Variant report

Variant	nsv865
Chromosome Location	chr12:104030102-104074864
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:209)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:209 , 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	chr12:104066332-104066931	HepG2	liver:	n/a	n/a
2	ATF1	chr12:104074575-104074806	K562	blood:	n/a	n/a
3	BACH1	chr12:104051260-104051267	K562	blood:	n/a	n/a
4	BHLHE40	chr12:104074439-104074809	K562	blood:	n/a	n/a
5	CCNT2	chr12:104074480-104074916	K562	blood:	n/a	n/a
6	CEBPB	chr12:104033972-104034044	K562	blood:	n/a	n/a
7	CEBPB	chr12:104066590-104066800	HepG2	liver:	n/a	n/a
8	CEBPB	chr12:104066532-104066907	HepG2	liver:	n/a	n/a
9	CEBPB	chr12:104073820-104074029	HepG2	liver:	n/a	n/a
10	CEBPB	chr12:104032689-104032897	A549	lung:	n/a	chr12:104032804-104032817 chr12:104032805-104032816
11	CEBPB	chr12:104066465-104067034	A549	lung:	n/a	n/a
12	CEBPB	chr12:104073906-104073971	IMR90	lung:	n/a	n/a
13	CEBPB	chr12:104065637-104065669	HepG2	liver:	n/a	n/a
14	CEBPB	chr12:104066580-104066895	A549	lung:	n/a	n/a
15	CEBPB	chr12:104060730-104060802	A549	lung:	n/a	chr12:104060750-104060759 chr12:104060748-104060761
16	CEBPB	chr12:104032791-104032879	H1-hESC	embryonic stem cell:	n/a	chr12:104032804-104032817 chr12:104032805-104032816
17	CEBPB	chr12:104066581-104066885	A549	lung:	n/a	n/a
18	CEBPB	chr12:104074525-104074832	K562	blood:	n/a	n/a
19	CEBPB	chr12:104032648-104032952	HepG2	liver:	n/a	chr12:104032804-104032817 chr12:104032805-104032816
20	CEBPD	chr12:104074446-104074808	K562	blood:	n/a	n/a
21	CEBPD	chr12:104074449-104074908	K562	blood:	n/a	n/a
22	CEBPZ	chr12:104033709-104033712	HepG2	liver:	n/a	n/a
23	CREB1	chr12:104074390-104074830	K562	blood:	n/a	n/a
24	CTCF	chr12:104036400-104036533	MCF-7	breast:	n/a	n/a
25	CTCF	chr12:104036340-104036490	Caco-2	colon:	n/a	n/a
26	CTCF	chr12:104047351-104047405	GM20000	blood:	n/a	n/a
27	CTCF	chr12:104036320-104036470	HEK293	kidney:	n/a	n/a
28	CTCF	chr12:104036380-104036530	GM12865	blood:	n/a	n/a
29	CTCF	chr12:104036460-104036610	HFF-Myc	foreskin:	n/a	n/a
30	CTCF	chr12:104036320-104036470	GM12872	blood:	n/a	n/a
31	CTCF	chr12:104036400-104036500	MCF-7	breast:	n/a	n/a
32	CTCF	chr12:104036340-104036490	GM06990	blood:	n/a	n/a
33	CTCF	chr12:104036380-104036530	K562	blood:	n/a	n/a
34	CTCF	chr12:104062320-104062470	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr12:104036400-104036550	GM12870	blood:	n/a	n/a
36	CTCF	chr12:104036380-104036530	HCT-116	colon:	n/a	n/a
37	CTCF	chr12:104036436-104036522	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr12:104036380-104036530	MCF-7	breast:	n/a	n/a
39	CTCF	chr12:104067885-104068007	HepG2	liver:	n/a	n/a
40	CTCF	chr12:104036380-104036530	GM12873	blood:	n/a	n/a
41	CTCF	chr12:104036480-104036630	GM12875	blood:	n/a	n/a
42	CTCF	chr12:104036349-104036561	HepG2	liver:	n/a	n/a
43	CTCF	chr12:104036420-104036570	MCF-7	breast:	n/a	n/a
44	CTCF	chr12:104036380-104036530	RPTEC	kidney:	n/a	n/a
45	CTCF	chr12:104036360-104036510	GM12868	blood:	n/a	n/a
46	CTCF	chr12:104062580-104062730	GM12869	blood:	n/a	n/a
47	CTCF	chr12:104036360-104036510	GM12869	blood:	n/a	n/a
48	CTCF	chr12:104036260-104036410	GM12867	blood:	n/a	n/a
49	CTCF	chr12:104067840-104067990	HepG2	liver:	n/a	n/a
50	CTCF	chr12:104036380-104036530	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:104063640-104063690	GM12878	blood:	n/a
2	chr12:104063640-104063690	MCF10A-Er-Src	breast:	n/a
3	chr12:104063640-104063690	HCF	heart:	n/a
4	chr12:104063640-104063690	HRCEpiC	kidney:	n/a
5	chr12:104063640-104063690	HRPEpiC	eye:	n/a
6	chr12:104063640-104063690	BE2_C	brain:	n/a
7	chr12:104063640-104063690	SK-N-SH_RA	brain:	n/a
8	chr12:104063640-104063690	U87	brain:	n/a
9	chr12:104063640-104063690	NHDF-neo	bronchial:	n/a
10	chr12:104063640-104063690	PANC-1	pancreas:	n/a
11	chr12:104063640-104063690	HCPEpiC	choroid plexus:	n/a
12	chr12:104063640-104063690	BJ	skin:	n/a
13	chr12:104063640-104063690	GM06990	blood:	n/a
14	chr12:104063640-104063690	A549	lung:	n/a
15	chr12:104063640-104063690	HEEpiC	esophagus:	n/a
16	chr12:104063640-104063690	IMR90	lung:	fetal
17	chr12:104063640-104063690	HAEpiC	amniotic membrane:	n/a
18	chr12:104063640-104063690	HPAEpiC	pulmonary alveolar:	n/a
19	chr12:104063640-104063690	LNCaP	prostate:	n/a
20	chr12:104063640-104063690	PFSK-1	brain:	n/a
21	chr12:104063640-104063690	HEK293	kidney:	embryo
22	chr12:104063640-104063690	HepG2	liver:	n/a
23	chr12:104063640-104063690	HRE	kidney:	n/a
24	chr12:104063640-104063690	MCF-7	breast:	n/a
25	chr12:104063640-104063690	NT2-D1	testis:	n/a
26	chr12:104063640-104063690	Jurkat	blood:	n/a
27	chr12:104063640-104063690	Caco-2	colon:	n/a
28	chr12:104063640-104063690	HUVEC	blood vessel:	n/a
29	chr12:104063640-104063690	AG09319	gingival:	n/a
30	chr12:104063640-104063690	GM12891	blood:	n/a
31	chr12:104063640-104063690	NH-A	brain:	n/a
32	chr12:104063640-104063690	ovcar-3	ovarian:	n/a
33	chr12:104063640-104063690	GM19239	blood:	n/a
34	chr12:104063640-104063690	H1-hESC	embryonic stem cell:	embryo
35	chr12:104063640-104063690	CMK	blood:	n/a
36	chr12:104063640-104063690	SKMC	muscle:	n/a
37	chr12:104063640-104063690	NB4	blood:	n/a
38	chr12:104063640-104063690	AG09309	skin:	n/a
39	chr12:104063640-104063690	HCM	heart:	n/a
40	chr12:104063640-104063690	T-47D	breast:	n/a
41	chr12:104063640-104063690	HIPEpiC	eye:	n/a
42	chr12:104063640-104063690	Hela-S3	cervix:	n/a
43	chr12:104063640-104063690	K562	blood:	n/a
44	chr12:104063640-104063690	NHBE	bronchial:	n/a
45	chr12:104063640-104063690	HMEC	breast:	n/a
46	chr12:104063640-104063690	ProgFib	skin:	n/a
47	chr12:104063640-104063690	GM12892	blood:	n/a
48	chr12:104063640-104063690	HCT-116	colon:	n/a
49	chr12:104063640-104063690	ECC-1	luminal epithelium:	n/a
50	chr12:104063640-104063690	SK-N-SH	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:104054220..104056283-chr12:104057216..104059364,2	K562	blood:
2	chr12:104056086..104059213-chr12:104060353..104063623,3	K562	blood:
3	chr12:104058121..104061173-chr12:104061276..104064386,3	K562	blood:
4	chr12:104025253..104027244-chr12:104037198..104039505,2	MCF-7	breast:
5	chr12:104026094..104026958-chr12:104035452..104036525,4	MCF-7	breast:
6	chr12:104061705..104063209-chr12:104063963..104066627,2	MCF-7	breast:
7	chr12:104031257..104033295-chr12:104039042..104040756,2	K562	blood:
8	chr12:104054220..104056283-chr12:104057216..104059364,2	K562	blood:
9	chr12:104031257..104033295-chr12:104039042..104040756,2	K562	blood:
10	chr12:104045851..104048485-chr12:104050145..104052057,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NT5DC3-3	chr12:104048558-104048646	ENSG00000257737.1
2	lnc-RP11-650K20.3.1-4	chr12:104066248-104066547	expReg_chr12_9712_+
3	lnc-NT5DC3-2	chr12:104062990-104063184	ENSG00000257766.1
4	lnc-NT5DC3-2	chr12:104062353-104062625	ENSG00000257766.1
5	lnc-NT5DC3-3	chr12:104051385-104051773	ENSG00000257737.1

No data

Variant related genes	Relation type
ENSG00000257766	TF binding region
ENSG00000257737	TF binding region
ENSG00000257766	CpG island
ENSG00000257737	CpG island
ENSG00000257737	chromatin interactions
ENSG00000257766	chromatin interactions

Extended variants
information (count: 1942 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1942 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149609465	chr12:104030120-104030121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs542157071	chr12:104030179-104030180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565740931	chr12:104030225-104030226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562053480	chr12:104030240-104030241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs539580161	chr12:104030274-104030275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78712116	chr12:104030276-104030277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547986572	chr12:104030286-104030287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs370184918	chr12:104030289-104030290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs76880940	chr12:104030416-104030417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs190479583	chr12:104030452-104030453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs374426191	chr12:104030523-104030524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550197804	chr12:104030545-104030546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs182260892	chr12:104030580-104030581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535862999	chr12:104030586-104030587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553591743	chr12:104030591-104030592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576377282	chr12:104030606-104030607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs831432	chr12:104030609-104030610	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs185984998	chr12:104030647-104030648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs11111691	chr12:104030652-104030653	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs113659113	chr12:104030658-104030659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148355566	chr12:104030714-104030715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs545539498	chr12:104030716-104030717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs7959003	chr12:104030717-104030718	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs575590970	chr12:104030728-104030729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs143265559	chr12:104030741-104030742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181342454	chr12:104030796-104030797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs147547637	chr12:104030822-104030823	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370856507	chr12:104030841-104030842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374054747	chr12:104030857-104030858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs367601744	chr12:104030860-104030861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370338110	chr12:104030883-104030884	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375917813	chr12:104030943-104030944	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs185424519	chr12:104030960-104030961	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs143944654	chr12:104030986-104030987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190632177	chr12:104030994-104030995	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs371942484	chr12:104030996-104030997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550260904	chr12:104030997-104030998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368808563	chr12:104031010-104031011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs112091107	chr12:104031014-104031015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs563778883	chr12:104031015-104031016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs182810214	chr12:104031023-104031024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs375394854	chr12:104031035-104031036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs369952698	chr12:104031055-104031056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373082148	chr12:104031064-104031065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs569973479	chr12:104031073-104031074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs549410506	chr12:104031086-104031087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs568246674	chr12:104031117-104031118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534120611	chr12:104031123-104031124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs547270097	chr12:104031146-104031147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs139443627	chr12:104031207-104031208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	22032731	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
Acute lymphoblastic leukemia	21339820	CNVD
lymphocytic leukemia	21291569	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Neurocytoma	17123091	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:337 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:104023600-104033800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:104027000-104037200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr12:104029600-104031600	Weak transcription	Spleen	Spleen
4	chr12:104030200-104032200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr12:104030400-104031400	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr12:104030800-104031000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr12:104030800-104031200	Enhancers	Brain Germinal Matrix	brain
8	chr12:104031600-104033200	Strong transcription	Spleen	Spleen
9	chr12:104033200-104062200	Weak transcription	Spleen	Spleen
10	chr12:104033800-104034200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr12:104033800-104034200	ZNF genes & repeats	GM12878-XiMat	blood
12	chr12:104034200-104035200	Flanking Active TSS	GM12878-XiMat	blood
13	chr12:104034200-104040600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr12:104034400-104034600	Enhancers	Colon Smooth Muscle	Colon
15	chr12:104034400-104035400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr12:104034400-104035400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr12:104035200-104035400	Enhancers	GM12878-XiMat	blood
18	chr12:104035600-104036000	Weak transcription	Colon Smooth Muscle	Colon
19	chr12:104036000-104036600	Enhancers	HepG2	liver
20	chr12:104036000-104036800	Enhancers	Stomach Smooth Muscle	stomach
21	chr12:104036200-104037400	Enhancers	Colon Smooth Muscle	Colon
22	chr12:104036200-104037400	Enhancers	Rectal Smooth Muscle	rectum
23	chr12:104036400-104036600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr12:104036800-104037400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr12:104037200-104037400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr12:104037400-104038400	Weak transcription	Rectal Smooth Muscle	rectum
27	chr12:104037400-104038800	Weak transcription	Colon Smooth Muscle	Colon
28	chr12:104037400-104039600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr12:104038400-104039600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr12:104038400-104041600	Enhancers	Rectal Smooth Muscle	rectum
31	chr12:104038600-104039600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr12:104038800-104039000	Enhancers	Muscle Satellite Cultured Cells	--
33	chr12:104038800-104041400	Enhancers	Colon Smooth Muscle	Colon
34	chr12:104038800-104042000	Enhancers	HSMM	muscle
35	chr12:104039000-104039200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr12:104039000-104039200	Enhancers	NH-A	brain
37	chr12:104039000-104040800	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr12:104039200-104040600	Enhancers	HSMMtube	muscle
39	chr12:104039400-104039800	Enhancers	Aorta	Aorta
40	chr12:104039400-104040600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr12:104039400-104040600	Weak transcription	NH-A	brain
42	chr12:104039600-104040000	Enhancers	Placenta Amnion	Placenta Amnion
43	chr12:104039600-104040600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr12:104039600-104040800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr12:104039600-104041400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr12:104040000-104040400	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr12:104040200-104041600	Enhancers	Fetal Heart	heart
48	chr12:104040400-104041000	Enhancers	Placenta Amnion	Placenta Amnion
49	chr12:104040400-104042000	Enhancers	NHEK	skin
50	chr12:104040400-104042200	Enhancers	HMEC	breast

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