Variant report

Variant	esv3421941
Chromosome Location	chr12:123556899-123561197
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:147)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:147 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr12:123560448-123560688	GM12878	blood:	n/a	n/a
2	CTCF	chr12:123560240-123560390	AG09319	gingival:	n/a	n/a
3	CTCF	chr12:123560201-123560372	MCF-7	breast:	n/a	n/a
4	CTCF	chr12:123560120-123560270	HA-sp	spinal cord:	n/a	n/a
5	CTCF	chr12:123560180-123560330	HA-sp	spinal cord:	n/a	n/a
6	CTCF	chr12:123560240-123560390	K562	blood:	n/a	n/a
7	CTCF	chr12:123560240-123560390	HEK293	kidney:	n/a	n/a
8	CTCF	chr12:123560198-123560343	NHEK	skin:	n/a	n/a
9	CTCF	chr12:123560180-123560330	HEEpiC	esophagus:	n/a	n/a
10	CTCF	chr12:123560211-123560350	MCF-7	breast:	n/a	n/a
11	CTCF	chr12:123560100-123560250	AG09319	gingival:	n/a	n/a
12	CTCF	chr12:123560204-123560352	LNCaP	prostate:	n/a	n/a
13	CTCF	chr12:123560160-123560310	AG10803	skin:	n/a	n/a
14	CTCF	chr12:123560554-123560601	GM19238	blood:	n/a	n/a
15	CTCF	chr12:123560160-123560310	AG04450	lung:	n/a	n/a
16	CTCF	chr12:123560240-123560390	HepG2	liver:	n/a	n/a
17	CTCF	chr12:123560062-123560478	K562	blood:	n/a	n/a
18	CTCF	chr12:123560046-123560549	K562	blood:	n/a	n/a
19	CTCF	chr12:123560300-123560450	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr12:123560040-123560290	NHEK	skin:	n/a	n/a
21	CTCF	chr12:123560200-123560350	HVMF	connective:	n/a	n/a
22	CTCF	chr12:123560140-123560290	SAEC	small airway:	n/a	n/a
23	CTCF	chr12:123560290-123560296	Spleen_OC	spleen:	n/a	n/a
24	CTCF	chr12:123560154-123560347	LNCaP	prostate:	n/a	n/a
25	CTCF	chr12:123560509-123560607	Lung_OC	lung:	n/a	n/a
26	CTCF	chr12:123560140-123560290	HPF	lung:	n/a	n/a
27	CTCF	chr12:123560100-123560250	AG09309	skin:	n/a	n/a
28	CTCF	chr12:123560103-123560372	HepG2	liver:	n/a	n/a
29	CTCF	chr12:123560479-123560629	GM19240	blood:	n/a	n/a
30	CTCF	chr12:123560135-123560357	Medullo	brain:	n/a	n/a
31	CTCF	chr12:123560260-123560410	MCF-7	breast:	n/a	n/a
32	CTCF	chr12:123560468-123560671	Spleen_OC	spleen:	n/a	n/a
33	CTCF	chr12:123558972-123559111	GM19239	blood:	n/a	n/a
34	CTCF	chr12:123560140-123560290	HMF	breast:	n/a	n/a
35	CTCF	chr12:123560180-123560330	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr12:123560220-123560370	AG04450	lung:	n/a	n/a
37	CTCF	chr12:123560479-123560610	GM12891	blood:	n/a	n/a
38	CTCF	chr12:123560427-123560700	GM12878	blood:	n/a	n/a
39	CTCF	chr12:123560260-123560410	HAc	cerebellar:	n/a	n/a
40	CTCF	chr12:123560500-123560650	GM12871	blood:	n/a	n/a
41	CTCF	chr12:123560280-123560430	BE2_C	brain:	n/a	n/a
42	CTCF	chr12:123560040-123560190	MCF-7	breast:	n/a	n/a
43	CTCF	chr12:123560154-123560355	HepG2	liver:	n/a	n/a
44	CTCF	chr12:123559112-123559116	GM19239	blood:	n/a	n/a
45	CTCF	chr12:123560121-123560443	K562	blood:	n/a	n/a
46	CTCF	chr12:123560218-123560331	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chr12:123560300-123560450	BE2_C	brain:	n/a	n/a
48	CTCF	chr12:123560090-123560457	K562	blood:	n/a	n/a
49	CTCF	chr12:123560480-123560630	GM12865	blood:	n/a	n/a
50	CTCF	chr12:123560140-123560290	HRPEpiC	eye:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:123560479-123560529	AG10803	skin:	n/a
2	chr12:123560479-123560529	HCPEpiC	choroid plexus:	n/a
3	chr12:123560479-123560529	SAEC	small airway:	n/a
4	chr12:123560479-123560529	U87	brain:	n/a
5	chr12:123560479-123560529	HEEpiC	esophagus:	n/a
6	chr12:123560479-123560529	LNCaP	prostate:	n/a
7	chr12:123560479-123560529	HepG2	liver:	n/a
8	chr12:123560479-123560529	Hepatocyte	liver:	n/a
9	chr12:123560479-123560529	PANC-1	pancreas:	n/a
10	chr12:123560479-123560529	AG04450	lung:	fetal
11	chr12:123560479-123560529	HEK293	kidney:	embryo
12	chr12:123560479-123560529	GM12878	blood:	n/a
13	chr12:123560479-123560529	BJ	skin:	n/a
14	chr12:123560479-123560529	HIPEpiC	eye:	n/a
15	chr12:123560479-123560529	AoSMC	blood vessel:	n/a
16	chr12:123560479-123560529	NHDF-neo	bronchial:	n/a
17	chr12:123560479-123560529	BE2_C	brain:	n/a
18	chr12:123560479-123560529	Jurkat	blood:	n/a
19	chr12:123560479-123560529	HRCEpiC	kidney:	n/a
20	chr12:123560479-123560529	GM19239	blood:	n/a
21	chr12:123560479-123560529	H1-hESC	embryonic stem cell:	embryo
22	chr12:123560479-123560529	HNPCEpiC	eye:	n/a
23	chr12:123560479-123560529	IMR90	lung:	fetal
24	chr12:123560479-123560529	HPAEpiC	pulmonary alveolar:	n/a
25	chr12:123560479-123560529	NT2-D1	testis:	n/a
26	chr12:123560479-123560529	NH-A	brain:	n/a
27	chr12:123560479-123560529	A549	lung:	n/a
28	chr12:123560479-123560529	Caco-2	colon:	n/a
29	chr12:123560479-123560529	MCF10A-Er-Src	breast:	n/a
30	chr12:123560479-123560529	CMK	blood:	n/a
31	chr12:123560479-123560529	MCF-7	breast:	n/a
32	chr12:123560479-123560529	HUVEC	blood vessel:	n/a
33	chr12:123560479-123560529	NB4	blood:	n/a
34	chr12:123560479-123560529	HRE	kidney:	n/a
35	chr12:123560479-123560529	GM12892	blood:	n/a
36	chr12:123560479-123560529	HRPEpiC	eye:	n/a
37	chr12:123560479-123560529	AG04449	skin:	fetal
38	chr12:123560479-123560529	HCT-116	colon:	n/a
39	chr12:123560479-123560529	SK-N-MC	brain:	n/a
40	chr12:123560479-123560529	SKMC	muscle:	n/a
41	chr12:123560479-123560529	PrEC	prostate:	n/a
42	chr12:123560479-123560529	SK-N-SH	brain:	n/a
43	chr12:123560479-123560529	GM12891	blood:	n/a
44	chr12:123560479-123560529	K562	blood:	n/a
45	chr12:123560479-123560529	ProgFib	skin:	n/a
46	chr12:123560479-123560529	HMEC	breast:	n/a
47	chr12:123560479-123560529	RPTEC	kidney:	n/a
48	chr12:123560479-123560529	HAEpiC	amniotic membrane:	n/a
49	chr12:123560479-123560529	HCM	heart:	n/a
50	chr12:123560479-123560529	GM06990	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:123544563..123545393-chr12:123557820..123558745,4	MCF-7	breast:
2	chr12:123558670..123560288-chr12:123570276..123571928,2	MCF-7	breast:
3	chr12:123547555..123551371-chr12:123552619..123557163,4	MCF-7	breast:
4	chr12:123558968..123563276-chr12:123716606..123719909,6	MCF-7	breast:
5	chr12:123557772..123560593-chr12:123574740..123576717,2	K562	blood:
6	chr12:123557220..123559958-chr12:123582515..123585405,2	MCF-7	breast:
7	chr12:123547184..123547743-chr12:123557921..123558809,2	MCF-7	breast:
8	chr12:123558228..123559870-chr12:123562881..123566276,3	K562	blood:
9	chr12:123560295..123563384-chr12:123563700..123566062,4	K562	blood:
10	chr12:123559703..123562585-chr12:123566918..123569407,2	K562	blood:
11	chr12:123555442..123558076-chr12:123754275..123756423,2	MCF-7	breast:
12	chr12:123558728..123560764-chr12:123563794..123566553,2	MCF-7	breast:
13	chr12:123560295..123563017-chr12:123563846..123566062,3	K562	blood:
14	chr12:123463143..123466030-chr12:123559790..123563075,3	MCF-7	breast:

No data

Variant related genes	Relation type
PITPNM2	TF binding region
ENSG00000251497	TF binding region
PITPNM2	CpG island
ENSG00000251497	CpG island
ENSG00000090975	chromatin interactions
ENSG00000111328	chromatin interactions
ENSG00000130921	chromatin interactions
ENSG00000182196	chromatin interactions
ENSG00000051825	chromatin interactions
ENSG00000251497	chromatin interactions

Extended variants
information (count: 154 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:154 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551013387	chr12:123556956-123556957	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs146226868	chr12:123556988-123556989	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs35002262	chr12:123557006-123557007	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs139593774	chr12:123557023-123557024	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs530251983	chr12:123557032-123557033	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs149320778	chr12:123557065-123557066	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs567499290	chr12:123557126-123557127	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs528366870	chr12:123557136-123557137	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs546834323	chr12:123557185-123557186	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs571212441	chr12:123557189-123557190	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs538220333	chr12:123557274-123557275	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs144616522	chr12:123557275-123557276	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs35745707	chr12:123557288-123557289	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs568599712	chr12:123557304-123557305	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs551513418	chr12:123557312-123557313	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs35171896	chr12:123557387-123557388	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs536376307	chr12:123557396-123557397	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs554863653	chr12:123557402-123557403	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs373456763	chr12:123557434-123557435	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs182320361	chr12:123557464-123557465	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs573344309	chr12:123557492-123557493	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs540471881	chr12:123557493-123557494	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs559263789	chr12:123557499-123557500	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs577625674	chr12:123557502-123557503	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs544601699	chr12:123557522-123557523	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs139462493	chr12:123557524-123557525	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs562898118	chr12:123557526-123557527	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs144212721	chr12:123557561-123557562	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs187053546	chr12:123557570-123557571	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs560393163	chr12:123557575-123557576	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs528244560	chr12:123557589-123557590	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs192753302	chr12:123557593-123557594	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs571173956	chr12:123557669-123557670	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs532309671	chr12:123557675-123557676	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs146567808	chr12:123557703-123557704	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs140070304	chr12:123557730-123557731	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs532941040	chr12:123557740-123557741	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs535957839	chr12:123557767-123557768	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs554601313	chr12:123557781-123557782	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs566464426	chr12:123557789-123557790	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs185005453	chr12:123557828-123557829	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs142367017	chr12:123557887-123557888	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs189931675	chr12:123557889-123557890	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs151300158	chr12:123557902-123557903	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs556587637	chr12:123557945-123557946	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs571452419	chr12:123557981-123557982	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs574736828	chr12:123558077-123558078	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs193196071	chr12:123558121-123558122	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs560606485	chr12:123558164-123558165	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs527799885	chr12:123558236-123558237	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 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
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
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
Ependymoma	20639864	CNVD
head and neck squamous cell carcinoma	24351288	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123542800-123563800	Enhancers	Left Ventricle	heart
2	chr12:123543800-123559000	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr12:123544000-123559000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr12:123546400-123562400	Enhancers	Liver	Liver
5	chr12:123549600-123561000	Weak transcription	Hela-S3	cervix
6	chr12:123549800-123560000	Weak transcription	Stomach Mucosa	stomach
7	chr12:123550000-123559800	Transcr. at gene 5' and 3'	Fetal Thymus	thymus
8	chr12:123550000-123562400	Enhancers	Fetal Heart	heart
9	chr12:123550600-123559400	Weak transcription	Primary hematopoietic stem cells	blood
10	chr12:123551000-123559000	Weak transcription	Primary B cells from cord blood	blood
11	chr12:123551000-123559200	Weak transcription	Primary B cells from peripheral blood	blood
12	chr12:123551000-123560200	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr12:123551200-123560400	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr12:123551200-123561800	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr12:123551400-123557600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr12:123551600-123557800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr12:123553400-123557400	Enhancers	Lung	lung
18	chr12:123553600-123560000	Transcr. at gene 5' and 3'	Thymus	Thymus
19	chr12:123553800-123557400	Enhancers	Brain Cingulate Gyrus	brain
20	chr12:123553800-123563800	Enhancers	Right Ventricle	heart
21	chr12:123554000-123557000	Enhancers	Spleen	Spleen
22	chr12:123554000-123559200	Enhancers	Primary T cells fromperipheralblood	blood
23	chr12:123554000-123563000	Enhancers	Right Atrium	heart
24	chr12:123554000-123563800	Enhancers	Brain Hippocampus Middle	brain
25	chr12:123554200-123557400	Enhancers	Brain Angular Gyrus	brain
26	chr12:123554200-123557400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
27	chr12:123554200-123557400	Enhancers	Fetal Muscle Leg	muscle
28	chr12:123554400-123557000	Enhancers	Stomach Smooth Muscle	stomach
29	chr12:123554400-123557200	Enhancers	Brain Anterior Caudate	brain
30	chr12:123554400-123557400	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr12:123554400-123557600	Enhancers	Esophagus	oesophagus
32	chr12:123554400-123558400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr12:123554400-123560400	Enhancers	Colon Smooth Muscle	Colon
34	chr12:123554600-123557000	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr12:123554600-123557000	Enhancers	Rectal Smooth Muscle	rectum
36	chr12:123554600-123559000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr12:123555000-123557200	Enhancers	Psoas Muscle	Psoas
38	chr12:123555000-123557800	Enhancers	Fetal Stomach	stomach
39	chr12:123555000-123558800	Enhancers	Fetal Brain Female	brain
40	chr12:123555000-123559000	Enhancers	Primary T helper cells fromperipheralblood	blood
41	chr12:123555000-123559200	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr12:123555200-123558200	Enhancers	HepG2	liver
43	chr12:123555200-123560000	Weak transcription	Fetal Intestine Large	intestine
44	chr12:123555400-123557200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr12:123555400-123557200	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr12:123555400-123557600	Genic enhancers	Primary T cells from cord blood	blood
47	chr12:123555600-123557200	Enhancers	Brain Substantia Nigra	brain
48	chr12:123555600-123557800	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr12:123555600-123559000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr12:123555600-123559000	Enhancers	Fetal Brain Male	brain

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