Variant report

Variant	nsv1243
Chromosome Location	chr1:67700289-67745337
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:254)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:254 , 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	ATF2	chr1:67740141-67740739	GM12878	blood:	n/a	n/a
2	ATF2	chr1:67740227-67740788	GM12878	blood:	n/a	n/a
3	BACH1	chr1:67728569-67728769	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr1:67736184-67736513	GM12878	blood:	n/a	n/a
5	BATF	chr1:67740286-67740662	GM12878	blood:	n/a	n/a
6	BATF	chr1:67740273-67740678	GM12878	blood:	n/a	n/a
7	BCL11A	chr1:67740262-67740713	GM12878	blood:	n/a	n/a
8	BCL11A	chr1:67740360-67740667	GM12878	blood:	n/a	n/a
9	BCL3	chr1:67740316-67740655	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:67740271-67740701	GM12878	blood:	n/a	n/a
11	CBX3	chr1:67715743-67716037	K562	blood:	n/a	n/a
12	CBX3	chr1:67715761-67716188	HCT-116	colon:	n/a	n/a
13	CBX3	chr1:67738329-67738604	K562	blood:	n/a	n/a
14	CEBPB	chr1:67739307-67739646	K562	blood:	n/a	chr1:67739480-67739491
15	CEBPB	chr1:67722586-67722846	IMR90	lung:	n/a	chr1:67722693-67722704
16	CEBPB	chr1:67722544-67722813	K562	blood:	n/a	chr1:67722693-67722704
17	CEBPB	chr1:67722566-67722863	H1-hESC	embryonic stem cell:	n/a	chr1:67722693-67722704
18	CEBPB	chr1:67739356-67739623	HepG2	liver:	n/a	chr1:67739480-67739491
19	CEBPB	chr1:67722539-67722805	A549	lung:	n/a	chr1:67722693-67722704
20	CEBPB	chr1:67722511-67722878	Hela-S3	cervix:	n/a	chr1:67722693-67722704
21	CEBPB	chr1:67739313-67739590	K562	blood:	n/a	chr1:67739480-67739491
22	CEBPB	chr1:67722538-67722847	HepG2	liver:	n/a	chr1:67722693-67722704
23	CEBPB	chr1:67739344-67739611	H1-hESC	embryonic stem cell:	n/a	chr1:67739480-67739491
24	CEBPB	chr1:67739373-67739601	MCF-7	breast:	n/a	chr1:67739480-67739491
25	CEBPB	chr1:67739387-67739629	IMR90	lung:	n/a	chr1:67739480-67739491
26	CEBPZ	chr1:67715824-67716040	HepG2	liver:	n/a	n/a
27	CHD2	chr1:67740359-67740627	GM12878	blood:	n/a	n/a
28	CHD2	chr1:67728727-67728757	K562	blood:	n/a	n/a
29	CTCF	chr1:67727487-67727635	HUVEC	blood vessel:	n/a	n/a
30	CTCF	chr1:67727440-67727590	GM12871	blood:	n/a	n/a
31	CTCF	chr1:67727500-67727648	HepG2	liver:	n/a	n/a
32	CTCF	chr1:67727480-67727630	GM12872	blood:	n/a	n/a
33	CTCF	chr1:67727520-67727670	GM12873	blood:	n/a	n/a
34	CTCF	chr1:67727460-67727610	HFF-Myc	foreskin:	n/a	n/a
35	CTCF	chr1:67727420-67727570	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr1:67727516-67727581	Pancreas_OC	pancreas:	n/a	n/a
37	CTCF	chr1:67727480-67727630	HFF	foreskin:	n/a	n/a
38	CTCF	chr1:67727480-67727630	HCFaa	heart:	n/a	n/a
39	CTCF	chr1:67727420-67727570	GM12865	blood:	n/a	n/a
40	CTCF	chr1:67727473-67727653	K562	blood:	n/a	n/a
41	CTCF	chr1:67727523-67727573	GM13976	blood:	n/a	n/a
42	CTCF	chr1:67727540-67727690	HRE	kidney:	n/a	n/a
43	CTCF	chr1:67727500-67727650	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr1:67727560-67727710	HAc	cerebellar:	n/a	n/a
45	CTCF	chr1:67727480-67727630	AG04449	skin:	n/a	n/a
46	CTCF	chr1:67727465-67727668	GM12878	blood:	n/a	n/a
47	CTCF	chr1:67727497-67727646	GM12892	blood:	n/a	n/a
48	CTCF	chr1:67727500-67727650	HMEC	breast:	n/a	n/a
49	CTCF	chr1:67727500-67727650	GM12878	blood:	n/a	n/a
50	CTCF	chr1:67727480-67727630	NHDF-neo	bronchial:	n/a	n/a

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:67720373..67722119-chr1:67724922..67726693,2	K562	blood:
2	chr1:67735715..67738245-chr1:67740488..67742574,2	K562	blood:
3	chr1:67699386..67700341-chr1:67965846..67966881,3	MCF-7	breast:
4	chr1:67720373..67722119-chr1:67724922..67726693,2	K562	blood:
5	chr1:67717674..67720281-chr12:80665322..80667474,2	MCF-7	breast:
6	chr1:67735715..67738245-chr1:67740488..67742574,2	K562	blood:
7	chr1:67726965..67727697-chr1:67966091..67966663,2	MCF-7	breast:
8	chr1:67699377..67700702-chr1:67965864..67966743,4	K562	blood:
9	chr1:67696114..67698357-chr1:67738401..67741074,2	K562	blood:
10	chr1:67733016..67734921-chr1:67736997..67739793,2	MCF-7	breast:
11	chr1:67723943..67726698-chr1:67962657..67965563,2	K562	blood:
12	chr1:67695892..67697817-chr1:67702175..67704682,3	K562	blood:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL12RB2-7	chr1:67705863-67705964	NONHSAT003779
2	lnc-IL12RB2-7	chr1:67705863-67705964	NONHSAT003777
3	lnc-IL12RB2-7	chr1:67721521-67721610	NONHSAT003777
4	lnc-IL12RB2-7	chr1:67702397-67702485	NONHSAT003778
5	lnc-IL12RB2-7	chr1:67724162-67724260	NONHSAT003773
6	lnc-IL12RB2-7	chr1:67724162-67724260	NONHSAT003775
7	lnc-IL12RB2-7	chr1:67721521-67721610	NONHSAT003775
8	lnc-IL12RB2-7	chr1:67702397-67702485	NONHSAT003776
9	lnc-IL12RB2-7	chr1:67721521-67721610	NONHSAT003773
10	lnc-IL12RB2-7	chr1:67702397-67702485	NONHSAT003773
11	lnc-IL12RB2-7	chr1:67721521-67721610	NONHSAT003778
12	lnc-IL12RB2-7	chr1:67724162-67724260	NONHSAT003776
13	lnc-IL23R-1	chr1:67743735-67744462	NONHSAT003783
14	lnc-IL12RB2-7	chr1:67721521-67721610	NONHSAT003779
15	lnc-IL12RB2-7	chr1:67705863-67705964	NONHSAT003773
16	lnc-IL12RB2-7	chr1:67702405-67702485	NONHSAT003777
17	lnc-IL12RB2-7	chr1:67705863-67705964	NONHSAT003778
18	lnc-IL12RB2-7	chr1:67702397-67702485	NONHSAT003775
19	lnc-IL12RB2-7	chr1:67724162-67724260	NONHSAT003777
20	lnc-IL12RB2-7	chr1:67724162-67724260	NONHSAT003778
21	lnc-IL12RB2-7	chr1:67705863-67705964	NONHSAT003775
22	lnc-IL12RB2-7	chr1:67724162-67724260	NONHSAT003779
23	lnc-IL12RB2-7	chr1:67702397-67702485	NONHSAT003779
24	lnc-IL12RB2-7	chr1:67721521-67721610	NONHSAT003776

No data

Variant related genes	Relation type
ENSG00000228523	TF binding region
ENSG00000221733	TF binding region
RNU4ATAC4P	TF binding region
C1orf141	TF binding region
ENSG00000203963	chromatin interactions
ENSG00000252116	chromatin interactions

Extended variants
information (count: 1515 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1515 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371456815	chr1:67700333-67700334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs577568841	chr1:67700388-67700389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs375731560	chr1:67700390-67700391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs397980410	chr1:67700408-67700409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs112949081	chr1:67700439-67700440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544929646	chr1:67700448-67700449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565177067	chr1:67700525-67700526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs138250234	chr1:67700544-67700545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs202113325	chr1:67700549-67700550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs149616038	chr1:67700650-67700651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs114740196	chr1:67700712-67700713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs147318853	chr1:67700732-67700733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569908478	chr1:67700741-67700742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532539928	chr1:67700867-67700868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564361896	chr1:67700911-67700912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112118491	chr1:67700912-67700913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs535018220	chr1:67700952-67700953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532249742	chr1:67700960-67700961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568332486	chr1:67700976-67700977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535927950	chr1:67701041-67701042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556228481	chr1:67701042-67701043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576104164	chr1:67701066-67701067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs367622305	chr1:67701080-67701081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs397860254	chr1:67701091-67701092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs397980411	chr1:67701092-67701093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs372165742	chr1:67701093-67701094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188150114	chr1:67701125-67701126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538621029	chr1:67701152-67701153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558622159	chr1:67701274-67701275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532268645	chr1:67701292-67701293	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs572350743	chr1:67701305-67701306	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs551939999	chr1:67701409-67701410	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs371452727	chr1:67701460-67701461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547469368	chr1:67701475-67701476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541361245	chr1:67701544-67701545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561028254	chr1:67701577-67701578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147138671	chr1:67701588-67701589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34667737	chr1:67701590-67701591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543502714	chr1:67701629-67701630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148621588	chr1:67701649-67701650	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs142091947	chr1:67701662-67701663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552136874	chr1:67701665-67701666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150745398	chr1:67701713-67701714	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs12030948	chr1:67701765-67701766	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs536236926	chr1:67701800-67701801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375711862	chr1:67701821-67701822	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548482335	chr1:67701914-67701915	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568515829	chr1:67702002-67702003	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537649261	chr1:67702023-67702024	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs112910229	chr1:67702042-67702043	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
CNS Malformation Syndrome	17530927	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	20459617	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal cancer	21851588	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:187 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:67692800-67702000	Weak transcription	K562	blood
2	chr1:67701600-67702000	Enhancers	Rectal Mucosa Donor 29	rectum
3	chr1:67701600-67702000	Enhancers	Sigmoid Colon	Sigmoid Colon
4	chr1:67701600-67702400	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr1:67701800-67702200	Enhancers	Fetal Intestine Large	intestine
6	chr1:67702000-67703800	Strong transcription	K562	blood
7	chr1:67703800-67722000	Weak transcription	K562	blood
8	chr1:67714400-67714800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr1:67714600-67716800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
10	chr1:67721800-67722000	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr1:67721800-67722000	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr1:67721800-67722200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
13	chr1:67721800-67723200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr1:67721800-67723200	Enhancers	Psoas Muscle	Psoas
15	chr1:67721800-67723600	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr1:67722000-67722400	Enhancers	H1 Cell Line	embryonic stem cell
17	chr1:67722000-67722400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr1:67722000-67722600	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr1:67722000-67723000	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr1:67722000-67723000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr1:67722000-67723000	Enhancers	HUVEC	blood vessel
22	chr1:67722000-67723200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr1:67722000-67723200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr1:67722000-67723200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:67722000-67723200	Strong transcription	K562	blood
26	chr1:67722000-67723400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr1:67722200-67722400	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chr1:67722200-67723000	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr1:67722200-67723000	Enhancers	Fetal Lung	lung
30	chr1:67722200-67723200	Enhancers	H9 Cell Line	embryonic stem cell
31	chr1:67722200-67723200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr1:67722200-67723400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr1:67722400-67726400	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr1:67722400-67727400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr1:67722600-67723000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr1:67722600-67723200	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr1:67722600-67723200	Enhancers	Fetal Thymus	thymus
38	chr1:67722800-67723000	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr1:67722800-67723200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
40	chr1:67722800-67723200	Enhancers	Brain Substantia Nigra	brain
41	chr1:67722800-67723200	Enhancers	Thymus	Thymus
42	chr1:67723000-67723200	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr1:67723000-67723400	Weak transcription	HUVEC	blood vessel
44	chr1:67723000-67727400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr1:67723000-67727400	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr1:67723200-67726000	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr1:67723200-67726200	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr1:67723200-67726200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr1:67723200-67726800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr1:67723200-67727600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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