Variant report

Variant	esv3409718
Chromosome Location	chr12:56696427-56696939
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:56695578-56696488	HepG2	liver:	n/a	n/a
2	BCLAF1	chr12:56696100-56696480	GM12878	blood:	n/a	n/a
3	CTCF	chr12:56696680-56696830	HVMF	connective:	n/a	n/a
4	CTCF	chr12:56696760-56696910	NB4	blood:	n/a	n/a
5	CTCF	chr12:56696280-56696430	GM06990	blood:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
6	CTCF	chr12:56696600-56696750	AoAF	blood vessel:	n/a	n/a
7	CTCF	chr12:56696680-56696830	HCM	heart:	n/a	n/a
8	CTCF	chr12:56696192-56696454	GM10266	blood:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
9	CTCF	chr12:56696300-56696450	HMEC	breast:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
10	CTCF	chr12:56696280-56696430	HFF	foreskin:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
11	CTCF	chr12:56696528-56696636	GM19240	blood:	n/a	n/a
12	CTCF	chr12:56696280-56696430	SK-N-SH_RA	brain:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
13	CTCF	chr12:56696198-56696465	K562	blood:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
14	CTCF	chr12:56696510-56696643	Spleen_OC	spleen:	n/a	n/a
15	CTCF	chr12:56696194-56696469	LNCaP	prostate:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
16	CTCF	chr12:56696300-56696450	NHEK	skin:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
17	CTCF	chr12:56696075-56696513	HepG2	liver:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
18	CTCF	chr12:56696522-56696664	GM13977	blood:	n/a	n/a
19	CTCF	chr12:56696145-56696508	A549	lung:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
20	CTCF	chr12:56696200-56696463	A549	lung:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
21	CTCF	chr12:56696700-56696850	WI-38	lung:	n/a	n/a
22	CTCF	chr12:56696176-56696577	T-47D	breast:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
23	CTCF	chr12:56696700-56696850	GM12864	blood:	n/a	n/a
24	CTCF	chr12:56696133-56696442	H1-hESC	embryonic stem cell:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
25	CTCF	chr12:56696184-56696483	HUVEC	blood vessel:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
26	CTCF	chr12:56696553-56696596	GM12891	blood:	n/a	n/a
27	CTCF	chr12:56696159-56696465	SK-N-SH_RA	brain:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
28	CTCF	chr12:56696199-56696437	GM10248	blood:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
29	CTCF	chr12:56696300-56696450	GM12869	blood:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
30	CTCF	chr12:56696216-56696438	Hela-S3	cervix:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
31	CTCF	chr12:56695763-56696742	SK-N-SH	brain:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
32	CTCF	chr12:56696560-56696710	HFF-Myc	foreskin:	n/a	n/a
33	CTCF	chr12:56696660-56696810	GM12864	blood:	n/a	n/a
34	CTCF	chr12:56696085-56696585	K562	blood:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
35	CTCF	chr12:56696501-56696625	LNCaP	prostate:	n/a	n/a
36	CTCF	chr12:56695635-56696796	A549	lung:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
37	CTCF	chr12:56696032-56696617	MCF-7	breast:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
38	CTCF	chr12:56696223-56696449	Pancreas_OC	pancreas:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
39	CTCF	chr12:56696117-56696527	IMR90	lung:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
40	CTCF	chr12:56696112-56696539	GM12878	blood:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
41	CTCF	chr12:56696740-56696890	A549	lung:	n/a	n/a
42	CTCF	chr12:56696300-56696450	GM06990	blood:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
43	CTCF	chr12:56696580-56696730	GM12865	blood:	n/a	n/a
44	CTCF	chr12:56696162-56696469	GM12878	blood:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
45	CTCF	chr12:56696700-56696850	HRE	kidney:	n/a	n/a
46	CTCF	chr12:56696720-56696870	AG10803	skin:	n/a	n/a
47	CTCF	chr12:56696680-56696830	Caco-2	colon:	n/a	n/a
48	CTCF	chr12:56696175-56696491	Spleen_OC	spleen:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
49	CTCF	chr12:56696086-56696453	K562	blood:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335
50	CTCF	chr12:56696225-56696433	GM13977	blood:	n/a	chr12:56696321-56696337 chr12:56696315-56696336 chr12:56696320-56696338 chr12:56696326-56696335 chr12:56696322-56696335

No.	Distal block	Cell Line	Cell type
1	chr12:56693640..56697163-chr12:56700934..56704368,3	MCF-7	breast:
2	chr12:56659486..56662634-chr12:56692106..56696696,6	MCF-7	breast:
3	chr12:56695752..56697519-chr12:56726820..56729640,2	MCF-7	breast:
4	chr12:56509513..56513531-chr12:56694540..56697702,5	K562	blood:
5	chr12:56625939..56627578-chr12:56694733..56696853,2	K562	blood:
6	chr12:56585782..56587966-chr12:56695653..56698357,2	K562	blood:
7	chr12:56618027..56618828-chr12:56696062..56696684,2	MCF-7	breast:
8	chr12:56690986..56698275-chr12:56706607..56711958,20	MCF-7	breast:
9	chr12:56692603..56696463-chr12:56860417..56864951,9	K562	blood:
10	chr12:56679574..56682384-chr12:56692383..56696875,5	K562	blood:
11	chr12:56696417..56698207-chr12:56857084..56858822,2	MCF-7	breast:
12	chr12:56679574..56681804-chr12:56694461..56697113,2	K562	blood:
13	chr12:56694767..56697892-chr12:56702654..56704783,4	K562	blood:
14	chr12:56694994..56697860-chr12:56698216..56699984,2	MCF-7	breast:
15	chr12:56692603..56696463-chr12:56860417..56864951,8	K562	blood:
16	chr12:56514975..56517772-chr12:56694804..56696732,2	MCF-7	breast:
17	chr12:56586878..56587381-chr12:56696043..56696785,2	K562	blood:
18	chr12:56692256..56696973-chr12:56707335..56712231,9	K562	blood:
19	chr12:56695853..56696434-chr12:56857361..56858155,2	K562	blood:
20	chr12:56690402..56700610-chr12:56705161..56712229,20	K562	blood:
21	chr12:56696025..56697572-chr12:56726476..56728778,2	K562	blood:
22	chr12:56652045..56652731-chr12:56695880..56696766,2	MCF-7	breast:
23	chr12:56509293..56514359-chr12:56692717..56696999,9	K562	blood:
24	chr12:56693116..56697525-chr12:56726716..56730598,5	K562	blood:
25	chr12:56617925..56618696-chr12:56695888..56696814,2	K562	blood:
26	chr12:56650147..56652111-chr12:56693703..56696656,2	MCF-7	breast:
27	chr12:56615624..56617857-chr12:56693691..56696506,3	K562	blood:

Variant related genes	Relation type
CS	TF binding region
ENSG00000135473	chromatin interactions
ENSG00000144785	chromatin interactions
ENSG00000257740	chromatin interactions
ENSG00000257727	chromatin interactions
ENSG00000139645	chromatin interactions
ENSG00000062485	chromatin interactions
ENSG00000181852	chromatin interactions
ENSG00000135469	chromatin interactions
ENSG00000135482	chromatin interactions
ENSG00000139641	chromatin interactions
ENSG00000176422	chromatin interactions
ENSG00000229117	chromatin interactions
ENSG00000135517	chromatin interactions
ENSG00000258345	chromatin interactions
ENSG00000139579	chromatin interactions

Extended variants
information (count: 23 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553763246	chr12:56696442-56696443	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
2	rs146365591	chr12:56696458-56696459	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
3	rs117824729	chr12:56696459-56696460	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
4	rs181798646	chr12:56696473-56696474	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
5	rs149373738	chr12:56696484-56696485	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
6	rs58179508	chr12:56696509-56696510	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
7	rs116934693	chr12:56696545-56696546	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	mRNA abundance
8	rs540270775	chr12:56696576-56696577	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
9	rs11171798	chr12:56696584-56696585	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
10	rs549096622	chr12:56696615-56696616	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
11	rs546795521	chr12:56696621-56696622	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
12	rs541437992	chr12:56696696-56696697	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
13	rs556279048	chr12:56696708-56696709	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
14	rs186099842	chr12:56696719-56696720	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
15	rs41392645	chr12:56696742-56696743	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs71459359	chr12:56696766-56696767	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
17	rs71459360	chr12:56696784-56696785	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
18	rs71459361	chr12:56696790-56696791	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
19	rs545224410	chr12:56696799-56696800	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
20	rs530435974	chr12:56696869-56696870	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs78057390	chr12:56696904-56696905	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
22	rs74842448	chr12:56696905-56696906	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
23	rs577040352	chr12:56696931-56696932	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
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
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Bladder cancer	21909424	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	20531469	CNVD
Rhabdomyosarcoma	16790082	CNVD
Renal cell carcinoma	18765545	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21138945	CNVD
Glioblastoma multiforme	21569311	CNVD
Glioblastoma multiforme	19115005	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	21509527	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glycogen storage disease	18421352	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD

Chromatin state (count:138 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:56694600-56704400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr12:56694600-56708400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr12:56694800-56696600	Enhancers	Primary B cells from cord blood	blood
4	chr12:56694800-56696600	Enhancers	Primary T helper cells PMA-I stimulated	--
5	chr12:56694800-56696600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
6	chr12:56694800-56696800	Enhancers	Primary T cells fromperipheralblood	blood
7	chr12:56694800-56697200	Enhancers	Primary B cells from peripheral blood	blood
8	chr12:56694800-56697600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr12:56694800-56708200	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr12:56694800-56708800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr12:56695000-56696800	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr12:56695000-56697000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr12:56695000-56697200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr12:56695000-56697200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr12:56695000-56697200	Weak transcription	Fetal Brain Female	brain
16	chr12:56695000-56697800	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr12:56695000-56698000	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr12:56695000-56698200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr12:56695000-56698600	Weak transcription	Brain Angular Gyrus	brain
20	chr12:56695000-56699000	Weak transcription	NH-A	brain
21	chr12:56695000-56700400	Weak transcription	Brain Germinal Matrix	brain
22	chr12:56695000-56700400	Weak transcription	Thymus	Thymus
23	chr12:56695000-56701800	Weak transcription	Ovary	ovary
24	chr12:56695000-56702000	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr12:56695000-56702800	Weak transcription	Small Intestine	intestine
26	chr12:56695000-56703600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr12:56695000-56703600	Weak transcription	Esophagus	oesophagus
28	chr12:56695000-56703600	Weak transcription	Gastric	stomach
29	chr12:56695000-56704600	Weak transcription	Aorta	Aorta
30	chr12:56695000-56708000	Weak transcription	Fetal Brain Male	brain
31	chr12:56695000-56708600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr12:56695200-56696600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr12:56695200-56697000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr12:56695200-56697000	Weak transcription	Fetal Lung	lung
35	chr12:56695200-56697800	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr12:56695200-56697800	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr12:56695200-56697800	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr12:56695200-56697800	Enhancers	Liver	Liver
39	chr12:56695200-56697800	Weak transcription	Placenta	Placenta
40	chr12:56695200-56697800	Weak transcription	Osteobl	bone
41	chr12:56695200-56698000	Weak transcription	Primary monocytes fromperipheralblood	blood
42	chr12:56695200-56698000	Weak transcription	NHEK	skin
43	chr12:56695200-56698200	Weak transcription	Primary hematopoietic stem cells	blood
44	chr12:56695200-56698200	Weak transcription	Brain Cingulate Gyrus	brain
45	chr12:56695200-56698200	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr12:56695200-56698200	Weak transcription	NHLF	lung
47	chr12:56695200-56698400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr12:56695200-56698600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr12:56695200-56698600	Weak transcription	Adipose Nuclei	Adipose
50	chr12:56695200-56698800	Weak transcription	Fetal Kidney	kidney

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