Variant report

Variant	esv3500918
Chromosome Location	chr12:122183269-122188067
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:239)
CpG islands
(count:61)
Chromatin interactive
region (count:33)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:239 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:122186826-122187121	HepG2	liver:	n/a	n/a
2	ATF1	chr12:122186507-122187146	K562	blood:	n/a	n/a
3	ATF3	chr12:122186598-122187199	K562	blood:	n/a	n/a
4	ATF3	chr12:122186269-122187325	A549	lung:	n/a	n/a
5	ATF3	chr12:122186372-122187225	A549	lung:	n/a	n/a
6	ATF3	chr12:122186757-122187099	K562	blood:	n/a	n/a
7	BACH1	chr12:122186766-122187106	K562	blood:	n/a	n/a
8	BCL3	chr12:122186184-122187268	A549	lung:	n/a	n/a
9	BCL3	chr12:122186167-122187242	A549	lung:	n/a	n/a
10	BHLHE40	chr12:122186503-122187102	K562	blood:	n/a	n/a
11	CBX3	chr12:122186272-122187455	K562	blood:	n/a	chr12:122187076-122187087
12	CEBPB	chr12:122183550-122183687	IMR90	lung:	n/a	chr12:122183646-122183657
13	CEBPB	chr12:122183527-122183755	HepG2	liver:	n/a	chr12:122183646-122183657
14	CEBPB	chr12:122186525-122187095	IMR90	lung:	n/a	n/a
15	CEBPB	chr12:122183471-122183812	K562	blood:	n/a	chr12:122183646-122183657
16	CEBPB	chr12:122186455-122187204	MCF-7	breast:	n/a	n/a
17	CEBPB	chr12:122186628-122187075	K562	blood:	n/a	n/a
18	CEBPB	chr12:122183515-122183798	K562	blood:	n/a	chr12:122183646-122183657
19	CHD2	chr12:122186660-122187076	K562	blood:	n/a	n/a
20	CHD2	chr12:122186791-122186962	HepG2	liver:	n/a	n/a
21	CREB1	chr12:122186377-122187286	K562	blood:	n/a	n/a
22	CREB1	chr12:122186341-122187470	HepG2	liver:	n/a	n/a
23	CREB1	chr12:122186068-122187186	A549	lung:	n/a	n/a
24	CREB1	chr12:122186439-122187258	HepG2	liver:	n/a	n/a
25	CREB1	chr12:122186422-122187139	A549	lung:	n/a	n/a
26	CREB1	chr12:122186119-122187271	K562	blood:	n/a	n/a
27	CTCF	chr12:122186480-122186630	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr12:122186520-122186670	Caco-2	colon:	n/a	n/a
29	CTCF	chr12:122186500-122186650	AG04449	skin:	n/a	n/a
30	CTCF	chr12:122186892-122186946	Spleen_OC	spleen:	n/a	n/a
31	CTCF	chr12:122185083-122185150	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr12:122186740-122186890	Caco-2	colon:	n/a	n/a
33	CTCF	chr12:122186280-122186430	HRE	kidney:	n/a	n/a
34	CTCF	chr12:122186480-122186630	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr12:122186500-122186650	HRE	kidney:	n/a	n/a
36	CTCF	chr12:122186547-122186667	Hela-S3	cervix:	n/a	n/a
37	CUX1	chr12:122186883-122187164	K562	blood:	n/a	chr12:122187144-122187158
38	E2F6	chr12:122186223-122187110	K562	blood:	n/a	chr12:122186694-122186703
39	E2F6	chr12:122186094-122187204	A549	lung:	n/a	chr12:122186694-122186703
40	E2F6	chr12:122186444-122187007	K562	blood:	n/a	chr12:122186694-122186703
41	EGR1	chr12:122186827-122187163	K562	blood:	n/a	n/a
42	EGR1	chr12:122186868-122187192	K562	blood:	n/a	n/a
43	ELF1	chr12:122186500-122187164	A549	lung:	n/a	chr12:122186675-122186687
44	ELF1	chr12:122186726-122187161	K562	blood:	n/a	n/a
45	ELF1	chr12:122186853-122187143	K562	blood:	n/a	n/a
46	ELF1	chr12:122186160-122187269	MCF-7	breast:	n/a	chr12:122186675-122186687
47	ELF1	chr12:122186721-122187138	HepG2	liver:	n/a	n/a
48	ELK1	chr12:122186794-122186977	K562	blood:	n/a	n/a
49	EP300	chr12:122186388-122187258	MCF-7	breast:	n/a	n/a
50	EP300	chr12:122186600-122187161	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:122186536-122186586	HMEC	breast:	n/a
2	chr12:122186536-122186586	ProgFib	skin:	n/a
3	chr12:122186536-122186586	NT2-D1	testis:	n/a
4	chr12:122186536-122186586	ovcar-3	ovarian:	n/a
5	chr12:122186536-122186586	GM12878	blood:	n/a
6	chr12:122186536-122186586	T-47D	breast:	n/a
7	chr12:122186536-122186586	GM12892	blood:	n/a
8	chr12:122186536-122186586	PrEC	prostate:	n/a
9	chr12:122186536-122186586	AG04450	lung:	fetal
10	chr12:122186536-122186586	GM06990	blood:	n/a
11	chr12:122186536-122186586	HEEpiC	esophagus:	n/a
12	chr12:122186536-122186586	SKMC	muscle:	n/a
13	chr12:122186536-122186586	HL-60	blood:	n/a
14	chr12:122186536-122186586	HCM	heart:	n/a
15	chr12:122186536-122186586	AG04449	skin:	fetal
16	chr12:122186536-122186586	MCF10A-Er-Src	breast:	n/a
17	chr12:122186536-122186586	HCPEpiC	choroid plexus:	n/a
18	chr12:122186536-122186586	PANC-1	pancreas:	n/a
19	chr12:122186536-122186586	NB4	blood:	n/a
20	chr12:122186536-122186586	HRPEpiC	eye:	n/a
21	chr12:122186536-122186586	SK-N-SH	brain:	n/a
22	chr12:122186536-122186586	GM12891	blood:	n/a
23	chr12:122186536-122186586	AG09309	skin:	n/a
24	chr12:122186536-122186586	HPAEpiC	pulmonary alveolar:	n/a
25	chr12:122186536-122186586	HIPEpiC	eye:	n/a
26	chr12:122186536-122186586	BE2_C	brain:	n/a
27	chr12:122186536-122186586	Hepatocyte	liver:	n/a
28	chr12:122186536-122186586	U87	brain:	n/a
29	chr12:122186536-122186586	NHBE	bronchial:	n/a
30	chr12:122186536-122186586	HCT-116	colon:	n/a
31	chr12:122186536-122186586	SK-N-SH_RA	brain:	n/a
32	chr12:122186536-122186586	AG09319	gingival:	n/a
33	chr12:122186536-122186586	GM19239	blood:	n/a
34	chr12:122186536-122186586	A549	lung:	n/a
35	chr12:122186536-122186586	AoSMC	blood vessel:	n/a
36	chr12:122186536-122186586	H1-hESC	embryonic stem cell:	embryo
37	chr12:122186536-122186586	SAEC	small airway:	n/a
38	chr12:122186536-122186586	NH-A	brain:	n/a
39	chr12:122186536-122186586	HCF	heart:	n/a
40	chr12:122186536-122186586	Jurkat	blood:	n/a
41	chr12:122186536-122186586	RPTEC	kidney:	n/a
42	chr12:122186536-122186586	Caco-2	colon:	n/a
43	chr12:122186536-122186586	HAEpiC	amniotic membrane:	n/a
44	chr12:122186536-122186586	AG10803	skin:	n/a
45	chr12:122186536-122186586	IMR90	lung:	fetal
46	chr12:122186536-122186586	HEK293	kidney:	embryo
47	chr12:122186536-122186586	PFSK-1	brain:	n/a
48	chr12:122186536-122186586	HRE	kidney:	n/a
49	chr12:122186536-122186586	CMK	blood:	n/a
50	chr12:122186536-122186586	HepG2	liver:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:122186813..122188581-chr12:122229620..122232767,4	MCF-7	breast:
2	chr12:122147215..122155218-chr12:122185094..122190846,22	MCF-7	breast:
3	chr12:122149421..122152814-chr12:122185119..122186671,3	MCF-7	breast:
4	chr12:116828326..116828938-chr12:122186633..122187345,3	MCF-7	breast:
5	chr12:122186484..122187293-chr12:122675389..122676074,2	MCF-7	breast:
6	chr12:122186493..122188379-chr12:122211134..122213755,2	K562	blood:
7	chr12:122181727..122184365-chr12:122185006..122187114,3	MCF-7	breast:
8	chr12:122185135..122187179-chr12:122190114..122193871,4	K562	blood:
9	chr12:122134794..122135634-chr12:122186324..122187082,2	MCF-7	breast:
10	chr12:122140564..122141337-chr12:122186461..122187284,3	MCF-7	breast:
11	chr12:122184924..122187179-chr12:122189642..122193871,5	K562	blood:
12	chr12:122185243..122188214-chr12:122238983..122240823,2	K562	blood:
13	chr12:122185267..122187971-chr12:122239677..122241444,2	MCF-7	breast:
14	chr12:122186669..122187298-chr12:122582252..122582922,2	MCF-7	breast:
15	chr12:122133742..122136740-chr12:122185481..122187047,2	MCF-7	breast:
16	chr12:122186590..122187486-chr12:122230711..122231592,3	MCF-7	breast:
17	chr12:122180307..122182295-chr12:122185324..122187863,3	K562	blood:
18	chr12:122186440..122186968-chr12:122237161..122237850,2	MCF-7	breast:
19	chr12:122184835..122196012-chr12:122235281..122245445,27	MCF-7	breast:
20	chr12:122180307..122183056-chr12:122185275..122189745,5	K562	blood:
21	chr12:122181102..122183945-chr12:122184844..122187780,3	MCF-7	breast:
22	chr12:122148459..122151159-chr12:122185562..122188129,3	K562	blood:
23	chr12:122182089..122184011-chr12:122191407..122193970,2	MCF-7	breast:
24	chr12:122125178..122127616-chr12:122187006..122188526,2	K562	blood:
25	chr12:121836861..121838700-chr12:122185043..122186944,2	K562	blood:
26	chr12:122184667..122189513-chr12:122211148..122219682,10	MCF-7	breast:
27	chr12:122125125..122127616-chr12:122187006..122188687,2	K562	blood:
28	chr12:122181727..122184365-chr12:122185006..122187114,3	MCF-7	breast:
29	chr12:122149138..122151891-chr12:122182134..122184327,2	MCF-7	breast:
30	chr12:122186548..122187486-chr12:122230661..122231592,4	MCF-7	breast:
31	chr12:122148875..122150670-chr12:122187534..122189442,2	MCF-7	breast:
32	chr12:122170327..122173309-chr12:122186416..122187977,2	K562	blood:
33	chr12:122186394..122187383-chr12:123554322..123555067,2	MCF-7	breast:

No data

Variant related genes	Relation type
TMEM120B	TF binding region
TMEM120B	CpG island
ENSG00000139725	chromatin interactions
ENSG00000170633	chromatin interactions
ENSG00000272849	chromatin interactions
ENSG00000089053	chromatin interactions
ENSG00000188735	chromatin interactions
ENSG00000212694	chromatin interactions
ENSG00000139718	chromatin interactions

Extended variants
information (count: 281 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:281 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528870375	chr12:122183281-122183282	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs544729269	chr12:122183290-122183291	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs547547223	chr12:122183328-122183329	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs142378553	chr12:122183337-122183338	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs144604825	chr12:122183370-122183371	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs557938327	chr12:122183451-122183452	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs186141317	chr12:122183455-122183456	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs6486775	chr12:122183531-122183532	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs190509406	chr12:122183539-122183540	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs555241313	chr12:122183550-122183551	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs573726740	chr12:122183616-122183617	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs541012198	chr12:122183623-122183624	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs552914845	chr12:122183655-122183656	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs142015048	chr12:122183659-122183660	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs533480272	chr12:122183677-122183678	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs551449580	chr12:122183693-122183694	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs7310523	chr12:122183798-122183799	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs575745471	chr12:122183802-122183803	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs543369395	chr12:122183806-122183807	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs139906377	chr12:122183822-122183823	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs528759233	chr12:122183832-122183833	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs183102861	chr12:122183854-122183855	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs143175118	chr12:122183859-122183860	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs559037151	chr12:122183876-122183877	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs533059722	chr12:122183889-122183890	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs147492481	chr12:122183966-122183967	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs535359987	chr12:122183986-122183987	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs569880155	chr12:122183998-122183999	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs536830130	chr12:122184009-122184010	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs548901357	chr12:122184020-122184021	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs188192388	chr12:122184066-122184067	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs192476003	chr12:122184072-122184073	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs201803913	chr12:122184087-122184088	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs552953468	chr12:122184094-122184095	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs188010174	chr12:122184095-122184096	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs71079090	chr12:122184110-122184111	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs577948308	chr12:122184124-122184125	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs539168056	chr12:122184157-122184158	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs145385958	chr12:122184196-122184197	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs575826991	chr12:122184197-122184198	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs578221745	chr12:122184202-122184203	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs561435397	chr12:122184204-122184205	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs148704427	chr12:122184218-122184219	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs372874300	chr12:122184219-122184220	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs540617454	chr12:122184246-122184247	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs559343670	chr12:122184281-122184282	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs532789832	chr12:122184300-122184301	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs551484884	chr12:122184313-122184314	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs563222294	chr12:122184334-122184335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530489561	chr12:122184335-122184336	Weak transcription	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
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
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:315 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:122151600-122186200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr12:122152000-122188000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr12:122152200-122186400	Weak transcription	Duodenum Mucosa	Duodenum
4	chr12:122152200-122188000	Weak transcription	Brain Germinal Matrix	brain
5	chr12:122152200-122188000	Weak transcription	Dnd41	blood
6	chr12:122152200-122191600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr12:122152200-122191600	Weak transcription	Rectal Smooth Muscle	rectum
8	chr12:122152200-122200200	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr12:122152400-122188000	Weak transcription	Stomach Smooth Muscle	stomach
10	chr12:122152800-122186200	Weak transcription	Pancreas	Pancrea
11	chr12:122154200-122200400	Weak transcription	Psoas Muscle	Psoas
12	chr12:122155200-122186400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr12:122155600-122186200	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr12:122158800-122186200	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr12:122158800-122186200	Weak transcription	NHDF-Ad	bronchial
16	chr12:122158800-122186400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr12:122159000-122186200	Weak transcription	NH-A	brain
18	chr12:122159200-122186400	Weak transcription	HSMM	muscle
19	chr12:122159400-122194800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr12:122163400-122186200	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr12:122163600-122186200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr12:122163600-122186200	Weak transcription	Liver	Liver
23	chr12:122163600-122186600	Weak transcription	HSMMtube	muscle
24	chr12:122163600-122188000	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr12:122163600-122188200	Weak transcription	Brain Anterior Caudate	brain
26	chr12:122163800-122186200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr12:122164800-122188200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr12:122166800-122186200	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr12:122166800-122186200	Weak transcription	Thymus	Thymus
30	chr12:122166800-122186400	Weak transcription	Colon Smooth Muscle	Colon
31	chr12:122167200-122186400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr12:122167600-122186200	Weak transcription	Spleen	Spleen
33	chr12:122170400-122186200	Weak transcription	Right Atrium	heart
34	chr12:122170600-122186200	Weak transcription	Placenta	Placenta
35	chr12:122172000-122186200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr12:122174200-122191800	Weak transcription	Brain Cingulate Gyrus	brain
37	chr12:122176600-122186400	Weak transcription	Hela-S3	cervix
38	chr12:122176600-122187200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr12:122177800-122186200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr12:122179200-122186200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr12:122179800-122211000	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr12:122180000-122186200	Weak transcription	Primary hematopoietic stem cells	blood
43	chr12:122180000-122186200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr12:122180000-122186200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr12:122180200-122191400	Weak transcription	Monocytes-CD14+_RO01746	blood
46	chr12:122180800-122186200	Weak transcription	Esophagus	oesophagus
47	chr12:122181000-122186200	Weak transcription	HUVEC	blood vessel
48	chr12:122181200-122186200	Weak transcription	Left Ventricle	heart
49	chr12:122181200-122186200	Weak transcription	Ovary	ovary
50	chr12:122181200-122186200	Weak transcription	HepG2	liver

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