Variant report

Variant	nsv976761
Chromosome Location	chr12:121202272-121210985
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:60)
CpG islands
(count:183)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:60 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr12:121205355-121205477	GM12878	blood:	n/a	n/a
2	CEBPB	chr12:121204797-121205275	ECC-1	luminal epithelium:	n/a	chr12:121205067-121205084
3	CEBPB	chr12:121204842-121205251	ECC-1	luminal epithelium:	n/a	chr12:121205067-121205084
4	CREB1	chr12:121205161-121205694	ECC-1	luminal epithelium:	n/a	chr12:121205418-121205431
5	CREB1	chr12:121205082-121205675	ECC-1	luminal epithelium:	n/a	chr12:121205418-121205431
6	CTCF	chr12:121205508-121205661	GM12878	blood:	n/a	n/a
7	CTCF	chr12:121205160-121205310	GM12872	blood:	n/a	n/a
8	CTCF	chr12:121205460-121205610	GM06990	blood:	n/a	n/a
9	CTCF	chr12:121204155-121204246	Pancreas_OC	pancreas:	n/a	chr12:121204226-121204239 chr12:121204202-121204223
10	CTCF	chr12:121205594-121205615	GM12892	blood:	n/a	n/a
11	CTCF	chr12:121205460-121205610	GM12870	blood:	n/a	n/a
12	CTCF	chr12:121204100-121204250	GM12868	blood:	n/a	chr12:121204226-121204239 chr12:121204202-121204223
13	CTCF	chr12:121205440-121205590	GM12872	blood:	n/a	n/a
14	CTCF	chr12:121205480-121205630	GM12872	blood:	n/a	n/a
15	CTCF	chr12:121205594-121205624	GM12891	blood:	n/a	n/a
16	CTCF	chr12:121205500-121205650	GM06990	blood:	n/a	n/a
17	CTCF	chr12:121204249-121204254	Pancreas_OC	pancreas:	n/a	n/a
18	CTCF	chr12:121205537-121205655	GM12878	blood:	n/a	n/a
19	CTCF	chr12:121209100-121209250	HCPEpiC	choroid plexus:	n/a	n/a
20	CTCF	chr12:121205480-121205630	GM12875	blood:	n/a	n/a
21	CTCF	chr12:121205460-121205610	GM12871	blood:	n/a	n/a
22	EP300	chr12:121204679-121205901	ECC-1	luminal epithelium:	n/a	chr12:121205086-121205095
23	EP300	chr12:121205592-121205723	GM12878	blood:	n/a	n/a
24	GATA2	chr12:121208127-121208452	SH-SY5Y	brain:	n/a	n/a
25	GATA3	chr12:121205249-121205676	T-47D	breast:	n/a	chr12:121205493-121205502 chr12:121205492-121205500
26	MAX	chr12:121204819-121205639	ECC-1	luminal epithelium:	n/a	n/a
27	MAX	chr12:121208921-121209334	NB4	blood:	n/a	n/a
28	MAX	chr12:121204798-121205654	ECC-1	luminal epithelium:	n/a	n/a
29	MYC	chr12:121204397-121204427	GM12878	blood:	n/a	n/a
30	MYC	chr12:121208892-121209328	NB4	blood:	n/a	n/a
31	NFIC	chr12:121204794-121205812	ECC-1	luminal epithelium:	n/a	n/a
32	NFIC	chr12:121204662-121205978	ECC-1	luminal epithelium:	n/a	n/a
33	NRF1	chr12:121205187-121205205	GM12878	blood:	n/a	n/a
34	PBX3	chr12:121205563-121205760	GM12878	blood:	n/a	n/a
35	POLR2A	chr12:121204580-121204769	K562	blood:	n/a	n/a
36	POLR2A	chr12:121206944-121207133	GM12891	blood:	n/a	n/a
37	POLR2A	chr12:121205518-121205892	H1-neurons	neurons:	n/a	n/a
38	POLR2A	chr12:121209626-121209675	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr12:121203245-121203343	HepG2	liver:	n/a	n/a
40	POLR2A	chr12:121205427-121205932	H1-neurons	neurons:	n/a	n/a
41	POLR2A	chr12:121204889-121205480	ECC-1	luminal epithelium:	n/a	n/a
42	POLR2A	chr12:121208236-121208617	GM12878	blood:	n/a	n/a
43	POLR2A	chr12:121209118-121209282	GM12878	blood:	n/a	n/a
44	POLR2A	chr12:121203863-121203968	K562	blood:	n/a	n/a
45	POLR2A	chr12:121206833-121207059	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr12:121204409-121204786	GM12878	blood:	n/a	n/a
47	POU2F2	chr12:121205425-121205751	GM12891	blood:	n/a	chr12:121205641-121205650 chr12:121205639-121205652 chr12:121205635-121205657 chr12:121205640-121205650 chr12:121205641-121205652 chr12:121205639-121205653 chr12:121205642-121205649 chr12:121205639-121205651 chr12:121205638-121205653 chr12:121205642-121205650 chr12:121205640-121205650 chr12:121205637-121205655 chr12:121205641-121205651
48	RAD21	chr12:121204752-121205665	ECC-1	luminal epithelium:	n/a	n/a
49	RAD21	chr12:121205530-121205672	GM12878	blood:	n/a	n/a
50	RCOR1	chr12:121204425-121204605	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:121210975-121211025	HRE	kidney:	n/a
2	chr12:121210975-121211025	AoSMC	blood vessel:	n/a
3	chr12:121202554-121202604	AG04449	skin:	fetal
4	chr12:121210975-121211025	AG10803	skin:	n/a
5	chr12:121203948-121203998	HEEpiC	esophagus:	n/a
6	chr12:121203948-121203998	GM19239	blood:	n/a
7	chr12:121210975-121211025	PANC-1	pancreas:	n/a
8	chr12:121210975-121211025	NHBE	bronchial:	n/a
9	chr12:121203948-121203998	A549	lung:	n/a
10	chr12:121210975-121211025	A549	lung:	n/a
11	chr12:121210975-121211025	CMK	blood:	n/a
12	chr12:121210975-121211025	RPTEC	kidney:	n/a
13	chr12:121202554-121202604	IMR90	lung:	fetal
14	chr12:121202554-121202604	U87	brain:	n/a
15	chr12:121202554-121202604	MCF10A-Er-Src	breast:	n/a
16	chr12:121202554-121202604	GM12891	blood:	n/a
17	chr12:121210975-121211025	NH-A	brain:	n/a
18	chr12:121210975-121211025	GM06990	blood:	n/a
19	chr12:121210975-121211025	NB4	blood:	n/a
20	chr12:121210975-121211025	SK-N-SH	brain:	n/a
21	chr12:121210975-121211025	LNCaP	prostate:	n/a
22	chr12:121203948-121203998	CMK	blood:	n/a
23	chr12:121210975-121211025	Caco-2	colon:	n/a
24	chr12:121210975-121211025	AG09309	skin:	n/a
25	chr12:121203948-121203998	HCPEpiC	choroid plexus:	n/a
26	chr12:121203948-121203998	K562	blood:	n/a
27	chr12:121210975-121211025	Jurkat	blood:	n/a
28	chr12:121202554-121202604	RPTEC	kidney:	n/a
29	chr12:121210975-121211025	T-47D	breast:	n/a
30	chr12:121210975-121211025	HEEpiC	esophagus:	n/a
31	chr12:121202554-121202604	NH-A	brain:	n/a
32	chr12:121202554-121202604	HRPEpiC	eye:	n/a
33	chr12:121203948-121203998	NHDF-neo	bronchial:	n/a
34	chr12:121210975-121211025	BE2_C	brain:	n/a
35	chr12:121203948-121203998	AG09319	gingival:	n/a
36	chr12:121203948-121203998	HCM	heart:	n/a
37	chr12:121203948-121203998	SAEC	small airway:	n/a
38	chr12:121203948-121203998	LNCaP	prostate:	n/a
39	chr12:121202554-121202604	HIPEpiC	eye:	n/a
40	chr12:121210975-121211025	HRPEpiC	eye:	n/a
41	chr12:121203948-121203998	SK-N-SH_RA	brain:	n/a
42	chr12:121202554-121202604	NHBE	bronchial:	n/a
43	chr12:121210975-121211025	NT2-D1	testis:	n/a
44	chr12:121202554-121202604	HRE	kidney:	n/a
45	chr12:121202554-121202604	HPAEpiC	pulmonary alveolar:	n/a
46	chr12:121210975-121211025	HMEC	breast:	n/a
47	chr12:121210975-121211025	HPAEpiC	pulmonary alveolar:	n/a
48	chr12:121210975-121211025	Hela-S3	cervix:	n/a
49	chr12:121203948-121203998	SK-N-MC	brain:	n/a
50	chr12:121203948-121203998	HRCEpiC	kidney:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:121203090..121205836-chr12:121209356..121211928,2	MCF-7	breast:
2	chr12:121208540..121211022-chr12:121211135..121213895,3	K562	blood:
3	chr12:121198595..121200409-chr12:121209397..121212163,2	MCF-7	breast:
4	chr12:121123033..121125000-chr12:121205934..121208435,2	K562	blood:
5	chr12:121202024..121204515-chr12:121206771..121210558,3	K562	blood:
6	chr12:121203090..121205836-chr12:121209356..121211928,2	MCF-7	breast:
7	chr12:121205065..121207154-chr12:121208257..121210269,2	K562	blood:
8	chr12:121199470..121201795-chr12:121202855..121205373,2	MCF-7	breast:
9	chr12:121210691..121212247-chr12:121214029..121215560,2	K562	blood:

No data

Variant related genes	Relation type
SPPL3	TF binding region
ENSG00000255946	TF binding region
SPPL3	CpG island
ENSG00000255946	CpG island
ENSG00000255946	chromatin interactions
ENSG00000157837	chromatin interactions
ENSG00000110917	chromatin interactions

Extended variants
information (count: 362 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:362 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571789879	chr12:121202320-121202321	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs570713584	chr12:121202331-121202332	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs6553	chr12:121202362-121202363	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs553205276	chr12:121202373-121202374	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs186571234	chr12:121202377-121202378	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs535554494	chr12:121202387-121202388	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs555775979	chr12:121202388-121202389	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs14445	chr12:121202390-121202391	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs563118509	chr12:121202409-121202410	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs372218050	chr12:121202410-121202411	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs377092397	chr12:121202420-121202421	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs550877248	chr12:121202432-121202433	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs11923	chr12:121202460-121202461	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs575671566	chr12:121202465-121202466	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs193103301	chr12:121202492-121202493	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs1801011	chr12:121202511-121202512	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs183902481	chr12:121202540-121202541	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs577931099	chr12:121202552-121202553	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs142377378	chr12:121202587-121202588	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs560067435	chr12:121202634-121202635	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs536544348	chr12:121202652-121202653	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs9431	chr12:121202664-121202665	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs572466767	chr12:121202684-121202685	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs562152174	chr12:121202719-121202720	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs368658291	chr12:121202727-121202728	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs371092255	chr12:121202752-121202753	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs550884116	chr12:121202773-121202774	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs570772722	chr12:121202774-121202775	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs188546176	chr12:121202775-121202776	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs201662278	chr12:121202793-121202794	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs373326481	chr12:121202794-121202795	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs193153002	chr12:121202835-121202836	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs146273163	chr12:121202886-121202887	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs201368977	chr12:121202897-121202898	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs373957771	chr12:121202900-121202901	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs74887195	chr12:121202917-121202918	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs6490303	chr12:121202952-121202953	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs538211612	chr12:121202953-121202954	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs116386051	chr12:121202965-121202966	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs138937457	chr12:121202974-121202975	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs527735012	chr12:121202994-121202995	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs184279843	chr12:121203005-121203006	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs560336618	chr12:121203015-121203016	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs141320890	chr12:121203034-121203035	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs542709503	chr12:121203069-121203070	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs574973611	chr12:121203073-121203074	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs11290474	chr12:121203093-121203094	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs531221872	chr12:121203098-121203099	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs550994159	chr12:121203128-121203129	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs150370811	chr12:121203138-121203139	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
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
Medulloblastoma	16783165	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
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:381 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121195600-121204200	Weak transcription	Stomach Mucosa	stomach
2	chr12:121195600-121207200	Strong transcription	Brain Germinal Matrix	brain
3	chr12:121196400-121207000	Strong transcription	Fetal Brain Female	brain
4	chr12:121196800-121203000	Strong transcription	Fetal Intestine Large	intestine
5	chr12:121196800-121212800	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr12:121197000-121203000	Strong transcription	Fetal Intestine Small	intestine
7	chr12:121197000-121207200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr12:121197200-121204200	Weak transcription	Fetal Brain Male	brain
9	chr12:121197200-121210000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr12:121197400-121203000	Strong transcription	Rectal Mucosa Donor 31	rectum
11	chr12:121197400-121203400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr12:121197400-121203400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr12:121197400-121203800	Strong transcription	Sigmoid Colon	Sigmoid Colon
14	chr12:121197400-121207000	Strong transcription	Pancreas	Pancrea
15	chr12:121197400-121209800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr12:121197400-121212600	Strong transcription	Thymus	Thymus
17	chr12:121197400-121220000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr12:121197600-121203000	Strong transcription	Rectal Mucosa Donor 29	rectum
19	chr12:121197600-121204400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr12:121197600-121205400	Strong transcription	GM12878-XiMat	blood
21	chr12:121197600-121207200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr12:121197600-121210400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr12:121197800-121203400	Strong transcription	Duodenum Mucosa	Duodenum
24	chr12:121197800-121209000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr12:121197800-121212400	Strong transcription	Liver	Liver
26	chr12:121197800-121220400	Strong transcription	Monocytes-CD14+_RO01746	blood
27	chr12:121198000-121202600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr12:121198000-121207200	Strong transcription	H9 Cell Line	embryonic stem cell
29	chr12:121198000-121207200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr12:121198000-121212000	Strong transcription	Adipose Nuclei	Adipose
31	chr12:121198200-121203800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr12:121198200-121204200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr12:121198200-121205600	Strong transcription	Primary B cells from peripheral blood	blood
34	chr12:121198200-121211400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr12:121198400-121207200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr12:121198400-121209800	Strong transcription	Dnd41	blood
37	chr12:121198400-121212200	Strong transcription	Primary B cells from cord blood	blood
38	chr12:121198400-121220800	Strong transcription	Primary monocytes fromperipheralblood	blood
39	chr12:121198600-121203000	Strong transcription	Colonic Mucosa	Colon
40	chr12:121198600-121209200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
41	chr12:121198800-121202600	Strong transcription	A549	lung
42	chr12:121198800-121207000	Strong transcription	HUES48 Cell Line	embryonic stem cell
43	chr12:121198800-121209000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr12:121199000-121202600	Weak transcription	Gastric	stomach
45	chr12:121199000-121206800	Strong transcription	Hela-S3	cervix
46	chr12:121199000-121207000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr12:121199000-121207200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr12:121199000-121211600	Strong transcription	Primary T cells fromperipheralblood	blood
49	chr12:121199200-121206600	Strong transcription	NHLF	lung
50	chr12:121199200-121209600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--

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