Variant report

Variant	esv34782
Chromosome Location	chr12:66933542-66971398
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:251)
CpG islands
(count:122)
Chromatin interactive
region (count:10)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:251 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:66944481-66944665	K562	blood:	n/a	n/a
2	ATF1	chr12:66948999-66949199	K562	blood:	n/a	n/a
3	ATF1	chr12:66944465-66944726	K562	blood:	n/a	n/a
4	ATF1	chr12:66956774-66956900	K562	blood:	n/a	n/a
5	CEBPB	chr12:66944454-66944708	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr12:66944409-66944714	K562	blood:	n/a	n/a
7	CTCF	chr12:66949071-66949221	MCF-7	breast:	n/a	n/a
8	CTCF	chr12:66942700-66942850	GM12878	blood:	n/a	n/a
9	CTCF	chr12:66942680-66942830	A549	lung:	n/a	n/a
10	CTCF	chr12:66942820-66942970	GM12870	blood:	n/a	n/a
11	CTCF	chr12:66942680-66942830	GM06990	blood:	n/a	n/a
12	CTCF	chr12:66942680-66942830	HBMEC	blood vessel:	n/a	n/a
13	CTCF	chr12:66942680-66942830	GM12871	blood:	n/a	n/a
14	CTCF	chr12:66942700-66942850	HA-sp	spinal cord:	n/a	n/a
15	CTCF	chr12:66942200-66942350	HPF	lung:	n/a	n/a
16	CTCF	chr12:66942700-66942850	GM12871	blood:	n/a	n/a
17	CTCF	chr12:66942580-66942730	GM12870	blood:	n/a	n/a
18	CTCF	chr12:66942721-66942803	LNCaP	prostate:	n/a	n/a
19	CTCF	chr12:66942640-66942790	NHDF-neo	bronchial:	n/a	n/a
20	CTCF	chr12:66942660-66942810	GM12870	blood:	n/a	n/a
21	CTCF	chr12:66942480-66942630	NHLF	lung:	n/a	n/a
22	CTCF	chr12:66949060-66949210	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr12:66942640-66942790	HEK293	kidney:	n/a	n/a
24	CTCF	chr12:66942680-66942830	AG09309	skin:	n/a	n/a
25	CTCF	chr12:66942640-66942790	Caco-2	colon:	n/a	n/a
26	CTCF	chr12:66942640-66942790	HA-sp	spinal cord:	n/a	n/a
27	CTCF	chr12:66949069-66949199	GM12878	blood:	n/a	n/a
28	CTCF	chr12:66942660-66942810	MCF-7	breast:	n/a	n/a
29	CTCF	chr12:66942658-66942803	GM13977	blood:	n/a	n/a
30	CTCF	chr12:66949180-66949330	HRPEpiC	eye:	n/a	n/a
31	CTCF	chr12:66942665-66942774	GM10248	blood:	n/a	n/a
32	CTCF	chr12:66942680-66942830	HVMF	connective:	n/a	n/a
33	CTCF	chr12:66942660-66942910	GM12801	blood:	n/a	n/a
34	CTCF	chr12:66948960-66949110	HMEC	breast:	n/a	n/a
35	CTCF	chr12:66942660-66942810	HCFaa	heart:	n/a	n/a
36	CTCF	chr12:66942680-66942830	GM12866	blood:	n/a	n/a
37	CTCF	chr12:66942589-66942946	K562	blood:	n/a	n/a
38	CTCF	chr12:66942640-66942790	AG10803	skin:	n/a	n/a
39	CTCF	chr12:66948874-66948895	Lung_OC	lung:	n/a	n/a
40	CTCF	chr12:66942720-66942870	HFF	foreskin:	n/a	n/a
41	CTCF	chr12:66942640-66942790	GM12878	blood:	n/a	n/a
42	CTCF	chr12:66949140-66949290	MCF-7	breast:	n/a	n/a
43	CTCF	chr12:66942260-66942410	GM12864	blood:	n/a	n/a
44	CTCF	chr12:66942700-66942850	HFF-Myc	foreskin:	n/a	n/a
45	CTCF	chr12:66942694-66942779	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr12:66949060-66949210	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr12:66935380-66935530	GM12866	blood:	n/a	n/a
48	CTCF	chr12:66942680-66942830	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr12:66942680-66942805	GM10266	blood:	n/a	n/a
50	CTCF	chr12:66942720-66942870	AG04450	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:66965991-66966041	HAEpiC	amniotic membrane:	n/a
2	chr12:66965641-66965691	A549	lung:	n/a
3	chr12:66965991-66966041	SK-N-MC	brain:	n/a
4	chr12:66965991-66966041	HepG2	liver:	n/a
5	chr12:66965991-66966041	Hela-S3	cervix:	n/a
6	chr12:66965991-66966041	ProgFib	skin:	n/a
7	chr12:66965991-66966041	HUVEC	blood vessel:	n/a
8	chr12:66965991-66966041	PANC-1	pancreas:	n/a
9	chr12:66965991-66966041	T-47D	breast:	n/a
10	chr12:66965641-66965691	PFSK-1	brain:	n/a
11	chr12:66965991-66966041	HRCEpiC	kidney:	n/a
12	chr12:66965641-66965691	AoSMC	blood vessel:	n/a
13	chr12:66965641-66965691	SK-N-SH	brain:	n/a
14	chr12:66965641-66965691	AG04450	lung:	fetal
15	chr12:66965641-66965691	NT2-D1	testis:	n/a
16	chr12:66965641-66965691	H1-hESC	embryonic stem cell:	embryo
17	chr12:66965641-66965691	GM12891	blood:	n/a
18	chr12:66965991-66966041	HEEpiC	esophagus:	n/a
19	chr12:66965641-66965691	PANC-1	pancreas:	n/a
20	chr12:66965641-66965691	HEK293	kidney:	embryo
21	chr12:66965991-66966041	SK-N-SH	brain:	n/a
22	chr12:66965991-66966041	AG04450	lung:	fetal
23	chr12:66965641-66965691	NH-A	brain:	n/a
24	chr12:66965641-66965691	GM19239	blood:	n/a
25	chr12:66965991-66966041	BE2_C	brain:	n/a
26	chr12:66965991-66966041	HCF	heart:	n/a
27	chr12:66965641-66965691	Jurkat	blood:	n/a
28	chr12:66965991-66966041	Jurkat	blood:	n/a
29	chr12:66965641-66965691	CMK	blood:	n/a
30	chr12:66965641-66965691	NB4	blood:	n/a
31	chr12:66965991-66966041	NH-A	brain:	n/a
32	chr12:66965991-66966041	NHBE	bronchial:	n/a
33	chr12:66965991-66966041	AG10803	skin:	n/a
34	chr12:66965991-66966041	LNCaP	prostate:	n/a
35	chr12:66965641-66965691	HAEpiC	amniotic membrane:	n/a
36	chr12:66965641-66965691	PrEC	prostate:	n/a
37	chr12:66965641-66965691	HUVEC	blood vessel:	n/a
38	chr12:66965991-66966041	HRPEpiC	eye:	n/a
39	chr12:66965641-66965691	Caco-2	colon:	n/a
40	chr12:66965991-66966041	Caco-2	colon:	n/a
41	chr12:66965991-66966041	PFSK-1	brain:	n/a
42	chr12:66965991-66966041	U87	brain:	n/a
43	chr12:66965641-66965691	T-47D	breast:	n/a
44	chr12:66965991-66966041	AG09309	skin:	n/a
45	chr12:66965641-66965691	AG04449	skin:	fetal
46	chr12:66965991-66966041	SK-N-SH_RA	brain:	n/a
47	chr12:66965991-66966041	HCPEpiC	choroid plexus:	n/a
48	chr12:66965991-66966041	BJ	skin:	n/a
49	chr12:66965641-66965691	GM12878	blood:	n/a
50	chr12:66965641-66965691	IMR90	lung:	fetal

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:66932403..66936111-chr12:66940757..66944323,3	K562	blood:
2	chr12:66940803..66943368-chr12:66944201..66946459,3	MCF-7	breast:
3	chr12:66940803..66943368-chr12:66944201..66946459,3	MCF-7	breast:
4	chr12:66930710..66933060-chr12:66933973..66935708,2	MCF-7	breast:
5	chr12:66942264..66943151-chr12:67082787..67083333,2	MCF-7	breast:
6	chr1:17014602..17017113-chr12:66936746..66938540,2	MCF-7	breast:
7	chr12:66934881..66936462-chr12:66943891..66946152,2	MCF-7	breast:
8	chr12:66934881..66936462-chr12:66943891..66946152,2	MCF-7	breast:
9	chr12:66938952..66941584-chr12:66945034..66947261,2	K562	blood:
10	chr12:66938952..66941584-chr12:66945034..66947261,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMBIM4-2	chr12:66957747-66957916	NONHSAT029232
2	lnc-TMBIM4-2	chr12:66961345-66962974	NONHSAT029232

No data

Variant related genes	Relation type
GRIP1	TF binding region
OSBPL9P4	TF binding region
OSBPL9P5	TF binding region
GRIP1	CpG island
OSBPL9P4	CpG island
OSBPL9P5	CpG island
ENSG00000155974	chromatin interactions

Extended variants
information (count: 1454 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1454 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7300413	chr12:66933542-66933543	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs11176251	chr12:66933557-66933558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs11176252	chr12:66933560-66933561	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534006556	chr12:66933612-66933613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs558504108	chr12:66933623-66933624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs11176253	chr12:66933637-66933638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576701976	chr12:66933671-66933672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537792288	chr12:66933672-66933673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs569342396	chr12:66933744-66933745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs556125966	chr12:66933807-66933808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574504931	chr12:66933860-66933861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548501154	chr12:66933863-66933864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554264536	chr12:66933889-66933890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs79907609	chr12:66933892-66933893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs546364989	chr12:66933915-66933916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185337702	chr12:66933923-66933924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs80312733	chr12:66933928-66933929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35414395	chr12:66933940-66933941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs544168092	chr12:66933962-66933963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs145808731	chr12:66934048-66934049	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs529714626	chr12:66934059-66934060	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs562329151	chr12:66934088-66934089	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs547942221	chr12:66934125-66934126	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs562774293	chr12:66934135-66934136	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs35145721	chr12:66934158-66934159	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs527422220	chr12:66934199-66934200	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs10878445	chr12:66934220-66934221	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs146535688	chr12:66934240-66934241	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs200436201	chr12:66934336-66934337	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs537703875	chr12:66934358-66934359	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs553724452	chr12:66934428-66934429	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs17102642	chr12:66934441-66934442	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs189796611	chr12:66934463-66934464	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs568087999	chr12:66934509-66934510	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs574009242	chr12:66934510-66934511	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs7487348	chr12:66934516-66934517	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs553915073	chr12:66934562-66934563	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs199551170	chr12:66934569-66934570	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs373791139	chr12:66934570-66934571	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs57465336	chr12:66934591-66934592	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs555677131	chr12:66934672-66934673	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs546029379	chr12:66934689-66934690	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs77969977	chr12:66934743-66934744	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs180682937	chr12:66934752-66934753	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs10784551	chr12:66934753-66934754	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs187428404	chr12:66934756-66934757	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs191924293	chr12:66934765-66934766	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs11837040	chr12:66934782-66934783	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs529594023	chr12:66934795-66934796	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs541786228	chr12:66934814-66934815	Weak transcription Enhancers	Chromatin interactive region	1 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
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
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
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
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21364760	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	22048815	CNVD
Congenital anomalies of the kidney and urinary tract	21113617	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Myxofibrosarcoma	16751306	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Lung cancer	17925434	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Disease	21505450	CNVD
craniofacial dysmorphism	21918468	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:66911400-66938200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:66930400-66938000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr12:66931000-66933600	Enhancers	Fetal Brain Female	brain
4	chr12:66932200-66934200	Enhancers	Fetal Brain Male	brain
5	chr12:66932800-66933600	Enhancers	Fetal Intestine Large	intestine
6	chr12:66932800-66933600	Enhancers	Fetal Intestine Small	intestine
7	chr12:66932800-66933800	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr12:66932800-66933800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr12:66932800-66934000	Enhancers	Brain Substantia Nigra	brain
10	chr12:66933000-66933600	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr12:66933000-66933800	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr12:66933000-66933800	Enhancers	Brain Anterior Caudate	brain
13	chr12:66933000-66934000	Enhancers	Brain Hippocampus Middle	brain
14	chr12:66933200-66934800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr12:66933600-66938200	Weak transcription	Fetal Brain Female	brain
16	chr12:66934200-66935200	Weak transcription	Fetal Brain Male	brain
17	chr12:66934800-66935000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr12:66935200-66936000	Enhancers	Fetal Brain Male	brain
19	chr12:66936000-66938400	Weak transcription	Fetal Brain Male	brain
20	chr12:66938000-66938600	Enhancers	Brain Germinal Matrix	brain
21	chr12:66938200-66938400	Enhancers	H9 Cell Line	embryonic stem cell
22	chr12:66938200-66938600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:66938200-66939000	Enhancers	Fetal Brain Female	brain
24	chr12:66938400-66938800	Enhancers	Fetal Brain Male	brain
25	chr12:66942000-66943600	Enhancers	Primary B cells from peripheral blood	blood
26	chr12:66942200-66942600	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr12:66942200-66943000	Enhancers	GM12878-XiMat	blood
28	chr12:66943000-66944600	Weak transcription	GM12878-XiMat	blood
29	chr12:66944400-66944600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr12:66944400-66944800	Enhancers	HUVEC	blood vessel
31	chr12:66944400-66945200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr12:66944600-66945200	Enhancers	GM12878-XiMat	blood
33	chr12:66945200-66948800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr12:66946400-66947000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr12:66948600-66949200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr12:66948800-66949400	Enhancers	HMEC	breast
37	chr12:66948800-66949600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr12:66949400-66956000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr12:66949600-66952600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr12:66952600-66953200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr12:66953200-66962200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr12:66956000-66956200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr12:66962200-66962800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr12:66962600-66964000	Weak transcription	Fetal Brain Female	brain
45	chr12:66962800-66981400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr12:66964800-66965800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr12:66965000-66965800	Enhancers	Brain Angular Gyrus	brain

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