1 Cell Line	embryonic stem cell

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