Variant report

Variant	esv3517152
Chromosome Location	chr12:64174867-64178831
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:21)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr12:64178705-64178967	HepG2	liver:	n/a	chr12:64178867-64178878 chr12:64178866-64178879 chr12:64178866-64178877 chr12:64178868-64178877
2	GATA3	chr12:64176068-64176194	SH-SY5Y	brain:	n/a	n/a
3	MAFK	chr12:64176612-64176699	HepG2	liver:	n/a	chr12:64176670-64176685
4	MAFK	chr12:64176566-64176750	HepG2	liver:	n/a	chr12:64176670-64176685
5	MXI1	chr12:64172589-64175771	SK-N-SH	brain:	n/a	n/a
6	MYC	chr12:64173966-64174922	MCF10A-Er-Src	breast:	n/a	chr12:64174158-64174171 chr12:64174158-64174168 chr12:64174160-64174167 chr12:64174162-64174169
7	MYC	chr12:64175044-64175163	MCF10A-Er-Src	breast:	n/a	n/a
8	POLR2A	chr12:64176306-64176603	MCF10A-Er-Src	breast:	n/a	n/a
9	POLR2A	chr12:64174818-64175185	MCF10A-Er-Src	breast:	n/a	n/a
10	POLR2A	chr12:64177351-64177740	GM12878	blood:	n/a	n/a
11	POLR2A	chr12:64177680-64177732	MCF10A-Er-Src	breast:	n/a	n/a
12	POLR2A	chr12:64175295-64175319	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr12:64175556-64175623	MCF10A-Er-Src	breast:	n/a	n/a
14	POLR2A	chr12:64173169-64175918	MCF10A-Er-Src	breast:	n/a	n/a
15	POLR2A	chr12:64178276-64178282	MCF10A-Er-Src	breast:	n/a	n/a
16	POLR2A	chr12:64177985-64178830	MCF10A-Er-Src	breast:	n/a	n/a
17	POLR2A	chr12:64178504-64178761	K562	blood:	n/a	n/a
18	POLR2A	chr12:64176162-64176412	MCF10A-Er-Src	breast:	n/a	n/a
19	RFX5	chr12:64176838-64176907	K562	blood:	n/a	n/a
20	STAT3	chr12:64175667-64175822	MCF10A-Er-Src	breast:	n/a	n/a
21	ZC3H11A	chr12:64175516-64175640	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:64177990-64178040	BE2_C	brain:	n/a
2	chr12:64177990-64178040	K562	blood:	n/a
3	chr12:64177990-64178040	HRCEpiC	kidney:	n/a
4	chr12:64177990-64178040	T-47D	breast:	n/a
5	chr12:64177990-64178040	HMEC	breast:	n/a
6	chr12:64177990-64178040	HCPEpiC	choroid plexus:	n/a
7	chr12:64177990-64178040	BJ	skin:	n/a
8	chr12:64177990-64178040	RPTEC	kidney:	n/a
9	chr12:64177990-64178040	SKMC	muscle:	n/a
10	chr12:64177990-64178040	Hela-S3	cervix:	n/a
11	chr12:64177990-64178040	HNPCEpiC	eye:	n/a
12	chr12:64177990-64178040	HEEpiC	esophagus:	n/a
13	chr12:64177990-64178040	Caco-2	colon:	n/a
14	chr12:64177990-64178040	HCM	heart:	n/a
15	chr12:64177990-64178040	HRPEpiC	eye:	n/a
16	chr12:64177990-64178040	HPAEpiC	pulmonary alveolar:	n/a
17	chr12:64177990-64178040	AG04449	skin:	fetal
18	chr12:64177990-64178040	AG09319	gingival:	n/a
19	chr12:64177990-64178040	CMK	blood:	n/a
20	chr12:64177990-64178040	GM12878	blood:	n/a
21	chr12:64177990-64178040	AoSMC	blood vessel:	n/a
22	chr12:64177990-64178040	IMR90	lung:	fetal
23	chr12:64177990-64178040	SK-N-SH_RA	brain:	n/a
24	chr12:64177990-64178040	NH-A	brain:	n/a
25	chr12:64177990-64178040	ProgFib	skin:	n/a
26	chr12:64177990-64178040	NT2-D1	testis:	n/a
27	chr12:64177990-64178040	HRE	kidney:	n/a
28	chr12:64177990-64178040	ECC-1	luminal epithelium:	n/a
29	chr12:64177990-64178040	NHBE	bronchial:	n/a
30	chr12:64177990-64178040	HIPEpiC	eye:	n/a
31	chr12:64177990-64178040	AG09309	skin:	n/a
32	chr12:64177990-64178040	GM12892	blood:	n/a
33	chr12:64177990-64178040	HEK293	kidney:	embryo
34	chr12:64177990-64178040	U87	brain:	n/a
35	chr12:64177990-64178040	AG10803	skin:	n/a
36	chr12:64177990-64178040	SAEC	small airway:	n/a
37	chr12:64177990-64178040	H1-hESC	embryonic stem cell:	embryo
38	chr12:64177990-64178040	HUVEC	blood vessel:	n/a
39	chr12:64177990-64178040	PrEC	prostate:	n/a
40	chr12:64177990-64178040	NB4	blood:	n/a
41	chr12:64177990-64178040	Jurkat	blood:	n/a
42	chr12:64177990-64178040	A549	lung:	n/a
43	chr12:64177990-64178040	GM12891	blood:	n/a
44	chr12:64177990-64178040	MCF-7	breast:	n/a
45	chr12:64177990-64178040	HepG2	liver:	n/a
46	chr12:64177990-64178040	PANC-1	pancreas:	n/a
47	chr12:64177990-64178040	AG04450	lung:	fetal
48	chr12:64177990-64178040	MCF10A-Er-Src	breast:	n/a
49	chr12:64177990-64178040	HAEpiC	amniotic membrane:	n/a
50	chr12:64177990-64178040	PFSK-1	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:64160929..64163621-chr12:64176185..64177955,2	K562	blood:
2	chr12:64172533..64176121-chr12:64194832..64198679,5	K562	blood:
3	chr12:64167616..64170565-chr12:64175638..64177734,2	MCF-7	breast:
4	chr12:64172802..64174995-chr12:64236940..64239856,2	MCF-7	breast:
5	chr12:64172589..64175160-chr12:64189373..64193026,5	MCF-7	breast:
6	chr12:64172631..64179011-chr12:64187703..64190145,6	MCF-7	breast:
7	chr12:64172395..64175865-chr12:64176316..64181928,12	K562	blood:
8	chr12:64173978..64177817-chr12:64182120..64184728,4	K562	blood:
9	chr12:64172395..64175865-chr12:64176316..64181928,12	K562	blood:

No data

Variant related genes	Relation type
TMEM5	TF binding region
TMEM5	CpG island
ENSG00000196935	chromatin interactions
ENSG00000118600	chromatin interactions
ENSG00000249753	chromatin interactions

Extended variants
information (count: 134 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:134 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368967532	chr12:64174878-64174879	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs141095352	chr12:64174881-64174882	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs557282296	chr12:64174885-64174886	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs144932093	chr12:64174897-64174898	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs73122634	chr12:64174904-64174905	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs397514546	chr12:64174908-64174909	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs114694892	chr12:64174923-64174924	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs550445278	chr12:64174925-64174926	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs373210870	chr12:64174967-64174968	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs377752245	chr12:64174971-64174972	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs201478556	chr12:64174982-64174983	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs377588524	chr12:64174990-64174991	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs572736957	chr12:64175001-64175002	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs35795914	chr12:64175023-64175024	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs375260708	chr12:64175063-64175064	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs529925217	chr12:64175073-64175074	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs541439035	chr12:64175119-64175120	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs377678481	chr12:64175184-64175185	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs555210814	chr12:64175196-64175197	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs113252149	chr12:64175223-64175224	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs78405797	chr12:64175228-64175229	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs543962305	chr12:64175299-64175300	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs191871233	chr12:64175389-64175390	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs533199699	chr12:64175418-64175419	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs183565771	chr12:64175446-64175447	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs559813831	chr12:64175513-64175514	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs528468783	chr12:64175560-64175561	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs547764286	chr12:64175563-64175564	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs538786261	chr12:64175576-64175577	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs201449460	chr12:64175579-64175580	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs369399392	chr12:64175606-64175607	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs531224686	chr12:64175621-64175622	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs551307085	chr12:64175706-64175707	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs188302383	chr12:64175713-64175714	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs139649969	chr12:64175726-64175727	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs552755968	chr12:64175766-64175767	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs144241822	chr12:64175792-64175793	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs535036264	chr12:64175865-64175866	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs537357585	chr12:64175939-64175940	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs35286858	chr12:64175968-64175969	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs575627781	chr12:64176037-64176038	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs371963950	chr12:64176041-64176042	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs554950415	chr12:64176069-64176070	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs574934139	chr12:64176107-64176108	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs77037942	chr12:64176112-64176113	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs180912457	chr12:64176139-64176140	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs577746760	chr12:64176228-64176229	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs56221188	chr12:64176235-64176236	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs112256531	chr12:64176282-64176283	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs573385070	chr12:64176334-64176335	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
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
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	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
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:64172800-64175200	Active TSS	K562	blood
2	chr12:64173000-64175000	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr12:64173000-64175000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr12:64173000-64175000	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr12:64173000-64175000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr12:64173200-64175000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr12:64173200-64175000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr12:64173200-64175000	Active TSS	NHLF	lung
9	chr12:64173200-64175200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr12:64173200-64175200	Active TSS	iPS-20b Cell Line	embryonic stem cell
11	chr12:64173200-64175600	Active TSS	Ovary	ovary
12	chr12:64173600-64175200	Active TSS	HMEC	breast
13	chr12:64174000-64175000	Flanking Active TSS	HUVEC	blood vessel
14	chr12:64174200-64175000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
15	chr12:64174200-64175000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr12:64174200-64175200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr12:64174200-64175400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr12:64174200-64175400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr12:64174400-64175000	Enhancers	Primary B cells from peripheral blood	blood
20	chr12:64174400-64175000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
21	chr12:64174400-64175000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
22	chr12:64174400-64175200	Weak transcription	Placenta	Placenta
23	chr12:64174400-64176000	Weak transcription	Primary T cells fromperipheralblood	blood
24	chr12:64174400-64176000	Weak transcription	Left Ventricle	heart
25	chr12:64174400-64176200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr12:64174400-64176200	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr12:64174400-64177200	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr12:64174400-64180600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr12:64174400-64180600	Weak transcription	Gastric	stomach
30	chr12:64174400-64184000	Weak transcription	Esophagus	oesophagus
31	chr12:64174400-64184000	Weak transcription	Lung	lung
32	chr12:64174400-64189200	Weak transcription	Pancreas	Pancrea
33	chr12:64174400-64200200	Weak transcription	Spleen	Spleen
34	chr12:64174400-64201800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr12:64174400-64203400	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr12:64174400-64204400	Weak transcription	Small Intestine	intestine
37	chr12:64174400-64204800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr12:64174600-64175000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
39	chr12:64174600-64175000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr12:64174600-64175000	Enhancers	Primary hematopoietic stem cells	blood
41	chr12:64174600-64175000	Active TSS	Primary hematopoietic stem cells short term culture	blood
42	chr12:64174600-64175000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr12:64174600-64175000	Enhancers	Primary T killer memory cells from peripheral blood	blood
44	chr12:64174600-64175000	Enhancers	Brain Anterior Caudate	brain
45	chr12:64174600-64175000	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr12:64174600-64175000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr12:64174600-64175000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr12:64174600-64175000	Enhancers	Fetal Intestine Small	intestine
49	chr12:64174600-64175000	Enhancers	Fetal Lung	lung
50	chr12:64174600-64175000	Enhancers	Fetal Stomach	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links